腰椎关节炎全髋关节置换术后屈曲受限的易感因素。

IF 2.9 3区 医学 Q2 RHEUMATOLOGY
Clinical Rheumatology Pub Date : 2025-03-01 Epub Date: 2025-01-27 DOI:10.1007/s10067-025-07338-7
Xiaoying Li, Jing Pan, Hongchao Li, Jun Zhang, Feng Pan, Siliang Man, Liang Zhang
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引用次数: 0

摘要

约有三分之一的轴性脊柱关节炎(axSpA)患者会出现髋关节受累的情况。我们评估了为治疗 axSpA 而进行全髋关节置换术(THA)后导致患者屈曲受限的可能因素的发生率。我们回顾性地检查了接受全髋关节置换术的 516 例 axSpA 患者(759 个髋关节)。我们回顾性地收集了患者的基线人口统计学资料以及临床、实验室和手术相关参数。比较了术前和最近一次随访的哈里斯髋关节评分(HHS)和髋关节屈曲能力。在记录最近一次随访时的术后髋关节屈曲程度后,我们将髋关节分为屈曲良好组(> 90°)和屈曲不良组(≤ 90°)。检查屈曲良好组和屈曲不良组基线参数的差异。然后将这些基线参数与 P 90°进行比较。有些不满意的患者有 147 个髋关节(19.4%),非常不满意的患者有 46 个髋关节(6.1%)。不满意的主要原因是活动范围(ROM)受限(323 个髋关节,80.1%)。多变量逻辑回归模型显示,术后髋关节屈曲不良的显著变量是发病年龄较小(OR = 0.967;P = 0.024)、银屑病(PSO)(OR = 2.071;P = 0.007)、C反应蛋白(CRP)升高(OR = 1.031;P = 0.007)、髋关节活动范围受限(ROM)(323 个髋关节,占 80.1%)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factors predisposing to limited flexion after total hip arthroplasty for the treatment of axial spondyloarthritis.

Hip involvement is a common condition in about one-third of patients with axial spondyloarthritis (axSpA). We assessed the incidence of possible factors that predispose patients to limited flexion after total hip arthroplasty (THA) for the treatment of axSpA. We retrospectively reviewed 516 patients with axSpA (759 hips) who underwent THA. Baseline patient demographics and clinical, laboratory, and surgery-related parameters were retrospectively collected. The preoperative and latest follow-up Harris hip score (HHS) and hip flexion ability were compared. After documenting the degree of postoperative hip flexion at the latest follow-up visit, we classified hips into good flexion group (> 90°) and poor flexion group (≤ 90°). The differences of baseline parameters between good flexion and poor flexion group were examined. Then those baseline parameters with P < 0.1 in intergroup comparisons were further included into the multivariate logistic models. The median duration of follow-up was 118.5 months (range, 25.0-269.1 months). The median HHS increased from 36.0 (25.0, 44.0) before surgery to 85.0 (77.0, 92.0) at the latest follow-up visit (P < 0.001). At the latest follow-up visit, 406 hips (53.5%) had hip flexion > 90°. The patients who were somewhat dissatisfied represented 147 hips (19.4%), and those who were very dissatisfied represented 46 hips (6.1%). The primary cause of dissatisfaction was limited range of motion (ROM) (323 hips, 80.1%). The multivariate logistic regression model revealed that the significant variables for postoperative poor hip flexion were the younger age of disease onset (OR = 0.967; P = 0.024), psoriasis (PSO) (OR = 2.071; P = 0.007), elevated C-reactive protein (CRP) (OR = 1.031; P < 0.001), and the lack of direct anterior approach (DAA) (OR = 0.372; P = 0.015). Although THA reconstruction for axSpA patients with end-stage hip involvement achieved encouraging clinical outcomes, it was prone to a restriction of hip flexion, which is closely associated with patient satisfaction. The younger age of disease onset, PSO, elevated CRP and the lack of DAA were significantly associated with limited postoperative hip flexion. Key Points • The restriction of hip flexion after THA reconstruction for axSpA patients is closely associated with patient satisfaction. • The younger age of disease onset, PSO, elevated CRP and the lack of DAA were significantly associated with limited postoperative hip flexion.

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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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