NORIP, Malmö 27/4-2004 Implementation phase of NORIP Gunnar Nordin, EQUALIS, Uppsala Common Nordic Reference Values, Session 15, NFKK 24 – 27 April 2004.

Slides:



Advertisements
Similar presentations
NORDIC BALTIC EAHIL WORKSHOP June 25-28, OSLO 2003 Evidence-based nursing and libraries: do we find what we are searching? Liisa Salmi Kuopio University.
Advertisements

Phone Bank Team Copyright-2013©Los Angeles Unified School District-All rights reserved.
NORIP, Malmø 27/ NOBIDA Nordic Reference Interval Project Biobank and Database Common Nordic Reference Intervals NFKK meeting 27/ Pål Rustad.
User verification of performance Zahra Khatami/Robert Hill BHR University Hospitals/Sheffield Teaching Hospitals Focus 2013.
HBB Status update – Performance Evaluation in Malawi Shivam Gupta Johns Hopkins University – Institute for International Programs.
Revalidation for nurses and midwives consultation phase 2
NORIP, Malmø 27/ NORIP concept Common Nordic Reference Intervals NFKK meeting 27/ Pål Rustad Fürst Medical Laboratory, Oslo
Science, Technology, Engineering, and Math all rolled up into iGEM Ung.igem.org/High_School_Division.
1 L U N D S U N I V E R S I T E T LUB OA Journals and publishers/hosts in the Nordic countries J ö rgen Eriksson, Lund University: project manager.
Nordic project on food contact materials (FCM) - presented by Project leader Ågot Li Senioradviser, The Norwegian Food Safety Authority.
Senior Lecturer in Pathology
THE ROLE OF EQA IN HARMONIZATION OF REFERENCE INTERVALS IN CROATIA LABQUALITY DAYS, 2015, HELSINKI FINLAND Department of Medical Biochemistry and Laboratory.
Module 5 Postanalytical Phase of Laboratory Testing.
Look First! Is there a pre-existing questionnaire which has been used for a similar purpose? Are there ‘question groups’ from validated questionnaires.
QC | Slide 1 of 16 June 2006 Good Practices for Quality Control Laboratories P art 4: Inspecting the laboratory Supplementary Training Modules on Good.
Björn Smedby – contributions to the Health Services Research and Classifications Björn Smedby, M.D., Ph.D., Professor Emeritus Health Services Research.
IFCC EQAS for Reference Laboratories ________________________________________
Method Selection and Evaluation Method Selection and Evaluation D. Kefaya EL- Sayed Mohamed Prof. Of Clinical Pathology (Clinical Chemistry), Mansoura.
Introduction to ISO New and modified requirements.
Development of Clinical Practice Guidelines for the NHS Dr Jacqueline Dutchak, Director National Collaborating Centre for Acute Care 16 January 2004.
Polio Update Pre Tender Meeting 11 th December 2008 UNICEF Supply Division.
Overweight at the GP surgery What do we need to proceed?
1 11th Nordic Conference on Information and Documentation, Rekjavik, Iceland, 30 May – 1 June 2001 Norwegian Librarian Ethics Revisited: The Case for.
Software Quality Assurance Lecture 4. Lecture Outline ISO ISO 9000 Series of Standards ISO 9001: 2000 Overview ISO 9001: 2008 ISO 9003: 2004 Overview.
Nationwide management of laboratory information with the NPU terminology Ulla Magdal, MI National Board of Health, Denmark.
Peter HinrichsEconomic Questions and Data Needs1 ELPEN. European Livestock Policy Evaluation Network.
Progress to date and Plans for Year 5 Overcoming HIV/AIDS epidemic in Ukraine Programme supported by the Global Fund 11 th Stakeholders’ meeting 22 nd.
 Enhance the capacity of the Department of Family Medicine to train Residents to design, implement, and evaluate an EB/QI plan  Focus on:  Rural practice.
Governance of a Department of Surgery – an Overview Using a Framework Reynaldo O. Joson, MD, MHA, MHPEd, MSc Surg Annual Conference of Tripartite Training.
Interferences - are some methods better than others? Graham Jones Department of Chemical Pathology St Vincent’s Hospital, Sydney.
BMH CLINICAL GUIDELINES IN EUROPE. OUTLINE Background to the project Objectives The AGREE Instrument: validation process and results Outcomes.
