Literature DB >> 20447801

Breakthrough pain in oncology: a longitudinal study.

Sebastiano Mercadante1, Vittoria Zagonel, Enrico Breda, Carlo Arcara, Vittorio Gebbia, Giampiero Porzio, Federica Aielli, Fabrizio David, Teresa Gammucci, Filomena Narducci, Gaetano Lanzetta, Rossella Restuccia, Alessandro Lembo, Virginia Passeri, Vladimir Virzì, Alessandra Casuccio.   

Abstract

CONTEXT: Existing studies on breakthrough pain (BP) have reported different prevalence rates because of different settings, populations, and assessment methods. These studies have used cross-sectional designs, and the relationship of BP with analgesic treatment has not been evaluated.
OBJECTIVES: The aim of this study was to longitudinally assess BP in cancer patients admitted to oncology units.
METHODS: A consecutive sample of patients admitted to oncology centers was selected. At admission (T0), three months after admission (T3), and six months after admission (T6), data on background pain and BP were recorded. BP was assessed in terms of its intensity, duration, number of episodes, onset with movement, spontaneous relief after stopping activity, limitation of physical activity, and effectiveness of analgesics.
RESULTS: Three hundred two patients completed the study. At T0, T3, and T6, 39%, 38%, and 33% patients, respectively, had continuous pain (P=0.294). Pain intensity significantly decreased (P=0.004 and 0.027 at T3 and T6, respectively). Most patients had BP at T0 (87.1%), T3 (80.9%), and T6 (73.2%), and there was a significant decrease in the prevalence of BP over time (P=0.016). Of 149 patients with BP, pain on movement was recorded in 43.6%, 43.4%, and 32.4% at T0, T3, and T6, respectively (P=0.228). Pain spontaneously decreased or ceased when stopping physical activity in 66%, 56%, and 62% at T0, T3, and T6, respectively (P=0.537). Pain on movement strongly limited physical activity in most patients.
CONCLUSION: These data expand current information about BP and underline the need for a longitudinal assessment of a phenomenon that is invariably dependent on stage of disease, patient, and therapeutic factors. Copyright (c) 2010 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20447801     DOI: 10.1016/j.jpainsymman.2010.01.010

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  16 in total

1.  [Experiences of cancer patients with breakthrough pain and pharmacological treatments].

Authors:  L Bertram; S Stiel; F Elsner; L Radbruch; A Davies; F Nauck; B Alt-Epping
Journal:  Schmerz       Date:  2010-12       Impact factor: 1.107

Review 2.  Breakthrough cancer pain.

Authors:  Andrew N Davies
Journal:  Curr Pain Headache Rep       Date:  2014-06

3.  Prevalence and characterization of breakthrough pain in cancer patients with proctalgia treated with 3D pelvic radiotherapy.

Authors:  V T Ferrero; M M Oset; J P Masferrer; E H Pardo; E J Sorolla; S C Largo
Journal:  Clin Transl Oncol       Date:  2019-04-05       Impact factor: 3.405

4.  Abstral (Fentanyl Sublingual Tablets for Breakthrough Cancer Pain).

Authors: 
Journal:  P T       Date:  2011-02

5.  The pain, the oncologist.

Authors:  Sebastiano Mercadante
Journal:  Support Care Cancer       Date:  2014-06-06       Impact factor: 3.603

6.  Active study: undetected prevalence and clinical inertia in the treatment of breakthrough cancer pain (BTcP).

Authors:  C Camps Herrero; J J Reina Zoilo; D Monge Martín; F Caballero Martínez; V Guillem Porta; E Aranda Aguilar; A Carrato Mena; E Díaz-Rubio García; J García-Foncillas López; M Feijóo Saus; R López López
Journal:  Clin Transl Oncol       Date:  2018-08-09       Impact factor: 3.405

Review 7.  Breakthrough pain and its treatment: critical review and recommendations of IOPS (Italian Oncologic Pain Survey) expert group.

Authors:  Sebastiano Mercadante; Paolo Marchetti; Arturo Cuomo; Massimo Mammucari; Augusto Caraceni
Journal:  Support Care Cancer       Date:  2015-10-05       Impact factor: 3.603

Review 8.  Pharmacotherapy for breakthrough cancer pain.

Authors:  Sebastiano Mercadante
Journal:  Drugs       Date:  2012-01-22       Impact factor: 9.546

9.  The non-selective cannabinoid receptor agonist WIN 55,212-2 attenuates responses of C-fiber nociceptors in a murine model of cancer pain.

Authors:  M L Uhelski; D M Cain; C Harding-Rose; D A Simone
Journal:  Neuroscience       Date:  2013-05-11       Impact factor: 3.590

10.  Opioid use and effectiveness of its prescription at discharge in an acute pain relief and palliative care unit.

Authors:  Sebastiano Mercadante; Giovanna Prestia; Maurizio Ranieri; Antonello Giarratano; Alessandra Casuccio
Journal:  Support Care Cancer       Date:  2013-02-12       Impact factor: 3.603

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