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1.
West Indian med. j ; 56(5): 394-397, Oct. 2007. ilus, tab
Article in English | LILACS | ID: lil-491692

ABSTRACT

OBJECTIVE: To present a quantitative risk assessment of West Nile (WNV) virus introduction into Barbados, West Indies. DESIGN AND METHODS: Three possible modes were considered: a) WNV infected mosquitoes via air transport, by city of departure, b) WNV infected mosquitoes via marine transport and c) viraemic migratory, birds. We estimated the number of WNV infected migratory birds as the product of the proportion of migratory birds infected and the number of migratory birds entering Barbados in three taxonomic groups. We further estimated the number of days these birds would be infectious as: [formula: see text]. We then estimated the number (#) of infectious mosquito-days for mosquitoes entering Barbados via air transport as: # infected mosquitoes = (total flights per week/city) x (duration of WNV season) x (number of Culex mosquitoes aboard each flight) x (Culex mosquito WNV infection prevalence) x (vector competence index) x (days infectious). The number of infected mosquitoes entering Barbados via marine transport was estimated using a similar expression as for air transport, except that the number of airplanes and mosquitoes/airplane were substituted with the # of sea containers during a 22-week mosquito season and # of mosquitoes/container. RESULTS: Migratory birds (approximately 69-101 infected birds/year) were associated with the highest introductory risk followed by mode (a) (approximately 2 infected mosquitoes/year) and mode (b) (0. 004 infected mosquitoes/year). CONCLUSIONS: Migratory birds and mosquitoes via air are imminent threats for virus introduction. Impending co-circulation of West Nile virus and four strains of dengue virus may present new challenges for public health.


OBJETIVO: Presentar una valoración del riesgo cuantitativa de la introducción del Virus del Nilo Occidental (VNO) en Barbados, West Indies. MÉTODOS E DISEÑO: Se consideraron tres posibles modos: a) mosquitos infectados con el VNO vía transporte aéreo, por ciudad de salida, b) mosquitos infectados con el VNO vía transporte marítimo, y c) aves migratorias virémicas. Calculamos el número de aves migratorias infectadas con el VNO como el producto de la proporción de aves migratorias infectadas por el número de aves migratorias que entran a Barbados en tres grupos taxonómicos. Luego calculamos el número de días en que estas aves serían infecciosas, de la forma siguiente:[fórmula: ver en el texto].Calculamos entonces el número de días-mosquito infeccioso para los mosquitos que entran en Barbados mediante transporte aéreo, como sigue: # mosquitos infectados = (vuelos totales por semana/ciudad) x (duración de la estación del VNO) x (número de mosquitos Culex a bordo de cada vuelo) x (prevalencia de infección con VNO por mosquito Culex) x (índice de competencia del vector) x (días infecciosos). El número de mosquitos infectados que entraron a Barbados por vía del transporte marítimo fue calculado usando una fórmula similar a la usada en relación con el transporte aéreo, excepto que el número de aeroplanos y mosquitos/ aeroplanos fueron sustituidos con el # de contenedores marítimos durante una temporada de mosquitos de 22 semanas y el # de mosquitos/contenedor RESULTADOS: Las aves migratorias ~ (69-101 aves infectadas/años) estuvieron asociadas con el riesgo de introducción más alto seguido del modo (a) (~2 mosquitos infectados/año), y finalmente el modo (b) (0.004 mosquitos infectados/año). CONCLUSIONES: Las aves migratorias y los mosquitos por vía aérea representan una amenaza inminente de introducción de virus. La co-circulación inminente del Virus del Nilo Occidental y cuatro cepas de virus de dengue pueden presentar nuevos desafíos a la salud pública.


Subject(s)
Humans , Animals , West Nile Fever/transmission , Risk Assessment/methods , West Nile virus , Birds , Barbados/epidemiology , Culicidae , Risk Factors , West Nile Fever/epidemiology , Animal Migration , Models, Theoretical , Public Health
2.
West Indian med. j ; 53(3): 198-200, Jun. 2004.
Article in English | LILACS | ID: lil-410463

ABSTRACT

Human infection with the sheep nasal botfly Oestrus ovis occurs sporadically. In most cases, there is a history of a strike in the eye by the adult fly. Human O. ovis has been reported rarely from the Americas. We report the first case of O. ovis infection in the Caribbean region, which occurred in an urban area of Barbados. The patient responded to removal of the larvae from the conjunctiva and symptomatic treatment


