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Cost Effectiveness Analysis of a Fixed Dose Combination Pill for Primary Prevention of Cardiovascular Disease From an Individual Participant Data Meta-Analysis Publisher



Lamy A1, 2 ; Tong W1 ; Joseph P1, 3 ; Gao P1 ; Huffman MD4, 5 ; Roshandel G6 ; Malekzadeh R7 ; Lopezjaramillo P8 ; Pais P9 ; Xavier D10 ; Avezum A11 ; Dans AL12 ; Gamra H13 ; Yusuf S1, 3
Authors
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Authors Affiliations
  1. 1. Population Health Research Institute, McMaster University, Hamilton, ON, Canada
  2. 2. Department of Surgery, McMaster University, Hamilton, ON, Canada
  3. 3. Department of Medicine, McMaster University, Hamilton, ON, Canada
  4. 4. The George Institute for Global Health, University of New South Wales, Sydney, Australia
  5. 5. Cardiovascular Division and Global Health Center, Washington University in St. Louis, St. Louis, United States
  6. 6. Golestan Research Center of Gastroenterology and Hepatology, Golestan University of Medical Sciences, Gorgan, Iran
  7. 7. Digestive Oncology Research Center, Digestive Disease Research Institute, Tehran University of Medical Sciences, Tehran, Iran
  8. 8. Masira Research Institute, Medical School, Universidad de Santander, Bucaramanga, Colombia
  9. 9. St. John's Research Institute, Bangalore, India
  10. 10. St. John's Medical College, Bangalore, India
  11. 11. International Research Center, Hospital Alemao Oswaldo Cruz, Sao Paulo, Brazil
  12. 12. University of the Philippines, Manila, Philippines
  13. 13. Fattouma Bourguiba Hospital and University of Monastir, Monastir, Tunisia

Source: eClinicalMedicine Published:2024


Abstract

Background: Cardiovascular disease (CVD) continues to impart a large burden on the global population, especially in lower income countries where affordability limits the use of cardiovascular medicines. A fixed dose combination strategy of at least 2 blood pressure lowering medications and a statin with aspirin in a single pill has been shown to reduce the risk of incident CVD by 38% in primary prevention in a recent meta-analysis. We report the in-trial (median follow-up: 5 years) cost-effectiveness of a fixed dose combination (FDC) pill in different income groups based on data from that meta-analysis. Methods: Countries were categorized using World Bank economic groups: Lower Middle Income Countries (LMIC), Upper Middle Income Countries (UMIC) and High Income Countries (HIC). Country specific costs were obtained for hospitalized events, procedures, and non-study medications (2020 USD). FDC price was based on the cheapest equivalent substitute (CES) for each component. Findings: For the CES-FDC pill versus control the difference in cost was $346 (95% CI: $294–$398) per participant in Lower Middle Income Countries, $838 (95% CI: $781–$895) in Upper Middle Income Countries and $42 (95% CI: −$155 to $239) (cost-neutral) in High Income Countries. During the study period the CES-FDC pill was associated with incremental gain in quality-adjusted life years of 0.06 (95% CI: 0.04–0.08) resulting in an incremental cost-effectiveness ratio (ICER) of $5767 (95% CI: 5735–$5799), $13,937 (95% CI: $13,893–$14,041) and $700 (95% CI: $662–$738) respectively. In subgroups analyses, the highest 10 years CVD risk subgroup had ICERs of $2033, $7322 and −$6000/QALY. Interpretation: A FDC pill produced at CES costs is cost-neutral in HIC. Governments of LMI and UMI countries should assess these results based on the ICER threshold accepted in their own country and own specific health care priorities but should consider prioritizing this strategy for patients with high 10 years CVD risk as a first step. Funding: Population Health Research Institute. © 2024 The Author(s)
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