P-815. A Randomized Trial of Doxycycline vs. Trimethoprim Sulfamethoxazole (TMP-SMX) for Uncomplicated Skin and Skin Structure Infections (SSSIs)

Abstract Background In the U.S., there are > 8 million visits for SSSIs annually, the vast majority of which are managed in the outpatient setting. However, safety and efficacy of doxycycline in comparison to other oral antibiotics for suppurative uncomplicated SSSIs (uSSSIs) remains unclear. Methods We performed a double-blind, randomized controlled clinical trial of adults and children > 8 years of age with suppurative uSSSIs managed in the outpatient setting at 3 sites, two in California and one in Missouri. All participants were required to have adequate source control of uSSSI and were randomized to doxycycline 100 mg po or 1 double strength (DS) tablet of TMP-SMX twice daily. Doses of study medication were modified for children < 40 kg. Primary outcome was early clinical response (ECR) at 48-72 hours in the intent to treat population. Secondary outcomes included clinical response at end of treatment (EOT), clinical response at one month (1M) and adverse effects. Results Among the 269 participants, 248 (92%) were adults and 21 (8%) were children; 132 (50%) were Hispanic, 93 (35%) African American, 33 (12%) white, 5 (2%) Asian, 1 (0.4%) Am. Indian/Alaskan Native, and 4 (1%) were other race/ethnicity. At the primary endpoint, ECR, cure rate was not significantly different between the two groups with a clinical response in 89/134 (66%) in the doxycycline arm in vs. 86/135 (64%) in the TMP-SMX arm (p=0.64). At the EOT visit, response was seen in 104 (78%) in the doxycycline arm and 104 (77%) in the TMP-SMX arm (p=0.91). Finally, at the 1M visit, clinical response was seen in 101 (75%) in the doxycycline arm in and 95 (70%) in the TMP-SMX arm (p=0.59). Adverse events were similar in the two groups with nausea (15 (11%) in the doxycycline arm vs. 10 (7%) in the TMP-SMX), headache (10 (7%) vs. 12 (9%)) and diarrhea (12 (9%) vs. 8 (6%)) being the most common. (Table) Conclusion In our multi-center randomized trial of outpatient treatment of suppurative uSSSI performed in a diverse population, we found no significant differences in clinical response between doxycycline and TMP-SMX. Safety and tolerability were also similar between groups. For adults and children with suppurative uSSSIs undergoing source control, doxycycline appears to be a safe and efficacious alternative to TMP/SMX. Disclosures Loren G. Miller, MD MPH, Armata: Grant/Research Support|GSK: Grant/Research Support|Merck: Grant/Research Support|Paratek: Grant/Research Support Gregory J. Moran, MD, FACEP, AbVacc: Grant/Research Support Mark Munekata, MD,MPH, Intuitive Surgical: Stocks/Bonds (Public Company)

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Journal
Open Forum Infectious Diseases
Published
2026-01-01
DOI
https://doi.org/10.1093/ofid/ofaf695.1023
Primary Topic
Hidradenitis Suppurativa and Treatments
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article

P-815. A Randomized Trial of Doxycycline vs. Trimethoprim Sulfamethoxazole (TMP-SMX) for Uncomplicated Skin and Skin Structure Infections (SSSIs)

Mary G. Boyle, Evelyn A Flores, Loren Gregory Miller, Mark Munekata et al.
Open Forum Infectious Diseases
Hidradenitis Suppurativa and Treatments
article

P-815. A Randomized Trial of Doxycycline vs. Trimethoprim Sulfamethoxazole (TMP-SMX) for Uncomplicated Skin and Skin Structure Infections (SSSIs)

Mary G. Boyle, Evelyn A Flores, Loren Gregory Miller, Mark Munekata, Stephanie A. Fritz, Donna Phan Tran, Gregory J. Moran, Buchen (Olivia) Han, Pluscedia Williams, Honghu Liu, Leo Fukunaga, Linyu Zhou, Kavitha Pathmarajah
article en

Abstract

Abstract Background In the U.S., there are > 8 million visits for SSSIs annually, the vast majority of which are managed in the outpatient setting. However, safety and efficacy of doxycycline in comparison to other oral antibiotics for suppurative uncomplicated SSSIs (uSSSIs) remains unclear. Methods We performed a double-blind, randomized controlled clinical trial of adults and children > 8 years of age with suppurative uSSSIs managed in the outpatient setting at 3 sites, two in California and one in Missouri. All participants were required to have adequate source control of uSSSI and were randomized to doxycycline 100 mg po or 1 double strength (DS) tablet of TMP-SMX twice daily. Doses of study medication were modified for children < 40 kg. Primary outcome was early clinical response (ECR) at 48-72 hours in the intent to treat population. Secondary outcomes included clinical response at end of treatment (EOT), clinical response at one month (1M) and adverse effects. Results Among the 269 participants, 248 (92%) were adults and 21 (8%) were children; 132 (50%) were Hispanic, 93 (35%) African American, 33 (12%) white, 5 (2%) Asian, 1 (0.4%) Am. Indian/Alaskan Native, and 4 (1%) were other race/ethnicity. At the primary endpoint, ECR, cure rate was not significantly different between the two groups with a clinical response in 89/134 (66%) in the doxycycline arm in vs. 86/135 (64%) in the TMP-SMX arm (p=0.64). At the EOT visit, response was seen in 104 (78%) in the doxycycline arm and 104 (77%) in the TMP-SMX arm (p=0.91). Finally, at the 1M visit, clinical response was seen in 101 (75%) in the doxycycline arm in and 95 (70%) in the TMP-SMX arm (p=0.59). Adverse events were similar in the two groups with nausea (15 (11%) in the doxycycline arm vs. 10 (7%) in the TMP-SMX), headache (10 (7%) vs. 12 (9%)) and diarrhea (12 (9%) vs. 8 (6%)) being the most common. (Table) Conclusion In our multi-center randomized trial of outpatient treatment of suppurative uSSSI performed in a diverse population, we found no significant differences in clinical response between doxycycline and TMP-SMX. Safety and tolerability were also similar between groups. For adults and children with suppurative uSSSIs undergoing source control, doxycycline appears to be a safe and efficacious alternative to TMP/SMX. Disclosures Loren G. Miller, MD MPH, Armata: Grant/Research Support|GSK: Grant/Research Support|Merck: Grant/Research Support|Paratek: Grant/Research Support Gregory J. Moran, MD, FACEP, AbVacc: Grant/Research Support Mark Munekata, MD,MPH, Intuitive Surgical: Stocks/Bonds (Public Company)

Open Forum Infectious DiseasesVol. 13(Supplement_1)
Los Angeles County Department of Public Health (US), University of California, Los Angeles (US), Washington University in St. Louis (US), UCLA Health (US), UCLA Medical Center (US), Olive View-UCLA Medical Center (US), Harbor–UCLA Medical Center (US), Charles R. Drew University of Medicine and Science (US)
Good health and well-being
Openalex Percentile: Top 91%
Hidradenitis Suppurativa and Treatments
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