Efficacy and safety of urate-lowering therapy in people with kidney impairment: a GCAN-initiated literature review

摘要

Objectives The aim was to evaluate the efficacy, defined as achieving target serum urate 6.0?mg/dl, and safety of urate-lowering therapies (ULTs) for people with gout and chronic kidney disease (CKD) stages 3–5. Methods PubMed, The Cochrane Library and EMBASE were searched from 1 January 1959 to 31 January 2018 for studies that enrolled people with gout, who had an estimated glomerular filtration rate (eGFR) or creatinine clearance (CrCl) of 60?ml/min and exposure to allopurinol, febuxostat, probenecid, benzbromarone, lesinurad or pegloticase. All study designs other than case reports were included, except for people on dialysis, for whom we did include case reports. Results There were 36 reports with an analysis of efficacy and/or safety based upon renal function: allopurinol ( n =?12), febuxostat ( n =?10), probenecid ( n =?3), benzbromarone ( n =?5), lesinurad ( n =?5) and pegloticase ( n =?1). There were 108 reports that involved people with gout and renal impairment but did not contain any analysis on efficacy and/or safety based upon renal function: allopurinol ( n =?84), febuxostat ( n =?14), benzbromarone ( n =?1), lesinurad ( n =?3) and pegloticase ( n =?6). Most studies excluded people with more severe degrees of renal impairment (eGFR or CrCl of 30?ml/min). For allopurinol, in particular, there was significant variability in the dose of drug used and the efficacy in terms of urate lowering, across all levels of renal impairment. Conclusion There is a lack of evidence regarding the efficacy and/or safety of currently used ULTs according to different levels of renal function. Future studies should include patients with CKD and should report study outcomes stratified by renal function.