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Dr Sarah Buckley

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Blog

Labour Induction: Making Choices

June 17, 2023 by Sarah Buckley

So many are being offered induction of labour, often without a good medical reason. This blog article will help you to make sense- and make informed choices- in this complex and controversial area.

So many inductions

In  Australia (2020) labour was induced in more than  1 in 3 pregnancies (35.5%), including almost half (45.8%) of first-time pregnancies. The US Vital Statistics (2021) reports 32.1% induction (2021), although women themselves report higher induction rates- as reported in the Listening to Mothers surveys. Rates are high in many other countries, suggesting that maternity-care interventions are being applied ‘too much, too soon’.

Why am I being offered an induction?

 If you have been offered an induction of labour without  a medical reason, especially in your first pregnancy, it is likely because of the 2019 ARRIVE trial.

This study found that routinely inducing labour at 39 weeks in a healthy, low-risk first-time pregnancy reduced the caesarean rate from 22.2% to 18.6% (16% reduction) with no other signficant benefits. (See my blog critique here and note the even greater reduction in caesareans- 25%-  from doula care.)

The ARRIVE trial has influenced practice world-wide because it provides supposedly the best evidence- a randomised controlled trial (RCT)- in this controversial area. However, RCTs have strict criteria for inclusion and treatment, and results may be different in real-life situations, outside experimental conditions. This problem is called ‘external validity.’ (See this discussion of the external validity of the ARRIVE trial.)

In fact, many studies have found that, in everyday practice settings, induction has minimal or even negative effects on caesarean rates, and may increase other risks. See this large study,  this study  and this high-quality review.  This is a controversial  area and results depend on the groups compared,  the timing of induction and the rates of induction in the group who were not initially induced  (‘expectantly managed.’) 

Has this improved outcomes?

Have the increasing numbers of inductions improved outcomes, as the ARRIVE trial suggested?

This study used US data to compare the outcomes for healthy, low-risk, first-time pregnancies before (2015-7) and after (2019) publication of the ARRIVE trial. Induction rates increased from 30% to 36% in this population, but their CS rate decreased only 0.6%. In addition, there were higher risks of some concerning outcomes in the induced groups, including more serious postpartum haemorrhage, lower newborn APGAR scores and more newborn breathing difficulties.

Could induction disrupt hormonal processes?

There are very complex and precise processes that lead to the physiological (spontaneous) onset of labour. These processes ensure that mother and baby are both perfectly prepared for an effective labour, birth and postpartum/newborn transitions, including breastfeeding and bonding. By definition, this readiness is not complete when birth is scheduled by induction or prelabour CS.

For a detailed review of the processes involved with the physiological onset of labour, see Chapter 2 , ‘Physiologic Onset of Labor and Scheduled Birth’ in my 2015 Hormonal Physiology report, linked from my website here and a more recent article here.

In addition, the method of induction may disrupt the natural hormonal flow of labour. As part of my PhD, I’ve been publishing studies with EU colleagues looking at oxytocin levels in women and babies in labour and the effects of interventions. Our upcoming reviews include studies of prostaglandins and rupture of membranes.

(To keep updated with my research, make sure to  sign up to my newsletter)

Oxytocin and Induction: My PhD research

In our most recent publication we summarised all the studies that measured plasma (blood) oxytocin levels in women receiving synthetic oxytocin (Pitocin, Syntocinon).

We found that, even with the highest doses in labour, maternal oxytocin levels were maximum 3-4 times higher than levels in physiological labour. This is not high enough to cross the placenta or into the maternal brain and cause direct harm. (However, indirect effects are possible, including effects from the additional stress and pain of induction- see our discussion here)

We also found that newborn babies have naturally high oxytocin levels in labour, likely due to the stress and massage-like effects of uterine contractions. These high oxytocin levels help the baby cope with labour and adapt to life outside the womb. Being exposed to synthetic oxytocin did not further increase newborn oxytocin levels, indicating that synthetic oxytocin does not cross to the baby in labour.

My next blog will discuss these findings further- stay tuned! We are also researching the effects of epidural, opioids and prostaglandins in upcoming publications.

Another important question is: could labour induction-whether with synthetic oxytocin or other methods- affect longer-term outcomes such as breastfeeding, bonding and postpartum depression?  These outcomes have not been well studied in the highest-quality randomised trials and are part of my PhD studies.

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Brain development in the womb

There are also a growing number of studies suggesting worse development and educational outcomes in children born at shorter gestation, even at 39 vs 40 or 41 weeks. This is not surprising when we consider that the unborn baby’s brain is growing at a very fast rate at the end of pregnancy, making those last weeks of brain development very precious. (See Every Week Counts) Shortening gestation with induction could limit full brain development.  See also my discussion here.

However, some studies looking at induction and longer-term offspring outcomes have not found negative effects. Induction rates in the expectant groups are an important consideration in these studies. It is also important to note that these population-wide studies do not mean that being induced will have effects on individual children.

