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Exploring the barriers and enablers to the standardized and routine use of patient-rated outcomes for clients presenting with hand injuries at an Australian public hospital.
IF 2.1 4区 医学 Q2 ORTHOPEDICS Pub Date : 2025-01-21 DOI: 10.1016/j.jht.2024.08.006
Laura Cowling, Dave Parsons, Cleo Bigwood, Sally Foster, Andrea Pinto, Yu Xuan Kong

Background: The utilization of standardized patient-rated outcome measures (PROMs) by hand therapists is essential to evaluate treatment and clinical outcomes and underpins evidence-based and patient-centered practice. However, research indicates that the routine use of PROMs is inconsistent in clinical practice.

Purpose: To explore the barriers and enablers experienced by hand therapists in the routine use of standardized and valid PROMs. Additionally, it aimed to describe appropriate strategies, based on the barriers and enablers identified, to improve the administration of PROMs in hand therapy practice.

Study design: Qualitative.

Methods: Semistructured interviews were used to explore the experiences of hand therapists in routinely using PROMs in clinical practice at two Australian tertiary public hospital hand clinics. Qualitative data were analyzed for themes using reflexive thematic analysis described by Braun and Clarke.

Results: Ten participants were interviewed. Interview findings generated three core themes-Culture is King, It's All Too Hard and When I do it, I value it. The core themes-Culture is King and It's All Too Hard reflected the cultural and institutional factors that present as barriers to the routine uptake of standardized PROMs, such as lack of infrastructure to support data collection and a lack of knowledge of PROMs. The third core theme, "When I do it, I value it" reflects the value and importance of completing PROMs to facilitate evidence-based practice and benefits in tracking treatment progress and providing feedback regarding their progression. Suggested strategies for addressing barriers included using appropriate and standardized methods of collecting and storing PROM data, improving accessibility to PROMs in clinical practice and forming peer education groups and training opportunities.

Conclusions: Hand therapists identify the value and importance of completing PROMs in daily practice; however, culture in the workplace and organizational infrastructure adversely influence the routine use of standardized PROMs by hand therapists.

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引用次数: 0
The 2021 American Hand Therapy Foundation research priorities survey. 2021年美国手部治疗基金会研究重点调查。
IF 2.1 4区 医学 Q2 ORTHOPEDICS Pub Date : 2025-01-16 DOI: 10.1016/j.jht.2024.11.007
April C Cowan, Marsha B Lawrence, Elaine E Fess, Caroline W Stegink-Jansen

Background: In 1998, the American Hand Therapy Foundation (AHTF) surveyed Certified Hand Therapists and active Charter Members of the American Society of Hand Therapists to identify hand rehabilitation research priorities, guide grant awards, and confirm alignment with the foundation's mission.

Purpose: The American Hand Therapy Foundation repeated the survey in 2021 to confirm that its award funding was consistent with hand therapists' research priorities.

Study design: Convergent parallel mixed method study design.

Methods: The survey was sent to 7093 hand therapists from the United States and overseas. Respondents' demographic information was captured using quantitative questions analyzed with descriptive statistics and weighted means. Research priorities and interests were captured using qualitative questions, Grounded Theory analysis, and Constant Comparative Methods.

Results: A total of 397 surveys were returned and analyzed (5.6% return rate, 95% confidence level, 5% margin of error). Participants' top research priorities were outcome studies and research grants. Tendon injuries and lateral epicondylitis were the highest prioritized diagnoses for further research. Intervention study priorities included hand rehabilitation management strategies and use of orthoses. Responses presented a need for funded outcomes research validating hand rehabilitation interventions. Level of interest in research participation was in data collection and as coauthor. Top barriers to participation in research activities were time constraints and lack of proficiency. Research education for clinicians and mentorship programs were identified as specific needs.

Conclusions: American Hand Therapy Foundation research award funding was consistent with practice and reported research concerns. Participants identified their top concerns for diagnostic and outcomes research and prioritized continuing Foundation involvement in funding clinical research.

