Skip to main content
. 2015 Aug 14;59(9):5830–5833. doi: 10.1128/AAC.04865-14

TABLE 2.

Medical conditions of the case and control groups

Variable Case group (n = 41)a Control group (n = 82)a P value
Duration of
    Hospitalization 100.2 ± 80.01 53.82 ± 33.70 0.001
    Hospitalization before the tigecycline use 33.66 ± 34.27 21.71 ± 18.56 0.042
    Tigecycline usage 20.80 ± 16.11 17.11 ± 11.59 0.195
Hospital exposure
    ICU stayb 18 (43.9) 21 (25.6) 0.040
    Surgical proceduresc 25 (61.0) 50 (61.0) 1.000
    Intervention proceduresd 17 (41.5) 41 (51.2) 0.307
Indwelling catheter or drainage
    Foley catheter 24 (58.5) 31 (39.0) 0.041
    Percutaneous drainage 22 (53.7) 50 (61.0) 0.437
    Suction drainage systeme 12 (29.3) 4 (4.9) 0.001
    Levin tube 18 (43.9) 25 (30.5) 0.141
Combined antibiotic therapy 7 (17.1) 17 (20.7) 0.629
Exposures to antimicrobial agents
    Narrow-, expanded-, and broad-spectrum cephalosporins 7 (17.1) 34 (41.5) 0.007
    Ampicillin-sulbactam and penicillin 2 (4.9) 11 (13.4) 0.147
    Glycopeptides and linezolid 19 (46.3) 40 (48.9) 0.799
    Metronidazole 11 (26.9) 15 (18.3) 0.274
    Antipseudomonal antibioticsf 33 (80.5) 58 (70.7) 0.245
a

Data are presented as means ± SD or number (%) of patients.

b

ICU stay at the start of tigecycline therapy.

c

Any surgical procedure under general anesthesia within 30 days prior to the administration of tigecycline.

d

Any intervention procedure except upper or lower GI endoscopy within 30 days prior to the administration of tigecycline.

e

Hemovac, sump, or vacuum dressing at infected site.

f

These include cefepime, piperacillin-tazobactam, carbapenems except ertapenem, colistin, quinolone, and aminoglycoside.