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首页> 外文期刊>Therapeutic Drug Monitoring >Therapeutic Drug Monitoring of Voriconazole After Intravenous Administration in Infants and Children With Primary Immunodeficiency.
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Therapeutic Drug Monitoring of Voriconazole After Intravenous Administration in Infants and Children With Primary Immunodeficiency.

机译:伏立康唑静脉给药后对婴幼儿原发性免疫功能低下患者的治疗药物监测。

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OBJECTIVE:: A voriconazole trough concentration (Ctrough) <1 mg/L is associated with a higher risk of treatment failure. The aim of this work was to describe the probability of not achieving this target concentration in infants and children receiving intravenous voriconazole. METHODS:: Voriconazole trough concentrations obtained during routine therapeutic drug monitoring over a 5-year period were collected retrospectively from infants and children receiving intravenous voriconazole for presumed or proven invasive fungal infections. RESULTS:: Sixty-two trough concentrations were obtained from 6 infants and 10 children. The risk of a Ctrough <1 mg/L was 77% and 47%, respectively. Daily doses between 20 and 32 mg/kg were necessary in some patients to achieve a Ctrough >1 mg/L, compared with the currently recommended 14-mg/kg regimen. CONCLUSIONS:: Routine therapeutic drug monitoring is potentially helpful in infants and children receiving voriconazole, even intravenously.
机译:目的:伏立康唑谷浓度(Ctrough)<1 mg / L与更高的治疗失败风险相关。这项工作的目的是描述接受静脉伏立康唑的婴幼儿未达到目标浓度的可能性。方法:回顾性收集5年期间常规治疗药物监测期间获得的伏立康唑谷浓度,这些婴儿和儿童接受了静脉伏立康唑的推定或已证实的侵袭性真菌感染。结果:从6婴儿和10儿童中获得了62谷浓度。 Ctrough <1 mg / L的风险分别是77%和47%。与目前建议的14 mg / kg方案相比,某些患者需要达到20-32 mg / kg的每日剂量才能达到Ctrough> 1 mg / L。结论:常规治疗药物监测可能对接受伏立康唑的婴儿和儿童,甚至静脉内治疗有帮助。

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