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The Effect of Once-Daily Gabapentin Extended Release Formulation in Patients With Postamputation Pain

OBJECTIVES: To compare gabapentin extended-release, a gastro-retentive formulation, in relieving postamputation pain among gabapentin-experienced and gabapentin-naïve patients. DESIGN: Open-labeled pilot study. SUBJECTS: Sixteen patients with postamputation pain (8 patients in the gabapentin-experie...

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Autores principales: Knezevic, Nebojsa Nick, Aijaz, Tabish, Candido, Kenneth D., Kovaleva, Svetlana, Lissounov, Alexei, Knezevic, Ivana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529536/
https://www.ncbi.nlm.nih.gov/pubmed/31156433
http://dx.doi.org/10.3389/fphar.2019.00504
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author Knezevic, Nebojsa Nick
Aijaz, Tabish
Candido, Kenneth D.
Kovaleva, Svetlana
Lissounov, Alexei
Knezevic, Ivana
author_facet Knezevic, Nebojsa Nick
Aijaz, Tabish
Candido, Kenneth D.
Kovaleva, Svetlana
Lissounov, Alexei
Knezevic, Ivana
author_sort Knezevic, Nebojsa Nick
collection PubMed
description OBJECTIVES: To compare gabapentin extended-release, a gastro-retentive formulation, in relieving postamputation pain among gabapentin-experienced and gabapentin-naïve patients. DESIGN: Open-labeled pilot study. SUBJECTS: Sixteen patients with postamputation pain (8 patients in the gabapentin-experienced and 8 patients in the gabapentin-naïve groups). METHODS: Patients were started on gabapentin extended-release and were followed up for 8 weeks. Patients reported their pain severity during rest and movement using a numeric rating scale (NRS), interference of pain with daily activities using the modified brief pain inventory (MBPI) questionnaire, and treatment satisfaction using the treatment satisfaction questionnaire for medication (TSQM). RESULTS: Patients from both gabapentin-experienced and gabapentin-naïve groups achieved a significant and sustainable pain relief over the course of therapy. The pain scores at rest decreased in both gabapentin-experienced and gabapentin-naïve groups from 5.88 ± 1.36 and 4.88 ± 2.95 to 1.88 ± 0.99 and 1.38 ± 1.51, respectively. An average percent of pain relief with gabapentin extended-release was noted to be significant (p < 0.01) after 8 weeks of therapy among gabapentin-experienced (81.25 ± 16.42%) and gabapentin-naïve groups (85 ± 17.73%) when compared to baseline for gabapentin-experienced (31.25 ± 29%) and gabapentin-naïve groups (36.25 ± 34.2%), respectively. Gabapentin-experienced and gabapentin-naïve groups had no significant difference in global satisfaction from treatment (79.14 ± 10.47 and 83.3 ± 20.82), convenience of treatment (73.78 ± 19.04 and 90.44 ± 11.66), effectiveness of treatment (72.6 ± 10.1 and 79.73 ± 11.6). The only statistically significant difference among gabapentin-experienced and gabapentin-naïve groups was found in adverse event tolerability (65.78 ± 10.36 and 85.8 ± 10.14, p < 0.01). CONCLUSION: Once-daily dosing of gabapentin-extended release showed significant improvement in pain severity and functional status, with no difference found between gabapentin-experienced versus gabapentin-naïve patients.
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spelling pubmed-65295362019-05-31 The Effect of Once-Daily Gabapentin Extended Release Formulation in Patients With Postamputation Pain Knezevic, Nebojsa Nick Aijaz, Tabish Candido, Kenneth D. Kovaleva, Svetlana Lissounov, Alexei Knezevic, Ivana Front Pharmacol Pharmacology OBJECTIVES: To compare gabapentin extended-release, a gastro-retentive formulation, in relieving postamputation pain among gabapentin-experienced and gabapentin-naïve patients. DESIGN: Open-labeled pilot study. SUBJECTS: Sixteen patients with postamputation pain (8 patients in the gabapentin-experienced and 8 patients in the gabapentin-naïve groups). METHODS: Patients were started on gabapentin extended-release and were followed up for 8 weeks. Patients reported their pain severity during rest and movement using a numeric rating scale (NRS), interference of pain with daily activities using the modified brief pain inventory (MBPI) questionnaire, and treatment satisfaction using the treatment satisfaction questionnaire for medication (TSQM). RESULTS: Patients from both gabapentin-experienced and gabapentin-naïve groups achieved a significant and sustainable pain relief over the course of therapy. The pain scores at rest decreased in both gabapentin-experienced and gabapentin-naïve groups from 5.88 ± 1.36 and 4.88 ± 2.95 to 1.88 ± 0.99 and 1.38 ± 1.51, respectively. An average percent of pain relief with gabapentin extended-release was noted to be significant (p < 0.01) after 8 weeks of therapy among gabapentin-experienced (81.25 ± 16.42%) and gabapentin-naïve groups (85 ± 17.73%) when compared to baseline for gabapentin-experienced (31.25 ± 29%) and gabapentin-naïve groups (36.25 ± 34.2%), respectively. Gabapentin-experienced and gabapentin-naïve groups had no significant difference in global satisfaction from treatment (79.14 ± 10.47 and 83.3 ± 20.82), convenience of treatment (73.78 ± 19.04 and 90.44 ± 11.66), effectiveness of treatment (72.6 ± 10.1 and 79.73 ± 11.6). The only statistically significant difference among gabapentin-experienced and gabapentin-naïve groups was found in adverse event tolerability (65.78 ± 10.36 and 85.8 ± 10.14, p < 0.01). CONCLUSION: Once-daily dosing of gabapentin-extended release showed significant improvement in pain severity and functional status, with no difference found between gabapentin-experienced versus gabapentin-naïve patients. Frontiers Media S.A. 2019-05-15 /pmc/articles/PMC6529536/ /pubmed/31156433 http://dx.doi.org/10.3389/fphar.2019.00504 Text en Copyright © 2019 Knezevic, Aijaz, Candido, Kovaleva, Lissounov and Knezevic. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Knezevic, Nebojsa Nick
Aijaz, Tabish
Candido, Kenneth D.
Kovaleva, Svetlana
Lissounov, Alexei
Knezevic, Ivana
The Effect of Once-Daily Gabapentin Extended Release Formulation in Patients With Postamputation Pain
title The Effect of Once-Daily Gabapentin Extended Release Formulation in Patients With Postamputation Pain
title_full The Effect of Once-Daily Gabapentin Extended Release Formulation in Patients With Postamputation Pain
title_fullStr The Effect of Once-Daily Gabapentin Extended Release Formulation in Patients With Postamputation Pain
title_full_unstemmed The Effect of Once-Daily Gabapentin Extended Release Formulation in Patients With Postamputation Pain
title_short The Effect of Once-Daily Gabapentin Extended Release Formulation in Patients With Postamputation Pain
title_sort effect of once-daily gabapentin extended release formulation in patients with postamputation pain
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529536/
https://www.ncbi.nlm.nih.gov/pubmed/31156433
http://dx.doi.org/10.3389/fphar.2019.00504
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