心电测量治疗小儿感染性休克:一项随机对照试验。

IF 2.7 Q4 Medicine
Critical care explorations Pub Date : 2025-03-31 eCollection Date: 2025-04-01 DOI:10.1097/CCE.0000000000001242
Suman Sudha Moharana, Lalitha Av, Santu Ghosh
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引用次数: 0

摘要

目的:评价在临床监测的基础上进行无创心电连续血流动力学监测与单独进行临床监测的儿童感染性休克前6小时复苏液量的差异。设计:随机对照试验。环境:三级护理医院的PICU。患者:2个月至18岁的儿童,败血症和首次输液后未解决的休克。干预措施:将患儿随机分为两组,即心电图联合临床监测组(B组)和单纯临床监测组(A组)。B组以心电图变量(心脏指数和全身血管阻力指数)和临床监测指导FB,并选择和滴定血管活性药物。按照标准指南,采用临床参数启动和滴定A组的液体复苏和血管活性治疗。测量和主要结果:共有119名儿童入组,其中A组60名,B组59名。A组对复苏液容量的要求(平均±sd)在最初6小时内(30±8.2 mL/kg)明显高于B组(22±9.2 mL/kg)。同样,在入组的前24小时,A组的维持和复苏液量(平均±sd)给药(56±13比46±10.7,p < 0.001)更高。与A组相比,B组的血管活性治疗开始时间更早(37±10.14分钟对47.33±12.41分钟),且该组的液体过载率更低(2.98%对1.7%)。然而,在休克消退时间、28天无icu天数、无住院天数和死亡率方面没有差异。结论:先进的血液动力学监测与心电图以及临床评估导致限制性液体策略,除了尽量减少液体过载的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Electrocardiometry for the Management of Pediatric Septic Shock: A Pilot Randomized Controlled Trial.

Electrocardiometry for the Management of Pediatric Septic Shock: A Pilot Randomized Controlled Trial.

Electrocardiometry for the Management of Pediatric Septic Shock: A Pilot Randomized Controlled Trial.

Objectives: To evaluate the difference in the resuscitation fluid volume in the initial 6 hours in pediatric septic shock between those undergoing noninvasive continuous hemodynamic monitoring with electrocardiometry in addition to clinical monitoring vs. clinical monitoring alone.

Design: Randomized control trial.

Setting: PICU in a tertiary care hospital.

Patients: Children from 2 months to 18 years with sepsis and unresolved shock after the initial fluid bolus (FB).

Interventions: Children were randomized to one of the two groups, that is, electrocardiometry with clinical monitoring group (group B) and clinical monitoring alone group (group A). In group B, electrocardiometry variables (cardiac index and systemic vascular resistance index) along with clinical monitoring were used to guide FB, as well as selection and titration of vasoactive agents. Clinical parameters were used to initiate and titrate fluid resuscitation and vasoactive therapy in group A as per standard guidelines.

Measurements and main results: One hundred nineteen children were enrolled in the study: 60 in group A and 59 in group B. There was a significantly higher requirement for resuscitation fluid volume (mean ± sd) within the initial 6 hours in the group A (30 ± 8.2 mL/kg) as compared with group B (22 ± 9.2 mL/kg). Similarly, maintenance along with resuscitation fluid volume (mean ± sd) administration (56 ±13 vs. 46 ±10.7, p < 0.001) was higher in group A in the first 24 hours of enrollment. Vasoactive therapy initiation was earlier in group B as compared with group A (37 ± 10.14 vs. 47.33 ± 12.41 min) with lower fluid overload percentage (2.98% vs. 1.7%) in this group. However, there was no difference in time to shock resolution, 28-day ICU-free days, hospital-free days, and mortality.

Conclusions: Advanced hemodynamic monitoring with electrocardiometry along with clinical assessment led to a restrictive fluid strategy in addition to minimizing the risk of fluid overload.

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CiteScore
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