Clinical and Experimental Endocrinology, KU Leuven, Leuven, Belgium.
Department of Endocrinology, University Hospitals Leuven, Leuven, Belgium.
Diabetes Care. 2024 Nov 1;47(11):2002-2011. doi: 10.2337/dc24-1320.
To determine efficacy and safety of intrapartum and early postpartum advanced hybrid closed-loop (AHCL) therapy compared with standard insulin therapy in pregnant women with type 1 diabetes (T1D).
CRISTAL was a double-arm, open-label, randomized controlled trial performed in Belgium and the Netherlands that assigned 95 pregnant participants with T1D 1:1 to a MiniMed 780G AHCL system (n = 46) or standard insulin therapy (n = 49). This prespecified, secondary observational analysis focused on differences in glycemic control and safety outcomes between participants from the original AHCL group who continued AHCL intrapartum (n = 27) and/or early postpartum (n = 37, until hospital discharge) and those from the original standard insulin therapy group using standard insulin therapy intrapartum (n = 45) and/or early postpartum (n = 34).
Of the 43 and 46 participants in the AHCL and standard insulin therapy groups, respectively, completing the trial, 27 (62.8%) in the AHCL group continued AHCL and 45 in the standard insulin therapy group (97.8%) continued standard insulin therapy intrapartum. Compared with standard insulin therapy, intrapartum AHCL was associated with more time in range 3.5-7.8 mmol/L (71.5 ± 17.7% vs. 63.1 ± 17.0%, P = 0.030) and numerically lower time above range >7.8 mmol/L (27.3 ± 17.4% vs. 35.3 ± 17.5%, P = 0.054), without increases in time below range <3.5 mmol/L (1.1 ± 2.4% vs. 1.5 ± 2.3%, P = 0.146). Early postpartum, 37 (86.0%) participants randomized to AHCL continued AHCL, with a median increase in insulin-to-carbohydrate ratios of 67% (interquartile range -14 to 126). Similar tight glycemic control (3.9-10.0 mmol/L: 86.8 ± 6.7% vs. 83.8 ± 8.1%, P = 0.124) was observed with AHCL versus standard insulin therapy. No severe hypoglycemia or diabetic ketoacidosis was reported in either group.
AHCL is effective in maintaining tight glycemic control intrapartum and early postpartum and can be safely continued during periods of rapidly changing insulin requirements.
比较经阴道分娩和产后早期应用强化混合闭环(AHCL)治疗与标准胰岛素治疗对 1 型糖尿病(T1D)孕妇的疗效和安全性。
CRISTAL 是一项在比利时和荷兰进行的双臂、开放标签、随机对照试验,将 95 名 T1D 孕妇按 1:1 随机分配至 MiniMed 780G AHCL 系统(n=46)或标准胰岛素治疗组(n=49)。本预设的二次观察性分析主要关注 AHCL 组中继续经阴道分娩(n=27)和/或产后早期(n=37,直至出院)的参与者(n=27)与继续使用标准胰岛素治疗组(n=45)和/或产后早期(n=34)的参与者之间在血糖控制和安全性结局方面的差异。
在分别完成试验的 43 名和 46 名 AHCL 组和标准胰岛素治疗组参与者中,27 名(62.8%)AHCL 组继续接受 AHCL,45 名标准胰岛素治疗组(97.8%)继续接受经阴道分娩的标准胰岛素治疗。与标准胰岛素治疗相比,经阴道分娩期间的 AHCL 治疗与更多的 3.5-7.8mmol/L 时间范围(71.5±17.7% vs. 63.1±17.0%,P=0.030)和更低的 7.8mmol/L 以上时间范围(27.3±17.4% vs. 35.3±17.5%,P=0.054)相关,而 3.5mmol/L 以下时间范围(1.1±2.4% vs. 1.5±2.3%,P=0.146)无增加。产后早期,37 名(86.0%)随机分配至 AHCL 组的参与者继续接受 AHCL,胰岛素与碳水化合物比值中位数增加 67%(四分位距-14 至 126)。同样,AHCL 组与标准胰岛素治疗组的血糖控制也相似(3.9-10.0mmol/L:86.8±6.7% vs. 83.8±8.1%,P=0.124)。两组均未报告严重低血糖或糖尿病酮症酸中毒。
AHCL 可有效维持经阴道分娩和产后早期的严格血糖控制,并可在胰岛素需求快速变化期间安全持续使用。