Outcome of trial of labour for vaginal birth after one caesarean section

Authors

  • Reefaat Rahman

    Department of Obstetrics and Gynaecology, Bangladesh Medical University, Dhaka, Bangladesh

  • Begum Nasrin

    Department of Obstetrics and Gynaecology, Bangladesh Medical University, Dhaka, Bangladesh

  • Tarafder Runa Laila

    Department of Obstetrics and Gynaecology, Bangladesh Medical University, Dhaka, Bangladesh

  • Farzana Aktar

    Department of Obstetrics and Gynaecology, Dhaka Medical College Hospital, Dhaka, Bangladesh

  • Nurun Nahar Khanam

    Department of Obstetrics and Gynaecology, Bangladesh Medical University, Dhaka, Bangladesh

DOI:

Keywords

VBAC, TOLAC, caesarean section, outcome  

Correspondence

Reefaat Rahman
Email: reefaatrahman@bmu.ac.bd

Publication history

Received: 13 June 2025
Accepted: 17 Nov 2025
Published online: 7 Jan 2026

Responsible editor

Reviewer

Funding

Funded by Bangabandhu Sheikh Mujib Medical University (currently, Bangladesh Medical University) Dhaka, Bangladesh, Ref No: BSMMU/2023/954(3),
Dated 25 Jan 2023

Ethical approval

Approved by IRB of Bangabandhu Sheikh Mujib Medical University (currently, Bangladesh Medical University) Dhaka, Bangladesh (Ref No: BSMMU/2022/7374, Dated 31 July 2022)

Trial registration number

Not applicable

Copyright

© The Author(s) 2025; all rights reserved. 
Published by Bangladesh Medical University (former Bangabandhu Sheikh Mujib Medical University).
Abstract
Background: Vaginal birth after cesarean section (VBAC) is a vital option for women with a prior cesarean section (C/S), but its success depends on some maternal factors, obstetric history, and labor conditions. This study aimed to find out the potential risks and benefits of vaginal birth after cesarean section.

Methods: This cross-sectional study was conducted in the Department of Obstetrics and Gynaecology, Bangabandhu Sheikh Mujib Medical University (currently, Bangladesh Medical University), Dhaka, Bangladesh, from January 2023 to December 2024. This study included 162 pregnant women with a history of one C/S attending the Obstetrics and Gynaecology department of BSMMU.

Results: Most of the participants (75.3%) were between 21–30 years old. Among the women who attempted TOLAC, 33.3% successfully had a VBAC, while 66.7% required an emergency repeat cesarean section. Fetal distress (51.3%) was the most common reason for the previous cesarean and the main cause of emergency repeat cesarean section after failed trial, which is 48.2%. Babies born through VBAC had satisfactory neonatal outcomes, with 90.7% having a good Apgar score (>7) compared to 75.9% in the emergency repeat caesarean section (ERCS) group.

Conclusion: This study found that fetal distress is a major factor leading to ERCS and underscores the better neonatal outcomes and lower postpartum hemorrhage rates in VBAC deliveries.
Key messages
This study shows that VBAC is a safe and effective option for appropriately selected women, with favourable maternal and neonatal outcomes. Implementing standardized counselling, strict eligibility criteria and continuous intrapartum monitoring can significantly increase VBAC success rates. Strengthening VBAC practices may help reduce unnecessary repeat caesarean sections and improve overall obstetric care quality in our setting.
Introduction

Vaginal birth after cesarean section (VBAC), the term that describes a vaginal delivery in a woman who has given birth via cesarean section in a previous pregnancy. Patients desiring VBAC delivery need to undergo a trial of labor, popularly known as a trial of labor after cesarean section (TOLAC). Delivery by cesarean section has increased significantly worldwide. In the United States, this rate increased from 5% in 1970 to 32.9% in 2009 and 31.9% in 2016 [1]. Several efforts failed to achieve the 15% cesarean delivery rate recommended by WHO [2].


The principal contributing factor to the overall increased cesarean section (CS) rates is repeat CS [3] Historically, the dictum "once a cesarean, always a cesarean" was introduced by Cragin in 1916, during the era of classical cesarean sections [4]. With the advent of lower-segment cesarean sections (LSCS), the safety of cesarean delivery has improved significantly. Modern practice now emphasises institutional delivery with proper monitoring and emergency support rather than routine repeat cesarean [5]. Vaginal delivery following cesarean surgery is a generally safe method compared to repeat CS, according to several studies [6], with the increasing rate of primary cesarean deliveries, more women are facing the prospect of repeat surgeries. A trial of labor after vaginal delivery can minimise the risk of repeated cesarean sections for women.

