Disparities in elexacaftor/tezacaftor/ivacaftor initiation in the US cystic fibrosis population
Fuente:
Wiley Open Access
Saved in:
| Main Authors: | Kamyron Jordan, Timothy Vigers, Jennifer L. Taylor‐Cousar, Scott D. Sagel |
|---|---|
| Format: | Artículo Open Access |
| Published: |
Wiley
2024
|
| Subjects: | |
| Online Access: | |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
Severe mental health changes in patients with cystic fibrosis on elexacaftor/tezacaftor/ivacaftor therapy
by: Cameron J. McKinzie, et al.
Published: (2024)
by: Cameron J. McKinzie, et al.
Published: (2024)
Mental health, sleep, and respiratory health after initiating elexacaftor/tezacaftor/ivacaftor treatment in children with cystic fibrosis
by: Hiep Pham, et al.
Published: (2024)
by: Hiep Pham, et al.
Published: (2024)
A survey of cystic fibrosis physicians' views on lung transplant referral in the era of elexacaftor/tezacaftor/ivacaftor
by: Nora Burdis, et al.
Published: (2024)
by: Nora Burdis, et al.
Published: (2024)
Effectiveness and safety of elexacaftor/tezacaftor/ivacaftor treatment in children aged 6‐11 years with cystic fibrosis in a real‐world setting
by: Valeria Daccò, et al.
Published: (2024)
by: Valeria Daccò, et al.
Published: (2024)
Medication utilization and lung function changes after initiation of treatment with elexacaftor/tezacaftor/ivacaftor
by: Richard De Vuyst, et al.
Published: (2024)
by: Richard De Vuyst, et al.
Published: (2024)
Diagnosis and treatment of ADHD in pediatric patients during the first year of elexacaftor/tezacaftor/ivacaftor
by: Kimberly Pasley, et al.
Published: (2024)
by: Kimberly Pasley, et al.
Published: (2024)
Clinical effectiveness of elexacaftor/tezacaftor/ivacaftor in a man with A559T and 3120+1G>CFTR variants
by: Emily Mitchell, et al.
Published: (2024)
by: Emily Mitchell, et al.
Published: (2024)
Clinical evidence of pancreatic recovery in children with cystic fibrosis on ivacaftor
by: Sydney Walker, et al.
Published: (2024)
by: Sydney Walker, et al.
Published: (2024)
Impact of Home Collection and Shipping of Respiratory Specimens on Bacterial Pathogen Detection in Children With Cystic Fibrosis
by: Jordana E. Hoppe, et al.
Published: (2025)
by: Jordana E. Hoppe, et al.
Published: (2025)
Home Cough Monitoring Reveals Higher Nighttime Cough Burden in Children With Cystic Fibrosis Compared With Healthy Children
by: Lilah D. Melzer, et al.
Published: (2025)
by: Lilah D. Melzer, et al.
Published: (2025)
The foregut in cystic fibrosis
by: Christopher Vélez, et al.
Published: (2024)
by: Christopher Vélez, et al.
Published: (2024)
Prevalence of cannabidiol use in persons with cystic fibrosis
by: Emma M. Tillman, et al.
Published: (2024)
by: Emma M. Tillman, et al.
Published: (2024)
The future of cystic fibrosis: A global perspective
by: Felix Ratjen
Published: (2024)
by: Felix Ratjen
Published: (2024)
Time to be blunt: Substance use in cystic fibrosis
by: Sanaz Vaziri, et al.
Published: (2024)
by: Sanaz Vaziri, et al.
Published: (2024)
Impact of elexacaftor/tezacaftor/ivacaftor on biomarkers of cystic fibrosis hepatobiliary involvement in the PUSH study
by: Wen Ye, et al.
Published: (2025)
by: Wen Ye, et al.
Published: (2025)
Lung T1 MRI assessments in children with mild cystic fibrosis lung disease
by: Clement L. Ren, et al.
Published: (2024)
by: Clement L. Ren, et al.
Published: (2024)
Predicting weight gain in patients with cystic fibrosis on triple combination modulator
by: Kelly L. Stewart, et al.
Published: (2024)
by: Kelly L. Stewart, et al.
Published: (2024)
Nutrition and behavioral health in cystic fibrosis: Eating and body image
by: Emma R. Lyons, et al.
Published: (2024)
by: Emma R. Lyons, et al.
Published: (2024)
Codevelopment of a model of care for adults living with cystic fibrosis‐related diabetes
by: Shanal Kumar, et al.
Published: (2024)
by: Shanal Kumar, et al.
Published: (2024)
The gastrointestinal microbiome, small bowel bacterial overgrowth, and microbiome modulators in cystic fibrosis
by: Nicole Green, et al.
Published: (2024)
by: Nicole Green, et al.
Published: (2024)
Me, myself, and I: A systematic review of cystic fibrosis and self‐concept
by: Maggie Harrigan, et al.
Published: (2024)
by: Maggie Harrigan, et al.
Published: (2024)
Validation of the Integrated Palliative Care Outcome Scale (IPOS) in adults with cystic fibrosis
by: Anna M. Georgiopoulos, et al.
Published: (2024)
by: Anna M. Georgiopoulos, et al.
Published: (2024)
BMI increase during early childhood in boys with cystic fibrosis and early adrenarche
by: Gizem Tamer, et al.
