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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptNIH Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
 
Clin Perinatol. Author manuscript; available in PMC Aug 28, 2012.
Published in final edited form as:
PMCID: PMC3428794
NIHMSID: NIHMS396118
Delivery After Prior Cesarean: Maternal Morbidity and Mortality
Yvonne W. Cheng, MD, MPH,a Karen B. Eden, PhD,b Nicole Marshall, MD,c Leonardo Pereira, MD,c Aaron B. Caughey, MD, PhD,d and Jeanne-Marie Guise, MD, MPHef*
aDivision of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco, 505 Parnassus Avenue, Box 0132, San Francisco, CA 94143, USA
bDepartment of Medical Informatics and Clinical Epidemiology, Oregon Evidence-based Practice Center, Oregon Health and Science University, Mail Code BICC, 3181 SW Sam Jackson Park Road, Portland, OR 97239, USA
c Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Oregon Health & Science University, Mail Code L458, 3181 SW Sam Jackson Park Road, Portland, OR 97239, USA
dDepartment of Obstetrics and Gynecology, Oregon Health & Science University, Mail Code L466, 3181 SW Sam Jackson Park Road, Portland, OR 97239, USA
eDivision of Maternal-Fetal Medicine, Departments of Obstetrics and Gynecology, Medical Informatics & Clinical Epidemiology, Public Health & Preventive Medicine, Oregon Evidence-based Practice Center, Oregon Health & Science University, Mail Code L466, 3181 SW Sam Jackson Park Road, Portland, OR 97239, USA
fQuality & Safety for Women’s Services, Health Services & Outcomes Research, Oregon BIRCWH K12, Comparative Effectiveness K12 & KM1, Institute for Patient Centered Comparative Effectiveness, State Obstetric and Pediatric Research Collaborative (STORC), OHSU Center of Excellence in Women’s Health, OHSU Hospital, Portland, OR 97239, USA
*Corresponding author. Division of Maternal-Fetal Medicine, Departments of Obstetrics and Gynecology, Medical Informatics & Clinical Epidemiology, Public Health & Preventive Medicine, Oregon Evidence-based Practice Center, Oregon Health & Science University, Mail Code L466, 3181 SW Sam Jackson Park Road, Portland, OR 97239. guisej/at/ohsu.edu
Keywords: VBAC, Pregnancy, Pregnancy complications, Cesarean section, Evidence review
The dictum “Once a cesarean, always a cesarean” has largely permeated the obstetric practice for most of the twentieth century and today.1 Although trial of labor after previous cesarean delivery (TOLAC) provides women who had a prior cesarean with an opportunity to achieve a vaginal birth after cesarean (VBAC), this was not considered a reasonable option until the 1970s to 1980s.24 As the annual incidence of cesarean delivery increased from less than 5 per 100 live births during the 1970s to 23.5 per 100 live births in the United States in 1988,5 the National Institute of Health (NIH) and the World Health Organization (WHO) held consensus conferences in the 1980s and concluded that cesarean delivery rates were too high and that VBAC was an acceptable approach for reducing cesarean delivery.6,7 With this change in recommendations, the annual incidence of VBAC (defined as the number of VBACs per 100 women with a prior cesarean delivery per year) increased from 5/100 (5%) in 1985 to 28.3/100 (28.3%) in 1996.8 At an individual level, successful VBAC is associated with a lower risk of maternal morbidity and fewer complications in future pregnancies; at a population level, VBAC is associated with an overall decrease in cesarean delivery.9,10 However, neither elective repeat cesarean delivery (ERCD) nor TOLAC is without risks. With increasing number of TOLAC, there were also reports of uterine scar dehiscence or rupture and associated maternal and/or neonatal morbidity and mortality.1113 In the next decade, there was a steep decline in the frequency of VBAC down to an incidence of 8.5/100 (8.5%) in 2006,14 likely caused by concern for perinatal morbidity and associated medical-legal liability.
The recent Practice Bulletin by the American College of Obstetricians and Gynecologists (ACOG) on Vaginal Birth After Previous Cesarean Delivery recommended that “most women with one previous cesarean delivery with a low transverse incision are candidates for and should be counseled about VBAC and offered TOLAC.”15 Despite this, the option of TOLAC is no longer available in one-third of hospitals16 and clinicians are less inclined to offer TOLAC.17 System-level changes, along with better identification of candidates of TOLAC, would likely be required to increase the VBAC rate.
This paper builds on a recent systematic evidence review conducted for the NIH Consensus Conference sponsored by the Agency for Healthcare Research and Quality (AHRQ) on VBAC18 and 2 meta-analyses on prediction of VBAC19 and associated perinatal outcomes.20 It particularly emphasizes the information that clinicians and patients need to make decisions.
PRACTICE OF VBAC
The overall TOLAC among US studies was 58%, with a range of 28% to 70%.18 For studies initiated after 1996, less than half of women (44%) had a TOLAC, compared with 62% of women in studies initiated before 1996.18 Many factors, including site of delivery (rural vs urban), type of hospital (teaching vs community), history of prior vaginal delivery (including prior VBAC), and race/ethnicity (black and other minorities vs white), had been identified to modify TOLAC rates.18,2125 The incidence of VBAC among people who had TOLAC is approximately 74% in the United States.18
One of the greatest challenges in counseling and managing women with previous cesarean delivery regarding whether to undergo TOLAC versus ERCD is the inability to accurately identify women who have a high probability of VBAC and those who have increased risk of morbidity with TOLAC and thus may be better candidates for ERCD. Several factors have been identified to influence the likelihood of successful VBAC; these, in turn, can influence the decision to either undergo a trial of labor or proceed with elective repeat cesarean.
