Cardiomyopathies in Pregnancy: Trends and Clinical Outcomes in Delivery Hospitalizations in the United States (2005-2020).

Adverse Pregnancy Outcomes Cardiomyopathy Cardiovascular Disease Pregnancy

Journal

Current problems in cardiology
ISSN: 1535-6280
Titre abrégé: Curr Probl Cardiol
Pays: Netherlands
ID NLM: 7701802

Informations de publication

Date de publication:
17 Sep 2024
Historique:
received: 04 09 2024
accepted: 16 09 2024
medline: 20 9 2024
pubmed: 20 9 2024
entrez: 19 9 2024
Statut: aheadofprint

Résumé

Cardiomyopathy (CDM) in pregnancy is associated with maternal morbidity and mortality. To explore trends and clinical outcomes in CDM subtypes during delivery hospitalizations. We used the National Inpatient Sample database to identify delivery hospitalizations between 2005-2020 by CDM subtypes: peripartum (PPCM), dilated (DCM), hypertrophic (HCM), and restrictive (RCM). Maternal and fetal outcomes were identified using International Classification of Diseases, 9th and 10th Revision, Clinical Modification codes. Baseline characteristics and temporal trends of CDM subtypes were analyzed. Maternal cardiovascular, pregnancy, and fetal outcomes were evaluated by CDM subtype using univariate logistic regression. The primary outcome was in-hospital mortality. During 2005-2020, 37,125 out of 61,811,842 delivery hospitalizations were complicated by CDM. Among CDM-related delivery hospitalizations, the most prevalent were DCM (46%), followed by PPCM (45.6%), HCM (4.6%), and RCM (3.9%). The rates of in-hospital mortality (1.7%), adverse cardiovascular events such as acute heart failure (17%), cardiogenic shock (3.4%), and cardiac arrest (3.1%), and adverse pregnancy outcomes such as preeclampsia (14.2%) and preterm labor (11%), were highest among PPCM (all p < 0.0001). The prevalence of PPCM (49.1% to 38.5%) decreased while the prevalence of HCM (2.7% to 8.8%) and DCM (48% to 52.2%) increased over time. Over a 15-year period, PPCM had higher rates of in-hospital mortality, cardiovascular events, and adverse pregnancy outcomes compared to other CDM subtypes. While the prevalence of PPCM decreased over time, the prevalence of HCM and DCM increased. Hence, further research on cardiomyopathies during pregnancy and prospective studies on this vulnerable patient cohort are urgently needed.

Sections du résumé

BACKGROUND BACKGROUND
Cardiomyopathy (CDM) in pregnancy is associated with maternal morbidity and mortality.
OBJECTIVES OBJECTIVE
To explore trends and clinical outcomes in CDM subtypes during delivery hospitalizations.
METHODS METHODS
We used the National Inpatient Sample database to identify delivery hospitalizations between 2005-2020 by CDM subtypes: peripartum (PPCM), dilated (DCM), hypertrophic (HCM), and restrictive (RCM). Maternal and fetal outcomes were identified using International Classification of Diseases, 9th and 10th Revision, Clinical Modification codes. Baseline characteristics and temporal trends of CDM subtypes were analyzed. Maternal cardiovascular, pregnancy, and fetal outcomes were evaluated by CDM subtype using univariate logistic regression. The primary outcome was in-hospital mortality.
RESULTS RESULTS
During 2005-2020, 37,125 out of 61,811,842 delivery hospitalizations were complicated by CDM. Among CDM-related delivery hospitalizations, the most prevalent were DCM (46%), followed by PPCM (45.6%), HCM (4.6%), and RCM (3.9%). The rates of in-hospital mortality (1.7%), adverse cardiovascular events such as acute heart failure (17%), cardiogenic shock (3.4%), and cardiac arrest (3.1%), and adverse pregnancy outcomes such as preeclampsia (14.2%) and preterm labor (11%), were highest among PPCM (all p < 0.0001). The prevalence of PPCM (49.1% to 38.5%) decreased while the prevalence of HCM (2.7% to 8.8%) and DCM (48% to 52.2%) increased over time.
CONCLUSIONS CONCLUSIONS
Over a 15-year period, PPCM had higher rates of in-hospital mortality, cardiovascular events, and adverse pregnancy outcomes compared to other CDM subtypes. While the prevalence of PPCM decreased over time, the prevalence of HCM and DCM increased. Hence, further research on cardiomyopathies during pregnancy and prospective studies on this vulnerable patient cohort are urgently needed.

Identifiants

pubmed: 39299364
pii: S0146-2806(24)00490-0
doi: 10.1016/j.cpcardiol.2024.102855
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

102855

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of competing interest Dr. Sharma is supported by the AHA grant 979,462. Dr. Ibrahim reports consulting income from Cytokinetics and honoraria from Applied Therapeutics. All other authors have no conflict of interest to report.

Auteurs

Danish Iltaf Satti (DI)

Division of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Eunjung Choi (E)

Division of Cardiovascular Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Harsh P Patel (HP)

Department of Cardiology, Southern Illinois University School of Medicine, Springfield, IL, USA.

Mohammed Faisaluddin (M)

Department of Internal Medicine, Rochester General Hospital, Rochester, NY, USA.

Adhya Mehta (A)

Department of Internal Medicine, Jacobi Medical Center, Albert Einstein College of Medicine, Bronx, NY, USA.

Bhavin Patel (B)

Department of Internal Medicine, Saint Joseph Mercy Oakland Hospital, Pontiac, MI, USA.

Chigolum Pamela Oyeka (CP)

Division of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Shruti Hegde (S)

Department of Cardiology, Southern Illinois University School of Medicine, Springfield, IL, USA.

Yaa Adoma Kwapong (YA)

Division of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Jeffrey Shi Kai Chan (JSK)

Cardiovascular Analytics Group, China-UK Collaboration, Hong Kong, China.

Shannon Anderson (S)

Division of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Nasrien E Ibrahim (NE)

Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Shashank S Sinha (SS)

Inova Schar Heart and Vascular, Inova Fairfax Medical Campus, Falls Church, Virginia, USA.

Sourbha S Dani (SS)

Division of Cardiovascular Medicine, Department of Medicine, Lahey Hospital and Medical Center, Burlington, MA, USA.

Garima Sharma (G)

Inova Schar Heart and Vascular, Inova Fairfax Medical Campus, Falls Church, Virginia, USA. Electronic address: Garima.Sharma@inova.org.

Classifications MeSH