Literature DB >> 11862500

How do we manage patients with refractory or breakthrough emesis?

Matti S Aapro1.   

Abstract

There is evidence that, in spite of the Perugia consensus, acute and delayed emesis are treated in a suboptimal way. Thus breakthrough and refractory emesis as defined in this paper may be related to inadequate therapy. Several interventions have been used in attempts to stop breakthrough emesis, including use or repeat use of setrons, corticosteroids, D2-receptor antagonists including neuroleptics, or sedatives. It has been documented that refractory emesis responds to various modifications of the original antiemetic regimen, including the addition of a D2-receptor antagonist or a switch to another setron. In conclusion, no level I or II evidence-based guidelines can be given, as few adequate studies have been performed in this area, which therefore remains poorly documented.

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Year:  2001        PMID: 11862500     DOI: 10.1007/s005200100288

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  11 in total

1.  Nausea and emesis: still an unsolved problem in cancer patients?

Authors:  Jørn Herrstedt
Journal:  Support Care Cancer       Date:  2002-01-31       Impact factor: 3.603

Review 2.  Antiemetic therapy for multiple-day chemotherapy and high-dose chemotherapy with stem cell transplant: review and consensus statement.

Authors:  Lawrence H Einhorn; Bernardo Rapoport; Jim Koeller; Steven M Grunberg; Petra Feyer; Cynthia Rittenberg; Matti Aapro
Journal:  Support Care Cancer       Date:  2004-10-09       Impact factor: 3.603

3.  Cross-national comparison of medical costs shared by payers and patients: a study of postmenopausal women with early-stage breast cancer based on assumption case scenarios and reimbursement fees.

Authors:  Shota Hamada; Shiro Hinotsu; Hiroshi Ishiguro; Masakazu Toi; Koji Kawakami
Journal:  Breast Care (Basel)       Date:  2013-08       Impact factor: 2.860

4.  Midazolam for acute emesis refractory to dexamethasone and granisetron after highly emetogenic chemotherapy: a phase II study.

Authors:  M Mandalà; M Cremonesi; A Rocca; M Cazzaniga; G Ferretti; S Di Cosimo; M Ghilardi; M Cabiddu; S Barni
Journal:  Support Care Cancer       Date:  2005-01-25       Impact factor: 3.603

5.  Computerized detection and analysis of cancer chemotherapy-induced emesis in a small animal model, musk shrew.

Authors:  Dong Huang; Kelly Meyers; Séverine Henry; Fernando De la Torre; Charles C Horn
Journal:  J Neurosci Methods       Date:  2011-03-15       Impact factor: 2.390

6.  Chemotherapy-induced nausea and vomiting in routine practice: a European perspective.

Authors:  Agnes Glaus; Cornelia Knipping; Rudolf Morant; Christel Böhme; Burkhard Lebert; Frank Beldermann; Bernhard Glawogger; Paz Fernandez Ortega; André Hüsler; Robert Deuson
Journal:  Support Care Cancer       Date:  2004-10       Impact factor: 3.603

7.  Chemotherapy agent cisplatin induces 48-h Fos expression in the brain of a vomiting species, the house musk shrew (Suncus murinus).

Authors:  Bart C De Jonghe; Charles C Horn
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2009-02-18       Impact factor: 3.619

8.  Food restriction, refeeding, and gastric fill fail to affect emesis in musk shrews.

Authors:  Charles C Horn; Liz Still; Christiana Fitzgerald; Mark I Friedman
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2009-11-05       Impact factor: 4.052

9.  Brain Fos expression induced by the chemotherapy agent cisplatin in the rat is partially dependent on an intact abdominal vagus.

Authors:  Charles C Horn
Journal:  Auton Neurosci       Date:  2009-04-10       Impact factor: 3.145

Review 10.  Options for the prevention and management of acute chemotherapy-induced nausea and vomiting in children.

Authors:  L Lee Dupuis; Paul C Nathan
Journal:  Paediatr Drugs       Date:  2003       Impact factor: 3.022

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