Epidemiology and susceptibility profiles of diabetic foot infections in five hospitals in Lebanon

Similar documents
Foot infections are now among the most

Foot infections in persons with diabetes are

Aerobic bacteria isolated from diabetic septic wounds

BACTERIOLOGICAL PROFILE OF DIABETIC FOOT INFECTIONS

Aerobic bacterial Profile of Diabetic Foot Ulcers and their Antibiotic Sensitivity Pattern

Analysis on distribution, drug resistance and risk factors of multi drug resistant bacteria in diabetic foot infection.

Correlation between the Treatment Result and Causative Bacteria in Amputation of Diabetic Foot

ISSN X (Print) Research Article

Prevalence of Bacteria Isolated from Type 2 Diabetic Foot Ulcers and the Antibiotic Susceptibility Pattern

Bone and Joint Infections in Diabetics: Diagnosis and Management of Diabetic Foot and Other Common Lower Extremity Infections

Treatment of febrile neutropenia in patients with neoplasia

Isolation and identification of bacterial pathogens from wounds of diabetic patients

Bacteriological Profile in Patients with Diabetic Foot Ulcers with special reference to their antibiotic sensitivity pattern

International Journal of Pharma and Bio Sciences

Bacteriology of Diabetic Foot Ulcer among an Egyptian Population: A Retrospective Study

Antimicrobial Guidelines for the Empirical Management of Diabetic Foot Infections

ORIGINAL ARTICLE SUSCEPTIBILITY PATTERNS IN GRAM NEGATIVE URINARY ISOLATES TO CIPROFLOXACIN, CO-TRIMOXAZOLE AND NITROFURANTOIN

Prevalence of ESBL producing enterobacteriaceae in diabetic foot ulcers

Comparison of bacterial etiology of non-healing ulcers in diabetic and non- diabetic patients.

University of Alberta Hospital Antibiogram for 2007 and 2008 Division of Medical Microbiology Department of Laboratory Medicine and Pathology

Sep Oct Nov Dec Total

Abstract. Introduction

Study on Bacterial Spectrum of Organism Causing Diabetic Foot Ulcers with its Antibiogram in Dr. B.R. Ambedkar Medical College, Bangalore, India

Diabetic Foot Infections

Microbiology and Treatment of Diabetic Foot Infections

Clinical observation study in 624 patients confirms good efficacy and tolerability

Author: Souha Kanj Andrew Whitelaw Michael J. Dowzicky. To appear in: International Journal of Antimicrobial Agents

JMSCR Vol 06 Issue 03 Page March 2018

Clinical observation study in 624 patients confirms good efficacy and tolerability

Affinity of Doripenem and Comparators to Penicillin-Binding Proteins in Escherichia coli and ACCEPTED

Cefotaxime Rationale for the EUCAST clinical breakpoints, version th September 2010

Microbiological Profile of Diabetic Foot Ulcer and Use of IL6 as a Predictor for Diabetic Foot Infection

INVESTIGATING: WOUND INFECTION

Bacteriology of Diabetic Foot Ulcers with Reference to Multidrug Resistance Strains at the Yaounde Central Hospital (Cameroon)

Mupirocin Rationale for the EUCAST clinical breakpoints, version th July 2010

Original article. Microorganisms Isolated From Foot Ulcers Infection Of Diabetic Iraqi Patients. Summary:

Tigecycline activity tested against 26, 474 bloodstream infection isolates: a collection from 6 continents

Laboratory CLSI M100-S18 update. Paul D. Fey, Ph.D. Associate Professor/Associate Director Josh Rowland, M.T. (ASCP) State Training Coordinator

Received 30 March 2005; returned 16 June 2005; revised 8 September 2005; accepted 12 September 2005

JMSCR Vol 05 Issue 08 Page August 2017

Bacteriological Profile of Post Traumatic Osteomyelitis in a Tertiary Care Centre

2012 Infectious Diseases Society of America Clinical Practice Guideline for the Diagnosis and Treatment of Diabetic Foot Infections a

(multidrug-resistant Pseudomonas aeruginosa; MDRP)

Outcome in Patients of Diabetic Foot Infection with Multidrug Resistant Organisms

A Decade of Limb Salvage Surgery. learning lessons afterwards

Characteristics of bacterial infection in patients with diabetic foot and its relationship with degree of vascular lesions in lower extremities.

