Lack of difference among terlipressin, somatostatin, and octreotide in the control of acute gastroesophageal variceal hemorrhage
Vasoactive drugs are recommended to be started as soon as possible in suspected variceal bleeding, even before diagnostic endoscopy. However, it is still unclear whether the therapeutic efficacies of the various vasoactive drugs used are comparable. The aim of this prospective, multicenter, randomiz...
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Veröffentlicht in: | Hepatology (Baltimore, Md.) Md.), 2014-09, Vol.60 (3), p.954-963 |
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creator | Seo, Yeon Seok Park, Soo Young Kim, Moon Young Kim, Ju Hyun Park, Jun Yong Yim, Hyung Joon Jang, Byoung Kuk Kim, Hong Soo Hahn, Taeho Kim, Byung Ik Heo, Jeong An, Hyonggin Tak, Won Young Baik, Soon Koo Han, Kwang Hyub Hwang, Jae Seok Park, Sang Hoon Cho, Mong Um, Soon Ho |
description | Vasoactive drugs are recommended to be started as soon as possible in suspected variceal bleeding, even before diagnostic endoscopy. However, it is still unclear whether the therapeutic efficacies of the various vasoactive drugs used are comparable. The aim of this prospective, multicenter, randomized, noninferiority trial was to characterize the effects of terlipressin, somatostatin, and octreotide when they are initiated before endoscopic treatment in patients with acute variceal bleeding. Patients with liver cirrhosis and significant upper gastrointestinal bleeding were randomly assigned to receive early administration of terlipressin, somatostatin, or octreotide, followed by endoscopic treatment. Patients with nonvariceal bleeding were excluded after endoscopy. The primary endpoint was 5‐day treatment success, defined as control of bleeding without rescue treatment, rebleeding, or mortality, with a noninferiority margin of 0.1. In total, 780 patients with variceal bleeding were enrolled: 261 in the terlipressin group; 259 in the somatostatin group; and 260 in the octreotide group. At the time of initial endoscopy, active bleeding was noted in 43.7%, 44.4%, and 43.5% of these patients, respectively (P = 0.748), and treatment success was achieved by day 5 in 86.2%, 83.4%, and 83.8% (P = 0.636), with similar rates of control of bleeding without rescue treatment (89.7%, 87.6%, and 88.1%; P = 0.752), rebleeding (3.4%, 4.8%, and 4.4%; P = 0.739), or mortality (8.0%, 8.9%, and 8.8%; P = 0.929). The absolute values of the lower bound of confidence intervals for terlipressin versus somatostatin, terlilpressin versus octreotide, and octreotide versus somatostatin were 0.095, 0.090, and 0.065, respectively. Conclusion: Hemostatic effects and safety did not differ significantly between terlipressin, somatostatin, and octreotide as adjuvants to endoscopic treatment in patients with acute gastroesophageal variceal bleeding. (Hepatology 2014;60:954–963) |
doi_str_mv | 10.1002/hep.27006 |
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However, it is still unclear whether the therapeutic efficacies of the various vasoactive drugs used are comparable. The aim of this prospective, multicenter, randomized, noninferiority trial was to characterize the effects of terlipressin, somatostatin, and octreotide when they are initiated before endoscopic treatment in patients with acute variceal bleeding. Patients with liver cirrhosis and significant upper gastrointestinal bleeding were randomly assigned to receive early administration of terlipressin, somatostatin, or octreotide, followed by endoscopic treatment. Patients with nonvariceal bleeding were excluded after endoscopy. The primary endpoint