Key result
Cardiac troponin I (cTnI-ultra) levels were significantly higher in term newborns with HIE compared to healthy controls (0.135 vs 0.0183 microg/l; p<0.0005).
Why the study?
Does early measurement of serum cardiac troponin I (cTnI-ultra) predict the presence, severity, and mortality of hypoxic-ischemic encephalopathy in term newborns?
Case-Control (n=91)
Does early measurement of serum cardiac troponin I (cTnI-ultra) predict the presence, severity, and mortality of hypoxic-ischemic encephalopathy in term newborns?
Absolute Event Rate: 0.135% vs 0.0183%
p-value: p=< 0.0005
Elevated cardiac troponin I levels in the first 24-48 hours after birth can serve as an early diagnostic and prognostic indicator for hypoxic-ischemic encephalopathy and associated mortality in term newborns.
INTRODUCTION: In the last few years the use of cardiac troponin I and T, as diagnostic and prognostic factors of ischemic myocardial injury both in adult and neonatal medicine has been of great interest. OBJECTIVE: The objective of our research was to investigate the significance of cardiac troponin I (cTnl) as an early indicator of the presence and severity of hypoxic-ischemic encephalopathy (HIE) in newborns. METHODS: We analyzed 55 term newborns with HIE diagnosed based on clinical findings and ultrasonographic examination of the central nervous system. Serum concentration of cTnl-ultra was determined by immunoenzyme method during the first 24-48 hours after birth, and the obtained findings were compared with the values of identical parameter in 36 healthy term newborns. RESULTS: During the first 24-48 hrs after birth, serum concentration of cTnI-ultra was significantly higher (p < 0.0005) in term newborns with HIE (0.135 +/- 0.207 microg/l) and median (0.07, 0.01-006 microg/l) in comparison to control group (0.0183 +/- 0.026 microg/l and median 0.01 (0.01-0.01 microg/l), with the cTnl-ultra level rising proportionally to the clinical HIE stages. The increase of cTnI-ultra of > 0.12 microg/l indicated the development of significant cerebral damage with the sensitivity of 75% and specificity of 72.2%, while the cTnI-ultra level of > 0.13 microg/l was a significant mortality predictor with sensitivity of 76.9% and specificity of 73.8%. CONCLUSION: The second generation cardiac troponin I assay highly correlates with clinical and ultrasonographic findings in neonates with HIE, so that it can be used as a significant diagnostic and prognostic indicator of this pathological condition.
No takes yet. Share an insight, caveat, or question.
Simović et al. (2012) conducted a case-control in Hypoxic-ischemic encephalopathy (HIE) after perinatal asphyxia (n=91). Cardiac troponin I (cTnI-ultra) level vs. Healthy term newborns was evaluated on Serum concentration of cTnI-ultra (p=< 0.0005). Cardiac troponin I (cTnI-ultra) levels were significantly higher in term newborns with HIE compared to healthy controls (0.135 vs 0.0183 microg/l; p<0.0005).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: