TRIAL
OF SCAR AND VAGINAL BIRTH AFTER CAESAREAN SECTION
Aisha
Hassan
Department of Gynaecology, Ayub Teaching Hospital,
Abbottabad
Background: The caesarean section rate
has increased to an alarming extent in the last three decades the world over
and fear of rupture of uterus in subsequent pregnancy and labour has led to a
high rate of repeat caesarean sections. The objective of this study was to
determine the final outcome of a trial of scar and Vaginal Birth After
Caesarean Section (VBAC) and develop guidelines to reduce the rate of unnecessary
repeat caesarean section. Methods: This
study was carried out in Obstetric and Gynecology Unit ‘A’ of Ayub Teaching
Hospital Abbottabad from 01.11.2002 to 31.10.2004. A total of 2652 patients
were delivered during this period, out of which 297 patients had history of one
previous caesarean section. A total of 53 patients had an elective repeat
caesarean section and rest of 244 was subjected to a trial of scar. Result: Out of 244 patients selected
for trial of scar, 165 (67.2%) had a successful uncomplicated vaginal delivery,
7 (3.2%) were delivered by forceps, 11 (5.2%) with vacuum extractor and 61 (24.4%)
required a repeat emergency caesarean section. 83% of the patients had a
spontaneous onset of labour and 17% needed induction of labour with
prostaglandin E2 pesseries and augmentation of the labour with oxytocin.
However repeat caesarean section rate was high in the later group. 71.2% of the
babies were born with Apgar score > 8 and 24.6% had an Apgar score between
6-8. There were 3 cases of scar dehiscence and one case of ruptured uterus and
one baby was lost due to this complication. No serious maternal complication
occurred. Conclusions: More than 75%
of the patients with previous one caesarean section for non-recurrent cause can
be successfully delivered vaginally. Antenatal booking and follow up, careful
case selection for trial of scar and close observations during labour will
achieve successful maternal and perinatal outcome. VBAC also saves any future
caesarean sections, as currently previous two caesarean sections is an
indication for elective caesarean section.
Key
wards:
Trial of Scar, Cesarean Section Rate,
VBAC,
INTRODUCTION
The caesarean section rate has increased, both in
the developed and developing countries alike. It is partly due to availability
of safe anaesthesia, excellent blood transfusion services, advance in operative
technology and development of broad spectrum antibiotics. The relative safety
of the operative procedure has led to relaxation of indications, resorting to
the procedure for relative indications and even ‘caesarean on demand’ by some
women. This tendency needs to be controlled as it puts a great drain on health
care resources, is costly and associated with serious risks to the mother and
the baby, all the recent advances notwithstanding. This rising caesarean
section rate has created an expanding high risk obstetric sub-population “Women
with scarred uterus”.1-6
Risk of rupture of uterus in
subsequent pregnancy led Craigin to introduce the concept “Once a caesarean,
always a caesarean” in 1916. This concept met a lot of criticism both in the East
and West and most obstetricians now favour a Trial of Scar policy in a well
equipped hospital for women who have undergone a caesarean section for non-recurrent
cause.7,8
Caesarean section is not
always a safe option, especially in a developing country like ours where the
patient profile is different, and there are less than adequate medical
facilities in many places. Ignorance and lack of education, poor understanding
of the operation and its subsequent management, both on the part of the patient
and her family leads to poor acceptance of both first and repeat caesarean
section. Failure to seek antenatal care in subsequent pregnancy, attempts of
delivery at home or report late in advanced labour, after unskilled vaginal
examina-tion and injudicious use of oxytocin at home leads to high maternal and
perinatal morbidity/ mortality. The risk of repeat caesarean section increases
in such cases with its own morbidity and mortality.
We carried out this study at
Ayub Teaching Hospital to assess safety of ‘Trial of Scar’ in ladies with
history of previous lower segment caesarean section.
