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. Author manuscript; available in PMC: 2019 Jan 1.
Published in final edited form as: Ann Emerg Med. 2017 Oct 5;71(1):21–30. doi: 10.1016/j.annemergmed.2017.07.483

Table 2.

Table 2a. Subgroup Analysis of Clinical Cure* Rates Through 7–14 days for Participants with a Drained Skin Abscess Treated with Trimethoprim-Sulfamethoxazole or Placebo by Presence or Absence of High-Risk Conditions.
Condition Cure (n/total no. [%]) Difference (95% CI)
Trimethoprim- sulfamethoxazole Placebo
Abscess cavity5 cm 69/77 (89.6) 54/71 (76.1) 14.7 (1.4 – 28.1)
Abscess cavity <5 cm 418/446 (93.7) 403/462 (87.2) 6.1 (2.1 – 10.1)
Erythema5 cm 357/390 (91.5) 338/399 (84.7) 6.8 (2.1 – 11.6)
Erythema <5 cm 130/134 (97.0) 119/134 (88.8) 8.2 (1.4 – 15.0)
History of MRSA infection 43/45 (95.6) 32/40 (80.0) 15.6 (−0.6 – 31.7)
No history of MRSA infection 444/479 (92.7) 425/493 (86.2) 6.5 (2.4 – 10.5)
Fever 93/102 (91.2) 78/98 (79.6) 14.3 (3.7 – 24.9)
No fever 391/418 (93.5) 374/430 (87.0) 5.9 (1.7 – 10.1)
Diabetes 50/58 (86.2) 47/57 (82.5) 3.8 (−11.3 – 18.8)
No diabetes 437/466 (93.8) 410/476 (86.1) 7.6 (3.6 – 11.7)
Co-morbidity§ 83/92 (90.2) 73/88 (83.0) 8.4 (−2.8 – 19.6)
No co-morbidity 404/432 (93.5) 384/445 (86.3) 7.0 (2.8 – 11.2)
MRSA|| 203/219 (92.7) 202/249 (81.1) 11.6 (5.2 – 18.0)
MSSA 78/86 (90.7) 71/86 (82.6) 8.1 (−3.1 – 19.4)
No MRSA or MSSA 203/216 (94.0) 181/195 (92.8) 1.2 (−4.1 – 6.5)
Table 2b. Subgroup Analysis of Composite Cure* Rates Through 7–14 days Among Participants with a Drained Skin Abscess Treated with Trimethoprim-Sulfamethoxazole or Placebo by Presence or Absence of High-Risk Conditions.
Condition Cure (n/total no. [%]) Difference (95% CI)
Trimethoprim- sulfamethoxazole Placebo
Abscess cavity5 cm 62/77 (80.5) 51/71 (71.8) 8.5 (−6.3 – 23.4)
Abscess cavity <5 cm 391/446 (87.7) 345/462 (74.7) 12.2 (7.0 – 17.4)
Erythema5 cm 335/390 (85.9) 295/399 (73.9) 11.5 (5.7 – 17.2)
Erythema <5 cm 118/134 (88.1) 101/134 (75.4) 11.9 (2.1 – 21.8)
History of MRSA infection 40/45 (88.9) 24/40 (60.0) 28.9 (8.8 – 49.0)
No history of MRSA infection 413/479 (86.2) 372/493 (75.5) 10.2 (5.1 – 15.2)
Fever 83/102 (81.4) 64/98 (65.3) 18.4 (5.4 – 31.3)
No fever 368/418 (88.0) 329/430 (76.5) 10.2 (4.9 – 15.5)
Diabetes 44/58 (75.9) 36/57 (63.2) 10.9 (−7.4 – 29.3)
No diabetes 409/466 (87.8) 360/476 (75.6) 11.7 (6.7 – 16.8)
Co-morbidity§ 71/92 (77.2) 55/88 (62.5) 13.5 (−0.8 – 27.9)
No co-morbidity 382/432 (88.4) 341/445 (76.6) 11.3 (6.2 – 16.5)
MRSA|| 186/219 (84.9) 163/249 (65.5) 18.3 (10.3 – 26.2)
MSSA 72/86 (83.7) 63/86 (73.3) 10.5 (−2.9 – 23.8)
No MRSA or MSSA 192/216 (88.9) 167/195 (85.6) 3.24 (−3.7 – 10.2)
Table 2c. Subgroup Analysis of Composite Cure* Rates Through 42–56 days Among Participants with a Drained Skin Abscess Treated with Trimethoprim-Sulfamethoxazole or Placebo by Presence or Absence of High-Risk Conditions.
Condition Cure (n/total no. [%]) Difference (95% CI)
Trimethoprim-sulfamethoxazole Placebo
Abscess cavity5 cm 55/70 (78.6) 47/70 (67.1) 11.4 (−4.61 – 27.5)
Abscess cavity <5 cm 361/434 (83.2) 311/440 (70.7) 12.5 (6.75 – 18.2)
Erythema >5 cm 307/376 (81.6) 269/383 (70.2) 11.4 (5.13 – 17.7)
Erythema <5 cm 109/129 (84.5) 89/127 (70.1) 14.4 (3.51 – 25.3)
History of MRSA infection 33/43 (76.7) 21/39 (53.8) 22.9 (0.34 – 45.4)
No history of MRSA infection 383/462 (82.9) 337/471 (71.5) 11.4 (5.81 – 16.9)
Fever 76/98 (77.6) 57/94 (60.6) 16.9 (2.99 – 30.8)
No fever 338/403 (83.9) 299/412 (72.6) 11.3 (5.44 – 17.2)
Diabetes 38/56 (67.9) 36/56 (64.3) 3.57 (−15.7 – 22.9)
No diabetes 378/449 (84.2) 322/454 (70.9) 13.3 (7.67 – 18.9)
Co-morbidity§ 61/88 (69.3) 54/86 (62.8) 6.53 (−8.7 – 21.7)
No co-morbidity 355/417 (85.1) 304/424 (71.7) 13.4 (7.71 – 19.2)
MRSA|| 166/208 (79.8) 139/235 (59.2) 20.7 (11.9 – 29.4)
MSSA 71/85 (83.5) 57/82 (69.5) 14.0 (0.11 – 27.9)
No MRSA or MSSA 176/209 (84.2) 160/190 (84.2) 0.0 (−7.71 – 7.71)

