Demaret Pierre, Tucci Marisa, Karam Oliver, Trottier Helen, Ducruet Thierry, Lacroix Jacques
1Division of Pediatric Critical Care Medicine, Department of Pediatrics, CHC, Liège, Belgium. 2Division of Pediatric Critical Care Medicine, Department of Pediatrics, Sainte-Justine Hospital and Université de Montréal, Montreal, QC, Canada. 3Pediatric Intensive Care Unit, Geneva University Hospital, Geneva, Switzerland. 4Department of Social and Preventive Medicine, Research Center, Sainte-Justine Hospital and Université de Montréal, Montreal, QC, Canada. 5Department of Pediatrics, Research Center, Sainte-Justine Hospital, Université de Montréal, Montreal, QC, Canada.
Pediatr Crit Care Med. 2015 Jul;16(6):505-14. doi: 10.1097/PCC.0000000000000423.
To identify the potential complications associated with RBC transfusions.
Prospective observational study.
PICU in a tertiary children's hospital.
All children consecutively admitted to our PICU during a 1-year period.
None.
Data were abstracted from medical charts prospectively. Outcomes possibly attributable to RBC transfusions were looked for daily. In transfused cases, it was considered that an outcome was associated with a transfusion only if it was observed after the first RBC transfusion. During the 1-year study period, 913 consecutive admissions were documented, 842 of which were included. Among them, 144 (17%) were transfused at least once. When comparing transfused cases with nontransfused cases, the odds ratio for new or progressive multiple organ dysfunction syndrome was 5.14 (95% CI, 3.28-8.06; p < 0.001). This association remained statistically significant in the multivariable analysis (odds ratio, 3.85; 95% CI, 2.38-6.24; p < 0.001). Transfused cases were ventilated longer than nontransfused cases (14.1 ± 32.6 vs 4.3 ± 9.6 d, p < 0.001), even after adjustment in a Cox model. The PICU length of stay was significantly increased for transfused cases (12.4 ± 26.2 vs 4.9 ± 10.2 d, p < 0.001), even after controlling for potential confounders. The paired analysis for comparison of pretransfusion and posttransfusion values showed that the arterial partial pressure in oxygen was significantly reduced within the 6 hours after the first RBC transfusion (mean difference, 25.6 torr, 95% CI, 5.7-45.4; p = 0.029). The paired analysis also showed an increased proportion of renal replacement therapy.
RBC transfusions in critically ill children were associated with prolonged mechanical ventilation and prolonged PICU stay. The risk of new or progressive multiple organ dysfunction syndrome was also increased in some transfused children. Furthermore, our study questions the ability of stored RBCs to improve oxygenation in critically ill children. Practitioners should take into account these data when prescribing an RBC transfusion to PICU patients.
确定与红细胞输血相关的潜在并发症。
前瞻性观察性研究。
一家三级儿童医院的儿科重症监护病房。
在1年期间连续入住我们儿科重症监护病房的所有儿童。
无。
前瞻性地从病历中提取数据。每天寻找可能归因于红细胞输血的结果。在输血病例中,仅当在首次红细胞输血后观察到某一结果时,才认为该结果与输血有关。在1年的研究期间,记录了913例连续入院病例,其中842例被纳入研究。其中,144例(17%)至少接受过一次输血。将输血病例与未输血病例进行比较时,新发或进行性多器官功能障碍综合征的比值比为5.14(95%可信区间,3.28 - 8.06;p < 0.001)。在多变量分析中,这种关联仍然具有统计学意义(比值比,3.85;95%可信区间,2.38 - 6.24;p < 0.001)。输血病例的机械通气时间比未输血病例长(14.1±32.6天对4.3±9.6天,p < 0.001),即使在Cox模型中进行调整后也是如此。输血病例的儿科重症监护病房住院时间显著延长(12.4±26.2天对4.9±10.2天,p < 0.001),即使在控制了潜在混杂因素之后。输血前后值比较的配对分析显示,首次红细胞输血后6小时内动脉血氧分压显著降低(平均差值,25.6托,95%可信区间,5.7 - 45.4;p = 0.029)。配对分析还显示肾脏替代治疗的比例增加。
危重症儿童的红细胞输血与机械通气时间延长和儿科重症监护病房住院时间延长有关。一些输血儿童发生新发或进行性多器官功能障碍综合征的风险也增加。此外,我们的研究对储存的红细胞改善危重症儿童氧合的能力提出了质疑。从业者在为儿科重症监护病房患者开具红细胞输血医嘱时应考虑这些数据。