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. Author manuscript; available in PMC: 2014 Jan 1.
Published in final edited form as: Paediatr Perinat Epidemiol. 2012 Nov 22;27(1):62–71. doi: 10.1111/ppe.12014

Mode of First Delivery and Women’s Intentions for Subsequent Childbearing: Findings from the First Baby Study

Kristen H Kjerulff a,b, Diana L Velott a, Junjia Zhu a, Cynthia H Chuang a,c, Marianne M Hillemeier a,d, Ian M Paul a,e, John T Repke b
PMCID: PMC3671865  NIHMSID: NIHMS410683  PMID: 23215713

Abstract

Background

More than a dozen studies have reported a reduced rate of childbearing after caesarean delivery (CD). It has been hypothesized that this is because women who deliver by CD are less likely to intend to have subsequent children than women who deliver vaginally -either before childbirth or as a consequence of CD. Little research has addressed either of these hypotheses.

Methods

As part of an ongoing prospective study, we interviewed 3006 women in their third trimester and 1 month after first childbirth to assess subsequent childbearing intentions.

Results

Women who delivered by CD were similar to those who delivered vaginally in intent to have at least one additional child, both before childbirth (90.1% vaginal, 89.9% CD; P=0.97) and after (87.8% vaginal, 87.1% CD; P=0.87); however, women who had CD were less likely to intend 2 or more additional children, both before childbirth (34.7% vaginal, 29.2% CD; P=0.03) and after (32.2% vaginal, 26.1% CD; P=0.01). Among women who intended to have at least 1 additional child before childbirth, 5.0% reported intending to have no additional children 1 month after delivery (5.1% vaginal, 4.6 % CD; P=0.52).

Conclusions

Women whose first delivery is by CD are less likely to intend a relatively large family of 3 or more children than those who deliver vaginally, but delivery by CD does not decrease women’s intentions to have at least one more child any more than does vaginal delivery, at least in the short-term.

Keywords: caesarean delivery, secondary infertility, first delivery, childbearing, prospective cohort study

Introduction

Previous studies, conducted both in the US and other countries, have found that women who deliver by caesarean (CD) are less likely to bear subsequent children and bear fewer subsequent children than women who deliver vaginally.114 However, nearly all of these studies were analyses of existing data sets,1, 3, 4, 6, 9, 10, 13, 14 such as birth registry data, or retrospective surveys,2, 7, 8, 11, 12 often many years after the index delivery. Consequently, it is not clear if women who deliver by caesarean are different from women who deliver vaginally prior to the delivery, or if there is something about the CD itself that affects their desire or ability to conceive or bear subsequent children.

It has been suggested that the deficit in childbearing subsequent to CD found in previous studies is voluntary, i.e. due to differences in subsequent childbearing intentions by mode of delivery.11, 13, 15, 16 If this deficit in childbearing subsequent to CD were voluntary one would hypothesize that either: (i) Women who deliver by CD are less likely to intend to have subsequent children prior to delivery than those who deliver vaginally; or (ii) Women who deliver by CD are more likely than those who deliver vaginally to decide that they intend to have no further children after childbirth, for reasons associated with the mode of delivery. The First Baby Study (FBS) is an ongoing, prospective interview study which was designed to investigate the association between mode of delivery and subsequent fertility over the course of a three year follow-up period after first childbirth. FBS participants were asked about their childbearing intentions both before and after first childbirth.

While most prior studies of childbearing subsequent to CD have compared CD to vaginal delivery,1, 2, 4, 5, 12, 14, 17 some have included instrumental vaginal delivery as a third mode – with conflicting results as to the effect of instrumental vaginal delivery on subsequent childbearing.6, 7, 911, 13 To better understand these findings, we investigated subsequent childbearing intentions in relation to two modes of delivery (CD versus vaginal) as well as three modes –spontaneous vaginal, instrumental vaginal and CD. Previous studies have generally measured subsequent childbearing as a dichotomous variable (no subsequent children versus one or more),17, 911, 17 but several have measured number of children born subsequent to the index delivery and reported fewer children born subsequent to caesarean delivery.13, 7, 10 Several studies have also investigated time from the index delivery to a subsequent childbirth,1, 2, 9, 17, 18 with some reporting longer time to a subsequent childbirth after caesarean, in comparison to vaginal delivery.2, 9, 17 Therefore, in this study we assessed women’s childbearing intentions in terms of whether or not they intended to have one or more children, the number of subsequent children intended, as well as the time frame for subsequent childbearing intentions.

