Impact of pharmacist-led collaborative gout clinic on timely achievement of serum uric acid goals

IF 0.4 Q3 MEDICINE, GENERAL & INTERNAL
Kah Mun Cheong, M. Sriranganathan, E. Lee
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Abstract

The concept of a pharmacist-led collaborative gout clinic is relatively new in Singapore. This study examined the impact of this pilot shared care model on providing dose titration of urate lowering therapy, gout education and patient support to achieve target serum uric acid (sUA) levels. A retrospective pre-post study was undertaken to compare outcomes in patients who were started on either allopurinol or febuxostat in the 24 months prior to (Group A: Pre implementation) or 33 months following launch of the collaborative gout clinic (Group B: Post implementation). The collaborative gout clinic comprises of a clinical pharmacist under the supervision of a rheumatologist. Of 98 eligible subjects enrolled in our study, there were 50 patients (all prescribed allopurinol) for Group A and 48 patients for Group B (allopurinol n = 29, febuxostat n = 19). Among patients who achieved target sUA level of 360 μmol/L or less at 1 year of drug initiation with use of allopurinol, the median [interquartile range, IQR] time taken to attain target sUA was shorter in Group B than Group A (111 [82–308] days vs. 293 [265–414] days, p = 0.016). As compared to Group A, Group B had lesser patients experiencing gout flare (41.3% vs. 70.0%, p = 0.018) and more patients achieving target sUA (75.9% vs. 22.0%, p < 0.001). Mean ± [standard deviation, SD] daily allopurinol dose to achieve target sUA levels was 276 mg ± [138 mg]. Our results demonstrate the use of a pharmacist-led collaborative gout clinic may help to achieve better clinical outcomes in gout management.
药剂师领导的合作痛风诊所对及时实现血清尿酸目标的影响
药剂师主导的合作痛风诊所的概念在新加坡相对较新。本研究考察了这种试点共享护理模式对提供降低尿酸盐治疗的剂量滴定、痛风教育和患者支持以达到目标血清尿酸(sUA)水平的影响。进行了一项回顾性前后研究,以比较在合作痛风诊所启动前24个月(A组:实施前)或启动后33个月(B组:实施后)开始服用别嘌呤醇或非布索坦的患者的结果。合作痛风诊所由一名临床药剂师在风湿病学家的监督下组成。在我们研究的98名符合条件的受试者中,A组有50名患者(均为处方别嘌醇),B组有48名患者(别嘌酚n=29,非布索坦n=19)。在使用别嘌醇开始用药1年时达到360μmol/L或更低的sUA目标水平的患者中,B组达到sUA目标所需的中位[四分位间距,IQR]时间比A组短(111[82-308]天对293[265-414]天,p=0.016)。与A组相比,B组发生痛风发作的患者较少(41.3%对70.0%,p=0.018),达到sUA目标的患者较多(75.9%对22.0%,p<0.001)。达到sUA水平的平均值±[标准差,SD]日别嘌醇剂量为276 mg±[138 mg]。我们的研究结果表明,使用药剂师领导的合作痛风诊所可能有助于在痛风管理中取得更好的临床结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Proceedings of Singapore Healthcare
Proceedings of Singapore Healthcare MEDICINE, GENERAL & INTERNAL-
CiteScore
0.90
自引率
0.00%
发文量
42
审稿时长
15 weeks
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