TY - JOUR
T1 - Cost-effectiveness of applying high-sensitivity troponin I to a score for cardiovascular risk prediction in asymptomatic population
AU - Jülicher, Paul
AU - Makarova, Nataliya
AU - Ojeda, Francisco
AU - Giusepi, Isabella
AU - Peters, Annette
AU - Thorand, Barbara
AU - Cesana, Giancarlo
AU - Jørgensen, Torben
AU - Linneberg, Allan
AU - Salomaa, Veikko
AU - Iacoviello, Licia
AU - Costanzo, Simona
AU - Söderberg, Stefan
AU - Kee, Frank
AU - Giampaoli, Simona
AU - Palmieri, Luigi
AU - Donfrancesco, Chiara
AU - Zeller, Tanja
AU - Kuulasmaa, Kari
AU - Tuovinen, Tarja
AU - Lamrock, Felicity
AU - Conrads-Frank, Annette
AU - Brambilla, Paolo
AU - Blankenberg, Stefan
AU - Siebert, Uwe
PY - 2024/7/19
Y1 - 2024/7/19
N2 - Risk stratification scores such as the European Systematic COronary Risk Evaluation (SCORE) are used to guide individuals on cardiovascular disease (CVD) prevention. Adding high-sensitivity troponin I (hsTnI) to such risk scores has the potential to improve accuracy of CVD prediction. We investigated how applying hsTnI in addition to SCORE may impact management, outcome, and cost-effectiveness. Characteristics of 72,190 apparently healthy individuals from the Biomarker for Cardiovascular Risk Assessment in Europe (BiomarCaRE) project were included into a discrete-event simulation comparing two strategies for assessing CVD risk. The standard strategy reflecting current practice employed SCORE (SCORE); the alternative strategy involved adding hsTnI information for further stratifying SCORE risk categories (S-SCORE). Individuals were followed over ten years from baseline examination to CVD event, death or end of follow-up. The model tracked the occurrence of events and calculated direct costs of screening, prevention, and treatment from a European health system perspective. Cost-effectiveness was expressed as incremental cost-effectiveness ratio (ICER) in € per quality-adjusted life year (QALYs) gained during 10 years of follow-up. Outputs were validated against observed rates, and results were tested in deterministic and probabilistic sensitivity analyses. S-SCORE yielded a change in management for 10.0% of individuals, and a reduction in CVD events (4.85% vs. 5.38%, p
AB - Risk stratification scores such as the European Systematic COronary Risk Evaluation (SCORE) are used to guide individuals on cardiovascular disease (CVD) prevention. Adding high-sensitivity troponin I (hsTnI) to such risk scores has the potential to improve accuracy of CVD prediction. We investigated how applying hsTnI in addition to SCORE may impact management, outcome, and cost-effectiveness. Characteristics of 72,190 apparently healthy individuals from the Biomarker for Cardiovascular Risk Assessment in Europe (BiomarCaRE) project were included into a discrete-event simulation comparing two strategies for assessing CVD risk. The standard strategy reflecting current practice employed SCORE (SCORE); the alternative strategy involved adding hsTnI information for further stratifying SCORE risk categories (S-SCORE). Individuals were followed over ten years from baseline examination to CVD event, death or end of follow-up. The model tracked the occurrence of events and calculated direct costs of screening, prevention, and treatment from a European health system perspective. Cost-effectiveness was expressed as incremental cost-effectiveness ratio (ICER) in € per quality-adjusted life year (QALYs) gained during 10 years of follow-up. Outputs were validated against observed rates, and results were tested in deterministic and probabilistic sensitivity analyses. S-SCORE yielded a change in management for 10.0% of individuals, and a reduction in CVD events (4.85% vs. 5.38%, p
KW - Humans
KW - Adult
KW - Troponin I - blood
KW - Female
KW - Quality-Adjusted Life Years
KW - Europe - epidemiology
KW - Male
KW - Cardiovascular Diseases - economics - blood - diagnosis
KW - Risk Assessment - methods
KW - Biomarkers - blood
KW - Middle Aged
KW - Aged
KW - Heart Disease Risk Factors
KW - Cost-Benefit Analysis
U2 - 10.1371/journal.pone.0307468
DO - 10.1371/journal.pone.0307468
M3 - Article
C2 - 39028718
SN - 1932-6203
VL - 19
JO - PLOS ONE
JF - PLOS ONE
IS - 7
M1 - e0307468
ER -