The Impact of Pediatric Rheumatic Diseases on Sexual Health, Family Planning, and Pregnancy

Edens, Cuoghi

doi:10.1016/j.rdc.2021.09.016

Cited by 1 publication

(1 citation statement)

References 155 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…The disease activity (causing pain, fatigue, and functional limitations) and treatments’ side effects (fatigue, vaginal dryness, and erectile dysfunction), may affect sexual function and lead to psychological distress (low self-esteem and impaired body image) [ 23 – 27 ]. Conversely, one comparative study of young adult women with JIA and healthy controls suggested only a minimal impact.…”

Section: Introductionmentioning

confidence: 99%

Survey of adolescents’ needs and parents’ views on sexual health in juvenile idiopathic arthritis

Savel,

Chausset,

Berland

et al. 2023

Pediatr Rheumatol

View full text Add to dashboard Cite

Background Although the advent of new therapeutics for juvenile idiopathic arthritis (JIA) patients has considerably lessened the impact of the disease and reduced its sequelae, the outcomes of JIA remain important in their lives. Disease repercussions and side effects of treatments may affect sexual health and cause psychological distress. This aim of the study was to determine the expectations of adolescent JIA patients and the perceptions of their parents regarding knowledge and communication with healthcare providers (HCPs) in the field of sexual health (SH). Methods In France, from September 2021 to April 2022, a survey was conducted, using anonymous self-administered questionnaires, among JIA patients (adults (aged 18–45 years) to provide insights from their recollection of their adolescence) and their parents in nine rheumatology centers and three patient associations. Results The responses to the 76 patient questionnaires and 43 parent questionnaires that were collected were analyzed. Half of the patients thought JIA impacted their romantic relationships, but the results were less clear-cut for their sexual activity; and 58.7% of the patients said they would be comfortable discussing the subject with HCPs, but only 26.3% had done so, mainly regarding biomedical issues. The patients and their parents thought that ideally, the topic should be addressed in an individual patient education session at the hospital (51.3% and 34.9%, respectively), in a regular consultation (47.4% and 53.5%), or in a dedicated consultation requested by the adolescent without the adolescent’s parents being informed (38.2% and 20.9%). Most of the respondents thought HCPs should be proactive in SH (77.6% of the patients and 69.8% of their parents). More patients than parents said the following digital information tools must be used: videos (29.0% vs. 9.3%, p = 0.0127) and smartphone applications (25.0% vs. 9.3%, p = 0.0372). Conclusion HCPs should consider addressing the unmet need for SH discussions during their patient encounters. To meet this need, we propose concrete actions in line with the wishes of patients and parents. Clinical trial registration number NCT04791189.

show abstract

Section: Introductionmentioning

confidence: 99%