The Microbiology of Diabetic Foot Infections in Korea

Article information

J Wound Manag Res. 2017;13(1):8-12
Publication date (electronic) : 2017 May 31
doi : https://doi.org/10.22467/jwmr.2017.00108
Department of Plastic Surgery, Korea University Guro Hospital, Seoul, Korea
Corresponding author: Seung-Kyu Han, M.D., Ph.D. Department of Plastic Surgery, Korea University Guro Hospital, 148 Gurodong-ro, Guro-gu, Seoul 08308, Korea Tel: +82-2-2626-3333 Fax +82-2-868-6698 E-mail: pshan@kumc.or.kr
Received 2017 May 9; Revised 2017 May 16; Accepted 2017 May 16.

Abstract

Background

In diabetic foot infection, causative pathogens differ in Western population as compared with Asian population. The aim of this study is to analyze microbiological data with respect to diabetic foot infection in Korea to help the choice adequate empirical antibiotics.

Methods

We enrolled 745 patients with diabetic foot infection, who were admitted to diabetic wound center of the Korea University Guro Hospital between January 2011 and December 2015. Deep tissue and/or bone biopsy cultures were taken during surgical debridement in the operating room and microbiological analysis was performed.

Results

Out of the 745 patients, 613 patients (82.2%) had isolated causative organisms and 832 microbial isolates were identified. Gram-positive aerobic bacteria were isolated in 57.5%, followed by Gram-negative aerobic bacteria (40.0%), anaerobes (1.4%), and fungus (1.1%). MRSA found most frequently identified (13.7%) in Gram-positive aerobes and Pseudomonas found most frequently identified (9.4%) in Gram-negative aerobes.

Conclusion

Microbiologic analysis in Korea differs from the reports from Western population. We propose the need of our own guidelines based on microbiology of Korea for better treatment.

Introduction

Diabetes mellitus is a serious health problem that is rapidly expanding worldwide. In 2000, according to the World Health Organization, at least 171 million people worldwide suffered from diabetes and due to increasing rates, this number is projected to double by 2030 [1]. Epidemiological studies suggest that 2.5% of diabetic patients develop diabetic foot ulcers each year and 15-25% during their lifetime [2]. Diabetic foot ulcer is a result of various risk factors such as peripheral neuropathy, peripheral vascular disease, trauma, and impaired resistance to infection [3,4]. Diabetic foot infection (DFI) is the most frequent and disastrous complication of the diabetic foot [5]. DFI is considered as a significant health and socioeconomic problem than any other diabetes-related complications and is the major cause of non-traumatic lower extremity amputations [6].

When surgeons are confronted with diabetic foot infection in clinics, they choose the management strategy using antibiotics or surgical debridement. Current clinical guidelines for the management of DFI, according to Infectious Disease Society of America (IDSA), recommend empirical antimicrobial treatment until wound cultures ascertain the causative pathogens and their antibiotic susceptibility patterns, allowing targeted antibiologic treatment [7]. The 3-5 days waiting period for results is the critical period for initial infection management, during which most of the clinicians use relatively broad-spectrum empirical antimicrobial therapy, which covers most of the causative pathogens.

The previous studies derived from Western population provided a leading consensus that Gram-positive aerobes, particularly Staphylococcus aureus (S. aureus), are the predominant causative organisms in DFI [8,9]. Furthermore, the frequency of methicillin-resistant S. aureus (MRSA) has increased dramatically over the past 15 years [5,10-12]. However, recent studies have demonstrated substantial variation in the etiology of DFI in different regions of the world. In contrast to Western population, investigations in Middle East, Asia, and Africa have found the most common isolates to be aerobic Gram-negative rods, particularly Pseudomonas aeruginosa [8,13-16]. The prevalence of causative organisms in DFI may vary from region to region, and empirical antibiotic therapy should be optimized for local clinical microbiology. Therefore, the objective of this study was to analyze the microbiologic profile of DFI in Korea.

Materials and Methods

Materials

Medical records of 745 patients with diabetic foot ulcers, who were admitted and treated at the Diabetic Wound Center of Korea University Guro Hospital between January 2011 and December 2015, were reviewed. A complete medical history was obtained at the first visit. For analysis of the demographic and clinical characteristics, 8 variables such as age, gender, smoking history, dialysis, HbA1C, wound duration, transcutaneous partial oxygen tension (TcpO2) and previous use of antibiotics were investigated (Table 1). For patients who were admitted several times for different episodes, only the first admission period was included in this study. This study protocol was approved by the Institutional Review Board of Korea University Guro Hospital.

