Ultrasound guided needling is becoming an accepted treatment for patients with shoulder pain due to calcifying tendinitis. However, evidence for this treatment is lacking. The investigators expect that patients treated with us guided needling with corticosteroid injection compared with patients treated with only corticosteroid injections in the subacromial bursa have better clinical outcome after one year follow-up.
Calcifying tendinitis of the shoulder is a common cause of shoulder pain with an incidence ranging from 2.7 % to 6.8 %. This disease of the rotator cuff tendons is characterised by calcifications in the tendons, most commonly in the supraspinatus tendon up to 82%. The aetiology remains unclear. Calcifying tendinitis is regarded as a self-healing condition with usually spontaneous resolution of the calcifications. But some patients have chronic or recurrent pain and disability of the shoulder which requires treatment. The treatment should be minimally invasive and effective in short and long term. Symptomatic treatment is indicated first using non-steroidal anti-inflammatory drugs, therapeutic exercise and non ultrasound guided subacromial corticosteroids injection. The role of corticosteroid injections is unknown due to the lack of good studies. Family doctors and orthopaedic surgeons inject corticosteroids in the shoulder without the guidance of ultrasound; with this method accurate needle placement in the subacromial bursa is not possible. When this treatment fails other therapeutical methods can be used. Ultrasound guided needling is a percutaneous technique of fragmentation or extraction of calcifications in the rotator cuff tendon. Literature shows favourable results but only a few randomized controlled trials were executed. Randomised controlled trials are needed to give more insight in the effectiveness of us guided needling. Comparing two groups of patients treated with us guided corticosteroid injection and one group combined with us guided needling can provide information of the usefulness of us guided needling.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
80
Us guided needling is a therapeutical technique treating calcifying tendinitis of the shoulder. Calcifications in the rotator cuff tendon are visualised with ultrasound. Under ultrasound guidance a 20 gauge needle is inserted in the calcification. Lidocaine 1% in a 1cc syringe is injected in the calcification and aspirated. The calcification is flushed until the fluid is clear. Sometimes it is not possible to flush the calcification. In this case the calcification will be fragmented. After flushing or fragmentation of the calcification, 20 mg triamcinolone with 1cc lidocaine 1% will be injected in de subacromial bursa under us guidance.
Us guided subacromial bursa injection with 20 mg triamcinolone with 1cc lidocaine 1%.
Medisch Spectrum Twente
Enschede, Netherlands
RECRUITINGVAS score on long term
Time frame: 1 year
Constant score on long term
The constant score is a validated scale, measuring the shoulder function. It is a objective measurement independent of the shoulder pain.
Time frame: 1 year
Constant score
To have a more insight over time the constant score will be measured at baseline, 6 weeks, 3 months and 6 months
Time frame: baseline,6 weeks, 3 months and 6 months
VAS score
To have a more insight over time the VAS score will be measured at baseline, 6 weeks, 3 months and 6 months. In practice patients seem to have a maximum pain shortly after the us guided needling. To measure this a VAS score will be taken after two weeks.
Time frame: Baseline, 2 weeks, 6 weeks, 3 months and 6 months
DASH score
This score measures the disability of the shoulder in daily life, work, sports and hobby over time.
Time frame: baseline, 6 weeks, 3 months, 6 months and 1 year.
Gärtner score of the shoulder calcifications on x-ray
Time frame: at baseline, directly post-interventional, at 6 weeks and one year.
Scoring system presented by Chiou et all. of the calcifications of the supraspinatus tendon on ultrasound
Time frame: at baseline, directly post-interventional, at 6 weeks and one year.
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