# The effect of prophylactic FVIII infusion combined with personalized rehabilitation on joint health and quality of life in children with hemophilia

**Authors:** Yaojin Sun, Qian Zhang, Xiaojie Gu, Yongjun Fang, Jie Huang, Heng Zhang

PMC · DOI: 10.3389/fped.2025.1578617 · 2025-07-10

## TL;DR

A 12-week personalized rehabilitation program combined with FVIII infusions improved joint health and quality of life in children with hemophilia.

## Contribution

This study introduces a personalized rehabilitation strategy for pediatric hemophilia patients, demonstrating significant improvements in joint health and quality of life.

## Key findings

- Median HEAD-US-C scores decreased significantly from 5.00 to 1.00 after treatment.
- Bleeding episodes dropped from 3.00 to 0.00, indicating reduced joint bleeding.
- CHO-KLAT quality of life scores improved from 71.51 to 79.15.

## Abstract

Hemophilia, a genetic disorder characterized by deficiencies in clotting factors VIII or IX, often results in joint and muscle bleeding, leading to hemophilic arthropathy and reduced quality of life. While multidisciplinary teams (MDTs) are widely used in hemophilia management, personalized rehabilitation strategies for pediatric patients remain underexplored. This study aimed to evaluate a 12-week individualized rehabilitation program targeting joint health in pediatric hemophilia patients.

This prospective study enrolled 59 children with hemophilia, implementing tailored rehabilitation plans based on specific joint pathologies. Assessments before and after treatment included joint ultrasound examinations (HEAD-US-C), Hemophilia Joint Health Scores (HJHS 2.1), and the CHO-KLAT tool for quality of life. Bleeding frequency was also recorded.

Post-treatment, median HEAD-US-C scores decreased from 5.00 to 1.00 (P < 0.001), and HJHS 2.1 scores decreased from 9.00 to 2.00 (P < 0.001). CHO-KLAT scores increased from 71.51 to 79.15 (P < 0.001). Median bleeding episodes dropped from 3.00 to 0.00 (P < 0.001), indicating enhanced joint health and reduced bleeding frequency.

Regular prophylactic FVIII administration combined with individualized rehabilitation significantly reduces joint bleeding and enhances joint function and quality of life in children with hemophilia. The MDT approach is integral to comprehensive care, but further studies are needed to assess the long-term efficacy and safety of this therapeutic strategy.

## Linked entities

- **Proteins:** F8 (coagulation factor VIII)
- **Diseases:** hemophilia (MONDO:0018660)

## Full-text entities

- **Genes:** F8 (coagulation factor VIII) [NCBI Gene 2157] {aka AHF, DXS1253E, F8B, F8C, FVIII, HEMA}
- **Diseases:** Hemophilia (MESH:D006467), joint and muscle bleeding (MESH:D019042), genetic disorder (MESH:D030342), deficiencies in clotting factors VIII or IX (MESH:C565024), hemophilic arthropathy (MESH:D007592), Bleeding (MESH:D006470)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12287007/full.md

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Source: https://tomesphere.com/paper/PMC12287007