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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 |
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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 & 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&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 & 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 & derivatives</topic><topic>Omeprazole - therapeutic use</topic><topic>Pharmacology. Drug treatments</topic><topic>Predictive Value of Tests</topic><topic>proton pump inhibitor</topic><topic>Recurrence</topic><topic>Stomach</topic><topic>Studies</topic><topic>Substance abuse treatment</topic><topic>Surgery</topic><topic>tranexamic acid</topic><topic>Tranexamic Acid - therapeutic use</topic><topic>Treatment Outcome</topic><topic>ulcer</topic><topic>upper gastrointestinal bleeding</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Gut</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hawkey, G M</au><au>Cole, A T</au><au>McIntyre, A S</au><au>Long, R G</au><au>Hawkey, C J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Drug treatments in upper gastrointestinal bleeding: value of endoscopic findings as surrogate end points</atitle><jtitle>Gut</jtitle><addtitle>Gut</addtitle><date>2001-09-01</date><risdate>2001</risdate><volume>49</volume><issue>3</issue><spage>372</spage><epage>379</epage><pages>372-379</pages><issn>0017-5749</issn><eissn>1468-3288</eissn><eissn>1458-3288</eissn><coden>GUTTAK</coden><abstract>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.</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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