The interaction between practice socioeconomic environment and patient-centered medical home (PCMH) implementation. A, Breast cancer (BC) screening. B, Cervical cancer (CC) screening. C, Colorectal cancer (CRC) screening. SES indicates socioeconomic status.
eTable 1. Capabilities Used to Calculate PCMH Implementation Scores, by PCMH Functional Domain
eTable 2. Multivariable Mixed Model Results for the Association Between Medical Home Implementation and Breast Cancer Screening in BCBSM PGIP Practices, July 2009 to June 2012
eTable 3. Multivariable Mixed Model Results for the Association Between Medical Home Implementation and Cervical Cancer Screening in BCBSM PGIP Practices, July 2009 to June 2012
eTable 4. Multivariable Mixed Model Results for the Association Between Medical Home Implementation and Colorectal Cancer Screening in BCBSM PGIP Practices, July 2009 to June 2012
eMethods. Primary Care Relationship Attribution
Markovitz AR, Alexander JA, Lantz PM, Paustian ML. Patient-Centered Medical Home Implementation and Use of Preventive ServicesThe Role of Practice Socioeconomic Context. JAMA Intern Med. 2015;175(4):598-606. doi:10.1001/jamainternmed.2014.8263
Copyright 2015 American Medical Association. All Rights Reserved. Applicable FARS/DFARS Restrictions Apply to Government Use.
The patient-centered medical home (PCMH) model of primary care is being implemented in a wide variety of socioeconomic contexts, yet there has been little research on whether its effects differ by context. Clinical preventive service use, including cancer screening, is an important outcome to assess the effectiveness of the PCMH within and across socioeconomic contexts.
To determine whether the relationship between the PCMH and cancer screening is conditional on the socioeconomic context in which a primary care physician practice operates.
Design, Setting, and Participants
A longitudinal study spanning July 1, 2009, through June 30, 2012, using data from the Blue Cross Blue Shield of Michigan Physician Group Incentive Program was conducted. Michigan nonpediatric primary care physician practices that participated in the Physician Group Incentive Program (5452 practice-years) were included. Sample size and outlier exclusion criteria were applied to each outcome. We examined the interaction between practices’ PCMH implementation scores and their socioeconomic context. The implementation of a PCMH was self-reported by the practice’s affiliated physician organizations and was measured as a continuous score ranging from 0 to 1. Socioeconomic context was calculated using a market-based approach based on zip code characteristics of the practice’s patients and by combining multiple measures using principal components analysis.
Main Outcomes and Measures
Breast, cervical, and colorectal cancer screening rates for practices’ Blue Cross Blue Shield of Michigan patients.
The implementation of a PCMH was associated with higher breast, cervical, and colorectal cancer screening rates across most market socioeconomic contexts. In multivariable models, the PCMH was associated with a higher rate of screening for breast cancer (5.4%; 95% CI, 1.5% to 9.3%), cervical cancer (4.2%; 95% CI, 1.4% to 6.9%), and colorectal cancer (7.0%; 95% CI, 3.6% to 10.5%) in the lowest socioeconomic group but nonsignificant differences in screening for breast cancer (2.6%; 95% CI, −0.1% to 5.3%) and cervical cancer (−0.5%; 95% CI, −2.7% to 1.7%) and a higher rate of colorectal cancer (4.5%; 95% CI, 1.8% to 7.3%) screening in the highest socioeconomic group. Because PCMH implementation was associated with larger increases in screening in lower socioeconomic practice settings, models suggest reduced disparities in screening rates across these contexts. For example, the model-predicted disparity in breast cancer screening rates between the highest and lowest socioeconomic contexts was 6% (77.9% vs 72.2%) among practices with no PCMH implementation and 3% (80.3% vs. 77.0%) among practices with full PCMH implementation.
Conclusions and Relevance
In our study, the PCMH model was associated with improved cancer screening rates across contexts but may be especially relevant for practices in lower socioeconomic areas.
