TY - JOUR
T1 - Survey of Mode of Delivery and Maternal and Perinatal Outcomes in Canada
AU - Canadian Mode of Delivery Study Group
AU - Yang, Jie
AU - Armson, B. Anthony
AU - Attenborough, Rebecca
AU - Carson, George D.
AU - da Silva, Orlando
AU - Heaman, Maureen
AU - Janssen, Patricia
AU - Murphy, Phil A.
AU - Pasquier, Jean Charles
AU - Sauve, Reg
AU - Von Dadelszen, Peter
AU - Walker, Mark
AU - Lee, Shoo K.
AU - Andruschak, John
AU - Dale, Sheryll
AU - Der, Kenny
AU - Pacheco, Terri
AU - Vida, Karen
AU - Frick, Corrine
AU - Bott, Nancy
AU - Carr, Lee Ann
AU - Bedard, Daniel
AU - Robert, Nicole
AU - Sprague, Ann
AU - Berthiaume, Maryse
AU - Beaudoin, Richard
AU - Fahey, John
AU - Gagnon, Irene
AU - Murphy, Phil
AU - Allen, Victoria
AU - Bocking, Alan
AU - Bottomley, Jim
AU - Bujold, Emmanuel
AU - Campbell, Karen
AU - Christilaw, Jan
AU - Crane, Joan
AU - Dodds, Linda
AU - Donner, Allan
AU - Dumont, Alexandre
AU - Dzakpasu, Susie
AU - Forson, Abigail
AU - Fraser, Bill
AU - Gagnon, Anita
AU - Joseph, K. S.
AU - Klein, Michael
AU - Kramer, Michael
AU - LaFrance, Martine
AU - Lemay, Karine
AU - Liu, Shiliang
AU - Moutquin, Jean Marie
N1 - Funding Information:
Disclosures: Funding for this study was provided by a Canadian Institutes of Health Research Operating Grant of $500 000 CAD. Organizational support for the Canadian Mode of Delivery Study Group was provided by the Maternal-infant Care Research Centre at Mount Sinai Hospital in Toronto, Ontario, Canada. MiCare is supported by a Canadian Institutes of Health Research Team Grant (CTP 87518) and Mount Sinai Hospital. The study sponsors had no role in the study design; the collection, analysis, or interpretation of data; the writing of the report; or the decision to submit the paper for publication. All authors confirm they had full access to all data in the study and accept responsibility to submit for publication.
Funding Information:
The authors thank the investigators and collaborators of the Canadian Mode of Delivery Study Group, including collaborators from the provincial perinatal programs in British Columbia, Alberta, Saskatchewan, Ontario, Québec, Nova Scotia, and Newfoundland and Labrador and those from the World Health Organization. Lists of individual collaborators and their affiliations are presented. The authors thank Heather McDonald Kinkaid, PhD, a scientific writer at the Maternal-infant Care Research Centre at Mount Sinai Hospital in Toronto, Ontario, Canada, for editorial support in preparing this manuscript. They also thank Priscilla Chan, project coordinator, Eugene Yoon, statistician, and other MiCare staff for data management and organizational support. Dr. McDonald Kinkaid's, Priscilla Chan's, and Eugene Yoon's contributions were within the scopes of their employment at MiCare, for which they receive salaries. Canadian Mode of Delivery Study Group Collaborators and Affiliations, Provincial Perinatal Programs, Perinatal Services BC, Provincial Health Services Authority: John Andruschak; Sheryll Dale; Kenny Der; Terri Pacheco; Karen Vida, Alberta Perinatal Health Program: Corrine Frick; Nancy Bott, Regina Qu'Appelle Health Region: Lee-Ann Carr, Better Outcomes Registry & Network (“BORN”), part of the Children's Hospital of Eastern Ontario: Daniel Bedard; Nicole Robert; Ann Sprague, Commission d'accès à l'information du Québec: Maryse Berthiaume; Richard Beaudoin, Reproductive Care Program of Nova Scotia: Rebecca Attenborough; John Fahey; Irene Gagnon, Newfoundland and Labrador Provincial Perinatal Program: Phil Murphy, Other Canadian Mode of Delivery Study Group Collaborators: Victoria Allen: Dalhousie University; Alan Bocking: University of Toronto; Jim Bottomley: Children's Hospital of Eastern Ontario; Emmanuel Bujold: Université Laval; Karen Campbell: University of Western Ontario; Jan Christilaw: University of British Columbia; Joan Crane: Memorial University; Linda Dodds: Dalhousie University; Allan Donner: University of Western Ontario; Alexandre Dumont: Université de Montréal; Susie Dzakpasu: Public Health Agency of Canada; Abigail Forson: Canadian Institutes of Health Research; Bill Fraser: Université de Montréal; Anita Gagnon: McGill University; KS Joseph: Dalhousie University; Michael Klein: University of British Columbia; Michael Kramer: Canadian Institutes of Health Research; Martine LaFrance: Canadian Institutes of Health Research; Karine Lemay: Canadian Institutes of Health Research; Shiliang Liu: Public Health Agency of Canada; Jean-Marie Moutquin: University of Sherbrooke; Carl Nimrod: University of Ottawa; Robert Platt: McGill University; Beverley O'Brien: University of Alberta; Arne Ohlsson: University of Toronto; Shi Wu Wen: University of Ottawa, World Health Organization: Metin Gulmezoghu; Archana Shah; Jose Villar Disclosures: Funding for this study was provided by a Canadian Institutes of Health Research Operating Grant of CAN $500 000. Organizational support for the Canadian Mode of Delivery Study Group was provided by the Maternal-infant Care Research Centre at Mount Sinai Hospital in Toronto, Ontario, Canada. MiCare is supported by a Canadian Institutes of Health Research Team Grant (CTP 87518) and Mount Sinai Hospital. The study sponsors had no role in the study design; the collection, analysis, or interpretation of data; the writing of the report; or the decision to submit the paper for publication. All authors confirm they had full access to all data in the study and accept responsibility to submit for publication.
