Prevalence of Positive Carriage of Tuberculosis, Methicillin-resistant Staphylococcus aureus, and Vancomycin-resistant Enterococci in Patients Transported by Ambulance: A Single Center Observational Study

Article information

J Prev Med Public Health. 2012;45(3):174-180
Publication date (electronic) : 2012 May 31
doi : https://doi.org/10.3961/jpmph.2012.45.3.174
1Department of Preventive Medicine, Graduate School of Public Health, Seoul National University, Seoul, Korea.
2Department of Emergency Medicine, Seoul National University College of Medicine, Seoul, Korea.
3Department of Emergency Medicine, Myongji Hospital, Kwandong University College of Medicine, Goyang, Korea.
4Department of Preventive Medicine, Kangwon National University College of Medicine, Chuncheon, Korea.
5Graduate School of Public Health and Institute of Health and Environment, Seoul National University, Seoul, Korea.
Corresponding author: Sang Do Shin, MD, PhD. 103 Daehak-ro, Jongno-gu, Seoul 110-799, Korea. Tel: +82-2-2072-3257, Fax: +82-2-741-7855, shinsangdo@medimail.co.kr
Received 2011 October 29; Accepted 2011 December 09.

Abstract

Objectives

An ambulance can be a potential source of contagious or droplet infection of a community. We estimated the prevalence of positive carriage of tuberculosis (TB), methicillin-resistant Staphylococcus aureus (MRSA), and vancomycin-resistant Enterococci (VRE) in patients transported by ambulance.

Methods

This was a retrospective observational study. We enrolled all patients who visited a tertiary teaching hospital emergency department (ED). Blood, sputum, urine, body fluid, and rectal swab samples were taken from patients when they were suspected of TB, MRSA, or VRE in the ED. The patients were categorized into three groups: pre-hospital ambulance (PA) group; inter-facility ambulance (IA) group; and non-ambulance (NA) group. Adjusted odds ratio (OR) and 95% confidence intervals (CI) were calculated using a multivariable logistic regression model for the prevalence of each infection.

Results

The total number of patients was 89206. Of these, 9378 (10.5%) and 4799 (5.4%) were in the PA and IA group, respectively. The prevalence of TB, MRSA, and VRE infection were 0.3%, 1.1%, and 0.3%, respectively. In the PA group, the prevalence of TB, MRSA, and VRE were 0.3%, 1.8%, and 0.4%. In the IA group, the prevalence of TB, MRSA, and VRE were 0.7%, 4.6%, and 1.5%, respectively. The adjusted ORs (95% CI) of the PA and IA compared to the NA group were 1.02 (0.69 to 1.53) and 1.83 (1.24 to 2.71) for TB, 2.24 (1.87 to 2.69) and 5.47 (4.63 to 6.46) for MRSA, 2.59 (1.78 to 3.77) and 8.90 (6.52 to 12.14) for VRE, respectively.

Conclusions

A high prevalence of positive carriage of TB, MRSA, and VRE in patients transported by metropolitan ambulances was found.

INTRODUCTION

Community-acquired methicillin-resistant Staphylococcus aureus (MRSA) infection has increased as along with hospital-acquired MRSA all over the world. According to the US Centers for Disease Control and Prevention (CDC), the number of MRSA-associated admissions was 126 000 from 1999 to 2000 and the number cases of invasive MRSA was 94 360 cases in 2005, which brought with it very high associated medical costs [1,2]. In Canada, 8.62 per 1000 admissions in 2007 were MRSA-associated, and vancomycin-resistant Enterococci (VRE) was isolated in 1.32 patients per 1000 admissions [3]. MRSA and VRE are typical nosocomial infections and can be transmitted to healthy individuals via person to person contact. Thus, MRSA and VRE were designated as nationally notifiable communicable diseases by the Korea CDC since 2010 because of their infectivity and fatality. Tuberculosis (TB) has been a serious public health problem inducing endemic infection in Korea. In 2007, the incidence rate and mortality rate of TB in Korea were 71.6 and 5.9 per 100 000 persons respectively [4]. The World Health Organization estimated that 9.2 million new cases and 1.7 million deaths from TB occurred in 2006, of which 0.7 million cases and 0.2 million deaths were in Human immunodeficiency virus-positive people globally [5,6].

