Neonatal severe bacterial infection impairment estimates in South Asia, sub-Saharan Africa, and Latin America for 2010

被引:111
作者
Seale, Anna C. [1 ,2 ]
Blencowe, Hannah [3 ]
Zaidi, Anita [4 ]
Ganatra, Hammad [4 ]
Syed, Sana [4 ]
Engnnann, Cyril [5 ]
Newton, Charles R. [2 ,6 ]
Vergnano, Stefania [7 ]
Stoll, Barbara J. [8 ]
Cousens, Simon N. [3 ]
Lawn, Joy E. [9 ,10 ]
机构
[1] Univ Oxford, Nuffield Dept Med, Ctr Trop Med, Oxford, England
[2] KEMRI Wellcome Trust Ctr Geog Med & Res Coast, Kilifi, Kenya
[3] London Sch Hyg & Trop Med, Fac Epidemiol & Populat Hlth, London WC1, England
[4] Aga Khan Univ, Dept Paediat & Child Hlth, Karachi, Pakistan
[5] Bill & Melinda Gates Fdn, Seattle, WA USA
[6] Univ Oxford, Dept Psychiat, Oxford, England
[7] St George Hosp, London, England
[8] Emory Univ, Sch Med, Emory & Childrens Healthcare Atlanta, Atlanta, GA USA
[9] Saving Newborn Lives Save Children, Washington, DC USA
[10] London Sch Hyg & Trop Med, Ctr Maternal Reprod & Child Hlth, London WC1, England
关键词
CLINICO-EPIDEMIOLOGIC PROFILE; INFANTS LESS-THAN-60 DAYS; SEVERE ILLNESS; SYSTEMATIC ANALYSIS; RANDOMIZED-TRIAL; SEPSIS; MORTALITY; DISTRICT; CHILDREN; BURDEN;
D O I
10.1038/pr.2013.207
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BACKGROUND: Survivors of neonatal infections are at risk of neurodevelopmental impairment (NDI), a burden not previously systematically quantified and yet important for program priority setting. Systematic reviews and meta-analyses were undertaken and applied in a three-step compartmental model to estimate NDI cases after severe neonatal bacterial infection in South Asia, sub-Saharan Africa, and Latin America in neonates of >32 wk gestation (or >1,500 g). METHODS: We estimated cases of sepsis, meningitis, pneumonia, or no severe bacterial infection from among estimated cases of possible severe bacterial infection ((pSBI) step 1). We applied respective case fatality risks ((CFRs) step 2) and the NDI risk among survivors (step 3). For neonatal tetanus, incidence estimates were based on the estimated deaths, CFRs, and risk of subsequent NDI. RESULTS: For 2010, we estimated 1.7 million (uncertainty range: 1.1-2.4 million) cases of neonatal sepsis, 200,000 (21,000-350,000) cases of meningitis, 510,000 cases (150,000 930,000) of pneumonia, and 79,000 cases (70,000-930,000) of tetanus in neonates >32 wk gestation (or >1,500 g). Among the survivors, we estimated moderate to severe NDI after neonatal meningitis in 23% (95% confidence interval: 19-26%) of survivors, 18,000 (2,700-35,000) cases, and after neonatal tetanus in 16% (6-27%), 4,700 cases (1,700-8,900). CONCLUSION: Data are lacking for impairment after neonatal sepsis and pneumonia, especially among those of >32 wk gestation. Improved recognition and treatment of pSBI will reduce neonatal mortality. Lack of follow-up data for survivors of severe bacterial infections, particularly sepsis, was striking. Given the high incidence of sepsis, even minor NDI would be of major public health importance. Prevention of neonatal infection, improved case management, and support for children with NDI are all important strategies, currently receiving limited policy attention.
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收藏
页码:73 / 85
页数:13
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