Original Research Article
DOI: http://dx.doi.org/10.18203/issn.2455-4510.IntJResOrthop20184389
A prospective study on results of bacterial culture from wound in type III compound fractures
Department of Orthopaedics, Government Medical College, Kottayam, Kerala, India
Received: 14 August 2018
Revised: 14 October 2018
Accepted: 15 October 2018
*Correspondence:
Dr. George Thomas,
E-mail: shawnshema@yahoo.com
Copyright: © the author(s), publisher and licensee Medip Academy. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
ABSTRACT
Background: Open fractures still represent a major challenge for the treating surgeon. Sound knowledge of the bacteriological epidemiology and antimicrobial susceptibility helps to prevent complications. Our aim is to study about the common bacteria causing open fracture infection and their antibiotic sensitivity in patients who are admitted in the department of Orthopedics, Government medical college, Kottayam.
Methods: A prospective study on 130 patients with type III open long bone fractures were studied for infection during study period of June 2016 to July 2017. After initial debridement and at third day during follow up wound inspection, swabs were taken from wound site. Swabs were send for microscopic examination, culture and antimicrobial susceptibility testing.
Results: Out of 130 type III open long bone fractures, 7.7% were having day 0 infection and 25.4% were having day 3 infection. 19.2% of patients developed infection from day 3 onwards. Staphylococcus aureus (37.1%) was the most commonly isolated bacteria from wound. Other organisms isolated were Acinetobacter, Pseudomonas, Klebsiella, E coli, Enterococcus, Streptococcus and Enterobacter. 100% of diabetic patients developed infection on day 3. Gentamicin, amikacin doxycycline, ciprofloxacin, vancomycin, piperacillin + tazobactum and cefoperazone + sulbactum were found to be effective against isolated organisms.
Conclusions: Gram positive Staphylococcus aureus was found to be the most common cause of wound infection in type III open fractures. An early adequate wound debridement, proper antibiotic therapy and aseptic post-operative wound care are essential for wound healing and fracture union in an open fracture.
Keywords: Open fracture, Infection, Antimicrobial susceptibility
INTRODUCTION
An open fracture is defined as an injury where the fracture and the fracture hematoma communicate with the external environment through a traumatic defect in the surrounding soft tissues and overlying skin. Apart from severe bone and soft tissue involvement, these injuries have other risk factors such as skin degloving, soft tissue crushing, contamination with dirt and debris and injury to neurovascular structures. Hence they are associated with a high risk of complications, including infection, non-union and amputation. 60–70% of compound fractures are believed to be contaminated with bacteria at the time of injury from both skin and environment. Infection of open fractures depends on the microbial and host factors.1
Open fractures have significant importance as poor outcome of treatment is associated with poor health status. Majority of open fractures are due to high velocity trauma like road traffic accidents especially in males of productive age group. These fractures frequently results in long term disability with potentially severe economic impact on the patient. According to Lee et al, wound infecting pathogens differ from country to country and from one hospital to another within the same country due to the difference in bacterial prevalence in different environments.2 Here is an effort to study the most prevalent pathogenic bacteria and there antibiotic sensitivity in type III compound fractures in our hospital and compare with other studies.
METHODS
This is a prospective observational study on 130 patients with type III open long bone fractures admitted in department of Orthopaedics, Government Medical College, Kottayam during the study period of June 2016 to July 2017. All patients were informed about the study in all respects and informed written consent was obtained.
Inclusion criteria
All patients with type III open long bone fractures.
Exclusion criteria
All patients who are immune compromised and with any other focus of infection.
Procedure
The study was approved by the Ethical and Research committee of Government medical college, Kottayam, Kerala. After finding the suitability as per inclusion and exclusion criteria, patients were selected for the study, briefed about the nature of study and written informed consent were obtained.
Further, demographic profile of patient, history of diabetes mellitus, mode of injury, clinical and radiological examination were recorded on predesigned proforma. First sample (D0) was collected from emergency room and second sample (D3) was taken on 3rd day during follow up wound inspection. Wound beds were prepared before specimen collection by using Levine’s technique, where the wound surface is cleansed of surface exudates and contaminants with a moistened sterile gauze and sterile normal saline solution.3 Dressed wounds were cleansed with non-bacteriostatic sterile normal saline after removing the dressing. The end of a sterile cotton-tipped applicator was rotated over a 1 cm2 area for 5 seconds with sufficient pressure to express fluid and bacteria to surface from within the wound tissue. The applicators were applied deep into the wounds in order to avoid contaminants that are usually found on the surface of the wounds. Two wound swabs were taken from each compound fracture wound at a time. Specimens were placed in a sterile container, properly labeled and transported to microbiology laboratory, Government medical college, Kottayam without any delay for further analysis. After taking D0 sample patients were started on empirical therapy with Cefotaxime, Gentamicin and Metronidazole. Microscopic examination for Gram staining, culturing of organisms and antimicrobial susceptibility were done from microbiology laboratory. Results were collected by hand from department of Microbiology, Government medical college Kottayam.
