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T h e j o u r n a l f o r h i g h a c u i t y, p ro g re s s i v e , a n d c r i t i c a l c a re n u r s i n g
CNE
Stroke Volume
Optimization
Therapeutic
Hypothermia
CNE
Delirium
Exertional
Heat Stroke
CNE
ECMO for
Pediatric
Cardiac Arrest
PAT I E N T S AT I S FA C T I O N
CANT BE COMPROMISED
think
of the ramications
CriticalCareNurse
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Contributing Editors
Advanced Practice
ANDREA M. KLINE-TILFORD, CPNP-AC/PC, CCRN, FCCM
Bariatric Care
BRENDA K. HIXON VERMILLION, RN, DNP, ACNS-BC,
ANP-BC, CCRN
End-of-Life Care
KATHLEEN OUIMET PERRIN, RN, PhD, CCRN
Evidence-Based Practice
MARCIA BELCHER, RN, MSN, BBA, CCRN-CSC, CCNS
Family-Centered Care
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MARIA CHRISTABELLE CASTRO, RN, MSHA, CCRN, NE-BC
Military Critical Care Nursing: Air Force
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Military Critical Care Nursing: Army
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Military Critical Care Nursing: Navy
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CriticalCareNurse
The journal for high acuity, progressive, and critical care nursing
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CNE
Stroke Volume
Optimization:
The New Hemodynamic
Algorithm
Alexander Johnson and Thomas Ahrens
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EDITORIAL
Improving Cardiac Arrest Resuscitation
Outcomes: A Valentine Worth Sending
Aortic cannula
vena c
71
Aorta
ava
Constant
mean
erior
Sup
Overestimated
systole
Normal
systole
Venous cannula
Left
atrium
Normal
diastole
Right
atrium
Right
ventricle
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ventricle
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with underdamped
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14. Iwami T, Kawamura T, Hiraide A, et al. Effectiveness of bystander-initiated cardiac-only resuscitation for patients with out-of-hospital cardiac
arrest. Circulation. 2007;116(25):2900-2907.
15. Iwami T, Kitamura T, Kawamura T, et al. Chest-compression-only cardiopulmonary resuscitation for out-of-hospital cardiac arrest with
public-access defibrillation. Circulation 2012;126:2844-2851. http://
circ.ahajournals.org/content/126/24/2844.full?sid=f1d8c729-f6cc-4041
-8d91-817fde1c97a0. Accessed December 2, 2014.
16. Yao L, Wang P, Zhou L, et al. Compression-only cardiopulmonary resuscitation vs standard cardiopulmonary resuscitation: an updated metaanalysis of observational studies. Am J Emerg Med. 2014;32(6):517-523.
17. American Heart Association. Two Steps to Staying Alive With HandsOnly CPR. http://www.heart.org/HEARTORG/CPRAndECC
/HandsOnlyCPR/Hands-Only-CPR_UCM_440559_SubHomePage.jsp.
Accessed December 2, 2014.
Corrections
In the December article by Chaisson
et al, Improving Patients Readiness for
Coronary Artery Bypass Graft Surgery
(Crit Care Nurse. 2014;34[6]:29-38),
the e-mail address listed for the corresponding author (Kristine Chaisson)
was invalid. The correct e-mail is
krischaisson@gmail.com.
2015 American Association of Critical-Care Nurses doi:
http://dx.doi.org/10.4037/ccn2015359
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Cover
Stroke Volume
Optimization: The New
Hemodynamic Algorithm
ALEXANDER JOHNSON, RN, MSN, ACNP-BC, CCNS, CCRN
THOMAS AHRENS, RN, PhD
Critical care practices have evolved to rely more on physical assessments for monitoring cardiac output
and evaluating fluid volume status because these assessments are less invasive and more convenient to
use than is a pulmonary artery catheter. Despite this trend, level of consciousness, central venous pressure,
urine output, heart rate, and blood pressure remain assessments that are slow to be changed, potentially
misleading, and often manifested as late indications of decreased cardiac output. The hemodynamic
optimization strategy called stroke volume optimization might provide a proactive guide for clinicians to
optimize a patients status before late indications of a worsening condition occur. The evidence supporting
use of the stroke volume optimization algorithm to treat hypovolemia is increasing. Many of the cardiac
output monitor technologies today measure stroke volume, as well as the parameters that comprise stroke
volume: preload, afterload, and contractility. (Critical Care Nurse. 2015;35[1]:11-28)
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11
CASE STUDY
Table 1
Class 1
Class 2
Class 3
Class 4
Blood loss, %
< 15%
15%-30%
30%-40%
> 40%
< 100
> 100
> 120
> 140
Normal
Normal
Decreased
Decreased
Normal or increased
Decreased
Decreased
Decreased
14-20
20-30
30-40
> 35
Slightly anxious
Mildly anxious
Anxious, confused
Confused, lethargic
Blood pressure, mm Hg
Pulse pressure
Respiratory rate, breaths per minute
Mental status
a Reprinted
Authors
Alexander Johnson is a clinical nurse specialist, Central DuPage Hospital, Cadence Health SystemNorthwestern Medicine, Winfield, Illinois.
Thomas Ahrens is a research scientist, Barnes-Jewish Hospital, St Louis, Missouri.
Corresponding author: Alexander Johnson, 4007 Schillinger Dr, Naperville, IL 60564 (e-mail: apjccrn@hotmail.com).
To purchase electronic or print reprints, contact the American Association of Critical-Care Nurses, 101 Columbia, Aliso Viejo, CA 92656. Phone, (800) 899-1712 or
(949) 362-2050 (ext 532); fax, (949) 362-2049; e-mail, reprints@aacn.org.
12
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A
BP = CO x SVR
MAP CVP x 80
CO
HR x SV
Preload
Afterload
Contractility
Rhythm
B
CO
SVR
Figure 1 A, Complexity of blood pressure (BP): interrelationship of variables comprising BP. BP is the cardiac
output (CO) multiplied by systemic vascular resistance
(SVR). CO is the product of heart rate (HR) and stroke
volume (SV). SV is influenced by preload, afterload,
contractility, and rhythm. SVR is calculated by dividing
the difference between mean arterial pressure (MAP)
and central venous pressure (CVP) by the CO and then
multiplying by 80. (Derivation of content as described in
Alspach.2) B, CO and SVR coexist in a balanced seesawtype relationship. In general, when one decreases, the other
increases (and vice versa) to maintain normal blood pressure.
CriticalCareNurse
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14
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Figure 2 Challenges associated with interpreting pulmonary artery occlusion pressure (PAOP). Left ventricular end-diastolic
volume (LVEDV) can be independent of PAOP. A, PAOP is 22 mm Hg. Normal left ventricle has very high LVEDV. B, PAOP is
22 mm Hg. Dilated right ventricle creates increased juxtacardiac pressure; LVEDV is normal. C, PAOP is 22 mm Hg. Left ventricular hypertrophy with noncompliant myocardium creates decreased space within the left ventricle; LVEDV is low. Use of PAOP
alone to reflect LVEDV may not be accurate.
Based on data from Marik et al27 and Turner.36
Illustration courtesy of Lisa Merry, RN, Merry Studio, Bloomington, Illinois.
Stroke volume, mL
120
100
SV 100 mL
75
SV 75 mL
50
SV 40 mL
25
Pulmonary artery
occlusive pressure
Fluid bolus administered
4 mm Hg
500 mL
12 mm Hg
1000 mL
18 mm Hg
1500 mL
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15
16
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Table 2
Technology
Manufacturer
Where used
Randomized controlled
trials regarding
patient outcome
Description
External
Doppler
imaging
USCOM, Sydney,
Australia
Anywhere
None
Esophageal
Doppler
imaging
Operating room,
intensive care
unit, emergency
department
Endotracheal
bioimpedance
ConMed Corporation,
Utica, New York
None
Operating room,
intensive care unit
Transcutaneous
bioimpedance
SonoSite, Bothell,
Washington
Anywhere
Pulse contour
FloTrac, Edwards
Lifesciences, Irvine
California
LidCo Ltd, Cambridge,
United Kingdom
PiCCO, Pulsion
Medical Systems,
Munich, Germany
None
Pulmonary artery
catheter
Operating room,
Several trials,59,60 with
intensive care unit both pro and con
findings
Operating room,
None
intensive care unit
Bioreactance
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Cheetah Medical,
Portland, Oregon
CriticalCareNurse
17
Velocity, cm/s
Flow time, ms
1/3 Systole
2/3 Diastole
1 Cardiac cycle
Figure 5 Waveform components for stroke volume optimization (SVO): aortic pulse waveform from an esophageal Doppler
examination. Corrected flow time (ie, the time spent in systole) corresponds to the width of the pulse waveform and is an index
of preload. Peak velocity corresponds to the height of the wave and is a measure of contractility. Stroke distance represents the
area under the curve and is used to compute stroke volume.
18
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Measurement of Afterload:
Systemic Vascular Resistance
Systemic vascular resistance (SVR) is the resistance
that must be overcome by the ventricles to develop force
and contract, propelling blood into the arterial circulation.2
Most of the newer hemodynamic monitoring technologies (eg, esophageal Doppler imaging, bioimpedance,
pulse contour methods) have the capability to calculate
SVR. However, SVR was not a major parameter in the
algorithms used in any of the SVO trials that showed
improved outcomes in surgical patients.44-52,73,74
Evidence of lack of inclusion suggests that SVR is a
more of a secondary monitoring parameter. Elevated SVR
usually occurs in response to systemic hypertension or
as a compensatory mechanism due to decreased cardiac
output, as in shock states (Figures 1A and 1B). Therefore,
nurses must know why the SVR is elevated. If the value is
elevated in response to low cardiac output, once cardiac
output is improved with treatment (eg, fluid, inotropes),
SVR should decrease because of a decreased need for
compensatory vasoconstriction. If SVR is elevated
because of systemic hypertension, treatment may include
administration of an afterload reducer.2
When SVR decreases, the left ventricular ejection of
blood encounters lower resistance. Low afterload states
may be less problematic when blood pressure and cardiac output are normal (Figure 1A). However, attempts
to increase low SVR generally include administration of
vasopressors.2 ScvO2 and stroke volume should also be
followed as end points to ensure that blood flow and tissue oxygenation improve in response to the vasopressor21
(Figure 6). Titrating the dose of a vasopressor used to
alter ScvO2 and stroke volume allows clinicians to focus
on optimizing blood flow to both the microcirculation
and the macrocirculation. Several studies of fluid replacement protocols that include use of vasopressors suggest
that optimizing ScvO231,33,75 and stroke volume47,76 improve
patients outcomes. However, further research is needed
to better establish how vasopressors and ScvO2 are best
used in SVO protocols.
Stroke Volume, Stroke Index, and
Stroke Distance
Stroke volume is one of the primary end points for
detecting fluid responsiveness and guiding goal-directed
therapy.27,32,62 Stroke index is a standardized parameter in
which a patients body surface area is taken into account.
CriticalCareNurse
19
Stroke volume, mL
75
50
25
10
5
50
15
55
20
60
65
Figure 6 Response of stroke volume to norepinephrine. Increasing vasopressor doses to previously established, prescribed
thresholds for mean arterial pressure (MAP) and systemic vascular resistance may in turn decrease stroke volume and overall
blood flow. The case example graph suggests that stroke volume is optimized at 8 g/min of norepinephrine, even though a
MAP of only 55 mm Hg is achieved at that dose. Note: patients responses to norepinephrine dosing may vary.
20
CriticalCareNurse
Table 3
Reference
range
Parameter
4-8
50-100
Stroke indexb
25-45
330-360
30-120
Stroke distance, cm
10-20
Cardiac
indexc
2.8-4.2
cm-5
900-1600
65-80
2-8
< 10-15
a Based
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Is the heart
pumping
enough blood?
Yes
(stroke volume
increased < 10%)
No
(stroke volume
increased > 10%)
If stroke volume
decreased > 10%
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CriticalCareNurse
21
Table 4
Interventions used and response of 59-year-old man admitted after a motor vehicle accident
Stroke
Peak
Heart rate, Central venous Central venous
Flow time,
volume,
velocity,
beats
oxygen
pressure,
corrected, ms
mL
cm/s
per minute saturation, %
mm Hg
Intervention
Administer 1000-mL
bolus of physiological saline
34
300
96
102
49
100/48 (64)
Administer 1000-mL
bolus of physiological saline
48
335
95
100
69
94/55 (68)
Response
49
337
95
99
70
100/60 (73)
after a motor vehicle accident (Table 4). On postoperative day 5, he was evaluated for discharge to a general
care unit. His urine output had decreased during the
preceding 12 hours, suggestive of hypovolemia. The
hypovolemia was evidenced by low stroke volume, low
FTc, and low ScvO2 in the presence of a normal peak
velocity. After injection of a 1000-mL bolus of physiological saline, stroke volume improved from 34 mL to 48
mL, more than a 10% (3.4 mL) improvement. So,
another bolus was given. Satisfactory response to the
bolus was manifested by normal FTc and ScvO2. Stroke
volume improved to 49 mL only with the second bolus
(<10% improvement), indicating the beginning of the
plateau along the Frank-Starling curve where increased
stretching of the ventricular myocytes does not improve
stroke volume. Thus, no further administration of fluid
was indicated.
Table 5
Intervention
Stroke
Peak
Heart rate, Central venous Central venous
Flow time,
volume,
velocity,
beats
oxygen
pressure,
corrected, ms
mL
cm/s
per minute saturation, %
mm Hg
Administer 1000-mL
bolus of 0.9%
normal saline
26
254
78
107
26
68/36 (47)
Administer 1000-mL
bolus of physiological saline
50
341
76
105
48
76/42 (53)
Administer
norepinephrine
10 g/min
51
341
76
105
50
80/44 (59)
Response
55
344
72
106
68
92/62 (72)
22
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Literature Supporting
Clinical Usefulness of SVO
Before they adopt a new practice, astute clinicians
want to know that the practice is strongly supported in
the literature. Randomized controlled trials are the
highest-level research design, and the number of welldesigned randomized controlled trials is directly correlated
with the level of evidence assigned to a given practice.83-85
The findings of 11 randomized controlled trials,44-52,73,74
including 9 prospective trials,44-52 suggest that SVO results
in improved patient outcomes. Despite a thorough literature review, we were unable to find a fluid replacement
strategy supported by more research. The results of the
9 prospective trials,44-52 which included a total of about
1000 patients, consistently suggested that compared with
conventional fluid replacement, SVO fluid replacement
protocols contribute to decreases in overall hospital length
of stay (by 2 days or more), complication rates, renal
insufficiency, infection, use of vasopressors, blood lactate
levels, and time-to-tolerance of oral intake. Appropriately
implemented SVO programs that replicate these outcomes
may also be associated with decreased costs.86
Notably, the sample in all 11 trials44-52,73,74 included
perioperative patients. Although 2 of these trials44,47 also
focused on postoperative care in the critical care unit,
more research is needed to indicate the efficacy of SVO
in nonsurgical patients. However, in perioperative
patients, the strength of the supporting evidence in
favor of SVO has been substantiated by large-scale systematic literature reviews conducted by the Agency for
Healthcare Research and Quality,87 the National Health
Service,86 and third-party payers such as the Centers for
Medicare and Medicaid Services88 and Aetna.89
In 3 of these studies,86-88 the agencies recommended
SVO protocols be used for monitoring cardiac output of
patients receiving mechanical ventilation in the critical
care unit and for surgical patients who require intraoperative fluid optimization. Esophageal Doppler imaging,88 bioimpedance,90 and PACs91 are all reimbursed by
the Centers for Medicare and Medicaid Services88 on the
basis of systematic literature reviews. However,
esophageal Doppler imaging is the only technology also
supported by the Agency for Healthcare Research and
Quality.87
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Nursing Considerations
Nursing considerations associated with incorporating SVO into bedside practice include acquiring and
evaluating hemodynamic data, maintenance of skin
integrity, sedation and analgesia, and nursing research.
Acquisition and Evaluation of
Hemodynamic Information
Clinical proficiency with applying or inserting the
hemodynamic monitoring device and adequate signal
acquisition are key.93 Each device has its own unique signal
acquisition technique and competency requirements.
