KOR

e-Article

A survey on transition from pediatric to adult care for patients with Wilson disease / 移行期医療に関するWilson病患者のアンケート調査結果
Document Type
Journal Article
Source
肝臓 / Kanzo. 2020, 61(12):700
Subject
15歳以上の患者
Wilson disease
Wilson病
patient's minds
patients aged over 15 years
survey
transition from pediatric to adult care
アンケート調査
患者の心理
移行期医療
Language
Japanese
ISSN
0451-4203
1881-3593
Abstract
We performed a survey of 109 patients with Wilson disease (male 57, female 52; mean age, 34 years [range, 8-67]; mean age of diagnosis, 12 years [range, 2-50]). Among these, 73 and 59 patients were diagnosed and currently seen by pediatricians, respectively, and 10 and 29 were diagnosed and currently seen by gastroenterologists, respectively. These numbers suggest that the number of patients currently being treated by pediatricians has decreased, while those currently being treated by gastroenterologists has increased, as compared with a diagnostician. Thirty-four percent (28/82) of patients aged ≥15 years have transitioned from pediatric to adult care; 10 were dissatisfied with their current physicians for reasons such as not having sufficient knowledge about Wilson disease. Sixty-six percent (54/82) of patients were still treated by their pediatricians (mean age, 33 years). These results suggest that problems at transition include independence support to the patients, provision of disease information, and cooperation with Wilson disease-related organizations.