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Ganciclovir therapy in cytomegalovirus (CMV) infection in immunocompetent pediatric patients

机译:更昔洛韦治疗免疫功能正常的小儿巨细胞病毒(CMV)感染

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Objectives: To evaluate the outcome of immunocompetent pediatric patients who had positive cytomegalovirus (CMV) antigenemia and received ganciclovir.Methods: A retrospective review was done of patients who had a CMV infection based on positive antigenemia. Medical charts were reviewed for the following information: age, sex, underlying disease, symptoms and signs, laboratory results, complementary diagnostic procedures, duration and dose of ganciclovir therapy, concomitant medications, complications, and outcome.Results: Sixty-four patients with positive CMV antigenemia were identified; 15 patients were excluded from the study because of their underlying diseases. Of the remaining 49 patients, 26 (53%) were female; the median age was 11.5 months (range 0.3–132 months). Sixty-one percent (30/49) of these patients received ganciclovir (5–10 mg/kg/day) for a median of 14 days (range 7–42 days). Clinical findings included: fever, anemia, hepatomegaly, failure to thrive, elevated liver enzymes, splenomegaly, seizures, and thrombocytopenia. Sixty-three percent (19/30) of the treated patients had negative antigenemia at the end of therapy. CMV antigenemia remained positive in six (20%) patients. Nine patients received a second course of ganciclovir.Conclusions: Ganciclovir was effective in 80% of patients, as determined by negative antigenemia at the end of therapy.
机译:目的:评估具有巨细胞病毒(CMV)抗原血症并接受更昔洛韦的免疫功能小儿患者的结果。方法:回顾性审查基于阳性抗原血症的CMV感染患者。审查了医学图表以获取以下信息:年龄,性别,潜在疾病,症状和体征,实验室结果,补充诊断程序,更昔洛韦治疗的持续时间和剂量,伴随用药,并发症和结局。结果:64例阳性确定了CMV抗原血症; 15名患者因其潜在疾病而被排除在研究之外。在其余的49位患者中,有26位(53%)是女性。中位年龄为11.5个月(范围0.3-132个月)。这些患者中有百分之六十一(30/49)接受更昔洛韦(5-10 mg / kg /天)治疗,中位数为14天(7-42天)。临床发现包括:发烧,贫血,肝肿大,无法存活,肝酶升高,脾肿大,癫痫发作和血小板减少。在治疗结束时,百分之六十三(19/30)的治疗患者抗原血症为阴性。六名(20%)患者的CMV抗原血症保持阳性。 9名患者接受了第二个更昔洛韦疗程。结论:更昔洛韦在80%的患者中有效,根据治疗结束时的阴性抗原血症确定。

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