Inappropriate application of the device may produce inaccurate hemodynamic readings, leading to improper treatment decisions.77,78 Once accurate readings are obtained,
understanding the appropriate application of normal
CriticalCareNurse
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24
CriticalCareNurse
Summary
The growing body of evidence supporting SVO
suggests that implementation of SVO into daily practice
should be considered.61,62,88 A new era is emerging in
which blood-flow monitoring is taking precedence over
the monitoring of blood pressures. Cardiac pressures
help provide estimates of blood volume; however, normal
cardiac pressures can be observed in a patient in shock
and provide little information about blood flow.30,95-97
Interpretation and treatment of blood pressures incorporate assumptions, whereas stroke volume may be
considered a more precise measure of fluid responsiveness and an earlier warning sign of volume depletion
than are urine output, altered mental status, CVP, heart
rate, and blood pressure.1-5 Earlier signals allow clinicians to anticipate rather than react to changes, improving the likelihood for maintaining a stable metabolic
state at the organ and cellular level. In addition to the
evidence supporting SVO, minimally invasive applications and improvements in accuracy also add to safety
advantages when inherent limitations of the various
methods are considered.
For years, strategies for use of SVO were not feasible
because no practical measurement method for SVO
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Financial Disclosures
Tom Ahrens has lectured for hemodynamic monitoring companies (including
Deltex Medical Inc) and is a hemodynamic monitoring consultant.
Now that youve read the article, create or contribute to an online discussion
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6. McCance KL, Huether SE, Brashers VL, Rote NS. Pathophysiology: The
Biologic Basis for Disease in Adults and Children. 6th ed. St Louis, MO:
Mosby, Elsevier: 2010.
7. Ahrens T, Rutherford K. Essentials of Oxygenation: Implication for Clinical
Practice. Boston, MA: Jones & Bartlett Publishers Inc; 1993:51.
8. Hillman KM, Bristow PJ, Chey T, et al. Antecedents to hospital deaths.
Intern Med J. 2001;31(6):343-348.
9. Kause J, Smith G, Prytherch D, et al; Intensive Care Society (UK); Australian and New Zealand Intensive Care Society Clinical Trials Group.
A comparison of antecedents to cardiac arrests, deaths and emergency
intensive care admissions in Australia and New Zealand, and the United
Kingdomthe ACADEMIA study. Resuscitation. 2004;62(3):275-282.
10. Connors AF Jr, Dawson NV, Shaw PK, Montenegro HD, Nara AR,
Martin L. Hemodynamic status in critically ill patients with and without
acute heart disease. Chest. 1990;98(5):1200-1206.
11. Dawson NV, Connors AF Jr, Speroff T, Kemka A, Shaw P, Arkes HR.
Hemodynamic assessment in managing the critically ill: is physician
confidence warranted? Med Decis Making. 1993;13(3):258-266.
12. Eisenberg PR, Jaffe AS, Schuster DP. Clinical evaluation compared to
pulmonary artery catheterization in the hemodynamic assessment of
critically ill patients. Crit Care Med. 1984;12(7):549-553.
13. Hoeft A, Schorn B, Weyland A, et al. Bedside assessment of intravascular
volume status in patients undergoing coronary bypass surgery. Anesthesiology. 1994;81(1):76-86.
14 Iregui MG, Prentice D, Sherman G, Schallom L, Sona C, Kollef MH.
Physicians estimates of cardiac index and intravascular volume based
on clinical assessment versus transesophageal Doppler measurements
obtained by critical care nurses. Am J Crit Care. 2003;12(4):336-342.
15. Neath SX, Lazio L, Guss DA. Utility of impedance cardiography to
improve physician estimation of hemodynamic parameters in the emergency department. Congest Heart Fail. 2005;11(1):17-20.
16. Staudinger T, Locker GJ, Laczika K, et al. Diagnostic validity of pulmonary
artery catheterization for residents at an intensive care unit. J Trauma.
1998;44(5):902-906.
17. Celoria G, Steingrub J, Vickers-Lahti M, et al. Clinical assessment of
hemodynamic values in two surgical intensive care units: effects of therapy. Arch Surg. 1990;125(8):1036-1039.
18. Bakker J, Jansen T. Dont take vitals, take a lactate. Intensive Care Med.
2007;33:1863-1865.
19. Howell MD, Donnino M, Clardy P, Talmor D, Shapiro NI. Occult hypoperfusion and mortality in patients with suspected infection. Intensive Care
Med. 2007;33(11):1892-1899.
20. Mikkelsen M, Miltiades A, Gaieski D, et al. Serum lactate is associated
with mortality in severe sepsis independent of organ failure and shock.
Crit Care Med. 2009;37(5):1670-1677.
21. Ahrens T. Hemodynamics in sepsis. AACN Adv Crit Care. 2006;17(4):
435-445.
22. Department of Health and Human Services, National Institutes of
Health, National Heart, Lung, and Blood Institute. The Seventh Report of
the Joint National Committee on Prevention, Detection, Evaluation, and
Treatment of High Blood Pressure. Bethesda MD: National Heart, Lung,
and Blood Institute; August 2004. NIH Publication No. 04-5230.
23. Connors A, Speroff T, Dawson N, et al. The effectiveness of right heart
catheterization in the initial care of critically ill patients. SUPPORT
Investigators. JAMA. 1996;276(11):889-897.
24. Smartt S. The pulmonary artery catheter: gold standard or redundant
relic. J Perianesth Nurs. 2005;20(6):373-379.
25. Pugsley J, Lerner A. Cardiac output monitoring: is there a gold standard
and how do the newer technologies compare? Semin Cardiothorac Vasc
Anesth. 2010;14(4):274-282.
26. Forrester JS, Diamond G, McHugh TJ, Swan HJ. Filling pressures in the
right and left sides of the heart in acute myocardial infarction: a reappraisal
of central-venous-pressure monitoring. N Engl J Med. 1971;285(4):190-193.
27. Marik P, Baram M, Vahid B. Does central venous pressure predict fluid
responsiveness? A systematic review of the literature and the tale of
seven mares. Chest. 2008;134(1):172-178.
28. Magdesian KG, Fielding CL, Rhodes DM, Ruby RE. Changes in central
venous pressure and blood lactate concentration in response to acute
blood loss in horses. J Am Vet Med Assoc. 2006;229(9):1458-1462.
29. Dellinger RP, Levy MM, Rhodes A, et al; Surviving Sepsis Campaign
Guidelines Committee including the Pediatric Subgroup. Surviving
Sepsis Campaign: International guidelines for management of severe
sepsis and septic shock: 2012. Crit Care Med. 2013;41(2):580-637.
30. Ahrens T. Stroke volume optimization vs central venous pressure in
fluid management. Crit Care Nurse. 2010;30(2):71-73.
31. Pope JV, Jones AE, Gaieski DF, Arnold RC, Trzeciak S, Shapiro NI; Emergency Medicine Shock Research Network (EMShockNet) Investigators.
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Multicenter study of central venous oxygen saturation (ScvO2) as a predictor of mortality in patients with sepsis. Ann Emerg Med. 2010;55(1):
40-46.e1.
Marik P. Surviving sepsis: going beyond the guidelines. Ann Intensive
Care. 2011;1(17):1-6.
Rivers E, Nguyen B, Havstad S, et al; Early Goal-Directed Therapy Collaborative Group. Early goal-directed therapy in the treatment of severe
sepsis and septic shock. N Engl J Med. 2001;345(19):1368-1377.
Benington S, Ferris P, Nirmalan M. Emerging trends in minimally invasive haemodynamic monitoring and optimization of fluid therapy. Eur J
Anaesthesiol. 2009;26(11):893-905.
Marik P, Monnet X, Teboul JL. Hemodynamic parameters to guide fluid
therapy. Ann Intensive Care. 2011;1(1):1-9.
Turner MA. Doppler-based hemodynamic monitoring: a minimally
invasive alternative. AACN Clin Issues. 2003;14(2):220-231.
Michard F, Teboul J. Predicting fluid responsiveness in ICU patients: a
critical analysis of the evidence. Chest. 2002;121:2000-2008.
Dnser M, Takala J, Brunauer A, Bakker J. Re-thinking resuscitation:
leaving blood pressure cosmetics behind and moving forward to permissive hypotension and a tissue perfusion-based approach. Crit Care. 2013;
17:326. doi:10.1186/cc12727.
Marik P, Bellomo R. Re-thinking resuscitation goals: an alternative
point of view! Crit Care. 2013;17:458. doi:10.1186/cc12775.
Knotzer H, Hasibeder W. Microcirculation function monitoring at the
bedsidea view from the intensive care. Physiol Meas. 2007;28(9):
R65-R86.
Marik P, Cavallazzi R, Vasu T, Hirani A. Dynamic changes in arterial
waveform derived variables and fluid responsiveness in mechanically
ventilated patients: a systematic review of the literature. Crit Care Med.
2009;37(9):2642-2647.
Marik P. Techniques for assessment of intravascular volume in critically
ill patients. Intensive Care Med. 2009;24(5):329-337.
Dark P, Singer M. The validity of trans-esophageal Doppler ultrasonography as a measure of cardiac output in critically ill adults. Intensive Care
Med. 2004;30:2060-2066.
Chytra I, Pradl R, Bosman R, Pelnar P, Kasal E, Zidkova A. Esophageal
Doppler-guided fluid management decreases blood lactate levels in
multiple-trauma patients: a randomized controlled trial. Crit Care.
2007;11(1):R24.
Conway DH, Mayall R, Abdul-Latif MS, Gilligan S, Tackaberry C. Randomized controlled trial investigating the influence of intravenous fluid
titration using esophageal Doppler monitoring during bowel surgery.
Anaesthesia. 2002;57(9):845-849.
Gan TJ, Soppitt A, Maroof M, et al. Goal-directed intraoperative fluid
administration reduces length of hospital stay after major surgery. Anesthesiology. 2002;97(4):820-826.
McKendry M, McGloin H, Saberi D, Caudwell L, Brady AR, Singer M.
Randomised controlled trial assessing the impact of a nurse delivered,
flow monitored protocol for optimisation of circulatory status after cardiac surgery. BMJ. 2004;329(7460):258-261.
Mythen MG, Webb AR. Perioperative plasma volume expansion
reduces the incidence of gut mucosal hypoperfusion during cardiac surgery. Arch Surg. 1995;130(4):423-429.
Sinclair S, James S, Singer M. Intraoperative intravascular volume optimisation and length of hospital stay after repair of proximal femoral
fracture: randomised controlled trial. BMJ. 1997;315(7113):909-912.
Venn R, Steele A, Richardson P, Poloniecki J, Grounds M, Newman P.
Randomized controlled trial to investigate influence of the fluid challenge on duration of hospital stay and perioperative morbidity in
patients with hip fractures. Br J Anaesth. 2002;88(1):65-71.
Wakeling HG, McFall MR, Jenkins CS, et al. Intraoperative oesophageal
Doppler guided fluid management shortens postoperative hospital stay
after major bowel surgery. Br J Anaesth. 2005;95(5):634-642.
Noblett S, Snowden C, Shenton B, Horgan A. Randomized clinical trial
assessing the effect of Doppler-optimized fluid management on outcome after elective colorectal resection. Br J Surg. 2006;93(9):1069-1076.
Pearse R, Dawson D, Fawcett J, Rhodes A, Grounds RM, Bennett ED.
Early goal-directed therapy after major surgery reduces complications
and duration of hospital stay: a randomized, controlled trial
[ISRCTN38797445]. Crit Care. 2005;9(6):R687-R693.
Mayer J, Boldt J, Mengistu AM, Rhm KD, Suttner S. Goal-directed
intraoperative therapy based on autocalibrated arterial pressure waveform analysis reduces hospital stay in high-risk surgical patients: a randomized, controlled trial. Crit Care. 2010;14(1):R18. doi:10.1186/cc8875.
Goepfert M, Richter H, Eulenburg C, et al. Individually optimized
hemodynamic therapy reduces complications and length of stay in the
intensive care unit: a prospective, randomized controlled trial. Anesthesiology. 2013;119(4):824-836.
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56. Salzwedel C, Puig J, Carstens A, et al. Perioperative goal-directed hemodynamic therapy based on radial arterial pulse pressure variation and
continuous cardiac index trending reduces postoperative complications
after major abdominal surgery: a multi-center, prospective, randomized
study. Crit Care. 2013;17(5):R191. doi:10.1186/cc12885.
57. Van der Linden PJ, Dierick A, Wilmin S, Bellens B, De Hert SG. A randomized controlled trial comparing an intraoperative goal-directed
strategy with routine clinical practice in patients undergoing peripheral
arterial surgery. Eur J Anaesthesiol. 2010;27(9):788-793.
58. Szakmany T, Toth I, Kovacs Z, et al. Effects of volumetric vs pressureguided fluid therapy on postoperative inflammatory response: a prospective, randomized clinical trial. Intensive Care Med. 2005;31(5):656-663.
59. Rajaram SS, Desai NK, Kalra A, et al. Pulmonary artery catheters for
adult patients in intensive care. Cochrane Database Syst Rev. 2013;2:
CD003408. doi:10.1002/14651858.CD003408.pub3.
60. Balk E, Raman G, Chung M, et al. Evaluation of the Evidence on Benefits
and Harms of Pulmonary Artery Catheter Use in Critical Care Settings.
Rockville, MD: Agency for Healthcare Research and Quality; March 28,
2008. http://www.cms.gov/determinationprocess/downloads/id55TA
.pdf. Accessed October 29, 2014.
61. Roche A, Miller T, Gan T. Goal-directed fluid management with transoesophageal Doppler. Best Pract Res Clin Anaesthesiol. 2009;23(3):327-334.
62. Schober P, Loer S, Schwarte L. Perioperative hemodynamic monitoring
with transesophageal Doppler technology. Anesth Analg. 2009;109:340-353.
63. Chew HC, Devanand A, Phua GC, Loo CM. Oesophageal Doppler ultrasound in the assessment of haemodynamic status of patients admitted
to the medical intensive care unit with septic shock. Ann Acad Med Singapore. 2009;38(8):699-703.
64. Bendjelid K. Assessing fluid responsiveness with esophageal Doppler
dynamic indices: concepts and methods [comment]. Intensive Care Med.
2006;32(7):1088.
65. Monnet X, Pinsky M, Teboul J. FTc is not an accurate predictor of fluid
responsiveness. Intensive Care Med. 2006;32:1090-1091.
66. Johnson A, Schweitzer D. Putting the wedge under pressure [comment].
Ann Acad Med Singapore. 2010;39(10):815.
67. Singer M. The FTc is not an accurate marker of left ventricular preload:
reply to the comment by Chemla and Nitenberg. Intensive Care Med.
2006;32(9):1456-1457.
68. Singer M. The FTc is not an accurate marker of left ventricular preload.
Intensive Care Med. 2006;32(7):1089.
69. Madan AK, UyBarreta VV, Aliabadi-Wahle S, et al. Esophageal Doppler
ultrasound monitor versus pulmonary artery catheter in the hemodynamic management of critically ill surgical patients. J Trauma. 1999;46(4):
607-611.
70. Seoudi H, Perkal M, Hanrahan A, Angood P. The esophageal Doppler
monitor in mechanically ventilated surgical patients: does it work
[abstract]? J Trauma. 1999;47(6):1171.
71. DiCorte CJ, Latham P, Greilich PE, Cooley MV, Grayburn PA, Jessen ME.
Esophageal Doppler monitor determinations of cardiac output and preload during cardiac operations. Ann Thoracic Surg. 2000;69(6):1782-1786.
72. Kincaid H, Fly M, Chang M. Noninvasive measurements of preload
using esophageal Doppler are superior to pressure-based estimates in
critically injured patients [abstract]. Crit Care Med. 1999;27(1):A111.
73. Mark JB, Steinbrook RA, Gugino LD, et al. Continuous noninvasive
monitoring of cardiac output with esophageal Doppler ultrasound during cardiac surgery. Anesth Analg. 1986;65(10):1013-1020.
74. Valtier B, Cholley BP, Belot JP, Coussay JE, Mateo J, Payen DM. Noninvasive monitoring of cardiac output in critically ill patients using transesophageal Doppler. Am J Respir Crit Care Med. 1998;158:77-83.