Publisher Copyright:
© 2022 The Society of Obstetricians and Gynaecologists of Canada/La Société des obstétriciens et gynécologues du Canada
PY - 2022/9
Y1 - 2022/9
N2 - Objective: To identify determinants of cesarean delivery (CD) and examine associations between mode of delivery (MOD) and maternal and perinatal outcomes. Methods: We conducted a retrospective analysis of a Canadian multicentre birth cohort derived from provincial data collected in 2008/2009. Maternal and perinatal characteristics and outcomes were compared between vaginal and cesarean birth and between the following MOD subgroups: spontaneous vaginal delivery (VD), assisted VD, planned cesarean delivery (CD), and intrapartum CD. Multivariate regression identified determinants of CD and the effects of MOD and previous CD on maternal and perinatal outcomes. Results: The cohort included 264 755 births (72.1% VD and 27.9% CD) from 91 participating institutions. Determinants of CD included maternal age, parity, previous CD, chronic hypertension, diabetes, urinary tract infection or pyelonephritis, gestational hypertension, vaginal bleeding, labour induction, pre-term gestational age, low birth weight, large for gestational age, malpresentation, and male sex. CD was associated with greater risk of maternal and perinatal morbidity and mortality. Subgroup analysis demonstrated higher risk of adverse pregnancy outcomes with assisted VD and intrapartum CD than spontaneous VD. Planned CD reduced the risk of obstetric wound hematoma and perinatal mortality but increased maternal and neonatal morbidity. Previous CD increased the risk of maternal and neonatal morbidity among multiparous women. Conclusions: The CD rate in Canada is consistent with global trends reflecting demographic and obstetric intervention factors. The risk of adverse pregnancy outcomes with CD warrants evaluation of interventions to safely prevent nonessential cesarean birth.
AB - Objective: To identify determinants of cesarean delivery (CD) and examine associations between mode of delivery (MOD) and maternal and perinatal outcomes. Methods: We conducted a retrospective analysis of a Canadian multicentre birth cohort derived from provincial data collected in 2008/2009. Maternal and perinatal characteristics and outcomes were compared between vaginal and cesarean birth and between the following MOD subgroups: spontaneous vaginal delivery (VD), assisted VD, planned cesarean delivery (CD), and intrapartum CD. Multivariate regression identified determinants of CD and the effects of MOD and previous CD on maternal and perinatal outcomes. Results: The cohort included 264 755 births (72.1% VD and 27.9% CD) from 91 participating institutions. Determinants of CD included maternal age, parity, previous CD, chronic hypertension, diabetes, urinary tract infection or pyelonephritis, gestational hypertension, vaginal bleeding, labour induction, pre-term gestational age, low birth weight, large for gestational age, malpresentation, and male sex. CD was associated with greater risk of maternal and perinatal morbidity and mortality. Subgroup analysis demonstrated higher risk of adverse pregnancy outcomes with assisted VD and intrapartum CD than spontaneous VD. Planned CD reduced the risk of obstetric wound hematoma and perinatal mortality but increased maternal and neonatal morbidity. Previous CD increased the risk of maternal and neonatal morbidity among multiparous women. Conclusions: The CD rate in Canada is consistent with global trends reflecting demographic and obstetric intervention factors. The risk of adverse pregnancy outcomes with CD warrants evaluation of interventions to safely prevent nonessential cesarean birth.
KW - cesarean section
KW - delivery, obstetric
KW - maternal outcomes
KW - obstetrical forceps
KW - pregnancy outcome
KW - vacuum extraction, obstetrical
UR - http://www.scopus.com/inward/record.url?scp=85133789142&partnerID=8YFLogxK
U2 - 10.1016/j.jogc.2022.04.017
DO - 10.1016/j.jogc.2022.04.017
M3 - Article
C2 - 35595024
AN - SCOPUS:85133789142
SN - 1701-2163
VL - 44
SP - 960
EP - 971
JO - Journal of Obstetrics and Gynaecology Canada
JF - Journal of Obstetrics and Gynaecology Canada
IS - 9
ER -