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      Neuraminidase inhibitors for the treatment of influenza infection in people with cystic fibrosis

      systematic-review
      , , ,
      Cochrane Cystic Fibrosis and Genetic Disorders Group
      The Cochrane Database of Systematic Reviews
      John Wiley & Sons, Ltd

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          Abstract

          Background

          Cystic fibrosis is the most common, life‐threatening, recessively inherited disease of Caucasian populations. It is a multisystem disorder caused by a mutation in the gene encoding the cystic fibrosis transmembrane conductance regulator protein which is important in producing sweat, digestive juices and mucus.The impaired or absent function of this protein results in the production of viscous mucus within the lungs and an environment that is susceptible to chronic airway obstruction and pulmonary colonization by a range of pathogenic bacteria. Morbidity and mortality of cystic fibrosis is related to chronic pulmonary sepsis and its complications by these bacteria.

          Influenza can worsen the course of the disease in cystic fibrosis by increasing the risk of pneumonia and secondary respiratory complications. Antiviral agents form an important part of influenza management and include the neuraminidase inhibitors zanamivir and oseltamivir. These inhibitors can limit the infection and prevent the spread of the virus.

          Objectives

          To assess the effects of neuraminidase inhibitors for the treatment of influenza infection in people with cystic fibrosis.

          Search methods

          We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group Trials Register comprising references identified from comprehensive electronic database searches and handsearches of relevant journals and abstract books of conference proceedings.

          Most recent search: 02 November 2015.

          Selection criteria

          Randomised controlled trials and quasi‐randomised controlled trials comparing neuraminidase inhibitors with placebo or other antiviral drugs.

          Data collection and analysis

          Two review authors had planned to independently screen studies, extract data and assess risk of bias using standard Cochrane methodologies. No studies were identified for inclusion.

          Main results

          No relevant studies were retrieved after a comprehensive search of the literature.

          Authors' conclusions

          We were unable to identify any randomised controlled studies or quasi‐randomised controlled studies on the efficacy of neuraminidase inhibitors for the treatment of influenza infection in people with cystic fibrosis. The absence of high level evidence for the effectiveness of these interventions emphasises the need for well‐designed, adequately powered, randomised controlled clinical studies.

          Plain language summary

          Antiviral treatment for influenza infection in people with cystic fibrosis

          Review question

          We looked for evidence for the use of antiviral treatment against influenza infection in people with cystic fibrosis.

          Background

          Cystic fibrosis is a genetic, life‐threatening disorder which affects many organs in the body. and people with cystic fibrosis have a higher risk of chronic lung disease. Influenza can worsen the course of the disease in cystic fibrosis by increasing the risk of pneumonia and secondary respiratory complications. During a pandemic (an epidemic occurring worldwide, or over a very wide area, crossing international boundaries and usually affecting a large number of people), flu symptoms may be more severe and complications more frequent. Severe cases of pandemic flu have occurred in people with underlying chronic conditions including people with cystic fibrosis. Although there is no evidence that people with cystic fibrosis are more likely to contract this infection than healthy people, the impact for them could be greater and the outcome worse as the lower airways are more often affected. Antiviral agents are important in managing influenza and include the neuraminidase inhibitors zanamivir and oseltamivir. These drugs can limit the infection and prevent the spread of the virus.

          Search date

          The evidence is current to: 02 November 2015.

          Study characteristics

          We did not find any studies looking at the use of neuraminidase inhibitors for influenza in people with cystic fibrosis.

          Key results

          Limited data from previous studies have shown that these drugs can be effective in healthy people and may be useful in high‐risk populations if used rationally. However, we are not able to answer the question of the safety and effectiveness of neuraminidase inhibitors for treating influenza in people with cystic fibrosis.

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          Author and article information

          Contributors
          kidzdoc311@gmail.com , kidzdoc311@yahoo.co.in
          Journal
          Cochrane Database Syst Rev
          Cochrane Database Syst Rev
          14651858
          10.1002/14651858
          The Cochrane Database of Systematic Reviews
          John Wiley & Sons, Ltd (Chichester, UK )
          1469-493X
          24 February 2016
          February 2016
          15 February 2016
          : 2016
          : 2
          : CD008139
          Affiliations
          American Mission Hospital deptDepartment of Paediatrics Manama Manama Bahrain PO Box 1
          University of Bahrain deptCollege of Health Sciences Salmaniya Medical Complex Manama Bahrain
          Cochrane deptBahrain Branch Box 25438 Awali Bahrain
          A Floor, Clarendon Wing, Leeds General Infirmary deptLeeds Regional Paediatric Cystic Fibrosis Centre Great George Street Leeds West Yorkshire UK LS1 3EX
          Article
          PMC7199381 PMC7199381 7199381 CD008139.pub4 CD008139
          10.1002/14651858.CD008139.pub4
          7199381
          26905631
          d7c33bc0-0455-42bd-84fc-571cd1cea53a
          Copyright © 2016 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
          History
          Categories
          CYSTIC FIBROSIS
          Child health
          Genetic disorders
          Infectious disease
          Lungs & airways

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