Skip to main content
Peer Review

Peer Reviewed

Original Research

Foot Abscesses With No Accompanying Wound: Clinical Presentation and Pathogens

July 2023
1943-2704
Wounds. 2023;35(7):E236-E239. doi:10.25270/wnds/23025

Abstract

Introduction. Acute bacterial infections of the skin and soft tissue are common and often pose serious complications, most commonly caused by Streptococcus species and Staphylococcus aureus. Objective. The authors report clinical presentation and pathogens in patients with a foot abscess and no wound. Methods. The authors retrospectively evaluated the demographics, clinical presentation, and microbiology from 20 patient records. Results. Twenty patients were identified. Fifteen were male (75%), and 10 patients (50%) had DM. Patients presented to the hospital 7.8 ± 4.8 days after onset of symptoms and underwent surgery 2.0 ± 0.9 days from admission. Patients underwent 2.4 ± 1.0 surgeries while admitted. Patients with DM presented with significantly higher erythrocyte sedimentation rate than patients without DM (66.6 ± 46.1 vs 43.3 ± 26.2; P = .02). There were no polymicrobial infections based on deep intraoperative tissue cultures. Seven patients had methicillin-sensitive S aureus (35%), 4 had Streptococcus agalactiae (20%), 3 had methicillin-resistant S aureus (15%), 1 had Streptococcus pyogenes (5%), 1 had Escherichia coli (5%), 1 had Streptococcus dysgalactiae (5%), 1 had an unidentified Streptococcus species (5%), and 2 had no growth (10%). Conclusion. Patients with foot abscess and no wounds had single-pathogen infections, predominantly Staphylococcus and Streptococcus

Abbreviations

CI, confidence interval; DM, diabetes mellitus

Introduction

Acute bacterial infections of the skin and soft tissue are common and often pose serious complications, most commonly caused by Streptococcus species and Staphylococcus aureus.1-3 Patients with soft tissue infections comprise 1% to 14% of emergency department visits and 4% to 7% of hospital admissions.4 An infection incidence rate of 24.6 per 1000 people per year has been reported, with a higher incidence among males and persons aged 45 to 64 years.5 In adults, foot infections are usually precipitated by a break in the cutaneous skin barrier such as interspace fissures, traumatic penetrating injuries, or ulcerations.6,7 It is uncommon for foot infection to occur when the integument is intact. Lavery et al8 reported that only 1 in 150 patients with foot infection did not have some type of wound as part of the presenting concern. The objective of the current study is to report the clinical presentation and pathogens of patients with a foot abscess and no accompanying wound.

Methods

Approval of this study was granted by the institutional review board at the University of Texas Southwestern Medical Center. The authors retrospectively evaluated 20 patients who were admitted to the hospital with a foot abscess and no wound. Patients younger than 18 years and older than 90 years were excluded. Demographic data including race and ethnicity, sex, and age; medical history; laboratory values; surgical cultures; and clinical presentation were collected. 

The diagnosis of DM was based on American Diabetes Association criteria.9 The Infectious Diseases Society of America Diabetic Foot Infection Classification was used to define foot infection.10 This definition includes clinical features of purulence or at least 2 local clinical signs of infection. Sensory neuropathy was defined as reduced sensation to vibrational stimuli using a tuning fork or inability to sense at least 1 testing point using a Semmes-Weinstein 10 g monofilament. Peripheral vascular disease was defined as an ankle-arm systolic blood pressure ratio of less than 0.90. 

Descriptive statistics, t test, and Fisher exact test were used for analysis. Dichotomous variables were reported as number (percent) and continuous variables as mean ± standard deviation. 

Table 1

Table 2

Results

Twenty patients were identified. Fifteen were male (75%), 10 (50%) had DM, and 16 (80%) were White. Patients presented to the hospital a mean of 7.8 ± 4.8 days after initial onset of foot symptoms. Surgery was performed within a mean of 2.0 ± 0.9 days from admission. The mean number of surgeries per patient during admission was 2.4 ± 1.0. 

Ten patients (50%) had DM. When comparing demographics of patients with DM, the only significant difference was the incidence of neuropathy (80% DM vs 10% no DM; P = .01). Laboratory values on admission are reported in Table 1. Patients with DM presented with a significantly higher erythrocyte sedimentation rate than patients without DM (66.60 mm/hour ± 46.05 vs 43.30 mm/hour ± 26.18; P = .02).

