The impact of copper impregnated wound dressings on surgical site infection following caesarean section: a double blind randomised controlled study

Abstract

ObjectiveTo investigate the effect of copper impregnated wound dressings on the surgical site infection (SSI) rate following caesarean section (CS). DesignSingle centre double blind randomised controlled trial. ParticipantsWomen aged 18 years or over who had a CS. InterventionsAll women were randomised to receive either a copper-oxide impregnated wound dressing (study group) or a non-copper wound dressing (control group). Main outcome measuresThe primary study outcome was the incidence of SSI within a 30-day period from CS, assessed via a telephone questionnaire. Secondary outcomes were length of hospital stay, and readmission rate. Results324 women were enrolled in the study of whom 159 were randomised to the study group and 165 to the control group. The follow up rate was 97.5%. A total of 78 women (24.1%) developed an SSI within 30 days following CS; 29 (18.2%) in the study group and 49 (29.7%) controls (P = 0.037, relative risk reduction (RRR) of 38.7%). The incidence of superficial/deep SSI was not significantly different (24.2% vs. 17.6%, P = 0.257), however a significant relative risk reduction of 80.3% for Organ/Space SSI was observed in the study group (12.7% vs. 2.5%, P = 0.002). Length of hospital stay, and readmission rate did not vary significantly between groups. ConclusionsThis is the first study to demonstrate a significant reduction in SSI rates following CS with the use of copper impregnated wound dressings. The high SSI rate confirms the importance of new strategies to reduce the infection rate. Copper is a natural remedy which could potentially reduce hospital acquired infections without the use of antibiotics and its associated risks of antibiotic resistance.