Division of Pediatric Emergency and Intensive Care, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, 160012, India.
Indian J Pediatr. 2022 Jan;89(1):7-12. doi: 10.1007/s12098-021-03707-7. Epub 2021 Apr 24.
To determine the efficacy and safety of intravenous (IV) labetalol in the management of hypertensive crisis in children.
A retrospective chart review of 56 consecutive children (age > 1 mo to ≤ 12 y) with hypertensive crisis admitted to a pediatric intensive care unit (PICU) from July 2009 to 2019.
The proportion of children attaining the primary endpoint (target 95th percentile in > 12 to ≤ 48 h) was significantly more in the group receiving labetalol as first-line or add-on (n = 23) as compared to those not receiving labetalol (n = 33) (62% vs. 30.3%, p = 0.03). Higher proportion of neurological recovery was seen in the labetalol group (56.2% vs. 18.7%, p = 0.02). The proportion of children with hypotension before 12 h was similar in both treatment groups (13% vs. 15%, p = 0.82). The practice variations between two periods of 5 y each (2009-2013 and 2014-2019) showed significantly more use of labetalol in the latter cohort (53% for 2014-2019 vs. 25% for 2009-2013, p = 0.03).
Labetalol, when used alone or as an add-on drug, was more efficacious than IV nitroprusside/nitroglycerine in attaining the primary endpoint in children up to ≤ 12 y of age with hypertensive crisis. Labetalol was safe and associated with higher neurological recovery.
确定静脉内(IV)拉贝洛尔治疗儿童高血压危象的疗效和安全性。
回顾性分析 2009 年 7 月至 2019 年期间,56 例连续入住儿科重症监护病房(PICU)的高血压危象儿童的病历。
与未使用拉贝洛尔的患儿(n=33)相比,首先使用或加用拉贝洛尔的患儿(n=23)达到主要终点(>12 至≤48 小时内达到 95%百分位数)的比例明显更高(62%比 30.3%,p=0.03)。拉贝洛尔组的神经恢复比例更高(56.2%比 18.7%,p=0.02)。两组患儿在 12 小时前出现低血压的比例相似(13%比 15%,p=0.82)。在 5 年的两个时间段(2009-2013 年和 2014-2019 年)之间的实践差异表明,在后一个队列中,拉贝洛尔的使用明显更多(2014-2019 年为 53%,2009-2013 年为 25%,p=0.03)。
拉贝洛尔单独使用或作为附加药物,在治疗年龄≤12 岁的儿童高血压危象时,比 IV 硝普钠/硝酸甘油更能达到主要终点。拉贝洛尔是安全的,并且与更高的神经恢复相关。