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National Collaborating Centre for Women's and Children's Health (UK). Caesarean Section. London: RCOG Press; 2011 Nov. (NICE Clinical Guidelines, No. 132.)

  • August 2012 NICE removed recommendations 40 and 41 from this guideline. The topic 'place of birth' will be addressed by the update of the clinical guideline 'Intrapartum care' which is currently in development. In this PDF document, the change is marked with black strikethrough. October 2012 NICE added a footnote to recommendation 113 to indicate that healthcare professionals should consult the guideline on surgical site infection for more recent recommendations on wound care. June 2018 The advice on which analgesia to use for post-operative pain has been updated. April 2019 Recommendation 1.4.6.17 has been updated by recommendation 1.3.21 in the NICE guideline on surgical site infection. August 2019: Recommendation 1.6.3.2 on patient-controlled analgesia after caesarean section has been withdrawn because of safety concerns and changes in practice in the UK. NICE will be looking at analgesia after caesarean section as part of the planned 2020 update of this guideline. September 2019: Recommendations 1.2.2.1 and 1.2.2.2 on multiple pregnancy have been updated. July 2021: We removed reference to the Joel-Cohen transverse incision in the recommendation on abdominal wall incision to clarify what should be done while the recommendation is being updated. See www.nice.org.uk/guidance/NG192 for more information, including the exceptional surveillance review on surgical opening technique

August 2012 NICE removed recommendations 40 and 41 from this guideline. The topic 'place of birth' will be addressed by the update of the clinical guideline 'Intrapartum care' which is currently in development. In this PDF document, the change is marked with black strikethrough. October 2012 NICE added a footnote to recommendation 113 to indicate that healthcare professionals should consult the guideline on surgical site infection for more recent recommendations on wound care. June 2018 The advice on which analgesia to use for post-operative pain has been updated. April 2019 Recommendation 1.4.6.17 has been updated by recommendation 1.3.21 in the NICE guideline on surgical site infection. August 2019: Recommendation 1.6.3.2 on patient-controlled analgesia after caesarean section has been withdrawn because of safety concerns and changes in practice in the UK. NICE will be looking at analgesia after caesarean section as part of the planned 2020 update of this guideline. September 2019: Recommendations 1.2.2.1 and 1.2.2.2 on multiple pregnancy have been updated. July 2021: We removed reference to the Joel-Cohen transverse incision in the recommendation on abdominal wall incision to clarify what should be done while the recommendation is being updated. See www.nice.org.uk/guidance/NG192 for more information, including the exceptional surveillance review on surgical opening technique

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11Pregnancy and childbirth after caesarean section

11.1. Implications of caesarean section for future pregnancies

Infertility

Infertility is defined as failure to conceive within 1–2 years of unprotected sexual intercourse. Most studies however have measured birth interval, reflecting future live birth rates and not rates of conception. These studies may not have been able to adjust for confounding factors such as use of contraception.

We found one systematic review603 which included 8 cohort studies in Northern Europe and USA and one further cohort study164 conducted in England which had addressed this question. Follow-up period in most studies ranged between 3.5 to 6 years, however one study had a follow up period between 1–19 years. Register information or interviews examined outcomes of at least one pregnancy, at least one live birth, all pregnancies, all live births, and fecundity. Almost all studies report that fewer women having a caesarean section (CS) will subsequently have children/or will have less children, due to a combination of a lessened desire for, or an incapability of having children. There is a 46% increase in the risk of having no more children five years after primary CS (risk ratio [RR] 1.46, 95% confidence interval [CI] 1.07 to 1.99).164 [evidence level 2b]

Sterilisation rates were higher after a CS in 3 studies. The increased risk ranged between 6% and 23%.604 [evidence level 2b]

Placenta praevia

We identified three recent cohort studies and an earlier systematic review. The incidence of placenta praevia in these studies ranges from 0.2%605 to 0.5%606,607 for women with a previous vaginal birth and 0.4%605 to 0.8%607 for women with a previous CS. These studies report a 30% to 60% increase in risk of placenta praevia in subsequent pregnancies for women who had had a previous CS compared to those who had had vaginal deliveries. Three case series608610 have reported on the incidence of placenta praevia and placenta accreta in women who have had previous CS. Overall the incidence of placenta accreta is estimated to be 1 in 2500 pregnancies, however, there is no comparative data for the incidence in women who have not had previous CS.

