Browsing by Author "Ubel, Peter A"
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Item Open Access Behavioral Economics and the Affordable Care Act: What States Should Know As They Design Health Insurance Exchanges(2013-04-17) Khan, ZarakEXECUTIVE SUMMARY One of the signature pieces of legislation passed under the Obama administration, the Patient Protection and Affordable Care Act (hereafter referred to as “ACA”) is a vast expansion of the healthcare system in the United States. Part of the law requires that states set up a health insurance exchanges. These exchanges are a key element of expanding coverage to those currently uninsured--particularly people who will be purchasing insurance on their own--and will be responsible for implementing several key aspects of the ACA. The ACA will bring many changes starting January 1, 2014 to people who don’t currently get their health coverage through their job. Part of the law requires that states set up health insurance exchanges. These exchanges are a key element of expanding coverage to those currently uninsured--particularly people who will be purchasing insurance on their own since they work in a small business that doesn’t offer coverage or are self-employed. A health insurance exchange is a governing body that sets standards for what health insurance plans are offered in a state. It is not itself an insurance company and does not offer any insurance plans, rather it ensures that the insurance market in a state is fair, transparent, competitive, and provides adequate benefits. It also provides an online marketplace where people can log on and purchase insurance. The way in which information is presented to people can significantly affect their decisions. When presented with the complicated information comprising a health insurance plan, people can struggle to process all that information. At times, they can be overwhelmed by the decision and choose a sub-optimal insurance plan. The ACA allows significant latitude in exchange design and research from the field of behavioral economics should play a role. Challenging the traditional economic assumption that humans are perfect utility-maximizing machines, behavioral economics melds psychology and neo-classical economics to understand how people make decisions. By understanding the places where people often struggle to make choices, policymakers can develop strategies to mitigate those problems. These recommendations are divided into two sections. The first two are relevant because the state has opted out of designing its own health insurance exchange. The next three are relevant to the design of an exchange and will be important if the state decides, after several years of federal control, that it wants to reassert its authority over its exchange. The first two deal with the responsibilities and rights of the state—both retained and foregone. The next three pertain to behavioral economics and the user interface of the exchange, a small but critical piece of the puzzle. 1. Enrollment will be key. North Carolina has opted to let the federal government set up their health insurance exchange (HIX). This means that the key responsibility retained by the state will be in enrolling residents. This is critical as one of the key assumptions behind a functioning market is full participation (hence the individual mandate). 2. North Carolina could set up a more effective HIX than the federal government. The federal government is overwhelmed and struggling to set up exchanges around the country. The state could be a more appropriate and responsive steward of this function. 3. Choice matters. Limits on the number of choices a person must make can lead them to a better decision (and one they feel better about). If, however, the limits are so prohibitive that they lead to a monopoly, they would be a hindrance to efficiency. 4. Setting robust minimum standards is important. Research on the Massachusetts HIX reveals that a majority of their enrollees choose the lowest level of coverage. As such, setting minimum standards is critical, as it is likely that a majority of enrollees will default to this option. 5. Issues of literacy and numeracy will affect consumers’ decisions. Consumers often do not understand the definitions of terms used in health plans. Reworking these definitions and then testing them for comprehensibility is a simple step that can make a great difference in how people choose their insurance.Item Open Access Empowering Patients as Decision Makers in the Context of Early Stage Prostate Cancer(2018) Scherr, Karen A.Patients with early stage prostate cancer face a difficult preference-sensitive decision. There are multiple treatment options, each of which is associated with a unique set of benefits and risks. For example, surgery may cure the cancer but also come with the risk of serious side effects, such as impotence and incontinence. Alternatively, active surveillance avoids those side effects but requires patients to live with an untreated cancer inside their body. The optimal treatment for each patient will thus depend not only on his medical characteristics but also on how he personally values those risks and benefits. Ideally, patients and their physicians would partner together in a process of shared decision making (SDM) to ensure that patients receive treatments that reflect their personal preferences (i.e., preference-concordant treatments). In this dissertation, I use both qualitative and quantitative methods to examine patients’ decision-making processes in the context of early stage prostate cancer, focusing on if and how patients and physicians work together in the decision-making process to incorporate patients’ preferences into their treatment choices.
