Halpern Rachel, Mody Reema R, Fuldeore Mahesh J, Patel Pankaj A, Mikuls Ted R
i3 Innovus, Eden Prairie, MN 55344, USA.
Curr Med Res Opin. 2009 Jul;25(7):1711-9. doi: 10.1185/03007990903017966.
To determine the association between allopurinol compliance and serum urate (sUA) level; and examine the association between sUA and gout-related healthcare costs in a large managed care population.
This retrospective administrative claims analysis examined subjects with gout (> or = 2 medical claims with ICD-9-CM diagnosis code 274.xx or > or = 1 claim with a gout diagnosis and > or = 1 pharmacy claim for allopurinol, probenecid, colchicine, or sulfinpyrazone) between January 1, 2002 and March 31, 2004. Each subject was observed during 1-year pre-index and 1-year post-index periods.
Outcomes were allopurinol medication possession ratio (MPR) and compliance (MPR > or = 0.80), sUA (mg/dL), and gout-related healthcare costs. 'Post-allopurinol' sUA was measured during three periods after the first observed allopurinol fill: 30-89 days; 90-149 days; > or = 150 days. A baseline sUA on or before the start of the post-index period was also identified. Outcomes were stratified by post-allopurinol or baseline sUA and compliance. Generalized linear modeling (GLM) regression measured the impact of baseline sUA on gout-related healthcare costs, controlling for demographic and health status variables.
The study sample comprised 18,243 subjects with mean age of 53.9 years. In all, 55% (n = 10,073) of subjects used allopurinol. There were 1473 (8.1%) subjects with a post-allopurinol sUA and 2438 (13.4%) subjects with a baseline sUA result. Among all subjects with a post-allopurinol sUA, 45.6% were compliant; between 49.3% and 56.8% of compliant subjects had an sUA < 6.0 mg/dL compared with 22.5-27.8% of non-compliant subjects, depending on the post-allopurinol time period (all p < 0.001). GLM results showed gout-related costs associated with baseline sUA > or = 6.0 and < 9.0 mg/dL were 58% higher (95% confidence interval (CI): 1.012 -2.456; p = 0.044) than were costs for sUA < 6.0 mg/dL. There was no significant difference in gout-related costs between baseline sUA < 6.0 mg/dL and > or = 9.0 mg/dL.
Analysis revealed an important associations between allopurinol compliance, sUA, and gout-related costs: compliance was positively associated with favorable sUA (<6.0 mg/dL) in unadjusted comparisons. GLM showed that baseline sUA < 6.0 was inversely associated with gout-related costs relative to baseline sUA > or = 6.0 and <9.0 mg/dL. Nevertheless, a substantial portion of subjects, even compliant ones, did not achieve sUA < 6.0 mg/dL. These results should be interpreted carefully in light of study limitations, including incomplete laboratory data, the potentially incorrect inference that medications were taken as prescribed, and lack of generalizability from Medicare managed care enrollees to the broader Medicare population.
确定别嘌醇依从性与血清尿酸(sUA)水平之间的关联;并在一个大型管理式医疗人群中研究sUA与痛风相关医疗费用之间的关联。
这项回顾性管理式医疗索赔分析研究了2002年1月1日至2004年3月31日期间患有痛风的受试者(国际疾病分类第九版临床修订本(ICD-9-CM)诊断代码为274.xx的≥2次医疗索赔,或≥1次痛风诊断索赔以及≥1次别嘌醇、丙磺舒、秋水仙碱或磺吡酮的药房索赔)。在索引前1年和索引后1年期间对每个受试者进行观察。
观察指标为别嘌醇药物持有率(MPR)和依从性(MPR≥0.80)、sUA(mg/dL)以及痛风相关医疗费用。“别嘌醇治疗后”的sUA在首次观察到别嘌醇配药后的三个时间段进行测量:30 - 89天;90 - 149天;≥150天。还确定了索引后时期开始时或之前的基线sUA。观察指标按别嘌醇治疗后或基线sUA以及依从性进行分层。广义线性模型(GLM)回归测量了基线sUA对痛风相关医疗费用的影响,并对人口统计学和健康状况变量进行了控制。
研究样本包括18243名受试者,平均年龄为53.9岁。总共有55%(n = 10073)的受试者使用别嘌醇。有1473名(8.1%)受试者有别嘌醇治疗后的sUA结果,2438名(13.4%)受试者有基线sUA结果。在所有有别嘌醇治疗后sUA的受试者中,45.6%的人依从;根据别嘌醇治疗后的时间段,依从受试者中有49.3%至56.8%的人sUA<6.0 mg/dL,而非依从受试者中这一比例为22.5% - 27.8%(所有p<0.001)。GLM结果显示,与基线sUA≥6.0且<9.0 mg/dL相关的痛风相关费用比sUA<6.0 mg/dL的费用高58%(95%置信区间(CI):1.012 - 2.456;p = 0.044)。基线sUA<6.0 mg/dL与≥9.0 mg/dL之间的痛风相关费用无显著差异。
分析揭示了别嘌醇依从性、sUA与痛风相关费用之间的重要关联:在未调整的比较中,依从性与良好的sUA(<6.0 mg/dL)呈正相关。GLM显示,相对于基线sUA≥6.0且<9.0 mg/dL,基线sUA<6.0与痛风相关费用呈负相关。然而,相当一部分受试者,即使是依从的受试者,sUA也未达到<6.0 mg/dL。鉴于研究的局限性,包括实验室数据不完整、药物按处方服用这一潜在的错误推断以及从医疗保险管理式医疗参保者到更广泛的医疗保险人群缺乏普遍性,这些结果应谨慎解读。