EBM

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS REGISTER
[Advanced]

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Add article to my folders
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kinzbrunner, B. M
Right arrow Search for Related Content
PubMed
Right arrow Articles by Kinzbrunner, B. M
Evidence-Based Medicine 2002; 7:25
© 2002 Evidence-Based Medicine


Therapeutics

Review: cannabinoids control chemotherapy-induced nausea and vomiting but increase the risk of side effects

Tramér MR, Carroll D, Campbell FA, et al. Cannabinoids for control of chemotherapy induced nausea and vomiting: quantitative systematic review. BMJ 2001 Jul 7;323:16–21.[Abstract/Free Full Text]

QUESTION: In patients with chemotherapy-induced sickness, what are the antiemetic efficacy and adverse effects of cannabinoids?

Data sources
Full publications of studies were identified by searching Medline (from 1966), EMBASE/Excerpta Medica (from 1982), and the Cochrane Library (2000, Issue 3) with the terms cannabinoids, cannabis, nabilone, tetrahydrocannabinol (THC), THC, marihuana, marijuana, levonantradol, dronabinol, randomized, and human. Bibliographies of relevant studies were checked.

Study selection
Studies were selected if they were randomised controlled trials (RCTs) comparing the antiemetic efficacy of cannabis with any other antiemetic agent or placebo in patients having chemotherapy.

Data extraction
Data were extracted on study quality, patients, interventions and regimens, and outcomes.

Main results
30 RCTs (1366 patients) published between 1975 and 1997 met the selection criteria. The mean number of patients per study was 46 (range 8 to 139 patients). 16 studies examined oral nabilone, 13 examined oral dronabinol, and 1 examined intramuscular levonantradol. The active control groups were administered prochlorperazine (12 studies), metoclopramide (4 studies), chlorpromazine (2 studies), thiethylperazine (1 study), haloperidol (1 study), domperidone (2 study), and alizapride . . . [Full text of this article]

Barry M Kinzbrunner, MD

Vitas Healthcare Corporation, Miami, Florida, USA







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS REGISTER
Terms and conditions relating to subscriptions purchased online  ¦  Website terms and conditions  ¦  Privacy policy
Copyright © 2002 by the BMJ Publishing Group Ltd.