44th European Cystic Fibrosis Conference


9-12 June 2021 Digital Conference
N. Poster
Poster title
Applicant name
  EPS2-001 Drug-induced liver injury from antibiotics administered to adult cystic fibrosis patients: is it a problem? A single-centre retrospective study Rachael Meredith Received Received
  EPS3-001 Is variation in Pseudomonas aeruginosa (Pa) surface-enhanced Raman spectroscopy (SERS) spectra related to phenotype? Danielle Allen Received Received
  EPS1-001 Physiotherapy practice of French cystic fibrosis children changed during lockdown due to COVID-19 pandemic Marie Mittaine Received Received
  P-001 TCR repertoire in monozygotic cystic fibrosis twins Burkhard Tmmler Received Received
  P-002 Genetic characteristics of the cystic fibrosis Polish patients registered in the public Matio Polish Cystic Fibrosis Foundation Karolina Surma Received Received
  EPS3-002 Using rapid evaporative ionisation mass spectrometry (REIMS) for biomarker discovery and mechanistic studies of Pseudomonas aeruginosa stress responses Rob Bradley Received Received
  EPS1-002 The impact of COVID-19 on the prescribing practice of specialist cystic fibrosis physiotherapist non-medical prescribers in the UK Catherine Brown Received Received
  EPS3-003 Using airway organoids and Air Liquid Interface cultures to profile the spatial and temporal dynamics of Pseudomonas aeruginosa infections Signe Lolle Received Received
  EPS1-003 Recommended shielding against COVID-19 impacts physical activity levels and adherence to airway clearance therapy in patients with cystic fibrosis Elpis Hatziagorou Received Received
  EPS2-003 Lumacaftor-ivacaftor therapy and its impact on glucose tolerance in children with cystic fibrosis Kathy McGrath Received Received
  EPS3-004 Depolarisation of the Pseudomonas aeruginosacytoplasmic membrane by Glatiramer acetate potentiates the antibacterial activity of tobramycin Ronan Murphy Received Received
  EPS1-004 Audit of virtual exercise class during COVID-19 in children with cystic fibrosis Zoe Johnstone Received Received
  EPS2-004 The role of Flash Glucose Monitoring System at annual review during the COVID-19 restrictions, within Cystic Fibrosis Diabetes Service at Blackpool Adult Cystic Fibrosis Centre. UK Julie Knowles Received Received
  EPS2-005 Arm circumference and skinfolds vs. body mass index: a single-centre experience over two decades Dorothea Appelt Received Received
  EPS1-005 Evaluating impacts of the change from clinic to home spirometry on clinicians and adults with cystic fibrosis Tracey Daniels Received Received
  P-005 Mild variants of the CFTR gene in Russian patients without clinical manifestations Yuliya Melyanovskaya Received Received
  P-006 The complex allele c.1399CT;1521_1523delCTT (L467F;F508del) of the CFTR gene in Russian cystic fibrosis patients Nataliya Kashirskaya Received Received
  EPS3-006 Low induction of Antibiotic resistance by two new drugs against Pseudomonas aeruginosa in a clinical cohort of cystic fibrosis patients Mette Kolpen Received Received
  EPS2-006 What do people with cystic fibrosis eat? Diet quality, macronutrient and micronutrient intakes compared to recommended guidelines in adults with cystic fibrosis: a systematic literature review Nicola Drummond Received Received
  EPS1-006 A retrospective audit of home-based spirometry quality in a large UK adult cystic fibrosis centre Ian Waller Received Received
  P-007 A novel cystic fibrosis-causing mutation identified in a newborn of African origin Natalia Cirilli Received Received
  EPS1-007 Impact of COVID-19 on cystic fibrosis physiotherapy outpatient clinics Emily Scott Received Received
  EPS2-007 How did the COVID-19 lockdown influence the nutritional status and body composition of cystic fibrosis patients in Poland? Monika Mielus Received Received
  EPS3-007 Predictors of eradication failure at first isolation of MRSA in children with cystic fibrosis Almala Pinar Ergenekon Received Received
  EPS2-008 The model for determining risk groups for the development of vitamin D deficiency and prevention algorithm in children with cystic fibrosis using the multifactor dimensionality reduction method Elena Zhekaite Received Received
  P-008 Identification of two novel mutations (c.3639dup and ex16-17a dup) in the CFTR gene in Polish patient with cystic fibrosis Sebastian Wardak Received Received
  EPS3-008 Evaluation of a fixed-step eradication regime in children with cystic fibrosis and detection of Pseudomonas aeruginosa Simon Florian Grewendorf Received Received
  EPS1-008 Exercising online a Beaming good initiative Gemma McCrea Received Received
  EPS3-009 Biofilm formation in methicillin-resistant Staphylococcus aureus isolated in cystic fibrosis patients is strain-dependent and differentially influenced by antibiotics Agathe Boudet Received Received
  P-009 The investigation of the effect of electrolyte disorder on sweat test in newborns with positive cystic fibrosis screening test Sevgi Pekcan Received Received
