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DOI: 10.1055/a-1926-0199
Provider Perspectives on Patient- and Provider-Facing High Blood Pressure Clinical Decision Support
- Abstract
- Background and Significance
- Objectives
- Methods
- Results
- Discussion
- Limitations
- Conclusion
- Clinical Relevance Statement
- Multiple Choice Questions
- References
Abstract
Background Hypertension, persistent high blood pressures (HBP) leading to chronic physiologic changes, is a common condition that is a major predictor of heart attacks, strokes, and other conditions. Despite strong evidence, care teams and patients are inconsistently adherent to HBP guideline recommendations. Patient-facing clinical decision support (CDS) could help improve recommendation adherence but must also be acceptable to clinicians and patients.
Objective This study aimed to partly address the challenge of developing a patient-facing CDS application, we sought to understand provider variations and rationales related to HBP guideline recommendations and perceptions regarding patient role and use of digital tools.
Methods We engaged hypertension experts and primary care respondents to iteratively develop and implement a pilot survey and a final survey which presented five clinical cases that queried clinicians' attitudes related to actions; variations; prioritization; patient input; importance; and barriers for HBP diagnosis, monitoring, and treatment. Analysis of Likert's scale scores was descriptive with content analysis for free-text answers.
Results Fifteen hypertension experts and 14 providers took the pilot and final version of the surveys, respectively. The majority (>80%) of providers felt the recommendations were important, yet found them difficult to follow-up to 90% of the time. Perceptions of relative amounts of patient input and patient work for effective HBP management ranged from 22 to 100%. Stated reasons for variation included adverse effects of treatment, patient comorbidities, shared decision-making, and health care cost and access issues. Providers were generally positive toward patient use of electronic CDS applications but worried about access to health care, nuance of recommendations, and patient understanding of the tools.
Conclusion At baseline, provider management of HBP is heterogeneous. Providers were accepting of patient-facing CDS but reported preferences for that CDS to capture the complexity and nuance of guideline recommendations.
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Keywords
hypertension - decision support systems - clinical - surveys and questionnaires - practice guideline - fast healthcare interoperable resourcesBackground and Significance
High blood pressure (HBP) is a common issue and hypertension, persistent high blood pressures leading to chronic physiologic changes, is a common condition among adults in the United States that, when uncontrolled, increases the risks of heart disease and stroke.[1] Medications can treat HBP but also have adverse events like hypotension and electrolyte derangements.[2] [3] HBP also can be reduced through lifestyle and behavioral changes such as diet, exercise, reducing stress, and avoiding alcohol and smoking, yet these changes require substantial effort.[4] Hypertension guidelines vary, reflecting risks and benefits in variable ways.[5] For example, goals for hypertension control vary from 150/90 to 120/80 across guidelines depending on their synthesis of the evidence for key populations, such as from the SPRINT trial.[6] From diagnosis to prescription, hypertension treatment is a complex interplay among provider intent, patient capacity, and best available data and knowledge.[7]
Clinical decision support (CDS) can provide the means to implement recommendations from hypertension guidelines but must consider variabilities in guidelines, clinical workflows, patient and provider preferences, and their attitudes and beliefs.[8] Past hypertension CDS efforts have had promising but mixed results and few are in current use, potentially due to these complexities.[9] CDS trials that involved multidisciplinary interventions yielded positive results and indicated hypertension CDS may have to balance needs and preferences to be effective.[10] [11] [12] [13] The Kaiser Permanente reports control rates of >80% with multifactorial approaches including CDS.[14] These efforts, however, are not easily implemented in different systems; this is especially due to lack of interoperability between clinical information systems, CDS logic, and data.[15] [16]
As part of research funded by Agency for Healthcare Research and Quality, our team has explored the way eight separate guidelines for hypertension can be translated into CDS recommendations; initially, we took 71 recommendations covering more than 36 domains, transformed them into machine-interpretable logic,[17] [18] [19] and determined the adequacy of standard EHR data to assess them.[20] We created a content implementation guide (see [Supplementary Figs. S1] and [S2] [available in the online version] for details)[21]; however, the implementation into an actual application requires consideration of many aspects such as usability, usefulness, adaptability, and, especially, the five rights of CDS, that is, right information to the right person in the right format to the right channel at the right time.[22] Given the complex, shared decision-making nature of hypertension, we sought to understand when the patient may be the right person to receive the alerts through the creation of a series of stakeholder surveys to implement the recommendations into an FHIR hypertension CDS application. This survey focused on the provider perspective, both hypertension experts and primary care providers, highlighting the variation in guidelines through different cases, their current practice preferences, and the potential approach when engaging patients with the CDS. Poorly designed CDS applications may exacerbate the variability and worsen clinical care and increase fatigue, while carefully designed CDS can aid in shared decision-making.[23]
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Objectives
Our objective for this paper was to understand the perception of hypertension experts and primary care providers in the role of the patient in responding to hypertension guideline recommendations to create a patient-facing clinical decision support tool.
