| Literature DB >> 35888010 |
Tomasz Wolny1, César Fernández-de-Las Peñas2, Tomasz Buczek3, Magdalena Domin1, Arkadiusz Granek4, Paweł Linek1.
Abstract
BACKGROUND: To date, various forms of physiotherapy are used in the treatment of cubital tunnel syndrome (CuTS). The effectiveness of physiotherapy for CuTS is inconclusive. The aim of this systematic review was to evaluate the effects of physiotherapy in the conservative treatment of CuTS.Entities:
Keywords: cubital tunnel syndrome; physiotherapy modalities; review; treatment outcomes; ulnar neuropathy
Year: 2022 PMID: 35888010 PMCID: PMC9318553 DOI: 10.3390/jcm11144247
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.964
Figure 1Flowchart.
Characteristics of included randomised clinical trials (RTCs).
| Study | Participants | Outcome Measures | Control/ | Intervention | Results |
|---|---|---|---|---|---|
| Svernlov et al. [ | Measurement at baseline and 6-month follow-up; | Three groups | Group A—elbow orthosis (3-month treatment); Group B—nerve gliding exercises (3-month treatment); Group C—information (exercise modification). | There was a significant improvement in each group after the applied therapy. There were no between-group differences. | |
| Badur et al. [ | Measurement at baseline, after treatment, and 1- and 3-month follow-up; | Two groups | Group 1—continuous shortwave diathermy (10 treatments); Group 2—placebo shortwave diathermy (10 treatments). | There were no changes in the assessed parameters in both groups after the applied therapy. | |
| Ozkan et al. [ | Measurement at baseline, after treatment, and 1- and 3-month follow-up; | Two groups | Group 1—low-level laser therapy (10 treatments); Group 2—ultrasound therapy (10 treatments). | There was a significant improvement in both groups after the applied therapy. There were no between-group. |
COPM—Canadian Occupational Performance Measure; VAS—visual analogue scale; NCS—nerve conduction study; DASH—Disabilities of the Arm, Shoulder, and Hand Outcome Measure.
Characteristics of included case studies design.
| Study | Participants | Outcome Measures | Control/ | Intervention | Results |
|---|---|---|---|---|---|
| Kearns and Wang [ | Measured at baseline and 4 weeks post-treatment; | No | Thrust manipulation (humeroulnar joint 2 treatments, radiocarpal joint 1 treatment). | After 3 treatment sessions, pain and paraesthesia were resolved; all other tests were negative. | |
| Oskay et al. [ | Measured at baseline, after treatment, and 12-month follow-up; | No | Cold application; pulsed ultrasound (10 treatments); nerve mobilisation techniques (10 treatments); strengthening exercises; postural adaptations; education; ergonomic modifications. | Pain, Tinel’s sign, and Disability of Arm, Shoulder, and Hand Index scores were decreased; grip and pinch strength increased during the observation period. | |
| Shen et al. [ | Measured at baseline and 4-, 8-, and 12-week follow-up; | No | Extracorporeal shock wave therapy (3 treatments). | The VAS and Quick DASH scores demonstrated improvements at all follow-up time points in all treated elbows. | |
| Anandkumar and Manivasagam [ | Measured at baseline, beginning of each treatment session, and at 6-month follow-up; | No | Dry needling (4 treatments, twice a week). | All patients achieved complete pain reduction and full recovery of function; the strength of the pain-free grip also improved; all self-reported significant improvement after therapy; the effect lasted 6 months after the therapy. | |
| Illes and Johnson [ | Measured at baseline and after treatment; | No | Chiropractic manipulative therapy; myofascial therapy (11 treatments); elastic therapeutic taping (no number specified); home exercises (8 treatments). | After 11 treatment sessions, symptoms resolved completely. | |
| Coppieters et al. [ | Measured at baseline, beginning of each treatment session, and at 6- and 10-month follow-up; | No | Neurodynamic mobilisation (5 treatments); | After the applied therapy, in each of the tests used, the symptoms were eliminated; The effect lasted 10 months after the therapy. | |
| Kwak et al. [ | Measured at baseline, after treatment, and at 1, 2, 3, and 6 months post-treatment; | No | PRF (1 treatment). | After 1 treatment session, the pain was completely relieved. At the 1-, 2-, 3-, and 6-month follow-up assessments after the procedure, the previously reported pain had not recurred. | |
| Fernández-de-Las-Peñas al. [ | Measured at baseline and at 1, 3, 6, and 12 months post-treatment; | No | PENS of the ulnar nerve (3 treatments); self-neural glides as a home program (2–3 weeks). | After three treatment sessions, there was an elimination of pain and symptoms and an improvement in functional status; the effect lasted 12 months after the therapy. |
NPRS—Numeric Pain Rating Scale; PSFS—Patient Specific Functional Scale; GROC—global rating of change; VAS—visual analogue scale; NPQ—Northwick–Park Questionnaire; DASH—Disabilities of the Arm, Shoulder, and Hand Outcome Measure; S-LANSS—Leeds Assessment of Neuropathic Symptoms and Signs; PENS—ultrasound-guided percutaneous electrical stimulation; STTT—selective tissue tension test; ULTT—upper-limb tension test; PAM—passive accessory movement; PRF—pulsed radiofrequency; NCS—nerve conduction study; MRI—magnetic resonance Imaging.
