Smith M S, Muir H, Hall R
Department of Anaesthesia, Dalhousie University, Halifax, Nova Scotia, Canada.
Drugs. 1996 Feb;51(2):238-59. doi: 10.2165/00003495-199651020-00005.
The objectives for the provision of a safe anaesthetic include rendering the patient analgesic for the procedure (amnesic if appropriate), with control of adverse haemodynamic perturbations, and muscle relaxation to facilitate surgery as necessary. This must be done with an understanding of the patient's pre-existing pathophysiology and drug therapy. This article focuses on the management of medications in the perioperative period from the practitioner's perspective. Areas of drug therapy examined include drugs affecting the cardiovascular, central nervous, haemostatic and endocrine systems. Review of the limited data available suggests that the safest course of action for the preoperative management of the vast majority of drug therapy is to continue such therapy until the time of surgery, particularly agents in which a withdrawal syndrome has been described, e.g. beta-adrenoceptor blocking agents, alpha 2-adrenoceptor agonists. Exceptions to this generalisation might include discontinuing ACE inhibitors prior to surgery as these agents may be associated with adverse haemodynamic changes during surgery. The management of drug therapy for patients receiving monoamine oxidase inhibitors (MAOIs) continues to be challenging due to the potential for drug interactions, e.g. severe hypertension with use of indirect-acting vasopressors and excitatory/depressive reactions with administration of pethidine (meperidine) or dextromethorphan. However, recent clinical experience has demonstrated the relative safety of continuing MAOIs prior to surgery by use of specific 'MAOI safe' anaesthetic techniques and/or substitution of short-acting MAOIs which do not irreversibly inhibit the enzyme. For drugs affecting the coagulation system, such as heparin and warfarin, prudence dictates discontinuing these agents whenever possible prior to surgery where it can be anticipated that haemorrhage will occur, e.g. vascular surgery, or where the consequences of even minor bleeding could be catastrophic, e.g. eye surgery. Controversy exists as to the management of patients receiving prophylactic low dose heparin for deep vein thrombosis prophylaxis or in whom intraoperative or postoperative anticoagulation is planned, e.g. aortic surgery, and in whom a regional anaesthetic technique is planned as part of the anaesthetic management. The data available suggest that, where prophylactic use of heparin is concerned, and provided the administration of the last dose of heparin and the institution of a regional anaesthetic nerve block does not occur at the same time, use of regional anaesthesia is not contraindicated in such circumstances. Where therapeutic anticoagulation is planned as part of the surgical management, there is a very small risk of the development of epidural or spinal haematoma when major central conduction nerve block is employed for anaesthesia, with resultant spinal cord compression and paralysis. These precautions do not apply to patients receiving aspirin or other nonsteroidal anti-inflammatory agents as there is a large clinical and published experience of the safety of regional anaesthesia in this group of patients. Patients treated with fibrinolytic agents are at increased risk for bleeding should surgery be required. For these patients, pre- and intraoperative use of agents with antifibrinolytic activity, e.g. aprotinin, has been demonstrated in case reports to be beneficial. Finally, recommendations for the management of patients who have received or are receiving glucocorticoids are given. Throughout the review, areas of uncertainty where further research is required are identified.
提供安全麻醉的目标包括使患者在手术过程中镇痛(必要时产生遗忘作用),控制不良血流动力学波动,并在必要时实现肌肉松弛以利于手术。这必须在了解患者既往病理生理学和药物治疗情况的基础上进行。本文从从业者的角度重点探讨围手术期药物的管理。所研究的药物治疗领域包括影响心血管、中枢神经、止血和内分泌系统的药物。对现有有限数据的回顾表明,绝大多数药物治疗术前管理的最安全做法是继续此类治疗直至手术时,特别是那些已描述有撤药综合征的药物,如β肾上腺素能受体阻滞剂、α2肾上腺素能激动剂。这一普遍原则的例外情况可能包括术前停用血管紧张素转换酶抑制剂,因为这些药物可能与手术期间的不良血流动力学变化有关。由于存在药物相互作用的可能性,如使用间接作用血管加压药时出现严重高血压,以及使用哌替啶(度冷丁)或右美沙芬时出现兴奋/抑郁反应,接受单胺氧化酶抑制剂(MAOI)治疗的患者的药物治疗管理仍然具有挑战性。然而,最近的临床经验表明,通过使用特定的“MAOI安全”麻醉技术和/或替代不会不可逆抑制该酶的短效MAOI,术前继续使用MAOI相对安全。对于影响凝血系统的药物,如肝素和华法林,谨慎起见,在可预见会发生出血的手术前,如血管手术,或即使轻微出血后果也可能是灾难性的手术前,如眼科手术,应尽可能停用这些药物。对于接受预防性低剂量肝素预防深静脉血栓形成或计划进行术中或术后抗凝的患者,如主动脉手术,以及计划将区域麻醉技术作为麻醉管理一部分的患者,其管理存在争议。现有数据表明,就肝素的预防性使用而言,只要最后一剂肝素的给药与区域麻醉神经阻滞的实施不同时进行,在这种情况下使用区域麻醉并无禁忌。如果手术管理计划包括治疗性抗凝,当采用主要的中枢传导神经阻滞进行麻醉时,发生硬膜外或脊髓血肿并导致脊髓压迫和瘫痪的风险非常小。这些预防措施不适用于接受阿司匹林或其他非甾体类抗炎药的患者,因为在这组患者中,区域麻醉的安全性已有大量临床和已发表的经验。接受纤维蛋白溶解剂治疗的患者如果需要手术,出血风险会增加。对于这些患者,病例报告显示术前和术中使用具有抗纤维蛋白溶解活性的药物,如抑肽酶,是有益的。最后,给出了对已接受或正在接受糖皮质激素治疗的患者的管理建议。在整个综述过程中,确定了需要进一步研究的不确定领域。