Pub Date : 2024-10-31eCollection Date: 2025-03-01DOI: 10.5606/tftrd.2024.14671
Zeynep Karakuzu Güngör, Erdal Güngör
Objectives: This study aims to investigate and compare the treatment efficacy of extracorporeal shockwave therapy (ESWT) and high-intensity laser therapy (HILT) regarding pain management and functionality in patients with de Quervain tenosynovitis (DQT).
Patients and methods: Between May 2022 and November 2022, a total of 60 patients with DQT (16 males, 34 females; mean age: 43.3±7.7 years; range, 18 to 65 years) were included in this study. The patients were randomly divided into two groups as follows: Group A (ESWT, n=29) and Group B (HILT, n=31). The patients were asked to refrain from all types of exercise 24 h before the experiment. The pain level of the patients at the time of presentation was evaluated via Visual Analog Scale (VAS), and the function outcome was evaluated with Quick Disabilities of Arm, Shoulder and Hand (QDASH) before and after the treatment. Muscle strength was evaluated with a Jamar hand dynamometer, and an algometer was used to measure pressure pain threshold (PPT). The Global Assessment Scale (GAS) was used to measure the treatment success.
Results: The intragroup comparisons revealed significant improvements in all parameters after the treatment in both groups (p<0.05). The VAS-rest score, the VAS-movement score, the QDASH score, pain-free grip strength (PFGS), and PPT showed a significant difference before treatment at three weeks and three months (p<0.01). The difference between the PPT values of the groups at three weeks was significant (p<0.01). The third-week PPT value of Group B was higher than the PPT value of Group A. The difference between GAS 1 and GAS 2 of both groups was statistically significant at three weeks and three months (p<0.05).
Conclusion: Both ESWT and HILT treatments are safe and effective in DQT treatment. The ESWT is a recent, non-invasive therapeutic modality which is effective, convenient, and safe in DQT. On the other hand, HILT is a non-invasive, reliable method which has a greater effect on DQT.
{"title":"The comparison of the efficacy of extracorporeal shockwave therapy and high-intensity laser therapy in the treatment of de Quervain tenosynovitis.","authors":"Zeynep Karakuzu Güngör, Erdal Güngör","doi":"10.5606/tftrd.2024.14671","DOIUrl":"https://doi.org/10.5606/tftrd.2024.14671","url":null,"abstract":"<p><strong>Objectives: </strong>This study aims to investigate and compare the treatment efficacy of extracorporeal shockwave therapy (ESWT) and high-intensity laser therapy (HILT) regarding pain management and functionality in patients with de Quervain tenosynovitis (DQT).</p><p><strong>Patients and methods: </strong>Between May 2022 and November 2022, a total of 60 patients with DQT (16 males, 34 females; mean age: 43.3±7.7 years; range, 18 to 65 years) were included in this study. The patients were randomly divided into two groups as follows: Group A (ESWT, n=29) and Group B (HILT, n=31). The patients were asked to refrain from all types of exercise 24 h before the experiment. The pain level of the patients at the time of presentation was evaluated via Visual Analog Scale (VAS), and the function outcome was evaluated with Quick Disabilities of Arm, Shoulder and Hand (QDASH) before and after the treatment. Muscle strength was evaluated with a Jamar hand dynamometer, and an algometer was used to measure pressure pain threshold (PPT). The Global Assessment Scale (GAS) was used to measure the treatment success.</p><p><strong>Results: </strong>The intragroup comparisons revealed significant improvements in all parameters after the treatment in both groups (p<0.05). The VAS-rest score, the VAS-movement score, the QDASH score, pain-free grip strength (PFGS), and PPT showed a significant difference before treatment at three weeks and three months (p<0.01). The difference between the PPT values of the groups at three weeks was significant (p<0.01). The third-week PPT value of Group B was higher than the PPT value of Group A. The difference between GAS 1 and GAS 2 of both groups was statistically significant at three weeks and three months (p<0.05).</p><p><strong>Conclusion: </strong>Both ESWT and HILT treatments are safe and effective in DQT treatment. The ESWT is a recent, non-invasive therapeutic modality which is effective, convenient, and safe in DQT. On the other hand, HILT is a non-invasive, reliable method which has a greater effect on DQT.</p>","PeriodicalId":56043,"journal":{"name":"Turkish Journal of Physical Medicine and Rehabilitation","volume":"71 1","pages":"28-36"},"PeriodicalIF":1.1,"publicationDate":"2024-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12012914/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144011329","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objectives: This study aimed to investigate the effects of different carrier frequencies of interferential current (IFC) treatment on a Visual Analog Scale (VAS) for pain, the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), 10-m walk test, and the amount of paracetamol taken.
