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Title: | Inter-Hematology Laboratory Quality Assessment with Reference to Hemoglobin Estimation, Packed Cell Volume and Total White Cell Counts |
Authors: | Moses, Dabah Lugos, Umanka, Yelpoji Polit, Mary-Jane, Nkechi Ofojekwu, Ogbonnaya, Ukegbu Nnanna James, Garba Damen |
Keywords: | Quality control Accuracy Precision |
Issue Date: | 2018 |
Publisher: | Insight Medical Publishing |
Series/Report no.: | Vol. 1;No. 4; Pp 1-6 |
Abstract: | Majority of clinical decisions are said to be based on
laboratory test results. Therefore, discrepant and
unreliable laboratory results may cause serious
consequences for the health of individuals and the
society. This study is designed to evaluate the degree of
accuracy and precision of laboratory test results from
different laboratories. Fifty blood samples were collected
from apparently healthy subjects and sent to 3 different
participating hospital laboratories designated as A, B and
C within northern Nigeria over a ten-week period. The
laboratories, all using standard hematology techniques,
undertook Hb estimation, total WBC counts and PCV
measurements in an inter-laboratory quality control
assessment. The study revealed that laboratories B and C
obtained significantly lower mean values of 13.20 g/dl
and 13.80 g/dl for hemoglobin respectively compared to
14.60 g/dl from the originating laboratory (p<0.01).
Meanwhile, the mean WBC values for laboratories B and C
appeared significantly higher than the accurate mean.
Two laboratories (B and C) also obtained mean values of
PCV slightly different from the accurate one while
laboratory A had similar mean PCV value to the accurate
one. Generally, higher variance ratios between
laboratories than between samples (P<0.01) was
observed in hemoglobin estimation and WBC count, while
PCV showed a high variance ratio between samples than
laboratories. However, the reproducibility of test results
of participating laboratories was good. With the
increasing reliance on laboratory test results for the
diagnosis of diseases, clinical laboratories must embark
on regular intra- and inter-laboratory quality evaluations
to minimize misdiagnosis. |
URI: | http://hdl.handle.net/123456789/2725 |
Appears in Collections: | Medical Laboratory Sciences
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