ABSTRACT
Each year, more than 167 million pigs in the European Union (EU) are tested for Trichinella spp. under the current meat hygiene regulations. This imposes large economic costs on countries, yet the vast majority of these pigs test negative and the public health risk in many countries is therefore considered very low. This work reviewed the current Trichinella status across the EU as well as the national level of monitoring and reporting. It also reviewed which animal species were affected by Trichinella and in which species it should be surveyed. This information was used to design a cost-effective surveillance programme that enables a standardised monitoring approach within the EU. The proposed surveillance programme relies on identifying sub-populations of animals with a distinct risk. Low-risk pigs are finisher pigs that originate from so-called controlled housing. All other pigs are considered high-risk pigs. Controlled housing is identified by the application of a specific list of management and husbandry practices. We suggest that member states (MS) be categorised into three classes based on the confidence that Trichinella can be considered absent, in the specified sub-population of pigs above a specified design prevalence which we set to 1 per million pigs. A simple and transparent method is proposed to estimate this confidence, based on the sensitivity of the surveillance system, taking into account the sensitivity of testing and the design prevalence. The probability of detecting a positive case, if present, must be high (>95 or >99%) to ensure that there is a low or negligible risk of transmission to humans through the food chain. In MS where the probability of a positive pig is demonstrated to be negligible, testing of fattening pigs from a sub-population consisting of pigs from controlled housing can be considered unnecessary. Furthermore, reduced testing of finishers from the sub-population consisting of pigs from non-controlled housing might even be considered, if conducted in conjunction with a proportionate sampling scheme and a risk-based wildlife surveillance programme where applicable. The proposed surveillance programme specifies the required number of samples to be taken and found negative, in a MS. A MS with no data or positive findings will initially be allocated to class 1, in which all pigs should be tested. When a MS is able to demonstrate a 95% or 99% confidence that Trichinella is absent, the MS will be allocated to class 2 or 3, in which the testing requirement is lower than in class 1.
Subject(s)
Animal Husbandry/standards , Sentinel Surveillance/veterinary , Swine Diseases/epidemiology , Trichinella/isolation & purification , Trichinellosis/veterinary , Animals , Cost-Benefit Analysis , European Union , Female , Hygiene , Male , Public Health , Swine , Swine Diseases/economics , Swine Diseases/prevention & control , Trichinellosis/economics , Trichinellosis/epidemiology , Trichinellosis/prevention & controlSubject(s)
Anthelmintics/pharmacology , Drug Resistance , Helminthiasis, Animal/drug therapy , Helminthiasis, Animal/parasitology , Sheep Diseases/drug therapy , Sheep Diseases/parasitology , Animals , Dose-Response Relationship, Drug , Feces/parasitology , Parasite Egg Count/veterinary , Parasitic Sensitivity Tests/veterinary , Sheep , Treatment Outcome , Wales/epidemiologyABSTRACT
No systematic studies of the occurrence of Trichinella in wildlife have been carried out in Northern Ireland (NI) in recent years, and the last reports of trichinellosis in livestock and human outbreaks in NI date back to 1979 and 1945, respectively. In this study, covering the period 2003/2004 and 2007/2008, a total of 443 red foxes (Vulpes vulpes) were collected throughout the country and screened for trichinellosis using a modified muscle digest method. One examined animal was found to be infected with larvae from Trichinella spiralis, indicating a national prevalence in NI of Trichinella in foxes of 0.2%. This prevalence compares well to the findings reported from the bordering Republic of Ireland [Rafter, P., Marucci, G., Brangan, P., Pozio, E., 2005. Rediscovery of Trichinella spiralis in red foxes (Vulpes vulpes) in Ireland after 30 years of oblivion. J. Infect. 50, 61-65] and could be a further indication for a sylvatic Trichinella life cycle existing independently from the domestic cycle.