was 5‐day treatment success, defined as control of bleeding without rescue treatment, rebleeding, or mortality, with a noninferiority margin of 0.1. In total, 780 patients with variceal bleeding were enrolled: 261 in the terlipressin group; 259 in the somatostatin group; and 260 in the octreotide group. At the time of initial endoscopy, active bleeding was noted in 43.7%, 44.4%, and 43.5% of these patients, respectively (P = 0.748), and treatment success was achieved by day 5 in 86.2%, 83.4%, and 83.8% (P = 0.636), with similar rates of control of bleeding without rescue treatment (89.7%, 87.6%, and 88.1%; P = 0.752), rebleeding (3.4%, 4.8%, and 4.4%; P = 0.739), or mortality (8.0%, 8.9%, and 8.8%; P = 0.929). The absolute values of the lower bound of confidence intervals for terlipressin versus somatostatin, terlilpressin versus octreotide, and octreotide versus somatostatin were 0.095, 0.090, and 0.065, respectively. Conclusion: Hemostatic effects and safety did not differ significantly between terlipressin, somatostatin, and octreotide as adjuvants to endoscopic treatment in patients with acute gastroesophageal variceal bleeding. (Hepatology 2014;60:954–963)</description><identifier>ISSN: 0270-9139</identifier><identifier>EISSN: 1527-3350</identifier><identifier>DOI: 10.1002/hep.27006</identifier><identifier>PMID: 24415445</identifier><identifier>CODEN: HPTLD9</identifier><language>eng</language><publisher>United States: Wolters Kluwer Health, Inc</publisher><subject>Acute Disease ; Adult ; Confidence intervals ; Endoscopy, Gastrointestinal ; Esophageal and Gastric Varices - complications ; Esophageal and Gastric Varices - drug therapy ; Female ; Gastrointestinal Hemorrhage - drug therapy ; Gastrointestinal Hemorrhage - etiology ; Hemorrhage ; Hemostasis - drug effects ; Hemostasis - physiology ; Hepatology ; Humans ; Liver cirrhosis ; Lypressin - analogs & derivatives ; Lypressin - therapeutic use ; Male ; Middle Aged ; Octreotide - therapeutic use ; Prospective Studies ; Somatostatin - therapeutic use ; Treatment Failure ; Vasoconstrictor Agents - therapeutic use</subject><ispartof>Hepatology (Baltimore, Md.), 2014-09, Vol.60 (3), p.954-963</ispartof><rights>2014 by the American Association for the Study of Liver Diseases</rights><rights>2014 by the American Association for the Study of Liver Diseases.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4586-1e008fef85bc92f7238d5b222d1b63e138aaac347e0a8c83901cb03ff8d4bf103</citedby><cites>FETCH-LOGICAL-c4586-1e008fef85bc92f7238d5b222d1b63e138aaac347e0a8c83901cb03ff8d4bf103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fhep.27006$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhep.27006$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24415445$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Seo, Yeon Seok</creatorcontrib><creatorcontrib>Park, Soo Young</creatorcontrib><creatorcontrib>Kim, Moon Young</creatorcontrib><creatorcontrib>Kim, Ju Hyun</creatorcontrib><creatorcontrib>Park, Jun Yong</creatorcontrib><creatorcontrib>Yim, Hyung Joon</creatorcontrib><creatorcontrib>Jang, Byoung Kuk</creatorcontrib><creatorcontrib>Kim, Hong Soo</creatorcontrib><creatorcontrib>Hahn, Taeho</creatorcontrib><creatorcontrib>Kim, Byung Ik</creatorcontrib><creatorcontrib>Heo, Jeong</creatorcontrib><creatorcontrib>An, Hyonggin</creatorcontrib><creatorcontrib>Tak, Won Young</creatorcontrib><creatorcontrib>Baik, Soon Koo</creatorcontrib><creatorcontrib>Han, Kwang Hyub</creatorcontrib><creatorcontrib>Hwang, Jae Seok</creatorcontrib><creatorcontrib>Park, Sang Hoon</creatorcontrib><creatorcontrib>Cho, Mong</creatorcontrib><creatorcontrib>Um, Soon Ho</creatorcontrib><title>Lack of difference among terlipressin, somatostatin, and octreotide in the control of acute gastroesophageal variceal hemorrhage</title><title>Hepatology (Baltimore, Md.)