自体富血小板血浆在髋关节血管性坏死 I 期和 II 期抢救中的应用:比较 82 例患者的 3 种手术技术的随机盲法试验

IF 1.1 4区 医学 Q3 ORTHOPEDICS
Nishit Palo, Binayak Ray, Mahima Lakhanpal, Naveen Jeyaraman, Abhishek Shukla, Abhishek Malik
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引用次数: 0

摘要

引言 股骨头血管坏死在常规骨科门诊中很常见。在处理无明显放射学证据的早期阶段(I 期和 II 期)时面临挑战。作者通过比较早期 AVN 患者的手术治疗方法,探索了这一新的研究领域。材料与方法 2020 年 11 月至 2023 年 2 月,对 82 例接受手术减压和辅助治疗的患者进行了前瞻性多中心研究,研究符合规定的纳入和排除标准。评估了放射性肿胀和骨内水肿的消退情况以及 THA 转换率。此外,还对髋关节疼痛VAS、腹股沟/大腿疼痛、盘腿坐困难发生率、无痛行走距离、Harris髋关节评分、30秒椅子测试和并发症进行了记录。男女比例为 3.9:1。8.5%的患者为双侧发病,48.78%的患者有阳性家族史。93.90%的患者表现为腹股沟疼痛和盘腿坐困难,85.3%的患者髋关节活动受限,54.87%的患者大腿疼痛。哈里斯髋关节评分最差的是第 3 组,其次是第 2 组和第 1 组。63.41% 和 36.58% 的患者分别患有 1 级和 2 级 AVN。术后 1 周,分别有 96.3% 和 93.9% 的患者腹股沟和大腿疼痛得到缓解(p < 0.001);趋势是第 3 组和第 2 组和第 1 组。4周时,第3组和第2组和第1组的Harris髋关节评分均有所改善;6个月时,趋势为第2组和第3组和第1组;第3组的30秒椅子测试结果、无痛行走距离和盘腿坐立时间更长。并发症发生率为 3.6%。6.09%的患者后来接受了全髋关节置换术。结论在 I 期和 II 期 AVN 中,双平面核心减压(双)和骨内注射 PRP 是一种很有前景的挽救方案;患者的早期髋关节评分(4 周)较好,腹股沟和大腿疼痛恢复较早。早期治疗的患者临床和放射学恢复效果更好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Augmentation of Autologous Platelet-Rich Plasma in Hip Salvage in Stages I and II of Avascular Necrosis: Randomized Blinded Trial Comparing 3 Surgical Techniques in 82 Patients

Augmentation of Autologous Platelet-Rich Plasma in Hip Salvage in Stages I and II of Avascular Necrosis: Randomized Blinded Trial Comparing 3 Surgical Techniques in 82 Patients

Introduction

Avascular necrosis of the femoral head is common in routine orthopedic clinics. The challenge arises in managing early stages (I and II) without obvious radiological evidence. Authors explore this naïve research area by comparing surgical procedures in early AVN patients.

Materials and Methods

A prospective multicentric study was performed from November 2020 to February 2023 on 82 patients treated with surgical decompression and adjuvants, concerning the defined inclusion and exclusion criteria. Radiopacity and intraosseous edema resolution and THA conversion rates were assessed. Hip pain VAS, groin/thigh pain, difficulty in sitting cross-legged incidence, pain-free walking distance, Harris hip scores, 30-s chair test, and complications were noted.

Results

Among 82 patients, the mean age was 28.46 years. Male:female ratio of 3.9:1. 8.5% had bilateral affection and 48.78% had a positive family history. 93.90% presented with groin pain and difficulty in sitting cross-legged, restricted hip movements in 85.3%, and thigh pain in 54.87%. Harris hip scored worst in Group 3 followed by Group 2 and Group 1. 63.41% and 36.58% of patients had Grades 1 and 2 AVN, respectively. At 1 week post-operatively, 96.3% and 93.9% of patients were relieved from groin and thigh pain, respectively (p < 0.001); the trend being Group 3 > Group 2 > Group 1. Hip pain VAS followed a similar trend. At 4 weeks, Harris hip scores improved in Group 3 > Group 2 > Group 1. At 6 months, the trend was Group 2 > Group 3 > Group 1. Group 3 had better 30-s chair test results, pain-free walking distance, and longer cross-legged sitting time. Complication rate of 3.6%. 6.09% of patients underwent THA later. Sclerotic patch and marrow edema resolution early in Group 3, i.e., 46 and 31 days respectively, followed by Group 2 and Group 1.

Conclusion

In Stages I and II AVN, biplanar core decompression (double) and intraosseous PRP injection is a promising salvage option; patients have better early hip scores (4 weeks), and early groin and thigh pain recovery. Patients treated early have better clinical and radiological recovery.

Graphical abstract

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来源期刊
CiteScore
1.80
自引率
0.00%
发文量
185
审稿时长
9 months
期刊介绍: IJO welcomes articles that contribute to Orthopaedic knowledge from India and overseas. We publish articles dealing with clinical orthopaedics and basic research in orthopaedic surgery. Articles are accepted only for exclusive publication in the Indian Journal of Orthopaedics. Previously published articles, articles which are in peer-reviewed electronic publications in other journals, are not accepted by the Journal. Published articles and illustrations become the property of the Journal. The copyright remains with the journal. Studies must be carried out in accordance with World Medical Association Declaration of Helsinki.
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