One of the strongest predictors of VBAC is previous vaginal delivery (Table 1). Studies consistently report that women with a history of vaginal delivery have a higher likelihood of VBAC than women who do not have prior vaginal deliveries. Although the probability of VBAC for women without history of vaginal delivery was 65%, women with prior vaginal delivery preceding cesarean had an 83% probability of achieving VBAC; for women with prior VBAC, the probability of subsequent successful VBAC was 94%.26 A recent meta-analysis that examined predictors of VBAC similarly reported that prior vaginal delivery increases the odds of VBAC by more than threefold (odds ratio [OR] 3.41; 95% confidence interval [CI] 2.56–4.54).19 More specifically, although having the experience of vaginal delivery is a favorable prognostic predictor of VBAC (a vaginal delivery preceding cesarean increased the odds of achieving VBAC [OR 1.60; 95% CI 1.22–2.09]), women who had prior VBAC had more than fourfold the odds of having VBAC again (OR 4.39; 95% CI 2.87–6.72).19 Data from the National Institute of Child Health and Human Development Maternal-Fetal Medicine Units Network (MFMU) suggest that the number of prior VBACs remains positively correlated with increasing success of VBAC, such that, for women with 0, 1, 2, 3, and 4 or more prior VBACs, the likelihood of achieving VBAC in the current pregnancy was 63.3%, 87.6%, 90.9%, 90.6%, and 91.6%, respectively (P<.001).27
Table 1
Table 1
Factors associated with VBAC (↑, favorable factors; ↓, unfavorable factors)
When the cesarean was performed for nonrecurrent indications, such as fetal mal-presentation or breech, the probability of VBAC was approximately 75%.18,19,2830 One retrospective study reported that a previous cesarean delivery performed for malpresentation significantly increased the likelihood of VBAC (OR 7.4; 95% CI 2.8–19.2).31 Another retrospective study also reported a similar association of VBAC for breech as the indication compared with nonbreech indications, although the estimated OR was smaller (OR 1.9; 95% CI 1.0–3.7).32 These results were not pooled for meta-analysis because of differences in designation of reference comparisons but, overall, previous cesarean attributable to malpresentation as an indication was considered a favorable predictor of VBAC (see Table 1).19 It was estimated that women with a previous cesarean for malpresentation carry a risk of repeat cesarean delivery that is similar to a nulliparous woman’s risk of primary cesarean in labor: the estimated odds of repeat cesarean delivery is 0.95 (95% CI 0.7–1.30).33
Although previous cesarean for nonrecurring indications as discussed earlier is a favorable predictor of VBAC, it seems that the probability of achieving VBAC is lower if prior indication of cesarean was related to cephalopelvic disproportion (see Table 1).18,19 More specifically, when failure to progress/active phase arrest, labor dystocia, arrest of descent, or cephalopelvic disproportion were the indications of previous cesarean, the likelihood of VBAC is about 54% (48%–60%).18 The likelihood of VBAC is around 60% (49%–69%) if fetal intolerance of labor/fetal distress was the reason for prior cesarean.18 Thus, compared with previous cesarean performed for nonrecurring indications (such as malpresentation/breech), women whose previous cesarean was performed for recurring indications had lower odds of achieving VBAC (adjusted OR [aOR] 0.42–0.8; 95% CI 0.3–0.6).18,32,34,35
Some obstetric factors (gestational age at delivery, birth weight) have been shown to modify the likelihood of VBAC (see Table 1). Infant birth weight is a strong predictor: as infant birth weight increases, the likelihood of VBAC decreases such that, for women whose infant weighed more than 4000 g, the probability of VBAC was reduced by 39% to 51% relative to that of women who had smaller infants.3538 A meta-analysis that examined 5 studies reported that women whose infant weighed more than 4000 g had nearly half the likelihood of VBAC (OR 0.55; 95% CI 0.49–0.61).19 However, infant birth weight is not known before delivery, and estimating fetal weight in the third trimester is notoriously challenging and inaccurate.39,40 Several studies also examined gestational age as a predictor of VBAC, but they varied in study design and thus pooled estimates of effect cannot be generated, although the overall trend seems to be that, as gestational age increases, the likelihood of VBAC is decreased, particularly when the pregnancy progresses beyond 41 weeks’ gestation.19
Several maternal demographic factors have been examined for their potential to improve the clinician’s ability to predict VBAC (see Table 1). Of the many demographic predictors, the strongest and most consistent seems to be race/ethnicity.19 Three cohort studies report that, compared with non-Hispanic white women, Hispanic women and African American women had a lower likelihood of achieving a VBAC: a reduction of 29% to 50% for Hispanic women and 20% to 52% for African Americans.34,41,42 When these studies were examined in a meta-analysis, Hispanic women had a significantly reduced odds of VBAC (pooled OR 0.59; 95% CI 0.50–0.71) as did African American women (pooled OR 0.62; 95% CI 0.48–0.80) compared with white women.19 Although nonwhite women were more likely to undergo a TOLAC, they were less likely to achieve VBAC; the reasons for this remain unclear.25 Studies that examined the association between maternal age and VBAC report an inverse relationship: older women are less likely to have a VBAC (see Table 1). Compared with women aged 40 years or younger, women older than 40 years had nearly half the likelihood of VBAC in a meta-analysis (OR 0.53; 95% CI 0.32–0.86).19 When age was examined as a continuous variable, for every 5-year incremental increase in maternal age, the odds of VBAC also decreased (OR 0.83; 95% CI 0.79–0.87).19 When maternal age was examined as a risk factor for needing emergency cesarean in the setting of TOLAC, a positive association was again seen (OR 1.22 per incremental 5-year increase in age; 95% CI 1.16–1.28).43
