Publications by Year: 2018

2018
Fedala A, Adjroud O, Saouli A. Contribution à la recherche des effets immunotoxiques du chrome hexavalent chez la rate gestante de la souche Albinos Wistar. Le Premier Séminaire International sur L’Agroalimentaire « SIA 2018 ». 2018.
Mehdid F, Rekkab N, Oukid S, Abad MT, Bradai M, Hamdi S, Boukhemia F, Hamladji RM, Nacer AR, Allouda M, et al. Epidemiological Study of Aplastic Anemia in Algeria for 844 Cases over 10 Years (2007-2016). Blood. 2018;132 (1) :5109.Abstract

Introduction: The aim of this work is to establish an epidemiological approach of aplastic anemia (AA) in Algeria, to identify the different therapeutic strategy and the patients outcomes.

Material and methods: This is a retrospective multi-center epidemiological study over 10 years (from 01 January 2007 to 31 December 2016). The source of information is represented by the medical files and the consultation sheets. The collection of information is ensured by the fact sheets established and distributed to the departments Hematology and Pediatrics at the national level.

Results: A total of 844 cards were received, concerning 844 patients including 746 adults and 94 children. The overall incidence of the disease is 0.21, it varies from 0.16 to 0.28 / 100000 inhabitants / year depending on the year. The average age is 34.7 years with extremes ranging from 1 month to 91 years, the sex ratio (M / F) is 1 (420/424). In adults there is a slight male predominance: sex ratio is 1.11 (421/378). AA is acquired in 806 patients (95.4%) and congenital in 38 patients (4.6%). Among the acquired AA: idiopathic = 694 (86.1%), toxic = 18 (2.23%), viral: 17 (2.1%): HBV = 13, HCV = 3, HIV = 1, drug = 13 (1.6%), gestational = 9, (1.1%), hematopoietic tuberculosis = 1. The presence of an HPN clone in 55 out of 261 patients studied was 21%, associated with a dysimmunitary disease = 5. In congenital AM, Fanconi anemia = 35, Blackfand-Diamond = 2, congenital dyskeratosis = 1. The prognostic classification according to the Camitta criteria and the EBMT criterion: out of 540 evaluable records found: very severe = 83 (15.3%), severe = 291 (53.8%), moderate = 166 (30.7%). CsA-SAL reference immunosuppressive therapy was instituted in only 49 pts (13.1%) with severe and very severe forms. It resulted in a hematologic response in 18 patients (36.5%), 15 patients died and 16 patients were probably lost to follow-up. Three hundred and twenty-seven pts (38.7%) received allogeneic hematopoietic stem cell transplant at CPMC (n = 316) and EHU (n = 11); = 277), Fanconi anemia (n = 44), amgacaryocytosis in its aplastic form (n = 3), erythroblastopenia in aplastic form (n = 2), untagged constitutional medullary aplasia (n = 1). As of 31/12/2016: 344 pts are alive, 208 died, 194 lost sight of and 98 pts whose fate is not specified on the cards.

Conclusion: AA is a rare , the incidence is 0.2 / 100000 inhabitants / year. It affects young adults with a slight male predominance in adults, idiopathic forms are in the foreground and severe forms predominat

Disclosures

No relevant conflicts of interest to declare.

Grifi F, Djenouni A, Bougherira S, Abad MT, Boucherit C, Boudjerra N, Zidani N, Aboura C, Aribi A, Belhani M, et al. Epidemiological Study on β-Thalassemia in Algeria. Blood. 2018;132 (1) :4902.Abstract

Introduction : Among genetic diseases in hematology, β Thalassemia ranks second after sickle cell disorders in Algeria. Given the seriousness and cost of the care that arises, a national action plan is needed. As a starting point, a national survey is essential to know the epidemiological situation of this disease.

Objective : To determine the soci-demographic, diagnosis and evolution characteristics of major and intermediate thalassemia in Algeria.

Materiels and Methods : This is a multicenter, retrospective, analytical study of 775 patients with thalassemia major (TM: 598 cases) and intermediate (TI: 177 cases). This national survey is representative of 21 services (Hematology: 19, Pediatrics: 03). The data was collected from medical records on a survey card distributed to all relevant services.

Results : As of January 1, 2017, the prevalence of β Thalassemia estimated from this study is of the order of 3.47 cases per 100 000 inhabitants. The current average age of major thalassemia (MT) is 17.90 years, with extremes of [1-44 years], that of intermediate form (IT) is 23 years old with extremes of [1-61 years], the sex ratio is 1.15. The concept of consanguinity is specified in 499 patients and is present in 49.30% of cases, the geographical origin of patients is variable, 53% are from the center of the country and 43% from the east. The circumstances of the diagnosis are known in 87.25% of subjects, these are clinical symptoms in 93.91% of patients, with an average age at diagnosis of 16.31 months for MT and 5.5 years for IT. The diagnosis is neonatal in only 5.68% of cases. Blood cells transfusion needs are known in 80% of our cohort, 86% receive a systematic and regular diet; 554 patients are on chelation therapy, the main modality being deferoxamine or Deferasirox type monotherapy. 40 MT patients received Hematopoetic Stem Cell Transplantation. The monitoring of iron overload was based mainly on the determination of ferritinemia, only 8.8% of patients received cardiac and hepatic MRI. Various complications associated with iron overload have been reported, the most common being: Hepatic injury (48%), heart disease (36%), diabetes (30%), hypothyroidism (29.17). %), with average ages of onset of 26.67, 18, 19, and 14.50 years, respectively. In addition, viral serology was performed in 536 patients, 64 (11.9%) of whom were carriers of anti-HCV Ab.

