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多沙普仑治疗早产儿难治性特发性呼吸暂停的剂量-反应关系。

Dose-response relationship of doxapram in the therapy for refractory idiopathic apnea of prematurity.

作者信息

Barrington K J, Finer N N, Torok-Both G, Jamali F, Coutts R T

出版信息

Pediatrics. 1987 Jul;80(1):22-7.

PMID:3110729
Abstract

Eighteen infants with idiopathic apnea of prematurity refractory to therapeutic levels of aminophylline were treated with incremental doses of doxapram beginning at 0.5 mg/kg/h. Continuous recording of heart rate, thoracic impedance, and transcutaneous PO2 demonstrated that 47% of the infants satisfied objective response criteria at the lowest dose, 53% responded at 1.0 mg/kg/h, 65% at 1.5 mg/kg/h, 82% at 2.0 mg/kg/h, and 89% at the highest allowed dose of 2.5 mg/kg/h. The mean serum doxapram concentration at the response dose was 2.9 +/- 1.3 micrograms/mL, and all infants who responded had levels greater than 1.5 micrograms/mL. BP was significantly elevated at doses higher than 1.5 mg/kg/h (P less than .05). Minute ventilation significantly increased and PCO2 significantly decreased as the doxapram dosage was increased (P = .02). Terminal elimination half-life was 9.9 +/- 2.9 hours. When doxapram is used for treatment of refractory neonatal apnea the starting dosage should be no more than 0.5 mg/kg/h.

摘要

18例对治疗剂量氨茶碱无反应的早产儿特发性呼吸暂停患儿,采用多沙普仑递增剂量治疗,起始剂量为0.5mg/kg/h。连续记录心率、胸阻抗和经皮氧分压,结果显示,47%的患儿在最低剂量时达到客观反应标准,53%在1.0mg/kg/h时反应,65%在1.5mg/kg/h时反应,82%在2.0mg/kg/h时反应,89%在最高允许剂量2.5mg/kg/h时反应。反应剂量时的多沙普仑平均血清浓度为2.9±1.3μg/mL,所有有反应的患儿浓度均大于1.5μg/mL。剂量高于1.5mg/kg/h时血压显著升高(P<0.05)。随着多沙普仑剂量增加,分钟通气量显著增加,二氧化碳分压显著降低(P=0.02)。终末消除半衰期为9.9±2.9小时。当多沙普仑用于治疗难治性新生儿呼吸暂停时,起始剂量不应超过0.5mg/kg/h。

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