Skip to main content
. 2011 Mar;13(3):216–225. doi: 10.1016/j.micinf.2010.10.016

Table 3.

Baseline demographics and clinical outcome in 39 patients with infective endocarditis stratified by the GPIIIa PlA1/A2 platelet receptor genotype.

GPIIIa PlA1/A2 genotype
P valuea
A1/A1, n = 29 A1/A2, n = 10
Age (y) 56 ± 17 56 ± 17 0.949
Male (%) 22 (76) 8 (80) 1.000
Native valve (%) 20 (69) 6 (60) 0.704
Valvular heart disease (%) 8 (28) 5 (50) 0.254
Previous infective endocarditis (%) 2 (7) 3 (30) 0.096
Intravenous drug abuser (%) 3 (10) 1 (10) 1.000
Affected valve (%)
 Mitral 11 (38) 4 (40) 0.524
 Aortic 10 (35) 3 (30)
 Mitral + aortic 5 (17) 1 (10)
 Tricuspid ± mitral/aortic 3 (10) 1 (10)
 Pulmonary 0 1 (10)
Presence of vegetations (%) 22 (76) 8 (80) 1.000
Vegetation length, mmb 14 ± 5 20 ± 12 0.166
Vegetation width, mmb 9 ± 4 9 ± 3 0.946
Organism (%)
 Streptococci 13 (45) 2 (20) 0.030
 Staphylococci 10 (35) 1 (10)
 Streptococci + staphylococci 2 (7) 0 (0)
 Enterococci 1 (3) 1 (10)
 Other 2 (7) 5 (50)
 Culture negative 1 (3) 1 (10)
Surgery (%) 18 (62) 7 (70) 0.721
Embolic phenomena (%) 8 (28) 7 (70) 0.027
Heart failure (%) 10 (34) 1 (10) 0.228
Death (%) 6 (21) 3 (30) 0.669
Composite clinical end-point (%)c 22 (73%) 8 (80%) 1.000
a

P values were determined using the Mann–Whitney U test for numerical variables, and Fisher’s exact test or the chi-squared test for categorical variables. Data for the one PlA2/A2 subject are not depicted and were excluded from all analyses.

b

Data on vegetation characteristics were available for 29 of the 30 subjects with vegetations.

c

The clinical end-point represents a composite of embolism, heart failure, need for surgery and mortality.

HHS Vulnerability Disclosure