Key result
Early elevated troponin I is linked to persistent encephalopathy in newborns with HIE with ~77% sensitivity.
Why the study?
The diagnostic and prognostic utility of early serum troponin I levels within 6 hours in newborns with HIE undergoing therapeutic hypothermia was unclear.
Does early elevation of serum troponin I predict persistent residual encephalopathy at discharge in newborns undergoing therapeutic hypothermia for hypoxic ischemic encephalopathy?
Observational
Does early elevation of serum troponin I predict persistent residual encephalopathy at discharge in newborns undergoing therapeutic hypothermia for hypoxic ischemic encephalopathy?
Effect estimate: Sensitivity 77%, specificity 78%
p-value: p=<0.001
Early elevation of troponin I within 6 hours of age serves as a predictive biomarker for high risk of residual encephalopathy at discharge in newborns with HIE undergoing therapeutic hypothermia.
OBJECTIVE: Elevation of serum troponin I has been reported in newborns with hypoxic ischemic encephalopathy (HIE), but it is diagnostic and prognostic utility for newborn under 6 hours is not clear. Study the predictive value of early serum troponin I levels in newborns with HIE undergoing therapeutic hypothermia (TH) for persistent residual encephalopathy (RE) at discharge. STUDY DESIGN: Retrospective chart review of newborns admitted with diagnosis of HIE to neonatal intensive care unit (NICU) for TH over a period of 3 years. Troponin levels were drawn with the initial set of admission laboratories while initiating TH. Newborns were followed up during hospital course and stratified into three groups based on predischarge examination and their electrical encephalography and cranial MRI findings: Group 1: no RE, Group 2: mild-to-moderate RE, and Group 3: severe RE or needing assisted medical technology or death. Demographic and clinical characteristics including troponin I levels were compared in each group. A cut-off level of troponin I ≥0.12 µg/L had a sensitivity of 77% and specificity of 78% for diagnosis of any RE, positive predictive value of 68%, and a negative predictive value of 84%. CONCLUSION: In newborns undergoing TH for HIE, the elevation of troponin within 6 hours of age predicts high risk of having RE at discharge. KEY POINTS: · Troponin I elevation is a biomarker of myocardial ischemia in adults and children.. · Myocardial ischemia may be part of multi-organ injury in neonatal HIE.. · Early elevation of troponin I level may correlate with the severity of neonatal HIE and predict residual encephalopathy in newborn at discharge from initial hospitalization..
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Munshi et al. (2020) conducted an observational in Hypoxic ischemic encephalopathy. Early serum troponin I levels was evaluated on Persistent residual encephalopathy (RE) at discharge (Sensitivity 77%, specificity 78%, p=<0.001). Early serum troponin I levels ≥0.12 µg/L predicted persistent residual encephalopathy at discharge in newborns with HIE with 77% sensitivity and 78% specificity (P<0.001).
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