背景:1998年,美国手部治疗基金会(AHTF)调查了美国手部治疗师协会的认证手部治疗师和活跃的特许会员,以确定手部康复研究的重点,指导拨款奖励,并确认与基金会使命的一致性。目的:美国手部治疗基金会在2021年重复了这项调查,以确认其奖励资金与手部治疗师的研究重点是一致的。研究设计:收敛平行混合方法研究设计。方法:对7093名来自美国及海外的手部治疗师进行问卷调查。受访者的人口统计信息是通过描述性统计和加权方法分析的定量问题来获取的。研究重点和兴趣是通过定性问题、扎根理论分析和持续比较方法来捕获的。结果:共回收分析问卷397份,回收率5.6%,置信水平95%,误差幅度5%。参与者的首要研究重点是结果研究和研究资助。肌腱损伤和外侧上髁炎是进一步研究的最高优先诊断。干预研究的重点包括手部康复管理策略和矫形器的使用。回应表明需要资助的结果研究来验证手部康复干预措施。参与研究的兴趣水平是数据收集和作为共同作者。参与研究活动的最大障碍是时间限制和缺乏熟练程度。临床医生的研究教育和指导计划被确定为特殊需求。结论:美国手部治疗基金会的研究资助与实践和报告的研究关注是一致的。与会者确定了他们最关心的诊断和结果研究,并优先考虑基金会继续参与资助临床研究。
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引用次数: 0
The case of a woman with bilateral Dupuytren's contractures who developed CRPS-1 after fasciectomy with no relapse on subsequent collagenase clostridium histolyticum injection and manipulation of the other hand: Considerations for implementing a Budapest criteria checklist and assessing vasomotor instability by measuring differences in skin temperature. 1例双侧Dupuytren挛缩患者在筋膜切除术后出现CRPS-1,随后注射溶组织梭菌胶原酶和另一只手的操作没有复发:实施布达佩斯标准检查表和通过测量皮肤温度差异评估血管舒缩不稳定性的考虑。
IF 2.1 4区 医学 Q2 ORTHOPEDICS Pub Date : 2025-01-16 DOI: 10.1016/j.jht.2024.09.002
Julianne W Howell

Background: For patients who experience atypical neurogenic pain thought to be complex regional pain syndrome (CRPS) after Dupuytren's fasciectomy early recognition has been reported to improve outcomes. Furthermore, given the progressive nature of Dupuytren's, individuals with a history of CRPS have been "at risk" for further surgical intervention.

Purpose: To familiarize therapists with a Budapest criteria (BC) checklist for early diagnosis of CRPS, describe how tracking sudomotor/vasomotor signs alongside differences in skin temperature were used to monitor vasomotor instability and intervention effectiveness for a patient with atypical pain after fasciectomy and to detail management of the same patient with a CRPS history who had collagenase clostridium histolyticum (CCH) injection of her other hand without exacerbating CRPS.

Study design: Case report.

Methods: Medical record review was done by the author. Part 1- patient-reported symptoms and therapist-observed signs were mined and scored against the BC. Part 2- vasomotor/sudomotor signs and differences in skin temperatures (>1˚C) were used to interpret response to therapy and medical interventions. Part3- description and pictures of the process this patient underwent for CCH and manipulation.

Results: Part 1- therapist documentation failed to satisfy the BC. Part 2- vasomotor/sudomotor signs and skin temperature differences of >1˚C reflected the patient's incomplete response to therapy and medication, thus strengthening need for percutaneous stellate ganglion sympathetic nerve blocks. Part 3- CRPS was not exacerbated with CCH procedure.

Conclusions: Use of a BC checklist may guide documentation, speed recognition for an earlier diagnosis of CRPS in patients with Dupuytren's and an atypical post-fasciectomy response. Once identified, observed signs and measures of skin temperature could be used to monitor response to therapy and medical interventions. The positive outcome for this woman with Dupuytren's and CRPS-I after CCH injection are encouraging.

背景:对于Dupuytren筋膜切除术后出现被认为是复杂区域疼痛综合征(CRPS)的非典型神经源性疼痛的患者,早期识别可以改善预后。此外,考虑到Dupuytren's的进行性,有CRPS病史的个体有进一步手术干预的“风险”。目的:让治疗师熟悉布达佩斯标准(BC)检查表,以便早期诊断CRPS,描述如何通过皮肤温度差异跟踪压迫性运动/血管舒缩体征来监测筋膜切除术后非典型疼痛患者的血管舒缩不稳定性和干预效果,并详细处理同一名有CRPS病史的患者,她的另一只手注射了溶组织梭菌胶原酶(CCH),而没有加重CRPS。研究设计:病例报告。方法:作者查阅病案资料。第1部分-患者报告的症状和治疗师观察到的体征被挖掘并对BC进行评分。第2部分-血管舒缩/舒缩体征和皮肤温度(bb0 - 1˚C)差异被用来解释对治疗和医疗干预的反应。第3部分-描述和图片的过程,该患者接受了CCH和操作。结果:第一部分-治疗师文件未能满足BC。第2部分:血管舒缩/舒缩体征及皮肤温度差异bb0℃反映患者对治疗和药物反应不完全,加强了对经皮星状神经节交感神经阻滞的需求。第3部分- CCH手术没有加重CRPS。结论:使用BC检查表可以指导文献记录,加速识别Dupuytren患者和非典型筋膜切除术后反应的CRPS的早期诊断。一旦确定,观察到的体征和皮肤温度测量可用于监测对治疗和医疗干预的反应。这名患有Dupuytren's和CRPS-I的妇女在注射CCH后的积极结果令人鼓舞。
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引用次数: 0
A collaborative interdisciplinary approach for trigger finger management. 扳机指管理的协作跨学科方法。
IF 2.1 4区 医学 Q2 ORTHOPEDICS Pub Date : 2025-01-15 DOI: 10.1016/j.jht.2024.12.003
Emma Yanko, Chris Thomson, Richard Bourassa, Curtis Gasmo, Thuy Le, Katie Crockett

