McNamara Colin, Bondar Kevin, Sullivan Thomas C, Clyburn Terry A, Park Kwan J, Brown Timothy S
Department of Orthopedics & Sports Medicine, Houston Methodist Hospital, Houston, TX, USA.
Arthroplast Today. 2023 Sep 18;23:101200. doi: 10.1016/j.artd.2023.101200. eCollection 2023 Oct.
Many institutions require the routine collection of pathology samples from every primary total knee arthroplasty (TKA) performed. These policies are controversial, and their cost-effectiveness is difficult to define. We sought to judge the cost-effectiveness of one such policy according to World Health Organization recommendations.
We analyzed 3200 consecutive primary TKAs, comparing our presumed preoperative diagnoses against the diagnoses made by the pathologist. Diagnoses were categorized as concordant (matching), discrepant (not matching but without impact to patient management), or discordant (not matching and resulting in a direct change to patient management). An incremental cost-utility ratio analysis was performed to determine the cost-effectiveness of our institution's policy to routinely collect pathology samples from every primary TKA performed. Cost-effectiveness was defined by World Health Organization guidelines as a cost of less than $228,090 per quality-adjusted life year gained.
Twelve pathology samples were lost before reaching a pathologist. From the remaining 3188 samples, we identified 3158 concordant cases, 29 discrepant diagnoses, and 1 discordant diagnosis. It cost an estimated $10,522.60 to identify each discrepant diagnosis and an estimated $305,155.36 to diagnose one discordant case in our cohort. Our incremental cost-utility ratio analysis revealed that we spent $305,155.36 to gain 0 quality-adjusted life years for our patients.
Routine histopathologic analysis of TKA samples was cost-ineffective in our patient cohort and may not be necessary during routine TKA.
许多机构要求对每例初次全膝关节置换术(TKA)常规采集病理样本。这些政策存在争议,其成本效益难以界定。我们试图根据世界卫生组织的建议来评判其中一项此类政策的成本效益。
我们分析了连续的3200例初次TKA病例,将我们术前推测的诊断与病理学家做出的诊断进行比较。诊断结果分为一致(匹配)、不一致(不匹配但对患者管理无影响)或不协调(不匹配且导致患者管理直接改变)。进行了增量成本效用比分析,以确定我们机构对每例初次TKA常规采集病理样本这一政策的成本效益。世界卫生组织指南将成本效益定义为每获得一个质量调整生命年的成本低于228,090美元。
有12份病理样本在送达病理学家之前丢失。在其余3188份样本中,我们确定了3158例一致病例、29例不一致诊断和1例不协调诊断。在我们的队列中,确定每例不一致诊断估计花费10,522.60美元,诊断1例不协调病例估计花费305,155.36美元。我们的增量成本效用比分析显示,我们花费305,155.36美元为患者获得了0个质量调整生命年。
在我们的患者队列中,TKA样本的常规组织病理学分析成本效益不佳,在常规TKA期间可能没有必要。