Sigma Metrics: A Powerful Tool for Performance Evaluation and Quality Control Planning in a Clinical Biochemistry Laboratory

Introduction: Any error in the laboratory testing processes can affect the diagnosis and patient management. Six Sigma is a data driven quality management system for identifying and reducing errors and variations in clinical laboratory processes. Aim: This study was carried out to estimate Sigma...

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Main Authors: TRUPTI DIWAN RAMTEKE, ANITA SHIVAJI CHALAK, SHALINI NITIN MAKSANE
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2021-03-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
Online Access:https://www.jcdr.net/articles/PDF/14722/47818_CE[Ra1]_F(KM)_PF1(ShG_SL)_PFA(KM)_PB(ShG_KM)_PN(KM).pdf
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spelling doaj-cfa308bbf91a481da90533202812ad6c2021-06-12T06:47:26ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2021-03-01153BC20BC2310.7860/JCDR/2021/47818.14722Sigma Metrics: A Powerful Tool for Performance Evaluation and Quality Control Planning in a Clinical Biochemistry LaboratoryTRUPTI DIWAN RAMTEKE0ANITA SHIVAJI CHALAK1SHALINI NITIN MAKSANE2Assistant Professor, Department of Biochemistry, Seth GS Medical College and KEM Hospital, Parel, Mumbai, Maharashtra, India.Professor and Head, Department of Biochemistry, Seth GS Medical College and KEM Hospital, Parel, Mumbai, Maharashtra , India.Assistant Professor, Department of Biochemistry, Seth GS Medical College and KEM Hospital, Parel, Mumbai, Maharashtra, India.Introduction: Any error in the laboratory testing processes can affect the diagnosis and patient management. Six Sigma is a data driven quality management system for identifying and reducing errors and variations in clinical laboratory processes. Aim: This study was carried out to estimate Sigma metrics of various biochemical analytes in order to evaluate performance of quality control and implement optimum quality control strategy for each analyte. Materials and Methods: This retrospective, observational study was conducted in year 2020 based on the data obtained for a period of six months (July 2019 to December 2019). Sigma metrics for 20 analytes was calculated by using internal quality control and external quality control data. Further, QGI was calculated for analytes having sigma value of <4 to identify imprecision or inaccuracy. Statistical analysis was performed using Microsoft office excel 2010 software. Results: Total protein, Glucose, Urea, Triglyceride (TAG), High Density Lipoprotein (HDL), and Low Density Lipoprotein (LDL) for normal (L1) and pathological (L2) controls achieved excellent performance (>6 sigma). Westgard rule (13s) with two control measurement (N2) per QC event and run size (R1000) i.e. 1000 patient samples between consecutive QC events was adopted for these analytes. For analytes with sigma value of 4-6, more rules (sigma 4-5: Westgardrules13s/22s/R4s/41s, N4 and R200 and for sigma value 5-6: 13S/22s/ R4s, N2 and R450) were adopted. The sigma values of six analytes (Creatinine, Sodium, Potassium, Calcium, Chloride, Inorganic phosphate) were <4 at one or more QC levels. For these analytes, strict QC procedures (Westgard rules13s/22s/R4s/41s/6x, N4 and R45) were incorporated. QGI of these analytes was <0.8 which indicated the problem of imprecision. Staff training programs and review of standard operating procedures were done for these analytes to improve method performance. Conclusion: Sigma Metrics estimation helps in designing optimum QC protocols, minimising unnecessary QC runs and reducing the cost for analytes having high sigma metrics. Focused and effective QC strategy for analytes having low sigma helps in improving the performance of those analytes.https://www.jcdr.net/articles/PDF/14722/47818_CE[Ra1]_F(KM)_PF1(ShG_SL)_PFA(KM)_PB(ShG_KM)_PN(KM).pdf: quality goal indexsix sigmatotal allowable error
collection DOAJ
