The Effect of Total Knee Replacement Surgery on Immune Functioning in Elderly
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Immunosenescence
- Sponsor
- Wageningen University
- Enrollment
- 14
- Locations
- 1
- Primary Endpoint
- Monocyte-derived TNFa production
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
The goal of this observational study is to determine changes in immune functioning after total knee replacement surgery in elderly. The study population consists of 14 patients aged 65 years or over undergoing primary total knee replacement surgery. Immune functioning will be assessed at multiple timepoints before and after surgery (i.e., ± 6 weeks before, and 1 day, 1 week, ± 2 weeks, and ± 6 weeks after surgery). Each patient will serve as his/her own control. Immune functioning will primarily be assessed by determining the change from baseline in monocyte-derived TNFα production at 1 week after surgery. Changes in monocyte responsiveness are considered indicative for changes in immune functioning. As secondary objective, additional parameters of immune functioning will be assessed. In addition, the course of immune functioning following total knee replacement surgery will be investigated. Burden and potential risks for the patient are estimated to be minor. During the study, 5 blood samples of 20 mL will be collected over a period of ± 12 weeks, resulting in a total blood draw of 100 mL. During surgery a sample of synovial fluid (± 2 mL) will be taken from surgical waste. Before and after surgery patients will report their pain medication intake and the presence of cold and flu-like symptoms in a diary. Patients do not directly benefit from the study.
Detailed Description
The world population is progressively aging. As humans age, their immune system becomes weaker through a process called immunosenescence. This age-related decline in immune functioning results in an increased susceptibility to infections. Elderly with chronic diseases or elderly who have experienced an incident, such as fall-related trauma or surgery, are particularly vulnerable to these infections, likely due to immunosuppression resulting from such an immune challenge. Currently, there are no standard interventions used to improve immune functioning in these immune-suppressed elderly. However, before the potential of such interventions can be explored, postoperative immune suppression in elderly first needs to be demonstrated. The goal of this prospective ex vivo study is therefore to determine changes in immune functioning after total knee replacement surgery in elderly. The study population consists of 14 patients (classified as ASA II or ASA III) aged 65 years or over, diagnosed with osteoarthritis, undergoing primary total knee replacement surgery under general anesthesia. Immune functioning will be assessed at multiple timepoints before and after surgery (i.e., ± 6 weeks before, and 1 day, 1 week, ± 2 weeks, and ± 6 weeks after surgery). Each patient will serve as his/her own control. Immune functioning will primarily be assessed by determining the change from baseline in monocyte-derived TNFα production at 1 week after surgery. TNFα production will be measured after ex vivo stimulation of whole blood with inflammatory stimuli and normalized for monocyte count. Changes in monocyte responsiveness are considered indicative for changes in immune functioning. As secondary objective, additional parameters of immune functioning will be assessed. In addition, the course of immune functioning following total knee replacement surgery will be investigated. Burden and potential risks for the patient are estimated to be minor. During the study, 5 blood samples of 20 mL will be collected over a period of ± 12 weeks, resulting in a total blood draw of 100 mL. Blood sampling will be combined with regular care visits, with the exception of one occasion where blood sampling will be performed at home. Patients could experience mild pain by the venipuncture, which occasionally leads to lightheadedness, fainting and hematoma. During surgery a sample of synovial fluid (± 2 mL) will be taken from surgical waste. Before and after surgery patients will report their pain medication intake and the presence of cold and flu-like symptoms in a diary. Patients do not directly benefit from the study.
Investigators
Klaske van Norren
Principle Investigator / Associate Professor
Wageningen University
Eligibility Criteria
Inclusion Criteria
- •Planned for primary total knee replacement surgery
- •Aged 65 years or over
- •Diagnosed with osteoarthritis
- •ASA Physical Status Classification of II or III
- •Willing to donate a blood sample at 5 different timepoints
- •Able to give written informed consent
Exclusion Criteria
- •Daily use of high doses NSAIDs within the 14 days before inclusion: Defined as higher than maintenance dose in the "farmacotherapeutisch kompas". For example: acetylsalicylic acid \> 4 g/day; diclofenac \> 75 mg/day; naproxen \> 500 mg/day; ibuprofen\> 1600 mg/day; celecoxib \> 200 mg/day
- •Use of systemic corticosteroids
- •Use of antibiotics within the 14 days before inclusion
- •Current diagnosis of cancer
- •Diagnosed with a primary immunodeficiency disorder (e.g., Severe Combined Immunodeficiency (SCID), Common Variable Immune Deficiency (CVID), X-linked agammaglobulinemia, selective immunoglobulin A deficiency, chronic granulomatous disease)
- •Vaccination (e.g., immunization against COVID-19, influenza, pneumonia, and travel-related infections) within the 14 days before inclusion and during the study period
- •Current participation in other scientific research
Outcomes
Primary Outcomes
Monocyte-derived TNFa production
Time Frame: Change from baseline at 1 week after surgery
TNFα production after ex vivo stimulation of whole blood with inflammatory stimuli corrected for monocyte count
Secondary Outcomes
- Monocyte-derived cytokine production(Change from baseline at ± 6 weeks after surgery)
- PBMC (peripheral blood mononuclear cell)-derived cytokine production(Change from baseline at 1 day after surgery)
- Systemic inflammation(Change from baseline at ± 6 weeks after surgery)
- PBMC-derived cytokine production(Change from baseline at ± 6 weeks after surgery)
- Composition of immune cell populations(Change from baseline at ± 6 weeks after surgery)
- Phagocytic function of monocytes(Change from baseline at ± 6 weeks after surgery)
- Monocyte HLA-DR expression(Change from baseline at ± 6 weeks after surgery)
- Synovial inflammation(During surgery)