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. 2011 Dec;55(12):5430–5432. doi: 10.1128/AAC.00706-11

Table 1.

Comparison of clinical characteristics and outcomes of patients treated with two different doses of TMP/SMX

Clinical parameter Result for TMP/SMX twice-daily dose of:
Odds ratio 95% confidence interval P value
160/800 mg (n = 170) 320/1,600 mg (n = 121)
Median (range) age (yr) 38 (24-52) 40 (28-52) 0.433
No. (%) female gender 87 (51.2) 52 (43.0) 0.72 0.45–1.15 0.19
Median (range) body wt (kg) 77 (44.5-156) 86 (42-141) 0.553
Median (range) body mass index 28 (16.8-54) 30 (18-58.8) 0.454
No. (%) of patients with:
    Diabetes mellitus 32 (18.8) 23 (19.0) 1.01 0.56–1.84 0.968
    Malignancy 3 (1.8) 0 (0.0) 0.269
    End-stage renal disease 0 (0.0) 0 (0.0)
    End-stage liver disease 4 (2.4) 1 (0.8) 0.35 0.04–3.13 0.406
    Human immunodeficiency virus infection 2 (1.2) 5 (4.1) 3.62 0.69–18.98 0.13
    Injection drug use 12 (7.1) 13 (10.7) 1.59 0.70–3.61 0.269
    Residence in a correctional facility 13 (7.6) 8 (6.6) 0.86 0.34–2.13 0.737
    Active tobacco smoking 64 (37.6) 45 (37.2) 0.98 0.61–1.59 0.937
    History of trauma on admission 4 (2.4) 9 (7.4) 3.34 1.00–11.09 0.046a
    History of MRSA colonization or infection within previous 1 yr 17 (10.0) 12 (9.9) 0.99 0.46–2.16 0.981
    Abscess 135 (79.4) 102 (84.3) 1.39 0.75–2.57 0.291
    Receipt of incision and drainage 82 (48.2) 77 (63.6) 1.88 1.17–3.03 0.009a
    Requirement for hospitalization for SSSI management 9 (5.3) 4 (3.3) 0.61 0.18–2.03 0.568
Median (range) treatment duration (days) 10 (7-13) 9 (6-12) 0.5
No. (%) of patients with clinical resolution 127 (74.7) 88 (72.7) 0.90 0.53–1.53 0.705
a

P ≤ 0.05.