Reduction of blood loss using high-dose aprotinin in major orthopaedic surgery: a prospective, double-blind, randomised and placebo-controlled study
- PMID: 12678347
- DOI: 10.1302/0301-620x.85b2.13303
Reduction of blood loss using high-dose aprotinin in major orthopaedic surgery: a prospective, double-blind, randomised and placebo-controlled study
Abstract
We have investigated in a prospective,randomised placebo-controlled study the effect of high-dose aprotinin on blood loss in patients admitted for major surgery (revision arthroplasty of the hip or knee, or for resection of a soft-tissue sarcoma). The mean intraoperative blood loss was reduced from 1957 ml in the control group to 736 ml in the aprotinin group (p = 0.002). The mean requirement for intraoperative homologous blood transfusion in the aprotinin group was 1.4 units (95% CI 0.2 to 2.7) and 3.1 units (95% CI 1.7 to 4.6) in the control group (p = 0.033). The mean length of hospital stay was reduced from 27.8 days in the control group to 17.6 days in the aprotinin group which was not statistically significant. The intraoperative use of aprotinin in major orthopaedic operations significantly reduced blood loss and the required amount of packed cells. It may result in in the length of hospital stay and costs.
Comment in
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A strategy for reducing blood-transfusion requirements in elective orthopaedic surgery.J Bone Joint Surg Br. 2004 Mar;86(2):309-10; author reply 310. J Bone Joint Surg Br. 2004. PMID: 15046454 No abstract available.
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Reduction of blood loss using high-dose aprotinin in major orthopaedic surgery.J Bone Joint Surg Br. 2004 May;86(4):620; author reply 620-1. J Bone Joint Surg Br. 2004. PMID: 15174566 No abstract available.
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