Literature DB >> 15973913

Acute pain management pharmacology for the patient with concurrent renal or hepatic disease.

E J Murphy1.   

Abstract

The clinical utility of most analgesic drugs is altered in the presence of patients with impaired renal or hepatic function not simply because of altered clearance of the parent drug, but also through production and accumulation of toxic or therapeutically active metabolites. Some analgesic agents may also aggravate pre-existing renal and hepatic disease. A search was performed, taking in published articles and pharmaceutical data to determine available evidence for managing acute pain effectively and safely in these two patient groups. The resulting information consisted mainly of small group pharmacokinetic studies or case reports, which included a large variation in degree of organ dysfunction. In the presence of renal impairment, those drugs which exhibit the safest pharmacological profile are alfentanil, buprenorphine, fentanyl, ketamine, paracetamol (except with compound analgesics), remifentanil and sufentanil. none of these deliver a high active metabolite load, or suffer from significantly prolonged clearance. Amitriptyline, bupivacaine, clonidine, gabapentin, hydromorphone, levobupivacaine, lignocaine, methadone, mexiletine, morphine, oxycodone and tramadol have been used in the presence of renal failure, but do require specific precautions, usually dose reduction. Aspirin, dextropropoxyphene, non-steroidal anti-inflammatory drugs and pethidine, should not be used in the presence of chronic renal failure due to the risk of significant toxicity. In the presence of hepatic impairment, most drugs are subject to significantly impaired clearance and increased oral bioavailability, but are poorly studied in the clinical setting. The agent least subject to alteration in this context is remifentanil; however the drugs' potency has other inherent dangers. Other agents must only be used with caution and close patient monitoring. Amitriptyline, carbamazepine and valproate should be avoided as the risk of fulminant hepatic failure is higher in this population, and methadone is contraindicated in the presence of severe liver disease.

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Year:  2005        PMID: 15973913     DOI: 10.1177/0310057X0503300306

Source DB:  PubMed          Journal:  Anaesth Intensive Care        ISSN: 0310-057X            Impact factor:   1.669


  20 in total

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Review 2.  The use of opioids in cancer patients with renal impairment-a systematic review.

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Journal:  Support Care Cancer       Date:  2016-10-15       Impact factor: 3.603

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Authors:  Joseph A Delaney; Nils Lehmann; Karl-Heinz Jöckel; Sammy Elmariah; Bruce M Psaty; Amir A Mahabadi; Matt Budoff; Richard A Kronmal; Khurram Nasir; Kevin D O'Brien; Stefan Möhlenkamp; Susanne Moebus; Nico Dragano; Almut G Winterstein; Raimund Erbel; Hagen Kälsch
Journal:  Atherosclerosis       Date:  2013-05-14       Impact factor: 5.162

Review 4.  Assessment and management of pain, with particular emphasis on central neuropathic pain, in moderate to severe dementia.

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5.  Future liver remnant volume is associated with postoperative fentanyl consumption following open donor hepatectomy: a retrospective multivariate analysis.

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8.  [Interdisciplinary guidance for pain management in nursing home residents].

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9.  Quality Assessment of Acute Inpatient Pain Management in an Academic Health Center.

Authors:  Richard J Lin; M Carrington Reid; Amy E Chused; Arthur T Evans
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10.  Analgesics in patients with hepatic impairment: pharmacology and clinical implications.

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