Showing posts with label Induction of labor. Show all posts
Showing posts with label Induction of labor. Show all posts

Saturday, September 15, 2018

What is the best approach for labor induction in a multiparous patient?


Simultaneous administration of oxytocin along with cervical ripening with balloon catheter minimized the time to vaginal delivery and increased the rate of delivery within 24 hours in multiparous patients with an unfavorable cervix. This has significant benefits regarding patient care and satisfaction reports the results of a randomized control trial published in September issue of the American Journal of Obstetrics and Gynecology.

The best method of induction of labor in a multiparous patient is debatable because of a paucity of data. Results available from the only previous RCT comparing the simultaneous vs. sequential use of balloon catheter and oxytocin found no difference in median time to delivery between the two groups (FIAT-M Trial).

In this RCT involving 180 patients, Bauer et al. sought to determine whether the simultaneous vs. sequential use of balloon catheter and oxytocin helps decrease the time to delivery in multiparous patients who present with an unfavorable cervix.

The study recruited multiparous women ≥18 years with prior vaginal delivery who needed induction of labor and presented with a non-anomalous, singleton fetus in cephalic presentation with intact membranes with cervical dilatation ≤2 cm on admission.

Women were randomized to receive either simultaneous (oxytocin with cervical ripening balloon) or sequential (oxytocin following cervical ripening balloon expulsion) regimen.

Investigators looked at the time from induction to delivery as the primary outcome measure while the secondary measures of interest were time to cervical ripening balloon expulsion, induction-to-delivery interval, mode of delivery and adverse maternal or neonatal outcomes.

Women who simultaneously received balloon and oxytocin were more likely to deliver within 24 hours as compared to those in whom oxytocin was started after the balloon expulsion (87.8% vs. 73.3%; P=0.02). The average induction-to-delivery interval in the simultaneous group was 12.5 h vs. 16.3 h with greater cervical dilatation when the balloon was expelled.

Both groups were comparable regarding mode of delivery, chorioamnionitis, or adverse maternal or neonatal outcomes.

The authors concluded that “The simultaneous use of oxytocin with cervical ripening balloon should be incorporated into the management for multiparous women who require cervical ripening while undergoing induction of labor.”

Presented as a poster at the 38th Annual Pregnancy Meeting of the Society for Maternal-Fetal Medicine, Dallas, TX, Jan. 29–Feb. 3, 2018.

Friday, January 27, 2017

Model developed to predict chances of vaginal delivery in nulliparous women undergoing induction of labor-- News from SMFM 2017, Las Vegas.

 

According to statistics by CDC, 23.3% of women in USA undergo induction of labor making it one of the most common obstetric procedure performed in US hospitals.

A study presented at the 37th  annual meeting of Society for Maternal-Fetal Medicine , January 23-28 , Las Vegas by Dr. Tetsuya Kawakita and his colleagues sought to  develop a model that could predict  the likelihood of successful induction of labor. [1]

The researchers used data from Consortium on Safe labor study, a retrospective multicenter study that extracted data on labor and delivery across 19 hospitals in United states. [2]

Of 12,413 nulliparous women at ≥37 weeks’ gestation who had labor undergone induction, 9,550 (76.9%) delivered vaginally.

The researchers studied the various demographic, obstetric and neonatal factors in these study group and by running stepwise logistic regression were able to identify factors associated with successful vaginal birth.

The maternal factors were maternal age, BMI, race, weeks at induction, gestational diabetes or prediabetes, cervical dilatation, effacement and consistency.  Fetal factors were station of fetal head, amount of liquor, IUGR and CTG at the beginning of the procedure. Taking all these factors into account a Nomogram was created, each maternal factor was allotted a fixed number of points. A maternal BMI of 70 received 8 points while a BMI of 20 received 95 points. Similarly, if maternal age at labor was 45 she received 4 points while 25 points were given if her age was 20.

The total points were calculated with a maximum of 317 points. The higher the number of points the patient received, the probability of vaginal delivery also increased.  


Adapted from SMFM 2017 abstracts 










[1] http://www.ajog.org/article/S0002-9378(16)31917-2/fulltext
[2] https://www.nichd.nih.gov/about/org/diphr/eb/research/Pages/safe-labor.aspx

Thursday, November 10, 2016

Combination of labor induction agents almost halves the time to delivery.

The cascade of spontaneous events that sets the wheels of labor in motion has remained a mystery despite all the recent advances in the field of maternal and fetal medicine. Researchers hypothesize that it’s blend of physiology and magic that sets the ball rolling. Maternal and fetal signals both play a part in starting the process.

