Induced sputum to detect lung pathogens in young children with cystic fibrosis

被引:34
作者
D'Sylva, Pamela [1 ]
Caudri, Daan [2 ,3 ]
Shaw, Nicole [3 ]
Turkovic, Lidija [3 ]
Douglas, Tonia [3 ,4 ]
Bew, Jane [5 ]
Keil, Anthony D. [5 ]
Stick, Stephen [2 ,3 ,6 ]
Schultz, Andre [2 ,3 ,6 ]
机构
[1] Princess Margaret Hosp Children, Dept Physiotherapy, Subiaco, WA, Australia
[2] Princess Margaret Hosp Children, Dept Resp & Sleep Med, Subiaco, WA, Australia
[3] Univ Western Australia, Telethon Kids Inst, Nedlands, WA, Australia
[4] Lady Cilento Childrens Hosp, Dept Resp & Sleep Med, South Brisbane, Qld, Australia
[5] Princess Margaret Hosp Children, PathWest Lab Med WA, Dept Microbiol, Subiaco, WA, Australia
[6] Univ Western Australia, Sch Paediat & Child Hlth, Nedlands, WA, Australia
关键词
bronchoscopy; cystic fibrosis; children; induced sputum; BRONCHOALVEOLAR LAVAGE; STAPHYLOCOCCUS-AUREUS; PRESCHOOL-CHILDREN; NASAL CARRIAGE; INFLAMMATION; INFECTION; INDUCTION; INFANTS; DIAGNOSIS; AIRWAYS;
D O I
10.1002/ppul.23636
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
IntroductionInduced sputum sampling holds promise as a method for obtaining samples representative of the lower airways in young children. Collection of induced sputum samples in young children differs from older children and adults' as pharyngeal suctioning is often required. Our aim was to determine the sensitivity and specificity of induced sputum with and without airway clearance techniques to detect lower airway pathogens in children less than age 7 with cystic fibrosis. MethodsMicrobiological culture results were compared between 61 paired induced sputum and bronchoalveolar lavage fluid samples from young children with cystic fibrosis. The first cohort received no airway clearance and the second cohort received airway clearance. Induced sputum was sampled within 7 days of bronchoscopy. ResultsMedian age (range) of participants was 3.3 years (0.9-6.7). Sensitivity and specificity (95%CI) of induced sputum was 36.8% (16.3, 61.6), and 69% (52.9, 82.4), respectively (N=61). In subgroup analysis, induced sputum with (N=31) and without airway clearance (N=30) demonstrated sensitivity of 50% (15.7, 84.3) and 27.3% (6.0, 61.0), respectively, and specificity of 60.9% (38.5, 80.3), and 78.9% (54.4, 93.9), respectively. ConclusionInduced sputum is not highly sensitive or specific as routine surveillance for detection of lower airway pathogens in young children with cystic fibrosis. Pediatr Pulmonol. 2017;52:182-189. (c) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:182 / 189
页数:8
相关论文
共 50 条
  • [31] The relationship between lung disease severity and the sputum proteome in cystic fibrosis
    Maher, Rosemary E.
    Barrett, Emma
    Beynon, Robert J.
    Harman, Victoria M.
    Jones, Andrew M.
    McNamara, Paul S.
    Smith, Jaclyn A.
    Lord, Robert W.
    RESPIRATORY MEDICINE, 2022, 204
  • [32] Adaptation and Evolution of Pathogens in the Cystic Fibrosis Lung
    Planet, Paul J.
    JOURNAL OF THE PEDIATRIC INFECTIOUS DISEASES SOCIETY, 2022, 11 : S23 - S31
  • [33] An Innovative Protocol for Metaproteomic Analyses of Microbial Pathogens in Cystic Fibrosis Sputum
    Graf, Alexander C.
    Striesow, Johanna
    Pane-Farre, Jan
    Sura, Thomas
    Wurster, Martina
    Lalk, Michael
    Pieper, Dietmar H.
    Becher, Dorte
    Kahl, Barbara C.
    Riedel, Katharina
    FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2021, 11
  • [34] Fungi in the cystic fibrosis lung: Bystanders or pathogens?
    Chotirmall, Sanjay H.
    McElvaney, Noel G.
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2014, 52 : 161 - 173
  • [35] Early Respiratory Bacterial Detection and Antistaphylococcal Antibiotic Prophylaxis in Young Children with Cystic Fibrosis
    Hurley, Matthew N.
    Fogarty, Andrew
    McKeever, Tricia M.
    Goss, Christopher H.
    Rosenfeld, Margaret
    Smyth, Alan R.
    ANNALS OF THE AMERICAN THORACIC SOCIETY, 2018, 15 (01) : 42 - 48
  • [36] Staphylococcus aureus Small-Colony Variants Are Independently Associated With Worse Lung Disease in Children With Cystic Fibrosis
    Wolter, Daniel J.
    Emerson, Julia C.
    McNamara, Sharon
    Buccat, Anne M.
    Qin, Xuan
    Cochrane, Elizabeth
    Houston, Laura S.
    Rogers, Geraint B.
    Marsh, Peter
    Prehar, Karandeep
    Pope, Christopher E.
    Blackledge, Marcella
    Deziel, Eric
    Bruce, Kenneth D.
    Ramsey, Bonnie W.
    Gibson, Ronald L.
    Burns, Jane L.
    Hoffman, Lucas R.
    CLINICAL INFECTIOUS DISEASES, 2013, 57 (03) : 384 - 391
  • [37] Safety and use of sputum induction in children with cystic fibrosis
    Suri, R
    Marshall, LJ
    Wallis, C
    Metcalfe, C
    Shute, JK
    Bush, A
    PEDIATRIC PULMONOLOGY, 2003, 35 (04) : 309 - 313
  • [38] Regional differences in the evolution of lung disease in children with cystic fibrosis
    Li, Zhanhai
    Sanders, Don B.
    Rock, Michael J.
    Kosorok, Michael R.
    Collins, Jannette
    Green, Christopher G.
    Brody, Alan S.
    Farrell, Philip M.
    PEDIATRIC PULMONOLOGY, 2012, 47 (07) : 635 - 640
  • [39] The evolution of lung disease in children with cystic fibrosis
    Le Bourgeois, M.
    ARCHIVES DE PEDIATRIE, 2009, 16 (06): : 576 - 577
  • [40] Association between early chronic methicillin-susceptible Staphylococcus aureus colonization and lung function in children with cystic fibrosis
    Sunman, Birce
    Yalcin, Ebru
    Ozsezen, Beste
    Tural, Dilber A.
    Buyuksahin, Halime N.
    Guzelkas, Ismail
    Emiralioglu, Nagehan
    Dogru, Deniz
    Ozcelik, Ugur
    Sener, Burcin
    Kiper, Nural
    PEDIATRIC PULMONOLOGY, 2022, 57 (12) : 2963 - 2970