混合闭环(HCL)胰岛素输送系统阳性预期的差异不能解释HCL使用的种族差异

IF 4.2 Q1 ENDOCRINOLOGY & METABOLISM Journal of Clinical and Translational Endocrinology Pub Date : 2023-06-01 DOI:10.1016/j.jcte.2023.100319
Jody B. Grundman , Amanda Perkins , Maureen Monaghan , Seema Meighan , Randi Streisand , Brynn E. Marks
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引用次数: 1

摘要

目的混合闭环(HCL)胰岛素输送系统可改善1型糖尿病(T1D)青年的血糖和生活质量,但在使用中存在不公平现象。我们旨在评估HCL系统阳性预期的差异是否可以解释使用差异。方法15名血红蛋白A1C(HbA1c)≥10%的公共保险非西班牙裔黑人(NHB)青年参加了一项研究,探讨在使用Control IQ技术的Tandem t:slim X2胰岛素泵6个月期间血糖和个人报告结果(PRO)的变化。在基线时,青少年和父母完成了PROs,包括评估HCL使用积极预期的胰岛素输送系统:感知、想法、反思和期望(INSPIRE)调查,以及评估糖尿病相关痛苦的糖尿病问题领域(PAID)调查。评估了该队列与串联控制IQ儿科关键试验(DCLP5)队列之间的差异。结果与DCLP5队列(0%NHB,10%公共保险)相比,基线血糖指标次优(MHbA1c 11.9±1.4%vs 7.6±0.9%,p<0.0001;连续血糖监测(CGM)时间高于范围>;180 mg/dL 82±15%vs 45±18%;0.0001)。与DCLP5队列相比,两个队列中的INSPIRE得分在青年(80±10 vs 77±13,p=0.41)和父母(88±14 vs 85±11,p=0.37)中同样高。PAID得分在父母中更高(68±19 vs 43±16,p<;0.0001),但在历史边缘化队列中青年(43±16 vs 35±16,p=0.09)除外。结论尽管血糖控制和糖尿病相关负担存在差异,但在历史上处于边缘地位的T1D青年和以非西班牙裔白人为主的私人保险DCLP5队列中,HCL系统的阳性预期具有可比性。这些发现表明,对HCL技术的认知差异可能无法解释使用中的不公平现象。
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Differences in positive expectancy of hybrid closed loop (HCL) insulin delivery systems do not explain racial differences in HCL use

Aims

Hybrid closed loop (HCL) insulin delivery systems improve glycemia and quality of life among youth with type 1 diabetes (T1D), however there are inequities in use. We aimed to evaluate whether differences in positive expectancy of HCL systems may explain differences in use.

Methods

Fifteen publicly-insured, non-Hispanic Black (NHB) youth with hemoglobin A1C (HbA1c) ≥ 10% enrolled in a study exploring changes in glycemia and person reported outcomes (PRO) during 6 months of Tandem t:slim X2 insulin pump with Control-IQ technology. At baseline youth and parents completed PROs, including Insulin Delivery Systems: Perceptions, Ideas, Reflections and Expectations (INSPIRE) survey assessing positive expectancy of HCL use, and Problem Areas in Diabetes (PAID) survey assessing diabetes-related distress. Differences between this cohort and the Tandem Control-IQ pediatric pivotal trial (DCLP5) cohort were assessed.

Results

As compared to the DCLP5 cohort (0% NHB, 10% publicly-insured), baseline glycemic indicators were suboptimal (MHbA1c 11.9 ± 1.4% vs 7.6 ± 0.9%, p < 0.0001; continuous glucose monitor (CGM) time-above-range > 180 mg/dL 82 ± 15% vs 45 ± 18%, p < 0.0001). INSPIRE scores in both cohorts were equally high among youth (80 ± 10 vs 77 ± 13, p = 0.41) and parents (88 ± 14 vs 85 ± 11, p = 0.37). PAID scores were higher among parents (68 ± 19 vs 43 ± 16, p < 0.0001), but not youth (43 ± 16 vs 35 ± 16, p = 0.09) in the historically marginalized cohort as compared to the DCLP5 cohort.

Conclusions

Despite differences in glycemic control and diabetes related burden, positive expectancy of HCL systems is comparable among historically marginalized youth with T1D and the predominantly non-Hispanic White, privately insured DCLP5 cohort. These findings suggest that differences in perceptions of HCL technology may not explain inequities in use.

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24
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16 weeks
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