Abstract
Background: Loss of skin as the first line of defence suppress immune system, extend hospital stay and makes burn patients more vulnerable to acquire healthcare associated infections. Such infections become the reason for mortality and morbidity in burn patients. Therefore, continuous monitoring of the pattern of nosocomial infection and drug resistance is necessary for assuring patient safety and healthcare quality improvement.
Aim: To describe the microbial profile of infections among burn patients admitted to Bahrain Defence Force Military Hospital.
Method: This is a retrospective cohort study involving 295burn patients. Wound swab method was used to isolate the microorganisms first on admission and then on suspicion of infection. The overall percentage of wound culture positive cases was 11.8% and the wound infection percentage was 5% of the total number of patients admitted to the unitA total of 126 swabs was performed from the burn wounds.
Results: Gram+ bacteria S.aureus was predominant in initial cultures. It was however, succeeded by Gram- bacteria, Pseudomonas, from third culture onwards. Fungal infection with Candida was most prevalent (n=21,16.7%). With TBSA >30% polymicrobial growth was observed which tend to increase with increase length of hospitalization. A greater proportion of patients (42.9%, n=15) had acquired healthcare associated infections and was negatively associated with increased length of hospitalization(r=-0.418, p=0.012).
Conclusion: 5% of the total patient population was categorized as health care associated infection cases. Gram negative bacteria, Pseudomonas were the prevalent microorganism isolated from wound infection of the burn patients.
Citation
Dahag MA, Louri NA, Dey N and Philip SS. Pattern of the Burn Wounds Infections in Bahrain Defence Force Military Hospital. Ann Burns and Trauma. 2018; 2(1): 1007.
Introduction
Till date,development of early bacterial infection remains one of the major challenges of patient safety in managing burn patients. Despite numerous advancements made in the antimicrobial medications, infection still accounts for approximately 75% of all the deaths in burn injuries among patients globally [1]. Burn destroys the first line of defense against microbes, the skin, and suppresses the immune system.Further, avascularized necrotic tissue in the burn area provides an excellent growth medium to the microbes. Together, these conditions make burn wound more prone to acquire infections and development of sepsis [2].
In the beginning, thermal injuries are supposed to be free of any infections. However, within 48 hrs, the endogenous microbial flora of the patients, which are mostly Gram positive bacteria, colonizes the wound followed by colonization with Gram negative bacteria from patient’s gastrointestinal and respiratory tract as well as hospital environment (i.e. of nosocomial origin).The spectrum of these microbial floras is dependent on individual hospital and varies with time as well as the prolonged length of hospital stay [3]. Moreover, prolonged use of antibiotics such as third generation cephalosporins, leads to selection of Multi Drug Resistant Strain (MDRS) of microbes [4-6]. Burn injuries when infected with MDRS become difficult to treat as less antimicrobial effective against them are available, thus resulting in prolonged hospital stay and greater mortality rate [7].
Therefore, periodic reviews of the bacterial flora of burn wounds should be carried out to know the pattern of predominant organisms and the treatment of the patients before getting the result of microbiological cultures in such a manner that the development of antibiotic resistance can be avoided against MDRS as well as effectively controlling infection in patients. This would be crucial to reduce the overall infection-related morbidity and mortality [8]. The aim of the present study is to estimate the incidence of burn wounds infections and describe the epidemiology profile of microbial flora among the burn patients in Bahrain Defense Force Military Hospital.
Materials and Methods
Study setting and population
This is a retrospective cohort study conducted in the burn unit of military hospital, Bahrain from February 2015 till April 2017. During this period, a total of 295 patients having acute burn injuries due to various reasons were admitted into the hospital burn unit.
Exclusion criteria includes
Pregnant women,diabetic patients,patients with immunosuppressive diseases or receiving any immunosuppressive therapy and patients who followed the open dressing method or underwent surgical coverage procedure as split thickness skin graft in the first 24 days post burn.
Sample collection procedures
All the samples were collected under complete aseptic conditions. Wound swabs were used to collect the infection data after thorough cleaning of the wound with sterile saline. A sterile cotton swab is moistened with sterile normal saline and rubbed onto the burn wound surface.Swabs are taken from deep areas, areas with discharge or thick eschar. The swabs were transported within 1 hr of collection to the Microbiology laboratory for bacteriological isolation and identification. Swabs for anaerobic culture were transported in thioglycolate broth in well-sealed bottles. Afterwards, the samples were plated on culture media as soon as possible.MacConkey agar, nutrient agar and blood agar media were used and were incubated at 37°C for 24 hours after inoculation.Samples from the burn wound were collected from patients when clinical signs of local infection was suspected or appeared and before skin grafting.
