scholarly journals An Often-Missed Laboratory Error

2019 ◽  
Vol 65 (6) ◽  
pp. 814-815
Author(s):  
Melissa M Budelier ◽  
Christopher W Farnsworth ◽  
Stephen M Roper
Keyword(s):  
1978 ◽  
Vol 39 (02) ◽  
pp. 455-465 ◽  
Author(s):  
Yvonne Stirling ◽  
D J Howarth ◽  
Marguerite Vickers ◽  
W R S North ◽  
T W Meade

SummaryTwo automated methods for two-stage factor VIII assays have been compared with one another, and evaluated in practice. The Depex method records the clotting time when an electric circuit is completed by the formation of a fibrin thread across a hook-type electrode; the Electra method is based on an optical density technique of clot detection. The two methods gave comparable results for measured levels of factor VIII when haemophilic or “normal” plasmas were assayed. Results from the two methods in practice also suggest that both are valid at low and “normal” factor VIII levels. The Electra method is also probably suitable for assays of concentrates; however, the Depex method appears to give falsely high values in these circumstances, and experimental findings suggest that the reason may be that increased viscosity due to the high fibrinogen levels in factor VIII concentrates causes premature closure of the circuit between the two ends of the Depex electrode. The main advantage of the Depex method is that, provided 3 or 4 machines are available, a given number of assays can be completed more quickly than on Electra. The main advantages of Electra are that it is probably subject to less laboratory error than Depex, and that it is suitable for assaying concentrates as well as haemophilic and “normal” plasmas.


2016 ◽  
Vol 5 (07) ◽  
pp. 4704
Author(s):  
Syed Riaz Mehdi* ◽  
Sharique Ahmad ◽  
Noorin Zaidi

Laboratory error is defined by ISO 22367 as “Failure of planned actions to be completed as intended or use a wrong plan to achieve an aim”. Lundeberg in 1981 outlined the concept of Total Testing Process (TTP) and Plebani elaborated it further and classified the whole testing process into five phases of Pre-Pre Analytic, Pre Analytic, Analytic, Post Analytic and Post - Post Analytic. The errors have to be identified and resolved in each phase of the process. The medical laboratories have to run Internal and External Quality Control programs and abide by the guidelines of ISO 15189 in order to be accredited by bodies like JCI, CAP or NABL. Active communication and regular interaction between the clinicians and the laboratory is recommended during Pre Analytic and Post Analytic phases of TTP in order to achieve the target of Best Laboratory Practices. 


1972 ◽  
Vol 18 (3) ◽  
pp. 250-257 ◽  
Author(s):  
J H Riddick ◽  
Roger Flora ◽  
Quentin L Van Meter

Abstract A system of quality-control data analysis by computer is described, in which two-way analysis of variance is used for partitioning sources of laboratory error into day-to-day, within-day, betweenpools and additivity variation. The partition for additivity is described in detail as to its advantages and applications. In addition, control charts based on two-way analysis of variance computations are prepared each month by computer. This computer program is designed to operate with the IBM 1800 or 1130 computers or any computer with a Fortran IV compiler. Examples are presented of use of the control charts and of tables of analysis of variance.


1981 ◽  
Vol 21 (108) ◽  
pp. 68
Author(s):  
E Seif ◽  
LN Balaam

The analysis of wheat protein data from ten homozygous genotypes grown at six locations in 4 years gave a heritability estimate of 50%, and another of 65% from a sub-set of genotypes of similar maturity. The first-order interactions, genotype x year and genotype x location, were small and nonsignificant. An examination of the variance of a genotype mean indicated that selection in regional testing programs could be based on data from as few as three trials. Laboratory error represented a large proportion of this variance, thus more than one laboratory determination will be necessary.


2020 ◽  
pp. 211-218
Author(s):  
Pat Croskerry

In this case, a middle-aged male presents to the emergency department (ED) of a general hospital with dizziness and weakness and a history of falling the previous day associated with seizures. There is also a possibility of head injury. He is well known to the department and has been seen previously by the head of the department regarding inappropriate use of the ED. Some difficulty ensues in terms of whether he has been having seizures or not, which, combined with a medication error and a laboratory error, results in him being overdosed with a significantly toxic drug. The case is an example of groupthink as well as fundamental attribution error.


1975 ◽  
Vol 21 (3) ◽  
pp. 309-314 ◽  
Author(s):  
E Melvin Gindler

Abstract Some rapid statistical tests give (a) rapid answers on how well methods agree and control chart evaluation (sign and run tests) and (b) evaluation of distribution of test results (Tukey's quick test and run test). These tests mainly require counting of data and the use of the given nomograms. An unusual distribution of patient test values—that is, unusual when compared with the generally observed distribution of the data seen in a particular laboratory—may indicate laboratory error, alteration of specimens (as from poor collection and/or storage techniques, such as evaporation), or an unusual patient population.


1958 ◽  
Vol 4 (6) ◽  
pp. 513-518 ◽  
Author(s):  
Wendell T Caraway

Abstract Some distillation processes may result in the inadvertent contamination of distilled water with free chlorine. One part per million of free chlorine in distilled water has been shown to inhibit markedly the color development in the usual determinations of uric acid and bilirubin. The effect of free chlorine on other clinical chemistry determinations is discussed and simple tests for the detection of free chlorine in water are reviewed.


1963 ◽  
Vol 9 (1) ◽  
pp. 1-18 ◽  
Author(s):  
Oscar Bodansky

Abstract In this paper we have attempted to define the relationships between clinical medicine and diagnostic or, as it is more frequently termed, clinical biochemistry. We have indicated first, the role that general biochemistry has played in elucidating mechanisms of disease and in providing the clinician with procedures that aid him in the diagnosis of disease and in the care of the patient. We have illustrated this role by reviewing very briefly some of the recent contributions such as the expanded diagnostic use of serum enzymes; the correlation of subcellular structure in human tissues with function at enzymatic levels; the investigation of enzyme variants; the metabolism of epinephrine and norepinephrine in pheochromocytoma; the metabolism of tryptophan in malignant carcinoid; and enzyme defects in hereditary disease. We noted the reservations with which the clinician frequently views the specific results that he obtains from the diagnostic biochemistry laboratory and have attempted to analyze the bases for these reservations. In this connection we considered the phenomenon of interlaboratory variability, the nature of the random and the constant errors that may exist within a laboratory, and the measures that the clinical biochemist may take to counteract these errors. We have tried to indicate the steps the clinician may take in a fuller and more knowledgeable utilization of the data from the diagnostic biochemistry laboratory. These involve a recognition of the efforts and advances that are being made in increasing precision and accuracy within the laboratory and the role that the clinician himself can play in contributing to this precision and accuracy. The phenomenon of intraindividual and interindividual variability of biochemical parameters, and the significance of this phenomenon in diagnosis, are also worthy of the clinicians attention. Finally, the clinician should abjure the concept that a seeming discrepancy between his formulation and laboratory results usually means a laboratory error. Thoughtful review, in cooperation with the biochemist, of such discrepancies are of value both for clinical medicine and clinical biochemistry.


1959 ◽  
Vol 169 (17) ◽  
pp. 2066
Author(s):  
S. Raymond Gambino
Keyword(s):  

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