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1 s with persistent hypercapnia after an acute COPD exacerbation.
2 sthma exacerbation and 131,974 patients with COPD exacerbation.
3 ts with asthma exacerbation and 162,899 with COPD exacerbation.
4 was the time to the first moderate or severe COPD exacerbation.
5 h increased respiratory symptoms and risk of COPD exacerbation.
6 on symptom, is useful in the confirmation of COPD exacerbation.
7 rticosteroids in the outpatient treatment of COPD exacerbations.
8 e primary outcome was the annual rate of all COPD exacerbations.
9 g NIV failure (25-15%) in severe hypercapnic COPD exacerbations.
10 hree dihexosylceramides were associated with COPD exacerbations.
11 a and glycosphingolipids are associated with COPD exacerbations.
12 d with a clinically significant reduction in COPD exacerbations.
13 ses in nocturnal symptoms and risk of severe COPD exacerbations.
14 f teeth and thus may reduce the frequency of COPD exacerbations.
15 s, rescue medication use, and risk of severe COPD exacerbations.
16 h increased respiratory symptoms and risk of COPD exacerbations.
17 ry tract contributes to approximately 50% of COPD exacerbations.
18 atio] of >1) would be associated with severe COPD exacerbations.
19 ondary bacterial infections in virus-induced COPD exacerbations.
20 as important cellular targets in controlling COPD exacerbations.
21 ve drugs for the prevention and treatment of COPD exacerbations.
22 inophilic airway inflammation contributes to COPD exacerbations.
23 acute chronic obstructive pulmonary disease (COPD) exacerbation.
24 er of chronic obstructive pulmonary disease (COPD) exacerbations.
25 9 (2.1-38), 23 (8.8-58), and 36 (12-105) for COPD exacerbations; 1.5 (0.9-2.2), 1.6 (1.0-2.4), and 2.
26 ropium patients were hospitalized because of COPD exacerbation (7.0% vs. 9.5%, respectively; differen
27 predictive value [NPV]; treatment efficacy (COPD exacerbations, all-cause mortality, quality of life
28 with chronic obstructive pulmonary disease (COPD) exacerbations among individuals with COPD in the g
29 oints were the percentage of patients with a COPD exacerbation and the percentage of patients with a
30 roup performed telephone-based assessment of COPD exacerbations and hospitalizations, and all hospita
34 d reduce the incidence of moderate or severe COPD exacerbations and upper respiratory infections.
35 uring chronic obstructive pulmonary disease (COPD) exacerbations and is a plausible target for MAIT c
40 ents did not cause a significant increase in COPD exacerbations, but did reduce total systemic cortic
41 rker to direct corticosteroid therapy during COPD exacerbations, but larger studies are required.
42 as superior in preventing moderate to severe COPD exacerbations compared with the single longacting a
44 lycopyrronium for rate of moderate to severe COPD exacerbations (defined by worsening symptoms and ca
45 he percentages of individuals experiencing a COPD exacerbation during the first year of observation w
46 ing the first 2 hrs of treatment of an acute COPD exacerbation failed to improve FEV1 faster than the
49 with respect to the first moderate or severe COPD exacerbation (hazard ratio, 1.06; 95% CI, 0.94 to 1
50 n the reduction of hospital readmissions for COPD exacerbations, health systems in the USA struggle t
51 ) for chronic obstructive pulmonary disease (COPD) exacerbations, helium/oxygen (heliox) reduces the
52 for an average period of 4.3 years regarding COPD exacerbations, hospital admissions, and mortality.
54 nt of chronic obstructive pulmonary disease (COPD) exacerbations improves outcomes; however, response
55 ease stages III-IV, and one or more moderate COPD exacerbation in the past year) were randomly assign
56 ss than 50%, at least one moderate-to-severe COPD exacerbation in the previous 12 months, and a COPD
57 wer than 50%, one or more moderate-to-severe COPD exacerbation in the previous 12 months, COPD Assess
62 ve than salmeterol-fluticasone in preventing COPD exacerbations in patients with a history of exacerb
64 ment Test [CAT] >/=10 vs <10) in addition to COPD exacerbations in the previous year (<2 vs >/= 2), a
65 d airway wall thickness were associated with COPD exacerbations, independent of the severity of airfl
66 ded blood eosinophils at baseline and future COPD exacerbations longitudinally, defined as moderate (
67 n in COPD and is associated with more severe COPD exacerbations, lower airway bacterial colonization,
68 pt that bacteria infecting the airway during COPD exacerbations mediate increased airway inflammation
69 inophil count is associated with the risk of COPD exacerbations, mortality, decline in FEV1, and resp
70 uenzae strains isolated from patients during COPD exacerbations often induce more airway inflammation
71 ADRB2 polymorphisms differentially affected COPD exacerbation outcomes in response to tiotropium ver
72 at tiotropium may lengthen the time to first COPD exacerbation (P = 0.028) and reduce health care uti
73 018), but no evidence of an association with COPD exacerbations (p=0.35) or the other indices of COPD
74 is common and clinically significant during COPD exacerbations, particularly in those with underlyin
76 nting to the emergency department with acute COPD exacerbation, past or present smokers (>/=20 pack-y
78 ma or chronic obstructive pulmonary disease (COPD) exacerbations, pneumonias, lung cancer, ischemic h
79 tware, could estimate joint heterogeneity in COPD exacerbation rate and severity and can have applica
82 ns (rate ratio, 1.01; 95% CI, 0.91 to 1.13), COPD exacerbations (rate ratio, 1.08; 95% CI, 0.98 to 1.
83 United States seem to be at greater risk for COPD exacerbation-related mortality than those living in
84 .5; P < 0.05), and to have increased risk of COPD exacerbation requiring an acute doctor visit (OR, 1
85 m Short-Form Physical Component (SF-12), and COPD exacerbations requiring health care utilization, ad
86 ough (OR, 4.20; P = 0.03), increased risk of COPD exacerbations requiring treatment with antibiotics
87 The most common serious adverse events were COPD exacerbation resulting in admission to hospital (ei
88 ed Trial of Simvastatin in the Prevention of COPD Exacerbations (STATCOPE) as a randomized, controlle
89 l Glycopyronium vs Fluticasone Salmeterol on COPD Exacerbations) study, which compared once-daily lon
90 ug vs. HandiHaler) and the risk of the first COPD exacerbation (superiority study, Respimat at a dose
91 uticasone in reducing the annual rate of all COPD exacerbations; the rate was 11% lower in the indaca
92 of the use of azithromycin for prevention of COPD exacerbations (United States and Canada, 2006-2010;
95 versus salmeterol-fluticasone on the rate of COPD exacerbations was independent of the baseline blood
96 A total of 215 patients hospitalized for a COPD exacerbation were randomized at hospital discharge
100 se of chronic obstructive pulmonary disease (COPD) exacerbation were examined by monitoring changes i
102 and reduced inflammation in a model of viral COPD exacerbation, which do not affect viral clearance.
103 re are no biomarkers to objectively diagnose COPD exacerbations, which are the major drivers of hospi
104 n rates after an index hospitalization for a COPD exacerbation will be penalized with reduced reimbur
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