Published: (2024)
by: Gizem Tamer, et al.
Published: (2024)
Overnutrition in persons with cystic fibrosis on modulator therapy and the relationship to obstructive sleep apnea
by: Aesha M. Jobanputra, et al.
Published: (2024)
by: Aesha M. Jobanputra, et al.
Published: (2024)
Effects on growth, weight and body composition after CFTR modulators in children with cystic fibrosis
by: CM. López Cárdenes, et al.
Published: (2024)
by: CM. López Cárdenes, et al.
Published: (2024)
Evaluation of otorhinolaryngologic, audiologic, and genetic findings in children with cystic fibrosis: A tertiary care experience
by: Halime Nayır Büyükşahin, et al.
Published: (2024)
by: Halime Nayır Büyükşahin, et al.
Published: (2024)
Preferences and perspectives regarding telehealth exercise interventions for adults with cystic fibrosis: A qualitative study
by: Megan Poulsen, et al.
Published: (2024)
by: Megan Poulsen, et al.
Published: (2024)
Successful treatment of Stenotrophomonas maltophilia with ceftazidime‐avibactam and aztreonam in an individual with cystic fibrosis: A case report
by: Stephanie Duehlmeyer, et al.
Published: (2024)
by: Stephanie Duehlmeyer, et al.
Published: (2024)
Clinical outcomes at 9–10 years of age in children born with cystic fibrosis transmembrane conductance regulator related metabolic syndrome
by: Brian J. Carroll, et al.
Published: (2024)
by: Brian J. Carroll, et al.
Published: (2024)
Comparison of particles in exhaled air and multiple breath washout for assessment of small airway function in children with cystic fibrosis
by: Annelies M. Zwitserloot, et al.
Published: (2024)
by: Annelies M. Zwitserloot, et al.
Published: (2024)
Diabetes remission in adults with cystic fibrosis commenced on Elexacaftor/Tezacaftor/Ivacaftor: A single center case‐series
by: Shanal Kumar, et al.
Published: (2024)
by: Shanal Kumar, et al.
Published: (2024)
Factors associated with pulmonary function decline of patients in the cystic fibrosis registry of Turkey: A retrospective cohort study
by: Nagehan Emiralioğlu, et al.
Published: (2024)
by: Nagehan Emiralioğlu, et al.
Published: (2024)
Adding fuel to the fire: The growing case for global access to cystic fibrosis transmembrane conductance regulator modulator therapy
by: Brenda M. Morrow, et al.
Published: (2024)
by: Brenda M. Morrow, et al.
Published: (2024)
Nebulized granulocyte macrophage‐colony stimulating factor to stabilize lung function in nontuberculous mycobacteria pulmonary disease in cystic fibrosis
by: Colette Biro, et al.
Published: (2024)
by: Colette Biro, et al.
Published: (2024)
Lung clearance index (LCI2.5) changes after initiation of Elexacaftor/Tezacaftor/Ivacaftor in children with cystic fibrosis aged between 6 and 11 years: The “real‐world” differs from trial data
by: Don S. Urquhart, et al.
Published: (2024)
by: Don S. Urquhart, et al.
Published: (2024)
The rebound effect: Reoccurrence of nasal polyps following discontinuation of a CFTR modulator in a patient with cystic fibrosis sinus disease
by: Brittany A. Wright, et al.
Published: (2024)
by: Brittany A. Wright, et al.
Published: (2024)
A comparison of aminoglycoside antibiotic serum concentrations collected by peripheral veins and peripherally inserted central catheters in adults with cystic fibrosis
by: Sabrina J. Sherwood, et al.
Published: (2024)
by: Sabrina J. Sherwood, et al.
Published: (2024)
Implementation and outcomes of a quality improvement project to systematically assess the gross motor skills in school‐aged children with cystic fibrosis
by: Abby Good, et al.
Published: (2024)
by: Abby Good, et al.
Published: (2024)
New York cystic fibrosis consortium newborn screening quality improvement: Development and implementation of a statewide consensus recommendations for management of infants with CFTR‐related metabolic syndrome
by: Saroj Choudhary, et al.
Published: (2024)
by: Saroj Choudhary, et al.
Published: (2024)
Improving implementation and team communication by integrating a cystic fibrosis transition readiness (CF R.I.S.E.) program into electronic health records
by: Catherine Enochs, et al.
Published: (2024)
by: Catherine Enochs, et al.
Published: (2024)
Similar Items
-
Severe mental health changes in patients with cystic fibrosis on elexacaftor/tezacaftor/ivacaftor therapy
by: Cameron J. McKinzie, et al.
Published: (2024) -
Mental health, sleep, and respiratory health after initiating elexacaftor/tezacaftor/ivacaftor treatment in children with cystic fibrosis
by: Hiep Pham, et al.
Published: (2024) -
A survey of cystic fibrosis physicians' views on lung transplant referral in the era of elexacaftor/tezacaftor/ivacaftor
by: Nora Burdis, et al.
Published: (2024) -
Effectiveness and safety of elexacaftor/tezacaftor/ivacaftor treatment in children aged 6‐11 years with cystic fibrosis in a real‐world setting
by: Valeria Daccò, et al.
Published: (2024) -
Medication utilization and lung function changes after initiation of treatment with elexacaftor/tezacaftor/ivacaftor
by: Richard De Vuyst, et al.
Published: (2024)