Tendency Prediction for Atonic Bleeding Following a Problem-Free Pregnancy

Atsushi Yanaihara, Shouta Hatakeyama, Shirei Ougi, Aguri Hirano, Takumi Yanaihara

Abstract


Background: The incidence of postpartum hemorrhage (PPH) has increased globally; however, the reasons for this are largely unknown. PPH is potentially fatal and atonic PPH can occur even in low-risk pregnancies. In this study, we aimed to identify the causes of atonic bleeding following a problem-free pregnancy.

Methods: One thousand, four hundred sixty-six patients with problem-free pregnancies who experienced total bleeding 2 h after vaginal delivery were divided into two groups based on the amount of blood loss: control group (n = 1,325), with a blood loss of < 800 mL and study group (n = 141) with a blood loss of ≥ 800 mL. Several factors that may correlate with atonic bleeding were divided into three groups: maternal demographic (MD) factors, intrapartum factors, and fatal factors. Comparisons were made between the control group and study group regarding these factors. A multivariate analysis and receiver operating characteristic (ROC) analysis were performed to identify the independent risk factors for atonic bleeding. The continuous net reclassification improvement (NRI) and integrated discrimination improvement (IDI) were also calculated.

Results: The independent factors being statistically significant that predicted over 800 mL of atonic bleeding were in vitro fertilization/intracytoplasmic sperm injection (IVF/ICSI) pregnancies (adjusted odd ratio (OR): 3.63; 95% confidence interval (CI): 2.46 - 5.36; P < 0.001), new-born weight (adjusted OR: 1.0016; 95% CI: 1.0011 - 1.0022; P < 0.001), and the cases of instrumental labor (IL) (adjusted OR: 2.48; 95% CI: 1.64 - 3.77; P < 0.001). ROCs for the final model (area under the curve (AUC): 0.765; 95% CI: 0.724 - 0.806), fatal model (AUC: 0.675; 95% CI: 0.627 - 0.723), intrapartum model (AUC: 0.654; 95% CI: 0.612 - 0.696) and MD model (AUC: 0.615; 95% CI: 0.575 - 0.656) were constructed. The NRI and IDI were 0.733 (95% CI: 0.565 - 0.901; P < 0.0001) and 0.073 (95% CI: 0.051 - 0.90; P < 0.0001) in the fatal model and final model, 0.057 (95% CI: -0.117 - 0.230; P = 0.288) and 0.015 (95% CI: -0.004 - 0.034; P = 0.521) in the MD model, and -0.146 (95% CI: -0.319 - 0.027; P = 0.098) and -0.003 (95% CI: -0.021 - 0.014; P = 0.700) in the intrapartum model.

Conclusions: We concluded that IVF/ICSI pregnancies, new-born weight, and IL were independent factors contributing to atonic bleeding. The coincidence of these three factors significantly predicts the likelihood of atonic bleeding.




J Clin Gynecol Obstet. 2019;8(2):39-43
doi: https://doi.org/10.14740/jcgo540


Keywords


Postpartum hemorrhage; Atonic bleeding; Delivery; Instrumental labor; IVF

Full Text: HTML PDF
 

Browse  Journals  

     

Journal of Clinical Medicine Research

Journal of Endocrinology and Metabolism

Journal of Clinical Gynecology and Obstetrics

World Journal of Oncology

Gastroenterology Research

Journal of Hematology

Journal of Medical Cases

Journal of Current Surgery

Clinical Infection and Immunity

Cardiology Research

World Journal of Nephrology and Urology

Cellular and Molecular Medicine Research

Journal of Neurology Research

International Journal of Clinical Pediatrics

 

 

 

 

 

Journal of Clinical Gynecology & Obstetrics, quarterly, ISSN 1927-1271 (print), 1927-128X (online), published by Elmer Press Inc.                     
The content of this site is intended for health care professionals.
This is an open-access journal, the authors retain the copyright, the journal is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International
License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Creative Commons Attribution license (Attribution-NonCommercial 4.0 International CC-BY-NC 4.0)


This journal follows the International Committee of Medical Journal Editors (ICMJE) recommendations for manuscripts submitted to biomedical journals,
the Committee on Publication Ethics (COPE) guidelines, and the Principles of Transparency and Best Practice in Scholarly Publishing.

website: www.jcgo.org   editorial contact: editor@jcgo.org    elmer.editorial2@hotmail.com
Address: 9225 Leslie Street, Suite 201, Richmond Hill, Ontario, L4B 3H6, Canada

© Elmer Press Inc. All Rights Reserved.


Disclaimer: The views and opinions expressed in the published articles are those of the authors and do not necessarily reflect the views or opinions of the editors and Elmer Press Inc. This website is provided for medical research and informational purposes only and does not constitute any medical advice or professional services. The information provided in this journal should not be used for diagnosis and treatment, those seeking medical advice should always consult with a licensed physician.