Literature DB >> 10998740

Breakthrough pain in cancer patients: new therapeutic approaches to an old challenge.

S K Reddy1, P Nguyen.   

Abstract

Breakthrough pain is a well recognized but ill-defined phenomenon that occurs commonly in the presence of otherwise stable, persistent pain. It is defined now as a "transient pain episode that occurs, or breaks through from the otherwise stable background pain." Breakthrough pain is usually associated with moderate to severe pain and may form a predictor of poor response to treatment with routine pharmacotherapy. Breakthrough pain is also associated with functional impairment and psychological distress. The assessment and treatment should be multidimensional. Although primary therapies such as chemotherapy, radiation treatment, and surgical options are explored, the mainstay of treatment is pharmacotherapy. Nonpharmacologic methods, such as orthotic devices and joint stabilizations along with behavioral methods, should be explored. Anesthetic and neurosurgical procedures are performed on a limited number of patients based on the prognosis, intractable nature of pain, and favorable risk/benefit ratio. Newer oral transmucosal fentanyl offers a favorable pharmacokinetic and pharmacodynamic profile and ease of administration.

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Year:  2000        PMID: 10998740     DOI: 10.1007/s11916-000-0086-3

Source DB:  PubMed          Journal:  Curr Rev Pain        ISSN: 1069-5850


  21 in total

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Authors:  H L Rosomoff; C J Brown; P Sheptak
Journal:  J Neurosurg       Date:  1965-12       Impact factor: 5.115

Review 2.  Management of breakthrough pain due to cancer.

Authors:  M A Simmonds
Journal:  Oncology (Williston Park)       Date:  1999-08       Impact factor: 2.990

3.  Breakthrough pain: definition, prevalence and characteristics.

Authors:  Russell K Portenoy; Neil A Hagen
Journal:  Pain       Date:  1990-06       Impact factor: 6.961

4.  The nature of opioid responsiveness and its implications for neuropathic pain: new hypotheses derived from studies of opioid infusions.

Authors:  Russell K Portenoy; Kathleen M Foley; Charles E Inturrisi
Journal:  Pain       Date:  1990-12       Impact factor: 6.961

5.  Role of rectal route in treating cancer pain: a randomized crossover clinical trial of oral versus rectal morphine administration in opioid-naive cancer patients with pain.

Authors:  F De Conno; C Ripamonti; L Saita; T MacEachern; J Hanson; E Bruera
Journal:  J Clin Oncol       Date:  1995-04       Impact factor: 44.544

Review 6.  Breakthrough pain in cancer patients: characteristics, prevalence, and treatment.

Authors:  R B Patt; N M Ellison
Journal:  Oncology (Williston Park)       Date:  1998-07       Impact factor: 2.990

7.  Predictive factors in advanced cancer pain treated only by analgesics.

Authors:  Sebastiano Mercadante; Salvatore Maddaloni; Salvina Roccella; Leonardo Salvaggio
Journal:  Pain       Date:  1992-08       Impact factor: 6.961

8.  Absorption and bioavailability of oral transmucosal fentanyl citrate.

Authors:  J B Streisand; J R Varvel; D R Stanski; L Le Maire; M A Ashburn; B I Hague; S D Tarver; T H Stanley
Journal:  Anesthesiology       Date:  1991-08       Impact factor: 7.892

9.  Dose-titration, multicenter study of oral transmucosal fentanyl citrate for the treatment of breakthrough pain in cancer patients using transdermal fentanyl for persistent pain.

Authors:  J M Christie; M Simmonds; R Patt; P Coluzzi; M A Busch; E Nordbrock; R K Portenoy
Journal:  J Clin Oncol       Date:  1998-10       Impact factor: 44.544

10.  The Edmonton staging system for cancer pain: preliminary report.

Authors:  E Bruera; K MacMillan; J Hanson; R N MacDonald
Journal:  Pain       Date:  1989-05       Impact factor: 6.961

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  2 in total

1.  Symptom masquerade: understanding the meaning of symptoms.

Authors:  Marlene Z Cohen; Lori Williams; Patti Knight; Julie Snider; Kavin Hanzik; Michael J Fisch
Journal:  Support Care Cancer       Date:  2004-01-20       Impact factor: 3.603

Review 2.  [Differential therapeutic aspects of analgesia with oral sustained-release strong opioids: application intervals, metabolism and immunosuppression].

Authors:  K Güttler; R Sabatowski
Journal:  Schmerz       Date:  2008-10       Impact factor: 1.107

  2 in total

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