Tanzer Timothy David, Brouard Thomas, Pra Samuel Dal, Warren Nicola, Barras Michael, Kisely Steve, Brooks Emily, Siskind Dan
Department of Pharmacy, Princess Alexandra Hospital, Brisbane, QLD, Australia.
Faculty of Medicine, The University of Queensland, Brisbane, QLD, Australia.
Ther Adv Psychopharmacol. 2022 May 24;12:20451253221092931. doi: 10.1177/20451253221092931. eCollection 2022.
Clozapine is the most effective medication for treatment-refractory schizophrenia but is associated with significant adverse drug effects, including hypotension and dizziness, which have a negative impact on quality of life and treatment compliance. Available evidence for the management of clozapine-induced hypotension is scant.
Due to limited guidance on the safety and efficacy of pharmacological treatments for clozapine-induced hypotension, we set out to systematically review and assess the evidence for the management of clozapine-induced hypotension and provide guidance to clinicians, patients, and carers.
We undertook a systematic review of the safety and efficacy of interventions for clozapine-induced hypotension given the limited available evidence.
PubMed, Embase, PsycINFO, CINAHL, and the Cochrane trial Registry were searched from inception to November 2021 for literature on the treatment strategies for clozapine-induced hypotension and dizziness using a PROSPERO pre-registered search strategy. For orthostatic hypotension, we developed a management framework to assist in the choice of intervention.
We identified nine case studies and four case series describing interventions in 15 patients. Hypotension interventions included temporary clozapine dose reduction, non-pharmacological treatments, and pharmacological treatments. Midodrine, fludrocortisone, moclobemide and Bovril combination, and etilefrine were associated with improvement in symptoms or reduction in orthostatic hypotension. Angiotensin II, arginine vasopressin, and noradrenaline successfully restored and maintained mean arterial pressure in critical care situations. A paradoxical reaction of severe hypotension was reported with adrenaline use.
Orthostatic hypotension is a common side effect during clozapine titration. Following an assessment of the titration schedule, salt and fluid intake, and review of hypertensive and nonselective α1-adrenergic agents, first-line treatment should be a temporary reduction in clozapine dose or non-pharmacological interventions. If orthostatic hypotension persists, fludrocortisone should be trialled with monitoring of potassium levels and sodium and fluid intake. Midodrine may be considered second-line or where fludrocortisone is contraindicated or poorly tolerated. For patients on clozapine with hypotension in critical care settings, the use of adrenaline to maintain mean arterial pressure should be avoided.
PROSPERO (Registration No. CRD42020191530).
氯氮平是治疗难治性精神分裂症最有效的药物,但会产生显著的药物不良反应,包括低血压和头晕,这对生活质量和治疗依从性有负面影响。关于氯氮平所致低血压管理的现有证据很少。
由于针对氯氮平所致低血压的药物治疗的安全性和有效性的指导有限,我们着手系统回顾和评估氯氮平所致低血压管理的证据,并为临床医生、患者及护理人员提供指导。
鉴于现有证据有限,我们对氯氮平所致低血压干预措施的安全性和有效性进行了系统回顾。
从数据库建立至2021年11月,使用PROSPERO预先注册的检索策略,在PubMed、Embase、PsycINFO、CINAHL和Cochrane试验注册库中检索关于氯氮平所致低血压和头晕治疗策略的文献。对于直立性低血压(体位性低血压),我们制定了一个管理框架以协助选择干预措施。
我们确定了9项病例研究和4个病例系列,描述了对15例患者的干预措施。低血压干预措施包括暂时减少氯氮平剂量、非药物治疗和药物治疗。米多君、氟氢可的松、吗氯贝胺与牛肉汁组合以及乙苯福林与症状改善或直立性低血压减轻有关。在重症监护情况下,血管紧张素II、精氨酸加压素和去甲肾上腺素成功恢复并维持了平均动脉压。有报告称使用肾上腺素会出现严重低血压的反常反应。
直立性低血压是氯氮平滴定过程中的常见副作用。在评估滴定方案、盐和液体摄入量,并复查高血压药物和非选择性α1-肾上腺素能药物后,一线治疗应为暂时减少氯氮平剂量或采取非药物干预措施。如果直立性低血压持续存在,应试用氟氢可的松并监测血钾水平以及钠和液体摄入量。米多君可被视为二线用药,或用于氟氢可的松禁忌或耐受性差的情况。对于在重症监护环境中服用氯氮平且出现低血压的患者,应避免使用肾上腺素来维持平均动脉压。
PROSPERO(注册号CRD42020191530)