Publications

A tale of three cities: Hospital and health system costs in the Midwest

A city at night

A Midwestern city at night with buildings lit up.

There is tremendous variation in health care spending by geographic region in the United States. To better understand this variation, CHRT analyzed health care markets, state-level regulation, and hospital cost variation in three Midwestern states, focusing on the largest city in each state: Detroit, Michigan; Indianapolis, Indiana; and Milwaukee, Wisconsin. These states were chosen for their diverse health care policies and market conditions. This brief describes trends in state-level health spending and factors that may contribute to the differences in spending among the three states.

Key findings include:

  • From 2001 to 2009, Michigan had the lowest overall health care cost per capita among the three Midwestern states in this analysis, while Wisconsin had the highest. Michigan also had the lowest average annual growth in spending per capita from 1991 to 2009, and Wisconsin had the highest. Many complex factors contributed to these differences, and likely included market conditions and regulations that varied by state.
  • In fiscal year 2013, Michigan had the lowest and Wisconsin had the highest per capita hospital spending among the three states in this analysis.
  • Market conditions and policies affecting the size of hospitals’ profit margins varied by state. See our report for details for Indiana, Michigan, and Wisconsin.
  • In fiscal year 2013, health system operating cost and total profit margins varied greatly in the three cities of the Midwestern states in this analysis. See our report for details for Detroit, Indianapolis, and Milwaukee.

Suggested citation: Dreyer, Theresa; Koss, Joseph; and Udow-Phillips, Marianne. A Tale of Three Cities: Hospital and Health System Costs in the Midwest. April 2015. Center for Healthcare Research & Transformation. Ann Arbor, MI.

Special thanks to Dean G. Smith, PhD, for guidance on the financial analysis.

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Cover Michigan Survey: Coverage and health care access trends in the wake of the ACA

2 females smiling

A patient smiles at a doctor.

This brief provides evidence of a dramatic change in Michigan’s health care landscape as a result of the first year of the ACA’s coverage expansions. Overall, the number of residents reporting they were uninsured, struggled to pay medical bills and/or delayed seeking needed medical care has dropped significantly compared to CHRT survey findings before the launch of the ACA coverage expansions. While most insured Michiganders reported easy access to primary care, they did, however, report a greater challenge in obtaining access to specialty care in 2014 than they reported before the ACA coverage expansions.

The Michigan health insurance landscape changed substantially in the wake of the Affordable Care Act’s coverage expansion provisions. Starting in January 2014, many eligible individuals could enroll in private insurance coverage through the Health Insurance Marketplace and receive financial assistance to lower their cost of coverage. On April 1, 2014, Michigan residents below 138 percent of the federal poverty level who were not previously eligible for Medicaid became eligible for the Healthy Michigan Plan, Michigan’s expanded Medicaid program.

Using data from two of the Center for Healthcare Research & Transformation’s Cover Michigan Surveys, this brief explores consumer experiences with insurance coverage and access to care within the state of Michigan between mid-2012 and late 2014. The 2014 survey was fielded beginning in September 2014, five months after the first Marketplace enrollment period ended and Healthy Michigan Plan enrollment had begun. By the end of the Marketplace’s first open enrollment period in March 2014, 272,000 Michigan residents had selected coverage through the Marketplace. By September 2014, 410,000 people were enrolled in the Healthy Michigan Plan, bringing the state’s total Medicaid enrollment to 2.2 million by that time.