Antibiotic Resistance Pattern of Blood and CSF Culture Isolates At NHLS Academic Laboratories (2005)

Bacterial distribution, changes of drug susceptibility and clinical characteristics in patients with diabetic foot infection

PATHWAY #4 DIABETIC FOOT DISORDERS VOLUME 45, NUMBER 5, SEPTEMBER/OCTOBER 2006 S 29

Culture of per-wound bone specimens: a simplified approach for the medical management of diabetic foot osteomyelitis

Objectives. Define classes of uncomplicated skin and soft tissue infection (SSTI) that drive empiric antimicrobial selection

Comparison of Super-oxidized Solution versus Povidone Iodine in Management of Infected Diabetic Ulcers: Our Experience

Activity of Ceftolozane/Tazobactam Against a Broad Spectrum of Recent Clinical Anaerobic Isolates

Clinical experience with ceftazidime in urology in Japan

Prevalence of Extended Spectrum -Lactamases In E.coli and Klebsiella spp. in a Tertiary Care Hospital

Giving the Proper Dose: How Can The Clinical and Laboratory Standards Institute(CLSI)Help?

Cefuroxime iv Rationale for the EUCAST clinical breakpoints, version th September 2010

Management of Diabetic Foot Ulcers. {Original Article (Diabetic Foot Ulcers)} 1. Ansar Latif 2. Anila Ansar 3. Sadia Waheed 4. Abdul Hamid ABSTRACT

Comparison of the Microbiology and Antibiotic Treatment Among Diabetic and Nondiabetic Patients Hospitalized for Cellulitis or Cutaneous Abscess

Surveillance of Surgical Site Infection in Surgical Hospital Wards in Bulgaria,

Bloodstream infection has been a primary

SURGICAL ANTISEPSIS. Overview FOUNDATIONS OF OPTOMETRIC SURGERY. Richard E. Castillo, OD, DO Consultative Ophthalmology and Procedural Optometry

UPDATES IN ANTIBIOTIC THERAPY OF BILIARY TRACT INFECTIONS

Efficacy of fresh Aloe vera gel against multi- drug resistant bacteria in infected leg ulcers

Wounds and Infections: Wound Management From the ID Physician Standpoint. Alena Klochko, MD Orlando VA Medical Center Infectious Disease Department

International Journal of Health Sciences and Research ISSN:

27/11/2012. Parainfuenza 1, 2 3 Rhinovirus Coronavirus Adenovirus Respiratory syncytial virus (RSV) Chlamydophila pneumoniae Mycoplasma pneumonite

CAP, HCAP, HAP, VAP. 1. In 1898, William Osler described community-acquired pneumonia as:

Microbiology and Antimicrobial Therapy for Diabetic Foot Infections

1430 West McCoy Lane Santa Maria, CA p:

Rochester Patient Safety C. difficile Prevention Collaborative: Long Term Care Antimicrobial Stewardship (funded by NYSDOH)

Jääskeläinen, Iiro H.

Clinical Comparison of Cefotaxime with Gentamicin plus Clindamycin in the Treatment of Peritonitis and Other Soft-Tissue Infections

Urinary Tract Infections: From Simple to Complex. Adriane N Irwin, MS, PharmD, BCACP Clinical Assistant Professor Ambulatory Care October 25, 2014

Changes in Etiologic Microorganisms in Thai Patients with Chemotherapy-Induced Neutropenia and Fever

Surveillance of Healthcare Associated Infections in Scottish Intensive Care Units

Outpatient treatment in women with acute pyelonephritis after visiting emergency department

A one year cross sectional study on role of Wagner s classification in predicting the outcome in diabetic foot ulcer patients

A Clinico-microbiological Study of Diabetic Foot Ulcers in an Indian Tertiary Care Hospital

2008 American Medical Association and National Committee for Quality Assurance. All Rights Reserved. CPT Copyright 2007 American Medical Association

Annual Surveillance Summary: Klebsiella species Infections in the Military Health System (MHS), 2017

Clinico-bacteriological study of diabetic foot: an observational study

Bacteriological Profile of Chronic Rhino Sinusitis

ESCMID Online Lecture Library. by author

Urinary tract infection. Mohamed Ahmed Fouad Lecturer of pediatrics Jazan faculty of medicine

EMPIRICAL TREATMENT OF SELECT INFECTIONS ADULT GUIDELINES. Refer to VIHA Algorithm for the empiric treatment of Urinary Tract Infection

