Cargando…

Is ranitidine therapy sufficient for healing peptic ulcers associated with non-steroidal anti-inflammatory drug use?

Long-term use of non-steroidal anti-inflammatory drugs (NSAIDs) increases the risk of serious gastroduodenal events. To minimise these risks, patients often require concomitant acid-suppressive therapy. We conducted a literature review of clinical trials examining use of ranitidine 150 mg twice dail...

Descripción completa

Detalles Bibliográficos
Autores principales: YEOMANS, N D, SVEDBERG, L-E, NAESDAL, J
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1636688/
https://www.ncbi.nlm.nih.gov/pubmed/17073837
http://dx.doi.org/10.1111/j.1742-1241.2006.01147.x
_version_ 1782130773551218688
author YEOMANS, N D
SVEDBERG, L-E
NAESDAL, J
author_facet YEOMANS, N D
SVEDBERG, L-E
NAESDAL, J
author_sort YEOMANS, N D
collection PubMed
description Long-term use of non-steroidal anti-inflammatory drugs (NSAIDs) increases the risk of serious gastroduodenal events. To minimise these risks, patients often require concomitant acid-suppressive therapy. We conducted a literature review of clinical trials examining use of ranitidine 150 mg twice daily to heal gastroduodenal ulcers (GU) in NSAID recipients. Seven studies were identified. After 8 weeks’ treatment with ranitidine, GU healing rates ranged from 50% to 74% and rates of duodenal ulcer (DU) healing ranged from 81% to 84%. Ranitidine was more effective when NSAIDs were discontinued (healing rates reaching 95% and 100%, respectively). The ulcer healing rate with sucralfate was similar to that of ranitidine. However, proton pump inhibitor (PPI) therapy was associated with significantly greater rates of both GU and DU healing than ranitidine; 8-week GU rates were 92% and 88% with esomeprazole 40 mg and 20 mg, respectively (vs. 74% with ranitidine, p < 0.01). For omeprazole, 8-week healing rates were 87% with omeprazole 40 mg and 84% with omeprazole 20 mg (vs. 64% for ranitidine, p < 0.001), and for lansoprazole the corresponding values were 73–74% and 66–69% for the 30 mg and 15 mg doses, respectively (vs. 50–53% for ranitidine, p < 0.05). In the PPI study reporting DU healing the values were 92% for omeprazole 20 mg (vs. 81% for ranitidine, p < 0.05) and 88% for omeprazole 40 mg (p = 0.17 vs. ranitidine). NSAID-associated GU are more likely to heal when patients receive concomitant treatment with a PPI rather than ranitidine.
format Text
id pubmed-1636688
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher Blackwell Publishing Ltd
record_format MEDLINE/PubMed
spelling pubmed-16366882006-11-17 Is ranitidine therapy sufficient for healing peptic ulcers associated with non-steroidal anti-inflammatory drug use? YEOMANS, N D SVEDBERG, L-E NAESDAL, J Int J Clin Pract Original Papers Long-term use of non-steroidal anti-inflammatory drugs (NSAIDs) increases the risk of serious gastroduodenal events. To minimise these risks, patients often require concomitant acid-suppressive therapy. We conducted a literature review of clinical trials examining use of ranitidine 150 mg twice daily to heal gastroduodenal ulcers (GU) in NSAID recipients. Seven studies were identified. After 8 weeks’ treatment with ranitidine, GU healing rates ranged from 50% to 74% and rates of duodenal ulcer (DU) healing ranged from 81% to 84%. Ranitidine was more effective when NSAIDs were discontinued (healing rates reaching 95% and 100%, respectively). The ulcer healing rate with sucralfate was similar to that of ranitidine. However, proton pump inhibitor (PPI) therapy was associated with significantly greater rates of both GU and DU healing than ranitidine; 8-week GU rates were 92% and 88% with esomeprazole 40 mg and 20 mg, respectively (vs. 74% with ranitidine, p < 0.01). For omeprazole, 8-week healing rates were 87% with omeprazole 40 mg and 84% with omeprazole 20 mg (vs. 64% for ranitidine, p < 0.001), and for lansoprazole the corresponding values were 73–74% and 66–69% for the 30 mg and 15 mg doses, respectively (vs. 50–53% for ranitidine, p < 0.05). In the PPI study reporting DU healing the values were 92% for omeprazole 20 mg (vs. 81% for ranitidine, p < 0.05) and 88% for omeprazole 40 mg (p = 0.17 vs. ranitidine). NSAID-associated GU are more likely to heal when patients receive concomitant treatment with a PPI rather than ranitidine. Blackwell Publishing Ltd 2006-11 /pmc/articles/PMC1636688/ /pubmed/17073837 http://dx.doi.org/10.1111/j.1742-1241.2006.01147.x Text en © 2006 The Authors Journal compilation © 2006 Blackwell Publishing Ltd
spellingShingle Original Papers
YEOMANS, N D
SVEDBERG, L-E
NAESDAL, J
Is ranitidine therapy sufficient for healing peptic ulcers associated with non-steroidal anti-inflammatory drug use?
title Is ranitidine therapy sufficient for healing peptic ulcers associated with non-steroidal anti-inflammatory drug use?
title_full Is ranitidine therapy sufficient for healing peptic ulcers associated with non-steroidal anti-inflammatory drug use?
title_fullStr Is ranitidine therapy sufficient for healing peptic ulcers associated with non-steroidal anti-inflammatory drug use?
title_full_unstemmed Is ranitidine therapy sufficient for healing peptic ulcers associated with non-steroidal anti-inflammatory drug use?
title_short Is ranitidine therapy sufficient for healing peptic ulcers associated with non-steroidal anti-inflammatory drug use?
title_sort is ranitidine therapy sufficient for healing peptic ulcers associated with non-steroidal anti-inflammatory drug use?
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1636688/
https://www.ncbi.nlm.nih.gov/pubmed/17073837
http://dx.doi.org/10.1111/j.1742-1241.2006.01147.x
work_keys_str_mv AT yeomansnd isranitidinetherapysufficientforhealingpepticulcersassociatedwithnonsteroidalantiinflammatorydruguse
AT svedbergle isranitidinetherapysufficientforhealingpepticulcersassociatedwithnonsteroidalantiinflammatorydruguse
AT naesdalj isranitidinetherapysufficientforhealingpepticulcersassociatedwithnonsteroidalantiinflammatorydruguse