Regulation of Cortisol in Patients Undergoing Total Joint Arthoplasty.


Journal

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
ISSN: 1938-2723
Titre abrégé: Clin Appl Thromb Hemost
Pays: United States
ID NLM: 9508125

Informations de publication

Date de publication:
Historique:
entrez: 18 5 2021
pubmed: 19 5 2021
medline: 20 11 2021
Statut: ppublish

Résumé

Osteoarthritis is a condition in which joint cartilage and bone degenerate progressively over time. Total joint arthroplasty is a definitive treatment. Cortisol is a hormone that is associated with pain and inflammation. This study aims to investigate the cortisol levels in patients undergoing total joint arthroplasty. Plasma samples were collected from 71 total joint arthroplasty (TJA) patients at baseline (pre-surgery), 24 hours post-operation, and 5 days post-operation. Cortisol levels were measured in each sample using a commercially available ELISA kit. All results were compiled as group means ± SD. The plasma cortisol level at baseline were 218.5 ± 12 ng/mL. The 24-hour post-surgical samples showed a marked increase in cortisol levels 240.7 ± 15 ng/mL. The blood samples drawn at the 5th day after surgery showed a downward trend (74 ± 12 ng/mL). At 5 days post-operation, cortisol levels were significantly lower than at baseline or 24 hours post-operation. These results point to the fact that prior to surgery, the patient's emotional stress contributes to increased serum cortisol levels. The higher level of cortisol persists at 24 hours post-operation due to inflammation from the procedure. This data also suggests that at 5 days post-operation, the inflammatory response from the surgery and emotional stress subside, resulting in a near normalization of the cortisol levels. Cortisol is a hormone that plays a major role in the body's response to surgery. The relevance between cortisol and different points in the surgical timeline has the potential to prognosticate and improve recovery measures.

Identifiants

pubmed: 34000837
doi: 10.1177/1076029621987614
pmc: PMC8135205
doi:

Substances chimiques

Hydrocortisone WI4X0X7BPJ

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1076029621987614

Subventions

Organisme : NIAID NIH HHS
ID : T35 AI125220
Pays : United States
Organisme : NHLBI NIH HHS
ID : T35 HL120835
Pays : United States

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Auteurs

Rajan Khanna (R)

Department of Pathology and Laboratory Medicine, Loyola University Medical Center, Maywood, IL, USA.

Hannah Slovacek (H)

Department of Pathology and Laboratory Medicine, Loyola University Medical Center, Maywood, IL, USA.

Jeffrey Liles (J)

Department of Orthopedic Surgery, Loyola University Medical Center, Maywood, IL, USA.

Sandra Haddad (S)

Department of Pathology and Laboratory Medicine, Loyola University Medical Center, Maywood, IL, USA.

Pavel Poredos (P)

Medical Clinic Division of Vascular Medicine, Ljubljana University Medical Center, Ljubljana, Slovenia.

Emily Bontekoe (E)

Department of Pathology and Laboratory Medicine, Loyola University Medical Center, Maywood, IL, USA.

Mateja Jezovnik (M)

Department of Advanced Cardiopulmonary Therapies and Transplantation, University of Texas Health Science Center at Houston, Houston, TX, USA.

Debra Hoppensteadt (D)

Department of Pathology and Laboratory Medicine, Cardiovascular Research Institute, Loyola University Chicago, Health Sciences Division, Maywood, IL, USA.

Jawed Fareed (J)

Cardiovascular Research Institute, Loyola University Chicago, Health Sciences Division, Maywood, IL, USA.

William Hopkinson (W)

Orthopaedic Surgery and Rehabilitation Department, Loyola University Chicago, Health Sciences Division, Maywood, IL, USA.

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Classifications MeSH