Key findings include:

  • More Michigan residents gained health care coverage—the proportion of adult Michiganders who reported being uninsured was cut in half, from 14 percent in 2012 to 7 percent in 2014 after the ACA.
  • Overall, from 2012 to 2014, those with insurance coverage reported access to primary care remained easy. Nearly 90 percent of insured adults reported having very or somewhat easy access to routine primary care appointments in 2012 and 2014.
  • Fewer people reported that they had delayed seeking medical care—22 percent of all respondents reported that they had not sought medical care they believed to be necessary in the previous six months in 2014, compared to 29 percent in 2012.
  • Between 2012 and 2014, Michiganders also reported fewer financial concerns associated with their health care:
    • In 2014, half as many respondents cited cost as a reason for not seeking needed medical care (21 percent, compared to 42 percent in 2012).
    • In 2014, 20 percent of respondents reported struggling to pay medical bills, compared to 27 percent in 2012.
  • Uninsured adults reported that it was more difficult to obtain primary care between 2012 and 2014. Those who reported very or somewhat easy access to primary care appointments declined from 67 percent in 2012 to 48 percent in 2014.
  • More people reported difficulty obtaining access to specialty care in 2014 compared to 2012. Specifically, 34 percent of adult Michiganders reported it was “very easy” to get an appointment with a specialist in 2012, compared to 24 percent in 2014.

Suggested Citation: Smiley, Mary L.; Riba, Melissa; Ndukwe, Ezinne G.; Udow-Phillips, Marianne. Cover Michigan Survey: Coverage and Health Care Access. (Ann Arbor, MI: Center for Healthcare Research and Transformation, March 2015).

Acknowledgements: The staff at the Center for Healthcare Research & Transformation would like to thank Thomas Buchmueller, Matthew M. Davis, Robert Goodman, Helen Levy, Renuka Tipirneni, and the staff of the Institute for Public Policy and Social Research (IPPSR) at Michigan State University for their assistance with the design and analysis of the survey.

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Primary care capacity in Michigan: How are physicians responding?

Someone having blood pressure and pulse taken

A primary care physician administers a blood pressure test.

On April 1, 2014, Michigan expanded access to Medicaid to people whose income was less than 138 percent of the Federal Poverty Level, or about $32,900 for a family of four. As of December 2014, over 470,000 Michiganders had enrolled in the expanded Medicaid program, known as Healthy Michigan, and over 270,000 Michiganders had enrolled in coverage through the Affordable Care Act’s Individual Marketplace. After Massachusetts expanded health insurance coverage in 2006, demand for primary care exceeded supply, raising the question of whether Michigan’s primary care providers have been able to keep up with increased demands for care after the Medicaid expansion.

In order to understand the current and anticipated capacity of Michigan physicians to take new patients, particularly those with Medicaid, the Center for Healthcare Research & Transformation (CHRT) collaborated with University of Michigan faculty to survey primary care physicians across the state about their practices, compensation models, and patient populations in late 2013 and early 2014 (2014 Michigan Physician Survey). CHRT collaborated with the Child Health Evaluation and Research Unit to conduct a similar survey in 2012, which provided comparison data.

Key findings include:

  • Michigan’s primary care physicians reported that they have the capacity to accept new patients—87 percent of Michigan primary care physicians reported that they were accepting new patients at the time of the survey.
  • More physicians reported accepting new Medicaid patients when surveyed in 2014 than did so in 2012—from 2012 to 2014, the share of physicians taking new Medicaid patients increased by almost one-fifth (19 percent), from 54 percent in 2012 to 64 percent in 2014.
  • Physicians reported that they expect the trend to continue and grow in the next year—22 percent of respondents expected their payer mix to include more than 30 percent Medicaid patients in the year following the survey, compared to the 15 percent who currently saw this high a volume of Medicaid patients (an increase of 45 percent).

Suggested Citation: Smiley, Mary L.; Riba, Melissa; Davis, Matthew M.; Kerr, Eve A.; Zikmund-Fisher, Brian J.; Ndukwe, Ezinne G.; Ward, Melanie; Udow-Phillips, Marianne. Primary Care Capacity in Michigan: How are Physicians Responding?. 2014 Michigan Physician Survey. (Ann Arbor, MI: Center for Healthcare Research & Transformation, 2014).

