Professional Documents
Culture Documents
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David Leaper, MD, ChM, FRCS, FACS, FLS1; Donald Fry, BSc, MD,
FACS2,3; Ojan Assadian, MD, DTMH4
ealth care-associated infections (HCAIs) are infections that are acquired through contact with any aspect of health care. They can
cause minor complications or serious disability or death, and can involve a wide variety of resistant or emergent organisms.1 Examples of HCAIs
include respiratory tract infections such as hospital- and ventilator-associated
pneumonias complicated by Gram-negative, nonfermenting bacilli that are resistant to almost all classes of antibiotics; and urinary tract infections caused
by microorganisms resistant to the quinolones and increased by the presence
of a catheter, mostly involving coliforms that can produce extended spectrum beta-lactamases (and, more worryingly, metallo-beta-lactamases, such as
the newly described New Delhi-metallo-beta-lactamase 1 [NDM-1],2,3 making bacteria resistant to a wide range of beta-lactam antibiotics, including all
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wound discharge (eg, after open hernia surgery) to being life threatening (eg, mediastinitis and sternal wound
infection).12 In between, HCAIs contribute to scars which
may be cosmetically unacceptable to the patient, cause
pain, require prolonged length of hospital stay with the
incurred expenses, and result in poor emotional well-being for the patient.13
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Organ/Space SSI
Infection occurs within 30 days of operation or within 1 year if an implant is present;
infection involves anatomic structures not opened or manipulated by the operation; and
at least 1 of the following:
o purulent drainage from a drain placed by a stab wound into the organ/space;
o organisms isolated from organ/space by aseptic culturing technique;
o identification of abscess in the organ/space by direct examination, during reoperation, or by histopathological or radiological examination; or
o diagnosis of organ/space SSI by surgeon or attending physician.
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Adapted from16 Horan TC, Gaynes RP, Martone WJ, Jarvis WR, Emori TG. CDC definitions of nosocomial surgical site infections, 1992: a
modification of CDC definitions of surgical wound infections. Infect Control Hosp Epidemiol. 1992;13(10):606-608.
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the National Nosocomial Infections Surveillance index included contaminated wound, the American Society of Anesthesiologists Physical Status classification system grade,
and duration of surgery. They have been compared28,29
and both were found capable of predicting SSI.
Apart from the unrecorded indirect costs related to loss
of productivity, reduced quality of life, and litigation, the
actual cost of an SSI can involve additional inpatient treatment and procedures that can run into many thousands
of pounds.30 The morbidity and mortality rates which follow sternal infection after cardiac surgery are just one
example.31 There is a paucity of prospective cost-benefit
analysis of the SSI, but retrospective analyses clearly identify that the economic costs of SSI are substantial.32
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i. Patient factors
age sex obesity smoking
immunosuppression
steroids, cancer, anticancer therapy (chemo and radiotherapy), HIV
nutritional indices
metabolic factors
diabetes mellitus, hepato0renal failure, serum albumin,
haemoglobin
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Adapted from85 Fry DE. Surgical site Infection. In: Fry DE, ed. Surgical Infections. London, UK: JP Medical Publishers Ltd;2013:4962.
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Conclusion
References
1.
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Microbiological investigations may support the diagnosis of SSI and surgical infections, provided specimens
are obtained appropriately. Thereby, microorganisms that
are potentially causative for infection are yielded, and not
colonized flora, which have no relevance for a suspected
infection. Optimal results are achieved from specimens
obtained directly from the infection site. Such material
may include explanted grafts, extra- or intra-operatively
obtained tissue biopsies from the infected area, and material aspirated from peri-graft fluid collection. Indirectly
obtained material, such as blood cultures, may also yield
important information. However, blood cultures may often be negative, particularly in late-onset infection, but
are more frequently positive in early-onset infection.76
Specimens may be processed using a number of techniques such as direct streaking swabs on agar plates, broth
culture, homogenization of tissue specimens with serial
dilution techniques, and sonication of the specimen to
enhance the recovery of biofilm-forming organisms from
graft or infected material.77 The report of processed microbiological specimens is decisive for a valuable evaluation
of therapy and clinical results.78,79 The demonstration of
specimens relevance from the pre-, intra- and postoperative phases is considered most valuable, if feasible and possible.80 Relevant preoperative samples include blood cultures taken from central and peripheral venous catheters
or direct vein puncture, wound specimens, drainage fluid,
nose and throat swabs in the case of MRSA colonization,
and urinary samples. In any case, all responsible microorganisms should be classified according to their type (eg,
Gram-positive or -negative, fungi, etc.) and specific therapy antibiograms offered for highly virulent microorganisms (eg, Pseudomonas aeruginosa). Careful assessment
is needed for microorganisms isolated from overlying
wounds or sinuses, as such microorganisms may represent
colonizing flora, (eg, MRSA), and may be wrongly interpreted as causative agents.76 Relevant intraoperative samples
are standard specimens obtained from the surgical site, the
peri-graft fluid/pus, or explanted prosthetic material.Worth
Microbiological Diagnosis
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2.