Numerous studies have reported that MRSA and VRE are common pathogens that can spread from patient to patient through surface contamination and healthcare workers [7]. TB can also be easily transmitted via the respiratory tract causing opportunistic infection, particularly in immune compromised patients.

Ambulances can be a potential source of contamination of various microorganisms because ambulances transport patients without having a prior knowledge of a patient's risk factors, or of the colonization or infection state of the ambulance. The space of an ambulance is small and closed, so there may be high probabilities of contamination between persons and between patients and equipment. A high call volume and lack of sufficient time for sterilization also make strict infection control difficult [8]. For these reasons, patients who are transported by ambulance are very vulnerable to infection. A high prevalence of infection among patients who are transported by ambulances is a risk factor of ongoing community transmission because it can be a source of infection of the next patient who is transported by the ambulance. We aimed to estimate the prevalence of positive carriage of TB, MRSA, and VRE among patients that present to the emergency department (ED) by mode of transportation.

METHODS

I. Study Design and Setting

This study was a retrospective observational study which was a review of patients' medical records among those who presented to the ED of one tertiary academic hospital. This study was reviewed and approved by the institutional review board of the study coordinating hospital and granted a waiver of signed informed consent.

This study was conducted at one tertiary academic hospital with 50000 annual visits and a 25% admission rate of ED visits. Pre-hospital ambulance services are operated by the fire department, which covers all emergency delivery. Inter-facility transports usually are performed by private ambulance companies. Ambulance crews in one delivery are composed of two or three, who have the license of emergency medical technician (EMT)-basic or EMT-intermediate. The ambulance authorities have their own infection control guidelines, which are declaratory rather than practical.

II. Data Collection and Processing

The patients who visited a study ED from January 2007 to December 2008 were enrolled. Doctors working in the ED ordered culture studies routinely when the patients had any sign of infection, such as fever, hypothermia, hypotension, leukocytosis, or elevation of c-reactive protein, although there are no standard rules for ordering cultures. Blood, sputum, urine, body fluid, and rectal swab samples were taken from patients when they were suspected of any infection in the ED.

Demographic data were extracted from the National Emergency Department Information System (NEDIS), which is a nationwide common registry for emergency patients. We collected the mode of transport to the ED from the NEDIS data, and we classified the study population according to their mode of transportation as the pre-hospital ambulance group, the inter-facility ambulance group, and the non-ambulance group. The microbiologic laboratory data was extracted from the microbiology registry of the study institute, which covered all microorganisms identified in ED patients as well as admitted patients. The data were selected using the time the sample was dropped off: the samples that were taken from patients immediately after arrival in the ED and before admission were included.

III. Outcome Measures and Data Analysis

For three microorganisms, the prevalence was calculated for all patients and for the ambulance utilization group. We determined the demographics of the groups, and we modeled the multivariable logistic regression analysis for the prevalence by the mode of visit (pre-hospital ambulance and inter-facility ambulance group) versus non-ambulance group adjusting for potential confounders. The adjusted odds ratio (OR) and 95% confidence intervals (CI) were calculated.

RESULTS

I. Demographic Findings

The total number of enrolled patients was 89 206. Of these, pre-hospital ambulances and inter-facility ambulances were used in 10.5% and 5.4% of patients, respectively. The median age of patients was 58 in the pre-hospital ambulance group, 62 in the inter-facility ambulance group, and 39 in the non-ambulance group. ED mortality was the highest in the inter-facility ambulance group (7.2%), followed by the pre-hospital ambulance group (1.9%) and the non-ambulance group (0.2%) (Table 1).

The characteristics of patients visiting the emergency department by type of transportation

II. Prevalence of Positive Carriage of TB, MRSA, and VRE

The prevalence of TB, MRSA, and VRE for all patients taken together were 0.3%, 1.1%, and 0.3%, respectively. TB was positive in 0.3% in the pre-hospital ambulance group and 0.7% in the inter-facility ambulance group and MRSA was positive in 1.8% in the pre-hospital ambulance group and 4.6% in the inter-facility ambulance group. VRE was positive in 0.4% in the pre-hospital ambulance group and 1.5% in the inter-facility ambulance group. There were statistical differences of age, gender, insurance, time and season of visit, and reason for visit between the positive and negative carriage of TB, MRSA, and VRE with older age, more ambulance use, and a higher proportion of disease as reason of visit in the positive cases (Table 2).