Background: Stenosing tenosynovitis, or trigger finger, is a common cause of hand disability. This study outlines a trigger finger management protocol that redirects referrals for surgical consultations to conservative management first.

Purpose: The primary outcome variable was the protocol endpoint based on the resolution of trigger finger symptoms (i.e. pain and triggering). Secondary outcome measures were to identify which patient characteristics were associated with an increased need for (i) surgical management and (ii) corticosteroid injections.

Study design: Retrospective chart review.

Methods: The study sample included all patients referred for surgical consultation for trigger finger who were redirected to physical therapy first between the dates of August 2018 and January 2023 (n = 72). Participants initially received a physical therapy assessment and three treatment sessions. Further management was determined based on patient presentation following our protocol. Descriptive analysis involved frequency calculations of studied variables. Comparison of patient characteristics and treatment modalities across different sub-groups was examined as well as associations between various patient characteristics and increased need for (i) surgical management and (ii) corticosteroid injection.

Results: Seventy-two patients were included in the study, and 60 patients completed the protocol. Of these patients, 22% (n = 16) resolved with physical therapy (PT) alone, 48.5% (n = 35) resolved with 1-2 corticosteroid injections following initial PT management and 12.5% (n = 9) were referred back for surgical consult. Sub-group comparisons revealed no significant differences in patient characteristics and treatment modalities across patients who resolved with physical therapy alone, physical therapy plus 1-2 injections, or in cases referred back for surgical consults.

Conclusion: The interdisciplinary care protocol in this study demonstrated that conservative management was successful in a majority of cases; facilitating timely access to evidence-based care, including corticosteroid injections and surgical management if necessary. Physical therapy treatment provides self-management and education strategies to those requiring further interventions, potentially reducing recurrence rates.