Patients and methods: The double-blind, randomized controlled study included 61 patients (16 males, 45 females; mean age: 63.7±9.8 years; range, 50 to 80 years) with knee osteoarthritis who were randomized to three treatment groups: 2,000 Hz, 4,000 Hz, and 8,000 Hz. The study was conducted between February 2019 and October 2019. Subjects received IFC treatment for 20 min five times per week for three weeks. All subjects were prescribed a home exercise program. Patients were evaluated at baseline and at three and seven weeks. The primary outcome was VAS to assess knee pain.
Results: Treatment with IFC yielded significant results in VAS pain, WOMAC pain, and WOMAC function parameters in all three groups, but no significant difference was shown among the three groups. The WOMAC stiffness parameter was found to benefit from the treatment only in the first group, while the 10-m walk test improved for the first and third groups. The number of paracetamol tablets taken differed significantly neither in nor among the treatment groups.
Conclusion: Previous trials have found a significant reduction in knee pain levels and an increase in function with IFC treatment, although there is no consensus on which carrier frequencies and duration to choose for IFC treatment. In this study, we detected significant benefits for all the different carrier frequency groups but were not able to show any to be superior to the others.
{"title":"The efficacy of interferential current treatment on knee osteoarthritis: A pilot randomized double-blind study comparing the effects of different carrier frequencies.","authors":"Benil Nesli Ata, Berrin Durmaz, Ece Çınar, Funda Atamaz Calis","doi":"10.5606/tftrd.2024.12390","DOIUrl":"https://doi.org/10.5606/tftrd.2024.12390","url":null,"abstract":"<p><strong>Objectives: </strong>This study aimed to investigate the effects of different carrier frequencies of interferential current (IFC) treatment on a Visual Analog Scale (VAS) for pain, the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), 10-m walk test, and the amount of paracetamol taken.</p><p><strong>Patients and methods: </strong>The double-blind, randomized controlled study included 61 patients (16 males, 45 females; mean age: 63.7±9.8 years; range, 50 to 80 years) with knee osteoarthritis who were randomized to three treatment groups: 2,000 Hz, 4,000 Hz, and 8,000 Hz. The study was conducted between February 2019 and October 2019. Subjects received IFC treatment for 20 min five times per week for three weeks. All subjects were prescribed a home exercise program. Patients were evaluated at baseline and at three and seven weeks. The primary outcome was VAS to assess knee pain.</p><p><strong>Results: </strong>Treatment with IFC yielded significant results in VAS pain, WOMAC pain, and WOMAC function parameters in all three groups, but no significant difference was shown among the three groups. The WOMAC stiffness parameter was found to benefit from the treatment only in the first group, while the 10-m walk test improved for the first and third groups. The number of paracetamol tablets taken differed significantly neither in nor among the treatment groups.</p><p><strong>Conclusion: </strong>Previous trials have found a significant reduction in knee pain levels and an increase in function with IFC treatment, although there is no consensus on which carrier frequencies and duration to choose for IFC treatment. In this study, we detected significant benefits for all the different carrier frequency groups but were not able to show any to be superior to the others.</p>","PeriodicalId":56043,"journal":{"name":"Turkish Journal of Physical Medicine and Rehabilitation","volume":"70 4","pages":"517-524"},"PeriodicalIF":1.1,"publicationDate":"2024-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11868852/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143544229","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-31eCollection Date: 2024-12-01DOI: 10.5606/tftrd.2024.13746
Zennure Adıgüzel Şahin, Mehmet Üzel, Fatma Güler Kahraman Yıldırım, Mahmut Ercan Tanyeli, Ahmet Ertaş, Deniz Palamar, Tuğçe Özekli Mısırlıoğlu, Kenan Akgün, Ahmet Dirican
Objectives: This study aimed to evaluate the accuracy of four clinical tests confirmed by ultrasonography (USG) and to evaluate the role of age, sex, handedness, subcutaneous tissue thickness (STT), tendon thickness (TT), and STT/TT in determining the absence of the palmaris longus muscle.
Patients and methods: In this descriptive study, 282 wrists of 141 healthy individuals (71 females, 70 males; mean age: 29±9.6 years; range, 21 to 55 years) were included between September 2021 and November 2022. The palmaris longus muscle tendon was identified by Schaeffer's test, Mishra's test I, Thompson's test, and Pushpakumar's test and then evaluated with USG. Before the tests, age, sex, and dominant hand information of the individuals were obtained. The STT and TT were measured with USG.