Sample processing
Discs with 30 mkg cefoxitin (Becton Dickinson) were used to distinguish between Methicillin-Resistant Staphylococci (MRS) and Methicillin-Susceptible Staphylococci (MSS).Those isolates that showed zone of inhibition <21 mm were considered as MRSA. In addition, oxacillin screen agar (bioMerieux) was utilized for detection of metyhicillin-resistant S. aureus (MRSA). S. aureus ATCC 25923 was included as a reference strain for quality control.The initial screening for ESBL production was carried out according to CLSI guidelines.
Fungal cultures were obtained on Sabouraud dextrose agar (Difco) and on “mycogel” agar (Oxoid) at 37°C and observed daily for 20 days.The characterization of fungi was done by the germ tube test, morphological examination and automated method Vitek YBC yeast identification system (bioMérieuxVitek, Inc., MI, US).
Sample quality control
All the samples were processed in triplicate to ensure reliability. Enterococcus faecalis (ATCC 29212),Staphylococcus aureus (ATCC 24923), Streptococcus pyogenes (ATCC 19615), E.coli (ATCC 25922),Pseudomonas aeruginosa (ATCC 27853) were used as quality control throughout the study for culture, Gram stain. All the strains were obtained from the ATCC, (The essential of live science research, USA).
Statistical analysis
All the data were entered and analyzed using Statistical Software for Social Sciences (SPSS) version 21.Frequency and percentage or Mean±standard deviations were used to describe the data. Comparisons between different groups were performed using Chi-squared test and Fischer’s exact test. Bivariate correlation (Pearson’s coefficient) was used to explore any significant association between study variables, and p value ≤0.05 was considered statistically significant.
Results
From February 2015 till April 2017,a total of 295 patients were admitted to the Burn unit of our hospital of which 35 cases (11.8%) were swab culture positive and were included in this study. Out of 35 cases,15 cases (5.08% of total patients) were considered as healthcare associated infection according to our hospital policy.The mean age of the patients included was 26±19.54 years (Range 2-79 years).Incidence of burn was more frequent in male (62.9%, n=22) than females (37.1% n=13).The Total Body Surface Area (TBSA) range from 1% -70%, 11-20% included highest number of patients (28.6%).
Majority of the patients had 2nd degree burns (74.3%, n=26) followed by 3rd degree (17.1%, n=6) and 1st degree burns (8.6%, n=3).The predominant cause of burn among the patients were flame (n=11, 28.9 %), followed by thermal (n=10, 26.3%), scald (n=9, 23.7%), electric (n=2, 5.3%) and others (n=2, 5.3%).The cause of burn in female was majorly hot liquid (scald burn, 41%) while in males,flame was the main cause of burn (36.4%). In children and adolescents (15 years) flame (40.9%) was the major cause of burn, see Table 1.
Table 1: Characteristics of patients included in the study.
Patient details | % (n) |
Total no. of admissions | 295 |
Swab culture positive case | 35 (11.8%) |
Total no. of infected case | 15 (5.08%) |
Mean age, (Range) | 26±19.54 years (2-79 years) |
Gender | |
Male | 62.9% (n=22) |
Female | 37.1% (n=13) |
TBSA | |
1-10% | 25% (n=8) |
11-20% | 28.1% (n-9) |
21-30% | 15.6% (n=5) |
31-40% | 21.9% (n=7) |
>40% | 9.4% (n=3) |
Degree of burn | |
1st | 8.6% (n=3) |
2nd | 74.3% (n=26) |
3rd | 17.1% (n=6) |
Burn cause | |
Flame | 31.4% (n=11) |
Thermal | 28.6% (n=10) |
Scald | 28.6% (n=10) |
Electric | 5.7% (n=2) |
Others | 5.7% (n=2) |
Prevalent burn cause in different age groups | |
<15 years | Scald (46.2%, n=6) |
>15 years | Flame (40.9%, n=9) |
A total of 126 wound swabs were collected from 35 patients.The overall percentage of positive cultures was 86.5% in comparison to the no growth 13.5% (Table 2). Total number of swabs collected per patient was considerably increased with increase in the duration of hospital stay (Pearson’s coefficient (r)=0.814, p30%, polymicrobial growth prevailed (p=0.05, Figure 1).