Other maternal characteristics that can modify the likelihood of VBAC are maternal weight and presence of medical conditions (see Table 1). Increasing maternal body mass index (BMI) at first prenatal visit or at delivery decreases the probability of VBAC.34,37 Each unit increase in BMI at first prenatal visit decreases the likelihood of VBAC (OR 0.94; 95% CI 0.93–0.95).34 Compared with nonobese women (BMI<30 kg/m2), women with a BMI greater than or equal to 30 kg/m2 at delivery have much lower odds of VBAC (OR 0.55; 95% CI 0.51–60).37 Because many medical conditions complicating pregnancy are associated with increased risk of cesarean delivery, 3 large cohort studies reported that women with medical diseases were less likely to have VBAC, by 17% to 58%, with the following aORs: chronic hypertension (OR 0.70; 95% CI 0.56–0.86); diabetes/gestational diabetes (OR 0.42; 95% CI 0.28–0.62); and presence of any hypertension, diabetes, asthma, seizures, renal disease, thyroid disease, or collagen vascular disease (OR 0.83; 95% CI 071–0.91).35,37,42
There is considerable interest in whether the number of prior cesareans affects the likelihood of VBAC (see Table 1). Because most studies of TOLAC/VBAC focus on women with 1 prior cesarean delivery, data on TOLAC in women with more than 1 previous cesarean delivery are less clear. Two large, multicenter cohort studies report that the probability of achieving successful VBAC appears to be similar for women with 1 prior cesarean (75.5%) or more than 1 cesarean delivery (74.6%), although 1 study reported higher risks of uterine rupture whereas the other did not.44,45 Thus, the ACOG practice bulletin on VBAC stated that, “it is reasonable to consider women with 2 previous low transverse cesarean deliveries to be candidates for TOLAC, and to counsel them based on the combination of other factors that affect their probability of achieving a successful VBAC.”15 Data on the risks and outcomes of women undergoing TOLAC with 3 or more previous cesarean deliveries are scant. One multicenter cohort study did not observe any cases of composite maternal morbidity and noted a similar probability of achieving VBAC (79.8%) for women with 3 or more previous cesareans as for women with 1 prior cesarean delivery (75.5%; aOR 1.4; 95% CI 0.81–2.41).46
Induction/Augmentation of Labor and VBAC
Induction of labor (IOL) for maternal or fetal indications is increasingly common in obstetric practice and has increased from 9.5% in 1990 to 22.8% in 2007 in the United States47 Although TOLAC remains an option in women for whom induction of labor is indicated, labor induction and augmentation is associated with a decreased likelihood of VBAC (OR 0.56; 95% CI 0.38–0.83.18,19 Most studies on this topic examined the use of prostaglandin E2 (PGE2) as the cervical ripening agent: the pooled estimates of VBAC rate in women with previous cesarean who received PGE2 for IOL was approximately 63% (95% CI 58%–69%).18 Data on misoprostol or mifepristone as IOL agents are more limited; the pooled estimates of VBAC rate range between 61% and 69%.18 Although oxytocin can be used alone for the purpose of induction or for augmentation of labor, studies that examined use of oxytocin as an induction agent estimated the probability of VBAC to be 62% (95% CI 53%–70%); as an augmentation agent, oxytocin is similarly associated with decreased probability of VBAC (68%; 95% CI 64%–72%).18 The pooled estimates from a meta-analysis report that women whose labor required oxytocin augmentation had nearly half the likelihood of VBAC compared with those who did not (OR 0.52; 95% CI 0.33–0.82).19
Cervical Status at Admission and VBAC
The likelihood of VBAC may be modified by intrapartum conditions such as cervical status and labor progression. Some studies have reported that women admitted with a more favorable cervical status (eg, cervical dilation >4 cm, advanced effacement) in spontaneous labor have a twofold increase in the likelihood of VBAC compared with those with unfavorable cervix (OR 2.2–2.6; 95% CI 1.7–2.8).19,37,48 When As a continuous variable, each centimeter in cervical dilatation at admission is associated with increased odds of VBAC (OR 1.89; 95% CI 1.13–3.22).49 More than 75% effacement of the cervix (compared with 25% effacement) at admission also increases the likelihood of VBAC (OR 2.72; 95% CI 2.00–3.71).48
Because a successful VBAC cannot be guaranteed, and because risks versus benefits may be disproportionately associated with a failed trial of labor after cesarean (in which a woman undergoes a repeat cesarean delivery after a trial of labor) compared with an elective repeat cesarean or a successful VBAC, the appropriate statistical comparison for both research and patient counseling regarding mode of delivery for women with a previous cesarean is by intention to deliver: TOLAC versus ERCD.18 This article focuses on the risks of morbidity associated with TOLAC and those associated with ERCD.