Methods

Recruitment

This study was approved by the Penn State College of Medicine Institutional Review Board (IRB) as well as the IRBs of participating hospitals located throughout the State of Pennsylvania. Recruitment methods included the placement of study brochures, flyers and posters in strategic locations at a variety of venues including hospitals, obstetricians’ offices, ultrasound centers, low-income clinics, community health and pregnancy support centers; press releases were sent to newspapers across the state and advertisements were placed in community newspapers and weekly publications; and the internet was used for hospital intranet postings and webpage announcements. Study recruiters described the study and distributed brochures to potential participants attending childbirth education classes and hospital tours associated with participating hospitals. Study brochures were mailed to potentially eligible women by a Medicaid insurer which served women across the State. Recruitment materials were also mailed to women reported to be nulliparous, pregnant, aged 18 to 35 and living in Pennsylvania, whose names and addresses were provided by a marketing company and compiled from information obtained from credit card companies, magazines, charities, organizations, manufacturers and retailers.

We began recruitment of study participants in January, 2009 and completed in April, 2011. There were 74 women who completed the baseline interview but did not complete the 1-month interview, some because of fetal demise, but most because they decided not to participate. Those who did not complete the 1 month interview were replaced until we had obtained our targeted enrollment number of 3,000 women. We over-enrolled slightly to obtain a final sample size of 3,006 study participants. Therefore, a total of 3,080 women were recruited, consented and completed the baseline interview, and 3,006 completed both the baseline and 1-month postpartum interviews. We used this method, to maximise participant retention. The 74 women who dropped out of the study after the first interview were different from those who completed the 1-month interview in that they were younger, less likely to be covered by private insurance and more likely to live in an urban area. They were not significantly different in race/ethnicity.

We obtained the birth certificate and hospital discharge data for the 3,006 study participants, with a match rate of 99.4% for the birth certificate data, 99.5% for the mothers’ hospital discharge data and 98.4% for the babies’ hospital discharge data.

Inclusion and Exclusion Criteria

The primary outcome of the FBS is childbirth subsequent to the first delivery. To maximise the likelihood of the occurrence of this outcome, we included only women having a first, singleton birth as was done in previous studies of fertility subsequent to CD.3, 6, 7, 9, 11, 13, 14, 18 To be included in this study, women needed to be aged 18 to 35 at the time of study recruitment, nulliparous, currently pregnant with a singleton pregnancy, speak English or Spanish and planning to deliver in a Pennsylvania hospital. Women who were planning to deliver at home or in a birthing center not associated with a hospital were not included. However, women under the care of a midwife were included in the study. Women were excluded if they planned for the infant to be adopted or planned to have a tubal ligation while hospitalized for delivery.

Interviews

The baseline interviews occurred prior to the beginning of labor, when participants were between 30 and 42 weeks gestation, at a median gestational age of 35 weeks. The baseline interview assessed reproductive and health history; pregnancy complications and health care utilization; mode of delivery preference; relationship factors; psychosocial factors; future birth desires and intentions; and socio-demographic factors. The 1-month postpartum telephone interview focused on the delivery experience and assessed factors related to labor and delivery; postpartum feelings about childbirth; in-hospital and post-discharge complications; and the health of the baby and the mother. The subsequent interviews (at 6, 12, 18, 24, 30 and 36 months postpartum) measure sexual relations and use of birth control; subsequent pregnancies; relationship factors; future birth desires and intentions; the health of the mother, the index child and all subsequent children; and socio-demographic factors. We completed the 12-month postpartum interviews in May 2012 and will complete the 36-month postpartum interviews in May 2014.

Future childbearing intentions were measured using questions adapted from the 2003 National Survey of Family Growth.19 In the baseline survey participants were asked “Not counting your current pregnancy, how many more babies do you intend to have?” and in the 1-month postpartum survey women were asked “Not counting your new baby, how many more babies do you intend to have?” At both data collection stages participants were asked “Do you have plans as to when you would like to have another baby?” and “If so, when do you plan on having another baby?”