Risk of Bias in randomised clinical trials (RTCs).
| Study | Domain 1 | Domain 2 | Domain 3 | Domain 4 | Domain 5 | Overall Risk of Bias |
|---|---|---|---|---|---|---|
| Svernlov et al. [ | Low | Some concerns | Low | High | Low | High |
| Badur et al. [ | Low | Some concerns | Low | Low | Low | Some concerns |
| Ozkan et al. [ | Low | Some concerns | Low | Low | Low | Some concerns |
Critical appraisal checklist for case studies design.
| Critical Appraisal Checklist | Kearns and Wang [ | Oskay et al. [ | Shen et al. [ | Anandkumar and Manivasagam [ | Illes and Johnson [ | Coppieters et al. [ | Kwak et al. [ | Fernández-de-Las-Peñas et al. [ |
|---|---|---|---|---|---|---|---|---|
| 1. Were the patient’s demographic characteristics clearly described? | Yes | Unclear | Yes | Yes | Yes | Yes | Yes | Yes |
| 2. Was the patient’s history clearly described and presented as a timeline? | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
| 3. Was the current clinical condition of the patient on presentation clearly described? | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
| 4. Were diagnostic tests or assessment methods and the results clearly described? | Unclear | Yes | Yes | Unclear | Unclear | Unclear | Yes | Unclear |
| 5. Was the intervention(s) or treatment procedure(s) clearly described? | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
| 6. Was the post-intervention clinical condition clearly described? | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
| 7. Were adverse events (harms) or unanticipated events identified and described? | No | Unclear | Unclear | Unclear | No | Unclear | Unclear | No |
| 8. Does the case report provide takeaway lessons? | No | Yes | Yes | Yes | No | No | Yes | Unclear |
Risk of bias in case studies design.
| Study | Bias Due to Confounding | Bias in Selection of Participants in the Study | Bias in Classification of Interventions | Bias Due to Deviations from Intended Interventions | Bias Due to Missing Data | Bias in Measurement of Outcomes | Bias in Selection of the Reported Result | Overall Bias |
|---|---|---|---|---|---|---|---|---|
| Kearns and Wang [ | Serious | Moderate | Serious | Serious | Moderate | Serious | Moderate | Serious |
| Oskay et al. [ | Serious | Moderate | Serious | Serious | Moderate | Serious | Moderate | Serious |
| Shen et al. [ | Moderate | Low | Moderate | Moderate | Low | Moderate | Moderate | Moderate |
| Anandkumar and Manivasagam [ | Moderate | Low | Moderate | Moderate | Low | Moderate | Moderate | Moderate |
| Illes and Johnson [ | Serious | Moderate | Serious | Serious | Moderate | Serious | Moderate | Serious |
| Coppieters et al. [ | Serious | Moderate | Serious | Serious | Moderate | Serious | Moderate | Serious |
| Kwak et al. [ | Moderate | Low | Moderate | Moderate | Low | Moderate | Moderate | Moderate |
| Fernández-de-Las-Peñas et al. [ | Serious | Moderate | Serious | Serious | Moderate | Serious | Moderate | Serious |