Postpartum psychiatric disorders and subsequent live birth: a population-based cohort study in Denmark.


Journal

Human reproduction (Oxford, England)
ISSN: 1460-2350
Titre abrégé: Hum Reprod
Pays: England
ID NLM: 8701199

Informations de publication

Date de publication:
28 04 2020
Historique:
received: 22 07 2019
revised: 08 01 2020
pubmed: 1 4 2020
medline: 28 4 2021
entrez: 1 4 2020
Statut: ppublish

Résumé

Are women with a history of first-onset postpartum psychiatric disorders after their first liveborn delivery less likely to have a subsequent live birth? Women with incident postpartum psychiatric disorders are less likely to go on to have further children. Women are particularly vulnerable to psychiatric disorders in the postpartum period. The potential effects of postpartum psychiatric disorders on the mother's future chances of live birth are so far under-researched. A population-based cohort study consisted of 414 571 women who had their first live birth during 1997-2015. We followed the women for a maximum of 19.5 years from the date of the first liveborn delivery until the next conception leading to a live birth, emigration, death, their 45th birthday or 30 June 2016, whichever occurred first. Postpartum psychiatric disorders were defined as filling a prescription for psychotropic medications or hospital contact for psychiatric disorders for the first time within 6 months postpartum. The outcome of interest was time to the next conception leading to live birth after the first liveborn delivery. Records on the death of a child were obtained through the Danish Register of Causes of Death. Cox regression was used to estimate the hazard ratios (HRs), stratified by the survival status of the first child. Altogether, 4327 (1.0%) women experienced postpartum psychiatric disorders after their first liveborn delivery. The probability of having a subsequent live birth was 69.1% (95% CI: 67.4-70.7%) among women with, and 82.3% (95% CI: 82.1-82.4%) among those without, postpartum psychiatric disorders. Women with postpartum psychiatric disorders had a 33% reduction in the rate of having second live birth (HR = 0.67, 95% CI: 0.64-0.69), compared to women without postpartum psychiatric disorders. The association disappeared if the first child died (HR = 1.01, 95% CI: 0.85-1.20). If postpartum psychiatric disorders required hospitalisations, this was associated with a more pronounced reduction in live birth rate, irrespective of the survival status of the first child (HR = 0.54, 95% CI: 0.47-0.61 if the first child survived, and HR = 0.49, 95% CI: 0.23-1.04 if the first child died). The use of population-based registers allows for the inclusion of a representative cohort with almost complete follow-up. The large sample size enables us to perform detailed analyses, accounting for the survival status of the child. However, we did not have accurate information on stillbirths and miscarriages, and only pregnancies that led to live birth were included. Our study is the first study to investigate subsequent live birth after postpartum psychiatric disorders in a large representative population. The current study indicates that postpartum psychiatric disorders have a significant impact on subsequent live birth, as women experiencing these disorders have a decreased likelihood of having more children. However, the variations in subsequent live birth rate are influenced by both the severity of the disorders and the survival status of the first-born child, indicating that both personal choices and decreased fertility may have a role in the reduced subsequent live birth rate among women with postpartum psychiatric disorders. This work was supported by the Danish Council for Independent Research (DFF-5053-00156B), the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No. 837180, AUFF NOVA (AUFF-E 2016-9-25), iPSYCH, the Lundbeck Foundation Initiative for Integrative Psychiatric Research (R155-2014-1724), Niels Bohr Professorship Grant from the Danish National Research Foundation and the Stanley Medical Research Institute, the National Institute of Mental Health (NIMH) (R01MH104468) and Fabrikant Vilhelm Pedersen og Hustrus Legat. The authors do not declare any conflicts of interest. N/A.

Identifiants

pubmed: 32227097
pii: 5811215
doi: 10.1093/humrep/deaa016
pmc: PMC7192534
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

958-967

Subventions

Organisme : NIMH NIH HHS
ID : R01 MH104468
Pays : United States

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For permissions, please e-mail: journals.permission@oup.com.

