Intensivmedizin up2date 2012; 8(1): 21-31
DOI: 10.1055/s-0030-1257074
Allgemeine Prinzipien der Intensivmedizin

© Georg Thieme Verlag KG Stuttgart · New York

Inhalative Antibiotika – eine Option für die Zukunft?

Jessica  Rademacher, Tobias  Welte
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
22. Dezember 2011 (online)

Kernaussagen

  • Inhalative Antibiotika haben bei der Behandlung der zystischen Fibrose einen eindeutigen Stellenwert. Für andere Erkrankungen (Bronchiektasen, beatmungsassoziierte Pneumonien) gibt es vielversprechende Daten. Weitere große Studien stehen noch aus.

  • Inhalatives Tobramycin ist das bislang am besten untersuchte inhalative Antibiotikum. Es hat eine gute Wirksamkeit gegen gramnegative Keime und nur wenige Nebenwirkungen.

  • Inhalatives Colistin findet bereits breite Anwendung bei der zystischen Fibrose. In Hochresistenzländern könnte es zur zusätzlichen Behandlung beatmungsassoziierter Pneumonien durch multiresistente Keime künftig an Bedeutung gewinnen.

  • Das kürzlich zugelassene inhalative Antibiotikum Aztreonam könnte den Handlungsspielraum bei chronischer Besiedlung erweitern.

  • Inhalative Antibiotika können in der Lunge eine hohe Konzentration erreichen und haben im Vergleich zur systemischen Therapie geringere Nebenwirkungen. Weitere randomisierte kontrollierte Studien sind jedoch erforderlich, um den Nutzen zu belegen.

