Author, date and country | Patient group | Study type (level of evidence) | Outcomes | Key results | Study Weaknesses |
---|---|---|---|---|---|
Valtonen EJ 1976 Finland | 60 patients in outpatient (Rheumatology clinic) with supraspinatus tendonitis Comparing triamcinolon acetonide versus methyl-Prednisolone | Clinical trial | Pain at 8 weeks | Triam. 3.83 to 1.41 p 0.001. Methyl 3.77 to 1.55 p 0.001. Triam 50% vs mthyl 41% NS between two drugs in reducing pain. | No randomisation No power calculation Not blinded Not in ED setting Side effects: Triam was more painful than methylprednisolone 33% triam required 2nd injection versus 63% in meth. Arm. |
Localised tenderness at 8 weeks | Triam 3.30 to 0.96 p 0.001. Methyl 3.17 to 0.45 p 0.01. Triam 29% vs methyl 14%. NS between two drugs. | ||||
Limitation of motion | Triam 2.90 to 0.78 p 0.001. Methyl 3.13 to 0.85 p 0.001. Triam 27% vs 27%. NS between two drugs. | ||||
Disturbance of sleep | Triam 3.33 to 1.17 p 0.001. Methyl 3.37 to 1.20 p 0.001. Triam 35% vs methyl 36%. NS between two drugs. | ||||
Valtonen EJ 1978 Finland | 180patients A- 90 pts received local injection of 6 mg betamethasone B- 60 pts intramuscular 6 mg betamethasone C- 30 pts received IM saline Comparing subacromial and gluteal single injection with placebo | Clinical trial | Pain relief, functional improvement at 1, 2, 4 weeks. Diff A-B | At (1) week: NS. At (2) week: NS. At (4) week: NS. | Not randomised Not powered Loss of follow up |
Diff A-C | At (1) week: 0.01 | ||||
Withrington et al 1985 England | 25 pts Rheumatology clinic Group 1 -12 pts received local injection of 80 mg (2ml) methyl prednisolone plus 2ml of 2% lignocaine. Group 2 -13 pts received 4 mls of 0.09% Nacl | Clinical trial | Shoulder movements and pain assessment at presentation 2 weeks and 8 weeks. Group 1. | 7 pts responded at (2) weeks (two relapsed at 8 weeks). Mean improvements in VAS of 3.71 cm between (0) and (20 weeks) P > 0.05 | Small trial Not powered Placebo vs methylpred. and local effect |
Group 2. | 4 pts responded at (2) weeks (1 pt relapsed at 8 weeks). Mean improvement in VAS of 1.16 cm at (0) and (2) weeks. P > 0.05 |