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Treatment drop-in in a contemporary cohort used to derive cardiovascular risk prediction equations
- Source :
- Heart; 2024, Vol. 110 Issue: 17 p1083-1089, 7p
- Publication Year :
- 2024
-
Abstract
- BackgroundNo routinely recommended cardiovascular disease (CVD) risk prediction equations have adjusted for CVD preventive medications initiated during follow-up (treatment drop-in) in their derivation cohorts. This will lead to underestimation of risk when equations are applied in clinical practice if treatment drop-in is common. We aimed to quantify the treatment drop-in in a large contemporary national cohort to determine whether equations are likely to require adjustment.MethodsEight de-identified individual-level national health administrative datasets in Aotearoa New Zealand were linked to establish a cohort of almost all New Zealanders without CVD and aged 30–74 years in 2006. Individuals dispensing blood-pressure-lowering and/or lipid-lowering medications between 1 July 2006 and 31 December 2006 (baseline dispensing), and in each 6-month period during 12 years’ follow-up to 31 December 2018 (follow-up dispensing), were identified. Person-years of treatment drop-in were determined.ResultsA total of 1 399 348 (80%) out of the 1 746 695 individuals in the cohort were not dispensed CVD medications at baseline. Blood-pressure-lowering and/or lipid-lowering treatment drop-in accounted for 14% of follow-up time in the group untreated at baseline and increased significantly with increasing predicted baseline 5-year CVD risk (12%, 31%, 34% and 37% in <5%, 5–9%, 10–14% and ≥15% risk groups, respectively) and with increasing age (8% in 30–44 year-olds to 30% in 60–74 year-olds).ConclusionsCVD preventive treatment drop-in accounted for approximately one-third of follow-up time among participants typically eligible for preventive treatment (≥5% 5-year predicted risk). Equations derived from cohorts with long-term follow-up that do not adjust for treatment drop-in effect will underestimate CVD risk in higher risk individuals and lead to undertreatment. Future CVD risk prediction studies need to address this potential flaw.
Details
- Language :
- English
- ISSN :
- 13556037 and 1468201X
- Volume :
- 110
- Issue :
- 17
- Database :
- Supplemental Index
- Journal :
- Heart
- Publication Type :
- Periodical
- Accession number :
- ejs67144838
- Full Text :
- https://doi.org/10.1136/heartjnl-2024-324179