language English
format Article
sources DOAJ
author TRUPTI DIWAN RAMTEKE
ANITA SHIVAJI CHALAK
SHALINI NITIN MAKSANE
spellingShingle TRUPTI DIWAN RAMTEKE
ANITA SHIVAJI CHALAK
SHALINI NITIN MAKSANE
Sigma Metrics: A Powerful Tool for Performance Evaluation and Quality Control Planning in a Clinical Biochemistry Laboratory
Journal of Clinical and Diagnostic Research
: quality goal index
six sigma
total allowable error
author_facet TRUPTI DIWAN RAMTEKE
ANITA SHIVAJI CHALAK
SHALINI NITIN MAKSANE
author_sort TRUPTI DIWAN RAMTEKE
title Sigma Metrics: A Powerful Tool for Performance Evaluation and Quality Control Planning in a Clinical Biochemistry Laboratory
title_short Sigma Metrics: A Powerful Tool for Performance Evaluation and Quality Control Planning in a Clinical Biochemistry Laboratory
title_full Sigma Metrics: A Powerful Tool for Performance Evaluation and Quality Control Planning in a Clinical Biochemistry Laboratory
title_fullStr Sigma Metrics: A Powerful Tool for Performance Evaluation and Quality Control Planning in a Clinical Biochemistry Laboratory
title_full_unstemmed Sigma Metrics: A Powerful Tool for Performance Evaluation and Quality Control Planning in a Clinical Biochemistry Laboratory
title_sort sigma metrics: a powerful tool for performance evaluation and quality control planning in a clinical biochemistry laboratory
publisher JCDR Research and Publications Private Limited
series Journal of Clinical and Diagnostic Research
issn 2249-782X
0973-709X
publishDate 2021-03-01
description Introduction: Any error in the laboratory testing processes can affect the diagnosis and patient management. Six Sigma is a data driven quality management system for identifying and reducing errors and variations in clinical laboratory processes. Aim: This study was carried out to estimate Sigma metrics of various biochemical analytes in order to evaluate performance of quality control and implement optimum quality control strategy for each analyte. Materials and Methods: This retrospective, observational study was conducted in year 2020 based on the data obtained for a period of six months (July 2019 to December 2019). Sigma metrics for 20 analytes was calculated by using internal quality control and external quality control data. Further, QGI was calculated for analytes having sigma value of <4 to identify imprecision or inaccuracy. Statistical analysis was performed using Microsoft office excel 2010 software. Results: Total protein, Glucose, Urea, Triglyceride (TAG), High Density Lipoprotein (HDL), and Low Density Lipoprotein (LDL) for normal (L1) and pathological (L2) controls achieved excellent performance (>6 sigma). Westgard rule (13s) with two control measurement (N2) per QC event and run size (R1000) i.e. 1000 patient samples between consecutive QC events was adopted for these analytes. For analytes with sigma value of 4-6, more rules (sigma 4-5: Westgardrules13s/22s/R4s/41s, N4 and R200 and for sigma value 5-6: 13S/22s/ R4s, N2 and R450) were adopted. The sigma values of six analytes (Creatinine, Sodium, Potassium, Calcium, Chloride, Inorganic phosphate) were <4 at one or more QC levels. For these analytes, strict QC procedures (Westgard rules13s/22s/R4s/41s/6x, N4 and R45) were incorporated. QGI of these analytes was <0.8 which indicated the problem of imprecision. Staff training programs and review of standard operating procedures were done for these analytes to improve method performance. Conclusion: Sigma Metrics estimation helps in designing optimum QC protocols, minimising unnecessary QC runs and reducing the cost for analytes having high sigma metrics. Focused and effective QC strategy for analytes having low sigma helps in improving the performance of those analytes.
topic : quality goal index
six sigma
total allowable error
url https://www.jcdr.net/articles/PDF/14722/47818_CE[Ra1]_F(KM)_PF1(ShG_SL)_PFA(KM)_PB(ShG_KM)_PN(KM).pdf
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