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1.
Public Health ; 182: 19-25, 2020 May.
Article in English | MEDLINE | ID: mdl-32120067

ABSTRACT

OBJECTIVES: To describe a cross-border foodborne outbreak of Shigella sonnei that occurred in Ireland and Northern Ireland (NI) in December 2016 whilst also highlighting the valuable roles of sales data and international collaboration in the investigation and control of this outbreak. STUDY DESIGN: A cross-border outbreak control team was established to investigate the outbreak. METHODS: Epidemiological, microbiological, and environmental investigations were undertaken. Traditional analytical epidemiological studies were not feasible in this investigation. The restaurant chain provided sales data, which allowed assessment of a possible increased risk of illness associated with exposure to a particular type of heated food product (product A). RESULTS: Confirmed cases demonstrated sole trimethoprim resistance: an atypical antibiogram for Shigella isolates in Ireland. Early communication and the sharing of information within the outbreak control team facilitated the early detection of the international dimension of this outbreak. A joint international alert using the European Centre for Disease Control's confidential Epidemic Intelligence Information System for Food- and Waterborne Diseases and Zoonoses (EPIS-FWD) did not reveal further cases outside of the island of Ireland. The outbreak investigation identified that nine of thirteen primary case individuals had consumed product A from one of multiple branches of a restaurant chain located throughout the island of Ireland. Product A was made specifically for this chain in a food production facility in NI. S. sonnei was not detected in food samples from the food production facility. Strong statistical associations were observed between visiting a branch of this restaurant chain between 5 and 9 December 2016 and eating product A and developing shigellosis. CONCLUSIONS: This outbreak investigation highlights the importance of international collaboration in the efficient identification of cross-border foodborne outbreaks and the value of using sales data as the analytical component of such studies.


Subject(s)
Disease Outbreaks/statistics & numerical data , Dysentery, Bacillary/epidemiology , Foodborne Diseases/epidemiology , Shigella sonnei , Adolescent , Adult , Aged , Aged, 80 and over , Child , Commerce/economics , Disease Outbreaks/economics , Dysentery, Bacillary/economics , Dysentery, Bacillary/microbiology , Female , Food Microbiology , Foodborne Diseases/economics , Foodborne Diseases/microbiology , Humans , Ireland/epidemiology , Male , Middle Aged , Northern Ireland/epidemiology , Restaurants , Young Adult
4.
Anaesthesia ; 72(6): 694-703, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28654138

ABSTRACT

Contemporary data are lacking for procedural practice, training provision and outcomes for awake fibreoptic intubation in the UK. We performed a prospective cohort study of awake fibreoptic intubations at a tertiary centre to assess current practice. Data from 600 elective or emergency awake fibreoptic intubations were collected to include information on patient and operator demographics, technical performance and complications. This comprised 1.71% of patients presenting for surgery requiring a general anaesthetic, with the majority occurring in patients presenting for head and neck surgery. The most common indication was reduced mouth opening (26.8%), followed by previous airway surgery or head and neck radiotherapy (22.5% each). Only five awake fibreoptic intubations were performed with no sedation, but the most common sedative technique was combined target-controlled infusions of remifentanil and propofol. Oxygenation was achieved with high-flow, heated and humidified oxygen via nasal cannula in 49.0% of patients. Most operators had performed awake fibreoptic intubation more than 20 times previously, but trainees were the primary operator in 78.6% of awake fibreoptic intubations, of which 86.8% were directly supervised by a consultant. The failure rate was 1.0%, and 11.0% of awake fibreoptic intubations were complicated, most commonly by multiple attempts (4.2%), over-sedation (2.2%) or desaturation (1.5%). The only significant association with complications was the number of previous awake fibreoptic intubations performed, with fewer complications occurring in the hands of operators with more awake fibreoptic intubation experience. Our data demonstrate that awake fibreoptic intubation is a safe procedure with a high success rate. Institutional awake fibreoptic intubation training can both develop and maintain trainee competence in performing awake fibreoptic intubation, with a similar incidence of complications and success compared with consultants.


Subject(s)
Bronchoscopy/methods , Fiber Optic Technology , Intubation, Intratracheal/methods , Adolescent , Adult , Aged , Aged, 80 and over , Airway Management/methods , Body Mass Index , Bronchoscopy/adverse effects , Bronchoscopy/instrumentation , Cohort Studies , Conscious Sedation , Female , Head/surgery , Humans , Hypnotics and Sedatives , Incidence , Intubation, Intratracheal/adverse effects , Male , Middle Aged , Neck/surgery , Prospective Studies , Tertiary Care Centers , Treatment Failure , Wakefulness , Young Adult
5.
Ir J Med Sci ; 175(4): 20-5, 2006.
Article in English | MEDLINE | ID: mdl-17312824

ABSTRACT

BACKGROUND: In rural areas it is impossible for eligible patients presenting with acute myocardial infarction (AMI) to receive thrombolysis within the recommended 90 minutes unless administered in the community by the general practitioner. AIMS: The aim of this study was to describe the attitudes of hospital staff and general practitioners towards pre-hospital administration of thrombolysis. METHOD: General practitioners, consultant physicians and nursing staff participated in the survey. RESULTS: General practitioners were convinced of the added benefits of administration of thrombolysis in the community and believed the hospital had a role to play. Likewise the hospital staff agreed with the benefits of pre-hospital thrombolysis. However, they felt that the decision to thrombolyse patients should be made in consultation with the hospital. CONCLUSIONS: Pre-hospital thrombolysis programmes must be continuously monitored and evaluated to identify important factors that may prevent wider use of thrombolytic treatment.


