Literature DB >> 35390177

Medical interventions for chronic rhinosinusitis in cystic fibrosis.

Tulasi Kota Karanth1, Veena Kota Laxminarayan Kl Karanth2, Bryan K Ward3, Bradford A Woodworth4, Laxminarayan Karanth5.   

Abstract

BACKGROUND: Chronic rhinosinusitis frequently occurs in people with cystic fibrosis. Several medical interventions are available for treating chronic rhinosinusitis in people with cystic fibrosis; for example, different concentrations of nasal saline irrigations, topical or oral corticosteroids, antibiotics - including nebulized antibiotics - dornase alfa and modulators of the cystic fibrosis transmembrane conductance regulator (CFTR) (such as lumacaftor, ivacaftor or tezacaftor). However, the efficacy of these interventions is unclear. This is an update of a previously published review.
OBJECTIVES: The objective of this review is to compare the effects of different medical interventions in people diagnosed with cystic fibrosis and chronic rhinosinusitis. SEARCH
METHODS: We searched the Cochrane Cystic Fibrosis Trials Register, compiled from electronic database searches and hand searching of journals and conference abstract books. Date of last search of trials register: 09 September 2021. We also searched ongoing trials databases, other medical databases and the reference lists of relevant articles and reviews. Date of latest additional searches: 22 November 2021. SELECTION CRITERIA: Randomized and quasi-randomized trials of different medical interventions compared to each other or to no intervention or to placebo. DATA COLLECTION AND ANALYSIS: Two review authors independently assessed trials identified for potential inclusion in the review. We planned to conduct data collection and analysis in accordance with Cochrane methods and to independently rate the quality of the evidence for each outcome using the GRADE guidelines. MAIN
RESULTS: We identified no trials that met the pre-defined inclusion criteria. The most recent searches identified 44 new references, none of which were eligible for inclusion in the current version of this review; 12 studies are listed as excluded and one as ongoing. AUTHORS'
CONCLUSIONS: We identified no eligible trials assessing the medical interventions in people with cystic fibrosis and chronic rhinosinusitis. High-quality trials are needed which should assess the efficacy of different treatment options detailed above for managing chronic rhinosinusitis, preventing pulmonary exacerbations and improving quality of life in people with cystic fibrosis.
Copyright © 2022 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

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Year:  2022        PMID: 35390177      PMCID: PMC8989145          DOI: 10.1002/14651858.CD012979.pub3

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


  60 in total

Review 1.  International Consensus Statement on Allergy and Rhinology: Rhinosinusitis Executive Summary.

Authors:  Richard R Orlandi; Todd T Kingdom; Peter H Hwang
Journal:  Int Forum Allergy Rhinol       Date:  2016-02-16       Impact factor: 3.858

2.  A phase I/II study of tgAAV-CF for the treatment of chronic sinusitis in patients with cystic fibrosis.

Authors:  J A Wagner; M L Moran; A H Messner; R Daifuku; C K Conrad; T Reynolds; W B Guggino; R B Moss; B J Carter; J J Wine; T R Flotte; P Gardner
Journal:  Hum Gene Ther       Date:  1998-04-10       Impact factor: 5.695

3.  Nasal saline as a placebo in chronic rhinosinusitis.

Authors:  Ahmet Karadag; Ferhat Catal
Journal:  J Cyst Fibros       Date:  2014-07-30       Impact factor: 5.482

4.  Maxillary sinusitis as a surrogate model for CF gene therapy clinical trials in patients with antrostomies.

Authors:  J A Wagner; I B Nepomuceno; N Shah; A H Messner; M L Moran; A M Norbash; R B Moss; J J Wine; P Gardner
Journal:  J Gene Med       Date:  1999 Jan-Feb       Impact factor: 4.565

5.  Distribution of mucus producing elements in the respiratory tract. Differences between upper and lower airway.

Authors:  M Tos
Journal:  Eur J Respir Dis Suppl       Date:  1983

6.  Physiologic and hypertonic saline solutions impair ciliary activity in vitro.

Authors:  W M Boek; N Keleş; K Graamans; E H Huizing
Journal:  Laryngoscope       Date:  1999-03       Impact factor: 3.325

7.  Efficacy and safety of lumacaftor and ivacaftor in patients aged 6-11 years with cystic fibrosis homozygous for F508del-CFTR: a randomised, placebo-controlled phase 3 trial.

Authors:  Felix Ratjen; Christopher Hug; Gautham Marigowda; Simon Tian; Xiaohong Huang; Sanja Stanojevic; Carlos E Milla; Paul D Robinson; David Waltz; Jane C Davies
Journal:  Lancet Respir Med       Date:  2017-06-09       Impact factor: 30.700

8.  A phase II, double-blind, randomized, placebo-controlled clinical trial of tgAAVCF using maxillary sinus delivery in patients with cystic fibrosis with antrostomies.

Authors:  John A Wagner; Ilynn B Nepomuceno; Anna H Messner; Mary Lynn Moran; Eric P Batson; Sue Dimiceli; Byron W Brown; Julie K Desch; Alexander M Norbash; Carol K Conrad; William B Guggino; Terence R Flotte; Jeffrey J Wine; Barrie J Carter; Thomas C Reynolds; Richard B Moss; Phyllis Gardner
Journal:  Hum Gene Ther       Date:  2002-07-20       Impact factor: 5.695

Review 9.  Asthma and the unified airway.

Authors:  John H Krouse; Randall W Brown; Stanley M Fineman; Joseph K Han; Andrew J Heller; Stephanie Joe; Helene J Krouse; Harold C Pillsbury; Matthew W Ryan; Maria C Veling
Journal:  Otolaryngol Head Neck Surg       Date:  2007-05       Impact factor: 3.497

Review 10.  Clinical chronic rhinosinusitis outcomes in pediatric patients with cystic fibrosis.

Authors:  Frank W Virgin
Journal:  Laryngoscope Investig Otolaryngol       Date:  2017-05-31
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