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Coordinated Care to Optimize Cardiovascular Preventive Therapies in Type 2 Diabetes: A Randomized Clinical Trial.
Pagidipati, Neha J; Nelson, Adam J; Kaltenbach, Lisa A; Leyva, Monica; McGuire, Darren K; Pop-Busui, Rodica; Cavender, Matthew A; Aroda, Vanita R; Magwire, Melissa L; Richardson, Caroline R; Lingvay, Ildiko; Kirk, Julienne K; Al-Khalidi, Hussein R; Webb, Laura; Gaynor, Tanya; Pak, Jonathan; Senyucel, Cagri; Lopes, Renato D; Green, Jennifer B; Granger, Christopher B.
Affiliation
  • Pagidipati NJ; Duke Clinical Research Institute, Durham, North Carolina.
  • Nelson AJ; Duke Clinical Research Institute, Durham, North Carolina.
  • Kaltenbach LA; Victorian Heart Institute, Monash University, Melbourne, Australia.
  • Leyva M; Duke Clinical Research Institute, Durham, North Carolina.
  • McGuire DK; Duke Clinical Research Institute, Durham, North Carolina.
  • Pop-Busui R; University of Texas Southwestern Medical Center, Dallas.
  • Cavender MA; Parkland Health and Hospital System, Dallas, Texas.
  • Aroda VR; University of Michigan Medical School, Ann Arbor.
  • Magwire ML; University of North Carolina, Chapel Hill.
  • Richardson CR; Brigham and Women's Hospital, Boston, Massachusetts.
  • Lingvay I; Saint Luke's Health System, Kansas City, Missouri.
  • Kirk JK; Warren Alpert Medical School, Brown University, Providence, Rhode Island.
  • Al-Khalidi HR; University of Texas Southwestern Medical Center, Dallas.
  • Webb L; School of Medicine, Wake Forest University, Winston-Salem, North Carolina.
  • Gaynor T; Duke Clinical Research Institute, Durham, North Carolina.
  • Pak J; Duke Clinical Research Institute, Durham, North Carolina.
  • Senyucel C; Boehringer Ingelheim Pharmaceuticals, Inc, Ridgefield, Connecticut.
  • Lopes RD; Boehringer Ingelheim Pharmaceuticals, Inc, Ridgefield, Connecticut.
  • Green JB; Eli Lilly and Company, Indianapolis, Indiana.
  • Granger CB; Duke Clinical Research Institute, Durham, North Carolina.
JAMA ; 329(15): 1261-1270, 2023 04 18.
Article in En | MEDLINE | ID: mdl-36877177
ABSTRACT
Importance Evidence-based therapies to reduce atherosclerotic cardiovascular disease risk in adults with type 2 diabetes are underused in clinical practice.

Objective:

To assess the effect of a coordinated, multifaceted intervention of assessment, education, and feedback vs usual care on the proportion of adults with type 2 diabetes and atherosclerotic cardiovascular disease prescribed all 3 groups of recommended, evidence-based therapies (high-intensity statins, angiotensin-converting enzyme inhibitors [ACEIs] or angiotensin receptor blockers [ARBs], and sodium-glucose cotransporter 2 [SGLT2] inhibitors and/or glucagon-like peptide 1 receptor agonists [GLP-1RAs]). Design, Setting, and

Participants:

Cluster randomized clinical trial with 43 US cardiology clinics recruiting participants from July 2019 through May 2022 and follow-up through December 2022. The participants were adults with type 2 diabetes and atherosclerotic cardiovascular disease not already taking all 3 groups of evidence-based therapies.

Interventions:

Assessing local barriers, developing care pathways, coordinating care, educating clinicians, reporting data back to the clinics, and providing tools for participants (n = 459) vs usual care per practice guidelines (n = 590). Main Outcomes and

Measures:

The primary outcome was the proportion of participants prescribed all 3 groups of recommended therapies at 6 to 12 months after enrollment. The secondary outcomes included changes in atherosclerotic cardiovascular disease risk factors and a composite outcome of all-cause death or hospitalization for myocardial infarction, stroke, decompensated heart failure, or urgent revascularization (the trial was not powered to show these differences).

Results:

Of 1049 participants enrolled (459 at 20 intervention clinics and 590 at 23 usual care clinics), the median age was 70 years and there were 338 women (32.2%), 173 Black participants (16.5%), and 90 Hispanic participants (8.6%). At the last follow-up visit (12 months for 97.3% of participants), those in the intervention group were more likely to be prescribed all 3 therapies (173/457 [37.9%]) vs the usual care group (85/588 [14.5%]), which is a difference of 23.4% (adjusted odds ratio [OR], 4.38 [95% CI, 2.49 to 7.71]; P < .001) and were more likely to be prescribed each of the 3 therapies (change from baseline in high-intensity statins from 66.5% to 70.7% for intervention vs from 58.2% to 56.8% for usual care [adjusted OR, 1.73; 95% CI, 1.06-2.83]; ACEIs or ARBs from 75.1% to 81.4% for intervention vs from 69.6% to 68.4% for usual care [adjusted OR, 1.82; 95% CI, 1.14-2.91]; SGLT2 inhibitors and/or GLP-1RAs from 12.3% to 60.4% for intervention vs from 14.5% to 35.5% for usual care [adjusted OR, 3.11; 95% CI, 2.08-4.64]). The intervention was not associated with changes in atherosclerotic cardiovascular disease risk factors. The composite secondary outcome occurred in 23 of 457 participants (5%) in the intervention group vs 40 of 588 participants (6.8%) in the usual care group (adjusted hazard ratio, 0.79 [95% CI, 0.46 to 1.33]). Conclusions and Relevance A coordinated, multifaceted intervention increased prescription of 3 groups of evidence-based therapies in adults with type 2 diabetes and atherosclerotic cardiovascular disease. Trial Registration ClinicalTrials.gov Identifier NCT03936660.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Cardiovascular Diseases / Disease Management / Diabetes Mellitus, Type 2 Type of study: Clinical_trials / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male Language: En Journal: JAMA Year: 2023 Type: Article

Full text: 1 Database: MEDLINE Main subject: Cardiovascular Diseases / Disease Management / Diabetes Mellitus, Type 2 Type of study: Clinical_trials / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male Language: En Journal: JAMA Year: 2023 Type: Article