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Peer-reviewedCC BY 4.0Journal of Clinical Medicine

Clinical and Laboratory Factors Associated with Exchange Transfusion in Neonates with Severe Hyperbilirubinaemia: A Retrospective Cohort Study

  1. 1Department of Paediatrics, Şanlıurfa Education and Research Hospital, 63200 Şanlıurfa, Türkiye
  2. 2Department of Paediatrics, Private Hospital, Osmangazi Cad. No:34 Sarigazi, Sancaktepe, 34885 İstanbul, Türkiye

Abstract

Background and Objectives: Exchange transfusion (ET) remains a critical intervention for severe neonatal hyperbilirubinaemia, yet laboratory associations with ET receipt require careful interpretation. We examined characteristics associated with ET and post-procedure laboratory changes. Materials and Methods: This retrospective tertiary-centre cohort included 98 neonates evaluated between January 2020 and December 2025 (65 received ET; 33 did not). A four-covariate logistic regression model assessed associations with ET receipt. Discrimination, bootstrap optimism, cross-validated calibration and an exploratory creatinine-containing model were examined. Results: Peak total serum bilirubin (TSB) was higher among ET recipients than non-recipients (33.69 ± 6.31 versus 26.19 ± 3.64 mg/dL; p < 0.001). In the primary model (n = 98), peak TSB was associated with ET receipt (adjusted odds ratio 1.31 per mg/dL, 95% confidence interval 1.16–1.48; p < 0.001). The apparent area under the receiver operating characteristic curve (AUC) was 0.860, decreasing to 0.837 after bootstrap optimism correction. An exploratory six-covariate model (n = 97) yielded an apparent AUC of 0.874 and an optimism-corrected AUC of 0.836. Creatinine showed an adjusted association (odds ratio 1.58 per 0.1 mg/dL, 95% confidence interval 1.07–2.32), but its incremental AUC was uncertain (difference 0.014, 95% confidence interval −0.022 to 0.053). Following ET, bilirubin, platelet count and total calcium decreased. Conclusions: Peak TSB strongly distinguished infants who received ET, but this association partly reflects the bilirubin-based indication for treatment. Creatinine did not demonstrate a reliable incremental discrimination benefit. These findings reinforce guideline-based ET assessment and post-exchange monitoring, not the adoption of new treatment thresholds or prediction tools.

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BibTeX
@article{izol2026clinical,
  title = {{Clinical and Laboratory Factors Associated with Exchange Transfusion in Neonates with Severe Hyperbilirubinaemia: A Retrospective Cohort Study}},
  author = {Aslıhan İzol and Selçuk Yazıcı and Sümeyya Ercan},
  journal = {Journal of Clinical Medicine},
  year = {2026},
  month = nov,
  doi = {10.3390/jcm15218762},
  url = {https://www.mdpi.com/2077-0383/15/21/8762},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Clinical and Laboratory Factors Associated with Exchange Transfusion in Neonates with Severe Hyperbilirubinaemia: A Retrospective Cohort Study
AU  - Aslıhan İzol
AU  - Selçuk Yazıcı
AU  - Sümeyya Ercan
PY  - 2026
DA  - 2026/11/09
JO  - Journal of Clinical Medicine
DO  - 10.3390/jcm15218762
UR  - https://www.mdpi.com/2077-0383/15/21/8762
AB  - Background and Objectives: Exchange transfusion (ET) remains a critical intervention for severe neonatal hyperbilirubinaemia, yet laboratory associations with ET receipt require careful interpretation. We examined characteristics associated with ET and post-procedure laboratory changes. Materials and Methods: This retrospective tertiary-centre cohort included 98 neonates evaluated between January 2020 and December 2025 (65 received ET; 33 did not). A four-covariate logistic regression model assessed associations with ET receipt. Discrimination, bootstrap optimism, cross-validated calibration and an exploratory creatinine-containing model were examined. Results: Peak total serum bilirubin (TSB) was higher among ET recipients than non-recipients (33.69 ± 6.31 versus 26.19 ± 3.64 mg/dL; p < 0.001). In the primary model (n = 98), peak TSB was associated with ET receipt (adjusted odds ratio 1.31 per mg/dL, 95% confidence interval 1.16–1.48; p < 0.001). The apparent area under the receiver operating characteristic curve (AUC) was 0.860, decreasing to 0.837 after bootstrap optimism correction. An exploratory six-covariate model (n = 97) yielded an apparent AUC of 0.874 and an optimism-corrected AUC of 0.836. Creatinine showed an adjusted association (odds ratio 1.58 per 0.1 mg/dL, 95% confidence interval 1.07–2.32), but its incremental AUC was uncertain (difference 0.014, 95% confidence interval −0.022 to 0.053). Following ET, bilirubin, platelet count and total calcium decreased. Conclusions: Peak TSB strongly distinguished infants who received ET, but this association partly reflects the bilirubin-based indication for treatment. Creatinine did not demonstrate a reliable incremental discrimination benefit. These findings reinforce guideline-based ET assessment and post-exchange monitoring, not the adoption of new treatment thresholds or prediction tools.
SN  - 2077-0383
ER  -