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1.
Zhonghua fu chan ke za zhi ; Zhonghua fu chan ke za zhi;(12): 41-48, 2024.
Article in Chinese | WPRIM | ID: wpr-1012302

ABSTRACT

Objective: To investigate the clinical characteristics of induced labor in twin pregnancy and the related factors of induced labor failure. Methods: The clinical data of twin pregnant women who underwent induced labor in Peking University Third Hospital from January 2016 to December 2022 were retrospectively analyzed. According to whether they had labor or not after induction, pregnant women were divided into the success group (pregnant women who had labor after induction, 72 cases) and the failure group (pregnant women who did not have labor after induction, 30 cases). Logistic regression was used to analyze the related factors of induction failure in twin pregnant women. Results: The parity and cervical Bishop score in the failure group were significantly lower than those in the success group, while the proportion of dichorionic diamniotic twins, assisted reproductive technology pregnancy and cervical Bishop score <6, postpartum hospital stay and total hospital stay in the failure group were significantly higher than those in the success group (all P<0.05). The proportion of induced labor by artificial rupture of membranes ± oxytocin intravenous infusion in the success group was 72.2% (52/72), which was significantly higher than that in the failure group (46.7%, 14/30; P=0.030). There were no significant differences between the two groups in the gestational age at delivery, the incidence of severe postpartum hemorrhage and blood transfusion, the amount of postpartum hemorrhage, the neonatal weight of two fetuses, the incidence of neonatal asphyxia, and the proportion of neonates admitted to the neonatal intensive care unit (all P>0.05). There were no severe perineal laceration and hysterectomy in all pregnant women. Multivariate logistic regression analysis showed that primipara (OR=3.064, 95%CI: 1.112-8.443; P=0.030) and cervical Bishop score <6 (OR=5.208, 95%CI: 2.008-13.508; P=0.001) were the independent risk factors for induction failure in twin pregnancy. Conclusions: Elective induction of labor in twin pregnancy is safe and feasible. It is helpful to improve the success rate of induction of labor by strictly grasping the timing and indications of termination of pregnancy, choosing the appropriate method of induction according to the condition of the cervix, and actively promoting cervical ripening .


Subject(s)
Infant, Newborn , Pregnancy , Female , Humans , Pregnancy Trimester, Third , Pregnancy, Twin , Postpartum Hemorrhage/etiology , Retrospective Studies , Labor, Induced/methods , Cervical Ripening
2.
Chin. med. j ; Chin. med. j;(24): 681-690, 2022.
Article in English | WPRIM | ID: wpr-927508

ABSTRACT

BACKGROUNDS@#At present, there is no consensus on the induction methods in term pregnancy with borderline oligohydramnios. This study aimed to compare the effectiveness and pregnancy outcomes of labor induction with dinoprostone or single-balloon catheter (SBC) in term nulliparous women with borderline oligohydramnios.@*METHODS@#We conducted a retrospective cohort study from January 2016 to November 2018. During the study period, a total of 244 cases were enrolled. Of these, 103 cases were selected for induction using dinoprostone and 141 cases were selected for induction with SBC. The pregnancy outcomes between the two groups were compared. Primary outcomes were successful vaginal delivery rates. Secondary outcomes were maternal and neonatal adverse events. Multivariate logistic regression was used to assess the risk factors for vaginal delivery failure in the two groups.@*RESULTS@#The successful vaginal delivery rates were similar between the dinoprostone group and the SBC group (64.1% [66/103] vs. 59.6%, [84/141] P = 0.475), even after adjustment for potential confounding factors (adjusted odds ratio [aOR]: 1.07, 95% confidence interval [CI]: 0.57-2.00, P = 0.835). The incidence of intra-amniotic infection was lower in the dinoprostone group than in the SBC group (1.9% [2/103] vs. 7.8%, [11/141] P < 0.001), but the presence of non-reassuring fetal heart rate was higher in the dinoprostone group than in the SBC group (12.6% [13/103] vs. 0.7%, [1/141] P < 0.001). Multivariate logistic regression showed that nuchal cord was a risk factor for vaginal delivery failure after induction with dinoprostone (aOR: 6.71, 95% CI: 1.96-22.95). There were three factors related to vaginal delivery failure after induction with SBC, namely gestational age (aOR: 1.51, 95% CI: 1.07-2.14), body mass index (BMI) >30 kg/m2 (aOR: 2.98, 95% CI: 1.10-8.02), and fetal weight >3500 g (aOR: 2.49, 95% CI: 1.12-5.50).@*CONCLUSIONS@#Term nulliparous women with borderline oligohydramnios have similar successful vaginal delivery rates after induction with dinoprostone or SBC, with their advantages and disadvantages. In women with nuchal cord, the risk of vaginal delivery failure is increased if dinoprostone is used in the induction of labor. BMI >30 kg/m2, large gestational age, and estimated fetal weight >3500 g are risk factors for vaginal delivery failure after induction with SBC.


Subject(s)
Female , Humans , Infant, Newborn , Pregnancy , Administration, Intravaginal , Catheters , Dinoprostone/therapeutic use , Fetal Weight , Labor, Induced/methods , Nuchal Cord , Oligohydramnios , Oxytocics , Pregnancy Outcome , Retrospective Studies
3.
Article in Spanish | LILACS, BIMENA | ID: biblio-1284516

ABSTRACT

Introducción: en la obstetricia se realizan algunas prácticas que producen daños significativos a la madre o a su bebé, aunque no siempre se admite su ejecución. Un ejemplo es la maniobra de Kristeller, cuya aplicación es controvertida. Objetivo: determinar la frecuencia con que se realizó la maniobra de Kristeller en una muestra de mujeres atendidas en la maternidad del Hospital San Felipe de Tegucigalpa. Metodología: estudio descriptivo, que se realizó en el período comprendido entre los meses de marzo a mayo del 2018. Se incluyeron un total de 376 pacientes. Las variables estudiadas fueron: hora del parto, paridad, profesional que atendió y supervisó el parto, profesional que realizó la maniobra de Kristeller, complicaciones maternas y neonatales observadas. Resultados: se encontró una frecuencia de maniobra de Kristeller de 12.2 % (46/376). Conclusiones: ser primigesta incrementó el riesgo de que se le aplicara la maniobra Kristeller (OR: 3.11, IC:95%, p=0.0002), dentro de los factores protectores se encontraron ser multípara (OR:0.25, IC:95%, p=0.00004) y, haber sido atendida por una licenciada en enfermería (OR: 0.34, IC:95%, p=0.0097). La maniobra de Kristeller aumentó el riesgo de complicaciones maternas en 12.5 veces (OR: 17.6, IC:95%, p=0.0000000019) y 6.5 veces en el neonato (OR: 7.7 IC:95%, p=0.0000578)...(AU)


