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Villeneuve, A., Joyal, J.-S., Proulx, F., Ducruet, T., Poitras, N., & Lacroix, J. (2016). Multiple organ
dysfunction syndrome in critically ill children: clinical value of two lists of diagnostic criteria. Annals of
Intensive Care, 6(1).
PEDIATRIC LOGISTIC ORGAN DYSFUNCTION SCORE
Table PELOD Scoring System.
Scoring System
Organ Dysfunction
and Variable 0 1 10 20
Neurologicala
Glasgow coma 12-15 and 7-11 4-6 or 3
score
Pupillary reactions Both reactive NA Both fixed NA
Cardiovascularb
Heart rate, bpm
<12 years 195 NA >195 NA
12 years 150 NA >150 NA
and or
Systolic blood pressure, mm Hg
<1 month >65 NA 35-65 <35
1 month-1 year >75 NA 35-75 <35
1-12 years >85 NA 45-85 <45
12 years >95 NA 55-95 <55
Renal
Creatinine, mmol/L
<7 days <140 NA 140 NA
7 days-1 year <55 NA 55 NA
1-12 years <100 NA 100 NA
12 years <140 NA 140 NA
Respiratory
Pao2, kPa/FiO2 >9.3 and NA 9.3 or NA
ratio
Paco2, kPa 11.7 and NA >11.7 NA
Mechanical No ventilation Ventilation NA NA
ventilation
Hematological
White blood cell
9
4.5 and 1.5-4.4 <1.5 NA
count, 10 /L9
Platelets, 10 /L 35 <35 NA NA
Hepatic
Aspartate <950 and 950 or NA NA
transaminase, IU/L
Prothrombin time <60 (<1.40) 60 ( 1.4) NA NA
(or INR)
PaO2: use arterial measurement only. PaO2/FiO2 ration cannot be assessed in patients with intracardiac shunts, is considered as normal in children with cyanotic heart
disease. PaCO2 may be measured from arterial, capillary, or venous samples. Mechanical ventilation: use of mask ventilation is not counted as mechanical ventilation.
a b
Glasgow coma score: use lowest value. If patient sedated, record estimated score before sedation. Pupillary reactions:non-reactive pupils must be > 3mm. Do not
assess heart rate and blood pressure during crying or iatrogenic agitation.
Abrreviations: PaO2, arterial oxygen pressure; FiO2, fraction inspired oxygen; NA, not significant; PaCO2, arterial carbon dioxide pressure; PELOD, Pediatric
Logistic Organ Dysfunction; IU, International Units; INR, international normalized ratio.
Russel RA, Jeffries HE, Ghanayem NS. Relationship Between Risk-Adjustment Tools and the Pediatric
Logistic Organ Dysfunction Score. World Journal for Pediatric and
Congenital Heart Surgery 2014, Vol 5(1) 16–21
aAll variables must be collected, but measurements can be done only if justified by the patient’s clinical status. If a variable is not measured, it should be considered
normal. If a variable is measured more than once in 24 h, the worst value is used in calculating the score;
bNeurologic dysfunction - Glasgow coma score: Use the lowest value. If the patient is sedated, record the estimated Glasgow coma score before sedation. Assess only
patients with known or suspected acute central nervous system disease. Pupillary reactions: Nonreactive pupils must be >3 mm. Do not assess after iatrogenic
pupillary dilatation;
cCardiovascular dysfunction: Heart rate and mean arterial pressure: Do not assess during crying or iatrogenic agitation;
dRespiratory dysfunction: PaO2: Use arterial measurement only. PaO2/FiO2 ratio is considered normal in children with cyanotic heart disease. PaCO 2 can be measured
from arterial, capillary, or venous samples. Invasive ventilation: the use of mask ventilation is not considered invasive ventilation. Logit (mortality)=−6.61+0.47 ×
PELOD-2 score; Probability of death=1/ (1+exp [−logit (mortality)]); FiO 2: Fraction of inspired oxygen; PELOD: Pediatric logistic organ dysfunction; PaO2: Arterial
oxygen pressure; WBC: White blood cell
Gulla KM, Sachdev A. Illness severity and organ dysfunction scoring in Pediatric Intensive Care Unit. Indian
J Crit Care Med 2016;20:27-35.
PEDIATRIC RISK OF MORTALITY III, PEDIATRIC INDEX OF MORTALITY 3
PRISM: pediatric risk of mortality; PIM: pediatric index of mortality; SBP: systolic blood pressure; FiO2: fraction of inspired oxygen; PaO2: arterial blood
oxygen partial pressure; BUN: blood urea nitrogen.
a
Low risk: asthma, bronchiolitis, croup, obstructive sleep apnea, diabetic ketoacidosis; high-risk: cardiac arrest, severe combined immune deficiency, leukemia or
lymphoma after fist induction, spontaneous cerebral hemorrhage, cardiomyopathy or myocarditis, hypoplastic left heart syndrome, hu-man immunodeficiency virus
infection, liver failure, neurodegenerative disorder; bLow risk: asthma, bronchiolitis, croup, obstructive sleep apnea, dia-betic ketoacidosis, seizure disorder; high risk:
spontaneous cerebral hemorrhage, cardiomyopathy or myocarditis, hypoplastic left heart syndrome, neu-rodegenerative disorder, necrotizing enterocolitis; very high-
risk: cardiac arrest, severe combined immune deficiency, leukemia or lymphoma after first induction, bone marrow transplant recipient, liver failure.
Jung JW, Soh IS, Kim MJ, et all. Validation of Pediatric Index of Mortality 3 for Predicting Mortality among
Patients Admitted to a Pediatric Intensive Care Unit. Acute and Critical Care 2018; 33(3): 170-177
Physiologic Stability Index (PSI)
Physiologic Stability index (PSI) was developed by a group of paediatric intensivists in 1984 from TISS
Table Physiologic stability Index:
Bhodaria P and Bhagwat AG. Severity Scoring Systems in Paediatric Intensive Care Units. Indian Journal of
Anaesthesia 2008;52:Suppl (5):663-675