Are there benefits from labour induction?

There is no doubt that induction of labour reduces the chances of stillbirth. Babies that have been induced and born are obviously not at risk of stillbirth. This has been a major motivation for induction past 40-41 weeks, although the actual risks (and therefore benefits of induction) are small.

Some babies that are overdue do not cope as well with labour. This has been used to disallow access to midwifery care in birth centres or homebirth past 41 or 42 weeks. However, again the risks are small. If you are labouring after 41-42 weeks, your care provider or midwife may want to monitor you more closely.

Based on these considerations, induction at 41-42 weeks may prevent 2 perinatal deaths (around the time of birth) per 1000 babies. Looked at another way, 544 inductions would be needed to prevent the death of one baby.  This information may be helpful if you are overdue and offered an induction of labour.

The best decision 

Ultimately the best decision is one you make with your heart and womb, connected to your baby, as well as with the information from here and the resources below.  

(To keep updated with my research, make sure to  sign up to my newsletter)

More induction resources:

Postdates induction of labour- balancing risks Rachel Reed- Midwife thinking

Ten things I wish women knew about induction- Sarah Wickham  and her books 

Induction of labour (Podcast)- Melanie the Midwife with Hannah Dahlen in The Great Birth Rebellion 

Inducing for due dates Evidence based birth   

Induction of labour articles Henci Goer  

Myth of the aging placenta –Sophie Messager 

Preventative induction of labor- does Mother Nature know best? (ARRIVE trial)  Lamaze international

Your body, your baby, your choice: Chapter 4 in  Gentle Birth, Gentle Mothering by Dr Sarah Buckley 

Acknowledgements:

Some of this information comes from a new publication as part of my PhD research: Maternal and newborn plasma oxytocin levels in response to maternal synthetic oxytocin administration during labour, birth and postpartum – a systematic review with implications for the function of the oxytocinergic system This was written with the good work and dedication of my colleagues Kerstin Uvnäs-Moberg, Zada Pajalic, Karolina Luegmair, Anette Ekström-Bergström, Anna Dencker, Claudia Massarotti, Alicja Kotlowska, Leonie Callaway, Sandra Morano, Ibone Olza & Claudia Meier Magistretti. This work was initiated within  EU COST IS1405 BIRTH: Building intrapartum research through health. 

Filed Under: Blog Tagged With: Pitocin myths and side-effects

Hormonal Physiology, Oxytocin and More

February 11, 2022 by Sarah Buckley

When we interact with our babiesSince the publication of her 2015 report Hormonal Physiology of Childbearing (more info and links here) Dr Buckley has continued to research and write about the hormones of physiological labour and the impacts of interventions.

She is currently a PhD candidate at the University of Queensland (Brisbane, Australia) studying oxytocin in childbearing.

This page lists the publications Sarah has co-authored, with links and descriptions. You can receive information about new publications by signing up to Sarah’s newsletters. 

Maternal and newborn plasma oxytocin levels in response to maternal synthetic oxytocin administration during labour, birth and postpartum – a systematic review with implications for the function of the oxytocinergic system. Buckley S, Uvnäs-Moberg K, Pajalic Z, Luegmair K, Ekström-Bergström A, Dencker A,Massarotti, C. Kotlovska, A Callaway, L Morano S, Olza Fernandez I, Meier-Magistretti C. BMC Pregnancy Childbirth. 2023;23(1):137. Full text here 

Maternal plasma levels of oxytocin during physiological childbirth – a systematic review with implications for uterine contractions and central actions of oxytocin. Uvnas-Moberg, K., A. Ekstrom-Bergstrom, M. Berg, S. Buckley, Z. Pajalic, E. Hadjigeorgiou, A. Kotlowska, L. Lengler, B. Kielbratowska, F. Leon-Larios, C. M. Magistretti, S. Downe, B. Lindstrom and A. Dencker (2019).  BMC Pregnancy Childbirth 19(1): 285  Full text here

Maternal plasma levels of oxytocin during breastfeeding-A systematic review. Uvnäs Moberg, K., A. Ekström-Bergström, S. Buckley, C. Massarotti, Z. Pajalic, K. Luegmair, A. Kotlowska, L. Lengler, I. Olza, S. Grylka-Baeschlin, P. Leahy-Warren, E. Hadjigeorgiu, S. Villarmea and A. Dencker (2020). PLoS One 15(8): e0235806. More info and full text links here

Birth as a neuro-psycho-social event: An integrative model of maternal experiences and their relation to neurohormonal events during childbirth. Olza, I., K. Uvnas-Moberg, A. Ekström-Bergström, P. Leahy-Warren, S. I. Karlsdottir, M. Nieuwenhuijze, S. Villarmea, E. Hadjigeorgiou, M. Kazmierczak, A. Spyridou and S. Buckley (2020) PLoS One 15(7): e0230992. More info and full text links here  

