The impaired healing hypothesis: a mechanism by which psychosocial stress and personal characteristics increase MSD risk?. Issue 4 (3rd April 2022)

• Record Type: Journal Article
• Authors: Gallagher, Sean; Barbe, Mary F.
• Is Part Of: Ergonomics. Volume 65:Issue 4(2022)
• Page Start: 573
• Page End: 586
• Publication Date: 2022-04-03
• Subjects: Musculoskeletal disorders -- fatigue failure -- psychological stress -- age -- sex -- obesity healing; Human engineering -- Periodicals; Cybernetics -- Periodicals; Industrial management -- Periodicals; Ergonomie -- Périodiques; Cybernétique -- Périodiques; Gestion d'entreprise -- Périodiques; 620.8205
• DOI: 10.1080/00140139.2021.1974103
• Languages: English
• ISSNs: 0014-0139

Abstract

Abstract: While the effects of physical risk factors on MSD development have been a primary focus of musculoskeletal research, psychological stressors, and certain personal characteristics (e.g. ageing, sex, and obesity) are also associated with increased MSD risk. The psychological and personal characteristics listed above share a common characteristic: all are associated with disruption of the body's neuroendocrine and immune responses resulting in an impaired healing process. An impaired healing response may result in reduced fatigue life of musculoskeletal tissues due to a diminished ability to keep pace with accumulating damage (perhaps reparable under normal circumstances), and an increased vulnerability of damaged tissue to further trauma owing to the prolonged healing process. Research in engineered self-healing materials suggests that decreased healing kinetics in the presence of mechanical loading can substantially reduce the fatigue life of materials. A model of factors influencing damage accrual and healing will be presented. Practitioner summary: This article provides a potential reason why musculoskeletal disorder risk is affected by psychosocial stress, age, sex, and obesity. The reason is that these factors are all associated with a slower than normal healing response. This may lead to faster damage development in musculoskeletal tissues resulting in higher MSD risk.