McEwan Phil, Hafner Marco, Jha Vivekenand, Correa-Rotter Ricardo, Chernin Gil, De Nicola Luca, Villanueva Russell, Wheeler David C, Barone Salvatore, Nolan Stephen, Garcia Sanchez Juan Jose
Health Economics and Outcomes Research Ltd, Cardiff, UK.
George Institute for Global Health India, New Delhi, India.
J Med Econ. 2023 Jan-Dec;26(1):1407-1416. doi: 10.1080/13696998.2023.2264715. Epub 2023 Oct 31.
Dapagliflozin was approved for use in patients with chronic kidney disease (CKD) based on results of the DAPA-CKD trial, demonstrating attenuation of CKD progression and reduced risk of cardio-renal outcomes and all-cause mortality (ACM) versus placebo, in addition to standard therapy. The study objective was to assess the potential medical care cost offsets associated with reduced rates of cardio-renal outcomes across 31 countries and regions.
A comparative cost-determination framework estimated outcome-related costs of dapagliflozin plus standard therapy versus standard therapy alone over a 3-year horizon based on the DAPA-CKD trial. Incidence rates of end-stage kidney disease (ESKD), hospitalizations for heart failure (HHF), acute kidney injury (AKI), and ACM were estimated for a treated population of 100,000 patients. Associated medical care costs for non-fatal events were calculated using sources from a review of publicly available data specific to each considered setting.
Patients treated with dapagliflozin plus standard therapy experienced fewer incidents of ESKD (7,221 vs 10,767; number needed to treat, NNT: 28), HHF (2,370 vs 4,684; NNT: 43), AKI (4,110 vs. 5,819; NNT: 58), and ACM (6,383 vs 8,874; NNT: 40) per 100,000 treated patients versus those treated with standard therapy alone. Across 31 countries/regions, reductions in clinical events were associated with a 33% reduction in total costs, or a cumulative mean medical care cost offset of $264 million per 100,000 patients over 3 years.
This analysis is limited by the quality of country/region-specific data available for medical care event costs. Based on the DAPA-CKD trial, we show that treatment with dapagliflozin may prevent cardio-renal event incidence at the population level, which could have positive effects upon healthcare service delivery worldwide. The analysis was restricted to outcome-associated costs and did not consider the cost of drug treatments and disease management.
基于DAPA-CKD试验的结果,达格列净被批准用于慢性肾脏病(CKD)患者,该试验表明,与安慰剂相比,在标准治疗的基础上,达格列净可延缓CKD进展,降低心肾结局风险和全因死亡率(ACM)。本研究的目的是评估31个国家和地区中心肾结局发生率降低所带来的潜在医疗费用抵消情况。
基于DAPA-CKD试验,采用比较成本确定框架,估计达格列净联合标准治疗与单纯标准治疗在3年内与结局相关的成本。估计了100,000例接受治疗患者的终末期肾病(ESKD)、心力衰竭住院(HHF)、急性肾损伤(AKI)和ACM的发生率。非致命事件的相关医疗费用使用针对每个特定环境的公开数据审查来源进行计算。
每100,000例接受治疗的患者中,接受达格列净联合标准治疗的患者发生ESKD(7,221例对10,767例;需治疗人数,NNT:28)、HHF(2,370例对4,684例;NNT:43)、AKI(4,110例对5,819例;NNT:58)和ACM(6,383例对8,874例;NNT:40)的事件少于接受单纯标准治疗的患者。在31个国家/地区,临床事件的减少与总成本降低33%相关,即每100,000例患者在3年内累计平均医疗费用抵消2.64亿美元。
本分析受到可用于医疗事件成本的特定国家/地区数据质量的限制。基于DAPA-CKD试验,我们表明,达格列净治疗可在人群水平上预防心肾事件的发生,这可能对全球医疗服务提供产生积极影响。该分析仅限于与结局相关的成本,未考虑药物治疗和疾病管理的成本。