The characteristics of patients visiting the emergency department by type of infection

The adjusted ORs (95% CI) for the potential confounders of the pre-hospital ambulance group and inter-facility ambulance compared to the non-ambulance group were 1.02 (0.69 to 1.53) and 1.83 (1.24 to 2.71) for TB, 2.24 (1.87 to 2.69) and 5.47 (4.63 to 6.46) for MRSA, and 2.59 (1.78 to 3.77) and 8.90 (6.52 to 12.14) for VRE, respectively (Table 3).

Results of multivariable logistic regression model of tuberculosis, MRSA, and VRE infection by type of transportation

III. The Identified Source of TB, MRSA, and VRE

The most commonly identified sources were sputum (60.5%) for TB, sputum (21.2%) for MRSA, and rectal swab (39.7%) for VRE (Table 4).

The identified source of TB, MRSA, and VRE

DISCUSSION

Antibiotic-resistant strains are an increasingly common and challenging public health issue in most of the world. In particular, MRSA is the most common strain of antibiotics-resistant infection, which varies in incidence according to geographic area and study institution. For example, Sweden and Norway reported less than 1% of MRSA, compared to high proportions in USA (25% to 50%), Canada (5% to 10%), and Hong Kong and Singapore (> 50%) [9]. VRE was reported at 7% in Germany and 16% in Switzerland and Greece [10]. In this study population, the overall prevalence of MRSA and VRE were 0.3% and 1.1%, which is not high compared to other countries. Although the incidence rates of TB have declined substantially in the United States, global efforts for TB control are being challenged by the steady increase in drug resistant TB, particularly multidrug resistant TB [11,12]. MRSA and VRE are also regarded as new challenging issues. Previous studies have reported that 51% to 59% of MRSA infections were found in purulent skin and soft tissue infections [13,14]. MRSA was found to be a potential risk factor with a 1.9 OR for the contamination of healthcare workers [13].

Several studies have reported positive MRSA findings in samples from ambulances [15-19]. These results also suggested that the patients with positive microorganisms who were transported by an ambulance could be a source of contamination of the ambulance. The ambulances which came into direct contact with patients were an important reservoir for these organisms. Furthermore, ambulances which transported the patients may be a potential risk factor of ongoing community transmission because it can be a source of infection to the next patients or ambulance crews who is transported by the ambulance. Regardless of whether the infection was community acquired or hospital acquired, therefore, patients with positive microorganisms who were transported by an ambulance can be another source of contamination of the ambulance, healthcare workers, and community contagion.

In particular, the inter-facility ambulance patients showed a much higher prevalence of MRSA and VRE than that in the ambulatory patients. The adjusted OR for MRSA of the pre-hospital ambulance group (2.24) was comparable with other studies, whereas the adjusted OR for MRSA of the inter-facility ambulance group (5.47) was very high. Patients who were transported from another hospital had a higher exposure to an infection risk of MRSA and VRE. It might be because there was no infection control program in the private ambulance services. Moreover, the patients transported between hospitals are more likely to be elderly and have a chronic disease or be in critical condition, and thus they are vulnerable for such infection. To decrease the spread of MRSA, patients with MRSA transported from another hospital were recommended to be isolated until being sterilized [20].

A higher rate of prevalence of MRSA and VRE does not always suggest that the ambulance is the source of contamination of community infection. However, these findings suggest that ambulance transport can be a potential source for infection for the next patients. To prevent this contagion, we should develop a strict infection control program for ambulance crews and services.

For ambulance infection control, the US Standard on Fire Department Occupational Safety and Health Program was introduced in 1987 [21,22]. To give enough ventilation in an ambulance, a strict ventilation time of 1.5 minutes or a high-efficiency particulate arresting filter was recommended [23]. Many ambulance infection control programs already suggested guidelines for an indepth program for sterilization, decontamination of material and equipment [23]. However, the actual adherence to these guidelines or the effect of these control programs remains unknown. In the setting of the present study, pre-hospital ambulances are operated by the fire department while inter-facility ambulances are operated by private companies or hospitals. According to the emergency medical service agency or ambulance authority, adherence to an infection control program could be variable. We do not know what kinds of screening and surveillance programs would be effective for ambulance infection control for each ambulance configuration.

