Pollack Murray M, Holubkov Richard, Funai Tomohiko, Berger John T, Clark Amy E, Meert Kathleen, Berg Robert A, Carcillo Joseph, Wessel David L, Moler Frank, Dalton Heidi, Newth Christopher J L, Shanley Thomas, Harrison Rick E, Doctor Allan, Jenkins Tammara L, Tamburro Robert, Dean J Michael
1Department of Pediatrics, Children's National Medical Center and the George Washington University School of Medicine and Health Sciences, Washington, DC. 2Department of Child Health, Phoenix Children's Hospital and the University of Arizona School of Medicine, Phoenix, AZ. 3Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT. 4Department of Pediatrics, Children's National Medical Center, Washington, DC. 5Department of Pediatrics, Children's Hospital of Michigan, Detroit, MI. 6Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA. 7Department of Critical Care Medicine, Children's Hospital of Pittsburgh, Pittsburgh, PA. 8Department of Pediatrics, Children's National Medical Center, Washington, DC. 9Department of Pediatrics, University of Michigan, Ann Arbor, MI. 10Department of Child Health, Phoenix Children's Hospital and University of Arizona College of Medicine-Phoenix, Phoenix, AZ. 11Department of Anesthesiology and Critical Care Medicine, Children's Hospital Los Angeles, Los Angeles, CA. 12Department of Pediatrics, University of California at Los Angeles, Los Angeles, CA. 13Department of Pediatrics, Washington University School of Medicine, St. Louis, MO. 14Department of Biochemistry, Washington University School of Medicine, St. Louis, MO. 15Pediatric Trauma and Critical Illness Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, the National Institutes of Health, Bethesda, MD.
Crit Care Med. 2015 Aug;43(8):1699-709. doi: 10.1097/CCM.0000000000001081.
Assessments of care including quality assessments adjusted for physiological status should include the development of new morbidities as well as mortalities. We hypothesized that morbidity, like mortality, is associated with physiological dysfunction and could be predicted simultaneously with mortality.
Prospective cohort study from December 4, 2011, to April 7, 2013.
General and cardiac/cardiovascular PICUs at seven sites.
Randomly selected PICU patients from their first PICU admission.
None.
Among 10,078 admissions, the unadjusted morbidity rates (measured with the Functional Status Scale and defined as an increase of ≥ 3 from preillness to hospital discharge) were 4.6% (site range, 2.6-7.7%) and unadjusted mortality rates were 2.7% (site range, 1.3-5.0%). Morbidity and mortality were significantly (p < 0.001) associated with physiological instability (measured with the Pediatric Risk of Mortality III score) in dichotomous (survival and death) and trichotomous (survival without new morbidity, survival with new morbidity, and death) models without covariate adjustments. Morbidity risk increased with increasing Pediatric Risk of Mortality III scores and then decreased at the highest Pediatric Risk of Mortality III values as potential morbidities became mortalities. The trichotomous model with covariate adjustments included age, admission source, diagnostic factors, baseline Functional Status Scale, and the Pediatric Risk of Mortality III score. The three-level goodness-of-fit test indicated satisfactory performance for the derivation and validation sets (p > 0.20). Predictive ability assessed with the volume under the surface was 0.50 ± 0.019 (derivation) and 0.50 ± 0.034 (validation) (vs chance performance = 0.17). Site-level standardized morbidity ratios were more variable than standardized mortality ratios.
New morbidities were associated with physiological status and can be modeled simultaneously with mortality. Trichotomous outcome models including both morbidity and mortality based on physiological status are suitable for research studies and quality and other outcome assessments. This approach may be applicable to other assessments presently based only on mortality.
对包括根据生理状态进行调整的质量评估在内的护理评估应涵盖新发病症以及死亡率。我们假设,与死亡率一样,发病率与生理功能障碍相关,并且可以与死亡率同时进行预测。
2011年12月4日至2013年4月7日的前瞻性队列研究。
七个地点的综合重症监护病房以及心脏/心血管重症监护病房。
从首次入住重症监护病房的患者中随机选取。
无。
在10078例入院病例中,未调整的发病率(采用功能状态量表测量,定义为从病前到出院时增加≥3)为4.6%(各地点范围为2.6 - 7.7%),未调整的死亡率为2.7%(各地点范围为1.3 - 5.0%)。在未进行协变量调整的二分法(生存和死亡)及三分法(无新发病症生存、有新发病症生存和死亡)模型中,发病率和死亡率与生理不稳定(采用儿童死亡风险III评分测量)显著相关(p < 0.001)。发病率风险随着儿童死亡风险III评分的增加而升高,然后在儿童死亡风险III值最高时降低,因为潜在的病症转变为死亡。进行协变量调整的三分法模型包括年龄、入院来源、诊断因素、基线功能状态量表以及儿童死亡风险III评分。三级拟合优度检验表明推导集和验证集的表现令人满意(p > 0.20)。用曲面下面积评估的预测能力在推导集中为0.50±0.019,在验证集中为0.50±0.034(与随机表现=0.17相比)。各地点层面的标准化发病率比标准化死亡率更具变异性。
新发病症与生理状态相关,并且可以与死亡率同时建模。基于生理状态的包括发病率和死亡率的三分法结局模型适用于研究以及质量和其他结局评估。这种方法可能适用于目前仅基于死亡率的其他评估。