Consultation on the Revision of Carbapenem Breakpoints

No Need to Agonize! Tips for the Diagnosis and Treatment of Complicated UTIs

Pressure Injury Complications: Diagnostic Dilemmas

Infections In Cirrhotic patients. Dr Abid Suddle Institute of Liver Studies King s College Hospital

December 3, 2015 Severe Sepsis and Septic Shock Antibiotic Guide

Ailyn T. Isais-Agdeppa, MD*, Lulu Bravo, MD*

HUSRES Annual Report 2009 Martti Vaara

Pneumonia Community-Acquired Healthcare-Associated

Sensitivity of Surveillance Testing for Multidrug-Resistant Gram-Negative Bacteria in the

Disclosures. Outpatient NPWT Options Free up Hospital Beds, but Do They Work? Objectives. Clinically Effective: Does it Work?

Diagnosis and Treatment of Diabetic Foot Infections

My Diabetic Patient Has No Pulses; What Should I Do?

Helen Heffernan and Rosemary Woodhouse Antibiotic Reference Laboratory, Institute of Environmental Science and Research Limited (ESR); July 2014.

Pharmacologyonline 1: (2010) ewsletter Singh and Kochbar. Optimizing Pharmacokinetic/Pharmacodynamics Principles & Role of

Transcription:

Original Article Epidemiology and susceptibility profiles of diabetic foot infections in five hospitals in Lebanon Michele Obeid 1, Eric Moughames 1, Petra Aboulhosn 1, Rashad Madi 1, Maya Farah 2, Jinia Feghali 2, Jacques Mokhbat 3, Anna Farra 3, Rima Moughnieh 4, Ziad Daoud 5, Rita Feghaleh 6, Edmond Abboud 7, Emma Abboud 8, Rola Husni-Samaha 3 1 Gilbert and Rose-Mary Chaghoury School of Medicine, Lebanese American University, Byblos, Lebanon 2 Department of Dermatology, Lebanese American University Medical Center, Beirut, Lebanon 3 Department of Internal Medicine, Division of Infectious Diseases, Lebanese American University Medical Center, Beirut, Lebanon 4 Department of Infectious Diseases, Makassed Hospital, Beirut, Lebanon 5 Department of Microbiology, Faculty of Medicine, University of Balamand and Centre Hospitalier du nord Hospital, Beirut, Lebanon 6 Department of Microbiology, Rafik Hariri University Hospital, Beirut, Lebanon 7 Department of Microbiology, Middle East Institute of Health, Mount Lebanon, Lebanon 8 Department of Microbiology, Mount Lebanon Hospital, Beirut, Lebanon Abstract Introduction: Approximately 80% of diabetes-related lower extremity amputations are preceded by a foot ulcer. Global studies on the epidemiology of diabetic foot ulcer (DFU) infections and guidelines detailing the most common pathogens and their respective antimicrobial susceptibilities are available. While Gram-positive cocci, mainly Staphylococcus species (spp.), were the most common organisms cultured from DFU in the United States, the Gram-negative Pseudomonas spp. were found to be the most common in some Middle Eastern countries. In Lebanon, however, such studies remain scarce. This study, conducted in Lebanon, investigated the most common organisms in DFU infections and their antimicrobial profiles. Methodology: We collected data from all documented diabetic foot infections between January 2015 and March 2016, 128 participants total, from 5 different hospitals in various regions of Lebanon. Results: Among all isolates, Enterobacteriaceae (42%), Pseudomonas spp. (18.6%) and methicillin-sensitive Staphylococcus aureus (MSSA) (15.3%) were the most frequent bacteria. In addition, 72% of Pseudomonas spp. were susceptible to ciprofloxacin and 63.6% of Enterobacteriaceae were susceptible to either amoxicillin/clavulanate or ciprofloxacin, 91% were susceptible to piperacillin/tazobactam. Methicillin-resistant Staphylococcus aureus (MRSA) was only found in hospitalized patients or those who received prior antibiotics. Polymicrobial infections were documented in only 38% of patients. Conclusion: In Lebanon, the most appropriate empirical oral outpatient treatment would be a combination of amoxicillin/clavulanate and ciprofloxacin. As for admitted patients who have failed the oral regimen, piperacillin/tazobactam would then be the treatment of choice. Key words: diabetes; foot; infection; Lebanon; antibiotics. J Infect Dev Ctries 2018; 12(5):347-351. doi:10.3855/jidc.10063 (Received 14 December 2017 Accepted 17 April 2018) Copyright 2018 Obeid et al. This is an open-access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Introduction Diabetes mellitus (DM) is a chronic disease and one of the leading causes of limb loss, currently affecting 382 million people worldwide [1]. It is predicted that by 2035, reported diabetes cases will reach 592 million [1]. The World Health Organization predicts that DM will be the seventh leading cause of death by 2030 [1]. In DM patients, when a foot ulcer develops; infection and peripheral artery disease are the major complications leading to subsequent amputation. Approximately 80% of diabetes-related lower extremity amputations are preceded by a foot ulcer [1]. Foot infections are a common and serious problem in diabetic patients. A classification system, specifying the depth and the severity of the foot infection, along with a vascular assessment helps determine which patients should be hospitalized and if they require special radiologic imaging or surgical intervention. According to the American Family Physician Association, the most common pathogens in diabetic