We used the 2009 Institute of Medicine guidelines for weight gain during pregnancy to classify the study participants into three categories of weight gain: less than recommended, recommended and more than recommended.20 These categories were based on the participant’s pre-pregnancy body mass index (BMI). The pre-pregnancy height, weight and gestational weight gain were obtained primarily by self-report. However, in the case of missing or unlikely self-report data we used the birth certificate data to calculate pre-pregnancy BMI and gestational weight gain. Mode of delivery was based on self-report, and verified by the birth certificate data. Instrumental vaginal delivery included delivery by forceps or vacuum extraction. Maternal height was categorized in quartiles.

We compared the participants in the First Baby Study to women aged 18 to 36 delivering their first, live birth, singleton child, gestation of 35 weeks or later, in Pennsylvania as a whole in 2008, using birth certificate data paired with hospital discharge data, excluding those with a code indicating prior caesarean delivery, or sterilization at the time of delivery. The population characteristics were compared to the sample characteristics for the variables of age, race/ethnicity, education, insurance coverage, marital status, preconception BMI, weight gained during pregnancy, maternal height and mode of delivery (CD, spontaneous vaginal and instrumental vaginal).

Statistical Power

Using a retrospective cohort of all women aged 18 to 35 having their first, singleton delivery in Pennsylvania in 2000 and followed to the end of 2004, we found that women whose first delivery was vaginal were more likely to have a subsequent delivery within 3 years than those who delivered by CD (age adjusted OR 1.29, 95% CI 1.28, 1.31). With a significance level of 0.05 power of 0.80, detectable/alternative OR of 1.29, the probability of exposure (caesarean delivery) of 0.29 (among women aged 18 to 35, having a first, singleton birth of 34 weeks gestation or later) and the probability of having a second delivery within 3 years if the first delivery is vaginal = 0 .39, the required sample size was 2,402.21 Estimating that there would be a sample attrition rate of 20% over the course of the 3 year follow-up period, we calculated that we would need to enroll 3,000 participants in order to have the required sample size of 2,402 by the end of the 3 year follow-up period.

Statistical Analysis

Chi-square test were used to investigate the associations between covariates and mode of delivery and childbearing intention before and after first childbirth. Z test for proportions were used to compare the study sample to the population of women aged 18 to 36 who had a first, singleton birth in Pennsylvania in 2008. Multivariable logistic regression models were used to estimate odds ratio (OR) and 95% confidence interval (CI) for the association between mode of delivery (in three categories) and intentions for subsequent childbearing (pre-delivery and post-delivery), with intentions in two categories (no more vs. one or more subsequent births), adjusting for maternal age.

Results

In general the participants in the FBS were different from the comparable population of women in Pennsylvania – they were older, more likely to be White, more educated, more likely to have private insurance and more likely to be married than the general population of women having their first, singleton birth, aged 18 to 36. They were not different in mode of delivery, preconception BMI or height.

As seen in Table 2, the older a women was at first childbirth the more likely she was to deliver by CD. There was a strong association between pre-pregnancy BMI category and delivery by CD: women who were obese prior to conception were the most likely to have CD and those who were underweight were the least likely. Gestational weight gain was also associated with mode of delivery – women who had gained more than recommended were more likely to have a CD than those who had gained as recommended or less than recommended.

Table 2.

