Comparison of Intravaginal Misoprostol Tablet (Prostaglandin E1) and Intracervical Dinoprostone (Prostaglandin E2) Gel in Induction of Labour
نویسنده
چکیده
Cervical ripening is an essential factor for initiation of normal labour for vaginal delivery. Prior to onset of spontaneous labour the cervix undergoes a gradual process of ripening. But in certain cases it does not occur spontaneously at term and sometimes induction of labour is required. Then cervical ripening means high bishop score in essential for successful induction of labour. This comparative study was conducted at Bikaner to compare induction of labour by vaginal prostaglandin E1 tablet (tablet Misoprostol 25 μg 4 hourly) and Intra cervical Dinoprostone gel 0.5 mg. For this purpose 100 clients were given vaginal prostaglandin E1 tablet (tablet Misoprostol 25 μg 4 hourly) and 100 clients were given Intra cervical Dinoprostone gel 0.5 mg. It was observed in this study that Dinoprostone gel is more efficacious for cervical ripening and labour induction in cases of nulliparous & primiparous at term with unfavourable cervix with intact membranes, as compared to misoprostol in terms of shorter total duration of labour, shorter mean induction delivery interval, more spontaneous vaginal deliveries, and reduced incidence of LSCS as well as instrumental deliveries. Keywords— Cervical Ripening, Induction of Labour, Intracervical Dinoprostone Gel, Intravaginal MisoprostolTablets.
منابع مشابه
A Randomized Comparison Between Intravaginal Misoprostol and Intracervical Dinoprostone for Cervical Ripening and Labour Induction in Participants with Unfavourable Cervices
The goal of obstetrics is a pregnancy that culminates in a healthy infant and a minimally traumatized mother. Ideally all pregnancies should go to term and labour should begin spontaneously. More often than not, the need for delivery is clear but the timing is not emergent and the route is not dictated by foetal demands. A method to initiate the normal process of labour at a time before labour ...
متن کاملMisoprostol: an effective agent for cervical ripening and labor induction.
OBJECTIVE Our purpose was to compare the safety and efficacy of intravaginal misoprostol versus intracervical prostaglandin E2 gel (dinoprostone) for preinduction cervical ripening and induction of labor. STUDY DESIGN Two hundred seventy-six patients with indications for induction of labor and unfavorable cervices were randomly assigned to receive either intravaginal misoprostol or intracervi...
متن کاملA Comparative Study of Intravaginal Misoprostol Vs Intra Cervical Dinoprostone Gel for Induction of Labour
Induction of labour is a common need in obstetrics ward. There are various complications and drug side effects associated with it. This study has been designed to compare the safety and efficacy of 50μg intra-vaginal misoprostol (PGE1 analogue)with 0.5mg intracervical dinoprostone gel (PGE2). . 40 pregnant women with different indications of induction of labour participated in the study. They w...
متن کاملEvaluation of non-pharmacological method-transcervical foley catheter to intravaginal misoprostol and Prostaglandin E2 gel for preinduction cervical ripening
The efficacy of intracervical Foley catheter with misoprostol (PGE1) and dinoprostone (PGE2) for preinduction cervical ripening, induction of labour, mode of delivery, induction to delivery interval and maternal complications has been compared.. Women who were admitted to hospital and met criteria for entrance in the trial were counseled and enrolled after informed consent. Inclusion criteria i...
متن کاملProstaglandin E2 Labour Induction with Intravaginal (Minprostin) versus Intracervical (Prepidil) Administration at Term: Randomized Study of Maternal and Neonatal Outcome and Patient's Perception Using the Osgood Semantic Differential Scales
AIM To compare the efficacy, safety, and patient's perception of two prostaglandin E2 application methods for induction of labour. METHOD Above 36th weeks of gestation, all women, who were admitted to hospital for induction of labour, were prospectively randomised to intravaginal 1 mg or intracervical 0.5 mg irrespective of cervical Bishop score. The main outcome variables were induction-to-d...
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