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1.
Obstet Gynecol ; 85(6): 993-8, 1995 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-7770272

RESUMO

OBJECTIVE: To study the sociodemographic risk factors and clinical features of Torulopsis glabrata vaginal infection. METHODS: We evaluated the sociodemographic and clinical characteristics of 86 consecutive symptomatic women attending a vaginitis clinic and isolated T glabrata. Case patients were compared with a control group of 174 asymptomatic women with negative vaginal cultures and an additional group of 625 symptomatic women with vaginal cultures positive for Candida albicans. In addition, the sensitivity of the isolates to the more common antimycotic agents used was tested by the modified Kirby-Bauer method. RESULTS: Patients with T glabrata vaginal infection were from lower socioeconomic backgrounds and had less education. They were more likely to use vaginal tampons and to be seropositive for human immunodeficiency virus than were negative controls. Compared with C albicans infection, T glabrata was more frequent among women over 38 years of age and in those with less education and of lower social class. In logistic regression analysis, T glabrata was associated more frequently with recurrent vaginal candidiasis than was C albicans (odds ratio 2.46, 95% confidence interval 1.33-4.54; P = .004). Six of the 86 (7%) T glabrata isolates and none of the C albicans isolates (P < .001 by Fisher exact test) were resistant to the imidazole derivatives tested. CONCLUSION: Torulopsis glabrata was isolated in 10% of women with vulvovaginal candidiasis attending a vaginitis clinic. This infection was associated with recurrent vaginitis in almost one-third of case patients presenting with symptoms.


Assuntos
Candidíase Vulvovaginal/epidemiologia , Vaginite/epidemiologia , Adulto , Estudos de Casos e Controles , Intervalos de Confiança , Feminino , Humanos , Modelos Logísticos , Razão de Chances , Fatores de Risco , Sensibilidade e Especificidade , Fatores Socioeconômicos , Vaginite/microbiologia
2.
J Hum Hypertens ; 8(10): 771-5, 1994 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-7837214

RESUMO

The relationship between smoking in pregnancy and the development of pre-eclampsia has not been well studied. Smoking habits were prospectively evaluated in 117 patients with pre-eclampsia and 468 normotensive control pregnancies. Twenty cases (17.1%) and 120 controls (25.6%) reported smoking at any time during pregnancy. In stepwise multiple logistic regression analysis, smoking in pregnancy was a significant protective factor against the occurrence of pre-eclampsia (adjusted odds ratio = 0.50; 95% confidence interval 0.28-0.80, P = 0.018). On the other hand, a history of pre-eclampsia in previous pregnancies, low (< 6th grade) educational level, a body mass index > 24 and maternal blood group AB were factors independently associated with an increased risk of pre-eclampsia. In conclusion, this study confirms that smoking in pregnancy reduces the risk of pre-eclampsia. However, the harmful consequences of smoking on pregnancy outcome far outweigh this risk reduction.


Assuntos
Pré-Eclâmpsia/etiologia , Fumar/efeitos adversos , Adolescente , Adulto , Estudos de Casos e Controles , Feminino , Humanos , Gravidez , Estudos Prospectivos , Fatores de Risco
3.
J Reprod Med ; 40(3): 209-15, 1995 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-7539849

RESUMO

We evaluated the impact of the severity of intrauterine growth retardation (IUGR) measured as the proportion of expected birth weight (birth weight x 100/median birth weight) on short-term neonatal complications and two-year infant neurodevelopmental outcome. The study was carried out on 236 singleton pregnancies complicated by idiopathic IUGR. The rates of bradycardia, respiratory distress syndrome, hypocalcemia, ventilatory support, apneic crises, transient neurologic signs and poor neonatal outcome (neonatal death or cerebral palsy) significantly correlated with the increasing severity of IUGR. In logistic regression analysis more severely growth retarded infants (< 67.5% of expected birth weight) had higher rates of bradycardia, respiratory distress syndrome, hypocalcemia and bacterial sepsis when compared with those less severely affected (84-67.5% of expected birth weight). In pregnancies complicated by idiopathic IUGR, most short-term neonatal complications are inversely related to the severity of growth failure as evaluated by the proportion of expected birth weight.


Assuntos
Peso ao Nascer , Deficiências do Desenvolvimento/etiologia , Retardo do Crescimento Fetal/complicações , Adulto , Pré-Escolar , Feminino , Humanos , Recém-Nascido , Modelos Logísticos , Estudos Longitudinais , Masculino , Razão de Chances , Gravidez , Resultado da Gravidez , Prognóstico , Índice de Gravidade de Doença
4.
Acta Obstet Gynecol Scand ; 73(8): 625-9, 1994 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-7941986

RESUMO

BACKGROUND: To evaluate the impact of the expectant management of hypertensive disorders of pregnancy on infant neurodevelopmental outcome. METHODS: The two-year neurodevelopmental outcome of infants delivered prematurely because of complications of maternal hypertension after expectant management was compared with that of infants of uncomplicated age-matched pregnancies delivered after spontaneous preterm labor or premature rupture of membranes. RESULTS: The rate of cerebral palsy was similar between the two groups. Conditional logistic regression analysis of the matched sets showed an increased risk of minor neurodevelopmental impairment among infants delivered after severe hypertension (odds ratio (OR) = 4.0, 95% confidence interval (CI) 1.34-12.1) or preeclampsia (OR = 4.0, 95% CI = 1.61-10.2). Fetal growth retardation was not associated with increasing infant neurodevelopmental morbidity. CONCLUSIONS: Infants delivered prematurely because of preeclampsia or severe hypertension are at increased risk of later minor neurodevelopmental problems.


