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Utility of posaconazole therapeutic drug monitoring and assessment of plasma concentration threshold for effective prophylaxis of invasive fungal infections: a meta-analysis with trial sequential analysis

机译:泊沙康唑治疗药物监测和血浆浓度阈值有效预防侵袭性真菌感染的效用:采用试验序贯分析的荟萃分析

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Posaconazole therapeutic drug monitoring (TDM) is increasingly used in clinical practice. However, the utility of posaconazole TDM and the target of posaconazole plasma concentration for clinical successful prophylaxis remain uncertain and controversial. The aim of this study was to evaluate posaconazole exposure-response relationship and determine an optimum posaconazole concentration for prophylaxis against invasive fungal infections (IFIs). Bibliographic databases were searched (from inception to September 2017) to select studies including the clinical outcomes below and above concentration cut-off value of 0.5?mg/L and 0.7?mg/L. The reliability of the results were evaluated with trial sequential analysis (TSA). Twenty-eight studies with 1930 patients included were analyzed. The results of our pooled analysis demonstrated that patients with posaconazole plasma concentrations over 0.5?mg/L were twice more likely to achieve successful responses compared with those with lower concentrations (odds ratio, OR?=?1.98, 95% confidence interval, CI 1.09–3.58, P?=?0.02) while the threshold, 0.7?mg/L showed no significant difference (OR?=?1.84, 95% CI 0.94–3.63, P?=?0.08). The TSA results showed that there was sufficient information to support these findings. An optimal posaconazole concentration target of 0.5?mg/L is suggested to ensure the clinical prophylactic efficacy and may help reduce the dosage and dose-dependent toxicity comparing with the target of 0.7?mg/L.
机译:泊沙康唑治疗药物监测(TDM)在临床实践中越来越多地使用。但是,泊沙康唑TDM的实用性和泊沙康唑血浆浓度在临床上成功预防的目标仍不确定和有争议。这项研究的目的是评估泊沙康唑的暴露-反应关系,并确定预防感染性真菌感染(IFIs)的最佳泊沙康唑浓度。搜索书目数据库(从成立到2017年9月)以选择研究,包括低于或超过浓度临界值0.5?mg / L和0.7?mg / L的临床结果。结果的可靠性通过试验序贯分析(TSA)进行了评估。分析了包括1930名患者的28项研究。我们汇总分析的结果表明,泊沙康唑血浆浓度超过0.5?mg / L的患者获得成功应答的可能性是低浓度患者的两倍(优势比,OR?=?1.98,95%置信区间,CI 1.09) -3.58,P <= 0.02。而阈值0.7?mg / L则无显着性差异(OR == 1.84,95%CI 0.94-3.63,P?= 0.08)。 TSA的结果表明,有足够的信息来支持这些发现。建议将泊沙康唑的最佳目标浓度设定为0.5?mg / L,以确保临床预防效果,并且与0.7?mg / L的目标浓度相比,可能有助于减少剂量和剂量依赖性毒性。

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