Outcomes and Care Quality Metrics for Women of Reproductive Age Living With Rheumatic Heart Disease in Uganda.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
21 04 2020
Historique:
pubmed: 17 4 2020
medline: 9 3 2021
entrez: 17 4 2020
Statut: ppublish

Résumé

Background Rheumatic heart disease disproportionately affects women of reproductive age, as it increases the risk of cardiovascular complications and death during pregnancy and childbirth. In sub-Saharan Africa, clinical outcomes and adherence to guideline-based therapies are not well characterized for this population. Methods and Results In a retrospective cohort study of the Uganda rheumatic heart disease registry between June 2009 and May 2018, we used multivariable regression and Cox proportional hazards models to compare comorbidities, mortality, anticoagulation use, and treatment cascade metrics among women versus men aged 15 to 44 with clinical rheumatic heart disease. We included 575 women and 252 men with a median age of 27 years. Twenty percent had New York Heart Association Class III-IV heart failure. Among patients who had an indication for anticoagulation, women were less likely than men to receive a prescription of warfarin (66% versus 81%; adjusted odds ratio, 0.37; 95% CI, 0.14-0.96). Retention in care (defined as a clinic visit within the preceding year) was poor among both sexes in this age group (27% for men, 24% for women), but penicillin adherence rates were high among those retained (89% for men, 92% for women). Mortality was higher in men than women (26% versus 19% over a median follow-up of 2.7 years; adjusted hazard ratio, 1.66; 95% CI, 1.18-2.33). Conclusions Compared with men, women of reproductive age with rheumatic heart disease in Uganda have lower rates of appropriate anticoagulant prescription but also lower mortality rates. Retention in care is poor among both men and women in this age range, representing a key target for improvement.

Identifiants

pubmed: 32295465
doi: 10.1161/JAHA.119.015562
pmc: PMC7428530
doi:

Substances chimiques

Anticoagulants 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e015562

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR002548
Pays : United States
Organisme : NCRR NIH HHS
ID : UL1 RR024989
Pays : United States
Organisme : NCATS NIH HHS
ID : TL1 TR001084
Pays : United States

Commentaires et corrections

Type : ErratumIn

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Auteurs

Andrew Y Chang (AY)

Division of Cardiovascular Medicine Stanford University Stanford CA.
Department of Medicine Stanford University Stanford CA.
Center for Innovation in Global Health Stanford University Stanford CA.

Juliet Nabbaale (J)

Uganda Heart Institute Mulago Hospital Kampala Uganda.
University Hospitals Harrington Heart & Vascular Institute Case Western Reserve University Cleveland OH.

Emmy Okello (E)

Uganda Heart Institute Mulago Hospital Kampala Uganda.

Isaac Ssinabulya (I)

Uganda Heart Institute Mulago Hospital Kampala Uganda.

Michele Barry (M)

Department of Medicine Stanford University Stanford CA.
Center for Innovation in Global Health Stanford University Stanford CA.

Andrea Z Beaton (AZ)

The Heart Institute Cincinnati Children's Hospital Medical Center & The University of Cincinnati School of Medicine Cincinnati OH.

Allison R Webel (AR)

Frances Payne Bolton School of Nursing Case Western Reserve University Cleveland OH.

Chris T Longenecker (CT)

University Hospitals Harrington Heart & Vascular Institute Case Western Reserve University Cleveland OH.

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