首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Efficacy and safety of itraconazole prophylaxis for fungal infections after orthotopic liver transplantation: a prospective, randomized, double-blind study.
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Efficacy and safety of itraconazole prophylaxis for fungal infections after orthotopic liver transplantation: a prospective, randomized, double-blind study.

机译:伊曲康唑预防原位肝移植术后真菌感染的有效性和安全性:一项前瞻性,随机,双盲研究。

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BACKGROUND: There is significant morbidity and mortality related to fungal infections in the solid-organ transplant population. METHODS: A prospective, randomized, double-blind, placebo-controlled, restricted sequential design trial was performed in 71 adults undergoing orthotopic liver transplantation. Patients were randomly assigned to receive either itraconazole (5.0 mg/kg orally, preoperatively, 2.5 mg/kg orally, two times a day, postoperatively) or placebo. Therapy continued for a maximum of 56 days or until patient was discharged from hospital or met a predefined endpoint. Measurements included incidence of fungal colonization, superficial or systemic fungal infections requiring systemic therapy, adverse events, and mortality rate. RESULTS: This trial design supported the superiority of itraconazole in preventing fungal infections; nine patients in the placebo group (24%; 95% confidence interval, 0.118-0.412) and one patient in the itraconazole group (4%; 95% confidence interval, 0.001-0.204) developed fungal endpoints requiring therapy with amphotericin B (P=0.04, Fisher's exact test). At the time of enrollment, fungal colonization occurred in 40% and 37% of itraconazole and placebo patients (P=0.43), respectively. Adverse events were reported by 97% and 100% of the intraconazole and placebo groups, respectively, and one itraconazole and six placebo-group patients died within the study period. There was no relation to trial medication for serious adverse events. CONCLUSION: Prophylaxis with itraconazole reduces fungal infections in patients undergoing orthotopic liver transplantation and is well tolerated.
机译:背景:在实体器官移植人群中,与真菌感染有关的发病率和死亡率均很高。方法:对71名接受原位肝移植的成年人进行了一项前瞻性,随机,双盲,安慰剂对照,限制性序贯设计试验。患者被随机分配接受伊曲康唑(术前口服5.0 mg / kg,术前口服2.5 mg / kg,每天两次,术后两次)或安慰剂。持续治疗最多56天,或直到患者出院或达到预定终点为止。测量包括真菌定植的发生率,需要全身治疗的浅表或全身性真菌感染,不良事件和死亡率。结果:该试验设计支持伊曲康唑在预防真菌感染方面的优势。安慰剂组的9例患者(24%; 95%的置信区间为0.118-0.412)和伊曲康唑组的1名患者(4%; 95%的置信区间为0.001-0.204)出现了需要使用两性霉素B治疗的真菌终点(P = 0.04,Fisher的精确检验)。在入组时,伊曲康唑和安慰剂患者分别发生真菌定植(40%)和37%(P = 0.43)。内康唑和安慰剂组分别报告有97%和100%的不良事件,在研究期内,伊曲康唑和6名安慰剂组患者死亡。与严重不良事件的试验药物无关。结论:伊曲康唑预防可减少原位肝移植患者的真菌感染,并且耐受性良好。

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