Subject(s)
Humans , Female , Pregnancy , Infant, Newborn , Obstetric Violence , Labor, Induced/methods , Violence Against Women , Postpartum Hemorrhage
4.
Rev. chil. obstet. ginecol. (En línea) ; Rev. chil. obstet. ginecol;85(supl.1): S28-S34, set. 2020. tab
Article in Spanish | LILACS | ID: biblio-1138646

ABSTRACT

INTRODUCCIÖN Y OBJETIVOS: Describir la experiencia de los partos en gestantes con diagnóstico confirmado de COVID 19 mediante RT-PCR asintomáticas o con sintomatología leve y aquellas sin la enfermedad, y determinar la tasa de éxito de parto vaginal en inducción de trabajo de parto. MÉTODOS: Análisis retrospectivo de pacientes que tuvieron su parto entre 15 de Abril y 03 de Julio del 2020 en el Hospital San Juan de Dios. Se incluyeron las pacientes inducidas con Dinoprostona, Oxitocina o ambas de manera secuencial y se dividieron según estatus COVID 19 mediante RT-PCR al ingreso. Se caracterizó demográficamente el grupo de pacientes positivas y se determinaron los datos de ambos grupos en relación a la necesidad de inducción de trabajo de parto y su éxito para parto vaginal. RESULTADOS: De un total de 657 nacimientos, hubo un 9.7% (n=64) de pacientes con COVID 19, de las cuales un 23.4% (n=15) requirió inducción de trabajo de parto, con una tasa de éxito para parto vaginal de un 66.7% (n=10). De estas pacientes, un 50% recibió Oxitocina, un 40% Dinosprostona y un 10% ambos medicamentos de forma secuencial. En las pacientes negativas, hubo un total de 568 nacimientos, con un 29.8% (n=169) de usuarias que requirieron inducción. La tasa de éxito para parto vaginal en este grupo fue de 72.2% (n=122), utilizando un 50% Oxitocina; un 27% Dinoprostona; un 14.8% ambas; y un 8.2% Balón de Cook. CONCLUSIONES: Sabemos que los resultados de este estudio están limitados por el bajo número de pacientes incluidas, sin embargo, podemos observar que, en nuestra experiencia con las pacientes que arrojaron PCR SARS-CoV-2 positivas, asintomáticas o con enfermedad leve, se logró realizar la inducción de trabajo de parto según protocolos habituales, obteniendo porcentajes de éxito para partos vaginales, similares a las pacientes sin la enfermedad.


INTRODUCTION AND OBJECTIVES: Describe the experience of deliveries in pregnant women with a confirmed diagnosis of COVID 19 by asymptomatic RT-PCR or with mild symptoms and those without the disease, and determine the success rate of vaginal delivery in the induction of labor. METHODS: Retrospective study of patients who had their delivery between 15th April and 03rd of July, 2020 in the San Juan de Dios Hospital. Patients induced with Dinoprostone, Oxytocin or both sequentially were included, and were divided according to COVID 19 status by RT-PCR on their admission process. The group of positive patients was demographically characterized and the data of both groups was determined in relation to the need for labor induction and its success for vaginal delivery. RESULTS: Of a total of 657 births, there were 9.7% (n = 64) of patients with COVID 19, of which 23.4% (n = 15) required labor induction, with a success rate for vaginal delivery of 66.7% (n = 10). Of these patients, 50% received Oxytocin, 40% Dinosprostone and 10% both drugs sequentially. In the negative patients, there were a total of 568 births, with 29.8% (n = 169) of users requiring labor induction. The success rate for vaginal delivery in this group was 72.2% (n = 122); 50% using Oxytocin; 27% Dinoprostone; 14.8% using both; and 8.2% using Cook's Catheter. CONCLUSIONS: We know that the results of this study are limited by the low number of patients included, however, in our experience, we can observe that, in patients with SARS-CoV-2 PCR positive, asymptomatic or with mild disease, it was possible to perform induction of labor according to standard protocols, achieving success rates for vaginal deliveries, similar to patients without the disease.


Subject(s)
Humans , Female , Pregnancy , Infant, Newborn , Adolescent , Adult , Middle Aged , Young Adult , Pneumonia, Viral/complications , Pregnancy Complications, Infectious/therapy , Pregnancy Complications, Infectious/virology , Coronavirus Infections/complications , Labor, Induced/methods , Oxytocin/administration & dosage , Pregnancy Outcome , Dinoprostone/administration & dosage , Cesarean Section , Retrospective Studies , Delivery, Obstetric , Pandemics , Betacoronavirus
5.
Pesqui. vet. bras ; Pesqui. vet. bras;40(4): 266-270, Apr. 2020. tab
Article in English | VETINDEX, LILACS | ID: biblio-1135618

ABSTRACT

The induction of labor aims to concentrate births to follow up better the parturient and the first care to the neonates. However, even if the labor induction technique with dexamethasone administration has been successfully described since the late 1970s, few studies report the technique of birth development and neonatal vitality in Santa Inês sheep. This study aimed to evaluate the efficiency of dexamethasone use in two doses (8 and 16mg) in labor induction of Santa Inês ewes at 145 days of gestation and to evaluate its effects on the birth characteristics. In this study, 58 ewes were used, raised in an extensive system in the experimental farms of UFBA, with confirmation pregnancy after fixed-time artificial insemination or controlled breeding. These female ewes were separated into three groups according to the dose of dexamethasone administered (G1 = 0mg, G2 = 8mg, and G3 = 16mg). From these births, 79 lambs were born. This study analyzed the period from induction of labor to birth, fetal presentation at birth, the weight of the placenta, and the period for placenta expulsion. The data were analyzed by the Statistical Analysis System (SAS v.9.1.3®, 2002), and the significance level considered for all analyzes was 5%. Births of induced groups occurred on average at 48.4±22.17 hours after induction, while the females with non-induced labor gave birth 131.96±41.9 hours on average after the placebo application (P<0.05), confirming the efficiency of both doses for induction of labor. The period from induction to birth did not differ (P>0.05) between the doses used. There were no differences in delivery about the fetal static relation, time to placental attachment, and weight. With this study, it can be concluded that the induction at 145 days of gestation with eight or 16mg of dexamethasone is a useful technique and does not alter the labor in Santa Inês sheep.(AU)


