Kikuchi Yuki, Tanifuji Hiroaki, Ueno Sota, Onuma Yoshifumi, Goto Masatomo, Ishihara Masato, Toraiwa Takeshi, Komatsu Hiroshi, Tomita Hiroaki
Department of Psychiatry, Graduate School of Medicine, Tohoku University, Sendai, Miyagi, Japan.
Department of Psychiatry, Kodama Hospital, Ishinomaki, Miyagi, Japan.
Front Psychiatry. 2024 Feb 21;15:1366621. doi: 10.3389/fpsyt.2024.1366621. eCollection 2024.
International guidelines for clozapine titration recommend measuring C-reactive protein (CRP) weekly for 4 weeks after clozapine initiation to prevent fatal inflammatory adverse events, including myocarditis. However, limited evidence exists regarding whether weekly CRP monitoring can prevent clozapine-induced inflammation.
We examined the relationship between CRP trends and the development of clozapine-induced inflammation. We also explored the usefulness and limitations of CRP monitoring during clozapine titration.
This study presents 17 and 4 cases of weekly and daily CRP monitoring during clozapine initiation, respectively.
Among 17 patients with weekly CRP measurements, 7 had fever. Elevated CRP levels were detected before the onset of fever in two of the seven patients. Of the five remaining patients, the CRP levels on a previous test had been low; however, the fever developed suddenly. Of the 10 patients with no fever under weekly CRP monitoring, three had elevated CRP levels >3.0 mg/dL. Refraining from increasing the clozapine dose may have prevented fever in these patients. Among four patients with daily CRP measurements, two became febrile. In both cases, CRP levels increased almost simultaneously with the onset of fever.
Weekly and daily CRP monitoring during clozapine titration is valuable for preventing clozapine-induced inflammation, assessing its severity, and guiding clozapine dose adjustments. Weekly CRP monitoring may not adequately predict clozapine-induced inflammation in some cases. Consequently, clinicians should be aware of the sudden onset of clozapine-induced inflammation, even if CRP levels are low. Daily CRP monitoring is better for detecting clozapine-induced inflammation.
氯氮平滴定的国际指南建议在氯氮平起始治疗后的4周内每周测量C反应蛋白(CRP),以预防包括心肌炎在内的致命性炎症不良事件。然而,关于每周监测CRP是否能预防氯氮平引起的炎症,证据有限。
我们研究了CRP变化趋势与氯氮平引起的炎症发展之间的关系。我们还探讨了氯氮平滴定期间CRP监测的有用性和局限性。
本研究分别介绍了氯氮平起始治疗期间每周和每日监测CRP的17例和4例病例。
在17例每周测量CRP的患者中,7例出现发热。7例患者中有2例在发热开始前检测到CRP水平升高。其余5例患者中,前一次检测时CRP水平较低;然而,发热突然出现。在每周CRP监测下未发热的10例患者中,3例CRP水平>3.0mg/dL。避免增加氯氮平剂量可能预防了这些患者的发热。在4例每日测量CRP的患者中,2例发热。在这两种情况下,CRP水平几乎与发热开始同时升高。
氯氮平滴定期间每周和每日监测CRP对于预防氯氮平引起的炎症、评估其严重程度以及指导氯氮平剂量调整具有重要价值。在某些情况下,每周监测CRP可能无法充分预测氯氮平引起的炎症。因此,即使CRP水平较低,临床医生也应意识到氯氮平引起的炎症可能突然发生。每日监测CRP更有利于检测氯氮平引起的炎症。