Effect of Rectus Sheath Block on Diaphragmatic Function After Elective Upper Abdominal Surgery

Assiut University

Status: Enrolling

Conditions: Acute Pain

Treatments: Procedure: Rectus Sheath Block

Study type: Interventional

Funder types: Other

Identifiers

NCT03725527

17100594

Details and patient eligibility

About

This study will be undertaken to investigate the respiratory and analgesic effects of ultrasound guided rectus sheath block analgesia after elective abdominal surgery with midline incision.

Full description

A major proportion of pain experienced by patients undergoing abdominal surgeries is due to somatic pain signals derived from the abdominal wall. The central portion of anterior abdominal wall components (skin, muscles and parietal peritoneum) is innervated by sensory neurons branching from the anterior rami of spinal nerves T7 to T1. These neurons lie between the rectus abdominis muscle and posterior rectus sheath, and pierce the rectus muscle close to the midline. The tendinous intersections of the rectus muscle do not fuse with the posterior rectus sheath, thereby allowing the injectate to spread cephalo-caudally within this potential space. Rectus sheath (RS) block has been described for any midline abdominal incisions (epigastric and umbilical hernia repairs). As visceral pain becomes attenuated by the 2nd postoperative day, rectus sheath block can also be administered for midline laparotomy.

However, the effects of rectus sheath block analgesia on the respiratory function after abdominal surgery with midline incisions are still under investigation.

Enrollment: 60 estimated patients

Sex: All

Ages: 18 to 50 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age: 18-50 years.
• Sex: both males and females.
• BMI< 30kg/m2.
• ASA physical status: 1, II and III.
• Elective abdominal surgery with midline incisions.

Exclusion criteria

• Patient refusal.
• Infection at injection site
• Coagulation disorders.
• Allergy to study medications.
• Pregnancy.
• Respiratory tract infection within the last 2 weeks.
• Urgent abdominal surgery

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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60 participants in 2 patient groups

Rectus sheath block

Active Comparator group

Description:

Patients will receive ultrasound-guided rectus sheath block' performed after induction of general anesthesia and before surgery.

Treatment:

Procedure: Rectus Sheath Block

control

No Intervention group

Description:

Patients will receive general anesthesia .