4.6 Article

Cost-Effectiveness of Dapagliflozin for Non-diabetic Chronic Kidney Disease

Journal

JOURNAL OF GENERAL INTERNAL MEDICINE
Volume 37, Issue 13, Pages 3380-3387

Publisher

SPRINGER
DOI: 10.1007/s11606-021-07311-5

Keywords

chronic kidney disease; cost-effectiveness analysis; health economics

Funding

  1. Veterans Administration (VA) Office of Academic Affairs Advanced Fellowship in Health Services Research
  2. Agency for Healthcare Research and Quality (AHRQ) [T32HS026128]
  3. Knight-Hennessy Scholars at Stanford University
  4. NIDDK [K24 DK085446]

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This study aimed to evaluate the cost-effectiveness of adding Dapagliflozin to standard care for patients with non-diabetic CKD. The results showed that using Dapagliflozin could prolong life expectancy, reduce CKD progression, and decrease the time on kidney replacement therapy. Additionally, the treatment was deemed cost-effective according to conventional criteria.
Background In the USA, chronic kidney disease (CKD) affects 1 in 7 adults and costs $100 billion annually. The DAPA-CKD trial found dapagliflozin, a sodium glucose co-transporter 2 (SGLT2) inhibitor, to be effective in reducing CKD progression and mortality in patients with diabetic and non-diabetic CKD. Currently, SGLT2 inhibitors are not considered standard of care for patients with non-diabetic CKD. Objective Determine the cost-effectiveness of adding dapagliflozin to standard management of patients with non-diabetic CKD. Design Markov model with lifetime time horizon and US healthcare sector perspective. Patients Patients with non-diabetic CKD Intervention Dapagliflozin plus standard care versus standard care only. Main Measures Quality-adjusted life years (QALYs), costs, and incremental cost-effectiveness ratios (ICERs), all discounted at 3% annually; total incidence of kidney failure on kidney replacement therapy; average years on kidney replacement therapy. Key Results Adding dapagliflozin to standard care improved life expectancy by 2 years, increased discounted QALYS (from 6.75 to 8.06), and reduced the total incidence of kidney failure on kidney replacement therapy (KRT) (from 17.4 to 11.0%) and average years on KRT (from 0.77 to 0.43) over the lifetime of the cohort. Dapagliflozin plus standard care was more effective than standard care alone while increasing lifetime costs (from $245,900 to $324,8900, or $60,000 per QALY gained). Results were robust to variations in assumptions about dapagliflozin's efficacy over time and by CKD stage, added costs of kidney replacement therapy, and expected population annual CKD progression rates and sensitive to the cost of dapagliflozin. The net 1-year budgetary implication of treating all US patients with non-diabetic CKD could be up to $21 billion. Conclusions Dapagliflozin improved life expectancy and reduced progression of CKD, the proportion of patients requiring kidney replacement therapy, and time on kidney replacement therapy in patients with non-diabetic CKD. Use of dapagliflozin meets conventional criteria for cost-effectiveness.

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