The Diabetes Staging System (DSS): A Pilot Study Assessing Feasibility, Provider Engagement and Implementation Challenges of a Novel Staging System for Type 2 Diabetes.

IF 3 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Moahad S Dar, Junhong Zhang, Anna Ashline, Swetha Kota, Sandra Woolson, Nadya T Majette, Hayden B Bosworth
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引用次数: 0

Abstract

Introduction and objective: Type 2 diabetes (DM2) currently lacks a standardized staging system that can be used to predict survival and guide providers towards guideline concordant care much like TNM staging does for cancer. We conducted a pilot study to assess the feasibility, provider engagement and implementation challenges of the DSS and examined if guideline concordant care improved especially SGLT2i/GLP-1a use in Veterans DM2 patients with cardiorenal disease.

Methods: A 6-month pilot study implemented DSS in VA primary care clinics between December 2023-September 2024. Study visits were at baseline and 6 months. Primary outcome: the initiation of SGLT2i/GLP-1a in Veteran DM2 patients with CVD/CKD compared to baseline. Secondary outcomes: weight, blood pressure, hemoglobin A1C, glomerular filtration rate (GFR), and medication adherence compared to baseline. Inclusion criteria: Male or female Veterans between the ages of 18-75 years with DM2 and ≥1 CV event and/or CKD and not on SGLT2i/GLP-1a. Exclusion criteria: Veterans with contraindications to SGLT2i/GLP-1 and/or a serious mental health disorder.

Results: After baseline visit, all providers prescribed to 14/14 patients at least one of the medications with 12/14 prescribed SGLT2i and 2/14 prescribed GLP-1a. We found 13/14 (93%) patients to still be on at least one of the medications at 6 months. At 6 months compared to baseline, weight (216 lbs. ± 41 → 213 lbs. ± 39), blood pressure (141/76 ± 20/10 → 132/73 ± 17/10), A1C (7.7% ± 1.5% → 7.4% ± 0.8%) modestly decreased but GFR remained stable (64 mL/min ± 17 → 64 mL/min ± 19). Medication adherence was continued for all 13 patients (Medication possession ratio was ≥80%).

Conclusion: DSS use was associated with increased SGLT2i/GLP-1a prescribing by VA primary care providers and medication adherence in Veterans DM2 patients with CVD/CKD. The DSS could help improve cardiorenal outcomes and guideline concordant in their DM2 patients in the future if larger studies can validate these findings.

Clinical trials registration number: NCT06142006.

糖尿病分期系统(DSS):一项评估2型糖尿病新型分期系统可行性、提供者参与和实施挑战的试点研究。
简介和目的:2型糖尿病(DM2)目前缺乏一个标准化的分期系统,该系统可用于预测生存,并指导提供者进行指导一致的护理,就像癌症的TNM分期一样。我们进行了一项试点研究,以评估DSS的可行性、提供者参与和实施挑战,并检查指南一致性护理是否改善,特别是SGLT2i/GLP-1a在退伍军人DM2心肾疾病患者中的使用。方法:在2023年12月至2024年9月期间,在VA初级保健诊所实施了为期6个月的DSS试点研究。研究访问分别在基线和6个月。主要结局:与基线相比,退伍军人DM2合并CVD/CKD患者中SGLT2i/GLP-1a的起始。次要结局:与基线相比,体重、血压、血红蛋白A1C、肾小球滤过率(GFR)和药物依从性。纳入标准:年龄在18-75岁之间的男性或女性退伍军人,患有DM2和≥1 CV事件和/或CKD,未服用SGLT2i/GLP-1a。排除标准:有SGLT2i/GLP-1禁忌症和/或严重精神健康障碍的退伍军人。结果:基线访问后,所有提供者给14/14的患者开了至少一种药物,其中12/14的患者开了SGLT2i, 2/14的患者开了GLP-1a。我们发现13/14(93%)的患者在6个月时仍在服用至少一种药物。6个月后,与基线相比,体重(216磅)。±41→213磅血压(141/76±20/10→132/73±17/10)、A1C(7.7%±1.5%→7.4%±0.8%)轻度下降,GFR保持稳定(64 mL/min±17→64 mL/min±19)。13例患者均坚持服药(药物持有率≥80%)。结论:DSS的使用与退伍军人DM2合并CVD/CKD患者的SGLT2i/GLP-1a处方增加和药物依从性相关。如果更大规模的研究可以验证这些发现,DSS可以帮助改善DM2患者的心肾结局和指南一致性。临床试验注册号:NCT06142006。
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来源期刊
Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy
Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
5.90
自引率
6.10%
发文量
431
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal. The journal is committed to the rapid publication of the latest laboratory and clinical findings in the fields of diabetes, metabolic syndrome and obesity research. Original research, review, case reports, hypothesis formation, expert opinion and commentaries are all considered for publication.
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