75. Micek ST, Roubinian N, Heuring T, et al. Before-after study of a standardized hospital order set for the management of septic shock. Crit
Care Med. 2006;34(11):2707-2713.
76. Saberi D, Caudwell L, McGloin H, Singer M. Proactive circulatory management in the first 4 hours postcardiac surgery: interim analysis of a
nurse-led, oesophageal Doppler-guided protocol [abstract]. Intensive
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Critical Care. 5th ed. St Louis, MO: Elsevier; 2005.
79. Edwards Lifesciences. Advanced hemodynamic monitoring. The FloTrac
sensor: stroke volume variation. http://www.edwards.com/products
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30, 2014.
80. Singer M. Continuous Haemodynamic Monitoring by Oesophageal Doppler
[doctoral dissertation]. London, England: University of London; April 1989.
81. Starling EH. The Linacre Lecture on the Law of the Heart. London, England:
Longmans, Green & Co; 1918.
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CriticalCareNurse
27
CNE Test Test ID C1513: Stroke Volume Optimization: The New Hemodynamic Algorithm
Learning objectives: 1. Discuss the use of stroke volume optimization in a hypovolemic patient 2. Define corrected flow time, peak velocity, stroke distance,
and stroke index 3. State various methods used to obtain blood flow measurement
Test answers: Mark only one box for your answer to each question. You may photocopy this form.
1. a
b
c
d
2. a
b
c
d
3. a
b
c
d
4. a
b
c
d
5. a
b
c
d
6. a
b
c
d
7. a
b
c
d
8. a
b
c
d
9. a
b
c
d
Test ID: C1513 Form expires: February 1, 2018 Contact hours: 1.0 Pharma hours: 0.0 Fee: AACN members, $0; nonmembers, $10 Passing score: 7 correct (78%)
Synergy CERP Category A Test writer: Carol Ann Brooks, BSN, RN, CCRN-K, CSC
Name
Program evaluation
Yes
No
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Address
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State
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Phone
E-mail
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The American Association of Critical-Care Nurses is accredited as a provider of continuing nursing education by the American Nurses Credentialing Centers Commission on Accreditation.
AACN has been approved as a provider of continuing education in nursing by the State Boards of Nursing of Alabama (#ABNP0062), California (#01036), and Louisiana (#ABN12). AACN
programming meets the standards for most other states requiring mandatory continuing education credit for relicensure.
Feature
Therapeutic hypothermia has become a widely accepted intervention that is improving neurological outcomes
following return of spontaneous circulation after cardiac arrest. This intervention is highly complex but infrequently used, and prompt implementation of the many steps involved, especially achieving the target body
temperature, can be difficult. A checklist was introduced to guide nurses in implementing the therapeutic
hypothermia protocol during the different phases of the intervention (initiation, maintenance, rewarming, and
normothermia) in an intensive care unit. An interprofessional committee began by developing the protocol, a
template for an order set, and a shivering algorithm. At first, implementation of the protocol was inconsistent,
and a lack of clarity and urgency in managing patients during the different phases of the protocol was apparent.
The nursing checklist has provided all of the intensive care nurses with an easy-to-follow reference to facilitate
compliance with the required steps in the protocol for therapeutic hypothermia. Observations of practice and
feedback from nursing staff in all units confirm the utility of the checklist. Use of the checklist has helped reduce
the time from admission to the unit to reaching the target temperature and the time from admission to continuous
electroencephalographic monitoring in the cardiac intensive care unit. Evaluation of patients outcomes as related
to compliance with the protocol interventions is ongoing. (Critical Care Nurse. 2015;35[1]:29-38)
n the United States, 359 400 people experience an out-of-hospital cardiac arrest each year, and
less than 9.5% of those people survive.1 Out-of-hospital cardiac arrest continues to be associated
with high mortality, and among those patients who do survive the initial cardiac arrest, two-thirds die
as a result of neurological injury.2 Postresuscitation care is increasingly recognized as an integral component
in improving the quality of survival and neurological outcomes. Although advances have been made in
initial resuscitative efforts; anoxic neurological injury remains a major concern after return of spontaneous
circulation (ROSC).2,3 Therapeutic hypothermia improves neurological outcomes after ROSC.3
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Background
In 2002, researchers in 2 studies5,6 reported improved
neurological outcomes and a decrease in mortality with
the use of therapeutic hypothermia after out-of-hospital
cardiac arrest. Recently published guidelines from both
the American Heart Association and the International
Liaison Committee on Resuscitation incorporated evidence from research
The effectiveness of a surgical safety and recommended
that clinicians implechecklist has been documented.
ment therapeutic
hypothermia to increase the likelihood of improved
neurological outcome.3,7 Brain cells die because of several
biochemical processes resulting from cardiac arrest and
the inflammatory process following that injury. Therapeutic hypothermia is believed to be effective because it reduces
cerebral metabolism, decreases cerebral blood flow, and
decreases intracranial pressure.8-10 The neuroprotective
Authors
Kathleen Ryan Avery is the clinical educator for the cardiac intensive
care unit and co-chair of the Therapeutic Hypothermia Committee
at Brigham and Womens Hospital, Boston, Massachusetts.
Molly OBrien is the research coordinator in the cardiac intensive
care unit at Shapiro Cardiovascular Center at Brigham and
Womens Hospital.
Carol Daddio Pierce is the clinical educator in the medical intensive
care unit at Brigham and Womens Hospital.
Priscilla K. Gazarian is the nursing program director for resuscitative clinical practice at Brigham and Womens Hospital and an
associate professor of nursing at Simmons College, Boston,
Massachusetts.
Corresponding author: Priscilla K. Gazarian, RN, PhD, The Center for Nursing Excellence, Brigham and Womens Hospital, 1 Brigham Circle, 4th Floor, Suite 6, Boston
MA 02120 (e-mail: pgazarian@partners.org).
To purchase electronic or print reprints, contact the American Association of CriticalCare Nurses, 101 Columbia, Aliso Viejo, CA 92656. Phone, (800) 899-1712 or (949)
362-2050 (ext 532); fax, (949) 362-2049; e-mail, reprints@aacn.org.
30
CriticalCareNurse
www.ccnonline.org
Local Problem
At our hospital, we have implemented therapeutic
hypothermia in 182 patients in the past 5 years. Until
2009, therapeutic hypothermia was exclusively implemented in the coronary care unit (CCU). Although most
patients who are treated with therapeutic hypothermia
continue to be admitted to the CCU (73%) or the medical
intensive care unit (18%), therapeutic hypothermia is
sometimes provided in the other intensive care units
(ICUs). The number of patients receiving therapeutic
hypothermia has increased steadily each year to a total
of 59 patients in 2013 (Figure 1). Because of the low frequency of therapeutic hypothermia cases and the large
number of nursing staff across different ICUs, months
can pass between case exposures, and each exposure
could be at a different phase of the protocol.
In a review of cases of therapeutic hypothermia at
our institution, we found inconsistencies in the implementation of the protocol and a lack of clarity and urgency in
managing the patients during the different phases of
the protocol (initiation, maintenance, rewarming, and
normothermia). Despite our having a standardized order
template and nursing policy for therapeutic hypothermia,
our data indicated a need for improvement in our implementation of the therapeutic hypothermia protocol.
Intended Improvement
Caring for patients after cardiac arrest in a critical
care unit is a complex, tense, and time-sensitive undertaking. Applying an infrequently used but multifaceted
procedure such as therapeutic hypothermia under these
conditions is challenging and may diminish reliable and
consistent implementation of the intervention. Barriers
to timely implementation exist, including a delayed
decision to implement therapeutic hypothermia, lack of
protocols to guide implementation, the volume of cardiac
www.ccnonline.org
No. of patients
40
35
30
25
20
15
10
5
0
2009
2010
2011
2012
2013
Year
CCU
MICU
SICU
Other
CriticalCareNurse
31
Table
Times needed to complete therapeutic hypothermia interventions after admission to coronary care unit
After checklist
(n = 61)
Goal time
7:00 (5:30-8:11)
6:30 (4:32-9:57)
< 4:00
5:47 (4:22-8:03)
4:00 (2:00-6:56)
< 3:00
Time measured
target temperature in fewer than 4 hours after the initiation of therapeutic hypothermia (see Table). We proposed
a checklist as an intervention to improve achieving the
desired temperature goal within the recommended 4
hours and to manage the various protocol interventions
and minimize complications.
Since the release of the World Health Organizations
surgical safety checklist study,23 checklists have gained
prominence in clinical care as visual tools for standardizing communiChecklists have been documented as cation, especially
effective tools to improve teamwork during high-risk
processes.24 Because
and communication.
checklists have been
documented as effective tools to improve teamwork
and communication,24 we theorized that a checklist
could improve performance in reaching target temperature during therapeutic hypothermia.
Study Purpose
The purpose of our checklist was to guide ICU nurses
and the health care team in safely, effectively, and efficiently implementing the therapeutic hypothermia
protocol during the different phases of the intervention
in the ICU to decrease the time required to achieve the
target temperature.
Methods
Ethics
Our cardiac arrest registry was reviewed by the
Human Research Committee and was approved as
research limited to health medical records. Data from
the cardiac arrest registry were collected and managed
by using REDCap electronic data capture tools hosted
at Brigham and Womens Hospital. REDCap (Research
32
CriticalCareNurse
1:05 (0:30-2:29)
0:30 (0:30-1:00)
37:27 (15:00-55:27)
14:17 (9:15-22:42)
< 18:00
Electronic Data Capture) is a secure, web-based application designed to support data capture for research
studies.36 All patient identifiers (date of birth, medical
record number) are restricted from data reporting
within REDCap to protect the confidentiality of the data.
Setting
Brigham and Womens Hospital is a 793-bed academic
medical center with 100 adult ICU beds in 6 units and a
total of 436 critical care staff nurses.
Planning the Intervention: Improving
Therapeutic Hypothermia Implementation
With a Checklist
To achieve optimal, consistent standardized care
for patients receiving therapeutic hypothermia in our
hospital, an interprofessional committee on therapeutic
hypothermia was established in 2008 with representation from nursing, pharmacy, cardiology, neurology,
pulmonary critical care, emergency medicine, and
interventional cardiology.37 Our committee began by
developing a protocol in 2009, an order template in
2010, and a shivering algorithm in 2011. These resources
had been developed as we gained experience with the
implementation of therapeutic hypothermia and were
based on current evidence. Nurses received ongoing
education on the therapeutic hypothermia protocol via
in-service training sessions and annual competency sessions. As we gained experience in caring for patients
receiving therapeutic hypothermia and as new data
were published, our hospitals protocol for therapeutic
hypothermia underwent annual revisions.
Based on the positive feedback from the ICU nursing
staff on the 1-page shivering algorithm and building on
the success of the World Health Organizations surgical
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CriticalCareNurse
33
Patient ID stamp
initiated:________
Date/Time TH
This is intended to be a quick reference onlyRefer to the ADM 1.4.18 and Nursing NCPM ICU-44 policies for details
on patient management of therapeutic hypothermia. This document is not part of the medical record.
Maintenance of cooling
4-24 hours
Normothermia x 48 hours
AFTER target temp 98.6F
BIS monitoring
Continue sedation/analgesia
infusions
BSAS q 1 hour
If BSAS 1, follow
shivering algorithm
BBG q 1 hour
If Glu > 200, start modified
BHIP
Turn insulin OFF if Glu < 200
MAP goal > 75 mm Hg
CVP goal > 12 mm Hg
Document hourly: Patient temp,
Arctic Sun flow, water temp
EEG performed
Draw labs q 4 hours after TH
initiation at:
____ 8 hours: Chem 7,
CBC, CK, CK-MB, cTnt,
lactic acid, ABG
____ 12 hours: Glu, K,
cultures: blood, sputum,
urine
____ 16 hours: Chem 7,
CBC, CK, CK-MB, cTnt,
lactic acid, ABG
____ 20 hours: Glu, K
____ 24 hours: Chem7,
CBC, CK, CK-MB, cTnt,
lactic acid, ABG
Hold K+ replacement 4 hours
prior to rewarming
(unless K < 3.5)
Figure 2 Therapeutic hypothermia (TH) after cardiac arrest: ICU nursing checklist.
Abbreviations: ABG, arterial blood gas analysis; BBG, bedside blood glucose; BHIP, Brigham and Womens Hospital intravenous insulin protocol; BICS OE, Brigham Integrated Computing System order entry; BIS, bispectral index monitoring; BSAS, Bedside Shivering Assessment Scale; Ca, calcium; CBC, complete blood cell count;
CK, creatine kinase; CK-MB, creatine kinaseMB fraction; cTnt, cardiac troponin T; CVP, central venous pressure; D/C, discontinue; EEG, continuous electroencephalographic monitoring; Glu, glucose; ICU, intensive care unit; IVB, intravenous bolus; K, potassium; labs, samples for laboratory tests; MAP, mean arterial pressure; Mg, magnesium; NMBA, neuromuscular blocking agent; q, every; temp, temperature; TOF, train of four.
Courtesy Brigham and Womens Hospital, Boston, Massachusetts.
34
CriticalCareNurse
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CASE STUDY
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Discussion
The use of the therapeutic hypothermia checklist helps
maintain consistent care of patients in the dynamic ICU
CriticalCareNurse
35
environment, where many team members need to collaborate with one another. Further, it supports nursing
practice by decreasing the uncertainty for nurses less
familiar with implementing the protocol in this complex
time-pressured situation.
We have introduced a novel checklist for the implementation of therapeutic hypothermia and demonstrated
further support for the growing body of evidence indicating that checklists and other types of cognitive aids
are effective in improving various complex processes.30
Using a checklist for therapeutic hypothermia has many
implications in addition to the potential to improve
patients outcomes. Given that checklists have been
documented as improving teamwork and communication, their use in therapeutic hypothermia could lead to
improved interdisciplinary collaboration. Further, this
type of support for nursing work increases nurses
autonomy and allows them more time to focus on providing holistic care to patients and patients families.
Limitations
This report of the implementation of an ICU nursing
checklist for therapeutic hypothermia to integrate the
evidence for therapeutic hypothermia into practice is
limited by the lack of control over possible confounding
variables that may have affected the time to achieve the
temperature target. Although our practice has improved,
we cannot conclude that this is solely a result of using
the checklist. Nonetheless, we easily integrated the
checklist into practice, and it can be adapted for use in
other institutions.
Summary
Thus far, the therapeutic hypothermia checklist for
intensive care nurses has helped the CCU improve 2
metrics related to the implementation of evidence-based
practice of therapeutic hypothermia: the time from CCU
admission to achieving the target temperature and the
time from CCU admission to continuous electroencephalographic monitoring.
Our next challenge will be to focus on the processes
within our system to continue the cooling initiated by
EMS and decrease the time from ROSC to ICU admission. Further evaluation of compliance with the therapeutic hypothermia checklist and the effects on
patients outcomes is needed for continuous quality
improvement. CCN
36
CriticalCareNurse
Acknowledgments
The authors thank Annmarie Chase, RN, MSN, CEN ED, clinical flow manager,
Benjamin M. Scirica, MD, MPH (co-chair), and all members of the Therapeutic
Hypothermia Committee at Brigham and Womens Hospital for their guidance
and support in the development of the therapeutic hypothermia checklist for
intensive care nurses and the nursing staff of the CCU and medical ICU for their
feedback on the implementation of the checklist.
Financial Disclosures
None reported.
Now that youve read the article, create or contribute to an online discussion about
this topic using eLetters. Just visit www.ccnonline.org and select the article you
want to comment on. In the full-text or PDF view of the article, click Responses
in the middle column and then Submit a response.
To learn more about therapeutic hypothermia, read Use of Therapeutic Hypothermia in Cocaine-Induced Cardiac Arrest: Further
Evidence by Scantling et al in the American Journal of Critical Care,
January 2014;23:89-92. Available at www.ajcconline.org.
References
1. Go AS, Mozaffarian D, Roger VL, et al. Heart disease and stroke statistics
2013 update: a report from the American Heart Association. Circulation.
2013;127(1):143-152.
2. Mongardon N, Dumas F, Ricome S, et al. Postcardiac arrest syndrome:
from immediate resuscitation to long-term outcome. Ann Intensive Care.
2011;1(1):45.