3.
4.
5.
6.
National Clinical Guideline Centre (UK). Infection: Prevention and Control of Healthcare-Associated Infections
in Primary and Community Care: Partial Update of NICE
Clinical Guideline 2. London, UK: Royal College of Physicians; 2012.
Johnson AP, Woodford N. Global spread of antibiotic resistance: the example of New Delhi metallo--lactamase
(NDM)-mediated carbapenem resistance.J Med Microbiol. 2013;62(Pt 4):499-513.
Nordmann P, Poirel L, Walsh TR, Livermore DM. The
emerging NDM carbapenemases. Trends Microbiol.
2011;19(12):588-595.
He M, Miyajima F, Roberts P, et al. Emergence and global
spread of epidemic healthcare-associated Clostridium difficile. Nat Genet. 2013;45(1):109-113.
World Health Organization. WHO Guidelines for Safe Surgery 2009: Safe Surgery Saves Lives. http://whqlibdoc.
who.int/publications/2009/9789241598552_eng.pdf. Accesssed October 31, 2013.
Plowman R, Graves N, Griffin MA, et al. The rate and cost
of hospital-acquired infections occurring in patients admitted to selected specialities of a district general hospi-
Leaper et al
11.
12.
13.
14.
N
O
15.
16.
17.
18.
TE
IC
PL
10.
9.
8.
7.
321
Leaper et al
IC
TE
46. Moran GJ, Krishnadasan A, Gorwitz RJ, et al. Methicillinresistant S. aureus infections among patients in the emergency department. N Engl J Med. 2006;355(7):666-674.
47. Tanner J, Woodings D, Moncaster K. Preoperative hair removal to reduce surgical site infection. Cochrane Database Syst Rev. 2006;19(3):CD004122.
48. Kurz A, Sessler DI, Lenhardt R. Perioperative normothermia to reduce the incidence of surgical-wound infection
and shorten hospitalization. Study of Wound Infection and
Temperature Group. N Engl J Med. 1996;334(19):12091215.
49. National Collaborating Centre for Nursing and Supportive Care.The management of inadvertent perioperative
hypothermia in adults. www.nice.org.uk/nicemedia/
live/11962/40429/40429.pdf. Published April 2008. Accessed October 31, 2013.
50. Kumar S,Wong PF, Melling AC, Leaper DJ. Effects of perioperative hypothermia and warming in surgical practice. Int
Wound J. 2005;2(3):193-204.
51. Furnary AP, Zerr KJ, Grunkemeier GL, Starr A. Continuous intravenous insulin infusion reduces the incidence
of deep sternal wound infection in diabetic patients
after cardiac surgical procedures. Ann Thorac Surg.
1999;67(2):352-362.
52. Qadan M, Battista C, Gardner SA, Anderson G, Akca O,
Polk HC Jr. Oxygen and surgical site infection: a study of
underlying immunologic mechanisms. Anesthesiology.
2010;113(2):369-377.
53. Greif R, Aka O, Horn EP, Kurz A, Sessler DI; Outcomes
Research Group. Supplemental perioperative oxygen to
reduce the incidence of surgical-wound infection. N Engl
J Med. 2000;342(3):161-167.
54. Belda FJ, Aguilera L, Garca de la Asuncin J, et al. Supplemental perioperative oxygen and the risk of surgical
wound infection: a randomized controlled trial. JAMA.
2005;294(16):2035-2042.
55. Pryor KO, Fahey TJ 3rd, Lien CA, Goldstein PA. Surgical
site infection and the routine use of perioperative hyperoxia in a general surgical population: a randomized controlled trial. JAMA. 2004;291(1):79-87.
56. Franz MG, Robson MC, Steed DL, et al. Guidelines to aid
healing of acute wounds by decreasing impediments of
healing. Wound Repair Regen. 2008;16(6):723-748.
57. Leaper DJ. Risk factors for and epidemiology of surgical
site infections Surg Infect (Larchmt). 2010;11(3):283-287.
58. Kaye KS, Schmit K, Pieper C, et al. The effect of increasing age on the risk of surgical site infection. J Infect Dis.
2005;191(7):1056-1062.
59. Bode LG, Kluytmans JA, Wertheim H, et al. Preventing sur-
N
O
PL
WOUNDS www.woundsresearch.com
Leaper et al
IC
TE
74. Wang ZX, Jiang CP, Cao Y, Ding YT. Systematic review and
meta-analysis of triclosan-coated sutures for the prevention of surgical site infection. Br J Surg. 2013;100(4):465473.
75. Leaper DJ, Assadian O, Hubner NO, et al. Antimicrobial
sutures and prevention of surgical site infection: assessment of the safety of the antiseptic triclosan. Int Wound J.
2011;8(6):556-566.
76. Miller LG, Perdreau-Remington F, Rieg G, et al. Necrotizing fasciitis caused by community-associated methicillinresistant Staphylococcus aureus in Los Angeles. N Engl J
Med. 2005;352(14):1445-1453.