The patient-centered medical home (PCMH) model of primary care has become a focus for innovation in the US health care system, with endorsements by the major primary care physician (PCP) societies1 and support in the Patient Protection and Affordable Care Act of 2010.2 As a holistic, patient-centered, team-based model of care, the PCMH promotes access, coordination, comprehensiveness, quality, and safety.3 This model emphasizes the core primary care function of providing clinical preventive services4 and a comprehensive approach to care over a patient’s life course rather than focusing on episodic treatment, a specific medical issue, or a particular body system.5 Increased clinical preventive service use is considered a key indicator for evaluating the success of the PCMH,6,7 and early evaluations8- 10 have shown consistent evidence of a positive association.
The PCMH model calls for practices to work within systems of care that are not restricted by organizational boundaries of the primary care practice but are coordinated across all elements of the health care system, patients’ day-to-day lives, and their communities.5 Because patient centeredness implies that patients are active partners in health care decision making,5 these contextual features may be especially relevant when evaluating the effect of the PCMH on clinical preventive services given persistent socioeconomic disparities in their use.11- 22 Some23,24 have argued that the PCMH model may be especially effective in lower socioeconomic status (SES) areas by overcoming some of the challenges that drive disparities by improving access to care, care coordination, and health literacy.
Implementation of the PCMH model is occurring in a wide variety of practice settings,25- 28 including areas with a predominance of low SES patients29,30; however, to our knowledge, no research to date has investigated whether the effects of PCMHs on preventive services differ by the SES contexts in which they were implemented.8 The SES context is typically defined based on residential neighborhoods or other geographic boundaries that have economic, educational, social, cultural, and political characteristics.31,32 Our study investigated (1) whether the relationship between the PCMH and cancer screening, an important type of clinical preventive service, is conditional on the socioeconomic context in which a physician practice operates and (2) whether the PCMH provides a boosting effect in lower socioeconomic contexts.
Cancer prevention services were chosen as the focus of our investigation.33,34 Several types of routine cancer screening tests are included in the Healthcare Effectiveness Data and Information (HEDIS) data set and are recommended by the US Preventive Services Task Force.35,36 This data set includes cervical cancer screening for women 21 years or older, breast cancer screening for women 50 years or older, and colorectal cancer screening for all adults 50 years or older. Results from studies that consider community socioeconomic context or area-based measures of SES are mixed, although several studies22,37,38 have reported significant positive associations between the odds of cancer screening and area SES.
This dynamic cohort study included a total of 2218 Michigan primary care practices that participated in the Blue Cross Blue Shield of Michigan (BCBSM) Physician Group Incentive Program (PGIP). The PGIP is a voluntary incentive and payment reform program designed to support physician organizations and their affiliated practices to achieve care transformation and value-based care delivery.39 Physician organizations participating in the PGIP report their affiliated practices semiannually to BCBSM. Using these data, we included practices that participated for at least 1 full year between July 1, 2009, and June 30, 2012, measured using the June reports, for a total of 5452 observed practice-years. We excluded practices in which specialists accounted for the majority of the physicians (n = 41), pediatric practices (n = 329), and practices with missing data on PCMH capability implementation or other predictor variables (n = 127). This study was approved by the University of Michigan Institutional Review Board and determined to be exempt for the purpose of program evaluation.
The PCMH model within the PGIP was created collaboratively with physician organization leaders based on the Joint Principles of the Patient-Centered Medical Home5 and the chronic care model40 and defined specific capabilities within 13 domains of PCMH functioning. The PGIP program supports PCMH implementation by providing physician organizations with financial incentives when their member practices initiate PCMH capabilities. Physician organizations identified PCMH capabilities begun in all affiliated practices. To validate these reports, BCBSM conducted site visits and, in 2012, confirmed that 95% of self-reported capabilities were in place at 323 randomly selected practices. Using 114 capabilities that were defined consistently from June 2009 through June 2012 (eTable 1 in the Supplement), we calculated practice-level PCMH implementation scores. Giving each domain an equal weight, we calculated continuous PCMH implementation scores ranging from 0 (no implementation) to 1 (full implementation); this calculation process is described in more detail elsewhere.41
We divided the study period into 3 study years: July 1, 2009, through June 30, 2010; July 1, 2010, through June 30, 2011; and July 1, 2011, through June 30, 2012. The PCMH implementation scores at the beginning of these study years were calculated using capabilities reported in the preceding June. In addition, the change in PCMH implementation scores between consecutive June reporting periods was used to measure the incremental implementation during the study year.
