Academic literature on the topic 'Clostridium difficile – Western Australia – Prevention'

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Journal articles on the topic "Clostridium difficile – Western Australia – Prevention"

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Collins, Deirdre A., and Thomas V. Riley. "Routine detection of Clostridium difficile in Western Australia." Anaerobe 37 (February 2016): 34–37. http://dx.doi.org/10.1016/j.anaerobe.2015.11.007.

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Riley, T. V., G. L. O'Neill, R. A. Bowman, and C. L. Golledge. "Clostridium difficile-associated diarrhoea: epidemiological data from Western Australia." Epidemiology and Infection 113, no. 1 (August 1994): 13–20. http://dx.doi.org/10.1017/s0950268800051414.

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SUMMARYThe incidence ofClostridium difficile-associated diarrhoea (CDAD) was investigated retrospectively at a 690-bed teaching hospital for the period 1983–92. Our aims were to determine: (i) the distribution by age and sex of patients with CDAD, (ii) the possibility of a seasonal trend and, (iii) the influence of infection control procedures, contamination of the hospital environment and the use of third-generation cephalosporins. The laboratory diagnosis of CDAD was based on demonstration of the organism by stool culture and/or detection of specific cytotoxin in stool filtrates.C. difficilewas detected in 917 patients who were being investigated for diarrhoeal illness. Yearly isolations varied from a low of 49 in 1983 to a high of 120 in 1990 (Chi square for linear trend 128·8;P <0·005). Most patients were elderly, with 63% aged 60 years or more; the majority (59%) were female. The relationship between culture ofC. difficileand detection of cytotoxin in faecal extracts was also examined. Sixty percent of a sample of 132 isolates from patients in whom faecal cytotoxin was not detected produced cytotoxinin vitro, suggesting that culture is a more sensitive indicator of infection withC. difficilethan cytotoxin detection. When the total number of faecal specimens received in the laboratory was used as a denominator there was an increase in the number of incident cases of CDAD between 1983 and 1990, apart from 1986. When occupied bed days was used as the denominator a similar trend was observed with a peak in 1990. These increases correlated with an increase in the use of third-generation cephalosporins at SCGH between 1983 and 1989 (Pearson's correlation coefficient, 0·90). The introduction of Body Substance Isolation in 1989, in conjunction with other infection control procedures, appears to have halted the rise, despite a continuing use of broad-spectrum cephalosporins. In order to reduce the number of cases of CDAD, either a reduction in levels of environmental contamination or a reduction in the use of third-generation cephalosporins is required. If this can be achieved the economic consequences, in terms of an opportunity cost, will be considerable.
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V Riley, Thomas, and Clayton L Golledge. "Probiotics and Clostridium difficile-associated diarrhoea." Microbiology Australia 24, no. 1 (2003): 20. http://dx.doi.org/10.1071/ma03120.

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Clostridium difficile is now recognised as the major cause of hospital acquired infectious diarrhoea. Data from Sir Charles Gairdner Hospital (SCGH) in Perth, Western Australia, is typical of many similar hospitals in developed countries. SCGH is a 600 bed adult university teaching hospital. During the period 1983 to 1992, C. difficile was detected in 917 patients who were being investigated for diarrhoeal illness. Up to 120 patients a year were infected, most of these being elderly females. Incidence rates increased from 23/100,000 occupied bed days in 1983 to 56/100,000 occupied bed days in 1990.
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Collins, Deirdre A., Linda A. Selvey, Antonio Celenza, and Thomas V. Riley. "Community-associated Clostridium difficile infection in emergency department patients in Western Australia." Anaerobe 48 (December 2017): 121–25. http://dx.doi.org/10.1016/j.anaerobe.2017.08.008.

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Lim, Su-Chen, Grace O. Androga, Daniel R. Knight, Peter Moono, Niki F. Foster, and Thomas V. Riley. "Antimicrobial susceptibility of Clostridium difficile isolated from food and environmental sources in Western Australia." International Journal of Antimicrobial Agents 52, no. 3 (September 2018): 411–15. http://dx.doi.org/10.1016/j.ijantimicag.2018.05.013.

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Knight, Daniel R., and Thomas V. Riley. "Prevalence of Gastrointestinal Clostridium difficile Carriage in Australian Sheep and Lambs." Applied and Environmental Microbiology 79, no. 18 (July 12, 2013): 5689–92. http://dx.doi.org/10.1128/aem.01888-13.

