Familial hypercholesterolemia nice guidelines for diabetes *246*

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    Heterozygous familial hypercholesterolemia (HeFH) is a monogenic disorder that affects about 1 in 500 people, with a higher prevalence in certain subpopulations such as people of Quebecois, Christian Lebanese and Dutch South Afrikaner extraction. Diagnostic guidelines for HeFH diagnosis in
    Implementing guidelines The Simon Broome criteria should be used to detect FH. 2010-12-01T00:00:00Z. Drs Kathy Greenough and Kate Cushing outline the NHS North of Tyne approach to implementing the NICE guideline on familial hypercholesterolaemia
    The 2018 guideline addresses the practical management of patients with high blood cholesterol and related disorders. Recommendations are based on the best available evidence from randomized controlled trials of cholesterol-lowering therapies and other sources of evidence. This guideline is a full update of the 2013 ACC/AHA cholesterol guideline.
    1. Jones LK, Kulchak Rahm A, Manickam K, et al. Healthcare utilization and patients’ perspectives after receiving a positive genetic test for familial hypercholesterolemia. Circ Genom Precis Med. 2018;11(8):e002146. 2. Raal FJ, Hovingh GK, Catapano AL. Familial hypercholesterolemia treatments: guidelines and new therapies.
    This collection features the best content from AFP, as identified by the AFP editors, on hyperlipidemia and related issues, including dyslipidemia, hypercholesterolemia, hypertriglyceridemia
    The NICE guideline recommends the use of statins for the initial treatment of FH, and the issue of counselling women with FH taking statins about the management of their fertility is important. Offspring from mothers versus fathers with familial hypercholesterolemia: is [SFD]), Diabetes
    Controversies in familial hypercholesterolaemia: recommendations of the NICE Guideline Development Group for the identification and management of familial hypercholesterolaemia R Minhas 1 , S E Humphries 2 ,
    The guideline gives PCSK9 inhibitors a low-cost value for patients at very high risk
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