Figure 1

Deep intraoperative tissue cultures showed no polymicrobial infections. Seven patients had methicillin-sensitive S aureus (35%), 4 had Streptococcus agalactiae (20%), 3 had methicillin-resistant S aureus (15%), 1 had Streptococcus pyogenes (5%), 1 had Escherichia coli (5%), 1 had Streptococcus dysgalactiae (5%), and 2 had no growth (10%). Results are shown in Table 2 and Figure 1

Figure 2

Patients with DM had an equal percentage of S aureus and Streptococcus infections (50% for each) (Figure 2). None of the Staphylococcus infections were due to resistant pathogens. In contrast, there were more S aureus than Streptococcus infections among patients who did not have DM (25% and 10%, respectively). The 1 E coli and 2 no growth cultures occurred in patients without DM.

Discussion

Results of this study show that only half the subjects who presented with abscesses and no wounds had DM. This was unexpected, because the majority of foot infections in the literature are due to wound infections in patients with DM.11 All foot abscesses in the current study were monomicrobial, in contrast to the polymicrobial results commonly reported in the foot infection literature.1,2 Kalan et al12 conducted a longitudinal, prospective study investigating the role of colonizing microbiomes in diabetic wound healing. They identified polymicrobial growth among diabetic foot infections and found that contaminants significantly affected wound severity and healing. It should be noted, however, that cultures of uninfected wounds do not predict outcomes.13,14

In the current study, the most common findings on presentation were subjective pain, with or without erythema. Patients received antibiotics for a mean of 2 days prior to incision and drainage in the operating room. It may be that the abscesses consolidated after administration of intravenous antibiotics. 

The authors of the current study did not identify any literature on abscesses without accompanying wounds. Since there is no prior literature outlining physical examination findings and outcomes for this condition, it is difficult to draw comparisons. A study by Venkata et al15 evaluated foot infections in patients with and without DM. In patients with DM the most common site of infection was the dorsum of the foot (40%), and in patients without DM the most common site was the toes (40%).5,15 Truong et al16 compared outcomes of foot infections secondary to puncture injuries in patients with and without DM. That study concluded that patients with DM took longer before presenting to the hospital (mean, 20.1 days ± 36.3 vs 18.8 days ± 34.8; P = .09; 95% CI, 13–26.5). This result was not statistically significant.

Limitations

This study has limitations. Owing to the retrospective nature of the study design, operational definitions for some variables may not be consistent throughout the medical documentation. However, since all the foot and ankle infections managed in the hospital of the study authors are evaluated by the limb salvage service, patients included in this cohort were evaluated based on a systematic format. The study population may not represent the general population, however, because Parkland Hospital is a safety-net hospital, serving a great number of patients who have a low income or no income, who are unfunded, and who are underfunded.17 

Conclusion

Foot abscesses without wounds are not frequently seen in practice. The authors of the current study did not identify any published reports describing clinical presentation or microbiological data associated with this pathology. Half of the subjects in the current study did not have DM. All the abscesses in this series had infection caused by a single pathogen, predominantly Staphylococcus and Streptococcus

Acknowledgments

Authors: Amanda L. Killeen, DPM; Katerina Grigoropoulos, DPM; Mehmet Suludere, MD; Peter Andrew Crisologo, DPM; and Lawrence A. Lavery, DPM, MPH

Affiliation: University of Texas Southwestern Medical Center, Dallas, TX

ORCID: Crisologo, 0000-0002-5367-9235; Grigoropoulos 0009-0002-0641-0572; Killeen, 0000-0002-8461-9139; Lavery, 0000-0002-7920-9952; Suludere, 0000-0002-2285-0909 

Disclosure: The authors disclose no financial or other conflicts of interest. 

Correspondence: Amanda L. Killeen, DPM; Assistant Professor, UT Southwestern: The University of Texas Southwestern Medical Center, Plastic Surgery, 5323 Harry Hines Blvd, F4.306a, Dallas, TX 75390; amanda.killeen@utsouthwestern.edu

How Do I Cite This?

