Pain management of cancer patients with transdermal fentanyl: A study of 1828 step I, II, & III transfers

被引:38
|
作者
Mystakidou, K
Parpa, E
Tsilika, E
Katsouda, E
Kouloulias, V
Kouvaris, J
Georgaki, S
Vlahos, L
机构
[1] Univ Athens, Sch Med, Areteion Hosp, Dept Radiol,Pain Relief & Palliat Care Unit, Athens 11526, Greece
[2] Univ Athens, Sch Med, Dept Gen Surg, Radiotherapy Unit, GR-11527 Athens, Greece
关键词
nociceptive; neuropathic; chronic pain; intolerable pain; analgesia;
D O I
10.1016/j.jpain.2003.12.003
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The aim of this observational study was to examine pain management outcomes and quality of life (QoL) measures in cancer patients with intolerable or chronic severe pain transferring from World Health Organization's step I, II, and III analgesics to the transdermal therapeutic fentanyl system (TTS-F). This study examines the safety and efficacy of TTS-F in long-term pain management, addressing the role of TTS-F in cancer pain. Pain measures were assessed in 1828 patients (step I [naive], 268; step II [codeine], 1239; and step III [morphine], 321) on the basis of selected questions from the Greek-Brief Pain Inventory. Overall treatment satisfaction (scale, 1 to 4), QoL, and European Collaborative Oncology Group (ECOG) status were also recorded. These were assessed in relation to TTS-F dose, stratified by transfer step, primary cancer, metastases, type of pain, and concomitant use of anti-inflammatory drugs. Of 1828 patients, 100 (5.5%) withdrew, and an addition 14 (0.8%) discontinued because of side effects. A total of 1714 continued on study; 744 patients died, and 970 departed during the study period. In total, 93.8% were satisfied with their pain relief, and complete patient satisfaction was obtained within 2 months. Pain, QoL, and treatment satisfaction measures demonstrated statistically significant improvements over time, independent of the step transfer. Although doses of TTS-F were higher for step III > II > I and for metastatic than nonmetastatic, the median dose for all groups remained 50 mug/h throughout the study period. Pain and QoL improvements were independent of patient characteristic(s). Direct transfer to TTS-F for patients with intolerable or chronic moderate to severe cancer pain offers an efficient and safe long-term analgesic option for palliative care patients. Careful selection and follow-up by experienced palliative care specialists are mandatory. TTS-F as a first-line analgesic approach for severe cancer pain should be considered a viable option because of its durable efficacy and low incidences of side effects. Perspective: At a fairly constant dose of 50 mug/h, the transdermal therapeutic fentanyl system offers a safe, well-tolerated pain relief treatment for carefully monitored patients with cancer pain. The authors stress that this includes patients who experience difficulties in their pain management while progressing through the WHO's ladder for pain management. (C) 2004 by the American Pain Society.
引用
收藏
页码:119 / 132
页数:14
相关论文
共 25 条
  • [21] Long-term management of chronic pain with transdermal buprenorphine: A multicenter, open-label, follow-up study in patients from three short-term clinical trials
    Likar, Rudolf
    Kayser, Hubertus
    Sittl, Reinhard
    CLINICAL THERAPEUTICS, 2006, 28 (06) : 943 - 952
  • [22] Usability Testing of a New Digital Integrated Health Ecosystem (PainRELife) for the Clinical Management of Chronic Pain in Patients With Early Breast Cancer: Protocol for a Pilot Study
    Masiero, Marianna
    Filipponi, Chiara
    Pizzoli, Silvia Francesca Maria
    Munzone, Elisabetta
    Guido, Luca
    Guardamagna, Vittorio Andrea
    Marceglia, Sara
    Caruso, Annamaria
    Prandin, Roberto
    Prenassi, Marco
    Manzelli, Vania
    Savino, Chiara
    Conti, Costanza
    Rizzi, Federica
    Casalino, Alice
    Candiani, Giulia
    Memini, Francesca
    Chiveri, Luca
    Vitali, Andrea Luigi
    Corbo, Massimo
    Milani, Alessandra
    Grasso, Roberto
    Traversoni, Silvia
    Fragale, Elisa
    Didier, Florence
    Pravettoni, Gabriella
    JMIR RESEARCH PROTOCOLS, 2023, 12
  • [23] Development of opioid-induced constipation: post hoc analysis of data from a 12-week prospective, open-label, blinded-endpoint streamlined study in low-back pain patients treated with prolonged-release WHO step III opioids
    Ueberall, Michael A.
    Mueller-Schwefe, Gerhard H. H.
    JOURNAL OF PAIN RESEARCH, 2015, 8 : 459 - 475
  • [24] Efficacy and Tolerability of Intranasal Fentanyl Spray 50 to 200 μg for Breakthrough Pain in Patients With Cancer: A Phase III, Multinational, Randomized, Double-Blind, Placebo-Controlled, Crossover Trial With a 10-Month, Open-Label Extension Treatment Period
    Kress, Hans Georg
    Oronska, Anna
    Kaczmarek, Zbigniew
    Kaasa, Stein
    Colberg, Torben
    Nolte, Thomas
    CLINICAL THERAPEUTICS, 2009, 31 (06) : 1177 - 1191
  • [25] Efficacy And Safety Of Controlled-Release Oxycodone For The Management Of Moderate-To-Severe Chronic Non-Cancer Pain In Japanese Patients: Results From An Open-Label Study
    Kawamata, Mikito
    Iseki, Masako
    Kawakami, Mamoru
    Yabuki, Shoji
    Sasaki, Takuma
    Ishida, Mitsuhiro
    Nishiyori, Atsushi
    Hida, Hideaki
    Kikuchi, Shin-ichi
    JOURNAL OF PAIN RESEARCH, 2019, 12 : 3423 - 3436