  EPS2-009 F508del genotype is an independent risk factor for reduced bone mineral density in children with cystic fibrosis JASNA RODMAN BERLOT Received Received
  EPS1-009 Adapting services during the COVID-19 pandemic a patient evaluation of physiotherapy telephone reviews within multidisciplinary team virtual clinics Sarah Fitzgerald Received Received
  P-010 Newborn screening for cystic fibrosis improves nutritional outcome: monocentric data of the first 4 years in Germany Katharina Schtz Received Received
  EPS2-010 Pregnancy and cystic fibrosis: patients experience from pre-conception to birth Marilyn Hagan Received Received
  EPS3-010 Clinical pharmacokinetics and dose recommendations for posaconazole gastro-resistant tablets in children with cystic fibrosis Sian Bentley Received Received
  P-011 Cystic fibrosis - newborn screening (CF-NBS) start-up in Flanders (Belgium): report of first evaluation after two years Marijke Proesmans Received Received
  P-012 Two years neonatal screening for cystic fibrosis in Republic of North Macedonia Stojka Fustik Received Received
  P-013 Evaluation of improvements of the cystic fibrosis newborn screening protocol in the Netherlands Marelle Bouva Received Received
  P-015 Evaluation of the specificity and sensitivity of the cut-off values of immunoreactive trypsinogen in the cystic fibrosis newborn screening program Tugba Ramasli Gursoy Received Received
  P-016 The role of clinical and laboratory findings in the diagnosis of cystic fibrosisin children with positive newborn screening Tugba Ramasli Gursoy Received Received
  P-017 Different ethnical distribution of the incidence of cystic fibrosis in Republic of North Macedonia Violeta Anastasovska Received Received
  P-018 Follow-up of children with Cystic Fibrosis Screen Positive, Inconclusive Diagnosis (CFSPID) in Switzerland Orell Imahorn Received Received
  P-019 Inconclusive Cystic Fibrosis Positive Neonatal Screening (CFSPID): clinical outcomes Silvia Gartner Received Received
  P-020 CFTR mutation panel in detecting cystic fibrosis screen positive inconclusive diagnosis patients (CFSPIDs) in the Marche Region, Italy Natalia Cirilli Received Received
  P-021 An evaluation of the cystic fibrosis newborn screening service at Royal Manchester Childrens Hospital - experience from a tertiary service provider in Northwest United Kingdom Anirban Maitra Received Received
  P-022 Evaluation of hearing and vestibular system in patients with cystic fibrosis Beste zsezen Received Received
  P-023 Characterisation of CFTR function in a patient with the F508del/CFTRdup1-3 genotype Senne Cuyx Received Received
  P-024 Pili annulati: is it a new finding in cystic fibrosis? SEVG&304; PEKCAN Received Received
  P-025 Systems biology modelling of CFTR maturation to predict possible active compound combinations Liza Vinhoven Received Received
  P-026 Characterisation of F508del-CFTR rescue by corrector MCG1516A Mafalda Bacalhau Received Received
  P-027 Identification of corrector combinations to increase the rescue of F508del-CFTR traffic and function Filipa Castela Ferreira Received Received
  P-028 Identification of novel F508del-CFTR correctors among triazole derivative compounds Mafalda Bacalhau Received Received
  P-029 First report: Kaftriovs. Symkeviin intestinal organoids Eva Furstova Received Received
  P-030 Metabolomic impact of the restoration of CFTR activity in the respiratory epithelium Emmanuelle Bardin Received Received
  P-031 The last 10: small molecule screening for correctors of rare CFTR processing mutations Marjolein Ensinck Received Received
  P-032 Chemical optimisation of a PI3Ky competing peptide for the therapy of cystic fibrosis Angela Della Sala Received Received
  P-033 Therapeutic approach by translational suppression of non-sens mutation in CFTR gene Sabrina Karri Received Received
  P-034 Novel insights into the therapeutic potential of antisense oligonucleotides as splicing modulators in respiratory and intestinal patient-derived model systems Noemie Stanleigh Received Received
  P-035 iPSC-derived macrophages from cystic fibrosis patients as a cell source to establish in vitro infection models and a drug screening platform Claudio Rodríguez-González Received Received
  P-036 Analysis of the dysfunction of cystic fibrosis macrophages Claudio Rodríguez-González Received Received
  P-037 Elexacaftor/tezacaftor/ivacaftor improve lung disease in patients with advanced cystic fibrosis homozygous for the F508del mutation Donatello Salvatore Received Received
  P-038 An Italian centre experience with elexacaftor-tezacaftor-ivacaftor therapy in cystic fibrosis patients with advanced lung disease Chiara Rosazza Received Received
  P-039 The clinical impact of triple CFTR modulator therapy in a cohort of people with CF and severe lung disease Orla Fanthorpe Received Received