3. Peberdy MA, Callaway CW, Neumar RW, et al. Part 9post-cardiac arrest
care: 2010 American Heart Association Guidelines for Cardiopulmonary
Resuscitation and Emergency Cardiovascular Care. Circulation. 2010;
122(18, suppl 3):S768-S786.
4. Neumar RW, Nolan JP, Adrie C, et al. Post-cardiac arrest syndrome:
epidemiology, pathophysiology, treatment, and prognostication. A consensus statement from the International Liaison Committee on Resuscitation (American Heart Association, Australian and New Zealand Council
on Resuscitation, European Resuscitation Council, Heart and Stroke Foundation of Canada, InterAmerican Heart Foundation, Resuscitation Council
of Asia, and the Resuscitation Council of Southern Africa); the American
Heart Association Emergency Cardiovascular Care Committee; the Council
on Cardiovascular Surgery and Anesthesia; the Council on Cardiopulmonary,
Perioperative, and Critical Care; the Council on Clinical Cardiology; and
the Stroke Council. Circulation. 2008;118(23): 2452-2483.
5. Bernard SA, Gray TW, Buist MD, et al. Treatment of comatose survivors
of out-of-hospital cardiac arrest with induced hypothermia. N Engl J Med.
2002;346(8):557-563.
6. The Hypothermia After Cardiac Arrest Study Group. Mild therapeutic
hypothermia to improve the neurologic outcome after cardiac arrest.
N Engl J Med. 2002;346:549-556.
7. Tagami T, Hirata K, Takeshige T, et al. Implementation of the fifth link of
the chain of survival concept for out-of-hospital cardiac arrest. Circulation.
2012;126(5):589-597.
8. Varon J, Acosta P. Therapeutic hypothermia: past, present, and future.
Chest. 2008;133(5):1267-1274.
9. Scirica BM. Therapeutic hypothermia after cardiac arrest. Circulation.
2013;127(2):244-250.
10. Simpson SQ, Peterson DA, OBrien-Ladner AR. Development and implementation of an ICU quality improvement checklist. AACN Adv Crit Care.
2007;18(2):183-189.
11. Nielsen N, Hovdenes J, Nilsson F, et al. Outcome, timing and adverse
events in therapeutic hypothermia after out-of-hospital cardiac arrest.
Acta Anaesthesiol Scand. 2009;53(7):926-934.
12. Mooney MR, Unger BT, Boland LL, et al. Therapeutic hypothermia after
out-of-hospital cardiac arrest: evaluation of a regional system to increase
access to cooling. Circulation. 2011;1224(2):206-214.
13. Brigham and Womens Hospital Therapeutic Hypothermia Committee.
Therapeutic Hypothermia After Cardiac Arrest: Guidelines of Care Administrative Policy. Boston, MA: Brigham and Womens Hospital; July 2011.
14. Laver SR, Padkin A, Atalla A, Nolan JP. Therapeutic hypothermia after
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CriticalCareNurse
37
CriticalCareNurse
The journal for high acuity, progressive, and critical care nursing
Avery KR, OBrien M, Pierce CD, Gazarian PK. Use of a Nursing Checklist to Facilitate Implementation of Therapeutic Hypothermia After Cardiac Arrest. Critical Care
Nurse. 2015;35(1):29-38.
38
CriticalCareNurse
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Feature
Nonpharmacological
Interventions to Prevent
Delirium: An EvidenceBased Systematic Review
RYAN M. RIVOSECCHI, PharmD
PAMELA L. SMITHBURGER, PharmD, MS, BCPS
SUSAN SVEC, RN, BSN, CCRN
SHAUNA CAMPBELL, RN, BSN
SANDRA L. KANE-GILL, PharmD, MS
Development of delirium in critical care patients is associated with increased length of stay, hospital costs, and
mortality. Delirium occurs across all inpatient settings, although critically ill patients who require mechanical
ventilation are at the highest risk. Overall, evidence to support the use of antipsychotics to either prevent or
treat delirium is lacking, and these medications can have adverse effects. The pain, agitation, and delirium
guidelines of the American College of Critical Care Medicine provide the strongest level of recommendation
for the use of nonpharmacological approaches to prevent delirium, but questions remain about which nonpharmacological interventions are beneficial. (Critical Care Nurse. 2015;35[1]:39-51)
elirium has a substantial impact on health care. This complication is associated with a
15-day increase in hospital length of stay (LOS),1 a financial impact of $4 billion to $16 billion
annually,2 and a 19% increase in 6-month mortality.3 Delirium is common across all patient
settings; the prevalence, however, varies according to acuity of illness. Delirium develops in general
medicine patients at rates ranging from 11% to 42%.4 The highest prevalence of delirium, as high as 87%,
occurs in critically ill patients.5 Understanding the impact of delirium on hospitalized patients makes
prevention and optimal treatment of this complication a priority. Two approaches are used to manage
delirium: use of pharmacological agents and application of nonpharmacological therapies.
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CriticalCareNurse
39
40
CriticalCareNurse
Methods
A literature search was completed by using MEDLINE
and EMBASE. With PubMed, the following terms were
used to search MEDLINE for material from 1946 to
October 15, 2013: delirium AND (critically ill, intensive
care, ICU, intensive care unit, OR critical illness), AND
(treatment, prevention, prophylaxis, adjunctive therapy,
OR adjunct therapy). Additional searches in MEDLINE
were then performed with the terms (mobility, animation,
exercise, rehabilitation, physical therapy, OR bicycle),
(light, window, curtains, shades, OR blinds), (earplugs,
ear, noise, OR hearing aid), (sleep, sleep hygiene, OR
sleep deprivation), (eyeglasses, glasses, OR magnifying
lens), orientation, and hydration, each combined with
AND delirium, AND (critically ill, intensive care, ICU,
intensive care unit, OR critical illness). EMBASE was
searched by using the same strategy. The search was
restricted to studies conducted in humans and reported
in English. A second reviewer independently performed
the same search for validation. The titles of all citations
retrieved from the search were reviewed for relevance.
On the basis of the relevance of the title, articles were
selected to be reviewed at the abstract level. Abstracts were
considered for full-text review if delirium was measured
as an outcome (incidence or severity), and the screening
for delirium was completed by using a standardized screening tool. No further review of an abstract was done if the
study covered was not original research, addressed exclusively pharmacological approaches, or used a combination
of pharmacological and nonpharmacological approaches.
If, after review, the abstract was still deemed applicable,
a full-text review was done in which the same inclusion
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EMBASE
1540 citations
MEDLINE
1104 citations
Limit to English
and humans 821
Titles screened for relevance
89 Selected for further
review of abstract
References
reviewed for
inclusion
54 Selected
for full-text
review
10 Included
7 Included
Results
44 Excluded
24 were not original research
6 did not measure delirium or did not
use standard delirium measurement
5 contained pharmacological intervention
5 were not full-text articles
4 did not involve an intervention
17 Included
in review
All Studies
A total of 17 articles7-24 met the
inclusion criteria and were selected
Figure Breakdown of articles selected in literature search.
for review (see Figure and Tables 1
and 2). Seven studies18-24 were done
in critically ill patients, 5 in geriatric
nonpharmacological intervention. Additionally, among
9-13
14-16
general medicine patients, 3 in postoperative patients,
the 6 evaluations7-10,13,18 of the severity of delirium, all but
7,8
and 2 in patients who had a hip fracture. A total of 13
1 study9 indicated a reduction in severity. Patients LOS
of the studies were prospective investigations,7-11,13,15,16,18,21-24
was examined in 6 studies.7,8,11,18-20 Of the 6 studies, the
14-16,24
and 4 were randomized control trials.
The Confusion
results of 2 revealed a decrease in LOS.11,19 Among the 3
Assessment Method or the Confusion Assessment Method
studies18-20
Delirium is associated with multiple negative
for the Intensive Care Unit (CAM-ICU) was the most fredone in the
consequences, including increased length
quently used tool and was used in 10 studies.7-10,13,19-23 The
ICU, only 1
of stay, higher health care costs, and even
Neelon and Champagne Confusion Scale was used in 4
indicated a
increased mortality.
evaluations,14-16,24 and the Intensive Care Delirium Screenreduction in
18
19
ing Checklist, the Diagnostic and Statistical Manual of
LOS. When
12
Mental Disorders (Fourth Edition; DSM-IV), and the
any outcome related to delirium (incidence, duration,
Delirium Screening Scale12 were each used once. The
severity) was examined, only 2 studies11,19 did not show
frequency of delirium screening ranged from less than
any benefit from the addition of a nonpharmacological
daily to 3 times per day.
intervention.
The incidence of delirium was determined in 12
A total of 28 unique nonpharmacological intervenstudies.7-15,18-21 Among these, 9 revealed a benefit of the
tions were used in the clinical studies. The most comnonpharmacological intervention.8-10,12-15,20,21 Table 3 gives
mon interventions associated with any clinical benefit
the interventions used in the individual studies. Among
were mobilization,8,10,20-23 reorientation,9,10,13,18,21 education
the interventions that were beneficial, the mean reducof nurses,7,10,12,18,23 and music therapy.9,16,18,20,21 A single
tion in the incidence of delirium was 24.7%, with a
nonpharmacological intervention was examined in 5
7,8,10,11,22,23
the durarange of 9.7% to 31.8%. In 6 studies,
studies,12,14-16,24 and multiple nonpharmacological intertion of delirium decreased after the addition of the
ventions were examined in 12 investigations.7-10,11,13,18-23
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CriticalCareNurse
41
Table 1
Reference,
year
Milisen et al,
2001
Design
Studies included that involved patients who were not critically ill
Screening tool
used (frequency)
Population (N)
Notable exclusions
Nonpharmacological interventions
Prospective
Marcantonio
et al,8 2001
Prospective,
randomized,
double-blind
CAM (daily)
Hip fracture,
65 years old
(126)
Metastatic cancer,
life expectancy
< 6 months
Inouye et al,9
1999
Prospective,
individual
matching
CAM (daily)
General medicine,
> 70 years old
(852)
Inability to complete
interview, low risk
for delirium
Vidn et al,10
2009
Prospective,
controlled
CAM (daily)
Expected hospital
stay <48 hours
Staff education
Poster in units
Orientation: clock, calendar, reason for
admission, date, place, family letter
Glasses, hearing aids
Sleep: warm drink, reschedule medications
and procedures
Mobilization: out of bed, catheter removal,
change positions, avoid restraints
Hydration: schedule water if ratio of blood urea
nitrogen to serum level of creatinine > 40
Nutrition
Lundstrm
et al,11 2005
Prospective
DSM-IV criteria
(days 1, 3, and 7)
Tabet et al,12
2005
Case-control,
single-blind
Reorientation
Cognitive stimulation activities
Feeding assistance
Hydration
Vision protocol
Hearing protocol
Prospective
Caplan and
Harper,13 2007
Ono et al,14
2011
Randomized,
NEECHAM (no com- Esophagectomy
randomized
ment on how often) (22)
controlled trial
NEECHAM
Taguchi et al,15 Prospective,
randomized
(twice a day)
2007
controlled trial
McCaffrey,16
2009
Prospective,
NEECHAM
randomized
(daily for 3 days)
controlled trial
Nursing education
Poster in units
Esophagectomy
(11)
Hip or knee
surgery, > 75
years old (22)
Music therapy
Abbreviations: CAM, Confusion Assessment Method; DSM-IV, Diagnostic and Statistical Manual of Mental Disorders (Fourth Edition); LOS, length of stay;
MDAS, Memorial Delirium Assessment Scale; NEECHAM, Neelon and Champagne Confusion Scale.
42
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Outcomes
Comments
Antipsychotic use
No difference in incidence
3-day reduction in duration
Reduction in the severity (2.94 points)
No difference in LOS
Not reported
Yes
Not reported
Not reported
Not reported
Not reported
Not reported
Not reported
Not reported
Not reported
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CriticalCareNurse
43
Table 2
Reference,
year
Design
Skrobik et al,
2010
18
Prospective
Screening tool
used (frequency)
Population (N)
Notable exclusions
Nonpharmacological interventions
ICDSC
(3 times a day)
Medical-surgical
ICU (1133)
Nursing education
Radio or compact disc player, reorientation
CAM, CAM-ICU
(3 times a day)
Cardiac surgery
(ICU/medicine)
(1010)
Kamdar et al,20
2013
Observational,
pre-post
design
CAM-ICU
(2 times a day)
Colombo
et al,21 2012
Prospective,
observational,
2 stage
CAM-ICU
(2 times a day)
Medical-surgical
ICU (314)
Schweickert
et al,22 2009
Prospective,
randomized
CAM-ICU (daily)
Needham
et al,23 2010
Prospective
CAM-ICU (daily)
No exclusions
Van Rompaey
et al,24 2012
Prospective,
NEECHAM (daily)
randomized
controlled trial
ICU (136)
Minimum score of
10 on Glasgow
Coma Scale
Hearing impairment
Sedation
Ear plugs
Abbreviations: CABG, coronary artery bypass graft; CAM, Confusion Assessment Method; ICDSC, Intensive Care Delirium Screening Checklist; ICU, intensive care unit;
LOS, length of stay; NEECHAM, Neelon and Champagne Confusion Scale; RASS, Richmond Agitation-Sedation Scale.
44
CriticalCareNurse
Discussion
ICU delirium is associated with numerous adverse
consequences, ranging from increased cost to mortality.3,5
As in a multitude of other ailments, prevention is the optimal strategy, especially when effective treatment options
are unavailable. Haloperidol has been studied for prevention and treatment of ICU delirium, but the results have
been inconclusive.25,26 Because of the unconvincing evidence
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Outcomes
Comments
Antipsychotic use
Yes
Not reported
Yes
Yes
Yes
Not reported
Not reported
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45
10
20
21
22
X
#
#
#
X
X
X
#
23
12
13
#
X
14
15
24
16
a Key:
X, trial in patients who were not critically ill; #, trial in critically ill patients.
46
X
#
Open blinds
Avoidance of restraints
Catheter removal
Eye mask
Adaptive equipment
Medication/procedure reschedule
Noise reduction
Light therapy
Back massage
Family
Warm drink
Calendar
Cognitive stimulation
Clock
Music
Hearing protocol
Reorientation
Eye protocol
X
#
Daily schedule
18
Mobility
Nutrition
Visual displays
Dentures
Nursing education
Hydration
Reference
Table 3
CriticalCareNurse
that encompassed 10 modules with at least 2 recommendations to be made for each module. Collectively, 31
recommendations potentially could have been used.
Implementation of the appropriate recommendations
for each patient resulted in one of the largest reductions
in both incidence and severity of delirium. Vidn et al10
also used a multicomponent intervention and had results
similar to those of Marcantonio et al.8 The inevitable
follow-up question becomes, Is a certain aspect of these
multicomponent interventions leading to the positive
results, and, if so, what aspect?
The importance of a protocol that includes multiple
interventions is evident when the outcomes of studies with
2 or fewer interventions7,11,12,14-16,18,19,22-24 are compared with
the outcomes of studies with many interventions.8-10,13,20,21
For incidence of delirium, the multi-interventional protocols resulted in a 15.9% mean reduction, whereas those
with 2 or fewer interventions showed an 11% reduction.
The 11% reduction is slightly misleading because 4 of the
11 studies7,11,18,19 with 2 or fewer interventions did not
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CriticalCareNurse
47
Conclusion
Use of nonpharmacological interventions is essential
for the prevention of delirium. These interventions can
be a low-risk, low-cost strategy that has shown a benefit
in most studies. Nonpharmacological therapy also has
the potential to decrease the off-label use of antipsychotics
for the treatment of delirium. The largest challenge in
developing a nonpharmacological protocol is determining what interventions to include. Although a one-sizefits-all protocol may not be available, a strong body of
evidence supports the inclusion of education of the medical team, reorientation with cognitive stimulation, and
48
CriticalCareNurse
Now that youve read the article, create or contribute to an online discussion
about this topic using eLetters. Just visit www.ccnonline.org and select the article
you want to comment on. In the full-text or PDF view of the article, click
Responses in the middle column and then Submit a response.
www.ccnonline.org
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25.
26.
27.
28.
29.
The effect of earplugs during the night on the onset of delirium and
sleep perception: a randomized controlled trial in intensive care patients.