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ABSTRACTRecently,Clostridium difficilehas been isolated from a wide variety of animals, particularly production animals, mainly cattle and pigs. Concurrently, the incidence ofC. difficileinfection (CDI) in humans has increased in the community, with some suggestions that food-borne transmission ofC. difficileis occurring. Interestingly, sheep and lambs appear not to have been investigated for carriage/colonization withC. difficile. The aim of this project was to determine the prevalence of carriage ofC. difficilein sheep and lambs in Australia by culturing fecal samples. A total of 371 sheep and lamb fecal samples were received in seven batches from three different geographic areas in eastern Australia and two in Western Australia. The overall rate of detection in sheep and lambs was low (4.0%); however, carriage/colonization in lambs (6.5%) was statistically significantly higher than that in sheep (0.6%) (P= 0.005). Seven distinct PCR ribotype patterns were observed, three of which were known international ribotypes (UK 056 [n= 1], UK 101 [n= 6], and UK 137 [n= 2]), while the remainder were unable to be matched with our available reference library. This low rate of carriage/colonization in Australian ovines suggests they are unlikely to be a major source/reservoir of human infections.
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Thomas, Claudia, Mark Stevenson, D. James Williamson, and Thomas V. Riley. "Clostridium difficile–Associated Diarrhea: Epidemiological Data from Western Australia Associated with a Modified Antibiotic Policy." Clinical Infectious Diseases 35, no. 12 (December 15, 2002): 1457–62. http://dx.doi.org/10.1086/342691.

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Foster, N. F., D. A. Collins, S. L. Ditchburn, C. N. Duncan, J. W. van Schalkwyk, C. L. Golledge, A. B. R. Keed, and T. V. Riley. "Epidemiology of Clostridium difficile infection in two tertiary-care hospitals in Perth, Western Australia: a cross-sectional study." New Microbes and New Infections 2, no. 3 (May 2014): 64–71. http://dx.doi.org/10.1002/nmi2.43.

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Legenza, Laurel, Susanne Barnett, Warren Rose, Monica Bianchini, Nasia Safdar, and Renier Coetzee. "Epidemiology and outcomes of Clostridium difficile infection among hospitalised patients: results of a multicentre retrospective study in South Africa." BMJ Global Health 3, no. 4 (July 2018): e000889. http://dx.doi.org/10.1136/bmjgh-2018-000889.

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IntroductionLimited data exist on Clostridium difficile infection (CDI) in low-resource settings and settings with high prevalence of HIV. We aimed to determine baseline CDI patient characteristics and management and their contribution to mortality.MethodsWe reviewed adult patients hospitalised with diarrhoea and a C. difficile test result in 2015 from four public district hospitals in the Western Cape, South Africa. The primary outcome measures were risk factors for mortality. Secondary outcomes were C. difficile risk factors (positive vs negative) and CDI treatment.ResultsCharts of patients with diarrhoea tested for C. difficile (n=250; 112 C. difficile positive, 138 C. difficile negative) were reviewed. The study population included more women (65%). C. difficile-positive patients were older (46.5 vs 40.7 years, p<0.01). All-cause mortality was more common in the C. difficile-positive group (29% vs 8%, p<0.0001; HR 2.0, 95% CI 1.1 to 3.6). Tuberculosis (C. difficile positive 54% vs C. difficile negative 32%, p<0.001), 30-day prior antibiotic exposure (C. difficile positive 83% vs C. difficile negative 46%, p<0.001) and prior hospitalisation (C. difficile positive 55% vs C. difficile negative 22%, p<0.001) were also more common in the C. difficile-positive group. C. difficile positive test result (OR 4.7, 95% CI 2.0 to 11.2; p<0.001), male gender (OR 2.8, 95% CI 1.1 to 7.2; p=0.031) and tuberculosis (OR 2.3, 95% CI 1.0 to 5.0; p=0.038) were independently associated with mortality. Of patients starting treatment, metronidazole was the most common antimicrobial therapy initiated (70%, n=78); 32 C. difficile-positive (29%) patients were not treated.ConclusionPatients testing positive for C. difficile are at high risk of mortality at public district hospitals in South Africa. Tuberculosis should be considered an additional risk factor for CDI in populations with high tuberculosis and HIV comorbidity. Interventions for CDI prevention and management are urgently needed.
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Suljagic, Vesna, Dragan Djordjevic, Srdjan Lazic, and Biljana Mijovic. "Epidemiological characteristics of nosocomial diarrhea caused by Clostridium difficile in a tertiary level hospital in Serbia." Srpski arhiv za celokupno lekarstvo 141, no. 7-8 (2013): 482–89. http://dx.doi.org/10.2298/sarh1308482s.

