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追求精准医学:先天性心脏病手术后未测量的患者因素与死亡率。

The Quest for Precision Medicine: Unmeasured Patient Factors and Mortality After Congenital Heart Surgery.

机构信息

Division of Cardiology, Department of Pediatrics and Communicable Diseases, University of Michigan C.S. Mott Children's Hospital, Ann Arbor, Michigan.

Division of Cardiology, Department of Pediatrics and Communicable Diseases, University of Michigan C.S. Mott Children's Hospital, Ann Arbor, Michigan.

出版信息

Ann Thorac Surg. 2019 Dec;108(6):1889-1894. doi: 10.1016/j.athoracsur.2019.06.031. Epub 2019 Aug 6.

Abstract

BACKGROUND

Emerging data across many fields suggest that unique patient characteristics can impact disease manifestation and response to therapy, supporting "precision medicine" approaches and more individualized and targeted therapeutic strategies. In children undergoing congenital heart surgery, current risk models primarily focus on the population level, and their utility in understanding precise characteristics that place individual patients at risk for poor outcome remains unclear.

METHODS

We analyzed index surgeries in the Pediatric Cardiac Critical Care Consortium (PC) registry (August 2014 to May 2016) and utilized a previously constructed model containing patient factors typically included in in-hospital mortality risk models (age, weight, prematurity, chromosomal anomalies/syndromes, preoperative factors, The Society of Thoracic Surgeons-European Association for Cardio-Thoracic Surgery score). Partitioned variances based on a hierarchical generalized linear model were used to estimate the proportion of variation in mortality explained by these factors.

RESULTS

A total of 8406 operations (22 hospitals) were included. We found that only 30% of the total between-patient variation in mortality in our cohort was explained by the patient factors included in our model. Age, The Society of Thoracic Surgeons-European Association for Cardio-Thoracic Surgery score, and preoperative mechanical ventilation explained the greatest proportion of variation. Of the variation that remained unexplained, 95% was attributable to unmeasured patient factors. In stratified analyses, these results were consistent across patient subgroups.

CONCLUSIONS

Patient factors typically included in congenital heart surgery risk models explain only a small portion of total variation in mortality. A better understanding of other underrecognized factors is critical in further defining risk profiles and in developing more individualized and tailored therapeutic strategies.

摘要

背景

许多领域的新兴数据表明,独特的患者特征可能会影响疾病的表现和对治疗的反应,支持“精准医学”方法以及更个体化和针对性的治疗策略。在接受先天性心脏病手术的儿童中,当前的风险模型主要侧重于人群水平,其在理解将个体患者置于不良预后风险中的精确特征方面的效用尚不清楚。

方法

我们分析了儿科心脏危重病护理联合会(PC)登记处(2014 年 8 月至 2016 年 5 月)的索引手术,并利用了先前构建的模型,该模型包含了通常包含在住院死亡率风险模型中的患者因素(年龄、体重、早产、染色体异常/综合征、术前因素、胸外科医师协会-欧洲心血管外科学会评分)。基于分层广义线性模型的方差划分用于估计这些因素解释死亡率差异的比例。

结果

共纳入 8406 例手术(22 家医院)。我们发现,我们队列中死亡率的总患者间差异只有 30%可以用我们模型中包含的患者因素来解释。年龄、胸外科医师协会-欧洲心血管外科学会评分和术前机械通气解释了最大的变异比例。未解释的变异中,有 95%归因于未测量的患者因素。在分层分析中,这些结果在患者亚组中是一致的。

结论

通常包含在先天性心脏病手术风险模型中的患者因素仅能解释死亡率总变异的一小部分。更好地了解其他未被充分认识的因素对于进一步定义风险特征以及开发更个体化和定制的治疗策略至关重要。

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