2019
DOI: 10.2215/cjn.05180418
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Clinical Pharmacology Considerations in Pain Management in Patients with Advanced Kidney Failure

Abstract: Pain is common and poorly managed in patients with advanced CKD, likely due to both under and over prescription of appropriate analgesics. Poorly managed pain contributes to patients' poor quality of life and excessive health care use. There is tremendous variability within and between countries in prescribing patterns of analgesics, suggesting that factors other than patient characteristics account for these differences. This article discusses the pharmacologic management of acute and chronic pain in patients… Show more

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Cited by 101 publications
(118 citation statements)
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References 55 publications
(53 reference statements)
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“…In the overall cohort, patients with other pre-ESRD non-opiate analgesic use had similar survival compared to those with no analgesic use, even after accounting for differences in pain severity and specific pain conditions (i.e., neuropathy); however, in analyses stratified by kidney function, those who used other non-opiate analgesics with lower eGFRs (i.e., <30 mL/min/1.73 m 2 ) in the prelude period had higher post-ESRD death risk. While our data suggest that non-opiate analgesics other than gabapentin/pregabalin may be a preferred analgesic alternative to opiates in patients with mild-to-moderate kidney dysfunction (eGFR ≥ 30 mL/ min/1.73 m 2 ), there should be cautious administration and/or consideration of nonpharmacologic interventions in advanced CKD patients given alterations in drug absorption, bioavailability, distribution, metabolism, and excretion [15].…”
Section: Discussionmentioning
confidence: 73%
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“…In the overall cohort, patients with other pre-ESRD non-opiate analgesic use had similar survival compared to those with no analgesic use, even after accounting for differences in pain severity and specific pain conditions (i.e., neuropathy); however, in analyses stratified by kidney function, those who used other non-opiate analgesics with lower eGFRs (i.e., <30 mL/min/1.73 m 2 ) in the prelude period had higher post-ESRD death risk. While our data suggest that non-opiate analgesics other than gabapentin/pregabalin may be a preferred analgesic alternative to opiates in patients with mild-to-moderate kidney dysfunction (eGFR ≥ 30 mL/ min/1.73 m 2 ), there should be cautious administration and/or consideration of nonpharmacologic interventions in advanced CKD patients given alterations in drug absorption, bioavailability, distribution, metabolism, and excretion [15].…”
Section: Discussionmentioning
confidence: 73%
“…Yet, several limitations of our study should be acknowledged. First, given the retrospective nature of our study, we were not able to precisely determine the indications for which opiate and non-opiate analgesics were prescribed (i.e., nociceptive vs. neuropathic pain) [15], nor if analgesics were administered for conditions other than pain (i.e., epilepsy and pruritus); however, upon examining pre-existing conditions associated with opiate use in our multivariable models (i.e., neuropathy), we observed robust associations between pre-ESRD opiate use and post-ESRD death. Second, due to data limitations we were unable to ascertain use of analgesics outside of the VA healthcare system (i.e., overthe-counter and prescription from non-VA providers), DOI: 10.1159/000509451 nor the type of analgesic prescribers (i.e., primary care and nephrology).…”
Section: Discussionmentioning
confidence: 99%
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“…The authors recognise that opioids are not considered appropriate for chronic pain. However, this is an acute pain arising in response to tissue injury and death [ 18 ] and therefore, we recommend an opioid as first line therapy.…”
Section: Recommendationsmentioning
confidence: 99%
“…The authors recommend alfentanil as it is not removed by dialysis, it does not cause toxicity in an ESRD population and it occupies a low volume in syringe drivers. This guidance is drawn from literature on the use of opioids in cancer patients with severe and end stage terminal illness (18)(19)(20) and is supported by the clinical pharmacology literature (17). Fentanyl by CSCI is an alternative.…”
Section: Background Pain Controlmentioning
confidence: 99%