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Drug treatments in upper gastrointestinal bleeding: value of endoscopic findings as surrogate end points

INTRODUCTION Pharmacotherapy for upper gastrointestinal bleeding has been difficult to evaluate because clinical end points are infrequent and affected by other factors. AIMS To evaluate whether blood in the stomach at endoscopy reflected severity of bleeding, predicted clinical outcomes, and could...

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Published in:Gut 2001-09, Vol.49 (3), p.372-379
Main Authors: Hawkey, G M, Cole, A T, McIntyre, A S, Long, R G, Hawkey, C J
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Cole, A T
McIntyre, A S
Long, R G
Hawkey, C J
description INTRODUCTION Pharmacotherapy for upper gastrointestinal bleeding has been difficult to evaluate because clinical end points are infrequent and affected by other factors. AIMS To evaluate whether blood in the stomach at endoscopy reflected severity of bleeding, predicted clinical outcomes, and could be altered by therapeutic agents. METHODS We studied 414 consecutive admissions with suspected upper gastrointestinal bleeding. Patients were randomised to receive lansoprazole 60 mg followed by 30 mg four times daily, tranexamic acid 2 g followed by 1 g four times daily, both drugs, or placebo for four days, until discharge or a clinical end point occurred. Logistic regression analysis was used to determine predictors of endoscopic changes and clinical outcomes, and to investigate the effects of drug treatments on blood in the stomach. RESULTS Of 414 patients with suspected upper gastrointestinal bleeding, 379 were endoscoped. Upper gastrointestinal bleeding was confirmed in 316. Sixteen required surgery within 30 days and 16 died on the index admission. Trial treatments were evaluable on a per protocol basis in 228 patients. The amount of blood in the stomach was found to reflect initial risk, with significant associations with high risk categorisation (odds ratio 3.7 (95% confidence interval 1.5–9.4) for more than a trace v none/trace), age (1.5 (1.1–1.9) per decade), and initial pulse (1.02 (1.00–1.04) per beat), and to predict rebleeding (9.2 (4.6–18.7)) and surgery (8.2 (2.9–22.9)). Other stigmata were less significant in these respects. The amount of blood in the stomach at endoscopy was reduced significantly by both lansoprazole (0.22 (0.07–0.63)) and tranexamic acid (0.27 (0.09–0.81)), although there was no evidence of synergy. CONCLUSIONS Blood in the stomach reflects clinical features in patients with acute upper gastrointestinal bleeding and is reduced by treatment with lansoprazole and tranexamic acid.
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AIMS To evaluate whether blood in the stomach at endoscopy reflected severity of bleeding, predicted clinical outcomes, and could be altered by therapeutic agents. METHODS We studied 414 consecutive admissions with suspected upper gastrointestinal bleeding. Patients were randomised to receive lansoprazole 60 mg followed by 30 mg four times daily, tranexamic acid 2 g followed by 1 g four times daily, both drugs, or placebo for four days, until discharge or a clinical end point occurred. Logistic regression analysis was used to determine predictors of endoscopic changes and clinical outcomes, and to investigate the effects of drug treatments on blood in the stomach. RESULTS Of 414 patients with suspected upper gastrointestinal bleeding, 379 were endoscoped. Upper gastrointestinal bleeding was confirmed in 316. Sixteen required surgery within 30 days and 16 died on the index admission. Trial treatments were evaluable on a per protocol basis in 228 patients. The amount of blood in the stomach was found to reflect initial risk, with significant associations with high risk categorisation (odds ratio 3.7 (95% confidence interval 1.5–9.4) for more than a trace v none/trace), age (1.5 (1.1–1.9) per decade), and initial pulse (1.02 (1.00–1.04) per beat), and to predict rebleeding (9.2 (4.6–18.7)) and surgery (8.2 (2.9–22.9)). Other stigmata were less significant in these respects. The amount of blood in the stomach at endoscopy was reduced significantly by both lansoprazole (0.22 (0.07–0.63)) and tranexamic acid (0.27 (0.09–0.81)), although there was no evidence of synergy. CONCLUSIONS Blood in the stomach reflects clinical features in patients with acute upper gastrointestinal bleeding and is reduced by treatment with lansoprazole and tranexamic acid.