Publication

Article

The American Journal of Managed Care

March 2024
Volume30
Issue 3
Pages: e78-e84

Improving Glycemic Control in Diabetes Through Virtual Interdisciplinary Rounds

Patients with diabetes whose providers received advice from remote, virtual interdisciplinary rounds had a greater 1-year reduction in hemoglobin A1c than comparable patients.

ABSTRACT

Objective: A team-based disease management approach that considers comorbid conditions, social drivers of health, and clinical guidelines improves diabetes care but can be costly and complex. Developing innovative models of care is crucial to improving diabetes outcomes. The objective of this analysis was to evaluate the efficacy of virtual interdisciplinary diabetes rounds in improving glycemic control.

Study Design: Retrospective cohort study using observational data from July 2018 to December 2021.

Methods: This study employed difference-in-differences analysis to compare change in hemoglobin A1c (HbA1c) in a group of patients whose providers received advice as part of virtual interdisciplinary rounds and a group of patients whose providers did not receive rounds advice. Patients with diabetes were identified for rounding (1) based on attribution to an accountable care organization along with an upcoming primary care appointment and an HbA1c between 8% and 9% or (2) via provider referral.

Results: The rounded group consisted of 481 patients and the comparison group included 1806 patients. There was a 0.3-point reduction in HbA1c (95% CI, 0.1-0.4) associated with rounds overall. In a subanalysis comparing provider adoption of recommendations among those rounded, provider adoption was associated with an HbA1c reduction of 0.5 points (95% CI, 0.1-0.9) at 6 months post rounds, although there was no significant difference in the full year post rounds.

Conclusions: Interdisciplinary rounds can be an effective approach to proactively provide diabetes-focused recommendations. This modality allows for efficient, low-cost, and timely access to an endocrinologist and team to support primary care providers in diabetes management.

Am J Manag Care. 2024;30(3):e78-e84. https://doi.org/10.37765/ajmc.2024.89449

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Takeaway Points

Virtual interdisciplinary rounds leveraged the expertise of an endocrinologist, pharmacist, and program coordinator to provide advice to primary care providers treating patients with diabetes who were either proactively identified based on clinical characteristics or referred to rounds for additional support (eg, optimization of medication therapy).

  • In the year after the intervention, patients’ mean hemoglobin A1c decreased 0.3 points (95% CI, 0.1-0.4) more than that of the comparison group.
  • Rounds proactively allowed for efficient, low-cost, and timely access to an endocrinologist and team to support primary care providers in diabetes management.

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Diabetes affects 37.3 million Americans and is anticipated to affect 60.6 million by 2060.1 Patients with diabetes have a higher rate of mortality, decreased quality of life, and increased risk of cardiovascular and chronic renal disease. Diabetes is predominant in the Black community, which contributes to health disparities.1,2 Consequently, diabetes is a major contributor to the total cost of care, directly responsible for $237 billion in medical costs in 2017.3 As such, care delivery models that reward health systems for reducing costs and improving quality, such as accountable care organizations (ACOs), incentivize diabetes care improvement at the population level.4,5

Using electronic health data to proactively identify patients at risk for costly complications, population health methods can focus on patient, provider, or system-level interventions to reduce risk.5-7 Provider-focused strategies include clinical decision support, active or passive reminders synchronous or asynchronous at the time of care, and provider education about guidelines, new medication, or technology.8 Treating diabetes on an individual or population basis requires addressing multiple pharmaceutical, behavioral, and lifestyle factors to reduce risk of complications. This puts primary care providers (PCPs) at the forefront of helping patients assess and individualize the risks and benefits of an array of interventions, including initiating prescriptions or referring to other experts who can.