This study had several limitations. The study was performed using a retrospective data review, which might result in the underestimation of the prevalence of TB, MRSA, and VRE. To determine the exact prevalence of these infections in the study hospital, we should test and culture the specimen for all patients of the study period. We know that the result cannot be generalized to all EDs because this study was from only a single tertiary teaching hospital ED. Future research should investigate the representative incidence and prevalence rate of across South Korea using data on the nationally notifiable communicable diseases that is collected by the Korea CDC. The tremendous efforts that have been made to improve surveillance of nosocomial infections like MRSA and VRE would be a good foundation for establishing preventive and public health policies. There were differences of severity such as admission and mortality rate, regardless of type of disease, between the pre-hospital ambulance group, inter-facility ambulance group, and non-ambulance group. The ORs of the ambulance-using groups might be overestimated if difference of disease severity between patients would be a potential confounder for positive carriage of TB, MRSA, and VRE. We could not conclude that the prevalence of these microorganism infections was associated with the direct probability of contamination to other patients using the ambulance; however, the data suggest that the high prevalence among patients who transported by ambulances may be a risk factor of ongoing community transmission because it can be a potential source of infection to the next patient who is transported by the ambulance. Future research should investigate the actual transmission rate by monitoring suspected cases that use ambulances and any rate of reduction that follows the initiation of an infection control program for ambulances.

In conclusion, ambulances can be a potential source of MRSA, VRE, and TB contamination. We found a much higher prevalence of those infections in the patient group transported from other hospitals, followed by the patient group transported by prehospital ambulances. Further study on the effectiveness of infection control programs should aim to identify the ways prehospital providers can reduce the risk of transmission of microorganisms among patients.

Notes

The authors have no conflicts of interest with the material presented in this paper.

This article is available at http://jpmph.org/.