MATERIAL AND METHODS
This study was carried out
in Obstetric and Gynecology Unit ‘A’ of Ayub Teaching Hospital Abbottabad from
01.11.2002 to 31.10.2004. We included the women who had lower segment cesarean
section for a non recurrent reason and offered them a Trial of Scar after
ruling out cephalo-pelvic disproportion. Obstetrical data was collected from
maternity notes and labour room record registers. Data obtained included
maternal age, parity, indication for previous caesarean section, previous
vaginal deliveries, gestational age, Bishop
score, details of labour (whether spontaneous, augmented or induced), timing
and onset of regular uterine contractions, rupture of membranes, mode of
delivery or indication for repeat caesarean section. In addition birth weight,
Apgar score of the baby, maternal febrile morbidity and mortality and length of
hospital stay were noted.
Patients who were declared
eligible for trial of Scar were figured out by having only one previous
caesarean section for a non recurrent cause, a low transverse uterine Scar,
adequate pelvis, a single fetus with vertex presentation, estimated weight of
the baby less than 3.8 kg and no absolute indication for caesarean section or
medical or obstetric complications.9-13
Patients who had contracted
pelvis, fetal macrosomia, placenta praevia, bad
obstetrical history or associated medical disorders were excluded from the
study. In our study all the patients with previous one scar were examined by
the senior Obstetricians. Circumstances surrounding previous deliveries were
noted. An elective caesarean section without cephalo-pelvic disproportion,
clean and regular uterine wound, smooth wound healing and absence of
post-operative sepsis were noted as favorable factors for a trial of scar. On
the other hand, an emergency procedure on patient with obstructed labour, with
attenuated devitalized lower segment and irregular wound were noted as poor
prognostic markers.
Good prognostic factor at
term included engaged head, average size of the baby, soft, central and dilated
cervix and adequate pelvis. The bad prognostic features include high and mobile
un-engaged head, good sized baby and unripe cervix. We preferred a digital
pelvimetry alone without resorting to X-rays and in the absence of any obvious
pelvic deformities allowed a trial of labour.
During trial of labour a
Senior House Officer or registrar who was fully aware of the antenatal record
of the patient was ensured to take care of the patient. At least 1 pint of
blood was typed and cross matched. Intravenous line with a 16-18 gauge cannula
was established and maintained. The
anesthetist, theatre staff and neonatologist was informed for the possibility
of a caesarean section. Fetal cardiac activity and maternal vital signs were
vigilantly monitored throughout the trial.
Patient’s informed consent
was taken for trial of scar. She was kept nil by mouth and an intravenous
infusion of 5% dextrose in water was started. The progress of labour and
relevant clinical observations was recorded on a partogram. Analgesia was given
during trial in the form of intra muscular injection of Tramadol Hcl. However,
epidural analgesia was not given due to non availability. Throughout the trial
patient was watched for lower abdominal tenderness (scar tenderness), acute
onset of severe abdominal pain, acute fetal distress, maternal tachycardia,
vaginal bleeding, loss of presenting part etc. Prostaglandin E2 (3 mg)
pesseries were used for induction of labour in cases of poor Bishop Score. Oxytocin was used both for induction (when
Bishop Score was favourable) and augmentation of labour to achieve optimal
uterine contractions.14,15
Vaginal delivery was
assisted with outlet forceps or vacuum extraction, in cases of poor maternal
efforts, when the fetal head was engaged (less then 1/5 palpable on abdominal
examination). Patients were kept under observation in the labour room for 2
hours after delivery to observe signs of post partum hemorrhage. Uterine atony
and maternal vital signs were recorded every half an hour for two hours. If
stable they were transferred to postnatal ward.
RESULTS
There were 5549 obstetric admissions during the 24
months study period. Total deliveries were 2652 including 297 cases with
previous one caesarean scar. Out of
these 2652 cases, 1065 cases were delivered by caesarean section, giving rise
to a caesarean section rate of 40.15%.
Out of 297 women with one previous scar, 244 (82.15%) fulfilled the
criteria for going through a trial of scar, and 53 (17.84%) had a repeat
elective caesarean section. Trial of
scar was discontinued when adequate progress was lacking after 6 hours of trial
in active phase of labour in spite of good uterine action and a repeat
emergency caesarean was performed in 61 patients (24.4%).
