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Objectives. List the indications and contraindications for cervical ripening and induction of labor.Discuss the different methods used for cervical ripening, labor induction and augmentation.Discuss the nurses role in the safe administration of cervical ripening and induction agents.. Definitions.
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1. Cervical Ripening andInduction/Augmentation of Labor
2. Objectives List the indications and contraindications for cervical ripening and induction of labor.
Discuss the different methods used for cervical ripening, labor induction and augmentation.
Discuss the nurses role in the safe administration of cervical ripening and induction agents.
3. Definitions What is cervical ripening?
Preparation of an unfavorable cervix for labor induction
What is induction?
Stimulation of uterine contractions before the spontaneous onset of labor
What is augmentation?
Correcting ineffective uterine contractions or hypocontractility
4. Incidence in the United States
Since 1989, there has been a 137% increase in induction and a 75% increase in augmentation rates.
NCHS, 2009
5. Risk-Benefit Risk of Cesarean Birth for Nulliparous Women:
17.2% spontaneous labor
30.4% induced labor
77.7% increase for induction
Reisner et al., 2009
Use of pharmacologic agents increases risk for tachysystole, indeterminate or abnormal FHR patterns and failure to progress
6. Cascade of Interventions Related to Induction of Labor
7. Economic Costs Spontaneous Labor/vaginal birth $4000
Induction of labor/vaginal birth
$5000
Cesarean Birth/scheduled
$7000
Cesarean Birth/failed induction
$7500
Simpson, KR., 2009
Simpson, 2009
8. Indeterminate/Abnormal FHR(Category II and Category III FHR) Nearly twice the risk, possibly related to:
Tachysystole
Early Amniotomy
Labor Dystocia
Longer Labor
Less Fetal Tolerance
Glantz, 2005, Simpson, KR., 2009
9. Risks to the Infant
10. Indications for Cervical Ripening and Induction of Labor
11. Contraindications-Induction of Labor Generally, the contraindications for labor induction are the same as those for spontaneous labor and vaginal birth
Vasa previa or complete placenta previa
Transverse fetal lie
Umbilical cord prolapse
Previous transfundal uterine incision
Active genital herpes infection
Pelvic structural deformities
Invasive cervical cancer
12. Situations Requiring Special Attention One or more previous low-transverse cesarean births
Breech presentation
Maternal heart disease
Multifetal pregnancy
Polyhydramnios
Presenting part above the pelvic inlet
Severe hypertension
Abnormal FHR patterns requiring emergent birth
A trial of labor after a previous cesarean birth or history of prior uterine scar
ACOG 2009, 2002
13. Indications for Augmentation of Labor Dystocia
Uterine Hypocontractility
Uterine hypocontractility should be augmented only after both the maternal pelvis and fetal presentation have been assessed.
ACOG 2009
14. Pre-induction/Ripening Criteria Availability of trained nursing and provider staff
Cervical ripening agents should be administered at or near the labor and birth suite where uterine activity and FHR can be monitored continually
Assessment of gestational age, cervical status, pelvic adequacy, fetal size and presentation
A physician capable of performing a cesarean birth should be readily available.
ACOG 2009
15. Criteria continued Considerations to any risks to mother or fetus
Patient counseling regarding indications, agents/methods, and possibility of repeat induction or cesarean birth
The medical record should document that a discussion was held between the pregnant woman and her health care provider
ACOG 2009
16. Bishop ScoreHas been shown to be an important determinant of the success or failure of induction
17. Cervical Status For women at term, a Bishop score of 6 or more may be useful in predicting onset of spontaneous labor within 7 days
Rozenberg, Goffinet & Hessabi, 2000
18. Cervical Ripening Agents These agents may soften the cervix and change the Bishop score
Mechanical/Non pharmacologic Methods
Pharmacologic Methods
19. Mechanical Dilators Laminaria Tents
Synthetic Osmotic Dilators
Foley Catheter
Double Balloon Cervical Ripening Catheter
Extraamniotic saline infusion- balloon catheter
20. Pharmacologic MethodsNot recommended for use in women with history prior c-birth or uterine scar Prostaglandin E1: Misoprostol (Cytotec)
Oral or vaginal use
Wide variations exist in time of onset of uterine contractions
Peak action is approximately 1-2 hours but can be up to 4-6 hours
May re-dose only if parameters met
21. Complications with Misoprostol (Cytotech) Tachysystole
Indeterminate/Abnormal FHR pattern
Precipitous Labors
Uterine Rupture
Need careful maternal/fetal assessments
Need consent/protocols
ACOG, 2009
22. Prostaglandin E2-Dinoprostone Prepidil
Cervidil
23. Cervical Ripening Agents Minimum safe interval from prostaglandin to oxytocin administration not established
Manufacturers guidelines recommend
Misoprostol- at least 4 hours after last dose
Prepidil- 6-12 hours after last dose
Cervidil-30-60 minutes after removal of vaginal insert
Not contraindicated with PROM
24. Induction and Augmentation of Labor Mechanical methods of Induction of Labor
Stripping the Membranes
Amniotomy Digital separation of the chorioamnionic membrane from the wall of the cervix and lower uterine segment during a vaginal examination (aka sweeping the membranes)
A finger is inserted into the cervical os and rotated 360 degrees.