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Methods
We iteratively created a unique survey that queried primary care providers and hypertension specialists about their attitudes toward clinical practice guidelines for hypertension and patient-facing CDS.
For the Human Subject Research Approval, the Oregon Health and Science University Institutional Review Board approved this study (approval number: STUDY00020522).
Survey Design
We used an iterative development process that focused on the constructs of high blood pressure guideline recommendations, variation, importance, challenges, and patient input and effort. We first searched the literature for similar surveys: we found work by Oliveria et al,[24] [25] Koopman et al,[26] Kerr et al,[27] Kim et al,[28] Turer et al,[29] and several studies that optimized their CDS implementation approach through surveys.[30] [31] [32] [33] We used the assessment of barriers to control by Kerr et al—clinical uncertainty, prioritization of BP, and organizational/system issues—and the five rights to drive the survey design. For demographics, shared decision-making, and use of hypertension tools, we used questions from these other surveys to assess these concepts.[34] However, since no surveys covered the most recent hypertension guidelines, we developed novel questions informed by the synthesis of hypertension guidelines into 71 recommendations described by Alper et al[5]. We organized the questions into five use cases that were meant to elicit provider preferences for diagnostic, monitoring, and treatment approaches to hypertension management with a focus on the five rights—especially the best person, channel, and time—and on variability in the guidelines, and barriers in following recommendations. [Table 1] highlights the cases and their objectives.
Abbreviations: BMI, body mass index; CKD, chronic kidney disease; DM, diabetes mellitus; MCA, middle cerebral artery.
The survey also asked providers to record their preferred hypertension care recommendations from four of the eight extant guidelines, eliminating those from outside the United States as follows: (1) Eighth Joint National Committee (JNC 8)[35]; (2) American College of Cardiology/American Heart Association (ACC/AHA)[36]; (3) American College of Physicians (ACP/AAFP)[2]; and (4) U.S. Department of Veterans Affairs (VA).[37] We presented providers with these cases and asked them to record their preferences for various therapeutic interventions, select one of the guideline-based recommendations from a list, and rate their selections by importance, frequency of use, difficulty, patient input required, and patient work required. Ratings were on a 7-point scale with 7 as the highest, 1 as the lowest, and 4 as neutral. The survey also asked participants to provide free text answers as to why they made the decisions they did for each use case, as well as share their overall impressions of CDS and shared decision-making in hypertension care.
As shown in [Fig. 1], we first fielded a pilot version of the survey to a convenience sample of “hypertension experts” who (1) had completed the American Hypertension Specialist Certification Program (AHSCP)[38] and (2) had public contact information (n = 280) to assess the understandability of the questions and the reliability of the responses (see [Supplementary Appendix A] “Draft Survey,” available in the online version). The pilot survey includes 90 questions within six sections with 14–18 questions per section. The pilot survey led to a final version of the survey with only 60 questions which we then administered to primary care providers. Results from both the pilot and final surveys guided our adaptation of the CDS application.
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Recruitment
We recruited hypertension experts who were nephrologists, cardiologists, internists, and family medicine physicians for the pilot survey from the AHSCP; and then between June 2020 and December 2020, we fielded the final survey to primary care providers from a convenience sample of 120 providers from 17 different primary care clinics.[39] Both groups received an e-mail invitation that included a consent form and a link to the online survey. Participants received $50.00 for completing the survey.