Patients with a previous cesarean have two options: planned repeat cesarean delivery (PRCD) or TOLAC, which may lead to either successful VBAC or unplanned cesarean. While successful VBAC reduces surgical risks, failed TOLAC can increase complications for both mother and baby more than an elective repeat CS [7]. The solution to this concern would be a careful selection of the patient for VBAC [8].

There are no official national VBAC statistics for Bangladesh. Instead, available data comes from specific hospital-based studies. Studies in various Bangladeshi hospitals report different success rates among selected, eligible patients attempting a trial of labor (TOLAC). One 2023 study in a private hospital found a success rate of 69.3% among cases enrolled in a trial of labor [9]. Another study done in a private hospital found a success rate of 64.8% among the patients who underwent a trial of labor [10].

In addition, with rising global cesarean section rates, promoting safe and successful VBAC can help reduce maternal morbidity, improve recovery times, and lower healthcare costs. However, the decision to pursue TOLAC is complex and influenced by multiple factors, including maternal characteristics, obstetric history, and hospital resources. Therefore, this study aimed to find out the potential risks and benefits of vaginal birth after cesarean section and to analyse the factors that influence the outcomes.  
  

Groups based on pre-test marks

Pretest
marks (%)

Posttest

Marks (%)

Difference in pre and post-test marks (mean improvement)

P

Didactic lecture classes

<50%

36.6 (4.8)

63.2 (9.4)

26.6

<0.001

≥50%

52.8 (4.5)

72.4 (14.9)

19.6

<0.001

Flipped classes

<50%

36.9 (4.7)

82.2 (10.8)

45.4

<0.001

≥50%

52.8 (4.6)

84.2 (10.3)

31.4

<0.001

Data presented as mean (standard deviation)

Background characteristics

Number (%)

Age at presentation (weeks)a

14.3 (9.2)

Gestational age at birth (weeks)a

37.5 (2.8)

Birth weight (grams)a

2,975.0 (825.0)

Sex

 

Male

82 (41)

Female

118 (59)

Affected side

 

Right

140 (70)

Left

54 (27)

Bilateral

6 (3)

Delivery type

 

Normal vaginal delivery

152 (76)

Instrumental delivery

40 (20)

Cesarean section

8 (4)

Place of delivery

 

Home delivery by traditional birth attendant

30 (15)

Hospital delivery by midwife

120 (60)

Hospital delivery by doctor

50 (25)

Prolonged labor

136 (68)

Presentation

 

Cephalic

144 (72)

Breech

40 (20)

Transverse

16 (8)

Shoulder dystocia

136 (68)

Maternal diabetes

40 (20)

Maternal age (years)a

27.5 (6.8)

Parity of mother

 

Primipara

156 (78)

Multipara

156 (78)

aMean (standard deviation), all others are n (%)

Background characteristics

Number (%)

Age at presentation (weeks)a

14.3 (9.2)

Gestational age at birth (weeks)a

37.5 (2.8)

Birth weight (grams)a

2,975.0 (825.0)

Sex

 

Male

82 (41)

Female

118 (59)

Affected side

 

Right

140 (70)

Left

54 (27)

Bilateral

6 (3)

Delivery type

 

Normal vaginal delivery

152 (76)

Instrumental delivery

40 (20)

Cesarean section

8 (4)

Place of delivery

 

Home delivery by traditional birth attendant

30 (15)

Hospital delivery by midwife

120 (60)

Hospital delivery by doctor

50 (25)

Prolonged labor

136 (68)

Presentation

 

Cephalic

144 (72)

Breech

40 (20)

Transverse

16 (8)

Shoulder dystocia

136 (68)

Maternal diabetes

40 (20)

Maternal age (years)a

27.5 (6.8)

Parity of mother

 

Primipara

156 (78)

Multipara

156 (78)

aMean (standard deviation), all others are n (%)

Mean escape latency of acquisition day

Groups                 

NC

SC

ColC

Pre-SwE Exp

Post-SwE Exp

Days

 

 