77. FitzGerald SF, Kelly C, Humphreys H. Diagnosis and treatment of prosthetic aortic graft infections: confusion and
inconsistency in the absence of evidence or consensus. J
Antimicrob Chemother. 2005;56(6):996-999.
78. Bergamini TM, Bandyk DF, Govostis D, Vetsch R, Towne
JB. Identification of Staphylococcus epidermidis vascular graft infections: a comparison of culture techniques. J
Vasc Surg. 1989;9(5):665-670.
79. Bisdas T, Wilhelmi M, Haverich A, Teebken OE. Cryopreserved arterial homografts vs silver-coated Dacron grafts
for abdominal aortic infections with intraoperative evidence of microorganisms. J Vasc Surg. 2011;53(5):12741281.
80. Moll FL, Powell JT, Fraedrich G, et al. Management of abdominal aortic aneurysms clinical practice guidelines of
the European Society for Vascular Surgery. Eur J Vasc Endovasc Surg. 2011;41:1-58.
81. Bisdas TE, Mattner F, Ella O, et al. Significance of infection
markers and microbiological findings during tissue processing of cryopreserved arterial homografts for the early
postoperative course. Vasa. 2009;38(4):365-373.
82. Batt M, Jean-Baptiste E, OConnor S, et al. In-situ revascularization for patients with aortic graft infection: a single
centre experience with silver coated polyester grafts. Eur
J Vasc Endovasc Surg. 2008;36(2):182-188.
83. OConnor S,Andrew P, Batt M, Becquemin JP.A systematic
review and meta-analysis of treatments for aortic graft infection. J Vasc Surg. 2006;44(1):38-45.
84. Tran NK, Wisner DH, Albertson TE, et al. Multiplex polymerase chain reaction pathogen detection in patients
with suspected septicemia after trauma, emergency, and
burn surgery. Surgery. 2012;151(3):456-463.
85. Fry DE. Surgical site infections. In: Fry DE, ed. Surgical
Infections. London, UK: JP Medical Publishes Ltd;2013;4962.
N
O
PL
gical site infection in nasal carriers of Staphylococcus aureus. N Engl J Med. 2010;362(1):9-17.
60. Guenaga KK, Matos D,Wille-Jrgensen P. Mechanical bowel preparation for elective colorectal surgery. Cochrane
Database Syst Rev. 2009;(1):CD001544.
61. Poth EJ. Historical development of intestinal antisepsis.
World J Surg. 1982;6(2):153-159.
62. Washington JA 2nd, Dearing WH, Judd ES, Elveback LR. Effect of perioperative antibiotic regimen on development
of infection after intestinal surgery; prospective, randomized, double- blind study. Ann Surg. 1974;180(4):567-572.
63. Clarke JS, Condon RE, Bartlett JG, Gorbach SL, Nichols
RL, Ochi S. Preoperative oral antibiotics reduce septic
complications of colon operations: results of prospective, randomized, double-blind clinical study. Ann Surg.
1977;186(3):251-259.
64. Lewis RT. Oral versus systemic antibiotic prophylaxis
in elective colon surgery: a randomized study and meta-analysis send a message from the 1990s. Can J Surg.
2002;45(3):173-180.
65. Fry DE. Colon preparation and surgical site infection. Am
J Surg. 2011;202(2):225-232.
66. Darouiche RO, Wall MJ Jr, Itani KM, et al. Chlorhexidine-alcohol versus povidone-iodine for surgical site antisepsis.
N Engl J Med. 2010;362(1):18-26.
67. Leaper DJ. Surgical-site infection. Br J Surg.
2010;97(11):1610-1602.
68. Noorani A, Rabey N, Walsh SR, Davies RJ. Systematic review and meta-analysis of preoperative antisepsis with
chlorhexidine versus povidoneiodine in clean-contaminated surgery. Br J Surg. 2010;97(11):1614-1620.
69. Fournel I, Tiv M, Soulias M, Hua C, Astruc K, Aho Glele
LS. Meta-analysis of intraoperative povidoneiodine application to prevent surgical-site infection. Br J Surg.
2010;97(11):1603-1613.
70. Rozzelle CJ, Leonardo J, Li V. Antimicrobial suture wound
closure for cerebrospinal fluid shunt surgery: a prospective, double-blinded, randomized controlled trial. J Neurosurg Pediatr. 2008;2(2):111-117.
71. Justinger C, Moussavian MR, Schlueter C, Kopp B, Kollmar
O, Schilling MK. Antibacterial [corrected] coating of abdominal closure sutures and wound infection. Surgery.
2009;145(3):330-334.
72. Galal I, El-Hindawy K. Impact of using triclosan-antibacterial sutures on incidence of surgical site infection. Am J
Sur. 2011;202(2):133-138.
73. Fleck T, Moidl R, Blacky A, et al. Triclosan-coated sutures
for the reduction of sternal wound infections: economic
considerations. Ann Thorac Surg. 2007;84(1):232-236.
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