Results: Sensitivity values by side were as follows (right/left respectively): Schaeffer's 92%/73%, Mishra's I 91%/93%, Thompson's 84%/87%, and Pushpakumar's 86%/91%. Specificity values by side were as follows (right/left respectively): Schaeffer's 87%/95%, Mishra's I 78%/82%, Thompson's 78%/79%, and Pushpakumar's 84%/82%. Sensitivity values by sex were as follows (female/male respectively): Schaeffer's 81%/96%, Mishra's I 92%/94%, Thompson's 85%/90%, and Pushpakumar's 91%/92%. Specificity values by sex were as follows (female/male respectively): Schaeffer's 68%/90%, Mishra's I 72%/90%, Thompson's 72%/85%, and Pushpakumar's 78%/85%. The intraclass correlation coefficient between clinical tests and USG was 0.94 for the left side and 0.95 for the right side.
Conclusion: Mishra's test I and Pushpakumar's test can be used in females, while Schaeffer's test and Mishra's test I can be used in males as a mutually supportive clinical test. Furthermore, while there may be false negative and false positive test results due to muscle variations, it should be noted that STT/TT is also effective, particularly on the right side.
目的:本研究旨在评估超声(USG)证实的四项临床检查的准确性,并评估年龄、性别、利手性、皮下组织厚度(STT)、肌腱厚度(TT)和STT/TT在判断掌长肌缺失中的作用。患者和方法:在这项描述性研究中,141名健康个体(71名女性,70名男性;平均年龄:29±9.6岁;范围为21至55岁),包括2021年9月至2022年11月。通过Schaeffer试验、Mishra试验I、Thompson试验和Pushpakumar试验确定掌长肌肌腱,然后用USG进行评估。测试前,获得受试者的年龄、性别和优势手信息。用USG测量STT和TT。结果:两侧敏感性值分别为:Schaeffer的92%/73%,Mishra的91%/93%,Thompson的84%/87%,Pushpakumar的86%/91%。两侧特异性值分别为(右/左):Schaeffer为87%/95%,Mishra为78%/82%,Thompson为78%/79%,Pushpakumar为84%/82%。性别敏感性值分别为:Schaeffer为81%/96%,Mishra为92%/94%,Thompson为85%/90%,Pushpakumar为91%/92%。性别特异性值分别为:Schaeffer为68%/90%,Mishra为72%/90%,Thompson为72%/85%,Pushpakumar为78%/85%。左侧和右侧临床试验与USG的类内相关系数分别为0.94和0.95。结论:Mishra’s test I和Pushpakumar’s test可用于女性,而Schaeffer’s test和Mishra’s test I可用于男性,作为一种相互支持的临床测试。此外,虽然由于肌肉变化可能会出现假阴性和假阳性的测试结果,但应该注意的是,STT/TT也是有效的,特别是在右侧。
{"title":"Sensitivity and specificity assessment of four clinical tests for palmaris longus muscle by ultrasound.","authors":"Zennure Adıgüzel Şahin, Mehmet Üzel, Fatma Güler Kahraman Yıldırım, Mahmut Ercan Tanyeli, Ahmet Ertaş, Deniz Palamar, Tuğçe Özekli Mısırlıoğlu, Kenan Akgün, Ahmet Dirican","doi":"10.5606/tftrd.2024.13746","DOIUrl":"https://doi.org/10.5606/tftrd.2024.13746","url":null,"abstract":"<p><strong>Objectives: </strong>This study aimed to evaluate the accuracy of four clinical tests confirmed by ultrasonography (USG) and to evaluate the role of age, sex, handedness, subcutaneous tissue thickness (STT), tendon thickness (TT), and STT/TT in determining the absence of the palmaris longus muscle.</p><p><strong>Patients and methods: </strong>In this descriptive study, 282 wrists of 141 healthy individuals (71 females, 70 males; mean age: 29±9.6 years; range, 21 to 55 years) were included between September 2021 and November 2022. The palmaris longus muscle tendon was identified by Schaeffer's test, Mishra's test I, Thompson's test, and Pushpakumar's test and then evaluated with USG. Before the tests, age, sex, and dominant hand information of the individuals were obtained. The STT and TT were measured with USG.</p><p><strong>Results: </strong>Sensitivity values by side were as follows (right/left respectively): Schaeffer's 92%/73%, Mishra's I 91%/93%, Thompson's 84%/87%, and Pushpakumar's 86%/91%. Specificity values by side were as follows (right/left respectively): Schaeffer's 87%/95%, Mishra's I 78%/82%, Thompson's 78%/79%, and Pushpakumar's 84%/82%. Sensitivity values by sex were as follows (female/male respectively): Schaeffer's 81%/96%, Mishra's I 92%/94%, Thompson's 85%/90%, and Pushpakumar's 91%/92%. Specificity values by sex were as follows (female/male respectively): Schaeffer's 68%/90%, Mishra's I 72%/90%, Thompson's 72%/85%, and Pushpakumar's 78%/85%. The intraclass correlation coefficient between clinical tests and USG was 0.94 for the left side and 0.95 for the right side.</p><p><strong>Conclusion: </strong>Mishra's test I and Pushpakumar's test can be used in females, while Schaeffer's test and Mishra's test I can be used in males as a mutually supportive clinical test. Furthermore, while there may be false negative and false positive test results due to muscle variations, it should be noted that STT/TT is also effective, particularly on the right side.