Taylor David, Vallianatou Kalliopi, Whiskey Eromona, Dzahini Olubanke, MacCabe James
Institute of Pharmaceutical Science, King's College London, Franklin-Wilkins Building, 150 Stamford Street, London, SE1 9NH, UK.
Pharmacy Department, Maudsley Hospital, Denmark Hill, London, SE5 8AZ, UK.
Schizophrenia (Heidelb). 2022 Mar 14;8(1):21. doi: 10.1038/s41537-022-00232-0.
The wider use of clozapine is limited by the risk of agranulocytosis and the associated requirement for monitoring of neutrophil counts. We searched local electronic patient records for cases of agranulocytosis occurring during clozapine treatment during the period 2007-2020. We found 23 episodes recorded as agranulocytosis in clozapine patients. Of these, nine met pre-defined criteria and were considered episodes of life-threatening agranulocytosis (LTA). These episodes of clozapine-induced LTA exhibited a distinct pattern of continuous and rapid neutrophil count decline to zero or near zero. Mean time for neutrophils to fall from ANC > 2 to ANC <0.5 × 10/L was 8.4 days (range 2-15 days). Each event was also characterised by a prolonged nadir and delayed recovery (range 4-16 days). Non-LTA episodes were, in contrast, brief and benign. We conclude that an important proportion of cases of agranulocytosis identified in people prescribed clozapine are not life-threatening and may not even be clozapine-related. Monitoring schemes should aim to identify true clozapine-induced LTA as opposed to threshold-defined nominal agranulocytosis. Genetics studies might benefit from examining associations with clozapine-induced LTA rather than with recorded cases of agranulocytosis or neutropenia.
氯氮平的广泛使用受到粒细胞缺乏症风险以及相关的中性粒细胞计数监测要求的限制。我们在本地电子病历中搜索了2007年至2020年期间氯氮平治疗期间发生的粒细胞缺乏症病例。我们在氯氮平患者中发现了23例记录为粒细胞缺乏症的病例。其中,9例符合预先定义的标准,被认为是危及生命的粒细胞缺乏症(LTA)发作。这些氯氮平诱导的LTA发作表现出一种独特的模式,即中性粒细胞计数持续快速下降至零或接近零。中性粒细胞从绝对中性粒细胞计数(ANC)>2降至ANC<0.5×10⁹/L的平均时间为8.4天(范围为2至15天)。每个事件的特点还包括最低点持续时间延长和恢复延迟(范围为4至16天)。相比之下,非LTA发作短暂且良性。我们得出结论,在服用氯氮平的人群中发现的粒细胞缺乏症病例,有很大一部分并非危及生命,甚至可能与氯氮平无关。监测方案应旨在识别真正由氯氮平诱导的LTA,而不是阈值定义的名义上的粒细胞缺乏症。遗传学研究可能会受益于研究与氯氮平诱导的LTA的关联,而不是与记录的粒细胞缺乏症或中性粒细胞减少症病例的关联。