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西多福韦在儿童腺病毒感染患者中的应用。

Use of cidofovir in pediatric patients with adenovirus infection.

作者信息

Ganapathi Lakshmi, Arnold Alana, Jones Sarah, Patterson Al, Graham Dionne, Harper Marvin, Levy Ofer

机构信息

Division of Infectious Diseases, Boston Children's Hospital, Boston, MA, USA; Harvard Medical School, Boston, MA, USA.

Division of Pharmacy, Boston Children's Hospital, Boston, MA, USA.

出版信息

F1000Res. 2016 Apr 26;5:758. doi: 10.12688/f1000research.8374.2. eCollection 2016.

DOI:10.12688/f1000research.8374.2
PMID:27239277
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4863673/
Abstract

: Adenoviruses contribute to morbidity and mortality among immunocompromised pediatric patients including stem cell and solid organ transplant recipients. Cidofovir (CDV), an antiviral compound approved by the FDA in 1996, is used for treatment of adenoviral (ADV) infections in immunocompromised patients despite concern of potential nephrotoxicity.   : We conducted a retrospective 5-year review at Boston Children's Hospital of 16 patients (mean age = 6.5 years) receiving 19 courses of CDV. During therapy all pertinent data elements were reviewed to characterize potential response to therapy and incidence of renal dysfunction.   Of the 19 CDV courses prescribed, 16 courses (84%) were in patients who had a positive blood ADV Polymerase chain reaction (PCR) alone or in combination with positive ADV PCR/ Direct Immunofluorescence Assay (DFA) at another site. Respiratory symptoms with or without pneumonia were the most common presentation (10/19, 53%). In the majority of blood positive courses (10/16, 63%), viral clearance was also accompanied by clinical response. This was not the case in four courses where patients expired despite viral clearance, including one in which death was directly attributable to adenovirus. There was reversible renal dysfunction observed during the use of CDV.   CDV appeared safe and reasonably tolerated for treatment of ADV in this pediatric population and was associated with viral response and clinical improvement in the majority of patients but reversible renal dysfunction was a side effect. Further studies of the efficacy of CDV for immunocompromised children with ADV infection are warranted.

摘要

腺病毒会导致免疫功能低下的儿科患者发病和死亡,这些患者包括干细胞和实体器官移植受者。西多福韦(CDV)是一种1996年获美国食品药品监督管理局批准的抗病毒化合物,尽管存在潜在肾毒性的担忧,但仍用于治疗免疫功能低下患者的腺病毒(ADV)感染。

我们对波士顿儿童医院16名接受19个疗程CDV治疗的患者(平均年龄 = 6.5岁)进行了为期5年的回顾性研究。治疗期间,对所有相关数据元素进行了审查,以确定潜在的治疗反应和肾功能障碍的发生率。

在开出的19个CDV疗程中,16个疗程(84%)用于单独血液ADV聚合酶链反应(PCR)呈阳性或在另一部位ADV PCR/直接免疫荧光测定(DFA)呈阳性的患者。有或无肺炎的呼吸道症状是最常见的表现(10/19,53%)。在大多数血液阳性疗程(10/16,63%)中,病毒清除也伴随着临床反应。在四个疗程中情况并非如此,尽管病毒已清除,但患者仍死亡,其中一例死亡直接归因于腺病毒。使用CDV期间观察到可逆性肾功能障碍。

在该儿科人群中,CDV用于治疗ADV似乎是安全且耐受性良好的,并且在大多数患者中与病毒反应和临床改善相关,但可逆性肾功能障碍是一种副作用。有必要对CDV治疗免疫功能低下的ADV感染儿童的疗效进行进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/157e/5166587/eed20a05e8f9/f1000research-5-11225-g0000.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/157e/5166587/eed20a05e8f9/f1000research-5-11225-g0000.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/157e/5166587/eed20a05e8f9/f1000research-5-11225-g0000.jpg

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