Distribution of maternal factors by mode of delivery

Overall n (%) Normal Vaginal (%) Instrumental Vaginal (%) Cesarean delivery (%) P-value
Maternal age (years) <0.001
 18 – 24 811 (27.0) 71.1 6.5 22.3
 25 – 29 1193 (39.7) 61.9 9.6 28.5
 30 – 36 1002 (33.3) 56.5 9.4 34.1
Race/Ethnicity 0.556
 White 2502 (83.2) 62.8 8.9 28.3
 Black 221 (7.4) 62.9 5.4 31.7
 Hispanic 166 (5.5) 61.4 8.4 30.1
 Other 117 (3.9) 59.0 11.1 30.2
Education 0.158
 High school degree or less 501 (16.7) 64.9 8.2 26.9
 Some college or technical 804 (26.7) 65.2 7.5 27.4
 College grad or higher 1701 (56.6) 60.7 9.4 29.9
Insurance 0.116
 Private 2307 (76.7) 61.4 8.9 29.6
 Public 687 (22.9) 66.5 7.7 25.8
 Self-Pay 12 (0.4) 66.7 16.7 16.7
Marital Status 0.357
 Married 2117 (70.4) 61.8 8.9 29.3
 Living with partner 544 (18.1) 63.1 9.7 27.2
 Not living with partner 187 (6.2) 65.8 7.0 27.3
 Unattached 157 (5.2) 67.5 4.5 28.0
Prepregnancy BMI <0.001
 Underweight (<18.5) 106 (3.5) 77.4 8.5 14.2
 Normal (18.5–24.9) 1609 (53.7) 66.1 10.3 23.7
 Overweight (25.0–29.9) 665 (22.2) 60.2 8.9 31.0
 Obese (≥30.0) 618 (20.6) 53.7 4.4 41.9
Pregnancy weight gain1 <0 .001
 Less than recommended 334 (11.2) 69.5 8.7 21.9
 Recommended 1039 (34.7) 68.0 9.4 22.5
 More than recommended 1618 (54.1) 57.7 8.2 34.1
Maternal height (inches) <0.001
 53–62 625 (20.8) 53.3 9.0 37.8
 63–65 1175 (39.1) 61.6 9.6 28.8
 66–67 726 (24.2) 67.4 8.1 24.5
 68–74 478 (15.9) 69.9 6.9 23.2
Prior miscarriages 0.211
 Yes 481 (16.0) 59.0 9.6 31.4
 No 2525 (84.0) 63.3 8.5 28.2
Prior induced abortions 0.096
 Yes 151 (5.0) 70.9 7.3 21.9
 No 2855 (95.0) 62.2 8.8 29.0
Pregnancy was intended 0.298
 Yes 1899 (63.4) 61.6 9.0 29.5
 No 1098 (36.6) 64.4 8.1 27.5
Fertility treatment 0.002
 Yes 335 (11.1) 54.3 9.0 36.7
 No 2671 (88.9) 63.6 8.6 27.7
Time to conception 0.029
 6 months or less2 2495 (83.0) 63.1 9.1 27.8
 More than 6 months 507(16.9) 60.0 6.9 33.1

Notes

1

based on 2009 IOM guidelines22

2

including unintended pregnancies.

Our first hypothesis that “Women who deliver by CD are less likely to be intending to have subsequent children prior to delivery than those who deliver vaginally” was not supported (Table 3). Although we found that women who delivered vaginally were more likely to be intending to have a relatively large family – two or more additional children beyond the first child - than those who delivered by CD (vaginal = 34.7 %, CD = 29.2%; P=0.034), women who delivered by CD were equally likely as those who delivered vaginally to be intending to have one or more subsequent children prior to first childbirth.

Table 3.

Mode of delivery and intentions for subsequent childbearing

Mode of Delivery Modes Overall
Overall n=3006 Normal Vaginal (%)n=1882 Instrumental Vaginal (%)n=261 Cesarean delivery (%)n=863 P-value Vaginal (%)n=2143 Cesarean delivery (%)n=863 P-value
Pre-delivery intentions 0.005 0.034
 No more children 6.2 5.8 8.4 6.4 6.1 6.4
 1 more child 57.0 55.8 52.9 60.7 55.4 60.7
 2 or more children 33.1 35.1 32.2 29.2 34.7 29.2
 Don’t know 3.7 3.4 6.5 3.7 3.7 3.7
Post-delivery intentions 0.006 0.011
 No more children 9.3 8.9 11.5 9.6 9.2 9.6
 1 more child 57.2 55.7 55.0 61.1 55.6 61.1
 2 or more children 30.4 32.7 28.5 26.1 32.2 26.1
 Don’t know 3.1 2.7 5.0 3.2 3.0 3.2
Pre-delivery versus postpartum intentions 0.710 0.954
 Fewer (post<pre) 15.5 15.1 17.9 15.7 15.4 15.7
 Same number 75.3 75.5 74.9 74.9 75.5 74.9
 More (post>pre) 9.2 9.3 7.2 9.4 9.1 9.4
Intend additional children postpartum but not prior to 1st birth1 26.3 28.4 18.2 25.5 0.737 26.7 25.5 0.958
No longer intend additional children2 5.0 5.0 5.4 4.6 0.377 5.1 4.6 0.520
Pre-delivery time frame for subsequent child3 0.285 0.293
 Within 1 year 5.6 5.2 8.0 5.6 5.6 5.6
 In about 2 years 38.2 38.2 38.2 38.1 38.2 38.1
 In about 3 years 16.0 16.1 16.3 15.7 16.1 15.7
 In about 4 years 4.9 5.1 2.8 4.9 4.8 4.9
 In about 5 or more years 7.5 8.3 7.2 5.8 8.2 5.8
 No plans or Don’t know 27.9 27.1 27.5 29.9 27.1 29.9
Postpartum time frame for subsequent child3 0.012 0.022
 Within 1 year 5.6 5.9 6.0 4.7 5.9 4.7
 In about 2 years 39.3 38.8 32.2 42.5 38.0 42.5
 In about 3 years 16.1 16.7 18.5 14.2 16.9 14.2
 In about 4 years 5.0 4.9 6.0 4.7 5.1 4.7
 In about 5 or more years 7.2 8.3 5.2 5.4 7.9 5.4
 No plans or Don’t know 26.8 25.3 32.2 28.5 26.1 28.5
Pre-delivery versus postpartum time frame 0.101 0.134
 Post sooner than pre 16.2 14.9 16.8 18.9 15.1 18.9
 Same 66.3 67.6 59.9 65.2 66.7 65.2
 Post later than pre 17.5 17.5 23.4 15.9 18.2 15.9