The use of therapies that improve outcomes is often delayed by clinical inertia, or inadequate treatment optimization in response to inadequate glycemic control or sustained hyperglycemia.7 Clinical inertia results from multiple barriers that stem from the provider (time constraints, lack of knowledge, variability in adherence to guideline recommendations), patient (financial constraints, transportation, nonadherence, adverse effects), and system levels (lack of affordable medication, health care, and clinical decision support).9,10 Innovative models that mitigate clinical inertia in diabetes care have emerged.11 A telementoring approach involving remote team-based training and ongoing support for PCPs and community health workers treating patients with diabetes demonstrated an improvement in hemoglobin A1c (HbA1c) compared with a matched cohort.12 For patients without the physical or financial means to access specialty care, a retrospective cohort study of patients with diabetes with an HbA1c of 8% or higher found that endocrinology e-consultations demonstrated improvement in HbA1c similar to in-person visits.13 Embedded pharmacists within primary care clinics improved prescribing for patients with diabetes.14 Finally, an extensive outpatient rounds model with 9 team members that included home visits and regular PCP follow-up has been described, but clinical outcomes are as yet unavailable.15 Although these existing models are promising, they all require providers to identify participating patients or intensive workforce needs. Systemwide identification of patients for proactive review by a team of specialists has not been extensively explored.

The purpose of this study was to describe and estimate the impact of diabetes-focused virtual interdisciplinary rounding (IDR) on glycemic control. We hypothesized that rounds would reduce clinical inertia and increase prescribing of appropriate medications to improve glycemic control through improved endocrinologist access and medication education via promotion of timely advice. We describe and evaluate this replicable innovation, which has the potential to provide health systems with a process to improve quality of care for patients with diabetes.

METHODS

This retrospective cohort study employed a difference-in-differences analysis using programmatic and clinical data from a clinically integrated network (CIN) to evaluate the impact of IDR on the HbA1c values of patients with diabetes. This analysis was deemed exempt by the Duke University Institutional Review Board protocol as a quality improvement project.

Quality Improvement Program

IDR is implemented within Duke Health’s Population Health Management Office, which provides care management and quality oversight to deliver value-based care within a CIN and ACO. The office employs an endocrinologist, pharmacist, and project manager to support PCPs by providing IDR.

Patients are identified for weekly IDR in 2 ways. First, patients may be referred by a PCP, care manager, or other health care team member. Second, and more frequently, patients are identified through a monthly report generated using electronic health record (EHR) data. The report includes patients who are 18 years or older, have received a diagnosis of diabetes, have an HbA1c between 8% and 9%, are not already under the care of an endocrinologist, and have an upcoming primary care appointment. Patients with an HbA1c between 8% and 9% were selected because previous iterations of IDR that included patients with higher HbA1c levels found they needed more intensive intervention (eg, motivational interviewing to discuss fear of insulin, more support around medication nonadherence). Although IDR often refers patients to additional resources, the program is optimized for patients who are managing relatively well but need updates to their medication regimen or help with paying for medications.

Each month, the project manager prioritizes patients from the monthly report by upcoming primary care visit and sends a list to the pharmacist. The pharmacist conducts a chart review for medication-related information, including EHR-integrated refill adherence data from Surescripts. She investigates alternatives for cost savings and possible therapeutic intensification. The 1-hour IDR among the pharmacist, endocrinologist, program coordinator, and occasionally the referring care manager includes a thorough review of 6 to 8 patients’ medical records.

The endocrinologist communicates the team’s suggestions to the PCP via secure communication through the patient’s EHR that becomes part of their medical record. Most recommendations are around medication initiation, discontinuation, titration, or affordability. For example, IDR providers often suggest titrating basal insulin with addition of a glucagon-like peptide 1 receptor agonist (GLP-1 RA) for prandial coverage in select patients. Addition of a GLP-1 RA is sometimes preferred over initiation or titration of prandial insulin to lessen hypoglycemia risks. A medication might be discontinued if the patient has developed a contraindication such as declining kidney function or if a new medication is recommended. The team may improve medication access by suggesting drugs aligned with the patient’s formulary, ensuring utilization of a preferred pharmacy or referral to a pharmacy technician to identify drug coupons or patient assistance programs.

Other IDR team recommendations may include reevaluation of current diabetes status through laboratory analysis or other care team referrals. For example, patients with a low body mass index or a history of diabetic ketoacidosis may be reevaluated for pancreatic insufficiency to guide therapy with insulin management. Referrals may include diabetes education, a nutritionist, or care management for any social (eg, food, transportation) or behavioral needs.

