Interventions for the eradication of meticillin-resistant Staphylococcus aureus (MRSA) in people with cystic fibrosis

David K.H. Lo*, Matthew N. Hurley, Marianne S. Muhlebach, Alan R. Smyth

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

25 Citations (Scopus)
3 Downloads (Pure)

Abstract

Background

Cystic fibrosis is an inherited recessive disorder of chloride transport that is characterised by recurrent and persistent pulmonary infections from resistant organisms that result in lung function deterioration and early mortality in sufferers.

Meticillin‐resistant Staphylococcus aureus (MRSA) has emerged as, not only an important infection in long‐term hospitalised patients, but also as a potentially harmful pathogen in cystic fibrosis, and has been increasing steadily in prevalence internationally. Chronic pulmonary infection with MRSA is thought to confer cystic fibrosis patients with a worse overall clinical outcome and, in particular, result in an increased rate of decline in lung function. Clear guidance for the eradication of MRSA in cystic fibrosis, supported by robust evidence from good quality trials, is urgently needed.

Objectives

To evaluate the effectiveness of treatment regimens designed to eradicate MRSA and to determine whether the eradication of MRSA confers better clinical and microbiological outcomes for people with cystic fibrosis.

Search methods

Randomised and quasi‐randomised controlled trials were identified by searching the Cochrane Cystic Fibrosis and Genetic Disorders Group's Cystic Fibrosis Trials Register, PUBMED, MEDLINE, Embase, handsearching article reference lists and through contact with local and international experts in the field.

Date of the last search of the Group's Cystic Fibrosis Trials Register: 04 September 2014.

Selection criteria

Randomised or quasi‐randomised controlled trials comparing any combinations of topical, inhaled, oral or intravenous antimicrobials with the primary aim of eradicating MRSA compared with placebo, standard treatment or no treatment.

Data collection and analysis

The authors independently assessed all search results for eligibility. No eligible trials were identified for inclusion.

Main results

No current published eligible trials were identified, although three ongoing clinical trials are likely to be eligible for inclusion in future updates of this review.

Authors' conclusions

We did not identify any randomised trials which would allow us to make any evidence‐based recommendations. Although the results of several non‐randomised studies would suggest that, once isolated, the eradication of MRSA is possible; whether this has a significant impact on clinical outcome is still unclear. Further research is required to guide clinical decision making in the management of MRSA infection in cystic fibrosis.

Original languageEnglish
Article numberCD009650
Number of pages25
JournalCochrane Database of Systematic Reviews
Volume2015
Issue number2
DOIs
Publication statusPublished - 24 Feb 2015
Externally publishedYes

Bibliographical note

Funding Information:
• National Institute for Health Research, UK. This systematic review was supported by the National Institute for Health Research, via Cochrane Infrastructure funding to the Cochrane Cystic Fibrosis and Genetic Disorders Group.

Publisher Copyright:
© 2015 The Cochrane Collaboration.

ASJC Scopus subject areas

  • Pharmacology (medical)

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