Imagine a new patient “Bill”, 62 years of age, comes to your clinic for a visit. You want to deliver guideline-recommended preventive care, and decide to use the U.S Preventive Services Task Force (USPSTF) guidelines. More than 10 separate guidelines are relevant to Bill. Following the guidelines you screen for hypertension, hyperlipidemia, colon cancer, depression, alcohol misuse, depression, diabetes, HIV, obesity, and tobacco use. You learn that Bill is obese, smokes, has high cholesterol, hypertension and diabetes. Given his risk factors, USPSTF guidelines indicate that Bill would be eligible for aspirin to prevent cardiovascular disease, management of obesity, diabetes, hypertension, and possibly counseling to promote a healthy diet and physical activity. Although the goal is to follow all of the guideline recommendations, it may simply not be possible to do everything. If that’s true, which of these guideline-recommended interventions are most important? Will smoking cessation, treatment of diabetes, or weight loss improve Bill’s health the most? How can we know, and what metric should we use to decide which interventions provide the most benefit?
How to prioritize what to do in the limited time of a clinical encounter is a pervasive problem in primary care. This question is the topic of a paper by Taksler and colleagues in this issue of the Annals (1). They address the question in the context of the benefits that accrue from delivery of preventive services and treatment for conditions identified through those services. The goal of their analysis is to identify, for Bill, and for other patients, which interventions result in the biggest increase in how long they can expect to live.
To do this, Taksler and colleagues develop a mathematical model that estimates how different interventions (e.g., treatment of diabetes, weight loss) would change Bill’s life expectancy. Life expectancy is the average time a group of people would live, and it’s an important measure of health benefit. Changes in life expectancy of a year or more are enormous, and even changes in life expectancy of a few days to weeks may be sufficient to justify an intervention (2). For example, biennial screening mammography from age 50 to 69 increases life expectancy by approximately 5 weeks (3). Taksler and colleagues do an admirable job considering all applicable preventive interventions for which the USPSTF has given an A or B recommendation (meaning they are recommended).
The first finding to note is that rather than a life expectancy of 19.1 years, which is expected for an average 62-year old white man, Bill’s life expectancy is only 9.6 years (the life expectancy of an average 77-year-old white man). This dramatically shorter life expectancy drives home the seriousness of Bill’s comorbid conditions. Of all the candidate interventions, the ones with most impact on life expectancy are control of diabetes (1.8 life-years gained), smoking cessation (1.5 life-years gained), and blood pressure control (1.4 life-years gained). Lowering cholesterol, use of daily aspirin, weight loss, and eating a healthier diet also provide substantial gains in life expectancy. Screening for colon cancer, HIV and abdominal aortic aneurysms provide much smaller gains. The rank order of the most important interventions change based on the comorbid conditions, ethnicity, and gender of the patient. For example, for a woman with Bill’s conditions, control of diabetes dropped from the first to the fourth largest impact on life expectancy. The change is because of women’s lower risk of coronary heart disease.
The value of the tool Taskler and colleagues developed is that it estimates the changes in health outcomes across many interventions, and thus enables us to understand the relative importance of different interventions for a specific patient. Although guideline development groups, such as the USPSTF, use models to help develop guidelines, by necessity, these models evaluate the effect of one intervention (e.g., mammography) on patients with different characteristics. These models can be very helpful in exploring how screening intervals and starting and stopping ages affect benefits and harms of an intervention delivered to different patient subpopulations (4). However, they are not intended to model multiple diseases or to directly prioritize across conditions and interventions.
Modeling the effect of interventions across many diseases is quite ambitious and requires numerous simplifying assumptions. As the authors note, their analysis is a proof-of-concept rather than a fully implemented tool, and there are extensions that would be valuable. They measure benefit in terms of life expectancy which only accounts for changes in mortality. Other metrics of impact could include a broader set of outcomes. Quality-adjusted life expectancy accounts for both mortality and morbidity and thus would have an advantage as a metric (5). If patients or clinicians were interested in high-value health care (6), the analysis could also account for costs, and interventions could be prioritized based on cost effectiveness. Regardless of the metric used, some interventions with high potential benefit (e.g., changing diet or lifestyle, weight loss) may be harder to realize in practice than others (e.g., blood pressure control), a factor that clinicians will likely consider. Some interventions may have synergies (or diminished benefits) when delivered together, another factor that may affect prioritization. In addition, some preventive interventions, such as screening for HIV, have a public health benefit (reduced transmission and consequent health benefits to individuals other than the patient) that is not captured in the framework. Finally, an analysis could incorporate detailed patient-specific information and preferences to provide individualized decision support (7). Although there is additional work that can be done, the study provides an important contribution.
