Patient-Accessible Tool for Shared Decision Making in Cardiovascular Primary Prevention Balancing Longevity Benefits Against Medication Disutility

被引:68
作者
Fontana, Marianna [1 ]
Asaria, Perviz [1 ]
Moraldo, Michela [1 ]
Finegold, Judith [1 ]
Hassanally, Khalil [1 ]
Manisty, Charlotte H. [1 ]
Francis, Darrel P. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Int Ctr Circulatory Hlth, Natl Heart & Lung Inst, London, England
基金
英国惠康基金;
关键词
compliance; hydroxymethylglutaryl-CoA reductase inhibitors; primary prevention; IMPROVE STATIN ADHERENCE; COST-EFFECTIVENESS; DISEASE RISK; FUTURE; TRIAL; SCORE;
D O I
10.1161/CIRCULATIONAHA.113.007595
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Primary prevention guidelines focus on risk, often assuming negligible aversion to medication, yet most patients discontinue primary prevention statins within 3 years. We quantify real-world distribution of medication disutility and separately calculate the average utilities for a range of risk strata. Method and Results We randomly sampled 360 members of the general public in London. Medication aversion was quantified as the gain in lifespan required by each individual to offset the inconvenience (disutility) of taking an idealized daily preventative tablet. In parallel, we constructed tables of expected gain in lifespan (utility) from initiating statin therapy for each age group, sex, and cardiovascular risk profile in the population. This allowed comparison of the widths of the distributions of medication disutility and of group-average expectation of longevity gain. Observed medication disutility ranged from 1 day to >10 years of life being required by subjects (median, 6 months; interquartile range, 1-36 months) to make daily preventative therapy worthwhile. Average expected longevity benefit from statins at ages 50 years ranges from 3.6 months (low-risk women) to 24.3 months (high-risk men). Conclusion We can no longer assume that medication disutility is almost zero. Over one-quarter of subjects had disutility exceeding the group-average longevity gain from statins expected even for the highest-risk (ie, highest-gain) group. Future primary prevention studies might explore medication disutility in larger populations. Patients may differ more in disutility than in prospectively definable utility (which provides only group-average estimates). Consultations could be enriched by assessing disutility and exploring its reasons.
引用
收藏
页码:2539 / 2546
页数:8
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