</p>","PeriodicalId":56043,"journal":{"name":"Turkish Journal of Physical Medicine and Rehabilitation","volume":"70 4","pages":"525-531"},"PeriodicalIF":1.1,"publicationDate":"2024-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11868856/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143543923","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objectives: This study aims to investigate the effect of extracorporeal shock wave therapy (ESWT) and manual therapy (MT) on active trigger points of the sternocleidomastoid muscle (SCM) in patients with cervicogenic headache (CEH).
Patients and methods: A total of 42 patients were included (27 females, 15 males; mean age: 33.2±7.7 years; range, 18 to 45 years) in the randomized controlled trial between March 2022 and December 2022. The patients were randomly divided into the ESWT group (n=21) and the MT group (n=21). Each group received therapy once a week for four weeks. The primary outcome measure was the Visual Analog Scale (VAS), and secondary outcome measures were pressure pain threshold (PPT), Neck Disability Index (NDI), and stiffness (shear elastic modulus) of the SCM measured at baseline, postintervention, and four weeks after treatment.
Results: One patient from the ESWT group was lost to follow-up. The missing data were imputed for intention-to-treat analysis. Significant decreases of VAS, NDI, and shear elastic modulus of SCM were found at postintervention and four weeks after treatment in both groups (p<0.01). The PPT scores markedly increased over time compared to baseline in both groups (p<0.01). The repeated measures of analysis of variance revealed a significant time effect (p<0.001) in each outcome variable for both groups. There were no significant differences between the two groups in VAS, PPT, NDI, and the stiffness of SCM at each time point.
Conclusion: Extracorporeal shock wave therapy and MT were equally effective in pain relief, functional recovery, and reduction of muscle stiffness. Extracorporeal shock wave therapy may be used as an alternative treatment method for CEH patients with active myofascial trigger points of the SCM.
{"title":"Comparison of extracorporeal shock wave therapy and manual therapy on active trigger points of the sternocleidomastoid muscle in cervicogenic headache: A randomized controlled trial.","authors":"Chunfeng Xia, Yanjun Zhao, Lizhen Lin, Yanni Yu, Jialiang Wang, Jiecheng Fan, Xiangzhen Yuan, Shuyun Zhang","doi":"10.5606/tftrd.2024.13994","DOIUrl":"https://doi.org/10.5606/tftrd.2024.13994","url":null,"abstract":"<p><strong>Objectives: </strong>This study aims to investigate the effect of extracorporeal shock wave therapy (ESWT) and manual therapy (MT) on active trigger points of the sternocleidomastoid muscle (SCM) in patients with cervicogenic headache (CEH).</p><p><strong>Patients and methods: </strong>A total of 42 patients were included (27 females, 15 males; mean age: 33.2±7.7 years; range, 18 to 45 years) in the randomized controlled trial between March 2022 and December 2022. The patients were randomly divided into the ESWT group (n=21) and the MT group (n=21). Each group received therapy once a week for four weeks. The primary outcome measure was the Visual Analog Scale (VAS), and secondary outcome measures were pressure pain threshold (PPT), Neck Disability Index (NDI), and stiffness (shear elastic modulus) of the SCM measured at baseline, postintervention, and four weeks after treatment.</p><p><strong>Results: </strong>One patient from the ESWT group was lost to follow-up. The missing data were imputed for intention-to-treat analysis. Significant decreases of VAS, NDI, and shear elastic modulus of SCM were found at postintervention and four weeks after treatment in both groups (p<0.01). The PPT scores markedly increased over time compared to baseline in both groups (p<0.01). The repeated measures of analysis of variance revealed a significant time effect (p<0.001) in each outcome variable for both groups. There were no significant differences between the two groups in VAS, PPT, NDI, and the stiffness of SCM at each time point.