  P-040 Compassionate use triple therapy CFTR modulation (Kaftrio) in severe disease. Single-centre, real-world clinical outcomes, safety and tolerability David Morrissy Received Received
  P-041 Effect of thetriplecombination of CFTR correctors and potentiatoron lung function, BMI and the Brasfield score in adolescents with cystic fibrosis Marina Praprotnik Received Received
  P-042 RECOVER - the Real World Clinical Outcomes with Novel Modulator therapy combinations in people with cystic fibrosis Paul McNally Received Received
  P-043 A snapshot of respiratory microbiology results pre- and post-commencing Kaftrio Laura Jenkins Received Received
  P-045 Are people with cystic fibrosis reducing their medication since Kaftrio initiation? Michael Dooney Received Received
  P-046 Menstrual abnormalities linked to Kaftrio Michael Dooney Received Received
  P-047 Impact of tezacaftor/ivacaftor/elexacaftor on outcome in a patient with I336Kmutation and a minimal function mutation R553X Sivagurunathan Sutharsan Received Received
  P-048 Olfactory dysfunction: impact of highly effective modulator therapy Daniel Beswick Received Received
  P-049 Tolerance induction (hyposensitisation) in drug intolerance to CFTR modulators Patience Eschenhagen Received Received
  P-050 Drug desensitisation for lumacaftor/ivacaftor - step-by-step to drug tolerance Julia Westhoff Received Received
  P-051 Rollout of Kaftrio to adult cystic fibrosis patients at the Royal Brompton Hospital during a global pandemic Elaine Bowman Received Received
  P-052 Managing the roll out of the cystic fibrosis modulator therapy Kaftrio at a large UK adult centre Constance (Connie) Takawira Received Received
  P-053 Real-life clinical effects of therapy with lumacaftor and ivacaftor in patients with cystic fibrosis Isabella Comello Received Received
  P-054 Clinical outcomes in people with cystic fibrosis treated with lumacaftor/ivacaftor in routine clinical practice in Sweden Anders Lindblad Received Received
  P-056 Intestinal current measurement (ICM) in cystic fibrosis paediatric patients - a pilot study Magdalena Postek Received Received
  P-057 Cystic fibrosis children not eligible for modulators therapy - data from a tertiary paediatric centre in Northwest United Kingdom Ghulam Mujtaba Received Received
  P-058 The effect of hypertonic saline treatment in preschoolers with cystic fibrosis on lung structure as measured by chest computed tomography (CT). SHIP-CT study: feasibility of CT scan protocol Harm A.W.M. Tiddens Received Received
  P-059 A double-blind randomised multicentre European study of linoleic acid supplementation for one year in patients with cystic fibrosis Birgitta Strandvik Received Received
  P-060 Phage therapy for chronic Pseudomonas aeruginosa infections in cystic fibrosis patients Maya Kahan-Hanum Received Received
  P-061 The UK Clinical Trials Accelerator Platform - a national cystic fibrosis clinical trials network increasing access to clinical trials for the UK cystic fibrosis community Rebecca Brendell Received Received
  P-062 Impact of the SARS-CoV-2 pandemic on clinical trials in the ECFS-CTN during 2020 Fiona Dunlevy Received Received
  P-063 Community involvement in shaping cystic fibrosis clinical trials Lorna Allen Received Received
  P-064 How does early weight gain explain the effect of childhood socioeconomic conditions on lung function for children with cystic fibrosis? A UK Registry-based study Daniela Schlter Received Received
  P-066 Lung function and pulmonary exacerbations among individuals with cystic fibrosis living near composting facilities in the United Kingdom Muhammad Saleem Khan Received Received
  P-067 Mechanisms for the effect of CFRD on mortality: a causal mediation analysis using UK cystic fibrosis Registry data Kamaryn Tanner Received Received
  P-068 Estimating the long-term effects of insulin on outcomes in cystic fibrosis-related diabetes: a target trial approach Emily Granger Received Received
  P-069 Cystic fibrosis-related liver disease a decade of experience Ana Mocic Pavic Received Received
  P-070 Epidemiology of nontuberculous mycobacteria in a single adult cystic fibrosis centre Ayesha Kumar Received Received
  P-071 Real-world pregnancy data and outcomes in an era post-CFTR modulation therapies: an Irish centres perspective Anina Ratjen Received Received
  P-072 Psychometric validation of the Cystic Fibrosis Impact Questionnaire: a patient-reported outcome instrument assessing the life impacts of cystic fibrosis Daniel Serrano Received Received
  P-073 Influence of assessment tool and publication type on the reported prevalence of depression and anxiety in adults with cystic fibrosis: a meta-analysis Louise Lord Received Received
  P-074 Setting up a framework for the collection of patient-reported outcomes in the real world: trials and tribulations Elise Lammertyn Received Received
  P-075 Are there lessons to be learned from cystic fibrosis patient deaths and the timing of lung transplant referral? Kavita Dave Received Received
