Department of Orthopaedic Surgery, University of California Davis School of Medicine, Sacramento, California, USA.
Department of Orthopedics, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
J Orthop Res. 2024 Oct;42(10):2149-2158. doi: 10.1002/jor.25874. Epub 2024 May 18.
Treating flexor tendon injuries within the digital flexor sheath (commonly referred to as palmar hand zone 2) presents both technical and logistical challenges. Success hinges on striking a delicate balance between safeguarding the surgical repair for tendon healing and initiating early rehabilitation to mitigate the formation of tendon adhesions. Adhesions between tendon slips and between tendons and the flexor sheath impede tendon movement, leading to postoperative stiffness and functional impairment. While current approaches to flexor tendon repair prioritize maximizing tendon strength for early mobilization and adhesion prevention, factors such as pain, swelling, and patient compliance may impede postoperative rehabilitation efforts. Moreover, premature mobilization could risk repair failure, necessitating additional surgical interventions. Pharmacological agents offer a potential avenue for minimizing inflammation and reducing adhesion formation while still promoting normal tendon healing. Although some systemic and local agents have shown promising results in animal studies, their clinical efficacy remains uncertain. Limitations in these studies include the relevance of chosen animal models to human populations and the adequacy of tools and measurement techniques in accurately assessing the impact of adhesions. This article provides an overview of the clinical challenges associated with flexor tendon injuries, discusses current on- and off-label agents aimed at minimizing adhesion formation, and examines investigational models designed to study adhesion reduction after intra-synovial flexor tendon repair. Understanding the clinical problem and experimental models may serve as a catalyst for future research aimed at addressing intra-synovial tendon adhesions following zone 2 flexor tendon repair.
治疗位于指深屈肌腱鞘内的屈肌腱损伤(通常称为手掌区 2 区)既具有技术挑战性,又具有后勤方面的挑战。成功的关键在于在保护肌腱愈合的手术修复和启动早期康复以减轻肌腱粘连形成之间取得微妙的平衡。肌腱束之间以及肌腱与屈肌腱鞘之间的粘连会阻碍肌腱运动,导致术后僵硬和功能障碍。虽然目前的屈肌腱修复方法侧重于最大限度地提高肌腱强度以实现早期活动和预防粘连,但疼痛、肿胀和患者依从性等因素可能会阻碍术后康复努力。此外,过早的活动可能会有修复失败的风险,需要进行额外的手术干预。药理学制剂为减轻炎症和减少粘连形成提供了一种潜在的途径,同时仍能促进正常的肌腱愈合。尽管一些系统和局部制剂在动物研究中显示出有希望的结果,但它们在临床上的疗效仍不确定。这些研究的局限性包括所选动物模型与人类群体的相关性以及工具和测量技术在准确评估粘连影响方面的充分性。本文概述了与屈肌腱损伤相关的临床挑战,讨论了目前用于最小化粘连形成的有和无标签制剂,并研究了旨在研究滑膜内屈肌腱修复后粘连减少的实验模型。了解临床问题和实验模型可能会成为未来研究的催化剂,旨在解决第 2 区屈肌腱修复后滑膜内肌腱粘连问题。