Antibiotic therapy for treatment in relapse of intestinal Crohn's disease. A prospective randomized study
We have undertaken a prospective randomized trial of one month's antimicrobial therapy for patients with symptomatic relapse of Crohn's disease. Criteria for entry included two major symptoms: fever, abdominal pain, diarrhea, weight loss, abdominal mass or complications (excluding perianal...
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Veröffentlicht in: | Diseases of the colon & rectum 1985-02, Vol.28 (2), p.81-85 |
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description | We have undertaken a prospective randomized trial of one month's antimicrobial therapy for patients with symptomatic relapse of Crohn's disease. Criteria for entry included two major symptoms: fever, abdominal pain, diarrhea, weight loss, abdominal mass or complications (excluding perianal disease); and two hematologic abnormalities: hemoglobin, ESR, albumin, C reactive protein, iron, or total iron binding capacity. Patients were monitored for the aforementioned clinical and hematologic (hemoglobin, albumin, CRP) parameters over six weeks and for changes in fecal flora. Randomization was to four groups: metronidazole alone (M), cotrimoxazole alone (C), metronidazole and cotrimoxazole (C plus M), or double placebo (P). Seventy-two patients entered the study (18 = M, 16 = C, 21 = C plus M, 17 = P). After two weeks, improvement was reported as follows: M = 67 percent, C = 17 percent, C plus M = 71 percent, P = 35 percent. In the metronidazole group, two patients required surgery and one had troublesome side effects. In the cotrimoxazole group, two had side effects. In the combined group (C plus M), four had troublesome side effects and two of the placebo group (P) required operation. By four weeks, there was no difference in response among the groups: (M = 44 percent, C = 62 percent, C plus M = 57 percent, P = 41 percent). Antimicrobials had no effect on fecal flora or hematologic parameters. These results indicate that antimicrobials have little therapeutic potential for relapse of intestinal Crohn's disease. |
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A prospective randomized study</title><source>MEDLINE</source><source>Journals@Ovid Complete</source><source>Alma/SFX Local Collection</source><creator>AMBROSE, N. S ; ALLAN, R. N ; KEIGHLEY, M. R. B ; BURDON, D. W ; YOUNGS, D ; BARNES, P ; LENNARD-JONES, J. E</creator><creatorcontrib>AMBROSE, N. S ; ALLAN, R. N ; KEIGHLEY, M. R. B ; BURDON, D. W ; YOUNGS, D ; BARNES, P ; LENNARD-JONES, J. E</creatorcontrib><description>We have undertaken a prospective randomized trial of one month's antimicrobial therapy for patients with symptomatic relapse of Crohn's disease. Criteria for entry included two major symptoms: fever, abdominal pain, diarrhea, weight loss, abdominal mass or complications (excluding perianal disease); and two hematologic abnormalities: hemoglobin, ESR, albumin, C reactive protein, iron, or total iron binding capacity. Patients were monitored for the aforementioned clinical and hematologic (hemoglobin, albumin, CRP) parameters over six weeks and for changes in fecal flora. Randomization was to four groups: metronidazole alone (M), cotrimoxazole alone (C), metronidazole and cotrimoxazole (C plus M), or double placebo (P). Seventy-two patients entered the study (18 = M, 16 = C, 21 = C plus M, 17 = P). After two weeks, improvement was reported as follows: M = 67 percent, C = 17 percent, C plus M = 71 percent, P = 35 percent. In the metronidazole group, two patients required surgery and one had troublesome side effects. In the cotrimoxazole group, two had side effects. In the combined group (C plus M), four had troublesome side effects and two of the placebo group (P) required operation. By four weeks, there was no difference in response among the groups: (M = 44 percent, C = 62 percent, C plus M = 57 percent, P = 41 percent). Antimicrobials had no effect on fecal flora or hematologic parameters. These results indicate that antimicrobials have little therapeutic potential for relapse of intestinal Crohn's disease.