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Treatment drop-in in a contemporary cohort used to derive cardiovascular risk prediction equations

Jingyuan Liang, Rodney T Jackson, Romana Pylypchuk, Yeunhyang Choi, Claris Chung, Sue Crengle, Pei Gao, Corina Grey, Matire Harwood, Anders Holt, Andrew Kerr, Suneela Mehta, Susan Wells, Katrina Poppe

1 Citation (Scopus)

Abstract

BACKGROUND: No 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.

METHODS: Eight 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.

RESULTS: A 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).

CONCLUSIONS: CVD 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.

Original languageEnglish
JournalHeart (British Cardiac Society)
Volume110
Issue number17
Pages (from-to)1083-1089
Number of pages7
ISSN1355-6037
DOIs
Publication statusPublished - 14 Aug 2024

Keywords

  • Humans
  • Middle Aged
  • Male
  • Female
  • Cardiovascular Diseases/epidemiology
  • Aged
  • Risk Assessment/methods
  • Adult
  • New Zealand/epidemiology
  • Heart Disease Risk Factors
  • Hypolipidemic Agents/therapeutic use
  • Antihypertensive Agents/therapeutic use

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