A indução do parto visa concentrar os nascimentos para melhor acompanhamento das parturientes e primeiros cuidados aos neonatos. Contudo, mesmo que a técnica de indução de parto, com administração de dexametasona, tenha sido descrita com sucesso desde o final da década de 70, existem estudos escassos que relatam a influência desta técnica sobre o parto em ovinos da raça Santa Inês. Dessa forma, o objetivo do estudo foi avaliar a eficácia da dexametasona em duas doses (8 e 16mg), para a indução do parto de ovelhas Santa Inês com 145 dias de gestação e avaliar os seus efeitos nas características de desencadeamento e finalização do parto. Para este estudo foram utilizadas 58 ovelhas, criadas em sistema extensivo nas fazendas experimentais da UFBA, com prenhez confirmada após inseminação artificial em tempo fixo ou monta controlada. Essas fêmeas foram separadas em três grupos, de acordo com a dose de dexametasona administrada (G1 = 0mg, G2 = 8mg e G3 = 16mg). Destes partos nasceram 79 cordeiros. Foram avaliados o período em horas da indução do parto aos nascimentos, a apresentação fetal ao nascimento, assim como o peso da placenta e o período para o delivramento. Os dados foram analisados pelo pacote estatístico Statistical Analysis System (SAS v.9.0®, 2002) sendo considerado para todas as análises o nível de significância de 5%. Os nascimentos dos grupos induzidos ocorreram em média com 48,4±22,1 horas após a indução, enquanto que as fêmeas com parto não induzido pariram em média 131,96±41,9 horas após aplicação do placebo (P<0,05), confirmando a eficácia de ambas as doses para indução do parto. O período da indução até o parto não diferiu (P>0,05) entre as doses utilizadas. Não ocorreram diferenças no parto em relação à estática fetal, tempo para o delivramento e peso da placenta nos diferentes grupos. Com este estudo, conclui-se que a indução de parto em ovelhas aos 145 dias de gestação com oito e 16 mg de dexametasona é uma técnica eficaz e que não altera o trabalho de parto nas ovelhas da raça Santa Inês.(AU)


Subject(s)
Animals , Female , Pregnancy , Dexamethasone , Sheep , Labor, Induced/methods , Labor, Induced/veterinary
6.
Rev. bras. ginecol. obstet ; Rev. bras. ginecol. obstet;40(9): 513-517, Sept. 2018. tab
Article in English | LILACS | ID: biblio-977819

ABSTRACT

Abstract Objective Induction of labor (IL) is a common obstetric procedure, but it is questionable whether or not it results in higher cesarean section (CS) rates. The present study aims to evaluate the impact of IL in the overall CS rates and to analyze these rates according to the method of IL employed and to the Robson group in which it was applied. Methods We have conducted a retrospective study including pregnant women whose labor was induced at a tertiary hospital in 2015 and 2016. All women were classified according to the Robson Classification System (RCS). The CS rates were analyzed and compared regarding the method of IL employed. Results A total of 1,166 cases were included. The CS rate after IL was 20.9%, which represented 23.1% of the total of CSs performed in 2015 and 2016. The highest CS rates were recorded in RCS groups 5 (65.2%) and 8 (32.3%). Group 2 was the highest contributor to the overall CS rate, since it represented 56.7% of the population. The intravaginal prostaglandins method was the most used (77%). Transcervical Foley catheter was the preferredmethod in group 5 and intravaginal prostaglandins in all the other groups. The CS rate was higher when transcervical Foley catheter was used (34.1%). Conclusion Transcervical Foley catheter induction was associated with a higher rate of CS, probably because it was the preferred method used in group 5.


Resumo Introdução A indução do trabalho de parto é uma prática comum e sua associação com o aumento da taxa de cesarianas tem sido questionada. O presente estudo surge com o objetivo de avaliar o impacto da indução do trabalho de parto na taxa global de cesarianas e de analisar as taxas de cesarianas de acordo com o método de indução do trabalho de parto utilizado e com o grupo de Robson. Métodos Realizamos umestudo retrospectivo cominclusão de grávidas submetidas a indução do trabalho de parto em um hospital terciário em 2015 e 2016. Todas as mulheres forram classificadas de acordo com a classificação de Robson. As taxas de cesarianas foram analisadas e comparadas em função do método de indução de trabalho de parto utilizado. Resultados Foram incluídos 1.166 casos. A taxa de cesarianas após a indução do trabalho de parto foi de 20,9%, correspondendo a 23,1% do total de cesarianas realizadas em 2015 e 2016. Os grupos 5 e 8 da classificação de Robson foram os que apresentaram as maiores taxas de cesarianas (65,2% e 32,3%, respectivamente). O grupo 2 foi o que mais contribuiu para a taxa global de cesarianas, por representar 56,7% do total da população. As prostaglandinas intravaginais foram o método mais utilizado (77%). O cateter de Foley transcervical foi o método mais utilizado no grupo 5 e as prostaglandinas intravaginais nos restantes. A taxa de cesarianas foi superior quando se utilizou o cateter de Foley transcervical (34,1%). Conclusão A indução do trabalho de parto com cateter de Foley transcervical associou-se a uma maior taxa de cesarianas, em provável relação com a sua maior utilização no grupo 5.


Subject(s)
Humans , Female , Pregnancy , Pregnancy Complications/classification , Cesarean Section/statistics & numerical data , Labor, Induced/methods , Retrospective Studies
7.
Prensa méd. argent ; Prensa méd. argent;104(4): 210-214, Jun2018. graf, tab
Article in Spanish | BINACIS, LILACS | ID: biblio-1052582

ABSTRACT

The labour induction is an intervention to initiate artificially the uterine contractions to produce the effacement and dilatation of the uterine cervix until the child-birth is achieved. It is indicated when the benefit of the termination of the pregnancy for the mother and the child is greater than its continuation. It is perfored in more or less the 20 % of the women. In our institution the rate oscillates in around the 9 % of the cases. It is understand as an successful induction the termination of the labour through the vaginal delivery. The methods for labour induction more commonly used at present are mechanical and pharmacological. Between the first group we can find the Hamilton maneuver and the amniotomy. And between the pharmacologicals we find the oxytocine. These elements are considered in the article


Subject(s)
Humans , Female , Pregnancy , Uterine Contraction , Labor Stage, First , Oxytocin/pharmacology , Cervix Uteri/embryology , Cesarean Section , Cervical Ripening , Parturition , Amniotomy/methods , Labor, Induced/methods
8.
Rev. chil. obstet. ginecol. (En línea) ; Rev. chil. obstet. ginecol;82(6): 681-691, Dec. 2017. tab
Article in Spanish | LILACS | ID: biblio-899961