</description><identifier>ISSN: 0017-5749</identifier><identifier>EISSN: 1468-3288</identifier><identifier>EISSN: 1458-3288</identifier><identifier>DOI: 10.1136/gut.49.3.372</identifier><identifier>PMID: 11511559</identifier><identifier>CODEN: GUTTAK</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and British Society of Gastroenterology</publisher><subject>2-Pyridinylmethylsulfinylbenzimidazoles ; acid suppression ; Acids ; Anti-Ulcer Agents - therapeutic use ; Antifibrinolytic Agents - therapeutic use ; Biological and medical sciences ; Blood Transfusion ; Blood Volume ; Clinical outcomes ; Digestive system ; Double-Blind Method ; Drug dosages ; Drug Synergism ; Drug therapy ; Drug Therapy, Combination ; Endoscopy ; Female ; fibrinolysis ; Gastrointestinal bleeding ; Gastrointestinal Hemorrhage - diagnosis ; Gastrointestinal Hemorrhage - etiology ; Gastrointestinal Hemorrhage - therapy ; Gastroscopy ; Hospitals ; Humans ; Laboratories ; Lansoprazole ; Logistic Models ; Male ; Medical sciences ; Middle Aged ; Mortality ; Odds Ratio ; Omeprazole - analogs &amp; derivatives ; Omeprazole - therapeutic use ; Pharmacology. Drug treatments ; Predictive Value of Tests ; proton pump inhibitor ; Recurrence ; Stomach ; Studies ; Substance abuse treatment ; Surgery ; tranexamic acid ; Tranexamic Acid - therapeutic use ; Treatment Outcome ; ulcer ; upper gastrointestinal bleeding</subject><ispartof>Gut, 2001-09, Vol.49 (3), p.372-379</ispartof><rights>British Society of Gastroenterology</rights><rights>2001 INIST-CNRS</rights><rights>COPYRIGHT 2001 BMJ Publishing Group Ltd.</rights><rights>Copyright: 2001 British Society of Gastroenterology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b675t-b57e2f7acae07d26b0b0d10a7097f6ff194dde64a246a5f47abfbb21ee1dda403</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1728427/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1728427/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1116199$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11511559$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hawkey, G M</creatorcontrib><creatorcontrib>Cole, A T</creatorcontrib><creatorcontrib>McIntyre, A S</creatorcontrib><creatorcontrib>Long, R G</creatorcontrib><creatorcontrib>Hawkey, C J</creatorcontrib><title>Drug treatments in upper gastrointestinal bleeding: value of endoscopic findings as surrogate end points</title><title>Gut</title><addtitle>Gut</addtitle><description>INTRODUCTION Pharmacotherapy for upper gastrointestinal bleeding has been difficult to evaluate because clinical end points are infrequent and affected by other factors. AIMS To evaluate whether blood in the stomach at endoscopy reflected severity of bleeding, predicted clinical outcomes, and could be altered by therapeutic agents. METHODS We studied 414 consecutive admissions with suspected upper gastrointestinal bleeding. Patients were randomised to receive lansoprazole 60 mg followed by 30 mg four times daily, tranexamic acid 2 g followed by 1 g four times daily, both drugs, or placebo for four days, until discharge or a clinical end point occurred. Logistic regression analysis was used to determine predictors of endoscopic changes and clinical outcomes, and to investigate the effects of drug treatments on blood in the stomach. RESULTS Of 414 patients with suspected upper gastrointestinal bleeding, 379 were endoscoped. Upper gastrointestinal bleeding was confirmed in 316. Sixteen required surgery within 30 days and 16 died on the index admission. Trial treatments were evaluable on a per protocol basis in 228 patients. The amount of blood