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Tramadol Extended-Release for the Management of Pain due to Osteoarthritis
Author(s) -
Chiara Angeletti,
Cristiana Guetti,
Antonella Paladini,
Giustino Varrassi
Publication year - 2013
Publication title -
isrn pain
Language(s) - English
Resource type - Journals
ISSN - 2314-4718
DOI - 10.1155/2013/245346
Subject(s) - tramadol , medicine , osteoarthritis , tapentadol , analgesic , tolerability , pain ladder , opioidergic , opioid , dosing , chronic pain , neuropathic pain , anesthesia , pharmacology , physical therapy , receptor , adverse effect , alternative medicine , (+) naloxone , pathology
Current knowledge on pathogenesis of osteoarticular pain, as well as the consequent several, especially on the gastrointestinal, renal, and cardiovascular systems, side effects of NSAIDs, makes it difficult to perform an optimal management of this mixed typology of pain. This is especially observable in elderly patients, the most frequently affected by osteoarthritis (OA). Tramadol is an analgesic drug, the action of which has a twofold action. It has a weak affinity to mu opioid receptors and, at the same time, can result in inhibition of the reuptake of noradrenaline and serotonin in nociceptorial descending inhibitory control system. These two mechanisms, “opioidergic” and “nonopioidergic,” are the grounds for contrasting certain types of pain that are generally less responsive to opioids, such as neuropathic pain or mixed OA pain. The extended-release formulation of tramadol has good efficacy and tolerability and acts through a dosing schedule that allows a high level of patients compliance to therapies with a good recovery outcome for the patients' functional status.

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