The incidence of placenta praevia ranges from 0.2% to 0.5% for women with a previous vaginal birth and 0.4% to 0.8% for women with a previous CS. [evidence level 2b].

Stillbirth

A large retrospective cohort study in Scotland (n = 120,633) investigated the association between previous CS and risk of stillbirth in subsequent pregnancies. The risk of antepartum stillbirth among women who had no previous CS was 2 per 1000 compared to 4 per 1000 among women who had a previous CS (hazard ratio 1.64, 95% CI 1.17 to 2.30). The risk of unexplained stillbirth associated with previous CS differed with gestational age, the excess risk was apparent from 34 weeks (hazard ratio 2.23, 95% CI 1.48 to 3.36).611 [evidence level 2b]

11.2. Pregnancy and childbirth after CS

Introduction

A recent study of 146 NHS trusts in England (Bragg et al., 2010) found that one in four women had a CS. The rise in primary CS rates has led to an increased proportion of women of reproductive age with a scarred uterus. Thus, the issue of the most appropriate mode of delivery following a CS continues to be the subject of research and debate.

This section presents the best available evidence to facilitate antenatal counselling and decision making when planning the mode of birth following one or more previous CSs.

Review question

What are the risks and benefits of planned caesarean section compared with planned vaginal birth for both women and babies in women who have had a previous caesarean section?

Overview of evidence

Four studies were included in this review (Guise et al., 2010; Cahill et al., 2010; Tahseen & Griffiths, 2010; Law et al., 2010).

Of the four studies, one is a systematic review (Guise et al., 2010), one was conducted in the USA (Cahill et al., 2010), one in the UK (Tahseen & Griffiths, 2010) and one in Hong Kong (Law et al., 2010). One study is a large, rigorous systematic review of observational studies (Guise et al., 2010). One study (Tahseen & Griffiths, 2010) performed a systematic review of observational studies of success rates and adverse maternal and neonatal outcomes of vaginal birth after one or two CSs and repeat CSs.

One study (Cahill et al., 2010) reported maternal morbidity in women with three or more prior caesarean births who attempt a vaginal birth (VBAC).

One study (Law et al., 2010) reported maternal psychological status among women with one previous caesarean birth who were randomised to planned vaginal birth or planned CS.

Evidence profile

One evidence profile summarises maternal outcomes from one systematic review plus one randomised trial of the risks and benefits of “elective” repeat CSs [ERCS] compared with trial of labour [TOL] (Guise et al., 2010, Law et al., 2010). One evidence profile summarises neonatal outcomes from one systematic review of the risks and benefits of ERCS compared with TOL (Guise et al., 2010). Three evidence profiles report maternal complications associated with repeat CS as reported by the same systematic review (Guise et al., 2010). One evidence profile reports maternal outcomes of vaginal birth or planned CS after two previous CSs compared with vaginal birth or planned CS after one previous CS (Tahseen & Griffiths, 2010). Maternal morbidity in women who plan vaginal birth after three or more prior CSs is detailed in one evidence profile reporting findings from one observational study (Cahill et al., 2010). All included studies were observational studies. Therefore, using the GRADE system, the quality of the evidence was moderate, low or very low for all studies.

Maternal outcomes

All of the data included in Table 11.1 have been taken from one systematic review and one randomised trial and details outcomes for women who have had one previous CS. The number in the first column indicates the number of studies within the review that contribute data to that outcome.

Table 11.1. GRADE summary of findings comparing planned CS with planned vaginal birth in women with a previous CS (maternal outcomes).

Table 11.1

GRADE summary of findings comparing planned CS with planned vaginal birth in women with a previous CS (maternal outcomes).

Repeat CS

Narrative discussions of maternal complications associated with multiple CSs were reported in one systematic review (Guise et al., 2010). All participants gave birth by CS. The number of studies contributing to the outcome in question is reported in the first column of the table. For Tables 11.2 to 11.4 just one study from within the systematic review (not the same study) contributed data to each outcome. All included studies involved women giving birth at any gestation.

Table 11.2. GRADE summary of findings for repeat CS (one prior CS compared with two prior CSs).

Table 11.2

GRADE summary of findings for repeat CS (one prior CS compared with two prior CSs).

