2017
DOI: 10.1007/s00520-017-3853-y
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Fentanyl buccal tablet for breakthrough cancer pain in clinical practice: results of the non-interventional prospective study ErkentNIS

Abstract: PurposeSeveral patients with advanced cancer suffer from breakthrough cancer pain (BTcP). BTcP is pain exacerbation despite opioid baseline therapy. Fentanyl buccal tablet (FBT) is a rapid-onset opioid for the treatment of BTcP. The aim of this study is to document the feasibility of FBT in patients with BTcP.MethodsThe study was performed in 64 centers. Basic pain score was rated on a numeric rating scale (NRS) before and after treatment. BTcP episodes, baseline opioid therapy, and FBT dose were rated as well… Show more

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Cited by 6 publications
(4 citation statements)
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“…These studies indicated that buccal fentanyl is well tolerated and may improve patient functioning, mood, and overall satisfaction in the management of breakthrough cancer pain. [37][38][39][40] The addition of intrathecal fentanyl to spinal anaesthesia decreases opioid consumption during the period of highest analgesic demand after caesarean section. 41 The transpulmonary fentanyl route remains an experimental phase for the management ofacute or chronic pain.…”
Section: Discussionmentioning
confidence: 99%
“…These studies indicated that buccal fentanyl is well tolerated and may improve patient functioning, mood, and overall satisfaction in the management of breakthrough cancer pain. [37][38][39][40] The addition of intrathecal fentanyl to spinal anaesthesia decreases opioid consumption during the period of highest analgesic demand after caesarean section. 41 The transpulmonary fentanyl route remains an experimental phase for the management ofacute or chronic pain.…”
Section: Discussionmentioning
confidence: 99%
“…Masel et al 35 Document the feasibility of fentanyl oral tablets for the treatment of patients with transitory exacerbation cancer pain.…”
Section: Discussionmentioning
confidence: 99%
“…The action time of each patch is 72 hours, remaining for 12 to 18 hours after its removal. The transmucosal formulation has short action duration, non-invasive administration route, and tolerable safety profile 14,17,25,26,34,35 .…”
Section: Fentanylmentioning
confidence: 99%
“…In a meta-analysis by Zeppetella et al, the difference in pain intensity control compared with placebo 15 min after intake was greater with all formulations of fentany than with other BTcP medications (20). Moreover, a reduction in the number of BTcP episodes was documented and patient satisfaction was rated as excellent or good (21,22). Patient satisfaction was also rated as high with fentanyl pectin nasal spray (23).…”
Section: Roos For Treatment Of Btcpmentioning
confidence: 99%