Alberta Health Services, Edmonton, AB, Canada.
Ann Pharmacother. 2010 Apr;44(4):727-32. doi: 10.1345/aph.1M398. Epub 2010 Mar 16.
To examine the pharmacokinetic implications and potential clinical effects of tobacco smoking cessation in patients on stable clozapine or olanzapine treatment.
A literature search of MEDLINE (1950-November 2009) and EMBASE (1980-November 2009) was conducted using the search terms smoking, tobacco, cigarette, cannabis, smoking cessation, cytochrome P450, antipsychotic, clozapine, and olanzapine. In addition, reference lists from publications identified were searched manually.
English-language articles and human studies were identified, yielding 111 returns. Articles that reported clinical outcomes following smoking cessation were selected. Pharmacokinetic data for these drugs were reviewed and articles that provided relevant background information were also included.
Pharmacokinetic studies have demonstrated more rapid clearance of olanzapine and lower clozapine and norclozapine (desmethylclozapine) concentrations in smokers compared to nonsmokers. These studies also found that smokers require higher doses of these agents than nonsmokers. There are case reports of adverse clinical outcomes following smoking cessation in patients being treated with olanzapine and clozapine. Reports that included serum concentrations consistently found elevations following smoking cessation, and dosage reductions of 30-40% were required to achieve pre-cessation concentrations. Worsening psychiatric symptoms, somnolence, hypersalivation, extreme fatigue, extrapyramidal effects, and seizures have all been reported following smoking cessation in this patient group.
Pharmacists need to be aware of potential risks associated with smoking cessation in patients stabilized on clozapine or olanzapine. Toxicity as a result of recent smoking reduction or cessation may be a reason for hospital admission. For hospitalized patients, pharmacists should obtain information concerning smoking status, including cessation attempts. Nonspecific signs and symptoms of elevated clozapine or olanzapine concentrations should be considered in relation to clinical status while the patient is hospitalized. Measurement of baseline serum clozapine concentrations and/or empiric dosage adjustment in patients expected to have a prolonged hospital stay with forced smoking cessation may be appropriate.
研究稳定期氯氮平和奥氮平治疗患者戒烟对药代动力学的影响及其潜在临床影响。
检索 MEDLINE(1950 年-2009 年 11 月)和 EMBASE(1980 年-2009 年 11 月),检索词为吸烟、烟草、香烟、大麻、戒烟、细胞色素 P450、抗精神病药、氯氮平和奥氮平。此外,还手工检索了从出版物中获得的参考文献列表。
选择报告戒烟后临床结局的英文文章和人类研究。对这些药物的药代动力学数据进行了回顾,并纳入了提供相关背景信息的文章。
药代动力学研究表明,与不吸烟者相比,吸烟者的奥氮平清除率更快,氯氮平和去甲氯氮平(去甲氯氮平)浓度更低。这些研究还发现吸烟者需要比不吸烟者更高的剂量。有奥氮平和氯氮平治疗患者戒烟后出现不良临床结局的病例报告。包括血清浓度的报告一致发现戒烟后浓度升高,需要减少 30-40%的剂量才能达到戒烟前的浓度。在该患者群体中,戒烟后出现精神病症状恶化、嗜睡、唾液分泌过多、极度疲劳、锥体外系症状和癫痫发作等情况均有报道。
药师需要了解稳定期氯氮平和奥氮平治疗患者戒烟相关的潜在风险。由于最近吸烟减少或戒烟导致的毒性可能是住院的原因。对于住院患者,药师应获取有关吸烟状况的信息,包括戒烟尝试。在患者住院期间,应根据临床状况考虑与升高的氯氮平和奥氮平浓度相关的非特异性体征和症状。对于预计需要长时间住院并被迫戒烟的患者,测量氯氮平的基线血清浓度和/或经验性剂量调整可能是合适的。