</title><addtitle>Hepatology</addtitle><description>Vasoactive drugs are recommended to be started as soon as possible in suspected variceal bleeding, even before diagnostic endoscopy. However, it is still unclear whether the therapeutic efficacies of the various vasoactive drugs used are comparable. The aim of this prospective, multicenter, randomized, noninferiority trial was to characterize the effects of terlipressin, somatostatin, and octreotide when they are initiated before endoscopic treatment in patients with acute variceal bleeding. Patients with liver cirrhosis and significant upper gastrointestinal bleeding were randomly assigned to receive early administration of terlipressin, somatostatin, or octreotide, followed by endoscopic treatment. Patients with nonvariceal bleeding were excluded after endoscopy. The primary endpoint was 5‐day treatment success, defined as control of bleeding without rescue treatment, rebleeding, or mortality, with a noninferiority margin of 0.1. In total, 780 patients with variceal bleeding were enrolled: 261 in the terlipressin group; 259 in the somatostatin group; and 260 in the octreotide group. At the time of initial endoscopy, active bleeding was noted in 43.7%, 44.4%, and 43.5% of these patients, respectively (P = 0.748), and treatment success was achieved by day 5 in 86.2%, 83.4%, and 83.8% (P = 0.636), with similar rates of control of bleeding without rescue treatment (89.7%, 87.6%, and 88.1%; P = 0.752), rebleeding (3.4%, 4.8%, and 4.4%; P = 0.739), or mortality (8.0%, 8.9%, and 8.8%; P = 0.929). The absolute values of the lower bound of confidence intervals for terlipressin versus somatostatin, terlilpressin versus octreotide, and octreotide versus somatostatin were 0.095, 0.090, and 0.065, respectively. Conclusion: Hemostatic effects and safety did not differ significantly between terlipressin, somatostatin, and octreotide as adjuvants to endoscopic treatment in patients with acute gastroesophageal variceal bleeding. (Hepatology 2014;60:954–963)</description><subject>Acute Disease</subject><subject>Adult</subject><subject>Confidence intervals</subject><subject>Endoscopy, Gastrointestinal</subject><subject>Esophageal and Gastric Varices - complications</subject><subject>Esophageal and Gastric Varices - drug therapy</subject><subject>Female</subject><subject>Gastrointestinal Hemorrhage - drug therapy</subject><subject>Gastrointestinal Hemorrhage - etiology</subject><subject>Hemorrhage</subject><subject>Hemostasis - drug effects</subject><subject>Hemostasis - physiology</subject><subject>Hepatology</subject><subject>Humans</subject><subject>Liver cirrhosis</subject><subject>Lypressin - analogs & derivatives</subject><subject>Lypressin - therapeutic use</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Octreotide - therapeutic use</subject><subject>Prospective Studies</subject><subject>Somatostatin - therapeutic use</subject><subject>Treatment Failure</subject><subject>Vasoconstrictor Agents - therapeutic use</subject><issn>0270-9139</issn><issn>1527-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU1v1DAQhq2qqF0Kh_6BylIvIJF2_JU4R1QVirQSHOAcOc541yWJU9sB9cZPJ2FbDkicZubVo0cjvYScM7hiAPx6j9MVrwDKI7JhileFEAqOyQaWsKiZqE_Jy5TuAaCWXJ-QUy4lU1KqDfm1NfY7DY523jmMOFqkZgjjjmaMvZ8ipuTHdzSFweSQssnrZcaOBpsjhuw7pH6keY_UhjHH0K82Y-eMdGfSEmAK097s0PT0h4nerssehxDjmr4iL5zpE75-mmfk24fbrzd3xfbzx08377eFlUqXBUMA7dBp1dqau4oL3amWc96xthTIhDbGWCErBKOtFjUw24JwTneydQzEGXlz8E4xPMyYcjP4ZLHvzYhhTg1TqgItKlUu6OU_6H2Y47h8t1KqklqW9UK9PVA2hpQiumaKfjDxsWHQrLU0Sy3Nn1oW9uLJOLcDdn_J5x4W4PoA_PQ9Pv7f1NzdfjkofwMmPJhm</recordid><startdate>201409</startdate><enddate>201409</enddate><creator>Seo, Yeon