1. Long‐term quality of life and surgical outcome of female congenital adrenal hyperplasia patients.
- Author
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Leung, Ling, Lui, Candace, Cheung, Ka Li, Chan, Ivy Hau Yee, and Wong, Kenneth Kak Yuen
- Abstract
Aim Methods Results Conclusions To investigate the long‐term quality of life and surgical outcome of female patients with congenital adrenal hyperplasia (CAH).Questionnaires for health‐related quality of life (HRQoL) outcome (WHO‐5, SF‐36), lower urinary tract symptoms (ICIQ‐FLUTS) and sexual outcome (ICIQ‐FLUTSsex) were administered to adult CAH patients. Paediatric CAH patients and their parents were invited to complete WHO‐5, PedsQL‐4.0‐SF15‐Generic Core Scales and ICIQ‐CLUTS.Six (46%) adults and 7 (54%) children with 21‐hydroxylase‐deficiency (age ranged from 8 years to 53 years) were recruited. Eleven (85%) had undergone a feminising genitoplasty. In the adult group, no statistically significant difference was identified in the HRQoL and ICIQ‐FLUTS scores. Mean overall score of ICIQ‐FLUTSsex was lower but not significantly in adult patients compared to controls (7.3 ± 2.9 vs. 2.9 ± 3.4, P = 0.06). A statistically significant negative correlation (r = −0.98, P = 0.02) was found between age at first operation and role limitations due to emotional problems in SF‐36. No statistically significant difference was identified in the self‐reported HRQoL and ICIQ‐CLUTS scores in the paediatric group compared to controls. However, parent's report showed a statistically significant difference in school functioning (73.8 ± 18.9 vs. 91.2 ± 18.7, P = 0.02) and emotional functioning (80.3 ± 15.9 vs. 94.7 ± 12.7, P = 0.007).Our data did not show an impaired HRQoL nor long‐term lower urinary tract symptoms in CAH patients' self‐reports. Healthcare team should pay more attention to adult patient's sexual function. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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