Effects of breast stimulation for spontaneous onset of labor on salivary oxytocin levels in low-risk pregnant women: A feasibility study

Kaori Takahata, Shigeko Horiuchi, Yuriko Tadokoro, Takuya Shuo, Erika Sawano, Kazuyuki Shinohara, Kaori Takahata, Shigeko Horiuchi, Yuriko Tadokoro, Takuya Shuo, Erika Sawano, Kazuyuki Shinohara

Abstract

Objectives: This preliminary study aimed to 1) determine changes in the salivary oxytocin (OT) level during breast stimulation for promoting the spontaneous onset of labor in low-risk term pregnancies, and 2) clarify the feasibility of the breast stimulation intervention protocol in terms of practicality and acceptability.

Methods: We used a single arm trial design. Sixteen low-risk pregnant women between 38 and 40 weeks of gestation with cephalic presentation participated. They performed breast stimulation for 3 days with an attendant midwife in a single maternity hospital. Each breast was stimulated for 15 minutes for a total of 1 hour per day. Saliva was collected 10 minutes before the intervention and 15, 30, 60, 75, and 90 minutes after the intervention, yielding 18 samples per woman.

Results: Among a total of 282 saliva samples from the 16 participants, OT level was measured in 142 samples (missing rate: 49.6%). The median OT level showed the highest values on day 3 of the breast stimulation, with a marked increase 30 min after the intervention. In the mixed models after multiple imputation for missing data, the OT level on the first day of intervention was significantly lower than that on the third day of intervention. Fatigue from breast stimulation decreased on subsequent days, and most of the women (75%) felt no discomfort with the protocol. Uterine hyperstimulation was not observed.

Conclusion: Following a 3-day breast stimulation protocol for spontaneous onset of labor, the mean OT level showed the highest values on day 3. The breast stimulation intervention protocol showed good feasibility in terms of practicality and acceptability among the pregnant women. Additional large-scale studies are warranted to confirm the protocol's effectiveness.

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Fig 1. Participant flow diagram.
Fig 1. Participant flow diagram.
Fig 2. Intervention procedure for days 1–3.
Fig 2. Intervention procedure for days 1–3.
Fig 3. Median levels of salivary oxytocin…
Fig 3. Median levels of salivary oxytocin on days 1–3.
Fig 4. Mean estimate levels of salivary…
Fig 4. Mean estimate levels of salivary oxytocin and 95% confidence intervals for first, second, and third days with linear mixed models after multiple imputation.