Notes:

1

among women who did not intend additional children prior to delivery;

2

among women who intended additional children prior to delivery

3

among women who report that they intend 1 or more subsequent children postpartum

The second hypothesis that “Women who deliver by CD are more likely to decide that they intend to have no further children after childbirth, for reasons associated with the mode of delivery” also was not supported (Table 3). Women who delivered by CD were equally likely as those who delivered vaginally to be intending to have one or more subsequent children after first childbirth, although they were less likely to be intending to have two or more subsequent children (vaginal = 32.2%, CD = 26.1%; P = 0.011).

After adjustment for maternal age, women who had an instrumental delivery were less likely to intend to have a subsequent child (P = 0.040) in comparison to those who delivered vaginally, prior to delivery (Table 4), as well as after delivery, although after delivery this was of borderline significance (P = 0.071). Mode of delivery (CD versus vaginal) was not associated with pre-delivery intentions for subsequent childbearing (OR 0.9, 95% CI 0.8, 1.1), or with post-delivery intentions (OR 1.0, 95% CI 0.9, 1.2).

Table 4.

Mode of delivery and maternal factors by subsequent childbearing intentions

Pre-delivery Intentions for Subsequent Childbearing Postpartum Intentions for Subsequent Childbearing
No more (%)n=186 1 or more (%)n=2706 Adjusted ORa [95% CI] No more (%)n=280 1 or more (%)n=2633 Adjusted ORa [95% CI]
Mode of delivery
 Normal vaginal 6.0 94.0 Reference 9.1 90.9 Reference
 Instrumental vaginal 9.0 91.0 0.6 [0.4, 1.0] 12.1 87.9 0.7 [0.5, 1.0]
 Cesarean delivery 6.6 93.4 0.9 [0.6, 1.2] 9.9 90.1 0.9 [0.7, 1.2]
Maternal age (years)
 18 – 24 9.0 91.0 Reference 13.7 86.3 Reference
 25 – 29 4.2 95.8 2.2 [1.5, 3.3] 6.0 94.0 2.5 [1.8, 3.4]
 30 – 36 7.0 93.0 1.3 [0.9, 1.9] 10.6 89.4 1.3 [1.0, 1.8]
Race/Ethnicity
 White 5.3 94.7 Reference 7.9 92.1 Reference
 Black 14.8 85.2 0.4 [0.2, 0.6] 20.5 79.5 0.4 [0.3, 0.6]
 Hispanic 10.8 89.2 0.5 [0.3, 0.9] 17.3 82.7 0.5 [0.4, 0.7]
 Other 10.0 90.0 0.5 [0.3, 1.0] 16.4 83.6 0.5 [0.3, 0.8]
Education
 HS degree or less 11.1 88.9 Reference 17.2 82.8 Reference
 Some college or technical school 7.8 92.2 1.5 [1.0, 2.2] 11.0 89.0 1.7 [1.2, 2.4]
 College grad or higher 4.4 95.6 3.1 [1.9, 4.9] 6.7 93.3 3.2 [2.2, 4.8]
Insurance
 Private 4.5 95.5 Reference 7.2 92.8 Reference
 Public 12.8 87.2 0.3 [0.2, 0.4] 17.8 82.3 0.3 [0.2, 0.4]
Self-Pay 14.3 85.7 0.4 [0.1, 3.4] 14.3 85.7 0.7 [0.1, 5.7]
Marital Status
 Married 4.2 95.8 Reference 7.1 92.9 Reference
 Living with partner 9.6 90.4 0.3[0.2, 0.4] 12.4 87.6 0.4 [0.3, 0.6]
 Not living with partner 13.6 86.4 0.2 [0.1, 0.3] 20.6 79.4 0.2 [0.1, 0.3]
