The Effect of rebamipide as adjunct therapy with proton-pump inhibitor in patients with upper gastrointestinal bleeding : (Record no. 10212)

MARC details
000 -LEADER
fixed length control field 02518nam a22002537a 4500
003 - CONTROL NUMBER IDENTIFIER
control field MED20160010
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20240720152931.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 171013b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Transcribing agency FEU-NRMF MEDICAL LIBRARY
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title ENGLISH
050 ## - LIBRARY OF CONGRESS CALL NUMBER
Classification number MED20160010
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name Andor, Julius M., MD.
Relator term author
245 ## - TITLE STATEMENT
Title The Effect of rebamipide as adjunct therapy with proton-pump inhibitor in patients with upper gastrointestinal bleeding :
Remainder of title a retrospective study /
Statement of responsibility, etc. Julius M. Ador and Roy Caballero.
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Place of publication, distribution, etc. Fairview, Quezon City
Name of publisher, distributor, etc. Department of Medicine, FEU-NRMF,
Date of publication, distribution, etc. 2016
300 ## - PHYSICAL DESCRIPTION
Extent 15 pages:
Other physical details illustrations;
Dimensions (in folder)
336 ## - CONTENT TYPE
Source text
Content type term rdacontent
337 ## - MEDIA TYPE
Source unmediated
Media type term rdamedia
338 ## - CARRIER TYPE
Source volume
Carrier type term rdacarrier
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc Includes bibliographical references.
520 ## - SUMMARY, ETC.
Summary, etc. ABSTRACT: Rebamipide, as a gastroprotective agent, is currently not included in the treatment recommendations of Upper Gastrointestinal Bleeding (UGIB). This retrospective cohort study determined the effect of Rebamipide as adjunct therapy with Proton-pump Inhibitor (PPI) in patients with UGIB admitted in FEU-NRMF Medical Foundation. A clear review was conducted within 5 years duration. Patients were divided into two groups: PPI alone vs. PPI + Rebamipide. 390 patients/cases were included in this study: 149 PPI alone cases and 241 PPI +Rebamipide cases. Resolution of signs of bleeding as to hematemesis, melena or hematochezia within 5 days duration was noted, as well as, the specific duration/time of resolution of signs of bleeding. Among 149 cases with PPI alone, 14.09% (21 cases) had resolution of signs within 5 days; while among those 241 cases with PPi + Rebamipide, the rate of resolution was 93% (224 cases). The rate difference was statistically significant wherein the resolution of signs of bleeding was significant association with PPI + Rebamipide intervention (p<0.001). In addition, the average time of resolution of the PPi alone group was 4.00 days +/-1.22, median days 4, and within an absolute range of 2-6 days resolution. On the other hand, the PPI + Remabipide group had average resolution time of 3.09 days +/ -0.95, with median days of 3, and within the absolute range of 2-5 days. In conclusion, Rebamipide + PPI is more effective than PPI alone in the treatment of UGIB. Also, Rebamipide may be an effective adjunct therapy with PPI in shortening the duration of UGIB.
521 ## - TARGET AUDIENCE NOTE
Target audience note Research - Department of Medicine
700 ## - ADDED ENTRY--PERSONAL NAME
Relator code supevising consultant
Personal name Caballero, Roy, MD.
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Library of Congress Classification
Koha item type Research
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Home library Current library Shelving location Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
    Library of Congress Classification     Far Eastern University - Nicanor Reyes Medical Foundation Far Eastern University - Nicanor Reyes Medical Foundation Research 10/13/2017   MED20160010 R000538 10/13/2017 10/13/2017 Research