Browsing by Author "Sharma, U B"
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Item Acute effects of alcohol on platelet functions.(1985-07-01) Singhal, B; Sharma, U B; Joshi, K C; Sharma, M L; Tambi, L KItem Congenital afibrinogenaemia.(1989-10-01) Mehta, S; Mehta, S R; Malhotra, H; Sharma, U B; Varma, A RA case of congenital afibrinogenaemia in a young female child is described. She had haemorrhagic tendency since birth in the form of markedly prolonged umbilical bleeding and easy bruising afterwards. Two of her brothers had bleeding tendencies, one died shortly after birth due to uncontrollable umbilical bleeding and other died at the age of 12 years from internal haemorrhage. The family study indicates the mode of inheritance to be probably autosomal recessive. The principal laboratory findings are complete non-coagulability of blood, grossly abnormal coagulation tests, zero ESR value, failure to detect fibrinogen by heat coagulation or chemical precipitation tests and biuret reaction and correction of thrombin time after fibrinogen infusion.Item Hemoglobinopathies in anemic children of eastern Rajasthan.(1988-10-01) Bansal, R K; Sharma, U B; Madhulika,; Singh, J; Saxena, SItem In vitro study of effect of glucose. Acetone and change in pH on phagocytic and bactericidal power of neutrophils.(1981-01-01) Sharma, U B; Sharma, M L; Sareen, P MItem In vitro study of phagocytic and bactericidal activity of neutrophils in cases of protein energy malnutrition.(1985-07-01) Chhangani, L; Sharma, M L; Sharma, U B; Joshi, NItem An open study to evaluate the efficacy of artemether in severe falciparum malaria.(1999-09-25) Sharma, P; Swarup, D; Saxena, G N; Bhandari, S; Sharma, U B; Tuteja, RAn open clinical trial was conducted in 30 patients of severe falciparum malaria with heavy parasitaemia (parasitized erythrocytes above 5%). Artemether (methyl ether of dihydroartemisinin-active principle isolated from Chinese plant Qinghaosu) was administered as 80 mg intramuscular injection twice on first day and then single dose of 80 mg intramuscular on 2nd to 5th day. The trial could be completed in 28 patients and two patients expired. In our observation falciparum malaria affected the young adults in their most productive period of life i.e. 25-44 yrs. All patients became afebrile by the 4th day with fever clearance time approximately 31.92 +/- 15.30 hr. Twenty-five patients (83.33%) became parasite free by 5th day with mean parasite clearance time approximately 47.04 +/- 19.95 hr. Deranged liver function and renal profile was observed in 63% and 50% patients respectively. Two patients, who died had very high degree of parasitaemia (50% and 16%) with cerebral malaria. One died due to multiorgan failure and other due to massive hematemesis and shock. The type of response achieved by artemether therapy was analysed as per WHO criteria suggested for chloroquine resistance. S response was observed in 25 patients (cure rate 83.33%). Two patients (6.66%) patients showed R II response, one patient (3.33%) showed R III response and R I response was not observed in any patient. No significant side effects were noted. This pilot study demonstrated that intramuscular artemether is a useful addition to antimalarial drugs in this era of multidrug resistant P. falciparum malaria showing high clinical potency with virtually no side effect.