Fung Mark, Haghamad Aya, Montgomery Elizabeth, Swanson Kathleen, Wilkerson Myra L, Stathakos Kimon, VanNess Richard, Nowak Sarah A, Wilburn Clayton, Kavus Haluk, Swid Mohammed Amer, Okoye Nkemakonam, Ziemba Yonah C, Ramrattan Girish, Macy Jonathan, McConnell John, Lewis Mary Jane, Bailey Beth, Shotorbani Khosrow, Crawford James M
Department of Pathology and Laboratory Medicine, University of Vermont College of Medicine, Burlington, VT, USA.
Department of Pathology and Laboratory Medicine, Northwell Health, New Hyde Park, NY, USA.
BMC Nephrol. 2024 Dec 6;25(1):447. doi: 10.1186/s12882-024-03869-4.
A retrospective observational study was conducted at 3 health care organizations to identify clinical gaps in care for patients with stage 3 or 4 chronic kidney disease (CKD), and financial opportunity from U.S. risk adjustment payment systems. Lack of evaluation for CKD in patients with diabetes was also assessed.
Outpatient longitudinal laboratory results and patient metadata available in the electronic medical record, laboratory information system, and/or laboratory billing or facility claims data for the calendar year 2021 were evaluated. Laboratory results were compared to billing data (ICD-10 codes) and risk adjustment scores including Hierarchical Condition Categories (HCC) to determine if laboratory-identified CKD was coded as a disease condition in the electronic medical record. Adults 18 to 75 years of age were included; inpatient laboratory results and pregnant individuals were excluded.
At the 3 institutions, 12,478 of 16,063 (78%), 487 of 1511 (32%) and 19,433 of 29,277 (66%) of patients with laboratory evidence of stage 3 or 4 CKD did not have a corresponding ICD-10 or HCC code for CKD in the electronic medical record. For patients at the 3 institutions with diabetes on the basis of an HbA1c value of ≥ 6.5%, 34,384 of 58,278 (59%), 2274 of 2740 (83%) and 40,378 of 52,440 (77%) had not undergone guideline-recommended laboratory testing for CKD during the same 12 months. Using publicly available data for calendar year 2021, an estimated 3246 of 32,398 patients (9.9%) at the 3 institutions with undocumented CKD stages 3-4 would be enrolled in Medicare Advantage or Affordable Care Act Marketplace programs. The imputed lost reimbursement under risk-adjusted payment systems for under-documentation of CKD in this subset of patients was $2.85 M for the three institutions combined, representing lost opportunity for both identification and proactive clinical management of these patients, and financial recovery for the costs of providing that care.
Clinical laboratories can provide value beyond routine diagnostics, helping to close gaps in care for identification and management of CKD, stratifying subgroups of patients to identify risk, and capturing missed reimbursement through risk adjustment factors.
在3家医疗保健机构进行了一项回顾性观察研究,以确定3期或4期慢性肾脏病(CKD)患者的护理临床差距,以及美国风险调整支付系统带来的财务机会。还评估了糖尿病患者中CKD评估的缺失情况。
对2021日历年电子病历、实验室信息系统和/或实验室计费或机构索赔数据中可用的门诊纵向实验室结果和患者元数据进行评估。将实验室结果与计费数据(ICD-10编码)和风险调整分数(包括分层条件类别(HCC))进行比较,以确定实验室确定的CKD在电子病历中是否被编码为疾病状态。纳入18至75岁的成年人;排除住院实验室结果和孕妇。
在这3家机构中,有实验室证据表明患有3期或4期CKD的患者中,16063例中的12478例(78%)、1511例中的487例(32%)以及29277例中的19433例(66%)在电子病历中没有对应的CKD的ICD-10或HCC编码。对于这3家机构中基于糖化血红蛋白(HbA1c)值≥6.5%诊断为糖尿病的患者,在同一12个月内,58278例中的34384例(59%)、2740例中的2274例(83%)以及52440例中的40378例(77%)未接受指南推荐的CKD实验室检测。利用2021日历年的公开数据,这3家机构中估计有32398例未记录CKD分期3 - 4期的患者中的3246例(9.9%)将参加医疗保险优势计划或《平价医疗法案》市场计划。在这部分患者中,由于CKD记录不全,风险调整支付系统估算的报销损失在这三家机构总计为285万美元,这既代表了识别和积极临床管理这些患者的机会丧失,也代表了提供该护理成本的财务回收损失。
临床实验室可以提供超出常规诊断的价值,有助于缩小CKD识别和管理方面的护理差距,对患者亚组进行分层以识别风险,并通过风险调整因素获取遗漏的报销。