Repeat low order caesarean delivery, risk factors for complications: A retrospective, longitudinal study

One-third of cesarean deliveries (CDs) are repeat operations, of which the majority are low-order, second (CD2) and third (CD3). The study objectives were to identify risk factors for a complicated maternal CD among women undergoing a repeat low-order CD and to develop a predictive model for at-risk...

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Veröffentlicht in:PloS one 2023-02, Vol.18 (2), p.e0276869-e0276869
Hauptverfasser: Reichman, Orna, Rottenstreich, Misgav, Sela, Hen Y, Michaelson-Cohen, Rachel, Ehrlich, Zvi, Rotem, Reut, Grisaru-Granovsky, Sorina
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Rottenstreich, Misgav
Sela, Hen Y
Michaelson-Cohen, Rachel
Ehrlich, Zvi
Rotem, Reut
Grisaru-Granovsky, Sorina
description One-third of cesarean deliveries (CDs) are repeat operations, of which the majority are low-order, second (CD2) and third (CD3). The study objectives were to identify risk factors for a complicated maternal CD among women undergoing a repeat low-order CD and to develop a predictive model for at-risk women. A retrospective longitudinal follow-up study was conducted in a single medical center, during 2005-2016. Women who underwent both CD2 and CD3 at the site were included. Those with placenta accreta or a caesarean hysterectomy were excluded. A composite complicated maternal CD was defined by either uterine rupture/dehiscence, blood transfusion, relaparotomy, admission to the intensive care unit or prolonged operative time >90th percentile. Data was analyzed comparing between CD2 to CD3, each woman served as her own control. Univariate analysis followed by a multivariate logistic regression modeling were performed with an OR of 95% CI defining significance. The study group comprised of 1,331 women. A complicated CD occurred in 159 (12%) vs. 226 (17%) of CD2 vs. CD3 respectively, (p
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The study objectives were to identify risk factors for a complicated maternal CD among women undergoing a repeat low-order CD and to develop a predictive model for at-risk women. A retrospective longitudinal follow-up study was conducted in a single medical center, during 2005-2016. Women who underwent both CD2 and CD3 at the site were included. Those with placenta accreta or a caesarean hysterectomy were excluded. A composite complicated maternal CD was defined by either uterine rupture/dehiscence, blood transfusion, relaparotomy, admission to the intensive care unit or prolonged operative time &gt;90th percentile. Data was analyzed comparing between CD2 to CD3, each woman served as her own control. Univariate analysis followed by a multivariate logistic regression modeling were performed with an OR of 95% CI defining significance. The study group comprised of 1,331 women. A complicated CD occurred in 159 (12%) vs. 226 (17%) of CD2 vs. CD3 respectively, (p&lt;0.001). Women with a complicated CD2 were at higher risk for complications in CD3, aOR 2.3 (95% CI 1.5, 3.3). Sub-Saharan African origin and preterm delivery at CD3 were both risk factors for a complicated CD3, aOR 3.7 (95% CI 1.9, 7.3) and aOR 1.7 (95% CI 1.1, 2.7), respectively. The multivariate regression model included 1328 cases, was statistically significant, χ2(7) = 50.760, p &lt;0.001, explained 6.3% of the variance of composite complicated maternal CD3 and correctly classified 82.9% of cases. Although a complicated CD2, Sub-Saharan African origin and preterm delivery are risk factors for maternal complications in CD3, it is hard to predict which specific women will experience complications. Sensitivity, specificity, positive and negative predictive value of a complicated CD2 for detecting complications in CD3 were 21%, 90%, 30% and 85% respectively.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0276869</identifier><identifier>PMID: 36753477</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Abdomen ; Adhesion ; Blood transfusion ; Blood transfusions ; CD3 antigen ; Cesarean section ; Cesarean Section - adverse effects ; Chi-square test ; Complications ; Complications and side effects ; Dehiscence ; Electronic health records ; Female ; Follow-Up Studies ; Health care facilities ; Health risks ; Humans ; Hysterectomy ; Infant, Newborn ; Infections ; Intensive care ; Longitudinal Studies ; Medical centers ; Medical records ; Medical research ; Medicine and Health Sciences ; Medicine, Experimental ; Multivariate analysis ; Obstetrics ; Patient outcomes ; Placenta ; Prediction models ; Pregnancy ; Premature Birth - etiology ; Regression models ; Retrospective Studies ; Risk Factors ; Skin ; Statistical analysis ; Vagina ; Variables</subject><ispartof>PloS one, 2023-02, Vol.18 (2), p.e0276869-e0276869</ispartof><rights>Copyright: © 2023 Reichman et al. 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The study objectives were to identify risk factors for a complicated maternal CD among women undergoing a repeat low-order CD and to develop a predictive model for at-risk women. A retrospective longitudinal follow-up study was conducted in a single medical center, during 2005-2016. Women who underwent both CD2 and CD3 at the site were included. Those with placenta accreta or a caesarean hysterectomy were excluded. A composite complicated maternal CD was defined by either uterine rupture/dehiscence, blood transfusion, relaparotomy, admission to the intensive care unit or prolonged operative time &gt;90th percentile. Data was analyzed comparing between CD2 to CD3, each woman served as her own control. Univariate analysis followed by a multivariate logistic regression modeling were performed with an OR of 95% CI defining significance. The study group comprised of 1,331 women. A complicated CD occurred in 159 (12%) vs. 226 (17%) of CD2 vs. CD3 respectively, (p&lt;0.001). Women with a complicated CD2 were at higher risk for complications in CD3, aOR 2.3 (95% CI 1.5, 3.3). Sub-Saharan African origin and preterm delivery at CD3 were both risk factors for a complicated CD3, aOR 3.7 (95% CI 1.9, 7.3) and aOR 1.7 (95% CI 1.1, 2.7), respectively. The multivariate regression model included 1328 cases, was statistically significant, χ2(7) = 50.760, p &lt;0.001, explained 6.3% of the variance of composite complicated maternal CD3 and correctly classified 82.9% of cases. Although a complicated CD2, Sub-Saharan African origin and preterm delivery are risk factors for maternal complications in CD3, it is hard to predict which specific women will experience complications. Sensitivity, specificity, positive and negative predictive value of a complicated CD2 for detecting complications in CD3 were 21%, 90%, 30% and 85% respectively.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>36753477</pmid><doi>10.1371/journal.pone.0276869</doi><tpages>e0276869</tpages><orcidid>https://orcid.org/0000-0003-0809-6089</orcidid><oa>free_for_read</oa></addata></record>
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subjects Abdomen
Adhesion
Blood transfusion
Blood transfusions
CD3 antigen
Cesarean section
Cesarean Section - adverse effects
Chi-square test
Complications
Complications and side effects
Dehiscence
Electronic health records
Female
Follow-Up Studies
Health care facilities
Health risks
Humans
Hysterectomy
Infant, Newborn
Infections
Intensive care
Longitudinal Studies
Medical centers
Medical records
Medical research
Medicine and Health Sciences
Medicine, Experimental
Multivariate analysis
Obstetrics
Patient outcomes
Placenta
Prediction models
Pregnancy
Premature Birth - etiology
Regression models
Retrospective Studies
Risk Factors
Skin
Statistical analysis
Vagina
Variables
title Repeat low order caesarean delivery, risk factors for complications: A retrospective, longitudinal study
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