Killeen AL, Grigoropoulos K, Suludere M, Crisologo PA, Lavery LA. Foot abscesses with no accompanying wound: clinical presentation and pathogens. Wounds. 2023;35(7):E236-E239. doi:10.25270/wnds/23025

References

1. van Asten SAV, La Fontaine J, Peters EJG, Bhavan K, Kim PJ, Lavery LA. The microbiome of diabetic foot osteomyelitis. Eur J Clin Microbiol Infect Dis. 2016;35(2):293-298. doi:10.1007/s10096-015-2544-1

2. Lavery LA, Sariaya M, Ashry H, Harkless LB. Microbiology of osteomyelitis in diabetic foot infections. J Foot Ankle Surg. 1995;34(1):61-64. doi:10.1016/S1067-2516(09)80103-8

3. Björnsdóttir S, Gottfredsson M, Thórisdóttir AS, et al. Risk factors for acute cellulitis of the lower limb: a prospective case-control study. Clin Infect Dis. 2005;41(10):1416-1422. doi:10.1086/497127

4. Dong SL, Kelly KD, Oland RC, Holroyd BR, Rowe BH. ED management of cellulitis: a review of five urban centers. Am J Emerg Med. 2001;19(7):535-540. doi:10.1053/ajem.2001.28330

5. Ellis Simonsen SM, van Orman ER, Hatch BE, et al. Cellulitis incidence in a defined population. Epidemiol Infect. 2006;134(2):293-299. doi:10.1017/S095026880500484X

6. Dupuy A, Benchikhi H, Roujeau JC, et al. Risk factors for erysipelas of the leg (cellulitis): case-control study. BMJ. 1999;318(7198):1591-1594. doi:10.1136/bmj.318.7198.1591

7. Roujeau JC, Sigurgeirsson B, Korting HC, Kerl H, Paul C. Chronic dermatomycoses of the foot as risk factors for acute bacterial cellulitis of the leg: a case-control study. Dermatology. 2004;209(4):301-307. doi:10.1159/000080853

8. Lavery LA, Armstrong DG, Peters EJG, Lipsky BA. Probe-to-bone test for diagnosing diabetic foot osteomyelitis: reliable or relic? Diabetes Care. 2007;30(2):270-274. doi:10.2337/dc06-1572

9. American Diabetes Association. (2) Classification and diagnosis of diabetes. Diabetes Care. 2017;40(suppl 1):S11-S24. doi:10.2337/dc15-S005

10. Lavery LA, Ryan EC, Ahn J, et al. The infected diabetic foot: re-evaluating the Infectious Diseases Society of America Diabetic Foot Infection Classification. Clin Infect Dis. 2020;70(8):1573-1579. doi:10.1093/cid/ciz489

11. Lavery LA, Armstrong DG, Wunderlich RP, Tredwell J, Boulton AJ. Diabetic foot syndrome: evaluating the prevalence and incidence of foot pathology in Mexican Americans and non-Hispanic whites from a diabetes disease management cohort. Diabetes Care. 2003;26(5):1435-1438. doi:10.2337/diacare.26.5.1435

12. Kalan LR, Meisel JS, Loesche MA, et al. Strain- and species-level variation in the microbiome of diabetic wounds is associated with clinical outcomes and therapeutic efficacy. Cell Host Microbe. 2019;25(5):641-655.e5. doi:10.1016/j.chom.2019.03.006

13. Gardner SE, Hillis SL, Heilmann K, Segre JA, Grice EA. The neuropathic diabetic foot ulcer microbiome is associated with clinical factors. Diabetes. 2013;62(3):923-930. doi:10.2337/db12-0771

14. Gardner SE, Haleem A, Jao YL, et al. Cultures of diabetic foot ulcers without clinical signs of infection do not predict outcomes. Diabetes Care. 2014;37(10):2693-2701. doi:10.2337/dc14-0051

15. Venkata RM, Varun DK P, Inamdar P. A comparative study of foot infections in diabetic and non-diabetic patients with reference to etiopathogenesis, clinical features and outcome. Int Surg J. 2020;7(5):1496-1502. doi:10.18203/2349-2902.isj20201858

16. Truong DH, Johnson MJ, Crisologo PA, et al. Outcomes of foot infections secondary to puncture injuries in patients with and without diabetes. J Foot Ankle Surg. 2019;58(6):1064-1066. doi:10.1053/j.jfas.2019.08.013

17. Parkland Health. Financial Summary. Accessed February 1, 2023. https://www.parklandhospital.com/financial-summary