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VBAC Calculator

Calculate your statistical probability of a successful vaginal birth after cesarean (VBAC) using the validated Grobman model.

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What is VBAC and the Trial of Labor After Cesarean (TOLAC)?

Vaginal Birth After Cesarean (VBAC) refers to giving birth vaginally after having had one or more previous deliveries by cesarean section. Attempting a vaginal birth after a prior cesarean is clinically known as a Trial of Labor After Cesarean (TOLAC). According to the American College of Obstetricians and Gynecologists (ACOG Practice Bulletin #205), attempting TOLAC is a safe, appropriate, and reasonable choice for most women with a prior low transverse uterine incision.

The Grobman MFMU VBAC Prediction Model

The most widely utilized and rigorously validated clinical algorithm for predicting VBAC success was developed by Dr. William Grobman and the Maternal-Fetal Medicine Units (MFMU) Network of the National Institute of Child Health and Human Development (NICHD). Based on prospective data from over 11,000 women undergoing TOLAC, the multivariable logistic regression model estimates individual success probability using key antenatal factors:

$$\text{Log-Odds } (w) = 3.655 - (0.040 \times \text{Age}) - (0.038 \times \text{BMI}) - \beta_{\text{Race}} + 0.893 \times (\text{Prior Vaginal Delivery}) + 0.681 \times (\text{Prior VBAC}) - 0.668 \times (\text{Recurring Indication}) - 0.413 \times (\text{Hypertension})$$

The predicted probability of a successful vaginal delivery (\(P\)) is then calculated as:

$$P(\text{VBAC}) = \frac{e^w}{1 + e^w} \times 100\%$$

Clinical Factors Influencing VBAC Success

Clinical Factor Favorable for VBAC Unfavorable for VBAC
Obstetric History Prior successful vaginal delivery or prior VBAC No prior vaginal deliveries
Prior C-Section Indication Non-recurring (breech presentation, fetal heart rate concern) Recurring (dystocia, arrest of dilation, cephalopelvic disproportion)
Maternal Demographics Younger maternal age, normal pre-pregnancy BMI Advanced maternal age, obesity (BMI > 30 kg/m²)
Labor Characteristics Spontaneous labor onset, favorable cervical Bishop score Need for cervical ripening / induction of labor

Interpreting Your VBAC Probability Score

Overall, 60% to 80% of women who attempt a trial of labor after one prior low-transverse cesarean achieve a successful vaginal delivery. Clinical research shows that when a patient's predicted success probability is 60% to 70% or greater, the maternal and neonatal complication rates of TOLAC are lower than or equal to those associated with an elective repeat cesarean delivery (ERCS).

For calculating other pregnancy timelines and milestones, explore the Pregnancy Due Date Calculator and the Pregnancy Conception Calculator.

Frequently Asked Questions

What is the success rate of a Trial of Labor After Cesarean (TOLAC)?

Across major obstetric studies, between 60% and 80% of eligible women who attempt TOLAC have a successful vaginal birth. A previous vaginal delivery—especially a previous VBAC—is the single strongest predictor of success, increasing success rates to approximately 85% to 90%.

What is the risk of uterine rupture during a VBAC trial of labor?

In women with one prior low-transverse uterine incision undergoing spontaneous labor, the risk of uterine rupture is low—typically between 0.5% and 0.9% (approximately 5 to 9 per 1,000 women). Because of this risk, TOLAC is conducted in hospital facilities equipped to perform emergency cesarean deliveries.

What are the benefits of a successful VBAC compared to a repeat cesarean?

A successful VBAC avoids major abdominal surgery, resulting in faster postpartum recovery, lower blood loss, decreased infection risk, shorter hospital stays, and reduced risks of placental complications (placenta previa and placenta accreta spectrum) in subsequent pregnancies.

Who is not a candidate for VBAC?

Contraindications to TOLAC include a prior classical (vertical) or T-shaped uterine incision, prior extensive transfundal uterine surgery (such as certain myomectomies), prior history of uterine rupture, or any standard obstetric contraindications to vaginal delivery (such as active genital herpes lesions or placenta previa).