# Comparative Perioperative Inflammatory and Functional Outcomes in Single Versus Multiple Joint Replacements for Hemophilic Arthritis: A Pilot Study

**Authors:** Maoye Shen, Ping Qian, Wenxue Jiang, Shanyou Yuan, Gaorui Cai, Zhenzhong Zhou, Xiaona Wu, Jinghua Wang, Xianjia Ning, Lixia Song

PMC · DOI: 10.1111/os.70045 · Orthopaedic Surgery · 2025-05-08

## TL;DR

This study compares surgical outcomes for hemophilia patients undergoing single or multiple joint replacements, finding that multiple joint replacements improve mobility without increasing risks.

## Contribution

The study provides novel comparative evidence on perioperative outcomes between single and multiple joint replacements in hemophilic arthritis patients.

## Key findings

- Multiple joint replacement (MJR) resulted in significantly better joint mobility scores compared to single joint replacement (SJR).
- No significant differences in infection, bleeding risks, or blood transfusion requirements were observed between SJR and MJR groups.
- Postoperative CRP levels declined significantly in both groups, while ESR showed an upward trend.

## Abstract

Hemophilic arthritis is a progressive joint disease often requiring surgical intervention in advanced stages. However, comparative evidence on perioperative inflammatory and coagulation responses between single joint replacement (SJR) and multiple joint replacement (MJR) remains scarce. This study aimed to assess the differences in perioperative outcomes, including inflammatory responses, blood transfusion requirements, and functional recovery, to guide surgical decision‐making for hemophilic arthritis patients.

This retrospective study included 29 male patients with moderate‐to‐severe hemophilic arthritis who underwent SJR (n = 12) or MJR (n = 17) at a single institution from October 2020 to October 2023. Data on inflammatory markers (CRP, ESR, IL‐6, WBC), hemoglobin levels, blood transfusion requirements, and joint mobility were collected for the immediate postoperative period (days 1–14). Trends in inflammatory markers were analyzed using average percent changes (APC), and differences in outcomes were evaluated using the Mann–Whitney U test for continuous variables and Fisher's exact test for categorical variables. Longitudinal changes were analyzed using mixed‐model repeated measures ANOVA with time points as fixed effects and subjects as random effects. Statistical significance was set at p < 0.05.

Postoperative CRP levels declined significantly in both groups, with APCs of −9.06% (95% CI: −15.63 to −1.98, p < 0.05) for the SJR group and −8.42% (95% CI: −16.18 to 0.06) for the MJR group. ESR showed a significant upward trend, with APCs of 10.82% (95% CI: 0.95–21.65, p < 0.05) in the SJR group and 17.54% (95% CI: 11.71–23.67, p < 0.05) in the MJR group. Blood transfusion requirements were comparable, with median transfusion volumes of 0.00 units (IQR: 3.50) for SJR and 0.00 units (IQR: 3.75) for MJR (p = 0.761). Notably, joint mobility scores were significantly better in the MJR group (mean: 31.88, SD: 19.31) compared to the SJR group (mean: 18.33, SD: 10.39; p = 0.030). Despite the larger surgical scope of MJR, no significant differences in infection or bleeding risks (SJR:median transfusion = 0.00 units, IQR: 3.50; MJR:median transfusion, 0.00 units, IQR: 3.75. p = 0.761) were observed between the groups.

This study demonstrates that MJR offers superior functional recovery compared to SJR, without increasing the risks of infection, bleeding, or transfusion. These findings support MJR as a safe and effective surgical option for hemophilic arthritis patients when appropriate perioperative management protocols are implemented. Future studies with larger sample sizes and long‐term follow‐up are needed to validate these results and explore extended outcomes.

This study reveals that, compared to single‐joint replacement, multi‐joint replacement enhances joint mobility in hemophilia patients without additional postoperative infection or transfusion risks.

## Linked entities

- **Diseases:** hemophilic arthritis (MONDO:0043240)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** coagulation (MESH:D001778), infection (MESH:D007239), Hemophilic Arthritis (MESH:D001168), bleeding (MESH:D006470), joint disease (MESH:D007592), Inflammatory (MESH:D007249)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC12146121/full.md

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Source: https://tomesphere.com/paper/PMC12146121