Exact mechanism is unknown- thought to release prostaglandins locally from the amnion/chorion/decidua
Risks include the potential for intraamniotic infection, unplanned rupture of membranes, disruption of an undiagnosed placenta previa and precipitous labor and birth
ACOG, 1999a; Hadi, 2000Digital separation of the chorioamnionic membrane from the wall of the cervix and lower uterine segment during a vaginal examination (aka sweeping the membranes)
A finger is inserted into the cervical os and rotated 360 degrees.
Exact mechanism is unknown- thought to release prostaglandins locally from the amnion/chorion/decidua
Risks include the potential for intraamniotic infection, unplanned rupture of membranes, disruption of an undiagnosed placenta previa and precipitous labor and birth
ACOG, 1999a; Hadi, 2000
25. Oxytocin Most commonly used induction agent in the United States and worldwide
Kelly & Tan, 2001
Synthetic oxytocin is chemically and physiologically identical to endogenous oxytocin
Half life between 10-12 minutes
Dawood, 1995a; Arias, 2000
3 4 half-lives to reach steady state
Full effects of oxytocin cannot be determined until steady-state concentration has been achieved.
Physiologic steady state 40 min, basis for dosing interval.
26. Endogenous Oxytocin First Stage Labor
Maternal circulating concentration 2-4 mU/min
Fetal Contribution
3 mU/min
Combined effects = 5-7 mU/min
Second Stage Labor
Surge of oxytocin at Fergusons reflex
Simpson, KR, 2009
27. Response to Oxytocin Prolonged exposure ? ? Oxytocin receptor sites compared with spontaneous labor
More oxytocin for dysfunctional labor will cause further desensitization. A rest period of 1-2 hours is recommended
Phaneuf et al., 2000
Continued oxytocin after active labor is established will not shorten labor. Active labor is self-sustaining.
28. Oxytocin Dosing
Considerable controversy exists about dosage and rate increase intervals-there is no consensus in the literature
You take the high road
and Ill take the low road
29. Oxytocin Dosing Only increase oxytocin rate if:
FHR is normal
Labor has not progressed 0.5 -1 cm/hr
Contractions are no closer than every 2-3 minutes
Excessive uterine activity over the course of 1 hour in first stage of labor is associated with an umbilical artery pH = 7.11 at birth
Decrease or discontinue oxytocin in active labor
Simpson, KR, 2009
30. Physiologic Dosage Start with doses of 0.5-1 mU/min
Increase in 1-2 mU/min increments every 30-40minutes until contractions are every 2-3 minutes apart and labor is progressing ACOG, 2009 SOGC, 2001
Current literature suggests that 90% of pregnant women at term will have labor successfully induced with 6mU/min or less of oxytocin
Dawood, 1995a, 1995b; Seitchik, Amico et al., 1984
31. Oxytocin Administration No maximal dose of oxytocin has been firmly established
Doses above 40mU/min are rarely used, except in cases of intrauterine fetal demise (IUFD).
Infusion rates >=20mU/min can decrease free water clearance by the kidney resulting in water intoxication.
Smith and Merrill, 2006
32. High Dose Oxytocin According to ACOG (2009), protocols that involve high-dose oxytocin are acceptable; however, high-dose oxytocin is associated with more uterine tachysystole
33. Oxytocin and Medication Safety
34. Nursing responsibilities Titrate oxytocin infusion drip to achieve three contractions in 10 minutes with a duration of 60-90 seconds
Closely monitor fetal response, uterine activity and resting tone
Monitor maternal vital signs and fluid balance
Closely monitor mean with dose changes, assess every 15 min, may summarize every 30 min when no more dose change.Closely monitor mean with dose changes, assess every 15 min, may summarize every 30 min when no more dose change.
35. Potential Complications-Oxytocin Tachysystole
>5 contractions in 10 minutes, averaged over a 30-minute window. Tachysystole should always be qualified as to the presence or absence of associated FHR decelerations.