Figure 1: Age-wise distribution of type of microorganism. Polymicrobial organisms were mainly present in patients of all age groups but maximally in age >30 years. Monomicrobial organisms were present in age <30 years.
As the length of stay in hospital increased,an increased tendency of being infected with more than one type of microorganisms was observed (Pearson’s coefficient (r)=0.307, p=0.07). New table is necessary to cross tabulate the mon/polymicrobials versus age, sex, length of stay, TBSA, swab rank, etc…
Table 2: Details of wound swabs.
Total no. of wound swabs | 126 |
Culture positive | 109 (86.5%) |
Culture negative | 17 (13.5%) |
Monomicrobial growth | 58 (46%) |
Polymicrobial growth | 51 (40.5%) |
The initial swab had mostly monomicrobial growth (n=16, 45.7%) of Gram+ type (n=14, 40%) which were replaced by Gram- type (n=11, 31.4%) in second swab culture, the time of which varied from 1 day to 1 month.The Gram- bacteria remained the dominant bacterial type thereafter (Figure 2).
Figure 2: Temporal prevalence of Gram+/- microorganism. Gram+ bacteria were prevalent in initial swab culture which was gradually replaced by Gram- bacteria. However, mix of Gram+ and Gram- bacteria were present from initial till last culture.
Of the total, fungal infection was present in only 9 patients (25.7%). From 126 wound swabs, fungal isolates were present in 23 (18.3%) cases. New table or graph is necessary to associate G+ve/-ve with swab rank and other variables.
A total of 156 bacterial isolates were obtained. Among them, Gram- bacteria, Pseudomonas (24.4%) was maximally isolated followed by Gram+ bacteria Staphylococcus aureus (16.03%) and MRSA (14.1%) (Figure 3).
Figure 3: Prevalence of bacteria in burn wounds. Gram- bacteria Pseudomonas was the most dominant bacteria isolated in burn wounds (p<0.001).
MRSA (N=15) was the dominating species in monomicrobial isolates, followed by Staphylococcus aureus (n=12) and Psedomonas (n=11) (Table 3). In polymicrobial isolates, Pseudomonas (n=28) was maximally isolated followed by K.pneumonia (n=13) and Staphylococcus aureus (n=13). Other low prevailing mono- and polybacterial isolates is shown in Table 1. The fungal and yeast infection was found in 20% (n=7) and 2.9% (n=1) of the patients respectively. The only fungal species isolated was Candida albicans (n=22) while Aspergillus (n=2) was the only mold isolated. Candida was isolated with Pseudomonas in highest frequency.
Table 3: Prevalence of microbial isolates with types of infection.
Polymicrobial | No. | % | Monomicrobial | No. | % |
K.pneumonia+ Enterococci spp. | 1 | 0.9 | K.pneumonia | 3 | 2.7 |
K.pneumonia+ Pseudomonas spp. | 1 | 0.9 | Pseudomonas | 11 | 10 |
spp. | |||||
K.pneumonia+ C.albicans | 1 | 0.9 | S.Aureus | 12 | 11 |
K.pneumonia+ MRSA | 1 | 0.9 | MRSA | 15 | 13.7 |
K.pneumonia+ S.aureus+ E.coli | 1 | 0.9 | Enterococcus | 4 | 3.6 |
spp. | |||||
K.pneumonia+ S.aureus+ | 3 | 2.7 | Enterobacterspp. | 7 | 6.4 |
Psudomonasspp. | |||||
K.pneumonia+ S.aureus+ BHS | 1 | 0.9 | E.coli | 1 | 0.9 |
K.pneumonia+ S.aureus+ Enterococci | 2 | 1.8 | S.maltophilia | 1 | 0.9 |
spp. | |||||
K.pneumonia+ Pseudomonas spp.+ | 1 | 0.9 | Acenitobacterspp. | 1 | 0.9 |
E.coli + A. fumigatus | |||||
K.pneumonia+ Enterobacter spp. + | 1 | 0.9 | C.albicans | 3 | 2.7 |
C.albicans | |||||
Pseudomonas spp. + S. aureus | 1 | 0.9 | |||
Pseudomonas spp. + E. coli | 1 | 0.9 | |||
Pseudomonas spp. + MRSA | 3 | 2.7 | |||
Pseudomonas spp. + P.misabilis | 1 | 0.9 | |||
Pseudomonas spp. + C. albicans | 7 | 6.4 | |||
Pseudomonas spp. + A. fumigatus | 1 | 0.9 | |||
Pseudomonas spp. + Candida spp. + | 4 | 3.6 | |||