Special thanks to Knoll Larkin for assistance with survey administration and to Thomas Buchmueller, Robert Goodman, Helen Levy, and Renuka Tipirneni for assistance with survey development and interpretation.

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Commercial accountable care organization products: Market leaders and trends

Magnifying glass with pen and papers of charts and graphs

Several pages with graphs and charts.In 2006, Elliott Fisher of Dartmouth coined the term “accountable care.” Accountable care arrangements are based on three principles:

  • Accountability for quality: A group of providers is clinically and financially responsible for the entire continuum of care for a group of patients. Depending on the arrangement, providers, hospitals, and health insurers may share responsibility for the patients’ care.
  • Shared savings: Payers share savings with providers if certain quality and cost goals are met and spending growth is slowed. In certain arrangements, providers may also face payment reductions if they don’t meet specified goals.
  • Performance measurement: Provider performance is tracked and rewarded based on process, outcome, and patient experience measures.

Accountable Care Organizations (ACOs) are networks of clinicians and hospitals who share medical and financial responsibility for the full continuum of patient care. The Affordable Care Act formalized the term by establishing the Medicare Accountable Care Organization (ACO) program and launching several other ACO models. More than 18 percent of hospitals across the country are estimated to be participating in some form of an ACO, with more expected by the end of 2014.

Simultaneously, many private sector health plans have launched an ACO network that they offer as a distinct insurance product option to individuals and employer groups. These products are based on contractual agreements with selected providers who are chosen based on financial and quality measures. Often, they are offered through Health Maintenance Organization (HMO) or Preferred Provider Organization (PPO) structures to encourage members to receive care from network providers.

This paper describes activity concerning commercial insurance products based on ACO networks.

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Autism spectrum disorder in Michigan

Child holding 2 puzzle pieces

Child's hands hold two white puzzle pieces, a symbol of ASD.Autism spectrum disorder (ASD) comprises a group of developmental disabilities that cause impairment in social interactions, communication skills, and behaviors that can have long-term health and social functioning costs for individuals with ASD and their families. In 2014, the Centers for Disease Control and Prevention (CDC) reported that approximately one in 68 children in the United States were diagnosed with autism spectrum disorder.

Researchers estimate that it costs between $1.4 and $2.4 million to support an individual with ASD over a lifetime for direct costs such as medical care or special education, and indirect costs such as lost employment. Federal agencies, advocacy groups, and states are paying more attention to the prevalence, diagnosis, and treatment costs for ASD, demonstrated by an influx in research and an increasing number of states that have mandated certain insurers to provide coverage for ASD diagnosis and treatment.

Autism spectrum disorder refers to a group of developmental disabilities that can cause substantial impairments in a person’s behaviors and social and communication skills. Signs of these impairments usually occur before
a child turns three years old, although children are often diagnosed between ages three and five. While the severity of symptoms may lessen by adulthood, core symptoms often last to some degree throughout the individual’s life. In recent years, researchers have found evidence that a small percentage of children with ASD, particularly those with milder symptoms, can overcome the diagnosis and reach social and cognitive functioning similar to that of their peers, though it is uncertain why some do and others do not.6,7 In 2013, the medical diagnosis for autism was redefined to include four autism-related disorders to better reflect the full “spectrum” of severity and complications associated with autism. Individuals with ASD will often have other medical conditions, including epilepsy, learning disabilities, anxiety, depression, sleep disorders, and gastrointestinal distress.9,10 As with other developmental disabilities, early diagnosis and intensive intervention can have a significant impact on the functional skills and quality of life for children with ASD.11 The American Academy of Pediatrics (AAP) recommends that all children be screened for developmental delays or disabilities during well-child visits at the age of 9 months, 18 months, and 24 or 30 months.

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Suggested Citation: Peters, Claire; Lausch, Kersten; and Udow-Phillips, Marianne. Autism Spectrum Disorder in Michigan. October 2014. Center for Healthcare Research & Transformation, Ann Arbor, MI.

