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美国成人系统性红斑狼疮直接成本的结构化文献综述。

A structured literature review of the direct costs of adult systemic lupus erythematosus in the US.

机构信息

Boston Healthcare Associates, Inc., Massachusetts 02110, USA.

出版信息

Arthritis Care Res (Hoboken). 2011 Sep;63(9):1224-32. doi: 10.1002/acr.20502.

DOI:10.1002/acr.20502
PMID:21584945
Abstract

OBJECTIVE

A structured review of the literature was undertaken to examine the direct costs of adult systemic lupus erythematosus (SLE) in a US population.

METHODS

English-language studies published from January 2000 to April 2010 were systematically reviewed from both Medline's PubMed and the Cochrane databases. Studies were included if they reported direct medical costs of SLE among adults in the US.

RESULTS

Seven studies published since January 2000 that reported direct medical costs associated with SLE in the US were identified. Studies examined main cost categories of inpatient, outpatient, and pharmacy services; each contributed substantially to total costs. Wide SDs were reported, consistent with variability in disease manifestation. Mean annual direct costs of SLE patients ranged from $13,735-$20,926; the costs of those with and without nephritis ranged from $29,034-$62,651 and $12,273-$16,575, respectively. Across studies of a general SLE population, pharmaceutical costs composed 19-30% of total expenditures, with inpatient costs accounting for 16-50% and outpatient costs accounting for 24-56% of overall costs. Methodologies varied across studies, with patient self-reported resource utilization generating the lowest estimates versus claims-based analyses; Medicaid claims analyses generated lower incremental cost estimates for SLE patients versus control patients compared to estimates based on commercial claims analysis.

CONCLUSION

SLE is associated with substantial annual direct cost burden in the US; however, little research has been done examining costs associated with specific treatments or cost variation by disease severity and disease manifestations. Future research elucidating the causes in variation of costs will help in the appraisal of emerging therapies and in developing clinical management strategies.

摘要

目的

对文献进行系统回顾,以考察美国成人系统性红斑狼疮(SLE)的直接成本。

方法

系统检索了 Medline 的 PubMed 和 Cochrane 数据库中 2000 年 1 月至 2010 年 4 月发表的英文文献。纳入的研究报告了美国成人 SLE 的直接医疗费用。

结果

共确定了 7 项自 2000 年 1 月以来发表的研究,报告了美国 SLE 相关的直接医疗费用。研究考察了住院、门诊和药房服务的主要费用类别;每个类别都对总费用有很大贡献。由于疾病表现的差异,报告了广泛的标准差。SLE 患者的年平均直接医疗费用范围为 13735 美元至 20926 美元;有和没有肾炎的患者的费用范围分别为 29034 美元至 62651 美元和 12273 美元至 16575 美元。在一般 SLE 人群的研究中,药物成本占总支出的 19-30%,住院成本占 16-50%,门诊成本占 24-56%。研究方法各不相同,患者自我报告的资源利用产生的估计值最低,而基于索赔的分析则产生的估计值最低;与基于商业索赔分析的估计值相比,SLE 患者的医疗补助索赔分析产生的增量成本估计值较低。

结论

SLE 在美国造成了巨大的年度直接经济负担;然而,很少有研究考察特定治疗相关的成本或疾病严重程度和疾病表现的成本变化。未来的研究阐明成本变化的原因将有助于评估新兴疗法,并制定临床管理策略。

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