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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.

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615000636550
Enrollment
60
Registered
2015-06-19
Start date
2014-04-29
Completion date
2015-04-27
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief 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.

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 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.

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.

Sponsors

Hoda Alsaid Ahmed Ezz
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Investigator)

Eligibility

Sex/Gender
All
Age
40 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

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 criteria

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.

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 2, 2026