References

1. Kuehnert MJ, Hill HA, Kupronis BA, Tokars JI, Solomon SL, Jernigan DB. Methicillin-resistant-Staphylococcus aureus hospitalizations, United States. Emerg Infect Dis 2005;11(6):868–872. 15963281.
2. Klevens RM, Morrison MA, Nadle J, Petit S, Gershman K, Ray S, et al. Invasive methicillin-resistant Staphylococcus aureus infections in the United States. JAMA 2007;298(15):1763–1771. 17940231.
3. Ofner-Agostini M, Johnston BL, Simor AE, Embil J, Matlow A, Mulvey M, et al. Vancomycin-resistant enterococci in Canada: results from the Canadian nosocomial infection surveillance program, 1999-2005. Infect Control Hosp Epidemiol 2008;29(3):271–274. 18241031.
4. Tuberculosis. Korea Centers for Disease Control and Prevention cited 2011 Sep 30. Available from: http://www.cdc.go.kr/kcdchome/jsp/home/health/dii/HEALDII0001Detail.jsp?menuid=100187&contentid=5007&pageNum=0&sub=0&boardid (Korean).
5. WHO/IUATLD Global Project on Anti-Tuberculosis Drug Resistance Surveillance. Anti-tuberculosis drug resistance in the world: fourth global report 2008. Geneva: World Health Organization. p. 10–20.
6. World Health Organization. Global tuberculosis control 2008: surveillance, planning, financing 2008. Geneva: World Health Organization. p. 1.
7. Zirakzadeh A, Patel R. Vancomycin-resistant enterococci: colonization, infection, detection, and treatment. Mayo Clin Proc 2006;81(4):529–536. 16610573.
8. Roline CE, Crumpecker C, Dunn TM. Can methicillin-resistant Staphylococcus aureus be found in an ambulance fleet? Prehosp Emerg Care 2007;11(2):241–244. 17454817.
9. Grundmann H, Aires-de-Sousa M, Boyce J, Tiemersma E. Emergence and resurgence of meticillin-resistant Staphylococcus aureus as a public-health threat. Lancet 2006;368(9538):874–885. 16950365.
10. Bouchillon SK, Johnson BM, Hoban DJ, Johnson JL, Dowzicky MJ, Wu DH, et al. Determining incidence of extended spectrum beta-lactamase producing Enterobacteriaceae, vancomycin-resistant Enterococcus faecium and methicillin-resistant Staphylococcus aureus in 38 centres from 17 countries: the PEARLS study 2001-2002. Int J Antimicrob Agents 2004;24(2):119–124. 15288309.
11. Bwanga F, Hoffner S, Haile M, Joloba ML. Direct susceptibility testing for multi drug resistant tuberculosis: a meta-analysis. BMC Infect Dis 2009;9:67. 19457256.
12. Yew WW, Leung CC. Update in tuberculosis 2008. Am J Respir Crit Care Med 2009;179(5):337–343. 19234321.
13. Moran GJ, Krishnadasan A, Gorwitz RJ, Fosheim GE, McDougal LK, Carey RB, et al. Methicillin-resistant S. aureus infections among patients in the emergency department. N Engl J Med 2006;355(7):666–674. 16914702.
14. Frazee BW, Lynn J, Charlebois ED, Lambert L, Lowery D, Perdreau-Remington F. High prevalence of methicillin-resistant Staphylococcus aureus in emergency department skin and soft tissue infections. Ann Emerg Med 2005;45(3):311–320. 15726056.
15. Noh H, Shin SD, Kim NJ, Ro YS, Oh HS, Joo SI, et al. Risk stratification-based surveillance of bacterial contamination in metropolitan ambulances. J Korean Med Sci 2011;26(1):124–130. 21218040.
16. Fischer D, Veldman A, Schäfer V, Diefenbach M. Bacterial colonization of patients undergoing international air transport: a prospective epidemiologic study. J Travel Med 2004;11(1):44–48. 14769287.
17. Nigam Y, Cutter J. A preliminary investigation into bacterial contamination of Welsh emergency ambulances. Emerg Med J 2003;20(5):479–482. 12954699.
18. Alves DW, Bissell RA. Bacterial pathogens in ambulances: results of unannounced sample collection. Prehosp Emerg Care 2008;12(2):218–224. 18379921.
19. Brown R, Minnon J, Schneider S, Vaughn J. Prevalence of methicillin-resistant Staphylococcus aureus in ambulances in southern Maine. Prehosp Emerg Care 2010;14(2):176–181. 20199231.
20. Van Belkum A, Verbrugh H. 40 years of methicillin resistant Staphylococcus aureus. BMJ 2001;323(7314):644–645. 11566814.
21. National Fire Protection Association. NFPA 1500: standard on fire department occupational safety and health program 2007. Quincy: National Fire Protection Association. p. 2.
22. National Fire Protection Association. NFPA 1521: standard for fire department safety officer 2008. Quincy: National Fire Protection Association. p. 2.
23. Guide to managing an emergency service infection control program. United States Fire Administration cited 2012 May 7. Available from: http://www.usfa.fema.gov/downloads/pdf/publications/fa-112.pdf.

Article information Continued

Table 1.

The characteristics of patients visiting the emergency department by type of transportation