Crit Care. 2012;16(3):R73.
Wang W, Li HL, Wang DX, et al. Haloperidol prophylaxis decreases
delirium incidence in elderly patients after noncardiac surgery: a randomized controlled trial. Crit Care Med. 2012;40(3):731-739.
Page VJ, Ely EW, Gates S, et al. Effect of intravenous haloperidol on the
duration of delirium and coma in critically ill patients (Hope-ICU): a
randomised, double-blind, placebo-controlled trial. Lancet Respir Med.
2013;1(7):515-523.
van den Boogaard M, Pickkers P, Slooter AJ, et al. Development and validation of PRE-DELIRIC (PREdiction of DELIRium in ICu patients)
delirium prediction model for intensive care patients: observational
multicentre study. BMJ. 2012;344:e420.
Devlin JW, Marquis F, Riker RR, et al. Combined didactic and scenariobased education improves the ability of intensive care unit staff to recognize delirium at the bedside. Crit Care. 2008;12(1):R19.
Gesin G, Russell BB, Lin AP, Norton HJ, Evans SL, Devlin JW. Impact of
a delirium screening tool and multifaceted education on nurses knowledge of delirium and ability to evaluate it correctly. Am J Crit Care. 2012;
21(1):e1-e11.
CriticalCareNurse
49
CriticalCareNurse
The journal for high acuity, progressive, and critical care nursing
Nonpharmacological Interventions to
Prevent Delirium: An Evidence-Based
Systematic Review
Facts
Development of delirium in critical care patients is
associated with increased length of stay, hospital costs,
and mortality. The pain, agitation, and delirium guidelines of the American College of Critical Care Medicine
provide the strongest level of recommendation for the
use of nonpharmacological approaches to prevent
delirium, but questions remain about which nonpharmacological interventions are beneficial.
Prevention is the optimal strategy, especially
when effective treatment options are unavailable.
Haloperidol has been studied for prevention and
treatment of intensive care unit (ICU) delirium,
but the results have been inconclusive.
A variety of interventions that benefit patients
who are not critically ill would still be useful in
an ICU. The evidence shows that targeting interventions to prevent or treat known risk factors
for delirium have the greatest benefit (eg, cognitive stimulation, reorientation), and a great deal
of overlap exists between risk factors for both
critically and noncritically ill patients.
Multicomponent intervention protocols to
combat delirium have proved beneficial. These
protocols should include early mobilization,
education of nurses, and cognitive stimulation
with reorientation.
Mobilization can be as complete as full physical
or occupational therapy treatments or merely
passive range-of-motion exercises. Bedside nurses
and other members of the medical team work
together to decide the level of mobilization a
patient can complete. Additionally, nurses can advocate for removal of tubes, catheters, or restraints that
may prevent early mobilization.
Education of nurses is an essential component of the
success of any new intervention. In order to include
the potentially large number of nurses who need to
be educated, education should be directed at all
types of learners.
Cognitive stimulation and reorientation is a broad
term that allows each nurse to develop an individual
strategy. Still, each nurses intervention should
incorporate a few key components, such as determining how the patient would like to be addressed,
frequent reorientation to date and time, providing
updates on the patients schedule and clinical status,
and conversing with the patient in a manner that
requires memory recall by the patient.
Obtaining nurses acceptance of and willingness to
support the new intervention is imperative.
One reason for resistance is a lack of time during the
nursing shift to add additional tasks. Assembling a
multidisciplinary team (physician, nurse, pharmacist, respiratory therapist) to determine which nonpharmacological interventions are feasible within
each specific unit is important.
Ultimately the success of a nonpharmacological protocol
to prevent delirium lies with the bedside nurses, who
have the most frequent contact with patients. CCN
Rivosecchi RM, Smithburger PL, Svec S, Campbell S, Kane-Gill SL. Nonpharmacological Interventions to Prevent Delirium: An Evidence-Based Systematic Review.
Critical Care Nurse. 2015;35(1):39-51.
50
CriticalCareNurse
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CNE Test Test ID C1512: Nonpharmacological Interventions to Prevent Delirium: An Evidence-Based Systematic Review
Learning objectives: 1. Describe the nursing literature on nonpharmacological interventions to prevent delirium 2. Discuss nonpharmacological interventions that have been shown to be effective in preventing delirium 3. Explain the tools developed for the measurement of delirium in intensive care unit patients
7. Which of the following is the nonpharmacological intervention specifically
discussed in the pain, agitation, and delirium guidelines of the American
College of Critical Care Medicine?
a. Music therapy
b. Reorientation
c. Nursing education
d. Early mobilization
9. The evidence-based literature supports which of the following nonpharmacological interventions to combat delirium?
a. Nursing education, mobility, and cognitive stimulation with reorientation
b. Nursing education, mobility, and art therapy
c. Mobility, cognitive stimulation with reorientation, and art therapy
d. Mobility, exercise therapy, and cognitive stimulation with reorientation
4. Which of the following tools was used most frequently in the delirium
research?
a. Delirium Screening Scale
b. Neelon and Champagne Confusion Scale
c. Intensive Care Delirium Screening Checklist
d. Confusion Assessment Method for the Intensive Care Unit
11. Which of the following is a strategy for educating nurses about nonpharmacological interventions that help reduce delirium?
a. Visual displays
b. Case study analysis
c. Excel spread sheet
d. PowerPoint self-learning modules
Test answers: Mark only one box for your answer to each question. You may photocopy this form.
1. a
b
c
d
2. a
b
c
d
3. a
b
c
d
4. a
b
c
d
5. a
b
c
d
6. a
b
c
d
7. a
b
c
d
8. a
b
c
d
9. a
b
c
d
10. a
b
c
d
11. a
b
c
d
12. a
b
c
d
Test ID: C1512 Form expires: February 1, 2018 Contact hours: 1.0 Pharma hours: 0.0 Fee: AACN members, $0; nonmembers, $10 Passing score: 9 correct (75%)
Synergy CERP Category A Test writer: Lynn C. Simko, PhD, RN, CCRN
Name
Program evaluation
Yes
No
Member #
Address
City
State
Country
ZIP
Phone
E-mail
RN Lic. 1/St
Payment by:
Card #
RN Lic. 2/St
Visa
M/C
AMEX
Discover
Check
Expiration Date
Signature
The American Association of Critical-Care Nurses is accredited as a provider of continuing nursing education by the American Nurses Credentialing Centers Commission on Accreditation.
AACN has been approved as a provider of continuing education in nursing by the State Boards of Nursing of Alabama (#ABNP0062), California (#01036), and Louisiana (#ABN12). AACN
programming meets the standards for most other states requiring mandatory continuing education credit for relicensure.
Although exertional heat stroke is considered a preventable condition, this life-threatening emergency affects
hundreds of military personnel annually. Because heat stroke is preventable, it is important that Navy critical
care nurses rapidly recognize and treat heat stroke casualties. Combined intrinsic and extrinsic risk factors
can quickly lead to heat stroke if not recognized by deployed critical care nurses and other first responders.
In addition to initial critical care nursing interventions, such as establishing intravenous access, determining
body core temperature, and assessing hemodynamic status, aggressive cooling measures should be initiated
immediately. The most important determinant in heat stroke outcome is the amount of time that patients
sustain hyperthermia. Heat stroke survival approaches 100% when evidence-based cooling guidelines are followed, but mortality from heat stroke is a significant risk when care is delayed. Navy critical care and other
military nurses should be aware of targeted assessments and cooling interventions when heat stroke is suspected during military operations. (Critical Care Nurse. 2015;35[1]:52-59)
52
CriticalCareNurse
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Table 1
Clinical condition
Definitiona
Core temperature
Related signs
Related symptoms
Heat syncope
Normal
Generalized weakness,
syncope
Heat cramps
Normal or elevated
but < 40C (104F)
Heat exhaustion
37C-40C
(98.6F-104F)
Authors
Carl Goforth is the clinical subject matter expert for the Marine Corps
Combat Development Command located in Quantico, Virginia.
He has more than 20 years of combined Navy and Marine service
and has deployed as a critical care and flight nurse attached to US
Marine units overseas.
Josh Kazman is a research associate with the Consortium for Health
and Military Performance at Uniformed Services University of the
Health Sciences. He has worked on a variety of projects and publications related to health disparities, heat tolerance, cardiovascular
disease, and injury prevention.
Corresponding author: CDR Carl Goforth, Combat Development & Integration,
HQMC, 3300 Russell Road, Quantico, VA 22134-5001 (e-mail: carl.goforth@
usmc.mil).
To purchase electronic or print reprints, contact the American Association of CriticalCare Nurses, 101 Columbia, Aliso Viejo, CA 92656. Phone, (800) 899-1712 or
(949) 362-2050 (ext 532); fax, (949) 362-2049; e-mail, reprints@aacn.org.
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CriticalCareNurse
53
Table 2
Intrinsic
(internal) factors
Extrinsic
(environmental) factors
Level of exertion
Alcohol consumption
Existing medical conditions
(ie, respiratory, hematologic,
or cardiovascular)
Dehydration
Table 3
Effect
Type of medication
Antihistamines
Anticholinergics
-Blocking medications
Calcium channel blockers
Lack of water
Temperature (ambient)
Humidity
Wet bulb globe temperature
Sleep deprivation
Medications or supplements
Obesity
Overmotivation
Inadequate acclimatization, poor
aerobic conditioning, or both
Sympathomimetics
Increases heat production
Amphetamines
(ergogenic), hypothalamic set
Ephedra
point, or both
1,3-dimethylamyamine
(sympathomimetic
properties)
Salicylates (supratherapeutic
doses)
a Based
on information from Howe and Boden,11 Seto et al,25 Kao et al,26 Lee,27
Lopez and Casa,28 Fink et al,29 Oh et al,30 and Eliason et al.31
Recent illness
Sickle cell trait
a Based
Risk Factors
Recognizing inherent risk factors can help Navy critical care nurses make informed clinical decisions during
training and deployments. Additionally, US Navy medical
missions, such as
disaster response,
Exertional heat stroke develops as a
usually include the
result of many complex factors and
care of diverse, vulcan vary from person to person.
nerable populations, such as the young and the elderly.19 EHS risk factors
(Table 2) are commonly classified into 1 of 2 areas:
intrinsic (related to the individual) and extrinsic (environmental, task-related, or contextual).
Intrinsic Risk Factors
In addition to a history of heat illness, intrinsic risk
factors can range from sickle cell trait to high motivation.6,16,22,23 Military training includes the indoctrination
of military culture, such as mission first, which can
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lead motivated persons to ignore important physiological warning signs. Other data from the US military show
that overweight military personnel have a higher risk
for sustaining heat injuries.22 Low aerobic fitness has
been cited as a predisposing factor for EHS.24 Poorly
conditioned athletes must work harder to keep up with
fit teammates and thus may ignore warning signs such
as dehydration, tachycardia, or sweating cessation.
Numerous classes of medications have also been implicated in heat stroke (Table 3).
The mechanism by which common medications
contribute to heat stroke depends on the class of drug.
Anticholinergics (antihistamines, antidepressants, or
antipsychotics) decrease production of sweat.11 Cardiovascular agents, such as antihypertensives or diuretics,
decrease the natural physiological responses to dehydration and hyperthermia.25 Of special concern to
young, healthy populations is the recent increase in
use of dietary supplements.
Recent publications indicate that US Marines are
among the highest military users of dietary supplements.26
Ergogenic stimulants, such as amphetamines or ephedra,
increase heat production. Ephedra, from the Chinese plant
ma-huang,27 along with 1,3-dimethylamyamine (DMAA),
is associated with serious heat injury in athletes28,29 and
with EHS30 and death31 in the military. Although the exact
mechanism underlying heat injury in many ergogenic
aids is not fully characterized, published reports clearly
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of the central nervous system and multiorgan dysfunction are typical of EHS (Figure 1). More extensive reviews
are available.13
Clinical Management
The extent and severity of EHS might not be readily apparent in the chaos of military operations.
Because mild forms of heat illness, if not recognized,
might rapidly progress to EHS, immediate evaluation
is necessary to assess the severity of symptoms and, if
needed, to initiate cooling rapidly. When cooling is
provided immediately, survival is near 100%.18 Reducing Tcore to less than 40.5C in less than 30 minutes is
the current recommendation.9
Hyperthermia
Hyperthermia is an increase in Tcore above the bodys
natural set point.6 Human homeostasis requires a narrow
operating temperature around 37C.34 To accomplish this,
a thermoregulatory system composed of compensatory
and noncompensatory systems communicate together for
thermoregulation when Tcore fluctuates.35 During strenuous physical activity, body temperature increases in
healthy persons, but as metabolic processes and/or environmental conditions exceed cardiovascular and central
nervous system compensation, hyperthermia (Tcore >
40C) ensues13 and the risk of EHS increases.10
Temperatures as high as 46.5C (116F) have been
reported in patients who have recovered from heat stroke,36
but survival at such an extreme Tcore is rare. The severity
of tissue injury due to hyperthermia depends on the critical thermal maximum,37 defined as the maximum intensity and duration of tissue heating before cellular death
occurs.38 At extreme core temperatures, thermoregulatory
mechanisms are overwhelmed, cellular proteins begin
denaturing, and apoptosis (programmed cellular death)
can occur within 5 minutes.39,40 Failure to promptly recognize and treat hyperthermia can lead to EHS within
minutes, a life-threatening medical emergency. The integrated effects of hyperthermia leading to derangement
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Supportive Interventions
The initial priorities most relevant to EHS are
hemodynamic status, Tcore, and mental status. Upon
presentation of EHS, critical care nursing staff must
assess and stabilize vital signs, correctly recognize
signs and symptoms of EHS, and begin cooling. The
hallmark of EHS is altered function of the central
nervous system, such as confusion and combativeness.
Nursing management for EHS starts with assessing airway, breathing,
and circulation
Central nervous system abnormalities
(ABCs). Baseline
such as confusion and agitation often
consciousness
are the first signs of heat stroke.
should also be
immediately established, along with an initial score on
the Glasgow Coma Scale. Additional assessments
include, when possible, medical history, medications,
and/or dietary supplements used, body temperature at
admission and maximum known temperature, clinical
features apparent at admission, and vital signs. Critical
care nursing interventions also include advanced
hemodynamic monitoring and initiating fluid resuscitation with crystalloid intravenous solutions per the institutions protocol, preferably chilled (4C) 0.9% sodium
chloride solution.41 Lactated Ringer solution is not
used, because liver function can be suppressed by overheated tissues, leading to unmetabolized lactate and
worsening lactic acidosis.20 Numerous studies42-44 have
demonstrated that axillary, aural (tympanic), oral, and
skin temperatures often indicate a falsely low Tcore,
especially after intense exercise in the heat. Rectal temperature remains the reference standard for assessment
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55
Intrinsic factors
Heat stress
Extrinsic factors
Compensatory
Sweat
Noncompensatory
Hypovolemia
Systemic inflammation
Core temperature
increase
ATP depletion
Circulatory collapse
Cellular anoxia
Core temperature
increase
CNS derangement
Heat stroke
*Liver dysfunction
*Renal failure
*Coagulopathy (DIC)
*Cardiac dysrythmia
*Myoglobin release
*Intestinal permeability
Death
Figure 1 The event sequence leading to heat stroke and death from the compensatory to the uncompensable phase. Physical
activity, especially during hot conditions, initiates a compensable thermoregulatory response (above the dashed horizontal line).
When individual ability to compensate is surpassed, central venous pressure decreases, core temperature increases leading to
thermoregulatory failure if prompt treatment is not initiated. This thermoregulatory failure triggers cellular death, intracellular
imbalance (energy depletion), and circulatory failure. The multiple body system failures, if not immediately treated, lead to death.
Abbreviations: ATP, adenosine triphosphate; CNS, central nervous system; DIC, dissemiated intravascular coagulation.
Adapted with permission from Epstein and Roberts,13 2011, John Wiley and Sons A/S.
