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Efficacy, safety, and tolerability of fentanyl pectin nasal spray in patients with breakthrough cancer pain

OBJECTIVE: Assessment of analgesic effectiveness, safety, and tolerability of fentanyl pectin nasal spray (FPNS) in the treatment of breakthrough cancer pain (BTcP) in routine clinical practice. METHODS: A prospective, open-label, noninterventional study (4-week observation period, 3 month follow-up...

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Autores principales: Ueberall, Michael A, Lorenzl, Stefan, Lux, Eberhard A, Voltz, Raymond, Perelman, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4993561/
https://www.ncbi.nlm.nih.gov/pubmed/27574463
http://dx.doi.org/10.2147/JPR.S106177
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author Ueberall, Michael A
Lorenzl, Stefan
Lux, Eberhard A
Voltz, Raymond
Perelman, Michael
author_facet Ueberall, Michael A
Lorenzl, Stefan
Lux, Eberhard A
Voltz, Raymond
Perelman, Michael
author_sort Ueberall, Michael A
collection PubMed
description OBJECTIVE: Assessment of analgesic effectiveness, safety, and tolerability of fentanyl pectin nasal spray (FPNS) in the treatment of breakthrough cancer pain (BTcP) in routine clinical practice. METHODS: A prospective, open-label, noninterventional study (4-week observation period, 3 month follow-up) of opioid-tolerant adults with BTcP in 41 pain and palliative care centers in Germany. Standardized BTcP questionnaires and patient diaries were used. Evaluation was made of patient-reported outcomes with respect to “time to first effect”, “time to maximum effect”, BTcP relief, as well as changes in BTcP-related impairment of daily life activities, quality-of-life restrictions, and health care resource utilization. RESULTS: A total of 235 patients were recruited of whom 220 completed all questionnaires and reported on 1,569 BTcP episodes. Patients reported a significant reduction of maximum BTcP intensity (11-stage numerical rating scale [0= no pain, 10= worst pain conceivable]) with FPNS (mean ± standard deviation = 2.8±2.3) compared with either that reported at baseline (8.5±1.5), experienced immediately before FPNS application (7.4±1.7), or that achieved with previous BTcP medication (6.0±2.0; P<0.001 for each comparison). In 12.3% of BTcP episodes, onset of pain relief occurred ≤2 minutes and in 48.4% ≤5 minutes; maximum effects were reported within 10 minutes for 37.9% and within 15 minutes for 79.4%. By the end of the study, there had been significant improvements versus baseline in BTcP-related daily life activities (28.3±16.9 vs 53.1±11.9), physical (35.9±8.4 vs 26.8±6.5), and mental quality of life (38.7±8.5 vs 29.9±7.9) (P<0.001 for each comparison vs baseline); in addition, health care resource utilization requirements directly related to BTcP were reduced by 67.5%. FPNS was well tolerated; seven patients (3.2%) experienced eight treatment-emergent adverse events of which none was serious. There were no indicators of misuse or abuse. CONCLUSION: FPNS provided rapid and highly effective BTcP relief in opioid-tolerant cancer patients with substantial improvements in daily functioning and quality of life. FPNS was well tolerated and associated with significant reductions in health care resource utilization and nursing assistance.
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spelling pubmed-49935612016-08-29 Efficacy, safety, and tolerability of fentanyl pectin nasal spray in patients with breakthrough cancer pain Ueberall, Michael A Lorenzl, Stefan Lux, Eberhard A Voltz, Raymond Perelman, Michael J Pain Res Original Research OBJECTIVE: Assessment of analgesic effectiveness, safety, and tolerability of fentanyl pectin nasal spray (FPNS) in the treatment of breakthrough cancer pain (BTcP) in routine clinical practice. METHODS: A prospective, open-label, noninterventional study (4-week observation period, 3 month follow-up) of opioid-tolerant adults with BTcP in 41 pain and palliative care centers in Germany. Standardized BTcP questionnaires and patient diaries were used. Evaluation was made of patient-reported outcomes with respect to “time to first effect”, “time to maximum effect”, BTcP relief, as well as changes in BTcP-related impairment of daily life activities, quality-of-life restrictions, and health care resource utilization. RESULTS: A total of 235 patients were recruited of whom 220 completed all questionnaires and reported on 1,569 BTcP episodes. Patients reported a significant reduction of maximum BTcP intensity (11-stage numerical rating scale [0= no pain, 10= worst pain conceivable]) with FPNS (mean ± standard deviation = 2.8±2.3) compared with either that reported at baseline (8.5±1.5), experienced immediately before FPNS application (7.4±1.7), or that achieved with previous BTcP medication (6.0±2.0; P<0.001 for each comparison). In 12.3% of BTcP episodes, onset of pain relief occurred ≤2 minutes and in 48.4% ≤5 minutes; maximum effects were reported within 10 minutes for 37.9% and within 15 minutes for 79.4%. By the end of the study, there had been significant improvements versus baseline in BTcP-related daily life activities (28.3±16.9 vs 53.1±11.9), physical (35.9±8.4 vs 26.8±6.5), and mental quality of life (38.7±8.5 vs 29.9±7.9) (P<0.001 for each comparison vs baseline); in addition, health care resource utilization requirements directly related to BTcP were reduced by 67.5%. FPNS was well tolerated; seven patients (3.2%) experienced eight treatment-emergent adverse events of which none was serious. There were no indicators of misuse or abuse. CONCLUSION: FPNS provided rapid and highly effective BTcP relief in opioid-tolerant cancer patients with substantial improvements in daily functioning and quality of life. FPNS was well tolerated and associated with significant reductions in health care resource utilization and nursing assistance. Dove Medical Press 2016-08-17 /pmc/articles/PMC4993561/ /pubmed/27574463 http://dx.doi.org/10.2147/JPR.S106177 Text en © 2016 Ueberall 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
Ueberall, Michael A
Lorenzl, Stefan
Lux, Eberhard A
Voltz, Raymond
Perelman, Michael
Efficacy, safety, and tolerability of fentanyl pectin nasal spray in patients with breakthrough cancer pain
title Efficacy, safety, and tolerability of fentanyl pectin nasal spray in patients with breakthrough cancer pain
title_full Efficacy, safety, and tolerability of fentanyl pectin nasal spray in patients with breakthrough cancer pain
title_fullStr Efficacy, safety, and tolerability of fentanyl pectin nasal spray in patients with breakthrough cancer pain
title_full_unstemmed Efficacy, safety, and tolerability of fentanyl pectin nasal spray in patients with breakthrough cancer pain
title_short Efficacy, safety, and tolerability of fentanyl pectin nasal spray in patients with breakthrough cancer pain
title_sort efficacy, safety, and tolerability of fentanyl pectin nasal spray in patients with breakthrough cancer pain
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4993561/
https://www.ncbi.nlm.nih.gov/pubmed/27574463
http://dx.doi.org/10.2147/JPR.S106177
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