Conte J E, Chernoff D, Feigal D W, Joseph P, McDonald C, Golden J A
School of Medicine, University of California, San Francisco.
Ann Intern Med. 1990 Aug 1;113(3):203-9. doi: 10.7326/0003-4819-113-3-203.
To evaluate the efficacy and toxicity of aerosolized pentamidine and of reduced-dose intravenous pentamidine for the treatment of mild to moderate Pneumocystis carinii pneumonia in patients with the acquired immunodeficiency syndrome (AIDS).
Randomized open study with serial pulmonary function testing and measurement of pentamidine concentrations in plasma and bronchoalveolar lavage fluid.
Of 44 men and 1 woman with a mild to moderate first episode of P. carinii pneumonia (Pao2 greater than or equal to 7.3 kPa [55 mm Hg]), 23 received aerosolized pentamidine and 22, intravenous pentamidine.
Pentamidine isethionate, 600 mg by inhalation using a Respirgard II nebulizer (Marquest Medical Products, Inc., Englewood, Colorado) or 3 mg/kg body weight intravenously, administered once daily for 2 to 3 weeks.
The planned 60-patient study was stopped after 45 patients had been enrolled. The rates (aerosolized compared with intravenous pentamidine) of initial failure, early recrudescence of symptoms, and relapse were 12% and 19% (difference, 7%; 99% confidence interval [CI], - 23% to 37%; P = 0.67), 35% and 0% (difference, 35%; CI, 13% to 58%; P = 0.02), and 24% and 0% (difference, 24%; CI, 4% to 49%; P = 0.03). The rates (aerosolized compared with intravenous pentamidine) of major toxicity were 0% (0 of 17 patients) and 10% (2 of 21 patients) (difference 10%; CI, -1% to 29%; P = 0.24). The mean (+/- SD) pentamidine concentration in bronchoalveolar lavage fluid for patients receiving aerosolized pentamidine was 96.6 +/- 65.1 ng/mL compared with 14.4 +/- 17.7 ng/mL for patients receiving intravenous treatment. Trough concentrations of pentamidine in plasma increased from 0 to 25.4 +/- 16.4, 56.5 +/- 26.1, and 61.1 +/- 56.0 ng/mL at the end of weeks 1, 2, and 3 of intravenous therapy, respectively.
The data suggest that reduced-dose intravenous pentamidine was more effective than aerosolized pentamidine for treating mild to moderate P. carinii pneumonia. Systemic absorption during aerosolized therapy was minimal; daily doses of intravenous pentamidine resulted in increased accumulation of pentamidine in plasma.
评估雾化喷他脒及小剂量静脉用喷他脒治疗获得性免疫缺陷综合征(AIDS)患者轻至中度卡氏肺孢子虫肺炎的疗效及毒性。
采用序贯肺功能检测以及测定血浆和支气管肺泡灌洗液中喷他脒浓度的随机开放研究。
44名男性和1名女性首次发生轻至中度卡氏肺孢子虫肺炎(动脉血氧分压大于或等于7.3 kPa [55 mmHg]),其中23例接受雾化喷他脒治疗,22例接受静脉喷他脒治疗。
使用Respirgard II雾化器(Marquest Medical Products, Inc., Englewood, Colorado)吸入600 mg 乙磺酸盐喷他脒,或静脉注射3 mg/kg体重,每日1次,持续2至3周。
在纳入45例患者后,原计划纳入60例患者的研究终止。初始治疗失败率、症状早期复发率及复发率(雾化喷他脒组与静脉喷他脒组相比)分别为12%和19%(差值为7%;99%置信区间[CI]为 - 23%至37%;P = 0.67),35%和0%(差值为35%;CI为13%至58%;P = 0.02),以及24%和0%(差值为24%;CI为4%至49%;P = 0.03)。主要毒性发生率(雾化喷他脒组与静脉喷他脒组相比)分别为0%(17例患者中的0例)和10%(21例患者中的2例)(差值为10%;CI为 - 1%至29%;P = 0.24)。接受雾化喷他脒治疗患者的支气管肺泡灌洗液中喷他脒平均(±标准差)浓度为96.6±65.1 ng/mL,而接受静脉治疗患者为14.4±17.7 ng/mL。静脉治疗第1、2、3周结束时,血浆中喷他脒的谷浓度分别从0增至25.4±16.4、56.5±26.1和61.1±56.0 ng/mL。
数据表明,小剂量静脉用喷他脒治疗轻至中度卡氏肺孢子虫肺炎比雾化喷他脒更有效。雾化治疗期间全身吸收极少;每日静脉注射喷他脒导致血浆中喷他脒蓄积增加。