Subject(s)
Foxes , Trichinella spiralis/isolation & purification , Trichinellosis/veterinary , Animals , Northern Ireland/epidemiology , Trichinellosis/epidemiology , Trichinellosis/parasitologyABSTRACT
The zoonotic disease trichinellosis is considered one of the re-emerging diseases with surveillance and control methods constantly gaining more importance worldwide. Recent change in European Union (EU) legislation introduces Trichinella-free production, and the possibility of risk-based monitoring for Trichinella in pigs. This has increased the role of wildlife surveillance programmes and their impact on protecting human health as well as highlighted the need for harmonised surveillance protocols and test methods for these infections. A modified digest method, based on the EU reference method for Trichinella testing of pig meat, was used to screen foxes present in Great Britain (England, Scotland and Wales) for trichinellosis. The method was validated using batched pools of 10 g foreleg muscle from up to 20 foxes (maximum amount 200 g). The method gave an average trichinae recovery rate of 71% for spiked samples. Assuming this recovery rate applies to all contaminated samples, then the test sensitivity would be 70% for all tissue samples with 0.1 trichinae per 10 g of foreleg muscle, 99.9% for samples with 1 trichinae per 10 g, and 100% for samples with 2 or more trichinae per 10 g. In two separate studies, conducted between 1999 to 2001 (Smith et al., 2003) and 2003 to 2007, over 3500 wild foxes have been screened for Trichinella with negative results. In the second study reported here, foxes were collected from locations throughout Great Britain using a stratified sampling method based on fox population densities. All work was conducted in compliance with appropriate quality assurance systems, latterly under ISO 9001. Results to date indicate the national prevalence of trichinellosis in foxes is <0.001 based on a 10 g individual sample size, an infection level of 1 larva per gram (l pg) and 95% confidence interval. This, together with no reports of trichinellosis in domesticated pigs, suggests that Britain can be considered a region of negligible risk of trichinellosis.
Subject(s)
Diagnostic Tests, Routine/veterinary , Foxes/parasitology , Helminthiasis, Animal/diagnosis , Trichinella/isolation & purification , Trichinellosis/veterinary , Animals , Diagnostic Tests, Routine/methods , Helminthiasis, Animal/epidemiology , Larva , Mice , Muscle, Skeletal/parasitology , Population Surveillance , Prevalence , Reproducibility of Results , Sensitivity and Specificity , Trichinellosis/diagnosis , Trichinellosis/epidemiology , United Kingdom/epidemiologyABSTRACT
Resistance to the benzimidazole (BDZ) class of anthelmintics in nematodes of sheep has become a common and global phenomenon. The rate at which the selection process and development of resistance occurs is influenced by a number of factors. Of these, the effects of stage-specific exposures to anthelmintic were investigated with a BDZ-resistant strain of Haemonchus contortus (HCR) over five parasite generations. Sheep were infected at each generation with the HCR strain and were treated with thiabendazole (TBZ), either 5 days post-infection (p.i.) (larval line), 21 days p.i. (adult line), or left untreated (no selection line). Additionally eggs from each generation were exposed to TBZ (egg line). Geometric worm burdens were calculated from post-mortem worm counts, both at the start of the study, and after the final selection studies for each of the selection lines. Egg hatch assays (EHAs) were also conducted throughout the study. All data relating to worm burdens and EHAs for each generation were analysed by linear regression to produce dose titration curves and lethal dose(50) (LD(50)) values for each of the selection lines. Over the five generations, LD(50) values on dose-response were increased and worm survival occurred at higher dose rates of TBZ irrespective of the parasite stage exposed to treatment. A similar picture was seen with ED(50) values, which showed a fluctuating but generally upward trend for each of the three selection lines. In contrast, LD(50) and ED(50) values were decreased in the no selection line, indicating some degree of reversion albeit to levels still considered to be BDZ-resistant.
