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
Hauptverfasser: AMBROSE, N. S, ALLAN, R. N, KEIGHLEY, M. R. B, BURDON, D. W, YOUNGS, D, BARNES, P, LENNARD-JONES, J. E
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container_end_page 85
container_issue 2
container_start_page 81
container_title Diseases of the colon & rectum
container_volume 28
creator AMBROSE, N. S
ALLAN, R. N
KEIGHLEY, M. R. B
BURDON, D. W
YOUNGS, D
BARNES, P
LENNARD-JONES, J. E
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.
doi_str_mv 10.1007/BF02552649
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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. 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A prospective randomized study</atitle><jtitle>Diseases of the colon &amp; 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. 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ispartof Diseases of the colon & rectum, 1985-02, Vol.28 (2), p.81-85
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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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