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Effects of angiotensin converting enzyme inhibitors and angiotensin II receptor antagonists on mortality and renal outcomes in diabetic nephropathy: systematic review.血管紧张素转换酶抑制剂和血管紧张素II受体拮抗剂对糖尿病肾病患者死亡率和肾脏结局的影响:系统评价
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Cost-effectiveness of early irbesartan treatment versus control (standard antihypertensive medications excluding ACE inhibitors, other angiotensin-2 receptor antagonists, and dihydropyridine calcium channel blockers) or late irbesartan treatment in patients with type 2 diabetes, hypertension, and renal disease.早期使用厄贝沙坦治疗与对照(标准抗高血压药物,不包括血管紧张素转换酶抑制剂、其他血管紧张素-2受体拮抗剂和二氢吡啶类钙通道阻滞剂)或晚期使用厄贝沙坦治疗对2型糖尿病、高血压和肾病患者的成本效益。
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基于氯沙坦的治疗对2型糖尿病终末期肾病发病率及相关费用的影响:英国一项回顾性成本效益分析

Effects of Losartan-based therapy on the incidence of end-stage renal disease and associated costs in type 2 diabetes mellitus: A retrospective cost-effectiveness analysis in the United Kingdom.

作者信息

Vora Jiten, Carides George, Robinson Paul

机构信息

Royal Liverpool Hospital, Liverpool, United Kingdom.

Health Economics Statistics, Merck & Co., Inc, Blue Bell, Pennsylvania.

出版信息

Curr Ther Res Clin Exp. 2005 Nov;66(6):475-85. doi: 10.1016/j.curtheres.2005.12.005.

DOI:10.1016/j.curtheres.2005.12.005
PMID:24678070
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3965974/
Abstract

BACKGROUND

In the Reduction of Endpoints in Non-Insulin-Dependent Diabetes Mellitus with the Angiotensin II Antagonist Losartan (RENAAL) study, the primary composite end point was the 2-fold increase in baseline serum creatinine concentration, the development of end-stage renal disease (ESRD), or death. The effects of losartan used for the prevention or delay of progression of diabetic nephropathy to ESRD were compared with those of conventional anti-hypertensive treatment (control) (calcium channel blockers, diuretics, α-blockers, β-blockers, and centrally acting agents), but not angiotensin-converting enzyme (ACE) inhibitors or angiotensin II antagonists (AIIAs), in 1513 adults with type 2 diabetes mellitus (DM-2) and nephropathy. Both treatment groups received conventional antihypertensive therapy (calcium channel blockers, diuretics, α-blockers, β-blockers, and/or centrally acting agents). ACE inhibitors and AIIAs were not allowed during the study period. The relative risk (RR) for composite outcome was 25% less, and the RR for ESRD was 28% less, in the losartantreated group compared with the control group.

OBJECTIVE

The aim of this retrospective cost-effectiveness analysis was to use data from the RENAAL study to determine the survival benefits and lifetime direct medical costs of a losartan-based regimen for the prevention of ESRD in patients with DM-2 and nephropathy in the setting of the UK National Health Service (NHS).

METHODS

This analysis used life-years saved as the effectiveness measure. The effect of losartan-based treatment on ESRD risk was confined to the trial period (3.5 years). However, survival and the lifetime direct medical costs of managing ESRD were projected beyond the trial period to incorporate the full effects of ESRD on survival and resource use. The effect of altering key variables was examined using 1-way sensitivity analyses.

RESULTS

ESRD-related costs were significantly lower in patients receiving losartan-based treatment compared with those in the control group (savings per patient, 7390 [95% CI, 11,366-3414; P< 0.001] [1 = US -$1.75]). Incorporation of the cost of losartan into the assessment found reduced net costs (savings per patient, 6622 [95% CI, 10,591-2653; P= 0.001]). The projected mean number of life years saved due to ESRD risk reduction with losartan was 0.44 years (95% CI, 0.16-0.71; P = 0.002). Losartan treatment was found to save costs in all cases, even if the cost of renal replacement therapy for patients with ESRD was reduced by 50%.

CONCLUSION

In this retrospective cost-effectiveness analysis using data from the RENAAL study, losartan-based treatment for the prevention or delay of progression of diabetic nephropathy to ESRD in patients with DM-2 and nephropathy was found to be potentially cost saving compared with conventional anti-hypertensive therapy from the perspective of the UK NHS.

摘要

背景

在使用血管紧张素II拮抗剂氯沙坦降低非胰岛素依赖型糖尿病患者终点事件(RENAAL)研究中,主要复合终点为基线血清肌酐浓度增加2倍、终末期肾病(ESRD)的发生或死亡。在1513例2型糖尿病(DM - 2)和肾病患者中,比较了氯沙坦用于预防或延缓糖尿病肾病进展至ESRD的效果与传统抗高血压治疗(对照)(钙通道阻滞剂、利尿剂、α受体阻滞剂、β受体阻滞剂和中枢作用药物)的效果,但未与血管紧张素转换酶(ACE)抑制剂或血管紧张素II拮抗剂(AIIAs)进行比较。两个治疗组均接受传统抗高血压治疗(钙通道阻滞剂、利尿剂、α受体阻滞剂、β受体阻滞剂和/或中枢作用药物)。研究期间不允许使用ACE抑制剂和AIIAs。与对照组相比,氯沙坦治疗组复合结局的相对风险(RR)降低了25%,ESRD的RR降低了28%。

目的

本回顾性成本效益分析的目的是利用RENAAL研究的数据,确定在英国国家医疗服务体系(NHS)背景下,基于氯沙坦的治疗方案对预防DM - 2和肾病患者发生ESRD的生存获益和终身直接医疗成本。

方法

本分析将挽救的生命年数作为有效性指标。基于氯沙坦的治疗对ESRD风险的影响仅限于试验期(3.5年)。然而,ESRD的生存情况和管理ESRD的终身直接医疗成本在试验期后进行了预测,以纳入ESRD对生存和资源使用的全部影响。使用单向敏感性分析检查改变关键变量的影响。

结果

与对照组相比,接受基于氯沙坦治疗的患者ESRD相关成本显著更低(每位患者节省7390[95%CI,11366 - 3414;P < 0.001][1 = 1.75美元])。将氯沙坦成本纳入评估后发现净成本降低(每位患者节省6622[95%CI,10591 - 2653;P = 0.001])。预计由于氯沙坦降低ESRD风险而挽救的平均生命年数为0.44年(95%CI,0.16 - 0.71;P = 0.002)。即使ESRD患者的肾脏替代治疗成本降低50%,氯沙坦治疗在所有情况下均能节省成本。

结论

在这项使用RENAAL研究数据的回顾性成本效益分析中,从英国NHS的角度来看,基于氯沙坦的治疗方案用于预防或延缓DM - 2和肾病患者的糖尿病肾病进展至ESRD,与传统抗高血压治疗相比可能具有成本节约效果。