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静脉用帕立骨化醇与口服骨化三醇治疗慢性肾脏病继发甲状旁腺功能亢进症的成本效果分析。

Cost-effectiveness analysis of intravenous paricalcitol vs. oral calcitriol in the treatment of hyperparathyroidism secondary to chronic kidney disease.

机构信息

Hospital das Clínicas da Faculdade de Medicina de Botucatu, Departamento de Gestão de Atividades Acadêmicas, Núcleo de Avaliação de Tecnologia em Saúde, Botucatu, SP, Brazil.

Ministério da Saúde, Departamento de Gestão e Incorporação de Tecnologias e Inovação em Saúde, Brasília, DF, Brazil.

出版信息

J Bras Nefrol. 2023 Jan-Mar;45(1):95-101. doi: 10.1590/2175-8239-JBN-2022-0049en.

DOI:10.1590/2175-8239-JBN-2022-0049en
PMID:35980102
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10139708/
Abstract

INTRODUCTION

Hyperparathyroidism (SHPT) secondary to chronic kidney disease (CKD) is characterized by high levels of parathyroid hormone (PTH), hyperplasia of the parathyroid glands and cardiovascular disease. Selective and non-selective and selective vitamin D-receptor activators, calcimimetics, are available in the Brazilian market to reduce PTH levels.

OBJECTIVES

To develop a cost-effectiveness (C/E) and budgetary impact (BI) analysis of intravenous paricalcitol vs. oral calcitriol for patients on dialysis with SHPT, from the perspective of the Brazilian Public Health Care System (SUS).

METHODOLOGY

We built a decision-tree model to analyze C/E, which considered the outcome of avoided death and a time horizon of 1 year. As for the BI analysis, two scenarios were considered, one of demand and one of epidemiological approach, based on data from the Brazilian Society of Nephrology.

RESULTS

The analysis showed that the C/E ratio was R$ 1,213.68 per year, and an incremental effectiveness of 0.032, referring to avoided death. The incremental C/E ratio was R$37,927.50 per death averted by paricalcitol. It was estimated that the incremental BI with the expansion of paricalcitol use will be between R$1,600,202.28 and R$4,128,565.65 in the first year, considering the main and epidemiological scenarios. At the end of 5 years after the expansion of its use, an incremental BI was estimated between R$ 48,596,855.50 and R$ 62,90,555.73.

CONCLUSION

Intravenous paricalcitol has superior efficacy and similar safety to oral calcitriol, reducing the overall mortality of dialysis patients, although it implies a higher cost.

摘要

简介

慢性肾脏病(CKD)继发甲状旁腺功能亢进症(SHPT)的特征是甲状旁腺激素(PTH)水平升高、甲状旁腺增生和心血管疾病。目前巴西市场上有选择性和非选择性维生素 D 受体激动剂、钙敏感受体激动剂,用于降低 PTH 水平。

目的

从巴西公共医疗保健系统(SUS)的角度出发,为透析并发 SHPT 的患者开发静脉用帕立骨化醇与口服骨化三醇的成本效益(C/E)和预算影响(BI)分析。

方法

我们构建了一个决策树模型来分析 C/E,该模型考虑了避免死亡的结果和 1 年的时间范围。对于 BI 分析,我们考虑了两种情况,一种是基于巴西肾病学会数据的需求情况,另一种是流行病学方法情况。

结果

分析表明,C/E 比为每年 1213.68 雷亚尔,增量有效性为 0.032,即避免死亡。帕立骨化醇每避免一例死亡的增量 C/E 比为 37927.50 雷亚尔。预计在帕立骨化醇使用扩大的情况下,第一年的增量 BI 将在 1600202.28 雷亚尔至 4128565.65 雷亚尔之间,考虑到主要和流行病学情况。在帕立骨化醇使用扩大后的 5 年内,预计增量 BI 为 48596855.50 雷亚尔至 62905555.73 雷亚尔之间。

结论

与口服骨化三醇相比,静脉用帕立骨化醇具有更好的疗效和相似的安全性,可以降低透析患者的整体死亡率,尽管它的成本更高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cef/10139708/ce3127cc25cd/0101-2800-jbn-2022-0049-gf01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cef/10139708/ce3127cc25cd/0101-2800-jbn-2022-0049-gf01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cef/10139708/ce3127cc25cd/0101-2800-jbn-2022-0049-gf01.jpg

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A comparative analysis of the efficacy and safety of paricalcitol versus other vitamin D receptor activators in patients undergoing hemodialysis: A systematic review and meta-analysis of 15 randomized controlled trials.比较分析甲状旁腺素与其他维生素 D 受体激动剂在血液透析患者中的疗效和安全性:系统评价和荟萃分析 15 项随机对照试验。
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KDIGO 2017 Clinical Practice Guideline Update for the Diagnosis, Evaluation, Prevention, and Treatment of Chronic Kidney Disease-Mineral and Bone Disorder (CKD-MBD).
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AMSTAR 2: a critical appraisal tool for systematic reviews that include randomised or non-randomised studies of healthcare interventions, or both.AMSTAR 2:一种用于系统评价的关键评估工具,该系统评价包括医疗保健干预措施的随机或非随机研究,或两者皆有。
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