We defined a medical practice’s socioeconomic context as the geographic environments in which its patients reside. We operationalized this market-based approach by calculating zip code characteristics for each practice, weighted by the proportion of the practice’s professional services provided to BCBSM members residing within that zip code. We identified 8 standard measures of socioeconomic position that were available at a zip code level and are relevant to population health31: (1) percentage of individuals with income below the poverty level, (2) median household income, (3) percentage of adults 25 years or older with less than a high school education, (4) percentage of individuals unemployed, (5) percentage of households with affordable housing (paying <30% of their income to housing), (6) percentage of families with single parents, (7) percentage of households with public assistance income, and (8) a foreclosure risk score. Measures 1 through 7 were identified using the 2011 American Community Survey.42 The foreclosure risk score was obtained from the Local Initiatives Support Corporation43 and combined measures of subprime lending, foreclosures, delinquency, and vacancy rates to assign a score relative to the neediest jurisdiction in the state, with a score of 100 representing the neediest jurisdiction and 0 the least needy. We calculated a weighted mean of these zip code characteristics for each practice using the locations of their patients and then used principal components analysis to combine these 8 measures into a single practice-level index of SES context. We assumed stability in zip code characteristics during the study period, but we calculated the practice’s scores separately for each study year to account for shifts in their patient populations over time. Thus, a practice could change SES categories during the study period. The SES index was standardized to have a mean (SD) of 0 (1).
The outcomes for this study were practice-level, age-appropriate breast, cervical, and colorectal cancer screening rates, defined using HEDIS.44- 46 Breast cancer screening was measured as the proportion of women aged 52 to 64 years who received a mammogram during the study year or the previous year. The lower age limit was modified from the HEDIS specifications to reflect the updated US Preventive Services Task Force recommendations.47 All upper age limits were 64 years because the BCBSM cohort of commercial members 65 years or older is small and the findings are likely not generalizable to the older population. Cervical cancer screening was based on the proportion of women aged 24 to 64 years who were evaluated in the previous 3 years. Colorectal cancer screening was measured as the proportion of patients aged 51 to 64 years who received a fecal occult blood test during the study year or a flexible sigmoidoscopy or colonoscopy in the previous 4 years and 9 months. The period used to identify colorectal screening was shortened from HEDIS specifications owing to limited historical claims data, but exclusion and continuous enrollment criteria were consistent with those of HEDIS.
Screening rates were calculated using the practice panels of adult BCBSM members, identified through a retrospective claims-based algorithm that assigns members to a single PCP based on administrative claims from the previous 24 months (eMethods in the Supplement). Outcomes were measured separately for each study year using administrative claims.
We controlled for characteristics of the practice, its patient population, its physician organization, and other geographic characteristics. Practice characteristics included (1) the number of physicians, (2) whether the practice contained nonprimary care specialists, (3) BCBSM patient volume, (4) mean number of years during which the practice’s PCPs participated in the PGIP, (5) physician turnover in the practice over time, and (6) whether the practice moved between physician organizations over time. Patient characteristics included (1) the proportion of adults who were female and (2) the mean prospective risk score (determined with OptumInsight Symmetry, version 8; OptumInsight). We operationalized physician organization size as the number of practices in the physician organization with PCPs. We also controlled for the following geographic characteristics, calculated using the market-based approach of weighting zip code characteristics based on the residences of the practices’ patients: (1) BCBSM market share, (2) percentage of residents living in a rural area, (3) number of PCPs per 1000 residents, and (4) percentage of nonwhite or Hispanic residents. Sensitivity analyses demonstrated that models excluding the race/ethnicity variable did not change the results.