</p><p><strong>Conclusion: </strong>Extracorporeal shock wave therapy and MT were equally effective in pain relief, functional recovery, and reduction of muscle stiffness. Extracorporeal shock wave therapy may be used as an alternative treatment method for CEH patients with active myofascial trigger points of the SCM.</p>","PeriodicalId":56043,"journal":{"name":"Turkish Journal of Physical Medicine and Rehabilitation","volume":"71 1","pages":"56-65"},"PeriodicalIF":1.1,"publicationDate":"2024-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12012926/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144000267","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-31eCollection Date: 2024-12-01DOI: 10.5606/tftrd.2024.14243
Merve Sekizkardes Tutuncu, Savas Sencan, Serdar Kokar, Osman Hakan Gunduz
{"title":"Inadvertent intradiscal flow during transforaminal epidural steroid injection.","authors":"Merve Sekizkardes Tutuncu, Savas Sencan, Serdar Kokar, Osman Hakan Gunduz","doi":"10.5606/tftrd.2024.14243","DOIUrl":"https://doi.org/10.5606/tftrd.2024.14243","url":null,"abstract":"","PeriodicalId":56043,"journal":{"name":"Turkish Journal of Physical Medicine and Rehabilitation","volume":"70 4","pages":"557-558"},"PeriodicalIF":1.1,"publicationDate":"2024-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11868861/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143544672","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-31eCollection Date: 2025-06-01DOI: 10.5606/tftrd.2024.14930
Burak Kamil Turan, Birkan Sonel Tur
In this case report, the rehabilitation process of a 38-year-old female patient who developed cauda equina syndrome due to spinal manipulation for the treatment of lumbar disc herniation was presented. The aim was to discuss the outcomes of rehabilitation after cauda equina syndrome, as well as the challenges associated with it. Despite the difficulties experienced during the rehabilitation process, a comprehensive multidisciplinary rehabilitation program is beneficial in terms of gaining independence and returning to daily activities, social life, and work for patients with cauda equina syndrome.
{"title":"Rehabilitation in a case with cauda equina syndrome after spinal manipulation: A long and difficult process.","authors":"Burak Kamil Turan, Birkan Sonel Tur","doi":"10.5606/tftrd.2024.14930","DOIUrl":"10.5606/tftrd.2024.14930","url":null,"abstract":"<p><p>In this case report, the rehabilitation process of a 38-year-old female patient who developed cauda equina syndrome due to spinal manipulation for the treatment of lumbar disc herniation was presented. The aim was to discuss the outcomes of rehabilitation after cauda equina syndrome, as well as the challenges associated with it. Despite the difficulties experienced during the rehabilitation process, a comprehensive multidisciplinary rehabilitation program is beneficial in terms of gaining independence and returning to daily activities, social life, and work for patients with cauda equina syndrome.</p>","PeriodicalId":56043,"journal":{"name":"Turkish Journal of Physical Medicine and Rehabilitation","volume":"71 2","pages":"250-254"},"PeriodicalIF":1.3,"publicationDate":"2024-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12305677/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144755224","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-16eCollection Date: 2024-12-01DOI: 10.5606/tftrd.2024.15350
Alper Mengi, Erkan Özduran
{"title":"Can ozone injections be blinded in research?","authors":"Alper Mengi, Erkan Özduran","doi":"10.5606/tftrd.2024.15350","DOIUrl":"https://doi.org/10.5606/tftrd.2024.15350","url":null,"abstract":"","PeriodicalId":56043,"journal":{"name":"Turkish Journal of Physical Medicine and Rehabilitation","volume":"70 4","pages":"559"},"PeriodicalIF":1.1,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11868866/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143544668","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objectives: This study aimed to compare the acute effects of radial extracorporeal shockwave therapy (r-ESWT) and focused extracorporeal shockwave therapy (f-ESWT) on pain, muscle strength, and function in patients with lateral epicondylitis (LE).
