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. 2014 Jan 30;14:47. doi: 10.1186/1471-2334-14-47

Table 1.

Comparisons of differences between patients with community-acquired K. pneumoniae bacteremia and control group

 
Community-acquired K. pneumoniae bacteremia
 
 
 
Variable
Invasive syndrome (%)
 
 
 
  Yes (n = 76) No (n = 332) p value Control (%) (n = 76) p value +
Hypermucoviscosity phenotype of K. pneumoniae
69 (90.8)
78 (23.5)
< 0.01*
   
Male
40 (52.6)
150 (45.2)
0.25
40 (52.6)
0.99
Age ≥ 60 yrs
39 (51.3)
128 (38.6)
0.05
39 (51.3)
0.99
Diabetes mellitus (DM)
41 (53.9)
134 (40.4)
0.04
25 (32.9)
0.01
DM with poor glycemic control (HbA1c ≥ 9%)
32 (42.1)
75 (22.6)
< 0.01*
17 (22.4)
0.02
Cardiovascular diseases
17 (22.4)
65 (19.6)
0.69
21 (27.6)
0.57
Liver cirrhosis
5 (6.6)
45 (13.6)
0.12
10 (13.2)
0.28
Chronic renal failure
10 (13.2)
35 (10.5)
0.54
18 (23.7)
0.14
Malignancy
4 (5.3)
33 (9.9)
0.27
18 (23.7)
< 0.01
Biliary tract diseases
2 (2.6)
20 (6.0)
0.39
8 (10.5)
0.10
Absence of underlying diseases
12 (15.8)
44 (13.3)
0.69
9 (11.8)
0.64
Therapy in the month prior to the infection
 
 
 
 
 
  Proton-pump inhibitors
8 (10.5)
24 (7.2)
0.47
15 (19.7)
0.17
  Aspirin
2 (2.6)
56 (16.9)
< 0.01*
8 (10.5)
0.10
  Antibiotics 5 (6.6) 28 (8.4) 0.76 12 (15.8) 0.12

+ Age-matched analysis (K. pneumoniae invasive syndrome vs. control group).

*Results of multivariate analysis indicated that community-acquired K. pneumoniae bacteremic patients who were infected by strains expressing the hypermucoviscosity phenotype (odds ratio [OR], 31.07; 95% confidence interval [CI], 13.55-71.22; p < 0.01) and diabetic patients with poor glycemic control (OR, 2.46; 95% CI, 1.27-4.77; p < 0.01) were at increased risk, whereas those who had recent therapy with aspirin (OR, 0.17; 95% CI, 0.04-0.79; p = 0.02) were at lower risk of acquiring K. pneumoniae-associated invasive syndrome.