Enterococci spp. | |||||
Pseudomonas spp. + MRSA + | 1 | 0.9 | |||
Enterobacter spp. | |||||
Pseudomonas spp. + E. coli + | 3 | 2.7 | |||
Enterococci spp. | |||||
Pseudomonas spp. + E. coli + | 1 | 0.9 | |||
C.albicans | |||||
S.aureus+C.albicans | 1 | 0.9 | |||
S.aureus+Enterobacterspp. | 1 | 0.9 | |||
S.aureus+ Enterococci spp. | 1 | 0.9 | |||
S.aureus+BHS | 1 | 0.9 | |||
S.aureus+ E. coli +P.misabilis | 1 | 0.9 | |||
Enterobacterspp. + S.paucimobilis | 1 | 0.9 | |||
Enterobacterspp. + C.albican | 1 | 0.9 | |||
Enterobacterspp. + Enterococci spp. | 1 | 0.9 | |||
Enterococci spp. + C.albican | 2 | 1.8 | |||
Enterococci spp. + E.coli | 1 | 0.9 | |||
MRSA + BHS | 1 | 0.9 | |||
MRSA + S.pneumonia | 1 | 0.9 | |||
Acinetobacterspp. +C.albicans | 1 | 0.9 | |||
E.coli+ S.maltophilia | 1 | 0.9 | |||
Total | 51 | 46 | 58 | 53 |
Gram + bacteria Staphylococcus aureus (2 %), Enterococci (14.9%) and Gram- bacteria Enterobacter (14.9%) were more prevalent in 1st swab taken immediately on admission. In 2nd swab culture, Staphylococcus aureus (14.7 %), Pseudomonas (14.7%), MRSA (11.7%), Klebsiella pneumonia (11.7%) and Candida (11.7%) were the dominant species.From 3rd culture onwards,Pseudomonas remained the dominant species (Table 4). Candida (n=2) and Aspergillus (n=1) infection could be detected very early (culture 1) in wound swabs (Table 2). Based on our hospital management policy, 40% (n=14) of the patients had acquired healthcare associated infection which consists primarily of Klebsiella pneumonia, Pseudomonas, Staphylococcus aureus, E.coli, and MRSA. Presence of nosocomial infection was inversely proportional to the length of stay in hospital (Pearson’s coefficient (r)=-0.418, p=0.012).
Table 4: Isolation pattern of microorganism from wound swab at different time period.
Microorganisms | Culture 1 | Culture 2 | Culture 3 | Culture 4 | Culture 5 | Culture 6 | ||||||
N | % | N | % | N | % | N | % | N | % | N | % | |
S.aureus | 12 | 25.5 | 5 | 14.7 | 3 | 11.1 | 1 | 6.6 | 1 | 7.7 | 1 | 11.1 |
Pseudomonas spp. | 4 | 8.5 | 5 | 14.7 | 6 | 22.2 | 4 | 26.2 | 3 | 23 | 3 | 33.3 |
MRSA | 3 | 6.3 | 4 | 11.7 | 5 | 18.5 | 2 | 13.3 | 2 | 15.3 | 1 | 11.1 |
K.pneumonia | 4 | 8.5 | 4 | 11.7 | 1 | 3.7 | 2 | 15.3 | 1 | 11.1 | ||
BHS | 2 | 4.3 | 1 | 6.6 | 1 | 7.7 | ||||||
Enterobacter spp. | 7 | 14.9 | 3 | 8.8 | 2 | 7.4 | 1 | 6.6 | ||||
A. fumigatus | 1 | 2.1 | 1 | 2.9 | ||||||||
Enterococci spp. | 7 | 14.9 | 3 | 8.8 | 4 | 14.8 | 1 | 6.6 | 2 | 15.3 | ||
C.albicans | 2 | 4.3 | 4 | 11.7 | 3 | 11.1 | 4 | 26.6 | 1 | 7.7 | 1 | 11.1 |
S.maltophilia | 1 | 2.1 | 1 | 2.9 | ||||||||
Acinitobacterspp. | 1 | 2.1 | 1 | 3.7 | ||||||||
S. pneumoniae | 1 | 2.1 | ||||||||||
P.misabilis | 1 | 2.1 | 1 | 2.9 | ||||||||
E.coli | 1 | 2.1 | 3 | 8.8 | 1 | 3.7 | 1 | 7.7 | 2 | 22.2 | ||
S.paucimobilis | 1 | 3.7 | ||||||||||
Total | 47 | 100 | 34 | 100 | 27 | 100 | 15 | 100 | 13 | 100 | 9 | 100 |
Discussion
Burn wound sepsis related complications remain the main cause of mortality and morbidity in burn patients. Ekrami and Kalantar [9] have reported a high incidence (82.2%) of sepsis in burn patients. Similarly, Al-Taie et al [10]. have shown an incidence of 89% of wound infections in burn patients. In contrast, our study showed an incidence of only 11.8% of sepsis in burn patients which is much lowers than the above two studies. Further, the healthcare associated infection in our study was approximately 5% which is lower than that reported by Ekrami and Kalantar [9] was (77.3%). This lower incidence of sepsis in burn patients in our study could be attributed to strict isolation techniques and infection prevention and control policies of our hospital.
