@article{542c19c47e714a9784f1d75eaa97c6e4,
title = "Chest radiograph findings in childhood pneumonia cases from the multisite PERCH study",
abstract = "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.",
keywords = "Chest radiograph, Mortality, Pediatrics, Pneumonia, Signs and symptoms",
author = "{PERCH Study Group} and Nicholas Fancourt and Knoll, {Maria Deloria} and Baggett, {Henry C.} and Brooks, {W. Abdullah} and Feikin, {Daniel R.} and Hammitt, {Laura L.} and Howie, {Stephen R.C.} and Kotloff, {Karen L.} and Levine, {Orin S.} and Madhi, {Shabir A.} and Murdoch, {David R.} and Scott, {J. Anthony G.} and Thea, {Donald M.} and Awori, {Juliet O.} and Breanna Barger-Kamate and James Chipeta and DeLuca, {Andrea N.} and Mahamadou Diallo and Driscoll, {Amanda J.} and Ebruke, {Bernard E.} and Higdon, {Melissa M.} and Yasmin Jahan and Karron, {Ruth A.} and Nasreen Mahomed and Moore, {David P.} and Kamrun Nahar and Sathapana Naorat and Ominde, {Micah Silaba} and Park, {Daniel E.} and Christine Prosperi and Somwe, {Somwe Wa} and Somsak Thamthitiwat and Zaman, {Syed M.A.} and Zeger, {Scott L.} and O'Brien, {Katherine L.} and Wei Fu and Kagucia, {E. Wangeci} and Mengying Li and Zhenke Wu and Watson, {Nora L.} and Jane Crawley and Endtz, {Hubert P.} and Khalequ Zaman and Doli Goswami and Lokman Hossain and Hasan Ashraf and Martin Antonio and Jessica McLellan and Eunice Machuka and Arifin Shamsul",
note = "Funding Information: Supplement sponsorship. This article appears as part of the supplement “Pneumonia Etiology Research for Child Health (PERCH): Foundational Basis for the Primary Etiology Results,” sponsored by a grant from the Bill & Melinda Gates Foundation to the PERCH study of Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland. Funding Information: Financial support. PERCH was supported by a grant from the Bill & Melinda Gates Foundation to the International Vaccine Access Center, Department of International Health, Johns Hopkins Bloomberg School of Public Health (grant 48968). J. A. G. S. was supported by a clinical fellowship from the Wellcome Trust of Great Britain (098532). N. F. was supported by an International Fulbright Science and Technology Fellowship from the US Department of State. Publisher Copyright: {\textcopyright} The Author 2017.",
year = "2017",
doi = "10.1093/cid/cix089",
language = "English (US)",
volume = "64",
pages = "S262--S270",
journal = "Clinical Infectious Diseases",
issn = "1058-4838",
publisher = "Oxford University Press",
}