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Hematological and biochemical parameters evaluation of healthy volunteers of the Clinical Pharmacology Unit of UFC / AvaliaÃÃo dos parÃmetros hematolÃgicos e bioquÃmicos de voluntÃrios sadios da Unidade de Farmacologia ClÃnica da UFCIsabele Bessera Santos Gomes 20 June 2005 (has links)
CoordenaÃÃo de AperfeiÃoamento de Pessoal de NÃvel Superior / Os valores de referÃncia de exames laboratoriais sÃo definidos com base em critÃrios estatÃsticos para uma amostra aleatÃria de indivÃduos. Os parÃmetros de referÃncia publicados sÃo provenientes de uma variedade de amostras, incluindo doadores de sangue, participantes de exames admissionais e voluntÃrios normais que fazem exames de rotina para ensaios clÃnicos. Esta pesquisa à do tipo documental com abordagem quantitativa. A amostra foi constituÃda por 1.947 exames laboratoriais dos voluntÃrios sadios, de ambos os sexos, com idade mÃdia de 25 anos, que participaram de ensaios clÃnicos na UNIFAC, entre os anos de 1999 e 2003. Para a realizaÃÃo do estudo, foram colhidos dos prontuÃrios as seguintes informaÃÃes: dados de identificaÃÃo do voluntÃrio, alÃm dos parÃmetros hematolÃgicos e bioquÃmicos. Foram investigados setenta e cinco ensaios clÃnicos, tendo os resultados demonstrado diferenÃa estatÃstica entre os sexo, para a maioria dos parÃmetros analisados. As faixas de referÃncia foram calculadas pelo mÃtodo dos percentis, sendo encontrado os seguintes valores para a anÃlise hematolÃgica para mulheres e homens, respectivamente: eritrÃcitos - de 3,9 a 5,0 milhÃes/mm3 e 4,4 a 5,7 milhÃes/mm3; hemoglobina - de 14,8 a 15,3 g/dL e 13,6 a 16,9 g/dL; leucÃcitos - de 4.400 a 10.500/ mm3 e 4.200 a 10.100/mm3; plaquetas â de 165.000 a 397.000/ mm3 e 155600 a 354400/ mm3. Jà para os parÃmetros bioquÃmicos, verificaram-se os seguintes valores para mulheres e homens, respectivamente: creatinina - de 0,5 a 0,9 mg/dL e 0,7 a 1,2 mg/dL; glicose - de 69 a 96 mg/dL e 71 a 100 mg/dL; colesterol - de 118 a 224 mg/dL e 112 a 219 mg/dL; triglicerÃdeos - de 38,0 a 171 mg/dL e 42 a 197 mg/dL. Os nossos achados sugerem que os valores de referÃncia dos parÃmetros investigados, para a populaÃÃo metropolitana de Fortaleza, sejam redefinidos como aqueles incluÃdos no intervalo entre os percentis 2,5o e 97o, os quais correspondem a 95% da distribuiÃÃo total dos valores de cada parÃmetro. / The values of reference of laboratorial parameters are defined on the basis of statistical criteria for a random sample of individuals. The published parameters of reference are proceeding from a variety of samples, including blood donors, participants of job admission examinations and normal voluntaries that are submitted to routine examinations for clinical assays. This research is of the documentary type with quantitative approach. The sample was constituted by 1.947 laboratorial parameters of healthy volunteers, of both genders, with average of 25 years, which had participated of clinical assays in the Clinical Pharmacological Unit (UNIFAC â UFC), between the years of 1999 and 2003. For the accomplishment of the study, the following information had been obtained from case report files: identification of the volunteer, besides the hematological and biochemical parameters. Seventy five clinical assays have been investigated. The results demonstrated statistical differences between the genders, for the majority of the analyzed parameters. The normal reference intervals have been calculated by the method of percentiles, being found the following values for the hematological analysis for women and men, respectively: erytrocytes â from 3.9 to 5.0 millions/mm3 and from 4.4 to 5.7 millions/mm3; hemoglobin â from 14.8 to 15.3 g/dL, and from 13.6 to 16.9 g/dL; leukocytes â between 4.400 and 10.500/mm3, and between 4.200 and 10.100//mm3; platelets â from 165.000 to 397.000/mm3, and from 155.600 to 354.400/mm3. For the biochemical parameters, there were found the following values for women and men, respectively: creatinine â from 0.5 to 0.9 mg/dL, and from 0.7 to 1.2 mg/dL; glucose â between 69 and 96 mg/dL, and between 71 and 100 mg/dL; cholesterol â between 118 and 224 mg/dL, and between 112 and 219 mg/dL; triglycerides â from 38 to 171 mg/dL, and from 42 to 197 mg/dL. Our findings suggest that the reference values of investigated parameters, for the metropolitan population of Fortaleza, must be redefined as that enclosed in the interval between the 2.5 and 97, which correspond to 95% of the total distribution of the values of each parameter.
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Effects of Dehydration and Blockade of the Renin-Angiotensin System in the One-humped Camel (Camelus dromedarius)Al Haj, Mahmoud January 2013 (has links)
The one-humped or the dromedarian camel is a pseudo-ruminant mammal, well adapted to the hot and dry climates of the desert. Its ability to withstand torrid heat and extreme desiccation is of paramount importance to its survival. The studies presented in this thesis were designed to investigate and document the effect of dehydration in the presence or absence of angiotensin II (Ang II) AT1 receptor blocker (losartan) on blood constituents, electrolytes, hormones, neurotransmitters as well as liver and kidney enzymes in a subset of dehydrated camels and to compare them with hydrated camels. Additionally, we studied the response of atrial natriuretic peptide (ANP) and B-type natriuretic peptide (BNP) and revealed for the first time the cardiac storage form of BNP in the camel heart. Dehydration induced significant increments in packed cell volume (PCV), white blood cells (WBC), gamma glutamyl-transferase (GGT), serum sodium, creatinine and urea levels, and a doubling in plasma cortisol and arginine vasopressin (AVP) levels. At the same time dehydration caused significant decrease in body weights, plasma insulin like growth factor-1 (IGF-1) and its binding protein-3 (IGFBP-3), and a 50% decrement in ANP and BNP levels. Moreover, dehydration with and without losartan resulted in significant changes in stress hormones and anti-oxidants in plasma, liver and kidney homogenates. Losartan on one hand enhanced the effect of dehydration resulting in significant increases in sodium, creatinine and urea levels. In addition losartan raised the binding affinity of Ang II AT2 receptors in the small intestine with 8-fold and with 16-fold for liver AT1 receptors, indicating that Ang II AT1 and AT2 receptor binding sites were present in camel's small intestine while only AT1 receptor binding sites were found in the camel liver. One the other hand losartan resulted in significant decrease in body weights impaired the rise in anti-diuretic hormone and reduced aldosterone level. Finally, we showed that the proBNP is the storage form of BNP in the camel heart.
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