Statistical analysis
Data is entered in Microsoft Excel software, and analysis done using SPSS version 20.0 software. The level of significance will be p<0.05 and high significance p<0.01. The results are analyzed at the end of the study and observations made.
RESULTS
Patients were divided into four groups according to the age (Table 1). Most of the patients were between 21 and 40 years (66.2%) of age. Mean age of the study population was 35.02 years. Among the study population 88.5% were men, with a male: female ratio of 7.67: 1. Mechanism of injury (Table 2) in majority of study population was road traffic accident (81%), fall from height (13.1%) and assault (5.4%). Only 6.2% of the study population was diabetic patients. Majority of the fractures (Table 3) were of type III-B (75.4%) followed by type III-A (23.1%) and type III-C (1.5%).
100% of diabetic patients had infection and it was found to be statistically significant with a Chi-Square value of 23.138 at p<0.001. Out of 130 patients 26.9% showed a positive culture for organism either on day 0 or day 3. Only 7.7% showed a positive wound culture on day 0. 24.5% of patient had positive culture on day 3. Among the cases who had infection on day 0, 20% got cured by day 3. In addition to this 19.2% developed infection by day 3, thus making the total number of cases with infection to be 24.5% of the study population (Table 4).
50% of the positive culture on day 0 showed Staphylococcus aureus. Remaining were 30% Acinetobacter, 20% Pseudomonas aeruginosa and Klebsiella, 10% were E. coli. In day 3 culture 33% were of Staphylococcus aureus, 30.3% were Acinetobacter, 27.3% were Pseudomonas, 18.2% were Klebsiella, 15.2% were E-coli, 9.1% were Enterococcus, 6.1% Streptococcus, 3% were Enterobacter respectively (Table 5). The antibiotic sensitivity pattern of various organisms isolated are shown in Table 6. 69.2% of Staphylococcus were sensitive to cloxacillin. 40% of Acinetobacter were sensitive to gentamicin and cefoperazone + sulbactum. 55.6% of Pseudomonas were sensitive to amikacin and ciprofloxacin. 83.3% of Klebsiella were sensitive to gentamicin. 80% of E-coli were sensitive to amikacin. 66.7% of Enterococcus were sensitive to ampicillin, amoxicillin + clavulanic acid and gentamicin. 50% of Streptococcus showed sensitivity to ceftriaxone, cefotaxime and gentamicin. 100% of Enterobacter showed sensitivity to ceftazidime and amikacin.
DISCUSSION
Infection still represents one of the major complications in the treatment of open fractures. Break down of the tissue barrier between the fracture zone and the environment leaves the underlying bone prone to direct contact with contaminating agents. Subsequent chronic osteitis and/or non-union still represent today a major source of disability and decreased quality of life for the individual patient as well as a socio-economic problem for public health systems.
In our study most of the patients were between 21 and 40 years of age with a mean age of 35.02±12.85 years. Age of the study population ranged from 11 years to 79 years. Ikem et al, reported similar finding in a study conducted in Ile-Ife, Nigeria.4 Among the study population 88.5% were men, with a male: female ratio of 7.6: 1. The male predominance in our study may be due to various social and demographic factors. The leading cause of open fracture was found to be road traffic accidents. Similar findings have been reported by Azam et al.5 Majority of the fractures were of type III-B followed by type III-A and type III-C. Among the diabetic patients 100% developed day 3 wound infection, which means diabetes is a strong precursor for infection.
The total bacterial isolation rate from the compound fracture wounds in this study was 26.9% which included both day 0 and day 3 cultures. This is lower than that (45%) reported from Chandigarh, by Sen et al, 45.8% reported from Ile-ife, Nigeria by Ikem et al and 30% reported by ketterl et al.4,6,7 Different factors related to wound bed preparation, sample collection, sample transportation and culturing technique might have an effect in the bacterial isolation rate. New culture positivity on day 3 observed in the study may also be due to inadequate debridement, improper wound care from the ward, insufficient antibiotic coverage.
The main bacterial isolate in open fracture wounds in this study was Staphylococcus aureus in both day 0 and day 3 cultures. The predominating prevalence of Staphylococcus aureus in wounds in general and compound fracture wounds have been also reported in other developing and developed countries like USA by Gustilo and Anderson, France by Carsenti-Etesse et al, England by Bowler et al, India by Dhawan et al, Brazil by Fonteset al, Romania by Purghel et al and in Iran by Khosravi et al.8-14 In the present study, Acinetobacter was the second most frequently isolated bacteria. Similar findings have been reported by Johnson et al.15 Other cultured organisms were Pseudomonas, Klebsiella, E-coli, Enterococcus, Streptococcus and Enterobacter. The comparison of results of our study with similar studies given in Table 7. The antibiotic susceptibility of bacteria were assed. It was found that Gentamicin, amikacin, doxycycline, ciprofloxacin, vancomycin, piperacillin + tazobactum and cefoperazone + sulbactum were sensitive against majority of the organisms.