Subject(s)
Humans , Animals , Female , Middle Aged , Diptera/growth & development , Eye Infections, Parasitic/diagnosis , Myiasis/diagnosis , Barbados , Goats/parasitology , Eye Infections, Parasitic/therapy , Larva , Sheep/parasitology , Zoonoses/parasitology
3.
West Indian med. j ; 51(1): 10-13, Mar. 2002.
Article in English | LILACS | ID: lil-333305

ABSTRACT

Leptospirosis is a zoonotic disease, maintained by chronic infection of the kidneys of reservoir animals, usually small mammals. Infection in humans is acquired from direct or indirect exposure to the urine of infected animals. Leptospirosis has a high incidence in tropical regions, and has been studied extensively in several Caribbean countries. We studied the carriage of Leptospira serovars by two small mammals which are potential maintenance hosts of the disease in Barbados. A total of 136 mongooses (Herpestes auropunctatus) and 97 mice (Mus musculus) were caught in live traps. Leptospiral antibodies were detected by microscopic agglutination test (MAT) using antigens representing 12 serogroups, and kidney tissues were inoculated into polysorbate medium for isolation of leptospires. The seroprevalence (at a titre of > or = 100) in mice was 28.2 (24/85, 95 CI 19.0, 39.1) and in mongooses 40.7 (48/118, 95 CI 31.7, 50.1). In mice, antibodies were detected predominantly against serogroups Ballum and Autumnalis, while in mongooses the predominant serogroup was Autumnalis. Leptospires were isolated from 28 mice (28.9, 95 CI 20.1, 39.0) and from 4 mongooses (2.9, 95 CI 0.8, 7.4). Mouse isolates were identified as serovars arborea (17) and bim (7). As in other parts of the world, common house mice (Mus musculus) represent a significant reservoir of leptospirosis. Although carriage of the Ballum serovar, arborea, was not unexpected, this represents the first time that an animal reservoir of serovar bim has been identified. This is significant because bim causes about 63 of human leptospirosis in Barbados, and control efforts and education for prevention can now be targeted at a specific reservoir.


Subject(s)
Animals , Male , Female , Leptospira , Leptospirosis , Mice , Herpestidae , Disease Vectors , Barbados , Urine , Carrier State , Kidney , Leptospira
4.
West Indian med. j ; 50(2): 137-139, Jun. 2001.
Article in English | LILACS | ID: lil-333393

ABSTRACT

Haemophilus influenzae is one of the common bacterial pathogens which affect children. Resistance to frequently used antibiotics is becoming a significant problem in community isolates of common pathogens. A retrospective review was conducted of the serotypes and antimicrobial sensitivity of H influenzae isolates from bacterial conjunctivitis, over an 18-month period. Data on antimicrobial sensitivity (obtained by the National Committee for Clinical Laboratory Standards disk diffusion method) and beta-lactamase production, and typing results, were analysed. Ninety-nine isolates were recovered, of which 87 were typed. Most isolates were recovered from children under one year of age. Ninety-three percent were unencapsulated and biotypes I and IV were most common. H influenzae type b was recovered only twice. beta-lactamase was produced by 41 isolates while four isolates were ampicillin-resistant but did not produce beta-lactamase. All isolates were sensitive to chloramphenicol and 45 were co-trimoxazole sensitive. H influenzae is commonly isolated from bacterial conjunctivitis in Barbados and, as elsewhere, the majority of isolates are from small children and are non-encapsulated. However, there is a high prevalence of beta-lactamase production, which may serve as a reservoir for transfer to more invasive encapsulated strains of H influenzae within the oropharyngeal flora.


Subject(s)
Humans , Infant , Adult , Conjunctivitis, Bacterial , Haemophilus influenzae , beta-Lactamases , Microbial Sensitivity Tests , Chloramphenicol , Haemophilus influenzae , Retrospective Studies , Anti-Infective Agents , Anti-Bacterial Agents/pharmacology , Trimethoprim, Sulfamethoxazole Drug Combination/pharmacology
5.
West Indian med. j ; 50(1): 50-54, Mar. 2001.
Article in English | LILACS | ID: lil-333413

