Monk J P, Benfield P
ADIS Drug Information Services, Auckland.
Drugs. 1990 May;39(5):741-56. doi: 10.2165/00003495-199039050-00008.
Pentamidine is an aromatic diamidine derivative which has become one of the standard therapies for Pneumocystis carinii pneumonia (PCP), particularly in patients with acquired immunodeficiency syndrome (AIDS). However, with parenteral administration of the drug there is a high risk of toxicity. Inhaled pentamidine produces much higher concentrations of drug on the bronchoalveolar surface with minimal systemic absorption. It has been used successfully for the treatment of PCP in AIDS patients, but its most valuable contribution has been as prophylaxis in AIDS patients at high risk of developing PCP. In prospective controlled studies there has been greater than 80% reduction in relapse rate with pentamidine. The reduction in relapse rate among patients who have experienced one previous episode of PCP has been 50 to 100% compared with historical control groups, over a follow-up period averaging about 6 months. Significant systemic adverse effects to inhaled pentamidine are rare. Respiratory effects associated with inhalation are common but usually controllable without treatment discontinuation. The ideal particle size for even distribution of pentamidine throughout the lung is considered to be 1 to 2 microns. Jet nebulisers such as the 'Respirgard II' system produce a mass median aerodynamic diameter (MMAD) of particles in this range. Ultrasonic nebulisers produce larger particles. The implication from this difference is that while ultrasonic nebulisers may have poorer alveolar distribution and the incidence of local side effects (common with all formulations) may be higher, total drug delivery may be more efficient allowing effective PCP prophylaxis with lower dosages (120 mg vs 300 mg monthly). However, there are no data available comparing the efficacies and tolerabilities of the different formulations of inhaled pentamidine. Nevertheless, inhaled pentamidine would seem poised to become routine prophylaxis in patients with AIDS or AIDS-related complex at risk of developing PCP.
喷他脒是一种芳香族双脒衍生物,已成为卡氏肺孢子虫肺炎(PCP)的标准治疗方法之一,尤其是在获得性免疫缺陷综合征(AIDS)患者中。然而,经肠道外给药时,该药物有很高的毒性风险。吸入喷他脒可在支气管肺泡表面产生更高浓度的药物,而全身吸收极少。它已成功用于治疗艾滋病患者的PCP,但其最有价值的贡献是作为预防有发生PCP高风险的艾滋病患者的药物。在前瞻性对照研究中,喷他脒使复发率降低了80%以上。与历史对照组相比,曾有过一次PCP发作的患者在平均约6个月的随访期内,复发率降低了50%至100%。吸入喷他脒产生的显著全身不良反应很少见。与吸入相关的呼吸道影响很常见,但通常无需停药即可控制。喷他脒在整个肺部均匀分布的理想粒径被认为是1至2微米。诸如“Respirgard II”系统之类的喷射雾化器产生的颗粒质量中位空气动力学直径(MMAD)在此范围内。超声雾化器产生的颗粒较大。这种差异的含义是,虽然超声雾化器的肺泡分布可能较差,局部副作用(所有制剂都常见)的发生率可能较高,但总药物递送可能更有效,从而可以用较低剂量(每月120毫克对300毫克)进行有效的PCP预防。然而,没有可用数据比较吸入喷他脒不同制剂的疗效和耐受性。尽管如此,吸入喷他脒似乎有望成为有发生PCP风险的艾滋病或艾滋病相关综合征患者的常规预防药物。