Evidence map›Paper›PMID 40078596›Full record

ArticleCanadian journal of respiratory therapy : CJRT = Revue canadienne de la therapie respiratoire : RCTR2025

Assessing respiratory therapists' compliance with cystic fibrosis guidelines in Saudi Arabia: A descriptive quantitative study.

Jameel Hakeem, Faisal Turkestani, Mohammed Alqahtani, Ziyad Al Nufaiei, Raid Al Zhranei, Fahad Alhadian, Rana Altabee, Mazen Homoud, Ayedh Ahmari, Ralph Zimmerman and 2 more

Abstract read
In one paragraph

Article in Canadian journal of respiratory therapy : CJRT = Revue canadienne de la therapie respiratoire : RCTR, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

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No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Jameel HakeemDepartment of Respiratory Therapy Georgia College & State University.
Faisal TurkestaniDepartment of Respiratory Therapy King Saud bin Abdulaziz University for Health Sciences.
Mohammed AlqahtaniDepartment of Respiratory Therapy King Saud bin Abdulaziz University for Health Sciences.
Ziyad Al NufaieiDepartment of Respiratory Therapy King Saud bin Abdulaziz University for Health Sciences.
Raid Al ZhraneiDepartment of Respiratory Therapy King Saud bin Abdulaziz University for Health Sciences.
Fahad AlhadianDepartment of Respiratory Therapy King Saud bin Abdulaziz University for Health Sciences.
Rana AltabeeDepartment of Respiratory Therapy King Saud bin Abdulaziz University for Health Sciences.
Mazen HomoudDepartment of Respiratory Therapy King Abdulaziz University.
Ayedh AhmariDepartment of Rehabilitation Sciences King Saud University.
Ralph ZimmermanDepartment of Respiratory Therapy Georgia College & State University.
Robert MurrayDepartment of Respiratory Therapy Georgia College & State University.
Douglas GardenhireDepartment of Respiratory Therapy Georgia College & State University.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Cystic fibrosis (CF) is a severe autosomal recessive disorder caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This condition disrupts chloride channels and leads to the production of thick, sticky mucus, affecting the respiratory and gastrointestinal systems. CF's prevalence is particularly high in Saudi Arabia, where the incidence has increased from 1 in 2,000 to 1 in 1,000 births. Effective management of CF is essential for improving patient outcomes, yet there is a notable lack of understanding regarding respiratory therapists' (RTs) adherence to established CF management protocols. Methods: This descriptive quantitative study aimed to assess RTs' adherence to the Cystic Fibrosis Foundation's guidelines. Using a convenience sampling technique, a self-report survey was distributed to 750 members of the Saudi Society for Respiratory Care (SSRC), resulting in 351 responses, of which 166 were fully completed and met the inclusion criteria. The survey focused on RTs' knowledge and management practices related to CF. Data analysis was conducted using SPSS version 25, with descriptive statistics (mean, standard deviation, frequency, percentage, and mode) and non-parametric tests. The Kruskal-Wallis Test was employed to evaluate differences in adherence scores across demographic groups (e.g., education level, years of experience). Chi-square analysis was applied to examine relationships between categorical demographic variables (e.g., region of practice) and adherence to guidelines. Results: The analysis revealed significant gaps in RTs' adherence to CF guidelines, with only 42.8% accurately identifying the sweat chloride threshold for CF diagnosis and a limited 36.1% recognizing Pseudomonas aeruginosa as a common CF pathogen. Additionally, just 56.6% correctly identified the gold-standard airway clearance therapy. The Wilcoxon signed-ranks test further highlighted a statistically significant disparity (p = 0.00) between RTs' theoretical knowledge and practical application of CF management techniques, emphasizing the need for improved training. Discussion: The findings suggest a need for enhanced training and resources to bridge the gap between theoretical knowledge and practical management of CF. The lack of adherence to clinical guidelines could impact patient outcomes and survival rates. Conclusion: Improving RTs' adherence to CF management guidelines through ongoing education and updated clinical standards is essential. Addressing these gaps could elevate the standard of care and contribute to better patient outcomes and survival rates in Saudi Arabia.

Indexed as

Cystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorPractice ManagementSurvival rates

Identifiers

PMID40078596
PMCPMC11901341

What Socratic holds

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LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.