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Gross overestimation of total allowable error based on biological variation

Clinical chemistry (Baltimore, Md.), 2011-09, Vol.57 (9), p.1334-1336

Oosterhuis, Wytze P

2011

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Six sigma in laboratory medicine: the unfinished symphony

Clinical chemistry and laboratory medicine, 2024-10

2024

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A survey of patients' views from eight European countries of interpretive support from Specialists in Laboratory Medicine

Clinical chemistry and laboratory medicine, 2017-08, Vol.55 (10), p.1496

2017

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Performance specifications for sodium should not be based on biological variation

Clinica chimica acta, 2023-02, Vol.540, p.117221-117221, Article 117221

2023

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Total error vs. measurement uncertainty: revolution or evolution?

Clinical chemistry and laboratory medicine, 2016-02, Vol.54 (2), p.235

2016

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Measurement uncertainty for practical use

Clinica chimica acta, 2022-06, Vol.531, p.352-360

2022

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Statistical distributions commonly used in measurement uncertainty in laboratory medicine

Biochemia medica, 2020-02, Vol.30 (1), p.010101-17

2020

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Why are clinical practice guidelines not followed?

Clinical chemistry and laboratory medicine, 2016-07, Vol.54 (7), p.1133-1139

2016

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Sigma metrics in laboratory medicine revisited: We are on the right road with the wrong map

Biochemia medica, 2018-06, Vol.28 (2), p.020503-020503

2018

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Proposal for the modification of the conventional model for establishing performance specifications

Clinical chemistry and laboratory medicine, 2015-05, Vol.53 (6), p.925

2015

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The use of error and uncertainty methods in the medical laboratory

Clinical chemistry and laboratory medicine, 2018, Vol.56 (2), p.209-219

2018

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Laboratory medicine in the European Union

Clinical chemistry and laboratory medicine, 2015-01, Vol.53 (1), p.5

2015

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Performance specifications and six sigma theory: Clinical chemistry and industry compared

Clinical biochemistry, 2018-07, Vol.57, p.12-17

2018

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ISO 15189 is a sufficient instrument to guarantee high-quality manufacture of laboratory developed tests for in-house-use conform requirements of the European In-Vitro -Diagnostics Regulation: Joint opinion of task force on European regulatory affairs and working group accreditation and ISO/CEN standards of the European Federation of Clinical Chemistry and Laboratory Medicine

Clinical chemistry and laboratory medicine, 2023-03, Vol.61 (4), p.608-626

2023

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Sigma metric or defects per million opportunities (DPMO): the performance of clinical laboratories should be evaluated by the Sigma metrics at decimal level with DPMOs

Clinical chemistry and laboratory medicine, 2016-08, Vol.54 (8), p.e217

2016

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ISO 15189 is a sufficient instrument to guarantee high-quality manufacture of laboratory developed tests for in-house-use conform requirements of the European In-Vitro -Diagnostics Regulation

Clinical chemistry and laboratory medicine, 2023-03, Vol.61 (4), p.608

2023

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The end of the laboratory developed test as we know it? Recommendations from a national multidisciplinary taskforce of laboratory specialists on the interpretation of the IVDR and its complications

Clinical chemistry and laboratory medicine, 2021-02, Vol.59 (3), p.491-497

2021

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Reflective testing – A randomized controlled trial in primary care patients

Annals of clinical biochemistry, 2021-03, Vol.58 (2), p.78-85

2021

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Awareness of drug laboratory test interactions is important for prevention of unnecessary additional diagnostics: An example

Clinica chimica acta, 2022-05, Vol.530, p.99-103

2022

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Clinical impact of direct HDLc and LDLc method bias in hypertriglyceridemia. A simulation study of the EAS-EFLM Collaborative Project Group

Atherosclerosis, 2014-03, Vol.233 (1), p.83-90

2014

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Added value of drug-laboratory test interaction alerts in test result authorisation

Clinical chemistry and laboratory medicine, 2022-04, Vol.60 (5), p.e108-e111

2022

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Clinical usefulness of drug-laboratory test interaction alerts: a multicentre survey

Clinical chemistry and laboratory medicine, 2021-06, Vol.59 (7), p.1239-1245

2021

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Real-time monitoring of drug laboratory test interactions: a proof of concept

Clinical chemistry and laboratory medicine, 2022-01, Vol.60 (2), p.235

2022

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Critical review of laboratory investigations in clinical practice guidelines: proposals for the description of investigation

Clinical chemistry and laboratory medicine, 2013-06, Vol.51 (6), p.1217-1226

2013

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Impact of interactions between drugs and laboratory test results on diagnostic test interpretation - a systematic review

Clinical chemistry and laboratory medicine, 2018-11, Vol.56 (12), p.2004-2009

2018

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Gross overestimation of total allowable error based on biological variation

Six sigma in laboratory medicine: the unfinished symphony

A survey of patients' views from eight European countries of interpretive support from Specialists in Laboratory Medicine

Performance specifications for sodium should not be based on biological variation

Total error vs. measurement uncertainty: revolution or evolution?

Measurement uncertainty for practical use

Statistical distributions commonly used in measurement uncertainty in laboratory medicine

Why are clinical practice guidelines not followed?

Sigma metrics in laboratory medicine revisited: We are on the right road with the wrong map

Proposal for the modification of the conventional model for establishing performance specifications

The use of error and uncertainty methods in the medical laboratory

Laboratory medicine in the European Union

Performance specifications and six sigma theory: Clinical chemistry and industry compared

Sigma metric or defects per million opportunities (DPMO): the performance of clinical laboratories should be evaluated by the Sigma metrics at decimal level with DPMOs

ISO 15189 is a sufficient instrument to guarantee high-quality manufacture of laboratory developed tests for in-house-use conform requirements of the European In-Vitro -Diagnostics Regulation

The end of the laboratory developed test as we know it? Recommendations from a national multidisciplinary taskforce of laboratory specialists on the interpretation of the IVDR and its complications

Reflective testing – A randomized controlled trial in primary care patients

Awareness of drug laboratory test interactions is important for prevention of unnecessary additional diagnostics: An example

Clinical impact of direct HDLc and LDLc method bias in hypertriglyceridemia. A simulation study of the EAS-EFLM Collaborative Project Group

Added value of drug-laboratory test interaction alerts in test result authorisation

Clinical usefulness of drug-laboratory test interaction alerts: a multicentre survey

Real-time monitoring of drug laboratory test interactions: a proof of concept

Critical review of laboratory investigations in clinical practice guidelines: proposals for the description of investigation

Impact of interactions between drugs and laboratory test results on diagnostic test interpretation - a systematic review

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