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1.
Obstet Gynecol ; 98(4): 550-4, 2001 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11576566

RESUMO

OBJECTIVE: To generate contemporary uterine activity and labor progress data for oxytocin-augmented labor, and assess whether 2 hours of active phase labor arrest with at least 200 Montevideo units justifies cesarean delivery. METHODS: Five hundred and one consecutive spontaneously laboring term women with abnormally progressive labor were managed by a standardized protocol: oxytocin and intrauterine pressure catheter with an intent to sustain at least 200 Montevideo units for 4 hours or more before cesarean for labor arrest. Uterine activity was measured, and maternal and neonatal outcomes were evaluated. With a sample of this size, the upper 95% confidence interval limit for an event with an observed rate of 1% is below 3%. RESULTS: During oxytocin augmentation, nulliparas who were delivered vaginally dilated at a median rate of 1.4 cm/hour versus 1.8 cm/hour for parous women. In both groups, the 5th percentile of cervical dilation rate was 0.5 cm/hour. Thirty-eight women experienced labor arrest for over 2 hours despite at least 200 sustained Montevideo units; 23 (61%) achieved a vaginal delivery. Rates of chorioamnionitis and endometritis for the 38 women were 26%. None of their infants sustained a serious complication, including brachial plexus injury, even though three of the 23 vaginal deliveries (13%) were complicated by shoulder dystocia. CONCLUSION: These data demonstrate that oxytocin-augmented labor proceeds at substantially slower rates than spontaneous labor, and support our previous contention that the criteria of labor arrest for 2 hours, despite at least 200 sustained Montevideo units, are insufficiently rigorous for the performance of cesarean.


Assuntos
Primeira Fase do Trabalho de Parto/efeitos dos fármacos , Complicações do Trabalho de Parto/tratamento farmacológico , Ocitocina/uso terapêutico , Adulto , Cesárea/estatística & dados numéricos , Corioamnionite , Intervalos de Confiança , Endometrite , Feminino , Humanos , Recém-Nascido , Trabalho de Parto Induzido , Ocitocina/farmacologia , Paridade , Gravidez , Resultado da Gravidez , Estudos Prospectivos , Fatores de Tempo , Contração Uterina/efeitos dos fármacos , Monitorização Uterina
2.
Am J Obstet Gynecol ; 183(5): 1100-2, 2000 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11084548

RESUMO

OBJECTIVE: Our aim was to evaluate the cardiovascular effects of high-dose intravaginal misoprostol administration by means of transthoracic electrical bioimpedance monitoring. STUDY DESIGN: Healthy women undergoing mid trimester pregnancy interruption with intravaginal misoprostol were eligible for this prospective observational study. Baseline blood pressure was obtained for 1 hour and transthoracic electrical bioimpedance monitoring was performed before misoprostol administration, 600 microg vaginally. Posttreatment assessments were made every 15 minutes for a total of 4 hours, with patients in a left lateral recumbent position. Heart rate, mean arterial pressure, cardiac index, stroke index, systemic vascular resistance index, and end-diastolic volume index were determined. Measurements were averaged for 30-minute intervals and reported as mean +/- SD. Statistical analyses included the paired t test and repeated-measures analysis of variance. RESULTS: Nine women consented to have transthoracic electrical bioimpedance monitoring, and no statistically significant changes in any of the measured cardiac parameters for the 4-hour monitoring interval were noted. Direct comparisons between the pretreatment and 2-hour posttreatment intervals (reported time peak of blood misoprostol levels) also revealed no significant differences in the cardiovascular index values. CONCLUSION: High-dose intravaginal misoprostol in the mid trimester does not alter maternal cardiac function as measured by transthoracic electrical bioimpedance.


Assuntos
Abortivos não Esteroides/administração & dosagem , Sistema Cardiovascular/efeitos dos fármacos , Misoprostol/administração & dosagem , Ocitócicos/administração & dosagem , Abortivos não Esteroides/efeitos adversos , Administração Intravaginal , Adulto , Relação Dose-Resposta a Droga , Impedância Elétrica , Feminino , Coração/efeitos dos fármacos , Coração/fisiologia , Humanos , Misoprostol/efeitos adversos , Monitorização Fisiológica/métodos , Ocitócicos/efeitos adversos , Gravidez , Segundo Trimestre da Gravidez , Estudos Prospectivos
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