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Mirtazapine for symptom control in refractory gastroparesis

INTRODUCTION: Gastroparesis symptoms can be severe and debilitating. Many patients do not respond to currently available treatments. Mirtazapine has been shown in case reports to reduce symptoms in gastroparesis. AIM: To assess the efficacy and safety of mirtazapine in gastroparetic patients. METHOD...

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Autores principales: Malamood, Mark, Roberts, Aaron, Kataria, Rahul, Parkman, Henry P, Schey, Ron
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384687/
https://www.ncbi.nlm.nih.gov/pubmed/28408802
http://dx.doi.org/10.2147/DDDT.S125743
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author Malamood, Mark
Roberts, Aaron
Kataria, Rahul
Parkman, Henry P
Schey, Ron
author_facet Malamood, Mark
Roberts, Aaron
Kataria, Rahul
Parkman, Henry P
Schey, Ron
author_sort Malamood, Mark
collection PubMed
description INTRODUCTION: Gastroparesis symptoms can be severe and debilitating. Many patients do not respond to currently available treatments. Mirtazapine has been shown in case reports to reduce symptoms in gastroparesis. AIM: To assess the efficacy and safety of mirtazapine in gastroparetic patients. METHODS: Adults with gastroparesis and poorly controlled symptoms were eligible. Participants were prescribed mirtazapine 15 mg PO qhs. Questionnaires containing the gastrointestinal cardinal symptom index (GCSI) and the clinical patient grading assessment scale (CPGAS) were completed by patients’ pretreatment, at 2 weeks, and at 4 weeks. Primary end point was nausea and vomiting response to mirtazapine using the GCSI. Secondary end point was nausea and vomiting severity assessment using the CPGAS. P-values were calculated using the paired two-tailed Student’s t-test. Intention to treat analysis was used. RESULTS: A total of 30 patients aged 19–86 years were enrolled. Of those, 24 patients (80%) completed 4 weeks of therapy. There were statistically significant improvements in nausea, vomiting, retching, and perceived loss of appetite at 2 and 4 weeks (all P-values <0.05) compared with pretreatment. There was a statistically significant improvement in the CPGAS score at week 2 (P=0.003) and week 4 (P<0.001). Of the total patients, 14 (46.7%) experienced adverse effects from mirtazapine and due to this, 6 patients stopped therapy. CONCLUSION: Mirtazapine significantly improved both nausea and vomiting in gastroparetics after 2 and 4 weeks of treatment. Side effects led to treatment self-cessation in a fifth of patients. From these data, we conclude that mirtazapine improves nausea and vomiting, among other symptoms, in patients with gastroparesis and might be useful in select patients.
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spelling pubmed-53846872017-04-13 Mirtazapine for symptom control in refractory gastroparesis Malamood, Mark Roberts, Aaron Kataria, Rahul Parkman, Henry P Schey, Ron Drug Des Devel Ther Original Research INTRODUCTION: Gastroparesis symptoms can be severe and debilitating. Many patients do not respond to currently available treatments. Mirtazapine has been shown in case reports to reduce symptoms in gastroparesis. AIM: To assess the efficacy and safety of mirtazapine in gastroparetic patients. METHODS: Adults with gastroparesis and poorly controlled symptoms were eligible. Participants were prescribed mirtazapine 15 mg PO qhs. Questionnaires containing the gastrointestinal cardinal symptom index (GCSI) and the clinical patient grading assessment scale (CPGAS) were completed by patients’ pretreatment, at 2 weeks, and at 4 weeks. Primary end point was nausea and vomiting response to mirtazapine using the GCSI. Secondary end point was nausea and vomiting severity assessment using the CPGAS. P-values were calculated using the paired two-tailed Student’s t-test. Intention to treat analysis was used. RESULTS: A total of 30 patients aged 19–86 years were enrolled. Of those, 24 patients (80%) completed 4 weeks of therapy. There were statistically significant improvements in nausea, vomiting, retching, and perceived loss of appetite at 2 and 4 weeks (all P-values <0.05) compared with pretreatment. There was a statistically significant improvement in the CPGAS score at week 2 (P=0.003) and week 4 (P<0.001). Of the total patients, 14 (46.7%) experienced adverse effects from mirtazapine and due to this, 6 patients stopped therapy. CONCLUSION: Mirtazapine significantly improved both nausea and vomiting in gastroparetics after 2 and 4 weeks of treatment. Side effects led to treatment self-cessation in a fifth of patients. From these data, we conclude that mirtazapine improves nausea and vomiting, among other symptoms, in patients with gastroparesis and might be useful in select patients. Dove Medical Press 2017-03-30 /pmc/articles/PMC5384687/ /pubmed/28408802 http://dx.doi.org/10.2147/DDDT.S125743 Text en © 2017 Malamood et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Malamood, Mark
Roberts, Aaron
Kataria, Rahul
Parkman, Henry P
Schey, Ron
Mirtazapine for symptom control in refractory gastroparesis
title Mirtazapine for symptom control in refractory gastroparesis
title_full Mirtazapine for symptom control in refractory gastroparesis
title_fullStr Mirtazapine for symptom control in refractory gastroparesis
title_full_unstemmed Mirtazapine for symptom control in refractory gastroparesis
title_short Mirtazapine for symptom control in refractory gastroparesis
title_sort mirtazapine for symptom control in refractory gastroparesis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384687/
https://www.ncbi.nlm.nih.gov/pubmed/28408802
http://dx.doi.org/10.2147/DDDT.S125743
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