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Opioids Switching with Transdermal Systems in Chronic Cancer Pain

BACKGROUND: Due to tolerance development and adverse side effects, chronic pain patients frequently need to be switched to alternative opioid therapy OBJECTIVE: To assess the efficacy and tolerability of an alternative transdermally applied (TDS) opioid in patients with chronic cancer pain receiving...

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Autores principales: Aurilio, C, Pace, MC, Pota, V, Sansone, P, Barbarisi, M, Grella, E, Passavanti, MB
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2684533/
https://www.ncbi.nlm.nih.gov/pubmed/19422676
http://dx.doi.org/10.1186/1756-9966-28-61
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author Aurilio, C
Pace, MC
Pota, V
Sansone, P
Barbarisi, M
Grella, E
Passavanti, MB
author_facet Aurilio, C
Pace, MC
Pota, V
Sansone, P
Barbarisi, M
Grella, E
Passavanti, MB
author_sort Aurilio, C
collection PubMed
description BACKGROUND: Due to tolerance development and adverse side effects, chronic pain patients frequently need to be switched to alternative opioid therapy OBJECTIVE: To assess the efficacy and tolerability of an alternative transdermally applied (TDS) opioid in patients with chronic cancer pain receiving insufficient analgesia using their present treatment. METHODS: A total of 32 patients received alternative opioid therapy, 16 were switched from buprenorphine to fentanyl and 16 were switched from fentanyl to buprenorphine. The dosage used was 50% of that indicated in equipotency conversion tables. Pain relief was assessed at weekly intervals for the next 3 weeks RESULTS: Pain relief as assessed by VAS, PPI, and PRI significantly improved (p < 0.0001) in all patients at all 3 follow up visits. After 3 weeks of treatment, the reduction in the mean VAS, PPI, and PRI scores in the fentanyl and buprenorphine groups was 68, 77, 74, and 69, 79, and 62%, respectively. Over the same time period the use of oral morphine as rescue medication was reduced from 27.5 ± 20.5 (mean ± SD) to 3.75 ± 8.06, and 33.8 ± 18.9 to 3.75 ± 10.9 mg/day in the fentanyl and buprenorphine groups, respectively. There was no significant difference in either pain relief or rescue medication use between the two patient groups The number of patient with adverse events fell during the study. After the third week of the treatment the number of patients with constipation was reduced from 11 to 5, and 10 to 4 patients in the fentanyl and buprenorphine groups, respectively. There was a similar reduction in the incidence of nausea and vomiting. No sedation was seen in any patient after one week of treatment. CONCLUSION: Opioid switching at 50% of the calculated equianalgesic dose produced a significant reduction in pain levels and rescue medication. The incidence of side effects decreased and no new side effects were noted. Further studies are required to provide individualized treatment for patients according to their different types of cancer.
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spelling pubmed-26845332009-05-20 Opioids Switching with Transdermal Systems in Chronic Cancer Pain Aurilio, C Pace, MC Pota, V Sansone, P Barbarisi, M Grella, E Passavanti, MB J Exp Clin Cancer Res Research BACKGROUND: Due to tolerance development and adverse side effects, chronic pain patients frequently need to be switched to alternative opioid therapy OBJECTIVE: To assess the efficacy and tolerability of an alternative transdermally applied (TDS) opioid in patients with chronic cancer pain receiving insufficient analgesia using their present treatment. METHODS: A total of 32 patients received alternative opioid therapy, 16 were switched from buprenorphine to fentanyl and 16 were switched from fentanyl to buprenorphine. The dosage used was 50% of that indicated in equipotency conversion tables. Pain relief was assessed at weekly intervals for the next 3 weeks RESULTS: Pain relief as assessed by VAS, PPI, and PRI significantly improved (p < 0.0001) in all patients at all 3 follow up visits. After 3 weeks of treatment, the reduction in the mean VAS, PPI, and PRI scores in the fentanyl and buprenorphine groups was 68, 77, 74, and 69, 79, and 62%, respectively. Over the same time period the use of oral morphine as rescue medication was reduced from 27.5 ± 20.5 (mean ± SD) to 3.75 ± 8.06, and 33.8 ± 18.9 to 3.75 ± 10.9 mg/day in the fentanyl and buprenorphine groups, respectively. There was no significant difference in either pain relief or rescue medication use between the two patient groups The number of patient with adverse events fell during the study. After the third week of the treatment the number of patients with constipation was reduced from 11 to 5, and 10 to 4 patients in the fentanyl and buprenorphine groups, respectively. There was a similar reduction in the incidence of nausea and vomiting. No sedation was seen in any patient after one week of treatment. CONCLUSION: Opioid switching at 50% of the calculated equianalgesic dose produced a significant reduction in pain levels and rescue medication. The incidence of side effects decreased and no new side effects were noted. Further studies are required to provide individualized treatment for patients according to their different types of cancer. BioMed Central 2009-05-07 /pmc/articles/PMC2684533/ /pubmed/19422676 http://dx.doi.org/10.1186/1756-9966-28-61 Text en Copyright © 2009 Aurilio et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Aurilio, C
Pace, MC
Pota, V
Sansone, P
Barbarisi, M
Grella, E
Passavanti, MB
Opioids Switching with Transdermal Systems in Chronic Cancer Pain
title Opioids Switching with Transdermal Systems in Chronic Cancer Pain
title_full Opioids Switching with Transdermal Systems in Chronic Cancer Pain
title_fullStr Opioids Switching with Transdermal Systems in Chronic Cancer Pain
title_full_unstemmed Opioids Switching with Transdermal Systems in Chronic Cancer Pain
title_short Opioids Switching with Transdermal Systems in Chronic Cancer Pain
title_sort opioids switching with transdermal systems in chronic cancer pain
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2684533/
https://www.ncbi.nlm.nih.gov/pubmed/19422676
http://dx.doi.org/10.1186/1756-9966-28-61
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