CompletedPhase 4ACTRN12615000636550

Postoperative analgesia of continuous wound catheters and ultrasound guided rectus sheath catheters for colorectal surgery.

Comparative study between continuous wound catheters and ultrasound guided rectus sheath catheters for postoperative analgesia in patients undergoing elective colorectal surgery.


Sponsor

Hoda Alsaid Ahmed Ezz

Enrollment

60 participants

Start Date

Apr 29, 2014

Study Type

Interventional

Conditions

Summary

The aim of the study was to compare the postoperative analgesia of continuous wound catheters and ultrasound guided rectus sheath catheters for colo-rectal surgery.


Eligibility

Sex: Both males and femalesMin Age: 40 YearssMax Age: 65 Yearss

Inclusion Criteria1

  • Adult patients of both sexes aged (40-65) years, (ASA) physical state class I and II scheduled for elective open colo-rectal surgery via midline exploratory abdominal incision in the general surgical department, Tanta University Hospital.

Exclusion Criteria1

  • Patients were excluded from the study if they were presented with coagulopathies and impaired platelet functions, cardiovascular instability, cerebral strokes, renal disease or liver disease. Patients with local infection at the site of the block or with history of allergy to local anesthetics were, also excluded from the study.

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Interventions

Group I: " Wound catheter continuous infusion group (CWCs) 30 patient": wound catheter was inserted before closure of wound. Technique: Two multi-orifice catheters were implanted by the surgeo

Group I: " Wound catheter continuous infusion group (CWCs) 30 patient": wound catheter was inserted before closure of wound. Technique: Two multi-orifice catheters were implanted by the surgeon into the subcutaneous layer on both sides of the surgical incision. The catheters were embedded into the wound to a length of approximately 6 - 10 cm and secured to the skin. A loading dose 10 mL of 0.25% bupivacaine was infused through each catheter just before closure of the incisional site. Analgesia was maintained by infusing 0.25% bupivacaine at a rate of 4 mL/h through two catheters (2 mL/hour per catheter) through electric infusion pump for 48 hours. Group II: "Rectus Sheath Catheters group (RSCs) 30 patient": Rectus sheath catheters were inserted bilaterally by the aid of ultrasonography at the end of surgery. Technique: The upper abdomen was prepared with 2% betadine, then the rectus muscle is imaged with a sheathed ultrasound probe in a longitudinal orientation above the level of the umbilicus. The probe was broadband (5-12MHz), 50 mm foot-print , linear array with an imaging depth of 4-6 cm. At first ultra-sonography probe identified the lina alba, then it was moved laterally to demonstrate the main body of the rectus abdominis muscle and the posterior rectus sheath, then 18G Tuohy needle was introduced few millimeters from the probe using an in plane technique at an angle of approximately 45 degrees to the skin just below the costal margin. The ultrasound allowed identification of the rectus muscle and posterior rectus sheath and fascia transversalis (two hyperechoic railway-like lines deep to it ). The needle tip was advanced to the desired position between the rectus muscle and the underlying posterior rectus sheath then 20 mL bupivacaine 0.25% (loading dose) were injected creating a space for the rectus sheath catheter to be introduced, causing hydro-dissection of the rectus muscle away from the posterior rectus sheath, and 4-8 cm of catheter was left in this space. The catheter depth at the skin is usually 12-15cm. To avoid interference with the surgical field the rest of the catheter was tunneled laterally. The same was repeated on the other side. Analgesia was maintained by injecting 10 ml bupivacaine 0.25% on each side every 6 h in the first 24 h postoperatively then every 12 h in the second 24 h to maintain analgesia. The catheters were removed after 48 hours post-operative.


Locations(1)

Tanta, El Gharbia Governorate, Egypt

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ACTRN12615000636550