SNAPSJIA study Survey of Adolescents' Needs and Parents' Views on Sexual Health in Juvenile Idiopathic Arthritis

Author:

SAVEL Carine1ORCID,CHAUSSET Aurélie1,BERLAND Pauline1,GUIGUET-AUCLAIR Candy1,CABANE Laura2,FAUTREL Bruno3,GAUDIN Philippe4,GUILLOT Pascale5,HAYEM Gilles6,LAFARGE Delphine7,MERLIN Etienne1,PEZIERE Nadine8,SORDET Christelle9,TROPE Sonia10,TOURNADRE Anne1,MALOCHET Sandrine1,COHEN Jean David11

Affiliation:

1. CHU Clermont-Ferrand: Centre Hospitalier Universitaire de Clermont-Ferrand

2. CHU Nice: Centre Hospitalier Universitaire de Nice

3. University Hospital Pitié Salpêtrière: Hopital Universitaire Pitie Salpetriere

4. CHU Grenoble: Centre Hospitalier Universitaire Grenoble Alpes

5. CHU Nantes: Centre Hospitalier Universitaire de Nantes

6. Hôpital Paris Saint-Joseph: Groupe hospitalier Paris Saint-Joseph

7. Association France Spondyloarthrite

8. Association KOURIR

9. CHU Strasbourg: Les Hopitaux Universitaires de Strasbourg

10. Association ANDAR

11. CHU Lapeyronie: Hopital Lapeyronie

Abstract

Abstract Background: Although the advent of new therapeutics for juvenile idiopathic arthritis (JIA) patients has considerably lessened the impact of the disease and reduced sequelae, the outcomes of JIA remain important in their lives and more specifically for sex life. According to the world health organization, sexual health (SH) is "a state of physical, emotional, mental and social well-being in relation to sexuality". The aim of the study was to determine the expectations of adolescents with JIA and the perceptions of their parents regarding knowledge and communication with healthcare providers (HCPs) in the field of SH. Methods: From September 2021 to April 2022, a French survey with anonymous self-administered questionnaires, was conducted among JIA patients and their parents in nine rheumatology centers and three patient associations. On the advice of a psychiatrist, we interviewed adults (age 18–45 years) for necessary hindsight from the subject. Results: 76 patient and 43 parent questionnaires were analyzed. Half the patients thought JIA impacted their love life, the results were less clearcut for their sex life. 58.7% would be comfortable discussing the subject with HCPs, but only 26.3% had done so, mainly regarding biomedical issues. Patients and parents thought the topic should ideally be addressed in hospital in an individual patient education session (51.3%, 34.9% respectively), a regular consultation (47.4%, 53.5%) or a dedicated consultation requested by the adolescent without parents being informed (38.2%, 20.9%). Most thought HCPs should be proactive (77.6% of patients, 69.8% of parents). The use of digital resources was significantly more cited by patients than by parents: video information (29.0% vs. 9.3%, p= 0.0127) smartphone application (25.0% vs. 9.3%, p = 0.0372). Conclusion: HCPs should address this unmet need for SH in hospital. The main difference between patients and parents was the use of digital tools, a preferred vector of communication for adolescents. Parents need to be reassured about their content. Clinical trial registration number: NCT04791189

Publisher

Research Square Platform LLC

Reference46 articles.

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