Essay 1 examines patients’ decision making processes within the context of a larger trial that was designed to assess the impact of a novel patient-centered (vs. standard) decision aid (DA) on patients’ decision making processes. The patient-centered DA increased patients’ desire to participate in the decision-making process and interest in active surveillance (Fagerlin et al., unpublished). However, regardless of which DA patients received, their treatment choices were primarily driven by physicians’ recommendation which, in turn, were driven by patients’ medical characteristics (e.g., cancer severity) and not their personal preferences (e.g., interest in sexual activity). Qualitative analyses of clinical appointments revealed relatively passive patients regardless of condition, suggesting that patients may not have known how to participate in clinical appointments and would benefit from pre-appointment communication skills training.
Essay 2 examines the effect of a novel patient communication skills intervention plus a patient-centered DA (vs. a patient-centered DA only) on several measures of patient empowerment using a randomized controlled trial. The intervention was a video (DVD) that modeled specific communication skills patients could use to participate in their upcoming appointments. The intervention increased patients’ intentions to use four process skills (e.g., taking notes) and sense of self-efficacy regarding their ability to ask for referrals and express personal concerns during their upcoming clinical appointments. It did not increase patients’ sense of self-efficacy regarding their ability to seek information or make assertive utterances.
Essay 3 examines focuses on a specific moment in clinical appointments: patients’ requests for treatment recommendations (data from Essay 1). Patient requests for recommendations are a pivotal and powerful moment in clinical appointments, yet no existing studies have examined how patients actually request recommendations nor what patient characteristics are associated with requests for recommendations. Patients or their companions requested recommendations in approximately 20% of appointments. Patients who requested recommendations had higher prostate cancer anxiety, placed increased importance on sex in their lives, preferred shared (vs. patient-led) decision making, and were more likely to prefer active treatment prior to appointments. When requesting recommendations, patients discussed physicians’ expertise and the role of their recommendations, asked physicians to engage in self-disclosure (e.g., “What would you do?”) and repeated their requests.
Truly empowering patients as decision makers in the context of early stage prostate cancer is difficult, and both patients and physicians may be uncertain how to behave in this new paradigm of patient empowerment. Patient communication skills interventions show promise, but continued research is needed to truly transform clinical medicine into a domain in which patients are empowered to fully participate in the medical decision-making process.
Item Embargo Examining How Patients Judge Their Physicians in Online Physician Reviews(2023) Madanay, Farrah LynnIn three essays, this dissertation examines how patients judge their physicians in online physician reviews and whether those judgements align with traditional gender stereotypes. Specifically, I qualitatively explore patients’ judgments of their physicians’ interpersonal manner and technical competence, and the predominant factors within the two dimensions. I then train a machine-learning algorithm to code patients’ judgments in online physician reviews at scale. Finally, I use the machine-coded sample to analyze physician gender differences in judgments received from patients and how those judgments affect physicians’ review star ratings. In Essay 1, I propose an elaborated theoretical framework to identify the predominant factors underlying patients’ interpersonal manner and technical competence judgments of their physicians. This framework expands on prior grounded theory work by Lopez et al. (2012) and uses findings from a qualitative content analysis of 2,000 reviews received by distinct physicians. For this framework, I draw on a larger, new dataset of physician reviews from Healthgrades.com, one of the leading physician review websites, and use a balanced sample of reviews representing primary care physicians and surgeons, male and female physicians, and low- and high-rated reviews. I provide rich descriptions and illustrative quotations of the factors comprising interpersonal manner and technical competence, and describe factors added to and removed from Lopez et al.’s original framework. This framework from Essay 1 demonstrates that patients value their physicians on a wide array of interpersonal manner and technical competence factors, including but not limited to bedside manner, going above and beyond, availability, knowledge, diagnostic skill, and open-mindedness about treatment. In Essay 2, I train, test, and validate an advanced natural language processing algorithm called Robustly Optimized BERT Pre-Training Approach (i.e., RoBERTa) for classifying the presence and positive or negative valence of patients’ interpersonal manner and technical competence judgments in online physician reviews. I use the 2,000 manually coded physician reviews from Essay 1 to train and test two classification models, one for interpersonal