Long-term maternal mortality risk following spontaneous preterm birth: A retrospective cohort study.


Journal

BJOG : an international journal of obstetrics and gynaecology
ISSN: 1471-0528
Titre abrégé: BJOG
Pays: England
ID NLM: 100935741

Informations de publication

Date de publication:
11 2023
Historique:
revised: 10 03 2023
received: 11 07 2022
accepted: 05 05 2023
pmc-release: 01 11 2024
medline: 26 10 2023
pubmed: 22 5 2023
entrez: 22 5 2023
Statut: ppublish

Résumé

To determine whether women with spontaneous preterm birth (PTB) have increased risks for long-term mortality. Retrospective cohort. Births in Utah between 1939 and 1977. We included women with a singleton live birth ≥20 weeks who survived at least 1 year following delivery. We excluded those who had never lived in Utah, had improbable birthweight/gestational age combinations, underwent induction (except for preterm membrane rupture) or had another diagnosis likely to cause PTB. Exposed women had ≥1 spontaneous PTB between 20 Overall and cause-specific mortality risks were compared using Cox regression. We included 29 048 exposed and 57 992 matched unexposed women. There were 3551 deaths among exposed (12.2%) and 6013 deaths among unexposed women (10.4%). Spontaneous PTB was associated with all-cause mortality (adjusted hazard ratio [aHR] 1.26, 95% confidence interval [CI] 1.21-1.31), death from neoplasms (aHR 1.10, 95% CI 1.02-1.18), circulatory disease (aHR 1.35, 95% CI 1.25-1.46), respiratory disease (aHR 1.73, 95% CI 1.46-2.06), digestive disease (aHR 1.33, 95% CI 1.12-1.58), genito-urinary disease (aHR 1.60, 95% CI 1.15-2.23) and external causes (aHR 1.39, 95% CI 1.22-1.58). Spontaneous PTB is associated with modestly increased risks for all-cause and some cause-specific mortality.

Identifiants

pubmed: 37212439
doi: 10.1111/1471-0528.17552
pmc: PMC10592573
mid: NIHMS1902309
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1483-1490

Subventions

Organisme : NIA NIH HHS
ID : R01AG022095
Pays : United States
Organisme : NIMHD NIH HHS
ID : R01 MD011609
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23HL159316
Pays : United States
Organisme : NIEHS NIH HHS
ID : K24ES031131
Pays : United States
Organisme : NIMHD NIH HHS
ID : R01MD011609
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG022095
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL159316
Pays : United States
Organisme : NIEHS NIH HHS
ID : K24 ES031131
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2023 John Wiley & Sons Ltd.

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Auteurs

Lauren H Theilen (LH)

Department of Obstetrics and Gynecology, University of Utah Health, Salt Lake City, Utah, USA.
Intermountain Healthcare, Women and Newborns Clinical Program, Salt Lake City, Utah, USA.

Ibrahim Hammad (I)

Department of Obstetrics and Gynecology, University of Utah Health, Salt Lake City, Utah, USA.
Intermountain Healthcare, Women and Newborns Clinical Program, Salt Lake City, Utah, USA.

Huong Meeks (H)

Huntsman Cancer Institute, Utah Population Database, Salt Lake City, Utah, USA.

Alison Fraser (A)

Huntsman Cancer Institute, Utah Population Database, Salt Lake City, Utah, USA.

Tracy A Manuck (TA)

Department of Obstetrics and Gynecology, University of Utah Health, Salt Lake City, Utah, USA.
Department of Obstetrics and Gynecology, University of North Carolina-Chapel Hill, Chapel Hill, North Carolina, USA.

Michael W Varner (MW)

Department of Obstetrics and Gynecology, University of Utah Health, Salt Lake City, Utah, USA.
Intermountain Healthcare, Women and Newborns Clinical Program, Salt Lake City, Utah, USA.

Ken R Smith (KR)

Huntsman Cancer Institute, Utah Population Database, Salt Lake City, Utah, USA.

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