 Unattached Prepregnancy body mass index category (kg/m2) 17.2 82.8 0.1 [0.1, 0.2] 20.9 79.1 0.2 [0.1, 0.3]
 Underweight (< 18.5) 6.9 93.1 1.0 [0.5, 2.3] 9.6 90.4 1.2 [0.6, 2.3]
 Normal (18.5 –24.9) 6.6 93.4 Reference 10.0 90.0 Reference
 Overweight (25.0– 29.9) 5.5 94.5 1.2 [0.8, 1.8] 8.3 91.7 1.2 [0.9, 1.7]
 Obese≥(=30.0) 6.9 93.1 1.0 [0.7, 1.4] 9.8 90.2 1.1 [0.8, 1.4]
Pregnancy weight gain1
 Less than Recommended 6.2 93.8 1.0 [0.6, 1.7] 11.2 88.8 0.8 [0.5, 1.2]
 Recommended 6.1 93.9 Reference 8.9 91.1 Reference
 More than Recommended 6.5 93.5 0.9 [0.7, 1.3] 9.6 90.4 0.9 [0.7, 1.2]
Maternal height (inches)
 53–62 9.1 90.9 Reference 12.0 88.0 Reference
 63–65 6.6 93.4 1.4 [1.0, 2.0] 10.9 89.1 1.1 [0.8, 1.5]
 66–67 3.7 96.3 2.5 [1.6, 4.1] 6.7 93.3 1.9 [1.3, 2.7]
 68–74 6.5 93.5 1.4 [0.9, 2.2] 7.6 92.4 1.6 [1.1, 2.5]
Prior Miscarriages
Yes 5.4 94.6 1.2 [0.8, 1.9] 11.2 88.8 0.8 [0.6,1.1]
No 6.6 93.4 Reference 9.3 90.7 Reference
Prior Induced Abortions
 Yes 9.1 90.9 0.7 [0.4, 1.3] 13.3 86.7 0.7 [0.4, 1.2]
 No 6.3 93.7 Reference 9.4 90.6 Reference
Pregnancy was intended
 Yes 4.0 96.0 Reference 7.1 92.9 Reference
 No 10.7 89.3 0.3 [0.2, 0.4] 14.1 85.9 0.5[0.4,0.6]
Fertility treatment
 Yes 5.3 94.7 1.2 [0.7, 2.1] 9.2 90.8 1.0 [0.7, 1.5]
 No 6.6 93.4 Reference 9.7 90.3 Reference
Time to conception
 6 months or less (including unplanned) 6.7 93.3 Reference 9.9 90.1 Reference
 More than 6 months 4.7 95.3 1.4 [0.9, 2.2] 8.1 91.9 1.2 [0.8, 1.7]
a

Adjusted for maternal age, except for the association of maternal age with subsequent childbearing intentions.

1

based on 2009 IOM gudelines22

Comment

In this interview study of more than 3,000 women at first childbirth we found little support for the hypothesis that women who deliver by CD are less likely to want subsequent children prior to or after childbirth than women who deliver vaginally. However, we did find that the women who delivered by CD were less likely to be intending to have a relatively large family, that is, two or more children subsequent to their first. It could be that women who intend to have only one more child are more likely to change their mind and not have a second child than women who intend to have two or more subsequent children.

Consistent with prior studies, we found that women who have difficulty conceiving and/or undergo fertility treatment were more likely to deliver by CD.17, 22 Difficulty conceiving one’s first child is a factor that could quite clearly increase a woman’s risk of being unable to conceive subsequent children. It has been hypothesized that for women who are borderline fertile, the “added stress of a CD (peritubal adhesions or intrauterine injury) may push these women over the threshold and result in infertility”.5 However, the women with difficulty conceiving were no less likely to be intending to have a subsequent child than those without difficulty conceiving.

