Author
Listed:
- Clara Marquina
(Monash University)
- Jedidiah I Morton
(Monash University
Baker Heart and Diabetes Institute)
- Melanie Lloyd
(Monash University
Royal Children’s Hospital Melbourne)
- Dina Abushanab
(Monash University
Hamad Medical Corporation)
- Yeji Baek
(Monash University)
- Tamrat Abebe
(Monash University)
- Adam Livori
(Monash University
Grampians Health)
- Padam Dahal
(Central Queensland University, Sydney Campus)
- Gerald F. Watts
(Central Queensland University, Sydney Campus
University of Western Australia
Royal Perth Hospital)
- Zanfina Ademi
(Monash University
Monash University)
Abstract
Background Objective This study aimed to systematically synthesise the cost-effectiveness of screening strategies to detect heterozygous familial hypercholesterolemia (FH). Methods We searched seven databases from inception to 2 February , 2023, for eligible cost-effective analysis (CEA) that evaluated screening strategies for FH versus the standard care for FH detection. Independent reviewers performed the screening, data extraction and quality evaluation. Cost results were adapted to 2022 US dollars (US$) to facilitate comparisons between studies using the same screening strategies. Cost-effectiveness thresholds were based on the original study criteria. Results A total of 21 studies evaluating 62 strategies were included in this review, most of the studies (95%) adopted a healthcare perspective in the base case, and majority were set in high-income countries. Strategies analysed included cascade screening (23 strategies), opportunistic screening (13 strategies), systematic screening (11 strategies) and population-wide screening (15 strategies). Most of the strategies relied on genetic diagnosis for case ascertainment. The most common comparator was no screening, but some studies compared the proposed strategy versus current screening strategies or versus the best next alternative. Six studies evaluated screening in children while the remaining were targeted at adults. From a healthcare perspective, cascade screening was cost-effective in 78% of the studies [cost-adapted incremental cost-effectiveness ratios (ICERs) ranged from dominant to 2022 US$ 104,877], opportunistic screening in 85% (ICERs from US$4959 to US$41,705), systematic screening in 80% (ICERs from US$2763 to US$69,969) and population-wide screening in 60% (ICERs from US$1484 to US$223,240). The most common driver of ICER identified in the sensitivity analysis was the long-term cost of lipid-lowering treatment. Conclusions Based on reported willingness to pay thresholds for each setting, most CEA studies concluded that screening for FH compared with no screening was cost-effective, regardless of the screening strategy. Cascade screening resulted in the largest health benefits per person tested.
Suggested Citation
Clara Marquina & Jedidiah I Morton & Melanie Lloyd & Dina Abushanab & Yeji Baek & Tamrat Abebe & Adam Livori & Padam Dahal & Gerald F. Watts & Zanfina Ademi, 2024.
"Cost-Effectiveness of Screening Strategies for Familial Hypercholesterolaemia: An Updated Systematic Review,"
PharmacoEconomics, Springer, vol. 42(4), pages 373-392, April.
Handle:
RePEc:spr:pharme:v:42:y:2024:i:4:d:10.1007_s40273-023-01347-7
DOI: 10.1007/s40273-023-01347-7
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