  P-076 Using the Cystic Fibrosis Foundation consensus guidelines to assess the timing of lung transplant referral for individuals with cystic fibrosis in a single large adult UK centre: do they help? Kavita Dave Received Received
  P-077 Clinical factors affecting timing of referral for lung transplantation for people with cystic fibrosis: a national comparison of opinions between adult cystic fibrosis and transplant centres Kavita Dave Received Received
  P-078 The burden of cystic fibrosis beyond medical costs in Switzerland Christina Tzogiou Received Received
  P-079 Using a learning health system to understand medicine waste in cystic fibrosis the Easy Medicines for Burden Reduction And Care Enhancement (EMBRACE) study Amanda Bevan Received Received
  P-081 30 years of organisation of care for cystic fibrosis patients in the Russian Federation Yuliya Melyanovskaya Received Received
  P-082 The National Cystic Fibrosis Patient Registry of the Russian Federation 9 years of experience (2011-2019) Nataliya Kashirskaya Received Received
  P-083 Clinical progression of SARS-CoV-2 infection in people with cystic fibrosis: a global observational study Elliot McClenaghan Received Received
  P-084 The impact of the SARS-CoV-2 pandemic on people living with cystic fibrosis in Ireland: real-world data from the Irish cystic fibrosis registry Huw Rees Received Received
  P-085 Impact of COVID-19 on hospital services and specialist care of adults with cystic fibrosis Rini Bhatnagar Received Received
  P-086 The impact of COVID-19 in people with cystic fibrosis a single-centre experience Georgina Aldous Received Received
  P-087 Impact of COVID-19 on mental health of children with cystic fibrosis and their parents Rini Bhatnagar Received Received
  P-088 Impact of COVID-19 and cocooning on employment of people with cystic fibrosis Rini Bhatnagar Received Received
  P-089 Coronavirus infection (COVID 19) in children with cystic fibrosis of the Russian Federation Yuliya Melyanovskaya Received Received
  P-090 A UK survey on changes in managing people with cystic fibrosis during the COVID-19 pandemic Saffana Hameed Received Received
  P-091 Regularity of check-ups at the cystic fibrosis centre in the time of COVID-19 pandemic Ivana Todori&263; Received Received
  P-092 Embedding an electronic patient record into a developing UK service and impact during the COVID-19 pandemic - Blackpool Adult Cystic Fibrosis Service (BACFS) Natasha Pickering Received Received
  P-094 Facilitating cystic fibrosis research during the COVID-19 pandemic Sharon Burnett Received Received
  P-095 Effect of age and genotype on lung function in children with cystic fibrosis Shadrina Vera Received Received
  P-096 Long-term follow-up of adolescent and adult patients with cystic fibrosis: a single centres experience Asl&305; &304;mran Y&305;lmaz Received Received
  P-097 Whos talking about cystic fibrosis? The changing landscape of internet postings related to cystic fibrosis: a two-year comparative study Tamara Vagg Received Received
  P-098 Change in FEV1 after standardised care algorithm for cystic fibrosis patients: quality improvement project Muruvvet Cenk Received Received
  P-100 Quality of home spirometry performance amongst adults with cystic fibrosis Jody Bell Received Received
  P-101 Provision of home spirometry in a physiologist-led service: experiences from a large adult cystic fibrosis centre Scott Hawkes Received Received
  P-102 Utility of Dynamic Chest Radiography (DCR) for calculating lung volume subdivisions in adult people with cystic fibrosis Thomas Simon FitzMaurice Received Received
  P-103 Longitudinal SF6 multiple breath washout testing in children aged 0-4 years with cystic fibrosis Rikke Sandvik Received Received
  P-104 Multiple-breath nitrogen washout test and structural lung damage in adult patients with cystic fibrosis Alexander Cherniak Received Received
  P-105 Lung clearance index in monitoring response to antibiotic therapy in children with cystic fibrosis Katarzyna Walicka-Serzysko Received Received
  P-106 Positioning may not affect lung clearance index TJ BAKER Received Received
  P-107 Lung clearance index in Bulgarian patients with cystic fibrosis Boryana Gospodinova Received Received
  P-108 Cross-sectional and longitudinal comparison of N2 and SF6 multiple breath washout in children with cystic fibrosis aged 2-45 months Rikke Sandvik Received Received
  P-109 Regional assessment of lung function using non-contrast MRI in people with cystic fibrosis Jonathan Brooke Received Received
  P-110 A soft, flexible, wearable device for cough detection in paediatric cystic fibrosis patients Andreas Tzavelis Received Received
  P-111 CT-signs and the effectiveness of surgical treatment of sinonasal disease in children with cystic fibrosis Yulia Gorinova Received Received
  P-112 Sleep disorders and exercise capacity in adult patients with cystic fibrosis in the Republic of North Macedonia Tatjana Jakovska Maretti Received Received
