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1.
Artigo em Inglês | IMSEAR | ID: sea-135351

RESUMO

Background & objectives: Measuring maternal mortality in developing countries poses a major challenge. In Nepal, vital registration is extremely deficient. Currently available methods to measure maternal mortality, such as the sisterhood method, pose problems with respect to validity, precision, cost and time. We conducted this field study to test a community-based method (the motherhood method), to measure maternal and child mortality in a developing country setting. Methods: Motherhood method was field tested to derive measures of maternal and child mortality at the district and sub-regional levels in Bara district, Nepal. Information on birth, death, risk factors and health outcomes was collected within a geographic area as in an unbiased census, but without visiting every household. The sources of information were a vaccination registry, focus group discussions with local health workers, and most importantly, interview in group setting with women who share social bonds formed by motherhood and aided by their peer memory. Such groups included all women who have given birth, including those whose babies died during the measurement period. Results: A total of 15161 births were elicited in the study period of two years. In the same period 49 maternal deaths, 713 infant deaths, 493 neonatal deaths and 679 perinatal deaths were also recorded. The maternal mortality ratio was 329 (95%CI:243-434)/100000 live birth, infant mortality rate was 48(44-51)/1000LB, neonatal mortality rate was 33(30-36)/1000LB, and perinatal mortality rate was 45(42-48)/1000 total birth. Interpretation & conclusions: The motherhood method estimated maternal, perinatal, neonatal and infant mortality rates and ratios. It has been field tested and validated against census data, and found to be efficient in terms of time and cost. Motherhood method can be applied in a time and cost-efficient manner to measure and monitor the progress in the reduction of maternal and child deaths. It can give current estimates of mortalities as well as averages over the past few years. It appears to be particularly well-suited to measuring and monitoring programmes in community and districts levels.


Assuntos
Criança , Mortalidade da Criança , Coleta de Dados/métodos , Países em Desenvolvimento , Feminino , Humanos , Lactente , Entrevistas como Assunto , Mortalidade Materna , Mães , Nepal , Sistema de Registros , Reprodutibilidade dos Testes , Características de Residência
2.
Saudi Journal of Gastroenterology [The]. 2010; 16 (3): 221-222
em Inglês | IMEMR | ID: emr-123582

RESUMO

Surgical mop retained in the abdominal cavity following surgery is a serious but avoidable complication. The condition may manifest either as an exudative inflammatory reaction with formation of abscess, or aseptically with a fibrotic reaction developing into a mass. Intraluminal migration is relatively rare. We report the case of a 23 year old woman who presented after a previous caesarean section with intestinal obstruction. Plain abdominal radiograph and computed tomography confirmed the presence of gossypiboma. The patient underwent laparatomy and sponge removal. This report discusses the approach to, and manifestations of, migratory surgical gossypiboma


Assuntos
Humanos , Feminino , Obstrução Intestinal , Cesárea , Tomografia Computadorizada por Raios X , Laparotomia
3.
Genet. mol. res. (Online) ; 6(2): 470-475, 2007. graf, ilus
Artigo em Inglês | LILACS | ID: lil-482022

RESUMO

Pyruvate kinase (PK) deficiency is a rare red cell glycolytic enzymopathy. The purpose of the present investigation was to offer prenatal diagnosis for PK deficiency to a couple who had a previous child with severe enzyme deficiency and congenital non-spherocytic hemolytic anemia. PK deficiency was identified in the family by assaying the enzyme activity in red cells. Chorionic villus sampling was performed in an 11-week gestation and the mutation was located in exon 10 of the PKLR gene characterized by polymerase chain reaction and using restriction endonuclease digestion with the MspI enzyme, which was confirmed by DNA sequencing on the ABI 310 DNA sequencer. Both the parents were heterozygous for the 1436G-->A [479 Arg-->His] mutation in exon 10 and the proband was homozygous for this mutation. The fetus was also heterozygous for this mutation and the pregnancy was continued. Prenatal diagnosis allowed the parents with a severely affected child with PK deficiency to have the reproductive choice of having the fetus tested in a subsequent pregnancy.


Assuntos
Humanos , Masculino , Feminino , Gravidez , Anemia Hemolítica Congênita não Esferocítica/diagnóstico , Diagnóstico Pré-Natal/métodos , Mutação , Piruvato Quinase/deficiência , Piruvato Quinase/genética , Anemia Hemolítica Congênita não Esferocítica/genética , Anemia Hemolítica/genética , Análise Mutacional de DNA , Enzimas de Restrição do DNA/metabolismo , Homozigoto , Primeiro Trimestre da Gravidez , Éxons , Índia
4.
Indian J Physiol Pharmacol ; 1983 Apr-Jun; 27(2): 135-40
Artigo em Inglês | IMSEAR | ID: sea-107751

RESUMO

In New Zealand rabbits a single intravenous injection of streptozotocin (STZ 65 mg/kg) elevated the levels of blood sugar to 340 mg percent, which was associated with glycolysis, ureamia, hypercholesterolemia, hypertriglyceridemia and loss of body weight. Oral administration of jambolan seed (1 g/kg) in casein diet significantly lowered the elevated postmeal (1 1/2 hr after) values of blood sugar, cholesterol, FFA and triglyceride down to levels comparable to phenformin. Jambolan seed treatment failed to check ureamia. Weight loss was checked by phenformin and jambolan seed but the gain was not equivalent to that recorded in nondiabetic control. Like phenformin, jambolan seed too failed to control glycogenolysis in STZ-induced diabetes.


Assuntos
Animais , Glicemia/metabolismo , Peso Corporal/efeitos dos fármacos , Diabetes Mellitus Experimental/sangue , Dieta , Lipídeos/sangue , Masculino , Fenformin/farmacologia , Plantas Medicinais , Coelhos , Ureia/sangue
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