foot infections are aerobic Gram-positive cocci, mainly Staphylococcus spp. [2]. More specifically, methicillinresistant Staphylococcus aureus (MRSA) is present in 10% to 32% of American diabetic s foot ulcer infections [2]. However, data has shown that moderate to severe infections and wounds that were previously treated with antibiotics are often polymicrobial, often including Gram-negative bacilli [2]. Moreover, obligate anaerobes may become co-pathogens in ischemic or necrotic wounds [3]. In a study conducted in Turkey [4], Pseudomonas spp. were the most frequently isolated organisms followed by S. aureus. Gram-positive and Gram-negative isolates represented 38.7% and 61.3% of the isolates, respectively. In addition, among the S. aureus isolates, MRSA scored as high as 44.2% [4]. Wound cultures usually take two to three days to produce results. In some instances, incubation is extended to give more opportunity for anaerobic bacteria to grow or to better assess the multiple organisms that are growing. This is why an empirical antimicrobial therapy that treats the most probable pathogens, and can be administered immediately, is key for the best management of diabetic foot ulcer infections [4]. As suggested by the Infectious Diseases Society of America (IDSA), the empirical antibiotic treatment for mild diabetic foot infections is dicloxacillin, clindamycin, cephalexin, levofloxacin, or amoxicillincalvulanate, assuming that the most probable pathogens are methicillin-sensitive Staphylococcus aureus (MSSA) and Streptococcus spp.. When MRSA is suspected, doxycycline and trimethoprim/sulfamethoxazole should be considered [3]. While according to the Scottish diabetic group, in antibiotic naïve patients, the most likely pathogens are beta-hemolytic streptococci [5]. The primary antibiotic is oral flucloxacillin with an increased prevalence of resistance after the first exposure to flucloxacillin. In a patient who is not antibiotic naïve (i.e. people with chronic infections, and have received antibiotics previously), infections are more likely to be polymicrobial and include aerobic Gram-negative bacilli. In that case, the first line of treatment is amoxicillin clavulanate [5]. DM affects developing countries disproportionately as more than 80% of diabetes deaths occur in low- and middle-income countries [1]. Some studies have shown that diabetes related complications are common in the Arab world with a higher prevalence in eastern Arab countries [6]. In Lebanon, epidemiological data about etiology and susceptibility profiles of bacteria that cause diabetic foot ulcers in in- and out-patients remains scarce. Some health care practitioners follow the American guidelines for treatment of diabetic foot ulcers while others follow the European guidelines. Local data and studies are crucial to empirical treatment and development of guidelines, which are essential in our fight against antimicrobial resistance in this region. DFU infections are one of the most serious infections in our country, so we decided to conduct a prospective multicenter study to document the local prevalence of the most common organisms incriminated in DFU infections along with their antimicrobial profiles. Methodology In our study, we collected demographic and microbiological data of all documented diabetic foot infections during the period between January 2015 and March 2016 from 5 different hospitals across various regions in Lebanon: 1-Mount Lebanon Hospital (City: Hazmieh, Governate: Mount Lebanon) 2- University Medical Center- Rizk Hospital (UMC-RH) (City: Beirut, Governate: Beirut) 3-Middle East Institute of Health (MEIH) (City: Bsalim, Governate: Mount Lebanon) 4-Sacré Coeur Hospital (City: Baabda; Governate: Mount Lebanon) 5-Nini Hospital (City: Tripoli; Governate: North) The research included 128 participants in total, outpatient and inpatient. Data collected included: Peripheral vascular disease Previous hospitalization in the past 3 months Previous antibiotics in the past 3 months Previous surgeries in the same area as the infection in the past 3 months Superficial culture samples were collected from all participants. Species identification and antibiograms were performed in the laboratories where the specimens were collected. However, susceptibility testing used either the European Committee on Antimicrobial Susceptibility Testing (EUCAST) or Clinical & Laboratory Standards Institute (CLSI) breakpoints. All data were entered, quantified and analyzed using Microsoft Excel. Results A total of 128 wound cultures from diabetic foot ulcers were collected from 128 patients between January 2015 and March 2016. In this study, the 128 patients were divided into two groups: those who had been hospitalized or have received antibiotics in the past 3 months (Group A; 66 patients (51.6%)); and those who had not (Group B; 62 patients (48.4%)). 348

