首页> 外文期刊>Drug Design, Development and Therapy >Sinonasal inhalation of tobramycin vibrating aerosol in cystic fibrosis patients with upper airway Pseudomonas aeruginosa colonization: results of a randomized, double-blind, placebo-controlled pilot study
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Sinonasal inhalation of tobramycin vibrating aerosol in cystic fibrosis patients with upper airway Pseudomonas aeruginosa colonization: results of a randomized, double-blind, placebo-controlled pilot study

机译:鼻咽吸入妥布霉素振动气雾剂在囊性纤维化患者上呼吸道铜绿假单胞菌定植:一项随机,双盲,安慰剂对照的试验研究结果

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Rationale: In cystic fibrosis (CF), the paranasal sinuses are sites of first and persistent colonization by pathogens such as Pseudomonas aeruginosa. Pathogens subsequently descend to the lower airways, with P. aeruginosa remaining the primary cause of premature death in patients with the inherited disease. Unlike conventional aerosols, vibrating aerosols applied with the PARI Sinus? nebulizer deposit drugs into the paranasal sinuses. This trial assessed the effects of vibrating sinonasal inhalation of the antibiotic tobramycin in CF patients positive for P. aeruginosa in nasal lavage. Objectives: To evaluate the effects of sinonasal inhalation of tobramycin on P. aeruginosa quantification in nasal lavage; and on patient quality of life, measured with the Sino-Nasal Outcome Test (SNOT-20), and otologic and renal safety and tolerability. Methods: Patients were randomized to inhalation of tobramycin (80 mg/2 mL) or placebo (2 mL isotonic saline) once daily (4 minutesostril) with the PARI Sinus? nebulizer over 28 days, with all patients eligible for a subsequent course of open-label inhalation of tobramycin for 28 days. Nasal lavage was obtained before starting and 2 days after the end of each treatment period by rinsing each nostril with 10 mL of isotonic saline. Results: Nine patients participated, six initially receiving tobramycin and three placebo. Sinonasal inhalation was well tolerated, with serum tobramycin <0.5 mg/L and stable creatinine. P. aeruginosa quantity decreased in four of six (67%) patients given tobramycin, compared with zero of three given placebo (non-significant). SNOT-20 scores were significantly lower in the tobramycin than in the placebo group (P=0.033). Conclusion: Sinonasal inhalation of vibrating antibiotic aerosols appears promising for reducing pathogen colonization of paranasal sinuses and for control of symptoms in patients with CF.
机译:原理:在囊性纤维化(CF)中,鼻旁窦是由铜绿假单胞菌等病原体首次和持续定殖的部位。病原体随后下降至下呼吸道,而铜绿假单胞菌仍然是遗传病患者过早死亡的主要原因。与传统的气雾剂不同,PARISinus®使用振动气雾剂?雾化器将药物沉积到鼻旁窦中。该试验评估了在鼻腔灌洗中振动通鼻鼻吸入抗生素妥布霉素对铜绿假单胞菌呈阳性的CF患者的影响。目的:评价鼻窦吸入妥布霉素对鼻灌洗中铜绿假单胞菌定量的影响;并通过鼻鼻息肉测试(SNOT-20)评估患者的生活质量,以及耳科和肾脏的安全性和耐受性。方法:患者被随机分配每天一次(4分钟/鼻孔)吸入妥布霉素(80 mg / 2 mL)或安慰剂(2 mL等渗盐水)与PARI窦?雾化器持续28天,所有患者均有资格接受随后28天的妥布霉素开放标签吸入疗程。在每个治疗期开始之前和结束后2天,通过用10 mL等渗盐水冲洗每个鼻孔获得洗鼻液。结果:9例患者参加,其中6例最初接受妥布霉素治疗,3例接受安慰剂治疗。鼻窦吸入耐受良好,血清妥布霉素<0.5 mg / L,肌酐稳定。接受妥布霉素治疗的六名患者中有四名(67%)的铜绿假单胞菌数量减少,相比之下,接受安慰剂的三名患者中有零名(无统计学意义)。妥布霉素组的SNOT-20评分显着低于安慰剂组(P = 0.033)。结论:鼻腔吸入振动性抗生素气雾剂有望减少CF患者鼻旁鼻窦的病原菌定植并控制症状。

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