The history of labor induction dates to time of Hippocrates' when mammary stimulation and mechanical cervical dilatation was used to bring about uterine contraction.[1]

Induction of labor for singleton births has seen a slight decline from 23.8% in 2010 and 23.3% in 2012 after seeing a steady increase in past 20 years. [2]  This translate to 932,000 women undergoing induction of labor for various maternal and fetal indication.

Various mechanical and chemical methods singly or in combination have been in use since long. The choice of method depends on state of cervix, previous obstetric history, indication of induction and gestational age at induction. Foley’s balloon catheter, Prostaglandin E2 and misoprostol are common methods used for cervical ripening. Amniotomy and oxytocin are used when the cervix is already ripened.[3]

A recent paper published on November 03, 2016 in Journal of Obstetrics & Gynecology evaluated the effectiveness of the four most commonly used method. [4] The paper was also presented at the Pregnancy Meeting, the 2016 Annual Meeting of the Society for Maternal-Fetal Medicine (SMFM).

Dr. Lisa Levine, MD, University of Pennsylvania’s Perelman School of Medicine, Philadelphia, Pennsylvania, and colleagues said in their presentation “This randomized trial is one of the first of its kind to compare 4 different induction methods in a head-to-head trial. We found that combination induction methods resulted in delivery in half the amount of time as single agents with no difference in caesarean delivery rates.”

The study called as Foley or Misoprostol for the Management of Induction (FOR MOMI) trial was a 4-armed randomized trial conducted between May 2013 and June 2015. The study recruited 492 women with singleton full-term pregnancy (37 weeks of gestation or greater), vertex-presentation, with no contraindication to vaginal delivery, intact membranes, Bishop score 6 or less, and cervical dilation 2 cm or less. These women were assigned to receive either misoprostol alone; or Foley catheter alone; Foley catheter and Pitocin concurrently or misoprostol and cervical Foley catheter concurrently.

The primary outcome measured was reduction in time to delivery with a reduction of more than 4 hours considered significant. Numerous secondary outcomes like time to vaginal delivery, rate of caesarean deliveries, time in active labor, defined as cervical dilation of 5 cm or more, delivery within 12 or 24 hours, and maternal length of stay were also looked at.

The demographics and clinical characteristics of the study participants were quite similar with a mean age of 27 years, 72% being nullipara, mean gestational age at induction being 39 weeks with mean bishop score 3 and mean cervical dilatation 1.

The median time to delivery for nulliparous and multiparous women in various arms of the study are (P<.001):
misoprostol–Foley group       13.1 hours
oxytocin–Foley group            14.5 hours
misoprostol only                    17.6 hours
Foley-only group                   17.7 hours

When the data was adjusted for parity and only vaginal deliveries analyzed, women in the misoprostol-Foley group where twice as likely to deliver earlier (HR=1.92) with reference to misoprostol only or Foley-only group.
  
Women in the combination arms of the study also had the maximum chance of delivering in 24 hours. (88% of women in the misoprostol/Foley group and 84% in the oxytocin/Foley group).
Rates of cesarean section and other maternal morbidities like perineal lacerations, endometritis, wound infection and dehiscence, readmission or length of stay were comparable in all the groups. No significant difference was found in neonatal morbidities too.

The authors opined that “This study has significant clinical implications for obstetric care. The ability to shorten the length of time women spend in labor without increasing morbidity has large clinical and financial implications given the cost and known maternal–neonatal risks associated with both prolonged labor and cesarean delivery."

The only study limitation was lack of blinding, because women had to be examined for application of different methods in 4 study arms. Also, individual arm lacked the statistical power to compare the cesarean section, maternal and neonatal morbidities across different groups.

In all, the findings could help millions of women and shorten thousands of hours in labor across the world. It is estimated that nearly 20% or 932,000 women undergo induction of labor in USA. If combination method is used in all of them, then there would be more than 3 million fewer hours, or more than 125,000 fewer days that women spend in labor in the United States alone. 

This has huge financial and health care utilization implications.




[1] www.glowm.com/section_view/heading/Induction%20of%20Labor/item/130
[2] http://www.cdc.gov/nchs/data/databriefs/db155.pdf
[3] https://sogc.org/wp-content/uploads/2013/08/September2013-CPG296-ENG-Online_REV-D.pdf
[4] http://journals.lww.com/greenjournal/Abstract/publishahead/Mechanical_and_Pharmacologic_Methods_of_Labor.98564.aspx

Tuesday, July 26, 2016

Induction of labor does not hike the risk for Autism Spectrum disorders.