Study of the Program

The data for the evaluation ranged from July 2018 through December 2021 and were obtained from 3 primary sources: programmatic data, a program management worksheet, and EHR data. Programmatic data provided a history of all patients identified as candidates for rounds, the patient’s ACO-attributed insurer at the time of review, the patient’s PCP, and the date of the patient’s next PCP appointment at the time they were on the rounds list. A program management worksheet included a complete list of all patients who were reviewed during rounds, the date of the rounds, an indication of whether each patient was referred, and an indication (based on chart review) of whether the PCP adopted rounds recommendations. Historical EHR data included all HbA1c levels in the 14 months before and after the review date and patient demographics.

This study included 2 primary groups: those included in IDR and a comparison group. The IDR or “rounded” group was made up of all patients reviewed between November 1, 2019, and June 1, 2021. In the rare case that a patient was rounded on more than once, only their first review was included. Patients may have been rounded on more than once if the patient was re-referred by their health care team or the IDR team requested additional laboratory tests or information. The comparison group contained all patients who were on the monthly report (ie, identified as eligible for rounds) with a PCP appointment scheduled within the next month. The comparison group was much larger because the IDR team, which covers between 6 and 8 patients per week, did not have sufficient time to review the complete list. A given patient cannot be in both the rounded and comparison groups.

To assess the HbA1c difference between the rounded and comparison groups, both groups were first assigned a “rounds date” (Figure 1). For the rounded group, this was the date of rounds. For the comparison group, the rounds date was the first date the patient appeared on the rounds list with an upcoming PCP appointment. The rounds date was followed by the index date, or the date a provider may act on rounds advice. The index date was the date of the next primary care visit within 90 days of rounds or the next HbA1c measurement if no primary care visit occurred. Because HbA1c tests calculate an average blood glucose level over 2 to 3 months, HbA1c levels were counted in the postindex period 3 months after the index date. HbA1c levels taken between the index date and the start of the postindex period were omitted from the analysis. The primary outcome was change in the patient’s HbA1c level between the preindex period and postindex period.

Statistical Analysis

The primary analysis was a generalized estimating equation with a gaussian family, identity link, and exchangeable correlation to account for the panel structure of the data (the patient-HbA1c level). The model was estimated as a difference-in-differences analysis where the main coefficient of interest was the interaction between indicators for pre-/postindex date plus 3 months and rounded group status. The model was adjusted for patient-level characteristics identified from the EHR and programmatic data including age, race/ethnicity, area deprivation index, health insurance, PCP practice type, calendar date, primary insurer, and chronic conditions (dementia, chronic kidney disease, congestive heart failure, coronary artery disease, and hypertension).

A secondary analysis tested whether the impact of rounds was persistent over time. This analysis employed a quarterly series of difference-in-differences equations comparing the difference in HbA1c level between the rounded group at 3 (> 1.5-4.5 months), 6 (> 4.5-7.5 months), 9 (> 7.5-10.5 months), and 12 (> 10.5-14 months) months post index date and the 14 months prior to the index date. This model was adjusted for the same covariates as the primary model.

Another secondary analysis used difference-in-differences to compare change in HbA1c in the 6 and 14 months post index for patients whose providers did and did not accept the rounds recommendations. In this case, the population included only patients who were in rounds and had recommendations from the rounds team that were actionable by a PCP (n = 438; eg, a recommendation to add a medication or refer to another provider). The model adjusted for the same variables as the primary analysis and also adjusted for whether the patient was referred by a provider. As with the primary analysis, both secondary analyses used generalized estimating equations with a gaussian family, identity link, and exchangeable correlation. Stata 17 (StataCorp LLC) was used for all calculations.

RESULTS

There were 481 patients in the rounded group and 1806 in the comparison group. Compared with the comparison group, the rounded group patients had a higher HbA1c in the preindex period (9.0% vs 8.3%; P < .001), were younger (mean age in years,60.8 vs 65.7; P < .001), were more often female (55.3% vs 48.4%; P = .007), and more often had unknown race (41.6% vs 11.7%; P < .001), with lower prevalence of coronary artery disease (14.6% vs 21.1%; P = .001), chronic kidney disease (30.6% vs 35.5%; P = .043), and hypertension (78.4% vs 85.2%; P < .001). Both groups had varying insurance plans, with fewer patients in the rounded group on Medicaid (0.6% vs 3.3%; P < .001). Both groups were similar with regard to area deprivation index score, prevalence of dementia, and congestive heart failure. Of the rounded group, 115 (23.9%) were referred by PCPs rather than identified from the rounds list (n = 295; 61.3%) or referred by care management (n = 71; 14.8%) (Table 1).

