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HLT 490 EVIDENCE-BASED INTERVENTION FOR CYSTIC FIBROSIS IN RESPIRATORY CARE (CASE STUDY)
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HLT 490 EVIDENCE-BASED INTERVENTION FOR CYSTIC FIBROSIS IN RESPIRATORY CARE (CASE STUDY)
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RUNNING HEAD. EVIDENCE-BASED INTERVENTION FOR CYSTIC FIBROSIS INRESPIRATORY CARE 1
HLT-490
EVIDENCE-BASED INTERVENTION FOR CYSTIC FIBROSIS IN RESPIRATORY CARE
Fabian Jolly
Grand Canyon University
HLT-490
,EVIDENCE-BASED INTERVENTION FOR CYSTIC FIBROSIS IN RESPIRATORY CARE 2
TABLE OF CONTENTS
Table of Contents
EVIDENCE-BASED INTERVENTION FOR CYSTIC FIBROSIS IN RESPIRATORY CARE..1
TABLE OF CONTENTS ................................................................................................................ 2
INTRODUCTION .......................................................................................................................... 3
The Importance of Evidence-Based Interventions ...................................................................... 4
The Global Perspective and Future of Cystic Fibrosis Care ....................................................... 5
Healthcare problem ..................................................................................................................... 5
Target patients ............................................................................................................................. 5
Impact of the Issue ...................................................................................................................... 6
PROBLEM OR ISSUE ................................................................................................................... 6
PICO QUESTIONS ...................................................................................................................... 10
LITERATURE REVIEW ..............................................................................................................11
RESEARCH QUESTIONS AND ETHICAL CONSIDERATIONS ............................................ 13
THEORY OR MODEL ................................................................................................................. 16
IMPLEMENTATION PLAN ........................................................................................................ 18
EVALUATION PLAN .................................................................................................................. 19
DISSEMINATION PLAN ............................................................................................................ 22
CONCLUSION/SUMMARY ....................................................................................................... 24
Key Project Highlights .............................................................................................................. 24
The primary discoveries and suggestions are as follows .......................................................... 25
The Way Ahead ............................................................................................................................... 26
, EVIDENCE-BASED INTERVENTION FOR CYSTIC FIBROSIS IN RESPIRATORY CARE 3
INTRODUCTION
Cystic Fibrosis (CF) is a multifaceted hereditary condition that predominantly impacts
the respiratory and gastrointestinal systems. The condition is distinguished by the buildup of
viscous and adhesive mucus in multiple organs, primarily the lungs, resulting in persistent
respiratory infections, inflammation, and gradual deterioration of lung function. Over the course
of time, notable progressions in medical expertise and technological advancements have resulted
in enhanced comprehension of cystic fibrosis (CF) pathophysiology and the formulation of
interventions grounded in empirical evidence, with the objective of enhancing the well-being and
lifespan of individuals affected by CF. The primary objective of this capstone project is to
investigate and execute evidence-based interventions for individuals diagnosed with cystic
fibrosis (CF) in the context of respiratory care.
Congestive heart failure (CF) continues to pose significant challenges in terms of its
management, primarily due to the variability in its clinical presentation and the progressive
nature of the disease. The respiratory bacteriology of individuals with cystic fibrosis (CF) has
been subject to alterations, as indicated by the European Cystic Fibrosis Society (ECFS) patient
registry. Consequently, there is a need for ongoing adaptation of treatment approaches
(Hatziagorou et al., 2020). In order to effectively manage CF-related lung disease, it is
imperative to adopt a comprehensive approach to care, especially for individuals who are in the
advanced stages of CF lung disease. This is because timely and appropriate interventions play a
crucial role in preserving respiratory function and promoting overall health and wellness
(Kapnadak et al., 2020).
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