56
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0.40
0.30
0.25
0.20
0.35
0.15
0.10
0.05
0.00
et
ge
ies
ies
nly
ion
ion
ion
ion
ion
lank
ers
ers
ers
ers
ers
lava
rter
rter
re o
b
a
a
c
m
m
m
m
m
u
i
t
r
r
g
r
a
m
t
im
im
im
im
jo
in
ajo
per
re i
ma
Gas
ool
ter
ter
ter
ater
at m
tem
ratu
Cc
-wa
-wa
-wa
s
s at
e
e-w
d
d
d
4
k
k
l
l
l
p
m
c
c
c
I
o
o
o
c
c
pa
pa
tem
-roo
Cc
8C
2C
ice
Ice
IVF
20
oom
r
re,
u
r
t
e
a
wat
per
tem
and
F
m
V
I
-roo
lled
IVF
Chi
Figure 2 Relative cooling rates by heat stroke nursing intervention. Optimal cooling rates (> 0.155C/min), acceptable cooling
rate (> 0.079C/min and < 0.154C/min), or unacceptable cooling rates (< 0.078C/min).
Abbreviation: IVF, intravenous fluids.
Adapted with permission from Pryor et al,9 2013 with permission from Elsevier.
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Conclusion
EHS requiring critical care nursing intervention represents a substantial risk of morbidity and mortality to
Navy and Marine Corps personnel. With military EHS
rates at high levels despite scientific advances, never
before has it been so clinically important to recognize
and rapidly treat potential EHS casualties. EHS rates in
the Marine Corps, for instance, were more than 5 times
higher than the rates in other military branches in
2011.49 Data also suggest that military heat stroke survivors have twice the mortality risk from cardiovascular,
kidney, and liver failure within 30 years of initial hospitalization compared with military survivors of nonheat
injuries.21 According to the best evidence available, icewater or cold-water immersion is the most effective cooling treatment and is recommended as the definitive
treatment.46 If this method is unavailable, case reports
demonstrate that continual water dousing combined
with fanning is a practical alternative until advanced treatment is available. Practical resources for the implementation of EHS prevention and emergency procedures can
CriticalCareNurse
57
Table 4
Resource
Website
Description
http://champ.usuhs.mil
http://www.usariem.army.mil
http://www.cs.amedd.army.mil
www.acsm.org
http://www.imef.marines.mil/portals
/68/Docs/IMEF/Surgeon/MCO_
6200.1E_W_CH_1_Heat_Injury
_Prevention.pdf
Financial Disclosures
Work on this manuscript was funded by the Office of Naval Research, grant
no. N0001411MP20023.
Now that youve read the article, create or contribute to an online discussion about
this topic using eLetters. Just visit www.ccnonline.org and select the article you
want to comment on. In the full-text or PDF view of the article, click Responses
in the middle column and then Submit a response.
To learn more about military critical care nursing, read Tales From
the Sea: Critical Care Nurses Serving Aboard the USNS Comfort
and USNS Mercy by Faulk and Hanly in Critical Care Nurse,
August 2013;33:61-67. Available at www.ccnonline.org.
References
1. Murakoshi M, Sekine M. Measures by local governmentactions to
take in dealing with heat stroke for firefighters. Nihon Rinsho. 2012;
70(6):1052-1056.
2. Armstrong LE, Johnson EC, Casa DJ, et al. The American football uniform:
uncompensable heat stress and hyperthermic exhaustion. J Athl Train.
2010;45(2):117-127.
3. Update: Heat Injuries, Active Component, US Armed Forces, 2012. MSMR.
2013;20(3):17-20.
4. Simpson R, Gray S, Florida-James G. Physiological variables and performance markers of serving soldiers from two elite units of the British
Army. J Sports Sci. 2006;24(6):597-604.
5. Chinevere T, Cadarette B, Goodman D, Ely B, Cheuvront S, Sawka M.
Efficacy of body ventilation system for reducing strain in warm and hot
climates. Eur J Appl Physiol. 2008;103(3):307-314.
58
CriticalCareNurse
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Electronic content is user friendly, mobile ready, can be posted to your company website, and/or
distributed via e-mail or social media campaigns.
Contact us today to discuss the many options available:
Matt Neiderer
Matt.neiderer@sheridan.com 800-635-7181 ext. 8265
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CriticalCareNurse
59
Pediatric Care
Extracorporeal
Membrane Oxygenation
for Pediatric Cardiac Arrest
JENNIE RYAN, MS, CPNP-AC
Extracorporeal cardiopulmonary resuscitation (ECPR) remains a promising treatment for pediatric patients
in cardiac arrest unresponsive to traditional cardiopulmonary resuscitation. With veno-arterial extracorporeal
support, blood is drained from the right atrium, oxygenated through the extracorporeal circuit, and transfused
back to the body, bypassing the heart and lungs. The use of artificial oxygenation and perfusion thus provides
the body a period of hemodynamic stability, while allowing resolution of underlying disease processes. Survival
rates for ECPR patients are higher than those for traditional cardiopulmonary resuscitation (CPR), although
neurological outcomes require further investigation. The impact of duration of CPR and length of treatment
with extracorporeal membrane oxygenation vary in published reports. Furthermore, current guidelines for
the initiation and use of ECPR are limited and may lead to confusion about appropriate use of this support.
Many ethical concerns arise with this advanced form of life support. More often than not, the dilemma is not
whether to withhold ECPR, but rather when to withdraw it. Although clinicians must decide if ECPR is
appropriate and when further intervention is futile, the ultimate burden of choice is left to the patients caregivers. Offering support and guidance to the patients family as well as the patient is essential. (Critical Care
Nurse. 2015;35[1]:60-70)
60
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Venous cannula
vena c
ava
Extracorporeal
Cardiopulmonary
Resuscitation
Aortic cannula
erior
Sup
Aorta
Left
atrium
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62
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Table
Population of
patients
Reference
No. of
patients
No. (%) of
Duration of
survivors to cardiopulmonary
discharge
resuscitation, min
Duration of
ECMO therapy
Aharon et al28
Postoperative,
cardiac
10
8 (80)
Mean (range),
42 (5-110)
> 30 min associated
with poor survival
Not reported
Alsoufi et al21
Postoperative,
cardiac
48
23 (46)
Not reported
Not reported
Alsoufi et al30
80
27 (34)
Median (range)
4 days for both survivors and
Survivors: 46 (14-95)
nonsurvivors
Nonsurvivors: 41 (19-110)
Cengiz et al4
ELSO registry
161
64 (40)
Not reported
Mean (SD)
Survivors: 4.7 (3.5) days
Nonsurvivors: 4.4 (6.4) days
Chan et al5
ELSO registry of
cardiac patients
492
208 (42)
Not reported
Median (IQR)
Survivors: 87 (51-137) hours
Nonsurvivors: 87 (37-171) hours
40
30 (75)
Median (IQR)
Survivors: 40 (25-50)
Nonsurvivors: 37 (35-50)
Median (IQR)
Survivors: 53 (29-98) hours
Nonsurvivors: 48 (28-102) hours
Not reported
Not reported
Conrad et al3
ELSO registry
de Mos et al10
ICU
151
Neonatal
282
Pediatric
Neonatal:
65 (43)
Pediatric:
111 (39)
2 (40)
Range
All: 31-77
Survivors: 35-48
Not reported
Cardiac
11
6 (55)
Delmo Walter et al
ICU
42
17 (40.4)
Mean (SD)
Survivors: 35 (1.3)
Nonsurvivors: 46 (4.2)
Mean (SD)
Survivors: 4.0 (2.2) days
Nonsurvivors: 6.0 (0.9) days
Duncan et al22
Cardiac
11
6 (55)
Median (range)
55 (20-103)
Not reported
Huang et al13
Pediatric
54
25 (46)
Mean (SD)
Survivors: 39 (17)
Nonsurvivors: 52 (45)
Not reported
Huang et al9
Pediatric
27
11 (41)
Median (IQR)
Survivors: 45 (25-50)
Nonsurvivors: 60 (37-81)
Joffe et al19
Meta-analysis
762
361 (49)
Not reported
Not reported
Kane et al
Cardiac
172
88 (51)
Pediatric
and cardiac
31
7 (23)
Kumar et al12
Postoperative,
cardiac
29
12 (41)
Del Nido23
11
20
Mean
Survivors: 4 days
Nonsurvivors: 6 days
Mean (SD)
Survivors: 42 (8)
Nonsurvivors: 51 (10)
Not reported
Continued
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63
Table
No. of
patients
Continued
No. (%) of
Duration of
survivors to cardiopulmonary
discharge
resuscitation, min
Reference
Population of
patients
Morris et al32
ICU
Paden et al2
ELSO registry
Polimenakos et al26
Cardiac single
ventricle,
neonates
14
8 (57)
Prodhan et al27
ICU, cardiac
32
Raymond et al8
AHA/NRCPR
Shah et al33
64
Median (range)
Survivors: 50 (5-105)
Nonsurvivors: 46 (15-90)
Median (range)
Survivors: 55 (2-359) hours
Nonsurvivors: 64 (1-506) hours
Not reported
Mean (SD)
Survivors: 38.6 (6.3)
Nonsurvivors: 42.1 (7.7)
Median (IQR)
Survivors: 4 (3-6.5) days
Nonsurvivors: 8 (5-11.5) days
24 (72)
Median (range)
Survivors: 43 (15-142)
Nonsurvivors: 60 (20-76)
Median (range)
Survivors: 122 (41-816) hours
Nonsurvivors: 59 (7-905)
hours
199
87 (44)
Median (range)
Survivors: 46 (26-68)
Nonsurvivors: 57 (38-71)
Not reported
Cardiac
27
9 (33)
Not reported
Mean (SD)
Survivors: 79.3 (40.7) hours
Nonsurvivors: 128.6 (193.3)
hours
Sivarajan et al34
Cardiac
37
14 (38)
Median
Survivors: 15
Nonsurvivors: 40
Not reported
Thiagarajan et al6
ELSO registry
682
261 (38)
Not reported
Meta-analysis
288
114 (39.6)
Not reported
Median (range)
4.3 (0.03-90) days
Wolf et al24
Cardiac
90
50 (55.5)
Survivors: 42 (16-98)
Nonsurvivors: 43 (20-75)
Median (range)
Survivors: 3 (1-20) days
Nonsurvivors: 5 (1-21) days
Thourani et al25
Cardiac
15
11 (73.3)
Not reported
Median (range)
66 (18-179)
Neonatal:
784
Pediatric:
1562
21 (33)
Duration of
ECMO therapy
Neonatal:
304 (39)
Pediatric:
630 (40)
Abbreviations: AHA/NRCPR, American Heart Association/National Registry of Cardiopulmonary Resuscitation; ELSO, Extracorporeal Life Support Organization; ICU,
intensive care unit; IQR, interquartile range.
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interesting are the multiple case reports24,27,30,32,37 of successful cannulation and survival to discharge in patients
receiving CPR of up to 90 to 220 minutes.
Other research has focused on parameters that may
act as predictors for positive outcome. ECPR patients
with a preexisting diagnosis of cardiac illness have
shown improved survival outcomes, when compared
with patients with noncardiac illnesses.5,6,8,30,32 Perhaps
patients with cardiac illness have less multiorgan dysfunction before cardiac arrest and therefore are more likely to
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Ethical Considerations
The judicious use of ECPR in pediatric critical care is
complicated by a vast number of factors, including the
high cost of care, questionable effectiveness, and intensified emotions of families and providers caring for a critically ill child. ECPR is an advanced form of life support,
so its use in patient care must be in accordance with the
principles of medical ethics. The first principle is beneficence, which requires that practitioners offer care that
is beneficial to their patients.40 Unnecessary surgical
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many professionals recognize that a psychological difference clearly exists.44 Based on this assumption, the Presidents Commission on Ethical Problems in Medicine
concluded that, contrary to widespread feelings on the
matter, withdrawing treatment was preferable to withholding treatment for 2 reasons.45,46 Primarily, withdrawing allows a time-limited trial of therapy in which the
patients status can be reassessed and prognosis determined.45,46 Second, a traditional reluctance to withdraw
treatment had led many practitioners to forgo lifesaving
therapies altogether for fear of eventual failure.44 For
this reason, most intensivists now offer advanced life
support to their patients with the hope that therapies
will be successful, or at the very least buy some time.44
Withholding ECPR is often a debate between physicians involved in the patients care. Most families are not
aware of ECPR and would not know to request that their
child be treated with ECPR. Often ECPR is recommended
by a physician, and therefore withholding ECPR may
come to mean simply not offering it. Withholding ECPR
often becomes an intraprofessional dilemma, where the
effectiveness of treatment is controversial. As discussed
previously, the lack of parameters to guide physicians is
detrimental to evidence-based practice, and decisions in
this scenario are often based on personal reasoning,
experience, and values. In these difficult situations, practitioners most often decide to treat, possibly against their
better judgment.44 Solomon et al44 examined perceptions
of physicians and nurses caring for critically ill children
and reported that 80% of critical care attending physicians
agreed that sometimes I feel we are saving children who
should not be saved, whereas only 8% agreed that
sometimes I feel we give up on children too soon.
The ethical dilemma of ECPR is therefore most often
not whether to withhold it, but when to withdraw it.
Again, the literature does not support a definitive
timetable for withdrawal of ECMO. Obviously, neurological devastation as evidenced by brain death is a definitive indicator for withdrawal of treatment. But no other
parameters exist, and the decision to withdraw is often
at the recommendation of the provider.40,47 Maintaining
ethical principles at this time is essential for practitioners
as they address the medical futility of further treatment.40
There must be a level of assurance that prolonged time
on ECMO will enhance patients outcomes and that this
possibility outweighs the risks of further suffering and
discomfort for the child.47
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Nursing Implications
The use of ECMO during CPR is a technologically
advanced and complex treatment that requires extensive
knowledge from every member of the health care team.
Bedside nurses should be well educated on the physiology of the patient, as well as the mechanical aspects of
the ECMO pump. Centers providing this treatment must
offer educational programs to train nurses in rapid
deployment of the ECMO circuit. Familiarity with the
circuit and experience with the cannulation procedure
will ensure a smooth transition from cardiopulmonary
resuscitation to artificial circulation.
Once the patient is cannulated, highly skilled nurses
are needed to manage daily treatment. Nursing care of
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ECMO patients is both physically and mentally demanding. These patients require frequent laboratory and
physical assessments, as well as frequent neurological
checks. Neurological injury is common in ECMO patients
owing to the acuity of their illness and the risk of cerebral
vascular injury from stroke or hemorrhage. Daily ultrasound imaging of the head are routine in most centers,
and continuous electroencephalographic monitoring is
also implemented with concerns for subclinical seizure
activity. Because
of the immense The importance of offering support and
workload associ- guidance can never be underestimated
ated with ECMO in this setting, where parents are very
aware that every moment with their
patients, 2
nurses are gener- child may be their last.
ally needed to
care for these acutely ill children. One nurse is tasked
with the care of the patient, while the other nurse tends
to the needs of the ECMO pump. Most centers have
implemented the use of perfusionists and specially
trained respiratory therapists to manage the ECMO circuit in an effort to reduce the strain on nursing staffing.
Furthermore, the bedside nurse is often depended on
to provide support to patients families. This responsibility is difficult and challenging, and it requires a large
amount of dedication. Most intensive care nurses are well
versed in end-of-life care and must continue to use this
skill during ECMO trials. Although the physical care of
these patients can be burdensome, bedside nurses must
strive to ensure that time is allocated for family support.
When needed, nurses should be aware of the resources
available for patients families, including palliative care
teams, social workers, and chaplain services. These services can help by offering assistance to family members
during periods of critical illness and end of life.
CriticalCareNurse
67
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13. Huang SC, Wu ET, Wang CC, et al. Eleven years of experience with
extracorporeal cardiopulmonary resuscitation for pediatric patients
with in-hospital cardiac arrest. Resuscitation. 2012;83(6):710-714.
14. Fuhrman BP, Zimmerman J. Pediatric Critical Care. 3rd ed. Philadelphia,
PA: Mosby; 2006.
15. Fiser RT, Morris MC. Extracorporeal cardiopulmonary resusciation in
refractory pediatric cardiac arrest. Pediatr Clin North Am. 2008;55(4):
929-941.
16. Young KD, Seidel JS. Pediatric cardiopulmonary resuscitation: a collective
review. Ann Emerg Med. 1999;33(2):195-205.