 

 

 

1st

26.2 (2.3)

30.6 (2.4) 

60.0 (0.0)b

43.2 (1.8)b

43.8 (1.6)b

2nd

22.6 (1.0) 

25.4 (0.6)

58.9 (0.5)b

38.6 (2.0)b

40.5 (1.2)b

3rd

14.5 (1.8) 

18.9 (0.4) 

56.5 (1.2)b

34.2 (1.9)b 

33.8 (1.0)b

4th

13.1 (1.7) 

17.5 (0.8) 

53.9 (0.7)b

35.0 (1.6)b

34.9 (1.6)b

5th

13.0 (1.2) 

15.9 (0.7) 

51.7 (2.0)b

25.9 (0.7)b 

27.7 (0.9)b

6th

12.2 (1.0) 

13.3 (0.4) 

49.5 (2.0)b

16.8 (1.1)b

16.8 (0.8)b

Average of acquisition days

5th and 6th 

12.6 (0.2)

14.6 (0.8)

50.6 (0.7)b

20.4 (2.1)a

22.4 (3.2)a

NC indicates normal control; SC, Sham control; ColC, colchicine control; SwE, swimming exercise exposure.

aP <0.05; bP <0.01.

Categories

Number (%)

Sex

 

   Male

36 (60.0)

   Female

24 (40.0)

Age in yearsa

8.8 (4.2)

Education

 

   Pre-school

20 (33.3)

   Elementary school

24 (40.0)

   Junior high school

16 (26.7)

Cancer diagnoses

 

Acute lymphoblastic leukemia

33 (55)

Retinoblastoma

5 (8.3)

Acute myeloid leukemia

4 (6.7)

Non-Hodgkins lymphoma

4 (6.7)

Osteosarcoma

3 (5)

Hepatoblastoma

2 (3.3)

Lymphoma

2 (3.3)

Neuroblastoma

2 (3.3)

Medulloblastoma

1 (1.7)

Neurofibroma

1 (1.7)

Ovarian tumour

1 (1.7)

Pancreatic cancer

1 (1.7)

Rhabdomyosarcoma

1 (1.7)

aMean (standard deviation)

Narakas classification

Total

200 (100%)

Grade 1

72 (36%)

Grade 2

64 (32%)

Grade 3

50 (25%)

Grade 4

14 (7%)

Complete recoverya

107 (54)

60 (83)

40 (63)

7 (14)

-

Near complete functional recovery but partial deformitya

22 (11)

5 (7)

10 (16)

6 (12)

1 (7)

Partial recovery with gross functional defect    and deformity

31 (16)

7 (10)

13 (20)

10 (20)

1 (7)

No significant improvement 

40 (20)

-

1 (1.5)

27 (54)

12 (86)

aSatisfactory recovery

bGrade 1, C5, 6, 7 improvement; Grade 2, C5, 6, 7 improvement; Grade 3, panpalsy C5, 6, 7, 8, 9, Grade 4, panpalsy with Hornon’s syndrome.

Narakas classification

Total

200 (100%)

Grade-1

72 (36%)

Grade-2

64 (32%)

Grade-3

50 (25%)

Grade-4

14 (7%)

Complete recoverya

107 (54)

60 (83)

40 (63)

7 (14)

-

Near complete functional recovery but partial deformitya

22 (11)

5 (7)

10 (16)

6 (12)

1 (7)

Partial recovery with gross functional defect    and deformity

31 (16)

7 (10)

13 (20)

10 (20)

1 (7)

No significant improvement 

40 (20)

-

1 (1.5)

27 (54)

12 (86)

aSatisfactory recovery

bGrade 1, C5, 6, 7 improvement; Grade 2, C5, 6, 7 improvement; Grade 3, panpalsy C5, 6, 7,8,9, Grade 4, panpalsy with Hornon’s syndrome.

Variables in probe trial day

Groups

NC

SC

ColC

Pre-SwE Exp

Post-SwE Exp

Target crossings

8.0 (0.3)

7.3 (0.3) 

1.7 (0.2)a

6.0 (0.3)a

5.8 (0.4)a

Time spent in target

18.0 (0.4) 

16.2 (0.7) 

5.8 (0.8)a

15.3 (0.7)a

15.2 (0.9)a

NC indicates normal control; SC, Sham control; ColC, colchicine control; SwE, swimming exercise exposure.

aP <0.01.

