A study on the relation of the severity of diabetic foot ulcers with the type of bacterial flora isolated from the wounds

Authors

  • Bikramjit Pal Assistant Professor, Department of Surgery, KPC Medical College, Jadavpur, Kolkata, India
  • Sumit Kumar Gupta Assistant Professor, Department of Surgery, KPC Medical College, Jadavpur, Kolkata, India

DOI:

https://doi.org/10.18203/2349-2902.isj20160224

Keywords:

Diabetic foot ulcer, Wagner classification of diabetic foot ulcers, Bacterial flora and diabetic wounds, Amputation and diabetic foot ulcer disease, Hospital stay and diabetic foot ulcer disease

Abstract

Background: The study is to determine the relation between severity of the diabetic foot ulcers and the organisms isolated from the wounds; its implications and prognosis with particular reference to the differences in the final outcome depending upon the type of organism infecting the wound. The study try to correlate the severity of the diabetic foot infection according to Meggit-Wagner classification, the incidence of amputation and the impact on the hospital stay with the difference of bacterial flora isolated from the wounds. This is an observational study done in 53 patients who were admitted in the surgical ward of a large private medical college in Jadavpur, India. It has been found from this study that the incidence and severity of diabetic foot ulcer is more in patients with some particular type of bacteria found in their wounds. A strong correlation is found in patients whose wounds were infected with some particular bacteria had resulted in more severe type of foot ulcers with higher incidence of amputation and concomitant longer hospital stay.

Methods: An observational study was done in 53 patients who were admitted in the surgical ward of a teaching hospital in Kolkata, India. The youngest patient was aged 28 years and the oldest patient was 83 years of age. All of them presented with clinically infected foot ulcers. The patients were explained about the study methods in their own language and due consent was taken. A standardized proforma in English, Hindi and the vernacular languages was made for recording the necessary data. The standard X-ray plates were taken into consideration for determination of the involvement of underlying bones. The microbiological studies were done in all patients from the wound swabs of the foot ulcers. The outcome of the diabetic foot ulcer was assessed from the severity of the disease, the presence of the different bacterial flora in their wounds, the incidence of amputation and the duration of hospital stay.

Results: The positive wound culture was found in 67.92 of patients, Methicillin resistant Staph. aureus (MRSA) was the commonest isolated organism (44.44%) followed by mixed bacterial flora (Staph. aureus, Streptococcus epidermidis, Peptococcus, and Bacteroides fragilis) in 16.98% of patients. ESBL Klebsiella was found in 13.89% of patients, Pseudomonas aeruginosa and Enterococcus feacalis were isolated in 8.33% of patients. 80% of ESBL infected wounds presented with Grade IV ulcers. The incidence of amputation was highest in patients whose wounds were colonized by MRSA and 60% of patients with ESBL Klebsiella infected wounds had hospital stay of more than three weeks.

Conclusions: The study observed that the prognosis and outcome of a diabetic foot ulcer vary considerably with the specific type of bacteria colonizing the wound.  

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References

Jeewanta M. A study to determine the knowledge and practice of foot care in patients with chronic diabetic ulcers. J Collaborative Research Int Med & Public Health. 2011;3(1).

Vishwanath V, Kumpatla S. Pattern and causes of amputation in diabetic patients – A multicentric study from India. J Assoc Physcians India. 2011;59:148-51.

Wagner FW. The Devascular Foot: A System for Diagnosis and Treatment. Foot Ankle. 1981;2(2):64-122.

Viswhanathan V. The Diabetic Foot: perspectives from Chennai, South India. Int J Low Extrem Wounds. 2007;6(1):34-6.

Voulgari C, Doupis J, Grigoropoulou P, Stylianou A, Georga A, Thomakos P. High rates of comorbid conditions in patients with type 2 diabetes and foot ulcers. Wounds. 2008;20:132-8.

Gershater L, Löndahl M, Nyberg P, Thörne J, Eneroth M. Complexity of factors related to outcome of neuropathic and neuroischaemic / ischaemic diabetic foot ulcers: a cohort study. Diabetologia. 2009;52:398-407.