  P-113 Integration of Qi Gong sessions into a respiratory rehabilitation program: the experience of the CF Centre in Roscoff (France) Laetitia Gueganton Received Received
  P-114 Neutrophil effector responses to cystic fibrosis clinical isolates of Pseudomonas aeruginosa Kayla Fantone Received Received
  P-115 Effectiveness of different eradication treatment protocols for the first Pseudomonas aeruginosa isolation in paediatric cystic fibrosis patients Birce Sunman Received Received
  P-116 Clinical characteristics of frequent and infrequent pulmonary exacerbations of cystic fibrosis lung disease Claire Houston Received Received
  P-118 Lung ultrasound in cystic fibrosis exacerbations Ioana Ciuca Received Received
  P-119 Improving Home IV outcomes Christina Ryan Received Received
  P-120 Bridging the gap enhancing a multidisciplinary team Home IV service to reduce discrepancy in cystic fibrosis care Victoria Kendall Received Received
  P-121 The effect of training about nebuliser cleaning and disinfection on the knowledge levels and practises of the caregivers of patients with cystic fibrosis Muruvvet Cenk Received Received
  P-122 The role of the clinical pharmacy specialist in monitoring adherence to inhaled therapies in patients with cystic fibrosis in the Republic of North Macedonia Marija Atanasova Nadzinska Received Received
  P-123 Adaptive immune response to Mycobacterium abscessus complex and cross-reactivity of BCG vaccination Renan Mauch Received Received
  P-124 Implementing an anti-emetic protocol improves morbidity associated with intravenous therapy for Mycobacterium abscessus in children Anupama Menon Received Received
  P-125 Impact of infection withAchromobacterspp.on clinical outcome in paediatric patients with cystic fibrosis Birce Sunman Received Received
  P-127 Pulsed intravenous methylprednisolone for allergic bronchopulmonary aspergillosis in cystic fibrosis Tamsin Thornton Received Received
  P-128 A review of inhaled corticosteroid prescribing in an adult cystic fibrosis population Claire McKeown Received Received
  P-129 Induced sputum as a minimally invasive sample to investigate airway inflammation in the early course of cystic fibrosis Vincent Giacalone Received Received
  P-130 Chronic inflammation biomarkers and lung function in cystic fibrosis patients Mihaela Dediu Received Received
  P-132 The Induced Immune response in CF patients Mads Lausen Received Received
  P-133 Impact of specialised pro-resolving lipid mediators on cystic fibrosis airway epithelial cell functions Malle Briottet Received Received
  P-134 SARS-CoV-2 infection in cystic fibrosis during the first pandemic wave in Italy: a multicentre prospective study with a control group Carla Colombo Received Received
  P-136 Relationship between cystic fibrosis disease severity and susceptibility to COVID-19 infection MERVE ATALAY Received Received
  P-137 COVID-19 in cystic fibrosis patients with and without lung transplantation: the Zurich cohort Carolin Steinack Received Received
  P-139 Evaluating the impact of a telemedicine service during the COVID-19 pandemic in people with cystic fibrosis Alex Bull Received Received
  P-140 TeCC (TeleMedicine, Cystic Fibrosis, Corona-Virus) study in a previous telemedicine-naive centre: clinical challenges, outcomes, and user experience in the first six months of a global pandemic David Morrissy Received Received
  P-142 Lung and gut microbiota signatures in cystic fibrosis mice challenged with Pseudomonas aeruginosa Annamaria Bevivino Received Received
  P-145 Unwanted effects of an essential oil component, citral, on the susceptibility of Pseudomonas aeruginosato antibiotics Alexandre Tetard Received Received
  P-146 Intra-patient evolution of a pulmonary strain of Pseudomonas aeruginosa,from primocolonisation until after lung transplant Susie Gaillot Received Received
  P-148 Different treatment regimens in first isolation of Pseudomonas aeruginosa Cansu Yilmaz Yegit Received Received
  P-149 Evolution of levofloxacin resistance and phenotypic characterisation of Pseudomonas aeruginosaclinical isolates from people with cystic fibrosis Callum Sloan Received Received
  P-150 Competitive fitness experiments of CF isolates of Pseudomonas aeruginosa in human and murine precision-cut lung slices (PCLS) Lion Wege Received Received
  P-151 Improved isolation yields for bacteriophage active against Staphylococcus aureus Joshua Iszatt Received Received
  P-152 Clinical findings and long-term effect of methicillin-resistant Staphylococcus aureus isolation in patients with cystic fibrosis Beste Ozsezen Received Received
  P-153 Exophiala dermatitidis infection in cystic fibrosis patients accelerates lung function decline: a retrospective single-centre review of historical lung function Gemma Ford Received Received
  P-154 Exophiala dermatitidis can undergo patient-patient transmission in cystic fibrosis patients Jonathan Ayling-Smith Received Received