Pain level

Number (%)

P

Pre

Post 1

Post 2

Mean (SD)a pain score

4.7 (1.9)

2.7 (1.6)

0.8 (1.1)

<0.001

Pain categories

    

   No pain (0)

-

(1.7)

31 (51.7)

<0.001

   Mild pain (1-3)

15 (25.0)

43 (70.0)

27 (45.0)

 

   Moderete pain (4-6)

37 (61.7)

15 (25.0)

2 (3.3)

 

   Severe pain (7-10)

8 (13.3)

2 (3.3)

-

 

aPain scores according to the visual analogue scale ranging from 0 to 10; SD indicates standard deviation

Surgeries

Number  

(%)

Satisfactory outcomes n (%)

Primary surgery (n=24)

 

 

Upper plexus

6 (25)

5 (83)

Pan-palsy

18 (75)

6 (33)

All

24 (100)

11 (46)

Secondary Surgery (n=26)

 

 

Shoulder deformity

15 (58)

13 (87)

Wrist and forearm deformity

11 (42)

6 (54)

All

26 (100)

19 (73)

Primary and secondary surgery

50 (100)

30 (60)

Mallet score 14 to 25 or Raimondi score 2-3 or Medical Research grading >3 to 5.

Narakas classification

Total

200 (100%)

Grade-1

72 (36%)

Grade-2

64 (32%)

Grade-3

50 (25%)

Grade-4

14 (7%)

Complete recoverya

107 (54)

60 (83)

40 (63)

7 (14)

-

Near complete functional recovery but partial deformitya

22 (11)

5 (7)

10 (16)

6 (12)

1 (7)

Partial recovery with gross functional defect    and deformity

31 (16)

7 (10)

13 (20)

10 (20)

1 (7)

No significant improvement 

40 (20)

-

1 (1.5)

27 (54)

12 (86)

aSatisfactory recovery

bGrade 1, C5, 6, 7 improvement; Grade 2, C5, 6, 7 improvement; Grade 3, panpalsy C5, 6, 7,8,9, Grade 4, panpalsy with Hornon’s syndrome.

Trials

Groups

NC

SC

ColC

Pre-SwE Exp

Post-SwE Exp

1

20.8 (0.6)

22.1 (1.8)

41.1 (1.3)b

31.9 (1.9)b

32.9 (1.8)a, b

2

10.9 (0.6)

14.9 (1.7)

37.4 (1.1)b

24.9 (2.0)b

26.8 (2.5)b

3

8.4 (0.5)

9.9 (2.0)

32.8 (1.2)b

22.0 (1.4)b

21.0 (1.4)b

4

7.8 (0.5)

10.4 (1.3)

27.6(1.1)b

12.8 (1.2)b

13.0 (1.4)b

Savings (%)c

47.7 (3.0)

33.0 (3.0)

10.0 (0.9)b

23.6 (2.7)b

18.9 (5.3)b

NC indicates normal control; SC, Sham control; ColC, colchicine control; SwE, swimming exercise exposure.

aP <0.05; bP <0.01.

cThe difference in latency scores between trials 1 and 2, expressed as the percentage of savings increased from trial 1 to trial 2

Methods

This study was conducted in the Department of Obstetrics and Gynaecology, Bangabandhu Sheikh Mujib Medical University (currently, Bangladesh Medical University) Dhaka, Bangladesh, from January 2023 to December 2024. This study included 162 pregnant women with a history of one cesarean section (C/S) between 37 weeks and 41 weeks of gestation who attended the inpatient and outpatient departments of Obstetrics and Gynaecology at Bangabandhu Sheikh Mujib Medical University (currently, Bangladesh Medical University) Dhaka, Bangladesh for obstetric management during the study period.


Initially, 192 women were included in the study at the beginning of their third trimester following the inclusion and exclusion criteria; among them, 30 patients were excluded near term due to various medical and obstetrical complications.

