Analysis of sequential aliquots of hypertonic saline solution-induced sputum from clinically stable patients with cystic fibrosis

被引:26
作者
Aitken, ML
Greene, KE
Tonelli, MR
Burns, JL
Emerson, JC
Goss, CH
Gibson, RL
机构
[1] Univ Washington, Dept Med, Div Pulm & Crit Care, Seattle, WA USA
[2] Childrens Hosp & Reg Med Ctr, Dept Pediat, Seattle, WA USA
[3] Univ Colorado, Denver, CO 80202 USA
关键词
cystic fibrosis; hypertonic saline; sputum;
D O I
10.1378/chest.123.3.792
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Study objectives: Sputum induction (SI) is a noninvasive tool for sampling inflamed airways. The purpose of this study was to determine the optimal duration of collection in patients with cystic fibrosis (CF). The hypothesis was that the duration of SI collection would quantitatively and qualitatively alter the content of the induced sputum. Methods: In 10 clinically stable patients with CF (mean+/-SD age, 28+/-7 years; mean FEV1, 2.6+/-0.7 L), SI was performed with 3% hypertonic saline solution at five time points over 20 min. Results: SI was well tolerated, with an average maximum fall in FEV1 of 7+/-7%. The sample volumes, urea concentrations, interleukin-8 concentrations, total cell counts, and nonsquamous cell counts remained constant (p>0.05). The percentage of neutrophils decreased from 89+/-5% to 86+/-4% (p=0.03), and the percentage of alveolar macrophages increased 5+/-2% to 8+/-4% (p<0.01). The mean quantitative microbiological counts of nonmucoid Pseudomonas aeruginosa and Staphylococcus aureus decreased over the 20-min time period each by half a log (p=0.05 and p<0.01, respectively). Surfactant protein-A concentration increased from 1.6+/-0.3 to 2.4+/-0.4 ng/mL (log(10); p<0.001). Conclusions: We conclude that aliquots of induced sputum are similar in clinically stable patients with CF during 4-min intervals, although there is more alveolar sampling after 20 min. When induced-sputum samples are fractionated for research monitoring of inflammatory or microbiologic indexes, power calculations accounting for these variations over time are required.
引用
收藏
页码:792 / 799
页数:8
相关论文
共 44 条
  • [1] A phase I study of aerosolized administration of tgAAVCF to cystic fibrosis subjects with mild lung disease
    Aitken, ML
    Moss, RB
    Waltz, DA
    Dovey, ME
    Tonelli, MR
    McNamara, SC
    Gibson, RL
    Ramsey, BW
    Carter, BJ
    Reynolds, TC
    [J]. HUMAN GENE THERAPY, 2001, 12 (15) : 1907 - 1916
  • [3] Armstrong DS, 1996, PEDIATR PULM, V21, P267, DOI 10.1002/(SICI)1099-0496(199605)21:5<267::AID-PPUL1>3.0.CO
  • [4] 2-K
  • [5] THE RELATIONSHIP BETWEEN INFECTION AND INFLAMMATION IN THE EARLY STAGES OF LUNG-DISEASE FROM CYSTIC-FIBROSIS
    BALOUGH, K
    MCCUBBIN, M
    WEINBERGER, M
    SMITS, W
    AHRENS, R
    FICK, R
    [J]. PEDIATRIC PULMONOLOGY, 1995, 20 (02) : 63 - 70
  • [6] Use of bronchoalveolar lavage semiquantitative cultures in cystic fibrosis
    Baughman, RP
    Keeton, DA
    Perez, C
    Wilmott, RW
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1997, 156 (01) : 286 - 291
  • [7] Comparison of spontaneous and induced sputum for investigation of airway inflammation in chronic obstructive pulmonary disease
    Bhowmik, A
    Seemungal, TAR
    Sapsford, RJ
    Devalia, JL
    Wedzicha, JA
    [J]. THORAX, 1998, 53 (11) : 953 - 956
  • [8] Longitudinal assessment of Pseudomonas aeruginosa in young children with cystic fibrosis
    Burns, JL
    Gibson, RL
    McNamara, S
    Yim, D
    Emerson, J
    Rosenfeld, M
    Hiatt, P
    McCcoy, K
    Castile, R
    Smith, AL
    Ramsey, BW
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2001, 183 (03) : 444 - 452
  • [9] Microbiology of sputum from patients at cystic fibrosis centers in the United States
    Burns, JL
    Emerson, J
    Stapp, JR
    Yim, DL
    Krzewinski, J
    Louden, L
    Ramsey, BW
    Clausen, CR
    [J]. CLINICAL INFECTIOUS DISEASES, 1998, 27 (01) : 158 - 163
  • [10] Sputum induction in young cystic fibrosis patients
    De Boeck, K
    Alifier, M
    Vandeputte, S
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2000, 16 (01) : 91 - 94