Seok</creator><creator>Park, Soo Young</creator><creator>Kim, Moon Young</creator><creator>Kim, Ju Hyun</creator><creator>Park, Jun Yong</creator><creator>Yim, Hyung Joon</creator><creator>Jang, Byoung Kuk</creator><creator>Kim, Hong Soo</creator><creator>Hahn, Taeho</creator><creator>Kim, Byung Ik</creator><creator>Heo, Jeong</creator><creator>An, Hyonggin</creator><creator>Tak, Won Young</creator><creator>Baik, Soon Koo</creator><creator>Han, Kwang Hyub</creator><creator>Hwang, Jae Seok</creator><creator>Park, Sang Hoon</creator><creator>Cho, Mong</creator><creator>Um, Soon Ho</creator><general>Wolters Kluwer Health, Inc</general><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>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201409</creationdate><title>Lack of difference among terlipressin, somatostatin, and octreotide in the control of acute gastroesophageal variceal hemorrhage</title><author>Seo, Yeon Seok ; Park, Soo Young ; Kim, Moon Young ; Kim, Ju Hyun ; Park, Jun Yong ; Yim, Hyung Joon ; Jang, Byoung Kuk ; Kim, Hong Soo ; Hahn, Taeho ; Kim, Byung Ik ; Heo, Jeong ; An, Hyonggin ; Tak, Won Young ; Baik, Soon Koo ; Han, Kwang Hyub ; Hwang, Jae Seok ; Park, Sang Hoon ; Cho, Mong ; Um, Soon Ho</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4586-1e008fef85bc92f7238d5b222d1b63e138aaac347e0a8c83901cb03ff8d4bf103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Acute Disease</topic><topic>Adult</topic><topic>Confidence intervals</topic><topic>Endoscopy, Gastrointestinal</topic><topic>Esophageal and Gastric Varices - complications</topic><topic>Esophageal and Gastric Varices - drug therapy</topic><topic>Female</topic><topic>Gastrointestinal Hemorrhage - drug therapy</topic><topic>Gastrointestinal Hemorrhage - etiology</topic><topic>Hemorrhage</topic><topic>Hemostasis - drug effects</topic><topic>Hemostasis - physiology</topic><topic>Hepatology</topic><topic>Humans</topic><topic>Liver cirrhosis</topic><topic>Lypressin - analogs & derivatives</topic><topic>Lypressin - therapeutic use</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Octreotide - therapeutic use</topic><topic>Prospective Studies</topic><topic>Somatostatin - therapeutic use</topic><topic>Treatment Failure</topic><topic>Vasoconstrictor Agents - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seo, Yeon Seok</creatorcontrib><creatorcontrib>Park, Soo Young</creatorcontrib><creatorcontrib>Kim, Moon Young</creatorcontrib><creatorcontrib>Kim, Ju Hyun</creatorcontrib><creatorcontrib>Park, Jun Yong</creatorcontrib><creatorcontrib>Yim, Hyung Joon</creatorcontrib><creatorcontrib>Jang, Byoung Kuk</creatorcontrib><creatorcontrib>Kim, Hong Soo</creatorcontrib><creatorcontrib>Hahn, Taeho</creatorcontrib><creatorcontrib>Kim, Byung Ik</creatorcontrib><creatorcontrib>Heo, Jeong</creatorcontrib><creatorcontrib>An, Hyonggin</creatorcontrib><creatorcontrib>Tak, Won Young</creatorcontrib><creatorcontrib>Baik, Soon Koo</creatorcontrib><creatorcontrib>Han, Kwang Hyub</creatorcontrib><creatorcontrib>Hwang, Jae Seok</creatorcontrib><creatorcontrib>Park, Sang Hoon</creatorcontrib><creatorcontrib>Cho, Mong</creatorcontrib><creatorcontrib>Um, Soon Ho</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Hepatology (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seo, Yeon Seok</au><au>Park, Soo Young</au><au>Kim, Moon Young</au><au>Kim, Ju Hyun</au><au>Park, Jun Yong</au><au>Yim, Hyung Joon</au><au>Jang, Byoung Kuk</au><au>Kim, Hong Soo</au><au>Hahn, Taeho</au><au>Kim, Byung Ik</au><au>Heo, Jeong</au><au>An, Hyonggin</au><au>Tak, Won Young</au><au>Baik, Soon Koo</au><au>Han, Kwang Hyub</au><au>Hwang, Jae Seok</au><au>Park, Sang Hoon</au><au>Cho, Mong</au><au>Um, Soon Ho</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lack of difference among terlipressin, somatostatin, and octreotide in the control of acute gastroesophageal variceal hemorrhage</atitle><jtitle>Hepatology (Baltimore, Md.)