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Granisetron Transdermal System for Treatment of Symptoms of Gastroparesis: A Prescription Registry Study

BACKGROUND/AIMS: Serotonin receptor (eg, 5-HT(3)) antagonists are used to treat nausea and vomiting from a variety of causes. Granisetron transdermal system (GTS) is an appealing delivery system for patients with gastroparesis. To assess if GTS improves nausea and vomiting and other gastroparesis sy...

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Detalles Bibliográficos
Autores principales: Midani, Deena, Parkman, Henry P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Neurogastroenterology and Motility 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5056574/
https://www.ncbi.nlm.nih.gov/pubmed/27400689
http://dx.doi.org/10.5056/jnm15203
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author Midani, Deena
Parkman, Henry P
author_facet Midani, Deena
Parkman, Henry P
author_sort Midani, Deena
collection PubMed
description BACKGROUND/AIMS: Serotonin receptor (eg, 5-HT(3)) antagonists are used to treat nausea and vomiting from a variety of causes. Granisetron transdermal system (GTS) is an appealing delivery system for patients with gastroparesis. To assess if GTS improves nausea and vomiting and other gastroparesis symptoms in patients with gastroparesis. METHODS: Patients with gastroparesis and symptoms of nausea and vomiting refractory to conventional treatment were treated with GTS. Symptoms of gastroparesis were assessed using a modified Gastroparesis Cardinal Symptom Index (GCSI). Following 2 weeks of treatment, patients were asked to assess their symptoms and indicate their therapeutic response using the Clinical Patient Grading Assessment Scale (CPGAS) reporting if symptoms of nausea and vomiting improved on a scale: 0 = no change to +7 = completely better. RESULTS: Fifty-one patients received GTS by prescription: average age was 40 ± 17 years, 44 female, 11 diabetics, 23 ± 20% retention at 4 hours on gastric emptying scintigraphy. Thirty-nine of the 51 (76%) patients stated improvement with GTS. There was significant improvement in nausea and vomiting as assessed with CPGAS at 2 weeks (2.28 ± 2.53; P < 0.05). Symptoms of nausea and vomiting significantly improved. Other symptoms including postprandial fullness, loss of appetite, upper abdominal pain, and early satiety improved. Side effects reported included redness at the site of the patch in 7 patients, pruritus in 5, and constipation in 5. CONCLUSIONS: GTS was moderately effective in reducing nausea and/or vomiting in 76% of gastroparesis patients. In addition to nausea and vomiting, symptoms of postprandial fullness, loss of appetite, upper abdominal pain, and early satiety also improved.
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spelling pubmed-50565742016-10-11 Granisetron Transdermal System for Treatment of Symptoms of Gastroparesis: A Prescription Registry Study Midani, Deena Parkman, Henry P J Neurogastroenterol Motil Original Article BACKGROUND/AIMS: Serotonin receptor (eg, 5-HT(3)) antagonists are used to treat nausea and vomiting from a variety of causes. Granisetron transdermal system (GTS) is an appealing delivery system for patients with gastroparesis. To assess if GTS improves nausea and vomiting and other gastroparesis symptoms in patients with gastroparesis. METHODS: Patients with gastroparesis and symptoms of nausea and vomiting refractory to conventional treatment were treated with GTS. Symptoms of gastroparesis were assessed using a modified Gastroparesis Cardinal Symptom Index (GCSI). Following 2 weeks of treatment, patients were asked to assess their symptoms and indicate their therapeutic response using the Clinical Patient Grading Assessment Scale (CPGAS) reporting if symptoms of nausea and vomiting improved on a scale: 0 = no change to +7 = completely better. RESULTS: Fifty-one patients received GTS by prescription: average age was 40 ± 17 years, 44 female, 11 diabetics, 23 ± 20% retention at 4 hours on gastric emptying scintigraphy. Thirty-nine of the 51 (76%) patients stated improvement with GTS. There was significant improvement in nausea and vomiting as assessed with CPGAS at 2 weeks (2.28 ± 2.53; P < 0.05). Symptoms of nausea and vomiting significantly improved. Other symptoms including postprandial fullness, loss of appetite, upper abdominal pain, and early satiety improved. Side effects reported included redness at the site of the patch in 7 patients, pruritus in 5, and constipation in 5. CONCLUSIONS: GTS was moderately effective in reducing nausea and/or vomiting in 76% of gastroparesis patients. In addition to nausea and vomiting, symptoms of postprandial fullness, loss of appetite, upper abdominal pain, and early satiety also improved. Korean Society of Neurogastroenterology and Motility 2016-10 2016-10-01 /pmc/articles/PMC5056574/ /pubmed/27400689 http://dx.doi.org/10.5056/jnm15203 Text en © 2016 The Korean Society of Neurogastroenterology and Motility This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Midani, Deena
Parkman, Henry P
Granisetron Transdermal System for Treatment of Symptoms of Gastroparesis: A Prescription Registry Study
title Granisetron Transdermal System for Treatment of Symptoms of Gastroparesis: A Prescription Registry Study
title_full Granisetron Transdermal System for Treatment of Symptoms of Gastroparesis: A Prescription Registry Study
title_fullStr Granisetron Transdermal System for Treatment of Symptoms of Gastroparesis: A Prescription Registry Study
title_full_unstemmed Granisetron Transdermal System for Treatment of Symptoms of Gastroparesis: A Prescription Registry Study
title_short Granisetron Transdermal System for Treatment of Symptoms of Gastroparesis: A Prescription Registry Study
title_sort granisetron transdermal system for treatment of symptoms of gastroparesis: a prescription registry study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5056574/
https://www.ncbi.nlm.nih.gov/pubmed/27400689
http://dx.doi.org/10.5056/jnm15203
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