Literatur

  • 1 MacLusky I B, Gold R, Corey M et al. Long-term effects of inhaled tobramycin in patients with cystic fibrosis colonized with Pseudomonas aeruginosa.  Pediatr Pulmonol. 1989;  7 42-48
  • 2 Wiesemann H G, Steinkamp G, Ratjen F et al. Placebo-controlled, double-blind, randomized study of aerosolized tobramycin for early treatment of Pseudomonas aeruginosa colonization in cystic fibrosis.  Pediatr Pulmonol. 1998;  25 88-92
  • 3 Ramsey B W, Pepe M S, Quan J M et al. Intermittent administration of inhaled tobramycin in patients with cystic fibrosis. Cystic Fibrosis Inhaled Tobramycin Study Group.  N Engl J Med. 1999;  340 23-30
  • 4 Moss R B. Long-term benefits of inhaled tobramycin in adolescent patients with cystic fibrosis.  Chest. 2002;  121 55-63
  • 5 Hodson M E, Gallagher C G, Govan J R. A randomised clinical trial of nebulised tobramycin or colistin in cystic fibrosis.  Eur Respir J. 2002;  20 658-664
  • 6 Gibson R L, Emerson J, McNamara S et al. Significant microbiological effect of inhaled tobramycin in young children with cystic fibrosis.  Am J Respir Crit Care Med. 2003;  167 841-849
  • 7 Angrill J, Agustí C, de Celis R et al. Bacterial colonisation in patients with bronchiectasis: microbiological pattern and risk factors.  Thorax. 2002;  57 15-19
  • 8 Drobnic M E, Suñé P, Montoro J B et al. Inhaled tobramycin in non-cystic fibrosis patients with bronchiectasis and chronic bronchial infection with Pseudomonas aeruginosa.  Ann Pharmacother. 2005;  39 39-44
  • 9 Hallal A, Cohn S M, Namias N et al. Aerosolized tobramycin in the treatment of ventilator-associated pneumonia: a pilot study.  Surg Infect. 2007;  8 73-82
  • 10 Gales A C, Reis A O, Jones R N. Contemporary assessment of antimicrobial susceptibility testing methods for polymyxin B and colistin: review of available interpretative criteria and quality control guidelines.  Clin Microbiol. 2001;  39 83-190
  • 11 Hogardt M, Schmoldt S, Götzfried M et al. Pitfalls of polymyxin antimicrobial susceptibility testing of Pseudomonas aeruginosa isolated from cystic fibrosis patients.  J Antimicrob Chemother. 2004;  54 1057-1061
  • 12 Herrmann G, Yang L, Wu H et al. Colistin-tobramycin combinations are superior to monotherapy concerning the killing of biofilm Pseudomonas aeruginosa.  J Infect Dis. 2010;  202 585-1592
  • 13 Valerius N H, Koch C, Høhiby N. Prevention of chronic Pseudomonas aeruginosa colonisation in cystic fibrosis by early treatment.  Lancet. 1991;  338 725-726
  • 14 Jensen T, Pedersen S S, Garne S et al. Colistin inhalation therapy in cystic fibrosis patients with chronic Pseudomonas aeruginosa lung infection.  J Antimicrob Chemother. 1987;  19 831-838
  • 15 Høiby N, Frederiksen B, Pressler T. Eradication of early Pseudomonas aeruginosa infection.  J Cyst Fibros. 2005;  4 49-54
  • 16 Rademacher J, Pletz M W, Welte T. Treatment of not-with cystic fibrosis associated forms bronchiectasis (non-CF bronchiectasis).  Internist. 2010;  51 1510-1515
  • 17 Steinfort D P, Steinfort C. Effect of long-term nebulized colistin on lung function and quality of life in patients with chronic bronchial sepsis.  Intern Med J. 2007;  37 495-498
  • 18 Dhar R, Anwar G A, Bourke S C et al. Efficacy of nebulised colomycin in patients with non-cystic fibrosis bronchiectasis colonised with Pseudomonas aeruginosa.  Thorax. 2010;  65 553
  • 19 Michalopoulos A, Kasiakou S K, Falagas M E. The significance of different formulations of aerosolized colistin.  Crit Care. 2005;  9 417-418
  • 20 Kwa A L, Loh C, Low J G et al. Nebulized colistin in the treatment of pneumonia due to multidrug-resistant Acinetobacter baumannii and Pseudomonas aeruginosa.  Clin Infect Dis. 2005;  41 754-757
  • 21 Berlana D, Llop J M, Fort E, Badia M B, Jódar R. Use of colistin in the treatment of multiple-drug-resistant gram-negative infections.  Am J Health Syst Pharm. 2005;  62 39-47
  • 22 Michalopoulos A, Fotakis D, Virtzili S et al. Aerosolized colistin as adjunctive treatment of ventilator-associated pneumonia due to multidrug-resistant Gram-negative bacteria: a prospective study.  Respir Med. 2008;  102 407-412
  • 23 McCoy K S, Quittner A L, Oermann C M et al. Inhaled aztreonam lysine for chronic airway Pseudomonas aeruginosa in cystic fibrosis.  Am J Respir Crit Care Med. 2008;  178 21-928
  • 24 Oermann C M, Retsch-Bogart G Z, Quittner A L et al. An 18-month study of the safety and efficacy of repeated courses of inhaled aztreonam lysine in cystic fibrosis.  Pediatr Pulmonol. 2010;  45 1121-1134
  • 25 Heinzl B, Eber E, Oberwaldner B et al. Effects of inhaled gentamicin prophylaxis on acquisition of Pseudomonas aeruginosa in children with cystic fibrosis: a pilot study.  Pediatr Pulmonol. 2002;  33 32-7
  • 26 Murray M P, Govan J R, Doherty C J et al. A randomized controlled trial of nebulized gentamicin in non-cystic fibrosis bronchiectasis.  Am J Respir Crit Care Med. 2011;  183 491-499
  • 27 Palmer L B, Smaldone G C, Simon S R et al. Aerosolized antibiotics in mechanically ventilated patients: delivery and response.  Crit Care Med. 1998;  26 31-39
  • 28 Ghannam D E, Rodriguez G H, Raad I I et al. Inhaled aminoglycosides in cancer patients with ventilator-associated Gram-negative bacterial pneumonia: safety and feasibility in the era of escalating drug resistance.  Eur J Clin Microbiol Infect Dis. 2009;  28 253-259
  • 29 Morgan J, Wannemuehler K A, Marr K A et al. Incidence of invasive aspergillosis following hematopoietic stem cell and solid organ transplantation: interim results of a prospective multicenter surveillance program.  Med Mycol. 2005;  43 49-58
  • 30 Drew R H. Aerosol and other novel administrations for prevention and treatment of invasive aspergillosis.  Med Mycol. 2009;  47 355-361
  • 31 Knechtel S A, Klepser M E. Safety of aerosolized amphotericin B.  Expert Opin Drug Saf. 2007;  6 523-532
  • 32 Sexauer W P, Fiel S B. Aerosolized antibiotics in cystic fibrosis.  Semin Respir Crit Care Med. 2003;  24 717-726
  • 33 Wilson R, Welte T, Polverinoet E et al.. Randomized, placebo-controlled, double-blind, multi-center study to evaluate the safety and efficacy of ciprofloxacin dry powder for inhalation (ciprofloxacin DPI) compared with placebo in patients with non-cystic fibrosis bronchiectasis. American Thoracic Society (ATS), annual meeting May 13 – 18, 2011 Denver, USA; Abstract No. 22 734

Dr. Jessica Rademacher

Transplant-Ambulanz
Med. Hochschule Hannover

Carl-Neuberg-Str. 1
30625 Hannover

eMail: rademacher.jessica@mh-hannover.de

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