Assuntos
Paralisia Cerebral/etiologia , Hipertensão/epidemiologia , Doenças do Sistema Nervoso/congênito , Complicações Cardiovasculares na Gravidez/epidemiologia , Resultado da Gravidez , Paralisia Cerebral/epidemiologia , Desenvolvimento Embrionário e Fetal , Feminino , Retardo do Crescimento Fetal/epidemiologia , Retardo do Crescimento Fetal/etiologia , Ruptura Prematura de Membranas Fetais/etiologia , Humanos , Hipertensão/complicações , Recém-Nascido de Baixo Peso , Recém-Nascido , Doenças do Sistema Nervoso/epidemiologia , Trabalho de Parto Prematuro , Pré-Eclâmpsia , Gravidez , Análise de Regressão
5.
Br J Obstet Gynaecol ; 101(11): 954-8, 1994 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-7999725

RESUMO

OBJECTIVE: To estimate the risk of fetal growth retardation resulting from the interaction between maternal smoking during pregnancy and other recognized risk factors. DESIGN: Case-control study of prospectively recorded data. SETTING: Department of Obstetrics and Gynaecology, University of Pavia, Italy. SUBJECTS: Three hundred and forty-seven singleton pregnancies with diagnosis of fetal growth retardation and 694 control pregnancies with appropriately grown fetuses. RESULTS: The overall odds ratio for fetal growth retardation associated with maternal smoking was 2.87 (95% confidence interval, 2.17-3.80). In logistic models the factors which independently increased the smoking-related risk of fetal growth retardation were a male fetus, nulliparity, maternal age 20 years or less, a history of first trimester haemorrhage and low (less than 50 kg) pre-pregnancy weight. The combined effect of smoking and caffeine consumption on the risk of fetal growth retardation was found to be additive rather than multiplicative. CONCLUSIONS: Several factors can affect the risk of fetal growth retardation associated with maternal smoking. The prenatal identification of these factors could help detect subgroups of women at high risk of fetal growth retardation.


Assuntos
Retardo do Crescimento Fetal/etiologia , Fumar/efeitos adversos , Adulto , Peso Corporal , Estudos de Casos e Controles , Café , Feminino , Humanos , Modelos Logísticos , Masculino , Idade Materna , Razão de Chances , Gravidez , Estudos Prospectivos , Fatores de Risco , Fatores Sexuais
6.
Hum Reprod ; 15(1): 21-3, 2000 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-10611182

RESUMO

It has recently been proposed that hyperinsulinaemic insulin resistance and increased ovarian cytochrome P-450c17alpha activity, two features of the polycystic ovary syndrome (PCOS), are pathogenetically linked. The aim of the present study was to test the hypothesis of the linkage between hyperinsulinaemia and supranormal activity of cytochrome P-450c17alpha using the human chorionic gonadotrophin (HCG) challenge, which is a more direct ovarian stimulus than gonadotrophin-releasing hormone (GnRH) in detecting modifications in ovarian steroidogenesis. Eleven women with insulin resistance-related PCOS were studied. HCG (10 000 IU) was given i.m., and blood samples were obtained 0, 8, 12, 16 and 24 h thereafter. Next day, metformin was given at a dose of 500 mg three times a day for 30-32 days, at which time the pretreatment study was repeated. Two women ovulated after metformin treatment. The administration of metformin was associated with a decrease in area under the curve for insulin during a 2h, 75g oral glucose tolerance test, in plasma free testosterone concentrations and an increase in plasma sex hormone binding globulin concentration. The plasma 17-hydroxyprogesterone response to HCG was significantly lower after metformin treatment. The present study gives a direct demonstration that metformin leads to a reduction in stimulated ovarian cytochrome P-450c17alpha activity in women with polycystic ovary syndrome.


Assuntos
Gonadotropina Coriônica , Resistência à Insulina , Metformina/farmacologia , Ovário/enzimologia , Síndrome do Ovário Policístico/complicações , Esteroide 17-alfa-Hidroxilase/metabolismo , 17-alfa-Hidroxiprogesterona/sangue , Adulto , Feminino , Humanos , Hiperinsulinismo/enzimologia , Hiperinsulinismo/etiologia , Hipoglicemiantes/administração & dosagem , Hipoglicemiantes/farmacologia , Insulina/sangue , Metformina/administração & dosagem , Testosterona/sangue
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