The aim of this study is to determine the surgical site infection rate and patient satisfaction for subcuticular versus interrupted mattress suture in closure of skin at Cesarean delivery in obese patients.
This is a randomized controlled trial conducted in Ain-Shams University Maternity Hospital on the period from March 2012 till August 2012. It included 130 pregnant women who underwent elective Cesarean section. The aim of this study is to determine the surgical site infection rate and patient satisfaction for subcuticular versus interrupted mattress suture in closure of skin at Cesarean delivery in obese patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
500
Skin is closed with interrupted mattress stitches using non-absorbable polypropylene \[Prolene®\]
Skin is closed with subcuticular stitches using non-absorbable polypropylene \[Prolene®\]
Surgical site infection
We used the definition devised and adopted by the Center for Disease Control and Prevention.
Time frame: 30 days after the operative procedure
Skin closure time
Time frame: 15 minutes
Postoperative pain
Measured by 10-cm visual analogue scale, zero being no pain and ten the worst possible pain
Time frame: 48 hours
Short-term cosmetic wound outcome
We used Stony Brook Scar Evaluation Scale
Time frame: 30 days
Overall women satisfaction
A questionnaire is used to check the patient satisfaction (satisfied versus unsatisfied) regarding the wound appearance and wound related pain
Time frame: 30 days
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