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High Body Mass Index and Use of Fentanyl Iontophoretic Transdermal System in Postoperative Pain Management: Results of a Pooled Analysis of Six Phase 3/3B Trials

INTRODUCTION: Postoperative pain management can be challenging in patients with a high body mass index (BMI) especially as a result of poor venous access and delayed ambulation that can result in serious complications. Fentanyl iontophoretic transdermal system (ITS) is a needle-free, patient-control...

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Autores principales: Viscusi, Eugene R., Ding, Li, Phipps, J. Bradley, Itri, Loretta M., Schauer, Philip R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5447541/
https://www.ncbi.nlm.nih.gov/pubmed/28004310
http://dx.doi.org/10.1007/s40122-016-0064-z
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author Viscusi, Eugene R.
Ding, Li
Phipps, J. Bradley
Itri, Loretta M.
Schauer, Philip R.
author_facet Viscusi, Eugene R.
Ding, Li
Phipps, J. Bradley
Itri, Loretta M.
Schauer, Philip R.
author_sort Viscusi, Eugene R.
collection PubMed
description INTRODUCTION: Postoperative pain management can be challenging in patients with a high body mass index (BMI) especially as a result of poor venous access and delayed ambulation that can result in serious complications. Fentanyl iontophoretic transdermal system (ITS) is a needle-free, patient-controlled analgesic method available for use in acute postoperative pain. The primary objective of these analyses was to determine if there were any differences between patients with high BMI (>40 kg/m(2)) and lower BMIs (<30 kg/m(2) and 35–40 kg/m(2)) in terms of efficacy or safety. METHODS: Data from three registration, placebo-controlled trials and three active-comparator trials using fentanyl ITS (IONSYS(®), The Medicines Company, Parsippany, NJ) for the management of postoperative pain were analyzed using BMI categories of <35 kg/m(2), 35–40 kg/m(2), and >40 kg/m(2). The majority of patients had lower abdominal or orthopedic surgery. For these analyses, the primary efficacy variables were assessed via patient global assessment of pain control (PGA) at 24 h and investigator global assessment (IGA) at study discharge. PGA and IGA are categorical 4-point scales (excellent, good, fair, or poor) with treatment “success” defined as either excellent or good. Safety was evaluated via treatment emergent adverse events (TEAEs). RESULTS: There were 1403 patients randomly assigned and treated with fentanyl ITS for at least 3 h (BMI <35 kg/m(2): 1180; 35–40 kg/m(2): 136, BMI >40 kg/m(2): 85; and 2 missing). PGA treatment success, which evaluates the method of pain control, at 24 h was consistent in the high and low BMI groups in patients treated with fentanyl ITS (<35 kg/m(2): 946/1180 [80.2%]; 35–40 kg/m(2): 103/136 [75.7%]; and >40 kg/m(2): 65/85 [76.5%]). The IGA results at study discharge were similar to the PGA. Safety appeared similar with fentanyl ITS across the BMI groups. CONCLUSION: In these analyses, fentanyl ITS was as efficacious, as assessed by the PGA ratings of treatment “success”, in patients with high BMI (>40 kg/m(2)) as it was for those with lower BMIs (<35 kg/m(2) or 35–40 kg/m(2)) and was generally well tolerated across all BMI categories.
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spelling pubmed-54475412017-06-13 High Body Mass Index and Use of Fentanyl Iontophoretic Transdermal System in Postoperative Pain Management: Results of a Pooled Analysis of Six Phase 3/3B Trials Viscusi, Eugene R. Ding, Li Phipps, J. Bradley Itri, Loretta M. Schauer, Philip R. Pain Ther Original Research INTRODUCTION: Postoperative pain management can be challenging in patients with a high body mass index (BMI) especially as a result of poor venous access and delayed ambulation that can result in serious complications. Fentanyl iontophoretic transdermal system (ITS) is a needle-free, patient-controlled analgesic method available for use in acute postoperative pain. The primary objective of these analyses was to determine if there were any differences between patients with high BMI (>40 kg/m(2)) and lower BMIs (<30 kg/m(2) and 35–40 kg/m(2)) in terms of efficacy or safety. METHODS: Data from three registration, placebo-controlled trials and three active-comparator trials using fentanyl ITS (IONSYS(®), The Medicines Company, Parsippany, NJ) for the management of postoperative pain were analyzed using BMI categories of <35 kg/m(2), 35–40 kg/m(2), and >40 kg/m(2). The majority of patients had lower abdominal or orthopedic surgery. For these analyses, the primary efficacy variables were assessed via patient global assessment of pain control (PGA) at 24 h and investigator global assessment (IGA) at study discharge. PGA and IGA are categorical 4-point scales (excellent, good, fair, or poor) with treatment “success” defined as either excellent or good. Safety was evaluated via treatment emergent adverse events (TEAEs). RESULTS: There were 1403 patients randomly assigned and treated with fentanyl ITS for at least 3 h (BMI <35 kg/m(2): 1180; 35–40 kg/m(2): 136, BMI >40 kg/m(2): 85; and 2 missing). PGA treatment success, which evaluates the method of pain control, at 24 h was consistent in the high and low BMI groups in patients treated with fentanyl ITS (<35 kg/m(2): 946/1180 [80.2%]; 35–40 kg/m(2): 103/136 [75.7%]; and >40 kg/m(2): 65/85 [76.5%]). The IGA results at study discharge were similar to the PGA. Safety appeared similar with fentanyl ITS across the BMI groups. CONCLUSION: In these analyses, fentanyl ITS was as efficacious, as assessed by the PGA ratings of treatment “success”, in patients with high BMI (>40 kg/m(2)) as it was for those with lower BMIs (<35 kg/m(2) or 35–40 kg/m(2)) and was generally well tolerated across all BMI categories. Springer Healthcare 2016-12-21 2017-06 /pmc/articles/PMC5447541/ /pubmed/28004310 http://dx.doi.org/10.1007/s40122-016-0064-z Text en © The Author(s) 2016 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research
Viscusi, Eugene R.
Ding, Li
Phipps, J. Bradley
Itri, Loretta M.
Schauer, Philip R.
High Body Mass Index and Use of Fentanyl Iontophoretic Transdermal System in Postoperative Pain Management: Results of a Pooled Analysis of Six Phase 3/3B Trials
title High Body Mass Index and Use of Fentanyl Iontophoretic Transdermal System in Postoperative Pain Management: Results of a Pooled Analysis of Six Phase 3/3B Trials
title_full High Body Mass Index and Use of Fentanyl Iontophoretic Transdermal System in Postoperative Pain Management: Results of a Pooled Analysis of Six Phase 3/3B Trials
title_fullStr High Body Mass Index and Use of Fentanyl Iontophoretic Transdermal System in Postoperative Pain Management: Results of a Pooled Analysis of Six Phase 3/3B Trials
title_full_unstemmed High Body Mass Index and Use of Fentanyl Iontophoretic Transdermal System in Postoperative Pain Management: Results of a Pooled Analysis of Six Phase 3/3B Trials
title_short High Body Mass Index and Use of Fentanyl Iontophoretic Transdermal System in Postoperative Pain Management: Results of a Pooled Analysis of Six Phase 3/3B Trials
title_sort high body mass index and use of fentanyl iontophoretic transdermal system in postoperative pain management: results of a pooled analysis of six phase 3/3b trials
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5447541/
https://www.ncbi.nlm.nih.gov/pubmed/28004310
http://dx.doi.org/10.1007/s40122-016-0064-z
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