The physician practice was the unit of analysis. To test the conditional effects of SES context, we analyzed the interaction between the level of PCMH implementation at the beginning of each study year and the market-based SES index for each practice in predicting the 3 practice-level cancer screening rates. We used multivariable, cross-classified linear models, with a random effect for the practice and a cumulative random effect for the physician organization. These random effects accounted for the longitudinal design, clustering of practices within physician organizations, and movement of practices between physician organizations over time.48
The market-based SES context index was stratified into 4 categories based on the number of SDs from the mean to account for potential nonlinearity in relationships. This approach captured the tail of the distribution while retaining sufficient sample sizes in each category. The groups were (1) greater than 1 SD above the mean (the highest SES category), (2) greater than the mean to 1 SD above, (3) the mean to 1 SD below, and (4) greater than 1 SD below the mean (the lowest SES category). We report estimates and 95% CIs of the effect of PCMH implementation scores on cancer screening for each of these SES index categories and the P value of the interaction term comparing each SES category with the highest SES category as the reference group. We also calculated marginal estimates for the mean of each cancer screening rate at different combinations of the PCMH score and SES index category. These marginal means are predictions from the model after controlling for all other covariates.
Both sample size and statistical outlier exclusion criteria were applied to each cancer screening outcome before constructing multivariable models. To be included in each model, practice-years had to have a minimum of 30 patients eligible for cancer screening (ie, meeting the HEDIS denominator criteria) and could not have a score that exceeded 2 interquartile range units from the median. Using residual diagnostics and models with categorized PCMH implementation scores, we found no departures from linear regression model assumptions including normality, homoscedasticity, and linearity. All analyses were performed using SAS, version 9.2 (SAS Institute Inc).
Across the 3-year study period, the median practice-level cancer screening rates were 75.0% for breast cancer, 75.0% for cervical cancer, and 50.0% for colorectal cancer. Screening rates for breast and cervical cancer decreased slightly during the study period from 76.1% in July 2009 to June 2010 to 74.6% in July 2011 to June 2012 for breast cancer and from 76.9% to 73.7% for cervical cancer; colorectal cancer screening rates remained constant from 50.3% in July 2009 to June 2010 to 50.0% in July 2011 to June 2012. Practices in higher market-based SES index categories had higher cancer screening rates (Table 1). The PCMH implementation scores increased from a median of 0.17 in June 2009 to 0.45 in June 2012 for a median increase of 0.07 per year. Table 2 reports the distribution of variables included in the SES index for each of the 4 SES index categories.
In multivariable analysis, practices in the highest market-based SES index category demonstrated a nonsignificant increase of 2.6% in breast cancer screening rates for an increase in the PCMH implementation score at the beginning of each study year from 0 (no implementation) to 1 (full implementation). The effect estimate in the lowest SES category (5.4%) was larger but not statistically significantly different from the effect in the highest SES category (P = .21), and the effect estimates in the middle categories were significantly larger than the effect in the highest SES category (P = .005 and P = .01), assessed using interaction terms (Table 3). A graphical representation of this relationship is demonstrated (Figure, A) using marginal estimates of the mean breast cancer screening rate at different combinations of PCMH score and SES category. For all SES categories, the model predicted an increase in breast cancer screening as PCMH scores increased, but the slope of the line was less for the highest SES category, illustrating the smaller predicted effect. In the Figure, the difference in the mean breast cancer screening rates between the highest and lowest SES categories is 6 percentage points at the lowest PCMH scores (77.9% vs 72.2%) and 3 percentage points at the highest PCMH scores (80.3% vs 77.0%). For cervical cancer screening, practices in the highest SES category revealed a small, nonsignificant (P = .64) decrease in screening rates (−0.5%) with an increase in the PCMH score from 0 to 1. All other SES categories had a statistically significant positive effect in conjunction with a monotonic relationship between lower SES categories and larger effect estimates (Table 3). At full PCMH implementation, the highest and lowest SES categories are predicted to have the same cervical cancer screening rates (77.0%) despite having a 4% absolute disparity in screening rates at the lowest PCMH score (77.4% vs 73.3%) (Figure, B).
