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1.
Article | IMSEAR | ID: sea-192758

ABSTRACT

Aim: The aim of the study was to determine the frequency of occurrence and percentage distribution of Kell blood group antigens in indigenes of Ogoni ethnic group of Rivers State, Nigeria. Study Design: This was a cross-sectional study carried out among indigenes of Ogoni whose first generational parental origin is Ogoni. A total of 101 subjects (49 females and 52 males), within the age of 30� years were recruited for the study and they were apparently healthy and free from transfusion transmissible infections upon serological screening. Place and Duration of Study: Ogoniland is located in an area along the Niger Delta Eastern edge, and to the north-east of the Imo River and Port Harcourt city. Ogoniland covers about 1036 Sq Km and borders the Bay of Guinea. All participants were recruited in Bori. Bori is the traditional headquarter of Ogoni. Bori is located on latitude: 4040?34.64? N and longitude: 7021?54.68? E. The analysis was carried out at the Post Graduate Laboratory of Rivers State University, Nkpolu-Oroworukwo, Port Harcourt, Rivers State, Nigeria. Port Harcourt, the capital of Rivers State, is located on latitude 4.750N and longitude 7.000E and lies along Bonny River in the Niger Delta. All subjects were recruited the same day and their blood samples collected on 2nd October, 2019, and analysis conducted on 3rd October, 2019. Methodology: Identification of Kell blood group antigens was done using Anti-Kell monoclonal reagent, prepared by Lorne Laboratories Ltd, UK. Lot No: 76090-A5; Expiry Date: 2021/02/21. Phenotyping of red cells was done using tube method as described by Lorne Laboratory Ltd. Results: The result showed zero frequency of occurrence and percentage distribution of Kell blood group antigen in the studied population (49 males and 52 females). Conclusion: The presence of Kell blood group antigens in indigenes of Ogoni recruited for the study which serve as representative of the Ogonis was rare. It is therefore necessary to take into cognizance that haemolytic transfusion reactions due to Kell antigens and antibodies will rarely occur, and as such Kell blood group is not significant in blood transfusion and in antenatal and blood group serology amongst the Ogonis.

2.
Article | IMSEAR | ID: sea-210136

ABSTRACT

Background and Purpose: Cellular component and clotting factors are involved in thrombotic events such as stroke, but the type and nature of alteration of those haemostatic parameters remain unclear. Our objective was to identify possible abnormal changes in some haemostatic parameters in established stroke patients.Materials and Methods: This was a prospective case-control study conducted at Braithwaite Memorial Specialist Hospital, Port Harcourt, Nigeria. Standard operating procedures were adopted to assayfibrinogen, antithrombin, tissue plasminogen activator, prothrombin time and activated partial thromboplastin time as well as the determination of platelet count and platelet indices.The data were analyzed using Statistical Package for Social Science (SPSS) version 17.0 software Results: A total of 108 individuals comprised of 54 stroke patients aged between 45 and 73 years(mean, 59± 13.04 years), 20 (37.04%) men and 34 (62.96%) women and another 54 age-and sex-matched healthy control subjects were studied. Significantly (p<0.05) higher mean values of mean platelet volume (MPPV), platelet distribution width (PDW), Platelet larger cell ratio (PLCR), antithrombin, tissue plasminogen activator and fibrinogen were observed in the stroke patients when compared to those of the control subjects. Whereas, significantly lower (p<0.05) mean values of platelet count, prothrombin time and activated partial thromboplastin time were observed in the stroke patients than in those of the control subjects. Conclusion: Several haemostatic parameters were found to be altered in stroke patients and have the potential to be risk factors but have not been demonstrated as being causative. Further work is needed to establish where they begin to contribute to stroke prognosis

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