While the present study focuses on helping clinicians prioritize which guideline-recommended prevention interventions to deliver, the goal of providing all guideline-recommended care remains very important, but challenging. Success may require multiple delivery strategies. Some interventions need not be delivered by physicians, and indeed, may best be performed by other healthcare professionals (8). While broader strategies are developed to provide all recommended care, the tool developed by Taksler and colleagues has promise to help make sure the highest impact interventions are delivered. Whether its use will improve patient outcomes is a question worthy of further study.
Acknowledgments
Dr. Owens is supported by the Department of Veterans Affairs. Dr. Goldhaber-Fiebert is supported by an NIH career development award (K01 AG037593).
Footnotes
Disclaimer: The views expressed in this article are those of the authors and do not necessarily reflect the position or policy of the Department of Veterans Affairs, the U.S. government, or the U.S. Preventive Services Task Force.
Contributor Information
Douglas K. Owens, VA Palo Alto Health Care System, Palo Alto, California, Center for Primary Care and Outcomes Research and Center for Health Policy, Stanford University, Stanford, California.
Jeremy D. Goldhaber-Fiebert, Center for Primary Care and Outcomes Research and Center for Health Policy, Stanford University, Stanford, California.
References
- 1.Taksler GB, Keshner M, Fagerlin A, Jajizadeh N, Braithwaite RS. Personalized estimates of benefit from preventive care guidelines: a proof of concept. Annals of Internal Medicine. 2013 doi: 10.7326/0003-4819-159-3-201308060-00005. (in press) [DOI] [PubMed] [Google Scholar]
- 2.Sanders GD, Bayoumi AM, Sundaram V, Bilir SP, Neukermans CP, Rydzak CE, et al. Cost effectiveness of screening for HIV in the era of highly active antiretroviral therapy. New England Journal of Medicine. 2005;352:570–585. doi: 10.1056/NEJMsa042657. [DOI] [PubMed] [Google Scholar]
- 3.Mandelblatt JS, Cronin KA, Bailey S, Berry DA, de Koning HJ, Draisma G, et al. Effects of mammography screening under different screening schedules: model estimates of potential benefits and harms. Annals of Internal Medicine. 2009;151:738–747. doi: 10.1059/0003-4819-151-10-200911170-00010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Zauber AG, Lansdorp-Vogelaar I, Knudsen AB, Wilschut J, van Ballegooijen M, Kuntz KM. Evaluating test strategies for colorectal cancer screening: a decision analysis for the U. S Preventive Services Task Force. Annals of Internal Medicine. 2008;149:659–669. doi: 10.7326/0003-4819-149-9-200811040-00244. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Owens DK, Shekelle PG. Quality of life, utilities, quality-adjusted life years, and health care decision making: Comment on “Estimating quality of life in acute venous thrombosis”. JAMA Intern Med. 2013 May;20:1–2. doi: 10.1001/jamainternmed.2013.7396. [Epub ahead of print] [DOI] [PubMed] [Google Scholar]
- 6.Owens DK, Qaseem A, Chou R, Shekelle P for the Clinical Guidelines Committee of the American College of Physicians. High-value, cost-conscious health care: concepts for clinicians to evaluate benefits, harms, and costs of medical interventions. Annals of Internal Medicine. 2011;154:174–80. doi: 10.7326/0003-4819-154-3-201102010-00007. [DOI] [PubMed] [Google Scholar]
- 7.Sox HC, Higgins MC, Owens DK. Medical Decision Making. 2. Chichester: John Wiley & Sons Ltd; 2013. pp. 330–332. [Google Scholar]
- 8.Anaya HD, Hoang T, Golden JF, Goetz MB, Gifford A, Bowman C, Osborn T, Owens DK, Sanders GD, Asch SM. Improving HIV screening and receipt of results by nurse-initiated streamlined counseling and rapid testing. Journal of General Internal Medicine. 2008;23:800–807. doi: 10.1007/s11606-008-0617-x. [DOI] [PMC free article] [PubMed] [Google Scholar]