Review of clinical pharmacokinetics and pharmacodynamics of clonidine as an adjunct to opioids in palliative care

可乐定 辅助 药效学 医学 药代动力学 缓和医疗 类阿片 药理学 麻醉 重症监护医学 内科学 护理部 受体 哲学 语言学
作者
Sarwat Amna,Thomas Øhlenschlæger,Eva Aggerholm Sædder,Jarl Sigaard,Troels K. Bergmann
出处
期刊:Basic & Clinical Pharmacology & Toxicology [Wiley]
卷期号:134 (4): 485-497 被引量:8
标识
DOI:10.1111/bcpt.13979
摘要

Abstract Clonidine is an α‐adrenoceptor agonist acting on receptors in the brain and peripheral tissues, leading to a reduction in sympathetic outflow and release of certain neurotransmitters. Clonidine has multiple uses across various medical conditions. One of its uses is as adjuvant to anaesthetic and analgesic agents specially opioids, mostly administered through intravenous and epidural routes. The opioids, effective in cancer pain management, are associated with various side effects such as sedation, pruritus, constipation, nausea, respiratory depression, tolerance and dependence. Combination of clonidine with opioids seems to help to achieve better pain management and less need of opioids. Use of clonidine in palliative care has been less common, but it is gradually gaining recognition for its potential benefits in managing symptoms like cancer pain and agitation. This combination approach has been explored in palliative care settings, including cancer pain and agitation, where patients experience complex and refractory symptoms. It seems to be well tolerated and gives better symptom relief. The available literature on clonidine's use in cancer pain and agitation management, especially in subcutaneous form, is limited and outdated. Therefore, the optimal dosing, safety profile and overall effectiveness of subcutaneous clonidine requires further exploration through prospective research studies.
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