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IPD1.10 Antifungal therapy in adults with cystic fibrosis: experience over ten years

Journal of cystic fibrosis, 2017-06, Vol.16, p.S57-S58

2017

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EPS6.6 Remote monitoring of home non-invasive ventilation during infective exacerbations of cystic fibrosis: a feasibility study

Journal of cystic fibrosis, 2017-06, Vol.16, p.S51-S51

2017

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115 Tolerability of nebulised non-liposomal amikacin for the treatment of Mycobacterium abscessus infection in adults with cystic fibrosis

Journal of cystic fibrosis, 2017-06, Vol.16, p.S94-S94

2017

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223 Iron status, disease severity and sputum microbiology in adults with cystic fibrosis

Journal of cystic fibrosis, 2017-06, Vol.16, p.S119-S119

2017

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WS21.5 “Real world” use of intermittent positive pressure breathing in the acute management of adults with cystic fibrosis

Journal of cystic fibrosis, 2016-06, Vol.15, p.S34-S34

2016

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112 Standard versus extended fungal culture for the detection of filamentous fungi in CF sputum samples

Journal of cystic fibrosis, 2016-06, Vol.15, p.S79-S79

2016

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232 Changes in nutritional status prior to lung transplantation – single centre experience over 10 years

Journal of cystic fibrosis, 2015-06, Vol.14, p.S118-S118

2015

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166 CF sputum rheology and the role of the airway mucin MUC5AC

Journal of cystic fibrosis, 2012-06, Vol.11, p.S99-S99

2012

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P328 Set-up and use of non-invasive ventilation for adults with cystic fibrosis: an exploratory survey of UK cystic fibrosis physiotherapists

Journal of cystic fibrosis, 2020-06, Vol.19, p.S147-S148

2020

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ePS1.02 Use of non-invasive ventilation in cystic fibrosis in the UK: developments over a decade

Journal of cystic fibrosis, 2020-06, Vol.19, p.S37-S37

2020

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P327 Estimating adherence with nebulised therapies: a challenge for people with cystic fibrosis and healthcare professionals

Journal of cystic fibrosis, 2020-06, Vol.19, p.S147-S147

2020

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WS19.6 Changes in the weather and the respiratory health of adults with cystic fibrosis

Journal of cystic fibrosis, 2013-06, Vol.12, p.S39-S39

2013

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122 The impact of human rhinovirus infection on the cystic fibrosis lung microbiome

Journal of cystic fibrosis, 2013-06, Vol.12, p.S79-S79

2013

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124 Ribosomal RNA intergenic spacer analysis (RISA) as a rapid and diagnostic means to profile microbial diversity in cystic fibrosis sputum

Journal of cystic fibrosis, 2013-06, Vol.12, p.S80-S80

2013

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134 Validity of a symptom questionnaire for the diagnosis of viral respiratory infection in adults with CF

Journal of cystic fibrosis, 2012-06, Vol.11, p.S90-S90

2012

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P077 Discontinuation of prophylactic flucloxacillin in young adults with cystic fibrosis

Journal of cystic fibrosis, 2018-06, Vol.17, p.S81-S81

2018

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P223 Totally implantable venous access device tip position and risk of venous complications in cystic fibrosis

Journal of cystic fibrosis, 2018-06, Vol.17, p.S122-S123

2018

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P308 Long-term tolerability of inhaled mannitol in adults with cystic fibrosis

Journal of cystic fibrosis, 2020-06, Vol.19, p.S142-S142

2020

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P310 Real-world use of inhaled mannitol in cystic fibrosis: patient-led dose modification

Journal of cystic fibrosis, 2020-06, Vol.19, p.S142-S143

2020

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P378 Psychosocial impact of Mycobacterium abscessus infection in adults with cystic fibrosis

Journal of cystic fibrosis, 2020-06, Vol.19, p.S162-S162

2020

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WS10.03 Impact of triple CFTR modulator therapy on urinary incontinence symptoms in adults with cystic fibrosis

Journal of cystic fibrosis, 2022-06, Vol.21, p.S20

2022

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WS10.01 Impact of triple CFTR modulator therapy on airway clearance and nebuliser adherence in adults with cystic fibrosis

Journal of cystic fibrosis, 2022-06, Vol.21, p.S19

2022

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208 Long-term non-invasive ventilation in adults with cystic fibrosis: experience over two decades

Journal of cystic fibrosis, 2011, Vol.10, p.S53-S53

2011

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P348 An insight into the confidence and skills needed to provide care at the end of life for people with cystic fibrosis

Journal of cystic fibrosis, 2020-06, Vol.19, p.S153-S153

2020

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IPD1.10 Antifungal therapy in adults with cystic fibrosis: experience over ten years

EPS6.6 Remote monitoring of home non-invasive ventilation during infective exacerbations of cystic fibrosis: a feasibility study

115 Tolerability of nebulised non-liposomal amikacin for the treatment of Mycobacterium abscessus infection in adults with cystic fibrosis

223 Iron status, disease severity and sputum microbiology in adults with cystic fibrosis

WS21.5 “Real world” use of intermittent positive pressure breathing in the acute management of adults with cystic fibrosis

112 Standard versus extended fungal culture for the detection of filamentous fungi in CF sputum samples

232 Changes in nutritional status prior to lung transplantation – single centre experience over 10 years

166 CF sputum rheology and the role of the airway mucin MUC5AC

P328 Set-up and use of non-invasive ventilation for adults with cystic fibrosis: an exploratory survey of UK cystic fibrosis physiotherapists

ePS1.02 Use of non-invasive ventilation in cystic fibrosis in the UK: developments over a decade

P327 Estimating adherence with nebulised therapies: a challenge for people with cystic fibrosis and healthcare professionals

WS19.6 Changes in the weather and the respiratory health of adults with cystic fibrosis

122 The impact of human rhinovirus infection on the cystic fibrosis lung microbiome

124 Ribosomal RNA intergenic spacer analysis (RISA) as a rapid and diagnostic means to profile microbial diversity in cystic fibrosis sputum

134 Validity of a symptom questionnaire for the diagnosis of viral respiratory infection in adults with CF

P077 Discontinuation of prophylactic flucloxacillin in young adults with cystic fibrosis

P223 Totally implantable venous access device tip position and risk of venous complications in cystic fibrosis

P308 Long-term tolerability of inhaled mannitol in adults with cystic fibrosis

P310 Real-world use of inhaled mannitol in cystic fibrosis: patient-led dose modification

P378 Psychosocial impact of Mycobacterium abscessus infection in adults with cystic fibrosis

WS10.03 Impact of triple CFTR modulator therapy on urinary incontinence symptoms in adults with cystic fibrosis

WS10.01 Impact of triple CFTR modulator therapy on airway clearance and nebuliser adherence in adults with cystic fibrosis

208 Long-term non-invasive ventilation in adults with cystic fibrosis: experience over two decades

P348 An insight into the confidence and skills needed to provide care at the end of life for people with cystic fibrosis

P079 Using a learning health system to understand medicine waste in cystic fibrosis – the Easy Medicines for Burden Reduction And Care Enhancement (EMBRACE) study

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