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Impact of Pneumatic Transport System on Preanalytical Phase Affecting Clinical Biochemistry Results

Introduction  PTS (pneumatic transport system) is extensively being used in modern hospitals for rapid transportation of blood samples and other specimens. However, it has a potential impact on blood components, which should be investigated and nullified accordingly. This study was part of a correct...

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Autores principales: Kumari, Sweta, Kumar, Santosh, Bharti, Neha, Shekhar, Ravi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Medical and Scientific Publishers Pvt. Ltd. 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104724/
https://www.ncbi.nlm.nih.gov/pubmed/37064988
http://dx.doi.org/10.1055/s-0042-1750077
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author Kumari, Sweta
Kumar, Santosh
Bharti, Neha
Shekhar, Ravi
author_facet Kumari, Sweta
Kumar, Santosh
Bharti, Neha
Shekhar, Ravi
author_sort Kumari, Sweta
collection PubMed
description Introduction  PTS (pneumatic transport system) is extensively being used in modern hospitals for rapid transportation of blood samples and other specimens. However, it has a potential impact on blood components, which should be investigated and nullified accordingly. This study was part of a correction program aimed at reducing hemolysis. It was done by comparing paired samples transported manually and by PTS. Materials and Methods  This study was initiated to monitor the impact of PTS on hemolysis of clinical biochemistry blood samples. It was performed in two phases—before and after the corrective action taken. Phase I: done after PTS installation but before the corrective action was taken. Duplicate samples from 100 healthy individuals were collected, one set transported by PTS and the other by human carriers. Both sets were assessed for 25 biochemistry analytes, hemolysis index (HI), and acceleration profiles using a data logger. Corrective measures were then taken, followed by phase II of the study. In phase II, the sample size and study design remained the same as phase I. All the test results of PTS and hand-carried samples were statistically analyzed for any significant difference. Result  In phase I, all the hemolysis-manifesting parameters, LDH (lactate dehydrogenase), potassium, AST (aspartate transaminase), and phosphorus, were raised in PTS samples as compared with the manual samples. Their differences were significant as the p -values were 0.001, 0.000, 0.025, and 0.047, respectively. The differences for LDH and potassium were clinically significant as well. HI (9%) and peak acceleration (15.7 g) were high in PTS samples. In phase II, no statistically significant difference between paired samples was found for all biochemistry parameters except for a few which were clinically nonsignificant. For PTS samples, HI was 2.5% and the peak acceleration was 11.2 g, whereas for manual samples, HI was 2%. Conclusion  Evidence of hemolysis was found in PTS samples as compared with handheld samples, which was resolved after several corrective actions were taken. Thereafter, PTS became reliable for sample delivery in a routine biochemistry laboratory. Hence, each hospital should scrutinize their PTS for its effects on sample integrity to get rid of PTS-induced preanalytical errors.
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spelling pubmed-101047242023-04-15 Impact of Pneumatic Transport System on Preanalytical Phase Affecting Clinical Biochemistry Results Kumari, Sweta Kumar, Santosh Bharti, Neha Shekhar, Ravi J Lab Physicians Introduction  PTS (pneumatic transport system) is extensively being used in modern hospitals for rapid transportation of blood samples and other specimens. However, it has a potential impact on blood components, which should be investigated and nullified accordingly. This study was part of a correction program aimed at reducing hemolysis. It was done by comparing paired samples transported manually and by PTS. Materials and Methods  This study was initiated to monitor the impact of PTS on hemolysis of clinical biochemistry blood samples. It was performed in two phases—before and after the corrective action taken. Phase I: done after PTS installation but before the corrective action was taken. Duplicate samples from 100 healthy individuals were collected, one set transported by PTS and the other by human carriers. Both sets were assessed for 25 biochemistry analytes, hemolysis index (HI), and acceleration profiles using a data logger. Corrective measures were then taken, followed by phase II of the study. In phase II, the sample size and study design remained the same as phase I. All the test results of PTS and hand-carried samples were statistically analyzed for any significant difference. Result  In phase I, all the hemolysis-manifesting parameters, LDH (lactate dehydrogenase), potassium, AST (aspartate transaminase), and phosphorus, were raised in PTS samples as compared with the manual samples. Their differences were significant as the p -values were 0.001, 0.000, 0.025, and 0.047, respectively. The differences for LDH and potassium were clinically significant as well. HI (9%) and peak acceleration (15.7 g) were high in PTS samples. In phase II, no statistically significant difference between paired samples was found for all biochemistry parameters except for a few which were clinically nonsignificant. For PTS samples, HI was 2.5% and the peak acceleration was 11.2 g, whereas for manual samples, HI was 2%. Conclusion  Evidence of hemolysis was found in PTS samples as compared with handheld samples, which was resolved after several corrective actions were taken. Thereafter, PTS became reliable for sample delivery in a routine biochemistry laboratory. Hence, each hospital should scrutinize their PTS for its effects on sample integrity to get rid of PTS-induced preanalytical errors. Thieme Medical and Scientific Publishers Pvt. Ltd. 2022-07-26 /pmc/articles/PMC10104724/ /pubmed/37064988 http://dx.doi.org/10.1055/s-0042-1750077 Text en The Indian Association of Laboratory Physicians. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. ( https://creativecommons.org/licenses/by-nc-nd/4.0/ ) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited.
spellingShingle Kumari, Sweta
Kumar, Santosh
Bharti, Neha
Shekhar, Ravi
Impact of Pneumatic Transport System on Preanalytical Phase Affecting Clinical Biochemistry Results
title Impact of Pneumatic Transport System on Preanalytical Phase Affecting Clinical Biochemistry Results
title_full Impact of Pneumatic Transport System on Preanalytical Phase Affecting Clinical Biochemistry Results
title_fullStr Impact of Pneumatic Transport System on Preanalytical Phase Affecting Clinical Biochemistry Results
title_full_unstemmed Impact of Pneumatic Transport System on Preanalytical Phase Affecting Clinical Biochemistry Results
title_short Impact of Pneumatic Transport System on Preanalytical Phase Affecting Clinical Biochemistry Results
title_sort impact of pneumatic transport system on preanalytical phase affecting clinical biochemistry results
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104724/
https://www.ncbi.nlm.nih.gov/pubmed/37064988
http://dx.doi.org/10.1055/s-0042-1750077
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