Tuberc Respir Dis.  2006 Aug;61(2):101-108.

Clinical Year Review of COPD

Affiliations
  • 1Division of Pulmonary-Allergology, Department of Internal Medicine Yeungnam University College of Medicine, Daegu, Republic of Korea. ghlee@med.yu.ac.kr

Abstract

No abstract available.


MeSH Terms

Pulmonary Disease, Chronic Obstructive*

Figure

  • Figure 1 Number of Papers of Respiratory Diseases from 2000 to 2005 years.

  • Figure 2 Comparison of nasal wash fluid IL-8 concentration in 35 patients with COPD and 12 control subjects of similar age, sex, and smoking status. Box plot represents median, IQR, and range (p=0.009).

  • Figure 3 Comparison of nasal bacterial load in 47 COPD patients with and without a lower airway colonizing PPM. Box plot represents median, IQR, and range (p=0.016).

  • Figure 4 Mean forced expiratory volume in one second (FEV1: adjusted for period, centre and patient within centre) before and during 24 h after the inhalation of tiotropium q.d. (●). Formoterol b.i.d. (◆), and tiotropium plus formoterol q.d. (■) at the end of the 6-week treatment periods.

  • Figure 5 Mean forced vital capacity (FVC: adjusted for period, centre and patient within centre) before and during 24 h after the inhalation of tiotropium q.d. (●). formoterol b.i.d. (◆), and tiotropium plus formoterol q.d. (■) at the end of the 6-week treatment periods.

  • Figure 6 Effect of early treatment on recovery of exacerbation symptoms. Patient mean total recovery time (days) plotted against the patient mean treatment delay (i.e., time from onset of exacerbation symptoms to initiation of therapy) (days) in 108 patients (regression coefficient 0.42 day/day delay; confidence interval, 0.19 to 0.65; p < 0.001).

  • Figure 7 The reported P values are for the entire study period based on a Cox proportional hazards regression stratified by center.

  • Figure 8 Kaplan-Meier estimates of the probability of remaining exacerbation-free. ------ : tiotropium, n=497; - - - - : placebo, n=506. Time to first exacerbation: p<0.001 versus placebo (calculated using the log-rank test).

  • Figure 9 Mean change in trough FEV1 (ml/year) in the tiotropium and placebo groups from days 8 to 344 (A) and from days 50 to 344 (B).

  • Figure 10 An algorithm showing which patients with an acute exacerbation of chronic obstructive pulmonary disease (COPD) should receive antibiotic treatment.

  • Figure 11 Comparative ROC Type II curves and C statistics value for IC/TLC ratio, FEV1, and BODE Index as predictors of mortality in patients with COPD. The sensitivity and specificity of IC/TLC are greater than that of the FEV1 but less than that of the BODE Index.


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