manner and one for technical competence. Both models perform with 90% accuracy, with high precision, recall, and weighted F1 scores. I validate the models using the full sample of 345,053 RoBERTa-coded reviews for 167,150 physicians by testing associations between the valence-coded judgments and review star ratings and by comparing review rating and gender analyses with extant results in the literature. The fine-tuned algorithm from Essay 2 allows us to code a large dataset of unstructured textual review data with high efficiency and accuracy, enabling subsequent large-scale text analysis. In Essay 3, I analyze whether patients’ judgments of their physicians’ interpersonal manner and technical competence align with traditional gender stereotypes. Drawing on the Stereotype Content Model, I hypothesize that patients’ judgments will conform with gender stereotypes, such that female physicians will be more likely to receive reviews with interpersonal manner judgments whereas male physicians will be more likely to receive reviews with technical competence judgments. Using the full sample of machine-coded reviews from Essay 2, I estimate multilevel logistic regressions to identify gender differences in interpersonal manner and technical competence judgments of physicians. Results from Essay 3 suggest that patients’ judgments partly align with traditional gender stereotypes: Female physicians are more likely to receive interpersonal manner judgments, but male physicians are not more likely to receive technical competence judgments. Whether female physicians are relatively more likely to receive praise or criticism for their interpersonal manner depends on their specialty. In stereotypically warm specialties, like primary care, females are penalized for seeming cold, whereas in stereotypically technical specialties, like surgery, females are advantaged for appearing warm. Last, female physicians, in some cases, are either not rewarded as much or penalized more than their male counterparts in their star ratings when receiving positive or negative interpersonal manner and technical competence judgments.
Item Open Access Garnering Support for the Sugar Sweetened Beverage Tax through Strategic Messaging(2018-01-18) Bandt, CarlyThis project aims to gain insight into public opinion regarding the Sugar Sweetened Beverage (SSB) tax, and how framing of the SSB tax can influence public opinion. This empirical evidence is valuable, as the U.S. is on the verge of SSB tax proposals emerging in cities nationwide. There has already been great variability in the ways the SSB tax has been framed since 2010, and there is still a large knowledge gap in determining what messages are most effective with which types of voters, which can be closed through rigorous testing. There is also little information on whether sociodemographic characteristics and political affiliation moderate the impact of attitudes toward the SSB tax, despite implications for health disparities in SSB consumption and related health outcomes. The central question is: how do differences in the way the sugar-sweetened beverage tax is presented impact the attitudes of voting-age Americans toward the tax?Item Open Access Medicaid Managed Care Programs and Healthcare Markets(2017) Chehal, Puneet KaurMy dissertation research offers insights about the effects of Medicaid managed care (MMC) programs from Kentucky’s statewide market-based program. Kentucky’s significant reforms to introduce a comprehensive MMC program just one year after the passage of the ACA can provide valuable lessons for other rural states with substantial poor populations.
In the first study, I explore Kentucky’s 2011 introduction of MMC and the quality of hospitals used by Medicaid recipients. Kentucky’s MMC program is a post-Affordable Care Act (ACA) market-based program that uses a small set of competing managed-care organizations (MCOs) to administer Medicaid benefits. Using a quasi-experimental research design, I explore whether the introduction of MMC changes the hospitals used by pregnant Medicaid-insured mothers for their deliveries and whether the quality of these hospitals is different compared to the hospitals used before the policy change. I also test whether the changes in hospitals used by pregnant Medicaid-insured mothers for their deliveries differ in smaller counties with fewer hospitals and Medicaid recipients compared to those in larger counties with more hospitals and Medicaid recipients. My analysis uses hospital quality measures designed by the Agency for Healthcare Research and Quality to measure hospital quality. I find that Medicaid-insured pregnant women from nonmetropolitan counties have an increased probability of delivering in the highest quality local hospitals as opposed to the lowest quality local hospitals. In contrast, I find that Medicaid-insured pregnant women from metropolitan counties have a decreased probability of delivering in the highest quality local hospitals and increased probability of delivering in lower quality local hospitals. Since Kentucky’s metropolitan counties have high quality hospitals and its nonmetropolitan counties have some of the poorest quality hospitals in the state, these findings may be positive for patient outcomes and program costs. Additional research evaluating patient outcomes and identifying the causal mechanisms responsible for changes in the hospitals used by Medicaid recipients is needed.