Patients who were rounded on decreased their HbA1c by 0.3 points (95% CI, 0.1-0.4; P < .01) more than the comparison group, adjusting for patient characteristics (Table 2). The quarterly series of equations estimates that the HbA1c improvement is persistent (Figure 2). The rounded group had significantly lower HbA1c levels at 6 months (0.3; 95% CI, 0.1-0.5; P = .04), 9 months (0.4; 95% CI, 0.2-0.7; P < .01), and 12 months (0.3; 95% CI, 0.05-0.6; P = .02); mean HbA1c levels were lower at 3 months, but the differences were not significant in the adjusted model.

There were 438 rounded patients whose providers received actionable rounds recommendations. Of these, 216 (49.3%) adopted rounds recommendations and 222 (50.7%) did not (Table 1). In the first 6 months of the postindex period, HbA1c decreased by 0.5 more points in the group whose providers accepted advice vs those whose providers did not (95% CI, 0.1-0.9; P < .01) (Table 3). However, there was no difference in HbA1c based on whether providers accepted rounds advice by 14 months after the rounded date (not shown); thus, the effect did not persist.

DISCUSSION

This analysis found a significant decrease in HbA1c associated with onetime, asynchronous, interdisciplinary rounds to support PCPs in treating patients with diabetes. HbA1c reductions appear to persist for over a year after the index date. These findings rise to the level of clinical significance. A 1-point reduction in HbA1c is associated with 1.7% decrease in annual health care costs along with significant reductions in diabetes-related complications.16,17 These findings suggest that rounds may be a simple and effective tool to improve clinical control of diabetes in an ACO.

The American Diabetes Association advises that the care team should avoid clinical inertia and prioritize timely and appropriate intensification of behavior change and/or pharmacologic therapy when patients are not at their recommended targets.7 Rounds support PCPs in overcoming inertia to provide better care by targeting the appropriate patient at an actionable time with an expert team. Rounds target patients with HbA1c levels higher than 8%, at which point physician-directed interventions such as education and audit-and-feedback have been shown to be effective, reducing HbA1c by 0.33 and 0.44 percentage points, respectively.8 Further limiting patients with HbA1c levels less than 9% narrows the population to patients who, IDR providers have found, have needs they are able to address with onetime provider advice. Outside the targeted group, patients referred by their PCP may also be responsive to change as the provider, in seeking help, signals a desire to improve diabetes control.

Timing the advice to arrive within 2 weeks prior to a patient’s primary care appointment ensures that the PCP receives the information in a timely manner for action. If the patient does not keep their appointment, the advice exists as part of the medical record labeled “Diabetes Virtual Rounds” so that it can be found easily by the provider who sees the patient next.

In addition to providing well-timed advice to the appropriate patients, the rounds team has the requisite skills to help PCPs combat therapeutic inertia in several ways as identified by the American Diabetes Association. Access to an endocrinologist is associated with patients achieving their HbA1c goal.18 However, there is a documented shortage of endocrinologists and an expected wait for a nonurgent visit of over 6 months in the Southeastern region of the US.19,20 Analogous to rounds, electronic consultations with an endocrinologist can provide the same support to patients, can reduce specialist access concerns, and have been shown to produce HbA1c reductions similar to in-person clinic visits.13,21 As such, the increase in access to an endocrinology expert’s opinion likely drives improvement and supports integration of evidence-based care. Inclusion of a pharmacist in rounds provides guidance with medication adherence, optimization, selection, and education. Pharmacist-clinician partnerships have been demonstrated to improve diabetes outcomes in clinic settings as well as increase implementation of guideline-directed medical therapy, which could reduce clinical inertia.14,22 Finally, the program coordinator is able to guide the team regarding patient resources. Together, the team is able to remind PCPs about upcoming health maintenance and diabetes education opportunities for patients and strategize about improving medication access.