Total Pre-hospital ambulance Inter-facility ambulance Non-ambulance p -value
Total 89 206 9378 4799 75 029
Gender < 0.01
 Male 47 929 (53.7) 5232 (55.8) 2751 (57.3) 39 946 (53.2)
 Female 41 277 (46.3) 4146 (44.2) 2048 (42.7) 35 083 (46.8)
Age (y) < 0.01
 Median (IQR) 44 (18, 63) 58 (40, 70) 62 (46, 72) 39 (13, 61)
Time of visits < 0.01
 8 am to 4 pm 41 413 (46.4) 3556 (37.9) 1998 (41.6) 35 859 (47.8)
 4 pm to MN 32 950 (36.9) 3384 (36.1) 2020 (42.1) 27 546 (36.7)
 MN to 8 am 14 843 (16.6) 2438 (26.0) 781 (16.3) 11 624 (15.5)
Season of visits 0.03
 Spring (Mar-May) 23 140 (25.9) 2383 (25.4) 1173 (24.4) 19 584 (26.1)
 Summer (Jun-Aug) 22 834 (25.6) 2353 (25.1) 1282 (26.7) 19 199 (25.6)
 Fall (Sep-Nov) 21 705 (24.3) 2372 (25.3) 1158 (24.1) 18 175 (24.2)
 Winter (Dec-Feb) 21 527 (24.1) 2270 (24.2) 1186 (24.7) 18 071 (24.1)
Insurance < 0.01
 National health insurance 80 853 (90.6) 7790 (83.1) 4300 (89.6) 68 763 (91.6)
 Automobile private insurance 1807 (2.0) 491 (5.2) 177 (3.7) 1139 (1.5)
 Medical aid program 4957 (5.6) 696 (7.4) 237 (4.9) 4024 (5.4)
 Other 1589 (1.8) 401 (4.3) 85 (1.8) 1103 (1.5)
Reason for visit < 0.01
 Disease 74 293 (83.3) 7251 (77.3) 4010 (83.6) 63 032 (84.0)
 Injury 14 913 (16.7) 2127 (22.7) 789 (16.4) 11 997 (16.0)
Length of stay in ED (h) < 0.01
 Mean±SD 6.9 ± 1.1 8.1 ± 16.5 9.4 ± 19.2 6.5 ± 1.1
Disposition from ED < 0.01
 Discharge 6 3037 (70.7) 5328 (56.8) 1120 (23.3) 56 589 (75.4)
 Transfer 2597 (2.9) 636 (6.8) 328 (6.8) 1633 (2.2)
 Admission 22 673 (25.4) 3212 (34.3) 3000 (62.5) 16 461 (21.9)
 Death 629 (0.7) 174 (1.9) 345 (7.2) 110 (0.1)
 Other 270 (0.3) 28 (0.3) 6 (0.1) 236 (0.3)

Data are presented as n (%).

IQR, inter-quartile range; MN, midnight; STD, standard deviation; ED, emergency department.

Table 2.

The characteristics of patients visiting the emergency department by type of infection

Total
Tuberculosis
MRSA
VRE
n % n % p - value1 n % p - value2 n % p - value3
Total 89 206 249 0.3 939 1.1 227 0.3
Gender 0.09 < 0.01 0.99
 Male 47 929 53.7 147 0.3 614 1.3 122 0.3
 Female 41 277 46.3 102 0.2 325 0.8 105 0.3
Age (y) < 0.01 < 0.01 < 0.01
 Median (IQR) 44 (18,63) 60 (42,73) 61 (39,72) 61 (45,72)
Transportation < 0.01 < 0.01 < 0.01
 Pre-hospital ambulance 9378 10.5 29 0.3 165 1.8 39 0.4
 Inter-facility ambulance 4799 5.4 31 0.6 221 4.6 74 1.5
 Non-ambulance 75 029 84.1 189 0.3 553 0.7 114 0.2
Time of visits < 0.01 < 0.01 < 0.01
 8 am to 4 pm 41 413 46.4 144 0.3 505 1.2 134 0.3
 4 pm to MN 32 950 36.9 83 0.3 310 0.9 67 0.2
 MN to 8 am 14 843 16.6 22 0.1 124 0.8 26 0.2
Season of visits < 0.01 0.22 < 0.01
 Spring (Mar-May) 23 140 25.9 51 0.2 242 1.0 80 0.3
 Summer (Jun-Aug) 22 834 25.6 63 0.3 222 1.0 45 0.2
 Fall (Sep-Nov) 21 705 24.3 85 0.4 254 1.2 36 0.2
 Winter (Dec-Feb) 21 527 24.1 50 0.2 221 1.0 66 0.3
Insurance < 0.01 0.03 0.01
 National health insurance 80 853 90.6 227 0.3 849 1.1 202 0.2
 Automobile private insurance 1807 2.0 0 0.0 11 0.6 2 0.1
 Medical aid program 4957 5.6 21 0.4 67 1.4 22 0.4
 Other 1589 1.8 1 0.1 12 0.8 1 0.1
Reason for visit < 0.01 < 0.01 < 0.01
 Disease 74 293 83.3 244 0.3 892 1.2 212 0.3
 Injury 14 913 16.7 5 0.0 47 0.3 15 0.1

MRSA, methicillin-resistant Staphylococcus aureus; VRE, vancomycin-resistant Enterococci; IQR, inter-quartile range; MN, midnight.