Motivated by my findings in the first chapter, in my second chapter I exploit Kentucky’s reforms to explore potential mechanisms that link MMC to changes in the hospitals used by Medicaid-insured pregnant women for their deliveries. I focus on hospital network status and physician-hospital arrangements, which are the terms by which physicians practice in hospitals. These arrangements can affect the hospital ultimately used by physicians’ patients and may be designed specifically for the purposes of joint contracting with insurers. After using reduced form hospital choice models to estimate the change in the hospitals used by pregnant women in Kentucky in response to the introduction of MMC, I introduce measures of hospital network status and physician-hospital arrangements to my analysis. The primary policy effects on the hospitals used by Medicaid-insured women for deliveries remain unchanged, including the two covariates that suggest that other mechanisms with opposing effects to hospital-network status and physician-hospital arrangements are responsible for the changes in hospitals used by Medicaid-insured women. Future research should consider the role of information in provider choice after the introduction of MMC.
In the third chapter, I shift my focus to considering how well Kentucky’s MMC program navigated expanding Medicaid eligibility. Specifically, I explore the impact of the ACA on disparities in access to medical providers in MMC programs. In states expanding Medicaid eligibility, low-income communities with pre-existing elevated numbers of uninsured people experienced larger gains in coverage from the ACA than other communities. While researchers have reported that there is increased physician participation in states that expanded Medicaid, researchers have yet to explore whether increases in physician participation coincided with areas experiencing the greatest increases in Medicaid coverage or inadequate access to medical services. In these programs, Medicaid recipients access care from provider networks created by the health maintenance organizations (HMOs) selected by states to administer Medicaid benefits. Using an original dataset on Kentucky’s Medicaid HMO networks, I use a difference-in-differences framework to compare provider network participation before and after the implementation of the ACA across counties. Specifically, I compare counties with differing levels of pre-ACA uninsured rates, medically underserved populations and poverty. I find provider network participation is greater in counties experiencing smaller increases in Medicaid coverage but subtly larger participation in counties with medically underserved areas or high poverty.
Item Open Access Online Crowdfunding Campaigns for Diabetes-Related Expenses.(Annals of internal medicine, 2023-07) Sloan, Caroline E; Campagna, Ada; Tu, Karissa; Doerstling, Steven; Davis, J Kelly; Ubel, Peter ABackground: More than 40% of patients with diabetes in the United States have trouble paying their medical bills. Among patients with health-related financial hardship, 56% have delayed or foregone care (1). By one estimate, an insulin-dependent patient with insurance spends about $4800 annually on medications, physicians’ visits, supplies, hospitalizations, and lost wages, equivalent to 15% of the median U.S. per capita income (2). Crowdfunding is increasingly being used by patients struggling with medical costs (3). Crowdfunding campaigns can shed light on the types of expenses that patients with diabetes may struggle to afford (3). Objective: To leverage the rich real-world testimonies available in crowdfunding campaigns in order to characterize the financial challenges of patients with diabetes who seek fundraising support. Methods and Findings: We scraped a random sample of 89 645 active U.S. medical crowdfunding campaigns posted on GoFundMe from 2010 to August 2020, using a previously published natural-language algorithm (4). Campaigns were included if they were in English and requested money for a single person whose primary condition was diabetes. We randomly selected 350 of 807 campaigns that met inclusion criteria, with oversampling of type 1 diabetes campaigns to obtain roughly equal proportions of type 1 and non–type 1 diabetes campaigns and ensure a wide breadth of experiences. Campaigns described patients’ medical situations, expenses, and fundraising goals. We conducted a directed content analysis to evaluate for the presence of predetermined fundraising request categories (Table 1). Two authors double-coded the first 100 campaigns and 10% of the remaining 250 campaigns. Intercoder reliability using the Cohen κ coefficient was 0.67 or higher for all coding categories and direct medical expense subcategories. After exclusions, our final sample included 313 campaigns; 89% were posted during 2015 to 2020. The median fundraising goal was $10 000 (IQR, $4500 to $15 000), the median fundraising amount was $2600 (IQR, $1670 to $4760), and 14% of campaigns reached their goal. Table 2 highlights campaign characteristics overall and by stated diabetes type. One quarter of fundraisers reported having insurance; of these, 49% said their insurance covered their medical expenses but out-of-pocket costs were still too high. Almost half of direct medical expenses were not directly related to glucose control (99 of 206 [48%]). Only 6% requested money specifically for insulin. One fifth of campaigns (21%) requested money for diabetic alert dogs; almost all were campaigns for type 1 diabetes. Indirect medical expenses included lost wages, healthy food, moving to a new city to be closer to state-of-the-art medical care, car repairs to enable transportation to physicians’ appointments, personal trainers, home modifications to support new physical disabilities, and funeral expenses. Campaigns that were not specifically for type 1 diabetes (type 2 or unspecified) mentioned indirect medical expenses more often than campaigns for type 1 diabetes (63% vs. 34%). Discussion: Crowdfunding campaigns provide a window into the wide range of financial struggles that patients with diabetes may face. First, many aspects of diabetes care beyond insulin can be cost-prohibitive, including indirect expenses that clinicians may not be equipped to address. Although the Inflation Reduction Act’s cap on out-of-pocket costs for insulin is an important step in making care more affordable, policymakers should address other diabetes-related costs as well. Second, even people who have insurance use crowdfunding due to lack of coverage for certain expenses or unaffordable copayments. Third, 35% of patients with type 1 diabetes started fundraising campaigns for diabetic alert dogs, which cost about $15 000 and are not covered by insurance because of high variability in effectiveness (5). Clinicians who learn of a patient’s intent to purchase a dog could redirect them toward proven management strategies, such as continuous glucose monitors. Our conclusions are not generalizable to financially distressed patients who may not seek crowdfunding because of older age (people who use crowdfunding are generally younger [3]), poor internet access, or other reasons. Our use of content analysis limited our ability to consider textual context. We could not evaluate for fraud or consider patients’ reported versus actual financial needs. The expenses for which patients use crowdfunding include life-sustaining expenses, such as food and hospitalizations; unproven therapies, such as diabetic alert dogs; and less essential indirect costs, such as personal trainers. Future research should evaluate whether and how these expenses contribute to financial distress in the larger population of patients with diabetes, including those who do not use crowdfunding.Item Open Access Palliative Care Consultations in Patients with Severe Traumatic Brain Injury: Who Receives Palliative Care Consultations and What Does that Mean for Utilization?(Neurocritical care, 2022-06) Williamson, Theresa L; Adil, Syed M; Shalita, Chidyaonga; Charalambous, Lefko T; Mitchell, Taylor; Yang, Zidanyue; Parente, Beth A; Lee, Hui-Jie; Ubel, Peter A; Lemmon, Monica E; Galanos, Anthony N; Lad, Shivanand P; Komisarow, Jordan MBackground
Palliative care has the potential to improve goal-concordant care in severe traumatic brain injury (sTBI). Our primary objective was to illuminate the demographic profiles of patients with sTBI who receive palliative care encounters (PCEs), with an emphasis on the role of race. Secondary objectives were to analyze PCE usage over time and compare health care resource utilization between patients with or without PCEs.Methods
The National Inpatient Sample database was queried for patients age ≥ 18 who had a diagnosis of sTBI, defined by using International Classification of Diseases, 9th Revision codes. PCEs were defined by using International Classification of Diseases, 9th Revision code V66.7 and trended from 2001 to 2015. To assess factors associated with PCE in patients with sTBI, we performed unweighted generalized estimating equations regression. PCE association with decision making was modeled via its effect on rate of percutaneous endoscopic gastrostomy (PEG) tube placement. To quantify differences in PCE-related decisions by race, race was modeled as an effect modifier.Results
From 2001 to 2015, the proportion of palliative care usage in patients with sTBI increased from 1.5 to 36.3%, with 41.6% White, 22.3% Black, and 25% Hispanic patients with sTBI having a palliative care consultation in 2015, respectively. From 2008 to 2015, we identified 17,673 sTBI admissions. White and affluent patients were more likely to have a PCE than Black, Hispanic, and low socioeconomic status patients. Across all races, patients receiving a PCE resulted in a lower rate of PEG tube placement; however, White patients exhibited a larger reduction of PEG tube placement than Black patients. Patients using palliative care had lower total hospital costs (median $16,368 vs. $26,442, respectively).Conclusions
