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Systematic Identification of Familial Hypercholesterolaemia in Primary Care—A Systematic Review

Silva, Luisa; Qureshi, Nadeem; Abdul-Hamid, Hasidah; Weng, Stephen; Kai, Joe; Leonardi-Bee, Jo

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Authors

Luisa Silva

Hasidah Abdul-Hamid

Stephen Weng

JO LEONARDI-BEE jo.leonardi-bee@nottingham.ac.uk
Professor of Evidence Synthesis



Abstract

Familial hypercholesterolaemia (FH) is a common inherited cause of premature cardiovascular disease, but the majority of patients remain undiagnosed. The aim of this systematic review was to assess the effectiveness of interventions to systematically identify FH in primary care. No randomised, controlled studies were identified; however, three non-randomised intervention studies were eligible for inclusion. All three studies systematically identified FH using reminders (on-screen prompts) in electronic health records. There was insufficient evidence that providing comments on laboratory test results increased the identification of FH using the Dutch Lipid Clinic Network (DLCN) criteria. Similarly, using prompts combined with postal invitation demonstrated no significant increase in definite FH identification using Simon-Broome (SB) criteria; however, the identification of possible FH increased by 25.4% (CI 17.75 to 33.97%). Using on-screen prompts alone demonstrated a small increase of 0.05% (95% CI 0.03 to 0.07%) in identifying definite FH using SB criteria; however, when the intervention was combined with an outreach FH nurse assessment, the result was no significant increase in FH identification using a combination of SB and DLCN criteria. None of the included studies reported adverse effects associated with the interventions. Currently, there is insufficient evidence to determine which is the most effective method of systematically identifying FH in non-specialist settings.

Citation

Silva, L., Qureshi, N., Abdul-Hamid, H., Weng, S., Kai, J., & Leonardi-Bee, J. (2021). Systematic Identification of Familial Hypercholesterolaemia in Primary Care—A Systematic Review. Journal of Personalized Medicine, 11(4), Article 302. https://doi.org/10.3390/jpm11040302

Journal Article Type Article
Acceptance Date Apr 10, 2021
Online Publication Date Apr 15, 2021
Publication Date Apr 15, 2021
Deposit Date Apr 20, 2021
Publicly Available Date Apr 20, 2021
Journal Journal of Personalized Medicine
Electronic ISSN 2075-4426
Publisher MDPI
Peer Reviewed Peer Reviewed
Volume 11
Issue 4
Article Number 302
DOI https://doi.org/10.3390/jpm11040302
Keywords familial hypercholesterolaemia; primary care; genetics
Public URL https://nottingham-repository.worktribe.com/output/5469712
Publisher URL https://www.mdpi.com/2075-4426/11/4/302

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