References

    1. Gulmezoglu AM, Crowther CA, Middleton P, Heatley E. Induction of labour for improving birth outcomes for women at or beyond term. Cochrane Database Syst Rev. 2012;(6):CD004945 CD004945. doi:
    1. Henderson J, Redshaw M. Women's experience of induction of labor: a mixed methods study. Acta Obstet Gynecol Scand. 2013;92: 1159–1167. doi:
    1. Waldenstrom U, Hildingsson I, Rubertsson C, Radestad I. A negative birth experience: prevalence and risk factors in a national sample. Birth. 2004;31: 17–27.
    1. Gregory SG, Anthopolos R, Osgood CE, Grotegut CA, Miranda ML. 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: 959–966. doi:
    1. Oberg AS, D'Onofrio BM, Rickert ME, Hernandez-Diaz S, Ecker JL, Almqvist C, et al. Association of labor induction with offspring risk of autism spectrum disorders. JAMA Pediatr. 2016;170: e160965 doi:
    1. Takahata K. Pregnant women's efforts to induce labor during the seven days before parturition. Journal of Japan Academy of Midwifery. 2015;29: 251–261 (In Japanese).
    1. Boulvain M, Stan C, Irion O. Membrane sweeping for induction of labour. Cochrane Database Syst Rev. 2005;(1): CD000451 doi:
    1. Kavanagh J, Kelly AJ, Thomas J. Breast stimulation for cervical ripening and induction of labour. Cochrane Database Syst Rev. 2005;(3): CD003392 doi:
    1. Curtis P, Resnick JC, Evens S, Thompson CJ. A comparison of breast stimulation and intravenous oxytocin for the augmentation of labor. Birth. 1999;26: 115–122.
    1. Adewole IF, Franklin O, Matiluko AA. Cervical ripening and induction of labour by breast stimulation. Afr J Med Med Sci. 1993;22: 81–85.
    1. Damania KK, Natu U, Mhatre PN, Mataliya M, Mehta AC, Daftary SN. Evaluation of two methods employed for cervical ripening. J Postgrad Med. 1992;38: 58–59.
    1. Demirel G, Guler H. The effect of uterine and nipple stimulation on induction with oxytocin and the labor process. Worldviews Evid Based Nurs. 2015;12: 273–280. doi:
    1. Elliott JP, Flaherty JF. The use of breast stimulation to prevent postdate pregnancy. Am J Obstet Gynecol. 1984;149: 628–632.
    1. Salmon YM, Kee WH, Tan SL, Jen SW. Cervical ripening by breast stimulation. Obstet Gynecol. 1986;67: 21–24.
    1. Singh N, Tripathi R, Mala YM, Yedla N. Breast stimulation in low-risk primigravidas at term: does it aid in spontaneous onset of labour and vaginal delivery? A pilot study. Biomed Res Int. 2014;2014: 695037 doi:
    1. Chayen B, Tejani N, Verma U. Induction of labor with an electric breast pump. J Reprod Med. 1986;31: 116–118.
    1. Amico JA, Finley BE. Breast stimulation in cycling women, pregnant women and a woman with induced lactation: pattern of release of oxytocin, prolactin and luteinizing hormone. Clin Endocrinol (Oxf). 1986;25: 97–106.
    1. Ross MG, Ervin MG, Leake RD. Breast stimulation contraction stress test: uterine contractions in the absence of oxytocin release. Am J Perinatol. 1986;3: 35–37. doi:
    1. White-Traut R, Watanabe K, Pournajafi-Nazarloo H, Schwertz D, Bell A, Carter CS. Detection of salivary oxytocin levels in lactating women. Dev Psychobiol. 2009;51: 367–373. doi:
    1. Christensson K, Nilsson BA, Stock S, Matthiesen AS, Uvnas-Moberg K. Effect of nipple stimulation on uterine activity and on plasma levels of oxytocin in full term, healthy, pregnant women. Acta Obstet Gynecol Scand. 1989;68: 205–210.
    1. Finley BE, Amico J, Castillo M, Seitchik J. Oxytocin and prolactin responses associated with nipple stimulation contraction stress tests. Obstet Gynecol. 1986;67: 836–839.
    1. Leake RD, Fisher DA, Ross M, Buster JE. Oxytocin secretory response to breast stimulation in pregnant women. Am J Obstet Gynecol. 1984;148: 259–262.
    1. Feldman R, Gordon I, Schneiderman I, Weisman O, Zagoory-Sharon O. Natural variations in maternal and paternal care are associated with systematic changes in oxytocin following parent-infant contact. Psychoneuroendocrinology. 2010;35: 1133–1141. doi:
    1. Feldman R, Gordon I, Zagoory-Sharon O. Maternal and paternal plasma, salivary, and urinary oxytocin and parent-infant synchrony: considering stress and affiliation components of human bonding. Dev Sci. 2011;14: 752–761. doi:
    1. Grewen KM, Davenport RE, Light KC. An investigation of plasma and salivary oxytocin responses in breast- and formula-feeding mothers of infants. Psychophysiology. 2010;47: 625–632. doi:
    1. Hoffman ER, Brownley KA, Hamer RM, Bulik CM. Plasma, salivary, and urinary oxytocin in anorexia nervosa: a pilot study. Eat Behav. 2012;13: 256–259. doi:
    1. Carter CS, Pournajafi-Nazarloo H, Kramer KM, Ziegler TE, White-Traut R, Bello D, et al. Oxytocin: behavioral associations and potential as a salivary biomarker. Ann N Y Acad Sci. 2007;1098: 312–322. doi:
    1. Feldman R, Zagoory-Sharon O, Weisman O, Schneiderman I, Gordon I, Maoz R, et al. Sensitive parenting is associated with plasma oxytocin and polymorphisms in the OXTR and CD38 genes. Biol Psychiatry. 2012;72: 175–181. doi:
    1. Terkawi AS, Jackson WM, Thiet MP, Hansoti S, Tabassum R, Flood P. Oxytocin and catechol-O-methyltransferase receptor genotype predict the length of the first stage of labor. Am J Obstet Gynecol. 2012;207: 184.e1–184.e8.
    1. Bowen DJ, Kreuter M, Spring B, Cofta-Woerpel L, Linnan L, Weiner D, et al. How we design feasibility studies. Am J Prev Med. 2009;36: 452–457. doi:
    1. Hewlett S, Dures E, Almeida C. Measures of fatigue: Bristol Rheumatoid Arthritis Fatigue Multi-Dimensional Questionnaire (BRAF MDQ), Bristol Rheumatoid Arthritis Fatigue Numerical Rating Scales (BRAF NRS) for severity, effect, and coping, Chalder Fatigue Questionnaire (CFQ), Checklist Individual Strength (CIS20R and CIS8R), Fatigue Severity Scale (FSS), Functional Assessment Chronic Illness Therapy (Fatigue) (FACIT-F), Multi-Dimensional Assessment of Fatigue (MAF), Multi-Dimensional Fatigue Inventory (MFI), Pediatric Quality Of Life (PedsQL) Multi-Dimensional Fatigue Scale, Profile of Fatigue (ProF), Short Form 36 Vitality Subscale (SF-36 VT), and Visual Analog Scales (VAS). Arthritis Care Res (Hoboken). 2011;63 Suppl 11: S263–86.
    1. Haefeli M, Elfering A. Pain assessment. Eur Spine J. 2006;15 Suppl 1: S17–24.
    1. Chen C, Lee SY, Stevenson HW. Response style and cross-cultural comparisons of rating scales among east asian and north american students. Psychological Science. 1995;6: 170–175.
    1. Lee JW, Jones PS, Mineyama Y, Zhang XE. Cultural differences in responses to a Likert scale. Res Nurs Health. 2002;25: 295–306. doi:
    1. Prevost M, Zelkowitz P, Tulandi T, Hayton B, Feeley N, Carter CS, et al. Oxytocin in pregnancy and the postpartum: relations to labor and its management. Front Public Health. 2014;2: 1 doi:

Source: PubMed

Подписаться