Nature and consequences of oxytocin and other neurohormones during the perinatal period.Buckley S, Uvnäs Moberg K Chapter in: Downe S, Byron S, editors. Squaring the Circle: Normal birth research, theory and practice in a technological age. London: Pinter and Martin; 2019. p. 19-31 More info and links to purchase this book here 

The initiation of labour at term gestation: Physiology and Practice implications. Hundley, V., S. Downe and S. J. Buckley (2020). Best Pract Res Clin Obstet Gynaecol Aug; 67:4-18  More info (This article is only available via subscription or payment

Physiologic Basis of Pain in Labour and Delivery: An Evidence-Based Approach to its Management. Practice Guideline No. 355 Bonapace, J., G. P. Gagne, N. Chaillet, R. Gagnon, E. Hebert and S. Buckley (2018). J Obstet Gynaecol Can 40(2): 2 DOI: 10.1016/j.jogc.2017.08.003  More info (This article is only available via subscription or payment

You can find more of Sarah’s science and wisdom in her  blogs  podcast interviews and books and DVDs

Filed Under: Blog, Childbirth, HPOC, Parenting, Pregnancy, Professional Development

Synthetic Oxytocin (Pitocin, Syntocinon): Unpacking the myths and side-effects

September 23, 2019 by Sarah Buckley


Synthetic oxytocin (Pitocin, Syntocinon) is widely used in maternity care around the world. It is commonly administered to induce or to speed up (augment) labour, and to prevent or treat bleeding after birth (postpartum haemorrhage).

Like all maternity-care interventions, synthetic oxytocin may be beneficial, even life-saving, for mothers and babies in some situations. However, because of its widespread use, including in many healthy mothers and babies, it is important to understand the possible risks and side-effects.

This blog explores some important questions, including:

  • Is synthetic oxytocin harmless because it mimics the natural oxytocin that women release during labour?
  • Do high doses of synthetic oxytocin impact the mother’s own natural oxytocin release in labour?

In upcoming blog posts: (make sure to sign up to my newsletter) 

  • Does synthetic oxytocin cross to the baby?
  • Could synthetic oxytocin impact the baby’s developing oxytocin system, as found in animal studies?
  • Could synthetic oxytocin even cause autism? (Also see this blog)

This information in this blog comes from a recent publication on Maternal oxytocin levels during physiological childbirth, which Dr Buckley is a co-author (more details below) and a new review from Dr Buckley and colleagues of oxytocin levels in women and newborns following maternal  synthetic oxytocin administration.

Is synthetic oxytocin harmless, because it mimics the natural oxytocin that women release during labour?

It is true that the chemical structure of synthetic oxytocin is identical to the chemical structure of the natural (endogenous) oxytocin that our bodies produce during labour, as shown in this picture.

However, our own natural (endogenous) oxytocin is made in the brain and is released during labour into both the body, where pulses of oxytocin reach the uterus and promote the rhythmic contractions of labour, and also locally into the brain, where it has calming and pain-relieving effects.

As labour progresses, high oxytocin levels released within the brain help to counter the stress and pain of the strengthening contractions, which are caused by oxytocin stimulating the labouring female’s uterus. At the same time, oxytocin is activating her brain’s pleasure and reward centres in preparation for bonding with her newborn baby. (These processes assist all mammals during labour, birth and postpartum.)

In contrast, synthetic oxytocin is administered by intravenous (IV) infusion and given in constant, high doses rather than in lower levels and pulses. This can lead to maternal plasma oxytocin levels that are more than double those in a natural (physiological) labour, as measured in the blood. (See Oxytocin levels during physiological childbirth)

For these reasons, IV synthetic oxytocin causes contractions that are stronger and closer together than natural contractions, especially in early labour. This makes the uterus work harder than normal and, like any muscle, it can get depleted of oxygen and lactic acid can accumulate. This tissue stress can activate the stress system, even if pain is relieved eg by an epidural. (See Figure 1 in this paper)

In addition, because synthetic oxytocin is administered into the body and not into the brain, it does not have the brain-based benefits of countering the extra labour stress and pain, as natural oxytocin does. (See Oxytocin levels during physiological childbirth.) Therefore, the maternal stress system may be more activated with high doses of synthetic oxytocin in labour, compared to physiological labour.

Those who are administered synthetic oxytocin also commonly receive epidurals to counter the increased pain, and epidurals reduce the natural release of oxytocin, as explained below and in this blog, which increases the need for synthetic oxytocin to fill the ‘hormonal gap.’

With this combination of epidural with synthetic oxytocin in labour, the natural stress-reducing benefits of endogenous oxytocin can be reduced or absent. (More about this below.) This combination might also explain some of the longer-term effects that have been reported for synthetic oxytocin such as mental health consequences, although these studies are not high quality.Image used with permission

For the baby, the stronger and more frequent contractions will inevitably reduce blood and oxygen supply more than during physiological labour, increasing the risks of hypoxia (low oxygen), which is especially risky for the baby’s brain at this time. For this reason, administration of synthetic oxytocin in labour always requires monitoring of the baby’s heart rate to check for indications of hypoxia.