背景:狭窄性腱鞘炎,或扳机指,是手部残疾的常见原因。本研究概述了一种触发手指管理方案,该方案将外科会诊的转诊重新定向到保守管理。目的:主要结局变量是基于触发指症状(即疼痛和触发)的解决的方案终点。次要结局指标是确定哪些患者特征与(i)手术治疗和(ii)皮质类固醇注射的需求增加有关。研究设计:回顾性图表回顾。方法:研究样本包括2018年8月至2023年1月期间所有因扳机指进行外科会诊的患者(n = 72)。参与者最初接受了物理治疗评估和三次治疗。进一步的治疗是根据病人的表现来决定的。描述性分析涉及研究变量的频率计算。比较了不同亚组的患者特征和治疗方式,以及不同患者特征与(i)手术治疗和(ii)皮质类固醇注射需求增加之间的关系。结果:72例患者纳入研究,60例患者完成了方案。在这些患者中,22% (n = 16)仅通过物理治疗(PT)解决,48.5% (n = 35)在初始PT治疗后通过1-2次皮质类固醇注射解决,12.5% (n = 9)再次转诊进行手术咨询。亚组比较显示,在单独进行物理治疗、物理治疗加1-2次注射或转介回外科会诊的患者中,患者特征和治疗方式没有显著差异。结论:本研究的跨学科治疗方案表明保守治疗在大多数病例中是成功的;促进及时获得循证护理,包括必要时进行皮质类固醇注射和手术治疗。物理治疗为那些需要进一步干预的患者提供了自我管理和教育策略,有可能降低复发率。
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引用次数: 0
Applying grip during isokinetic testing significantly impacts the concentric and eccentric strength of the wrist flexors. 在等速测试中应用握力会显著影响腕屈肌的同心和偏心强度。
IF 2.1 4区 医学 Q2 ORTHOPEDICS Pub Date : 2025-01-14 DOI: 10.1016/j.jht.2024.12.019
Smadar Peleg, Eitan Shemy, Takashi Okada, Michal Arnon, Zeevi Dvir
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引用次数: 0
The intermetacarpal distance method for assessment of active thumb radial abduction has excellent test-retest agreement, reliability, and precision in persons with non-operative thumb carpometacarpal osteoarthritis. 在非手术拇指腕掌骨关节炎患者中,评估拇指主动桡骨外展的掌间距离法具有极好的复测一致性、可靠性和准确性。
IF 2.1 4区 医学 Q2 ORTHOPEDICS Pub Date : 2025-01-14 DOI: 10.1016/j.jht.2024.12.002
Halil Ibrahim Ergen, Karl Dischinger, Corey McGee
<p><strong>Background: </strong>Limitations in thumb radial abduction (i.e., carpometacarpal extension) are commonly experienced by persons with thumb carpometacarpal osteoarthritis. Restoring this deficit is often a focus of surgical and rehabilitative interventions. Because of this, clinical measures of radial abduction are needed. The ''gold-standard'' assessment of thumb radial abduction is goniometry however it has modest reliability in persons with thumb carpometacarpal osteoarthritis. Conversely, the intermetacarpal distance (IMD) method of assessing radial abduction has promising reliability in healthy persons and excellent inter-rater reliability in those with thumb carpometacarpal osteoarthritis. However, to date, there has been no exploration of its test-retest reliability and precision in persons with thumb carpometacarpal osteoarthritis. Further, while multiple trials are often performed in various hand therapy assessments, it is common practice to take a single measurement of hand joint range of motion. Yet, we do not know if multiple trials might enhance the reliability of these range of motion measurements.</p><p><strong>Purpose: </strong>The current study aimed to (1) assess the test-retest agreement, reliability, and precision of the IMD method when measuring thumb radial abduction and (2) compare these psychometric properties when reporting one trial, the mean of two trials, and the mean of three trials of the IMD method in people with thumb carpometacarpal (CMC1) osteoarthritis (OA).</p><p><strong>Study design: </strong>Prospective Cohort study of test-retest reliability.</p><p><strong>Methods: </strong>Purposive sampling was used to recruit adults with radiographically confirmed CMC1 OA. Participants' radial abduction was assessed using the IMD method to measure radial abduction of the affected hand on two separate occasions approximately two weeks apart. Three trials of the assessment were administered at each visit. The Bland Altman method was uses to assess agreement, the intraclass correlation coefficient (ICC<sub>2,3</sub>) was calculated to examine the reliability, and the standard error of the measurement (SEM), minimum detectable change (MDC) and MDC percentage were calculated to determine the precision of the IMD method for one trial, the mean of two trials, and the mean of three. Descriptive data on demographics and IMD values of the sample were presented.</p><p><strong>Results: </strong>Forty persons with CMC1 OA participated. The mean difference between trials ranged from 0.21 to 0.30 mm, no significant fixed biases (p≥0.48) or proportional biases (p≥0.41) existed between mean test and retest scores, and 38/40 (95%) of test-retest differences fell within the 95% limits of agreement. The Intraclass Correlation Coefficient (ICC<sub>2,3</sub>) values were 0.942 (0.893-0.968), 0.970 (0.943-0.984), and 0.970 (0.942-0.984) for 1 trial, the mean of two trials, and then mean of three trials respectively. The ICC value of
