The tourniquet's effects on skeletal muscle during total knee arthroplasty

Author:

Johnsen Magnus1ORCID,Mousavizadeh Rouhollah2,Scott Alex3,Havik Steinar1,Husby Vigdis S.4,Winther Siri B.5,Husby Otto S.6,Lian Øystein67

Affiliation:

1. Orthopedic Department Trondheim University Hospital Trondheim Norway

2. Department of Physical Therapy, Faculty of Medicine The University of British Columbia Vancouver British Columbia Canada

3. Department of Physical Therapy, Faculty of Medicine The University of British Columbia, Vancouver Campus Vancouver British Columbia Canada

4. Department of Health Sciences Aalesund, Faculty of Medicine and Health Science Norwegian University of Science and Technology Aalesund Norway

5. Orthopedic Research Department Trondheim University Hospital Trondheim Norway

6. Department of Neuromedicine and Movement Science, Faculty of Medicine and Health Science Norwegian University of Science and Technology Trondheim Norway

7. Department of Orthopedic Surgery Kristiansund Hospital Kristiansund Norway

Abstract

AbstractThis study investigates the impact of perioperative tourniquet on skeletal muscle cells during total knee arthroplasty (TKA) and its effects on the gene expression of apoptotic, inflammatory, and angiogenic pathways. The randomized controlled trial included 44 patients undergoing TKA. The patients were randomized to undergo surgery with (n = 23) or without (n = 21) tourniquet. The tourniquet was inflated before skin incision and deflated before wound closure in the tourniquet group. Biopsies from the lateral vastus muscle were obtained from both groups before wound closure and 8 weeks after surgery. The messenger ribonucleic acid (mRNA) expression and protein levels of angiopoietin‐like 4 (ANGPTL4), Hypoxia‐inducible Factor 1α, and Vascular Endothelial Growth Factor Alpha (VEGF‐A) in the biopsies were examined by reverse transcription‐quantitative polymerase chain reaction and tissue microarray, respectively. Differences in mean values (ΔCt for mRNA expression and staining positivity for protein expression) were compared with t‐tests. The apoptotic marker BID and the angiogenic marker VEGF‐A were significantly lower in the tourniquet group compared to the control group (p = 0.03, p = 0.047). However, there was a significant upregulation of VEGF‐A 8 weeks after surgery in the tourniquet group compared to perioperative biopsies (p = 0.002), indicating persistent changes. A significant upregulation in protein expression of the angiogenic marker ANGPTL4 was found perioperatively in the tourniquet group (p = 0.02). Our results demonstrate that the angiogenic gene expression is significantly altered by the tourniquet, the effects of which might contribute to postoperative interstitial edema, increased pain, and decreased muscle strength. These effects could lead to delayed rehabilitation and ultimately reduced patient satisfaction after TKA.

Funder

Zimmer Biomet

Publisher

Wiley

Reference36 articles.

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