Oral trasmucosal fentanyl citrate for breakthrough pain treatment in cancer patients

被引:6
作者
Mercadante, Sebastiano [1 ,2 ,3 ]
机构
[1] Univ Palermo, La Maddalena Canc Ctr, I-90145 Palermo, Italy
[2] Dept Anesthesia Intens Care & Emergencies, Anesthesia & Intens Care Unit, I-90145 Palermo, Italy
[3] Dept Anesthesia Intens Care & Emergencies, Pain Relief & Palliat Care Unit, I-90145 Palermo, Italy
关键词
breakthrough pain; opioids; oral transmucosal fentanyl citrate; TRANSMUCOSAL FENTANYL; DOSE-TITRATION; MANAGEMENT; TRIAL; PHARMACOKINETICS; MULTICENTER; MORPHINE; OTFC(R); OPIOIDS;
D O I
10.1517/14656566.2012.663353
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Breakthrough cancer pain has been defined as a transitory increase in pain intensity that occurs either spontaneously or in relation to a specific predictable or unpredictable trigger, despite relatively stable and adequately controlled background pain. The availability of supplemental doses of oral opioids, in addition to the continuous analgesic medication, is the main treatment suggested to manage pain flares. Areas covered: Oral transmucosal fentanyl citrate (OTFC) is the first product of a new generation of delivery systems, named rapid-onset opioids (ROOs), characterized by rapidity of effect and the short duration of analgesia. Controlled studies and long-term experience have shown that OTFC is an effective treatment for breakthrough pain management and its use should be considered in any patient experiencing breakthrough pain related to cancer. Expert opinion: The onset of action of OTFC - demonstrated to start within 15 min - and the short time to maximum concentration make it a useful indication for breakthrough pain; dose titration is commonly recommended. However, it is likely that patients receiving high doses of opioids for background analgesia will not be candidates for titration with minimal initial doses of OTFC, as they are opioid tolerant and the process would be time consuming.
引用
收藏
页码:873 / 878
页数:6
相关论文
共 27 条
[1]   Evidence-based oral transmucosal fentanyl citrate (OTFC®) dosing guidelines [J].
Aronoff, GM ;
Brennan, MJ ;
Pritchard, DD ;
Ginsberg, B .
PAIN MEDICINE, 2005, 6 (04) :305-314
[2]   ORAL TRANSMUCOSAL FENTANYL - HELP OR HINDRANCE [J].
ASHBURN, MA ;
STREISAND, JB .
DRUG SAFETY, 1994, 11 (05) :295-300
[3]   Oral transmucosal fentanyl citrate in the outpatient management of severe cancer pain crises - A retrospective case series [J].
Burton, AW ;
Driver, LC ;
Mendoza, TR ;
Syed, G .
CLINICAL JOURNAL OF PAIN, 2004, 20 (03) :195-197
[4]   Dose-titration, multicenter study of oral transmucosal fentanyl citrate for the treatment of breakthrough pain in cancer patients using transdermal fentanyl for persistent pain [J].
Christie, JM ;
Simmonds, M ;
Patt, R ;
Coluzzi, P ;
Busch, MA ;
Nordbrock, E ;
Portenoy, RK .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (10) :3238-3245
[5]   Breakthrough cancer pain:: a randomized trial comparing oral transmucosal fentanyl citrate (OTFC®) and morphine sulfate immediate release (MSIR®) [J].
Coluzzi, PH ;
Schwartzberg, L ;
Conroy, JD ;
Charapata, S ;
Gay, M ;
Busch, MA ;
Chavez, J ;
Ashley, J ;
Lebo, D ;
McCracken, M ;
Portenoy, RK .
PAIN, 2001, 91 (1-2) :123-130
[6]  
Csaba N, 2006, EXPERT OPIN DRUG DEL, V91, P463
[7]   Oral transmucosal fentanyl citrate and xerostomia [J].
Davies, AN ;
Vriens, J .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2005, 30 (06) :496-497
[8]   The management of cancer-related breakthrough pain: Recommendations of a task group of the Science Committee of the Association for Palliative Medicine of Great Britain and Ireland [J].
Davies, Andrew N. ;
Dickman, Andrew ;
Reid, Colette ;
Stevens, Anna-Marie ;
Zeppetella, Giovambattista .
EUROPEAN JOURNAL OF PAIN, 2009, 13 (04) :331-338
[9]   Multiple dose pharmacokinetics of oral transmucosal fentanyl citrate in healthy volunteers [J].
Egan, TD ;
Sharma, A ;
Ashburn, MA ;
Kievit, J ;
Pace, NL ;
Streisand, JB .
ANESTHESIOLOGY, 2000, 92 (03) :665-673
[10]   Oral transmucosal fentanyl citrate: Randomized, double-blinded, placebo-controlled trial for treatment of breakthrough pain in cancer patients [J].
Farrar, JT ;
Cleary, J ;
Rauck, R ;
Busch, M ;
Nordbrock, E .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (08) :611-616