Evaluation of the sexual health in people living with hemophilia.


Journal

Haemophilia : the official journal of the World Federation of Hemophilia
ISSN: 1365-2516
Titre abrégé: Haemophilia
Pays: England
ID NLM: 9442916

Informations de publication

Date de publication:
Nov 2021
Historique:
revised: 26 08 2021
received: 18 07 2018
accepted: 31 08 2021
pubmed: 20 9 2021
medline: 11 11 2021
entrez: 19 9 2021
Statut: ppublish

Résumé

Knowledge about sexual health, difficulty with sexual activity and intimacy (sexual difficulty), in people with hemophilia is little understood. The objectives were to determine the prevalence of sexual difficulty in people living with hemophilia (PWH) compared to people with no bleeding disorders (PWNoBD), and to determine factors associated with it. This was an analysis of the PROBE study. We recruited individuals who had hemophilia A or B (PWH) and PWNoBD who were 18 years old or older. We calculated proportions of participants with sexual difficulty and odds ratios (ORs) adjusted for sex and age with 95% confidence intervals. There were 2007 PWH and 1972 PWNoBD. Mean (standard deviation) age was 41 (15) years in PWH and 42 (13) years in PWNoBD. Sexual difficulty was reported in 302 (15.1%) PWH and 79 (4.0%) PWNoBD. The odds of sexual difficulty were significantly higher in PWH (OR 3.82, 95% CI 2.85, 5.11). Among PWH, older age, experiencing acute or chronic pain in the past 12 months, bleeds within the past two weeks, ≥3 spontaneous joint bleeds (past six months), limitation of range of motion of any joints, and any life- or limb-threatening bleeds in the past 12 months were associated with sexual difficulty. Sexual difficulty is more prevalent in people living with hemophilia and associated with markers of disease severity. Sexual health issues should be incorporated in comprehensive hemophilia care, future research, and hemophilia related health policy.

Sections du résumé

BACKGROUND BACKGROUND
Knowledge about sexual health, difficulty with sexual activity and intimacy (sexual difficulty), in people with hemophilia is little understood.
OBJECTIVES OBJECTIVE
The objectives were to determine the prevalence of sexual difficulty in people living with hemophilia (PWH) compared to people with no bleeding disorders (PWNoBD), and to determine factors associated with it.
METHODS METHODS
This was an analysis of the PROBE study. We recruited individuals who had hemophilia A or B (PWH) and PWNoBD who were 18 years old or older. We calculated proportions of participants with sexual difficulty and odds ratios (ORs) adjusted for sex and age with 95% confidence intervals.
RESULTS RESULTS
There were 2007 PWH and 1972 PWNoBD. Mean (standard deviation) age was 41 (15) years in PWH and 42 (13) years in PWNoBD. Sexual difficulty was reported in 302 (15.1%) PWH and 79 (4.0%) PWNoBD. The odds of sexual difficulty were significantly higher in PWH (OR 3.82, 95% CI 2.85, 5.11). Among PWH, older age, experiencing acute or chronic pain in the past 12 months, bleeds within the past two weeks, ≥3 spontaneous joint bleeds (past six months), limitation of range of motion of any joints, and any life- or limb-threatening bleeds in the past 12 months were associated with sexual difficulty.
CONCLUSIONS CONCLUSIONS
Sexual difficulty is more prevalent in people living with hemophilia and associated with markers of disease severity. Sexual health issues should be incorporated in comprehensive hemophilia care, future research, and hemophilia related health policy.

Identifiants

pubmed: 34538001
doi: 10.1111/hae.14410
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

993-1001

Informations de copyright

© 2021 John Wiley & Sons Ltd.

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Auteurs

Federico Germini (F)

Department of Medicine, McMaster University, Hamilton, ON, Canada.
Department of HEI, McMaster University, Hamilton, ON, Canada.

Chatree Chai-Adisaksopha (C)

Department of Medicine, McMaster University, Hamilton, ON, Canada.
Department of HEI, McMaster University, Hamilton, ON, Canada.

Drashti Pete (D)

Department of HEI, McMaster University, Hamilton, ON, Canada.

Randall Curtis (R)

Factor VIII Computing, Berkeley, USA.

Neil Frick (N)

National Hemophilia Foundation, New York, USA.

Michael B Nichol (MB)

Sol Price School of Public Policy, University of Southern California, Los Angeles, USA.

Declan Noone (D)

Irish Haemophilia Society, Dublin, Ireland.

Brian O'Mahony (B)

Irish Haemophilia Society, Dublin, Ireland.
Trinity College Dublin, Dublin, Ireland.

David Page (D)

Canadian Hemophilia Society, Montreal, Canada.

Jeffrey S Stonebraker (JS)

Poole College of Management, North Carolina State University, Raleigh, USA.

Lehana Thabane (L)

Department of HEI, McMaster University, Hamilton, ON, Canada.
Biostatistics Unit, St Joseph's Healthcare, Hamilton, Canada.

Mark A Crowther (MA)

Department of Medicine, McMaster University, Hamilton, ON, Canada.
Department of HEI, McMaster University, Hamilton, ON, Canada.

Mark W Skinner (MW)

Department of HEI, McMaster University, Hamilton, ON, Canada.
Institute for Policy Development Ltd, Washington, USA.

Alfonso Iorio (A)

Department of Medicine, McMaster University, Hamilton, ON, Canada.
Department of HEI, McMaster University, Hamilton, ON, Canada.

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