The Italian external quality assessment program for Cystic Fibrosis sweat chloride test: CFTR modulators and the impact of a new sweat test report form.

Cystic fibrosis Report form Sweat test

Journal

Practical laboratory medicine
ISSN: 2352-5517
Titre abrégé: Pract Lab Med
Pays: Netherlands
ID NLM: 101690848

Informations de publication

Date de publication:
May 2024
Historique:
received: 19 03 2024
revised: 14 05 2024
accepted: 17 05 2024
medline: 31 5 2024
pubmed: 31 5 2024
entrez: 31 5 2024
Statut: epublish

Résumé

The advent of CFTR modulators highlighted that the sweat test (ST) for CF can be used also as an outcome measure for the basic defect of CFTR. Despite the technological advances, ST still remains operator-dependent and its execution should be strongly paired with guidelines. In 2022, due to the advent of CFTR modulators, the Italian CF Society introduced a specific ST report. The aim of the present paper is to discuss the impact of this new report in the 2022-23 round of the Italian External Quality Assessment program for ST (I-EQA-SCT). The scheme of the I-EQA-SCT is prospective, enrolment is voluntary, the payment of a fee is required and results are shared through a web-facility. Assessment covers analysis, interpretation, and reporting of results. In the 2022-23 round, 2 out of the 3 mock clinical information referred to patients who started modulators. Fourteen laboratories completed the 2022-23 I-EQA-SCT round. Three of them failed in the interpretation of results from these two mock cases and/or used a wrong report not consistent with the more recent Italian Sweat Test Recommendations. The overall results obtained from the laboratories involved in the I-EQA-SCT program clearly showed that the laboratories' qualitative and quantitative performance improved significantly. Results emerged from this round highlighted an issue in the report form used for monitoring patients on CFTR modulator therapy thus stressing the importance of these programs in improving both the performance of lab services and ameliorating the sweat test recommendations.

Sections du résumé

Background UNASSIGNED
The advent of CFTR modulators highlighted that the sweat test (ST) for CF can be used also as an outcome measure for the basic defect of CFTR. Despite the technological advances, ST still remains operator-dependent and its execution should be strongly paired with guidelines. In 2022, due to the advent of CFTR modulators, the Italian CF Society introduced a specific ST report. The aim of the present paper is to discuss the impact of this new report in the 2022-23 round of the Italian External Quality Assessment program for ST (I-EQA-SCT).
Methods UNASSIGNED
The scheme of the I-EQA-SCT is prospective, enrolment is voluntary, the payment of a fee is required and results are shared through a web-facility. Assessment covers analysis, interpretation, and reporting of results. In the 2022-23 round, 2 out of the 3 mock clinical information referred to patients who started modulators.
Results UNASSIGNED
Fourteen laboratories completed the 2022-23 I-EQA-SCT round. Three of them failed in the interpretation of results from these two mock cases and/or used a wrong report not consistent with the more recent Italian Sweat Test Recommendations.
Conclusions UNASSIGNED
The overall results obtained from the laboratories involved in the I-EQA-SCT program clearly showed that the laboratories' qualitative and quantitative performance improved significantly. Results emerged from this round highlighted an issue in the report form used for monitoring patients on CFTR modulator therapy thus stressing the importance of these programs in improving both the performance of lab services and ameliorating the sweat test recommendations.

Identifiants

pubmed: 38818249
doi: 10.1016/j.plabm.2024.e00403
pii: S2352-5517(24)00049-0
pmc: PMC11137549
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e00403

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

The authors certify that they have NO affiliations with or involvement in any organization or entity with any financial interest (such as honoraria; educational grants; participation in speakers’ bureaus; membership, employment, consultancies, stock ownership, or other equity interest; and expert testimony or patent-licensing arrangements), or non-financial interest (such as personal or professional relationships, affiliations, knowledge or beliefs) in the subject matter or materials discussed in this manuscript.

Auteurs

Natalia Cirilli (N)

Cystic Fibrosis Centre, Department of Gastroenterology and Transplantation, Marche University Hospital, Ancona, Italy.

Giovanna Floridia (G)

Unità di Bioetica, Istituto Superiore di Sanità, 00161, Rome, Italy.

Annalisa Amato (A)

National Center Rare Diseases, Undiagnosed Rare Diseases Interdepartmental Unit, Istituto Superiore di Sanità, 00161, Rome, Italy.

Rita Padoan (R)

Italian Cystic Fibrosis Registry, Scientific Board, Rome, Italy.

Federica Censi (F)

National Center Rare Diseases, Undiagnosed Rare Diseases Interdepartmental Unit, Istituto Superiore di Sanità, 00161, Rome, Italy.

Gianluca Ferrari (G)

National Center Rare Diseases, Undiagnosed Rare Diseases Interdepartmental Unit, Istituto Superiore di Sanità, 00161, Rome, Italy.

Valeria Raia (V)

Pediatric Unit, Department of Translational Medical Sciences, Regional Cystic Fibrosis Center, University Naples Federico II, Naples, Italy.

Giuseppe Castaldo (G)

CEINGE-Advanced Biotechnology, Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy.

Ettore Capoluongo (E)

Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy.
Department of Clinical Pathology, San Giovanni Addolorata Hospital, Rome, Italy.

Domenica Taruscio (D)

National Center Rare Diseases, Undiagnosed Rare Diseases Interdepartmental Unit, Istituto Superiore di Sanità, 00161, Rome, Italy.

Marco Salvatore (M)

National Center Rare Diseases, Undiagnosed Rare Diseases Interdepartmental Unit, Istituto Superiore di Sanità, 00161, Rome, Italy.

Classifications MeSH