Objective. To evaluate the effectiveness of spironolactone as a treatment for osteoarthritis (OA)-related
knee effusion in comparison to ibuprofen, cold compresses, and placebo.
Methods. This study was carried out on 200 patients, aged 40 years or older, attending the outpatient
clinic of the Rheumatology Department of Sohag University Hospital with unilateral knee effusion
related to OA based on clinical examination, musculoskeletal ultrasonography (US), and synovial
fluid analysis. In group 1, 50 patients received spironolactone 25 mg daily for 2 weeks; in group 2,
50 patients took ibuprofen 1200 mg daily for 2 weeks; in group 3, 50 patients used cold compresses
2 times daily for 2 weeks; and in group 4, 50 patients received placebo for the same duration. Fluid
> 4 mm was considered as effusion. Decrease in fluid to reach below 4-mm thickness was considered
complete improvement, and any decrease that did not reach below 4 mm thickness was considered
partial improvement.
Results. The mean age of the participants was 51.2 ± 8.1 years. The mean duration of effusion was
16.5 ± 3.6 days. In group 1, 66% had complete improvement, 20% partial improvement, and 14% no
response. In group 2, 24% had complete improvement, 12% partial improvement, and 64% no
response. In group 3, 28% had complete improvement, 14% partial improvement, and 58% no
response. In group 4, only 6% had complete improvement, 10% partial improvement, and 84% no
response.
Conclusion. Low-dose spironolactone is a safe and effective medical treatment for OA-related knee
effusion. (First Release April 1 2016; J Rheumatol 2016;43:1114–20; doi:10.3899/jrheum.151200)