Subject(s)
Anthelmintics/pharmacology , Benzimidazoles/pharmacology , Drug Resistance , Haemonchus/drug effects , Selection, Genetic , Sheep Diseases/parasitology , Sheep/parasitology , Aging , Animals , Anthelmintics/therapeutic use , Dose-Response Relationship, Drug , Haemonchiasis/drug therapy , Haemonchiasis/parasitology , Haemonchiasis/veterinary , Haemonchus/growth & development , Lethal Dose 50 , Logistic Models , Sheep Diseases/drug therapy , Time FactorsABSTRACT
The development of species and populations of parasitic helminths with resistance to one or more anthelmintics is an increasing problem world-wide. The majority of currently available anthelmintics used to control parasitic nematodes of cattle and sheep belong to only three main groups, the benzimidazoles, imidazothiazoles and the avermectins/milbemycins. The successful implementation of helminth control programmes designed to limit the development of resistance in nematode populations depends to some degree on the availability of effective and sensitive methods for its detection and monitoring. A variety of in vivo and in vitro tests have been developed for the detection of nematode populations resistant to the main anthelmintic groups, but each suffers to some degree from reliability, reproducibility, sensitivity and ease of interpretation. This review covers those tests that have been reported and described and highlights some of their strengths and weaknesses.
Subject(s)
Anthelmintics/pharmacology , Helminthiasis, Animal/drug therapy , Helminths/drug effects , Parasitic Sensitivity Tests/veterinary , Animals , Animals, Domestic , Anthelmintics/therapeutic use , Cattle , Cattle Diseases/diagnosis , Cattle Diseases/drug therapy , Cattle Diseases/parasitology , Drug Resistance , Helminthiasis, Animal/diagnosis , Helminths/growth & development , Parasite Egg Count/veterinary , Parasitic Sensitivity Tests/methods , Sensitivity and Specificity , Sheep , Sheep Diseases/diagnosis , Sheep Diseases/drug therapy , Sheep Diseases/parasitology , Species SpecificitySubject(s)
Faculty, Medical , Personal Satisfaction , Radiology/trends , Data Collection , Professional PracticeABSTRACT
RATIONALE AND OBJECTIVES: The purpose of this study was to obtain long-term follow-up data on women with benign histologic results of a breast stereotactic core needle biopsy (CNB). MATERIALS AND METHODS: Mammography charts of 300 consecutive women who underwent prone stereotactic CNB with digital radiography were reviewed. Women with frankly malignant or suspicious histologic findings (51 patients) or a technically unsuccessful stereotactic CNB (one patient) were excluded. The remaining 248 benign core biopsies in 229 women were included in the study. RESULTS: Follow-up mammograms were obtained for 152 lesions with benign histologic results following stereotactic CNB. The mean length of follow-up after stereotactic CNB was 34.6 months. Cancer was diagnosed in six women who underwent surgical biopsies 1/2 to 30 months after benign stereotactic CNB. An initial chart review demonstrated that no follow-up data were available for 64 lesions, and information was missing for an additional seven. CONCLUSION: SCNB remains a sampling procedure that can result in false-negative histologic results. Intrinsic procedural issues were identified that could minimize the potential for missing a malignancy. Goals for patient compliance with follow-up recommendations fell short of expectations.
Subject(s)
Biopsy, Needle/methods , Breast Diseases/pathology , Adult , Aged , Aged, 80 and over , Breast Diseases/diagnostic imaging , Breast Neoplasms/diagnostic imaging , Breast Neoplasms/pathology , Calcinosis/diagnostic imaging , Calcinosis/pathology , Carcinoma in Situ/diagnostic imaging , Carcinoma in Situ/pathology , Carcinoma, Ductal, Breast/diagnostic imaging , Carcinoma, Ductal, Breast/pathology , Diagnosis, Differential , Diagnostic Errors , Disease Progression , False Negative Reactions , Female , Follow-Up Studies , Humans , Hyperplasia/diagnostic imaging , Hyperplasia/pathology , Mammography , Middle Aged , Predictive Value of Tests , Retrospective Studies , Stereotaxic TechniquesABSTRACT
RATIONALE AND OBJECTIVES: The purpose of this study was to survey academic radiology departments to determine how emergency radiology coverage is handled and whether there are any prerequisites for those individuals providing this coverage. MATERIALS AND METHODS: The authors developed a simple two-page survey and sent it to a total of 608 program directors, chiefs of diagnostic radiology, chairpersons, and chief residents at academic departments of radiology. RESULTS: Of the 608 surveys sent, 278 (46%) were returned. More than half of the departments have an emergency radiology section that provides "wet read" coverage during the day, and most academic departments cover the emergency department during the night and on weekends. Nighttime and weekend coverage is handled mostly by residents. Most departments give time off for lunch, with few other prerequisites for faculty who provide emergency coverage. Sixty percent of the departments have teleradiology capability, and many use it for emergency department coverage. CONCLUSION: These results can serve as the basis for discussion and comparison with other institutions regarding a variety of aspects of emergency department coverage.
