Comparison of Periprosthetic Joint Infection Incidence and Microbial Profiles in Obese vs Non-Obese Patients After Total Knee Arthroplasty
This observational study aims to compare the incidence of periprosthetic joint infections and their microbial profiles in obese patients versus non-obese patients after undergoing total knee arthroplasty.
Data Collection
Body Weight+5
+ Nutrition Disorders
+ Nutritional and Metabolic Diseases
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: January 1, 2025
Actual date on which the first participant was enrolled.This study focuses on understanding the risk of joint infection after a knee replacement surgery, specifically comparing obese and non-obese patients. The research aims to determine if obesity increases the likelihood of a periprosthetic joint infection (PJI) within two years following the surgery. By identifying the microbial profiles in obese patients, the study hopes to aid in selecting appropriate preventive measures and tailoring antibiotic treatments for this group. This research is important as it could lead to improved care for obese patients undergoing knee replacement surgery. The study involves adult patients with primary or secondary osteoarthritis who have undergone knee replacement surgery between 2011 and 2021. Patients are categorized into two groups based on their Body Mass Index (BMI): obese and non-obese. The primary outcome of interest is revision due to prosthetic joint infection within 730 days following surgery. Secondary outcomes include revision due to all causes within the same timeframe and the type of microbial infection in both obese and non-obese patients within the first 90 days and from 91 days to 730 days post-surgery. The study will use statistical analyses to compare the results between the two groups, taking into account factors such as age, sex, education, income, and comorbidities.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.101299 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: * Adults with available BMI data recieved knee arthroplasty due to osteoarthritis Exclusion Criteria: \-
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Department of Orthopedic surgery and traumatology, Bispebjerg Hospital, Copenhagen, Denmark
Copenhagen NV, DenmarkOpen Department of Orthopedic surgery and traumatology, Bispebjerg Hospital, Copenhagen, Denmark in Google Maps