背景:拇指桡侧外展受限(即腕掌骨外展)是拇指腕掌骨关节炎患者常见的症状。修复这一缺陷通常是手术和康复干预的重点。因此,需要对桡骨外展进行临床测量。拇指桡骨外展的“金标准”评估是角度测量,但对于患有拇指腕掌骨关节炎的人来说,它的可靠性并不高。相反,评估桡骨外展的掌间距离(IMD)方法在健康人群中具有良好的可靠性,在拇指腕掌骨关节炎患者中具有良好的趾间可靠性。然而,到目前为止,还没有对其在拇指腕掌骨关节炎患者中的重测信度和准确性进行探索。此外,虽然在各种手部治疗评估中经常进行多项试验,但通常的做法是对手部关节活动范围进行单一测量。然而,我们不知道多次试验是否可以提高这些运动范围测量的可靠性。目的:本研究旨在(1)评估IMD方法在测量拇指桡骨外展时的测试-重测一致性、可靠性和准确性;(2)在报道拇指腕掌骨关节炎(CMC1)患者的IMD方法的一次试验、两次试验的平均值和三次试验的平均值时,比较这些心理测量特性。研究设计:重测信度的前瞻性队列研究。方法:采用目的抽样方法招募影像学证实的成人CMC1 OA患者。参与者的桡骨外展是用IMD方法评估的,在两个不同的场合,大约相隔两周,测量受影响的手的桡骨外展。每次访问时进行三次评估试验。采用Bland Altman方法评估一致性,计算类内相关系数(ICC2,3)检验信度,计算测量的标准误差(SEM)、最小可检测变化(MDC)和MDC百分比,确定IMD方法在一次试验、两次试验的平均值和三次试验的平均值的精度。提供了样本的人口统计学和IMD值的描述性数据。结果:40例CMC1型OA患者参与。试验之间的平均差异范围为0.21 ~ 0.30 mm,平均检验和重测分数之间不存在显著的固定偏差(p≥0.48)或比例偏差(p≥0.41),38/40(95%)的重测差异在95%的一致性范围内。组内相关系数(ICC2,3)分别为0.942(0.893-0.968)、0.970(0.943-0.984)、0.970(0.942-0.984),分别为1个试验、2个试验的平均值和3个试验的平均值。两个试验的平均值的ICC值显著高于1个试验的平均值,表明可靠性较好,但每种方法的可靠性均落入优秀范围(即>0.90)。1次试验(MDC%=13.0)的精度在可接受范围内,2次试验(MDC%=9.1)和3次试验(MDC%=9.1)的平均值精度在优范围内。结论:评估CMC1骨外展的IMD方法在CMC1骨关节炎患者中进行一次试验、两次试验的平均值或三次试验的平均值时具有可接受的一致性、优异的重测信度和可接受到优异的精度。两个或三个试验的平均值的精度和可靠性不高,但两个试验的平均值比单个试验的可靠性和精度高。分别进行一项或两项试验时,IMD测量值1.9 mm和1.4 mm的变化需要超过测量误差,而在进行一项或两项试验时,变化必须超过5.3 mm和3.8 mm才能超过临床有意义的阈值。当使用IMD方法评估CMC1型OA患者的CMC1型桡骨外展时,我们建议采用两次试验的平均值而不是一次试验。
{"title":"The intermetacarpal distance method for assessment of active thumb radial abduction has excellent test-retest agreement, reliability, and precision in persons with non-operative thumb carpometacarpal osteoarthritis.","authors":"Halil Ibrahim Ergen, Karl Dischinger, Corey McGee","doi":"10.1016/j.jht.2024.12.002","DOIUrl":"https://doi.org/10.1016/j.jht.2024.12.002","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Limitations in thumb radial abduction (i.e., carpometacarpal extension) are commonly experienced by persons with thumb carpometacarpal osteoarthritis. Restoring this deficit is often a focus of surgical and rehabilitative interventions. Because of this, clinical measures of radial abduction are needed. The ''gold-standard'' assessment of thumb radial abduction is goniometry however it has modest reliability in persons with thumb carpometacarpal osteoarthritis. Conversely, the intermetacarpal distance (IMD) method of assessing radial abduction has promising reliability in healthy persons and excellent inter-rater reliability in those with thumb carpometacarpal osteoarthritis. However, to date, there has been no exploration of its test-retest reliability and precision in persons with thumb carpometacarpal osteoarthritis. Further, while multiple trials are often performed in various hand therapy assessments, it is common practice to take a single measurement of hand joint range of motion. Yet, we do not know if multiple trials might enhance the reliability of these range of motion measurements.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Purpose: &lt;/strong&gt;The current study aimed to (1) assess the test-retest agreement, reliability, and precision of the IMD method when measuring thumb radial abduction and (2) compare these psychometric properties when reporting one trial, the mean of two trials, and the mean of three trials of the IMD method in people with thumb carpometacarpal (CMC1) osteoarthritis (OA).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Study design: &lt;/strong&gt;Prospective Cohort study of test-retest reliability.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;Purposive sampling was used to recruit adults with radiographically confirmed CMC1 OA. Participants' radial abduction was assessed using the IMD method to measure radial abduction of the affected hand on two separate occasions approximately two weeks apart. Three trials of the assessment were administered at each visit. The Bland Altman method was uses to assess agreement, the intraclass correlation coefficient (ICC&lt;sub&gt;2,3&lt;/sub&gt;) was calculated to examine the reliability, and the standard error of the measurement (SEM), minimum detectable change (MDC) and MDC percentage were calculated to determine the precision of the IMD method for one trial, the mean of two trials, and the mean of three. Descriptive data on demographics and IMD values of the sample were presented.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Forty persons with CMC1 OA participated. The mean difference between trials ranged from 0.21 to 0.30 mm, no significant fixed biases (p≥0.48) or proportional biases (p≥0.41) existed between mean test and retest scores, and 38/40 (95%) of test-retest differences fell within the 95% limits of agreement. The Intraclass Correlation Coefficient (ICC&lt;sub&gt;2,3&lt;/sub&gt;) values were 0.942 (0.893-0.968), 0.970 (0.943-0.984), and 0.970 (0.942-0.984) for 1 trial, the mean of two trials, and then mean of three trials respectively. The ICC value of ","PeriodicalId":54814,"journal":{"name":"Journal of Hand Therapy","volume":" ","pages":""},"PeriodicalIF":2.1,"publicationDate":"2025-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143016619","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Positive clinical tests for medial epicondylalgia are more common than tests for lateral epicondylalgia in recreational pickleball players: A cross-sectional study. 在娱乐性匹克球运动员中,内侧上髁痛的阳性临床测试比外侧上髁痛的测试更常见:一项横断面研究。
IF 2.1 4区 医学 Q2 ORTHOPEDICS Pub Date : 2025-01-14 DOI: 10.1016/j.jht.2024.12.013
Betsy A Myers, June Hanks