Among the 128 culture samples, a total of 182 bacteria were identified. Of the 128 samples, 49 (38%) were found to have polymicrobial infections. Among Group A, 20 patients (30.3%) and among Group B, 28 patients (45%) carried polymicrobial DFU infections. From the collected organisms, there were 60 (33%) Gram-positive isolates, 120 (66%) Gram-negative isolates and 2 (1%) yeasts. Among all isolates, Pseudomonas spp. (n = 34, 18.6%) and MSSA (n = 28, 15.3%) were the most common bacteria, followed by Proteus spp. (n = 23; 12.6%) and E. coli (n = 22; 12.1%) (Figure 1). It is important to note that from the polymicrobial isolates 74% were Enterobacteriaceae, 39% were Pseudomonas spp. and 11% were MRSA. Amongst all the isolates, 34 (18.7%) were S. aureus; of those, 28 were MSSA and 6 were MRSA. S. aureus was the most commonly isolated Gram-positive organism (57%), of which 17.6% were MRSA. Enterococcus spp. (n = 11; 18%) was the second most isolated (Figure 2). Of the S. aureus isolated from patients in Group A, 6 (42.9%) were MRSA. Of the MRSA, 5 were tested for clindamycin susceptibility, of which 4 (80%) were susceptible and 1 (20%) was resistant. MSSA showed 100% susceptibility to clindamycin. It is important to note that MRSA were only found in Group A patients. The most common Gram-negative isolate was Pseudomonas spp. (including P. aeruginosa) (28%) followed by E. coli (19%) and Proteus spp. (17%). Of Pseudomonas spp. Tested, 69% were susceptible to ciprofloxacin and 28% were resistant, whereas 3% had intermediate susceptibility. Escherichia coli, Klebsiella, Proteus, Enterobacter, Serratia, Citrobacter constituted 42% of the pathogens collected from the patients in this study. The data showed that 48.6% of the Enterobacteriaceae tested were susceptible to ciprofloxacin. Of the 38 Enterobacteriaceae isolated in Group A ulcers, 16 (42%) were susceptible to ciprofloxacin. Out of 32 Enterobacteriaceae isolated from Group B ulcers, 18 (56%) were susceptible to ciprofloxacin. In addition, 96%, 91%, 70% and 43.7% of all Enterobacteriaceae tested were susceptible to imipenem, piperacillin/tazobactam, ceftazidime and amoxicillin/clavulanate, respectively. Also, 63.6% were susceptible to ciprofloxacin and/or amoxicillin/clavulanate. Figure 1. Number of pathogens isolated in the study. data, collected form 5 different hospitals in Greater Beirut, Tripoli and Mount Lebanon, showed different results. Among 182 species isolated, 66% were Gramnegative bacteria, compared to 61.3% in a study done in Turkey [4]. Our results also showed that of the 128 patients, 38% had polymicrobial infections, a finding that was in accordance with a similar study by Tiwari et al. [7]. Interestingly, patients who had neither been admitted to the hospital nor had received antibiotics in the past 3 months, had more polymicrobial infections. This may be due to prior antibiotic treatment selecting for one single organism. Pseudomonas spp. were the most common (28%) among the Gram-negative organisms, followed by E. coli (19%). The increased incidence of Pseudomonas spp. has been reported in another study conducted in Turkey which reported 48.7% of Pseudomonas spp. among Gram-negatives and 29.8% among all isolates, compared to 18.6% in our study [4]. Similar results have been reported in other parts of the world such as India, where a study showed that the most commonly Figure 2. Overall Gram-positive percentages. Discussion Most studies on diabetic foot ulcer infections reports that Gram-positive cocci are the most common organisms, followed by Gram-negative organisms. Our 349

