The Leeds Method of Management. April, 2008. Nebulised antibiotics [online]. Leeds Regional Adult and Paediatric Cystic Fibrosis Units, St James’s University Hospital, Leeds, UK. Available from http://www.cysticfibrosismedicine.com
The advantages of nebulised antibiotic therapy for Pseudomonas aeruginosa infection in CF have been recognised for over 30 years (Mearns, 1970). An antibiotic delivered directly to the site of infection should be most effective. The altered lung environment consequent on inadequate CFTR protein function may reduce drug accumulation by the bacteria, and aminoglycoside efficacy may be reduced by binding to the excess extracellular neutrophil DNA (Levy et al, 1983). Sputum concentrations 25 times greater than the minimum inhibitory concentration (MIC) may be necessary to achieve a bactericidal effect (Mendelman et al, 1985). These levels cannot be reached by intravenous administration without unacceptable risks of systemic toxicity, but can be realised by inhalation of aerosolised antibiotics which, because of their minimal systemic absorption are unlikely to cause ototoxicity or nephrotoxicity (Smith et al, 1989).
Patients should be assessed before and after a test dose of a nebulised antibiotic. In children chest auscultation and, where possible, respiratory function tests are performed. In adults pre and post respiratory function tests are performed. Some patients will develop bronchospasm and may benefit from bronchodilator inhalation given before the antibiotic (Dodd et al, 1997; Cunningham et al, 2001; Alothman et al, 2002). A mouthpiece is preferable to a mask to maximise pulmonary deposition.
Nebulised antibiotics should be taken after physiotherapy to ensure maximum deposition.
Tobramycin crosses the placenta and there is a theoretical risk of damage to the VIII cranial nerve and of nephrotoxicity. Avoidance of parenteral administration is recommended during pregnancy but the risks from nebulised administration are much less. A decision whether or not to continue nebulised antibiotic treatment during pregnancy should be made on an individual basis and in consultation with the patient. The minimal but theoretical risks to the baby of continued treatment should be weighed against the risks to the mother’s health of stopping treatment.
i) Delay or prevention of chronic infection with P. aeruginosa
ii) Prevention of clinical deterioration in patients chronically infected with P. aeruginosa
Regular nebulised antibiotics reduce the rate of decline of respiratory function in patients chronically infected with P. aeruginosa. In 1981, Hodson et al compared six months of treatment with twice-daily nebulised gentamicin (80mg) and carbenicillin (1gm) versus placebo (Hodsonet al, 1981). Treated patients had significantly improved respiratory function and a non-significant trend towards fewer hospital admissions. Follow-up studies confirmed the benefits of treatment for chronic pseudomonas infection; improved lung function, a slower decline in lung function, fewer hospital admissions, better clinical scores and weight, and decreased P. aeruginosa density and virulence factors (Conway, 1999). There was no renal toxicity, ototoxicity or increase in bacterial resistance (Touw et al, 1995; Mukhopadhyay et al, 1996).
Low systemic and high local concentrations of colistin after nebulised delivery (Ratjen et al, 2006), and a randomised double blind study of TOBI® (Ramsey et al, 1999) support their use in patients with chronic P. aeruginosa infection. In the TOBI® study the first cycle of treatment produced a 12% increase in FEV1 which was maintained through the study. There was also a significant fall in colony forming units per gram of sputum, and patients required fewer intravenous antibiotic treatments. Sputum drug concentrations greater than 25 times the MIC value were seen in 95% of patients. Adolescent patients responded particularly well with 14% improvement in FEV1 compared with 1.8% for controls (Moss, 2002). Increasing P. aeruginosa tobramycin resistance was not associated with reduced clinical efficacy (Ramsey et al, 1999). There was no increased isolation of intrinsically tobramycin resistant micro-organisms (Burns et al, 1999). Colistin resistance is rare (Denton et al, 2002; Govan, 2002), and in our experience sensitivity returns when colistin inhalation and intravenous use is suspended for six months. A comparative study of twice-daily nebulised TOBI® (300mg) and nebulised colistin (1 mega unit), at present the only antibiotics licensed in the UK for nebulisation in CF, showed that both treatments reduced the bacterial content of the sputum significantly, and FEV1increased by 6.7% with TOBI® and 0.37% with colistin (Hodson et al, 2002; Govan, 2002 ).