Subject(s)
Emergency Service, Hospital/organization & administration , Radiology Department, Hospital/organization & administration , Data Collection , Humans , Personnel Staffing and Scheduling/organization & administrationSubject(s)
Antinematodal Agents/pharmacology , Gastrointestinal Diseases/veterinary , Ivermectin/pharmacology , Nematode Infections/veterinary , Sheep Diseases/drug therapy , Animals , Antinematodal Agents/administration & dosage , Antinematodal Agents/therapeutic use , Female , Gastrointestinal Diseases/drug therapy , Injections, Subcutaneous , Ivermectin/administration & dosage , Ivermectin/therapeutic use , Nematode Infections/drug therapy , Sheep , Sheep Diseases/prevention & controlABSTRACT
A survey in 1992 showed that 44 per cent of the sheep farms tested in the south west and 15 per cent of those in the north east of England had parasitic nematode worm burdens which were resistant to benzimidazole anthelmintics, and that 65 per cent of the non-dairy goat farms tested in England and Wales had resistant worms. Ostertagia circumcincta was the main species in sheep and Haemonchus contortus in goats. The resistance to benzimidazoles was diagnosed by a combination of an egg hatch assay and a larval development test. A simplified faecal egg count reduction test was used to investigate sheep and goat farms for signs of ivermectin resistance but no positive cases were detected. The initial identification of levamisole resistance on one farm, both from a faecal egg count reduction test and a positive larval development test, was confirmed by a 'dose and slaughter' trial.
Subject(s)
Anthelmintics/therapeutic use , Benzimidazoles/therapeutic use , Goats/parasitology , Haemonchiasis/veterinary , Ivermectin/therapeutic use , Ostertagiasis/veterinary , Sheep/parasitology , Animals , Disease Outbreaks/veterinary , Drug Resistance , England/epidemiology , Feces/parasitology , Haemonchiasis/drug therapy , Haemonchiasis/epidemiology , Ostertagiasis/drug therapy , Ostertagiasis/epidemiology , Prevalence , Wales/epidemiologyABSTRACT
The faecal egg count reduction test (FECRT) is widely used to assess the presence or absence of levamisole resistance in gastrointestinal nematodes in sheep flocks. However, in a recent study the FECRT appeared to falsely indicate the presence of levamisole resistance. One possible explanation for this result could have been that the anthelmintic failed to completely remove all immature stages of levamisole-susceptible strains, which then developed into egg laying adults and gave misleading results in the FECRT. Artificial infection of lambs with levamisole-susceptible, benzimidazole-resistant strains of Ostertagia circumcincta, Haemonchus contortus and Trichostrongylus colubriformis was followed by treatment with levamisole when the infections were between 2 and 10 days old. Levamisole was 84%, 88% and 98% effective against these immature stages of three species, respectively. The positive control, ivermectin, was more than 99% effective against all three species. The percentage faecal egg count reduction on samples taken 11 and 20 days post-treatment with levamisole was 80% and 78%, respectively. These results demonstrate that, due to the maturation of immature stages, the FECRT based on faecal eggs counts taken 11 or more days after treatment may give results indicative of levamisole resistance despite the absence of levamisole resistant strains of gastrointestinal nematodes.
