Variation in treatment preferences of pulmonary exacerbations among Australian and New Zealand cystic fibrosis physicians

Background Despite advances in cystic fibrosis (CF) management and survival, the optimal treatment of pulmonary exacerbations remains unclear. Understanding the variability in treatment approaches among physicians might help prioritise clinical uncertainties to address through clinical trials.Method...

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Main Authors: Andre Schultz, Tom Snelling, Grace Currie, Anna Tai
Format: Article
Language:English
Published: BMJ Publishing Group 2021-08-01
Series:BMJ Open Respiratory Research
Online Access:https://bmjopenrespres.bmj.com/content/8/1/e000956.full
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spelling doaj-72c4ff045c5e44b18575514e326249e12021-08-10T11:31:02ZengBMJ Publishing GroupBMJ Open Respiratory Research2052-44392021-08-018110.1136/bmjresp-2021-000956Variation in treatment preferences of pulmonary exacerbations among Australian and New Zealand cystic fibrosis physiciansAndre Schultz0Tom Snelling1Grace Currie2Anna Tai3Telethon Kids Institute, Wal-yan Respiratory Research Centre, Perth, Western Australia, AustraliaWesfarmers Centre of Vaccines and Infectious Diseases, Telethon Kids Institute, Nedlands, Western Australia, AustraliaWesfarmers Centre of Vaccines and Infectious Diseases, Telethon Kids Institute, Nedlands, Western Australia, AustraliaDepartment of Respiratory Medicine, Sir Charles Gairdner Hospital, Nedlands, Western Australia, AustraliaBackground Despite advances in cystic fibrosis (CF) management and survival, the optimal treatment of pulmonary exacerbations remains unclear. Understanding the variability in treatment approaches among physicians might help prioritise clinical uncertainties to address through clinical trials.Methods Physicians from Australia and New Zealand who care for people with CF were invited to participate in a web survey of treatment preferences for CF pulmonary exacerbations. Six typical clinical scenarios were presented; three to paediatric and another three to adult physicians. For each scenario, physicians were asked to choose treatment options and provide reasons for their choices.Results Forty-nine CF physicians (31 paediatric and 18 adult medicine) participated; more than half reported 10+ years of experience. There was considerable variation in primary antibiotic selection; none was preferred by more than half of respondents in any scenario. For secondary antibiotic therapy, respondents consistently preferred intravenous tobramycin and a third antibiotic was rarely prescribed, except in one scenario describing an adult patient. Hypertonic saline nebulisation and twice daily chest physiotherapy was preferred in most scenarios while dornase alfa use was more variable. Most CF physicians (>80%) preferred to change therapy if there was no early response. Professional opinion was the most common reason for antibiotic choice.Conclusions Variation exists among CF physicians in their preferred choice of primary antibiotic and use of dornase alfa. These preferences are driven by professional opinion, possibly reflecting a lack of evidence to base policy recommendations. Evidence from high-quality clinical trials is needed to inform physician decision making.https://bmjopenrespres.bmj.com/content/8/1/e000956.full
collection DOAJ
language English
format Article
sources DOAJ
author Andre Schultz
Tom Snelling
Grace Currie
Anna Tai
spellingShingle Andre Schultz
Tom Snelling
Grace Currie
Anna Tai
Variation in treatment preferences of pulmonary exacerbations among Australian and New Zealand cystic fibrosis physicians
BMJ Open Respiratory Research
author_facet Andre Schultz
Tom Snelling
Grace Currie
Anna Tai
author_sort Andre Schultz
title Variation in treatment preferences of pulmonary exacerbations among Australian and New Zealand cystic fibrosis physicians
title_short Variation in treatment preferences of pulmonary exacerbations among Australian and New Zealand cystic fibrosis physicians
title_full Variation in treatment preferences of pulmonary exacerbations among Australian and New Zealand cystic fibrosis physicians
title_fullStr Variation in treatment preferences of pulmonary exacerbations among Australian and New Zealand cystic fibrosis physicians
title_full_unstemmed Variation in treatment preferences of pulmonary exacerbations among Australian and New Zealand cystic fibrosis physicians
title_sort variation in treatment preferences of pulmonary exacerbations among australian and new zealand cystic fibrosis physicians
publisher BMJ Publishing Group
series BMJ Open Respiratory Research
issn 2052-4439
publishDate 2021-08-01
description Background Despite advances in cystic fibrosis (CF) management and survival, the optimal treatment of pulmonary exacerbations remains unclear. Understanding the variability in treatment approaches among physicians might help prioritise clinical uncertainties to address through clinical trials.Methods Physicians from Australia and New Zealand who care for people with CF were invited to participate in a web survey of treatment preferences for CF pulmonary exacerbations. Six typical clinical scenarios were presented; three to paediatric and another three to adult physicians. For each scenario, physicians were asked to choose treatment options and provide reasons for their choices.Results Forty-nine CF physicians (31 paediatric and 18 adult medicine) participated; more than half reported 10+ years of experience. There was considerable variation in primary antibiotic selection; none was preferred by more than half of respondents in any scenario. For secondary antibiotic therapy, respondents consistently preferred intravenous tobramycin and a third antibiotic was rarely prescribed, except in one scenario describing an adult patient. Hypertonic saline nebulisation and twice daily chest physiotherapy was preferred in most scenarios while dornase alfa use was more variable. Most CF physicians (>80%) preferred to change therapy if there was no early response. Professional opinion was the most common reason for antibiotic choice.Conclusions Variation exists among CF physicians in their preferred choice of primary antibiotic and use of dornase alfa. These preferences are driven by professional opinion, possibly reflecting a lack of evidence to base policy recommendations. Evidence from high-quality clinical trials is needed to inform physician decision making.
url https://bmjopenrespres.bmj.com/content/8/1/e000956.full
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