Thai Helen, Preobrazenski Nicholas, Hsieh TiChen, Robertson Carrie, Owoeye Olabisi
Department of Psychology, McGill University, Montreal, Quebec, Canada.
Faculty of Medicine, Department of Psychiatry, University of Ottawa, Ottawa, Ontario, Canada.
Schizophr Bull. 2025 Mar 14;51(2):493-500. doi: 10.1093/schbul/sbae113.
In response to Health Canada's March 2020 directive, patients on clozapine for over 12 months were allowed to extend hematological testing intervals from 4 to 8 weeks during the COVID-19 pandemic. We hypothesized that this change would not affect the timely detection of hematological abnormalities in patients with severe mental illness.
A chart review was conducted of patients at the Royal Ottawa who were prescribed clozapine from March 2019 to March 2021. We analyzed clinical and hematological data from electronic health records and Clozaril Support and Assistance Network database to compare occurrences of hematological abnormalities [leukopenia (white blood cell count <3.5 × 109/L) and agranulocytosis (absolute neutrophil count <0.5 × 109/L)] from March 17, 2020 to March 16, 2021, between standard and extended monitoring protocols using binomial logistic and zero-inflated negative binomial regressions.
Of 621 patients, 196 were on extended blood monitoring, and 425 followed standard blood monitoring. Clozapine dose did not differ between groups (standard: 370 ± 201 mg; extended: 352 ± 172 mg; P = .14, ds = 0.10). Clozapine treatment duration up to March 2021 was 12.6 ± 8.3 years, with the extended group (10 ± 7.9 years) having a significantly (P < .01, ds = 0.50) shorter duration than the standard (14 ± 8.2 years). Extended monitoring did not significantly impact likelihood of detecting hematological abnormalities (OR = 0.83, 95% CI [0.58,1.41], P = .55) after controlling for age, sex, total bloodwork, and other psychotropics associated with neutrophil counts (ie, valproate, olanzapine). No patient on the extended regimen developed agranulocytosis.
Reducing blood monitoring frequency in patients on clozapine for more than 12 months did not compromise detection of hematological abnormalities.
为响应加拿大卫生部2020年3月的指令,在新冠疫情期间,服用氯氮平超过12个月的患者的血液学检测间隔时间从4周延长至8周。我们假设这一变化不会影响对重症精神疾病患者血液学异常的及时检测。
对2019年3月至2021年3月期间在渥太华皇家医院开具氯氮平处方的患者进行了病历审查。我们分析了电子健康记录和氯氮平支持与援助网络数据库中的临床和血液学数据,以比较2020年3月17日至2021年3月16日期间,使用二项逻辑回归和零膨胀负二项回归,标准监测方案与延长监测方案下血液学异常[白细胞减少症(白细胞计数<3.5×10⁹/L)和粒细胞缺乏症(绝对中性粒细胞计数<0.5×10⁹/L)]的发生率。
621例患者中,196例接受延长血液监测,425例遵循标准血液监测。两组间氯氮平剂量无差异(标准组:370±201mg;延长组:352±172mg;P = 0.14,ds = 0.10)。截至2021年3月,氯氮平治疗时长为12.6±8.3年,延长组(10±7.9年)的治疗时长显著短于标准组(14±8.2年)(P<0.01,ds = 0.50)。在控制年龄、性别、全血细胞检查以及其他与中性粒细胞计数相关的精神药物(即丙戊酸盐、奥氮平)后,延长监测对检测血液学异常的可能性没有显著影响(OR = 0.83,95%CI[0.58,1.41],P = 0.55)。接受延长方案的患者中无粒细胞缺乏症发生。
将服用氯氮平超过12个月患者的血液监测频率降低,并未影响对血液学异常的检测。