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Data Analysis
Primary analysis summarized provider and clinic characteristics, and generated descriptive statistics for aggregates of each of the five cases. We generated binary values for questions with a 7-point scale by selecting answers that were scored five or higher. Two researchers (J.R. and C.D.) qualitatively reviewed all text answers and generated preliminary themes which were vetted and finalized by the research team.
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Results
In all, 15 hypertension experts responded to the pilot survey (see [Supplementary Appendix A]: “Draft Survey,” available in the online version); significant revisions were made based on their feedback. We shortened and clarified the cases, provided clearer text from the recommendations, and expanded options where they suggested other treatments. The pilot questions related to screening, monitoring, and challenges were retained and are presented with the final survey. For the final survey ([Supplementary Appendix B]: “Main Survey,” available in the online version), 14 primary care providers responded: 10 physicians and 4 advanced practice providers (two physician assistants and two nurse practitioners). A slight majority worked in urban practices (n = 8, 57%) versus rural practices (n = 6, 43%). Nine of the 14 (64%) had been practicing medicine for 5 years or longer.
All the experts and 8 out of 14 primary care respondents were very or extremely familiar with the process to develop guidelines. Half of the primary care providers (50%) reported their clinics primarily followed the Eighth Joint National Committee (JNC 8) guideline, while four (28%) used the ACC/AHA guideline, one (7%) followed the ACP/AAFP guideline, and two respondents (14%) were unsure. Experts were more likely to follow ACC/AHA guidelines. We next report the results for each of the five use cases. [Fig. 2] summarizes the actions taken for each case.
Diagnosis and Monitoring (Case 1)
Case 1 presented recommendations for diagnosis and monitoring ([Table 2]); here, the guidelines suggest home or ambulatory blood pressure monitoring. Of the primary care respondents, only one-third suggested that the patient should use home monitoring of blood pressure (HMBP) and half of them recommended ambulatory blood pressure monitoring (ABPM). In contrast, 100% of hypertension experts recommended monitoring, predominantly recommending ABPM (73%).
Abbreviations: BMI, Body Mass Index; DBP, diastolic blood pressure; SBP, systolic blood pressure.
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Nonpharmacologic Treatment (Case 2)
Case 2 presented nonpharmacologic treatment options ([Table 3]); all options were potentially valid selections. Participants were asked to rank nonpharmacologic recommendations in order of priority for the patient. Of the primary care providers responding, a majority prioritized recommendations for smoking cessation (>80%), moderating alcohol consumption (>50%), and increasing physical activity (>50%) in their top three priorities, whereas less than half prioritized salt restriction, weight loss, and dietary changes.
Abbreviations: BMI, body mass index; DBP, diastolic blood pressure; SBP, systolic blood pressure.
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Pharmacologic Treatment: Cases 3–5 (in Order of Increasing Complexity)
Case 3 presented a patient with moderate severity hypertension ([Table 4]); most guidelines recommend several medications as potential initial options. However, 71% of primary care providers recommended treating with a calcium channel blocker (CCB). Eighty-six percent of primary care respondents (n = 12) would have prescribed an angiotensin-converting enzyme (ACE)-inhibitor or angiotensin receptor blocker (ARB) if the patient had diabetes and 50% (n = 7) would have recommended a thiazide-type diuretic or CCB if the patient happened to be Black (following JNC8 and VA guidelines).
Abbreviations: BMI, body mass index; CKD, chronic kidney disease; DM, diabetes mellitus; eGFR, estimated glomerular filtration rate; HDL, high-density lipoprotein; LDL, low-density lipoprotein; MCA, middle cerebral artery.
Case 4 provided a scenario where patient had several comorbidities, including chronic kidney disease (CKD). In response, 67% (n = 8) of primary care respondents selected the therapeutic option of an ACE Inhibitor, congruent with all guidelines. Case 5 described an older adult with complex comorbidities and a likely adverse event (hypotension) from treatment. No single recommendation received a majority of responses, the selection with the highest proportion at 45% of primary care providers was, “In adults with hypertension and CKD with proteinuria, target a BP of <130/80 mm Hg.” When asked about preferred pharmacologic treatment actions, only one option achieved 50% agreement among the 14 primary care providers, “Add treatment with an ACE-Inhibitor.”
