Glucagon-like peptide-1 receptor agonists and upper endoscopy: a real-world experience

被引:1
|
作者
Jirapinyo, Pichamol [1 ,2 ]
Siranart, Noppachai [1 ]
Thompson, Christopher C. [1 ,2 ]
机构
[1] Brigham & Womens Hosp, Div Gastroenterol Hepatol & Endoscopy, Boston, MA USA
[2] Harvard Med Sch, Boston, MA USA
关键词
D O I
10.1002/oby.24190
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ObjectiveIncreased use of glucagon-like peptide-1 receptor agonists (GLP-1RAs) has raised safety concerns during endoscopy due to their mechanism of delaying gastric emptying. This study aims to evaluate the impact of GLP-1RAs on technical success and safety of esophagogastroduodenoscopy (EGD).MethodsThis was a retrospective study of bariatric patients who underwent EGD between January 2022 and December 2023. Only patients on GLP-1RAs were included and were categorized into those who held GLP-1RAs prior to EGD (GLP-HELD group) and those who did not (GLP-CONTINUED group). The primary outcome was technical success, defined as completion of EGD without interruption. Secondary outcomes included the presence of residual gastric contents during EGD and aspiration rates.ResultsA total of 629 patients were included. Baseline age and BMI were mean (SD) 54.9 (13.0) years and 37.3 (8.0) kg/m2, respectively. Of 629 patients, 146 (23%) were in the GLP-HELD group, and 483 (77%) were in the GLP-CONTINUED group. For the primary outcome, rates of early termination of EGD were similar between groups (1.4% for GLP-CONTINUED vs. 0% for GLP-HELD; p = 0.36). For secondary outcomes, incidence of residual gastric contents was similar between groups (6.4% for GLP-CONTINUED vs. 2.7% for GLP-HELD; p = 0.09). There were no aspiration events in either group.ConclusionsContinuation of GLP-1RAs did not appear to be associated with an increased incidence of residual gastric contents, early procedural termination, or aspiration events.
引用
收藏
页码:250 / 256
页数:7
相关论文
共 50 条
  • [41] Is Glucagon-like peptide-1 for real?
    Murr, Michel M.
    SURGERY FOR OBESITY AND RELATED DISEASES, 2014, 10 (05) : 786 - 786
  • [42] Hydrocarbon-Stitched Peptide Agonists of Glucagon-Like Peptide-1 Receptor
    Bird, Gregory H.
    Fu, Accalia
    Escudero, Silvia
    Godes, Marina
    Opoku-Nsiah, Kwadwo
    Wales, Thomas E.
    Cameron, Michael D.
    Engen, John R.
    Danial, Nika N.
    Walensky, Loren D.
    ACS CHEMICAL BIOLOGY, 2020, 15 (06) : 1340 - 1348
  • [43] Effects of gastric inhibitory polypeptide, glucagon-like peptide-1 and glucagon-like peptide-1 receptor agonists on Bone Cell Metabolism
    Hansen, Morten S. S.
    Tencerova, Michaela
    Frolich, Jacob
    Kassem, Moustapha
    Frost, Morten
    BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2018, 122 (01) : 25 - 37
  • [44] Glucagon-like peptide-1 receptor
    Krashes, Michael
    CURRENT BIOLOGY, 2024, 34 (23) : R1163 - R1164
  • [45] Glucagon-like peptide-1 receptor agonists during pregnancy and lactation
    Zipursky, Jonathan S.
    Bogler, Tali
    Maxwell, Cynthia
    CANADIAN MEDICAL ASSOCIATION JOURNAL, 2024, 196 (43) : E1413 - E1413
  • [46] Glucagon-like peptide-1 receptor agonists and safety in the preconception period
    Minis, Evelyn
    Stanford, Fatima Cody
    Mahalingaiah, Shruthi
    CURRENT OPINION IN ENDOCRINOLOGY DIABETES AND OBESITY, 2023, 30 (06) : 273 - 279
  • [47] Synthesis and biological evaluation of glucagon-like peptide-1 receptor agonists
    Zhang, Yu-Juan
    Shen, Liu-Lan
    Cheon, Hyae-Gyeong
    Xu, Yong-Nan
    Jeong, Jin-Hyun
    ARCHIVES OF PHARMACAL RESEARCH, 2014, 37 (05) : 588 - 599
  • [48] Online Advertising of Compounded Glucagon-Like Peptide-1 Receptor Agonists
    Chetty, Ashwin K.
    Chillakanti, Mahima
    Ramachandran, Reshma
    Ross, Joseph S.
    Chen, Alissa S.
    JAMA HEALTH FORUM, 2025, 6 (01):
  • [49] Glucagon-like peptide-1 receptor agonists and risk of breast cancer
    Bolen, Shari D.
    Maruthur, Nisa M.
    BMJ-BRITISH MEDICAL JOURNAL, 2016, 355
  • [50] Glucagon-Like Peptide-1 Receptor Agonists and Strategies To Improve Their Efficiency
    Alavi, Seyed Ebrahim
    Cabot, Peter J.
    Moyle, Peter M.
    MOLECULAR PHARMACEUTICS, 2019, 16 (06) : 2278 - 2295