Maternal Death
Despite improvement in medical technology and care, maternal mortality increased from 7 to 9 per 100,000 in the 1980s and 1990s to 12 to 15 per 100,000 since 2003.50,51 Although the absolute risk of maternal death remains low, a meta-analysis found that maternal mortality is higher for ERCD, at 13.4 per 100,000 (95% CI 4.3–41.6 per 100,000 ERCD) compared with 3.8 per 100,000 TOLAC (95% CI 0.9–15.5 per 100,000 TOLAC).18,20 One study examined whether hospitals with low delivery volumes (defined as fewer than 500 deliveries per year) were associated with increased odds of maternal mortality with TOLAC and did not observe a statistical significance because of the small number of maternal deaths.52
Uterine Rupture
Uterine rupture is potentially life threatening and catastrophic for the expecting mother and her fetus(es), and it is the outcome associated with TOLAC that most significantly increases the risk of perinatal morbidity and mortality.9,18 Among studies that examined uterine rupture for both TOLAC and ERCD groups, the overall incidence of uterine rupture was 0.30% (95% CI 0.23%–0.40%); however, 96% of ruptures occurred in women who had TOLAC.18 Thus, despite the absolute risk of uterine rupture remaining low, the risk of uterine rupture is higher for women undergoing TOLAC than ERCD (Table 2). In addition, the occurrence of uterine rupture was higher for studies limited to term pregnancies compared with studies that included women of any gestational age at delivery (0.78% vs 0.32%, respectively; P = .03).18 When the direction of previous uterine incision was examined as a risk factor for uterine rupture, one multicenter cohort study reported that women with a low, transverse cesarean delivery or an unknown scar have the lowest risk of rupture (0.63%–0.75%).18,53
Table 2
Table 2
Maternal outcomes associated with TOLAC versus ERCD
Another factor that may modify the risk of uterine rupture is IOL. More specifically, the risk of uterine rupture among women who had induction was lowest with oxytocin (1.1%), followed by PGE2 (2%), and highest with misoprostol (6%); however, these risk estimations may be imprecise given the consistency in study design and methodology, so these results should be interpreted with caution.18 In particular, the method of induction is likely associated with the cervical status as well as the duration of induction, which may confound the strength of the associations reported in many studies. Individual factors associated with uterine rupture included increasing maternal age, prior vaginal delivery or VBAC, increased number of previous cesarean deliveries, increased gestational age at delivery, shorter interpregnancy interval, induction/augmentation of labor, epidural anesthesia, and having a single-layer uterine closure on previous cesarean.18
Although the presence of risk factors may help identify women at higher risk of uterine rupture, the diagnosis of rupture can be challenging because there is no single sign that reliably indicates the occurrence of rupture. Fetal heart rate tracing abnormalities, especially fetal bradycardia (reported in 33%–100% of uterine ruptures), are the most commonly observed signs of uterine rupture.3,5456 Others include maternal vaginal bleeding, pain, and abnormal uterine contraction patterns.48
Hysterectomy
Among the 8 studies that examined the risk of hysterectomy among women with previous cesarean, the summary incidence was 0.28% for women who had ERCD (95% CI 0.12%–0.67%) and 0.17% for women who had a trial of labor (95% CI 0.12%–0.26%), which were not statistically significantly different (see Table 2).18 Among term pregnancies, the incidence of hysterectomy among women who had TOLAC and ERCD were similar (0.14% vs 0.16%, respectively; P = .67). When the risk of hysterectomy was compared among women who had TOLAC after 1 cesarean, TOLAC after 2 or more cesareans, and ERCD, the incidence of hysterectomy was lowest among women with TOLAC after 1 cesarean delivery (0.2%), whereas it was 0.4% among women who had ERCD, and highest (0.6%) among women who had TOLAC after multiple previous cesareans.36
Hemorrhage and Transfusion
Studies report increased rates of hemorrhage associated with ERCD (0.3%–29%) compared with TOLAC, but none found a statistically significant difference between the 2 groups (see Table 2).18 Inconsistent definitions of hemorrhage used by various studies probably contributed to the wide range of hemorrhage rates reported. In addition, physicians’ estimation of blood loss has been known to be imprecise and this adds to the challenge of studying this topic.18 Because these studies did not use similar definitions to diagnose hemorrhage, these data were not combined to provide pooled estimates.