These are the following criteria to be eligible for enrollment as our study participants: a) Patients aged between 20 to 45 years; b) Patients with term pregnancy between 37 weeks to 41 weeks of gestation; c) Patients with a history of previous cesarean section; d) Patients who were willing to participate were included in the study  And a) Patients with comorbidities like DM (FBS above 5.3mmol/L or 2HA 75 mg glucose  above 8.5 mmol/L), morbid obesity  (pre pregnancy BMI  above 40) & hypertensive disorder( blood pressure above 140/90 on at least two occasions 4 hours apart) b) Patients with fetal macrosomia and abnormal presentation like breech, face, transverse lie, etc.; c) Patients with cephalopelvic disproportion (CPD), dystocia or failure to progress of labor and failed induction; d) Patients with standard contraindications to labor or vaginal birth (eg, placenta previa, CPD, previous successful repair of VVF, etc.); e) Patients with a high risk of intrapartum uterine rupture were excluded from our study.

All patients of this study had a spontaneous onset of labour; induction was not given to any patient. The labour process was observed meticulously, following the standard labour care guide. The labour monitoring was done mainly by the resident doctors with the presence of a consultant gynaecologist. Most of the deliveries were spontaneous vaginal deliveries, only two required vacuum extraction. Fetal wellbeing was monitored using Doppler and intermittent CTG. Fetal distress was identified by CTG. Provision for emergency caesarean section was kept ready in case of any impending rupture.

Statistical analysis

All data were systematically recorded using a preformatted data collection form. Quantitative variables were presented as mean (standard deviation), while qualitative data were shown as frequencies and percentages. The chi-square test was used to assess fetal outcomes in vaginal deliveries and the repeat cesarean group. Analyses were performed using SPSS version 26 for Windows. Ethical approval was obtained from the Institutional Review Board of Bangabandhu Sheikh Mujib Medical University (currently, Bangladesh Medical University) Dhaka, Bangladesh. The procedure with benefits and risks were explained. All the patients participated voluntarily and informed written consent were taken. There was no conflict of interest. Honesty, accuracy, and freedom from bias were ensured. 

Group

Didactic posttest marks (%)

Flipped posttest marks (%)

Difference in marks (mean improvement)

P

<50%

63.2 (9.4)

82.2 (10.8)

19.0

<0.001

≥50%

72.4 (14.9)

84.2 ( 10.3)

11.8

<0.001

Data presented as mean (standard deviation)

Results

 Characteristics

Total samples (n)

Negative

n (%)a

HAV infection

n (%)b

HEV infection

n (%)b

HAV and HEV infection

n (%)b

 

42791

32244 (75.3)

5767 (29.6)

4780 (20.5)

85 (0.6)

Gender

Male

29756

22369 (69.4)

3755 (65.1)

3632 (76.0)

62 (72.9)

Female

13035

9875 (30.6)

2012 (34.9)

1148 (24.0)

23 (27.1)

Age (Years)

≤10

7198

4675 (14.5)

2183 (37.9)

340 (7.1)

10 (11.8)

11-20

10477

7046 (21.9)

2186 (37.9)

1245 (26.0)

41 (48.2)

21-30

10828

7990 (24.8)

898 (15.6)

1940 (40.6)

27 (31.8)

31-40

5539

4596 (14.3)

230 (4.0)

713 (14.9)

5 (5.9)

41-50

3786

3368 (10.4)

115 (2.0)

303 (6.3)

2 (2.4)

>50

4963

4569 (14.2)

155 (2.7)

239 (5.0)

0 (0)

an= number of participants, % in bracket; bTotal samples tested for HAV infection=19452, HEV infection=23249 and both HAV & HEV infection = 13997; cPercentages for the HAV, HEV and both (HAV & HEV) infection were calculated from the total tested samples, respectively. The percentages within the group in the Gender and Age categories were calculated.

Table 1 shows that the majority of women (75.3%) were between 21–30 years of age, followed by 17.3% in the 31–40 age group, and only 7.41% were over 40. Regarding BMI, half of the participants (50%) had a normal BMI (18.5–25 kg/m²), 45.06% were overweight (BMI 26–30 kg/m²), and 4.9% were obese (BMI >30). A history of previous vaginal delivery was noted in 19.8% of women. Among those who underwent a trial of labor, 33.3% achieved a successful vaginal birth after cesarean (VBAC), while 66.7% required an emergency repeat cesarean section.


