Jacobs Marshall Lewis, Jacobs Jeffrey Phillip, Jenkins Kathy J, Gauvreau Kimberlee, Clarke David R, Lacour-Gayet Francois
Drexel University College of Medicine, Philadelphia, Pennsylvania 19073, USA.
Cardiol Young. 2008 Dec;18 Suppl 2:163-8. doi: 10.1017/S1047951108002904.
Meaningful evaluation of quality of care must account for variations in the population of patients receiving treatment, or "case-mix". In adult cardiac surgery, empirical clinical data, initially from tens of thousands, and more recently hundreds of thousands of operations, have been used to develop risk-models, to increase the accuracy with which the outcome of a given procedure on a given patient can be predicted, and to compare outcomes on non-identical patient groups between centres, surgeons and eras. In the adult cardiac database of The Society of Thoracic Surgeons, algorithms for risk-adjustment are based on over 1.5 million patients undergoing isolated coronary artery bypass grafting and over 100,000 patients undergoing isolated replacement of the aortic valve or mitral valve. In the pediatric and congenital cardiac database of The Society of Thoracic Surgeons, 61,014 operations are spread out over greater than 100 types of primary procedures. The problem of evaluating quality of care in the management of pediatric patients with cardiac diseases is very different, and in some ways a great deal more challenging, because of the smaller number of patients and the higher number of types of operations. In the field of pediatric cardiac surgery, the importance of the quantitation of the complexity of operations centers on the fact that outcomes analysis using raw measurements of mortality, without adjustment for complexity, is inadequate. Case-mix can vary greatly from program to program. Without stratification of complexity, the analysis of outcomes for congenital cardiac surgery will be flawed. Two major multi-institutional efforts have attempted to measure the complexity of pediatric cardiac operations: the Risk Adjustment in Congenital Heart Surgery-1 method and the Aristotle Complexity Score. Both systems were derived in large part from subjective probability, or expert opinion. Both systems are currently in wide use throughout the world and have been shown to correlate reasonably well with outcome. Efforts are underway to develop the next generation of these systems. The next generation will be based more on objective data, but will continue to utilize subjective probability where objective data is lacking. A goal, going forward, is to re-evaluate and further refine these tools so that, they can be, to a greater extent, derived from empirical data. During this process, ideally, the mortality elements of both the Aristotle Complexity Score and the Risk Adjustment in Congenital Heart Surgery-1 methodology will eventually unify and become one and the same. This review article examines these two systems of stratification of complexity and reviews the rationale for the development of each system, the current use of each system, the plans for future enhancement of each system, and the potential for unification of these two tools.
对医疗质量进行有意义的评估必须考虑接受治疗的患者群体差异,即“病例组合”。在成人心脏手术中,最初来自数万例、最近来自数十万例手术的经验性临床数据已被用于开发风险模型,以提高预测特定患者接受特定手术结果的准确性,并比较不同中心、外科医生和时代的不同患者群体的手术结果。在胸外科医师协会的成人心脏数据库中,风险调整算法基于150多万例接受单纯冠状动脉搭桥手术的患者以及10多万例接受单纯主动脉瓣或二尖瓣置换手术的患者。在胸外科医师协会的儿科和先天性心脏病数据库中,61,014例手术分布在100多种主要手术类型中。由于儿科心脏病患者数量较少且手术类型较多,评估儿科心脏病患者护理质量的问题非常不同且在某些方面更具挑战性。在小儿心脏外科领域,手术复杂性量化的重要性集中在这样一个事实上,即使用未经复杂性调整的原始死亡率测量进行结果分析是不够的。病例组合在不同项目之间可能有很大差异。如果不按复杂性进行分层,则先天性心脏手术的结果分析将存在缺陷。两项主要的多机构研究试图衡量小儿心脏手术的复杂性:先天性心脏病手术风险调整-1方法和亚里士多德复杂性评分。这两种系统在很大程度上都源自主观概率或专家意见。这两种系统目前在全世界广泛使用,并且已被证明与结果有合理的相关性。正在努力开发这些系统的下一代版本。下一代将更多地基于客观数据,但在缺乏客观数据的情况下仍将使用主观概率。未来的一个目标是重新评估并进一步完善这些工具,以便在更大程度上从经验数据中得出。在此过程中,理想情况下,亚里士多德复杂性评分和先天性心脏病手术风险调整-1方法的死亡率要素最终将统一并变得相同。这篇综述文章研究了这两种复杂性分层系统,并回顾了每个系统的开发原理、当前使用情况、每个系统未来改进的计划以及这两种工具统一的可能性。