Author, date and country | Patient group | Study type (level of evidence) | Outcomes | Key results | Study Weaknesses |
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Vulpiari et al, 2009, Italy | 105 patients (127 achilles tendons) treated with ESWT. All patients underwent clinical and instrumental diagnosis. Symptomatology classified using Visual Analogical Scale (VAS) and 5 stage clinical evaluation range. Shock wave therapy consisted of an average of 4 sessions at 2/7 day intervals. | Follow up, type C study. | VAS score Subjective clinical evaluation score. | Satisfactory results in 47.2% of cases (60/127 tendons) at 2 months follow up Satisfactory results in 73.2% at medium term (2-12 months) follow up (93/127) Satisfactory results in 76% at long term (13-24 months) follow up (92/121). | There was not a control group in this study undergoing a placebo and they were unable to achieve 100% patient recall. |
Rasumussen et al, 2008, Denmark | 48 patients assigned to non-operative treatment of Achilles tendinopathy were randomised to either receive extra corporeal shock-wave therapy (ESWT) or sham ESWT over 4 weeks. Assessed before treatment, during 4-week treatment block and at 4,8 and 12 weeks of follow up | Randomised, double-blind, placebo-controlled trial. | American Orthopaedic Foot and Ankle Society (AOFAS) score Pain score. | Both groups increased during the treatment and follow up period Mean AOFAS score increased from 74 (SD 12) to 81 (16) in placebo group Mean AOFAS score increased from 70 (6.8) to 88 (10) in ESWT group Better results were seen in intervention group at 8 and 12 weeks Pain reduced in both groups, but not significant difference between the groups. | ESWT treatment area was too small compared to extent of tendinopathy. Also the location of the lesion and energy level used was not documented. |
Rompe et al, 2009, | 68 patients with chronic Achilles tendinopathy were enrolled. All of these had undergone unsuccessful management for >3 months, including at least: peritendinous local injection, non-steroidal anti-inflammatory drugs (NSAIDs) and physiotherapy. They were randomly assigned to receive either eccentric loading only or eccentric loading plus shock-wave treatment. | Randomised controlled trial Level of evidence, 1. | Victorian Institute of Sport Assessment- Achilles (VISA-A) score. | VISA-A score increased in both groups at 4 months. 50 to 73 points in group 1 (eccentric loading) 51 to 87 points in group 2 (eccentric loading plus shock wave treatment). | Patients were fully aware of the active treatment they received Relatively small numbers of patients included in the study. |
Furia 2005, USA | 35 patients with chronic insertional Achilles tendinopathy were treated with one dose of high energy shock wave therapy whilst 33 patients were managed with traditional non-operative methods. All shock wave therapy performed with local analgesic field block or a non-local anaesthesia. | Case control study Level of evidence,3 | Mean visual analogue score (VAS), Roles and Maudsley score. These were recorded at 1, 3 and 12 months after surgery. | The VAS score for control group at 1, 3 and 12 months was 8.2, 7.2 and 7 respectively. The VAS score for shock wave group at 1,3 and 12 months was 4.2, 2.9 and 2.8 respectively. At 12 months after treatment, the number of patients with successful Roles and Maudsley scores was statistically greater in shock wave group compared with control group. | Subjective assessment scores MRI scans not performed Relatively small numbers involved. |
Costa et al, 2005, UK | 49 patients with Achilles tendinopathy consented to participate in the trial. 22 randomised to shock wave therapy. 20 of these patients were followed up for 1 year. 27 patients were randomised to placebo- control group. 23 of these patients were followed up at 1 year. Each patient treated once a month for 3 months. | Randomised, placebo-controlled trial Level of evidence, 1 | Primary outcome was a reduction in Achilles tendon pain during walking. | At end of trial, no difference in pain relief between the shock wave therapy group and the control group. 2 patients in the treatment group with tendon ruptures. These patients were aged 62 and 65 respectively. | Relatively small numbers and number of patients lost to follow up Large confidence intervals, making it difficult to establish effect |