Age‐specific incidence of joint disease in paediatric patients with haemophilia: A single‐centre real‐world outcome based on consecutive US examination

Author:

Mizoguchi Yoko1ORCID,Tani Chihiro2,Aizawa Mika3ORCID,Tomioka Keita4,Shimomura Maiko1,Nishimura Shiho5,Matsubara Yoshiko2,Iwaki Daisuke6,Tanaka Kiyoto1,Kawaguchi Hiroshi1ORCID,Nakashima Yuko7,Mikami Yukio8,Okada Satoshi1,Kobayashi Masao9

Affiliation:

1. Department of Pediatrics Hiroshima University Graduate School of Biomedical and Health Sciences Hiroshima Japan

2. Department of Diagnostic Radiology Hiroshima University Hospital Hiroshima Japan

3. Graduate School of Advanced Science and Engineering Hiroshima University Hiroshima Japan

4. Department of Pediatrics Hiroshima Prefectural Rehabilitation Center Hiroshima Japan

5. Department of Pediatrics Hiroshima City Hiroshima Citizens Hospital Hiroshima Japan

6. Division of Rehabilitation Department of Clinical Practice and Support Hiroshima University Hospital Hiroshima Japan

7. Collaborative Research laboratory of Musculoskeletal Ultrasound in Medicine Hiroshima University Hospital Hiroshima Japan

8. Department of Rehabilitation Medicine Hiroshima University Hospital Hiroshima Japan

9. Japanese Red Cross Chugokushikoku Block Blood Center Hiroshima Japan

Abstract

AbstractIntroductionJoint health is one of the most important factors contributing to a healthy life in patients with haemophilia. Recent study revealed that starting early prophylaxis was not enough to prevent joint disease in most paediatric patients with haemophilia.AimIn this study, we aimed to determine the age‐specific incidence of acute joint disease during childhood at single haemophilia treatment centre (HTC).MethodThe joint health in 48 patients was evaluated based on consecutive US testing for 5 years at annual multidisciplinary comprehensive care.ResultsDuring the study period, 23 patients (47.9%) had no joint disease since the initial examination, whereas 13 patients (27.0%) showed development from negative to positive findings. The incidence of joint disease increased with age: 0% in preschool, 5.3% in elementary school, 14.3% in junior high school and 35% beyond high school age. Among the 13 patients who developed joint disease, two experienced acquired synovitis that resolved during the follow‐up period. Statistical analysis revealed that the patients who routinely underwent follow‐up by the HTC exhibited a significantly lower incidence of joint disease than did those followed up at other institutions (p < .001).ConclusionThese results indicated that close check‐up, including routine joint examination using US as well as frequent assessment of pharmacokinetic profile at the HTC, might play an important role in avoiding joint disease among paediatric patients with haemophilia.

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

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