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Association of Adult Congenital Heart Disease With Pregnancy, Maternal, and Neonatal Outcomes

IMPORTANCE: With the help of medical advances, more women with adult congenital heart disease (ACHD) are becoming pregnant. Adverse maternal, obstetric, and neonatal events occur more frequently in women with ACHD than in the general obstetric population. Adult congenital heart disease is heterogene...

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Autores principales: Ramage, Kaylee, Grabowska, Kirsten, Silversides, Candice, Quan, Hude, Metcalfe, Amy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Association 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6512464/
https://www.ncbi.nlm.nih.gov/pubmed/31074818
http://dx.doi.org/10.1001/jamanetworkopen.2019.3667
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author Ramage, Kaylee
Grabowska, Kirsten
Silversides, Candice
Quan, Hude
Metcalfe, Amy
author_facet Ramage, Kaylee
Grabowska, Kirsten
Silversides, Candice
Quan, Hude
Metcalfe, Amy
author_sort Ramage, Kaylee
collection PubMed
description IMPORTANCE: With the help of medical advances, more women with adult congenital heart disease (ACHD) are becoming pregnant. Adverse maternal, obstetric, and neonatal events occur more frequently in women with ACHD than in the general obstetric population. Adult congenital heart disease is heterogeneous, yet few studies have assessed whether maternal and neonatal outcomes differ across ACHD subtypes. OBJECTIVE: To assess the association of ACHD and its subtypes with pregnancy, maternal, and neonatal outcomes. DESIGN, SETTING, AND PARTICIPANTS: This cross-sectional study used data from the Discharge Abstract Database, which contains information on all hospitalizations in Canada (except Quebec) from fiscal years 2001-2002 through 2014-2015. Discharge Abstract Database information was linked with maternal and infant hospital records across Canada. All women who gave birth in hospitals during the study period were included in the study. Data were analyzed from December 18, 2017, to March 22, 2019. EXPOSURES: Women with ACHD were identified using diagnostic and procedural codes. Subtypes of ACHD were classified using the Anatomic and Clinical Classification of Congenital Heart Defects scheme. MAIN OUTCOMES AND MEASURES: Primary outcomes were defined a priori and included severe maternal morbidity (measured using the Maternal Morbidity Outcomes Indicator), neonatal morbidity and mortality (measured using the Neonatal Adverse Outcomes Indicator), ischemic placental disease, preterm birth, congenital anomalies, and small-for-gestational-age births. Absolute and relative rates of each outcome were calculated overall and by ACHD subtype. Logistic regression using generalized estimating equations assessed crude and adjusted odds ratios (aORs) for each outcome in women with ACHD compared with women without ACHD after adjustment for comorbidities, mode of delivery, and study year. RESULTS: The 2114 women with ACHD included in the analysis (mean [SD] age, 29.4 [5.7] years) had significantly higher odds of maternal morbidity (aOR, 2.7; 95% CI, 2.2-3.4) and neonatal morbidity and mortality (aOR, 1.8; 95% CI, 1.6-2.1) compared with women without ACHD (n = 2 682 451). Substantial variation was observed between women with different subtypes of ACHD. For example, the aORs of preterm birth (<37 weeks) varied from 0.4 (95% CI, 0.4-0.5) for women with anomalies of atrioventricular junctions and valves to 4.7 (95% CI, 2.9-7.5) for women with complex anomalies of atrioventricular connections. CONCLUSIONS AND RELEVANCE: These results suggest that women with different subtypes of ACHD are not uniformly at risk for adverse maternal and neonatal outcomes. Although some women with ACHD can potentially expect healthy pregnancies, it appears that clinical care should be modified to address the heightened risks of certain ACHD subtypes.