The effect of the PCMH score on colorectal cancer screening was positive and statistically significant for all SES categories. Similar to breast cancer screening, lower SES categories generally had larger effect estimates, but the effect was not monotonic. Only the effect estimate for the third SES category was statistically significantly different from the highest SES category (P = .04). A similar larger disparity in screening rates was demonstrated at the lowest PCMH scores (52.6% vs 48.2%; 4 percentage points between the highest and lowest SES categories) than at the highest PCMH scores (56.6% vs 54.6%; 2 percentage points between the highest and lowest SES categories) (Figure, C). Full multivariable model results for each screening type are reported in eTables 2 through 4 in the Supplement.
These research results suggest that increased implementation of a PCMH model has a greater potential to increase cancer screening in physician practices operating within lower SES contexts. Our multivariable models predicted that disparities across SES contexts in medical practice screening rates could be halved or, in the case of cervical cancer, eliminated as a result of full implementation of the PCMH model. The observed greater increases in cancer screening rates in lower SES practice contexts may indicate that individuals in these environments benefit more from the PCMH model for this type of preventive service. The greater changes in the lower SES contexts could also occur because there is less room for improvement in cancer screening rates in higher SES environments. Although the observed reduction in disparities attributable to the PCMH implementation score (2%-4%) was modest, this reduction could translate into important gains in early detection at the population level. In addition, this modest decrease in cancer screening disparities should be considered along with the other potential benefits of implementing the PCMH model.
In almost all SES context categories, we found a significant effect of PCMH implementation on improved cancer screening outcomes. This finding is consistent with literature8- 10 describing evidence of a positive association between the PCMH model and preventive service use, including cancer screening rates. In contrast to many previous studies,8- 10 we quantified progression toward the PCMH model of care through implementation of relevant capabilities as opposed to measuring the dichotomous effect of a PCMH intervention. In addition, many of the previous studies were cross-sectional while ours was strengthened by 3 years of longitudinal data.
We did not observe significant associations between PCMH implementation and improved screening rates for breast and cervical cancer in practices in the highest SES contexts. Breast and cervical cancer screening rates in the United States are relatively high, but colorectal cancer screening rates have lagged.49,50 It is possible that in higher SES contexts, physicians have reached a ceiling effect whereby it is much more difficult to improve breast and cervical cancer screening rates. It is also possible that patients and physicians in higher SES practice contexts are more aware of changes in guidelines that recommend less frequent screening for breast and cervical cancer. However, the US Preventive Services Task Force guidelines36 for cervical cancer screening were not released until March 2012, which was past the data collection period for the present study. In addition, mammography guideline changes and controversy have only addressed the 40- to 49-year-old age group.51 Cancer screening rates in any practice will never reach 100% owing to contraindications not observable in available data.
The observed significant effects of the PCMH on cancer screening rates could be explained by the general shift in focus of physicians implementing the PCMH model toward more preventive and comprehensive care. This shift is especially important considering that a physician’s recommendation is one of the greatest predictors of screening.52,53 The observed impact could also reflect specific capabilities included in the BCBSM PCMH implementation approach, such as the focus on coordination of care across the health system including community resources, increased access to the practice, reminder systems for needed services, and performance reports tracking preventive service use, all of which may be relevant for increasing preventive service use.33,54- 62 This model of care may be especially relevant in lower SES contexts where there are greater patient- and system-level barriers to screening. The idea that health care interventions can have a greater effect on lower SES populations is consistent with findings from Rothman et al,63 who demonstrated that patients with low literacy derived more benefit from a diabetes mellitus disease management program than did patients with higher literacy. Health care interventions in the racial disparities literature64- 66 have been mixed, with some interventions increasing and others reducing disparities, suggesting that the specific characteristics of the interventions, including the amount of cultural competency, may be important for disparity reduction. Our study did not try to determine the specific components of the model that are related to improving cancer screening rates since we considered that many of these processes are interrelated within the PCMH model.