Abbreviations: MRSA = methicillin-resistant Staphylococcus aureus; MSSA = methicillin-susceptible S. aureus

*

Overall, for trimethoprim-sulfamethoxazole and placebo groups, clinical cure rate at 7–14 days was 92.9% and 85.7% (difference, 7.2; 95% CI 3.2–11.2), composite cure rate at 7–14 was 86.5% and 74.3% (difference, 12.2; 95% CI 7.2–17.1) and extended composite cure at 42–56 days was 82.4% and 70.2% (difference, 12.2; 95% CI 6.8–17.6), respectively. Outcomes were defined as follows: clinical cure was defined as resolution of all symptoms and signs of infection, or improvement such that no new antibiotics were prescribed (through 7–14 days after the end of treatment); composite cure was defined as resolution of all symptoms and signs of infection, or improvement such that no additional antibiotics and/or surgical drainage procedure were required (through 7–14 days and 42–56 days after the end of treatment).

Abscess cavity and erythema dimensions were defined as the maximal dimension (length or width).

Fever was defined as history of fever within the preceding week or temperature >38°C measured in the ED (0.8%).

§

Co-morbidities were defined as those present in >0.5% of study participants: diabetes (10.9%); eczema or other chronic skin condition (3.4%); chronic obstructive pulmonary disease (1.1%); congestive heart failure (0.9%); human immunodeficiency virus infection (1.6%); and cancer (0.9%).

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Culture results were those based on the organism isolated from primary wound specimen.