</description><identifier>ISSN: 0012-3706</identifier><identifier>EISSN: 1530-0358</identifier><identifier>DOI: 10.1007/BF02552649</identifier><identifier>PMID: 3882364</identifier><identifier>CODEN: DICRAG</identifier><language>eng</language><publisher>Secaucus, NJ: Springer</publisher><subject>Adult ; Aged ; Antibacterial agents ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Biological and medical sciences ; Clinical Trials as Topic ; Crohn Disease - drug therapy ; Crohn Disease - microbiology ; Double-Blind Method ; Drug Combinations - administration & dosage ; Drug Therapy, Combination ; Feces - microbiology ; Humans ; Medical sciences ; Metronidazole - administration & dosage ; Middle Aged ; Pharmacology. Drug treatments ; Random Allocation ; Recurrence ; Sulfamethoxazole - administration & dosage ; Trimethoprim - administration & dosage ; Trimethoprim, Sulfamethoxazole Drug Combination</subject><ispartof>Diseases of the colon & rectum, 1985-02, Vol.28 (2), p.81-85</ispartof><rights>1985 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c270t-61970a1a95561c0b3d2ed0c1082a58b3b3cbf9229a4334316bf10b448659c69a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=9218785$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3882364$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>AMBROSE, N. S</creatorcontrib><creatorcontrib>ALLAN, R. N</creatorcontrib><creatorcontrib>KEIGHLEY, M. R. B</creatorcontrib><creatorcontrib>BURDON, D. W</creatorcontrib><creatorcontrib>YOUNGS, D</creatorcontrib><creatorcontrib>BARNES, P</creatorcontrib><creatorcontrib>LENNARD-JONES, J. E</creatorcontrib><title>Antibiotic therapy for treatment in relapse of intestinal Crohn's disease. A prospective randomized study</title><title>Diseases of the colon & rectum</title><addtitle>Dis Colon Rectum</addtitle><description>We have undertaken a prospective randomized trial of one month's antimicrobial therapy for patients with symptomatic relapse of Crohn's disease. Criteria for entry included two major symptoms: fever, abdominal pain, diarrhea, weight loss, abdominal mass or complications (excluding perianal disease); and two hematologic abnormalities: hemoglobin, ESR, albumin, C reactive protein, iron, or total iron binding capacity. Patients were monitored for the aforementioned clinical and hematologic (hemoglobin, albumin, CRP) parameters over six weeks and for changes in fecal flora. Randomization was to four groups: metronidazole alone (M), cotrimoxazole alone (C), metronidazole and cotrimoxazole (C plus M), or double placebo (P). Seventy-two patients entered the study (18 = M, 16 = C, 21 = C plus M, 17 = P). After two weeks, improvement was reported as follows: M = 67 percent, C = 17 percent, C plus M = 71 percent, P = 35 percent. In the metronidazole group, two patients required surgery and one had troublesome side effects. In the cotrimoxazole group, two had side effects. In the combined group (C plus M), four had troublesome side effects and two of the placebo group (P) required operation. By four weeks, there was no difference in response among the groups: (M = 44 percent, C = 62 percent, C plus M = 57 percent, P = 41 percent). Antimicrobials had no effect on fecal flora or hematologic parameters. These results indicate that antimicrobials have little therapeutic potential for relapse of intestinal Crohn's disease.</description><subject>Adult</subject><subject>Aged</subject><subject>Antibacterial agents</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Biological and medical sciences</subject><subject>Clinical Trials as Topic</subject><subject>Crohn Disease - drug therapy</subject><subject>Crohn Disease - microbiology</subject><subject>Double-Blind Method</subject><subject>Drug Combinations - administration & dosage</subject><subject>Drug Therapy, Combination</subject><subject>Feces - microbiology</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Metronidazole - administration & dosage</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>Random Allocation</subject><subject>Recurrence</subject><subject>Sulfamethoxazole - administration & dosage</subject><subject>Trimethoprim - administration & dosage</subject><subject>Trimethoprim, Sulfamethoxazole Drug