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1.
Bull Soc Pathol Exot ; 108(3): 191-6, 2015 Aug.
Article in French | MEDLINE | ID: mdl-26141497

ABSTRACT

This study is the first one that describes the situation of Legionnaires' disease (LD) in Tunisia, with its clinical and epidemiological characteristics and investigates the risk factors associated with Legionella infections in our country. We conducted a retrospective multicentric study during 5 years (2008-2012) concerning all confirmed LD cases in Tunisia and we investigated risk factors for infection. The total of confirmed LD cases was 14. Incidence was 0.03. Mean age: 53.1, sex ratio (M/F): 2.6. Summer-autumnal peak was noted. Risk factors for infection were: the great humidity at home (n=4), living in community (n=3) and practice ablutions (before prayer) in public places (n=4). Community acquired legionellosis (n=9) and nosocomial (n=2). Pulmonary symptoms (n=11)+/-gastrointestinal (n=6) and/or neurological signs (n=4). Beta lactams therapy failed (n=11). CXR showed bilateral lesions (n=6). Abnormalities in laboratory values were noted: hyponatremia (n=9), high CPK levels (n=9). Diagnosis was confirmed by positive urinary Legionella antigens test (n=10) and by direct immunofluorescence (n=1). Treatment was based on bitherapy (n=10). Five patients died. The incidence of LD appears lower than other countries. Some risk factors, as ablutions, are different from that reported in Western countries and seem to be specific to our society. Given the seriousness of its consequences, it is strongly recommended to improve the national surveillance system up and register LD as notifiable disease.


Subject(s)
Intensive Care Units/statistics & numerical data , Legionnaires' Disease/epidemiology , Aged , Anti-Bacterial Agents/therapeutic use , Antigens, Bacterial/urine , Baths , Bronchoalveolar Lavage Fluid/microbiology , Community-Acquired Infections/epidemiology , Comorbidity , Cross Infection/epidemiology , Disease Susceptibility , Female , Hospitals, University/statistics & numerical data , Housing , Humans , Humidity , Incidence , Legionella/isolation & purification , Legionnaires' Disease/diagnosis , Legionnaires' Disease/drug therapy , Legionnaires' Disease/transmission , Length of Stay/statistics & numerical data , Male , Middle Aged , Retrospective Studies , Risk Factors , Seasons , Smoking/epidemiology , Socioeconomic Factors , Tunisia , Water Microbiology
2.
J Fr Ophtalmol ; 37(9): 695-701, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25199482

ABSTRACT

PURPOSE: To assess vision loss, identify affected anatomical sites, determine etiologies and potentially avoidable causes in students attending two institutions for the visually disabled in Tunis city. METHODS: A visit for a complete ophthalmological examination was performed. All students attending these schools were recruited in our study. The World Health Organisation Programme for the Prevention of Blindness (WHO/PBL) examination record for children was used. Data was analysed by the SPSS version 17 statistical software. RESULTS: A total of 172 students were recruited with mean age of 11.9±3.3 years (between 6 and 18 years). One hundred and thirty-seven (79.6%) were under 16 years. The sex-ratio was 1.17. Ninety students (52.3%) had low vision and eighty-two (47.7%) were blind. We reported retina (29%), whole globe (29%), globe appears normal (11%) and optic nerve (9.8%) as the common sites of ocular abnormalities. Retinal dystrophy (22.7%) and congenital glaucoma (22.7%) were the most reported ocular diseases. The main etiologies were hereditary (54.1%) and unknown (30.8%). Consanguinity was reported in 108 students (62.8%), and fifty-five students (32%) had a positive family history. Overall, 50.5% (87/172) of ocular diseases were potentially treatable or preventable. CONCLUSION: Retinal dystrophy and congenital glaucoma were the most common eye diseases. Heredity was the main etiology, and consanguinity was high. To decrease their incidence, awareness of the family members of the risks of consanguinous marriage and appropriate therapy for congenital glaucoma/cataract may significantly improve the child's visual prognosis.