  P-155 Identification of an evolutionary split in Burkholderia multivorans using phylogenomics: does it have any impacts on the ability to cause cystic fibrosis lung infection? Kasia Parfitt Received Received
  P-156 Mycobacterium abscessus treatment in adult patients with cystic fibrosis: case series and review Amel Alameeri Received Received
  P-157 Monitoring the distribution and genotypic diversity of Burkholderiales bacteria in Russian cystic fibrosis patients in the year of the COVID-19 pandemic Olga Voronina Received Received
  P-158 Fungal airway colonisation in cystic fibrosis patients in the Institute for Respiratory Diseases in Children - Skopje, Republic of North Macedonia Ivana Arnaudova Danevska Received Received
  P-159 Relationship between clinical and environmental strains of emerging opportunistic pathogens in cystic fibrosis and diversity in the home environment Quentin Menetrey Received Received
  P-160 Detection and management of non-tuberculous mycobacteria in cystic fibrosis patients in a tertiary paediatric centre Harriet Wayman Received Received
  P-162 Pneumococcal and influenza vaccination coverage level: data from a cystic fibrosis centre Elpis Hatziagorou Received Received
  P-163 Effects of the SARS-CoV-2 pandemic on attendance at the cystic fibrosis centre and the definition of the microbiological status of cystic fibrosis patients in Tuscany Daniela Dolce Received Received
  P-164 What is the tolerance of antibiotic dry powder inhalers in patients with cystic fibrosis? Paul Wilson Received Received
  P-165 Improvement in antibiotic usage and ppFEV1 with compassionate use of elexacaftor, tezacaftor and ivacaftor (ETI) for patients with cystic fibrosis Olivia Baker Received Received
  P-166 Prevalence of cystic fibrosis-associated liver disease in Albanian cystic fibrosis patients Irena Kasmi Received Received
  P-167 Prevalence of liver disease in cystic fibrosis patients in the Institute for Respiratory Diseases in Children - Skopje, Republic of North Macedonia Ivana Arnaudova Danevska Received Received
  P-168 Use of faecal elastase in patients with cystic fibrosis and mutation analysis in the Republic of North Macedonia Tatjana Jakovska Maretti Received Received
  P-169 Trends in Glycaemic Control in a Cohort of Patients with Cystic Fibrosis Related Diabetes Rahana Khanam Received Received
  P-170 Current status of cystic fibrosis-related diabetes in the Bulgarian cystic fibrosis population GUERGANA PETROVA Received Received
  P-171 Adult cystic fibrosis diabetes patient education and care needs: have your say - a patient survey Katrin Kosbab-Jackson Received Received
  P-172 Patient experience of Manchester Virtual Cystic Fibrosis-Related Diabetes Clinic during the COVID-19 pandemic Amanda Brennan Received Received
  P-173 Investigation of cyproheptadine as an appetite stimulator in 6 children with cystic fibrosis with a suboptimal nutritional status Sara Van Meerbeeck Received Received
  P-174 The association between body composition and respiratory outcomes for patients with cystic fibrosis Lidia Sheibani Received Received
  P-175 Nutritional status, lung function and adequacy of micronutrient supplementation in children with cystic fibrosis Tena Niseteo Received Received
  P-176 The benefits of changing to a cystic fibrosis-specific combined fat-soluble vitamin supplement: vitamin status, tablet burden and adherence Katie Marsden Received Received
  P-177 A review of vitamin levels in children with cystic fibrosis following the introduction of a multi-vitamin preparation harriet gledhill Received Received
  P-180 Food access challenges and social needs for people with cystic fibrosis Cristen Clemm Received Received
  P-181 Nutrition support at an adult cystic fibrosis centre Mandisa Mitchell-Whyte Received Received
  P-182 Developing a model for self-care support of diet and the gut in the routine care of children with cystic fibrosis: a qualitative study Laurie Cave Received Received
  P-183 The role of the nutritionist in care of adult patients with cystic fibrosis in Republic of North Macedonia Sonja Panovska Received Received
  P-184 Going green: patient awareness of inhaler indication, usage and environmental impact Kizzy Snow Received Received
  P-185 Health literacy in children with cystic fibrosis Cherie Millar Received Received
  P-186 The use of Recombinant human DNase in a large adult cystic fibrosis centre: a quality improvement review Alison Orr Received Received
  P-187 Measuring the effect of airway clearance in adults with cystic fibrosis a systematic review Gemma Stanford Received Received
  P-188 Non-invasive ventilation use and management of adult cystic fibrosis patients at end of life Lucy E Wadsworth Received Received
  P-189 Impact of triple CFTR modulation therapy on non-invasive ventilation use in adults with cystic fibrosis Lucy E Wadsworth Received Received
  P-190 Adherence 50 to prescribed nebulisers in children with cystic fibrosis is associated with increased hospital admissions and lower FEV1 Z-Score Kieren James Lock Received Received