Abruptio placentae
Uterine rupture
Hyponatremia (water intoxicaiton)
I & O when on oxytocin
36. Nursing Interventions for Tachysystole with Normal FHR pattern Lateral positioning of mother
Increase IV fluid (LR)
If uterine activity not returned to normal after 10 minutes, ? oxytocin by half
If tachysystole persists, D/C oxytocin until tachysystole resolves
Consider terbutaline 0.25 mg SQ, with order
ACOG, 2010, AWHONN, 2008
37. Nursing Interventions for Tachysystole with Indeterminate or Abnormal FHR pattern Discontinue or reduce oxytocin
Lateral positioning of Mother
IV fluid bolus (LR)
If hypotensive, (as with epidural) contact anesthesia provider, prepare to administer epinephrine, with order
Oxygen, 10 LPM, non-rebreather mask
Consider terbutaline 0.25 SQ, with order
If unresolved, inform provider immediately, possibly prepare for C/S.
(ACOG 2010)
38. Resuming Oxytocin
39. Women attempting VBAC Should women with a previous cesarean birth undergo induction or augmentation of labor?
Spontaneous labor more likely to result in successful VBAC
Some studies show women with oxytocin administration undergoing TOLAC may be at increased risk of uterine rupture than spontaneous labor. Other studies have not.
Use of prostaglandins are associated with a higher rate of uterine rupture and are NOT RECOMMENDED
ACOG, 2010
40. VBAC Success Rates
41. VBAC Induction Physician and surgical team must be immediately available throughout active labor
Recommend 1:1 nursing care with an experienced RN
Continuous EFM
Must have ability to perform emergency C/birth
42. Nursing Implications with VBAC Induction/Augmentation Access to operating room readily available
Monitor as for high risk
Signs and symptoms of uterine rupture/dehiscence of prior scar
Patient c/o increasing pain and tenderness even with epidural
Presentation may take place over period of time or suddenly like something has given away
Vomiting, syncope, vaginal bleeding, tachycardia, fetal bradycardia or absent fetal heart rate
43. Management Maternal stabilization and immediate cesarean birth
Key to diagnosis is suspicion of uterine rupture
Simpson, K.R & Creehan, P., 2001
44. Conflict? No way!
45. Summary Evidence suggests that cervical ripening can increase the chances of successful induction
Misoprostol (cytotec) is becoming more widely used for cervical ripening and labor induction
No elective inductions before 39 completed weeks of gestation
Protocols should be based on ACOG/AHWONN standards and guidelines
Multiple factors contribute to the steady increase in the rate of induction in the United States
Consider implementation of an Induction of Labor Patient Safety Bundle.
46. References American College of Obstetricians and Gynecologists. (August, 2009). Induction of Labor, Practice Bulletin, Clinical Management Guidelines for Obstetrician-Gynecologists, Number107. Washington DC: Author.
American College of Obstetricians and Gynecologists. (November, 2010). Management of Intrapartum Fetal Heart Rate Tracings, Number116. Washington DC: Author.
American College of Obstetricians and Gynecologists. (August 2010).Vaginal Birth After Previous Cesarean Delivery, Practice Bulletin, Clinical Management Guidelines for Obstetrician-Gynecologists, Number115, Washington DC: Author.
Simpson, K.R., (2008). Cervical Ripening and Induction and Augmentation of Labor. 3rd edition. Association of Womens Health, Obstetric and Neonatal Nurses. Washington DC.
American Academy of Pediatrics & American College of Obstetricians and Gynecologists. (2007). Guidelines for Perinatal Care (6th Ed.). Elk Grove, IL, Washington DC: Authors.
National Center for Health Statistics (NCHS) year 2000 - 2009 data
Tita, A.,et al. (2009). Timing of elective preterm and neonatal outcomes. (Electronic Version). NEJM. 360:2, 111-120
Joint Commission. (2010). Specifications Manual for Joint Commission Quality Core Measures http://jointcommission.org/releases/TJC2010A/MIF0166.html
Phaneuf S., et al, Loss of myometrial oxytocin receptors during oxytocin-induced and oxytocin-augmented labour. Journal of Reproduction & Fertility 2000;120(1):91-97.
Glantz, J (April 2005). Elective Induction vs. spontaneous labor Associations and Outcomes. Ele Med. 50(4):235-240.
International Classification of Diseases, Code ICD-9-CM Description Shortened Description Table Number 11.07: Conditions Possibly Justifying Elective Delivery Prior to 39 Weeks Gestation (Ver. 2011A)