Validation of a Handprint for Clinical Evaluation of Dupuytren's Contracture.

IF 0.3 Q4 SURGERY Journal of Hand and Microsurgery Pub Date : 2021-08-25 eCollection Date: 2023-06-01 DOI:10.1055/s-0041-1735347
Takashi Ajiki, Akira Murayama, Yukinori Hayashi, Katsushi Takeshita
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Abstract

Objective  We have developed a handprint-based method for visualizing and quantifying the palmar contact of patients with Dupuytren's contracture. The purpose of this study was to examine whether the generated handprint was useful for assessing the severity of flexion contracture of the fingers and for evaluating the therapeutic effects of collagenase clostridium histolyticum (CCH) injection for Dupuytren's contracture. Methods  The handprint was created by applying medical-grade ethanol-containing hand sanitizer over the entire palmar surface of the affected hand and then pressing it on thermal paper for word processors. The reliability of the handprint was evaluated through test-retest of 10 healthy volunteers at an interval of 10 days, and the validity of the handprint was assessed using a flexion contracture model in which the little finger was fixed in an Alfence splint. In addition, we obtained handprints of the affected hand in 33 patients with unilateral Dupuytren's contracture both before CCH injection and at the final observation after injection to investigate the contact area of the hand (CAH) and the length of the hand (LH). The relationships between CAH, LH, total extension deficit angle (TEDA), and patient-reported outcome measures (Japanese Society for Surgery of the Hand Version of the Quick Disability of Arm, Shoulder, and Hand Questionnaire [Quick DASH-JSSH] and Hand20) were examined. Results  The test-retest correlation coefficient was 0.9187 ( p  < 0.001) for CAH and 0.9052 ( p  < 0.001) for LH, indicating high reliability of the handprint. The ratios of CAH and LH decreased gradually as the contracture angle of the splinted finger increased. The handprint revealed a marked improvement of palmar contact after CCH injection for Dupuytren's contracture. Furthermore, the ratios of CAH and LH were strongly correlated with TEDA, Quick DASH-JSSH, and Hand20 before treatment. Conclusion  Our handprint-based assessment method was extremely useful for clinical evaluation of CCH treatment for Dupuytren's contracture. Type of Study/Level of Evidence  Therapeutic.

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验证用于杜普伊特伦挛缩症临床评估的手印。
目的 我们开发了一种基于手印的方法,用于观察和量化杜普伊特伦挛缩症患者的手掌接触情况。本研究的目的是检验生成的手印是否有助于评估手指屈曲挛缩的严重程度,以及评估胶原酶溶解梭菌(CCH)注射治疗杜普伊特伦挛缩症的疗效。方法 将医用乙醇洗手液涂抹在患手的整个掌面,然后将其按压在文字处理机的热敏纸上,以此制作手印。我们对 10 名健康志愿者进行了间隔 10 天的重测,评估了手印的可靠性,并使用屈曲挛缩模型评估了手印的有效性,在该模型中,小指被固定在 Alfence 夹板中。此外,我们还采集了 33 名单侧杜普伊特伦挛缩症患者在注射 CCH 前和注射后最后观察期间的患手手纹,以研究手的接触面积(CAH)和手的长度(LH)。研究了CAH、LH、总伸展缺损角(TEDA)和患者报告的结果指标(日本手外科学会快速手臂、肩部和手部残疾问卷[Quick DASH-JSSH]和Hand20)之间的关系。结果 测试-重复相关系数为 0.9187 ( p p 结论 我们基于手印的评估方法对于杜普伊特伦挛缩症的 CCH 治疗的临床评估非常有用。研究类型/证据级别 治疗。
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CiteScore
1.00
自引率
25.00%
发文量
39
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