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中性 pH、低葡萄糖降解产物腹膜透析液与标准液的经济学评价:BALANZ 试验的二次分析。

Economic evaluation of neutral-pH, low-glucose degradation product peritoneal dialysis solutions compared with standard solutions: a secondary analysis of the balANZ Trial.

机构信息

Sydney School of Public Health, University of Sydney, NSW, Australia.

Centre for Kidney Disease Research, Translational Research Institute at University of Queensland, QLD, Australia; Department of Nephrology, Princess Alexandra Hospital, Brisbane, QLD, Australia.

出版信息

Am J Kidney Dis. 2015 May;65(5):773-9. doi: 10.1053/j.ajkd.2014.12.017. Epub 2015 Mar 4.

Abstract

BACKGROUND

Biocompatible solutions may lower peritonitis rates, but are more costly than conventional solutions. The aim of the present study was to assess the additional costs and health outcomes of biocompatible over conventional solutions in incident peritoneal dialysis patients to guide practice decisions.

STUDY DESIGN

Secondary economic evaluation of a randomized controlled trial.

SETTING & POPULATION: 185 participants in the balANZ trial.

MODEL, PERSPECTIVE, & TIMEFRAME: Cost-effectiveness of biocompatible compared to standard solution over the 2 years using an Australian health care funder perspective.

INTERVENTION

Intervention group received biocompatible solutions and control group received standard solutions over 2 years.

OUTCOMES

Costs included dialysis charges, costs of treating peritonitis, non-peritonitis-related hospital stays, and medication. Peritonitis was the health outcome of interest; incremental cost-effectiveness ratios were reported in terms of the additional cost per additional patient avoiding peritonitis at 2 years.

RESULTS

Mean total per-patient costs were A$57,451 and A$53,930 for the biocompatible and standard-solution groups, respectively. The base-case analysis indicated an incremental cost of A$17,804 per additional patient avoiding peritonitis at 2 years for biocompatible compared to standard solution. In a sensitivity analysis excluding extreme outliers for non-peritonitis-related hospitalizations, mean per-patient costs were A$49,159 and A$52,009 for the biocompatible and standard-solution groups, respectively. Consequently, the incremental cost-effectiveness ratio also was reduced significantly: biocompatible solution became both less costly and more effective than standard solution and, in economic terms, was dominant over standard solution.

LIMITATIONS

Peritonitis was a secondary outcome of the balANZ trial. Health outcomes measured only in terms of patients avoiding peritonitis over 2 years may underestimate the longer term benefits (eg, prolonged technique survival).

CONCLUSIONS

Biocompatible dialysis solutions may offer a cost-effective alternative to standard solutions for peritoneal dialysis patients. Reductions in peritonitis-related hospital costs may offset the higher costs of biocompatible solution.

摘要

背景

生物相容性溶液可能会降低腹膜炎的发生率,但成本高于传统溶液。本研究旨在评估生物相容性溶液相对于传统溶液在新进入腹膜透析患者中的额外成本和健康结果,以指导实践决策。

研究设计

一项随机对照试验的二次经济评估。

研究地点和人群

balANZ 试验中的 185 名参与者。

模型、观点和时间范围:使用澳大利亚医疗保健资金提供者的观点,在 2 年内比较生物相容性与标准溶液的成本效益。

干预措施

干预组在 2 年内接受生物相容性溶液,对照组接受标准溶液。

结果

包括透析费用、腹膜炎治疗费用、非腹膜炎相关住院费用和药物费用。腹膜炎是关注的健康结果;增量成本效益比以每 2 年避免 1 例腹膜炎的额外患者的额外成本表示。

结论

生物相容性透析溶液可能为腹膜透析患者提供一种具有成本效益的标准溶液替代方案。降低腹膜炎相关住院费用可能会抵消生物相容性溶液的较高成本。

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