Evidence map›Paper›PMID 35210925›Full record

ReviewBiochemia medica2022

National Guidelines for the Performance of the Sweat Test in Diagnosis of Cystic Fibrosis on behalf of the Croatian Society of Medical Biochemistry and Laboratory Medicine and the Cystic Fibrosis Centre - Paediatrics and adults, University Hospital Centre Zagreb.

Jasna Leniček Krleža, Merica Aralica, Duška Tješić-Drinković, Karolina Crneković, Jelena Culej, Gordana Fressl Juroš, Verica Horvat, Dara Metzner, Dijana Pamuković Jaram, Alma Pipić Kitter and 4 more

Abstract readReview
In one paragraph

Review in Biochemia medica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

14 authors.

Jasna Leniček KrležaDepartment of Laboratory Diagnostics, Children's Hospital Zagreb, Zagreb, Croatia.
Merica AralicaClinical Department of Laboratory Diagnostics, Clinical Hospital Center Rijeka, Rijeka, Croatia.
Duška Tješić-DrinkovićCystic Fibrosis Centre - Paediatrics and Adults, University Hospital Centre Zagreb and University of Zagreb - School of Medicine, Zagreb, Croatia.
Karolina CrnekovićDepartment of Medical Laboratory Diagnostics, General Hospital "Dr. Ivo Pedišić", Sisak, Croatia.
Jelena CulejPoliklinika Breyer, Zagreb, Croatia.
Gordana Fressl JurošDepartment of Clinical Laboratory Diagnostics, Children's Hospital Srebrnjak, Zagreb, Croatia.
Verica HorvatDepartment of Medical Laboratory Diagnostics, General Hospital Varaždin, Varaždin, Croatia.
Dara MetznerClinical Department of Laboratory Diagnostics, Clinical Hospital Center Rijeka, Rijeka, Croatia.
Dijana Pamuković JaramDepartment of Medical Laboratory Diagnostics, General Hospital Šibenik, Šibenik, Croatia.
Alma Pipić KitterDepartment of Medical Laboratory Diagnostics, General Hospital "Dr. Josip Benčević", Slavnoski Brod, Croatia.
Fran SmaićDepartment of Medical Laboratory Diagnostics, General Hospital "Dr. Josip Benčević", Slavnoski Brod, Croatia.
Sanela Šimić VojakDepartment of Medical Laboratory Diagnostics, County Hospital Požega, Požega, Croatia.
Livija ŠimičevićCinical Department of Laboratory Diagnostics, University Hospital Centre Zagreb, Zagreb, Croatia.
Valentina VerićDepartment of Medical Laboratory Diagnostics, General Hospital Bjelovar, Bjelovar, Croatia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The sweat test (ST) is a cornerstone in the diagnosis of cystic fibrosis (CF), together with newborn screening and genetic testing. However, the performance of the ST can depend on the operator's skill, so several international guidelines have been published to standardise the ST, but inconsistencies remain. The joint Working Group for ST Standardisation (WG STS) of the Croatian Society of Medical Biochemistry and Laboratory Medicine, in association with cistic fybrosis health professional and the Cistic Fibrosis Centre for Paediatrics and Adults, have issued National Guidelines for the Performance of the Sweat Test in order to ensure consistency in ST performance and accuracy of reported results. Many of the standards were taken from the 2nd Edition of the UK Guidelines for Performance of the ST for the Diagnosis of CF, while others were taken from independent consensus statements from the WG STS based on local ST equipment and practices. The standards cover every step of the ST, from the indications for testing to reporting of results and their interpretation, including the analytical phase and quality control. In addition, National Guidelines include appendices with practical examples in order to aid implementation of the recommendations in routine practice.

Indexed as

Cystic FibrosisPediatricsChildHospitals, UniversityHumansInfant, NewbornLaboratoriesSweat

Identifiers

PMID35210925
PMCPMC8833251

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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 OpenQuestion graph.