International Council for Standardization in Haematology (ICSH): Laboratory guidance for the evaluation of haemostasis analyser-reagent test systems.  Part 1: Instrument-specific issues and commonly used coagulation screening tests.

Authors & Contributors

Chris Gardiner - Robyn Coleman - Moniek P. M. de Maat - Akbar Dorgalaleh - Marión Echenagucia - Robert C. Gosselin - Masahiro Ieko - Steve Kitchen

Published In

International Journal of Laboratory Hematology. 2021; Volume 43: 169-183

First Published

29 November 2020

Publisher

Wiley

DOI

Abstract

Before a new method is used for clinical testing, it is essential that it is evaluated for suitability for its intended purpose.

 

This document gives guidance for the performance of verification, validation and implementation processes required by regulatory and accreditation bodies.

 

It covers the planning and execution of an evaluation of the commonly performed screening tests (prothrombin time, activated partial thromboplastin time, thrombin time and fibrinogen assay), and instrument-specific issues. Advice on selecting an appropriate haemostasis analyser, planning the evaluation, and assessing the reference, interval, precision, accuracy, and comparability of a haemostasis test system are also given.

 

A second companion document will cover specialist haemostasis testing.

This article continues in full online at Wiley Online Library - use 'continue reading' button below

(opens as a new browser tab)