Literature DB >> 4039775

[Benefit and risk of high-dose metoclopramide in comparison to high-dose haloperidol or triflupromazine in cisplatin-induced vomiting].

R Saller, D Hellenbrecht.   

Abstract

The antiemetic efficacy of metoclopramide (MCL, Paspertin, loading infusion 0.5 mg/kg body wt./h over 2 h, maintenance infusion 0.25 mg/kg/h over 24 h) has been compared with haloperidol (HAL, Haldol, 1/10 of MCL dosage) and with triflupromazine (TFP, Psyquil, 1/2 of MCL dosage) in two sequential analyses, against the emetic effects of cisplatin (60-90 mg/m2). After treating 14 and 8 pairs of patients respectively, MCL was significantly (alpha = 0.05) more effective than HAL or TFP. Only 1 of the 14 patients in the HAL group and 0 of 8 in the TFP group were totally protected against emesis, in contrast to 6 of 14 patients and 3 of 8 in the MCL groups. In order to quantify the benefit/risk relationship of the antiemetic drugs studied the number of prevented emetic episodes (in comparison to previous insufficient treatment) was related to the incidence of major undesired effects (i.e. dystonia and/or akathisia). This relationship was 17.8 and 12.1 for the two MCL groups; for HAL and TFP it was only 5.8 and 4.6, respectively. The high antiemetic selectivity of MCL against cisplatin-induced emesis is probably related to the still unknown action of MCL on the gastrointestinal motility. A high neuroleptic potency, with or without additional anticholinergic activity, is apparently not essential for high antiemetic protection against cisplatin.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 4039775     DOI: 10.1007/bf01733669

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN: 0023-2173


  16 in total

Review 1.  Multiple receptors for dopamine.

Authors:  J W Kebabian; D B Calne
Journal:  Nature       Date:  1979-01-11       Impact factor: 49.962

2.  Neuropharmacology of chemotherapy-induced emesis.

Authors:  H L Borison; L E McCarthy
Journal:  Drugs       Date:  1983-02       Impact factor: 9.546

3.  The gastrointestinal tract in chemotherapy-induced emesis. A final common pathway.

Authors:  O E Akwari
Journal:  Drugs       Date:  1983-02       Impact factor: 9.546

4.  The pharmacology and clinical effectiveness of phenothiazines and related drugs for managing chemotherapy-induced emesis.

Authors:  G Wampler
Journal:  Drugs       Date:  1983-02       Impact factor: 9.546

5.  The action of commonly used antiemetics on the lower oesophageal sphincter.

Authors:  J G Brock-Utne; J Rubin; S Welman; G E Dimopoulos; M G Moshal; J W Downing
Journal:  Br J Anaesth       Date:  1978-03       Impact factor: 9.166

6.  Comparison of the antiemetic effect of high-dose intravenous metoclopramide and high-dose intravenous haloperidol in a randomized double-blind crossover study.

Authors:  S M Grunberg; K V Gala; M Lampenfeld; D Jamin; K Johnson; P Cariffe; D Strych; M Krailo
Journal:  J Clin Oncol       Date:  1984-07       Impact factor: 44.544

7.  Antagonism of cisplatin induced emesis in the dog.

Authors:  J A Gylys; K M Doran; J P Buyniski
Journal:  Res Commun Chem Pathol Pharmacol       Date:  1979-01

8.  Metoclopramide. A review of antiemetic trials.

Authors:  R J Gralla
Journal:  Drugs       Date:  1983-02       Impact factor: 9.546

9.  Lorazepam as an adjunct to antiemetic therapy with haloperidol in patients receiving cytotoxic chemotherapy.

Authors:  M L Friedlander; J H Kearsley; K Sims; A Coates; D Hedley; D Raghavan; R M Fox; M H Tattersall
Journal:  Aust N Z J Med       Date:  1983-02

10.  Specific antiemetics for specific cancer chemotherapeutic agents: haloperidol versus benzquinamide.

Authors:  J A Neidhart; M Gagen; D Young; H E Wilson
Journal:  Cancer       Date:  1981-03-15       Impact factor: 6.860

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.