Electric cautery does not reduce blood loss in primary total knee arthroplasty compared with scalpel only surgery a double-blinded randomized controlled trial
The purpose of this study was to systematically compare blood loss between the electric cautery and scalpel used in primary total knee arthroplasty (TKA).
We performed a double-blind trial randomizing osteoarthritic knee patients undergoing unilateral TKA done by either using scalpel (group S) or cautery (group C). Primary outcomes were total blood loss calculated from maximum haemoglobin drop and blood loss collected in drain. Secondary outcomes were systemic inflammatory response (serum C-reactive protein), wound complications, and functional outcomes assessed over three months.
A total of 80 patients were recruited. Group S had similar calculated total blood loss compared to group C (1070 (S) vs 1128 (C) mL, 95% CI − 219 to 103, p = 0.47). There was no difference in the mean drain-collected blood loss between the two groups (443 (S) vs 486 (C) mL, 95% CI − 128 to 47, p = 0.36). Group C had higher serum C-reactive protein level at 48 hours after TKA compare to group S (105 vs 140 mg/dL, 95% CI − 66 to − 4, p = 0.03). Wound complications and functional outcomes at three months were also similar between the two groups.
Using electric cautery does not reduce total blood loss as we thought it would be in primary TKA compare to scalpel only surgery and it is also associated with a greater systemic inflammatory response. Cautery used in TKA which operated under tourniquet may not be worthwhile for the risk of hazardous smoke and the increasing cost.
KeywordsScalpel Knife Electric cautery Blood loss Total knee arthroplasty
We thank Dr. Bob Taylor and Professor Norman Hangnail for reviewing the article and language help. We also thank all participants for providing the data used in this study.
Our institution provided the funding for this study.
Compliance with ethical standards
The institutional review board approved the study protocol before the first patient enrollment (MTU-EC-OT-1-125/56). The study protocol was also registered in clinicaltrials.gov (Identifier: NCT02108327). All patients provided written informed consent and agreed to participate in this trial.
Conflict of interest
The authors declare that they have no conflicts of interest.
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