</jtitle><addtitle>Hepatology</addtitle><date>2014-09</date><risdate>2014</risdate><volume>60</volume><issue>3</issue><spage>954</spage><epage>963</epage><pages>954-963</pages><issn>0270-9139</issn><eissn>1527-3350</eissn><coden>HPTLD9</coden><abstract>Vasoactive drugs are recommended to be started as soon as possible in suspected variceal bleeding, even before diagnostic endoscopy. However, it is still unclear whether the therapeutic efficacies of the various vasoactive drugs used are comparable. The aim of this prospective, multicenter, randomized, noninferiority trial was to characterize the effects of terlipressin, somatostatin, and octreotide when they are initiated before endoscopic treatment in patients with acute variceal bleeding. Patients with liver cirrhosis and significant upper gastrointestinal bleeding were randomly assigned to receive early administration of terlipressin, somatostatin, or octreotide, followed by endoscopic treatment. Patients with nonvariceal bleeding were excluded after endoscopy. The primary endpoint was 5‐day treatment success, defined as control of bleeding without rescue treatment, rebleeding, or mortality, with a noninferiority margin of 0.1. In total, 780 patients with variceal bleeding were enrolled: 261 in the terlipressin group; 259 in the somatostatin group; and 260 in the octreotide group. At the time of initial endoscopy, active bleeding was noted in 43.7%, 44.4%, and 43.5% of these patients, respectively (P = 0.748), and treatment success was achieved by day 5 in 86.2%, 83.4%, and 83.8% (P = 0.636), with similar rates of control of bleeding without rescue treatment (89.7%, 87.6%, and 88.1%; P = 0.752), rebleeding (3.4%, 4.8%, and 4.4%; P = 0.739), or mortality (8.0%, 8.9%, and 8.8%; P = 0.929). The absolute values of the lower bound of confidence intervals for terlipressin versus somatostatin, terlilpressin versus octreotide, and octreotide versus somatostatin were 0.095, 0.090, and 0.065, respectively. Conclusion: Hemostatic effects and safety did not differ significantly between terlipressin, somatostatin, and octreotide as adjuvants to endoscopic treatment in patients with acute gastroesophageal variceal bleeding. (Hepatology 2014;60:954–963)</abstract><cop>United States</cop><pub>Wolters Kluwer Health, Inc</pub><pmid>24415445</pmid><doi>10.1002/hep.27006</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acute Disease Adult Confidence intervals Endoscopy, Gastrointestinal Esophageal and Gastric Varices - complications Esophageal and Gastric Varices - drug therapy Female Gastrointestinal Hemorrhage - drug therapy Gastrointestinal Hemorrhage - etiology Hemorrhage Hemostasis - drug effects Hemostasis - physiology Hepatology Humans Liver cirrhosis Lypressin - analogs & derivatives Lypressin - therapeutic use Male Middle Aged Octreotide - therapeutic use Prospective Studies Somatostatin - therapeutic use Treatment Failure Vasoconstrictor Agents - therapeutic use |
title | Lack of difference among terlipressin, somatostatin, and octreotide in the control of acute gastroesophageal variceal hemorrhage |
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