Real-World Comparison of Oral Versus Injectable Semaglutide for the Reduction of Hemoglobin A1C and Weight in Patients with Type 2 Diabetes.

IF 1.1 Q4 PHARMACOLOGY & PHARMACY
Maria Pinto, Lillian Brennan, Katie Diehl, Shally Lin, Samantha Heacock
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引用次数: 0

Abstract

Background: No head-to-head comparisons of semaglutide formulations currently exist in the literature. In practice, many may think that oral and injectable semaglutide formulations are interchangeable, although there is currently limited real-world data to determine whether this is accurate.

Objective: The purpose of this study was to determine the effect of oral versus injectable semaglutide on hemoglobin A1C (HbA1C) and weight in patients with type 2 diabetes (T2D).

Methods: This was a retrospective single-center review of adult patients who had a diagnosis of T2D and were treated with oral or injectable semaglutide between November 1, 2019, and July 31, 2022. Primary outcome was a comparison of changes in HbA1C (%) and weight (kg) from baseline to 6 months between patients receiving oral versus injectable semaglutide, stratified according to highest dose received. Secondary outcomes included frequency of dose reductions and discontinuations, achievement of clinical goals, and presence of an embedded clinical pharmacist at patients' primary care office.

Results: A total of 105 patients were included. Patients experienced mean decreases in HbA1C and weight from baseline to 6 months of -1.75% (P < 0.001) and -3.64 kg (P = 0.015), respectively, in the oral semaglutide group and -1.35% (P < 0.001) and -5.26 kg (P < 0.001), respectively, in the injectable semaglutide group. When directly comparing semaglutide formulations, oral semaglutide demonstrated a 0.4% greater numerical reduction in HbA1C (P = 0.523) and injectable semaglutide demonstrated a 1.62-kg greater numerical reduction in weight (P = 0.312). Adverse events (AEs) occurred more frequently with oral semaglutide than with injectable semaglutide (16.7% vs 4.9%). Discontinuation due to AEs was more common with oral semaglutide.

Conclusion: In this study, patients with T2D who received oral semaglutide demonstrated greater reductions in HbA1C, whereas those treated with injectable semaglutide had greater reductions in weight, although there were no statistically significant reductions in HbA1C or weight between the 2 formulations. Rates of AEs and discontinuation were more common in the oral semaglutide group.

口服塞马鲁肽与注射塞马鲁肽在降低 2 型糖尿病患者血红蛋白 A1C 和体重方面的真实世界比较。
背景:目前尚无文献对塞马鲁肽制剂进行头对头比较。在实践中,许多人可能会认为口服和注射的塞马鲁肽制剂是可以互换的,尽管目前只有有限的实际数据来确定这种说法是否准确:本研究旨在确定口服与注射塞马鲁肽对 2 型糖尿病(T2D)患者血红蛋白 A1C(HbA1C)和体重的影响:这是对2019年11月1日至2022年7月31日期间确诊为T2D并接受口服或注射塞马鲁肽治疗的成年患者进行的回顾性单中心研究。主要结果是比较接受口服与注射塞马鲁肽治疗的患者从基线到6个月的HbA1C(%)和体重(kg)变化,根据接受的最高剂量进行分层。次要结果包括减量和停药频率、临床目标的实现情况以及在患者的初级保健诊所派驻临床药师的情况:结果:共纳入 105 名患者。从基线到6个月期间,口服塞马鲁肽组患者的HbA1C和体重平均降幅分别为-1.75%(P < 0.001)和-3.64 kg(P = 0.015),注射塞马鲁肽组患者的HbA1C和体重平均降幅分别为-1.35%(P < 0.001)和-5.26 kg(P < 0.001)。如果直接比较两种塞马鲁肽配方,口服塞马鲁肽的HbA1C数值降低幅度比注射塞马鲁肽大0.4%(P = 0.523),体重数值降低幅度比注射塞马鲁肽大1.62公斤(P = 0.312)。口服塞马鲁肽发生不良事件(AE)的频率高于注射塞马鲁肽(16.7% vs 4.9%)。因不良反应而停药的情况在口服塞马鲁肽中更为常见:在这项研究中,接受口服塞马鲁肽治疗的T2D患者的HbA1C降低幅度更大,而接受注射塞马鲁肽治疗的患者的体重降低幅度更大,尽管两种制剂之间的HbA1C或体重降低幅度没有统计学意义。口服塞马鲁肽组的不良反应率和停药率更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Pharmacy Technology
Journal of Pharmacy Technology PHARMACOLOGY & PHARMACY-
CiteScore
1.50
自引率
0.00%
发文量
49
期刊介绍: For both pharmacists and technicians, jPT provides valuable information for those interested in the entire body of pharmacy practice. jPT covers new drugs, products, and equipment; therapeutic trends; organizational, legal, and educational activities; drug distribution and administration; and includes continuing education articles.
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