ABSTRACT

INTRODUCCIÓN: La rotura prematura de membranas (RPM) ocurre en un 8 a 10% de las embarazadas, y de ellas, un 20% corresponde a embarazos de pretérmino. El mayor riesgo para el feto luego de una RPM pretérmino son las complicaciones propias de la prematurez. Por debajo de las 34 semanas se favorece el manejo expectante, y el uso de antibióticos y corticoides. Entre las 34 y 37 semanas, sin embargo, las prácticas varían, no habiendo un consenso claro sobre la conducta óptima. OBJETIVO: El objetivo de esta revisión es explorar la evidencia actualmente disponible respecto de la conducta activa versus la expectante en embarazos con RPM entre las 34 y 37 semanas (36 semanas más 6 días). METODOLOGÍA: Se realizó una búsqueda de literatura médica en distintas bases de datos, dentro de las cuales se incluye "PubMed" y "Cochrane", usando los siguientes términos: "Fetal Membranes, Premature Rupture", "Premature Birth", "34 and 37 weeks" y "Clinical Trial". Se limitó la búsqueda a artículos que fueran ensayos clínicos aleatorizados. De un total de 31 trabajos, se seleccionaron 3, a los cuales se les aplicó la pauta de análisis crítico para evaluación de estudios de terapia. RESULTADOS: Se incluyeron 3 estudios que respondían a la pregunta planteada. En el primer estudio se concluyó que en pacientes en que hay interrupción inmediata la incidencia de sepsis neonatal es baja y no es posible demostrar que esta conducta mejore los resultados en comparación con el manejo expectante (2.6% vs. 4.1%). El manejo activo en este estudio se asoció a mayor incidencia de hiperbilirrubinemia, hipoglicemia, y mayor estadía hospitalaria neonatal. En el segundo artículo se planteó que la incidencia de sepsis neonatal sigue siendo baja, lo cual no disminuyó con la inducción del trabajo de parto. Esta tampoco disminuyó el riesgo de otros resultados neonatales o maternos. Finalmente, el tercer estudio concluyó que la interrupción inmediata aumenta las complicaciones neonatales sin disminución de la sepsis neonatal, pero a expensas de mayor frecuencia de fiebre materna y de hemorragia intraparto. CONCLUSIONES: El manejo expectante no es inferior al manejo activo en el contexto de RPM entre las semanas 34 a 37 de edad gestacional.


INTRODUCTION: Premature rupture of membranes (PROM) occur in eight to ten percent of pregnancies, and 20 percent of them occur in preterm pregnancies. Biggest fetal risks after preterm PROM are complications due to prematurity. Before 34 weeks of gestation it is preferred an expectant management, and the use of antibiotics and steroids. Between 34 and 37 weeks, however, practices are variable without a clear consensus about the best management. OBJECTIVE: The objective of this review is to explore the available evidence about active versus expectant management in pregnancies with PROM between 34 and 37 weeks (36 weeks plus 6 days). METHODS: Different databases were searched for medical literature, including 'PubMed' and 'Cochrane', using the following terms: 'Fetal Membranes, Premature Rupture', 'Premature Birth', '34 and 37 weeks' and 'Clinical Trial'. The search was limited to clinical randomized trials. From a total of 31 studies, three were selected, in which critical analysis guidelines for evaluation of therapy studies were applied. RESULTS: Three clinical trials which answered our question were included in this review. The first study concluded that in patients whose pregnancies were interrupted immediately, the incidence of neonatal sepsis was low but is was not able to demonstrate that this action improved outcomes compared to expectant management (2.6% vs 4.1%). Active management in this study was associated to greater incidences of hyperbilirubinemia, hypoglycemia and longer neonatal hospital stay. In the second article the incidence of neonatal sepsis was low and didn't decrease with induction of labor. It also didn't reduce the risk of other maternal nor neonatal outcomes. Finally, the third study concluded that induction of labor increased neonatal complications without reducing neonatal sepsis, but at the expense of increased frequency of intrapartum hemorrhage and maternal fever. CONCLUSION: After analyzing the selected articles, it is possible to conclude that there is enough evidence to say that expectant management is not inferior to active management in relation to PROM between 34 and 37 weeks of gestational age.


Subject(s)
Humans , Female , Pregnancy , Fetal Membranes, Premature Rupture/therapy , Watchful Waiting/methods , Neonatal Sepsis/prevention & control , Labor, Induced/methods , Pregnancy Trimester, Third , Pregnancy Outcome , Randomized Controlled Trials as Topic , Multicenter Studies as Topic , Gestational Age , Premature Birth/prevention & control , Clinical Decision-Making , Neonatal Sepsis/etiology
9.
Rev. bras. ginecol. obstet ; Rev. bras. ginecol. obstet;39(10): 523-528, Nov. 2017. tab
Article in English | LILACS | ID: biblio-898828

ABSTRACT

Abstract Purpose To assess cases of labor induction with vaginal 25-μg tablets of misoprostol and maternal outcomes in a tertiary hospital in southeastern Brazil. Methods This was a retrospective cohort study of 412 pregnant women with indication for labor induction. Labor induction was performed with vaginal 25-μg tablets ofmisoprostol in pregnant women with Bishop scores < 6. Stepwise regression analysis was used to identify the factors present at the beginning of induction that could be used as predictors of successful labor induction. Results A total of 69% of the pregnant women who underwent labor induction progressed to vaginal delivery, and 31% of the women progressed to cesarean section. One or two misoprostol tablets were used in 244 patients (59.2%). Of the 412 patients, 197 (47.8%) required oxytocin later on in the labor process, after induction with misoprostol. The stepwise regression analysis showed that only Bishop scores of 4 and 5 and previous vaginal delivery were independent factors with statistical significance in the prediction of successful vaginal labor induction (β = 0.23, p < 0.001, for a Bishop score of 4 and 5, and β = 0.22, p < 0.001, for previous vaginal delivery). Conclusion Higher Bishop scores and previous vaginal delivery were the best predictors of successful labor induction with vaginal 25-μg tablets of misoprostol.


Resumo Objetivo Avaliar os casos de indução do trabalho de parto com misoprostol 25 mcg por via vaginal e seus desfechos maternos em um hospital terciário do Sudeste do Brasil. Métodos Realizou-se um estudo retrospectivo de coorte com 412 gestantes com indicações para indução de trabalho de parto. A indução do trabalho de parto foi realizada com misoprostol 25 mcg vaginal em gestantes com índice de Bishop < 6. Realizou-se análise de regressão stepwise para identificar os fatores presentes ao início da indução que poderiam ser usados como prognosticadores do sucesso da indução do trabalho de parto. Resultados A indução de trabalho de parto determinou 69% de partos normais, sendo que 31% evoluíram para cesárea. Em relação ao número de comprimidos de misoprostol, 1 ou 2 comprimidos foram utilizados em 244 pacientes (59,2%). Das 412 pacientes, 197 (47,8%) necessitaramde ocitocina após a indução commisoprostol para dar continuidade ao trabalho de parto. Na análise de regressão stepwise, apenas a presença de índice de Bishop 4 e 5 e parto vaginal prévio foram fatores independentes com significância estatística na predição do sucesso da indução emobter parto vaginal (β = 0,23, p < 0,001, para índice de Bishop 4 e 5, e β = 0,22, p < 0,001, para parto vaginal prévio). Conclusão Maiores índices de Bishop e parto vaginal prévio são os maiores prognosticadores do sucesso de indução de trabalho de parto com misoprostol 25 mcg vaginal.


