Time-related Concordance Between Swab and Biopsy Samples in the Microbiological Assessment of Burn Wounds
- Wed, 3/25/09 - 3:27pm
- 0 Comments
- 3220 reads
Abstract: The aim of this study was to investigate the concordance between swab and tissue biopsy samples in terms of microbiological isolates and their time-related changes. A total of 156 samples (78 swab and 78 biopsy) were collected from 39 cases of partial- or full-thickness burns and compared at days 7 and 14 after admission regarding the type of microorganisms and their time-related changes. Pseudomonas aeruginosa and Citrobacter freundii were the two most common microorganisms found by both sampling methods. While the majority of swab and biopsy samples were concordant in day 7, the rate of concordance in day 14 was less than day 7—87.1% versus 66.6%, respectively. After comparing the ratio of P aeruginosa and C freundii in positive swab and biopsy cultures on days 7 and 14, unlike the swab samples, the biopsy samples yielded similar results both times (75% P aeruginosa and 25% C freundii, respectively). The results of this study show that the swab is a sufficient tool for burn wound monitoring during the first week and could defer the need for invasive biopsy sampling. For patients who remain in the burn unit for a longer period, biopsy samples are justified for monitoring the bacterial activity in burn wounds.
Address correspondence to:
Ghasemali Khorasani, MD
Mazandaran University of Medical Sciences
Emam Square, Valliasr Blvard
Sari, Mazandaran, 48157-33971
Iran
Phone: +98 151 2262342
E-mail: gakhorasani@yahoo.com
A severe burn is a serious injury that bacterial colonization often complicates. Infection impairs the healing process, and microorganism invasion of neighboring healthy tissue can lead to sepsis, which is the most frequent cause of death in burn injuries.1,2 Early detection of invasive burn wound infection could be helpful in reducing the mortality for these patients. Although tissue biopsy is considered the most appropriate sampling method for identifying wound infection and its causative pathogens,3–6 the procedure is potentially traumatic and is not routinely available, particularly for slow- or non-healing wounds that require frequent, long-term care. For these reasons, the use of a more conventional and readily available sampling method such as swab sampling could be considered as an alternative method for monitoring burn wounds. Since there are arguments to support the use of the swab sample as a useful method for routinely assessing the microbiology of appropriate wounds,7–11 we conducted this study to investigate the value of swab samples versus biopsy samples in terms of microbiological isolates and their time-related patterns of change.
Material and Methods
Setting and patients. Our burn center is a part of a 75-bed tertiary referral university-dependent hospital located in northern Iran. This prospective cross-sectional study was conducted on patients with partial- or full-thickness burns who were enrolled from September 2006 through March 2007. The Mazandaran University of Medical Sciences review board approved this study. Surface swabs and wound biopsies for bacteriological assessment of the burn wounds were performed at the end of weeks 1 and 2. Seven of the 39 patients in this study were septic based on the following clinical criteria: body temperature < 36˚C or > 39˚C, blood pressure < 90 mmHg or a reduction of 40 mmHg or more, and pulse rate > 90 beats per minute. Blood samples were taken 3 times and cultured in patients who had signs and symptoms of septicemia.
Biopsy samples. Under anesthesia, about 1 cm3 of tissue, along with the underlying live tissue, was removed from each wound and suspended in 2-mL physiological saline and homogenized. Samples were inoculated on blood and MacConkey agar.
1. Pruitt BA Jr, McManus AT, Kim SH, Goodwin CW. Burn wound infections: current status. World J Surg. 1998;22(2):135–145.
2. Mzezewa S, Jonsson K, Aberg M, Salemark L. A prospective study on the epidemiology of burns in patients admitted to the Harare burn units. Burns. 1999;25(6):499–504.
3. Brentano L, Gravens DL. A method for the quantitation of bacteria in burn wounds. Appl Microbiol. 1967;15(3):670–671.
4. Volenec FJ, Clark GM, Mani MM, Humphrey LJ. Burn wound biopsy bacterial quantitation: a statistical analysis. Am J Surg. 1979;138(5):695–697.
5. Basak S, Dutta SK, Gupta S, Ganguly AC, De R. Bacteriology of wound infection: evaluation by surface swab and quantitative full thickness wound biopsy culture. J Indian Med Assoc. 1992;90(2):33–34.
6. Loebl EC, Marvin JA, Heck EL, Curreri PW, Baxter CR. The method of quantitative burn-wound biopsy cultures and its routine use in the care of the burned patient. Am J Clin Pathol. 1974;61(1):20–24.
7. Bornside GH, Bornside BB. Comparison between moist swab and tissue biopsy methods for quantitation of bacteria in experimental incisional wounds. J Trauma. 1979;19(2):103–105.
8. Lawrence JC. The bacteriology of burns. J Hosp Infect. 1985;(6 Suppl B):3–17.
9. 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(2):89–94.
10. Thomson PD, Smith DJ Jr. What is infection? Am J Surg. 1994;167(1A):7S–10S.
11. Vindenes H, Bjerknes R. Microbial colonization of large wounds. Burns. 1995;21(8):575–579.
12. Barrow GI, Feltham RKA, eds. Cowan and Steel’s Manual for the Identification of Medical Bacteria. 3rd ed. New York, NY; Cambridge University Press; 1993:50–90.
