[Research progress of mechanism and prevention of peritendinous adhesions]

Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2013 May;27(5):633-6.
[Article in Chinese]

Abstract

Objective: To review the research progress of mechanism and prevention of peritendinous adhesions. Methods Recent literature about peritendinous adhesions was reviewed, and the results from experiments about the mechanism and prevention of peritendinous adhesions were analyzed.

Results: The molecular mechanism of peritendinous adhesions is related to overexpressions of transforming growth factor beta 1, early growth response protein 1, matrix metallopeptidase 9, and so on. The present methods of prevention of peritendinous adhesions include drugs, barrier, optimizing rehabilitation, gene therapy, and so on. These methods have achieved good results in experiments, but the clinical applications have not been confirmed yet.

Conclusion: It is necessary to pay more attention to the research of mechanism of peritendinous adhesions and methods of its prevention and subsequently to convert them into clinical applications, which is significant to the prevention of peritendinous adhesions in the future.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / administration & dosage*
  • Biocompatible Materials / administration & dosage
  • Genetic Therapy / methods
  • Humans
  • Hyaluronic Acid / administration & dosage
  • Ibuprofen / administration & dosage
  • Matrix Metalloproteinase 9 / metabolism
  • Membranes, Artificial
  • Motion Therapy, Continuous Passive
  • Postoperative Complications / etiology
  • Postoperative Complications / prevention & control
  • Tendon Injuries / pathology
  • Tendon Injuries / surgery*
  • Tissue Adhesions / etiology*
  • Tissue Adhesions / metabolism
  • Tissue Adhesions / prevention & control*
  • Transforming Growth Factor beta1 / metabolism
  • Wound Healing / physiology

Substances

  • Anti-Inflammatory Agents
  • Biocompatible Materials
  • Membranes, Artificial
  • Transforming Growth Factor beta1
  • Hyaluronic Acid
  • Matrix Metalloproteinase 9
  • Ibuprofen