Effect of pulmonary exacerbations on long-term lung function decline in cystic fibrosis

被引:208
作者
Waters, Valerie [1 ]
Stanojevic, Sanja
Atenafu, Eshetu G. [4 ]
Lu, Annie [1 ]
Yau, Yvonne [3 ]
Tullis, Elizabeth [5 ,6 ]
Ratjen, Felix [2 ]
机构
[1] Hosp Sick Children, Div Infect Dis, Toronto, ON M5G 1X8, Canada
[2] Hosp Sick Children, Div Resp Med, Dept Pediat, Toronto, ON M5G 1X8, Canada
[3] Hosp Sick Children, Div Microbiol, Dept Pediat Lab Med, Toronto, ON M5G 1X8, Canada
[4] Univ Hlth Network, Princess Margaret Hosp, Dept Biostat, Toronto, ON, Canada
[5] Univ Toronto, St Michaels Hosp, Div Respirol, Toronto, ON M5B 1W8, Canada
[6] Univ Toronto, St Michaels Hosp, Dept Med, Li Ka Shing Knowledge Inst,Keenan Res Ctr, Toronto, ON M5B 1W8, Canada
关键词
Forced expiratory volume in 1 s; cystic fibrosis; pulmonary exacerbation; STENOTROPHOMONAS-MALTOPHILIA; PSEUDOMONAS-AERUGINOSA; ADULT PATIENTS; FEV1; DECLINE; CHILDREN; MORTALITY; OUTCOMES;
D O I
10.1183/09031936.00159111
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
It is unknown what proportion of long-term lung function decline in cystic fibrosis (CF) is explained by pulmonary exacerbations. The aim of this study was to determine how exacerbations requiring hospitalisation contribute to the course of CF lung disease. This was a retrospective cohort study. The primary outcome was the rate of decline of forced expiratory volume in 1 s (FEV1) % predicted. Out of 851 subjects, 415 (48.8%) subjects had >= 1 exacerbation. After adjustment for confounders, the annual rate of FEV1 decline in those without an exacerbation was 1.2% per yr (95% CI 1.0-1.5), compared with 2.5% per yr (95% CI 2.1-2.8) in those with an exacerbation. The proportion of overall FEV1 decline associated with >= 1 exacerbation was 52% (95% CI 35.0-68.9). For a given number of exacerbations, the annual rate of FEV1 decline was greatest in subjects with <= 6 months between exacerbations. Half of FEV1 decline seen in CF patients was associated with pulmonary exacerbations. Time between exacerbations, specifically <= 6 months between exacerbations, plays an important contribution to overall lung function decline. These findings support using time to next exacerbation as a clinical end-point for CF trials.
引用
收藏
页码:61 / 66
页数:6
相关论文
共 26 条
  • [11] Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis
    Konstan, Michael W.
    Morgan, Wayne J.
    Butler, Steven M.
    Pasta, David J.
    Craib, Marcia L.
    Silva, Stefanie J.
    Stokes, Dennis C.
    Wohl, Mary Ellen B.
    Wagener, Jeffrey S.
    Regelmann, Warren E.
    Johnson, Charles A.
    [J]. JOURNAL OF PEDIATRICS, 2007, 151 (02) : 134 - 139
  • [12] EFFECT OF HIGH-DOSE IBUPROFEN IN PATIENTS WITH CYSTIC-FIBROSIS
    KONSTAN, MW
    BYARD, PJ
    HOPPEL, CL
    DAVIS, PB
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (13) : 848 - 854
  • [13] Kuczmarski RJ., 2002, VITAL HLTH STAT, V11, P1, DOI [DOI 10.1016/J.BBRC.2015.06.114, 10.1590/S1516-35982002000600018]
  • [14] Predictive 5-year survivorship model of cystic fibrosis
    Liou, TG
    Adler, FR
    FitzSimmons, SC
    Cahill, BC
    Hibbs, JR
    Marshall, BC
    [J]. AMERICAN JOURNAL OF EPIDEMIOLOGY, 2001, 153 (04) : 345 - 352
  • [15] Pulmonary exacerbations in cystic fibrosis - It's time to be explicit!
    Marshall, BC
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 169 (07) : 781 - 782
  • [16] Inflammatory and microbiologic markers in induced sputum after intravenous antibiotics in cystic fibrosis
    Ordoñez, CL
    Henig, NR
    Mayer-Hamblett, N
    Accurso, FJ
    Burns, JL
    Chmiel, JF
    Daines, CL
    Gibson, RL
    McNamara, S
    Retsch-Bogart, GZ
    Zeitlin, PL
    Aitken, ML
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 168 (12) : 1471 - 1475
  • [17] Improving rate of decline of FEV1 in young adults with cystic fibrosis
    Que, C
    Cullinan, P
    Geddes, D
    [J]. THORAX, 2006, 61 (02) : 155 - 157
  • [18] Intermittent administration of inhaled tobramycin in patients with cystic fibrosis
    Ramsey, BW
    Pepe, MS
    Quan, JM
    Otto, KL
    Montgomery, AB
    Williams-Warren, J
    Vasiljev-K, M
    Borowitz, D
    Bowman, CM
    Marshall, BC
    Marshall, S
    Smith, AL
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (01) : 23 - 30
  • [19] Defining a pulmonary exacerbation in cystic fibrosis
    Rosenfeld, M
    Emerson, J
    Williams-Warren, J
    Pepe, M
    Smith, A
    Montgomery, AB
    Ramsey, B
    [J]. JOURNAL OF PEDIATRICS, 2001, 139 (03) : 359 - 365
  • [20] Azithromycin in, patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa -: A randomized controlled trial
    Saiman, L
    Marshall, BC
    Mayer-Hamblett, N
    Burns, JL
    Quittner, AL
    Cibene, DA
    Coquillette, S
    Fieberg, AY
    Accurso, FJ
    Campbel, PW
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2003, 290 (13): : 1749 - 1756