Mode of Delivery
|
No. of patients |
% |
Spontaneous Vaginal
Deliveries |
165 |
67.2 |
Vacuum
delivery |
11 |
5.2 |
Forceps delivery |
7 |
3.2 |
Repeat caesarean for failed
trial of scar |
61 |
24.4 |
Table-2: Indications for emergency
caesarean section after failed trial of scar (n=61)
Indications
|
Number |
% |
Failure
to progress during 1st stage of labour |
34 |
52 % |
Fetal distress |
18 |
31 % |
Scar Dehiscence |
4 |
6.5% |
Others |
5 |
8.1% |
Table-3:
Indications for previous caesarean section (non recurrent cause) versus outcome
in present pregnancy
Indication
For Primary Caesarean Section |
Total No=
244 |
% |
Vaginal
Delivery |
Caesarean
Section |
||
No. |
% |
No. |
% |
|||
Breech and abnormal lie |
70 |
29 |
61 |
87.1 |
09 |
12.9 |
Fetal
distress |
63 |
26.2 |
47 |
74.6 |
16 |
25.4 |
Failure to progress: a. In first stage of labour b. In second
stage of labour |
52 31 21 |
21.2 |
37 |
71 |
15 |
29 |
Placenta
Praevia |
22 |
8.8 |
16 |
72.7 |
06 |
27.3 |
Precious Pregnancy |
14 |
5.6 |
09 |
64.2 |
05 |
35.8 |
Fetal
compromise (reduced fetal movements, poor biophysical profile) |
14 |
5.6 |
9 |
64.2 |
07 |
35.8 |
Pregnancy induced
hypertension |
9 |
3.6 |
06 |
66.6 |
03 |
33.4 |
Table-4: APGAR Score in trial of scar
babies at 1-minute
Apgar Score |
Number 182 |
Percentage |
Apgar Score > 8 |
128 |
71.2 % |
Apgar Score 6 – 8 |
45 |
24.6% |
Apgar Score < 6 |
9 |
4.2% |
Table-5: Maternal complication
Types of Complications
|
Complications
|
||
Vaginal Delivery |
Emergency Caesarean section |
Elective Caesarean Section |
|
Puerperal Pyrexia
(endometritis) |
6 (3.27%) |
23 (37.7%) |
12 (22.6%) |
Wound sepsis |
- |
11 (18%) |
7 (13.2%) |
Gaped
Episiotomy |
5 (4%) |
0 |
- |
Thrombophlebitis |
- |
5 (8.19%) |
1 (1.8%) |
Rupture uterus |
- |
4 (6.55%) |
- |
Transfusion |
7 (5.73%) |
32 (52.45%) |
15 (28.3%) |
Other infection |
2 (1.63%) |
18 (29.5%) |
7 (13.2%) |
|
1 – 2 days
(0.82 – 1.63%) |
8 – 12 day
(13-19.6%) |
6-8 Days (17%) |
The indication for previous
caesarean section has a considerable impact on outcome of trial of scar. Table-3
shows that highest vaginal delivery rate (87%) was achieved in cases of prior
caesarean section for mal-presentations. It was followed by failure to progress
(74.6%), placenta praevia (72.7%) and fetal distress (71.6%). Minimum vaginal
delivery rate (64%) was achieved in cases of fetal compromise.
Women,
who had previous experience of vaginal deliveries in addition to caesarean
section were 104 and 90 (88.3%) of them achieved a successful vaginal delivery
compared to 140 women without previous vaginal delivery in whom 93 (71.1%)
could achieve a vaginal delivery
Various parameters of
maternal morbidity that occurred during study are compared in Table 5. There were
three cases of scar dehiscence, detected and managed well in time, with
uneventful maternal and perinatal outcome. Only one patient had complete
uterine rupture, whose cesarean section was decided due to acute abdominal pain
and tenderness and fetal distress. Uterine rupture occurred because of
non-availability of theatre table in emergency for more than six hours due to
work overload.
