Introduction: Pain is the primary symptom associated with cartilage damage in the knee. It can lead to impaired function and lower quality of life. Symptomatic management is the primary focus of treatment. Platelet rich plasma and hialuronic acid can be used as methods to reduce pain and improve knee function. Purpose: The purpose of this study was to evaluate the effects of platelet rich plasma on the reduction of pain and improvement of quality of life in patients with knee cartilage damage. Methods: A clinical intervention without a control group was conducted in 54 participants with knee cartilage damage. They recieved one injection of platelet rich plasma. Measurements were made before and six months after the intervention. Numeric rating scale was used to asses pain at rest and in movement, the Knee Injury and Osteoarthritis Outcome Score, the Western Ontario and McMaster Universities Osteoarthritis Index for quality of life and knee function. Tegner Activity Scale was used to asses physical activity. Statistical analysis was made using program R. To compare results we used the paired t test. Mixed linear models were used to indentify associations between participants characteristics and changes over time. Results: Statistically significant differences were observed in all questionnaires between baseline and after six months. P-values were less than or equal to 0,025. Clinically meaningful differences in pain at rest and movement on Numeric Analog Scale and quality of life on Knee Injury and Osteoarthritis Outcome Score were included in the 95-% confidence interval for mean differences. Pain assessment on the Knee Injury and Osteoarthritis Outcome Score and activity level on Tegner Scale did not include clinically meaningful differences. Discussion and conclusion: Platelet rich plasma may contribute to pain reduction and improvement of quality of life in patients with knee cartilage damage. Analysis suggest that pain score on the Knee Injury and Osteoarthritis Outcome Score and physical activity on Tegner did not improve to a clinically significant degree after six months. It is essential to highlight that this was a six month observational study without control group, so findings cannot be generalized. Further studies with a larger sample sizes and standardized protocol of preparation and injection of the platelet rich plasma are needed.
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