in the stomach was found to reflect initial risk, with significant associations with high risk categorisation (odds ratio 3.7 (95% confidence interval 1.5–9.4) for more than a trace v none/trace), age (1.5 (1.1–1.9) per decade), and initial pulse (1.02 (1.00–1.04) per beat), and to predict rebleeding (9.2 (4.6–18.7)) and surgery (8.2 (2.9–22.9)). Other stigmata were less significant in these respects. The amount of blood in the stomach at endoscopy was reduced significantly by both lansoprazole (0.22 (0.07–0.63)) and tranexamic acid (0.27 (0.09–0.81)), although there was no evidence of synergy. CONCLUSIONS Blood in the stomach reflects clinical features in patients with acute upper gastrointestinal bleeding and is reduced by treatment with lansoprazole and tranexamic acid.</description><subject>2-Pyridinylmethylsulfinylbenzimidazoles</subject><subject>acid suppression</subject><subject>Acids</subject><subject>Anti-Ulcer Agents - therapeutic use</subject><subject>Antifibrinolytic Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Blood Transfusion</subject><subject>Blood Volume</subject><subject>Clinical outcomes</subject><subject>Digestive system</subject><subject>Double-Blind Method</subject><subject>Drug dosages</subject><subject>Drug Synergism</subject><subject>Drug therapy</subject><subject>Drug Therapy, Combination</subject><subject>Endoscopy</subject><subject>Female</subject><subject>fibrinolysis</subject><subject>Gastrointestinal bleeding</subject><subject>Gastrointestinal Hemorrhage - diagnosis</subject><subject>Gastrointestinal Hemorrhage - etiology</subject><subject>Gastrointestinal Hemorrhage - therapy</subject><subject>Gastroscopy</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Laboratories</subject><subject>Lansoprazole</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Odds Ratio</subject><subject>Omeprazole - analogs &amp; derivatives</subject><subject>Omeprazole - therapeutic use</subject><subject>Pharmacology. Drug treatments</subject><subject>Predictive Value of Tests</subject><subject>proton pump inhibitor</subject><subject>Recurrence</subject><subject>Stomach</subject><subject>Studies</subject><subject>Substance abuse treatment</subject><subject>Surgery</subject><subject>tranexamic acid</subject><subject>Tranexamic Acid - therapeutic use</subject><subject>Treatment Outcome</subject><subject>ulcer</subject><subject>upper gastrointestinal bleeding</subject><issn>0017-5749</issn><issn>1468-3288</issn><issn>1458-3288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNp90t-L1DAQB_AiireevvksQQVf7Jq0adP4IBzrbw6FQ8_HMG0nvaxtUpP20P_eLFvuVlgkhUDnwzeZMEnymNE1Y3n5qpunNZfrfJ2L7E6yYrys0jyrqrvJilIm0kJweZI8CGFLKa0qye4nJ4wV8SvkKrl66-eOTB5hGtBOgRhL5nFETzoIk3fGThgmY6EndY_YGtu9JtfQz0icJmhbFxo3moZoY3fFQCCQMHvvOphwB8i4CwkPk3sa-oCPlv00-f7-3bfNx_T864dPm7PztC5FMaV1ITDTAhpAKtqsrGlNW0ZBUCl0qTWTvG2x5JDxEgrNBdS6rjOGyNoWOM1Pkzf73HGuB2yb2JSHXo3eDOD_KAdG_Vux5kp17loxkVU8EzHg2RLg3a85Nq-2bvbxAUIkQkpOS8qierpXHfSojNUuhjWDCY06ExXPM86KiF4eQR1ajAc7i9rE34c8PcLjanEwzTG_xDfeheBR33TJqNrNhoqzobhUuYqzEfmTw5e5xcswRPB8ARAa6LUH25hw4FjJpLy9pgkT_r4pg_-pSpGLQn253KiL7LMUF_ml-hH9i72vh-3_b_gXsDjfsA</recordid><startdate>20010901</startdate><enddate>20010901</enddate><creator>Hawkey, G M</creator><creator>Cole, A T</creator><creator>McIntyre, A S</creator><creator>Long, R G</creator><creator>Hawkey, C J</creator><general>BMJ Publishing Group Ltd and British Society of Gastroenterology</general><general>BMJ</general><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>5PM</scope></search><sort><creationdate>20010901</creationdate><title>Drug treatments in upper gastrointestinal bleeding: value of endoscopic findings as surrogate end points</title><author>Hawkey, G M ; Cole, A T ; McIntyre, A S ; Long, R G ; Hawkey, C J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b675t-b57e2f7acae07d26b0b0d10a7097f6ff194dde64a246a5f47abfbb21ee1dda403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>2-Pyridinylmethylsulfinylbenzimidazoles</topic><topic>acid suppression</topic><topic>Acids</topic><topic>Anti-Ulcer Agents - therapeutic use</topic><topic>Antifibrinolytic Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Blood Transfusion</topic><topic>Blood Volume</topic><topic>Clinical outcomes</topic><topic>Digestive system</topic><topic>Double-Blind Method</topic><topic>Drug dosages</topic><topic>Drug Synergism</topic><topic>Drug therapy</topic><topic>Drug Therapy, Combination</topic><topic>Endoscopy</topic><topic>Female</topic><topic>fibrinolysis</topic><topic>Gastrointestinal bleeding</topic><topic>Gastrointestinal Hemorrhage - diagnosis</topic><topic>Gastrointestinal Hemorrhage - etiology</topic><topic>Gastrointestinal Hemorrhage - therapy</topic><topic>Gastroscopy</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Laboratories</topic><topic>Lansoprazole</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Odds Ratio</topic><topic>Omeprazole - analogs &amp; derivatives</topic><topic>Omeprazole - therapeutic use</topic><topic>Pharmacology. 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AIMS To evaluate whether blood in the stomach at endoscopy reflected severity of bleeding, predicted clinical outcomes, and could be altered by therapeutic agents. METHODS We studied 414 consecutive admissions with suspected upper gastrointestinal bleeding. Patients were randomised to receive lansoprazole 60 mg followed by 30 mg four times daily, tranexamic acid 2 g followed by 1 g four times daily, both drugs, or placebo for four days, until discharge or a clinical end point occurred. Logistic regression analysis was used to determine predictors of endoscopic changes and clinical outcomes, and to investigate the effects of drug treatments on blood in the stomach. RESULTS Of 414 patients with suspected upper gastrointestinal bleeding, 379 were endoscoped. Upper gastrointestinal bleeding was confirmed in 316. Sixteen required surgery within 30 days and 16 died on the index admission. Trial treatments were evaluable on a per protocol basis in 228 patients. The amount of blood in the stomach was found to reflect initial risk, with significant associations with high risk categorisation (odds ratio 3.7 (95% confidence interval 1.5–9.4) for more than a trace v none/trace), age (1.5 (1.1–1.9) per decade), and initial pulse (1.02 (1.00–1.04) per beat), and to predict rebleeding (9.2 (4.6–18.7)) and surgery (8.2 (2.9–22.9)). Other stigmata were less significant in these respects. The amount of blood in the stomach at endoscopy was reduced significantly by both lansoprazole (0.22 (0.07–0.63)) and tranexamic acid (0.27 (0.09–0.81)), although there was no evidence of synergy. CONCLUSIONS Blood in the stomach reflects clinical features in patients with acute upper gastrointestinal bleeding and is reduced by treatment with lansoprazole and tranexamic acid.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and British Society of Gastroenterology</pub><pmid>11511559</pmid><doi>10.1136/gut.49.3.372</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects 2-Pyridinylmethylsulfinylbenzimidazoles
acid suppression
Acids
Anti-Ulcer Agents - therapeutic use
Antifibrinolytic Agents - therapeutic use
Biological and medical sciences
Blood Transfusion
Blood Volume
Clinical outcomes
Digestive system
Double-Blind Method
Drug dosages
Drug Synergism
Drug therapy
Drug Therapy, Combination
Endoscopy
Female
fibrinolysis
Gastrointestinal bleeding
Gastrointestinal Hemorrhage - diagnosis
Gastrointestinal Hemorrhage - etiology
Gastrointestinal Hemorrhage - therapy
Gastroscopy
Hospitals
Humans
Laboratories
Lansoprazole
Logistic Models
Male
Medical sciences
Middle Aged
Mortality
Odds Ratio
Omeprazole - analogs & derivatives
Omeprazole - therapeutic use
Pharmacology. Drug treatments
Predictive Value of Tests
proton pump inhibitor
Recurrence
Stomach
Studies
Substance abuse treatment
Surgery
tranexamic acid
Tranexamic Acid - therapeutic use
Treatment Outcome
ulcer
upper gastrointestinal bleeding
title Drug treatments in upper gastrointestinal bleeding: value of endoscopic findings as surrogate end points
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