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分析泊沙康唑作为 12 岁以下异基因造血干细胞移植后患儿的口服抗真菌预防用药。

Analysis of posaconazole as oral antifungal prophylaxis in pediatric patients under 12 years of age following allogeneic stem cell transplantation.

机构信息

Department of Pediatric Hematology and Oncology, University Children's Hospital Tübingen, Tübingen, Germany.

出版信息

BMC Infect Dis. 2012 Oct 19;12:263. doi: 10.1186/1471-2334-12-263.

Abstract

BACKGROUND

Pediatric patients undergoing hematopoietic stem cell transplantation (HSCT) are at high risk of acquiring fungal infections. Antifungal prophylaxis shortly after transplantation is therefore indicated, but data for pediatric patients under 12 years of age are scarce. To address this issue, we retrospectively assessed the safety, feasibility, and initial efficacy of prophylactic posaconazole in children.

METHODS

60 consecutive pediatric patients with a median age of 6.0 years who underwent allogeneic HSCT between August 2007 and July 2010 received antifungal prophylaxis with posaconazole in the outpatient setting. 28 pediatric patients received an oral suspension at 5 mg/kg body weight b.i.d., and 32 pediatric patients received the suspension at 4 mg/kg body weight t.i.d. The observation period lasted from start of treatment with posaconazole until its termination (maximum of 200 days post-transplant).

RESULTS

Pediatric patients who received posaconazole at 4 mg/kg body weight t.i.d. had a median trough level of 383 μg/L. Patients who received posaconazole at 5 mg/kg body weight b.i.d. had a median trough level of 134 μg/L. Both regimens were well tolerated without severe side effects. In addition, no proven or probable invasive mycosis was observed.

CONCLUSION

Posaconazole was a well-tolerated, safe, and effective oral antifungal prophylaxis in pediatric patients who underwent high-dose chemotherapy and HSCT. Posaconazole at a dosage of 12 mg/kg body weight divided in three doses produced consistently higher morning trough levels than in patients who received posaconazole 5 mg/kg body weight b.i.d. Larger prospective trials are needed to obtain reliable guidelines for antifungal prophylaxis in children after HSCT.

摘要

背景

接受造血干细胞移植(HSCT)的儿科患者存在发生真菌感染的高风险。因此,在移植后不久进行抗真菌预防是必要的,但针对 12 岁以下儿科患者的数据却很少。为解决这一问题,我们回顾性评估了预防性泊沙康唑在儿科患者中的安全性、可行性和初步疗效。

方法

2007 年 8 月至 2010 年 7 月期间,我们对 60 例中位年龄为 6.0 岁的接受异基因 HSCT 的连续儿科患者进行了研究,这些患者在门诊接受泊沙康唑抗真菌预防。28 例儿科患者接受 5mg/kg 体重的混悬液,每日 2 次(bid),32 例儿科患者接受 4mg/kg 体重的混悬液,每日 3 次(tid)。观察期从开始使用泊沙康唑至其结束(移植后最多 200 天)。

结果

接受泊沙康唑 4mg/kg 体重 tid 的儿科患者的中位谷浓度为 383μg/L。接受泊沙康唑 5mg/kg 体重 bid 的儿科患者的中位谷浓度为 134μg/L。两种方案均耐受良好,无严重副作用。此外,未观察到确诊或疑似侵袭性真菌感染。

结论

泊沙康唑是一种耐受性良好、安全且有效的口服抗真菌预防药物,适用于接受大剂量化疗和 HSCT 的儿科患者。与接受泊沙康唑 5mg/kg 体重 bid 的儿科患者相比,接受泊沙康唑 12mg/kg 体重分 3 次剂量的儿科患者清晨谷浓度更高。需要更大规模的前瞻性试验来获得 HSCT 后儿童抗真菌预防的可靠指南。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a88/3514296/4ea7c0d2e82e/1471-2334-12-263-1.jpg

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