Some studies suggest increased risks of hypoxia and possible long-term consequences for babies exposed to synthetic oxytocin in labour, compared to physiological labour, although this area is not well studied. (See studies below.)

Prolonged, high doses of synthetic oxytocin may also reduce activity in the uterine oxytocin receptors, although the mechanisms is not certain. This can decrease the effectiveness of oxytocin (natural or synthetic) to cause strong contractions, including after the birth. This explains why receiving synthetic oxytocin in labour increases the chance of postpartum haemorrhage and requires extra medications (including more synthetic oxytocin) to counter this risk.

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Do high doses of synthetic oxytocin impact the natural oxytocin release in labour?

It is sometimes presumed that administering high doses of synthetic oxytocin in labour will reduce maternal natural (endogenous) oxytocin production. This is not likely, according to our current understandings, although this is very hard to measure as natural and synthetic oxytocin can’t be differentiated in the blood.

It is important to understand that oxytocin release from the brain in labour is not controlled by the usual ‘negative feedback’ systems, whereby high levels of a hormone or biological marker stimulate feedback systems that eventually bring levels and systems back to normal. For example, our heart rate and blood pressure are controlled such that sudden increases are detected by our body systems and lead to changes that bring them back down to what is normal for each of us. This negative feedback is operative in most biological systems, and contributes to homeostasis- the maintaining of physiological stability in the face of changes.

However, labour is not a homeostatic process! In labour, contractions need to strengthen rather than remain stable, and eventually be strong enough to push the baby from the mother’s uterus. This strengthening requires positive, rather than negative, feedback systems, also called ‘feed-forward cycles.’

This diagram shows one positive-feedback cycle in labour, where strong uterine contractions cause pressure on the cervix area  and generate sensory feedback to the brain that increases brain  oxytocin release, including release to the uterus. This causes even stronger contractions and sensations, more sensory feedback and more oxytocin release.

This positive-feedback cycle, also known as the Ferguson reflex, provides the high levels of oxytocin (average 3-4-fold increased at birth) that are needed for the birthing mother to have an effective pushing stage.(See Oxytocin levels during physiological childbirth)

The administration of synthetic oxytocin (without epidurals) will not reduce this cycle, or directly reduce natural oxytocin release. In fact, in some circumstances, synthetic oxytocin may even accelerate this positive-feedback cycle (and increase brain oxytocin) by causing stronger contractions with greater sensations.

However, when epidurals are co-administered, the sensations from contractions, which fuel this feed-forward cycle, are abolished. This slows or even stops the cycle, and consequently slows or stops oxytocin release, as described in this blog.

The combination of epidurals with high doses of synthetic oxytocin can therefore increase physiological stress in labour,  even if there is no pain, but reduce oxytocin release, including within the brain, which would usually counteract this stress in labour.

In summary

Synthetic oxytocin is chemically identical to the natural oxytocin released in labour and birth. However it has different effects because it is administered IV rather than into the brain.

In contrast, natural oxytocin  is released from and into the brain in labour, and gives calming, pain relieving effects that counteract labour stress and pain. Within the brain, natural oxytocin released in labour also activates reward and pleasure centres in preparation for bonding with the newborn baby.

While synthetic oxytocin may not directly reduce the natural release of oxytocin, the common co-intervention of epidural analgesia does significantly reduce oxytocin release. Epidurals can slow labour and reduce oxytocin’s anti-stress, anti-inflammatory and anti-oxidant benefits. This combination might explain some of the longer-term effects that have been found for synthetic oxytocin.

In addition,  prolonged, high doses of synthetic oxytocin increase the risk of bleeding after birth (postpartum haemorrhage). This likely reflects disruption to uterine oxytocin receptors, making the uterus less responsive to oxytocin and increasing the risk of bleeding, although the mechanism is debated.

(For more great articles like this, make sure to  sign up to my newsletter)

References and resources

Much of this information comes from a new publication on Maternal oxytocin levels during physiological childbirth: A systematic review with implications for uterine contractions and central actions of oxytocin  This was written with the good work and dedication of colleagues Kerstin Uvnas Moberg, Anette Ekstrom-Bergstrom  and other European co-authors. This work was partly funded by  EU COST IS1405 BIRTH: Building intrapartum research through health. 

Ecstatic Birth ebook

Hormonal Physiology of Childbearing report Sarah’s 2015 report with lots of information about oxytocin (Free download)

Sarah’s 2-part blog on epidural effects, including oxytocin

Impacts of synthetic oxytocin in labour:

  • Oscarsson 06: Higher newborn risks in a population study
  • Clark 2008: Preventable adverse newborn outcomes 
  • Buchanan 12:  Worse outcomes for mothers and babies
  • Drummond 18: Legal views on synthetic oxytocin in labour

Note that these studies are observational and do not imply causation. However, there is very little high-quality research available in this area, despite the widespread use of synthetic oxytocin. 

