Comparing nose-throat swabs and nasopharyngeal aspirates collected from children with symptoms for respiratory virus identification using real-time polymerase chain reaction

被引:125
作者
Lambert, Stephen B. [1 ,2 ,3 ]
Whiley, David M. [1 ,2 ,3 ]
O'Neill, Nicholas T. [1 ,2 ]
Andrews, Emily C. [1 ,2 ]
Canavan, Fiona M. [1 ,2 ]
Bletchly, Cheryl [5 ]
Siebert, David J. [5 ]
Sloots, Theo P. [1 ,2 ,3 ,4 ,5 ]
Nissen, Michael D. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Royal Childrens Hosp, Queensland Paediat Infect Dis Lab, Sir Albert Sakzewski Virus Res Ctr, Herston, Qld 4029, Australia
[2] Hlth Serv Dist, Herston, Qld, Australia
[3] Univ Queensland, Clin Med Virol Ctr, Brisbane, Qld, Australia
[4] Univ Queensland, Dept Pediat & Child Hlth, Brisbane, Qld, Australia
[5] Royal Brisbane Hosp Campus, Div Microbiol, Clin & Statewide Serv Div, Herston, Qld, Australia
关键词
respiratory viruses; real-time PCR; diagnostic methods; children;
D O I
10.1542/peds.2008-0691
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
OBJECTIVES. The objective of this study was to calculate sensitivity values for the detection of major respiratory viruses of childhood by using combined nose-throat swabs and nasopharyngeal aspirates. METHODS. Children who had symptoms and presented to a pediatric teaching hospital and had a diagnostic respiratory specimen collected were enrolled, and paired nose-throat swab and nasopharyngeal aspirate specimens were collected. Parents were asked to collect the nose-throat swab specimen in the first instance but could defer to a health care worker if unwilling. Nose-throat swab collectors were asked to rate perceived quality of collection. All nasopharyngeal aspirates were collected by a health care worker by using a standard protocol. Real-time polymerase chain reaction for 8 respiratory viruses was performed in our hospital's diagnostic laboratory. RESULTS. Paired nose-throat swab/nasopharyngeal aspirate specimens were collected during 303 illnesses, with at least 1 respiratory virus identified in 186 (61%). For the major pathogens of childhood, influenza A virus and respiratory syncytial virus, collection by using the nose-throat swab had a sensitivity of 91.9% and 93.1%, respectively. A health care worker collected 219 (72%) of the nose-throat swab specimens; concordance with the nasopharyngeal aspirate was not related to health care worker collection or perceived quality of collection. CONCLUSIONS. Nose-throat swab specimens, in combination with sensitive molecular testing, are a less invasive diagnostic respiratory specimen with adequate sensitivity for use in the clinic and hospital outpatient settings and large-scale community studies through parent collection. For children who present to a hospital in which an avian or pandemic strain of influenza virus is reasonably part of the differential diagnosis, nasopharyngeal aspirates or a similar collection technique (eg, nasal washes) should continue to be used.
引用
收藏
页码:E615 / E620
页数:6
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