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Safety, Tolerability, and Efficacy of Pain Reduction by Gabapentin for Acute Headache and Meningismus After Aneurysmal Subarachnoid Hemorrhage: A Pilot Study

Introduction: Severe, often sudden-onset headache is the principal presenting symptoms of aneurysmal subarachnoid hemorrhage (aSAH). We hypothesized that gabapentin would be safe and tolerable for aSAH-induced headaches and would reduce concurrent opioid use. Methods: We performed a single-center, d...

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Autores principales: Dhakal, Laxmi P., Turnbull, Marion T., Jackson, Daniel A., Edwards, Emily, Hodge, David O., Thottempudi, Neeharika, Kamireddi, Prasuna, Akinduro, Oluwaseun O., Miller, David A., Meschia, James F., Freeman, William D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399216/
https://www.ncbi.nlm.nih.gov/pubmed/32849209
http://dx.doi.org/10.3389/fneur.2020.00744
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author Dhakal, Laxmi P.
Turnbull, Marion T.
Jackson, Daniel A.
Edwards, Emily
Hodge, David O.
Thottempudi, Neeharika
Kamireddi, Prasuna
Akinduro, Oluwaseun O.
Miller, David A.
Meschia, James F.
Freeman, William D.
author_facet Dhakal, Laxmi P.
Turnbull, Marion T.
Jackson, Daniel A.
Edwards, Emily
Hodge, David O.
Thottempudi, Neeharika
Kamireddi, Prasuna
Akinduro, Oluwaseun O.
Miller, David A.
Meschia, James F.
Freeman, William D.
author_sort Dhakal, Laxmi P.
collection PubMed
description Introduction: Severe, often sudden-onset headache is the principal presenting symptoms of aneurysmal subarachnoid hemorrhage (aSAH). We hypothesized that gabapentin would be safe and tolerable for aSAH-induced headaches and would reduce concurrent opioid use. Methods: We performed a single-center, double-blind, randomized, placebo-controlled trial (registered at ClinicalTrials.gov; NCT02330094) from November 24, 2014, to June 24, 2017, where aSAH patients received either dose-escalating gabapentin or oral placebo, both alongside a standard of care pain regimen. After 7 days, patients had the option to continue in an open-label period until 14 days after enrollment or until discharge from the intensive care unit. Our primary endpoint was the efficacy of gabapentin in reducing headache numeric pain scores and opioid usage in patients with aSAH compared to the placebo group. We identified 63 potential patients with aSAH for the study. After applying stringent exclusion criteria, 16 eligible patients were enrolled into one of two arms. Results: The study ended prematurely after reaching a pre-specified funding period and an unexpected drop in aSAH cases. There was a trend toward lower headache numeric pain scores and opioid use in the gabapentin treated arm; however this was not significantly different. Gabapentin was well tolerated by participants and no adverse effects were reported. Conclusions: While there was a trend toward lower pain scores and opioid requirement in the gabapentin group, the study was underpowered to detect a difference. Larger multicenter trials are required to evaluate the efficacy of gabapentin to reduce opioid requirements after aSAH.
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spelling pubmed-73992162020-08-25 Safety, Tolerability, and Efficacy of Pain Reduction by Gabapentin for Acute Headache and Meningismus After Aneurysmal Subarachnoid Hemorrhage: A Pilot Study Dhakal, Laxmi P. Turnbull, Marion T. Jackson, Daniel A. Edwards, Emily Hodge, David O. Thottempudi, Neeharika Kamireddi, Prasuna Akinduro, Oluwaseun O. Miller, David A. Meschia, James F. Freeman, William D. Front Neurol Neurology Introduction: Severe, often sudden-onset headache is the principal presenting symptoms of aneurysmal subarachnoid hemorrhage (aSAH). We hypothesized that gabapentin would be safe and tolerable for aSAH-induced headaches and would reduce concurrent opioid use. Methods: We performed a single-center, double-blind, randomized, placebo-controlled trial (registered at ClinicalTrials.gov; NCT02330094) from November 24, 2014, to June 24, 2017, where aSAH patients received either dose-escalating gabapentin or oral placebo, both alongside a standard of care pain regimen. After 7 days, patients had the option to continue in an open-label period until 14 days after enrollment or until discharge from the intensive care unit. Our primary endpoint was the efficacy of gabapentin in reducing headache numeric pain scores and opioid usage in patients with aSAH compared to the placebo group. We identified 63 potential patients with aSAH for the study. After applying stringent exclusion criteria, 16 eligible patients were enrolled into one of two arms. Results: The study ended prematurely after reaching a pre-specified funding period and an unexpected drop in aSAH cases. There was a trend toward lower headache numeric pain scores and opioid use in the gabapentin treated arm; however this was not significantly different. Gabapentin was well tolerated by participants and no adverse effects were reported. Conclusions: While there was a trend toward lower pain scores and opioid requirement in the gabapentin group, the study was underpowered to detect a difference. Larger multicenter trials are required to evaluate the efficacy of gabapentin to reduce opioid requirements after aSAH. Frontiers Media S.A. 2020-07-28 /pmc/articles/PMC7399216/ /pubmed/32849209 http://dx.doi.org/10.3389/fneur.2020.00744 Text en Copyright © 2020 Dhakal, Turnbull, Jackson, Edwards, Hodge, Thottempudi, Kamireddi, Akinduro, Miller, Meschia and Freeman. 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 Neurology
Dhakal, Laxmi P.
Turnbull, Marion T.
Jackson, Daniel A.
Edwards, Emily
Hodge, David O.
Thottempudi, Neeharika
Kamireddi, Prasuna
Akinduro, Oluwaseun O.
Miller, David A.
Meschia, James F.
Freeman, William D.
Safety, Tolerability, and Efficacy of Pain Reduction by Gabapentin for Acute Headache and Meningismus After Aneurysmal Subarachnoid Hemorrhage: A Pilot Study
title Safety, Tolerability, and Efficacy of Pain Reduction by Gabapentin for Acute Headache and Meningismus After Aneurysmal Subarachnoid Hemorrhage: A Pilot Study
title_full Safety, Tolerability, and Efficacy of Pain Reduction by Gabapentin for Acute Headache and Meningismus After Aneurysmal Subarachnoid Hemorrhage: A Pilot Study
title_fullStr Safety, Tolerability, and Efficacy of Pain Reduction by Gabapentin for Acute Headache and Meningismus After Aneurysmal Subarachnoid Hemorrhage: A Pilot Study
title_full_unstemmed Safety, Tolerability, and Efficacy of Pain Reduction by Gabapentin for Acute Headache and Meningismus After Aneurysmal Subarachnoid Hemorrhage: A Pilot Study
title_short Safety, Tolerability, and Efficacy of Pain Reduction by Gabapentin for Acute Headache and Meningismus After Aneurysmal Subarachnoid Hemorrhage: A Pilot Study
title_sort safety, tolerability, and efficacy of pain reduction by gabapentin for acute headache and meningismus after aneurysmal subarachnoid hemorrhage: a pilot study
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399216/
https://www.ncbi.nlm.nih.gov/pubmed/32849209
http://dx.doi.org/10.3389/fneur.2020.00744
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