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本文引用的文献

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Improving patient outcomes in psoriasis: strategies to ensure treatment adherence.改善银屑病患者的治疗效果:确保治疗依从性的策略
Psoriasis (Auckl). 2015 Jul 17;5:109-115. doi: 10.2147/PTT.S54070. eCollection 2015.
2
Impact of prior biologic use on persistence of treatment in patients with psoriatic arthritis enrolled in the US Corrona registry.美国Corrona注册研究中既往使用生物制剂对银屑病关节炎患者治疗持续性的影响。
Clin Rheumatol. 2017 Apr;36(4):895-901. doi: 10.1007/s10067-017-3593-x. Epub 2017 Mar 7.
3
The risk of fracture among patients with psoriatic arthritis and psoriasis: a population-based study.银屑病关节炎和银屑病患者的骨折风险:一项基于人群的研究。
Ann Rheum Dis. 2017 May;76(5):882-885. doi: 10.1136/annrheumdis-2016-210441. Epub 2017 Jan 16.
4
Psoriasis and Associated Psychiatric Disorders: A Systematic Review on Etiopathogenesis and Clinical Correlation.银屑病及相关精神障碍:关于病因发病机制和临床相关性的系统综述
J Clin Aesthet Dermatol. 2016 Jun;9(6):36-43. Epub 2016 Jun 1.
5
Depression and Insomnia in Patients With Psoriasis and Psoriatic Arthritis Taking Tumor Necrosis Factor Antagonists.使用肿瘤坏死因子拮抗剂的银屑病和银屑病关节炎患者的抑郁与失眠
Medicine (Baltimore). 2016 May;95(22):e3816. doi: 10.1097/MD.0000000000003816.
6
Patient Characteristics, Health Care Resource Utilization, and Costs Associated with Treatment-Regimen Failure with Biologics in the Treatment of Psoriasis.治疗银屑病的生物制剂治疗失败相关的患者特征、医疗资源利用和成本。
J Manag Care Spec Pharm. 2016 Apr;22(4):396-405. doi: 10.18553/jmcp.2016.22.4.396.
7
Biologic therapy adherence, discontinuation, switching, and restarting among patients with psoriasis in the US Medicare population.美国医疗保险人群中银屑病患者的生物治疗依从性、停药、换药及重新开始治疗情况。
J Am Acad Dermatol. 2016 Jun;74(6):1057-1065.e4. doi: 10.1016/j.jaad.2016.01.048. Epub 2016 Mar 4.
8
Economic and Comorbidity Burden Among Patients with Moderate-to-Severe Psoriasis.中重度银屑病患者的经济负担和合并症负担。
J Manag Care Spec Pharm. 2015 Oct;21(10):874-88. doi: 10.18553/jmcp.2015.21.10.874.
9
Healthcare utilization and costs associated with dabigatran compared to warfarin treatment in newly diagnosed patients with non-valvular atrial fibrillation.在新诊断的非瓣膜性心房颤动患者中,与华法林治疗相比,达比加群的医疗保健利用情况及成本。
Curr Med Res Opin. 2015 Dec;31(12):2189-95. doi: 10.1185/03007995.2015.1092124. Epub 2015 Sep 24.
10
Treatment patterns and annual biologic costs in US veterans with rheumatic conditions or psoriasis.美国患有风湿性疾病或银屑病的退伍军人的治疗模式和年度生物制剂成本。
J Med Econ. 2016;19(1):34-43. doi: 10.3111/13696998.2015.1086774. Epub 2015 Sep 30.

评估治疗持续性对美国国防部人群中中重度银屑病和/或银屑病关节炎患者经济负担的影响。

Evaluating the Effect of Treatment Persistence on the Economic Burden of Moderate to Severe Psoriasis and/or Psoriatic Arthritis Patients in the U.S. Department of Defense Population.

机构信息

1 Janssen Scientific Affairs, Lawrenceville, New Jersey.

2 Research, Ann Arbor, Michigan.

出版信息

J Manag Care Spec Pharm. 2018 Jul;24(7):654-663. doi: 10.18553/jmcp.2018.24.7.654.

DOI:10.18553/jmcp.2018.24.7.654
PMID:29952710
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10398301/
Abstract

BACKGROUND

Psoriasis is a chronic, hyper-proliferative dermatological condition associated with joint symptoms known as psoriatic arthritis (PsA). In a 2013 review, the total economic burden of PsA was estimated at $51.7-$63.2 billion. The economic burden of moderate to severe psoriasis patients has reduced significantly with the advent of biologics, but there remains a dearth of real-world evidence of the impact of treatment persistence on the economic burden of moderate to severe psoriasis and/or PsA patients.

OBJECTIVE

To evaluate the overall and psoriasis and/or PsA-related health care utilization and costs among patients who were persistent versus those nonpersistent on index biologic among the moderate to severe psoriasis and/or PsA population.

METHODS

Adult patients with ≥ 2 claims with diagnosis of psoriasis and/or PsA during the period of November 2010-October 2015 were identified from the U.S. Department of Defense database; the first diagnosis date during November 2011-October 2014 was defined as the index date. As of the index date, patients were considered to have moderate to severe psoriasis or PsA if they had ≥ 1 nontopical systemic therapy or phototherapy during the 1-year pre- or 1-month post-index date. Persistence to index therapy, defined as the first biologic used (etanercept, adalimumab, ustekinumab, infliximab) on or within 30 days post-index date, was determined based on the biologic dosing schedule and a 90-day gap. Generalized linear models were used to compare the health care utilization and costs between persistent and nonpersistent patients during the 1-year post-index period.

