Journal
LANCET
Volume 394, Issue 10199, Pages 663-671Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/S0140-6736(19)31359-5
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Funding
- National Institute for Health Research (NIHR) Post-doctoral Research Fellowship [PDF-2016-09-029]
- Wellcome Trust [107731/Z/15/Z]
- Royal Society [107731/Z/15/Z]
- NIHR Biomedical Research Centre at University College London Hospitals (London, UK)
- New Zealand Health Research Council
- New Zealand Heart Foundation
- New Zealand National Science Challenge Healthier Lives research programme
- Health Data Research UK - UK Medical Research Council, Engineering and Physical Sciences Research Council
- Economic and Social Research Council, Department of Health and Social Care (England), Chief Scientist Office of the Scottish Government Health and Social Care Directorates, Health and Social Care Research and Development Division (Welsh Government)
- Public Health Agency (Northern Ireland)
- British Heart Foundation
- National Institutes of Health Research (NIHR) [PDF-2016-09-029] Funding Source: National Institutes of Health Research (NIHR)
- Wellcome Trust [107731/Z/15/Z] Funding Source: Wellcome Trust
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Background Worldwide treatment recommendations for lowering blood pressure continue to be guided predominantly by blood pressure thresholds, despite strong evidence that the benefits of blood pressure reduction are observed in patients across the blood pressure spectrum. In this study, we aimed to investigate the implications of alternative strategies for offering blood pressure treatment, using the UK as an illustrative example. Methods We did a retrospective cohort study in primary care patients aged 30-79 years without cardiovascular disease, using data from the UK's Clinical Practice Research Datalink linked to Hospital Episode Statistics and Office for National Statistics mortality. We assessed and compared four different strategies to determine eligibility for treatment: using 2011 UK National Institute for Health and Care Excellence (NICE) guideline, or proposed 2019 NICE guideline, or blood pressure alone (threshold >= 140/90 mm Hg), or predicted 10-year cardiovascular risk alone (QRISK2 score >= 10%). Patients were followed up until the earliest occurrence of a cardiovascular disease diagnosis, death, or end of follow-up period (March 31, 2016). For each strategy, we estimated the proportion of patients eligible for treatment and number of cardiovascular events that could be prevented with treatment. We then estimated eligibility and number of events that would occur during 10 years in the UK general population. Findings Between Jan 1, 2011, and March 31, 2016, 1 222 670 patients in the cohort were followed up for a median of 4.3 years (IQR 2.5-5.2). 271 963 (22.2%) patients were eligible for treatment under the 2011 NICE guideline, 327 429 (26.8%) under the proposed 2019 NICE guideline, 481 859 (39.4%) on the basis of a blood pressure threshold of 140/90 mm Hg or higher, and 357 840 (29.3%) on the basis of a QRISK2 threshold of 10% or higher. During follow-up, 32 183 patients were diagnosed with cardiovascular disease (overall rate 7.1 per 1000 person-years, 95% CI 7.0-7.2). Cardiovascular event rates in patients eligible for each strategy were 15.2 per 1000 person-years (95% CI 15.0-15.5) under the 2011 NICE guideline, 14.9 (14.7-15.1) under the proposed 2019 NICE guideline, 11.4 (11.3-11.6) with blood pressure threshold alone, and 16.9 (16.7-17.1) with QRISK2 threshold alone. Scaled to the UK population, we estimated that 233 152 events would be avoided under the 2011 NICE guideline (28 patients needed to treat for 10 years to avoid one event), 270 233 under the 2019 NICE guideline (29 patients), 301 523 using a blood pressure threshold (38 patients), and 322 921 using QRISK2 threshold (27 patients). Interpretation A cardiovascular risk-based strategy (QRISK2 >= 10%) could prevent over a third more cardiovascular disease events than the 2011 NICE guideline and a fifth more than the 2019 NICE guideline, with similar efficiency regarding number treated per event avoided. Copyright (C) 2019 The Author(s). Published by Elsevier Ltd.
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