13. Sjöberg T, Mzezewa S, Jönsson K, Robertson V, Salemark L. Comparison of surface swab cultures and quantitative tissue biopsy cultures to predict sepsis in burn patients: a prospective study. J Burn Care Rehabil. 2003;24(6):365–370.
14. Uppal SK, Ram S, Kwatra B, Garg S, Gupta R. Comparative evaluation of surface swab and quantitative full thickness wound biopsy culture in burn patients. Burns. 2007;33(4):460–463.
15. Zanetti G, Blanc DS, Federli I, et al. Importation of Acinetobacter baumannii into a burn unit: a recurrent outbreak of infection associated with widespread environmental contamination. Infect Control Hosp Epidemiol. 2007;28(6):723–725.
16. Stratchounski LS, Dekhnich AV, Kretchikov VA, et al. Antimicrobial resistance of nosocomial strains of Staphylococcus aureus in Russia: results of a prospective study. J Chemother. 2005;17(1):54–60.
17. Altoparlak U, Erol S, Akcay MN, Celebi F, Kadanali A. The time-related changes of antimicrobial resistance patterns and predominant bacterial profiles of burn wounds and body flora of burned patients. Burns. 2004;30(7):660–664.
18. Reboli AC, John JF Jr, Platt CG, Cantey JR. Methicillin-resistant Staphylococcus aureus outbreak at a Veterans’ Affairs Medical Center: importance of carriage of the organism by hospital personnel. Infect Control Hosp Epidemiol. 1990;11(6):291–296.
19. Agnihotri N, Gupta V, Joshi RM. Aerobic bacterial isolates from burn wound infections and their antibiograms—a five-year study. Burns. 2004;30(3):241–243.
20. Fuchs PC, Kopp J, Häfner H, Kleiner U, Pallua N. MRSA-retrospective analysis of an outbreak in the burn centre Aachen. Burns. 2002;28(6):575–578.
21. Meier PA, Carter CD, Wallace SE, Hollis RJ, Pfaller MA, Herwaldt LA. A prolonged outbreak of methicillin-resistant Staphylococcus aureus in the burn unit of a tertiary medical center. Infect Control Hosp Epidemiol. 1996;17(12):798–802.
22. Xu Y, Li T, Qi S, et al. [An investigation of bacterial epidemiology and an analysis of bacterial resistance to antibiotics in a burn unit from 1993 to 1999]. [Article in Chinese]. Zhonghua Shao Shang Za Zhi. 2002;18(3):159–162.
23. de Macedo JL, Rosa SC, Castro C. Sepsis in burned patients. Rev Soc Bras Med Trop. 2003;36(6):647–652.
24. Oliveira GA, Dell’Aquila AM, Masiero RL, et al. Isolation in Brazil of nosocomial Staphylococcus aureus with reduced susceptibility to vancomycin. Infect Control Hosp Epidemiol. 2001;22(7):443–448.
25. Ferreira AC, Gobara S, Costa SE, et al. Emergence of resistance in Pseudomonas aeruginosa and Acinetobacter species after the use of antimicrobials for burned patients. Infect Control Hosp Epidemiol. 2004;25(10):868–872.
26. Zhang X, Zhao BC. [Infective pathogens and drug resistance in burned patients]. [Article in Chinese]. Hunan Yi Ke Da Xue Xue Bao. 2003;28(4):405–408.
27. Arens S, Verbist L. Differentiation and susceptibility of Citrobacter isolates from patients in a university hospital. Clin Microbiol Infect. 1997;3(1):53–57.
28. Fillaux J, Dubouix A, Conil JM, Laguerre J, Marty N. Retrospective analysis of multidrug-resistant Acinetobacter baumannii strains isolated during a 4-year period in a university hospital. Infect Control Hosp Epidemiol. 2006;27(7):647–653.
29. Shih CC, Chen YC, Chang SC, Luh KT, Hsieh WC. Bacteremia due to Citrobacter species: significance of primary intraabdominal infection. Clin Infect Dis. 1996;23(3):543–549.
30. Song W, Lee KM, Kang HJ, Shin DH, Kim DK. Microbiologic aspects of predominant bacteria isolated from the burn patients in Korea. Burns. 2001;27(2):136–139.
31. Kaushik R, Kumar S, Sharma R, Lal P. Bacteriology of burn wounds-the first three year in a new burn unit at the Medical College Chandigarh. Burns. 2001;27(6):595–597.
32. Rastegar Lari A, Bahrami Honar H, Alaghehbandan R. Pseudomonas infection in Tohid Burn Center, Iran. Burns. 1998;24(7):637–641.
33. Haberal M, Ucar N, Bayraktar U, Oner Z, Bilgin N. Visceral injuries, wound infection and sepsis following electrical injuries. Burns. 1996;22(2):158–161.
34. Livermore DM. Multiple mechanisms of antimicrobial resistance in Pseudomonas aeruginosa: our worst nightmare? Clin Infect Dis. 2002;34(5):634–640.







