Abstract
Bleeding caused by coagulopathy is common in children undergoing cardiac surgery and causes adverse outcomes. Coagulation testing assists selection of treatments to stop bleeding but has an uncertain role for predicting bleeding. We aimed to evaluate how well prospective coagulation testing predicted excessive bleeding during and after cardiac surgery compared to prediction using clinical characteristics alone. The study was a single-center, prospective cohort study in children having a range of cardiac surgery procedures with coagulation testing at anesthetic induction and immediately after cardiopulmonary bypass. The primary outcome was clinical concern about bleeding (CCB), a composite of either administration of prohemostatic treatments in response to bleeding or a high chest drain volume after surgery. In 225 children, CCB occurred in 26 (12%) during surgery and in 68 (30%) after surgery. Multivariable fractional polynomial models using the clinical characteristics of the children alone predicted CCB during surgery (c-statistic 0.64; 95% confidence interval 0.53, 0.76) and after surgery (0.74; 0.67, 0.82). Incorporating coagulation test results into these models improved prediction (c-statistics 0.79; 0.70, 0.87, and 0.80; 0.74, 0.87, respectively). However, this increased the overall proportion of children classified correctly as CCB or not CCB during surgery by only 0.9% and after surgery by only 0.4%. Incorporating coagulation test results into predictive models had no effect on prediction of blood transfusion or postoperative complications. Prospective coagulation testing marginally improves prediction of CCB during and after cardiac surgery but the clinical impact of this is small when compared to prediction using clinical characteristics.
| Original language | English |
|---|---|
| Number of pages | 12 |
| Journal | Seminars in Thoracic and Cardiovascular Surgery |
| Early online date | 12 Jan 2021 |
| DOIs | |
| Publication status | E-pub ahead of print - 12 Jan 2021 |
Bibliographical note
Funding Information:Funding: The study was supported by the UK National Institute for Health Research through the Biomedical Research Centre at University Hospitals Bristol NHS Foundation Trust and the University of Bristol , and the British Heart Foundation . This study was designed and delivered in collaboration with the Clinical Trials and Evaluation Unit, Bristol Trials Centre, a UKCRC registered clinical trials unit, which is in receipt of NIHR CTU support funding. The views expressed are those of the author(s) and not necessarily those of the NIHR or the Department of Health and Social Care. The British Heart Foundation provided additional support.
Publisher Copyright:
© 2021
Research Groups and Themes
- Bristol Heart Institute
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