Table 11.3. GRADE summary of findings for repeat CS (one prior CS compared with two or more prior CSs).

Table 11.3

GRADE summary of findings for repeat CS (one prior CS compared with two or more prior CSs).

Table 11.4. GRADE summary of findings for repeat CS (one prior CS compared with three prior CSs).

Table 11.4

GRADE summary of findings for repeat CS (one prior CS compared with three prior CSs).

Vaginal birth attempt following two or more CS

All of the data included in this section have been taken from two studies (Cahill et al., 2010; Tahseen & Griffiths, 2010) that reported maternal morbidity in women who attempted VBAC. The range of successful VBACs was 74% to 80% in one observational study (Cahill et al., 2010) and 72% to 76% in the other study (Tahseen & Griffiths, 2010). For the systematic review (Tahseen & Griffiths, 2010) the number of studies reported in the first columns of Tables 11.5 and 11.6 corresponds to the number of included studies contributing findings to each reported outcome.

Table 11.5. GRADE summary of findings for planned VBAC after two prior CSs compared with planned repeat CS after two prior CSs.

Table 11.5

GRADE summary of findings for planned VBAC after two prior CSs compared with planned repeat CS after two prior CSs.

Table 11.6. GRADE summary of findings for planned VBAC after three or more prior CSs compared with planned repeat CS after three or more prior CSs.

Table 11.6

GRADE summary of findings for planned VBAC after three or more prior CSs compared with planned repeat CS after three or more prior CSs.

Neonatal outcomes

All of the data included in Table 11.7 have been taken from one systematic review (Guise et al., 2010). The number in the first column indicates the number of studies from that review which report on those outcomes.

Table 11.7. GRADE summary of findings comparing planned CS with planned vaginal birth in women with a previous CS (neonatal outcomes).

Table 11.7

GRADE summary of findings comparing planned CS with planned vaginal birth in women with a previous CS (neonatal outcomes).

No pooled data was reported in the systematic review (Guise et al., 2010) for neonatal intensive care unit [NICU] admission, hypoxic-ischemic encephalopathy (HIE) and neonates' Apgar score. There were narrative discussions for these outcomes which are summarised here.

There was evidence that the rate of NICU admission was higher in neonates born by planned repeat CS compared with neonates born following planned vaginal birth (eight studies, low quality, pooled data not reported).

There was very low quality evidence from three studies that reported lower rates of HIE among neonates born by planned repeat CS compared with neonates born following planned vaginal birth (pooled data not reported) .

There was low quality evidence from four studies that found no difference in the proportion of babies with an Apgar score of 7 or below at 5 minutes in neonates born by planned repeat CS compared with neonates born following a planned vaginal birth (pooled data not reported).

Evidence statements

Maternal outcomes following one CS

The evidence for all outcomes other than maternal mortality was of very low quality.

Maternal mortality

One systematic review found that the maternal mortality rate was higher in women who had undergone planned repeat CS at term compared with women who had undergone a planned vaginal birth at term. This finding was statistically significant. The evidence for this outcome was of moderate quality.

One systematic review found that the mortality rate was significantly higher in women who had undergone planned repeat CS at any gestational age compared with women who had undergone a planned vaginal birth at any gestational age. This finding was statistically significant. The evidence for this outcome was of moderate quality.

Uterine rupture

One systematic review found that the rate of uterine rupture was lower among women with planned repeat CS at term compared with women who had undergone a planned vaginal birth at term. This finding was statistically significant.

One systematic review found that the rate of uterine rupture was lower among women with planned repeat CS at any gestational age compared with women who had undergone a planned vaginal birth at any gestational age. This finding was statistically significant.

Blood transfusion

One systematic review found that the rate of blood transfusion was lower among women who had a planned repeat CS at term when compared with women who had undergone a planned vaginal birth at term. This finding was statistically significant.

One systematic review found that the rate of blood transfusion was lower among women who had a planned repeat CS at any gestational age when compared with women who had undergone a planned vaginal birth at any gestational age. This finding was statistically significant.

Hysterectomy

One systematic review did not find a statistically significant difference in the rates of hysterectomy among women who had a planned CS at term compared with women who had undergone a planned vaginal birth at term.

One systematic review did not find a statistically significant difference in the rates of hysterectomy among women who had a planned CS at any gestational age compared with women who had undergone a planned vaginal birth at any gestational age.