There are several limitations in our research approach. Our study was set in the context of the PGIP, which provided financial incentives related to PCMH implementation and for breast and cervical cancer screening. Incentive structures did not differ by the context of the practice. This study also used a self-selected group of practices by virtue of participating in the PGIP that may not be generalizable. The PGIP does, however, comprise almost two-thirds of the PCP practices in Michigan, including a mixture of practice sizes, organizational structures, and rural and urban geographies. In addition, patients included in the practice-level cancer screening rates were all commercially insured, so their experiences may differ from those of uninsured or publically insured patients. The use of administrative claims data, combined with a limited data collection period of 4 years and 9 months, may have caused some misclassification of patients in terms of their cancer screening behavior and needs. However, this misclassification is likely nondifferential with respect to PCMH score and SES category. In addition, few practices (2%) were excluded from the analysis because of missing covariate data. These practices were mostly lacking PCMH capability data (92%). Covariate data were more likely to be missing in earlier periods of the study and for smaller practices as well as those that had recently moved to a different physician organization. It is unlikely that missing data were systematically related to cancer screening rates, so the exclusion is unlikely to have caused substantial bias.
The Institute of Medicine’s 2001 report, Crossing the Quality Chasm:A New Health System for the 21st Century,67 considers equity to be a core dimension of a high-quality health care system; nevertheless, interventions to reduce socioeconomic disparities in health and health care have been difficult to implement.68,69 Previous studies23,70- 72 examining the role of the PCMH in reducing health disparities have focused on whether the patient had a regular source of primary care rather than looking at the level of practice transformation by a patient’s PCP. Our study provides additional support for the idea that the PCMH model can help close socioeconomic gaps in the quality of preventive care. Many practices in lower socioeconomic areas face resource constraints, including lower payments received for Medicaid and uninsured patients and difficulty recruiting highly qualified physicians and staff,73- 75 that lead to reduced PCMH implementation.65 Thus, it is important that reimbursement models provide sufficient support for practices with fewer resources to maximize the potential benefit of the PCMH.
The results of this study suggest that the PCMH model has potential to increase cancer screening rates. However, our findings also suggest that the effects of the PCMH model on cancer screening rates vary depending on the socioeconomic context of the practice, with greater effects occurring in lower socioeconomic contexts. Thus, the PCMH model could also contribute to reductions in disparities in cancer screening rates across socioeconomic contexts.
Accepted for Publication: November 25, 2014.
Corresponding Author: Michael L. Paustian, PhD, Department of Clinical Epidemiology and Biostatistics, Blue Cross Blue Shield of Michigan, 2311 Green Rd, Mail Code A112, Ann Arbor, MI 48105 (email@example.com).
Published Online: February 16, 2015. doi:10.1001/jamainternmed.2014.8263.
Author Contributions: Dr Paustian had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Study concept and design: Markovitz, Alexander, Paustian.
Acquisition, analysis, or interpretation of data: Markovitz, Lantz, Paustian.
Drafting of the manuscript: All authors.
Critical revision of the manuscript for important intellectual content: All authors.
Statistical analysis: Markovitz, Alexander, Paustian.
Administrative, technical, or material support: Paustian.
Study supervision: Alexander, Paustian.
Conflict of Interest Disclosures: Ms Markovitz and Dr Paustian were employed by Blue Cross Blue Shield of Michigan during the time of this study. No other disclosures were reported.
Funding/Support: Funding was received from the Agency for Healthcare Research and Quality (grant R18 RFA-HS-10-002) for our foundational work on this topic. Ms Markovitz was supported by training grant T32HD060454 in Reproductive, Perinatal, and Pediatric Epidemiology from the National Institute of Child Health and Human Development, National Institutes of Health.
Role of the Funder/Sponsor: The funding organizations had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
Correction: This article was corrected on February 17, 2015, to fix an author’s affiliation.