Subject(s)
Antinematodal Agents/therapeutic use , Digestive System/parasitology , Drug Resistance , Feces/parasitology , Levamisole/therapeutic use , Nematode Infections/veterinary , Parasite Egg Count/veterinary , Sheep Diseases , Animals , Haemonchus , Larva , Nematode Infections/prevention & control , Ostertagia , Reproducibility of Results , Sheep , TrichostrongylusABSTRACT
The ivermectin sustained release bolus (IVSRB), when used at turnout as recommended, will provide season-long control of parasitic bronchitis, thus obviating the need for use of a lungworm vaccine. However, some concerns have been expressed that calves treated with an IVSRB will receive so little exposure to Dictyocaulus viviparus that it will compromise their immunity in subsequent grazing seasons, which would be of particular importance in dairy herds. Although there is evidence that IVSRB-treated calves can develop immunity to D. viviparus when exposed to pasture infection, it was considered worthwhile to evaluate the compatibility of the IVSRB and lungworm vaccination to allow veterinary surgeons the option of using these products concurrently when they have particular concerns about the long term immune status of replacement dairy heifers. Thirty-two dairy replacement heifers were vaccinated with two doses of lungworm vaccine and, at turnout, half the calves received an IVSRB and the remainder an oxfendazole pulse release bolus (OPRB). At the end of the grazing season four replicate bolus treated pairs and four parasite-naive calves were challenged with 1000 D. viviparus infective larvae. At slaughter there was a 95% and 93% reduction in D. viviparus burdens in the IVSRB and OPRB treated calves respectively, compared with the unvaccinated, untreated controls. These results indicate that where it is considered necessary to use lungworm vaccination in addition to an IVSRB or an OPRB, the compatibility of these products with lungworm vaccine will allow development of a protective level of immunity to D. viviparus.
Subject(s)
Anthelmintics/administration & dosage , Benzimidazoles/administration & dosage , Cattle Diseases , Dictyocaulus Infections/prevention & control , Dictyocaulus/isolation & purification , Vaccination , Animals , Anthelmintics/therapeutic use , Benzimidazoles/therapeutic use , Cattle , Delayed-Action Preparations , Dictyocaulus/immunology , Dictyocaulus Infections/immunology , Female , Larva , Parasite Egg CountABSTRACT
OBJECTIVE: To examine the occurrence of breast fibroadenomas in postmenopausal patients referred for breast biopsy. DESIGN: A retrospective review of breast biopsy outcome and of patient demographics, including menstrual and hormonal status. SETTING: The Tucson Breast Center, a large outpatient breast cancer detection clinic affiliated with the University of Arizona Health Sciences Center in Tucson, Arizona. PARTICIPANTS: All women seen at the Tucson Breast Center between 1985 and 1990 who were referred for breast biopsy. RESULTS: A total of 100 fibroadenomas were found in 709 breast biopsies whose results were known. Fifty-two of these were in premenopausal women and 44 in postmenopausal women; the menopausal status of four women was unknown. In postmenopausal women, 11 of the 44 patients reported hormone use. Fibroadenomas constituted 20% (39 of 195) of the benign masses and 12% (39 of 339) of all breast masses in postmenopausal women. Fibroadenomas constituted 10% (44 of 447) of all biopsies in postmenopausal women, including those with breast masses, abnormal calcifications, or other lesions. CONCLUSION: Noncalcified fibroadenomas of the breast are not confined to young women and may constitute a small but noteworthy proportion of lesions coming to breast biopsy in postmenopausal women.
Subject(s)
Breast Neoplasms/epidemiology , Breast Neoplasms/pathology , Fibroadenoma/epidemiology , Fibroadenoma/pathology , Adult , Aged , Aged, 80 and over , Arizona , Biopsy , Breast Neoplasms/diagnostic imaging , Calcinosis/diagnostic imaging , Calcinosis/pathology , Female , Fibroadenoma/diagnostic imaging , Humans , Incidence , Mammography , Middle Aged , Postmenopause , Retrospective StudiesABSTRACT
On five farms identified by in vitro tests to have benzimidazole resistance, and on one farm with apparent anthelmintic failure, faecal egg count reduction tests were performed using benzimidazoles, levamisole and ivermectin. With benzimidazoles efficacy was less than 70 per cent on all farms, confirming the validity of the in vitro tests to detect benzimidazole resistance. On two farms levamisole had an efficacy of less than 90 per cent but laboratory tests failed to demonstrate levamisole resistance. Ivermectin reduced egg counts by 100 per cent on all farms.