Patients and methods: Fifty-six patients (31 males, 25 females; mean age: 44.6±8.4 years; range, 19 to 60 years) who were diagnosed with LE participated in the randomized study between August 2023 and October 2023. The patients were stratified by pain level to have four r-ESWT or f-ESWT treatments once a week. Patients were evaluated on the first day of treatment and one week after the last treatment. The outcome measures used were the Visual Analog Scale for pain, isokinetic dynamometer for wrist muscle strength measurement, the DASH (Disabilities of the Arm, Shoulder, and Hand) score for functional status, and the 36-item Short-Form Health Survey (SF-36) for health-related quality of life.
Results: After the treatment, the pain at rest and during activity decreased in both groups (p=0.018, p=0.001, p=0.003, and p<0.001). Nocturnal pain was found to be lower in the f-ESWT group (p=0.028). The isokinetic muscle strength of the wrist extensors was higher in the r-ESWT group compared to the f-ESWT group (p=0.002 and p=0.017). The DASH performance score of the r-ESWT group was higher compared to the f-ESWT group (p=0.009). Both groups showed improvements in SF-36 scores (p<0.05).
Conclusion: Both groups showed a decrease in pain levels, but the effects were superior in the f-ESWT group. However, r-ESWT was found to present better results in terms of its effect on isokinetic muscle strength. While f-ESWT may be more effective in reducing pain, r-ESWT may be more effective in increasing muscle strength.
{"title":"Radial versus focused extracorporeal shockwave therapy in lateral epicondylitis: Acute effects on pain, muscle strength, upper extremity function, and quality of life.","authors":"Bihter Akınoğlu, Aydan Örsçelik, Ayfer Ezgi Yılmaz, Salman Usman Shehu, Şeyma Özal, Hüseyin Günaydın, Tuğba Kocahan","doi":"10.5606/tftrd.2024.14060","DOIUrl":"https://doi.org/10.5606/tftrd.2024.14060","url":null,"abstract":"<p><strong>Objectives: </strong>This study aimed to compare the acute effects of radial extracorporeal shockwave therapy (r-ESWT) and focused extracorporeal shockwave therapy (f-ESWT) on pain, muscle strength, and function in patients with lateral epicondylitis (LE).</p><p><strong>Patients and methods: </strong>Fifty-six patients (31 males, 25 females; mean age: 44.6±8.4 years; range, 19 to 60 years) who were diagnosed with LE participated in the randomized study between August 2023 and October 2023. The patients were stratified by pain level to have four r-ESWT or f-ESWT treatments once a week. Patients were evaluated on the first day of treatment and one week after the last treatment. The outcome measures used were the Visual Analog Scale for pain, isokinetic dynamometer for wrist muscle strength measurement, the DASH (Disabilities of the Arm, Shoulder, and Hand) score for functional status, and the 36-item Short-Form Health Survey (SF-36) for health-related quality of life.</p><p><strong>Results: </strong>After the treatment, the pain at rest and during activity decreased in both groups (p=0.018, p=0.001, p=0.003, and p<0.001). Nocturnal pain was found to be lower in the f-ESWT group (p=0.028). The isokinetic muscle strength of the wrist extensors was higher in the r-ESWT group compared to the f-ESWT group (p=0.002 and p=0.017). The DASH performance score of the r-ESWT group was higher compared to the f-ESWT group (p=0.009). Both groups showed improvements in SF-36 scores (p<0.05).</p><p><strong>Conclusion: </strong>Both groups showed a decrease in pain levels, but the effects were superior in the f-ESWT group. However, r-ESWT was found to present better results in terms of its effect on isokinetic muscle strength. While f-ESWT may be more effective in reducing pain, r-ESWT may be more effective in increasing muscle strength.</p>","PeriodicalId":56043,"journal":{"name":"Turkish Journal of Physical Medicine and Rehabilitation","volume":"71 1","pages":"19-27"},"PeriodicalIF":1.1,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12012923/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144064592","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-17eCollection Date: 2025-06-01DOI: 10.5606/tftrd.2024.14692
Ezgi Yıldız Güvercin, Yeşim Kirazlı, Hale Üzümcügil, Ece Çınar, Musa Baklacı, Gülce Kirazlı, Tayfun Kirazlı, Neşe Çelebisoy, Figen Gökçay
Objectives: The aim of this study was to investigate the effect of neck exercises in addition to vestibular rehabilitation treatment in unilateral peripheral vestibular system (PVS) diseases accompanied by neck pain and to evaluate the relationship between neck pain severity and clinical balance parameters in this patient population.
