S100B as a biomarker of brain injury in premature neonates. A prospective case – control longitudinal study

2020 ◽  
Vol 510 ◽  
pp. 781-786
Author(s):  
Dimitra Metallinou ◽  
Grigorios Karampas ◽  
Georgia Nyktari ◽  
Nikoletta Iacovidou ◽  
Katerina Lykeridou ◽  
...  
2021 ◽  
Vol 11 (9) ◽  
pp. 1243
Author(s):  
Dimitra Metallinou ◽  
Grigorios Karampas ◽  
Eleftheria Lazarou ◽  
Nikoletta Iacovidou ◽  
Panagiota Pervanidou ◽  
...  

Disruption of normal intrauterine brain development is a significant consequence of premature birth and may lead to serious complications, such as neonatal brain injury (NBI). This prospective case-control longitudinal study aimed at determining the levels and prognostic value of serum activin A during the first three days of life in human premature neonates which later developed NBI. It was conducted in a single tertiary hospital and eligible participants were live-born premature (<34 weeks) neonates. Each case (n = 29) developed NBI in the form of an intraventricular haemorrhage, or periventricular leukomalacia, and was matched according to birth weight and gestational age to one neonate with normal head ultrasound scans. Serum activin A levels in both groups showed a stable concentration during the first three days of life as no difference was observed within the two groups from the first to the third day. Neonates diagnosed with NBI had significantly higher activin A levels during the first two days of life compared to control neonates and its levels correlated to the severity of NBI during the second and third day of life. Although serum activin A on the second day was the best predictor for neonates at risk to develop NBI, the overall predictive value was marginally fair (area under the ROC-curve 69.2%). Activin A, in combination with other biomarkers, may provide the first clinically useful panel for the early detection of premature neonates at high risk of NBI.


2017 ◽  
Vol 98 (11) ◽  
pp. 2118-2125.e1 ◽  
Author(s):  
Pradeep Suri ◽  
Kelly Stolzmann ◽  
Katherine M. Iverson ◽  
Rhonda Williams ◽  
Mark Meterko ◽  
...  

2018 ◽  
Vol 61 (1) ◽  
pp. 18-26 ◽  
Author(s):  
Gian Candrian ◽  
Andreas Müller ◽  
Patrizia Dall’Acqua ◽  
Kyveli Kompatsiari ◽  
Gian-Marco Baschera ◽  
...  

2017 ◽  
Vol 31 (4) ◽  
pp. 306-312 ◽  
Author(s):  
Yoshitaka Suzuki ◽  
Caroline Arbour ◽  
Samar Khoury ◽  
Jean-François Giguère ◽  
Ronald Denis ◽  
...  

2015 ◽  
Vol 16 (5) ◽  
pp. 508-514 ◽  
Author(s):  
Maroun J. Mhanna ◽  
Wael EI Mallah ◽  
Margaret Verrees ◽  
Rajiv Shah ◽  
Dennis M. Super

OBJECT Decompressive craniectomy (DC) for the management of severe traumatic brain injury (TBI) is controversial. The authors sought to determine if DC improves the outcome of children with severe TBI. METHODS In a retrospective, case-control study, medical records of all patients admitted to the pediatric ICU between May 1998 and May 2008 with severe TBI and treated with DC were identified and matched to patients who were treated medically without DC. Medical records were reviewed for patients’ demographic data and baseline characteristics. RESULTS During the study period, 17 patients with severe TBI treated with DC at a median of 2 hours (interquartile range [IQR] 1–14 hours) after admission were identified and matched to 17 contemporary controls. On admission, there were no differences between DC and control patients regarding age (10.2 ± 5.9 years vs 12.4 ± 5.4 years, respectively [mean ± SD]), sex, weight, Glasgow Coma Scale score (median 5 [IQR 3–7] vs 4 [IQR 3–6], respectively; p = 0.14), or the highest intracranial pressure (median 42 [IQR 22–54] vs 30 [IQR 21–36], respectively; p = 0.77). However, CT findings were significant for a higher rate of herniation and cerebral edema among patients with DC versus controls (7/17 vs 2/17, respectively, had herniation [p = 0.05] and 14/17 vs 6/17, respectively, had cerebral edema [p = 0.006]). Overall there were no significant differences in survival between patients with DC and controls (71% [12/17] vs 82% [14/17], respectively; p = 0.34). However, among survivors, at 4 years (IQR 1–6 years) after the TBI, 42% (5/12) of the DC patients had mild disability or a Glasgow Outcome Scale score of 5 vs none (0/14) of the controls (p = 0.012). CONCLUSIONS In this retrospective, small case-control study, the authors have shown that early DC in pediatric patients with severe TBI improves outcome in survivors. Future prospective randomized controlled studies are needed to confirm these findings.


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