Buerkle H, Wilhelm W
Klinik und Poliklinik für Anästhesiologie und operative Intensivmedizin, Westfälische Wilhelms-Universität Münster, Münster, Germany.
Curr Opin Anaesthesiol. 2000 Jun;13(3):271-5. doi: 10.1097/00001503-200006000-00006.
Recently, with the introduction of the novel mu-opioid receptor agonist remifentanil, anaesthesiologists have acquired a unique tool to provide adequate, titratable and predictable analgesia throughout surgery, without the risk of opioid-related delay in postoperative recovery. This new compound will therefore mandate a change in anaesthesia practice from opioid-restricted to opioid-dominated anaesthesia. It is the first in the class of esterase-metabolized opioids within the 4-anilidopiperidine series of drugs, and it possesses an analgesic potency similar to that of fentanyl. The advantages of remifentanil are mainly related to its unique pharmacokinetics, whereas its pharmacodynamics are the same as those of fentanyl. Because of these characteristics, remifentanil-based anaesthesia allows profound opioid analgesia intraoperatively, with rapid and predictable awakening thereafter. Review of the recent literature reveals the potential of remifentanil for improving analgesia in gynaecological procedures and its theoretical advantage in obstetric procedures.
最近,随着新型μ-阿片受体激动剂瑞芬太尼的引入,麻醉医生获得了一种独特的工具,可在整个手术过程中提供充分、可滴定且可预测的镇痛效果,而不存在与阿片类药物相关的术后恢复延迟风险。因此,这种新化合物将促使麻醉实践从限制使用阿片类药物转变为以阿片类药物为主导的麻醉方式。它是4-苯胺基哌啶系列药物中首个酯酶代谢型阿片类药物,其镇痛效力与芬太尼相似。瑞芬太尼的优势主要与其独特的药代动力学有关,而其药效动力学与芬太尼相同。由于这些特性,基于瑞芬太尼的麻醉可在术中实现深度阿片类镇痛,随后快速且可预测地苏醒。对近期文献的回顾揭示了瑞芬太尼在妇科手术中改善镇痛的潜力及其在产科手术中的理论优势。