CONCLUSION
With the development of new operative and aseptic techniques as well as a deeper understanding of the pathophysiology of fractures with soft tissue compromise the results can be improved. Gram positive Staphylococcus aureus were found to be the most common cause of wound infection in type III open compound fractures followed by Gram negative Acinetobacter, as the emerging cause of infection The careful handling of soft tissues with radical debridement of all necrotic tissues, proper antibiotic therapy and aseptic wound care from ward contributes to the avoidance of infection and non-union.
ACKNOWLEDGEMENTS
I express my thanks and gratitude to Professor M.A Thomas and thankful Dr. George Thomas, Associate Professor, Orthopedics.
Funding: No funding sources
Conflict of interest: None declared
Ethical approval: The study was approved by the institutional ethics committee
REFERENCES
- 1. Rajasekaran S, Devendra A, Perumal R, Dheenadayalan J, Sundararajan SR. Initial management of open fractures. Court-Brown CM, Heckman JD, McQueen MM, Ricci WM, editors. Micheald. McKee associate editor. Rockwood and Green Fractures in adults Volume 1.8thed Philadelphia, Baltimore, New York, London. Buenos Aires, Hong Kong, Sydney, Tokyo. Wolters Kluwer; 2015: 353– 365.
- 2. Lee J. Efficacy of cultures in the management of open fractures. Clin Orthop Relat Res. 1997;339:71-5.
- 3. Levine NS, Lindberg RB, Mason AD Jr, Pruitt BA Jr. The quantitative swab culture and smear: A quick, simple method for determining the number of viable aerobic bacteria on open wounds. J Trauma. 1976;16:89-94.
- 4. Ikem IC, Oginni LM, Bamgboye EA, Ako-Nai AK, Onipade AO. The bacteriology of open fractures in Ile-Ife, Nigeria. Niger J Med. 2004;13:359-65.
- 5. Azam Q, Sherwani M, Abbas M, Gupta R, Asif N, Sabir AB. Internal fixation in compound type III fractures presenting after golden period. Indian J Orthop. 2007;41:204-8.
- 6. Sen RK, Murthy NRS, Gill SS, Nagi ON. Bacterial load in tissues and its predictive value for infection in open fractures. J Orthop Surg. 2000;8:1-5.
- 7. Ketterl RL, Steinau HU, Feller AM, Stübinger B, Claudi BF. Aggressive debridement and early soft-tissue coverage in grade III open tibial fractures. Zentralblatt Fur Chirurgie Journal. 1990;115:209–18.
- 8. Gustilo R.B, Anderson J.T. Prevention of infection in the treatment of one thousand and twenty-five open fractures of long bones: Retrospective and prospective analyses. J Bone Joint Surg Am. 1976;58:453–538.
- 9. Carsenti-Etesse H, Doyon F, Desplaces N. Epidemiology of bacterial infection during management of open leg fractures. Eur J ClinMicrobiol Infect Dis. 1999;18:315–23.
- 10. Bowler P.G, Duerden B.I, Armstrong D.G. Wound microbiology and associated approaches to wound management. ClinMicrobiol Rev. 2001;14:244-69.
- 11. Dhawan B, Mohanty S, Das B.K, Kapil A. Bacteriology of orthopaedic wound infections in an Indian Tertiary Care Hospital. Indian J Med Res. 2005;121:784-5.
- 12. Fontes C.O, Carvalho M.A.R, Nicoli J.R, Hamdan J.S, Mayrink W, Genaro O, Carmo L.S, Farias L.M. Identification and antimicrobial susceptibility of micro-organisms recovered from cutaneous lesions of human American tegumentary leishmaniasis in Minas Gerais, Brazil. J Med Microbiol. 2005;54:1071-6.
- 13. Purghel F, Badea R, Ciuvica R, Anastasiu A. The use of antibiotics in traumatology and orthopaedic surgery. Clin Med. 2006;1:58-65.
- 14. Khosravi AD, Ahmadi F, Salmanzadeh S, Dashtbozorg A, AbasiMontazeri E. Study of bacteria isolated from orthopedic implant infections and their antimicrobial susceptibility pattern. Res J Microbiol. 2009;4:158-63.
- 15. Johnson EN, Burns TC, Hayda RA, Hospenthal DR, Murray CK. Infectious complications of open type III tibial fractures among combat casualities. Clin Infect Dis. 2007;45:409-15.
- 16. Patzakis MJ, Wilkins J. Factors influencing infection rate in open fracture wounds. Clin Orthop. 1989;243:36–40,
- 17. Russell GG, Henderson R, Arnett G. Primary or delayed closure for open tibial fractures. J Bone Jt Surg. 1990;72:125–8.
- 18. Muhr G. Therapeutic strategies in fractures with soft tissue damage. Chirurg. 1991;62:361–6.
- 19. Rajasekaran S, Dheenadhayalan J, Babu JN, Sundararajan SR, Venkatramani H, Sabapathy SR. Immediate primary skin closure in type-III A and B open fractures Results after a minimum of five years. J Bone Joint Surg [Br]. 2009;91:217-24.