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小儿感染性休克中有无间歇性上腔静脉血氧饱和度监测的早期目标导向治疗:一项随机对照试验

Early Goal-Directed Therapy With and Without Intermittent Superior Vena Cava Oxygen Saturation Monitoring in Pediatric Septic Shock: A Randomized Controlled Trial.

作者信息

Jain Puneet, Rameshkumar Ramachandran, Satheesh Ponnarmeni, Mahadevan Subramanian

机构信息

Division of Pediatric Critical Care, Department of Pediatrics, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Puducherry.

Division of Pediatric Critical Care, Department of Pediatrics, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Puducherry. Correspondence to: Dr Rameshkumar R, Associate Professor, Division of Pediatric Critical Care, Department of Pediatrics, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Puducherry 605 006.

出版信息

Indian Pediatr. 2021 Dec 15;58(12):1124-1130. Epub 2021 May 28.

Abstract

OBJECTIVE

To compare early goal-directed therapy (EGDT) 'with' and 'without' intermittent superior vena cava oxygen saturation (ScvO2) monitoring in pediatric septic shock.

DESIGN

Open label randomized controlled trial.

SETTING

Pediatric intensive care unit in a tertiary care center.

PARTICIPANTS

Children aged 1 month to 12 year with septic shock.

INTERVENTION

Patients not responding to fluid resuscitation (up to 40 mL/kg) were randomized to EGDT 'with' (n=59) and 'without' (n=61) ScvO2 groups. Resuscitation was guided by ScvO2 monitoring at 1-hour, 3-hour, and later on six-hourly in the 'with' ScvO2 group, and by clinical variables in the 'without' ScvO2 group.

OUTCOME

Primary outcome was all-cause 28-day mortality. Secondary outcomes were time to and proportion of patients achieving therapeutic endpoints (at 6 hours and PICU stay), need for organ supports, new organ dysfunction (at 24 hours and PICU stay), and length of PICU and hospital stay.

RESULTS

The study was stopped after interim analysis due to lower mortality in the intervention group. There was significantly lower all-cause 28-day mortality in EDGT with ScvO2 than without ScvO2 group [37.3% vs. 57.5%, adjusted hazard ratio 0.57, 95%CI 0.33 to 0.97, P=0.04]. Therapeutic endpoints were achieved early in 'with' ScvO2 group [mean (SD) 3.6 (1.6) vs. 4.2 (1.6) h, P=0.03]. Organ dysfunction by sequential organ assessment score during PICU stay was lower in 'with' ScvO2 group [median (IQR) 5 (2,11) vs. 8 (3,13); P=0.03]. There was no significant difference in other secondary outcomes.

CONCLUSIONS

EGDT with intermittent ScvO2 monitoring was associated with reduced mortality and improved organ dysfunction in pediatric septic shock.

摘要

目的

比较在儿童感染性休克中,进行与不进行间歇性上腔静脉血氧饱和度(ScvO2)监测的早期目标导向治疗(EGDT)。

设计

开放标签随机对照试验。

地点

三级医疗中心的儿科重症监护病房。

参与者

年龄在1个月至12岁的感染性休克儿童。

干预措施

对液体复苏(高达40 mL/kg)无反应的患者被随机分为有ScvO2监测的EGDT组(n = 59)和无ScvO2监测的EGDT组(n = 61)。在有ScvO2监测的组中,复苏在1小时、3小时进行指导,之后每6小时根据ScvO2监测进行指导;在无ScvO2监测的组中,根据临床变量进行指导。

结果

主要结局是全因28天死亡率。次要结局是达到治疗终点的时间和患者比例(6小时和在儿科重症监护病房住院期间)、器官支持需求、新的器官功能障碍(24小时和在儿科重症监护病房住院期间)以及儿科重症监护病房和住院时间。

结果

由于干预组死亡率较低,中期分析后研究提前终止。有ScvO2监测的EGDT组全因28天死亡率显著低于无ScvO2监测的组[37.3%对57.5%,调整后风险比0.57,95%可信区间0.33至0.97,P = 0.04]。有ScvO2监测的组更早达到治疗终点[平均(标准差)3.6(1.6)对4.2(1.6)小时,P = 0.03]。在儿科重症监护病房住院期间,根据序贯器官评估评分,有ScvO2监测的组器官功能障碍更低[中位数(四分位间距)5(2,11)对8(3,13);P = 0.03]。其他次要结局无显著差异。

结论

在儿童感染性休克中,进行间歇性ScvO2监测的EGDT与降低死亡率和改善器官功能障碍相关。

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