Despite this variability, primary care providers chose guideline-supported recommendations, the majority of the time: in all, 70% of the time for diagnosis and monitoring (case 1), although only 50% used the ambulatory blood pressure monitoring option preferred by some guidelines; 100% for nonpharmacologic options (case 2); and 65% for pharmacologic options (case 3–5).
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Attitudes toward the Recommendations and Reasons for Variation
[Fig. 3] highlights the attitudes toward the recommendations in each case: their perceived importance, the frequency they are followed, the difficulty in following them, the amount of patient input, and the amount of patient effort. When averaged across the cases, more than 80% of primary care respondents rated the guidelines as important; however, the values were slightly lower for the simplest case (case 1) where the guidelines only called for monitoring. Primary care respondents reported being able to adhere to guidelines from 10 to 78% of the time, with nonpharmacologic recommendations followed the least frequently. Patient input and effort were highest for nonpharmacologic treatments; these are largely self-managed. However, the amount of patient effort and input did not increase with the complexity of their situation.
When primary care providers were asked for free-text reasons for varying from guidelines, 30% of those who responded focused on drug allergies or side effects, while 28% focused on patient comorbidities. The remainder of responses focused on items such as family history, patient compliance or preferences, shared decision-making, cost or access concerns, or deferring to a specialist. Seventy-one percent of hypertension experts focused on allergies or side effects and 21% on comorbidities. Shared decision-making and age were suggested once while patient preference, cost/access, or other factors were not mentioned.
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Main Themes from Free Text Responses
The hypertension experts and primary care providers described their preferences and experiences with CDS and shared decision-making in the context of hypertension management through free text. Primary themes were needs for effective communication and patient education materials, having consensus among provider and patient recommendations, and having clear understanding of risk and benefit in this process (see [Supplementary Table S1], available in the online version). For instance, one provider requested, “a nuanced tool that accounts for fall risk, non-life-threatening side effects, like erectile dysfunction (ED),” and then asked, “how much lifestyle change is really possible?” Several respondents mentioned wanting risk tools (like an atherosclerotic cardiovascular disease [ASCVD] risk calculator) that could provide “simple visualizations.” Others reported the desire to have consensus targets for treatment and be sure that recommendations were from updated guidelines.
Diagnosis and monitoring challenges were commonly reported. Although participants described the importance of home monitoring, they had many concerns, including financial or insurance barriers to obtaining a home cuff or ABPM, the need for calibration of home devices over time, lack of available ABPM devices, and physical or mental challenges to completing home monitoring. This was balanced against the potential inaccuracy of office measurements (e.g., white coat effect, the physical/mental stresses of a visit) and limited patient follow-up or access to the clinic.
For treatment variations, many identified narrative recommendations embedded in the guidelines that we did not transform into logic; for instance, secondary hypertension, motivation, psychiatric comorbidities, social factors, and mental health (e.g., stress reduction, sleep, and psychiatric care). Similarly, other variations in treatment included known allergies, cost, knowledge about patient compliance, or other patient context (including estimated glomerular filtration rate [eGFR] for CKD and more details related to frailty and fall risk).
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Discussion
Our objective was to identify ways that hypertension guideline recommendations could be implemented in a patient-facing CDS tool, given the need to vary from guidelines and diversity of opinions about the role of the patient; to that end, hypertension experts and primary care providers identified several potential options. Providers found recommendations for hypertension guidelines to be important (>80%) and, when provided cases, had substantial variation in their responses despite primarily following guideline recommendations. Primary care providers identified nonpharmacologic options as challenging and requiring the most patient effort and input; less patient input and effort was thought to be needed from pharmacologic approaches. Diagnosis and monitoring had several challenges, from the unreliability of office blood pressures to the burden on patients to monitor reliably and accurately. ABPM was infrequently chosen despite guidelines recommending its use, providers noted barriers to cost and availability.