Infection (endometritis)

One systematic review found that the rate of infection was lower among women with planned repeat CS when compared with women who had a planned vaginal birth. However, the paper did not provide enough data to determine if this difference was statistically significant.

Length of hospital stay

One systematic review found that the mean length of hospital stay was longer among women with planned repeat CS when compared with women who had a planned vaginal birth. However, the paper did not provide enough data to determine if this difference was statistically significant.

Postnatal depression

One randomised trial did not find a statistically significant difference in the rates of postnatal depression 6 months postpartum among women who had a planned CS compared with women who had a planned vaginal birth using the Edinburgh Postnatal Depression Scale and Beck Depression Inventory scales..

Client satisfaction

One randomised trial did not find a statistically significant difference in the rates of client satisfaction 6 months postpartum among women who had a planned CS compared with women who had a planned vaginal birth using Client Satisfaction Questionnaires scores.

Repeat caesarean sections

No pooled data was reported in the systematic review (Guise et al., 2010) for maternal complications associated with repeat CS. There were narrative discussions of each included study for the following outcomes:

One prior CS compared with two prior CSs

The evidence for all outcomes was of low quality.

Blood transfusion

One study found that the rate of blood transfusion was lower among women giving birth by CS following one prior CS compared with women who had undergone two prior CSs at any gestational age. This finding was statistically significant.

Infection (endometritis)

One study did not find a statistically significant difference in infection rates in women giving birth by CS following one prior CS compared with women who had undergone two prior CSs at any gestational age.

Wound complication

One study found that the wound complication rate was lower among women giving birth by CS following one prior CS compared with women who had undergone two prior CSs at any gestational age. This finding was statistically significant.

Surgical injuries

One study found that the rate of surgical injuries was lower among women giving birth by CS following one prior CS at any gestational age when compared with women who had two prior CSs. This finding was statistically significant.

One prior CS compared with two or more prior CSs

The evidence for both outcomes was of low quality.

Blood transfusion

One study found that fewer women giving birth by CS following one prior CS at any gestational age required a blood transfusion when compared with women who had two or more prior CSs. This finding was statistically significant.

Hysterectomy

One study did not find a statistically significant difference in the rate of hysterectomy among women giving birth by CS following one prior CS at any gestational age when compared with women who had two or more prior CSs.

One prior CS compared with three prior CSs

The evidence for all outcomes was of low quality.

Surgical injuries

One study found that the rate of surgical injuries was lower among women giving birth by CS following one prior CS at any gestational age when compared with women who had three prior CSs. This finding was statistically significant.

Infection (endometritis)

One study did not find a statistically significant difference in the infection rates among women giving birth by CS following one prior CS compared with women who had undergone three prior CSs at any gestational age.

Wound complication

One study did not find a statistically significant difference in the wound complication rates among women giving birth by CS following one prior CS compared with women who had undergone three prior CSs at any gestational age.

Planned VBAC after two prior CSs versus planned repeat CS after two prior CSs

The evidence for all outcomes was of very low quality.

Blood transfusion

One systematic review did not find a statistically significant difference in the rate of blood transfusions among women who planned a vaginal birth following two prior CSs compared with women who had a planned CS following two prior CSs.

Febrile morbidity

One systematic review did not find a statistically significant difference in the rate of febrile morbidity among women who planned a vaginal birth following two prior CSs compared with women who had a planned CS following two prior CSs.

Hysterectomy

One systematic review did not find a statistically significant difference in the rate of hysterectomy in women who planned a vaginal birth following two prior CSs compared with women who had a planned CS following two prior CSs.

Planned VBAC after three or more prior CSs versus planned repeat CS after three or more prior CSs

The evidence for all outcomes was of very low quality.

Blood transfusion

One study did not find a statistically significant difference in the blood transfusion rates among women who planned a vaginal birth following three or more prior CSs compared with women who had a planned CS following three or more prior CSs.

Fever

One study did not find a statistically significant difference in fever rates in women who planned a vaginal birth following three or more prior CSs compared with women who had a planned CS following three or more prior CSs.

Bladder injury

One study did not find a statistically significant difference in the rate of bladder injuries among women who planned a vaginal birth following three or more prior CSs compared with women who had a planned CS following three or more prior CSs.

