Safety and Efficacy of an Amniotic Suspension Allograft Injection Over 12 Months in a Single-Blinded, Randomized Controlled Trial for Symptomatic Osteoarthritis of the Knee.

この研究はインパクトが大きい可能性があると判断されました。 OEのAIによるハイインパクト指標は、論文が掲載されたジャーナルと論文自体の科学的内容の両方からのシグナルを統合することで、論文の影響力を推定します。 最先端の自然言語処理を用いて開発されたOEハイインパクトモデルは、ジャーナルのインパクトファクターのみよりも、研究の将来の引用実績をより正確に予測します。 これにより、臨床的に意義のある研究をより早く認識することができ、読者は将来の診療を形成する可能性が最も高い論文に焦点を当てることができます。

研究概要

Two-hundred patients with moderate, symptomatic knee osteoarthritis were randomized to receive an intra-articular injection of amniotic suspension allograft (ASA; n=68), hyaluronic acid (HA; n=64) or normal saline (n=68). Outcomes of interest included the change from baseline at 12 months in the Knee Injury and Osteoarthritis Outcome Score (KOOS) subsets (pain; symptoms; activities of daily living; sports and recreation; quality of life), as well as Visual Analog Scale (VAS) pain scores overall, during strenuous work, during sedentary work, and during normal daily living. Immunoglobulin levels and C-reactive protein (CRP) levels, as well as the presence of serum anti human leukocyte antigen (HLA) levels, were recorded up to 6 months post-injection. Results revealed significantly greater improvement in all KOOS subsets and VAS pain scores from baseline at 12 months in the ASA group compared to the HA and saline groups. However, severe patient drop-out after 3 months in the HA and saline groups was observed, and a last observation carried forward method was used for analysis. No significant differences between the ASA group and the HA and saline groups were observed in all immunoglobulin levels, with the exception of IgE at 6 months which was significantly higher in the saline group vs ASA. The rate of treatment-emergent adverse event cases was similar between the ASA (2.9%) and HA (3.1%) groups, with none observed in the saline group.