Patient demographics

Microbiological methods

Only intraoperative samples collected from surgical procedures were included in the study. Surgical debridement was performed to remove all non-viable tissue from the wounds. Deep tissue and/or bone specimens were obtained and immediately stored in aseptic tube for culture. The specimens were sent to microbiologic laboratory in our hospital and incubated at 35°C for 24-48 hours in Sheep blood agar plate. Furthermore, MacConkey II agar plate was used for aerobes and Chocolate agar plate for anaerobes.

Results

Out of the 745 patients enrolled in this study, 613 patients (82.2%) had isolated causative organisms and 832 microbial isolates were identified which are presented in Table 2. Overall, 478 organisms (57.5%) were Gram-positive and 333 organisms (40.0%) were Gram-negative. In Gram-positive aerobes, MRSA was identified as the most commonly isolated organisms (13.7%) followed by Enterococcus faecalis (12.6%), Methicillin-sensitive S. aureus (MSSA) (12.5%), Streptococcus agalactiae (6.5%) and Methicillin-resistant Staphylococcus epidermidis (MRSE) (3.5%). With reference to the Gram-negative organisms, Pseudomonas aeruginosa was identified as the most commonly isolated organisms (9.4%) followed by Escherichia coli (7.2%), Klebsiella pneumonia (3.2%), Enterobacter cloacae (3.0%), and Serratia marcescens (2.4%).

Microorganisms isolated from wound

Discussion

Diabetic foot infection is common and complex public health problem, particularly of importance in diabetes mellitus patients [17]. To the best of our knowledge, this is the first single-center based microbiological study of DFI comprising of a large population in Korea (745 patients). Only deep tissue or bone culture obtained in operating room during surgical debridement were employed for this study, thus ensuring presence of reliable results on true pathogen of DFI.

The predominant causative microbiological organisms of DFI in Western population are Gram-positive aerobes, especially S. aureus, and the infection rate of MRSA has increased dramatically over the past 15 years [5,7,10,12-14,18]. A large multi-center study from the United States in 2008 discovered that 77% of DFIs were caused by Gram-positive aerobes, while 21.2% were caused by Gram-negative aerobes [9]. Analogously, a more recent multi-center study involving microbiological survey of DFI from Portugal revealed that 66% of DFIs were caused by aerobic Gram-positives, 19% by aerobic Gram-negatives, and 13.6% by obligate anaerobes [8].

On the other hand, recent studies have demonstrated different etiological distribution of causative organisms of DFI in different regions of the world [13-15,18,19]. Investigations from Middle East, Asia, and Africa have found the most common isolates to be aerobic Gram-negative rods, particularly Pseudomonas aeruginosa [8,13-16]. A large study from Kuwait on DFI found that the major proportion of DFIs (51.2%) were caused by aerobic Gram-negatives, while aerobic Gram-positives caused only 32.3% and obligate anaerobes only 15.3% [18]. Similarly, a recent study from India revealed that 51.4% of DFIs were caused by aerobic Gram-negatives, 33.3% were caused by aerobic Gram-positives and 15.3% were caused by anaerobic bacteria [20].

Our study found that Gram-positive aerobes (57.5%) were isolated more frequently than Gram-negative aerobes (40.0%) and MRSA (13.7%) was a predominant pathogen, but the proportion of MRSA was relatively small when compared to Western population (30.1-48.8%) [9,21,22].

This microbiological data was analyzed for comparing to our previous data obtained from same center in 2007, which estimated microbiological transition trend of diabetic foot infection. The distribution of microbial isolates between 2007 and 2016 is reported in Table 3. It can be seen from the data that the majority of identified organisms were Gram-positive (76.4% in 2007, 57.9% in 2016), and MRSA was most commonly isolated organisms (29.4% in 2007, 13.7% in 2016) which exhibited a decreasing trend in contrary to the data reported in most of the Western population. The rate of MRSA as a cause of DFI has increased in Western population in recent years [12]. In a study conducted in Manchester, UK in 2003, the rate of MRSA isolates was 30.2%, which was almost double the proportion of MRSA infected patients at their center 3 years back [10,11,20].

