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Effects of tourniquet inflation on peri- and postoperative cefuroxime concentrations in bone and tissue.

Authors :
Hanberg, Pelle
Bue, Mats
Kabel, Jesper
Jørgensen, Andrea René
Jessen, Christian
Søballe, Kjeld
Stilling, Maiken
Source :
Acta Orthopaedica; Dec 2021, Vol. 92 Issue 6, p746-752, 7p, 1 Illustration, 1 Diagram, 4 Charts
Publication Year :
2021

Abstract

Background and purpose — Tourniquet is widely used in orthopedic surgery to reduce intraoperative bleeding and improve visualization. We evaluated the effect of tourniquet application on peri- and postoperative cefuroxime concentrations in subcutaneous tissue, skeletal muscle, calcaneal cancellous bone, and plasma. The primary endpoint was the time for which the free cefuroxime concentration was maintained above the clinical breakpoint minimal inhibitory concentration (T > MIC) for Staphylococcus aureus (4 µg/mL). Patients and methods — 10 patients scheduled for hallux valgus or hallux rigidus surgery were included. Microdialysis catheters were placed for sampling of cefuroxime concentrations bilaterally in subcutaneous tissue, skeletal muscle, and calcaneal cancellous bone. A tourniquet was applied on the thigh of the leg scheduled for surgery (tourniquet duration time [range]: 65 minutes [58–77]). Cefuroxime (1.5 g) was administered intravenously 15 minutes prior to tourniquet inflation, followed by a second dose 6 hours later. Dialysates and venous blood samples were collected for 12 hours. Results — A cefuroxime concentration of 4 µg/mL was reached within 23 minutes in all compartments and patients. For cefuroxime the T > MIC (4 µg/mL) ranged between 4.8 and 5.4 hours across compartments, with similar results for the tourniquet and non-tourniquet leg. Comparable T > MIC and penetration ratios were found for the first and second dosing intervals. Interpretation — Administration of cefuroxime (1.5 g) 15 minutes prior to tourniquet inflation is safe in order to achieve tissue concentrations above 4 µg/mL throughout surgery. A tourniquet application time of approximately 1 hour did not affect the cefuroxime tissue penetration in the following dosing interval. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17453674
Volume :
92
Issue :
6
Database :
Complementary Index
Journal :
Acta Orthopaedica
Publication Type :
Academic Journal
Accession number :
153736705
Full Text :
https://doi.org/10.1080/17453674.2021.1942620