Huang Lyen C, Myer Landon, Jaspan Heather B
Desmond Tutu HIV Centre, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Anzio Road, Observatory 7925, Cape Town, South Africa.
BMC Infect Dis. 2008 Sep 24;8:127. doi: 10.1186/1471-2334-8-127.
Mortality among HIV-infected children in developing countries remains high after serious bacterial infections despite the use of antibiotics. Intravenous immunoglobulin (IVIG) has been used as an adjuvant therapy to treat these infections, but little data exists regarding its efficacy, and previous studies have focused on IVIG as a prophylactic agent. We examined the impact of IVIG as an adjuvant therapy in reducing mortality and length of hospital stay in HIV-infected children with serious bacterial infections.
This retrospective study focused on pediatric admissions at a large urban hospital between 2002 and 2006. Children between the ages of one month and nine years of age with laboratory confirmed HIV-status, serious bacterial infection, no prior exposure to IVIG, and a hospital length of stay of 5 days or more, were eligible for inclusion.
A total of 140 children (median age 1.2 years) met inclusion criteria; lower respiratory tract infection was diagnosed in 94 (67%) of the children, while 74 (53%) had bacterial sepsis. Fifty-four (39%) children were receiving antiretroviral therapy and 39 (28%) were receiving tuberculosis treatment. Overall 73 (52%) were treated with IVIG, with the majority (74%) of children receiving a single dose. Thirteen (9%) died during their hospital admission. In crude analysis IVIG was significantly associated with increased mortality was (Odds Ratio (OR): 5.8; 95% Confidence Interval (CI): 1.2-27.1) and this association was weakened by adjustment for other predictors of mortality (OR 4.3, 95% CI 0.7-27.9, p = 0.123). IVIG use was also associated with longer hospital stays.
Administration of one to three doses of IVIG during the acute phase of illness does not appear to reduce mortality or the length of hospital stays in HIV-infected children with serious bacterial infections. However, the retrospective nature of this study makes confounding by indication difficult to control and further studies regarding the timing, dosing, and method of administration are required. Nonetheless the routine use of IVIG in resource-limited settings should be carefully considered given its high cost.
在发展中国家,尽管使用了抗生素,但感染严重细菌的艾滋病毒感染儿童死亡率仍然很高。静脉注射免疫球蛋白(IVIG)已被用作治疗这些感染的辅助疗法,但关于其疗效的数据很少,而且以往的研究主要集中在将IVIG作为预防剂。我们研究了IVIG作为辅助疗法对降低感染严重细菌的艾滋病毒感染儿童死亡率和住院时间的影响。
这项回顾性研究聚焦于2002年至2006年期间一家大型城市医院的儿科住院病例。年龄在1个月至9岁之间、实验室确诊感染艾滋病毒、患有严重细菌感染、此前未接触过IVIG且住院时间为5天或更长时间的儿童符合纳入标准。
共有140名儿童(中位年龄1.2岁)符合纳入标准;94名(67%)儿童被诊断为下呼吸道感染,74名(53%)患有细菌性败血症。54名(39%)儿童正在接受抗逆转录病毒治疗,39名(28%)正在接受结核病治疗。总体而言,73名(52%)儿童接受了IVIG治疗,大多数(74%)儿童接受了单剂量治疗。13名(9%)儿童在住院期间死亡。在粗分析中,IVIG与死亡率增加显著相关(比值比(OR):5.8;95%置信区间(CI):1.2 - 27.1),通过对其他死亡率预测因素进行调整后,这种关联有所减弱(OR 4.3,95% CI 0.7 - 27.9,p = 0.123)。使用IVIG还与更长的住院时间相关。
在疾病急性期给予1至3剂IVIG似乎并不能降低感染严重细菌的艾滋病毒感染儿童的死亡率或住院时间。然而,本研究的回顾性性质使得因适应症导致的混杂难以控制,需要进一步研究给药时间、剂量和给药方法。尽管如此,鉴于其成本高昂,在资源有限的环境中应谨慎考虑IVIG的常规使用。