Clinical Pearls:

  • Contrary to the findings of earlier study, Induction of labor does not increase the risk for development of Autism Spectrum disorders(ASD).


Autism Spectrum disorders(ASD) is a group of complex developmental disability that affects a person ability to interact and communicate socially. It includes several conditions that were earlier diagnosed separately and include autistic disorder, pervasive developmental disorder not otherwise specified (PDD-NOS), and Asperger syndrome.

According to CDC about 1% of world population have ASD. It is the fastest growing developmental disability in US and the current prevalence is 1 in 64 births and has increased 119.4 percent from 2000 (1 in 150) to 2010 (1 in 68).[1] An article published in JAMA Pediatric 2014 by Buescher et al. estimated that about 3.5 million people in US live with ASD.[2]

Numerous pregnancy related risk factors have been attributed in putting the children at high risk for ASD like children that were born to older parents,  were preterm or low birth weight, born with other chromosomal disorders like  Down syndromefragile X syndrometuberous sclerosis and  those delivered by cesarean section.

A study published in Annals of Epidemiology attributed three perinatal risk factors like being born too early, too small, and/or by Cesarean delivery to be responsible for 12-13% of ASD in children.[3]
Many other studies have examined the mother’s use of  serotonin uptake  inhibitors (SSRIs) and increasing use of ART as a causative factor for  sudden increase in prevalence of ASD.

Another large population based study published in JAMA pediatrics in October,2013 concluded that “Compared with children born to mothers who received neither labor induction nor augmentation, children born to mothers who were induced and augmented, induced only, or augmented only experienced increased odds of autism after controlling for potential confounders related to socioeconomic status, maternal health, pregnancy-related events and conditions, and birth year. The observed associations between labor induction/augmentation were particularly pronounced in male children.”[4]

This study sparked a widespread debate between physicians and researchers and the lead author of the study Dr. Gregory proposed the culprit to be oxytocin in induced or augmented labors, putting these children at high risk for ASD. After this controversy ACOG put out a committee opinion (597) in 2014 stating that “Current evidence does not support a conclusion that labor induction or augmentation causes autism spectrum disorder (ASD) in newborns, available evidence is inconsistent and does not demonstrate causation.”[5]

A recent study conducted by researchers at Harvard T.H. Chan School of public health in Boston and published in JAMA pediatrics online first on July 25, 2016 found no association between induction of labor and ASD. This large nationwide study performed in Sweden, followed up a cohort of 1,362,950 children born between 1992-2005. Out of which 1.6% (22077) children were diagnosed with ASD by ages 8 years through 21 years.  

In 11% of the mothers’ labor induction was done due to preeclampsia, gestational diabetes and chronic hypertension. After the statistical analysis, the study found an association between labor induction and ASD but when the analysis was performed between siblings and close relatives the association was not documented.

Siblings share many genetic, socioeconomic and maternal characteristics that may increase the risk for development of ASD, so if association is not documented when comparing with them, the association probably does not exist.

The finding of this large study suggests that if clinically indicated, decision to induce labor should not be withheld in fear of baby developing ASD. Not to induce the labor when indicated may have adverse neonatal consequences.

Dr. Bateman concludes "Overall, these findings should provide reassurance to women who are about to give birth, that having their labor induced will not increase their child's risk of developing autism spectrum disorders."




[1] https://www.cdc.gov/ncbddd/autism/facts.html
[2] http://www.ncbi.nlm.nih.gov/pubmed/24911948
[3] Schieve LA, Tian LH, Baio J, Rankin K, Rosenberg D, Wiggins L, Maenner MJ, Yeargin-Allsopp M, Durkin M, Rice C, King L, Kirby RS, Wingate MS, Devine O. Annals of Epidemiology. January 2014. [epub ahead of print]
[4] Gregory SG, Anthopolos R, Osgood CE, Grotegut CA, Miranda M. Association of Autism With Induced or Augmented Childbirth in North Carolina Birth Record (1990-1998) and Education Research (1997-2007) Databases. JAMA Pediatr.2013;167(10):959-966. doi:10.1001/jamapediatrics.2013.2904.
[5] http://www.acog.org/Resources-And-Publications/Committee-Opinions/Committee-on-Obstetric-Practice/Labor-Induction-or-Augmentation-and-Autism