Office-based ambulatory cervical ripening prior to inpatient induction of labor - MDedge
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EDITORIAL Office-based ambulatory cervical ripening prior to inpatient induction of labor There is growing literature to support the use of ambulatory cervical ripening (CR) for low-risk women—initiating CR in the office, sending the patient home to complete the first phase of the CR process, and then admitting her to the labor unit for additional CR or induction of labor Robert L. Barbieri, MD Chair Emeritus, Department of Obstetrics and Gynecology Interim Chief, Obstetrics Brigham and Women’s Hospital Kate Macy Ladd Distinguished Professor of Obstetrics, Gynecology and Reproductive Biology Harvard Medical School Boston, Massachusetts F or women with a Bishop morning or is sent home in the effectiveness of ambulatory versus score ≤6, CR is an important morning to return for IOL in the eve- inpatient Foley catheter CR.1 A total of first step in planned induc- ning or at night. A secondary benefit 130 women with a Bishop score
EDITORIAL Streptococcus group B infection, and Ausbeck and colleagues ran- by direct visualization using a vagi- HIV infection. Prostaglandin CR was domly assigned 126 nulliparous nal speculum. After placement of not used if the woman had a previous women with a Bishop score
In another study of outpatient CR Two systematic reviews and baseline Bishop score of 2.9, had with the Cook double-balloon cath- meta-analyses reported that out- Dilapan-S placed for approximately eter, 695 women with a Bishop score comes were similar when using the 15 hours prior to oxytocin IOL. The
EDITORIAL 425 women at 37 to 42 weeks’ gesta- outpatient CR with oral misopro- birthing unit. If they had no regular tion were assigned randomly to out- stol (100 µg) or placebo.23 Fol- contractions they were discharged patient or inpatient CR.18 All women lowing administration of the oral home. For nulliparous women, the had CTG monitoring for 20 minutes misoprostol, the women had 2 hours time from intervention to delivery in before and after vaginal placement of CTG monitoring. The treatment the misoprostol group was 4.9 days, of the PGE2 gel. The PGE2 dose was was repeated daily for up to 3 days and 8.1 days in the control group. For 2 mg for nulliparous and 1 mg for if there was no change in the cervix. parous women, the times from inter- parous women. The cesarean deliv- If labor occurred, the patient was vention to delivery in the two groups ery rates were similar in the outpa- admitted to the labor unit for oxy- were 3.8 and 6.9 days, respectively. tient and inpatient groups—22.3% tocin IOL. The times from first dose and 22.9%, respectively. Among the of misoprostol or placebo to deliv- women randomized to outpatient ery were 46 and 84 hours (P
Safety of office-based Two systematic reviews have misoprostol, the transcervical bal- ambulatory CR among reported that, compared with bal- loon catheter is associated with a low low-risk women loon CR, misoprostol CR is associ- rate of uterine tachysystole. It may Safety is a complex concept with ated with an increased risk of uterine be a preferred method for outpatient experts often disagreeing on what tachysystole.33-34 In a large retrospec- CR. If placement of a transcervi- level of safety is required to accept a tive study, compared with inpatient cal balloon catheter is challenging, new medical procedure. Establish- CR, outpatient CR with dinoprostone for example when the patient has ing the safety of office-based ambu- vaginal insert was not associated a tightly closed cervix, oral miso- latory CR among low-risk women with an increased risk of newborn prostol ambulatory CR may be an would require a very large cohort or admission to the neonatal intensive option if CTG monitoring is available randomized studies with at least a care unit or a low Apgar score at in the office. thousand participants. Only a few 5 minutes after birth.35 During the COVID pandemic, large studies focused on the safety of many in-person office visits have CR have been reported. Sciscione and transitioned to virtual visits with colleagues