Burn wounds consisting of necrotic tissue and protein rich exudates provide an excellent growth medium for multiplication of microorganisms and hence are more susceptible to microorganism invasion [11]. Additionally, compromised immune system in burn patients and longer hospital stay helps in perpetuating the growth of microorganisms. Wound infections in such patients are so fast that even after thorough cleaning with antimicrobial solution; microorganisms were isolated from most of the wounds on 1st culture made immediately on admission [12,13]. On the same note, 86.5% of swabs collected were positive for microorganisms in our study. In the present research, polymicrobial pattern of growth was considerably associated with length of hospital stay which is in agreement with study by Altoparlak et al [14].
A great disparity is observed in dominance of gender in burn units of different geographical regions of the world. In countries where female predominantly work in kitchen, a prevalence of female patients is seen in the burn units as there is more chances of getting burn due to flame or hot water and objects [15,16]. According to research by Al-Aali [1],in our study also, males were predominantly admitted to burn unit.This can be attributed to the study setting which is a military hospital with male dominance.
Saha et al. [17] have reported initial prevalence of Gram+ bacteria in burn wounds which is gradually superseded by Gram- opportunistic bacteria having more proclivities to invade. Accordingly in our study, Gram+ S.aureus were most frequently isolated on 1st day of hospital admission. On second swab culture, Gram+, S.aureus and Gram- bacteria, Pseudomonas, were equally prevalent.From third culture onwards,Pseudomonas continued to be the most prevalent microorganisms.
Burn wounds are considered sterile however, infection is mostly acquired in burns wounds while patient transportation in combat cases and while staying in hospital which are mostly unavoidable [18]. Chances of being infected with nosocomial microorganisms increases as the duration of hospital stay increases [19]. On the contrary, our study showed a negative correlation between healthcare associated infection and duration of stay in hospital. Further, according to our hospital policy, Klebsiella pneumonia, S.aureus, MRSA, Pseudomonas, and E.coli constitute the major nosocomial microorganisms. Presence of all of these microorganisms in1st swab culture indicates that either the patients infected with them have been transported from other hospitals from where the infection is carried or presence of these organisms in high numbers in our hospital. The hospital management should focus in controlling these microorganisms.
Fungal infections tend to appear later in microbial invasion of burn wounds and was associated with longer duration of hospitalization [20,21]. Candida is the most common nosocomial fungal infection reported [22]. Nonetheless, in our study,infection with Candida and Aspergillus was seen as early as day 1.Further,Candida was isolated mostly with Pseudomonas.This should be taken into consideration while determining the treatment regime in burn patients of our hospital.
Conclusion
Approximately half of the infections acquired by the burn patients were hospital associated.Gram negative bacteria were the dominating bacterial type in the burn patients during the study period specially, Pseudomonas. S.aureus and MRSA were the major Gram positive bacteria while Candida was the main fungi identified in our burn patients.The findings of this study will aid in designing useful guideline for deciding the effective therapy for burn patients in our hospital. Further studies, evaluating antimicrobial resistance pattern in these microorganisms is however warranted.
References
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8. Chan M. Antimicrobial resistance in the European Union and the World. Conference on Combating Antimicrobial Resistance. Time for action. Copenhagen. Denmark. March 2012.
22. Macedo JLS. Imunodepressão do queimado: patogênese e fator de riscoparasepse. Rev Bras Queimadura. 2003; 3: 26-35.