European survey on preanalytical sample handling - Part 2: Practices of European laboratories on monitoring and processing haemolytic, icteric and lipemic samples. On behalf of the European Federation of Clinical Chemistry and Laboratory Medicine (EFLM) Working Group for the Preanalytical Phase (WG-PRE).


Journal

Biochemia medica
ISSN: 1846-7482
Titre abrégé: Biochem Med (Zagreb)
Pays: Croatia
ID NLM: 9610305

Informations de publication

Date de publication:
15 Jun 2019
Historique:
received: 22 11 2018
accepted: 12 03 2019
entrez: 22 6 2019
pubmed: 22 6 2019
medline: 31 8 2019
Statut: ppublish

Résumé

No guideline currently exists on how to detect or document haemolysis, icterus or lipemia (HIL) in blood samples, nor on subsequent use of this information. The EFLM WG-PRE has performed a survey for assessing current practices of European laboratories in HIL monitoring. This second part of two coherent articles is focused on HIL. An online survey, containing 39 questions on preanalytical issues, was disseminated among EFLM member countries. Seventeen questions exclusively focused on assessment, management and follow-up actions of HIL in routine blood samples. Overall, 1405 valid responses from 37 countries were received. A total of 1160 (86%) of all responders stating to analyse blood samples - monitored HIL. HIL was mostly checked in clinical chemistry samples and less frequently in those received for coagulation, therapeutic drug monitoring and serology/infectious disease testing. HIL detection by automatic HIL indices or visual inspection, along with haemolysis cut-offs definition, varied widely among responders. A quarter of responders performing automated HIL checks used internal quality controls. In haemolytic/icteric/lipemic samples, most responders (70%) only rejected HIL-sensitive parameters, whilst about 20% released all test results with general comments. Other responders did not analysed but rejected the entire sample, while some released all tests, without comments. Overall, 26% responders who monitored HIL were using this information for monitoring phlebotomy or sample transport quality. Strategies for monitoring and treating haemolytic, icteric or lipemic samples are quite heterogeneous in Europe. The WG-PRE will use these insights for developing and providing recommendations aimed at harmonizing strategies across Europe.

Identifiants

pubmed: 31223259
doi: 10.11613/BM.2019.020705
pii: bm-29-2-020705
pmc: PMC6559623
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

020705

Déclaration de conflit d'intérêts

Potential conflict of interest: None declared.

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Auteurs

Janne Cadamuro (J)

Department of Laboratory Medicine, Paracelsus Medical University, Salzburg, Austria.

Giuseppe Lippi (G)

Section of Clinical Chemistry, University of Verona, Verona, Italy.

Alexander von Meyer (A)

Institute of Laboratory Medicine, Kliniken Nordoberpfalz AG and Klinikum St. Marien, Weiden and Amberg, Germany.

Mercedes Ibarz (M)

Department of Laboratory Medicine, University Hospital Arnau de Vilanova, IRBLleida, Lleida, Spain.

Edmee van Dongen (E)

Department of Laboratory Medicine, Paracelsus Medical University, Salzburg, Austria.
Section of Clinical Chemistry, University of Verona, Verona, Italy.
Institute of Laboratory Medicine, Kliniken Nordoberpfalz AG and Klinikum St. Marien, Weiden and Amberg, Germany.
Department of Laboratory Medicine, University Hospital Arnau de Vilanova, IRBLleida, Lleida, Spain.
Department of Clinical Chemistry, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Clinical Chemistry Department, Worcestershire Acute Hospitals NHS Trust, Worcester, UK.
Department of Clinical Biochemistry and Pharmacology, Odense University Hospital, Odense, Denmark.
Clinical Department of Laboratory Medicine, University Hospitals Leuven, Leuven, Belgium.
Department of Medical Biosciences, Clinical Chemistry, Umea University, Umea, Sweden.
Department of Clinical Pathology, São João Hospital Center, Department of Biomedicine, Faculty of Medicine, and EPI Unit, Institute of Public Health, University of Porto, Porto, Portugal.
Norwegian Quality Improvement of laboratory examinations (Noklus), Bergen, Norway.
UK NEQAS Haematology, West Hertfordshire Hospitals NHS Trust, operating UK NEQAS for Haematology and Transfusion, Watford, UK.
Department of Medical Laboratory Diagnostics, University Hospital Sveti Duh, Zagreb, Croatia.

Michael Cornes (M)

Clinical Chemistry Department, Worcestershire Acute Hospitals NHS Trust, Worcester, UK.

Mads Nybo (M)

Department of Clinical Biochemistry and Pharmacology, Odense University Hospital, Odense, Denmark.

Pieter Vermeersch (P)

Clinical Department of Laboratory Medicine, University Hospitals Leuven, Leuven, Belgium.

Kjell Grankvist (K)

Department of Medical Biosciences, Clinical Chemistry, Umea University, Umea, Sweden.

Joao Tiago Guimaraes (JT)

Department of Clinical Pathology, São João Hospital Center, Department of Biomedicine, Faculty of Medicine, and EPI Unit, Institute of Public Health, University of Porto, Porto, Portugal.

Gunn B B Kristensen (GBB)

Norwegian Quality Improvement of laboratory examinations (Noklus), Bergen, Norway.

Barbara de la Salle (B)

UK NEQAS Haematology, West Hertfordshire Hospitals NHS Trust, operating UK NEQAS for Haematology and Transfusion, Watford, UK.

Ana-Maria Simundic (AM)

Department of Medical Laboratory Diagnostics, University Hospital Sveti Duh, Zagreb, Croatia.

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