17. Nadkarni VM, Larkin GL, Peberdy MA, et al. First documented rhythm
and clinical outcome from inhospital cardiac arrest among children and
adults. JAMA. 2006;295(1):50-57.
18. Topijan AA, Nadkarni VM, Berg RA. Cardiopulmonary resuscitation in
children. Curr Opin Crit Care. 2009;15(3):203-208.
19. Joffe AR, Lequier L, Robertson CMT. Pediatric outcomes after extracorporeal membrane oxygenation for cardiac disease and for cardiac arrest:
a review. ASAIO J. 2012;58(4):297-310.
20. Kane DA, Thiagarajan RR, Qypij D et al. Rapid response extracorporeal
membrane oxygenation to support cardiopulmonary resuscitation in
children with cardiac disease. Circulation. 2010;122(11 suppl):S241-S248.
21. Alsoufi B, Al-Radi O, Gruenwald C, et al. Extracorporeal life support
following cardiac surgery in children: analysis of risk factors and survival in a single institution. Eur J Cardiothorac Surg. 2009;35(6):1004-1011.
22. Duncan B, Ibrahim A, Hraska V, et al. Use of rapid-deployment extracorporeal oxygenation for the resuscitation of pediatric patients with
heart disease after cardiac arrest. J Thorac Cardiovasc Surg. 1998;116(2):
305-311.
23. Del Nido P. Extracorporeal membrane oxygenation for cardiac support
in children. Ann Thorac Surg. 1996;61(1):336-339.
24. Wolf MJ, Kanter KR, Kirshbom PM, Kogon BE, Wagoner SF. Extracorporeal cardiopulmonary resuscitation for pediatric cardiac patients. Ann
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25. Thourani VH, Kirshbom PM, Kanter KR, et al. Venoarterial extracorporeal membrane oxygenation (VA-ECMO) in pediatric cardiac support.
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26. Polimenakos AC, Wojtyla P, Smith PJ, et al. Post-cardiotomy extracorporeal resuscitation in neonates with complex single ventricle: analysis of
outcomes. Eur J Cardiothorac Surg. 2011;40(6):1395-1404.
27. Prodhan P, Fiser RT, Dyamenahalli U, et al. Outcomes after extracorporeal cardiopulmonary resuscitation (ECPR) following refractory
pediatric cardiac arrest in the intensive care unit. Resuscitation. 2009;80(10):
1124-1129.
28. Aharon AS, Drinkwater DC, Churchwell KB, et al. Extracorporeal membrane oxygenation in children after repair of congenital cardiac lesions.
Ann Thorac Surg. 2001;72(6):2095-2101.
29. Chrysostomou C, Morell VO, Kuch BA, OMalley E, Munoz R, Wearden
PD. Short- and intermediate-term survival after extracorporeal membrane
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30. Alsoufi B, Al-Radi O, Nazer R, et al. Survival outcomes after rescue
extracorporeal resuscitation in pediatric patients with refractory cardiac
arrest. J Cardiovasc Surg. 2007;134(4):952-959.
31. Kelly RB, Harrison RE. Outcome predictors of pediatric extracorporeal
cardiopulmonary resuscitation. Pediatr Cardiol. 2010;31(5):626-633.
32. Morris MC, Wernovsky G, Nadkarni VM. Survival outcomes following
extracorporeal cardiopulmonary resuscitation from inhospital pediatric
cardiac arrest. Pediatr Crit Care Med. 2004;5(5):440-446.
33. Shah SA, Shankar V, Churchwell KB, et al. Clinical outcomes of 84 children with congenital heart disease managed with extracorporeal membrane oxygenation after cardiac surgery. ASAIO J. 2005;51(5):504-507.
34. Sivarajan VB, Best D, Brizard CP, et al. Duration of resuscitation prior
to rescue extracorporeal membrane oxygenation impacts outcome in
children with heart disease. Intensive Care Med. 2011;37(5):853-860.
35. American Heart Association. 2005 American Heart Association guideline
for cardiopulmonary resuscitation and emergency cardiovascular care.
Circulation. 2005;112(24):47-50.
36. de Caen AR, Kleinman ME, Chameides L, et al. Part 10: Pediatric basic
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treatment recommendations. Resuscitation. 2010;81(suppl 1):e213-e259.
37. Kelly RB, Porter PA, Meier AH, Myers JL, Thomas NJ. Duration of cardiopulmonary resuscitation before extracorporeal rescue: how long is
not long enough? ASAIO J. 2005;51(5):665-667.
38. Merril ED, Schoeneberg L, Sandesara P, et al. Outcomes after prolonged
extracorporeal membrane oxygenation support in children with cardiac
disease: Extracorporeal Life Support Organization registry study. J Thorac
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CriticalCareNurse
69
CNE Test Test ID C151: Extracorporeal Membrane Oxygenation for Pediatric Cardiac Arrest
Learning objectives: 1. Determine the difference between venovenous and venoarterial extracorporeal membrane oxygenation (ECMO) 2. Describe the
benefits of extracorporeal cardiopulmonary resuscitation 3. Discuss the ethical considerations related to management of patients undergoing ECMO
7. The use of ECPR in pediatric critical care is complicated by all except which of
the following?
a. High cost of care
b. Questionable effectiveness
c. Intensified emotions of families and providers
d. Absence of standardized clinical guidelines for withdrawal
8. Which of the following is the term for the concept of initiating and removing
advanced life support?
a. Initiating
b. Withholding
c. Withdrawing
d. All of the above
10. Which of the following can help nurses assist families with emotional
support during hospitalization?
a. Child life specialists
b. Palliative care, social workers, and chaplain services
c. Physician support
d. Leadership support
4. ECPR is recommended for use in which of the following types of patient settings?
a. Heart transplant surgery
b. Brief no-flow cardiac arrest in the hospital setting
c. Severe hyperthermia
d. Prolonged cardiopulmonary resuscitation with spontaneous return of circulation
11. Studies examining parents experiences with ECMO report which of the
following?
a. Parents felt they had no other choice as death was the only other option.
b. ECMO is one of several treatments available to improve their childs condition.
c. Parents preferred optimistic reports on their childs condition over reasonable prognosis.
d. Parents relied heavily on the physicians to guide them through the daily stressors
of having a child undergoing supportive measures.
Test answers: Mark only one box for your answer to each question. You may photocopy this form.
1. a
b
c
d
2. a
b
c
d
3. a
b
c
d
4. a
b
c
d
5. a
b
c
d
6. a
b
c
d
7. a
b
c
d
8. a
b
c
d
9. a
b
c
d
10. a
b
c
d
11. a
b
c
d
12. a
b
c
d
Test ID: C151 Form expires: February 1, 2018 Contact hours: 1.0 Pharma hours: 0.0 Fee: AACN members, $0; nonmembers, $10 Passing score: 9 correct (75%)
Synergy CERP Category A Test writer: Tina Cronin
Name
Program evaluation
Yes
No
Member #
Address
City
State
Country
ZIP
Phone
E-mail
RN Lic. 1/St
Payment by:
Card #
RN Lic. 2/St
Visa
M/C
AMEX
Discover
Check
Expiration Date
Signature
The American Association of Critical-Care Nurses is accredited as a provider of continuing nursing education by the American Nurses Credentialing Centers Commission on Accreditation.
AACN has been approved as a provider of continuing education in nursing by the State Boards of Nursing of Alabama (#ABNP0062), California (#01036), and Louisiana (#ABN12). AACN
programming meets the standards for most other states requiring mandatory continuing education credit for relicensure.
hirty years ago this month (February 1985) I took the CCRN
exam. Achieving and maintaining my critical care certification
is one of the accomplishments, in my 34 years as a critical care
nurse, of which I am most proud. Many of the nurses who are reading this column were not yet born when I became certified. My
efforts to help others prepare for and achieve this coveted certification is exciting and humbling. The recent changes that have
occurred in the eligibility criteria have allowed more nurses to
obtain and maintain their CCRN certification. Now all nurses who
affect the care of critically ill patients and their families, whether
electronically (CCRN-e), in the classroom, at the bedside, or from an
administrative office (CCRN-K), can proudly wear the CCRN credential. I feel honored to be a member of this group. Please join me in
celebrating my anniversary and remember to celebrate your own!
RAUEN
CEBALLOS
RISCH
Contributors
Carol Rauen, RN, MS, CCNS, CCRN, PCCN, CEN, RN-BC, the department editor,
is an independent clinical nurse specialist in The Outer Banks of North Carolina.
Carol welcomes feedback from readers and practice questions from potential
contributors at rauen.carol104@gmail.com.
Kirtley Ceballos, MSN, RNC-NIC, PCNS-BC, clinical nurse specialist in the
neonatal intensive care unit at University of Colorado Hospital, University of
Colorado Health, Colorado Institute for Maternal Fetal Health, Aurora, Colorado,
contributed the pediatric CCRN questions.
Steve Risch, RN, MSN, CCRN, CCNS, a critical care clinical nurse specialist at
Holy Cross Hospital, Silver Spring, Maryland, contributed the adult CCRN
questions.
2015 American Association of Critical-Care Nurses doi: http://dx.doi.org/10.4037/ccn2015495
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71
72
CriticalCareNurse
2. Correct Answer: D
Rationale
3. Correct Answer: C
Rationale
www.ccnonline.org
4. Correct Answer: D
Rationale
5. Correct Answer: A
Rationale
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CriticalCareNurse
73
lower quadrant. Hyponatremia (C) should always be considered in patients with central nervous system infection
and can be a result of adrenal insufficiency. Cushing syndrome (D) is rare in children and most often caused by
steroid therapy.
Source
4. Correct Answer: C
1. Correct Answer: C
Rationale
Rationale
Source
Potts NL, Mandleco BL. Pediatric Nursing: Caring for Children and Their Families.
Independence, KY: Cengage Learning; 2011:723.
Source
Hockenberry MJ, Wilson D. Wong's Nursing Care of Infants and Children. St
Louis, MO: Elsevier Health Sciences; 2013:857-858.
5. Correct Answer: D
Rationale
2. Correct Answer: B
Rationale
3. Correct Answer: A
Rationale
Because the patient is most likely receiving pain medication for the fracture, increased pain and tenderness may
not be perceived. The nurse should monitor for signs of
acute infection and alterations in thermoregulation while
continuing to provide pain-relief measures.
Source
Potts NL, Mandleco BL. Pediatric Nursing: Caring for Children and Their Families.
Independence, KY: Cengage Learning; 2011:1312.
74
CriticalCareNurse
www.ccnonline.org
Author
Barbara McLean is a critical care clinical
nurse specialist at Grady Health Systems
in Atlanta, Georgia.
Corresponding author: Barbara McLean, RN, MN,
CCNS-BC, NP-BC, CCRN, Grady Health Systems, 80 Jesse
Hill Jr. Drive SE, Atlanta, GA 30303 (e-mail:
bmclean1@gmh.edu).
To purchase electronic and print reprints, contact the
American Association of Critical-Care Nurses, 101
Columbia, Aliso Viejo, CA 92656. Phone, (800) 8092273 or (949) 362-2050 (ext 532); fax, (949) 3622049; e-mail, reprints@aacn.org.
2015 American Association of Critical-Care Nurses
doi: http://dx.doi.org/10.4037/ccn2015557
www.ccnonline.org
replies:
Many critically ill patients are
monitored with continuous blood
pressure measurements, which
provide clinicians with the important measures of systolic blood
pressure (reflecting the change of
pressure in the artery related to
ventricular stroke volume) and
diastolic blood pressure (related
to vascular tone), as well as the
calculated mean arterial pressure
and pulse pressure. The physiology
of blood pressure monitoring is
quite complex, and the meanings
of the different values are often
misunderstood. Although most
providers use target end points for
pressure monitoring and intervention, little evidence supports the
use of a single blood pressure target. When measuring noninvasively,
the points of measure are static,
versus the invasive measures, which
are dynamic (beat to beat). The
CriticalCareNurse
75
Doppler Flow
Systems that operate on the
Doppler principle take advantage
of the change in frequency of an
echo signal when there is movement between 2 objects. Doppler
devices emit brief pulses of sound
at a high frequency that are reflected
back to the transducer. In an uncompressed artery, the small amount
of motion of the artery wall does
not cause a change in frequency of
the reflected signal. The compressed
artery exhibits a large amount of
wall motion when flow first appears
in the vessel distal to the inflated
cuff, which changes the frequency
of the signal, causing what is known
as a Doppler shift. The first appearance of flow in the distal part of the
artery represents systolic pressure.
When the Doppler shift in the echo
signal disappears, that represents
diastolic pressure.
Infrasound
Infrasound devices use a
microphone to detect low-frequency
(20-30 Hz) sound waves associated
with the oscillation of the arterial
wall. These sounds are processed by
76
CriticalCareNurse
Oscillometry
Most automated NIBP devices
are based on oscillometry. Oscillometric devices operate on the same
principle as manual oscillometric
measurements. The cuff senses
pressure fluctuations caused by
vessel wall oscillations in the presence of pulsatile blood flow. Maximum oscillation is seen at mean
pressure, whereas wall movement
greatly decreases below diastolic
pressure. As with the other automated methods described, the
signals produced by the system
are processed electronically and
displayed in numeric form.3 In
oscillometry, variations in cuff
pressure resulting from arterial
pulsations during cuff deflation
are sensed by the monitor and
used to determine arterial blood
pressure values. The pressure at
which the peak amplitude of arterial pulsations occurs corresponds
closely to directly measured mean
arterial pressure, and values of
systolic and diastolic pressure are
derived from proprietary formulas
that examine the rate of change of
the pressure pulsations. Consequently, systolic and diastolic values obtained with this technique
are less reliable than mean arterial
pressure values.
Indirectly measured pressures
vary depending on the size of the
cuff used. Cuffs of inadequate width
and length can provide falsely elevated measurements. Bladder width
should equal 40% and bladder
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that forces itself (via cardiac ejection) into the resistant arteries. For
most trials conducted in humans
or animals, blood pressure measures obtained by using a wide variety of methods correlate poorly with
invasive arterial pressure measurements, particularly in patients
with edema, who are receiving
vasoactive medications, or who
have significant hypoperfusion.7-9
In the clinical environment,
monitoring of direct arterial
pressure uses an underdamped
catheter-transducer system. The
arterial response to ventricular
ejection is a frequency response,
that is, the stroke volume bolus of
blood goes into the artery, generating a vibration column that emits
many responses (arterial wall
oscillations) that are averaged into
the systolic pressure. These frequencies transmit into the system,
which transmits the frequencies
through the fluid-filled tubing and
transducer.10 Nowadays, monitors
offer internal calibration, filtering
of artifacts, and printouts of the
display. The digital display shows
an average of values over time and
thus does not show beat-to-beat
variability accurately. Beat-to-beat
differences in amplitude can be
measured precisely by freezing the
monitor display with on-screen
calibration, allowing assessment
of the effect of ectopic beats on
blood pressure, variations in pulse
pressure or systolic pressure, and
the severity of pulsus paradoxus.
Direct measurement of arterial
blood pressure requires that the
pressure waveform from the cannulated artery be reproduced
CriticalCareNurse
77
300 mm Hg
Systole
Dicrotic
notch
Systolic
Mean
Diastolic
Pressure
Diastole
Time
Figure 1 Crisp systole, dicrotic notch, and diastole. When flush test is applied, 2 oscillations follow before return to baseline.
78
CriticalCareNurse
www.ccnonline.org
300 mm Hg
Square wave or flush test
Normal
systole
Constant
mean
Underestimated
systole
Oscillations absent,
indicates overdamping
Systolic
Mean
Pressure
Diastolic
Normal diastole
Overestimated
diastole
Comparing normal
with overdamped
Time
Figure 2 When the arterial pressure loses its sharp visualization or the digital measure is lower than oscillated or anticipated,
check the patient first. Then check all connections on the monitoring system, starting at the patient all the way to the transducer
and then the pressure bag. An overdamped picture can occur when connections are loose, the pressure bag is inflated at less
than 300 mm Hg, there is air in the tubing, or a clot forms on the tip. Validate the mean pressure of both the arterial catheter
and the oscillated pressure.
www.ccnonline.org
CriticalCareNurse
79
300 mm Hg
Systolic
Overestimated
systole
Normal
systole
Constant
mean
Mean
Ringing oscillations
indicate underdamping
Pressure
Diastolic
Normal
diastole
Comparing normal
with underdamped
Underestimated
diastole
Time
Figure 3 Spiked systole with a lower diastole should alert the provider to a possible underdamping issue. Underdamping usually
occurs when the tubing is too long or the catheter is the wrong size. The problem is usually not physiologic. Reduce the tubing
length and stabilize or replace the catheter. Observe that the mean pressure remains constant between oscillated and invasive.
