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Outpatient Based Misoprostol to Prevent Prolonged Pregnancy, Paperback
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The study group receiving single low dose misoprostol vaginally at 40 weeks of gestation showed a significant decrease in the need for induction compared to the control group, with no observed side effects.
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What Stands Out
Product Details
- Open randomized controlled trial using single low dose (25 μg) misoprostol vaginally at 40 weeks of gestation
- Intervention to prevent prolonged pregnancy in uncomplicated singleton pregnancies
- Significantly fewer women in study group required induction compared to control group
- Shorter mean duration from enrolment to delivery in study group compared to control group
- Comparable rates of cesarean section, meconium stained liquor, NICU admission, and neonatal morbidity in both groups
- No observed neonatal or perinatal mortality in either group
| Package Weight | 1 Pound |
Who Should Buy?
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Healthcare Providers
Medical professionals seeking effective methods for managing prolonged pregnancies in outpatient settings will benefit significantly from this guide.
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Expectant Mothers
Pregnant women at risk of prolonged pregnancies can use this resource to understand treatment options available to them.
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Medical Students
Students studying obstetrics can gain insight into practical approaches to labor management and the use of Misoprostol.
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Casual Readers
Individuals without a medical background may find the content too technical and difficult to understand effectively.
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Individuals Without Pregnancy Issues
Those not facing prolonged pregnancy concerns may not find the information applicable to their situation or needs.
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Non-Healthcare Professionals
People unrelated to the medical field may struggle to apply the clinical insights presented in this book.
Product Description
Outpatient Based Misoprostol to Prevent Prolonged Pregnancy, Paperback
Customer Questions & Answers
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Question:
What was the main finding of the study?
Answer: The main finding was a decreased need for induction in the group receiving misoprostol compared to the control group. -
Question:
Were there any side effects observed in the study group?
Answer: No side effects were observed in the study group receiving misoprostol at 40 weeks of gestation. -
Question:
Was there any difference in neonatal outcomes between the study and control groups?
Answer: No significant difference was observed in neonatal outcomes such as birth weight, meconium stained liquor rate, NICU admission rate, and neonatal morbidity between the study and control groups.
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Features & Benefits
- Significantly lower need for induction in the study group
- Study group had no observed side effects
- Comparable birth weight, meconium stained liquor rate, NICU admission rate, and neonatal morbidity in both groups
- No neonatal or perinatal mortality observed in either group
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