Background: Epicondylalgia is a common overuse injury in tennis. However, little is known regarding epicondylalgia in pickleball.

Purpose: This study examined the prevalence of positive epicondylalgia tests in recreational pickleball players and the relationship between positive tests and player characteristics.

Study design: Cross-sectional study.

Methods: Clinical tests for epicondylalgia were performed courtside on the dominant arm of 129 recreational pickleball players. Participants completed a survey with questions related to demographics and play characteristics. Descriptive data were reported for epicondylalgia testing and survey performance. Chi-squared analysis and Fisher's exact test were used to determine associations between testing and survey responses. Relative risk estimates for positive tests for epicondylalgia were calculated based on pickleball playing characteristics.

Results: The prevalence of positive tests was 7% for medial epicondylalgia, 5.4% for lateral epicondylalgia, and 2.3% for both medial epicondylalgia and lateral epicondylalgia. Ninety-two participants (71.3%) completed the survey. Those who participated in tournaments were less likely to have a positive test for medial epicondylalgia (Fisher's exact test, p = 0.017). The relative risk of having a positive epicondylalgia test was lower for those who have played for at least 4 years (medial = 0.875 [CI 0.81-0.95] and lateral 0.913 [CI 0.866-0.979]). Epicondylalgia testing was not associated with age, sex, hand dominance, level of play, location of play, warm-up performance, frequency of play, or length of play.

Conclusions: Among pickleball players, there was a lower prevalence of positive tests for lateral epicondylalgia than for medial epicondylalgia. Compared to tennis, lateral epicondylalgia may be less common due to a lower elbow torque, while medial epicondylalgia may be more common due to methods to impart spin. Given the differences among sports, clinicians may need to utilize different prevention and intervention strategies when working with pickleball players.

背景:上髁痛是网球运动中常见的过度使用损伤。然而,对匹克球的上髁痛知之甚少。目的:本研究探讨休闲匹克球运动员上髁痛测试阳性率及其与运动员特征的关系。研究设计:横断面研究。方法:对129名休闲匹克球运动员的主臂进行场边上髁痛临床试验。参与者完成了一项与人口统计和游戏特征相关的调查。报告了上髁痛测试和调查表现的描述性数据。使用卡方分析和Fisher精确检验来确定测试和调查反应之间的关联。根据匹克球运动特征计算上髁痛阳性测试的相对风险估计。结果:内上髁痛的阳性率为7%,外上髁痛为5.4%,内上髁痛和外上髁痛均为2.3%。92名参与者(71.3%)完成了调查。参加比赛的患者内侧上髁痛检测呈阳性的可能性较小(Fisher精确检验,p = 0.017)。对于那些至少踢了4年球的人来说,上髁痛测试呈阳性的相对风险较低(内侧= 0.875 [CI 0.81-0.95],外侧= 0.913 [CI 0.866-0.979])。上髁痛测试与年龄、性别、手优势、游戏水平、游戏位置、热身表现、游戏频率或游戏时长无关。结论:在匹克球运动员中,外上髁痛的阳性检测率低于内上髁痛。与网球相比,由于肘关节扭矩较低,外侧上髁痛可能不太常见,而内侧上髁痛可能由于施加旋转的方法而更常见。鉴于运动之间的差异,临床医生在治疗匹克球运动员时可能需要使用不同的预防和干预策略。
{"title":"Positive clinical tests for medial epicondylalgia are more common than tests for lateral epicondylalgia in recreational pickleball players: A cross-sectional study.","authors":"Betsy A Myers, June Hanks","doi":"10.1016/j.jht.2024.12.013","DOIUrl":"https://doi.org/10.1016/j.jht.2024.12.013","url":null,"abstract":"<p><strong>Background: </strong>Epicondylalgia is a common overuse injury in tennis. However, little is known regarding epicondylalgia in pickleball.</p><p><strong>Purpose: </strong>This study examined the prevalence of positive epicondylalgia tests in recreational pickleball players and the relationship between positive tests and player characteristics.</p><p><strong>Study design: </strong>Cross-sectional study.</p><p><strong>Methods: </strong>Clinical tests for epicondylalgia were performed courtside on the dominant arm of 129 recreational pickleball players. Participants completed a survey with questions related to demographics and play characteristics. Descriptive data were reported for epicondylalgia testing and survey performance. Chi-squared analysis and Fisher's exact test were used to determine associations between testing and survey responses. Relative risk estimates for positive tests for epicondylalgia were calculated based on pickleball playing characteristics.</p><p><strong>Results: </strong>The prevalence of positive tests was 7% for medial epicondylalgia, 5.4% for lateral epicondylalgia, and 2.3% for both medial epicondylalgia and lateral epicondylalgia. Ninety-two participants (71.3%) completed the survey. Those who participated in tournaments were less likely to have a positive test for medial epicondylalgia (Fisher's exact test, p = 0.017). The relative risk of having a positive epicondylalgia test was lower for those who have played for at least 4 years (medial = 0.875 [CI 0.81-0.95] and lateral 0.913 [CI 0.866-0.979]). Epicondylalgia testing was not associated with age, sex, hand dominance, level of play, location of play, warm-up performance, frequency of play, or length of play.</p><p><strong>Conclusions: </strong>Among pickleball players, there was a lower prevalence of positive tests for lateral epicondylalgia than for medial epicondylalgia. Compared to tennis, lateral epicondylalgia may be less common due to a lower elbow torque, while medial epicondylalgia may be more common due to methods to impart spin. Given the differences among sports, clinicians may need to utilize different prevention and intervention strategies when working with pickleball players.</p>","PeriodicalId":54814,"journal":{"name":"Journal of Hand Therapy","volume":" ","pages":""},"PeriodicalIF":2.1,"publicationDate":"2025-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143016603","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effects of high-intensity laser therapy in patients with De Quervain's tenosynovitis: A systematic review and meta-analysis. 高强度激光治疗对De Quervain氏腱鞘炎患者的影响:系统回顾和荟萃分析。
IF 2.1 4区 医学 Q2 ORTHOPEDICS Pub Date : 2025-01-14 DOI: 10.1016/j.jht.2024.10.001
Hernán Andrés de la Barra Ortiz, Nivaldo Antonio Parizotto, Claudio Chamorro Lange, Richard Eloin Liebano