reported a large observa- Will you consider the patient in their home. Histori- tional study of inpatient transcervi- office-based CR in your cally, most cases of CR have been cal Foley catheter for CR involving obstetric practice? performed on labor and deliv- 1,905 women.31 They reported no As reviewed in this editorial, evolv- ery units. It may be time for your adverse outcomes among term, sin- ing data suggest that it is feasible to practice to consider office-based gleton, uncomplicated pregnancies. initiate CR in the office ambulatory ambulatory CR for low-risk women They calculated that the 95% con- setting prior to admission to the planning an IOL. Office-based fidence interval (CI) for an adverse labor unit for additional CR or IOL. ambulatory CR is a win for labor event was between 0.0% and 0.2%. In Many women prefer to complete CR nurses who generally prefer to man- a meta-analysis of 26 studies includ- at home after initiation in the office, age laboring patients rather than ing 5,563 women, the risk of chorio- rather than have CR in a labor unit or patients undergoing prolonged in- amnionitis during IOL was equivalent hospital setting.36 The transcervical hospital CR. Outpatient CR is also with pre-IOL Foley catheter CR (7.2%) balloon catheter has the most pub- a win for low-risk patients who or prostaglandin CR (7.2%) (relative lished data supporting the feasibility prefer to be at home rather than risk, 0.96; 95% CI, 0.66–1.38).32 of ambulatory CR. Compared with in a labor unit. ● References 1. Policiano C, Pimenta M, Martins D, et al. Outpa- 8. Wilkinson C, Adelson P, Turnbull D. A compari- 14. Blumenthal PD, Rmanauskas R. Randomized trial tient versus inpatient cervix priming with Foley son of inpatient with outpatient balloon catheter of Dilapan and Laminaria as cervical ripening catheter: a randomized trial. Eur J Obstet Gynecol cervical ripening: a pilot randomized controlled agents before induction of labor. Obstet Gynecol. Repro Biol. 2017;210:1-6. trial. BMC Pregnancy Childbirth. 2015;15:126. 1990;75:365-368. 2. Ausbeck EB, Jauk VC, Xue Y, et al. Outpatient 9. Beckmann M, Gibbons K, Flenady V, et al. Induc- 15. Gupta J, Chodankar R, Baev O, et al. Synthetic Foley catheter for induction of labor in nullipa- tion of labor using prostaglandin E2 as an inpa- osmotic dilators in the induction of labour—an rous women. Obstet Gynecol. 2020;136:597-606. tient versus balloon catheter as an outpatient: a international multicenter observational study. 3. Wilkinson C, Adelson P, Turnbull D. A compari- multicenter randomised controlled trial. BJOG. Eur J Obstet Gynecol Repro Biol. 2018;229:70-75. son of inpatient with outpatient balloon catheter 2020;127:571-579. 16. Saad AF, Villarreal J, Eid J, et al. A randomized con- cervical ripening: a pilot randomized controlled 10. Liu X, Wang Y, Zhange F, et al. Double- versus trolled trial of Dilapan-S vs Foley balloon for pre- trial. BMC Pregnancy Childbirth. 2015;15:126. single-balloon catheters for labour induction and induction cervical ripening (DILAFOL trial). Am J 4. Sciscione AC, Muench M, Pollock M, et al. Tran- cervical ripening: a meta-analysis. BMC Preg- Obstet Gynecol. 2019;220:275.e1-e9. scervical Foley catheter for preinduction cervical nancy Childbirth. 2019;19:358. 17. de Vaan MD, Eikleder MLT, Jozwiak M, et al. ripening in an outpatient versus inpatient setting. 11. Yang F, Huan S, Long Y, et al. Double-balloon Mechanical methods for induction of labour. Obstet Gynecol. 2001;98:751-756. versus single-balloon catheter for cervical ripen- Cochrane Database Syst Rev. 2019;CD001233. 5. Henry A, Madan A, Reid R, et al. Outpatient Foley ing and labor induction: a systematic review and 18. Wilkinson C, Bryce R, Adelson P, et al. A random- catheter versus inpatient prostaglandin E2 gel meta-analysis. J Obstet Gynaecol Res. 2018;44: ized controlled trial of outpatient compared with for induction of labour: a randomised trial. BMC 27-34. inpatient cervical ripening with prostaglandin E2 Pregnancy Childbirth. 2013;13:25. 12. Goldberg AB, Fortin JA, Drey EA, et al. Cervi- (OPRA study). BJOG. 2015;122:94-104. 