Goldfien Robert, Pressman Alice, Jacobson Alice, Ng Michele, Avins Andrew
Chair of the Chiefs of Rheumatology for The Permanente Medical Group in Richmond, CA.
Director of Analytics and Evaluation in the Department of Research, Development, and Dissemination for Sutter Health in Walnut Creek, CA.
Perm J. 2016 Summer;20(3):15-234. doi: 10.7812/TPP/15-234. Epub 2016 Jul 1.
Relatively few patients with gout receive appropriate treatment.
To determine whether a pharmacist-staffed gout management program is more effective than usual care in achieving target serum uric acid (sUA) levels in gout patients.
A parallel-group, randomized controlled trial of a pharmacist-staffed, telephone-based program for managing hyperuricemia vs usual care. Trial duration was 26 weeks.
Primary outcome measure was achieving sUA levels at or below 6 mg/dL at the 26-week visit. Secondary outcome was mean change in sUA levels in the control and intervention groups. Participants were adults with recurrent gout and sUA levels above 6.0 mg/dL. Participants were randomly assigned to management by a clinical pharmacist following protocol or to monitoring of sUA levels but management of their gout by their usual treating physician.
Of 102 patients who met eligibility criteria, 77 subjects obtained a baseline sUA measurement and were entered into the trial. Among 37 participants in the intervention group, 13 (35%) had sUA levels at or below 6.0 mg/dL at 26 weeks, compared with 5 (13%) of 40 participants in the control group (risk ratio = 2.8, 95% confidence interval [CI] = 1.1 to 7.1, p = 0.03). The mean change in sUA levels among controls was +0.1 mg/dL compared with -1.5 mg/dL in the intervention group (sUA difference = -1.6, 95% CI = -0.9 to -2.4, p < 0.001).
A structured pharmacist-staffed program was more effective than usual care for achieving target sUA levels. These results suggest a structured program could greatly improve gout management.
相对较少的痛风患者接受了适当的治疗。
确定由药剂师参与的痛风管理项目在使痛风患者达到目标血清尿酸(sUA)水平方面是否比常规护理更有效。
一项平行组、随机对照试验,比较由药剂师参与的基于电话的高尿酸血症管理项目与常规护理。试验持续时间为26周。
主要结局指标是在26周访视时达到sUA水平在6mg/dL或以下。次要结局是对照组和干预组sUA水平的平均变化。参与者为患有复发性痛风且sUA水平高于6.0mg/dL的成年人。参与者被随机分配接受临床药剂师按照方案进行的管理,或接受sUA水平监测但由其常规治疗医生管理痛风。
在102名符合资格标准的患者中,77名受试者获得了基线sUA测量值并进入试验。干预组的37名参与者中,13名(35%)在26周时sUA水平在6.0mg/dL或以下,而对照组的40名参与者中有5名(13%)达到该水平(风险比=2.8,95%置信区间[CI]=1.1至7.1,p=0.03)。对照组sUA水平的平均变化为+0.1mg/dL,而干预组为-1.5mg/dL(sUA差异=-1.6,95%CI=-0.9至-2.4,p<0.001)。
由药剂师参与的结构化项目在实现目标sUA水平方面比常规护理更有效。这些结果表明结构化项目可大大改善痛风管理。