Although the younger a woman was at first childbirth the less likely she was to deliver by CD, the women in the youngest age group in this study (age 18 to 24) were less likely to intend to have subsequent children prior to first birth, in comparison to women aged 25–29, and not significantly different from the women in the oldest age group (30–36). These are relevant findings because studies on the association of CD with a decrement in subsequent childbearing have considered maternal age to be an important confounder because the risk for CD increases with age while the likelihood of a subsequent childbirth decreases with age (regardless of mode of delivery), even among women under the age of 35.6 The results of this study suggest that a decrement in childbearing subsequent to first birth for women of older age at first birth may not be because older women are less likely to be intending to have a subsequent child, but due to other factors, such as age-related sub-fecundity.

This study has several limitations. Unlike some of the previous large-scale studies using birth certificate or other types of administrative data, this is not a population-based study. The participants in this study are of higher socioeconomic status than women delivering their first, singleton child in the State of Pennsylvania as a whole. It was not feasible to conduct probability sampling, such as via random-digit dialing or random sampling of households, as is done with national surveys. To use probability sampling to identify and enroll more than 3,000 pregnant women prior to first childbirth would have been prohibitively expensive because we would have had to contact thousands of individuals to identify each woman aged 18 to 35, pregnant with her first, singleton child and otherwise eligible and willing to participate. Participation studies tend to include more educated and affluent individuals than in the general population, as seen in our study.23, 24 One bias which could arise from the higher socioeconomic status of our sample could be a greater ability to seek fertility treatment in case of difficulty conceiving subsequent to first childbirth than women in the state overall. Another source of selection bias, inherent to observational treatment outcome studies, is differences between those who receive one treatment versus another (treatment-selection bias). As this study illustrates, women who have caesarean section at first childbirth are different from those who deliver vaginally. When we assess the primary outcome of interest in this study (childbearing over the course of the follow-up period) we will investigate the usefulness of weighting methods commonly used to adjust for participant-selection bias,25, 26 as well as propensity scoring and other types of methods used to adjust for treatment-selection bias.27, 28

Another limitation of this study is that the postpartum assessment of childbearing intentions reported here occurred only one month after first childbirth. As the glow of new motherhood begins to fade over the course of time, women may change their minds about subsequent childbearing. In addition, women who delivered by caesarean section may be more likely to decide that they do not want to go through childbirth again because of the lengthier recovery period, or the development of painful scar tissue, or some other factor that would not be evident at 1-month postpartum.

After more than a dozen studies have reported a deficit in childbearing subsequent to CD, it is important that prospective, longitudinal interview studies be conducted in order to investigate why this deficit occurs. The results reported here suggest that women’s pre-first-delivery intentions for more children are not substantially different for women who deliver by CD in comparison to those who deliver vaginally. In addition, we found no evidence at 1-month postpartum that delivery by CD causes women to decide that they no longer want subsequent children any more than does vaginal delivery.

As we follow this cohort of more than 3000 women forward in time, with interviews every 6 months over the course of a three year period, we will be able to measure the extent to which such factors as pre-delivery and 1-month postpartum childbearing intentions play out in determining the occurrence of the primary outcome of interest – subsequent childbearing.

Table 1.

Study sample in comparison to population of first, singleton births among women Aged 18–36 in Pennsylvania in 2008

Characteristics Study Sample % (n=3,006) Population % (n=43,430) P-value
Mode of delivery 0.100
 Normal vaginal 62.6 61.1
 Instrumental vaginal 8.7 8.9
 Cesarean 28.7 30.0
Maternal age (years) < 0.001
 18 – 24 27.0 46.2
 25 – 29 39.7 31.0
 30 – 36 33.3 22.9
Race/ethnicity < 0.001
 White 83.2 76.0
 Black 7.4 13.2
 Hispanic 5.5 5.8
 Other 3.9 5.0
Education < 0.001
 High school degree or less 16.7 36.2
 Some college or technical 26.7 28.9
 College grad or higher 56.6 34.8
Insurance < 0.001
 Private 76.7 64.8
 Public 22.9 29.8
 Self-pay 0.4 5.5
Marital status < 0.001
 Married 70.4 52.5
 Not married 29.6 47.5

Acknowledgments

We acknowledge the support of this research by grant (R01-HD052990) from the Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, USA.

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