Table 1 Demographic and obstetric characteristics of study participants (n=162)

Characteristics

Number (%)

Maternal age, years

 

21–30 years

122 (75.3)

31–40 years

28 (17.3)

>40 years

12 (7.4)

Mean (Standard deviation)

28.7 (4.8)

Body mass index, kg/m²

 

18.5–25

81 (50.0)

26–30

73 (45.6)

>30

8 (4.9)

Mean (Standard deviation)

25.1 (3.4)

History of vaginal delivery

32 (19.8)

Type of delivery 

Vaginal birth after cesarean 

54 (33.3)

Emergency repeat cesarean section

108 (66.7)


As given in Table 2, the most common indication for the initial cesarean section was fetal distress (51.2%), followed by post-maturity (19.8%), breech presentation (8.0%), and transverse lie (4.3%). In emergency repeat cesarean sections, fetal distress remained the leading cause (48.2%), followed by scar tenderness (19.4%), prolonged labor (17.59%), and maternal exhaustion or personal preference (14.8%).


Table 2 Indications of caesarean sections

Characteristics

Number (%)

First ever cesarean section 

 

Fetal distress

83 (51.2)

Post maturity

32 (19.8)

Breech presentation

13 (8.0)

Transverse lie

7 (4.3)

Prolonged labor

8 (4.9)

Antepartum hemorrhage 

5 (3.1)

Elective caesarean sections (by maternal request)

14 (8.6) 

Repeat cesarean section 

 

Fetal distress

52 (48.2)

Scar tenderness

21 (19.4)

Prolonged/failed progress of labor

19 (17.6)

Maternal exhaustion / own request

16 (14.8)


Table 3 shows that in the VBAC group (n=54), fetal distress was observed in only 3 cases (5.6%), indicating a significantly lower incidence compared to the ERCS group (n=108), where 52 cases (48.2%) experienced fetal distress (P<0.001). The fetal weight range was comparable between the two groups, with VBAC neonates weighing between 2.4–3.5 kg and ERCS neonates ranging from 2.5–3.4 kg. Assessment of Apgar scores showed that a good Apgar score (>7) was more frequently observed in the VBAC group, with 49 neonates (90.7%) scoring in the normal range, whereas only 82 neonates (75.9%) in the ERCS group had similarly favorable scores (P=0.024). Conversely, average Apgar scores (<7) were recorded in 5 neonates (9.7%) in the VBAC group and 26 neonates (24.1%) in the ERCS group (P=0.024). 


Table 3 Neonatal outcomes among study participants (n=162)

Parameters

VBACa

(n=54)

ERCSa

(n=108)

P

Fetal distress

 

 

 

n (%)

3 (5.6)

52 (48.2)

<0.001

Fetal weight (kg)

 

 

 

Range

2.4 – 3.5

2.5 – 3.4

0.27

Mean (SD)a

3.0 (0.3) 

3.0 (28.0)

 

Apgar score at 5 min

 

 

 

Good (>7)

49 (90.7)

82 (75.9)

0.02

Average (<7)

5 (9.3)

26 (24.1)

0.02

Mean (SD)a

8.4 (0.6) 

8.0 (0.7)

 

aVBAC indicates vaginal birth after cesarean section; ERCS, emergency repeat caesarean section; SD, standard deviation


Discussion

This study explored the outcome of a trial of labour after one previous caesarean section in a tertiary care hospital. It particularly focused on the clinical results and the practical realities that influence decision-making by both clinicians and patients. The findings provide a realistic view of current VBAC practice in Bangladesh, where the success of TOLAC is shaped not only by obstetric factors but also by physicians’ attitudes, patient preferences, and the readiness of the health system.


In this study, the success rate of VBAC was 33.3%, which is lower than the success rates reported in most international studies, usually ranging from 60% to 80.0% [11]. This difference probably reflects the cautious approach commonly taken in our setting, where both clinicians and patients tend to prefer a planned repeat caesarean section due to fear of complications. Limited availability of continuous fetal monitoring also contributes to this conservative tendency. The novelty of this study lies in identifying these local barriers, highlighting that institutional and cultural contexts are as important as medical indications when considering VBAC.

The mindset of the clinician plays a central role in the outcome of TOLAC. Many obstetricians, even in tertiary hospitals, are hesitant to allow labour after caesarean because of the perceived risk of uterine rupture and the potential medicolegal consequences if complications occur. Similar findings were reported [12, 13], who observed that clinician confidence and institutional policies strongly influence the decision to offer TOLAC. In our experience, many repeat caesarean deliveries are performed pre-emptively, even in women with favorable conditions, because of this underlying fear. However, our findings show that with proper case selection and close monitoring, VBAC can be achieved safely, with good neonatal outcomes and minimal maternal morbidity.