Special thanks to Lisa Grost.

Best Practices in Care Management for Senior Populations

5 wooden stars ascending on stair steps

Care Management is a service designed to help patients and their caregivers manage medical conditions more effectively, in order to improve health and reduce the need for hospitalizations and emergency department visits. The concept arose in the past decade from disease management programs of the 1990s, which focused on individual diseases rather than more comprehensive consideration of patients’ needs. Care managers are generally nurses or social workers who work closely with patients and caregivers to assess health risks and needs, collaboratively develop care plans, and coach patients in self-care.[footnote list=”1″ style=”lower-alpha”]All references in this paper correspond to item numbers in the Annotated Bibliography, which details the research on care management.

This seminal report offers a wealth of information about the evidence base for care management, detailing what works in research and practice. The authors considered evidence from randomized controlled trials (RCTs), Medicare demonstration projects, and programs initiated by health systems and private insurers. They concluded that while most care management programs successfully improved quality of care, few achieved cost savings. The authors identified four key elements needed to both save money and improve quality: (1) targeting only high-risk patients, (2) incorporating in-person contact between patients and care managers (including home visits), (3) hiring highly-trained care managers to work with primary care physicians (PCPs) in multidisciplinary teams, and (4) coaching patients in self-care.

The authors concluded that hospital-to-home care transitions programs are most effective at reducing cost and improving quality. Two successful models—Eric Coleman’s Care Transitions Intervention and Mary Naylor’s Transitional Care Model (as described below in items 8 and 9)—demonstrated cost-savings in RCTs and have been adapted to real-world settings by health systems and plans.Care managers strive to ensure close communication between patients and physicians, and among all providers involved in patients’ care.

Health care providers increasingly offer care management, driven in part by reimbursement changes under the Affordable Care Act that sparked provider interest. Health plans are encouraging this trend through reimbursement policies and are moving away from offering care management directly or through vendor-supplied services. This analysis focuses on the question: do care management programs work for senior populations and, if so, what characteristics are shared by the most effective programs?

Key Research Findings

Research shows that care management programs generally improve quality of care, but cost reduction is hard to achieve, especially for patients age 85 and older.6 The research also identifies several key attributes that can increase the likelihood of a program to achieve improved quality and efficiency.

Randomized Controlled Trials

Hospital-to-home care transition programs delivered in health systems are most effective at reducing costs and improving quality.[footnote list=”1″]For additional detail on care transitions, see the CHRT report Care Transitions: Best Practices and Evidence-based Programs. Two proven models are Eric Coleman’s Care Transitions Intervention and Mary Naylor’s Transitional Care Model. In the Coleman program, advanced practice nurses contacted high-risk elderly patients as they were discharged from the hospital, then followed up with the patients by conducting one home visit and three phone calls over a four-week period. In a 2006 study, this program showed a 30 percent reduction in 30-day admissions and a 20 percent reduction in patient costs.

Naylor’s more intensive model provided high-risk, high-cost elderly patients with care management for three months after discharge from the hospital. Advanced practice nurses regularly visited patients’ homes and met with their primary care physicians, and patients could reach care managers by phone seven days a week. As reported in a 2004 study, readmissions dropped by 36 percent and patient costs by 39 percent (nearly $5,000 per patient) within one year.

Care management delivered in other provider settings, including primary care and multispecialty groups, has shown quality improvements but little evidence of cost reduction in RCTs. Evaluations of vendor-supported care management are inconclusive. The Congressional Budget Office determined that the methodologies that vendors used to evaluate their own products were too weak for cost or quality claims to be reliable,1 and the few independent studies of vendor-delivered programs showed limited quality impacts with no evidence of cost reduction.

Demonstration Projects

The Centers for Medicare and Medicaid Services (CMS) runs demonstration projects to test innovative health programs for seniors and measure their impact. Few CMS demonstration projects of care management programs have achieved sufficient cost-savings to offset implementation expenditures. Of the 34 CMS-funded care management demonstration projects since 1999, two raised costs and 31 had no statistically significant impact on reducing costs. There are, however, two programs that did improve quality and produce savings: the Program of All-Inclusive Care for the Elderly (PACE), which began as a CMS demonstration in the 1970s, and a recent demonstration project at Massachusetts General Hospital.

PACE programs generally save money over time but have substantial start-up costs. PACE provides integrated care to elderly, high-risk patients through multidisciplinary teams. Enrollees’ care is managed in adult day care centers, with home care offered as needed. The program dramatically improves patients’ functional status and quality of life, decreases mortality, and reduces hospital and nursing home use. PACE programs have grown slowly, however, largely due to strict program requirements. These requirements include leaving personal physicians in favor of PACE physicians and mandatory attendance at adult day care. Programs that modify the PACE model to increase patient flexibility have not produced the same magnitude of cost savings or quality improvements. For example, in a comparison of a Wisconsin PACE program to a more flexible local competitor based on the PACE model, PACE participants were 68 percent less likely to be hospitalized and 59 percent less likely to be admitted for preventable conditions.

Massachusetts General Hospital ran the only other CMS demonstration that achieved statistically significant cost savings within three years, reducing Medicare expenditures by an estimated 7 to 11 percent by decreasing hospital admissions and emergency department visits. The program enrolled high-risk patients receiving care from the health system and affiliated primary care clinics. Care managers were employed by primary care physicians and managed patients’ care both in person and by phone. The care managers also had access to the health system’s electronic medical records to facilitate communication between providers.

Patient-Centered Medical Homes

Patient-Centered Medical Homes (PCMHs) are the preferred care management delivery model for many health systems, insurers, and state Medicaid agencies. PCMHs are new ways of organizing primary care practices to promote quality of care, coordination between providers, and increased responsiveness to patients’ needs. Care management is a central component of most PCMH demonstration projects. As of 2010, 14 PCMH interventions had demonstrated at least a 10 percent improvement in quality and cost metrics, although some cost measures were not statistically significant. Most successful PCMH programs integrated care managers within practices as part of multidisciplinary teams, aligned financial incentives between providers and payers, and leveraged electronic medical records to increase communication between providers.

Best Practices

Care management programs that successfully reduced costs and improved quality did the following:

  • Provided face-to-face contact between patients and care managers. The frequency of in-person contact varied from an initial appointment in the PCP’s office to regular home visits.
  • Integrated care management within primary care practices. In the best programs, care managers were co-located with primary care physicians or, at minimum, regularly visited the physicians and managed the care of all eligible patients in the practice. In one model, care managers worked in up to three small practices with space set aside for them in each, in order to build strong communication with all physicians.
  • Targeted patient selection. High-risk patients with multiple chronic conditions—generally a subset of the elderly—benefit most and have the greatest potential for cost savings.
  • Stratified services based on patient needs. Stratifying high-risk patients allows more complex patients to receive more intensive services; care managers that manage the most high-risk patients require lower caseloads.
  • Focused on transitions of care from the hospital to other settings. Hospital-to-home transitions are one of the best cost-saving measures, and engage patients when they may be most receptive to behavior change.
  • Coached patients in self-management techniques. Coaching helps patients engage in self-care, manage their medications, and recognize and respond to “red flags” for their conditions.
  • Used electronic medical records. Electronic medical records can be leveraged to assess patients’ health risks, reduce duplication, facilitate communication between providers, and provide feedback to primary care physicians.

While including these elements does not guarantee programs’ success, the research is strong that these features do create the foundation for high-quality, cost-saving care management services.

Conclusion

Care management can help patients and caregivers mitigate the impact of chronic conditions, and reduce the need for expensive health care services such as hospitalizations and emergency department visits. However, while many care management programs have improved quality of care, relatively few have achieved cost savings. This paper outlines best practices that can help providers and health plans invest in care management programs that are designed to promote both quality and efficiency.

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Access to mental health care in Michigan

Female in contemplation

A young woman looking out a window, suffering from a mental health disease.One in five Michigan residents report having been diagnosed with depression at some point in their lives. Mental health disorders cause more disability among Americans than any other illness group.

Using data from the Cover Michigan Survey and the Michigan Primary Care Physician Survey, both fielded in calendar year 2012, this brief explores issues related to the prevalence of mental health disease, specifically depression and anxiety, and the capacity of the Michigan health care system to serve people with these conditions.

Overall, it is clear that there is high need for mental health services in Michigan and the capacity to serve those in need is not adequate to the task. Without addressing increased capacity for care, the increased mental health coverage provided to many under the Affordable Care Act will do little to help those most in need.

Key findings include:

  • Depression and anxiety are prevalent in Michigan and higher than the U.S. average. Twenty percent of Michiganders reported ever being diagnosed with depression, compared to 18 percent of Americans. Prevalence is greater when diagnoses of depression and/or anxiety are combined
    • Depression and/or anxiety were reported in Michigan at particularly high rates among those with Medicaid (59 percent) and the uninsured (33 percent).
  • People with depression and/or anxiety had greater difficulty completing everyday activities, including work, than did Michiganders with other or no chronic conditions.
    • Respondents with depression and/or anxiety reported twice as many limited activity days compared to those who reported having other chronic conditions. Respondents with depression and/or anxiety reported an average of five days in which poor health limited their activity.
  • The health care system in Michigan is inadequate to serve adults and children with mental health needs.
    • Fifty-seven percent of primary care physicians reported that availability of mental health services in their community was inadequate for adults and 68 percent reported it was inadequate for children.
      • Adult mental health services in the St. Joseph, Muskegon, and Petoskey regions had the highest inadequacy ratings (89, 82 and 77 percent, respectively).
      • Child mental health services received the poorest ratings in the Muskegon and Petoskey regions (100 and 94 percent respectively).
      • Even in regions where primary care physicians reported the best access (Pontiac and Royal Oak), more than a third noted that access was inadequate.
    • The availability of psychiatric beds in Michigan is extremely low compared to other states—Michigan was ranked 42nd among the 50 states and the District of Columbia in availability of inpatient psychiatric beds.

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Suggested Citation: Smiley, Mary; Young, Danielle; Udow- Phillips, Marianne; Riba, Melissa; Traylor, Joshua. Access to Mental Health Care in Michigan. Cover Michigan Survey 2013. December 2013. Center for Healthcare Research & Transformation. Ann Arbor, MI.

Federally qualified health centers: Are they effective?

Empty waiting room

Chairs in an empty waiting room of a federally qualified health center.In 1964, the Office of Economic Opportunity established federally qualified health centers (FQHCs), which were initially called neighborhood health centers, as part of President Lyndon B. Johnson’s “War on Poverty.” The legislative goals for neighborhood health centers were to:

  • Provide comprehensive, high-quality health services.
  • Be accessible to low-income residents.
  • Be responsive to patient needs.
  • Offer employment, education and social assistance.

These goals, with the exception of providing employment assistance, continue today and have expanded to include additional services such as oral health, mental health, and pharmaceutical services.

The number of FQHCs has grown over the past 40 years. In 1965, there were two FQHCs in the country; today there are more than 1,200 FQHCs with more than 8,500 service sites. The growth has largely resulted from a view that FQHCs can achieve the original goals as well as help curb health care costs by reducing emergency department visits and hospitalizations. Indeed, the Patient Protection and Affordable Care Act (ACA) provides an $11 billion Health Center Trust Fund because of their perceived importance in serving the Medicaid population. In fiscal year (FY) 2011 and FY 2012, however, the federal government cut annual health center appropriations by 27 percent (from $2.2 billion to $1.6 billion). To offset the funding cuts, the Obama administration diverted $600 million from the Health Center Trust Fund each year, preventing those funds from creating new access points and expanding services as intended. In FY 2013, the federal government again held health center appropriations to $1.6 billion, which necessitated another diversion of trust fund dollars.

The core question is: What does the evidence say about the impact FQHCs have had on the legislative goals listed above? A companion piece to this summary provides a comprehensive overview of FQHCs.

The bottom line answer to this question is that FQHCs are generally meeting their original goals by serving low-income populations with quality, cost-effective health care.

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Federally qualified health centers: An overview

Female pushing someone in a wheelchair through a crowded space

Two people wait in a busy waiting room at a federally qualified health center.Health center is an all-encompassing term for federally qualified health centers (FQHCs) and FQHC look-alikes; they are a key component of the health care safety net that provided care to more than 20 million Americans in 2011.

The Patient Protection and Affordable Care Act of 2010 (ACA) has positioned health centers to play a crucial role in the future health care environment. Expansions in Medicaid and privately insured populations are expected to put a significant demand on primary care, particularly in underserved, low-income communities where large increases to the number of newly insured are anticipated. Despite the expected growth in coverage, an estimated 23 million people (or more if states opt out of the allowed Medicaid expansion) will remain uninsured.

Newly insured and uninsured populations will depend on FQHCs and FQHC look-alikes for primary care. Despite bipartisan political and financial support, FQHCs face challenges. To achieve long-term sustainability, FQHCs need to become financially self-sufficient, find ways to address the growing health professional shortages, advance collaborative efforts with provider networks, and improve cost and quality outcomes.

This paper describes the FQHC model and how FQHCs operate nationally; it then provides a look at the future of FQHCs within the context of health care reform, and concludes by summarizing the challenges facing FQHCs. A companion piece examines whether FQHCs are effective.

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Access to health care in Michigan

Female caregiver smiling at older, smiling female patient in wheelchair

A nurse and patient smile at each other.Understanding the impact of health care coverage (or the lack of it) on health care access is crucial to improving health care in Michigan.

The Center for Healthcare Research & Transformation (CHRT), in partnership with the Institute for Public Policy and Social Research (IPPSR) at Michigan State University, surveyed Michigan residents three times (in 2009, 2010, and 2012) on key issues relating to health care coverage, access to care, and health status. The latest survey, Cover Michigan Survey 2013, was fielded in the third quarter of 2012.

This report compares data from 2010 and 2012 and focuses on one aspect of that survey: The relationship between coverage status and access to care. Future reports will cover other aspects of health care in Michigan.

Key findings include:

  • More respondents said they had an identified primary care provider than in 2010; the greatest increase was found among those with Medicaid coverage.
  • Those with Medicaid coverage reported a significantly easier time in scheduling appointments for primary and specialty care than in 2010—now on par with those with employer-sponsored coverage.
  • Those with individually-purchased coverage reported greater difficulty scheduling appointments for primary care than in 2010.
  • Respondents reported using public or community health clinics as their usual sources of care at significantly higher rates than in 2010.
  • Respondents who lacked coverage reported using emergency rooms and urgent care centers as their usual sources of care at considerably higher rates than those who had coverage.

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Suggested Citation: Young, Danielle; Stadler, Phillip; Udow-Phillips, Marianne; Riba, Melissa. Access to Health Care in Michigan. Cover Michigan Survey 2013. March 2013. Center for Healthcare Research & Transformation. Ann Arbor, MI.

Acknowledgements: The staff at the Center for Healthcare Research & Transformation would like to thank Matthew M. Davis, MD, MAPP, and Helen Levy, PhD, at the University of Michigan; Robert Goodman, DO, at Blue Care Network of Michigan; and the staff of the Institute for Public Policy and Social Research (IPPSR) at Michigan State University for their assistance with the design of the survey and data collection.