We used this work to adapt the CDS application. The major step we took, given the variability from providers, was focused on shared decision-making between patients and providers. We did so by making the application entirely patient facing in design (although accessible directly by providers) and focus on nonpharmacologic recommendations ([Supplementary Fig. S3], available in the online version). We also created mechanisms to input preferences and goals, such as blood pressure goals, and drove screening and monitoring based off these goals ([Supplementary Figs. S4] and [S5], available in the online version). Given the substantial expectation of monitoring and clinical uncertainty expressed, we built the capacity to self-monitor home blood pressures and incorporated metrics for when enough blood pressures from home and office were present to be confident of the assessment for control.[14] [26] [27] We opted not to suggest specific blood pressure medication changes but instead prompted for when a change should be made and presented current treatments. Our previous work in data adequacy also highlighted the need for key data to be added before the recommendations could be processed, we prompted for these data first.[40]
One limitation of this survey approach was the relatively small sample size which limits generalizability. However, the respondents did identify multiple different areas where they would potentially diverge from the standards and the reasons for these decisions. Varying from the recommendations reflected variation between guidelines (lack of consensus) and specific patient characteristics (like social need, comorbidities, adherence issues, or frailty). Although some recommendations can encode these differences (common comorbidities, for instance), adjusting recommendations for these factors require accurate, clear data which was not available in two out of four cases in our prior work,[20] and consensus on how to include these factors. Providers' response to increasing complexity was sometimes to get more input from the patients and acknowledge their effort, and sometimes to decide to vary more frequently. The challenges in managing guidelines with multiple comorbidities has been well studied; however, more recent work has highlighted the value in sharing the decision-making for these cases by eliciting patient priorities and values and deciding the best course of action together.[41] [42]
The impact of these findings on CDS systems are substantial. First, presenting the recommendations in certain situations, recommending nonpharmacologic therapy, could be highly successful if issues around workflow and patient input could be addressed. Providing self-management support through patient-facing applications, for instance, that are tied to clinical teams' support may be one way to accomplish this. Second, many providers asked for visualization tools and guidance on consensus or agreement which could be presented as part of the recommendations to help guide the discussions. Third, support for the challenges of home monitoring to get information reliable for diagnosis and overcome challenges could address a major gap. Finally, even when there is not consensus from guidelines, prioritization is still possible and highlighting potential patient factors that could aid in prioritization while referencing the most frequently chosen options could improve personalization and social trust, both factors that impact behavior and could increase adherence. Work in cognitive psychology and behavioral economics indicate social norms and nudging toward highly prioritized options while still providing choices may increase responsiveness while not diminishing autonomy.[43] [44]
Based on the survey results, we have adapted the CDS application which we call COACH, the Collaboration Oriented Approach to Controlling High blood pressure. These changes, shown in the [Supplementary Figure S2] (available in the online version) section, led to prioritization of patient-facing elements (largely home blood pressure monitoring and nonpharmacologic counseling, goal setting, and follow-up), given the need for input and work for patients, allowance for variation in pharmacologic treatment, and the capture of “nuance” or personalization like previous adverse events or blood pressure goals in the CDS application. In addition, the prioritized clinician recommendations for lifestyle changes, like smoking cessation and alcohol moderation if relevant to the patient, are presented with the level of support (e.g., 80% of providers recommend).
Gaining end-user perspectives and preferences is fundamental to user-centered design, particularly for new technologies such as shareable and interoperable CDS.[45] [46] [47] These data are informing the designs of our provider-facing CDS tool which we anticipate will increase the likelihood of provider adoption. Using this survey method in which providers ranked preferences for guideline-based recommendations given patient scenarios has provided important insights as to how providers perceive the benefits of some recommendations over others when weighed against specific patient scenarios. We used these insights to transform our CDS application, now implemented at our institution.
Furthermore, surveys like ours may be sufficient for designing CDS applications; however we encourage informaticians to incorporate more advanced methods. For example, methods from cognitive science may better elucidate user perceptions and replicate real-world decisions around guideline-based care for hypertension management.[44] [48]
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Limitations
This study has limitations that are important to note. First, we recruited providers from a convenience sample rather than a random sample[49]; however, this is common in qualitative and user acceptance designs. Similarly, we did not intend to validate the survey beyond its utility in adapting the tool. Second, our analysis incorporated a “top three” approach to represent priority recommendations which has the potential to conflate priority recommendations. Also, we reported summary scores for each of the cases but due to the variety of nonresponses throughout the survey, we only removed survey scores when any provider did not answer an entire battery of survey questions. Lastly, we did not vet our qualitative themes (“member check”) based on participants' free-text answers.