The difference in pooled incidences of transfusion among women who had TOLAC (0.9%) and women who had ERCD (1.2%) was not statistically significant (see Table 2).18 However, when data were limited to only term pregnancies, the risk of transfusion was higher for TOLAC (0.7%; 95% CI 0.2%–2.2%) than for ERCD (0.5%; 95% CI 0.2%–1.3%), with a relative risk (RR) that is higher for TOLAC (RR 1.30; 95% CI 1.15 to 1.4).18 When the risk of transfusion was stratified among women who had ERCD and women who had indicated repeat cesarean (IRCD) with or without labor, women who had IRCD without labor had a higher risk of transfusion, suggesting that maternal comorbid conditions contribute to the risk of transfusion.53
Infection
There was no significant difference in the overall infection risk between women who had TOLAC and women who had ERCD (see Table 2).18 When infection was further stratified by type (endometritis, chorioamnionitis, wound infection, and fever), a higher risk of endometritis was seen in women who had TOLAC (0.8%–30%) than those who had ERCD (1.2%–18%).18 There was a significant increase in the rate of endometritis with increasing BMI such that, in morbidly obese women (BMI >40 kg/m2), TOLAC is associated with more than twice the odds of endometritis than ERCD (aOR 2.4; 95% CI 1.7–3.5).57 Similarly, a higher incidence of chorioamnionitis was seen in women who had TOLAC compared with those who had ERCD.58,59 There was no statistically significant difference in the risk of wound infection in TOLAC compared with ERCD.18 The pooled incidence of febrile morbidity was 6.5% (95% CI 4.4%–9.3%) for women who had TOLAC and 7.2% (2.5%–18.9%) for women who had ERCD; the relative risk of fever for TOLAC was significantly lower than ERCD (RR 0.63; 95% CI 0.43–0.91).18 When the association of fever was further evaluated by outcomes of TOLAC, women who had either cesarean after a trial of labor or ERCD had higher risk compared with those who had successful VBAC, thus suggesting surgery as a risk factor for febrile morbidity.18,59,60
Surgical Injury
Surgical injury is a rare complication during delivery. Secondary data analyses from a multicentered large cohort study suggest that the risk of surgical injury between TOLAC and ERCD was not statistically significantly different (see Table 2).18,46,53,57,61
Women who choose an ERCD or those who have an unsuccessful TOLAC will likely require cesarean delivery for all future pregnancies, making it important to understand the risks, including hysterectomy and placental abnormalities, associated with multiple prior cesareans.
Hysterectomy
Hysterectomy rates increased with each additional cesarean in all studies. 4,13,16,17,19,20,22 The OR for hysterectomy increased with the number of prior cesareans, from 0.7 to 2.14 with 1 prior cesarean, 1.4 to 7.9 with 1 or more prior cesareans, and to 3.8 to 18.6 with 2 or more prior cesareans. The association between increased risk of hemorrhage, blood transfusion, surgical injury, and adhesions with increasing number of cesarean deliveries was consistently reported in all studies.18,20 Increasing number of cesarean deliveries was not associated with a change in perioperative infection or wound complications.
Placenta Previa
Prior cesarean was a statistically significant risk factor for placenta previa compared with prior normal spontaneous vaginal delivery (NSVD; OR 1.48–3.95).18 The pooled analysis estimated the absolute risk of previa associated with any number of cesareans as 12 per 1000 (95% CI 8, 15 per 1000; P<.001).20 The incidence with each additional prior cesarean delivery increased from 10 per 1000 with 1 prior cesarean delivery (95% CI 6, 13 per 1000) to 28 per 1000 (95% CI 18, 37 per 1000) with 3 or more cesarean deliveries. Women with no prior cesarean delivery and previa required hysterectomy in 0.7% to 4% of cases compared with 50% to 67% in women with 3 or more prior cesarean deliveries.34,6264
Placenta Accreta
The incidence of placenta accreta increased with increasing number of cesarean deliveries. The increased incidence did not reach statistical significance until women had at least 2 prior cesarean deliveries compared with no prior cesarean delivery (OR 8.6–29.8).18 Women with 1 prior cesarean delivery had a rate of accreta of 0.3% to 0.6%. In comparison with women without prior cesarean delivery, the OR for accreta with 1 prior cesarean delivery was 1.3 to 2.16, which was not statistically significant. The incidence of accreta continued to increase with increasing prior cesarean delivery up to 6.74% for women with 5 or more prior cesarean delivery compared with no prior cesarean delivery, with an OR of 29.8.18
Two studies noted a statistically significant increase in accreta in women with previa and prior cesarean delivery.3,4 As the number of prior cesarean delivery increased, the presence of placenta previa increased the likelihood of placenta accreta from 3.3% to 4% in women undergoing their first cesarean delivery to 50% to 67% in women with 4 or more prior cesarean delivery. The risk of hysterectomy in women with accreta and prior cesarean delivery was not reported separately, but 2 studies found that accreta was a significant risk factor for hysterectomy (OR 43–99.5; 95% CI 19.0,∞).13,16
Each additional cesarean is associated with increased maternal morbidity in a dose-response fashion, especially for women with 3 or more prior cesareans, who are at statistically significant increased risk of previa, accreta, and hysterectomy.
For most of the twentieth century, “Once a cesarean, always a cesarean” was the standard obstetric practice. Although TOLAC is deemed an appropriate option in women with previous cesarean delivery, assessment of individual risks and the likelihood of successful VBAC are important in determining who may be appropriate candidates for TOLAC. Much effort has been put forth to improve the identification of prognostic factors associated VBAC and to develop normograms for predicting VBAC and associated morbidity.31,34,49,65 In addition, patient involvement in the decision-making process and counseling of TOLAC/VBAC has been associated with increased choice of TOLAC as well as increased patient satisfaction. Early timing of counseling is likely to be important because nearly half of the women with prior cesarean make decisions about future TOLAC before becoming pregnant again.19
Ideally, good candidates for planned TOLAC are women in whom the balance between risks (desirably as low as possible) and success (as high as possible) is acceptable both to the patient and the clinician. However, this is often an individual decision, and what is considered acceptable for 1 patient may be different for another. Thus, counseling of women with previous cesarean delivery who are considering their delivery options involves personalized information. The key in facilitating a woman’s decision with respect to undergoing a TOLAC is proper counseling regarding her chances of success, a uterine rupture, and injury to herself or fetus if she experiences a uterine rupture.
