Literature DB >> 27907224

Single versus combination intravenous anti-pseudomonal antibiotic therapy for people with cystic fibrosis.

Heather E Elphick1, Alison Scott1.   

Abstract

BACKGROUND: Choice of antibiotic, and the use of single or combined therapy are controversial areas in the treatment of respiratory infection due to Pseudomonas aeruginosa in cystic fibrosis (CF). Advantages of combination therapy include wider range of modes of action, possible synergy and reduction of resistant organisms; advantages of monotherapy include lower cost, ease of administration and reduction of drug-related toxicity. Current evidence does not provide a clear answer and the use of intravenous antibiotic therapy in cystic fibrosis requires further evaluation. This is an update of a previously published review.
OBJECTIVES: To assess the effectiveness of single compared to combination intravenous anti-pseudomonal antibiotic therapy for treating 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 of the Group's Trials Register: 14 October 2016. SELECTION CRITERIA: Randomised controlled trials (RCTs) comparing a single intravenous anti-pseudomonal antibiotic with a combination of that antibiotic plus a second anti-pseudomonal antibiotic in people with CF. DATA COLLECTION AND ANALYSIS: Two authors independently assessed trial quality and extracted data. MAIN
RESULTS: We identified 45 trials, of which eight trials (356 participants) comparing a single anti-pseudomonal agent to a combination of the same antibiotic and one other, were included.There was a wide variation in the individual antibiotics used in each trial. In total, the trials included seven comparisons of a beta-lactam antibiotic (penicillin-related or third generation cephalosporin) with a beta-lactam-aminoglycoside combination and three comparisons of an aminoglycoside with a beta-lactam-aminoglycoside combination. These two groups of trials were analysed as separate subgroups.There was considerable heterogeneity amongst these trials, leading to difficulties in performing the review and interpreting the results. The meta-analysis did not demonstrate any significant differences between monotherapy and combination therapy, in terms of lung function; symptom scores; adverse effects; and bacteriological outcome measures.These results should be interpreted cautiously. Six of the included trials were published between 1977 and 1988; these were single-centre trials with flaws in the randomisation process and small sample size. Overall, the methodological quality was poor. AUTHORS'
CONCLUSIONS: The results of this review are inconclusive. The review raises important methodological issues. There is a need for an RCT which needs to be well-designed in terms of adequate randomisation allocation, blinding, power and long-term follow up. Results need to be standardised to a consistent method of reporting, in order to validate the pooling of results from multiple trials.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 27907224      PMCID: PMC6463970          DOI: 10.1002/14651858.CD002007.pub4

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


  52 in total

1.  Cystic fibrosis lung inflammation: early, sustained, and severe.

Authors:  A Cantin
Journal:  Am J Respir Crit Care Med       Date:  1995-04       Impact factor: 21.405

2.  Reduction of sputum Pseudomonas aeruginosa density by antibiotics improves lung function in cystic fibrosis more than do bronchodilators and chest physiotherapy alone.

Authors:  W E Regelmann; G R Elliott; W J Warwick; C C Clawson
Journal:  Am Rev Respir Dis       Date:  1990-04

Review 3.  Single versus combination intravenous antibiotic therapy for people with cystic fibrosis.

Authors:  H E Elphick; A Tan
Journal:  Cochrane Database Syst Rev       Date:  2005-04-18

4.  The efficacy and safety of meropenem and tobramycin vs ceftazidime and tobramycin in the treatment of acute pulmonary exacerbations in patients with cystic fibrosis.

Authors:  Jeffrey L Blumer; Lisa Saiman; Michael W Konstan; David Melnick
Journal:  Chest       Date:  2005-10       Impact factor: 9.410

5.  Piperacillin and tobramycin in the treatment of Pseudomonas lung infections in cystic fibrosis.

Authors:  J A Hoogkamp-Korstanje; J van der Laag
Journal:  J Antimicrob Chemother       Date:  1983-08       Impact factor: 5.790

6.  Distribution and elimination of tobramycin administered in single or multiple daily doses in adult patients with cystic fibrosis.

