Pharmacokinetics and lung delivery of PDDS-aerosolized amikacin (NKTR-061) in intubated and mechanically ventilated patients with nosocomial pneumonia

被引:117
作者
Luyt, Charles-Edouard [1 ]
Clavel, Marc [2 ]
Guntupalli, Kalpalatha [3 ]
Johannigman, Jay [4 ]
Kennedy, John I. [5 ]
Wood, Christopher [6 ]
Corkery, Kevin [7 ]
Gribben, Dennis [8 ]
Chastre, Jean [1 ]
机构
[1] Univ Paris 06, Grp Hosp Pitie Salpetriere, Serv Reanimat Med, AP HP, F-75651 Paris 13, France
[2] Ctr Hosp Dupuytren, Serv Reanimat Med, F-87000 Limoges, France
[3] Baylor Coll Med, Houston, TX 77030 USA
[4] Univ Cincinnati, Div Trauma Crit Care, Dept Surg, Cincinnati, OH 45221 USA
[5] Univ Alabama Birmingham, Div Pulm & Crit Care Med, Birmingham, AL 35249 USA
[6] Univ Tennessee, Hlth Sci Ctr, Crit Care Dept, Memphis, TN 38163 USA
[7] Novartis Pharmaceut, San Carlos, CA 94070 USA
[8] Talima Therapeut, San Carlos, CA 94070 USA
关键词
LINING FLUID; NEBULIZED AMIKACIN; BRONCHOALVEOLAR LAVAGE; TISSUE CONCENTRATIONS; TOBRAMYCIN; PIGLETS; ANTIBIOTICS; PENETRATION; DEPOSITION; DIAGNOSIS;
D O I
10.1186/cc8206
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Introduction Aminoglycosides aerosolization might achieve better diffusion into the alveolar compartment than intravenous use. The objective of this multicenter study was to evaluate aerosol-delivered amikacin penetration into the alveolar epithelial lining fluid (ELF) using a new vibrating mesh nebulizer (Pulmonary Drug Delivery System (PDDS), Nektar Therapeutics), which delivers high doses to the lungs. Methods Nebulized amikacin (400 mg bid) was delivered to the lungs of 28 mechanically ventilated patients with Gram-negative VAP for 7-14 days, adjunctive to intravenous therapy. On treatment day 3, 30 minutes after completing aerosol delivery, all the patients underwent bronchoalveolar lavage in the infection-involved area and the ELF amikacin concentration was determined. The same day, urine and serum amikacin concentrations were determined at different time points. Results Median (range) ELF amikacin and maximum serum amikacin concentrations were 976.1 (135.7-16127.6) and 0.9 (0.62-1.73) mu g/mL, respectively. The median total amount of amikacin excreted in urine during the first and second 12-hour collection on day 3 were 19 (12.21-28) and 21.2 (14.1-29.98) mu g, respectively. During the study period, daily through amikacin measurements were below the level of nephrotoxicity. Sixty-four unexpected adverse events were reported, among which 2 were deemed possibly due to nebulized amikacin: one episode of worsening renal failure, and one episode of bronchospasm. Conclusions PDDS delivery of aerosolized amikacin achieved very high aminoglycoside concentrations in ELF from radiography-controlled infection-involved zones, while maintaining safe serum amikacin concentrations. The ELF concentrations always exceeded the amikacin minimum inhibitory concentrations for Gram-negative microorganisms usually responsible for these pneumonias. The clinical impact of amikacin delivery with this system remains to be determined.
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页数:10
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