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Buccal acetaminophen provides fast analgesia: two randomized clinical trials in healthy volunteers

BACKGROUND: Acetaminophen (APAP) by oral or intravenous (iv) routes is used for mild to moderate pain but may take time to be effective. When fast relief is required and/or oral or iv routes are not available because of the patient’s condition, the transmucosal route may be an alternative. METHODOLO...

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Autores principales: Pickering, Gisèle, Macian, Nicolas, Libert, Frédéric, Cardot, J Michel, Coissard, Séverine, Perovitch, Philippe, Maury, Marc, Dubray, Claude
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189711/
https://www.ncbi.nlm.nih.gov/pubmed/25302017
http://dx.doi.org/10.2147/DDDT.S63476
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author Pickering, Gisèle
Macian, Nicolas
Libert, Frédéric
Cardot, J Michel
Coissard, Séverine
Perovitch, Philippe
Maury, Marc
Dubray, Claude
author_facet Pickering, Gisèle
Macian, Nicolas
Libert, Frédéric
Cardot, J Michel
Coissard, Séverine
Perovitch, Philippe
Maury, Marc
Dubray, Claude
author_sort Pickering, Gisèle
collection PubMed
description BACKGROUND: Acetaminophen (APAP) by oral or intravenous (iv) routes is used for mild to moderate pain but may take time to be effective. When fast relief is required and/or oral or iv routes are not available because of the patient’s condition, the transmucosal route may be an alternative. METHODOLOGY: A new transmucosal/buccal (b) pharmaceutical form of APAP dissolved in 50% wt alcohol is compared with other routes of administration. Two consecutive randomized, crossover, double-blind clinical trials (CT1: NCT00982215 and CT2: NCT01206985) included 16 healthy volunteers. CT1 compared the pharmacology of 250 mg bAPAP with 1 g iv APAP. CT2 compared the pharmacodynamics of 125 mg bAPAP with 1 g iv and 125 mg sublingual (s) APAP. Mechanical pain thresholds are recorded in response to mechanical stimuli applied on the forearm several times during 120 minutes. The objective is to compare the time of onset of antinociception and the antinociception (area under the curve) between the routes of administration with analysis of variance (significance P<0.05). RESULTS: bAPAP has a faster time of antinociception onset (15 minutes, P<0.01) and greater antinociception at 50 minutes (P<0.01, CT1) and 30 minutes (P<0.01, CT2) than ivAPAP and sAPAP. All routes are similar after 50 minutes. CONCLUSION: bAPAP has a faster antinociceptive action in healthy volunteers. This attractive alternative to other routes would be useful in situations where oral or iv routes are not available. This finding must now be confirmed in patients suffering from acute pain of mild and moderate intensity.
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spelling pubmed-41897112014-10-09 Buccal acetaminophen provides fast analgesia: two randomized clinical trials in healthy volunteers Pickering, Gisèle Macian, Nicolas Libert, Frédéric Cardot, J Michel Coissard, Séverine Perovitch, Philippe Maury, Marc Dubray, Claude Drug Des Devel Ther Original Research BACKGROUND: Acetaminophen (APAP) by oral or intravenous (iv) routes is used for mild to moderate pain but may take time to be effective. When fast relief is required and/or oral or iv routes are not available because of the patient’s condition, the transmucosal route may be an alternative. METHODOLOGY: A new transmucosal/buccal (b) pharmaceutical form of APAP dissolved in 50% wt alcohol is compared with other routes of administration. Two consecutive randomized, crossover, double-blind clinical trials (CT1: NCT00982215 and CT2: NCT01206985) included 16 healthy volunteers. CT1 compared the pharmacology of 250 mg bAPAP with 1 g iv APAP. CT2 compared the pharmacodynamics of 125 mg bAPAP with 1 g iv and 125 mg sublingual (s) APAP. Mechanical pain thresholds are recorded in response to mechanical stimuli applied on the forearm several times during 120 minutes. The objective is to compare the time of onset of antinociception and the antinociception (area under the curve) between the routes of administration with analysis of variance (significance P<0.05). RESULTS: bAPAP has a faster time of antinociception onset (15 minutes, P<0.01) and greater antinociception at 50 minutes (P<0.01, CT1) and 30 minutes (P<0.01, CT2) than ivAPAP and sAPAP. All routes are similar after 50 minutes. CONCLUSION: bAPAP has a faster antinociceptive action in healthy volunteers. This attractive alternative to other routes would be useful in situations where oral or iv routes are not available. This finding must now be confirmed in patients suffering from acute pain of mild and moderate intensity. Dove Medical Press 2014-09-26 /pmc/articles/PMC4189711/ /pubmed/25302017 http://dx.doi.org/10.2147/DDDT.S63476 Text en © 2014 Pickering et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. 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
Pickering, Gisèle
Macian, Nicolas
Libert, Frédéric
Cardot, J Michel
Coissard, Séverine
Perovitch, Philippe
Maury, Marc
Dubray, Claude
Buccal acetaminophen provides fast analgesia: two randomized clinical trials in healthy volunteers
title Buccal acetaminophen provides fast analgesia: two randomized clinical trials in healthy volunteers
title_full Buccal acetaminophen provides fast analgesia: two randomized clinical trials in healthy volunteers
title_fullStr Buccal acetaminophen provides fast analgesia: two randomized clinical trials in healthy volunteers
title_full_unstemmed Buccal acetaminophen provides fast analgesia: two randomized clinical trials in healthy volunteers
title_short Buccal acetaminophen provides fast analgesia: two randomized clinical trials in healthy volunteers
title_sort buccal acetaminophen provides fast analgesia: two randomized clinical trials in healthy volunteers
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189711/
https://www.ncbi.nlm.nih.gov/pubmed/25302017
http://dx.doi.org/10.2147/DDDT.S63476
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