isolated pathogen was Pseudomonas aeruginosa, constituting 20.1% of all isolated pathogens [8]. In a similar study from Kuwait on the microbiology of diabetic foot infections, Pseudomonas aeruginosa constituted 17.4% of all isolates [9]. These results common among developing countries, possibly explained by the poor water sanitation systems and increased temperatures and humidity in these regions. Conditions where Pseudomonas spp. will be more likely to colonize and cause infections in diabetic patients than in developed countries with colder climates and where water sanitation systems is quality controlled. Furthermore, the data collected in this study showed that a high percentage of Pseudomonas spp. (72%) were susceptible to ciprofloxacin, and these numbers are similar in Group A (61% susceptible to ciprofloxacin) and Group B (75% susceptible to ciprofloxacin). These findings indicate that ciprofloxacin should be included as part of the empirical treatment for diabetic foot infections in an outpatient setting in Lebanon to better cover the frequent Pseudomonas spp. infections. Reviewing data related to Enterobacteriaceae collected from diabetic foot ulcer infections, there was a good susceptibility (96%, 91% and 70%) of these organisms to imipenem, piperacillin/tazobactam and ceftazidime, respectively. However, the susceptibility of Enterobacteriaceae to ciprofloxacin was only 48.6%. These numbers show that Enterobacteriaceae has significant resistance to ciprofloxacin in Lebanon, and the combination of ciprofloxacin and amoxicillin/clavulanate provide better coverage for our patient population (63.6%). Piperacillin/tazobactam is more likely to be used as an empirical therapy for inpatients who were admitted due to failure of the oral regimen. Moreover, while S. aureus are the most prevalent pathogens in diabetic foot infections in the Western world, in Lebanon these constituted only 18.7% of overall isolates, a number similar to that found in a study in 35 centers in Turkey, which revealed that only 11.4% of the isolates were S. aureus [10]. Of the S. aureus isolated in our study, 17.6% were MRSA compared to 44.2% in another study done in Turkey [4]. Additionally, MRSA was only found in Group A patients. Rates of MRSA in Lebanon (3.3% of all isolates) are significantly lower than in Western countries where some studies found MRSA in 32% of all diabetic foot infections [2,11]. A study done in Israel found MRSA in only 3% of diabetic foot ulcer infections [12]. Therefore, since S. aureus does not constitute one of the most common pathogens isolated from diabetic foot ulcers in our study, MRSA coverage should only be considered for patients with high risk of acquiring the bacteria. Those are patients with prior use of antibiotics, previous hospitalization [13], long duration of foot infection, deeper ulcers reaching bone with signs of osteomyelitis and positive nasal MRSA carriage [11]. This study had some limitations, the most significant one being the small sample size. Despite the fact that the clinical data collected was from 5 major hospitals in Beirut, Tripoli and Mount Lebanon, representing 3 of the 5 regions in Lebanon, these hospitals are considered referral centers, so the population studied may cover more regions in Lebanon. Next, most Lebanese laboratories take diabetic foot ulcer culture samples from superficial tissue instead of collecting deeper specimens. However, with only 38% of cultures taken found to be polymicrobial, and single isolates were pathogenic organisms, we can assume that the organisms cultured were the true pathogens. In fact, S. epidermidis which is a widespread skin colonizer, was infrequently isolated (3%) in our study. Also, although some laboratories used EUCAST breakpoints while others used CLSI breakpoints, the latest guidelines of both were very similar to each other [14]. Finally, some laboratories reported only species of certain organisms but this did not affect our results and the data were sufficient to be analyzed as documented above. Conclusion Our study demonstrates that in Lebanon, Gramnegatives are the most common organisms isolated from DFU infections with Pseudomonas spp. being the most common followed by E. coli. In the era of antimicrobial resistance, combined treatment may provide a solution. Pseudomonas spp. were shown to have high susceptibility to ciprofloxacin, however in order to also cover the highly prevalent Enterobacteriaceae, the combination of amoxicillin/clavulanate and ciprofloxacin would be the recommended empirical regimen for outpatients. As for patients who are admitted due to failure of that oral regimen, piperacillin/tazobactam is then recommended. MRSA was found to be less frequent in Lebanon and should be empirically treated in high risk patients only. These results may be an incentive to check local DFU susceptibilities in the neighboring countries, instead of using European and American guidelines that do not necessarily apply. Obviously, the epidemiology of DFU differs from one country to another; therefore, local guidelines for treating diabetic foot infections are 350