Bugg 13 : Augmentation with synthetic oxytocin has minimal benefits (Cochrane review)

Rahm 2012 : Epidurals reduce oxytocin 

Filed Under: Blog Tagged With: Pitocin myths and side-effects

How to Have the Best Cesarean

March 24, 2019 by Sarah Buckley


It’s true that our female bodies are superbly designed, and that gentle, natural birth is the best possible start. But birth is ultimately mysterious and unpredictable, and can sometimes take its own unexpected direction.

For example, the peaceful natural birth that you planned with a midwife, in a birth centre, or at home, may become less safe because of extra risks for you or your baby, or a situation can arise that sends you clearly towards a surgical birth. Or maybe you have known from the start that a cesarean is your best or only safe option.

What can you do to make the best of these circumstances? How can you compensate for the labour and birth that you and your baby will miss, to a greater or lesser extent, when a cesarean is needed? And how can you address the inevitable ‘hormonal gaps’ for you and your baby?

The answers can be surprisingly simple, from a hormonal perspective, and are important considerations, however you plan to give birth. (Personally I had a cesarean birth plan with each of my home births!)

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Hormonal gaps

Cesareans and other maternity-care interventions can be necessary, and even life-saving, for mother and/or baby in some situations. However, in these situations, there will inevitably be a gap between what our bodies and babies naturally expect in this major biological transition, and what actually happens.

Hormonal gaps occur because mother and baby miss significant and even vital processes. For example, if the cesarean occurs before labour onset (sometimes called a pre-labour, scheduled, or elective cesarean), mother and baby will not be fully ready for labour and the transitions of birth.

The baby can miss important preparations for the enormous transition to breathing, including hormonally-driven clearing of the lung fluid, which all babies have in the womb. This significantly contributes to newborn breathing difficulties, which are 2x more likely following a prelabour cesarean, even at 39 weeks, compared to vaginal birth (see study below). Breathing difficulties can necessitate separation and admission to special care facilities, and mother and baby will miss being together during the sensitive hours after birth.

Another hormonal gap for the caesarean newborn is lack of the ‘catecholamine surge.’ This huge in-labour increase in adrenaline and noradrenaline, the fight or flight or catecholamine hormones, activates the baby on every level as labour advances. The catecholamine surge also protects from low oxygen, further clears lung fluid, and ensures that the baby is wide-eyed and alert at birth, and ready to initiate breastfeeding. Babies born by cesarean and especially pre-labour cesarean, miss this activation and tend to be drowsy and not ready for interactions or feeding.

For the mother, the processes of labour activate her oxytocin system, in both body and brain. Her uterus will be sensitive and responsive to oxytocin, and capable of the strong postpartum contractions that prevent haemorrhage.  Oxytocin released in her brain also ensures that she will be calm and connected as she meets her baby for the first time.

Pleasure and reward

Oxytocin also acts on the mother’s brain reward centres, which are maximally sensitive at this time because of prelabour preparations. Her pre-labour preparations plus in-labour processes ensure full reward centre activation as she meets her baby for the first time. This produces the brain-based pleasure that is a critical part of bonding for all mammals, establishing irresistible brain pathways that will reward and motivate new mothers to give the dedicated care that all newborn mammals require for survival.

This process can be seen in mammalian mothers who adopt the babies of another species, if introduced during this biologically sensitive period. While human mothers can obviously bond with and love a baby that they have not birthed (or been with in this sensitive period) there can still be a hormonal gap in this ‘biological bonding,’ and  the pleasure (’reward salience’) that the mother receives from her baby can be reduced, even into the future.

Closing the gaps: in hospital

How can we close these hormonal gaps for mother and baby? An ideal solution is to allow labour to begin naturally, then perform an in-labour non-emergency cesarean. This ensures that the baby has maximum readiness, and may reduce the risk of newborn breathing difficulties (see study below). An in-labour, non-emergency cesarean is also ideal for maternal readiness, including maximising sensitivity to oxytocin in her uterus and brain.

If this is not possible, the major hormonal gaps involved in prelabour cesarean can be significantly addressed in the operating theatre. For the baby, the stress (and stress hormones) that accompany the sudden loss of the womb environment can be soothed by early–ideally immediate–skin-to-skin contact with the mother. This can occur even as the surgeon is finishing the operation. (Some surgeons have shown that the baby can even push itself out, with a little time and patience, and delayed clamping of the cord gives additional benefits- see Natural Caesarean study and video below.)

Ongoing, uninterrupted contact with the mother will help to switch on the baby’s ‘rest and digest’ system  and ability to initiate breastfeeding. Because of the hormonal gaps, it is necessary to be patient and allow the baby to come to the breast in their own time. The new mother’s breastfeeding and attachment hormones can also be affected by a cesarean, and liberal skin-to-skin and breastfeeding will help this as well.

If the baby cannot be placed on the mother’s chest, the ‘cheek-to-cheek’ position is recommended (see below). Any of these positions will begin to establish the biological bond between mother and baby. If this is not possible, skin-to-skin with father or partner is also valuable.