Although targeting, timing, and the integration of an interdisciplinary clinical team show promise in supporting PCPs in reducing HbA1c levels, the exact pathway for HbA1c reduction is not immediately clear from this study. Although providers following IDR advice was associated with an HbA1c reduction at 6 months, only half of providers followed advice, and the reduction was not maintained among this group for the full study period. As such, there may be additional, unexamined ways in which rounds might spur HbA1c improvement. For example, having the rounds note, through colleague interactions, may leverage PCPs’ professionalism to encourage diabetes management, whether or not the management exactly follows rounds recommendations.23 Rerounding at 6 months to identify barriers (eg, affordability of medication, adverse effects, medication titration) or a qualitative study discussing perceptions of rounds with PCPs could further illuminate this pathway.

Limitations

This study has several limitations. First, the patient population included in this analysis is from 1 CIN and may lack applicability to other institutions. However, many health systems are forming networks and may have similar infrastructure to enact such a program. Second, the rounded group included referred patients who had higher HbA1c levels and different characteristics overall from the patients identified proactively (both rounded and comparison groups). We mitigated this concern by adjusting for important patient characteristics, such as comorbidities, that are associated with difficulty in attaining glycemic control. Finally, we assessed whether the provider indicated in the patient’s chart that they followed rounds recommendations, not whether the patient adhered to them (eg, through filling new medications). These would be difficult to ascertain, and provider recommendation is a reasonable surrogate.

CONCLUSION

IDR may reduce HbA1c by improving access to endocrinology and pharmacist expert advice to PCPs regarding diabetes management. This model is unique because it combines e-consultation with a population-based service through proactive identification of patients with elevated HbA1c levels. The small team–based approach provides efficiency in workflow, with 6 to 8 patients per hour vs 2 to 3 in traditional practice; a focused goal on the management of diabetes; and consistency in recommendations with minimal health system burden. Rationale for PCP nonadoption of recommendations may be explored to further assess improvement in workflow for HbA1c reduction and barriers to implementation. IDR may provide a sustainable and replicable part of the solution in removing barriers to providing optimal diabetes care.

Acknowledgments

The authors thank Brooke Alhanti and Amanda Brucker for their input on evaluation methods, as well as Andi Endriga for her work retrieving electronic health record data.

Author Affiliations: Duke Population Health Management Office (AFH, CLR, PC, JY, PG, SES), Durham, NC; Express Scripts (VLJ), Durham, NC; Division of General Internal Medicine (JY) and Division of Endocrinology, Metabolism, and Nutrition (SES), Department of Medicine, Duke University School of Medicine, Durham, NC; Eshelman School of Pharmacy, University of North Carolina at Chapel Hill (PG), Chapel Hill, NC; Duke University School of Medicine (SW), Durham, NC.

Source of Funding: This project was supported by Duke Health’s Population Health Management Office as part of its routine quality improvement work.

Author Disclosures: Ms Cohen owns shares of Novo Nordisk. Dr Jackson owns stock in several pharmaceutical companies via a mutual fund. Dr Spratt owns stock in the following companies, which may or may not sell or produce diabetes-related products: Amgen, GE, Johnson & Johnson, Medtronic, Merck, Pfizer, Procter & Gamble, Organon, Viatris, and Walmart. The remaining authors report no relationship or financial interest with any entity that would pose a conflict of interest with the subject matter of this article.

Authorship Information: Concept and design (AFH, CLR, PG, SES); acquisition of data (AFH, CLR, PC, VLJ, PG, SES); analysis and interpretation of data (AFH, PC, VLJ, PG, SES); drafting of the manuscript (AFH, CLR, PC, VLJ, SW); critical revision of the manuscript for important intellectual content (AFH, CLR, JY, PG, SW, SES); statistical analysis (AFH); provision of patients or study materials (CLR, PC, JY, SW); obtaining funding (JY); administrative, technical, or logistic support (PC); and supervision (PG, SES).

Address Correspondence to: Susan E. Spratt, MD, Duke Population Health Management Office, 3100 Tower Blvd, Ste 1100, Durham, NC 27707. Email: Susan.Spratt@duke.edu.

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