Background: De Quervain's tenosynovitis (QT) is common among individuals performing repetitive manual tasks and significantly affects daily activities due to pain. While traditional treatments often provide limited relief, high-intensity laser therapy (HILT) shows as a potential analgesic resource.

Purpose: This systematic review aimed to evaluate the analgesic effects of HILT in patients with QT.

Study design: This study is a systematic review with meta-analysis with an observational, retrospective, and secondary design.

Methods: The search was conducted in PubMed, Web of Science, Scopus, EBSCOhost, Embase, Cochrane Library, Physiotherapy Evidence Database (PEDro), and Google Scholar (last updated September 17, 2024) to identify clinical trials comparing HILT with other treatments for QT. Pain intensity, measured with a Visual Analog Scale (VAS), was the main outcome. Disability and handgrip strength, measured with the quick disabilities of the arm, shoulder and hand (Q-DASH) and patient-rated wrist and hand evaluation (PRWE) questionnaires and dynamometry, were the secondary outcomes. Study quality was assessed using the Cochrane Risk of Bias Tool 2 (RoB2), and a meta-analysis was performed using mean difference (MD) or standardized mean difference (SMD). The GRADE approach guided evidence-based recommendations for statistically significant outcomes.

Results: Three studies were included, demonstrating an overall low bias (66%), with outcome measurements being the principal sources of bias. The meta-analysis did not reveal statistically significant advantages for HILT in terms of pain intensity and disability (VAS MD=0.21 cm; 95% CI: -1.43,1.86) (SMD=-0.31; 95% CI: -0.75,0.13). Despite individual studies reporting significant differences favoring HILT, the meta-analysis lacks statistical significance, preventing definitive recommendations.

Conclusions: Despite the potential benefits of HILT in managing QT, the current evidence does not support its superiority over conventional treatments like splinting or splinting combined with exercise. Further clinical trials are necessary to confirm HILT's efficacy and refine treatment guidelines in line with the dosage proposed by the included studies.