Subject(s)
Humans , Female , Pregnancy , Adult , Young Adult , Abortifacient Agents, Nonsteroidal/administration & dosage , Misoprostol/administration & dosage , Labor, Induced/methods , Administration, Intravaginal , Brazil , Pregnancy Outcome , Retrospective Studies , Cohort Studies , Tertiary Care Centers
10.
Medisan ; 21(9)set. 2017.
Article in Spanish | LILACS | ID: biblio-995148

ABSTRACT

La inducción del parto resulta un procedimiento elemental en la práctica obstétrica, que se aplica en un grupo importante de pacientes para interrumpir con éxito el embarazo debido a riesgos materno y perinatal. En este artículo se expone brevemente un nuevo método que permite abordar con efectividad la respuesta a la oxitocina, después del uso del Misofar® en función facilitadora para inducir el parto, acortando la latencia en la rotura prematura de membranas y condicionando las estructuras cervicales en gestantes con preeclampsia para obtener una mejor respuesta. Esta nueva herramienta se pone a disposición de la comunidad médica, en beneficio materno y perinatal.


Labor induction is an elementary procedure in obstetrics that is applied in an important group of patients to successfully interrupt pregnancy due to maternal and perinatal risks. In this work, a new method that allows to approach with effectiveness the oxytocin response is briefly exposed, after the use of Misofar® in facilitator function to induce labor, shortening the latency in early break of membranes and conditioning the cervical structures in pregnant women with pre-eclampsia to obtain a better response. This new tool is at medical community disposal for the maternal and perinatal benefit.


Subject(s)
Humans , Female , Pregnancy , Prostaglandins , Misoprostol/therapeutic use , Delivery, Obstetric/methods , Labor, Induced/methods , Oxytocin/therapeutic use , Communication
11.
Rev. bras. ginecol. obstet ; Rev. bras. ginecol. obstet;39(2): 53-59, Feb. 2017. tab, graf
Article in English | LILACS | ID: biblio-843913

ABSTRACT

Abstract Purpose To evaluate blood loss during misoprostol-induced vaginal births and during cesarean sections after attempted misoprostol induction. Methods We conducted a prospective observational study in 101 pregnant women indicated for labor induction; pre- and postpartum hemoglobin levels were measured to estimate blood loss during delivery. Labor was induced by administering 25 μg vaginal misoprostol every 6 hours (with a maximum of 6 doses). The control group included 30 patients who spontaneously entered labor, and 30 patients who underwent elective cesarean section. Pre- and postpartum hemoglobin levels were evaluated using the analysis of variance for repeated measurements, showing the effects of time (pre- and postpartum) and of the group (with and withoutmisoprostol administration). Results Therewere significant differences between pre- and postpartum hemoglobin levels (p < 0.0001) with regard to misoprostol-induced vaginal deliveries (1.6 ± 1.4 mg/dL), non-induced vaginal deliveries (1.4 ± 1.0 mg/dL), cesarean sections after attempted misoprostol induction (1.5 ± 1.0 mg/dL), and elective cesarean deliveries (1.8 ± 1.1 mg/dL). However, the differences were proportional between the groups with and without misoprostol administration, for both cesarean (p = 0.6845) and vaginal deliveries (p = 0.2694). Conclusions Labor induction using misoprostol did not affect blood loss during delivery.


Resumo Objetivo Avaliar a perda sanguínea em partos vaginais induzidos com misoprostol, e em cesáreas com tentativa prévia de indução do parto com misoprostol. Métodos Realizou-se estudo prospectivo observacional com 101 gestantes com indicação para indução do trabalho de parto, as quais foram avaliadas pela dosagem de hemoglobina pré e pós-parto para estimativa da perda sanguínea no parto. Procedeu-se à indução do trabalho de parto com misoprostol 25 μg, via vaginal, a cada 6 horas, em um número máximo de 6 doses. O grupo controle foi composto por 30 pacientes que entraram emtrabalho de parto espontaneamente, e por 30 pacientes que se submeteram a cesárea eletiva. O estudo da hemoglobina, antes e depois do parto, foi avaliado por ANOVA paramedidas repetidas, no qual foi verificado o efeito do tempo (pré e pós-parto) e o efeito do grupo (com e sem uso do misoprostol). Resultados Existem diferenças significativas entre os níveis de hemoglobina pré e pós-parto (p < 0,0001) nos partos vaginais induzidos pelo misoprostol (1,6 ± 1,4 mg/ dL), nos partos vaginais não induzidos (1,4 ± 1,0 mg/dL), nas cesáreas com tentativa prévia de indução (1,5 ± 1,0mg/dL), e nas cesáreas eletivas (1,8 ± 1,1mg/dL). Porém, as diferenças foram proporcionais em ambos os grupos, ou seja, ocorreu diferença tanto no grupo que fez uso do misoprostol quanto no grupo que não fez uso do medicamento, tanto na cesárea (p = 0,6845) quanto no parto vaginal (p = 0,2694). Conclusões A indução do parto com misoprostol não alterou a perda sanguínea durante o parto.


Subject(s)
Humans , Female , Pregnancy , Adolescent , Adult , Young Adult , Blood Loss, Surgical , Cesarean Section , Labor, Induced/methods , Misoprostol/adverse effects , Oxytocics/adverse effects , Postpartum Hemorrhage/chemically induced , Prospective Studies
12.
Rev. cuba. obstet. ginecol ; 42(3): 344-353, jul.-set. 2016.
Article in Spanish | LILACS | ID: biblio-845019

ABSTRACT

Introducción: el síndrome de anticuerpos antifosfolípidos es un estado protrombótico adquirido determinado por la presencia de anticuerpos antifosfolípidos en pacientes con trombosis venosa o arterial y una morbilidad incrementada durante el embarazo. Objetivos: describir los principales aspectos epidemiológico-clínicos del síndrome durante el embarazo y los resultados perinatales. Métodos: se realizó un estudio descriptivo y analítico de una serie de pacientes con síndrome de anticuerpos antifosfolípidos y embarazo en el Centro de Investigaciones Médico Quirúrgicas y el Centro Nacional de Reumatología, en La Habana, Cuba. La serie estudiada se constituyó con 188 mujeres. Se revisaron los expedientes clínicos de las gestantes internadas y de consultas externas de ambas instituciones, diagnosticadas como patología primaria o secundaria y se conformó una base de datos con variables epidemiológicas como: características del embarazo y desenlace materno fetal. Resultados: del total de pacientes estudiadas de la serie, 32 sufrieron trombosis con morbilidad obstétrica. Se diagnosticó síndrome de anticuerpos antifosfolípidos primario en seis pacientes y secundario en 26 (17,5 por ciento). La edad promedio fue de 27 años. Según el color de la piel; seis de cada 10 eran blancas y el resto, mestizas y negras. Entre estas pacientes hubo 81 embarazos; con una razón de 2,53 embarazos/paciente; 76 por ciento nacieron vivos, 18 por ciento tuvo un aborto espontáneo y hubo 5 por ciento de muertes fetales. De ellas, 16 por ciento tuvo parto pretérmino y 10 por ciento desarrolló preeclampsia. No hubo muertes maternas. Conclusiones: el embarazo en pacientes con síndrome de anticuerpos antifosfolípidos es de elevado riesgo, y se constató una elevada morbimortalidad materno fetal(AU)


