Office-based ambulatory cervical ripening prior to inpatient induction of labor - MDedge

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Office-based ambulatory cervical ripening prior to inpatient induction of labor - MDedge
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.

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EDITORIAL
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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.

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