Heistein Lisa C, Ramaciotti Claudio, Scott William A, Coursey Melanie, Sheeran Paul W, Lemler Matthew S
Division of Cardiology, Department of Pediatrics, University of Texas Southwestern Medical Center and Children's Medical Center, Dallas, Texas, USA.
Pediatrics. 2006 Mar;117(3):e434-41. doi: 10.1542/peds.2005-1445. Epub 2006 Feb 15.
The physiologic responses to chloral hydrate sedation in the setting of a pediatric echocardiography laboratory have not been well documented; neither has the population at risk been identified adequately. The purpose of this study was to describe the physiologic responses to chloral hydrate sedation, to report the occurrence of adverse events, and to identify any risk factors that predicted these adverse events in children who underwent sedation for echocardiography at our institution.
We analyzed retrospectively 1095 patients who were sedated for echocardiography. Vital signs and oxygen saturations were recorded every 5 minutes, and adverse events were noted. Potential risk factors for sedation-related adverse events were analyzed.
Thirty-eight percent of patients were classified as American Society of Anesthesiologists class 3 or 4, reflecting the significant comorbidity in the study population. Hemodynamic responses to chloral hydrate sedation included > or = 20% decreases in heart rate (24% of the patients) and blood pressure (59% of the patients). There were no deaths or permanent morbidity. Adverse events occurred in 10.8% of patients and included apnea (n = 3 [0.3%]), airway obstruction (n = 15 [1.4%]), hypoxia (n = 65 [5.9%]), hypercarbia (n = 40 of 603 [6.6%]), hypotension with poor perfusion (n = 4 [0.4%]), vomiting (n = 4 [0.4%]), and prolonged sedation (n = 36 [3.3%]). No intervention was required in 92.5%, minor interventions were necessary in 7%, and major interventions were required in 0.5% of all patients. Multivariate analysis identified only age younger than 6 months as a predictor for adverse events, whereas cyanosis, hospitalization, American Society of Anesthesiologists class, fasting time, oxygen requirement, and use of additional sedation were not predictors.
Moderate decreases in heart rate and blood pressure, in the absence of clinical deterioration, are expected responses to chloral hydrate sedation in this pediatric population. The majority of adverse events were minor, and major events were uncommon. Infants who were younger than 6 months were found to be at higher risk for serious adverse events.
儿科超声心动图实验室中,水合氯醛镇静的生理反应尚未得到充分记录;高危人群也未得到充分识别。本研究的目的是描述水合氯醛镇静的生理反应,报告不良事件的发生情况,并确定在我院接受超声心动图检查镇静的儿童中预测这些不良事件的任何风险因素。
我们回顾性分析了1095例接受超声心动图检查镇静的患者。每5分钟记录生命体征和血氧饱和度,并记录不良事件。分析了与镇静相关不良事件的潜在风险因素。
38%的患者被归类为美国麻醉医师协会3或4级,这反映了研究人群中显著的合并症。水合氯醛镇静的血流动力学反应包括心率降低≥20%(24%的患者)和血压降低(59%的患者)。没有死亡或永久性发病情况。10.8%的患者发生了不良事件,包括呼吸暂停(n = 3 [0.3%])、气道阻塞(n = 15 [1.4%])、低氧血症(n = 65 [5.9%])、高碳酸血症(603例中有40例 [6.6%])、低血压伴灌注不良(n = 4 [0.4%])、呕吐(n = 4 [0.4%])和镇静时间延长(n = 36 [3.3%])。92.5%的患者无需干预,7%的患者需要轻微干预,0.5%的患者需要重大干预。多因素分析仅确定6个月以下的年龄是不良事件的预测因素,而发绀、住院、美国麻醉医师协会分级、禁食时间、氧气需求和使用额外镇静剂不是预测因素。
在该儿科人群中,在无临床恶化的情况下,心率和血压适度降低是水合氯醛镇静的预期反应。大多数不良事件为轻微事件,重大事件不常见。发现6个月以下的婴儿发生严重不良事件的风险较高。