Conclusion : The quality and life expectancy of thalassemic patients has improved significantly in recent years; complications related to iron overload remain the leading cause of death, the means of evaluation remain insufficient in our country. In addition, the care of our patients must be standardized on the national territory.

Disclosures

No relevant conflicts of interest to declare.

BOUKHTACHE NAOUAL, BACHIR ABDELKRIMSI, BELHAMRA MOHAMED, Chafaa S, GHAZI CHERIF, OUCHEN SAWSEN. DYNAMIQUE DES POPULATIONS ET MODALITES D’INFESTATION DE POLLINIA POLLINI COSTA, 1857 (HOMOPTERA, ASTEROLECANIIDAE) SUR L’OLIVIER OLEA EURPAEA L. DANS LA REGION SEMI-ARIDE D’ARRIS (BATNA, NORD-EST D’ALGERIE). Courrier du Savoir. 2018;26.Abstract

Le suivi démo-écologique de la cochenille Pollinia pollini est réalisée dans une oliveraie de la région semi-aride d’Arris (Nord-est Algérie) durant une période d’une année, allant de janvier à décembre 2015. L’étude du mode d’infestation de l’olivier Olea eurpaea par la cochenille est basée sur des dénombrements des différents stades de développement de l’espèce sur les rameaux. Ces dénombrements sont réalisés suivant les orientations de l’arbre (Nord, Est, Sud, Ouest et Centre) et suivant le mode d’installation de la cochenille sur les rameaux (à la surface des rameaux, aux aisselles des rameaux et des feuilles ou à l’intérieur du bois). Ce travail montre que P. pollini évolue en une seule génération annuelle. La parution des larves du premier stade commence à la troisième décade de mars et se poursuit jusqu’à la mi-août. Les larves du deuxième stade apparaissent à la troisième décade d’avril et enregistrent leur pic en juillet. Les femelles adultes, qui sont présentes le long de la période d’étude, enregistrent leurs effectifs maximaux en octobre et en novembre. L’étude de l’abondance globale de P. pollini en fonction des orientations montre que l’espèce s’installe préférentiellement dans les parties Nord, Est et Ouest de l’arbre, avec des proportions relativement proches allant de 20 % à 22 %. Le suivi de l’emplacement de P. pollini sur les rameaux de l’olivier montre que la cochenille s’installe dans trois emplacements différents. Elle préfère s’installer aux aisselles des rameaux et des feuilles (43,23 %), à la surface des rameaux (29,15 %) et à l’intérieur du bois (27,62 %).

Mimeche F, Zedam A, Chafaa S, Mimeche H, Biche M. Seasonal study of the diet of the barbel Luciobarbus callensis (Valencienne1842) in the K'sob reservoir (M'Sila, Algeria). Journal of Water Science . 2018;31 (2) : 89-171 .Abstract

The composition of the diet of the barbel (Luciobarbus callensis) was studied in the K'sob reservoir near the town of M'Sila (Algeria). The capture of the barbels was carried out between September 2010 and August 2011.The diet was studied from 379 specimens collected by trammel net. During the study period, it was noted that the food spectrum essentially consisted of Chironomids, Ephemeroptera and Copepods, which are abundant in the environment. The barbel of the K'sob reservoir has a seasonal food pattern influenced by climatic and ecological conditions and by its reproductive cycle. The diet of L. callensis in the study area is omnivorous, with a zoo-benthophage tendency.

Mimeche F, Zedam A, Chafaa S, Mimeche H, Biche M. Étude saisonnière du régime alimentaire du barbeau Luciobarbus callensis (Valencienne 1842) dans le réservoir de K'sob (M'Sila, Algérie). Revue des sciences de l’eau. 2018;31 (2) :89-171 .Abstract

The composition of the diet of the barbel (Luciobarbus callensis) was studied in the K'sob reservoir near the town of M'Sila (Algeria). The capture of the barbels was carried out between September 2010 and August 2011.The diet was studied from 379 specimens collected by trammel net. During the study period, it was noted that the food spectrum essentially consisted of Chironomids, Ephemeroptera and Copepods, which are abundant in the environment. The barbel of the K'sob reservoir has a seasonal food pattern influenced by climatic and ecological conditions and by its reproductive cycle. The diet of L. callensis in the study area is omnivorous, with a zoo-benthophage tendency.

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