No adverse events were observed in clozapine‐treated patients on extended hematologic monitoring intervals during the coronavirus pandemic in four psychiatric centers in Japan

Hata, Masahiro; Fujimoto, Michiko; Kanai, Koji; Yoshiyama, Kenji; Nakatani, Yoshitaka; Nakabayashi, Daiji; Maemura, Saki; Kawata, Shinya; Hakozaki, Takaaki; Nishikura, Shuya; Umemoto, Aiko; Sasada, Toru; Iwata, Kazuhiko; Tanaka, Hideki; Mamoto, Akiko; Toi, Yuuki; Taniguchi, Norio; Saito, Makiko; Kimura, Yoshio; Kishimoto, Kazuko; Hayami, Megumi; Ikeda, Manabu

AIM: As an emergency measure during the coronavirus disease pandemic, the monitoring interval for clozapine use was temporarily extended beyond the regulatory requirement in Japan, which is the safest monitoring interval worldwide. In this study, we aimed to explore the effect of this measure on patients undergoing clozapine treatment. METHODS: This retrospective chart review study included patients with treatment‐resistant schizophrenia (TRS) who were undergoing clozapine treatment at four psychiatric institutions in Japan. Demographic characteristics and clinical information of these patients were collected on April 27, 2020, when Japanese psychiatrists were virtually allowed to prescribe clozapine beyond the regulatory requirement. Furthermore, information of adverse events related to the emergency measure was collected and analyzed. RESULTS: Of the 41 patients with TRS included in this study, 19 patients underwent extended hematological monitoring during clozapine treatment. No psychiatric or hematological adverse events were observed in the patients during the extended monitoring interval. CONCLUSION: This study suggested that there were few adverse events of clozapine‐treated patients related to emergency measures in Japan. However, hematological monitoring intervals during clozapine treatment have been emergently extended worldwide; hence, it is necessary to verify the results of these measures.