Subject(s)
Blindness/etiology , Glaucoma/congenital , Retinal Dystrophies/complications , Adolescent , Blindness/epidemiology , Child , Consanguinity , Disabled Children , Female , Genetic Predisposition to Disease , Humans , Male , Tunisia
3.
Ophthalmic Res ; 49(4): 177-84, 2013.
Article in English | MEDLINE | ID: mdl-23306536

ABSTRACT

To evaluate a possible association between the complement factor H (CFH) Y402H polymorphism and susceptibility to age-related macular degeneration (AMD) in the Tunisian population, as well as the impact of the genotype distribution among different phenotypes and the response to treatment with intravitreal bevacizumab, exon 9 of CFH was analyzed for the Y402H polymorphism by direct sequencing in 135 healthy controls and 127 sporadic unrelated AMD patients classified into the following groups: 12 atrophic AMD (group G1), 115 exudative AMD (G2) and 10 AMD patients who had fibrovascular scarring (G3) that did not allow a precise grading of the phenotype. Seventy patients in G2 were treated with 1.25 mg intravitreal bevacizumab at 6-week intervals until choroidal neovascularization (CNV) was no longer active. The frequency of the CFH 402H allele was significantly higher in AMD patients than in controls (p = 2.62 × 10(-16)). However, subgroup analysis does not reveal any association between the variant allele H and phenotypes of AMD or CNV. Also, there was no significant difference in response to bevacizumab treatment according to Y402H CFH genotype (p = 0.59). A strong association of the 402H allele with susceptibility to AMD in the Tunisian population was confirmed; however, this variant does not appear to be involved in the clinical progression of this disease or in the postintravitreal bevacizumab response.


Subject(s)
Macular Degeneration/genetics , Polymorphism, Single Nucleotide , Aged , Aged, 80 and over , Angiogenesis Inhibitors/therapeutic use , Antibodies, Monoclonal, Humanized/therapeutic use , Bevacizumab , Case-Control Studies , Complement Factor H/genetics , Female , Fluorescein Angiography , Gene Frequency , Genotype , Humans , Intravitreal Injections , Macular Degeneration/diagnosis , Macular Degeneration/drug therapy , Male , Middle Aged , Polymerase Chain Reaction , Tunisia , Vascular Endothelial Growth Factor A/antagonists & inhibitors , Visual Acuity/physiology
4.
Diabetes Metab ; 27(5 Pt 1): 613-7, 2001 Nov.
Article in French | MEDLINE | ID: mdl-11694863

ABSTRACT

OBJECTIVE: Study the diabetes prevalence on children because, in Tunisia there are not any available data concerning the epidemiological profile of diabetes in the population aged less than 19 years. MATERIAL AND METHODS: We undertook an epidemiological survey on a representative sample of 1,569 pupils from Sousse in Tunisia aged between 13 and 19 years with a global answer rate of 95.4%. Fasting blood glucose was measured by the glucose oxidase method. RESULTS: The main results showed that prevalences of the moderate hyperglycaemia on an empty stomach (2%) and of the mellitus diabetes (0.4%) did not reveal any significant statistical difference between girls and boys. The moderate hyperglycaemia prevalence varied according to the existence of other cardiovascular risk factors such as hypercholesterolemia (3.3%), arterial hypertension (2.1%) and overweight (3.4%). CONCLUSION: Our survey has provided a first evaluation related to a population of youngsters on the diabetes prevalence and other cardiovascular risk factors. This would help to sensitise health authorities on the importance of primary prevention and its setting in health clubs at schools.


Subject(s)
Diabetes Mellitus, Type 1/epidemiology , Blood Glucose/analysis , Child , Fasting , Female , Humans , Hyperglycemia/epidemiology , Male , Middle Aged , Prevalence , Sex Characteristics , Tunisia/epidemiology
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