Critical Care Group - Portex Unit, Institute of Child Health, University College London, London, Great Britain.
PLoS One. 2013;8(2):e57478. doi: 10.1371/journal.pone.0057478. Epub 2013 Feb 28.
Atropine has is currently recommended to facilitate haemodynamic stability during critical care intubation. Our objective was to determine whether atropine use at induction influences ICU mortality.
METHODOLOGY/PRINCIPAL FINDINGS: A 2-year prospective, observational study of all first non-planned intubations, September 2007-9 in PICU and Intensive Care Transport team of Hôpital Robert Debré, Paris, 4 other PICUs and 5 NICUs in the Paris Region, France. Follow-up was from intubation to ICU discharge. A propensity score was used to adjust for patient specific characteristics influencing atropine prescription. 264/333 (79%) intubations were included. The unadjusted ICU mortality was 7.2% (9/124) for those who received atropine compared to 15.7% (22/140) for those who did not (OR 0.42, 95%CI 0.19-0.95, p=0.04). One child died during intubation (1/264, 0.4%). Two age sub-groups of neonates (≤28 days) and older children (>28 days, <8 years) were examined. This difference in mortality arose from the higher mortality in children aged over one month when atropine was not used (propensity score adjusted OR 0.22, 95%CI 0.06-0.85, p=0.028). No effect was seen in neonates (propensity score adjusted OR 1.3, 95%CI 0.31-5.1 p=0.74). Using the propensity score, atropine maintained the mean heart rate 45.9 bpm above that observed when no atropine was used in neonates (95%CI 34.3-57.5, p<0.001) and 43.5 bpm for older children (95%CI 25.5-61.5 bpm, p<0.001).
CONCLUSIONS/SIGNIFICANCE: Atropine use during induction was associated with a reduction in ICU mortality in children over one month. This effect is independent of atropine's capacity to attenuate bradycardia during intubation which occurred similarly in neonates and older children. This result needs to be confirmed in a study using randomised methodology.
目前推荐使用阿托品来促进重症监护插管期间的血流动力学稳定。我们的目的是确定诱导时使用阿托品是否会影响 ICU 死亡率。
方法/主要发现:这是一项为期 2 年的前瞻性、观察性研究,纳入了 2007 年 9 月至 2009 年 9 月在巴黎罗伯特·德布雷医院儿科重症监护病房 (PICU) 和重症监护转运团队、巴黎地区的 4 个其他 PICU 和 5 个新生儿重症监护病房进行的所有首次非计划性插管。随访时间从插管到 ICU 出院。使用倾向评分来调整影响阿托品处方的患者特定特征。共纳入 264/333(79%)例插管。接受阿托品治疗的患者 ICU 死亡率为 7.2%(9/124),而未接受阿托品治疗的患者为 15.7%(22/140)(OR 0.42,95%CI 0.19-0.95,p=0.04)。有 1 例患儿在插管过程中死亡(1/264,0.4%)。检查了新生儿(≤28 天)和年龄较大的儿童(>28 天,<8 岁)这两个年龄亚组。这种死亡率差异源于未使用阿托品时年龄较大儿童(1 个月以上)的死亡率更高(倾向评分调整后的 OR 0.22,95%CI 0.06-0.85,p=0.028)。在新生儿中未见此效果(倾向评分调整后的 OR 1.3,95%CI 0.31-5.1,p=0.74)。使用倾向评分,阿托品使新生儿的平均心率比未使用阿托品时高 45.9 次/分(95%CI 34.3-57.5,p<0.001),使年龄较大儿童的平均心率高 43.5 次/分(95%CI 25.5-61.5,p<0.001)。
结论/意义:诱导时使用阿托品与 1 个月以上儿童 ICU 死亡率降低相关。这种效果独立于阿托品在插管期间减轻心动过缓的能力,这种作用在新生儿和年龄较大的儿童中相似。需要使用随机方法进行的研究来证实这一结果。