Surgical injury

One study did not find a statistically significant difference in the rate of surgical injuries among women who planned a vaginal birth following three or more prior CSs compared with women who had a planned CS following three or more prior CSs.

Uterine rupture

One study did not find a statistically significant difference in the rate of uterine rupture in women who planned a vaginal birth following three or more prior CSs compared with women who had a planned CS following three or more prior CSs.

Neonatal outcomes

The evidence for all outcomes was of very low quality.

Perinatal mortality

One systematic review did not find a statistically significant difference in the perinatal mortality rate among infants born to women who planned a repeat CS at term compared with infants born at term to women who planned a vaginal birth.

Neonatal mortality

One systematic review found that the neonatal mortality rate was lower for infants born at term to women who planned a repeat CS compared with infants born at term to women who planned a vaginal birth. This finding was statistically significant.

Bag and mask ventilation

One systematic review found that the use of bag and mask ventilation was lower among neonates born at term to women who planned a repeat CS compared with neonates born at term to women who planned a vaginal birth. This finding was statistically significant.

Transient tachypnea

One systematic review did not find a statistically significant difference in the incidence of neonatal transient tachypnoea between neonates born to women who planned a repeat CS and those born at term to women who planned a vaginal birth.

Health economics

A model was developed to compare the cost effectiveness of VBAC versus a planned CS in women with one previous CS and with no plans for further children. A summary of this analysis is provided below (see Chapter 13 for further details).

In addition to the costs of birth, the model also estimated ‘downstream’ costs and quality adjusted life years (QALYs) based on the risk of adverse events for each planned mode of birth. The base case analysis considered only the outcomes that were reported in the review undertaken for this guideline to determine the risks and benefits for both women and babies of planned CS compared with planned vaginal birth in women who have had a previous CS. Secondary analyses also used outcomes that were only reported in the review which compared the risk and benefits of planned CS compared with planned vaginal birth. However, it should be recognised that these risks are likely to be underestimated for this population and that the relative risk for these adverse outcomes may also be different in this population.

The results tended to show that VBAC was more likely to be cost effective, although this was a borderline finding and considerable uncertainty remains, especially with respect to all the outcomes that may differ between the different modes of planned birth in this population.

Evidence to recommendations

Relative value placed on outcomes considered

It was noted that findings from studies of babies born at term were very similar to those that included babies born at any gestational age. This was thought to reflect the relatively low numbers of preterm babies included in the studies involving all gestational ages. The extra statistical power afforded by the larger numbers where studies of all gestational ages have been included meant the GDG was happy to consider this evidence when making recommendations.

Maternal mortality is clearly a vitally important outcome at an individual level, but in terms of informing decision making for a whole population, the very low numbers of deaths reported in the studies (absolute numbers range from 1.9 to 7.5 per 100,000) mean this outcome does not necessarily drive the recommendations made. Other important outcomes, including uterine rupture and neonatal mortality, were more common, although still rare, meaning that although differences between study groups were statistically significant, the low incidence meant that they were also considered less clinically significant in terms of driving clinical practice and advice to women. In the context of low actual risk, then absolute risk will be a more important consideration than relative risk.

The reported neonatal outcomes of bag and mask ventilation and transient tachypnoea were felt to be of limited value as it was not possible to determine how these outcomes related to ongoing health problems or disability.

Trade-off between clinical benefits and harms

Mortality-related outcomes are very rare. However, the GDG noted that for women planning birth following one previous CS, maternal mortality is statistically significantly higher for women planning a repeat CS while neonatal mortality is statistically significantly higher for women planning a vaginal birth. Perinatal mortality is not statistically different between the two groups.

The GDG agreed that although it is right to give women all available information when planning mode of birth, the important thing to emphasise to women planning birth after one previous CS is that serious adverse outcomes, including maternal and neonatal mortality, uterine rupture, need for blood transfusion and hysterectomy, are rare, no matter whether women choose a planned repeat CS or VBAC.

The GDG noted that the relative risk of adverse outcomes may vary from woman to woman depending upon her obstetric history, including reasons for previous CS(s) and whether or not a woman has previously given birth vaginally. These individual considerations need to be taken into account when discussing mode of birth following one or more previous CSs.