Palliative care usage for sTBI has increased dramatically this century and it reduces resource utilization. This is true across races, however, its usage rate and associated effect on decision making are race-dependent, with White patients receiving more PCE and being more likely to decline the use of a PEG tube if they have had a PCE.Item Open Access Patients want to talk about their out-of-pocket costs-Can real-time benefit tools help?(Journal of the American Geriatrics Society, 2023-05) Sloan, Caroline E; Ubel, Peter AThis editorial comments on the article by Mattingly et al.Item Open Access Physician-Patient Cost Conversations in Rheumatoid Arthritis: The Patient Experience at the Intersection of High Cost and Health Policy(2016-01-26) Stayman, MaxThe out-of-pocket cost burden associated with healthcare in the United States imposes broad hardship on patients. One quarter of Americans struggle to pay their healthcare bills, and over half of personal bankruptcy filings in the United States cite healthcare expenses as a contributing factor. This study examined 268 transcripts of audio-recorded clinic encounters between rheumatoid arthritis patients and their rheumatologists to better understand the patient experience in the face of high cost and begin to inform high-impact areas for policy solutions moving forward. Qualitative analysis of the transcripts identified three themes – emotional response, difficulty managing complexity, and cost-induced non-adherence – that characterize the patient experience when dealing with high cost. Informed by these transcript findings, subject matter expert interviews directed the policy recommendations. In the future, policymakers should continue to leverage the patient experience to motivate policy changes that reduce the cost burden associated with expensive medical care.Item Open Access Poor Consumer Comprehension and Plan Selection Inconsistencies Under the 2016 HealthCare.gov Choice Architecture.(MDM policy & practice, 2017-01) Wang, Annabel Z; Scherr, Karen A; Wong, Charlene A; Ubel, Peter ABackground
Many health policy experts have endorsed insurance competition as a way to reduce the cost and improve the quality of medical care. In line with this approach, health insurance exchanges, such as HealthCare.gov, allow consumers to compare insurance plans online. Since the 2013 rollout of HealthCare.gov, administrators have added features intended to help consumers better understand and compare insurance plans. Although well-intentioned, changes to exchange websites affect the context in which consumers view plans, or choice architecture, which may impede their ability to choose plans that best fit their needs at the lowest cost.Methods
By simulating the 2016 HealthCare.gov enrollment experience in an online sample of 374 American adults, we examined comprehension and choice of HealthCare.gov plans under its choice architecture.Results
We found room for improvement in plan comprehension, with higher rates of misunderstanding among participants with poor math skills (P < 0.05). We observed substantial variations in plan choice when identical plan sets were displayed in different orders (P < 0.001). However, regardless of order in which they viewed the plans, participants cited the same factors as most important to their choices (P > 0.9).Limitations
Participants were drawn from a general population sample. The study does not assess for all possible plan choice influencers, such as provider networks, brand recognition, or help from others.Conclusions
Our findings suggest two areas of improvement for exchanges: first, the remaining gap in consumer plan comprehension and second, the apparent influence of sorting order - and likely other choice architecture elements - on plan choice. Our findings inform strategies for exchange administrators to help consumers better understand and select plans that better fit their needs.Item Open Access Price Transparency in American Healthcare: Public Policies to Support Market-Based Solutions(2014-05-04) Mortimer, LauraThe United States has the most expensive healthcare system in the world. We pay more money per capita for care than any other country – around three times the OECD average. Healthcare accounts for nearly a quarter of our federal budget, and the average family of four in America pays over $20,000 out-of-pocket each year for care. And yet, our health outcomes are no better than those of countries that spend far less money on care; we receive considerably less bang for our buck. As prices rise and we spend both more public and private dollars on healthcare, policy makers and other stakeholders must find ways to build more rational economic decision-making into the system. Unfortunately, the fee-for-service model makes this change difficult because it