1

p-value is the statistical difference between the positive and negative carriage of tuberculosis.

2

p-value is the statistical difference between the positive and negative carriage of MRSA.

3

p-value is the statistical difference between the positive and negative carriage of VRE.

Table 3.

Results of multivariable logistic regression model of tuberculosis, MRSA, and VRE infection by type of transportation

Total (n) Tuberculosis
OR 95% CI
AOR1 95% CI
n % Lower limit Upper limit Lower limit Upper limit
Non-ambulance 75 029 189 0.3 1.00 1.00
Pre-hospital ambulance 9378 29 0.3 1.23 0.83 1.82 1.02 0.69 1.53
Inter-facility ambulance 4799 31 0.6 2.58 1.76 3.77 1.83 1.24 2.71

Total (n) MRSA
OR 95% CI
AOR1 95% CI
n % Lower limit Upper limit Lower limit Upper limit

Non-ambulance 75 029 553 0.7 1.00 1.00
Pre-hospital ambulance 9378 165 1.8 2.41 2.02 2.87 2.24 1.87 2.69
Inter-facility ambulance 4799 221 4.6 6.50 5.55 7.62 5.47 4.63 6.46

Total (n) VRE
OR 95% CI
AOR1 95% CI
n % Lower limit Upper limit Lower limit Upper limit

Non-ambulance 75 029 114 0.2 1.00 1.00
Pre-hospital ambulance 9378 39 0.4 2.74 1.91 3.95 2.59 1.78 3.77
Inter-facility ambulance 4799 74 1.5 10.29 7.67 13.81 8.90 6.52 12.14

Total (n) Any of 3 infections
OR 95% CI
AOR1 95% CI
n % Lower limit Upper limit Lower limit Upper limit

Non-ambulance 75 029 804 1.1 1.00 1.00
Pre-hospital ambulance 9378 211 2.2 2.13 1.82 2.48 1.95 1.66 2.28
Inter-facility ambulance 4799 290 6.0 5.94 5.18 6.81 4.90 4.24 5.66

MRSA, methicillin-resistant Staphylococcus aureus, VRE; vancomycin-resistant Enterococci; OR, odds ratio; CI, confidence intervals; AOR, adjusted adds ratio.

1

Adjusted for the gender, age, time of visit, season of visit, insurance, and reason for visit.

Table 4.

The identified source of TB, MRSA, and VRE

TB MRSA VRE
Total 294 (100.0) 1569 (100.0) 398 (100.0)
Blood, peripheral 1 (0.3) 138 (8.8) 24 (6.0)
Blood, central catheter 0 (0.0) 68 (4.3) 15 (3.8)
Broncho-alveolar lavage 33 (11.2) 34 (2.2) 2 (0.5)
Endotracheal aspiration 21 (7.1) 274 (17.5) 0 (0.0)
Sputum 178 (60.5) 333 (21.2) 0 (0.0)
Nasopharynx, oral 2 (0.7) 86 (5.5) 0 (0.0)
Urine, catheter 0 (0.0) 21 (1.3) 23 (5.8)
Urine, clean-voided 3 (1.0) 79 (5.0) 64 (16.1)
Stool 1 (0.3) 00 (0.0) 29 (7.3)
Rectal swab 0 (0.0) 00 (0.0) 158 (39.7)
Wound, abscess 16 (5.4) 225 (14.3) 30 (7.5)
Skin 2 (0.7) 49 (3.1) 5 (1.3)
Tissue 15 (5.1) 28 (1.8) 4 (1.0)
Body fluid 21 (7.1) 66 (4.2) 18 (4.5)
Drainage 1 (0.3) 141 (9.0) 21 (5.3)
Other 0 (0.0) 27 (1.7) 5 (1.3)

Data are presented as n (%).

TB, tuberculosis; MRSA, methicillin-resistant Staphylococcus aureus; VRE, vancomycin-resistant Enterococci.