Blood AJ, Chang LS, Hassan S, Chasse J, Stern G, Gabovitch D, Zelle D, Colling C, Aronson SJ, Figueroa C, Collins E, Ruggiero R, Zacherle E, Noone J, Robar C, Plutzky J, Gaziano TA, Cannon CP, Wexler DJ, and Scirica BM
Background: Several SGLT2i (sodium-glucose transport protein 2 inhibitors) and GLP1-RA (glucagon-like peptide-1 receptor agonists) reduce cardiovascular events and improve kidney outcomes in patients with type 2 diabetes; however, utilization remains low despite guideline recommendations., Methods: A randomized, remote implementation trial in the Mass General Brigham network enrolled patients with type 2 diabetes with increased cardiovascular or kidney risk. Patients eligible for, but not prescribed, SGLT2i or GLP1-RA were randomly assigned to simultaneous virtual patient education with concurrent prescription of SGLT2i or GLP1-RA (ie, Simultaneous) or 2 months of virtual education followed by medication prescription (ie, Education-First) delivered by a multidisciplinary team driven by nonlicensed navigators and clinical pharmacists who prescribed SGLT2i or GLP1-RA using a standardized treatment algorithm. The primary outcome was the proportion of patients with prescriptions for either SGLT2i or GLP1-RA by 6 months., Results: Between March 2021 and December 2022, 200 patients were randomized. The mean age was 66.5 years; 36.5% were female, and 22.0% were non-White. Overall, 30.0% had cardiovascular disease, 5.0% had cerebrovascular disease, and 1.5% had both. Mean estimated glomerular filtration rate was 77.9 mL/(min‧1.73 m 2 ), and mean urine/albumin creatinine ratio was 88.6 mg/g. After 2 months, 69 of 200 (34.5%) patients received a new prescription for either SGLT2i or GLP1-RA: 53.4% of patients in the Simultaneous arm and 8.3% of patients in the Education-First arm ( P <0.001). After 6 months, 128 of 200 (64.0%) received a new prescription: 69.8% of patients in the Simultaneous arm and 56.0% of patients in Education-First ( P <0.001). Patient self-report of taking SGLT2i or GLP1-RA within 6 months of trial entry was similarly greater in the Simultaneous versus Education-First arm (69 of 116 [59.5%] versus 37 of 84 [44.0%]; P <0.001) Median time to first prescription was 24 (interquartile range [IQR], 13-50) versus 85 days (IQR, 65-106), respectively ( P <0.001)., Conclusions: In this randomized trial, a remote, team-based program identifies patients with type 2 diabetes and high cardiovascular or kidney risk, provides virtual education, prescribes SGLT2i or GLP1-RA, and improves guideline-directed medical therapy. These findings support greater utilization of virtual team-based approaches to optimize chronic disease management., Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT06046560., Competing Interests: Disclosures Dr Blood reports grants from Boehringer Ingelheim, Novo Nordisk, Eli Lilly, General Electric Health; consulting for Color Health, Arsenal Capital Partners, Walgreens Health, Medscape, Novo Nordisk; and equity in Knownwell. Dr Chang reports research grants via Brigham and Women’s Hospital from Applied Therapeutics, Better Therapeutics, Boehringer Ingelheim, Corcept Therapeutics, Eli Lilly, Fractyl Health, Novo Nordisk, Rhythm Pharmaceuticals, and Sanofi. Dr Hassan reports grants from Better Therapeutics, Boehringer Ingelheim, and Novo Nordisk. J. Chasse reports grants from Boehringer Ingelheim and Novo Nordisk. S. J. Aronson reports research grants via Brigham and Women’s Hospital from Better Therapeutics, Boehringer Ingelheim, and NovoNordisk; via Mass General Brigham from the National Institutes of Health; and consulting for Nest Genomics. Drs Noone and Robar and E. Zacherle are employees of Novo Nordisk. Dr Plutzky reports grant support from Boehringer Ingelheim; and consulting for Janssen and Novo Nordisk. Dr Gaziano reports grant support from the National Institutes of Health and Novartis; and consulting for Novartis, Multiply Labs, Amgen, DalCor, and Dimagi. Dr Cannon reports research grants from Amgen, Better Therapeutics, Boehringer Ingelheim, Daiichi Sankyo, Merck, Novo Nordisk, and Pfizer; and consulting for Amryt/Chiesi, Alnylam, Amarin, Amgen, Applied Therapeutics, Ascendia, Biogen, Boehringer Ingelheim, Bristol Myers-Squibb, CSL Behring, Eli Lilly, Janssen, Lexicon, Merck, Milestone, Pfizer, Rhoshan, and Sanofi. Dr Wexler reports participating in the data monitoring committee for Novo Nordisk; and is Co-Investigator (Putman, Principal Investigator) of Vertex VX22-264-101 Study at the Diabetes Research Center. Dr Scirica reports research grants via Brigham and Women’s Hospital from Amgen, Better Therapeutics, Boehringer Ingelheim, Merck, NovoNordisk, and Pfizer; consulting for Abbvie (Data Safety Monitoring Board [DSMB]), AstraZeneca (DSMB), Bayer, Boehringer Ingelheim, Better Therapeutics, Bristol Myers-Squibb, Elsevier Practice Update Cardiology, Esperion, Hanmi (DSMB), Lexeo (DSMB), Lexicon, and NovoNordisk; and equity in Doximity and Health [at] Scale. The other authors report no disclosures.