Nordic guidelines? An idea within NFOG Anette Tønnes Pedersen, Gyn. Klinik / Fertilitetsklinikken, Rigshospitalet.
Tessy Badriyah Healthy Computing, 1 nd June 2011 Aim : to contribute to the building of effective and efficient methods to predict clinical outcome that.
International Scientific Workshop on the Standardization of Genome Amplification Techniques for the Safety Testing of Blood, Tissues and Organs With Regard.
Performance criteria or ”quality specifications” Gunnar Nordin Dubrovnik Course in Zagreb 2015.
Use of Reference Materials in Medical Testing SLAB 10th Anniversary Celebrations Accreditation Conference 10 th November 2015 Dr Deepani Siriwardhana Senior.
Mauro Panteghini Who, what and when to do in validation/verification of methods.
CBSS - Task Force against Trafficking in Human Beings with focus on adults Stop Trafficking and Stand for Health! Conference 20 September 2010 Riga, Latvia.
SMC and the role of Public Involvement Action Duchenne Scottish Mini Conference 4 December 2015 Lindsay Lockhart Public Involvement Officer.
Prospects for promoting health and performance by school meals in Nordic countries NordForsk #
© The Strategic Projects Team Hosted by the Greater East Midlands Commissioning Support Unit National Pathology Programme Standardisation and Harmonisation.
Data collection Cynthia Tavares Task Force meeting Luxembourg, 2- 3 March 2006.
Patients access to investigational drugs Steinar Aamdal Dept. of Clinical Cancer Research Oslo University Hospital.
Quality Care Standards Mrs. Bente Frokjaer Secretary Community Pharmacy Section of FIP and Mr. Robert L. Grant Pharmacy Guild of New South Wales Australia.
 Remember Chemistry panel Quality Control:-  In a medical laboratory, it is a statistical process used to monitor and evaluate the analytical process.
TF_Arusha_Jun10/1 Framework for Evaluation of Male Circumcision Devices Tim Farley Department of Reproductive Health and Research World Health Organization.
Redesign/ Change Management Team 3. Point of Actions  Joint Application Design (JAD) session (2 weeks)  Representatives from each department  Overview.
Session 6: Data Flow, Data Management, and Data Quality.
Clinical Utility of EQA Dr. Angela Amayo UON27/11/2008.
CENTRAL FINLAND HEALTH CARE DISTRICT HEALTH THROUGH KNOWLEDGE, EXPERTISE AND CO-OPERATION
ICF in Finland – background Verdana 36 Bold Title Conclusions The ICF was translated to Finnish in However, lack of systematic education, clinical.
Method comparisons - what do we learn from the Nordic Reference Interval Project 2000 (NORIP) Pål Rustad Fürst Medical Laboratory Labquality Days 12/
Diagnostic clinical chemistry
Principles of Good Laboratory Practice and Reliability Requirements
SPIMEU newsletter May 2017 Work Package 4
ROUTINE HEALTH INFORMATION SYSTEMS
Mosby items and derived items © 2005 by Mosby, Inc.
BOND PROGRAM- Door Lock & Building Access
This teaching material has been made freely available by the KEMRI-Wellcome Trust (Kilifi, Kenya). You can freely download,
Nordic Perspective on SS7
Rubicon Q&A May 9th, 2017.
Controversial aspects of NORIP
Uncertainty: the biochemistry perspective
Secondary Science - Integrated Physics and Chemistry
Towards International Harmonized Nomenclature for Medical Devices
Mosby items and derived items © 2005 by Mosby, Inc.
STANDARDISATION, HARMONISATION AND TRACEABILITY
Reporting of critical potassium results reporting in hyperkalaemia: Audit and survey of practice in Scotland Neil Greig 24/04/17.
Postanalytical Phase of Laboratory Testing
Presentation transcript:

NORIP, Malmö 27/ Implementation phase of NORIP Gunnar Nordin, EQUALIS, Uppsala Common Nordic Reference Values, Session 15, NFKK 24 – 27 April 2004

NORIP, Malmö 27/ NORIP For the first time fully documented and traceable reference limit values Information needed to –Colleagues in the field of laboratory medicine –All requesters of tests in the health care systems –Others, e.g. organizers of multi center studies

NORIP, Malmö 27/4-2004

How should X be used?

