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A Comprehensive Analysis of Reported Adverse Events and Device Failures Associated with Esophageal Self-Expandable Metal Stents: An FDA MAUDE Database Study

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Al-Azhar University – Gaza
Jaber F.; Alsakarneh S.; Alsharaeh T.; Salahat A.-J.; Jaber M.; Mohamed I.; Gangwani M.K.; Aldiabat M.; Kilani Y.; Ahmed M.; Madi M.; Numan L.; Bazarbashi A.N.
Jaber, Fouad (57927659200); Alsakarneh, Saqr (57919358400); Alsharaeh, Tala (58791721900); Salahat, Ahmed-Jordan (58791133800); Jaber, Mohammad (58774780400); Mohamed, Islam (58299799300); Gangwani, Manesh Kumar (57196117639); Aldiabat, Mohammad (57218678146); Kilani, Yassine (57556786600); Ahmed, Mohamed (57226385509); Madi, Mahmoud (57209181750); Numan, Laith (57211013456); Bazarbashi, Ahmad Najdat (57203949950)
57927659200; 57919358400; 58791721900; 58791133800; 58774780400; 58299799300; 57196117639; 57218678146; 57556786600; 57226385509; 57209181750; 57211013456; 57203949950
2024
Digestive Diseases and Sciences
A Comprehensive Analysis of Reported Adverse Events and Device Failures Associated with Esophageal Self-Expandable Metal Stents: An FDA MAUDE Database Study
69
8
2765
2774
Springer
Department of Internal Medicine, University of Missouri Kansas City, Kansas City, MO, United States; Department of Medical Education, Faculty of Medicine, The University of Jordan, Amman, Jordan; Department of Medical Education, Faculty of Medicine, Al-Azhar University, Gaza, Palestine; Department of Internal Medicine, University of Toledo, Toledo, OH, United States; Department of Internal Medicine, Washington University in St. Louis, St. Louis, MO, United States; Department of Epidemiology, Harvard School of Public Health, Boston, MA, United States; Department of Internal Medicine, NYC Health + Hospitals | Lincoln - Weill Cornell Medical College, Bronx, NY, United States; Division of Gastroenterology and Hepatology, Saint Louis University School of Medicine, St. Louis, MO, United States; Division of Gastroenterology and Hepatology, Washington University, St. Louis, MO, United States; Division of Gastroenterology and hepatology, University of Missouri-Kansas City, Kansas City, MO, United States
Jaber F., Department of Internal Medicine, University of Missouri Kansas City, Kansas City, MO, United States; Alsakarneh S., Department of Internal Medicine, University of Missouri Kansas City, Kansas City, MO, United States; Alsharaeh T., Department of Medical Education, Faculty of Medicine, The University of Jordan, Amman, Jordan; Salahat A.-J., Department of Medical Education, Faculty of Medicine, The University of Jordan, Amman, Jordan; Jaber M., Department of Medical Education, Faculty of Medicine, Al-Azhar University, Gaza, Palestine; Mohamed I., Department of Internal Medicine, University of Missouri Kansas City, Kansas City, MO, United States; Gangwani M.K., Department of Internal Medicine, University of Toledo, Toledo, OH, United States; Aldiabat M., Department of Internal Medicine, Washington University in St. Louis, St. Louis, MO, United States, Department of Epidemiology, Harvard School of Public Health, Boston, MA, United States; Kilani Y., Department of Internal Medicine, NYC Health + Hospitals | Lincoln - Weill Cornell Medical College, Bronx, NY, United States; Ahmed M., Division of Gastroenterology and hepatology, University of Missouri-Kansas City, Kansas City, MO, United States; Madi M., Division of Gastroenterology and Hepatology, Saint Louis University School of Medicine, St. Louis, MO, United States; Numan L., Division of Gastroenterology and Hepatology, Saint Louis University School of Medicine, St. Louis, MO, United States; Bazarbashi A.N., Division of Gastroenterology and Hepatology, Washington University, St. Louis, MO, United States
F. Jaber; Department of Internal Medicine, University of Missouri Kansas City, Kansas City, United States; email: fouad.jaber.md@gmail.com
4
10.1007/s10620-024-08483-w
Adverse events; Esophageal stents; FDA MAUDE database; MAUDE; Post-market surveillance; SEMS
Databases, Factual; Esophageal Stenosis; Humans; Product Surveillance, Postmarketing; Prosthesis Failure; Self Expandable Metallic Stents; United States; United States Food and Drug Administration; Article; bleeding; clinical outcome; comparative study; device failure; device removal; dysphagia; Food and Drug Administration; human; odynophagia; pain; perforation; postmarketing surveillance; stent complication; stent fracture; stent migration; adverse event; epidemiology; esophagus stenosis; etiology; factual database; Food and Drug Administration; postmarketing surveillance; prosthesis complication; self expandable metallic stent; therapy; United States