Combination</subject><issn>0012-3706</issn><issn>1530-0358</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkM1LAzEUxIMotVYv3oUcREHY-pJsdjfHWvyCghc9L9nsWxrZL5NUqH-9kZZ6egzzY5g3hFwymDOA_P7hCbiUPEvVEZkyKSABIYtjMgVgPBE5ZKfkzPvPKIFDPiETURRcZOmU2EUfbGWHYA0Na3R63NJmcDQ41KHDPlDbU4etHj3SoYkqoA-21y1dumHd33paW4_a45wu6OgGP6IJ9hup0309dPYHa-rDpt6ek5NGtx4v9ndGPp4e35cvyert-XW5WCWG5xCSjKkcNNNKyowZqETNsQbDoOBaFpWohKkaxbnSqRCpYFnVMKjStMikMpnSYkZudrmxzNcmli076w22re5x2PgylypXAngE73agia29w6Ycne2025YMyr9dy_9dI3y1T91UHdYHdD9k9K_3vvZGt0383lh_wBRnRV5I8QtjM38x</recordid><startdate>198502</startdate><enddate>198502</enddate><creator>AMBROSE, N. S</creator><creator>ALLAN, R. N</creator><creator>KEIGHLEY, M. R. B</creator><creator>BURDON, D. W</creator><creator>YOUNGS, D</creator><creator>BARNES, P</creator><creator>LENNARD-JONES, J. E</creator><general>Springer</general><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>7X8</scope></search><sort><creationdate>198502</creationdate><title>Antibiotic therapy for treatment in relapse of intestinal Crohn's disease. A prospective randomized study</title><author>AMBROSE, N. S ; ALLAN, R. N ; KEIGHLEY, M. R. B ; BURDON, D. W ; YOUNGS, D ; BARNES, P ; LENNARD-JONES, J. 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Drug treatments</topic><topic>Random Allocation</topic><topic>Recurrence</topic><topic>Sulfamethoxazole - administration & dosage</topic><topic>Trimethoprim - administration & dosage</topic><topic>Trimethoprim, Sulfamethoxazole Drug Combination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>AMBROSE, N. S</creatorcontrib><creatorcontrib>ALLAN, R. N</creatorcontrib><creatorcontrib>KEIGHLEY, M. R. B</creatorcontrib><creatorcontrib>BURDON, D. W</creatorcontrib><creatorcontrib>YOUNGS, D</creatorcontrib><creatorcontrib>BARNES, P</creatorcontrib><creatorcontrib>LENNARD-JONES, J. 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A prospective randomized study</atitle><jtitle>Diseases of the colon & rectum</jtitle><addtitle>Dis Colon Rectum</addtitle><date>1985-02</date><risdate>1985</risdate><volume>28</volume><issue>2</issue><spage>81</spage><epage>85</epage><pages>81-85</pages><issn>0012-3706</issn><eissn>1530-0358</eissn><coden>DICRAG</coden><abstract>We have undertaken a prospective randomized trial of one month's antimicrobial therapy for patients with symptomatic relapse of Crohn's disease. Criteria for entry included two major symptoms: fever, abdominal pain, diarrhea, weight loss, abdominal mass or complications (excluding perianal disease); and two hematologic abnormalities: hemoglobin, ESR, albumin, C reactive protein, iron, or total iron binding capacity. Patients were monitored for the aforementioned clinical and hematologic (hemoglobin, albumin, CRP) parameters over six weeks and for changes in fecal flora. Randomization was to four groups: metronidazole alone (M), cotrimoxazole alone (C), metronidazole and cotrimoxazole (C plus M), or double placebo (P). Seventy-two patients entered the study (18 = M, 16 = C, 21 = C plus M, 17 = P). After two weeks, improvement was reported as follows: M = 67 percent, C = 17 percent, C plus M = 71 percent, P = 35 percent. In the metronidazole group, two patients required surgery and one had troublesome side effects. In the cotrimoxazole group, two had side effects. In the combined group (C plus M), four had troublesome side effects and two of the placebo group (P) required operation. By four weeks, there was no difference in response among the groups: (M = 44 percent, C = 62 percent, C plus M = 57 percent, P = 41 percent). Antimicrobials had no effect on fecal flora or hematologic parameters. These results indicate that antimicrobials have little therapeutic potential for relapse of intestinal Crohn's disease.</abstract><cop>Secaucus, NJ</cop><pub>Springer</pub><pmid>3882364</pmid><doi>10.1007/BF02552649</doi><tpages>5</tpages></addata></record> |
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subjects | Adult Aged Antibacterial agents Antibiotics. Antiinfectious agents. Antiparasitic agents Biological and medical sciences Clinical Trials as Topic Crohn Disease - drug therapy Crohn Disease - microbiology Double-Blind Method Drug Combinations - administration & dosage Drug Therapy, Combination Feces - microbiology Humans Medical sciences Metronidazole - administration & dosage Middle Aged Pharmacology. Drug treatments Random Allocation Recurrence Sulfamethoxazole - administration & dosage Trimethoprim - administration & dosage Trimethoprim, Sulfamethoxazole Drug Combination |
title | Antibiotic therapy for treatment in relapse of intestinal Crohn's disease. A prospective randomized study |
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