Houston Methodist Orthopedics and Sports Medicine, Houston, Texas, U.S.A.
Department of Orthopedics, University of Colorado School of Medicine, Aurora, Colorado, U.S.A.
Arthroscopy. 2022 May;38(5):1658-1663. doi: 10.1016/j.arthro.2021.11.045. Epub 2021 Dec 7.
To determine whether there are differences in (1) the incidence of post-related complications following hip arthroscopy between prospective and retrospective publications; and (2) between post-assisted and postless techniques.
A systematic review was performed using PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines to characterize post-related complications following hip arthroscopy for central or peripheral compartment hip pathology, including femoroacetabular impingement syndrome and chondrolabral injury. Inclusion criteria were prospective and retrospective Level I-IV evidence investigations that reported results of hip arthroscopy performed in the supine position. Exclusion criteria included open or extra-articular endoscopic hip surgery. Post-related complications included pudendal nerve injury (sexual dysfunction, dyspareunia, perineal pain or numbness) or perineum/external genitalia soft-tissue injury.
Ninety-four studies (12,212 hips; 49% male, 51% female; 52% Level IV evidence) were analyzed. Prospective studies (3,032 hips) report a greater incidence of post-related complications compared with retrospective (8,116 hips) studies (7.1% vs 1.4%, P < .001). Three studies (1,064 hips) used a postless technique and all reported a 0% incidence of pudendal neurapraxia or perineal soft tissue injury. Most pudendal nerve complications were transient, resolving by 3 months, but permanent nerve injury was reported in 4 cases. Only 19%, 22%, 7%, and 4% of studies reported a total surgery time, traction time, traction force, and bed Trendelenburg angle for their study samples, respectively.
The incidence of post-related complications is 5 times greater in prospective (versus retrospective) hip arthroscopy literature. Postless distraction resulted in a 0% incidence of post-related injuries.
IV, systematic review of Level I-IV evidence.
确定髋关节镜检查后相关并发症的发生率在以下方面是否存在差异:(1)前瞻性和回顾性出版物之间;(2)辅助后和无辅助后技术之间。
使用 PRISMA(系统评价和荟萃分析的首选报告项目)指南进行系统评价,以描述髋关节镜检查治疗中央或周围隔室髋关节病变(包括股骨髋臼撞击综合征和软骨盂唇损伤)后相关并发症。纳入标准为前瞻性和回顾性 I-IV 级证据研究,报告仰卧位髋关节镜手术结果。排除标准包括开放式或关节外内镜髋关节手术。后相关并发症包括阴部神经损伤(性功能障碍、性交困难、会阴疼痛或麻木)或会阴/外生殖器软组织损伤。
分析了 94 项研究(12212 髋;49%为男性,51%为女性;52%为 IV 级证据)。前瞻性研究(3032 髋)报告后相关并发症的发生率高于回顾性研究(8116 髋)(7.1%比 1.4%,P<.001)。有 3 项研究(1064 髋)采用无辅助后技术,所有研究均报告阴部神经麻痹或会阴软组织损伤的发生率为 0%。大多数阴部神经并发症是短暂的,在 3 个月内缓解,但有 4 例报告了永久性神经损伤。只有 19%、22%、7%和 4%的研究分别报告了其研究样本的总手术时间、牵引时间、牵引力和床 Trendelenburg 角度。
前瞻性(与回顾性)髋关节镜检查文献中后相关并发症的发生率高 5 倍。无辅助后牵伸导致后相关损伤的发生率为 0%。
IV,I-IV 级证据的系统评价。