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Respiratory and systemic infections in children with severe aplastic anemia on immunosuppressive therapy

机译:免疫抑制治疗患儿患儿呼吸系统呼吸系统感染

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In the present study we investigated the occurrence of systemic and respiratory infections in a cohort of 123 children with severe acquired aplastic anemia (SAA) on immunosuppressive therapy (IST). We recorded 101 episodes of infection in 77 patients (62.6 %). Pneumonia was among the most frequently observed clinical forms of infection (17 cases-16.8 %). In the entire group, 23 children died, mostly in the course of fatal sepsis (15/23) and in 3 cases because of pneumonia complications. All patients were treated with horse (h-ATG) or rabbit antithymocyte globulin (r-ATG) supplemented with cyclosporine and corticosteroids. The crude incidence rate for serious infections in h-ATG group and r-ATG group was comparable. The relative risk of infectious complications was lower in patients treated with granulocyte colony stimulating factors (G-CSF) by 36 % (RR 0.64; p < 0.0001). The analysis confirmed that respiratory tract and disseminated infections comprise a very serious clinical problem and are the leading cause of death of SAA children. Active surveillance and the analysis of associated risk factors are required to detect opportunistic infections in this group of patients.
机译:在本研究中,我们研究了在免疫抑制治疗(IST)的严重获得性血栓性贫血(SAA)的123名儿童队列中系统性和呼吸道感染的发生。我们在77名患者中记录了101个感染剧集(62.6%)。肺炎是最常观察到的临床形式的感染(17例-16.8%)。在整个组中,23名儿童死亡,主要是在致命败血症(15/23)的过程中,因为肺炎并发症3例。所有患者均用HINGS(H-ATG)或兔antithymyte球蛋白(R-ATG)处理,所述马孢菌素和皮质类固醇。 H-ATG组和R-ATG组严重感染的原始发病率可比。用粒细胞菌落刺激因子(G-CSF)处理36%(RR 0.64; P <0.0001),感染性并发症的相对风险较低。分析证实,呼吸道和播散的感染包括一个非常严重的临床问题,是Saa儿童死亡的主要原因。主动监测和相关危险因素的分析需要检测该组患者的机会主义感染。

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