Chest Radiograph Findings in Childhood Pneumonia Cases From the Multisite PERCH Study

被引:56
|
作者
Fancourt, Nicholas [1 ,2 ,3 ]
Knoll, Maria Deloria [1 ]
Baggett, Henry C. [4 ,5 ]
Brooks, W. Abdullah [6 ,7 ,8 ]
Feikin, Daniel R. [1 ,9 ]
Hammitt, Laura L. [1 ,10 ]
Howie, Stephen R. C. [11 ,12 ,13 ]
Kotloff, Karen L. [14 ]
Levine, Orin S. [1 ,15 ]
Madhi, Shabir A. [17 ]
Murdoch, David R. [18 ,19 ]
Scott, J. Anthony G. [10 ,20 ]
Thea, Donald M. [21 ]
Awori, Juliet O. [10 ]
Barger-Kamate, Breanna [22 ,23 ]
Chipeta, James [24 ,25 ]
DeLuca, Andrea N. [1 ,26 ]
Diallo, Mahamadou [27 ]
Driscoll, Amanda J. [1 ]
Ebruke, Bernard E. [11 ]
Higdon, Melissa M. [1 ]
Jahan, Yasmin [7 ,8 ]
Karron, Ruth A. [28 ]
Mahomed, Nasreen [16 ,29 ]
Moore, David P. [16 ,17 ,30 ,31 ]
Nahar, Kamrun [7 ,8 ]
Naorat, Sathapana [4 ]
Ominde, Micah Silaba [10 ]
Park, Daniel E. [1 ,32 ]
Prosperi, Christine [1 ]
Somwe, Wa Somwe [24 ]
Thamthitiwat, Somsak [4 ]
Zaman, Syed M. A. [11 ,33 ]
Zeger, Scott L. [34 ]
O'Brien, Katherine L. [1 ]
机构
[1] Johns Hopkins Bloomberg Sch Publ Hlth, Int Vaccine Access Ctr, Dept Int Hlth, Baltimore, MD USA
[2] Murdoch Childrens Res Inst, 50 Flemington Rd, Melbourne, Vic 3052, Australia
[3] Royal Childrens Hosp, Melbourne, Vic, Australia
[4] Thailand Minist Publ Health US Centers Dis Contro, Global Dis Detect Ctr, Nonthaburi, Thailand
[5] Ctr Dis Control & Prevent, Div Global Hlth Protect, Ctr Global Hlth, Atlanta, GA USA
[6] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Int Hlth, Baltimore, MD USA
[7] Int Ctr Diarrhoeal Dis Res, Dhaka, Bangladesh
[8] Int Ctr Diarrhoeal Dis Res, Matlab, Bangladesh
[9] Ctr Dis Control & Prevent, Div Viral Dis, Natl Ctr Immunizat & Resp Dis, Atlanta, GA USA
[10] Kenya Med Res Inst Wellcome Trust Res Programme, Kilifi, Kenya
[11] MRC Unit, Basse, Gambia
[12] Univ Auckland, Dept Paediat, Auckland, New Zealand
[13] Univ Otago, Ctr Int Hlth, Dunedin, New Zealand
[14] Univ Maryland, Sch Med, Inst Global Hlth, Ctr Vaccine Dev,Dept Pediat,Div Infect Dis & Trop, Baltimore, MD 21201 USA
[15] Bill & Melinda Gates Fdn, Seattle, WA USA
[16] Univ Witwatersrand, Resp & Meningeal Pathogens Res Unit, MRC, Johannesburg, South Africa
[17] Univ Witwatersrand, Vaccine Preventable Dis Unit, Dept Sci & Technol, Natl Res Fdn, Johannesburg, South Africa
[18] Univ Otago, Dept Pathol, Christchurch, New Zealand
[19] Canterbury Hlth Labs, Microbiol Unit, Christchurch, New Zealand
[20] London Sch Hyg & Trop Med, Dept Infect Dis Epidemiol, London, England
[21] Boston Univ, Sch Publ Hlth, Ctr Global Hlth & Dev, Boston, MA 02215 USA
[22] Johns Hopkins Sch Med, Div Emergency Med, Dept Paediat, Baltimore, MD USA
[23] Spokane Emergency Phys, Washington, DC USA
[24] Univ Zambia, Sch Med, Dept Paediat & Child Hlth, Lusaka, Zambia
[25] Univ Teaching Hosp, Lusaka, Zambia
[26] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
[27] Ctr Dev Vaccins CVD Mali, Bamako, Mali
[28] Johns Hopkins Bloomberg Sch Publ Hlth, Ctr Immunizat Res, Dept Int Hlth, Baltimore, MD USA
[29] Univ Witwatersrand, Dept Diagnost Radiol, Johannesburg, South Africa
[30] Chris Hani Baragwanath Acad Hosp, Dept Paediat & Child Hlth, Johannesburg, South Africa
[31] Univ Witwatersrand, Johannesburg, South Africa
[32] George Washington Univ, Dept Epidemiol & Biostat, Milken Inst Sch Publ Hlth, Washington, DC 20052 USA
[33] London Sch Hyg & Trop Med, London, England
[34] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Biostat, Baltimore, MD USA
基金
英国惠康基金;
关键词
chest radiograph; pneumonia; pediatrics; signs and symptoms; mortality; ETIOLOGY RESEARCH; STANDARDIZED INTERPRETATION; PEDIATRIC PNEUMONIA; CONFIRMED PNEUMONIA; CLINICAL-FEATURES; CONJUGATE VACCINE; CHILDREN; DIAGNOSIS; CRITERIA; DEFINITION;
D O I
10.1093/cid/cix089
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Chest radiographs (CXRs) are frequently used to assess pneumonia cases. Variations in CXR appearances between epidemiological settings and their correlation with clinical signs are not well documented. Methods. The Pneumonia Etiology Research for Child Health project enrolled 4232 cases of hospitalized World Health Organization (WHO)-defined severe and very severe pneumonia from 9 sites in 7 countries (Bangladesh, the Gambia, Kenya, Mali, South Africa, Thailand, and Zambia). At admission, each case underwent a standardized assessment of clinical signs and pneumonia risk factors by trained health personnel, and a CXR was taken that was interpreted using the standardized WHO methodology. CXRs were categorized as abnormal (consolidation and/or other infiltrate), normal, or uninterpretable. Results. CXRs were interpretable in 3587 (85%) cases, of which 1935 (54%) were abnormal (site range, 35%-64%). Cases with abnormal CXRs were more likely than those with normal CXRs to have hypoxemia (45% vs 26%), crackles (69% vs 62%), tachypnea (85% vs 80%), or fever (20% vs 16%) and less likely to have wheeze (30% vs 38%; all P < .05). CXR consolidation was associated with a higher case fatality ratio at 30-day follow-up (13.5%) compared to other infiltrate (4.7%) or normal (4.9%) CXRs. Conclusions. Clinically diagnosed pneumonia cases with abnormal CXRs were more likely to have signs typically associated with pneumonia. However, CXR-normal cases were common, and clinical signs considered indicative of pneumonia were present in substantial proportions of these cases. CXR-consolidation cases represent a group with an increased likelihood of death at 30 days post-discharge.
引用
收藏
页码:S262 / S270
页数:9
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