Patients and methods: In this prospective, randomized-controlled study, a total of 70 patients (30 males, 40 females; mean age: 52.6±14.9 years; range, 37 to 68 years) who were diagnosed with unilateral PVS disease with concomitant neck pain were included between September 2019 and May 2022. The patients were randomized into two equal groups. Group 1 (n=35) received a vestibular rehabilitation program for four weeks, and Group 2 (n=35) received neck exercises in addition to the standard rehabilitation protocol. As the compensation improved in the vestibular rehabilitation treatment, additional compelling exercises were added to the program. At Week 4, all patients were evaluated with clinical parameters including the severity of balance, neck pain, dizziness, Dizziness Handicap Inventory (DHI), Functional Gait Assessment (FGA), Activity-specific Balance Confidence (ABC) scale, Dynamic Gait Index (DGI), Berg Balance Scale (BBS), Timed Up-and-Go (TUG) test, Falls Efficacy Scale (FES)-International, postural stability, and Neck Disability Index (NDI).
Results: After the rehabilitation program, a statistically significant improvement was observed in all clinical parameters in both groups (p<0.05). Compared to Group 1, there was a statistically significant difference in all other clinical parameters in Group 2, except for the two parameters: the Romberg eye-open time and TUG test (p<0.05). A significant correlation was found between the severity of neck pain and the severity of dizziness, BBS, DHI, FGA, and NDI (p<0.05).
Conclusion: Neck exercises may yield positive clinical outcomes when combined with vestibular rehabilitation and should be taken into consideration for planning rehabilitation program in patients with unilateral PVS disease and neck pain.
{"title":"The impact of cervical exercises in addition to vestibular rehabilitation on unilateral peripheral vestibular system disorders accompanied by neck pain: A prospective, randomized-controlled trial.","authors":"Ezgi Yıldız Güvercin, Yeşim Kirazlı, Hale Üzümcügil, Ece Çınar, Musa Baklacı, Gülce Kirazlı, Tayfun Kirazlı, Neşe Çelebisoy, Figen Gökçay","doi":"10.5606/tftrd.2024.14692","DOIUrl":"10.5606/tftrd.2024.14692","url":null,"abstract":"<p><strong>Objectives: </strong>The aim of this study was to investigate the effect of neck exercises in addition to vestibular rehabilitation treatment in unilateral peripheral vestibular system (PVS) diseases accompanied by neck pain and to evaluate the relationship between neck pain severity and clinical balance parameters in this patient population.</p><p><strong>Patients and methods: </strong>In this prospective, randomized-controlled study, a total of 70 patients (30 males, 40 females; mean age: 52.6±14.9 years; range, 37 to 68 years) who were diagnosed with unilateral PVS disease with concomitant neck pain were included between September 2019 and May 2022. The patients were randomized into two equal groups. Group 1 (n=35) received a vestibular rehabilitation program for four weeks, and Group 2 (n=35) received neck exercises in addition to the standard rehabilitation protocol. As the compensation improved in the vestibular rehabilitation treatment, additional compelling exercises were added to the program. At Week 4, all patients were evaluated with clinical parameters including the severity of balance, neck pain, dizziness, Dizziness Handicap Inventory (DHI), Functional Gait Assessment (FGA), Activity-specific Balance Confidence (ABC) scale, Dynamic Gait Index (DGI), Berg Balance Scale (BBS), Timed Up-and-Go (TUG) test, Falls Efficacy Scale (FES)-International, postural stability, and Neck Disability Index (NDI).</p><p><strong>Results: </strong>After the rehabilitation program, a statistically significant improvement was observed in all clinical parameters in both groups (p<0.05). Compared to Group 1, there was a statistically significant difference in all other clinical parameters in Group 2, except for the two parameters: the Romberg eye-open time and TUG test (p<0.05). A significant correlation was found between the severity of neck pain and the severity of dizziness, BBS, DHI, FGA, and NDI (p<0.05).</p><p><strong>Conclusion: </strong>Neck exercises may yield positive clinical outcomes when combined with vestibular rehabilitation and should be taken into consideration for planning rehabilitation program in patients with unilateral PVS disease and neck pain.</p>","PeriodicalId":56043,"journal":{"name":"Turkish Journal of Physical Medicine and Rehabilitation","volume":"71 2","pages":"187-198"},"PeriodicalIF":1.3,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12305684/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144755227","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-26eCollection Date: 2024-09-01DOI: 10.5606/tftrd.2024.13140
Nataša Kalebota, Nadica Laktašić Žerjavić, Kristina Kovač Durmiš, Milan Milošević, Antun Andreić, Biljana Končar, Mladen Vedriš, Petar Turković, Nikolino Žura, Iva Žagar, Mislav Pap, Porin Perić
Objectives: This study aims to assess the impact of a Tai Chi exercise program (TCEP) on pain, spinal flexibility, muscle strength, stability and balance, functional status, and quality of life (QoL) among home-dwelling patients with osteoarthritis (OA) or inflammatory arthritis (iA).
