http://uk.reuters.com/article/health...1?feedType=RSS
What do you all think of this new study? Has anyone seen the actual study?
What do you all think of this new study? Has anyone seen the actual study?
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Here's a link to the full article.
Here's a link to the study. *The pilot study for this project was funded by Forest Pharmaceuticals, Inc., in 2000. In addition, Forest Pharmaceuticals has provided, at no cost, its dinoprostone vaginal insert cervical ripening product for use in an ongoing randomized clinical trial of AMOR-IPAT * Pretty much obvious what I think... at least I would hope it is. |
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Here's a link to the full article.
Here's a link to the study. *The pilot study for this project was funded by Forest Pharmaceuticals, Inc., in 2000. In addition, Forest Pharmaceuticals has provided, at no cost, its dinoprostone vaginal insert cervical ripening product for use in an ongoing randomized clinical trial of AMOR-IPAT * Pretty much obvious what I think... at least I would hope it is. |


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I think, having skimmed it, that it boils down to 'this particular set of interventions leads to fewer c-sections than this other set of more typical interventions'. As per usual, the proper control group (women who are JUST LEFT ALONE) isn't included...
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| Because most of the patients who were delivered by family physicians at our institution had been exposed to the AMOR-IPAT method of care, all nonexposed subjects came from offices that were staffed by obstetricians. |
| Between 1993 and 1997, different hospital practitioners used risk-guided prostaglandin-assisted preventive labor induction with differing intensity. We used a retrospective cohort design, based on the practitioner providing prenatal care, to compare birth outcomes in women exposed to this alternative method of care with those in women not exposed. Multiple logistic regression analysis controlled for patient characteristics and clustering by practitioner. |
| Randomized controlled trials of this method of care are warranted. |
| From one study, although most women would choose to achieve vaginal birth, those women who were interested in elective cesarean would do so for such reasons as scheduling and concerns about pain, as well as recovery from labor. These potential concerns about vaginal delivery pale in comparison to the higher rates of maternal hemorrhage, infection, and even death associated with cesarean delivery Further, current cesarean delivery affects maternal and neonatal outcomes in subsequent pregnancies.12,13 One management scheme that may appease women interested in enhancing their chances of achieving vaginal birth while affording more control to the parturient with respect to scheduling is elective or preventive induction of labor. |
| To reduce the likelihood iatrogenic fetal lung immaturity caused by preventive labor induction the lower limit of the optimal time of delivery (LLOTD) was set at 38 weeks 0 days of gestation. |