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Pulmonary deposition of nebulised pentamidine isethionate: effect of nebuliser type dose and volume of fill.

机译:雾化喷他戊is羟乙磺酸盐的肺部沉积:雾化器类型剂量和填充量的影响。

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摘要

An estimate of the absolute pulmonary deposition of nebulised pentamidine isethionate was obtained in nine patients with AIDS. Two nebuliser systems were compared, System 22 Mizer (Medic-Aid) and Respirgard II (Marquest), with 50 and 150 mg doses of pentamidine in a 3 ml solution driven by an air flow of 6 l/min with the patient in the sitting position. The 50 mg pentamidine dose was repeated with a 6 ml fill with both devices. The nebuliser cloud was labelled with technetium-99m human serum albumin (Ventocol) and lung deposition was measured with a gamma camera. Of the two nebulisers studied, System 22 Mizer delivered more drug to the lungs as a whole and to each individual lung region, including the peripheral and upper zones. For the 50 mg dose the mean (SEM) total pulmonary deposition with the 3 and the 6 ml fill respectively was 2.63 (0.34) and 3.71 (0.41) mg for the System 22 Mizer and 1.37 (0.26) and 1.45 (0.18) mg for the Respirgard II. For the 150 mg dose the System 22 Mizer delivered 7.16 (1.02) mg and the Respirgard II 4.34 (0.57) mg. Increasing the volume of fill from 3 to 6 ml increased pulmonary deposition with System 22 Mizer, and this was related to an increase in nebuliser output. Neither pulmonary deposition nor nebuliser output was increased by using a 6 ml solution in the Respirgard II. Increasing the volume of fill prolonged the time required for nebulisation with both nebulisers. The System 22 Mizer produced more nonpulmonary (gastric and oropharyngeal) deposition of drug, more frequent local adverse effects (cough, burning in the throat, and a metallic taste), and small reductions in lung function, particularly with the 150 mg pentamidine dose. Thus nebuliser type, volume of fill, and nebuliser dose affect the pulmonary deposition of pentamidine. A 300 mg dose of pentamidine via a Respirgard II is generally recommended as providing effective prophylaxis; our results suggest that similar pulmonary deposition can be produced with System 22 Mizer and 150 mg pentamidine. A clinical trial would be needed to show whether this regimen provides similar prophylactic benefit.
机译:估算了9名艾滋病患者中雾化的喷他戊idine羟乙磺酸盐的绝对肺部沉积。比较了两种雾化器系统,分别是System 22 Mizer(Medic-Aid)和Respirgard II(Marquest),分别将50和150 mg喷他idine定在3 ml溶液中,由6 l / min的气流驱动,让患者坐下位置。两种设备均以6 ml填充液重复50 mg喷他idine剂量。雾化器云用tech 99m人体血清白蛋白(Ventocol)标记,并用伽马相机测量肺部沉积。在研究的两个雾化器中,System 22 Mizer向整个肺部以及每个单个的肺部区域(包括外围和上部区域)输送了更多的药物。对于50 mg剂量,System 22 Mizer的平均(SEM)总肺沉积量为3和6 ml,分别为2.63(0.34)和3.71(0.41)mg,而对于22 mg,则为1.37(0.26)和1.45(0.18)mg Respirgard II。对于150 mg剂量,System 22 Mizer递送7.16(1.02)mg,而Respirgard II递送4.34(0.57)mg。使用System 22 Mizer将填充量从3 ml增加到6 ml,可增加肺部沉积,这与雾化器输出量的增加有关。通过在Respirgard II中使用6 ml溶液,肺沉积和雾化器输出均不会增加。增加填充量会延长使用两个雾化器进行雾化所需的时间。 System 22 Mizer产生更多的非肺部(胃和口咽)药物沉积,更频繁的局部不良反应(咳嗽,喉咙灼热和金属味),以及肺功能的轻微降低,特别是使用150 mg喷他tam剂量时。因此,雾化器的类型,填充量和雾化器剂量都会影响喷他idine的肺部沉积。通常建议通过Respirgard II服用300毫克喷他idine,以提供有效的预防。我们的结果表明,使用System 22 Mizer和150 mg喷他idine可以产生类似的肺部沉积。需要进行临床试验以表明该方案是否可提供类似的预防益处。

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