Clinical outcomes associated with Staphylococcus aureus and Pseudomonas aeruginosa airway infections in adult cystic fibrosis patients

被引:62
作者
Ahlgren, Heather G. [1 ]
Benedetti, Andrea [1 ,3 ,4 ]
Landry, Jennifer S. [1 ,4 ]
Bernier, Joanie [5 ]
Matouk, Elias [1 ,5 ]
Radzioch, Danuta [1 ,2 ,6 ]
Lands, Larry C. [7 ]
Rousseau, Simon [1 ,2 ]
Nguyen, Dao [1 ,2 ]
机构
[1] McGill Univ, Dept Med, Montreal, PQ, Canada
[2] McGill Univ, Dept Med, Res Inst, Ctr Hlth, Montreal, PQ, Canada
[3] McGill Univ, Dept Epidemiol Biostat & Occupat Hlth, Montreal, PQ, Canada
[4] McGill Univ, Ctr Hlth, Resp Epidemiol & Clin Res Unit, Montreal, PQ, Canada
[5] McGill Univ, Ctr Hlth, Adult CF clin, Montreal, PQ, Canada
[6] McGill Univ, Dept Human Genet, Montreal, PQ, Canada
[7] McGill Univ, Ctr Hlth, Res Inst, Dept Pediat, Montreal, PQ, Canada
来源
BMC PULMONARY MEDICINE | 2015年 / 15卷
关键词
Cystic fibrosis; Microbiology; Staphylococcus aureus; Pseudomonas aeruginosa; Lung function; Pulmonary exacerbation; Retrospective cohort; SMALL-COLONY VARIANTS; PULMONARY-FUNCTION; LUNG-DISEASE; YOUNG-CHILDREN; OROPHARYNGEAL CULTURES; SCORING SYSTEM; FEV1; DECLINE; INFANTS; INFLAMMATION; SURVIVAL;
D O I
10.1186/s12890-015-0062-7
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Staphylococcus aureus (SA) is the most prevalent organism infecting the respiratory tract of CF children, and remains the second most prevalent organism in CF adults. During early childhood, SA infections are associated with pulmonary inflammation and decline in FEV1, but their clinical significance in adult CF patients is poorly characterized. Methods: We conducted a retrospective cross-sectional study to determine the association between airway microbiology and clinical outcomes (FEV1, rate of pulmonary exacerbations, CRP levels and clinical scores). Results: In a cohort of 84 adult CF patients, 24 % were infected with SA only, 60 % were infected with PA, and 16 % had neither PA nor SA. CF patients with SA experienced fewer pulmonary exacerbations and lower CRP levels than those with PA. Conclusion: In adult CF patients, SA infections alone, in the absence of PA, are a marker of milder disease.
引用
收藏
页数:6
相关论文
共 44 条
  • [11] Association Between Respiratory Tract Methicillin-Resistant Staphylococcus aureus and Survival in Cystic Fibrosis
    Dasenbrook, Elliott C.
    Checkley, William
    Merlo, Christian A.
    Konstan, Michael W.
    Lechtzin, Noah
    Boyle, Michael P.
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2010, 303 (23): : 2386 - 2392
  • [12] Inflammatory Responses to Individual Microorganisms in the Lungs of Children With Cystic Fibrosis
    Gangell, Catherine
    Gard, Samantha
    Douglas, Tonia
    Park, Judy
    de Klerk, Nicholas
    Keil, Tony
    Brennan, Siobhain
    Ranganathan, Sarath
    Robins-Browne, Roy
    Sly, Peter D.
    [J]. CLINICAL INFECTIOUS DISEASES, 2011, 53 (05) : 425 - 432
  • [13] Pathophysiology and management of pulmonary infections in cystic fibrosis
    Gibson, RL
    Burns, JL
    Ramsey, BW
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 168 (08) : 918 - 951
  • [14] Complex molecular epidemiology of methicillin-resistant Staphylococcus aureus isolates from children with cystic fibrosis in the era of epidemic community-associated methicillin-resistant S aureus
    Glikman, Daniel
    Siegel, Jane D.
    David, Michael Z.
    Okoro, Ngozi M.
    Boyle-Vavra, Susan
    Dowell, Maria L.
    Daum, Robert S.
    [J]. CHEST, 2008, 133 (06) : 1381 - 1387
  • [15] Review: Staphylococcus aureus and MRSA in cystic fibrosis
    Goss, Christopher H.
    Muhlebach, Marianne S.
    [J]. JOURNAL OF CYSTIC FIBROSIS, 2011, 10 (05) : 298 - 306
  • [16] Selection for Staphylococcus aureus small-colony variants due to growth in the presence of Pseudomonas aeruginosa
    Hoffman, Lucas R.
    Deziel, Eric
    D'Argenio, David A.
    Lepine, Francois
    Emerson, Julia
    McNamara, Sharon
    Gibson, Ronald L.
    Ramsey, Bonnie W.
    Miller, Samuel I.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (52) : 19890 - 19895
  • [17] PROGNOSTIC IMPLICATIONS OF INITIAL OROPHARYNGEAL BACTERIAL-FLORA IN PATIENTS WITH CYSTIC-FIBROSIS DIAGNOSED BEFORE THE AGE OF 2 YEARS
    HUDSON, VL
    WIELINSKI, CL
    REGELMANN, WE
    [J]. JOURNAL OF PEDIATRICS, 1993, 122 (06) : 854 - 860
  • [18] PULMONARY-FUNCTION AND CLINICAL COURSE IN PATIENTS WITH CYSTIC-FIBROSIS AFTER PULMONARY COLONIZATION WITH PSEUDOMONAS-AERUGINOSA
    KEREM, E
    COREY, M
    GOLD, R
    LEVISON, H
    [J]. JOURNAL OF PEDIATRICS, 1990, 116 (05) : 714 - 719
  • [19] Factors associated with FEV1 decline in cystic fibrosis: analysis of the ECFS Patient Registry
    Kerem, Eitan
    Viviani, Laura
    Zolin, Anna
    MacNeill, Stephanie
    Hatziagorou, Elpis
    Ellemunter, Helmut
    Drevinek, Pavel
    Gulmans, Vincent
    Krivec, Uros
    Olesen, Hanne
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2014, 43 (01) : 125 - 133
  • [20] Longitudinal development of mucoid Pseudomonas aeruginosa infection and lung disease progression in children with cystic fibrosis
    Li, ZH
    Kosorok, MR
    Farrell, PM
    Laxova, A
    West, SEH
    Green, CG
    Collins, J
    Rock, MJ
    Splaingard, ML
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2005, 293 (05): : 581 - 588