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. 2019 Sep 5;9(9):CD006682.
doi: 10.1002/14651858.CD006682.pub6.

Duration of intravenous antibiotic therapy in people with cystic fibrosis

Affiliations

Duration of intravenous antibiotic therapy in people with cystic fibrosis

Linsey Abbott et al. Cochrane Database Syst Rev. .

Abstract

Background: Progressive lung damage from recurrent exacerbations is the major cause of mortality and morbidity in cystic fibrosis. Life expectancy of people with cystic fibrosis has increased dramatically in the last 40 years. One of the major reasons for this increase is the mounting use of antibiotics to treat chest exacerbations caused by bacterial infections. The optimal duration of intravenous antibiotic therapy is not clearly defined. Individuals usually receive intravenous antibiotics for 14 days, but treatment may range from 10 to 21 days. A shorter duration of antibiotic treatment risks inadequate clearance of infection which could lead to further lung damage. Prolonged courses of intravenous antibiotics are expensive and inconvenient. The risk of systemic side effects such as allergic reactions to antibiotics also increases with prolonged courses and the use of aminoglycosides requires frequent monitoring to minimise some of their side effects. However, some organisms which infect people with cystic fibrosis are known to be multi-resistant to antibiotics, and may require a longer course of treatment. This is an update of previously published reviews.

Objectives: To assess the optimal duration of intravenous antibiotic therapy for treating chest exacerbations in people with cystic fibrosis.

Search methods: We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group Trials Register which comprises references identified from comprehensive electronic database searches, handsearches of relevant journals, abstract books and conference proceedings. Most recent search of the Group's Cystic Fibrosis Trials Register: 30 May 2019.We also searched online trials registries. Most recent search of the ClinicalTrials.gov and WHO International Clinical Trials Registry Platform (ICTRP) portal: 06 January 2019.

Selection criteria: Randomised and quasi-randomised controlled trials comparing different durations of intravenous antibiotic courses for acute respiratory exacerbations in people with CF, either with the same drugs at the same dosage, the same drugs at a different dosage or frequency or different antibiotics altogether, including studies with additional therapeutic agents.

Data collection and analysis: No eligible trials were identified for inclusion. A trial looking at the standardised treatment of pulmonary exacerbations is currently ongoing and will be included when the results are published. MAIN RESULTS: No eligible trials were included.

Authors' conclusions: There are no clear guidelines on the optimum duration of intravenous antibiotic treatment. Duration of treatment is currently based on unit policies and response to treatment. Shorter duration of treatment should improve quality of life and adherence, result in a reduced incidence of drug reactions and be less costly. However, the shorter duration may not be sufficient to clear a chest infection and may result in an early recurrence of an exacerbation. This systematic review identifies the need for a multicentre, randomised controlled trial comparing different durations of intravenous antibiotic treatment as it has important clinical and financial implications. The currently ongoing STOP2 trial is expected to provide some guidance on these questions when published.

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Conflict of interest statement

Martin Wildman works intensively in the area of adherence working to understand how preventative nebulised treatment can decrease the need for IV antibiotics. He has received support from Respironics in terms of salary support for a research fellow who has worked on adherence research. He has also received funding from Smiths Medical for work around adherence device developments, funding from Pari to develop software to measure drug duration, and funding from Philips to use airflow data to try to predict exacerbations. He has also been paid for consultancy relating to adherence by Vertex Inc (Vertex do not manufacture or market antibiotics).

Amanda Plummer has received an honrarium from Profile Pharmaceuticals and from the Chiesi advisory board related to preventative nebulised treatment; these do not constitute a conflict of interest for this review which is looking at the duration of intravenous antibiotic treatment.

Linsey Abbott declares no known potential conflict of interest.

Zhe Hui Hoo declares funding from a CF Trust clinical fellowship (Award Identifier CF007).

Figures

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Study flow diagram.

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References

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References to other published versions of this review

Plummer 2011
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