NORIP, Malmö 27/ How should X be used? Evaluation and verification of the performance of routine clinical measurement procedures Make routine results traceable to common reference intervals for the Nordic countries (NORIP data) Laboratories not able to reproduce the stated values of X – try to find the reason! (together with the supplier!)

NORIP, Malmö 27/ Evaluation of results from X by the Excel sheet

NORIP, Malmö 27/ How should X not be used? X is not a substitute for the calibrators supplied by IVD manufacturers!

NORIP, Malmö 27/ Status of IFCC enzymes April 2004 Norway 100% (since May 2003) Denmark 50% Sweden 15% Finland (May 2004) Iceland (Autumn 2004?)

NORIP, Malmö 27/ Implementation of NORIP in Norway Implementation of clinical chemistry will start after publication and information in “Tidsskrift for Norsk Legeforening” June Checklist published on NKK website Implementation of haematology to be discussed.

NORIP, Malmö 27/ Implementation of NORIP in Sweden Implementation during 2004 recommended by SFKK. March 04 information in “Läkartidningen” Checklist on EQUALIS Website Users of Jaffémethods for creatinine are recommended by SFKK and EQUALIS to use creatinine free serum (see poster 78) April 04 full implementation by the pioneer laboratories

NORIP, Malmö 27/ Implementation* of NORIP in Sweden April 04 *) Exceptions for Potassium and Calcium made in two districts. Several districts plan for implementation during summer and autumn 04

NORIP, Malmö 27/4-2004

Analysens CV% = 2,6 ?

NORIP, Malmö 27/ Why might data not fit? Optimal preanalytical conditions in NORIP NORIP used serum tubes without gel Multiple tubes collected during venepunction ????

NORIP, Malmö 27/ Implementation of NORIP in Finland –Haematology implemented Jan 04 –Finnish Society recommends implementation in clinical chemistry May 04 –HUCS/HUS plan to implement May 04 –Other laboratories probably autumn 04

NORIP, Malmö 27/ Implementation of NORIP in Iceland Iceland: –Information will be given to clinicians and in ‘Lægeforeningens’ journal later this year

NORIP, Malmö 27/ Implementation of NORIP in Denmark DSKB has not yet recommended time for implementation of non-enzymes clinical chemistry.

NORIP, Malmö 27/ Secondary effects of NORIP General clinical chemistry: –Harmonization of Jaffé and enzymatic methods for creatinine –Test of the validity of the NPU system for the systematic nomenclature and codes for measured properties Haematology: –Common recommendation to use dry K 2 -EDTA –Replacement of the old fashioned ‘% haematocrit’ with EVF (Sweden)

NORIP, Malmö 27/ NPU system for nomenclature and codes used in Denmark and Sweden NPU01807 P—Creatininium; subst.c.(Jaffé) = ? µmol/l NPU04998 P—Creatininium; subst.c.(enz.) = ? µmol/l Two different codes for creatininium in plasma: NPU04998 should be used for Jaffé-creatinine after calibration with creatinine free serum!

NORIP, Malmö 27/ NPU system for nomenclature and codes used in Denmark and Sweden New NPU codes because new traceability New codes for new methods

NORIP, Malmö 27/ The future Evaluation of potential limitations of NORIP reference intervals, e.g. potassium, calcium and LD. –National EQA organizers should collect experiences from implementation –The NORIP working group (NOBIDA?) should be asked by NFKK to evaluate the final implementation Complete use of the collected data in the NORIP –E.g. reference intervals for the differential count, reticulocytes and other haematological properties Reference intervals for children. –Working group established by NFKK Further harmonization (???) –The unit katal for enzymes –Substance concentration for B-Haemoglobin (mmol/L)