Introduction: antiphospholipid antibody syndrome (APS) is an acquired prothrombotic state characterized by the presence of antiphospholipid antibodies in patients with venous or arterial thrombosis and increased morbidity during pregnancy. Objectives: describe the main clinical and epidemiological features of the syndrome during pregnancy as well as its perinatal outcomes. Methods: a descriptive analytical study was conducted of a series of patients with antiphospholipid antibody syndrome and pregnancy at the Center for Medical Surgical Research and the National Rheumatology Center in Havana, Cuba. The study series was composed of 188 women. Examination was performed of the medical records of pregnant women either hospitalized or attending outpatient consultation at the two institutions who had been diagnosed with the syndrome as a primary or a secondary condition. A database was developed with epidemiological variables such as characteristics of the pregnancy and maternal fetal outcome. Results: of the total patients studied in the series, 32 had thrombosis with obstetric morbidity. Primary antiphospholipid antibody syndrome was diagnosed in six patients, whereas secondary APS was diagnosed in 26 (17.5 percent). Mean age was 27 years. With respect to skin color, six out of every ten patients were white, and the rest were either brown or black. There were 81 pregnancies in the series, i.e. 2.53 patients / pregnancy, with 76 percent live births, 18 percent spontaneous abortions and 5 percent fetal deaths. 16 percent had a preterm delivery and 10 percent developed preeclampsia. There were no maternal deaths. Conclusions: pregnancy in patients with antiphospholipid antibody syndrome is highly risky, with increased maternal and fetal morbidity and mortality(AU)


Subject(s)
Humans , Female , Pregnancy , Pregnancy Complications/etiology , Antiphospholipid Syndrome/diagnosis , Antiphospholipid Syndrome/epidemiology , Laboratory and Fieldwork Analytical Methods/methods , Indicators of Morbidity and Mortality , Preconception Care/methods , Observational Study , Labor, Induced/methods
13.
Radiol. bras ; Radiol. bras;48(2): 81-85, Mar-Apr/2015. tab, graf
Article in English | LILACS | ID: lil-746613

ABSTRACT

Objective: To evaluate the incidence and spectrum of abdominal computed tomography imaging findings in patients with paracoccidioidomycosis. Materials and Methods: Retrospective analysis of abdominal computed tomography images of 26 patients with disseminated paracoccidioidomycosis. Results: Abnormal abdominal tomographic findings were observed in 18 patients (69.2%), while no significant finding was observed in the other 8 (30.8%) patients. Conclusion: Computed tomography has demonstrated to play a relevant role in the screening and detection of abdominal abnormalities in patients with disseminated paracoccidioidomycosis. .


Objetivo: Avaliar a frequência e variedade de achados de imagem por exames de tomografia computadorizada de abdome em indivíduos com paracoccidioidomicose disseminada. Materiais e Métodos: Estudo retrospectivo dos exames de tomografia computadorizada de abdome de 26 pacientes com paracoccidioidomicose disseminada. Resultados: Foram encontradas alterações tomográficas abdominais em 18 pacientes (69,2%) dos casos analisados e 8 pacientes (30,8%) apresentaram exames normais. Conclusão: A tomografia computadorizada de abdome mostrou grande importância no rastreamento e identificação de alterações abdominais nos pacientes com paracoccidioidomicose disseminada. .


Subject(s)
Adult , Female , Humans , Infant, Newborn , Pregnancy , Abortifacient Agents, Nonsteroidal , Fetal Death , Misoprostol , Oxytocics , Infusions, Intravenous , Labor, Induced/methods , Pregnancy Outcome , Randomized Controlled Trials as Topic , Uganda
14.
Rev. bras. ginecol. obstet ; Rev. bras. ginecol. obstet;37(3): 127-132, 03/2015. tab
Article in Portuguese | LILACS | ID: lil-741862

ABSTRACT

OBJETIVO: Descrever os desfechos materno-fetais com o uso da sonda de Foley para indução do trabalho de parto em gestantes de alto risco com cesariana anterior. MÉTODOS: Foi realizado um estudo de intervenção e descritivo, no período de novembro de 2013 a junho de 2014. Foram incluídas 39 gestantes a termo, com feto vivo, apresentação cefálica, peso estimado <4.000 g, cesariana prévia, com indicação de indução do trabalho de parto, escore de Bishop ≤6 e índice de líquido amniótico >5 cm. A sonda de Foley nº 16F foi introduzida, por no máximo 24 horas, sendo considerado satisfatória quando a paciente entrou em trabalho de parto nas primeiras 24 horas. RESULTADOS: O trabalho de parto foi induzido satisfatoriamente em 79,5% das gestantes. Nove mulheres evoluíram para parto vaginal (23,1%), com uma frequência de 18% de partos vaginais ocorridos dentro de 24 horas. As principais indicações da indução do parto foram as síndromes hipertensivas (75%). As médias dos intervalos entre a colocação da sonda de Foley e o início do trabalho de parto e o parto foram de 8,7±7,1 e 14,7±9,8 horas, respectivamente. A eliminação de mecônio foi observada em 2 pacientes e o escore de Apgar <7 no primeiro minuto foi observado em 5 recém-nascidos (12,8%). CONCLUSÕES: A sonda de Foley é uma alternativa para indução do trabalho de parto em gestantes com cesariana anterior, apesar da baixa taxa de parto vaginal. .


PURPOSE: To describe the maternal and fetal outcomes with the use of the Foley catheter for induction of labor in high-risk pregnant women with previous caesarean section. METHODS: An interventive and descriptive study was conducted from November 2013 to June 2014. A total of 39 pregnant women at term, with a live fetus, cephalic presentation, estimated fetal weight <4,000 g, with previous cesarean section, medical indications for induction of labor, Bishop score ≤6 and amniotic fluid index >5 cm were included. A number 16F Foley catheter was introduced for a maximum of 24 hours, and was considered to be satisfactory when the patient began labor within 24 hours. RESULTS: Labor was successfully induced in 79.5% of pregnant women. Nine women achieved vaginal delivery (23.1%), with a frequency of 18% of vaginal births occurring within 24 hours. The main indications for the induction of labor were hypertensive disorders (75%). The mean interval between the placement of the Foley catheter and the beginning of labor and delivery were 8.7±7.1 and 14.7±9.8 hours, respectively. Meconium-stained amniotic fluid was observed in two patients; and an Apgar score <7 in the first minute was detected in 5 newborns (12.8%). CONCLUSIONS: The Foley catheter is an alternative for the induction of labor in women with previous caesarean section, despite the low vaginal delivery rate. .


