Intraoperative pneumatic tourniquet application reduces soft-tissue microcirculation, but without affecting wound healing in calcaneal fractures.

Ali Modabber, Boyko Gueorguiev, Torsten Pastor, Matthias Knobe, Frank Hildebrand, Bergita Ganse, Filippo Migliorini, Philipp Lichte, Felix M Bläsius, Sven Nebelung, Kajetan Klos, Mario F Scaglioni, Clemens Schopper

Journal: European journal of medical research 2024;29(1):462

PMID: 39289760

Abstract

BACKGROUND

Wound healing complications are a major challenge following the extended lateral approach in calcaneal fractures. Soft-tissue microcirculation plays an important role via the delivery of oxygen, nutrients, and the regulation of a local milieu. The aim of this clinical study was to examine the effect of intraoperative pneumatic tourniquet application on skin and subcutaneous microcirculation, and its impact on wound healing progression.

METHODS

Patients with calcaneal fractures were randomly assigned to two groups defined by a surgery conducted either with use or without use of a tourniquet. Blood flow (BF [AU]), tissue oxygen saturation (SO[%]) and the relative amount of haemoglobin (rHb[AU]) were intraoperatively measured at two depths (2 and 8 mm) non-invasively by spectrophotometry (Micro-Lightguide O2C, LEA Medizintechnik, Giessen, Germany). Time points were before and after inflation of the pneumatic tourniquet and also at the end of surgery before deflation. A linear mixed model (LMM) was fitted for statistical analysis.

RESULTS

Thirty-four patients (3 women and 31 men) with 37 calcaneal fractures were included. In 22 of them, the surgery was conducted with a tourniquet and in the other 15 without its use. A significant decrease of microcirculation, characterized by decreases in blood flow (p = 0.011) and tissue oxygenation (p = 0.023) was measured in 8 mm depth after inflating the tourniquet. However, these changes did not influence the time of postoperative wound healing.

CONCLUSION

The use of a pneumatic tourniquet reduces deep microcirculation without affecting postoperative wound healing. Trial registration The study was registered in www.

CLINICALTRIALS

gov (NCT01264146).

© 2024. The Author(s).

Address: Department of Orthopaedics, Trauma and Reconstructive Surgery, University Hospital RWTH Aachen, Aachen, Germany. [email protected].; Department of Orthopaedics, Trauma and Reconstructive Surgery, University Hospital RWTH Aachen, Aachen, Germany.; Werner Siemens Foundation Endowed Chair of Innovative Implant Development, Saarland University, Homburg, Germany.; Department of Trauma, Hand and Reconstructive Surgery, Saarland University, Homburg, Germany.; AO Research Institute Davos, 7270, Davos, Switzerland.; Department of Orthopaedic and Trauma Surgery, Cantonal Hospital Lucerne, 6000, Lucerne, Switzerland.; Department of Diagnostic and Interventional Radiology, Aachen University Hospital, 52074, Aachen, Germany.; Gelenkzentrum Rhein-Main, Hochheim, Germany.; Department of Trauma, Hand and Reconstructive Surgery, Jena University Hospital, Friedrich Schiller University Jena, 07747, Jena, Germany.; Department of Oral and Maxillofacial Surgery, University Hospital of Aachen, Aachen, Germany.; Department of Hand- and Plastic Surgery, Lucerne Cantonal Hospital, Lucerne, Switzerland.; Department for Orthopedics and Traumatology, Kepler University Hospital GmbH, Johannes Kepler University Linz, Linz, Austria.; Medical Faculty, University of Zurich, 8091, Zurich, Switzerland. [email protected].; Medical Faculty, RWTH Aachen University Hospital, 52074, Aachen, Germany. [email protected].; Department of Orthopaedic Trauma, Westmuensterland Hospital, 48683, Ahaus, Germany. [email protected].
Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.