fundamentally misaligns incentives between patients, payers, and providers. Absent a complete overhaul of fee-for-service, several regulatory reforms and market innovations are essential to bending the healthcare cost curve. Health policy experts agree that lack of price transparency is a major part of the problem. Patients often do not know the amount they will pay for care until they receive a bill, weeks or even months later. As consumer-driven healthcare becomes more the norm and patients pay more out-of-pocket for care, their ability to make value-based decisions is severely limited by the absence of treatment cost information. Functional, competitive markets require that all participants have access to complete, correct information regarding their choices. The American healthcare market is far from this ideal. This paper reviews the price transparency problem in four parts. Part One explains the issue in more detail and provides a basic economic framework through which to understand the problem. Part Two presents an overview of government involvement in healthcare price transparency and includes policy initiatives at both the state and federal levels. Part Three covers private market involvement in the price transparency movement and shows how digital, cloud-based private market tools are making patients better healthcare consumers. Part Four looks ahead to future challenges in healthcare price transparency and outlines policy recommendations to ensure the movement’s success. The following chart summarizes these key policy recommendations. State governments may be better positioned to implement some of these changes, such as establishing all-payer claims databases, whereas federal policy makers should enact others, such as Medicare data disclosure guidelines. These policies can all support market-based healthcare price transparency reforms and effectively allow for public-private incentive alignment and collaboration. As long as fee-for-service payment remains in United States healthcare, these types of policies and partnerships are essential to creating more competitive markets and ultimately improving population health. Policy Recommendations to Support Healthcare Price Transparency: ➢ Mandate disclosure of physician quality and patient outcomes data alongside price information to illustrate value or cost-effectiveness ➢ Simplify payment models and offer clinical decision aids to help patients – particularly those with high deductible insurance plans – understand financial toxicity of treatment options and make decisions as savvy consumers ➢ Use value-based insurance design to better align payers’ and patients’ incentives and nudge patients towards higher value care ➢ Ban gag clauses in contractual agreements between insurers and providers ➢ Establish mandatory all-payer claims databases in every state ➢ Revise the Qualified Entity program under ACA Section 10332 to ensure all entities – public, private, or nonprofit – access to Medicare claims data ➢ Standardize public disclosure process and clarify data management guidelines to prevent abuse and misunderstanding of medical claims data ➢ Limit time period or scope of financial data released to prevent provider collusion around healthcare prices ➢ Provide additional resources to study the effects of price transparency on patients’ treatment and insurance purchasing decisionsItem Open Access Understanding How Language, Design, and Processing Fluency Affect Cognition(2018) Santistevan-Swett, StephanieJudgment and decision-making in a healthcare context often involve complex information and difficult tradeoffs. In order to understand key concepts and receive help with difficult decisions, patients may turn to written materials, like informed consent forms. Unfortunately, these materials can actually increase confusion. This dissertation explores the relationship between written health materials and cognitive processes, specifically comprehension, memory, judgment, and decision-making. The first goal was to investigate how language and design affect cognition for informed consent forms. We developed a Standard informed consent form and two Enhanced versions that had simplified language and modified design, and compared comprehension and memory between the three versions. As written health materials undergo changes to make their content more accessible to readers, they also become more fluent. The second goal was to explore how this fluency affects judgments and decision-making, especially for materials that have a negative valence. This question was studied in the context of two competing fluency theories, the Hedonic Fluency Model and the Fluency Amplification Model. We manipulated the fluency of various materials, including medications, diseases, and risks, and asked participants to make several judgments about the fluent and disfluent materials. Our results highlight the complexities and nuances that characterize fluency’s effects.