  P-191 The use of technology and web-based exercise programmes to improve engagement and quality of exercise sessions delivered to paediatric inpatients during an admission Louisa Wallbridge Received Received
  P-192 The introduction of a quality improvement focus group in a large UK adult cystic fibrosis centre Jocelyn Choyce Received Received
  P-193 Audit of cough swab sampling techniques in children with cystic fibrosis Zoe Johnstone Received Received
  P-194 Implementation of a cystic fibrosis-specific virtual pulmonary rehab program Catherine Fordyce Received Received
  P-195 Using remote access musculoskeletal consultations within a cystic fibrosis specialist physiotherapy service: a pilot Becky Dunphy Received Received
  P-196 Evaluation of the efficiency of Frequencer and Vest airways clearance devices in adult cystic fibrotic patients Peter Borka Received Received
  P-197 Dysglycaemia and changes in aerobic function in cystic fibrosis Owen Tomlinson Received Received
  P-198 Physical activity is associated with aerobic capacity and lung function in adults with cystic fibrosis Maire Curran Received Received
  P-199 Assessing the effectiveness of a six-month partially supervised outpatient exercise programme for adults with cystic fibrosis: a service evaluation Ann Banks Received Received
  P-200 Supporting exercise services in cystic fibrosis: five years of the UK CF & Exercise Network Owen Tomlinson Received Received
  P-201 The effectiveness of exercise interventions to increase physical activity in cystic fibrosis: a systematic review Maire Curran Received Received
  P-202 The evaluation of sinonasal and health symptoms in children with cystic fibrosis on Orkambi or Symkevi using the SNOT-22 Gemma Murray Received Received
  P-203 Fertile ground: pregnancies in a post-Kaftrio pandemic era Aoife Lillis Received Received
  P-204 The what-ifs....considering the psychological impacts of CFTR modulators Michele Puckey Received Received
  P-205 Patient-reported outcome measures in the current context of new generation modulator therapies in cystic fibrosis Kate Hayes Received Received
  P-206 Patient feedback following the introduction of a dedicated Symkevi Initiation Clinic prior to starting modulator therapy Lynette Haigh Received Received
  P-207 Depression and inflammation in people with cystic fibrosis: a pilot study Fabiana Ciciriello Received Received
  P-208 Anxiety, depression and resilience during COVID-19 in Dutch patients with cystic fibrosis or primary ciliary dyskinesia and their caregivers Marieke Verkleij Received Received
  P-209 Key priorities in mental health research: results of a community and provider survey across the US Beth Smith Received Received
  P-210 COACH project - screening for psychological comorbidity in adolescents with cystic fibrosis Svenja Temming Received Received
  P-211 Use of telemedicine for mental health screening during the COVID-19 pandemic Heather Bruschwein Received Received
  P-212 Understanding (the experiences of) how mindfulness is used by people with cystic fibrosis: barriers and enablers Sophia Kauser Received Received
  P-213 Can we attend anywhere? Evaluation of multi-disciplinary team (MDT) remote consultations Lisa Morrison Received Received
  P-214 Virtual cystic fibrosis doctor: design, development, and user experience pilot study David Morrissy Received Received
  P-215 Contrasting patient and paediatric cystic fibrosis team perception of telemedicine consultations Ema Kavaliunaite Received Received
  P-217 Delivering quality improvement coaching in a virtual world: the use of digital technology to empower and engage CFDigiCare clinicians to undertake quality improvement activities nationally Charlotte Carolan Received Received
  P-218 Detection of anxiety and depression through mental health screening questionnaires in cystic fibrosis patients and their families during the COVID-19 pandemic Ana Morales Tirado Received Received
  P-219 Before and during the COVID-19 pandemic: a review of health of our paediatric cystic fibrosis patients Lois Powell Received Received
  P-220 Experiences of virtual cystic fibrosis clinics during the Covid-19 pandemic at one UK adult cystic fibrosis centre Louise Warnock Received Received
  P-221 Quality of life in adult and children with cystic fibrosis during the COVID-19 pandemic in Croatia Tihana Odobasic Palkovic Received Received
  P-222 Supporting children with cystic fibrosis: building social networks through the pandemic Ellie Mindel Received Received
  P-223 The role of psychologist in a cystic fibrosis centre during the COVID-19 pandemic experience of a Polish paediatric centre Urszula Borawska-Kowalczyk Received Received
  P-224 Change in care during the COVID-19 pandemic: single-centre experience in a middle-income setting Ilektra Toulia Received Received