背景:De Quervain的腱鞘炎(QT)在重复性体力劳动的个体中很常见,并且由于疼痛而显著影响日常活动。而传统的治疗方法往往提供有限的缓解,高强度激光治疗(HILT)显示出一种潜在的镇痛资源。目的:本系统综述旨在评价hirt对qt患者的镇痛作用。研究设计:本研究是一项采用观察性、回顾性和二次设计的荟萃分析系统综述。方法:检索PubMed, Web of Science, Scopus, EBSCOhost, Embase, Cochrane Library,物理治疗证据数据库(PEDro)和谷歌Scholar(最后更新于2024年9月17日),以确定将HILT与其他QT治疗方法进行比较的临床试验,以视觉模拟量表(VAS)测量疼痛强度为主要结果。残障和握力,用手臂、肩膀和手的快速残障(Q-DASH)和患者评定的手腕和手评估(PRWE)问卷和动力测量法测量,是次要结果。采用Cochrane风险偏倚工具2 (RoB2)评估研究质量,并采用均差(MD)或标准化均差(SMD)进行meta分析。GRADE方法为统计上显著的结果提供循证建议。结果:纳入3项研究,显示总体偏倚低(66%),结果测量是偏倚的主要来源。meta分析并未显示HILT在疼痛强度和残疾方面的统计学显著优势(VAS MD=0.21 cm;95% ci: -1.43,1.86) (smd =-0.31;95% ci: -0.75,0.13)。尽管个别研究报告了支持HILT的显著差异,但meta分析缺乏统计学意义,因此无法给出明确的建议。结论:尽管HILT治疗QT有潜在的益处,但目前的证据并不支持其优于夹板或夹板联合运动等传统治疗方法。需要进一步的临床试验来证实HILT的疗效,并根据纳入研究建议的剂量完善治疗指南。
{"title":"Effects of high-intensity laser therapy in patients with De Quervain's tenosynovitis: A systematic review and meta-analysis.","authors":"Hernán Andrés de la Barra Ortiz, Nivaldo Antonio Parizotto, Claudio Chamorro Lange, Richard Eloin Liebano","doi":"10.1016/j.jht.2024.10.001","DOIUrl":"https://doi.org/10.1016/j.jht.2024.10.001","url":null,"abstract":"<p><strong>Background: </strong>De Quervain's tenosynovitis (QT) is common among individuals performing repetitive manual tasks and significantly affects daily activities due to pain. While traditional treatments often provide limited relief, high-intensity laser therapy (HILT) shows as a potential analgesic resource.</p><p><strong>Purpose: </strong>This systematic review aimed to evaluate the analgesic effects of HILT in patients with QT.</p><p><strong>Study design: </strong>This study is a systematic review with meta-analysis with an observational, retrospective, and secondary design.</p><p><strong>Methods: </strong>The search was conducted in PubMed, Web of Science, Scopus, EBSCOhost, Embase, Cochrane Library, Physiotherapy Evidence Database (PEDro), and Google Scholar (last updated September 17, 2024) to identify clinical trials comparing HILT with other treatments for QT. Pain intensity, measured with a Visual Analog Scale (VAS), was the main outcome. Disability and handgrip strength, measured with the quick disabilities of the arm, shoulder and hand (Q-DASH) and patient-rated wrist and hand evaluation (PRWE) questionnaires and dynamometry, were the secondary outcomes. Study quality was assessed using the Cochrane Risk of Bias Tool 2 (RoB2), and a meta-analysis was performed using mean difference (MD) or standardized mean difference (SMD). The GRADE approach guided evidence-based recommendations for statistically significant outcomes.</p><p><strong>Results: </strong>Three studies were included, demonstrating an overall low bias (66%), with outcome measurements being the principal sources of bias. The meta-analysis did not reveal statistically significant advantages for HILT in terms of pain intensity and disability (VAS MD=0.21 cm; 95% CI: -1.43,1.86) (SMD=-0.31; 95% CI: -0.75,0.13). Despite individual studies reporting significant differences favoring HILT, the meta-analysis lacks statistical significance, preventing definitive recommendations.</p><p><strong>Conclusions: </strong>Despite the potential benefits of HILT in managing QT, the current evidence does not support its superiority over conventional treatments like splinting or splinting combined with exercise. Further clinical trials are necessary to confirm HILT's efficacy and refine treatment guidelines in line with the dosage proposed by the included studies.</p>","PeriodicalId":54814,"journal":{"name":"Journal of Hand Therapy","volume":" ","pages":""},"PeriodicalIF":2.1,"publicationDate":"2025-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143016598","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A valid and reliable 3D-printed electronic grip strength assessment tool. 一个有效和可靠的3d打印电子握力评估工具。
IF 2.1 4区 医学 Q2 ORTHOPEDICS Pub Date : 2025-01-14 DOI: 10.1016/j.jht.2024.11.010
Amelia Sorensen, Lily Brosnan, Yong Hao Pua, Julian Thumboo, Yee Sien Ng, Laura Tay Bee Gek, Ross Clark
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引用次数: 0
Is it prudent to interpret findings from nonblinded RCTs relying solely on patient-reported outcome measures for outcome assessment? 仅仅依靠患者报告的结果评估来解释非盲随机对照试验的结果是否谨慎?
IF 2.1 4区 医学 Q2 ORTHOPEDICS Pub Date : 2025-01-14 DOI: 10.1016/j.jht.2024.09.001
Manigandan Chockalingam, Laura Pearson, Orla Daly
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引用次数: 0
期刊
Journal of Hand Therapy
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