Detection of Pneumococcal DNA in Blood by Polymerase Chain Reaction for Diagnosing Pneumococcal Pneumonia in Young Children From Low- and Middle-Income Countries.

Susan C Morpeth ; Maria Deloria Knoll ; J Anthony G Scott ORCID logo ; Daniel E Park ; Nora L Watson ; Henry C Baggett ; W Abdullah Brooks ; Daniel R Feikin ; Laura L Hammitt ; Stephen RC Howie ; +29 more... Karen L Kotloff ; Orin S Levine ; Shabir A Madhi ; Katherine L O'Brien ; Donald M Thea ; Peter V Adrian ; Dilruba Ahmed ; Martin Antonio ORCID logo ; Charatdao Bunthi ; Andrea N DeLuca ; Amanda J Driscoll ; Louis Peter Githua ; Melissa M Higdon ; Geoff Kahn ; Angela Karani ; Ruth A Karron ; Geoffrey Kwenda ; Sirirat Makprasert ; Razib Mazumder ; David P Moore ; James Mwansa ; Sammy Nyongesa ; Christine Prosperi ; Samba O Sow ; Boubou Tamboura ; Toni Whistler ; Scott L Zeger ; David R Murdoch ; PERCH Study Group ; (2017) Detection of Pneumococcal DNA in Blood by Polymerase Chain Reaction for Diagnosing Pneumococcal Pneumonia in Young Children From Low- and Middle-Income Countries. Clinical infectious diseases, 64 (suppl_). S347-S356. ISSN 1058-4838 DOI: 10.1093/cid/cix145
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BACKGROUND.: We investigated the performance of polymerase chain reaction (PCR) on blood in the diagnosis of pneumococcal pneumonia among children from 7 low- and middle-income countries. METHODS.: We tested blood by PCR for the pneumococcal autolysin gene in children aged 1-59 months in the Pneumonia Etiology Research for Child Health (PERCH) study. Children had World Health Organization-defined severe or very severe pneumonia or were age-frequency-matched community controls. Additionally, we tested blood from general pediatric admissions in Kilifi, Kenya, a PERCH site. The proportion PCR-positive was compared among cases with microbiologically confirmed pneumococcal pneumonia (MCPP), cases without a confirmed bacterial infection (nonconfirmed), cases confirmed for nonpneumococcal bacteria, and controls. RESULTS.: In PERCH, 7.3% (n = 291/3995) of cases and 5.5% (n = 273/4987) of controls were blood pneumococcal PCR-positive (P < .001), compared with 64.3% (n = 36/56) of MCPP cases and 6.3% (n = 243/3832) of nonconfirmed cases (P < .001). Blood pneumococcal PCR positivity was higher in children from the 5 African countries (5.5%-11.5% among cases and 5.3%-10.2% among controls) than from the 2 Asian countries (1.3% and 1.0% among cases and 0.8% and 0.8% among controls). Among Kilifi general pediatric admissions, 3.9% (n = 274/6968) were PCR-positive, including 61.7% (n = 37/60) of those with positive blood cultures for pneumococcus. DISCUSSION.: The utility of pneumococcal PCR on blood for diagnosing childhood pneumococcal pneumonia in the 7 low- and middle-income countries studied is limited by poor specificity and by poor sensitivity among MCPP cases.


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