MALARIA;

Objectives: To see the effects of malaria infection on platelet count and haemoglobin in children suffering from malaria.Design: Descriptive study. Setting: CMH Okara and CMH Pano Aqil Cantt. Period: July 2008 to June 2012. Methodology: Childrenadmitted with fever of less than seven days duration who had positive smear for malaria parasite were included in the study. After detailedhistory and thorough examination, patients were investigated to find out the cause of fever. All the patients with localizing cause for feverand history of drug intake were excluded. All patients were investigated with complete blood counts and serial peripheral smears formalaria parasite. Peripheral blood smear examination for malarial parasite was taken as gold standard for the diagnosis of malaria. Cut off9 value for low hemoglobin (anemia) was taken as 10gm/dl and platelet count of less than 150x10 /L, was used to definethrombocytopenia. Patients with thrombocytopenia were divided in to three categories. Mild thrombocytopenia was defined as patients9 9 9 with platelet count of 150x10 /L, moderate thrombocytopenia included patients with platelet counts of 50x10 /L and severe thrombocytopenia consisted of patients with platelet counts of <20x10 /L. Results: A total of one hundred andfourteen smear positive patients were analyzed, out of which 93% had low and 7% had normal platelet count. 95% had Vivax and only 5%9 9 9 had Falciparum malaria. Mean platelet count was 87x10 /L. Mean platelet count in Falciparum was 42x10 /L whereas it was 88 x10 /L inVivax malaria. Sixty two (54%) patients had anaemia. Mean haemoglobin was 9.54gm/dl. Mean Hb in Falciparum malaria was 7.5gm/dland in Vivax it was 9.6gm/dl. Conclusions: Higher frequency of mild to moderate thrombocytopenia and anaemia was observed inhospitalized children suffering from malaria. Plasmodium Vivax was found to be the most common species.