The Cochrane Review found insufficient evidence to claim superiority for either TOBI® or colistin. Eleven trials met the inclusion criteria. The review concluded that nebulised antibiotic treatment improves lung function and reduces the frequency of respiratory exacerbations. There was no evidence of clinically important adverse events (Ryan et al, 2003).
Long term treatment is effective with patients having fewer hospital admissions and intravenous antibiotic use, and better preservation of respiratory function (Moss, 2001). Long term treatment is generally very safe but patients show an unpredictable range of systemic antibiotic absorption. The possibility of toxic drug levels resulting from nebulised antibiotic delivery should be remembered. Acute renal failure after one week of TOBI® and concurrent ciprofloxacin, and reversible vestibular dysfunction in a patient receiving haemodialysis have been reported (Hoffmann et al, 2002; Edson et al, 2004). Following inhaled gentamicin children showed significantly raised, but reversible, urinary N-acetyl-b-D-glucosaminidase (NAG) activity indicating renal tubular damage, compared to control children who had never received inhaled gentamicin or who had discontinued the drug at least three months previously. There was a positive correlation between NAG levels and cumulative antibiotic dose (Ring et al, 1998).
There is no published evidence to support concern that nebulised antibiotics may be a health hazard to medical personnel or the hospital and home environment.
Some drug solutions/suspensions show physico-chemical compatibility and may be mixed in the nebuliser chamber for simultaneous inhalation (Kamin et al, 2006).
There are no trials showing that nebulised antibiotics are as effective as intravenous antibiotics for treating infective exacerbations, or that they are useful adjuncts to intravenous therapy (Stephens et al, 1983; Schaad et al, 1987; Semsarian, 1990).
Nonetheless, clinicians may wish to use TOBI® for the treatment of exacerbations associated with multi-resistant P. aeruginosa because of the high endobronchial antibiotic levels achieved. The high sputum drug concentrations may render the usual laboratory breakpoints meaningless (Saiman et al, 1996; Lang et al, 2000).
Twice daily inhaled gentamicin in a small group of very young children prevented chronic infection for a mean of 78 months (Heinzl et al, 2002). Regular use of nebulised TOBI®, colistin, injectable forms of tobramycin or amikacin are associated with a chronic P. aeruginosainfection rate of <3% in Belgian children (Lebecque et al, 2006). There are, however, important negative effects to be considered before adopting this proactive approach, e.g. the increased risks of bacterial resistance, the risk of emergence of fungal organisms, the potential toxicity of treatment and the impact on daily life of long term nebulised antibiotic treatments. We can also prevent chronic P. aeruginosa infection in the majority of children with less invasive protocols aimed at eradicating new P. aeruginosa infection.
We recommend that specific treatment should be considered for patients who are smear positive, and for those with persistent positive cultures and symptoms despite routine antibiotic treatment.
Nebulised amikacin is part of the complex and long term antibiotic regimens for the treatment of the “rapid growers” e.g. M. abscessus (Cullen et al, 2000). There is no evidence base for dosage but 500mg bd is recommended. This may need reducing to 250mg bd in younger children. The injectable preparation (250mg/ml) should be used and made up to 4mls with sodium chloride 0.9%.
The role of nebulised vancomycin remains uncertain. There are anecdotal reports of efficacy in eradicating MRSA from the respiratory tract of patinets with CF (Maiz et al, 1998), but there are concerns regarding the possible impact of widespread and longer term use on the emergence of resistance.
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