Subject(s)
Attitude of Health Personnel , Emergency Treatment , Myocardial Infarction/drug therapy , Physicians, Family , Rural Health Services , Thrombolytic Therapy , Decision Making , Humans , Ireland
6.
Ir J Med Sci ; 174(3): 9-12, 2005.
Article in English | MEDLINE | ID: mdl-16285331

ABSTRACT

BACKGROUND: Patients with an acute myocardial infarction require a rapid response to their symptoms and the earlier fibrinolysis is given (where indicated), the better the outcome. AIMS: The aim of this study is to compare 'door to needle times' for fibrinolysis in Acute Myocardial Infarction (AMI) in three phases of one year each, at Letterkenny General Hospital. METHODS: In the PREINTERVENTION year all fibrinolysis was performed in the Coronary Care Unit (CCU). In the INTERVENTION year Emergency Department (ED) fast track fibrinolysis was introduced and in the POST INTERVENTION year most fibrinolysis was performed on fast track in the ED. RESULTS: The time saved by the introduction of ED fibrinolysis was significant, 41 minutes on average per patient. Elderly, female patients were more likely to bypass ED fast track fibrinolysis and to be brought to CCU for fibrinolysis, with attendant delays. This has educational implications in relation to the variation in clinical presentation of AMI with age and sex. CONCLUSION: The ED fast track fibrinolysis system is recommended as an effective, safe, achievable and worthwhile intervention towards improving 'door to needle times' for fibrinolysis in AMI.


Subject(s)
Coronary Care Units/standards , Emergency Service, Hospital/standards , Fibrinolytic Agents/therapeutic use , Myocardial Infarction/drug therapy , Thrombolytic Therapy/statistics & numerical data , Time and Motion Studies , Acute Disease , Aged , Female , Humans , Ireland , Male , Middle Aged , Outcome and Process Assessment, Health Care , Practice Guidelines as Topic , Retrospective Studies , Thrombolytic Therapy/standards , Time Factors
7.
Ir Med J ; 95(10): 308-10, 2002.
Article in English | MEDLINE | ID: mdl-12537326

ABSTRACT

Legionnaires' disease is a multi-system illness that can have widespread clinical symptoms, though the principle manifestation is pneumonia. A review of all legionnaires' disease case notifications in Ireland in the 4 year period 1998-2001 was undertaken to assess the degree of concern health authorities here should have in relation to this disease. There were 17 cases of legionnaires' disease (all were legionella pneumophila serogroup 1) notified to the National Disease Surveillance Centre in the period 1998-2001. Nine cases were travel-associated cases with the majority of cases occurring during the summer months. There were 2 deaths. It would appear that legionnaires' disease is rare in Ireland but when compared with other European countries Ireland is conspicuous by its low rate. This would suggest that a major degree of under diagnosis and under reporting of legionnaires' disease currently exists in Ireland.


Subject(s)
Disease Notification/statistics & numerical data , Legionnaires' Disease/epidemiology , Population Surveillance , Adult , Aged , Female , Humans , Ireland/epidemiology , Male , Middle Aged
11.
12.
Cancer Cells ; 3(5): 200-2, 1991 May.
Article in English | MEDLINE | ID: mdl-1892730
13.
Cancer Cells ; 3(3): 110-2, 1991 Mar.
Article in English | MEDLINE | ID: mdl-2054259
14.
Ir J Med Sci ; 160 Suppl 9: 45-9, 1991 Jan.
Article in English | MEDLINE | ID: mdl-1938322

ABSTRACT

The Kilkenny Faculty of the Irish College of General Practitioners and the Kilkenny Health Project have established a Health Assessment Programme (HAP) to standardise the examination and recording of coronary heart disease (CHD) risk factors in general practice. Criteria were agreed for classification and coding of demographic data, relevant medical history and risk behaviours. Height, weight and blood pressure are measured and venous blood sample is taken for total cholesterol estimation. The assessment is followed by appropriate counselling. The HAP was first targetted at men and women aged 40 to 49 years. During the first 16 months of the programme, 2102 assessments were carried out by 41 general practitioners, which represents 29% of the target group. Those taking part had a lower social class distribution when compared with participants in the KHP baseline survey in 1985. There were no significant differences between the two groups in smoking prevalence or in the distribution of body mass index. Median cholesterol was 5% lower in the HAP group than at the baseline survey. 16% of the HAP clients had diastolic blood pressures of 90 mm Hg or more. The HAP has demonstrated that it is feasible to measure CHD risk factors in a variety of general practice settings. The format facilitates a preventive orientation and has proved acceptable to patients.


Subject(s)
Coronary Disease/prevention & control , Health Status , Adult , Family Practice , Female , Humans , Ireland , Male , Middle Aged , Risk Factors
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