ABSTRACT

The susceptibility of 39 toxin producing Clostridium difficile isolates from stools of hospitalized patients was determined, by disc diffusion, to six antibiotics. All but one isolate (toxin A negative) produced toxin A and toxin B. A wide variation in susceptibility to clindamycin, tetracycline and chloramphenicol was noted. Erythromycin and cotrimoxazole showed a clear-cut discrimination in resistance and susceptibility, while all isolates were sensitive to vancomycin. Erythromycin sensitive isolates demonstrated a significant association with diarrhoea (60.9, 14/23, p < 0.001). These strains were predominantly found at the University Hospital of the West Indies (UHWI, 94.1, 16/17). Strains resistant to erythromycin and clindamycin together were commonly found at the National Chest Hospital (NCH, 68.2, 15/22). All erythromycin sensitive strains found at the NCH were from patients transferred to that hospital. These findings suggest that there is a common strain of C difficile (erythromycin resistant) at the NCH different from that found at the UHWI; the resistant pattern seen with isolates from the NCH was typical of toxigenic serogroup C strain and could be typed by the the disc diffusion method. Patients at the NCH who were colonized with either of the two strains of C difficile were likely to get diarrhoea, once there was suppression of the normal microflora by antibiotics and colonic overgrowth with C difficile.


Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Enterocolitis, Pseudomembranous , Microbial Sensitivity Tests , Clostridioides difficile , Diarrhea , Anti-Bacterial Agents/pharmacology , Bacterial Toxins , Aged, 80 and over , Enterocolitis, Pseudomembranous , Clostridioides difficile , Treatment Outcome , Enterotoxins , Jamaica
6.
West Indian med. j ; 49(4): 340-343, Dec. 2000.
Article in English | LILACS | ID: lil-333429

ABSTRACT

Leptospirosis is relatively uncommon in children. Two cases of severe leptospirosis occurred in teenaged boys who shared a common exposure via immersion in fresh water. While both patients had laboratory-confirmed leptospirosis, their symptoms differed in many respects.


Subject(s)
Adolescent , Child , Humans , Male , Leptospirosis , Swimming , Penicillins , Ampicillin , Leptospirosis , Fresh Water , Diagnosis, Differential , Severity of Illness Index , Water Microbiology , Disease Outbreaks/statistics & numerical data , Serologic Tests
7.
West Indian med. j ; 48(1): 16-19, Mar. 1999.
Article in English | LILACS | ID: lil-473126

ABSTRACT

Organisms of the Mycobacterium fortuitum complex are recognised but uncommon causes of pulmonary disease, primary cutaneous disease and a wide spectrum of nosocomial infections. M fortuitum was isolated from 20 patients over a 15 month period, with an apparent clustering of isolates occurring from January to March 1994. The molecular epidemiology of this clustering was investigated using an arbitrary primer polymerase chain reaction method (AP-PCR). 21 isolates were studied, which yielded 13 distinct profiles. Multiple isolates from a single patient yielded identical profiles. All of seven isolates recovered during the six week period from January to March 1994 shared a common profile which was distinct from all other isolates, suggesting that a single strain was isolated from specimens from all seven patients. The source of this cluster is uncertain. We can find no epidemiological basis for an episode of cross-infection within the hospital environment, and it is assumed that contamination of the specimens during collection, transport or processing was responsible for the [quot ]pseudo-outbreak[quot ] of M fortuitum.


Subject(s)
Humans , Cross Infection/diagnosis , Mycobacterium Infections, Nontuberculous/diagnosis , Mycobacterium fortuitum/classification , Specimen Handling , Bronchiectasis/microbiology , Molecular Epidemiology , Sputum/microbiology , Retrospective Studies , Feces/microbiology , AIDS-Related Opportunistic Infections/diagnosis , Respiratory Tract Infections/diagnosis , Mycobacterium fortuitum/genetics , Pneumonia, Bacterial/diagnosis , Lung Diseases, Obstructive/microbiology , Polymerase Chain Reaction , Vasculitis/microbiology
8.
West Indian med. j ; 47(1): 15-17, Mar. 1998.
Article in English | LILACS | ID: lil-473428