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Introduction. Among the most important causes of diarrhea in modern hospitals is Clostridium difficile (C. difficile). A wide spectrum of diseases caused by this bacterium is now known as C. difficile associated disease (CDAD). The development of CDAD is usually preceded by the administration of antimicrobial therapy and fecal-oral infections with C. difficile. Over the last years epidemiology of CDAD has significantly changed. Recently, a hypervirulent BI/NAP1/027 strain, the cause of severe epidemics in North America and Western Europe, has been identified. Objective. The aim of this study was to identify risk factors for CDAD in patients operated on at the Military Medical Academy (MMA). Methods. The study included all patients who underwent surgery at the MMA during 2010. Nested case-control study design was used. The subjects were divided into groups of operated patients with and without CDAD. The patients were under prospective follow-up, while their data were collected using a questionnaire during a routine epidemiological control. Results. During 2010 the incidence rate of CDAD was 3.3 per 10,000 hospital days. Univariate regression analysis showed that the length of administration of one or two antibiotics, as well as concurrent administration of two antibiotics, were far more frequently observed in the patients with than in the patients without CDAD. Independent risk factor for the development of CDAD was the length of the administration of one antibiotic. Conclusion Reduction in the incidence rate of CDAD can be achieved by using reliable measures of prevention and control; the rational use of antibiotics, early diagnosis and therapy of infected patients, contact isolation of infected persons, proper disinfection, and continued education of medical and non-medical personnel.
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Dissertations / Theses on the topic "Clostridium difficile – Western Australia – Prevention"

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Thomas, Claudia. "The epidemiology and control of Clostridium difficile infection in a Western Australian hospital." University of Western Australia. School of Population Health, 2003. http://theses.library.uwa.edu.au/adt-WU2004.0011.

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[Truncated abstract] The prinicipal aim of this thesis was to explore the relationship between 3rd generation cephalosporin antibiotics and hospital-acquired Clostridium difficile-associated diarrhoea (CDAD). This antibiotic class has been implicated in the aetiology of CDAD; therefore restriction of these antibiotics via antibiotic policies represents a potential strategy for prevention and control of CDAD. Successful control of CDAD in hospitals translates to improved quality of care for patients, and a reduction of pressure on hospital resources. Therefore, the objectives of this study were to determine whether 3rd generation cephalosporins were related to CDAD, to evaluate the effect of changes to antibiotic policy on the incidence of CDAD, and to determine the impact of CDAD on patient length of stay and hospital costs. The study was conducted in Sir Charles Gairdner Hospital (SCGH), a public teaching hospital located in Perth, the capital city of the state of Western Australia. Evidence for an association between 3rd generation cephalosporins and CDAD was obtained from studies of ecologic- and individual-level data. A time series analysis of the relationship between monthly consumption of 3rd generation cephalosporins and the incidence of CDAD in SCGH was undertaken covering the period 1994 to 2000. The results demonstrated a positive relationship between the use of 3rd generation cephalosporins and CDAD. A matched case-control study that involved 193 adult inpatients diagnosed with CDAD and 386 adult inpatients without CDAD, selected from the period 1996 to 2000, was conducted. Information was collected on exposure to 3rd generation cephalosporin antibiotics during hospitalisation, as well as exposure to other antibiotics and medications, procedures, and comorbidities. Results from conditional logistic regression analyses found CDAD cases were six times more likely to be exposed to 3rd generation cephalosporins during their admission, prior to the onset of diarrhoea, than controls (adjusted odds ratio [OR] = 6.17, 95% confidence interval [CI] = 1.56-24.37). Approximately one third of CDAD in the study population could be attributed to 3rd generation cephalosporins. CDAD cases were also four times more likely to have been exposed to either amoxicillin-clavulanate or ticarcillin-clavulanate (adjusted OR=4.23, 95% CI=1.81-9.93). In October 1998, an antibiotic policy was introduced at SCGH that restricted the use of ceftriaxone, the 3rd generation cephalosporin most commonly used by the hospital. During 1999 and 2000, the incidence of CDAD halved as ceftriaxone consumption fell in response to this policy. The effect of this policy was demonstrated in the time series model; during the post-policy period the relationship between ceftriaxone and CDAD that was evident prior to the policy was cancelled out. From the individual-level data, obtained from the case-control study, a reduction in the prevalence of exposure to 3rd generation cephalosporins from 11% to 1% accounted for a 30% reduction in the incidence of CDAD. Data from the case-control study was also used to analyse the independent contribution of CDAD to length of stay and admission costs using multiple linear regression
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