Authors:  A Aminimanizani; P M Beringer; J Kang; L Tsang; R W Jelliffe; B J Shapiro
Journal:  J Antimicrob Chemother       Date:  2002-10       Impact factor: 5.790

7.  Clinical and bacteriological responses to three antibiotic regimens for acute exacerbations of cystic fibrosis: ticarcillin-tobramycin, azlocillin-tobramycin, and azlocillin-placebo.

Authors:  F J McLaughlin; W J Matthews; D J Strieder; B Sullivan; A Taneja; P Murphy; D A Goldmann
Journal:  J Infect Dis       Date:  1983-03       Impact factor: 5.226

8.  Is anti-Pseudomonas therapy warranted in acute respiratory exacerbations in children with cystic fibrosis?

Authors:  P H Beaudry; M I Marks; D McDougall; K Desmond; R Rangel
Journal:  J Pediatr       Date:  1980-07       Impact factor: 4.406

9.  Controlled trial of ceftazidime vs. ticarcillin and tobramycin in the treatment of acute respiratory exacerbations in patients with cystic fibrosis.

Authors:  R Gold; A Overmeyer; B Knie; P C Fleming; H Levison
Journal:  Pediatr Infect Dis       Date:  1985 Mar-Apr

Review 10.  Management of acute pulmonary exacerbations in cystic fibrosis: a critical appraisal.

Authors:  J D Nelson
Journal:  J Pediatr       Date:  1985-06       Impact factor: 4.406

View more
  7 in total

Review 1.  Cystic Fibrosis Airway Microbiome: Overturning the Old, Opening the Way for the New.

Authors:  George A O'Toole
Journal:  J Bacteriol       Date:  2018-01-24       Impact factor: 3.490

2.  Pseudomonas aeruginosa antimicrobial susceptibility test (AST) results and pulmonary exacerbation treatment responses in cystic fibrosis.

Authors:  Donald R VanDevanter; Sonya L Heltshe; Jay B Hilliard; Michael W Konstan
Journal:  J Cyst Fibros       Date:  2020-06-04       Impact factor: 5.482

Review 3.  The Epidemiology and Pathogenesis and Treatment of Pseudomonas aeruginosa Infections: An Update.

Authors:  Dan Reynolds; Marin Kollef
Journal:  Drugs       Date:  2021-11-07       Impact factor: 9.546

4.  Mutational background influences P. aeruginosa ciprofloxacin resistance evolution but preserves collateral sensitivity robustness.

Authors:  Sara Hernando-Amado; Pablo Laborda; José Ramón Valverde; José Luis Martínez
Journal:  Proc Natl Acad Sci U S A       Date:  2022-04-06       Impact factor: 12.779

5.  Protocol for establishing a core outcome set for evaluation in studies of pulmonary exacerbations in people with cystic fibrosis.

Authors:  Charlie McLeod; Alan Robert Smyth; Mitch Messer; Andre Schultz; Jamie Wood; Richard Norman; Christopher C Blyth; Steve Webb; Zoe Elliott; Donald Van Devanter; Anne L Stephenson; Allison Tong; Thomas L Snelling
Journal:  BMJ Open       Date:  2022-09-23       Impact factor: 3.006

6.  Association Between Number of Intravenous Antipseudomonal Antibiotics and Clinical Outcomes of Pediatric Cystic Fibrosis Pulmonary Exacerbations.

Authors:  Jonathan D Cogen; Anna V Faino; Frankline Onchiri; Lucas R Hoffman; Matthew P Kronman; David P Nichols; Margaret Rosenfeld; Ronald L Gibson
Journal:  Clin Infect Dis       Date:  2021-11-02       Impact factor: 20.999

Review 7.  Pulmonary Exacerbations in Adults With Cystic Fibrosis: A Grown-up Issue in a Changing Cystic Fibrosis Landscape.

Authors:  Gemma E Stanford; Kavita Dave; Nicholas J Simmonds
Journal:  Chest       Date:  2020-09-20       Impact factor: 9.410

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.