Literature DB >> 11309214

Advances in cancer pain management.

F J McDonnell1, J W Sloan, S R Hamann.   

Abstract

Control of malignant pain and related symptoms is paramount to clinical success in caring for cancer patients. To achieve the best quality of life for patients and families, oncologists and palliative care clinicians must work together to understand problems related to psychologic, social, and spiritual pain. Pain is the primary problem targeted for control using the World Health Organization's (WHO) analgesic ladder. This article focuses on increased knowledge of analgesic action that may enable expansion of the WHO analgesic ladder to fulfill the broader objectives of palliative medicine. We discuss clinical experience with several classes of drugs that are currently used to treat cancer pain: 1) nonsteroidal anti-inflammatory drugs, with emphasis on cyclooxygenase-2 inhibitors; 2) opioid analgesics, with specific emphasis on methadone and its newly recognized value in cancer pain; 3) ketamine, an antagonist at N-methyl-d-aspartate receptors; and 4) bisphosphonates, used for pain resulting from bone metastases. New concepts that compare molecular actions of morphine at excitatory opioid receptors, and methadone at nonopioid receptor systems, are presented to underscore the importance of balancing central nervous system excitatory (anti-analgesic) versus inhibitory (analgesic) influences.

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Year:  2001        PMID: 11309214     DOI: 10.1007/s11916-001-0041-y

Source DB:  PubMed          Journal:  Curr Pain Headache Rep        ISSN: 1534-3081


  60 in total

1.  The need for ketamine.

Authors:  P G Lawlor; Y Tarumi
Journal:  J Pain Symptom Manage       Date:  2000-01       Impact factor: 3.612

2.  Opioid hyperexcitability: the application of alternate opioid therapy.

Authors:  Neil MacDonald; Linda Der; Sharon Allan; Phillip Champion
Journal:  Pain       Date:  1993-06       Impact factor: 6.961

Review 3.  Mechanism of action of nonsteroidal anti-inflammatory drugs.

Authors:  J R Vane; R M Botting
Journal:  Am J Med       Date:  1998-03-30       Impact factor: 4.965

4.  d-Methadone blocks morphine tolerance and N-methyl-D-aspartate-induced hyperalgesia.

Authors:  A M Davis; C E Inturrisi
Journal:  J Pharmacol Exp Ther       Date:  1999-05       Impact factor: 4.030

5.  Analgesic effects of nonsteroidal anti-inflammatory drugs in cancer pain due to somatic or visceral mechanisms.

Authors:  S Mercadante; A Casuccio; A Agnello; S Pumo; J Kargar; S Garofalo
Journal:  J Pain Symptom Manage       Date:  1999-05       Impact factor: 3.612

Review 6.  Pharmacology and mechanisms of opioid analgesic activity.

Authors:  T L Yaksh
Journal:  Acta Anaesthesiol Scand       Date:  1997-01       Impact factor: 2.105

7.  Different doses of pamidronate in patients with painful osteolytic bone metastases.

Authors:  S Cascinu; F Graziano; P Alessandroni; M Ligi; E Del Ferro; D Rossi; R Ficarelli; G Catalano
Journal:  Support Care Cancer       Date:  1998-03       Impact factor: 3.603

8.  The combination of NMDA antagonism and morphine produces profound antinociception in the rat dorsal horn.

Authors:  V Chapman; A H Dickenson
Journal:  Brain Res       Date:  1992-02-28       Impact factor: 3.252

Review 9.  Nonsteroidal anti-inflammatory drug-associated toxicity of the liver, lower gastrointestinal tract, and esophagus.

Authors:  D Bjorkman
Journal:  Am J Med       Date:  1998-11-02       Impact factor: 4.965

10.  Lack of analgesic effect of opioids on neuropathic and idiopathic forms of pain.

Authors:  S Arnér; B A Meyerson
Journal:  Pain       Date:  1988-04       Impact factor: 6.961

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  2 in total

1.  Spinal cord NMDA receptor-mediated activation of mammalian target of rapamycin is required for the development and maintenance of bone cancer-induced pain hypersensitivities in rats.

Authors:  Ming-Hung Shih; Sheng-Chin Kao; Wei Wang; Myron Yaster; Yuan-Xiang Tao
Journal:  J Pain       Date:  2012-02-15       Impact factor: 5.820

2.  An open-label, 1-year extension study of the long-term safety and efficacy of once-daily OROS(R) hydromorphone in patients with chronic cancer pain.

Authors:  Magdi Hanna; Alberto Tuca; John Thipphawong
Journal:  BMC Palliat Care       Date:  2009-09-15       Impact factor: 3.234

  2 in total

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