  P-225 Parents feedback on virtual paediatric cystic fibrosis clinics during Covid-19 pandemic Rachel Evans Received Received
  P-226 A survey of family experience of cystic fibrosis care during the COVID-19 pandemic Jill Watkinson Received Received
  P-227 Cystic fibrosis social workers experience of working during COVID-19 Fiona Dowdall Received Received
  P-228 Concerns for people with cystic fibrosis when travelling pre-COVID-19 Cherie Millar Received Received
  P-229 Children and young people with cystic fibrosis enhanced multi-disciplinary pathways to address their educational needs during the evolving COVID-19 pandemic Chandran Suja Received Received
  P-230 A review of paediatric cystic fibrosis care during the COVID-19 pandemic Lois Powell Received Received
  P-231 Patient experience of accessing a virtual cystic fibrosis service during the 2020 SARS-CoV-2 pandemic in Blackpool, North West of England Tarek Saba Received Received
  P-232 The impact of COVID-19 on the relationships between parents of young people diagnosed with cystic fibrosis and the cystic fibrosis multidisciplinary team Steve Jones Received Received
  P-233 Treatment outcome preferences among people with cystic fibrosis: a discrete choice experiment Rory Cameron Received Received
  P-234 CFHealthHub a digital learning health system supporting virtual clinics and self-care across 60 of UK adult CF centres: a survey to understand benefits amongst the national CFDigiCare community Josie Cunningham Received Received
  P-235 Using a 1,500-patient learning health system (LHS) to support virtual clinics and medicines optimisation: a UK seven-centre Patient and Public Involvement (PPI) project to understand user experience Sophie Dawson Received Received
  P-236 Quantifying the under-served or hard to reach but reachable people with cystic fibrosis (CF) in two UK adult CF centres Sophie Dawson Received Received
  P-237 The role of beliefs in predicting adherence to nebulised medications in adolescents with cystic fibrosis Bronwyn Stirzaker Received Received
  P-238 EMBRACEing Medicines Optimisation: working collaboratively to identify barriers and share solutions in the medication pathway across 12 sites within the CFHealthHub Charlotte Carolan Received Received
  P-239 Pulmonary medication adherence among children and adults with cystic fibrosis Elpis Hatziagorou Received Received
  P-240 Improving the accuracy of nebulizer prescriptions (and update where necessary) during the medication reconciliation process on CFHealthHub (within 24-hours) Rianna White Received Received
  P-241 Middle-aged cystic fibrosis patients experiences of living with cystic fibrosis: a qualitative study Lena Backstrm Eriksson Received Received
  P-242 Ageing with cystic fibrosis: how do older adults with cystic fibrosis adapt to change? Steven Stirk Received Received
  P-243 The psychological impact of the late diagnosis of atypical cystic fibrosis patients Guergana Petrova Received Received
  P-244 Moving from paediatric to adult care: resources to support transition Jacqueline Ali Received Received
  P-246 Transition in cystic fibrosis: international trends Daniel Office Received Received
  P-247 Improved quality of care increases lung function and growth parameters in children with cystic fibrosis Fabien Beaufils Received Received
  P-248 Patient Science: a new citizen science approach for health and medical research involving people affected by cystic fibrosis Johanna Gardecki Received Received
  P-249 Mens health in cystic fibrosis in the modern era: a qualitative study Traci Kazmerski Received Received
  P-250 Correlation between care allowance levels and antibiotic treatment at the Stockholm Cystic Fibrosis Centre Eleonora Falk Received Received
  P-251 The experience of adults with cystic fibrosis engaging in a complex health management regime: a meta-ethnography Steven Stirk Received Received
  P-252 Evaluation of a dashboard-style 1-page coloured CF annual review summary as a novel feedback method to improve communication with families and aid MDT working. Alison Coates Received Received
  P-253 Share the Sunshine to Improve Staff Wellbeing Sarah Simmons Received Received
  P-254 Development of a primary palliative care model that includes a novel approach to address the needs of caregivers of adults with cystic fibrosis - improving life with cystic fibrosis: a primary palliative care partnership Anna Georgiopoulos Received Received
  P-255 Parenthood experience of cystic fibrosis patients and their spouses - An explorative study Anne Jacob Received Received
  P-256 Waiting for double lung transplantation: psychological impact (review) Trudy Havermans Received Received
  P-257 Directions of psychological and pedagogical support of children with cystic fibrosis Sviridova Tatiana Received Received
  P-258 Integrating a diabetes service within the Adult Cystic Fibrosis Service at Blackpool Victoria Hospital, UK Julie Knowles Received Received
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