Literature DB >> 27582394

Duration of intravenous antibiotic therapy in people with cystic fibrosis.

Amanda Plummer1, Martin Wildman, Tim Gleeson.   

Abstract

BACKGROUND: Respiratory disease 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 and the incidence of allergic reactions to antibiotics also increases with prolonged courses. The use of aminoglycosides requires frequent monitoring to avoid 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: 05 May 2016. 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. MAIN
RESULTS: No eligible trials were identified. 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 compliance; result in a reduced incidence of drug reactions; and be less costly. However, this 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.

Entities:  

Year:  2016        PMID: 27582394      PMCID: PMC6457596          DOI: 10.1002/14651858.CD006682.pub5

Source DB:  PubMed          Journal:  Cochrane Database Syst Rev        ISSN: 1361-6137


  60 in total

Review 1.  Antibiotic therapy against Pseudomonas aeruginosa in cystic fibrosis: a European consensus.

Authors:  G Döring; S P Conway; H G Heijerman; M E Hodson; N Høiby; A Smyth; D J Touw
Journal:  Eur Respir J       Date:  2000-10       Impact factor: 16.671

2.  Meta-analyses involving cross-over trials: methodological issues.

Authors:  Diana R Elbourne; Douglas G Altman; Julian P T Higgins; Francois Curtin; Helen V Worthington; Andy Vail
Journal:  Int J Epidemiol       Date:  2002-02       Impact factor: 7.196

3.  Predictors of deterioration of lung function in cystic fibrosis.

Authors:  C Schaedel; I de Monestrol; L Hjelte; M Johannesson; R Kornfält; A Lindblad; B Strandvik; L Wahlgren; L Holmberg
Journal:  Pediatr Pulmonol       Date:  2002-06

4.  Burkholderia cepacia in cystic fibrosis. Variable disease course.

Authors:  D D Frangolias; E Mahenthiralingam; S Rae; J M Raboud; A G Davidson; R Wittmann; P G Wilcox
Journal:  Am J Respir Crit Care Med       Date:  1999-11       Impact factor: 21.405

5.  Spread of a multiresistant strain of Pseudomonas aeruginosa in an adult cystic fibrosis clinic.

Authors:  A M Jones; J R Govan; C J Doherty; M E Dodd; B J Isalska; T N Stanbridge; A K Webb
Journal:  Lancet       Date:  2001-08-18       Impact factor: 79.321

6.  Alginate overproduction affects Pseudomonas aeruginosa biofilm structure and function.

Authors:  M Hentzer; G M Teitzel; G J Balzer; A Heydorn; S Molin; M Givskov; M R Parsek
Journal:  J Bacteriol       Date:  2001-09       Impact factor: 3.490

Review 7.  Treatment of cystic fibrosis in the adult.

Authors:  M E Hodson
Journal:  Respiration       Date:  2000       Impact factor: 3.580

Review 8.  Prospects for the prevention and control of pseudomonal infection in children with cystic fibrosis.

Authors:  N Høiby
Journal:  Paediatr Drugs       Date:  2000 Nov-Dec       Impact factor: 3.022

9.  Efficacy of once-daily tobramycin monotherapy for acute pulmonary exacerbations of cystic fibrosis: a preliminary study.

Authors:  V Master; G W Roberts; K P Coulthard; P A Baghurst; A Martin; M E Roberts; C R Onishko; A J Martin; R J Linke; M Holmes; A Jarvinen; D Kennedy; K A Colebatch; D Hansman; D W Parsons
Journal:  Pediatr Pulmonol       Date:  2001-05

10.  Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis.

Authors:  Julia Emerson; Margaret Rosenfeld; Sharon McNamara; Bonnie Ramsey; Ronald L Gibson
Journal:  Pediatr Pulmonol       Date:  2002-08
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  5 in total

Review 1.  Clinically Promising Biomarkers in Cystic Fibrosis Pulmonary Exacerbations.

Authors:  L Keith Scott; Robert Toner
Journal:  Lung       Date:  2017-06-16       Impact factor: 2.584

Review 2.  The future of cystic fibrosis care: a global perspective.

Authors:  Scott C Bell; Marcus A Mall; Hector Gutierrez; Milan Macek; Susan Madge; Jane C Davies; Pierre-Régis Burgel; Elizabeth Tullis; Claudio Castaños; Carlo Castellani; Catherine A Byrnes; Fiona Cathcart; Sanjay H Chotirmall; Rebecca Cosgriff; Irmgard Eichler; Isabelle Fajac; Christopher H Goss; Pavel Drevinek; Philip M Farrell; Anna M Gravelle; Trudy Havermans; Nicole Mayer-Hamblett; Nataliya Kashirskaya; Eitan Kerem; Joseph L Mathew; Edward F McKone; Lutz Naehrlich; Samya Z Nasr; Gabriela R Oates; Ciaran O'Neill; Ulrike Pypops; Karen S Raraigh; Steven M Rowe; Kevin W Southern; Sheila Sivam; Anne L Stephenson; Marco Zampoli; Felix Ratjen
Journal:  Lancet Respir Med       Date:  2019-09-27       Impact factor: 30.700

3.  Duration of intravenous antibiotic therapy in people with cystic fibrosis.

Authors:  Linsey Abbott; Amanda Plummer; Zhe Hui Hoo; Martin Wildman
Journal:  Cochrane Database Syst Rev       Date:  2019-09-05

4.  Optimising Antibiotic Usage to Treat Bacterial Infections.

Authors:  Iona K Paterson; Andy Hoyle; Gabriela Ochoa; Craig Baker-Austin; Nick G H Taylor
Journal:  Sci Rep       Date:  2016-11-28       Impact factor: 4.379

Review 5.  A comprehensive overview of the cystic fibrosis on the island of São Miguel (Azores, Portugal).

Authors:  Joana Rosa; Patrícia Gaspar-Silva; Paula Pacheco; Conceição Silva; Cláudia C Branco; Barbara S Vieira; Alexandra Carreiro; Juan Gonçalves; Luisa Mota-Vieira
Journal:  BMC Pediatr       Date:  2020-01-03       Impact factor: 2.125

  5 in total

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