When considering increasing numbers of previous CSs, the evidence showed no difference between planned vaginal birth and planned CS in rates of blood transfusion, fever and hysterectomy after two prior CSs. However, with an increasing number of CSs, there is an increasing risk of need for blood transfusion, wound complications and injuries to the bladder, regardless of the mode of birth.

Trade-off between net health benefits and resource use

An economic model developed for this guideline to compare the cost effectiveness of planned CS versus planned vaginal birth in women who have had a previous CS did not strongly suggest a preferred mode of birth. As a result, this model would, given the current state of evidence, support a recommendation allowing women to choose their preferred method of birth in consultation with the healthcare professionals responsible for her care. Considerations about any future pregnancies may be an important factor in the decisions made, given the increased risks in, for example, incidence of placenta praevia and morbidly adherent placenta, which are associated with repeat CSs.

Quality of evidence

The evidence for outcomes following one previous CS was drawn from one large meta-analysis of observational studies and one randomised controlled trial (RCT), and ranged from moderate to very low. The large sample sizes reported for the meta-analysis meant the GDG felt more confident in the validity of the findings regarding rare outcomes.

The evidence examining outcomes following more than one previous CS is of low and very low quality. While evidence comparing outcomes for women having a CS following one, two or more previous CSs is interesting and can be used to provide general information about increasing risks following two or more CSs, it does not help a woman decide the level of risk associated with her choice of mode of birth in the current pregnancy. However, this information is helpful for decision making about future births. The evidence comparing outcomes for women choosing a planned vaginal birth compared with those choosing a planned CS after two or more previous CSs is useful in this respect as this reflects the choice women have. Unfortunately, this evidence is of very low quality, thus lowering the validity of the reported findings.

No good quality evidence was available for women planning birth following five or more previous CSs.

Other considerations

The GDG noted that many women leave hospital following a caesarean birth without understanding the implications for planning future pregnancies and births. It was felt that it is important to provide this information to women and their partners so that they can have an accurate picture of what this means for them when planning their family, including options for future modes of birth. The GDG agreed that there is a benefit to providing this information to women and their partners prior to leaving the hospital because the medical records are easily available to refer to. As a result, the GDG recommended that this discussion take place with women after the CS. However, the GDG also recognised that some women may prefer to have this discussion at a later date, so highlighted that this discussion can be deferred. Due to the large amount of information women and their partners receive during the immediate postnatal period, this information should be provided both verbally and in written formats. It is important to emphasise to women that, regardless of future choice of mode of birth, poor outcomes are very rare.

Recommendations

NumberRecommendation
119When advising about the mode of birth after a previous CS consider:
  • maternal preferences and priorities
  • the risks and benefits of repeat CS
  • the risks and benefits of planned vaginal birth after CS, including the risk of unplanned CS. [new 2011]
120Inform women who have had up to and including four CS that the risk of fever, bladder injuries and surgical injuries does not vary with planned mode of birth and that the risk of uterine rupture, although higher for planned vaginal birth, is rare. [new 2011]
121Offer women planning a vaginal birth who have had a previous CS:
  • electronic fetal monitoring during labour
  • care during labour in a unit where there is immediate access to CS and onsite blood transfusion services. [GPP] [2011]
122During induction of labour, women who have had a previous CS should be monitored closely, with access to electronic fetal monitoring and with immediate access to CS, because they are at increased risk of uterine rupture. [GPP] [2004]
123Pregnant women with both previous CS and a previous vaginal birth should be informed that they have an increased likelihood of achieving a vaginal birth than women who have had a previous CS but no previous vaginal birth. [B] [2004]
124While women are in hospital after having a CS, give them the opportunity to discuss with healthcare professionals the reasons for the CS and provide both verbal and printed information about birth options for any future pregnancies. If the woman prefers, provide this at a later date. [new 2011]

For recommendations on methods of induction for women who have had a previous CS, see the Induction of labour guideline (NICE, 2008)

NumberResearch recommendation
RR 46A comparison of the long term psychological and physical outcomes between women who have chosen and/or been advised towards a VBAC or a planned repeat CS.
RR 47An evaluation of the effectiveness of continuity of carer on the proportion of women planning and achieving a VBAC, and the short and long term psychological and physical outcomes of women following a planned VBAC.
Copyright © 2011, National Collaborating Centre for Women's and Children's Health.

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Bookshelf ID: NBK115291

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