Informed consent today for any woman who desires a TOLAC must address 4 specific questions: (1) what is her chance of having a successful VBAC? (2) What is the risk that she will have a uterine rupture if she does attempt a VBAC? (3) What is the chance of harm or death to her baby if the uterus ruptures? (4) What are the risks of undergoing a repeat cesarean delivery? In addition, future fertility/family plans present as a key factor that should be considered because multiple cesareans increase a woman’s risk for future pregnancy complications. In particular, the risk of placenta previa, accreta, and hysterectomy increases in a dose-response fashion with increasing number of cesarean deliveries, so clinicians should elucidate future pregnancy/family plans and incorporate such in the decision-making process with the patient.
The annual incidence of cesarean delivery in the United States continues to increase such that today, nearly 1 in 3 pregnant women undergo cesarean.48 This trend is contrary to the national goal of decreasing cesarean delivery in low-risk women.66,67 Although there are many potential causes, the decline in VBACs contributes to the continual increase in cesarean deliveries. Prior cesarean delivery is the most common indication for cesarean and accounts for more than one-third of all cesareans. As the most common inpatient surgical procedure performed in the United States, cesarean delivery also accounts for nearly half of the childbirth-related expenses of hospitalization, at $7.8 billion annually.18 Thus, the appropriate use and safety of cesarean and VBAC are of concern not only at the individual patient and clinician level but they also have far-reaching public health and policy implications at the national level. Although TOLAC/VBAC is a reasonable and safe option for most women with prior cesarean delivery, careful consideration of risks/benefits and assessment of individual factors is vital in this decision-making process.
Acknowledgments
Financial disclosure: this work was funded by the Agency for Healthcare Research and Quality, contract no. HHSA 290-2007-10057-I, task order no. 4 for the Office of Medical Applications of Research at the National Institutes of Health.
1. Cragin EB. Conservatism in obstetrics. NY Med J. 1916;104:1–3.
2. Lavin JP, Stephens RJ, Miodovnik M, et al. Vaginal delivery in patients with a prior cesarean section. Obstet Gynecol. 1982;59:135–148. [PubMed]
3. Flamm BL, Newman LA, Thomas SJ, et al. Vaginal birth after cesarean delivery: results of a 5-year multicenter collaborative study. Obstet Gynecol. 1990;76:750–754. [PubMed]
4. Miller DA, Diaz FG, Paul RH. Vaginal birth after cesarean: a 10-year experience. Obstet Gynecol. 1994;84:255–258. [PubMed]
5. Centers for Disease Control and Prevention (CDC) Rates of cesarean delivery— United States 1991. MMWR Morb Mortal Wkly Rep. 1993;42:285–289. [PubMed]
6. Cesarean Childbirth: report of a Consensus Development Conference. Sponsored by the NICHD in conjunction with the National Center for Health Care Technology and assisted by the Office for Medical Applications of Research. Washington, DC: NIH Publication; 1981. pp. 82–2067.
7. Appropriate technology for birth. Lancet. 1985;2:436–437. [PubMed]
8. Menacker F, Declercq E, Macdorman MF. Cesarean delivery: background, trends, and epidemiology. Semin Perinatol. 2006;30:235–241. [PubMed]
9. American College of Obstetricians and Gynecologists. Practice Bulletin: Clinical management guidelines for obstetrician-gynecologists. Vaginal birth after previous cesarean delivery. Obstet Gynecol. 2010;116:450–463. [PubMed]
10. Curtin SC. Rates of cesarean birth and vaginal birth after previous cesarean, 1991–95. Mon Vital Stat Rep. 1997;45(11 Suppl 3):1–12.
11. Sachs BP, Kobelin C, Castro MA, et al. The risks of lowering the cesarean-delivery rate. N Engl J Med. 1999;340:54–57. [PubMed]
12. Phelan JP. VBAC: time to reconsider? OBG Management. 1996;8:64–68.
13. Caughey AB, Shipp TD, Repke JT, et al. Rate of uterine rupture during a trial of labor in women with one or two prior cesarean deliveries. Am J Obstet Gynecol. 1999;181:872–876. [PubMed]
14. Martin JA, Hamilton EB, Sutton PD, et al. Births: final data for 2006. Natl Vital Stat Rep. 2009;57:1–104.
15. The American College of Obstetricians and Gynecologists Practice Bulletin—Clinical Guidelines for Obstetrician-Gynecologists. Vaginal birth after previous cesarean delivery. No 115, August 2010 (replaces Practice Bulletin No 54, July 2004 and Committee Opinion No 342, August 2006) Obstet Gynecol. 2010;116:450–463. [PubMed]
16. National Institutes of Health. Consensus Development Conference statement. Bethesda (MD): NIH; 2010. [Accessed November 9, 2010]. NIH Consensus Development Conference: vaginal birth after cesarean: new insights. Available at: http://consensus.nih.gov/2010/images/vbac/vbac_statement.pdf.