80
CriticalCareNurse
4. Bruner JM, Krenis LJ, Kunsman JM, Sherman AP. Comparison of direct and indirect
methods of measuring arterial blood pressure: Pt III. Med Instrum. 1981;15(3):182-188.
5. Bogert LW, van Lieshout JJ. Non-invasive
pulsatile arterial pressure and stroke volume
changes from the human finger. Exp Physiol.
2005;90:437-446.
6. Van Egmond J, Hasenbros M, Crul JF. Invasive v. non-invasive measurement of arterial
pressure. Br J Anaesth. 1985;57(4):434-444.
7. Aarnes TK, Hubbell JAE, Lerche P, Bednarski RM. Comparison of invasive and
oscillometric blood pressure measurement
techniques in anesthetized sheep, goats, and
cattle. Vet Anaesth Analg. 2014;41:174-185.
8. Hohn A, Defosse JM, Becker S, et al. Noninvasive continuous arterial pressure monitoring with Nexfin does not sufficiently
replace invasive measurements in critically
ill patients. Br J Anaesth. 2013;111(2):178-184.
9. Stover JF, Stocker R, Lenherr R, et al. Noninvasive cardiac output and blood pressure
monitoring cannot replace an invasive
monitoring system in critically ill patients.
BMC Anesthesiol. 2009;9:6.
10. Troy P, Smyrnios NA, Howell MD. Routine
monitoring of critically ill patients. In:
Irwin RS, Rippe JM, eds. Irwin and Rippes
Intensive Care Medicine. Philadelphia, PA:
Lippincott Williams & Wilkins; 2011:258-276.
11. McGhee BH, Bridges EJ. Monitoring arterial blood pressure: what you may not
know. Crit Care Nurse. 2002;22(2):60-79.
12. Kim SH, Lilot M, Sidhu KS, Rinehart J, Yu
Z, Canales C, Cannesson M. Accuracy and
precision of continuous noninvasive arterial
pressure monitoring compared with invasive
arterial pressure: a systematic review and
meta-analysis. Anesthesiology. 2014;120(5):
1080-1097.
Hold it in your
hand, like the
print copy
Easy navigation
with flippable
pages
Financial Disclosures
None reported.
References
1. Magder SA. The highs and lows of blood
pressure: toward meaningful clinical targets
in patients with shock. Crit Care Med. 2014;
42(5):1241-1251.
2. Pierce EC. Percutaneous arterial catheterization in man with special reference to aortography. Surg Gynecol Obstet. 1951;93:56.
3. Borow KM, Newberger JW. Non-invasive
estimation of central aortic pressure using
the oscillometric method for analyzing
systemic artery pulsatile blood flow: comparative study of indirect systolic, diastolic, and mean brachial artery pressure
with simultaneous direct ascending aortic
pressure measurements. Am Heart J.
1982;103:879.
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In Our Unit
Implementation of Early Exercise and
Progressive Mobility: Steps to Success
Melody R. Campbell, RN, DNP, CEN, CCRN, CCNS
Julie Fisher, PT, MPT
Lyndsey Anderson, MOT, OTR/L
Erin Kreppel, PT, MPT
Authors
Melody R. Campbell is a critical care clinical nurse specialist and trauma program
manager at Kettering Medical Center, Kettering, Ohio.
Julie Fisher is a physical therapist and the lead therapist in the physical medicine
and rehabilitation department at Good Samaritan Hospital, Dayton, Ohio.
Lyndsey Anderson is an occupational therapist in the physical medicine and
rehabilitation department at Good Samaritan Hospital, Dayton, Ohio.
Erin Kreppel is a physical therapist in the physical medicine and rehabilitation
department at Little Company of Mary Hospital, Evergreen Park, Illinois.
Corresponding author: Melody R. Campbell, RN, DNP, CEN, CCRN, CCNS, Trauma Program, Kettering Medical
Center, 3535 Southern Blvd, Kettering, Ohio 45429 (e-mail: melody.campbell@khnetwork.org).
To purchase electronic or print reprints, contact the American Association of Critical-Care Nurses,
101 Columbia, Aliso Viejo, CA 92656. Phone, (800) 899-1712 or (949) 362-2050 (ext 532); fax,
(949) 362-2049; e-mail, reprints@aacn.org.
2015 American Association of Critical-Care Nurses doi: http://dx.doi.org/10.4037/ccn2015701
82
CriticalCareNurse
Literature Review,
Appraisal, and Synthesis
Electronic databases searched for
evidence included Cochrane, PubMed,
and CINAHL. Key words included
mechanical ventilation, critically ill,
critical illness, early mobilization protocol, delirium, intensive care unit, early
mobility, sedation, physical rehabilitation, and physical therapy. In CINAHL,
limits included research, English,
human, and all adults. Related citations were reviewed in PubMed with
limitations of clinical trials, human,
English, and publication between 2007
and 2012. References from key articles
were reviewed to search for additional
evidence. Articles were included in
the appraisal if content focused on
early mobility in critically ill patients
receiving mechanical ventilation.
Articles were rated by strength of
evidence.4 Level 1 evidence, that established by meta-analysis or systemic
review (and also the highest level of
evidence) was not found. No Cochrane
reviews or national practice guidelines
that were related to the subject had
been published between 2007 and
2012. Since that time, a clinical practice
guideline2 related to pain, agitation,
and delirium in the critically ill has
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Human Institutional Review Committee and the universitys institutional review board. We wanted to
collect patient data during the implementation of our project to monitor
process and outcomes and wanted
to ensure the safety of that data collection and dissemination of results.
The final aspects of planning for
practice change included creating
an aim statement. Using our EBPI
model, an aim statement would
help us to know whether we had
reached a short-term goal in our
implementation. Working with our
medical director, we determined
that our aim statement would be:
By month 3 of the project, early
mobility would be incorporated
into the care of 25% of patients
receiving mechanical ventilation
(as appropriate). The implementation steps in accordance with our
EBPI model are listed in Table 1.
CriticalCareNurse
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84
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Assess wakefulness
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CriticalCareNurse
85
Table 1
1. Describe the problem: Need for implementation of early mobility into practice.
2. Formulate focused clinical question: What is the effect of an early mobility protocol
on delirium and length of stay in the intensive care unit over the course of 3 months?
3. Search for evidence.
4. Appraise and synthesize evidence.
5. Develop aim statement: By month 3 of project, early mobility will be incorporated
into care of 25% of patients receiving mechanical ventilation (as appropriate).
6. Engage in small tests of change.
Ensure safety: high-fidelity human simulation
Ensure safety and reproducibility: protocol refinement
7. Disseminate practice to all staff and patients.
8. Utilize plan-do-study-act process to monitor/evaluate implementation of new practice.
a Based
86
CriticalCareNurse
Implementation
Small tests of change were used
to begin the implementation. After
each test, the multidisciplinary
team reviewed how things went.
The protocol flowed well and was
easily understood. The team, having
gained confidence through the use
of simulation, worked well together
and the patients were safe. Next steps
involved teaching others about early
mobility and disseminating the
practice. The physical medicine and
rehabilitation department conducted
several in-service training sessions
with their staff and added written
and oral competencies to ensure staff
knowledge and patient safety. Nurses
and respiratory therapists conducted
www.ccnonline.org
Table 2
Cardiac monitor
Ventilator
Simulation
Instructor
content
Expectations of
student group
Important learning
considerations
Normal sinus
Assist control Oral endotracheal Patient is improv- Verbalize the contraindirhythm
Fraction of
tube to subglottic
ing. Yesterday
cations to initiating
Heart rate = 80/min
inspired
suction
patient was able
early mobility. Examine
Noninvasive blood
oxygen=40%
to sit and dangle
patient and infusions.
Sequential compressure = 130/80 Positive endlegs at bedside,
Review ventilator settings
pression device
mm Hg
expiratory
sit to stand with
and vital signs.
(both legs)
Oxygen saturation
pressure =
2-person assist.
Verbalize preparing patient
(pulse oximetry) =
5 cm H2O
Gait was steady.
Nasogastric
for early mobility.
98%
Plan for today is
tubetube
Respiratory rate =
to march in place, Prepare patient for sit to
feeding/pump
16/min
weight shift,
stand, march in place,
Urinary catheter
and determine
weight shift, possible
if patient can
ambulation in room.
Peripherally
ambulate in room. Verbalize:
inserted central
Secure all devices
catheter
Turn off tube feeding
Infusions:
Move urinary catheter,
Dexmedetomidine
and intravenous poles
(Precedex)
to side of bed next to
0.7 g/kg per hour
ventilator.
Remove unnecessary
devices (eg, sequential
compression system)
Obtain portable ventilator
Walker with support
for portable cardiac
monitor
Recumbent wheelchair
Inadvertent
endotracheal
tube removal,
patient is
anxious,
tachypneic.
Sustaining Practice
Creating organizational memory
and knowledge reservoirs were
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CriticalCareNurse
87
Lessons Learned
After 3 months, we were excited
that we had met our aim. More
than 25% of critically ill patients
receiving mechanical ventilation in
that third month had received early
mobility. No serious adverse events
had occurred. Staff were not only
readily identifying patients who were
appropriate for early mobility but
also were obtaining orders for
physical and occupational therapy
for patients who were not receiving
mechanical ventilation. A physical
therapist and an occupational therapist were assigned to the ICU daily.
We had collected data related to
incidence and duration of delirium
and found a problem with the flowsheet design in our electronic medical
record. Additional changes were
88
CriticalCareNurse
Summary
Our purposeful approach to the
implementation of early mobility by
using an EBPI model resulted in sustainment of the practice a year later.
Critical appraisal and synthesis of
the literature resulted in a good protocol for early mobility. High-fidelity
human simulation built confidence
with working together, and this
translated to experiences with early
mobility in actual patients. Lessons
learned from others related to the
use of unit champions and multidisciplinary rounding to help support
the practice change. We continue to
find opportunities to improve our
practice related to the care of patients
receiving mechanical ventilation. CCN
Acknowledgments
The authors acknowledge the leadership and support of Mary Jo Trout, PharmD, RPh, BCPS, Robyn R.
Razor, RN, MSN, and Thomas M. Yunger, Jr, MD,
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
13.
14.
FCCP, DABSM.
Financial Disclosures
None reported.
References
1. Vasilevskis EE, Ely EW, Speroff T, et al.
Reducing iatrogenic risks: ICU-acquired
delirium and weaknesscrossing the quality chasm. Chest. 2012;138(5):1224-1233.
2. Barr J, Fraser GL, Puntillo K, et al. Clinical
practice guidelines for management of pain,
agitation and delirium in adult patients in
In Our Unit
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Book Reviews
Becoming Nursey
Kleber K. Portland, OR: Book Baby
Publishing; 2014. Paperback; 186 pages;
$12.99 (print), $7.99 (eBook). ISBN-13:
978-1483542460
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Anatomy of
Research for
Nurses
Hedges C, Williams B.
Indianapolis, IN: Sigma
Theta Tau International;
2014. Paperback; 352
pages. ISBN-13: 978-1938835117
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Foundations of
Clinical Nurse
Specialist
Practice
2nd edition
Fulton JS, Lyon BL,
Goudreau KA, eds.
New York, NY: Springer Publishing; 2014.
Paperback; 512 pages. ISBN-13: 9780826129666
This book is both a text for educating new clinical nurse specialists
(CNSs) and for the benefit of CNSs
in practice to continue their professional development journey. While
giving the history and context of the
role, this edition reaches into the
present and future opportunities
within the health care system for the
unique contributions of the CNS. As
health care continues to change, so
do the ways in which a CNS affects
patients and families, nurses, and
systems in the 3 spheres of influence.
The authors also discuss entrepreneurship, billing and reimbursement, and regulation of practice.
Finally, short exemplar chapters
demonstrate how the CNS role can
be implemented to achieve positive
outcomes in multiple settings.
Palliative Care
Nursing: Quality
Care to the
End of Life
4th edition
Matzo M, Sherman DW,
eds. New York, NY:
Springer Publishing; 2015. Hardcover;
704 pages. ISBN-13: 978-9826196354
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Education Directory
FLORIDA
Miami
CCRN/PCCN Review Course
Date: February 20-21, 2015. Place: Nova Southeastern University.
Address: 8585 SW 124th Ave, FL 33183. Keynote Speaker: Mary Ann
Cammy Fancher. Sponsor: Greater Miami Area Chapter of AACN.
Contact: Joe Falise. Phone: (954) 594-1427. E-mail: jfalise@med.miami
.edu. Fee: Members, $140; nonmembers, $170; groups of 3 or more,
$130/person; 1-day course (all attendees), $100. Credits: 14 CEUs
Miami
SCRN (Stroke Certified Registered Nurse) Review Course
Date: February 20-21, 2015. Place: Nova Southeastern University.
Address: 8585 SW 124th Ave, FL 33183. Keynote Speaker: Kendra
Kent. Sponsor: Greater Miami Area Chapter of AACN. Contact:
Ruth Salathe. Phone: (305) 586-4203. E-mail: ruthsalathe@gmail.com.
Fee: Members, $150; nonmembers, $175; groups of 3 or more,
$140/person (applies only if registration received together); 1-day
course (all attendees), $100. Credits: 14 CEUs
Orlando
Certification in Legal Nurse Consulting (5-day Seminar and Online)
Date: April 13-17, 2015. Place: Marriott Orlando Airport. Address:
7499 Augusta National Dr, Orlando, FL 32822. Keynote Speaker:
Vickie L. Milazzo. Sponsor: Vickie Milazzo Institute. Phone: (800)
880-0944. Fax: (713) 942-8075. E-mail: mail@LegalNurse.com.
Website: www.LegalNurse.com. Fee: Varies. Credits: 25.3 CEUs
(5-day seminar); 40 CEUs (online)
Plantation
40th Annual Spring Seminar
Date: April 18, 2015. Place: Renaissance Hotel. Address: 1230 South
Pine Island, Plantation, FL 33324. Keynote Speakers: Teri Lynn Kiss,
Kendra Menzies-Kent, Douglas Houghton, Mary Ann Cammy
Fancher. Sponsor: Broward County Chapter of AACN. Contact:
Patty Kelly. Phone: (954) 722-8020. E-mail: pattykelly7 @att.net.
Fee: Members, $75; nonmembers, $100 before April 1, 2015.
Credits: 6.5 CEUs
OREGON
Eugene
PCCN/CCRN Review
Date: February 11-12, 2015. Place: Valley River Inn. Address:
1000 Valley River Way, Eugene, OR 97401. Keynote Speaker:
Nicole Kupchik. Sponsor: Willamette Valley Chapter of AACN.
Contact: Denise Hendrickson. Phone: (541) 868-6620. E-mail:
willamettevalleychapter@gmail.com. Credits: Applied
TEXAS
Tyler
CCRN/PCCN Review
Date: February 26-27, 2015. Place: Wisenbaker Conference
Center, Trinity Mother Frances Hospital, Tyler, TX. Keynote
Speaker: Julie Miller. Sponsor: Greater East Texas Chapter of
AACN. Contact: Kim Thompson. E-mail: getaacn@gmail.com.
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NATIONWIDE
Nurse Leaders/Managers/Directors
The improving economy will require more interim Nurse Leaders.
Contact Nielsen Healthcare Group for a variety of opportunities. You choose your assignment; there are no fees or contract
to limit your options.
Send resume to: nhcg@primary.net
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ILLINOIS
Itasca
Midwest Conference
Date: March 23-24, 2015. Place: Eaglewood Resort and SPA.
Address: 1401 Nordic Rd, Itasca, IL 60143. Keynote Speakers: TBA.
Sponsor: Midwest Chicago Area Chapter of AACN. Contact: Jenny
A. Zaker. Phone: (847) 309-0662. E-mail: zakerj46@gmail.com.
Fee: TBA. Credits: TBD
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