Randomized Evaluation of a Remote Management Program to Improve Guideline-Directed Medical Therapy: The DRIVE Trial

被引:7
作者
Blood, Alexander J. [1 ,2 ,3 ,7 ]
Chang, Lee-Shing [4 ,7 ]
Hassan, Shahzad [2 ,3 ]
Chasse, Jacqueline [2 ,3 ]
Stern, Gretchen [2 ]
Gabovitch, Daniel [2 ]
Zelle, David [2 ]
Colling, Caitlin [7 ]
Aronson, Samuel J. [2 ,5 ]
Figueroa, Christian [2 ]
Collins, Emma [2 ]
Ruggiero, Ryan [2 ]
Zacherle, Emily [8 ]
Noone, Joshua [8 ]
Robar, Carey [8 ]
Plutzky, Jorge [2 ,3 ,7 ]
Gaziano, Thomas A. [2 ,3 ,7 ]
Cannon, Christopher P. [2 ,3 ,6 ,7 ]
Wexler, Deborah J. [6 ,7 ]
Scirica, Benjamin M. [1 ,2 ,3 ,7 ]
机构
[1] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Accelerator Clin Transformat, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Div Cardiovasc Med, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Endocrinol Diabet & Hypertens, Boston, MA 02115 USA
[5] Mass Gen Brigham, Personalized Med, Cambridge, MA USA
[6] Massachusetts Gen Hosp, Diabet Ctr, Boston, MA USA
[7] Harvard Med Sch, Boston, MA 02115 USA
[8] Novo Nordisk Inc, Plainsboro, NJ USA
关键词
cardiovascular diseases; diabetes mellitus; type; 2; drug therapy; glucagon-like peptide receptors; sodium-glucose transport proteins; telemedicine; COST;
D O I
10.1161/CIRCULATIONAHA.124.069494
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:1802 / 1811
页数:10
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