Prioritising cardiovascular disease risk assessment to high risk individuals based on primary care records.
Prioritising cardiovascular disease risk assessment to high risk individuals based on primary care records.
复制标题
DOI:
10.1371/journal.pone.0292240
复制
发表时间:
2023
期刊:
影响因子:
3.7
通讯作者:
中科院分区:
文献类型:
--
作者:
To provide quantitative evidence for systematically prioritising individuals for full formal cardiovascular disease (CVD) risk assessment using primary care records with a novel tool (eHEART) with age- and sex- specific risk thresholds. eHEART was derived using landmark Cox models for incident CVD with repeated measures of conventional CVD risk predictors in 1,642,498 individuals from the Clinical Practice Research Datalink. Using 119,137 individuals from UK Biobank, we modelled the implications of initiating guideline-recommended statin therapy using eHEART with age- and sex-specific prioritisation thresholds corresponding to 5% false negative rates to prioritise adults aged 40–69 years in a population in England for invitation to a formal CVD risk assessment. Formal CVD risk assessment on all adults would identify 76% and 49% of future CVD events amongst men and women respectively, and 93 (95% CI: 90, 95) men and 279 (95% CI: 259, 297) women would need to be screened (NNS) to prevent one CVD event. In contrast, if eHEART was first used to prioritise individuals for formal CVD risk assessment, we would identify 73% and 47% of future events amongst men and women respectively, and a NNS of 75 (95% CI: 72, 77) men and 162 (95% CI: 150, 172) women. Replacing the age- and sex-specific prioritisation thresholds with a 10% threshold identify around 10% less events. The use of prioritisation tools with age- and sex-specific thresholds could lead to more efficient CVD assessment programmes with only small reductions in effectiveness at preventing new CVD events.
登录
查看更多内容
影响因子:
105.7
作者:
Chamnan, Parinya;Simmons, Rebecca K.;Griffin, Simon J.
通讯作者:
Griffin, Simon J.
影响因子:
105.7
作者:
Hippisley-Cox, Julia;Coupland, Carol;Brindle, Peter
通讯作者:
Brindle, Peter
DOI:
10.1056/nejmoa1107477
发表时间:
2012-10-04
期刊:
The New England journal of medicine
影响因子:
--
作者:
Emerging Risk Factors Collaboration;Kaptoge S;Di Angelantonio E;Pennells L;Wood AM;White IR;Gao P;Walker M;Thompson A;Sarwar N;Caslake M;Butterworth AS;Amouyel P;Assmann G;Bakker SJ;Barr EL;Barrett-Connor E;Benjamin EJ;Björkelund C;Brenner H;Brunner E;Clarke R;Cooper JA;Cremer P;Cushman M;Dagenais GR;D'Agostino RB Sr;Dankner R;Davey-Smith G;Deeg D;Dekker JM;Engström G;Folsom AR;Fowkes FG;Gallacher J;Gaziano JM;Giampaoli S;Gillum RF;Hofman A;Howard BV;Ingelsson E;Iso H;Jørgensen T;Kiechl S;Kitamura A;Kiyohara Y;Koenig W;Kromhout D;Kuller LH;Lawlor DA;Meade TW;Nissinen A;Nordestgaard BG;Onat A;Panagiotakos DB;Psaty BM;Rodriguez B;Rosengren A;Salomaa V;Kauhanen J;Salonen JT;Shaffer JA;Shea S;Ford I;Stehouwer CD;Strandberg TE;Tipping RW;Tosetto A;Wassertheil-Smoller S;Wennberg P;Westendorp RG;Whincup PH;Wilhelmsen L;Woodward M;Lowe GD;Wareham NJ;Khaw KT;Sattar N;Packard CJ;Gudnason V;Ridker PM;Pepys MB;Thompson SG;Danesh J
通讯作者:
Danesh J
影响因子:
37.8
作者:
Lloyd-Jones, Donald M.
通讯作者:
Lloyd-Jones, Donald M.
影响因子:
1.9
作者:
LAIRD, NM;WARE, JH
通讯作者:
WARE, JH