Subject(s)
Humans , Female , Pregnancy , Infant, Newborn , Adolescent , Adult , Young Adult , Catheters , Labor, Induced/instrumentation , Labor, Induced/methods , Pregnancy, High-Risk , Vaginal Birth after Cesarean , Pregnancy Outcome , Prospective Studies
15.
Article in English | IMSEAR | ID: sea-157570

ABSTRACT

Induction of labour means initiation of uterine contractions (after the period of viability) by any method (medical, surgical or combined) for the purpose of vaginal delivery. It is helpful when the risks of continuation of pregnancy either to the mother or the fetus is more. Some unfavourable conditions like IUGR, PROM, Post –term pregnancy, IUD, Chorioamnionitis, Maternal medical problems like PIH, Diabetes Mellitus, Renal diseases, COPD, Cardiac diseases may call for induction of labour. Various Pharmacological methods have been introduced for both pre-induction cervical ripening and induction of labour are as follows- 1) Prostaglandins 2) Oxytocin 3) Steroid receptor antagonist-Mifepristone 4) Relaxin This study was conducted on nulliparous females in the age group of 20-30yrs, with gestational age more than 34 wks in the Dept. Of Obstetrics and Gynaecology, Index Medical College Hospital and Research Centre Khudel, Indore over a period of 1 year with a sample size of 100 and they were randomized into Group A-receiving 50mcg of misoprost tablet vaginally and Group B -receiving endocervical cerviprime gel. Hence the purpose of this study is to emphasize that misoprostol is a better alternative than dinoprostone for induction of labour at rural hospital setup by comparing their- 1) Success Rate 2) Induction –delivery interval 3) Number of doses required, their cost effectiveness 4) Maternal complications 5) Fetal complications Among these prostaglandins especially prostaglandin E1,because of their short induction delivery interval, easy availability, low price, easy storage at room temperature, low maternal and fetal complication appear to be especially useful.


Subject(s)
Adult , Delivery, Obstetric/drug effects , Dinoprostone/therapeutic use , Female , Fetus/complications , Gestational Age , Humans , Labor, Induced/complications , Labor, Induced/methods , India , Misoprostol/therapeutic use , Pregnancy , Pregnancy Complications , Pregnancy Outcome , Vagina/physiology , Young Adult
16.
Femina ; 41(1): 47-54, jan-fev. tab
Article in Portuguese | LILACS | ID: lil-694478

ABSTRACT

Os métodos de indução do parto podem ser divididos em estímulos naturais, estímulos exógenos diretos ou mecânicos e estímulos exógenos indiretos ou farmacológicos, cada qual apresenta suas particularidades nas indicações e contraindicações. O objetivo deste artigo foi realizar uma revisão da literatura consultando Medline/Pubmed e a Biblioteca Cochrane para avaliar a eficácia e segurança na utilização dos principais métodos de indução do trabalho de parto. Apurou-se não haver método ideal de indução do trabalho de parto. Os estímulos naturais e os métodos alternativos carecem de maiores estudos para incentivo de seu uso rotineiro. As prostaglandinas, em destaque o misoprostol, está indicada no Índice de Bishop desfavorável e a ocitocina em condições cervicais favoráveis. Os avanços no campo da biologia molecular tem corroborado que o método ideal deve atuar em sincronismo com a contratilidade uterina e a maturação cervical.(AU)


Methods of labor induction can be classified as natural stimuli, direct exogenous stimuli or mechanical and indirect exogenous stimuli or pharmacological. Which one has its peculiarities in relation to indications and contraindications. The objective of this article was to assess the efficacy and safety of the main methods of induction of labor trough the analysis of the medical literature in Medline/Pubmed and the Cochrane Library to. No ideal method of inducing labor was found. Further studies are required to encourage natural stimuli and alternative methods more often. According to Bishop scores, prostaglandins, (especially misoprostol) are unfavorable and oxytocin in case of favorable cervical environment. Advances in the field of molecular biology have confirmed that the ideal method should work simultaneously with uterine contraction and cervical ripening.(AU)


Subject(s)
Humans , Female , Pregnancy , Uterine Contraction/drug effects , Labor Stage, First/metabolism , Oxytocin/metabolism , Cervix Uteri/metabolism , Labor, Induced/methods , Prostaglandins/metabolism , Databases, Bibliographic , Laminaria/metabolism
17.
Femina ; 41(2)março - abril.
Article in Portuguese | LILACS | ID: lil-694481

ABSTRACT

Métodos de maturação cervical são utilizados há décadas, apresentando mecanismos, efetividade e riscos diversos. Para reconhecer os métodos existentes e delimitar quais possuem os menores riscos, melhor efetividade e disponibilidade na prática médica, foi realizada uma revisão crítica, que buscou artigos nas bases Medline/Pubmed, biblioteca Cochrane e LILACS/SciELO, referentes à maturação cervical mecânica ou farmacológica em gestantes com termos e palavras-chave relacionadas à maturidade cervical, misoprostol e parto induzido. Constatou-se que os métodos mais utilizados na prática são a prostaglandina sintética (misoprostol) e a sonda de Foley. Estes se mostraram superiores aos demais métodos encontrados, uma vez que são efetivos, têm baixo custo, são fáceis de armazenar e utilizar, especialmente o misoprostol. Ambos apresentaram uma efetividade similar, mas os métodos mecânicos estão relacionados a um maior risco de infecção.


Cervical ripening methods have been used for decades, showing different mechanisms, risks and effectiveness. To recognize the existing methods and delineate which have the lower risks, best availability and effectiveness in clinical practice, a critical review was conducted, which sought articles in Medline / Pubmed, Cochrane Library, and LILACS/SciELO regarding mechanical or pharmacological cervical ripening in pregnant women, with terms and keywords related to cervical ripening, misoprostol and induced labor. It was found that the most used methods in practice are synthetic prostaglandin (misoprostol) and the Foley catheter. They seem to be superior to other methods because they are effective, inexpensive and easy to store and use, especially misoprostol. Both showed a similar efficacy, but mechanical methods are related to a higher risk of infection.


Subject(s)
Humans , Female , Cervical Ripening , Misoprostol/administration & dosage , Misoprostol/pharmacology , Abortifacient Agents, Nonsteroidal/administration & dosage , Catheterization/methods , Cervix Uteri , Dinoprostone/administration & dosage , Prostaglandins, Synthetic/therapeutic use , Labor, Induced/methods
18.
Rev. bras. ginecol. obstet ; Rev. bras. ginecol. obstet;35(2): 60-65, fev. 2013. tab
Article in English | LILACS | ID: lil-666189

ABSTRACT

PURPOSE: To evaluate the effectiveness and the safety of orally administered misoprostol in comparison to intravenously infused oxytocin for labor induction in term pregnant women. METHODS: Between 2008 and 2010, a total of 285 term pregnant women whom were candidate for vaginal delivery were assessed for eligibility to enter the study. Twenty five patients were excluded for different reasons; and 260 included women were randomly assigned to one of the two groups according to the method of treatment, misoprostol or oxytocin. The misoprostol group received 25 µg every 2 hours for up to 24 hours for induction. The oxytocin group received an infusion of 10 IU which was gradually increased. The time from induction to delivery and induction to the beginning of the active phase and successful inductions within 12, 18, and 24 hours were recorded. The trial is registered at irct.ir, number IRCT2012061910068N1. RESULTS: Failure of induction, leading to caesarean section was around 38.3% in the oxytocin group and significantly higher than that of the misoprostol group (20.3%) (p<0.001). Despite the more prevalent failure in the oxytocin group, the mean time intervals from induction to active phase and labor of this group were both significantly less than the misoprostol group (10.1±6.1 and 13.2±7.7 versus 12.9±5.4 and 15.6±5.1 hours respectively, both p-values were <0.05). Maternal and fetal complications were comparable between groups except gastrointestinal symptoms which were encountered more frequently in the misoprostol (10.9 versus 3.9%, p=0.03). CONCLUSIONS: Misoprostol is a safe and effective drug with low complications for the induction of labor. Failure is seen less with misoprostol and caesarean sections are less frequently indicated as compared to oxytocin.