needed in Lebanon and should be periodically revised because of the changing nature of bacterial resistance. References 1. Hingorani A, LaMuraglia G, Henke P, Meissner M, Loretz L, Zinszer K, Driver V, Frykberg R, Carman T, Marston W, Mills J, Murad MH (2016) The management of diabetic foot: A clinical practice guideline by the Society for Vascular Surgery in collaboration with the American Podiatric Medical Association and the Society for Vascular Medicine. J Vasc Surg 63: Suppl 2: 3-21. 2. Gemechu FW, Seemant F, Curley CA (2013) Diabetic foot infections. Am Fam Physician 88: 177-184. 3. Lipsky BA, Berendt A, Cornia P, Pile J, Peters E, Armstrong D, Deery G, Embil J, Joseph W, Karchmer A, Pinzur M, Senneville E (2012) 2012 Infectious Diseases Society of America Clinical Practice Guideline for the Diagnosis and Treatment of Diabetic Foot Infections. Clin Infect Dis 54: 32-73. 4. Turhan V, Mutluoglu M, Acar A, Hatipoğlu M, Önem Y, Uzun G, Ay H, Öncül O, Görenek L(2013) Increasing incidence of Gram-negative organisms in bacterial agents isolated from diabetic foot ulcers. J Infect Dev Ctries 7: 707-712. doi: 10.3855/jidc.2967. 5. Edmonds M, Doxford M, Londahl M, Apelqvist J, Leese G, Nathwani D (2009) Opinions on antibiotic therapy for the infected diabetic foot. Diabetic Foot J 12: 112-118. 6. Al-Wahbi AM (2006) The diabetic foot. In the Arab world. Saudi Med J 27: 147-53. 7. Tiwari S, Pratyush D, Dwivedi A, Gupta S, Rai M, Singh S (2012) Microbiological and clinical characteristics of diabetic foot infections in northern India. J Infect Dev Ctries 6: 329-332. doi: https://doi.org/10.3855/jidc.1827 8. Hayat A, Masood N and Shaik N (2011) Study for microbiological pattern and in vitro antibiotic susceptibility in patients having diabetic foot infections at tertiary care hospital in Abbottabad. Worl Appl Sci J 12: 123-131. 9. AL-Benwan K, AL-Mulla A, and Rotimi VO (2012) A study of the microbiology of diabetic foot infections in a teaching hospital in Kuwait. J Infect Public Heal 5: 1-8. 10. Hatipoglu M, Mutluoglu M, Turhan V, Uzun G, Lipsky B, Sevim E, Demiraslan H, Eryilmaz E, Ozuguz C, Memis A, Ay H, Arda B, Uysal S, Motor V, Kader C, Erturk A, Coskun O, Sengoz G (2016) Causative pathogens and antibiotic resistance in diabetic foot infections: A prospective multi-center study. J Diabetes Complicat 30: 910-916. 11. Stanaway S, Johnson D, Moulik P, Gill G (2007) Methicillinresistant Staphyloccocus aureus (MRSA) isolation from diabetic foot ulcers correlates with nasal MRSA carriage. Diabetes Res Clin Pr 75: 47-50. 12. Katz DE, Friedman ND, Ostrovki E, Ravid D, Amrami N, Avivi D, Mengesha B, Zaindenstein R, Lazarovitch T, Dadon M, Marchaim D (2016) Diabetic foot infection in hospitalized adults. J Infect Chemother 22: 167-173. 13. Lavery LA, Fontaine J, Bhavan K, Kim PJ, William JR, Junt NA (2014) Risk factors for methicillin-resistant Staphylococcus aureus in diabetic foot infections. Diabetic Foot Ankle 5 (1): 23575 14. Turnidge J and Paterson DL (2007) Setting and revising antibacterial susceptibility breakpoints. Clin Microbiol Rev 20: 391-408 Corresponding author Rola Husni-Samaha, MD Chief of Infectious Diseases Head of Infection Control Lebanese American University Medical Center- Rizk Hospital Zahar Street, Achrafieh Beirut, Lebanon P.O. Box 11-3288 Phone: +9613924800 Fax: +961 1 200816 Email: roula.samaha@umcrh.com Conflict of interests: No conflict of interests is declared. 351