Patients’ attitudes and expectations also have a major influence on the mode of delivery. In urban areas, women often consider caesarean section a more predictable and comfortable option, while others express a strong desire for normal delivery because of faster recovery and lower cost. The decision is therefore a balance between convenience and risk perception. Proper counselling plays a vital role here. As highlighted in previous studies [14], shared decision-making that clearly explains both the benefits and risks of TOLAC can increase the rate of successful VBAC while maintaining patient safety. In our setting, patient education remains limited, and many women decide based on anecdotal experience rather than medical advice.

Health system preparedness is another crucial determinant of success. Safe TOLAC requires continuous intrapartum monitoring, prompt access to emergency theatre, and the presence of skilled personnel. In many hospitals in developing countries, these facilities are not always consistently available, which understandably makes obstetricians reluctant to take the risk of allowing labour to continue after a previous caesarean. Strengthening hospital infrastructure, ensuring the presence of experienced obstetric and anaesthetic teams, and introducing standard operating protocols for VBAC could greatly improve outcomes.

Our results reaffirm that VBAC is not only a clinical choice but also a reflection of trust—between patient and clinician—and the capability of the health system. Consistent with previous findings, favorable predictors such as previous vaginal delivery and optimal fetal weight were associated with better outcomes. Yet, the broader implication of this study is the need to change our professional mindset and institutional culture from the old dictum of “once a caesarean, always a caesarean” to an evidence-based, patient-centred approach. Encouraging safe VBAC practices, supported by structured counselling and institutional preparedness, may help reduce unnecessary repeat caesarean sections and improve maternal and neonatal health in the long term.

Limitations

This study has several limitations. First, it was conducted in a single tertiary hospital with a relatively small sample size. Therefore, the findings may not be generalizable to other healthcare settings, particularly private or rural institutions with different patient characteristics and resource availability.

Second, only women who were willing to undergo a trial of labour were included, while those opting for elective repeat caesarean section were excluded. This introduces potential selection bias, which may have influenced the observed VBAC success rate.

Third, continuous electronic fetal monitoring and 24–hour anaesthetic or surgical support were not always available. These limitations might have prompted earlier decisions for repeat caesarean section in cases where close observation could have resulted in a successful VBAC.

Fourth, this study focused on immediate maternal and neonatal outcomes. Long-term follow-up of subsequent pregnancies or uterine scar integrity was not undertaken, which limits the understanding of extended maternal health outcomes.

Finally, labour progress and clinical decisions were made by different obstetricians on duty, which may have led to observer variation in case management.

Despite these limitations, this study provides valuable local evidence on VBAC practice in Bangladesh and highlights the importance of institutional preparedness, clinician confidence, and patient counselling in improving outcomes for women with a previous caesarean section.

Conclusion

This study found that VBAC can be a safe and feasible option for many women, especially those with a history of vaginal delivery and favorable obstetric factors. However, failed TOLAC carries significant risks, including increased maternal morbidity. Predictive factors such as prior vaginal delivery, Bishop score, fetal weight, and maternal age should be considered when counseling women about TOLAC. Further research, particularly RCTs, is essential to refine selection criteria and improve VBAC success rates, ultimately reducing unnecessary repeat cesarean sections. Further prospective, longitudinal studies with larger sample sizes are required to improve VBAC success rates and minimise unnecessary repeat cesarean deliveries. 

Acknowledgements
We were grateful to the staff of the Department of Obstetrics and Gynaecology and the University Research Board of Bangabandhu Sheikh Mujib Medical University (currently, Bangladesh Medical University) Dhaka, Bangladesh.
Author contributions

Concept or design of the work; or the acquisition, analysis, or interpretation of data for the work: RR, NNK, BN, TRL, FA. Drafting the work or reviewing it critically for important intellectual content: RR, NNK, BN, TRL, FA. Final approval of the version to be published: RR, NNK, BN, TRL, FA. Accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved: RR, NNK, BN, TRL, FA.

Conflict of interest
We do not have any conflict of interest.
Data availability statement
We confirm that the data supporting the findings of the study will be shared upon reasonable request. 
AI disclosure
None
Supplementary file
None
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