Boulton, Young MJ, AJM, Medead AF. Amulticentre study of prevalence of diabetic peripheralneuropathyin the United Kingdom hospital clinic population. Diabetologia. 1993;36:150-4.

Umadevi S, Kumar S, Joseph NM, Easow JM, Kandhakumari G, Srirangaraj S, et al. Microbiological study of diabetic foot infections. Indian Journal of Medical Specialities 2011;2(1):12-7.

Babypadmini S, Appalaraju B. Extended-spectrum β-lactamases in urinary isolates of Escherichia coli and Klebsiella pneumoniae - prevalence and susceptibility pattern in a tertiary care hospital. Indian J Med Microbiol. 2004;22:172-4.

Mathai D, Rhomberg PR, Bledenbach DJ, Jones RN. Evaluation of the in vitro activity of six broad-spectrums beta-lactam antimicrobial agents against recent clinical isolates from India; A survey of ten medical center laboratories. Diagn Microbiol Infect Dis. 2002;44:367-77.

Mansouri M, Ramazanzadeh R. Spread of extended-spectrum β-lactamase producing Escherichia coli clinical isolates in Sanandaj hospitals. J Biol Sci. 2009;9:362-6.

Selvakumar BN, Jasmine R. Antibiotic susceptibility of ESBL-producing urinary isolates at a tertiary care hospital in Tiruchirappali, South India. J Med Sci. 2007;7:443-6.

Arabaci F, Oldacay M, Berber D. Evaluation of ESBL positivity rates for Escherichia coli and Klebsiella pneumoniae strains with the sensititre ESBL antimicrobic susceptibiity plates in a public hospital, Turkey. J Med Sci. 2009;9:103-7.

Ramani A, Ramani R, Shivananda PG, Kundaje GN. Bacteriology of diabetic foot ulcers. Indian J Pathol Microbiol. 1991;34(2):81-7.

Bansal E, Garg A, Bhatia S, Attri A. Spectrum of microbial flora, in diabetic foot ulcers. Ind J of Microbiology and Pathology. 2008;51(2):204-8.

Lavery LA, Fontaine JL, Bhavan K, Kim PJ, Williams JR, Hunt NA. Risk factors for methicillin-resistant Staphylococcus aureus in diabetic foot infections. Diabet Foot Ankle. 2014;5:10.

Papia G, Louie M, Tralla A, Johnson C, Collins V, Simor AE. Screening high-risk patients for methicillin-resistant Staphylococcus aureus on admission to the hospital: is it cost effective? Infect Control Hosp Epidemiol. 1999;20:473-7.

Reddy SL, Grayson AD, Smith G, Warwick R, Chalmers JA. Methicillin resistant Staphylococcus aureus infections following cardiac surgery: incidence, impact and identifying adverse outcome traits. Eur J Cardiothorac Surg. 2007;32:113-7.

Aragon-Sanchez J, Lazaro-Martinez JL, Quintana-Marrero Y. Are diabetic foot ulcers complicated by MRSA osteomyelitis associated with worse prognosis? Outcomes of a surgical series. Diabet Med. 2009;26:552-5.

Shahi SK, Singh VK, Kumar A, Khan AU. Detection of Escherichia coli and Associated β-Lactamases Genes from Diabetic Foot Ulcers by Multiplex PCR and Molecular Modeling and Docking of SHV-1, TEM-1, and OXA-1 β-Lactamases with Clindamycin and Piperacillin-Tazobactam. PLoS One. 2013;8(7):e68234.

Kiratisin P, Apisarnthanarak A, Laesripa C, Saifon P. Molecular characterization and epidemiology of extended-spectrum ß-lactamase producing Escherichia coli and Klebsiella pneumoniae isolates causing health care-associated infection in Thailand, where the CTX-M family is endemic. Antimicrob Agents Chemother. 2008;52:2818-24.

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Published

2016-12-13

How to Cite

Pal, B., & Gupta, S. K. (2016). A study on the relation of the severity of diabetic foot ulcers with the type of bacterial flora isolated from the wounds. International Surgery Journal, 3(1), 189–194. https://doi.org/10.18203/2349-2902.isj20160224

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Original Research Articles