RESULTS

A total of 2,945 moderate to severe psoriasis and/or PsA patients were identified. Of those, 1,899 (64.5%) were persistent and 1,046 (35.5%) were nonpersistent. Compared with nonpersistent patients, persistent patients were older (49.2 vs. 45.5 years; P < 0.001) and more likely to be male (52% vs. 45%; P < 0.001). More persistent patients were diagnosed with dyslipidemia (40% vs. 35%; P = 0.002), had lower antidepressant use (23.4% vs. 27.4%; P < 0.001), and had lower anxiolytic use (30% vs. 37%; P < 0.001) compared with nonpersistent patients. After adjusting for demographic and clinical characteristics, nonpersistent patients had higher total medical costs ($12,457 vs. $8,964; P < 0.001) compared with persistent patients, and ambulatory visits (23.9 vs. 21.4; P = 0.007) were a major contributor. Approximately 40% of the total overall medical costs were attributed to psoriasis and PsA. Although persistent patients incurred higher pharmacy costs ($10,684 vs. $7,849; P < 0.001) due to higher biologic use and the potentially high per-unit cost of biologics, their psoriasis- and/or PsA-related medical costs were significantly lower than those of nonpersistent patients ($3,395 vs. $5,041; P < 0.001). Total overall costs combining medical and pharmacy costs were similar between the cohorts ($22,678 vs. $21,477; P = 0.122).

CONCLUSIONS

Moderate to severe psoriasis and/or PsA patients who were persistent on index biologic treatment had higher pharmacy utilization and costs, albeit with lower medical costs and similar total costs, compared with nonpersistent patients.

DISCLOSURES

This study was funded by Janssen Scientific Affairs. Lee is a paid employee of Janssen Scientific Affairs. Xie, Wang, Vaidya, and Baser are paid employees of STATinMED Research, which is a paid consultant to Janssen Scientific Affairs. This study was presented as an abstract at the Academy of Managed Care Pharmacy 2017 Annual Meeting, March 27-30, 2017, in Denver, CO.

摘要

背景

银屑病是一种与关节症状相关的慢性、过度增殖性皮肤病,被称为银屑病关节炎(PsA)。在 2013 年的一项综述中,估计 PsA 的总经济负担为 517 亿至 632 亿美元。随着生物制剂的出现,中重度银屑病患者的经济负担显著减轻,但关于治疗持久性对中重度银屑病和/或 PsA 患者的经济负担的影响的真实世界证据仍然不足。

目的

评估中度至重度银屑病和/或 PsA 患者中,与指数生物制剂相比,持久性与非持久性患者的总体和银屑病及/或 PsA 相关的医疗保健利用和成本。

方法

从美国国防部数据库中确定了≥2 项银屑病和/或 PsA 诊断的成年患者;2011 年 11 月至 2014 年 10 月期间的第一个诊断日期被定义为索引日期。截至索引日期,如果患者在 1 年的预索引或索引后 1 个月期间有≥1 种非局部全身治疗或光疗,则被认为患有中度至重度银屑病或 PsA。根据生物制剂的剂量方案和 90 天的间隔,将持久性定义为首次使用的生物制剂(依那西普、阿达木单抗、乌司奴单抗、英夫利昔单抗)或在索引日期后的 30 天内使用。使用广义线性模型比较了索引后 1 年内持久性和非持久性患者的医疗保健利用和成本。

结果

共确定了 2945 名中度至重度银屑病和/或 PsA 患者。其中,1899 名(64.5%)为持久性患者,1046 名(35.5%)为非持久性患者。与非持久性患者相比,持久性患者年龄较大(49.2 岁 vs. 45.5 岁;P<0.001),且更可能为男性(52% vs. 45%;P<0.001)。与非持久性患者相比,更多的持久性患者被诊断为血脂异常(40% vs. 35%;P=0.002),抗抑郁药使用率较低(23.4% vs. 27.4%;P<0.001),抗焦虑药使用率较低(30% vs. 37%;P<0.001)。调整人口统计学和临床特征后,非持久性患者的总医疗费用(12457 美元 vs. 8964 美元;P<0.001)高于持久性患者,且门诊就诊次数较多(23.9 次 vs. 21.4 次;P=0.007)是主要原因。大约 40%的总医疗费用归因于银屑病和 PsA。尽管由于生物制剂的使用频率较高和潜在的高单位生物制剂成本,持久性患者的药物费用较高(10684 美元 vs. 7849 美元;P<0.001),但其银屑病和/或 PsA 相关的医疗费用明显低于非持久性患者(3395 美元 vs. 5041 美元;P<0.001)。结合医疗和药物成本的总总体费用在两组之间相似(22678 美元 vs. 21477 美元;P=0.122)。

结论

与非持久性患者相比,索引生物制剂治疗中持久性较高的中重度银屑病和/或 PsA 患者的药物利用和成本较高,尽管医疗成本较低,总体成本相似。

披露

这项研究由杨森科学事务部资助。李是杨森科学事务部的受薪员工。谢、王、瓦伊迪亚和巴泽是 STATinMED Research 的受薪员工,STATinMED Research 是杨森科学事务部的付费顾问。这项研究以摘要形式在 2017 年 3 月 27 日至 30 日于科罗拉多州丹佛市举行的管理式医疗药房协会 2017 年年会上进行了介绍。