Références

Nat Rev Dis Primers. 2018 Apr 26;4:18022
pubmed: 29695824
Am J Psychiatry. 2016 Feb 1;173(2):117-27
pubmed: 26514657
Arch Gen Psychiatry. 2003 Jan;60(1):29-36
pubmed: 12511170
Acta Obstet Gynecol Scand. 2019 Jun;98(6):753-760
pubmed: 30648732
Clin Epidemiol. 2015 Nov 17;7:449-90
pubmed: 26604824
Scand J Public Health. 2011 Jul;39(7 Suppl):91-4
pubmed: 21775362
Scand J Public Health. 2011 Jul;39(7 Suppl):54-7
pubmed: 21775352
JAMA. 2006 Dec 6;296(21):2582-9
pubmed: 17148723
J Adv Nurs. 2018 Jun;74(6):1236-1244
pubmed: 29394456
Hum Reprod. 2018 Aug 1;33(8):1557-1565
pubmed: 30010921
Scand J Public Health. 2011 Jul;39(7 Suppl):26-9
pubmed: 21775346
BMJ. 2012 Nov 08;345:e7085
pubmed: 23137820
Am J Epidemiol. 1988 Dec;128(6):1352-63
pubmed: 3195572
Int J Eat Disord. 2016 Mar;49(3):260-75
pubmed: 26711005
Scand J Public Health. 2011 Jul;39(7 Suppl):95-8
pubmed: 21775363
Am J Psychiatry. 2016 Dec 1;173(12):1179-1188
pubmed: 27609245
Am J Psychiatry. 2002 Jun;159(6):991-7
pubmed: 12042188
Evol Med Public Health. 2016 Mar 14;2016(1):71-84
pubmed: 26976787
Arch Gen Psychiatry. 2000 Dec;57(12):1157-62
pubmed: 11115329
J Obstet Gynecol Neonatal Nurs. 2004 Jul-Aug;33(4):410-20
pubmed: 15346666
Int J Epidemiol. 2017 Jun 1;46(3):798-798f
pubmed: 27789670
Birth. 2002 Mar;29(1):40-6
pubmed: 11843788
Clin Epidemiol. 2018 Aug 28;10:1073-1082
pubmed: 30214312
Eur J Epidemiol. 2018 Jan;33(1):27-36
pubmed: 29349587
Am J Psychiatry. 2012 Jun;169(6):609-15
pubmed: 22407083
Transl Psychiatry. 2016 Oct 18;6(10):e919
pubmed: 27754485
JAMA Psychiatry. 2019 Oct 16;:
pubmed: 31617870
Biostatistics. 2000 Dec;1(4):423-39
pubmed: 12933565
Acta Obstet Gynecol Scand. 1999 Apr;78(4):305-9
pubmed: 10203297
Scand J Public Health. 2011 Jul;39(7 Suppl):22-5
pubmed: 21775345
BJPsych Open. 2016 Sep 7;2(5):294-300
pubmed: 27703792
Obstet Gynecol. 2015 May;125(5):1224-35
pubmed: 25932852
Infant Behav Dev. 2010 Feb;33(1):1-6
pubmed: 19962196
PLoS One. 2015 Jul 10;10(7):e0132280
pubmed: 26162087

Auteurs

X Liu (X)

The National Centre for Register-based Research, Aarhus University, Aarhus, Denmark.

O Plana-Ripoll (O)

The National Centre for Register-based Research, Aarhus University, Aarhus, Denmark.

K G Ingstrup (KG)

The National Centre for Register-based Research, Aarhus University, Aarhus, Denmark.

E Agerbo (E)

The National Centre for Register-based Research, Aarhus University, Aarhus, Denmark.
CIRRAU-Centre for Integrated Register-based Research, Aarhus University, Aarhus, Denmark.
Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Denmark.

R Skjærven (R)

Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
Centre for Fertility and Health, Norwegian Institute of Public Health, Oslo, Norway.

T Munk-Olsen (T)

The National Centre for Register-based Research, Aarhus University, Aarhus, Denmark.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH