Win-Win-Win: Incorporating Integrated Care for the Benefit of All

Posted by Amanda Slack on 05:04 AM

Imagine this for a moment. You have been experiencing some unsettling symptoms and are struggling to know what is real and what is not. Your friends and family convince you to get some help, and you go to a local behavioral health organization where you are prescribed a medication that falls into the Second-Generation Antipsychotics (SGA) category1. This drug helps with your with your symptoms and allows you to feel some sense of normalcy, however, you are now experiencing symptoms of diabetes. A scary situation resulting in a trip to the ER confirms that you do, in fact, have Type 2 diabetes, and it could be a side effect of the medication you’re on. Now, you need both behavioral and physical health care regularly and could face severe health consequences or premature death. That is a lot of serious life changes to manage, and it is hard to imagine how there could be an approach to this in which anyone wins. While this may not happen to everyone, it is not an unusual situation. It is estimated that people on SGA medications have at least twice the risk of developing Type 2 diabetes2, and the World Health Organization reports that people with severe and persistent mental illness have a staggering 10- to 20- year reduction in life expectancy compared to the general population3. Reasons for this include medication side effects, barriers to accessing treatment, physical inactivity, and high rates of tobacco or alcohol use. In the past, behavioral and physical health care were kept separate in the treatment world. This resulted in people bouncing between providers with little communication about overlap in conditions. Now, funding sources, governing bodies, and regulatory agencies are incentivizing models of coordinated care to address this issue. So how does a system set up to be very one-dimensional shift to incorporate other disciplines? Frameworks4 for integration typically include care coordination and care management as part of the solution. How do we incorporate framework into real life– particularly in this era of staffing shortages and red tape? Companies have to get creative in developing successful care coordination strategies. TBD Solutions recently worked with a CCBHC to create a system that utilizes data to assist care coordinators (sometimes called care managers, case managers, etc.) in prioritizing need. The Risk Factor Queue uses documents in a person’s chart to identify potential risk factors and calculate an overall risk score. Risk factors are categorized into physical, behavioral, and medication-related buckets. Complexity of need increases as the number of identified risk categories increase. In our earlier example about developing Type 2 diabetes, you would have, at minimum, risk factors noted for your diagnosis and your medications, resulting in a score that is higher due to its complexity. The care coordinator does not need to read through your chart to find all the areas you may need help managing; it is readily available in one spot. Now they can use that information to inform decisions and discuss potential care needs with you. A conversation might look like this,“You don’t have a primary care physician on record? Let’s get you set up with one. You are out of refills on your prescriptions? We will make an appointment to review your medications and refill what is needed.” Integrated care doesn’t require people to have expertise in behavioral and physical health care practices, but it does require that processes and systems be put in place to address the clear relationship between physical and behavioral health. Creative solutions must be developed to meet specific needs and incorporate the organization’s strengths. In this case, the need for efficiency from all involved parties was addressed. The care coordinator doesn’t have to spend as much time digging for information in the hopes, they are not missing a client5 who could benefit from their service, and you (the client) aren’t trying to manage your complex needs alone. This is a win-win-win in the eyes of the client, the care coordinator, and the continued quest for integrated care.
1 Antipsychotics, Second Generation: Drug Class, Uses, Side Effects, Drug Names (rxlist.com) 2 Stubbs, B., Vancampfort, D., De Hert, M., and Mitchell, A. J. (2015). The prevalence and predictors of type two diabetes mellitus in people with schizophrenia: a systematic review and comparative meta-analysis. Acta Psychiatr. Scand. 132, 144–157 doi: 10.1111/acps.12439. 3 Guidelines for the management of physical health conditions in adults with severe mental disorders. Geneva: World Health Organization; 2018. License: CC BY-NC-SA 3.0 IGO. 4 04.22.2022_MDI-CHI-Paper_Reduced.pdf (thenationalcouncil.org) 5Individuals receiving behavioral health treatment are referred to by many different labels, including patient, client, consumer, resident, guest, individual, and person served. This writing is predicated upon the foundation of recovery-oriented principles in mental health treatment and choosing the least stigmatizing language. While TBD Solutions understands the potential breadth and diversity of this post’s audience, the language “client” or “person served” will be used when referring to a person receiving services as it is universally understood and less stigmatizing than words like “patient” or “consumer.”

Four Tips for Initiating a More Meaningful Disparities Analysis

Posted by Claudia Vredeveld on 07:40 AM

From Healthy People 2030 to CCBHC to organization-level strategic planning, a common theme across behavioral and physical health care today is a push for greater equity. This often takes the form of initiatives to better understand the social determinants of health and disparities between populations. This is certainly not the first push for health equity, though; studies of health disparities can be found as early as the mid-1800s. Even with an increase in focus during recent decades, the past 20 years have seen very little progress made toward health equity. While only part of a broader solution, one way organizations can better support current equity efforts is to improve the way we analyze disparities.

Unfortunately, instead of leading to meaningful change, disparities analyses have the tendency to simply reinforce what we already know about the world. Findings are often too broad for one organization to take action on or not nuanced enough to describe a community’s unique characteristics. This is especially true if not enough attention is paid at the beginning of an analysis, before any numbers are crunched. This article outlines a few things you can do when initiating a new disparities analysis to make sure your findings are actionable and meaningful for your community.

Start broad.

Perhaps you are interested in assessing whether there are disparities in access to behavioral health services at your organization. It can be tempting to dive right into available data sources, calculating standard measures by race, sex, and age and churning out visuals. Taking this approach, however, can lead to missed opportunities to better understand the people in your community. Instead, practice starting from the broadest view, considering the full scope of the question and the environment in which you are asking it.

You might start by considering: Why might some populations have an easier time accessing services than other populations?

Next, take note of existing sources of knowledge: What does your own experience tell you about who may not be receiving the services they need and why? What have your colleagues noticed? What are other experts, journalists, and community leaders saying about this topic?

By stepping back and starting broad, you let real people and experiences drive your analyses, and avoid moving too quickly into a line of questioning. You create openings for new perspectives and questions that a narrower lens might have otherwise missed.

Document the specific question(s) you are trying to answer.

Once you identify an area of focus, document the specific question or set of questions you want answered. Questions that are too broad tend to spiral off in many directions and can lead to answers that don’t address the original intent of the question. Good data questions are precise, measurable, and lead to either meaningful answers or new questions.

Broad question: Are there disparities in access to behavioral health services at my organization?

Data question: Does the number service encounters provided per month at my organization differ by race, neighborhood, or income of persons served?

Throughout the analysis, check in to make sure you are still working toward answering the original question.

Be critical of your data sources.

Once you identify what you want to know and which population groupings are important to include, consider what data is available to you.

  • Do the population measures in your datasets accurately represent and describe your populations of focus? Was race data self-reported or observer-coded? What response options were available? Variation exists in racial/ethnic categories used in reporting, even at the federal level. Answer options may not fully match how individuals self-identify or individuals may be misclassified on administrative records, leading to data that might not be reflective of your community. Similarly, what answer options were available in your measure of gender? Is it a measure of gender identify or really a measure of sex? How is poverty measured? Even the federal poverty line, a standard measure used for eligibility determination for Medicaid along with numerous other programs, is rife with flaws and could lead to underestimates of need.

  • What population groupings are missing from your dataset? There are some populations that are often left out of standard reporting, either through exclusion during data collection or a lack of relevant identifying measures. LGBTQ and justice-involved populations are at high risk for behavioral health conditions, yet there is little data available (publicly or otherwise) on their experiences. What are some creative ways that you could reach out to those populations for whom you don’t currently have data?

Because getting nuanced population-level data can be time consuming and challenging, we are often limited to whatever major reports and EHR systems can provide. Where it is feasible, think creatively about how you could enhance or add data sources to better describe your populations of focus. Where it is not feasible, be cognizant–and explicitly state–the limitations of your data.

Map out hypothesized relationships.

After you document specific questions and before the analysis begins, a helpful practice is to map out your hypotheses. While often skipped, this step can play an important role in making sure your findings are interpreted in context and can lead to action. Consider how, specifically, the population measure you are interested in is related to the outcome. Continue asking how until you feel you can clearly draw the line from one variable to the other. Create a mental framework, or better yet, physically draw out the relationships.

The intermediary variables you identify in this process are often more actionable than the initial population measure. Consider how you might include these concepts in your analysis, whether in the first iteration or as part of a refinement process. Do you have data related to these variables? Could these concepts inform qualitative efforts, where you are reaching out and getting input from the individuals who belong to this population?

These hypothesized relationships add important context for interpreting and presenting your findings as well. Too often, results from disparities analyses are misinterpreted in ways that perpetuate the discrimination faced by marginalized populations. Findings of racial disparities are frequently communicated as “the effect of race on _____”, drawing a direct causal link between race and an outcome variable. Mapping out the full pathway, however, we would see that race is a strong predictor of outcomes because it is an excellent measure of exposure to racism. Racism is what feeds disparities in housing, education, wealth, and employment, which in turn fuel physical and behavioral health disparities. Without this context, differences in outcomes between racial groups are too often misinterpreted as stemming from a biological difference–a theory with its roots in slavery. Mapping out relationships between population measures and outcomes draws focus to the social factors which drive disparities.

By starting broad, documenting the specific question(s) you are trying to answer, being critical of your data sources, and mapping out hypothesized relationships, your analyses are more likely to result in findings that you can take meaningful action on, creating a clearer path to equity in your organization and your community.