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Conclusion
In general, providers had highly variable approaches to HBP management and were accepting of patient-facing CDS tools, but emphasized the importance of CDS recommendations that capture the complexity and nuance of the recommendations. The results from our survey are informing the project team's decisions around designing a SMART-on-FHIR CDS application that supports provider and patient needs for hypertension management.
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Clinical Relevance Statement
This study assessed attitudes toward clinical decision support and treatment priorities of clinicians who treat hypertension (high blood pressure), assessing how participants would monitor, diagnose, or treat five fictional patients with conditions including and related to hypertension. The results of this survey have been used to inform the development of a new clinical decision support tool for hypertension diagnosis and treatment.
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Multiple Choice Questions
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Which domain of high blood pressure guideline recommendations did providers find most difficult to follow?
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Screening
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Monitoring
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Pharmacologic treatments
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Nonpharmacologic treatments
Correct Answer: The correct answer is option d. Providers found nonpharmacologic recommendations, on the whole, most difficult to follow; this was partially.
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What challenges to prescribing ambulatory blood pressure monitoring (ABPM) did providers note as barriers to its use in practice?
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Challenges related to interpreting the results
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Clinical practice guidelines not supporting its use
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Cost and availability
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Patient reluctance to monitor blood pressure
Correct Answer: The correct answer is option c. Providers noted that cost and availability of ambulatory blood pressure monitoring presented the primary challenges to prescribing it in clinical practice.
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Conflict of Interest
None declared.
Protection of Human and Animal Subjects
This research was performed in compliance with current standards for human subjects research and was reviewed by the Oregon Health & Science University Institutional Review Board.
The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health or Agency for Healthcare Research and Quality.
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- 43 Shaffer VA. Nudges for health policy: effectiveness and limitations. Miss Law Rev 2017; 82: 727
- 44 Shaffer VA, Wegier P, Valentine KD. et al. Patient judgments about hypertension control: the role of variability, trends, and outliers in visualized blood pressure data. J Med Internet Res 2019; 21 (03) e11366
- 45 Chokshi SK, Belli HM, Troxel AB. et al. Designing for implementation: user-centered development and pilot testing of a behavioral economic-inspired electronic health record clinical decision support module. Pilot Feasibility Stud 2019; 5: 28
- 46 Chokshi SK, Mann DM. Innovating from within: a process model for user-centered digital development in academic medical centers. JMIR Human Factors 2018; 5 (04) e11048
- 47 Mann D, Hess R, McGinn T. et al. Adaptive design of a clinical decision support tool: What the impact on utilization rates means for future CDS research. Digit Health 2019; 5: 2055207619827716
- 48 Shaffer VA, Wegier P, Valentine KD. et al. Use of Enhanced Data Visualization to Improve Patient Judgments about Hypertension Control. Med Decis Making 2020; 40 (06) 785-796
- 49 Nielsen J, Landauer TK. A mathematical model of the finding of usability problems. Proceedings of the INTERACT '93 and CHI '93 Conference on Human Factors in Computing Systems; Amsterdam, The Netherlands: Association for Computing Machinery; 1993: 206-213
Address for correspondence
Publication History
Received: 27 December 2021
Accepted: 11 August 2022
Accepted Manuscript online:
17 August 2022
Article published online:
30 November 2022
© 2022. Thieme. All rights reserved.
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- 44 Shaffer VA, Wegier P, Valentine KD. et al. Patient judgments about hypertension control: the role of variability, trends, and outliers in visualized blood pressure data. J Med Internet Res 2019; 21 (03) e11366
- 45 Chokshi SK, Belli HM, Troxel AB. et al. Designing for implementation: user-centered development and pilot testing of a behavioral economic-inspired electronic health record clinical decision support module. Pilot Feasibility Stud 2019; 5: 28
- 46 Chokshi SK, Mann DM. Innovating from within: a process model for user-centered digital development in academic medical centers. JMIR Human Factors 2018; 5 (04) e11048
- 47 Mann D, Hess R, McGinn T. et al. Adaptive design of a clinical decision support tool: What the impact on utilization rates means for future CDS research. Digit Health 2019; 5: 2055207619827716
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