Wound Infection Clinical Trial
Official title:
Negative Pressure Wound Therapy to Prevent Post Operative Wound Complications Following Cesarean Delivery in Women at High Risk for Wound Complications
This study is aimed at determining whether or not the use of a wound suction device placed on
the cesarean incision instead of a standard sterile dressing will decrease the prevalence of
wound complications and wound infections in women at high risk for post operative
complications. The study will first look at the infection and wound complication rate in
women 6 months prior to the start date of the study by reviewing charts of women who have
undergone a cesarean section. The study involves placing a single use, portable wound vacuum
over the cesarean section incision and keeping it in place for 72h. The investigators will
then compare the rates of wound infection and wound complications between these two groups.
It is our hypothesis that negative pressure wound systems will decrease the wound infection
and complication rate in this high risk population.
Infectious complications have been found to be five times higher in women undergoing a
cesarean delivery compared to a vaginal delivery. Known risk factors for wound complications
are obesity, premature rupture of membranes, diabetes mellitus, hypertensive disorders,
emergency cesarean delivery, twin delivery, chorioamnionitis, increased surgical blood loss
and preeclampsia.
This study is aimed at determining whether or not the use of a suction device placed on the
wound instead of a standard sterile dressing will decrease the prevalence of wound
complications and wound infections in women at high risk for post operative complications.
The investigators will compare the results from the participants of this study to an existing
data set of historical controls who underwent cesarean delivery. The study involves placing a
single use, portable negative wound pressure system kept in place while in the hospital after
surgery (on average 48-72 hours) in women who meet criteria for increased risk of wound
complications. The investigators will then compare the rates of wound infection and wound
complications between these two groups.
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