Bronzan Rachel N, Taylor Terrie E, Mwenechanya James, Tembo Madalitso, Kayira Kondwani, Bwanaisa Lloyd, Njobvu Alfred, Kondowe Wendy, Chalira Chipo, Walsh Amanda L, Phiri Amos, Wilson Lorna K, Molyneux Malcolm E, Graham Stephen M
Blantyre Malaria Project, Blantyre, Malawi.
J Infect Dis. 2007 Mar 15;195(6):895-904. doi: 10.1086/511437. Epub 2007 Feb 2.
Previous prospective studies of bacteremia in African children with severe malaria have mainly included children with cerebral malaria, and no study has examined the impact of human immunodeficiency virus (HIV) infection. We examined the prevalence and etiology of bacteremia and the impact of HIV infection on bacteremia in Malawian children with severe malaria, as well as the impact of bacteremia and HIV infection on outcome.
From 1996 until 2005, blood for culture was obtained on admission from all children admitted with severe malaria during the rainy season to the Paediatric Research Ward at the Queen Elizabeth Central Hospital in Blantyre, Malawi. HIV testing was performed prospectively from 2001 to 2005 and retrospectively for those admitted from 1996 to 2000. Multivariate regression analysis examined independent risk factors for bacteremia and death.
Sixty-four (4.6%) of 1388 children with severe malaria had bacteremia; nontyphoidal Salmonellae (NTS) accounted for 58% of all bacteremias. The prevalence of any bacteremia and of NTS bacteremia was highest in children with severe malarial anemia (11.7% and 7.6%), compared with the prevalence in children with cerebral malaria and severe anemia (4.7% and 3.8%) and in those with cerebral malaria alone (3.0% and 0.9%). HIV infection status was determined in 1119 patients. HIV prevalence was 16% (and was highest in those with severe malaria anemia, at 20.4%), but HIV infection was not significantly associated with bacteremia. Neither bacteremia nor HIV infection was associated with death.
Antibiotics are not routinely indicated for children with severe malaria in this region, in which HIV is endemic. However, antibiotic therapy should be used to treat NTS infection if bacteremia is suspected in children with severe malarial anemia.
以往针对患有严重疟疾的非洲儿童菌血症的前瞻性研究主要纳入了患有脑型疟疾的儿童,尚无研究探讨人类免疫缺陷病毒(HIV)感染的影响。我们研究了马拉维患有严重疟疾的儿童菌血症的患病率和病因、HIV感染对菌血症的影响,以及菌血症和HIV感染对预后的影响。
1996年至2005年期间,在雨季,从马拉维布兰太尔伊丽莎白女王中央医院儿科研究病房收治的所有患有严重疟疾的儿童入院时采集血样进行培养。2001年至2005年进行前瞻性HIV检测,对1996年至2000年入院的患者进行回顾性检测。多变量回归分析研究菌血症和死亡的独立危险因素。
1388例患有严重疟疾的儿童中有64例(4.6%)发生菌血症;非伤寒沙门氏菌(NTS)占所有菌血症的58%。与患有脑型疟疾和严重贫血的儿童(4.7%和3.8%)以及仅患有脑型疟疾的儿童(3.0%和0.9%)相比,患有严重疟疾贫血的儿童中任何菌血症和NTS菌血症的患病率最高(分别为11.7%和7.6%)。对1119例患者进行了HIV感染状况检测。HIV患病率为16%(在患有严重疟疾贫血的患者中最高,为20.4%),但HIV感染与菌血症无显著关联。菌血症和HIV感染均与死亡无关。
在这个HIV流行的地区,对于患有严重疟疾的儿童,抗生素并非常规必需。然而,如果怀疑患有严重疟疾贫血的儿童发生菌血症,应用抗生素治疗NTS感染。