Patients and methods: Between October 2018 and April 2019, a total of 28 participants (4 males, 24 females; median age: 62 years; range, 34 to 79 years) who completed the training program participating in at least 18 sessions were included. The TCEP consisted of 50 sessions for 60 min twice a week. The average attendance rate was high (78%, 39 sessions).
Results: Chest mobility (breathing index, p<0.001), sagittal mobility of cervical (p<0.001), thoracic (p=0.009), and lumbar spine (Schober's test, p<0.001) improved significantly in participants with OA and iA. The improvement in functional status was significant only in participants with OA (Lequesne index, p=0.014). Although the change in Lequesne index was statistically significant, the median value remained in the range of severe disability and the change did not reach the minimal clinically important difference. Although the trends were positive, the changes in pain (Visual Analog Scale pain, p=0.599), stability and balance (functional reach test, p=0.341), muscular strength (wall sit test, p=0.069), and health-related QoL (15D, p=0.065) were non-significant in participants with OA and iA.
Conclusion: Our study results suggest that a 25-week TCEP is safe and can improve chest and spinal mobility in home-dwelling individuals with OA or iA.
研究目的本研究旨在评估太极锻炼计划(TCEP)对居家骨关节炎(OA)或炎性关节炎(iA)患者的疼痛、脊柱柔韧性、肌肉力量、稳定性和平衡性、功能状态以及生活质量(QoL)的影响:在2018年10月至2019年4月期间,共纳入28名完成培训计划的参与者(4名男性,24名女性;中位年龄:62岁;范围:34至79岁),他们至少参加了18次课程。TCEP 共有 50 节课,每周两次,每次 60 分钟。平均出勤率很高(78%,39 节课):结果:胸廓活动度(呼吸指数、肺活量指数我们的研究结果表明,为期 25 周的 TCEP 是安全的,可以改善居家的 OA 或 iA 患者的胸部和脊柱活动度。
{"title":"Effects of Tai Chi exercise on pain, functional status, and quality of life in patients with osteoarthritis or inflammatory arthritis.","authors":"Nataša Kalebota, Nadica Laktašić Žerjavić, Kristina Kovač Durmiš, Milan Milošević, Antun Andreić, Biljana Končar, Mladen Vedriš, Petar Turković, Nikolino Žura, Iva Žagar, Mislav Pap, Porin Perić","doi":"10.5606/tftrd.2024.13140","DOIUrl":"10.5606/tftrd.2024.13140","url":null,"abstract":"<p><strong>Objectives: </strong>This study aims to assess the impact of a Tai Chi exercise program (TCEP) on pain, spinal flexibility, muscle strength, stability and balance, functional status, and quality of life (QoL) among home-dwelling patients with osteoarthritis (OA) or inflammatory arthritis (iA).</p><p><strong>Patients and methods: </strong>Between October 2018 and April 2019, a total of 28 participants (4 males, 24 females; median age: 62 years; range, 34 to 79 years) who completed the training program participating in at least 18 sessions were included. The TCEP consisted of 50 sessions for 60 min twice a week. The average attendance rate was high (78%, 39 sessions).</p><p><strong>Results: </strong>Chest mobility (breathing index, p<0.001), sagittal mobility of cervical (p<0.001), thoracic (p=0.009), and lumbar spine (Schober's test, p<0.001) improved significantly in participants with OA and iA. The improvement in functional status was significant only in participants with OA (Lequesne index, p=0.014). Although the change in Lequesne index was statistically significant, the median value remained in the range of severe disability and the change did not reach the minimal clinically important difference. Although the trends were positive, the changes in pain (Visual Analog Scale pain, p=0.599), stability and balance (functional reach test, p=0.341), muscular strength (wall sit test, p=0.069), and health-related QoL (15D, p=0.065) were non-significant in participants with OA and iA.</p><p><strong>Conclusion: </strong>Our study results suggest that a 25-week TCEP is safe and can improve chest and spinal mobility in home-dwelling individuals with OA or iA.</p>","PeriodicalId":56043,"journal":{"name":"Turkish Journal of Physical Medicine and Rehabilitation","volume":"70 3","pages":"300-308"},"PeriodicalIF":1.1,"publicationDate":"2024-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11639501/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142831159","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}