If mother and baby are separated, whether routinely or because of illness, skin-to-skin contact and breastfeeding as soon as possible, and as much as possible, is still the magic glue!

Closing the gaps: oxytocin and more oxytocin!

Breastfeeding is Mother Nature’s back-up system. Breastfeeding releases oxytocin and other feel-good hormones that reinforce pleasure and reward for both mother and baby. Early and frequent feeding will benefit the new mother, switching on her pleasure centres and reinforcing the bond with her baby with every episode.

Oxytocin released during breastfeeding also promotes wound healing and the immune system, reduces inflammation and has antioxidant properties, which are all beneficial in recovering from surgery. Oxytocin switches off stress and switches on relaxation and growth. Oxytocin will help you to relax and ease into new motherhood.

Liberal skin-to-skin contact also activates the oxytocin system and, according to one study, reduces the chance of postpartum depression in the early months. Soft carriers can be used under clothing so that mother and baby are skin-to-skin most of the time. Skin-to-skin is an ideal way to close hormonal gaps for the weeks and even months after a cesarean, and is particularly important if formula feeding or breast pumping.

Co-sleeping is our evolutionary norm, and maintains the continuum of mother-baby contact and hormonal release, as well as supporting breastfeeding- and gives mothers better sleep too!  (See below for safe co-sleeping guidelines)

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In summary

In summary, a cesarean birth creates significant gaps between the biological expectations for mother and baby and their experiences.

Mother-newborn skin-to-skin contact, beginning as early as possible after cesarean birth, will initiate and build the biological bonding that mother and baby may otherwise miss.  Early and liberal breastfeeding is Mother Nature’s back up system!

More resources

Ecstatic Birth ebook

Hormonal Physiology of Childbearing report Sarah’s 2015 report with lots of information about the hormones and caesareans (Free download)

Belly Belly: Mother-friendly caesarean.  

Belly Belly: Gentle C-sections for mothers and babies

American Pregnancy Positive caesarean

Childbirth connection Excellent information about all aspects of caesarean

Penny Simkin Best cesarean possible handout (under articles and handouts)

UK motherandbaby.co.uk, some good tips

Caesarean recovery https://www.mamanatural.com/c-section-recovery/

Cheek-to-cheek newborn contact post cesarean  (Questions 2.6 and 2.10)

Breastfeeding and cosleeping information

Safe cosleeping guidelines

Study: The natural caesarean: a woman-centred technique: a great article to give to your care provider from a OB team in the UK

Study: In labour caesarean benefits baby’s breathing

Study: Newborn breathing difficulties following cesarean 

Study: Skin-to-skin reduces postpartum depression

Videos

Natural caesarean UK, teaching; Includes good information for care providers: ‘walking the baby out,’ delayed cord clamping, immediate skin to skin contact, keeping the baby warm, and early breastfeeding

Skin to skin after CS (teaching)

One family’s gentle C-section with early skin to skin

 

 

Filed Under: Blog

Does Synthetic Oxytocin (Pitocin) Cause Autism?

December 12, 2018 by Sarah Buckley

Image courtesy of MyDvija https://mydvija.com

Does exposure in labour to synthetic oxytocin (Pitocin, Syntocinon) cause autism? Or could exposure at least increase the risks of an autism spectrum condition, including milder forms of autism, for genetically vulnerable children?

This question has been asked for many years, beginning with natural birth pioneer and surgeon Michel Odent in the 1980s. Dr Odent noted similarities between the social behaviours that autistic individuals tend to have (reduced eye contact and reading of  social cues) and the functions of our brain-based oxytocin system, which helps us with social behaviours, among other effects.

These concerns have been echoed by many researchers, who have wondered: Could exposure to synthetic oxytocin at this vulnerable time impact the baby’s developing oxytocin system? Could it disrupt oxytocin receptors, or mis-set the oxytocin system in other significant ways, with long-term effects? Could this even explain the worldwide increase in autism diagnosis among our children?

A recent study by Gustella and colleagues has addressed this question using a 20-year study that tracked children’s behavioural and emotional development. Researchers analysed this against the amount of synthetic oxytocin administered to their mothers during labour.

The overall finding was that there was no relationship between exposure to synthetic oxytocin in labour and autistic behaviours. This was also supported by the research finding that the dosage of synthetic oxytocin was not related to the presence or degree of autistic behaviours.(If synthetic oxytocin. really did cause autism, we would expect to get a ‘dose-response ‘effect, such that higher dosages would increase the risk and/or severity.)

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Researchers are obviously keen to find biological causes for autism, or at least factors that might increase the risks.  There are several other studies that have looked at exposure to synthetic oxytocin during labour and birth as a possible cause, with mixed results.

This is an important study because it has reliable data for the synthetic oxytocin dosage, which was extracted from hospital records, and  and for autism diagnosis, which is based on behavioural assessments at two or more times up to age 17.

