Impact of Liraglutide to Semaglutide Conversion on Glycemic Control and Cost Savings at a Veterans Affairs Medical Center.

Maiah Hardin, Fiona Adanse, Chandler Schexnayder, Janeca Malveaux, Sylvester Agbahiwe
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Abstract

Background: Semaglutide and liraglutide are glucagon-like peptide 1 receptor agonists (GLP-1 RAs) approved by the US Food and Drug Administration for patients with type II diabetes mellitus (T2DM). Patients with T2DM treated with liraglutide at the Michael E. DeBakey Veterans Affairs Medical Center (MEDVAMC) were converted to semaglutide. The primary objective was to assess changes in glycemic control and cost savings that resulted from this conversion.

Methods: We conducted a retrospective chart review of veterans without retinopathy treated at MEDVAMC between March 1, 2021, and November 30, 2021, who were converted from liraglutide 0.6 mg and 1.2 mg daily to semaglutide 0.25 mg weekly (titrated to 0.5 mg weekly after 4 weeks). We compared hemoglobin A1c (HbA1c) values at baseline and 3 to 12 months following conversion to assess glycemic control. Cost savings were evaluated using outpatient pharmacy data.

Results: During the study, 411 patients were converted from liraglutide to semaglutide; 49 additional patients met the criteria for clinician education, and 14 were converted as a result. In total, 304 patients met the criteria for inclusion. At baseline, patients' mean (SD) levels included: HbA1c, 8.1% (1.5); blood glucose, 187.4 (44.2) mg/dL; and body weight, 112.9 (23.0) kg. Three to 12 months postconversion, patients' mean (SD) HbA1c significantly decreased to 7.6% (1.4) (P < .001), blood glucose decreased to 172.6 (39.0) mg/dL (P < .001), and body weight decreased to 105.2 (32.3) kg (P < .001). Cost savings exceeding $400,000 resulted from liraglutide to semaglutide conversion.

Conclusions: Conversion of liraglutide to semaglutide led to significant HbA1c decrease and weight loss and resulted in minimal changes to patients' antihyperglycemic regimen. Common adverse effects included hypoglycemia and gastrointestinal intolerance. Due to the low conversion rate of liraglutide to semaglutide following education, a more effective method of education for clinicians to promote teleretinal imaging before conversion is warranted. Lastly, although the semaglutide cost savings initiative at MEDVAMC resulted in significant savings for the institution, a full cost-effective analysis is needed for further conclusion.

退伍军人事务医疗中心将利拉鲁肽转换为赛马鲁肽对血糖控制和成本节约的影响。
背景:塞马鲁肽和利拉鲁肽是美国食品和药物管理局批准用于治疗II型糖尿病(T2DM)患者的胰高血糖素样肽1受体激动剂(GLP-1 RAs)。Michael E. DeBakey退伍军人事务医疗中心(MEDVAMC)接受利拉鲁肽治疗的T2DM患者转用了赛马鲁肽。主要目的是评估血糖控制的变化以及转换后节省的成本:我们对 2021 年 3 月 1 日至 2021 年 11 月 30 日期间在 MEDVAMC 接受治疗的无视网膜病变的退伍军人进行了回顾性病历审查,他们从每天服用利拉鲁肽 0.6 毫克和 1.2 毫克转为每周服用塞马鲁肽 0.25 毫克(4 周后滴定为每周服用 0.5 毫克)。我们比较了基线和转换后 3 至 12 个月的血红蛋白 A1c (HbA1c) 值,以评估血糖控制情况。我们还利用门诊药房数据对成本节约情况进行了评估:研究期间,411 名患者从利拉鲁肽转为塞马鲁肽;另外 49 名患者符合临床医生教育标准,14 名患者因此转为塞马鲁肽。共有 304 名患者符合纳入标准。基线时,患者的平均(标度)水平包括HbA1c,8.1% (1.5);血糖,187.4 (44.2) mg/dL;体重,112.9 (23.0) kg。转换后 3 至 12 个月,患者的平均(标清)HbA1c 显著降至 7.6% (1.4) (P < .001),血糖降至 172.6 (39.0) mg/dL (P < .001),体重降至 105.2 (32.3) kg (P < .001)。将利拉鲁肽转换为塞马鲁肽可节省超过40万美元的成本:结论:将利拉鲁肽转换为塞马鲁肽可显著降低 HbA1c 和减轻体重,对患者降糖治疗方案的改变极小。常见的不良反应包括低血糖和胃肠道不耐受。由于利拉鲁肽在接受教育后转换为塞马鲁肽的比例较低,因此有必要为临床医生提供更有效的教育方法,在转换前推广远程视网膜成像。最后,虽然 MEDVAMC 的semaglutide 成本节约计划为该机构节省了大量成本,但仍需进行全面的成本效益分析才能得出进一步结论。
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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