OBJETIVO: Avaliar a eficácia e segurança do misoprostol administrado por via oral em comparação à infusão de oxitocina para a indução do trabalho de parto em gestantes a termo. MÉTODOS: Entre 2008 e 2010, um total de 285 gestantes a termo candidatas para parto vaginal foram avaliadas quanto à eligibilidade para inclusão no estudo. Vinte e cinco pacientes foram excluídas por várias razões, e as 260 mulheres incluídas foram divididas aleatoriamente em dois grupos de acordo com o método de tratamento, misoprostol ou oxitocina. O grupo tratado com o misoprostol recebeu 25 µg cada 2 horas durante um máximo de 24 horas para indução. O grupo tratado com oxitocina recebeu infusão de 10 UI, que foi aumentada gradativamente. O tempo a partir da indução até o início da fase ativa e as induções bem-sucedidas dentro de 12, 18 e 24 horas foram registrados. O ensaio foi registrado em irct.ir, número IRCT2012061910068N1. RESULTADOS: A falha de indução levando à necessidade de cesariana foi de aproximadamente 38.3% no grupo tratado com oxitocina, sendo significativamente maior em relação ao grupo tratado com misoprostol (20,3%) (p<0,001). Apesar da falha mais prevalente no grupo tratado com oxitocina, os intervalos médios entre indução e fase ativa e trabalho de parto nesse grupo foram ambos significativamente menores em relação ao grupo tratado com misoprostol (10,1±6,1 e 13,2±7,7 versus 12,9±5,4 and 15,6±5,1 horas, respectivamente, sendo ambos os p-valores <0,05). Complicações maternas e fetais foram comparáveis entre grupos, com exceção dos sintomas gastrointestinais, que foram encontrados mais frequentemente no grupo tratado com misoprostol (10,9 versus 3,9%, p=0,03). CONCLUSÕES: O misoprostol é droga segura e eficaz para a indução do parto, com poucas complicações. Falhas são menos observadas e cesáreas são indicadas menos frequentemente com o misoprostol em relação à oxitocina.


Subject(s)
Adult , Female , Humans , Pregnancy , Labor, Induced/methods , Misoprostol/administration & dosage , Oxytocics/administration & dosage , Oxytocin/administration & dosage , Administration, Oral , Infusions, Intravenous , Pregnancy Trimester, Third
19.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;46(1): 91-97, 11/jan. 2013. tab, graf
Article in English | LILACS | ID: lil-665800

ABSTRACT

Hormone-mediated quiescence involves the maintenance of a decreased inflammatory responsiveness. However, no study has investigated whether labor induction with prostanoids is associated with changes in the levels of maternal serum hormones. The objective of this study was to determine whether labor induction with dinoprostone is associated with changes in maternal serum progesterone, estradiol, and estriol levels. Blood samples were obtained from 81 pregnant women at term. Sixteen patients had vaginal birth after spontaneous labor, 12 required cesarean section after spontaneous labor and 16 underwent elective cesarean. Thirty-seven patients had labor induction with dinoprostone. Eligible patients received a vaginal insert of dinoprostone (10 mg) and were followed until delivery. Serum progesterone (P4), estradiol (E2) and estriol (E3) levels and changes in P4/E2, P4/E3 and E3/E2 ratios were monitored from admission to immediately before birth, and the association of these measures with the resulting clinical classification outcome (route of delivery and induction responsiveness) was assessed. Progesterone levels decreased from admission to birth in patients who underwent successful labor induction with dinoprostone [vaginal and cesarean birth after induced labor: 23% (P < 0.001) and 18% (P < 0.025) decrease, respectively], but not in those whose induction failed (6.4% decrease, P > 0.05). Estriol and estradiol levels, P4/E2, P4/E3 and E3/E2 ratios did not differ between groups. Successful dinoprostone-induced labor was associated with reduced maternal progesterone levels from induction to birth. While a causal relationship between progesterone decrease and effective dinoprostone-induced labor cannot be established, it is tempting to propose that dinoprostone may contribute to progesterone withdrawal and favor labor induction in humans.


Subject(s)
Adult , Female , Humans , Infant, Newborn , Pregnancy , Dinoprostone , Estradiol/blood , Estriol/blood , Labor, Induced/methods , Oxytocics , Progesterone/blood , Pregnancy Outcome , Term Birth/blood
20.
Medical Forum Monthly. 2013; 24 (2): 39-41
in English | IMEMR | ID: emr-142546

ABSTRACT

The unripe cervix may present a problem when delivery is indicated prior to the Spontaneous onset of labour. To assess the role of Foleys, catheter in improving cervical score prior to Induction of labour. Observational type of study. This study was conducted in the Department of Obstetrics and Gynecology, Ghulam Muhammad Mahar Medical College Teaching Hospital Khairpur, Sindh during six months period from January to June 2012. Foley,s catheter was used for pre-induction cervical Ripening in fifty patients with medical and Obstetrical indication for induction of labour with unfavorable cervix. The study group comprised 35[70%] primigravida and 15[30%] multigravida. The mean maternal age was 20-35 years. Foleys catheter No: 18-22 was inserted in fully aseptic condition extra amniotic up to the level of Internal cervical os and was removed after 24 hours. Pre and post treatment cervical Condition was assessed by Bishop,s score. Foleys was inserted in 50 patients for pre-induction ripening of cervix. Thirty [60%] out of 50 patients delivered spontaneous vaginal delivery, 11[22%]Delivered by caesarean section due to failure to progress, fetal distress and CPD. Mean induction to delivery interval was 12.72hours.There were no cases of infection, Ruptured membranes, hemorrhage or other complications attributed to balloon Catheter used. Pre-induction cervical ripening with extra amniotic Foleys catheter Balloon has the advantages of being effective, simple, economical and free of Systemic serious side effects


Subject(s)
Humans , Female , Cervical Ripening , Labor, Induced/methods , Treatment Outcome , Hospitals, Teaching
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