17. Angelini DJ, Greenwald L. Closed claims analysis of 65 medical malpractice cases involving nurse-midwives. J Midwifery Womens Health. 2005;50:454–460. [PubMed]
18. Guise JM, Eden K, Emeis C, et al. Vaginal birth after cesarean: new insights. Evidence Report/Technology Assessment No. 191 (Prepared by the Oregon Health & Science University Evidence-based Practice Center under contract no. 290-2008-10057-I). AHRQ Publication No. 10-E003. Rockville (MD): Agency for Healthcare Research and Quality; 2010.
19. Eden KB, McDonagh M, Denman MA, et al. New insights on vaginal birth after cesarean: can it be predicted? Obstet Gynecol. 2010;116:967–981. [PubMed]
20. Guise JM, Denman MA, Emeis C, et al. Vaginal birth after cesarean: new insights on maternal and neonatal outcomes. Obstet Gynecol. 2010;115:1267–1278. [PubMed]
21. McMahon MJ, Luther ER, Bowes WA, Jr, et al. Comparison of a trial of labor with an elective second cesarean section. N Engl J Med. 1996;335:689–695. [PubMed]
22. Cameron CA, Roberts CL, Peat B. Predictors of labor and vaginal birth after cesarean section. Int J Gynaecol Obstet. 2004;85:267–269. [PubMed]
23. Hueston WJ, Rudy M. Factors predicting elective repeat cesarean delivery. Obstet Gynecol. 1994;83:741–744. [PubMed]
24. Pang MW, Law LW, Leung TY, et al. Sociodemographic factors and pregnancy events associated with women who declined vaginal birth after cesarean section. Eur J Obstet Gynecol Reprod Biol. 2009;143:24–28. [PubMed]
25. Selo-Ojeme D, Abulhassan N, Mandal R, et al. Preferred and actual delivery mode after cesarean in London UK. Int J Gynaecol Obstet. 2008;102:156–159. [PubMed]
26. Elkousy MA, Sammel M, Stevens E, et al. The effect of birthweight on vaginal birth after cesarean delivery success rates. Am J Obstet Gynecol. 2003;188:824–830. [PubMed]
27. Mercer BM, Gilbert S, Landon MB, et al. Labor outcomes with increasing number of prior vaginal births after cesarean delivery. Obstet Gynecol. 2008;111:285–291. [PubMed]
28. Van Gelderen CJ, England MJ, Naylor GA, et al. Labour in patients with a cesarean section scar. The place of oxytocin augmentation. S Afr Med J. 1998;70:529–532. [PubMed]
29. Horenstein JM, Eglinston GS, Tahilramaney MP, et al. Oxytocin use during a trial of labor in patients with previous cesarean section. J Reprod Med. 1984;29:26–30. [PubMed]
30. Flamm BL, Goings JR, Fuelberth NJ, et al. Oxytocin during labor after previous cesarean section: results of a multicenter study. Obstet Gynecol. 1987;70:709–712. [PubMed]
31. Gonen R, Tamir A, Degani S, et al. Variables associated with successful vaginal birth after one cesarean section: a proposed vaginal birth after cesarean section score. Am J Perinatol. 2004;21:447–453. [PubMed]
32. Weinstein D, Benshushan A, Tanos V, et al. Predictive score for vaginal delivery after cesarean section. Am J Obstet Gynecol. 1996;174:192–198. [PubMed]
33. Shipp TD, Zelop CM, Repke JT, et al. Labor after previous cesarean: influence of prior indication and parity. Obstet Gynecol. 2000;95:913–916. [PubMed]
34. Grobman WA, Lai Y, Landon MB, et al. Development of a nomogram for prediction of vaginal birth after cesarean delivery. Obstet Gynecol. 2007;109:806–812. [PubMed]
35. Gyamfi C, Juhasz G, Gyamfi P, et al. Increased success of trial of labor after previous vaginal birth after cesarean. Obstet Gynecol. 2004;104:715–719. [PubMed]
36. Landon MB, Spong CY, Thom E, et al. Risk of uterine rupture with a trial of labor in women with multiple and single prior cesarean delivery. Obstet Gynecol. 2006;108:12–20. [PubMed]
37. Landon MB, Leindecker S, Spong CY, et al. The MFMU Cesarean Registry: factors affecting the success of trial of labor after previous cesarean delivery. Am J Obstet Gynecol. 2005;193:1016–1023. [PubMed]
38. Zelop CM, Shipp TD, Cohen A, et al. Trial of labor after 40 weeks’ gestation in women with prior cesarean. Obstet Gynecol. 2001;97:391–393. [PubMed]
39. Chauhan SP, Cowan BD, Magann EF, et al. Intrapartum detection of a macrosomic fetus: clinical versus 8 sonographic models. Aust N Z J Obstet Gynaecol. 1995;35:266–270. [PubMed]
40. Hiratal GI, Medearis AL, Horenstein J, et al. Ultrasonographic estimation of fetal weight in the clinically macrosomic fetus. Am J Obstet Gynecol. 1990;162:238–242. [PubMed]
41. King DE, Lahiri K. Socioeconomic factors and the odds of vaginal birth after cesarean delivery. JAMA. 1994;272:524–529. [PubMed]
42. Srinivas SK, Stamilio DM, Stevens EJ, et al. Predicting failure of a vaginal birth attempt after cesarean delivery. Obstet Gynecol. 2007;109:800–805. [PubMed]