Some of these concern about long-term effects of synthetic oxytocin comes from animal studies, particularly studies in prairie voles, which are small North American rodents with a complex oxytocin system not unlike ours. Researchers  have found effects on adult social and sexual behaviours, when newborn prairie voles are injected with synthetic oxytocin. However, it is important to consider that the dosage used in these newborn animals is 100 times or more higher than would be safe to give to a labouring woman. (In labour, a woman’s uterus is very sensitive to oxytocin. An excessive dose will cause overly strong contractions that will endanger her baby.)

In addition, there has been a debate about whether synthetic oxytocin- or the natural oxytocin that the mother releases in labour- can cross the placenta to the baby. Animal studies have found that maternal oxytocin does cross to the baby in labour and even reaches the baby’s brain, where it switches on factors that protect the brain from low oxygen.

However, human babies have a more mature brain at birth, and  actually produce their own oxytocin, so this mechanism is unlikely to affect human babies, (However there are many other factors that help to protect our baby’s brains- see my report below for more).

In addition, even if synthetic oxytocin administered in labour did reach the baby’s brain, levels would be very low– around 1/1000 of effective levels in the blood. Such low levels may be more beneficial than harmful. For example, low doses of synthetic oxytocin administered daily to newborn rats reduces their blood pressure and stress responses in adulthood.

However, its is also true that synthetic oxytocin could have detrimental effects for mothers and/or babies by other mechanisms.

If doses are too high and cause excessive contractions, there could be risks of too-low oxygen for the baby (hypoxia). This can cause long-term harms, including brain damage. However, this should  be detected by routine monitoring of the baby’s heart rate when synthetic oxytocin is given, and action quickly taken if needed.

Harms usually relate to poor monitoring and/or inadequate actions taken.Some hospitals and care provides have recognised these risks and have protocols for the safe administration of synthetic oxytocin, with dosages kept as low as possible to avoid such risks.

Synthetic oxytocin could also affect the baby indirectly, including via the mother. Stronger contractions cause more stress and pain, leading to more interventions for pain relief, including epidurals. which significantly affect the mother’s oxytocin system- see my blog here.

And because epidurals reduce the mothers own oxytocin production, labour tends to slow and women are often administered  synthetic oxytocin to speed labour. For these reasons,  it can be hard to separate the effects of epidurals and synthetic oxytocin for mothers and babies.

Synthetic oxytocin (and /or epidurals) could also impact breastfeeding success, which would impact the long-term health and wellbeing of the baby. (See review articles below) These have not been well studied, despite synthetic oxytocin being very widely used in labour, and also after birth.

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To conclude: the best evidence that we have does not show a connection between synthetic oxytocin in labour and autism. Synthetic oxytocin may have other negative impacts for mothers and/or babies that have not been well studied.

Supporting gentle, natural  birth is likely to be the safest long-term strategy to promote health and wellbeing for mothers, babies, fathers and families, with  extra support for those who require interventions.

More information and references

Gustella et al 2015 Does perinatal exposure to exogenous oxytocin influence child behavioural problems and autistic-like behaviours to 20 years of age?

Clark 2009 Oxytocin: New perspectives on an old drug. (Risks of synthetic oxytocin)

Erickson 2017 Breastfeeding Outcomes After Oxytocin Use During Childbirth: An Integrative Review

French 2016 Labor Epidural Analgesia and Breastfeeding: A Systematic Review

Petersson 2008 Postnatal oxytocin treatment of spontaneously hypertensive male rats decreases blood pressure and body weight in adulthood

Note for those who have read my 2015 Hormonal Physiology of Childbearing report. Some of this information, and my opinions, are different to my report, where I discuss possible mechanisms by which synthetic oxytocin might contribute to autism. This study was not published at that time, and I have also has the opportunity to read more about oxytocin for my my PhD studies, including discussion with my PhD advisor Professor Kerstin Uvnas Moberg.  

Filed Under: Blog

Should Every Mother be Induced at 39 Weeks? The ARRIVE Trial

October 4, 2018 by Sarah Buckley

If you are pregnant right now, you can’t have missed it. For maternity care providers, it’s been the topic of the year.  Should healthy, low-risk women should be routinely induced at 39 weeks?

On August 9, the ARRIVE study (A Randomized Trial of Induction Versus Expectant Management) was finally published in full, reigniting a media storm on this topic.

But what is this based on? What are the benefits? And, most importantly, should we all be getting on the ‘induction express’?

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The ARRIVE study was designed to test whether inducing healthy mothers in their first pregnancy was a benefit (or not) for themselves and their babies. Women were randomised to routine induction at 39 weeks or ‘expectant management’ (more about this below) and outcomes for women and babies were recorded and analysed.

Researchers found similar outcomes for both groups of mothers and babies, with somewhat lower caesarean rates in the induced women (18.6 vs 22.2%) as well as a slight reduction in late pregnancy complications such as high blood pressure. (This makes sense, as the induced women had a shorter time in late pregnancy to develop these complications.)

