Shao Hui, Fonseca Vivian, Furman Roy, Meneghini Luigi, Shi Lizheng
Department of Pharmaceutical Outcomes and Policy, College of Pharmacy, University of Florida, Gainesville, FL.
Department of Medicine and Pharmacology, School of Medicine, Tulane University, New Orleans, LA
Diabetes Care. 2020 Nov;43(11):2847-2852. doi: 10.2337/dc20-0465. Epub 2020 Sep 4.
We successfully implemented the American Diabetes Association's (ADA) Diabetes INSIDE (INspiring System Improvement with Data-Driven Excellence) quality improvement (QI) program at a university hospital and safety-net health system (Tulane and Parkland), focused on system-wide improvement in poorly controlled type 2 diabetes (HbA >8.0% [64 mmol/mol]). In this study, we estimated the 5-year risk reduction in complications and mortality associated with the QI program.
The QI implementation period was 1 year, followed by the postintervention period of 6 months to evaluate the impact of QI on clinical measures. We measured the differences between the baseline and postintervention clinical outcomes in 2,429 individuals with HbA >8% (64 mmol/mol) at baseline and used the Building, Relating, Assessing, and Validating Outcomes (BRAVO) diabetes model to project the 5-year risk reduction of diabetes-related complications under the assumption that intervention benefits persist over time. An alternative assumption that intervention benefits diminish by 30% every year was also tested.
The QI program was associated with reductions in HbA (-0.84%) and LDL cholesterol (LDL-C) (-5.94 mg/dL) among individuals with HbA level >8.0% (64 mmol/mol), with greater reduction in HbA (-1.67%) and LDL-C (-6.81 mg/dL) among those with HbA level >9.5% at baseline (all < 0.05). The implementation of the Diabetes INSIDE QI program was associated with 5-year risk reductions in major adverse cardiovascular events (MACE) (relative risk [RR] 0.78 [95% CI 0.75-0.81]) and all-cause mortality (RR 0.83 [95% CI 0.82-0.85]) among individuals with baseline HbA level >8.0% (64 mmol/mol), and MACE (RR 0.60 [95% CI 0.56-0.65]) and all-cause mortality (RR 0.61 [95% CI 0.59-0.64]) among individuals with baseline HbA level >9.5% (80 mmol/mol). Sensitivity analysis also identified a substantially lower risk of diabetes-related complications and mortality associated with the QI program.
Our modeling results suggest that the ADA's Diabetes INSIDE QI program would benefit the patients and population by substantially reducing the 5-year risk of complications and mortality in individuals with diabetes.
我们在一家大学医院和安全网医疗系统(杜兰大学和帕克兰医院)成功实施了美国糖尿病协会(ADA)的糖尿病内部质量改进(QI)项目(通过数据驱动的卓越表现激发系统改进),该项目聚焦于改善控制不佳的2型糖尿病(糖化血红蛋白[HbA]>8.0%[64 mmol/mol])的全系统情况。在本研究中,我们估计了该QI项目在5年内降低并发症和死亡率的风险。
QI实施期为1年,随后是6个月的干预后期,以评估QI对临床指标的影响。我们测量了2429例基线时HbA>8%(64 mmol/mol)的个体在基线和干预后的临床结局差异,并使用构建、关联、评估和验证结局(BRAVO)糖尿病模型,在干预效益随时间持续存在的假设下,预测糖尿病相关并发症5年风险的降低情况。还测试了另一种假设,即干预效益每年递减30%。
在HbA水平>8.0%(64 mmol/mol)的个体中,QI项目与HbA(-0.84%)和低密度脂蛋白胆固醇(LDL-C)(-5.94 mg/dL)的降低相关,在基线时HbA水平>9.5%的个体中,HbA(-1.67%)和LDL-C(-6.81 mg/dL)降低幅度更大(均P<0.05)。糖尿病内部QI项目的实施与基线HbA水平>8.0%(64 mmol/mol)的个体5年主要不良心血管事件(MACE)风险降低(相对风险[RR]0.78[95%CI 0.75-0.81])和全因死亡率降低(RR 0.83[95%CI 0.82-0.85])相关,与基线HbA水平>9.5%(80 mmol/mol)的个体MACE(RR 0.60[95%CI 0.56-0.65])和全因死亡率降低(RR 0.61[95%CI 0.59-0.64])相关。敏感性分析还发现与QI项目相关的糖尿病相关并发症和死亡率风险显著降低。
我们的模型结果表明,ADA的糖尿病内部QI项目将通过大幅降低糖尿病患者5年的并发症和死亡风险,使患者和人群受益。