Comparative analysis with a previous study

On the other hand, Gram-negative aerobes (33.3% in 2007, 40.0% in 2016) and Pseudomonas aeruginosa (7.8% in 2007, 9.4% in 2016) exhibited a similar trend of occurrence like other Asian population. Recent prospective study conducted in India showed the isolation from DFI as 62% for all aerobic Gram-negatives, and 13% specifically for Pseudomonas aeruginosa [23]. This ratio is relatively higher than Western population. Published data in North America have reported the rate of Pseudomonas aeruginosa isolated from DFI as 4.5-6.5% [9,24,25]. Some studies suggested the reasons for the high prevalence of DFI in Asian population as compared to Western population, which include hot climatic conditions leading to foot sweating, use of poor footwear, a high incidence of patient self-treatment with antimicrobials, frequent foot washing, and suboptimal perineal/hand hygiene [26].

Current clinical guidelines, according to IDSA, for the management of DFI recommend empirical antibiotics classified by the fact whether Pseudomonas was isolated or not. The local rate of isolation of Pseudomonas is important for clinicians, because therapy directed for these species is usually different for other organisms

Conclusion

The results of microbiologic analysis in Korean DFI patients differ from the reports from Western population. Although MRSA was the most common causative organism, Pseudomonas had also been identified as a very important causative organism in Korea. These outcomes are expected to change empiric antibiotic therapy regimens for DFIs in Korea, as they need to be optimized for local clinical practice, and not only follow the guidelines of the Western population.

Notes

No potential conflict of interest relevant to this article was reported.

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Table 1.

Patient demographics

Variable Total (n = 745)
Age (year) 62 ± 12.1
Gender
 Male 540 (72.5%)
 Female 205 (27.5%)
Smoking history
 Yes 245 (32.9%)
 No 500 (67.1%)
Dialysis
 Yes 176 (23.6%)
 No 569 (76.4%)
HbA1C (%) 8.0 ± 1.8
Wound duration (week) 19.1 ± 8.3
TcpO2 (mmHg) 34.6 ± 20.7
Previous use of antibiotics
 Yes 534 (71.7%)
 No 211 (28.3%)

TcpO2, Transcutaneous partial oxygen tension.

Table 2.

Microorganisms isolated from wound

Name of isolates Number (%)
Gram positive aerobes 478 (57.5)
Staphylococcus aureus (MRSA) 114 (13.7)
Enterococcus faecalis 105 (12.6)
Staphylococcus aureus (MSSA) 104 (12.5)
Streptococcus agalactiae 54 (6.5)
Staphylococcus epidermidis (MRSE) 29 (3.5)
Corynebacterium striatum 14 (1.7)
Enterococcus faecium 8 (1.0)
Enterococcus faecium (VRE) 5 (0.6)
 Others 45 (5.4)
Gram negative aerobes 333 (40.0)
Pseudomonas aeruginosa 78 (9.4)
Escherichia coli 60 (7.2)
Klebsiella pneumonia 27 (3.2)
Enterobacter cloacae 25 (3.0)
Serratia marcescens 20 (2.4)
Proteus mirabilis 17 (2.0)
Acinetobacter baumannii 13 (1.6)
Citrobacter freundii 13 (1.6)
Morganella morganii ssp. morganii 12 (1.4)
Stenotrophomonas maltophilia 10 (1.2)
 Others 58 (7.0)
Fungal 9 (1.1)
Candida albicans 7 (0.8)
 Others 2 (0.2)
Anaerobes 12 (1.4)
Total 832

Table 3.

Comparative analysis with a previous study

Microorganism 2007 2016
Gram positive aerobes 76.4% 57.5%
Staphylococcus aureus (MRSA) 29.4% 13.7%
Staphylococcus aureus (MSSA) 15.6% 12.5%
Enterococcus faecalis 13.5% 12.6%
Streptococcus agalactiae 15.9% 6.5%
Corynebacterium striatum 2.0% 17.0%
Gram negative aerobes 33.3% 40.0%
Pseudomonas aeruginosa 7.8% 9.4%
Escherichia coli 7.3% 7.2%
Klebsiella pneumonia 6.9% 3.2%
Enterobacter cloacae 4.5% 3.0%
Serratia marcescens 4.3% 2.4%
Acinetobacter baumannii 2.3% 1.6%
Fungal 2.0% 1.1%
Anaerobes 0.0% 1.4%