6. Kuhlmann MJ, Spencer N, Garcia-Jasso C, et al. cal preparation before dilation and evacuation 19. Blair R, Harvey MA, Pudwell J, et al. Retrospec- Foley bulb insertion by blind placement com- using adjunctive misoprostol and mifepristone tive comparison of PGE2 vaginal insert and Foley pared with direct visualization. Obstet Gynecol. compared with overnight osmotic dilators alone: catheter for outpatient cervical ripening. J Obstet 2021;137:139-145. a randomized controlled trial. Obstet Gynecol. Gynaecol Can. 2020;42:1103-1110. 7. Delaney S, Shaffer BL, Chen YW, et al. Labor 2015;126:599-609. 20. Thomas J, Fairclough A, Kavanagh J, et al. Vaginal induction with a Foley balloon inflated to 30 13. 1Upadhyaya NB, Childs KD, Neiger R, et al. prostaglandin (PGE2 or PGF2alpha) for induction mL compared with 60 mL. Obstet Gynecol. Ambulatory cervical ripening in term pregnancy. of labour at term. Cochrane Database Syst Rev. 2015;115:1239-1245. J Reprod Med. 1999;44:363-366. 2014;CD003101. CONTINUED ON PAGE 14 mdedge.com/obgyn Vol. 33 No. 3 | March 2021 | OBG Management 13
EDITORIAL CONTINUED FROM PAGE 13 21. O’Brien JM, Mercer BM, Cleary NT, et al. Efficacy 26. Stitely ML, Browning J, Fowler M, et al. Outpatient The timing of adverse events with Foley catheter of outpatient induction with low-dose intra- cervical ripening with intravaginal misoprostol. preinduction cervical ripening; implications for vaginal prostaglandin E2: a randomized, double- Obstet Gynecol. 2000;96:684-688. outpatient use. Am J Perinatol. 2014;31:781-786. blind, placebo controlled trial. Am J Obstet Gyne- 27. McKenna DS, Ester JB, Proffitt M, et al. Misopro- 32. McMaster K, Sanchez-Ramos L, Kaunitz AM. Eval- col. 1995;173:1855-1859. stol outpatient cervical ripening without sub- uation of a transcervical Foley catheter as a source 22. Biem SR, Turnell RW, Olatunbosun O, et al. sequent induction of labor: a randomized trial. of infection. Obstet Gynecol. 2015;126:539-551. A randomized controlled trial of outpatient Obstet Gynecol. 2004;104:579-584. 33. Fox NS, Saltzman DH, Roman AS, et al. Intravagi- versus inpatient labour induction with vaginal 28. PonMalar J, Benjamin SJ, Abraham A, et al. Ran- nal misoprostol versus Foley catheter for labour controlled-release prostaglandin-E2: effective- domized double-blind placebo controlled study induction: a meta-analysis. BJOG. 2011;118: ness and satisfaction. J Obstet Gynaecol Can. of preinduction cervical priming with 25 µg of 647-654. 2003;25:23-31. misoprostol in the outpatient setting to prevent 34. Hofmeyr GJ, Gulmezoglu AM, Pileggi C. Vaginal 23. Gaffaney CA, Saul LL, Rumney PJ, et al. Outpa- formal induction of labor. Arch Gynecol Obstet. misoprostol for cervical ripening and induc- tient oral misoprostol for prolonged pregnan- 2017;295:33-38. tion of labour. Cochrane Database Syst Rev. cies: a pilot investigation. Am J Perinatol. 2009;26: 29. Chang DW, Velazquez MD, Colyer M, et al. Vagi- 2010:CD000941. 673-677. nal misoprostol for cervical ripening at term: 35. Salvador SC, Simpson ML, Cundiff GW. Dino- 24. Kipikasa JH, Adair CD, Williamson J, et al. Use of comparison of outpatient vs inpatient adminis- prostone vaginal insert for labour induction: a misoprostol on an outpatient basis for postdate tration. Obstet Gynecol Surv. 2006;61:167-168. comparison of outpatient and inpatient settings. pregnancy. Int J Gynaecol Obstet. 2005;88:108-111. 30. Meyer M, Pflum J, Howard D. Outpatient miso- J Obstet Gynaecol Can. 2009;31:1028-1034. 25. Oboro VO, Tabowei TO. Outpatient misoprostol prostol compared with dinoprostone gel for pre- 36. Sutton C, Harding J, Griffin C. Patient attitudes cervical ripening without subsequent induction induction cervical ripening: a randomized con- towards outpatient cervical ripening prior to of labor to prevent post-term pregnancy. Acta trolled trial. Obstet Gynecol. 2005;105:466-472. induction of labour at an Australian tertiary hos- Obstet Gynecol Scand. 2005;84:628-631. 31. Sciscione AC, Bedder CL, Hoffman MK, et al. pital. J Obstet Gynaecol. 2016;36:921-928. 14 OBG Management | March 2021 | Vol. 33 No. 3 mdedge.com/obgyn
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