Adverse Events in Pediatric Critical Care Nonsurvivors With a Low Predicted Mortality Risk: A Multicenter Case Control Study*

被引:3
|
作者
Verlaat, Carin [1 ]
Zegers, Marieke [1 ]
Klein, Richard [2 ]
van Waardenburg, Dick [3 ]
Kuiper, Jan Willem [4 ]
Riedijk, Maaike [5 ]
Kneyber, Martin [6 ]
Timmers, Brigitte [7 ]
van Heerde, Marc A. [5 ]
Hazelzet, Jan [8 ]
van der Hoeven, Johannes [1 ]
Lemson, Joris [1 ]
机构
[1] Radboud Univ Nijmegen, Dept Intens Care, Med Ctr, Nijmegen, Netherlands
[2] Leiden Univ, Dept Intens Care, Med Ctr, Leiden, Netherlands
[3] Maastricht Univ, Dept Pediat Intens Care, Med Ctr, Maastricht, Netherlands
[4] Erasmus Univ, Sophia Childrens Hosp, Dept Pediat Intens Care, Med Ctr, Rotterdam, Netherlands
[5] Univ Amsterdam, Dept Pediat Intens Care, Med Ctr, Amsterdam, Netherlands
[6] Univ Med Ctr Groningen, Dept Pediat Intens Care, Groningen, Netherlands
[7] Univ Med Ctr Utrecht, Dept Pediat Intens Care, Utrecht, Netherlands
[8] Erasmus Univ, Dept Publ Hlth, Med Ctr, Rotterdam, Netherlands
关键词
adverse events; cohort studies; outcome; patient safety; pediatric critical care; PATIENT SAFETY; PREVENTABLE DEATHS; CHILDREN; UNIT; PREVALENCE; HOSPITALS; INDEX; PICU;
D O I
10.1097/PCC.0000000000003103
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
OBJECTIVES:Some patients with a low predicted mortality risk in the PICU die. The contribution of adverse events to mortality in this group is unknown. The aim of this study was to estimate the occurrence of adverse events in low-risk nonsurvivors (LN), compared with low-risk survivors (LS) and high-risk PICU survivors and nonsurvivors, and the contribution of adverse events to mortality. DESIGN:Case control study. Admissions were selected from the national Dutch PICU registry, containing 53,789 PICU admissions between 2006 and 2017, in seven PICUs. PICU admissions were stratified into four groups, based on mortality risk (low/high) and outcome (death/survival). Random samples were selected from the four groups. Cases were "LN." Control groups were as follows: "LS," "high-risk nonsurvivors" (HN), and "high-risk survivors" (HS). Adverse events were identified using the validated trigger tool method. SETTING:Patient chart review study. PATIENTS:Children admitted to the PICU with either a low predicted mortality risk (< 1%) or high predicted mortality risk (>= 30%). INTERVENTIONS:None. MEASUREMENTS AND MAIN RESULTS:In total, 419 patients were included (102 LN, 107 LS, 104 HN, and 106 HS). LN had more complex chronic conditions (93.1%) than LS (72.9%; p < 0.01), HN (49.0%; p < 0.001), and HS (48.1%; p < 0.001). The occurrence of adverse events in LN (76.5%) was higher than in LS (13.1%) and HN (47.1%) (p < 0.001). The most frequent adverse events in LN were hospital-acquired infections and drug/fluid-related adverse events. LN suffered from more severe adverse events compared with LS and HS (p < 0.001). In 30.4% of LN, an adverse event contributed to death. In 8.8%, this adverse event was considered preventable. CONCLUSIONS:Significant and preventable adverse events were found in low-risk PICU nonsurvivors. 76.5% of LN had one or more adverse events. In 30.4% of LN, an adverse event contributed to mortality.
引用
收藏
页码:4 / 16
页数:13
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