ABSTRACT

Rodents, particularly rats, are widely held to be the source of most human cases of leptospirosis. Feral rats were trapped at sites throughout Barbados during two six month surveys: from October to March 1986/87 and from October to March 1994/95. During the first survey, 63 rats were trapped, of which 26 (41) were identified as Rattus rattus and 37 (59) as Rattus norvegicus. In the second study, 100 rats were trapped, of which R. rattus comprised 24(24) and R. norvegicus 76(76). Cultures of blood, urine and kidney were made in EMJH medium. Leptospires were isolated from 12/63 (19) and from 16/100 (16) of the rats during 1986/87 and 1994/95, respectively; 27/28 isolates were recovered from the kidneys or urine or both, while only one isolate was recovered from the blood. During the first study, isolates were identified as serovars copenhageni (11) and arborea (1), while in the second study, serovars copenhageni (9), arborea (5) and bim (1) were identified; one isolate was lost before it could be identified. In the first study, antibodies were detected by microscopic agglutination at a titre of > or = 100 in 26/62 (42) of rats tested, while in the second survey, 5/100 (5) of rats had similar titres. In two surveys, conducted eight years apart, we confirmed that rats in Barbados are commonly infected with leptospires, and that viable organisms are found in the kidneys and urine, evidence of chronic infection and thus excretion of leptospires in rodent urine. Moreover, the predominant serovar isolated was copenhageni, of which Rattus spp. are the worldwide reservoir. There was little evidence that rats act as a reservoir for the serovar bim, the most common cause of human leptospirosis in Barbados.


Subject(s)
Humans , Male , Female , Animals , Animals, Wild/microbiology , Leptospira/isolation & purification , Leptospirosis/transmission , Rats/microbiology , Disease Vectors , Barbados , Rodent Control , Leptospirosis/prevention & control , Kidney/microbiology , Urine/microbiology
9.
West Indian med. j ; 44(3): 81-4, Sept. 1995.
Article in English | LILACS | ID: lil-152460

ABSTRACT

A pharmacoeconomic study of 15 antibiotics available in Barbados was performed. The antibiotics studied were amoxycillin/clavulanate, ampicillin/sulbactam, cefazolin, cefotaxime, ceftazidime, ceftriaxone, clindamycin, cloxacillin, cotrimoxazole, gentamicin, imipenem, metronidazole, piperacillin/tazobactam, and vancomycin. The costs of use of these compound were calculated for a five-day course using a formula comprising eight categories: antibiotic purchase cost, maintenance of intravenous access, drug delivery cost, drug monitoring cost, dose readjustment, general monitoring cost, 'sharps' disposal cost and adverse effects. The cost of adverse effects were not included in this study due to lack of accurate data. The total cost of antibiotic use (in U.S. dollars) ranged from $42.52 to $463.73 per five-day course. Generic compound were less expensive ($45.52-$98.23) than brand-name compounds ($106.18 - $463.73). Antibiotic purchase costs accounted for proportions of total costs ranging from 7 to 93 percent. Non-drug costs represented a much greater proportion of total costs of generic compounds. For most compound the non-drug costs were related to the frequency of dosing, but for gentamicin the non-drug costs were relatively higher because of the need for monitoring of serum gentamicin levels. Efficacy and freedom from side-effects will remain the most important determinants in the choice of antibiotic therapy. However, pharmacoeconomic analyses can provide prescribers with the information required to make cost-effective choices for treatment of their patients


Subject(s)
Bacterial Infections/drug therapy , Economics, Pharmaceutical , Anti-Bacterial Agents/economics , Barbados , Infusions, Intravenous/economics , Efficacy , Drug Costs , Costs and Cost Analysis , Fees, Pharmaceutical , Anti-Bacterial Agents/therapeutic use
10.
West Indian med. j ; 38(3): 126-32, Sept. 1989. ilus
Article in English | LILACS | ID: lil-81189

ABSTRACT

Bacterial vaginosis is a common, non-inflammatory infection of the vagina. It is characterised by the presence of a thin, homogenous, greyish-white discharge. The differencial diagnosis includes infection with Trichomonas vaginalis and Candida albicans. A diagnosis of bacterial vaginosis may be made by the detection of three of the following: characteristic discharge, pH of 5 or greater, clue cells and a positive KOH amine test. Culture of vaginal discharge is not necessary to effect a diagnonsis. Bacterial vaginosis respondes readily to treatment with metronidazole at a dosage of 400 mg twce daily for sevem days, although a proportion of patient suffer a recurrence of symptoms. Treatment of sexual partners may be necessary in such cases. Bacterial vaginosis results from the synergistic interaction of Gardnerella vginalis and obligate anerobes, including Bacteroides and Mobiluncus species. The pathogenesis, laboratory diagnosis, treatment, and the mechanisms by which these organisms produce the symptoms of bacterial vaginosis are discussed


Subject(s)
Humans , Female , Vaginal Diseases/diagnosis , Bacterial Infections/diagnosis , Recurrence , Metronidazole/therapeutic use , Diagnosis, Differential , Vaginal Diseases/physiopathology , Vaginal Diseases/drug therapy , Bacterial Infections/physiopathology , Bacterial Infections/drug therapy
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