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QUALITY IMPROVEMENT
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QUALITY IMPROVEMENT
QUALITY IMPROVEMENT
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(57) QI: Improving Access to Mental Health Services in the Cystic Fibrosis Population
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(58) The limited clinical value of ongoing microbiological surveillance for children with cystic fibrosis admitted for antibiotic treatment
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(59) Improving Mycobacterial sputum culture (MSCx) collection in adult patients during the highly effective modulator therapy (HEMT) era
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(60) Improving Cystic Fibrosis Related Diabetes Annual Screening in Adult CF Patients
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(61) High Dose (Stoss) Vitamin D Supplementation in Cystic Fibrosis: A Quality Improvement Project
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(62) Lessons learned from the experience of patients and parents of the adaptations in cystic fibrosis care during COVID-19 pandemic in France
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(63) The Development of a Standardized Approach for Providing Reproductive Health Education to Adolescents and Young Adults with Cystic Fibrosis
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(64) Successful Creation of a Home Spirometry Program within an Adult CF Clinic
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(65) Utilizing Quality Improvement tools to increase participation in a large CF Center’s Parent Advisory Council
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(66) Implementation of Standardized
Pseudomonas aeruginosa
Eradication Protocol
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(67) Implementation of a health screening process for cystic fibrosis care during the COVID-19 pandemic
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(68) Increasing Care Coordination between the Primary Cystic Fibrosis Team and Gastroenterology in a Pediatric Cystic Fibrosis Care Center Utilizing the Model of Improvement
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(69) The Multi-Disciplinary Team Approach to Screening for Bone Health in Children with Cystic Fibrosis (CF)
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(70) Improving identification and evaluation of adult cystic fibrosis patients with advanced lung disease to increase timely referral for lung transplantation.
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(71) Verification of co-morbid diagnosis of Depression and Anxiety in adolescents with Cystic Fibrosis after change in Electronic Medical Record (EMR)
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(72) The DCC Challenge: Utilizing a Network Learning model to test implementation of the Daily Care Check-In
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(73) Decreasing Sweat Test QNS Percent Rates at Atrium Health CF Center: QI work always in progress
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(74) Implementation of routine point-of-care liver ultrasound elastography as quality improvement in a multi-disciplinary cystic fibrosis clinic
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(75) Quality Improvement Initiative in Sweat Chloride Testing at the WMed Health Cystic Fibrosis Program and Bronson Methodist Hospital
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(76) Increased dietitian/patient contact improves anthropometric outcomes in 0-24 month old children with cystic fibrosis (CF)
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(77) Improving Transition from Pediatric to Adult Cystic Fibrosis Care: A Quality Improvement Initiative
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(78) Pre-visit planning initiative in partnership with pediatric Cystic Fibrosis patients and families
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(79) Impact of Providing At-Home Medical Device Kits on Remote Monitoring of Individuals with Cystic Fibrosis
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(80) Development of a National Cystic Fibrosis Patient and Caregiver Experience of Care (XoC) Survey
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(81) Results from the National CF Foundation Experience of Care (XoC) survey
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(82) Screening for Sleep Disorders in Pediatric Patients with Cystic Fibrosis: Improved Knowledge and Early intervention
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(83) Performance Improvement Initiative to Decrease QNS rates for Sweat testing at a Community Hospital
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(84) Reducing Appointment Duration Through Monitoring Clinic Flow
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(85) Quality Improvement Project: Human Milk feeding and Lactation Support in a Large Pediatric Cystic Fibrosis (CF) Clinic
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(86) Identifying Knowledge Gaps by Usıng Adapted CF R.I.S.E in a Low Resource Setting
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(87) Increasing inhaled hypertonic saline therapy in pediatric patients with
cystic fibrosis.
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(88) Best practices for CFF Patient Registry: From consent to annual review
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(89) A Novel CF-Pregnancy Service: Two year review following introduction of elexacaftor/tezacaftor/ivacaftor (Kaftrio)
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(90) Advancing Patient-Family Partnership through Shared Co-Production Tools in Two CF Learning Network Sites
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(91) CF Learning Network (CFLN) Learning Structure for Multicenter Spread of Co-Production and Timely Patient Registry Data Entry Practices
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(92) Developing a Sustainable Team Model During Uncertain Times
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(93) Developing Individualized State-Level Reports for the Evaluation of the CF Newborn Screening: From Specimen Collection to Follow-up Over 10 Years
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(94) Enhancing Clinical Research Practices Utilizing eQUIP-CR at Baylor College of Medicine
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(95) Improvement of Vitamin D Levels and DEXA Screening Using a Microsystems Approach
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(96) Improving Cystic Fibrosis Related Diabetes Treatment Initiation through Pulmonary Nurse Intervention
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(97) Improving oral glucose tolerance testing rate through a cross-disciplinary quality improvement collaboration
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(98) Improving Quarterly Out-Patient Pediatric Cystic Fibrosis (CF) Clinic Visits
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(99) Improving Screening for Cystic Fibrosis-Related Diabetes in a Pediatric Cystic Fibrosis Clinic
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(100) Improving the Experience for Patients and Families with New Diagnoses of Cystic Fibrosis
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(101) Investigation of the educational needs of people with a new diagnosis of CFTR-Related Disease
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(102) Nebulizer care and maintenance QI: Role of re-educating patients on the cleaning of nebulizer equipment and replacement supplies
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(103) Patients and family partners can become leaders on their quality improvement teams
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(104) Provider Involvement in Research Conversations with Patients: Quality Improvement (QI)
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(105) Quality Improvement Process to Increase Compliance with Influenza Vaccination in Adult Cystic Fibrosis Patients
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(106) Real time use of a CFTR modulator tracking report can identify problems with adherence
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(107) Rebuilding a Culture of Research
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(108) Streamlining Workflow Among Multiple Registered Dietitians to Improve Care for Patients with Cystic Fibrosis
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(109) The Cystic Fibrosis Learning Network: A mixed methods analysis of program goals, features, and impact
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(110) The Inadequacy of Targeted Hearing Screening for Children with Cystic Fibrosis
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(111) Using Real-Time Data to Improve Patient No-Shows and Late Cancellations
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