43. Smith GC, White IR, Pell JP, et al. Predicting cesarean section and uterine rupture among women attempting vaginal birth after prior cesarean section. PLoS Med. 2005;2:e252. [PMC free article] [PubMed]
44. Macones GA, Cahill A, Pare E, et al. Obstetric outcomes in women with two prior cesarean deliveries: is vaginal birth after cesarean delivery a viable option? Am J Obstet Gynecol. 2005;192:1223–1228. [PubMed]
45. Asakura H, Myers SA. More than one previous cesarean delivery: a 5-year experience with 435 patients. Obstet Gynecol. 1995;95:924–929. [PubMed]
46. Cahill AG, Tuuli M, Odibo AO, et al. Vaginal birth after cesarean for women with three or more prior cesareans: assessing safety and success. BJOG. 2010;117:422–427. [PubMed]
47. Martin JA, Hamilton BE, Sutton PD, et al. Birth: final data for 2007. Natl Vital Stat Rep. 2010;58:1–125. [PubMed]
48. Flamm BL, Geiger AM. Vaginal birth after cesarean delivery: an admission scoring system. Obstet Gynecol. 1997;90:907–910. [PubMed]
49. Macones GA, Hausman N, Edelstein R, et al. Predicting outcomes of trials of labor in women attempting vaginal birth after cesarean delivery: a comparison of multivariate methods with neural networks. Am J Obstet Gynecol. 2001;194:409–413. [PubMed]
50. Hoyert DL. Maternal mortality and related concepts. Vital Health Stat. 2007;33:1–13. [PubMed]
51. Kung HC, Hoyert DL, Xu J, et al. Death: final data for 2005. Natl Vital Stat Rep. 2008;56:1–120. [PubMed]
52. Wen SW, Rusen ID, Walker M, et al. Maternal Health Study Group, Canadian Perinatal Surveillance System. Comparison of maternal mortality and morbidity between trial of labor and elective cesarean section among women with previous cesarean delivery. Am J Obstet Gynecol. 2004;191:1263–1269. [PubMed]
53. Spong CY, Landon MB, Gilbert S, et al. National Institute of Child Health and Human Development (NICHD) Maternal-Fetal Medicine Units (MFMU) Network. Risk of uterine rupture and adverse perinatal outcome at term after cesarean delivery. Obstet Gynecol. 2007;110:801–807. [PubMed]
54. Guise JM, McDonagh MS, Hashima J, et al. Vaginal birth after cesarean (VBAC) Evid Rep Technol Assess (Summ) 2003;(71):1–8. [PubMed]
55. Cowan RK, Kinch RA, Ellis B, et al. Trial of labor following cesarean delivery. Obstet Gynecol. 1994;83:933–936. [PubMed]
56. Flamm BL, Lim OW, Jones C, et al. Vaginal birth after cesarean section: results of a multicenter study. Am J Obstet Gynecol. 1998;158:1079–1084. [PubMed]
57. Hibbard JU, Gilbert S, Landon MB, et al. Trial of labor or repeat cesarean delivery in women with morbid obesity and previous cesarean delivery. Obstet Gynecol. 2006;108:125–133. [PubMed]
58. Kugler E, Shoham-Vardi I, Burstein E, et al. The safety of a trial of labor after cesarean section in a grandmultiparous population. Arch Gynecol Obstet. 2008;277:339–344. [PubMed]
59. Dumwald C, Mercer B. Vaginal birth after cesarean delivery: predicting success, risks of failure. J Matern Fetal Neonatal Med. 2004;15:388–393. [PubMed]
60. Eglinton GS, Phelan JP, Yeh S, et al. Outcome of a trial of labor after prior cesarean delivery. J Reprod Med. 1984;29:3–8. [PubMed]
61. Silver RM, Landon MB, Rouse DJ, et al. Maternal morbidity associated with multiple repeat cesarean deliveries. Obstet Gynecol. 2006;107:1226–1232. [PubMed]
62. Zelop CM, Harlow BL, Frigoletto FD, Jr, et al. Emergency peripartum hysterectomy. Am J Obstet Gynecol. 1993;168:1443–1448. [PubMed]
63. Juntunen K, Makarainen L, Kirkinen P. Outcome after a high number (4–10) of repeat cesarean sections. BJOG. 2004;111:561–563. [PubMed]
64. Lynch CM, Kearney R, Turner MJ. Maternal morbidity after elective repeat cesarean section after two or more previous procedures. Eur J Obstet Gynecol Reprod Biol. 2003;106:10–13. [PubMed]
65. Grobman WA, Lai Y, Landon MB, et al. Can a prediction model for vaginal birth after cesarean also predict the probability of morbidity related to a trial of labor? Am J Obstet Gynecol. 2009;200:56, e1–e6. [PMC free article] [PubMed]
66. Healthy People. Maternal, infant, and child health. Department of Health and Human Services; 2010. [Accessed November 9, 2010]. Available at: http://www.healthypeople.gov/2010/Data/midcourse/html/focusareas/FA16ProgressHP.htm.
67. Healthy People. Maternal, infant, and child health. Department of Health and Human Services; 2020. [Accessed November 9, 2010]. Available at: http://www.healthypeople.gov/HP2020/Objectives/ViewObjective.aspx?Id=161&TopicArea=Maternal%2c+Infant+and+Child+Health&Objective=MICH+HP2020%e2%80%936&TopicAreaId=32.