Friday, 22 November 2024

DEALING WITH CAESAREAN SCAR DEHISCENCE

Caesarean scar dehiscence refers to the partial separation or thinning of the uterine scar from a previous Caesarean section. It is typically asymptomatic and discovered incidentally during imaging or subsequent surgery. It differs from uterine rupture, which involves a full-thickness tear of the uterine wall and often leads to significant complications.



Pathophysiology:

• Occurs due to poor healing of the Caesarean     

           section scar.

 Risk increases with excessive tension, poor 

           surgical technique, or inadequate vascularization 

           of the scar tissue.


Risk Factors:

1. Previous Caesarean section:

 Higher risk with classical or T-incisions.

 Multiple Caesarean deliveries.

2. Interdelivery interval: Short intervals (<18   

        Fmonths) between pregnancies.

3. Uterine overdistension:

 Multiple pregnancies.

 Polyhydramnios.

4. Infection: Postpartum or post-surgical infection impairs healing.

5. Other factors:

 Use of corticosteroids.

 Smoking or poor nutrition.

 Advanced maternal age.


Clinical Features:

 Often asymptomatic.

 Occasionally presents with: 

 Mild lower abdominal pain.

 Vaginal bleeding (rare).

 Feeling of pressure in the pelvis.


Diagnosis:

1. Ultrasound (US):

 Thinning of the myometrium at the scar site (<2.5 mm considered high risk).

 Hypoechoic defect in the uterine wall.

2. MRI: Useful for detailed evaluation if US is inconclusive.

3. Intraoperative findings:

Seen during a repeat Caesarean section as a thin, translucent scar or partial separation.


Management:

1. Asymptomatic cases:

 Observation and regular antenatal monitoring.

 Advise delivery at 37–39 weeks via planned 

           Caesarean section.

2. Symptomatic or detected during pregnancy:

 Requires evaluation for uterine rupture risk.

 May necessitate early Caesarean delivery.

3. Severe cases:

Surgical repair may be indicated if detected outside of pregnancy.


Complications:

 Increased risk of uterine rupture in subsequent 

           pregnancies.

 Abnormal placentation (e.g., placenta accreta 

           spectrum).

 Adhesions or scarring in the pelvis