Neonatal morbidity was also
increased in cases requiring emergency caesarean section after failed trial of
scar. There was stillbirth of only 1 baby out of 244, this one baby died due to
uterine rupture. One had congenital malformation
and died after few minutes. This gives the perinatal mortality of 7.3/1000
total births.
Discussion
The
overall Caesarean section rate in our hospital during study period was 40.15%.
This is apparently very high and unacceptable rate as compared to current
caesarean section rate of 12 % in
Ayub Teaching Hospital is the biggest tertiary care
level
From the result of Table-3 it can be postulated that
even when the indication for previous caesarean section was failure to progress
in first or second stage of labour or cephalo- pelvic disproportion, a trial of
scar should be considered, because in most such cases an element of relative
cephalo- pelvic disproportion exist due to good size baby or fetal mal
positions (occipito-posterior and occipito-transverse) or mal presentations
like braw or face presentation which may not necessarily occur in subsequent
pregnancy. Moreover, with the help of partogram and drawing alert and action
lines and labour curves, one can identify the abnormal labour patterns earlier
and timely and accurate action can result in safety of both mother and fetus.3
Although in cases of previous caesarean sections,
X-ray pelvimetry gives information about the pelvic diameters at various
levels, its draw back is that it provides static radiographs; whereas labour is
a dynamic process, in which laxity of pelvic ligaments offers relaxation of
pelvic diameters. In addition uterine contractions, flexion of fetal head to
more favourable diameters and moulding are important determinants of the
outcome of labour. Therefore too much reliance cannot be placed on pelvimetry.
In a retrospective review of women who had post caesarean section X-ray
pelvimetry, Murthy et al found that 66% of women with radiological inadequate
pelvis delivered normally in subsequent pregnancy.20 Computerized
axial tomography and Magnetic Resonance Imaging have the advantage of much
better resolution and being less or totally free of hazards of Ionizing
radiations, but both are expensive and not widely available with inherent
drawback of poor reflection of possible outcome of labour, which is dependent
mainly on intra-partum events.20,21
There were three cases of scar dehiscence and one case
of uterine rupture in spontaneous labour group, possibly due to lack of
physiological strength of scar tissue. Similarly, it was interesting to note in
this study that women who had experienced previous vaginal delivery in addition
to caesarean section, had a better chance of achieving VBAC (90% vs 71%),
indicating that a history of previous vaginal delivery should be noted as a
favourable factor for trial of scar.22 Perinatal outcome in cases
delivered vaginally was encouraging as 71% of babies were born with Apgar score
of 8. Only 6 babies (4.2%) had an Apgar score less than 6 and all were
successfully resuscitated. This finding confirms that VBAC is completely safe
for the babies as is reported in international studies.4
Conclusions & Recommendations
It
was concluded from this study that not permitting a trial of labour in an
eligible candidate is simply not justified on the basis of fear of uterine
rupture. The likelihood of a successful trial of scar in carefully selected
patients was similar to that reported in developed countries (62-84%), thus
resulting in decreased incidence of repeat caesarean section. Benefits of
vaginal over abdominal delivery include less post partum morbidity, shorter
hospital stay, fewer operative and anesthetic risks, financial savings and of
immeasurable value is the earlier and easier neonatl -maternal interaction and
bonding.
It was also concluded from this study that risk of
repeat caesarean section arises from an injudicious primary caesarean section
in non booked obstetric patients. It is recommended that nation wide measures
should be taken to improve antenatal care at primary and tertiary level
hospitals. Traditional birth attendants and other paramedical staff involved in
taking care of these patients during labour and delivery should be properly
trained and issued certificates allowing them obstetric clinical practice so
that they are able to make timely referrals in appropriate cases.
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_____________________________________________________________________________________________________________________
Address for Correspondence:
Dr. Aisha Hassan, Department of Gynaecology, Ayub Teaching Hospital, Abbottabad. Ph: Res:92-992-351-4716,