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接受研究性支气管镜检查的哮喘患者的血清利多卡因浓度。

Serum lidocaine concentrations in asthmatics undergoing research bronchoscopy.

作者信息

Langmack E L, Martin R J, Pak J, Kraft M

机构信息

Department of Medicine, National Jewish Medical and Research Center, Denver, CO 80206, USA.

出版信息

Chest. 2000 Apr;117(4):1055-60. doi: 10.1378/chest.117.4.1055.

DOI:10.1378/chest.117.4.1055
PMID:10767239
Abstract

STUDY OBJECTIVES

To determine how often serum lidocaine concentrations (SLC) fall into the potentially toxic range (> 5 mg/L) in asthmatics undergoing research bronchoscopy, and to determine whether subject or procedure characteristics are associated with higher SLC.

DESIGN

Prospective, observational study.

SETTING

Academic research center.

PARTICIPANTS

Fifty-one volunteers with mild to moderate asthma enrolled in three separate bronchoscopy protocols to study airway inflammation in asthma.

INTERVENTIONS

Lidocaine was administered topically to the upper airway and tracheobronchial tree to achieve local anesthesia for bronchoscopy. Venous blood was sampled during bronchoscopy, 30 min after upper airway anesthesia was completed (time 1), and 30 min after bronchoscopy was completed (time 2).

MEASUREMENTS AND RESULTS

The mean total amount of lidocaine administered was 600 +/- 122 mg (8.2 +/- 2.0 mg/kg). No signs or symptoms of lidocaine toxicity were observed in any of the subjects. SLC ranged between 0.10 and 2.90 mg/L at time 1 and 0.50 and 3.20 mg/L at time 2. SLC was significantly correlated with the total amount of lidocaine (milligrams/kilogram) administered at both points (time 1, r = 0.33, p = 0.021; time 2, r = 0.33, p = 0.023). No statistically significant relationship was observed between SLC and subject age, sex, weight, baseline FEV(1), procedure length, or study protocol. No statistically significant relationship was found between subject FEV(1) and either total lidocaine dose or procedure length.

CONCLUSIONS

An average total dose of 600 mg (8.2 mg/kg) of lidocaine appears to be safe in mild to moderate asthmatics undergoing research bronchoscopy.

摘要

研究目的

确定在接受研究性支气管镜检查的哮喘患者中,血清利多卡因浓度(SLC)落入潜在中毒范围(>5mg/L)的频率,并确定受试者或操作特征是否与较高的SLC相关。

设计

前瞻性观察性研究。

地点

学术研究中心。

参与者

51名轻度至中度哮喘志愿者,参加了三项独立的支气管镜检查方案,以研究哮喘中的气道炎症。

干预措施

将利多卡因局部应用于上呼吸道和气管支气管树,以实现支气管镜检查的局部麻醉。在支气管镜检查期间、上呼吸道麻醉完成后30分钟(时间1)和支气管镜检查完成后30分钟(时间2)采集静脉血样。

测量和结果

利多卡因的平均总给药量为600±122mg(8.2±2.0mg/kg)。在任何受试者中均未观察到利多卡因中毒的体征或症状。时间1时SLC范围为0.10至2.90mg/L,时间2时为0.50至3.20mg/L。在两个时间点,SLC与利多卡因给药总量(毫克/千克)均显著相关(时间1,r = 0.33,p = 0.021;时间2,r = 0.33,p = 0.023)。未观察到SLC与受试者年龄、性别、体重、基线FEV(1)、操作时长或研究方案之间存在统计学显著关系。未发现受试者FEV(1)与利多卡因总剂量或操作时长之间存在统计学显著关系。

结论

对于接受研究性支气管镜检查的轻度至中度哮喘患者,平均总剂量600mg(8.2mg/kg)的利多卡因似乎是安全的。

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