While overall this study was well funded and conducted, it raises many more questions than we currently have answers, and is certainly not a reason to start inducing every mother and baby.

Firstly, over 50 000 women were considered for this study but less than half were eligible because the definition of ‘low risk’ was very tight. Of these women, only 6 000 agreed to participate, suggesting that being randomly assigned to induction was not popular. Are these 6000 women representative enough of the general population that we can apply the findings to other low-risk, first-time mothers?

In addition, these 6000 women gave birth in well-resourced, high-level hospitals, where everyone was keen to apply the criteria and especially the strict protocols for induction. Would this apply to other maternity hospitals, with different protocols and less motivated staff?

And given that these women were generally low-risk enough to birth outside the hospital, there were some surprisingly poor outcomes. In both groups, around 1 in 9 babies were admitted to NICU and only 1 in 3 women were exclusively breastfeeding at 4-8 weeks. While the caesarean rate was lower for induced women, 18% is still quite high for such a low-risk group. If these women had planned to give birth at home, for example, the chance of caesarean would have been less than 10%.

It is possible that some of these poorer outcomes happened in both groups relatively equally because the groups were actually not so different. In this study, ‘expectant management’ included possible induction after 40 weeks and 5 days, which is actually shorter than the average gestation for first-time mothers – 41 weeks and 1 day, and all women in this expectant management group were required to be induced no later than 42 weeks and 2 days. Consequently, many women who were assigned to ’expectant management’ may later have been induced, although this number has not yet been revealed.

Women who were in the induced group spent many more hours in the labour and delivery unit (20 hours vs 14). This may reflect that women who were induced at 39 weeks were not as ready for labour, compared to the expectant group who would have given birth at a later gestation, even if induced. This means that their bodies (and babies) had greater readiness for labour.

It is likely that many care providers will now start to recommend routine induction at 39 weeks. You may have even been encouraged to accept induction, which is certainly more convenient for hospitals and care providers than waiting for labour to begin. However, this would put huge pressures on maternity care resources, and with the main benefit being possibly 4 fewer women per 100 having a caesarean.

In contrast, the best scientific studies that we have suggest that having your own supportive birth companion (doula) will reduce your need for a caesarean, while supporting, rather than disrupting, the natural processes for you and your baby. For example, the Cochrane systematic review for supportive birth companion (see links below) shows a 25% reduction in caesarean risk in women with continuous labour support vs a 16% reduction in this study.

In addition, choosing care with your own midwife, from pregnancy through labour and birth, lessens your need for analgesia, while also reducing risks of preterm birth and increasing satisfaction. (Midwifery care also decreased caesarean rates in most studies included in the Cochrane systematic review- see link below-but this was not statistically significant in the overall review- see below)

As I describe in my report, Hormonal Physiology of Childbearing, the natural (physiological) onset of labour is a pivotal time. While we don’t fully understand the processes that initiate human labour, we believe that the baby signals readiness for labour, birth and life outside the womb to the mother through placental hormones. These signals promote ‘prelabour physiologic preparations’ for mother and baby, which will make labour and birth as efficient, pleasurable, and safe as possible, for both.

Physiologic labour onset, by definition, allows the full maturity of the baby’s body and brain, which is also growing rapidly in the final weeks in the womb. Could disrupting these final weeks of brain development have longer-term effects? Several studies have found better developmental and academic outcomes for every extra week of pregnancy, even up to 41 weeks (see studies below).

You can read a lot more about this controversial study in the links below.

In the meantime, please don’t be swayed or scared into an unnecessary induction because of this study.

More Information and Resources

The ARRIVE Study: free abstract and accompanying editorial

Responses from maternity care providers and consumer groups

  • “That’s a feminist issue!” from Milli Hill and Positive Birth (UK)
  •  What women need to know from BellyBelly
  • Great infographic from Mindful Childbirth Santa Cruz
  • In-depth critique from Henci Goer in Science and Sensibility
  • “Why Induction Matters” book and Midwife Thinking blog from Rachel Reed

Professional group responses:

  • Response from Australian professionals in Women and Birth journal
  • Response from the Society for Maternal-Fetal Medicine (US)
  • Response from American College of Obstetricians and and Gynecologists (ACOG)
  • Response from American College of Nurse-Midwives (ACNM)

Other research

  • Hormonal Physiology of Childbearing
  • Benefits of midwifery care
  • Benefits of supportive birth companion (doula)
  • benefits of home birth
  • Benefits of longer gestation for academic achievement
    • Academic achievement varies with gestational age among children born at term
    • Gestational age and school achievement: a population study
    • A whole-of-population study of term and post-term gestational age at birth and children’s development

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Filed Under: Blog

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Sarah is a Medical Doctor, with an M.B Ch.B from University of Otago, New Zealand, equivalent to MB BS (Australia) and MD(US). She also holds a Diploma of Obstetrics (University of Auckland) and a Diploma of Family Planning (Family Planning Victoria).

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