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spelling pubmed-65124642019-05-28 Association of Adult Congenital Heart Disease With Pregnancy, Maternal, and Neonatal Outcomes Ramage, Kaylee Grabowska, Kirsten Silversides, Candice Quan, Hude Metcalfe, Amy JAMA Netw Open Original Investigation IMPORTANCE: With the help of medical advances, more women with adult congenital heart disease (ACHD) are becoming pregnant. Adverse maternal, obstetric, and neonatal events occur more frequently in women with ACHD than in the general obstetric population. Adult congenital heart disease is heterogeneous, yet few studies have assessed whether maternal and neonatal outcomes differ across ACHD subtypes. OBJECTIVE: To assess the association of ACHD and its subtypes with pregnancy, maternal, and neonatal outcomes. DESIGN, SETTING, AND PARTICIPANTS: This cross-sectional study used data from the Discharge Abstract Database, which contains information on all hospitalizations in Canada (except Quebec) from fiscal years 2001-2002 through 2014-2015. Discharge Abstract Database information was linked with maternal and infant hospital records across Canada. All women who gave birth in hospitals during the study period were included in the study. Data were analyzed from December 18, 2017, to March 22, 2019. EXPOSURES: Women with ACHD were identified using diagnostic and procedural codes. Subtypes of ACHD were classified using the Anatomic and Clinical Classification of Congenital Heart Defects scheme. MAIN OUTCOMES AND MEASURES: Primary outcomes were defined a priori and included severe maternal morbidity (measured using the Maternal Morbidity Outcomes Indicator), neonatal morbidity and mortality (measured using the Neonatal Adverse Outcomes Indicator), ischemic placental disease, preterm birth, congenital anomalies, and small-for-gestational-age births. Absolute and relative rates of each outcome were calculated overall and by ACHD subtype. Logistic regression using generalized estimating equations assessed crude and adjusted odds ratios (aORs) for each outcome in women with ACHD compared with women without ACHD after adjustment for comorbidities, mode of delivery, and study year. RESULTS: The 2114 women with ACHD included in the analysis (mean [SD] age, 29.4 [5.7] years) had significantly higher odds of maternal morbidity (aOR, 2.7; 95% CI, 2.2-3.4) and neonatal morbidity and mortality (aOR, 1.8; 95% CI, 1.6-2.1) compared with women without ACHD (n = 2 682 451). Substantial variation was observed between women with different subtypes of ACHD. For example, the aORs of preterm birth (<37 weeks) varied from 0.4 (95% CI, 0.4-0.5) for women with anomalies of atrioventricular junctions and valves to 4.7 (95% CI, 2.9-7.5) for women with complex anomalies of atrioventricular connections. CONCLUSIONS AND RELEVANCE: These results suggest that women with different subtypes of ACHD are not uniformly at risk for adverse maternal and neonatal outcomes. Although some women with ACHD can potentially expect healthy pregnancies, it appears that clinical care should be modified to address the heightened risks of certain ACHD subtypes. American Medical Association 2019-05-10 /pmc/articles/PMC6512464/ /pubmed/31074818 http://dx.doi.org/10.1001/jamanetworkopen.2019.3667 Text en Copyright 2019 Ramage K et al. JAMA Network Open. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the CC-BY License.
spellingShingle Original Investigation
Ramage, Kaylee
Grabowska, Kirsten
Silversides, Candice
Quan, Hude
Metcalfe, Amy
Association of Adult Congenital Heart Disease With Pregnancy, Maternal, and Neonatal Outcomes
title Association of Adult Congenital Heart Disease With Pregnancy, Maternal, and Neonatal Outcomes
title_full Association of Adult Congenital Heart Disease With Pregnancy, Maternal, and Neonatal Outcomes
title_fullStr Association of Adult Congenital Heart Disease With Pregnancy, Maternal, and Neonatal Outcomes
title_full_unstemmed Association of Adult Congenital Heart Disease With Pregnancy, Maternal, and Neonatal Outcomes
title_short Association of Adult Congenital Heart Disease With Pregnancy, Maternal, and Neonatal Outcomes
title_sort association of adult congenital heart disease with pregnancy, maternal, and neonatal outcomes
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6512464/
https://www.ncbi.nlm.nih.gov/pubmed/31074818
http://dx.doi.org/10.1001/jamanetworkopen.2019.3667
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