Biochemical test as an efficient system to improve safety in parenteral nutrition for premature infants
Objective: The biochemical test validation process of parenteral nutrition bags is described to verify the correct composition of critical compounds before its administration, as well as its impact on safety after two years since its implantation in a population of premature infants. Method: For...
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2018-11-01
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doaj-45d9f9666ae3408eae518188098093282020-11-24T21:53:58ZengGrupo Aula MédicaFarmacia Hospitalaria1130-63432171-86952018-11-0142623924310.7399/fh.11004Biochemical test as an efficient system to improve safety in parenteral nutrition for premature infantsCarlota Salazar-Santander 0Maria Teresa Miana-Mena 1Bernardino González-de-la-Presa 2Carmen López-Cabezas 3Pharmacy Service, Hospital Clínic, Barcelona. SpainPharmacy Service, Hospital Clínic, Barcelona. SpainCORE Laboratory, CBD, Hospital Clínic, Barcelona. SpainPharmacy Service, Hospital Clínic, Barcelona. SpainObjective: The biochemical test validation process of parenteral nutrition bags is described to verify the correct composition of critical compounds before its administration, as well as its impact on safety after two years since its implantation in a population of premature infants. Method: For the validation of the technique, 35 samples of parenteral nutrition without lipids were processed by the emergency laboratory, following the routine procedures used to measure the concentrations of glucose and electrolytes in plasma and urine. To analyze its impact on safety, pre-implantation and post- implantation risk analysis was carried out using failure mode, effects and criticality analysis (FMECA). Likewise, all out-of-range results and their potential repercussions on patient safety were evaluated. Results: Regression analysis showed no systematic measurement error for glucose, calcium and potassium; however, there is a constant systematic error for sodium and magnesium, thus both were discarded for routine analysis. Failure mode, effects and criticality analysis results showed a decrease in the risk of the process of 11% for the biochemical test. We tested 1,734 parenteral nutritions from 218 premature neonates; 58 (3.3%) results were out of the acceptance range, and 7 were considered to be potentially dangerous compounding errors. Conclusions: The biochemical test of glucose and electrolytes is an efficient and reproducible method that prevents possible compounding errors from reaching the patient. http://www.aulamedica.es/fh/pdf/11004.pdfChemical analysishealthcare failure modeeffect and criticality analysisInfantParenteral nutritionQuality controlPrematureSafety |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Carlota Salazar-Santander Maria Teresa Miana-Mena Bernardino González-de-la-Presa Carmen López-Cabezas |
spellingShingle |
Carlota Salazar-Santander Maria Teresa Miana-Mena Bernardino González-de-la-Presa Carmen López-Cabezas Biochemical test as an efficient system to improve safety in parenteral nutrition for premature infants Farmacia Hospitalaria Chemical analysis healthcare failure mode effect and criticality analysis Infant Parenteral nutrition Quality control Premature Safety |
author_facet |
Carlota Salazar-Santander Maria Teresa Miana-Mena Bernardino González-de-la-Presa Carmen López-Cabezas |
author_sort |
Carlota Salazar-Santander |
title |
Biochemical test as an efficient system to improve safety in parenteral nutrition for premature infants |
title_short |
Biochemical test as an efficient system to improve safety in parenteral nutrition for premature infants |
title_full |
Biochemical test as an efficient system to improve safety in parenteral nutrition for premature infants |
title_fullStr |
Biochemical test as an efficient system to improve safety in parenteral nutrition for premature infants |
title_full_unstemmed |
Biochemical test as an efficient system to improve safety in parenteral nutrition for premature infants |
title_sort |
biochemical test as an efficient system to improve safety in parenteral nutrition for premature infants |
publisher |
Grupo Aula Médica |
series |
Farmacia Hospitalaria |
issn |
1130-6343 2171-8695 |
publishDate |
2018-11-01 |
description |
Objective: The biochemical test validation process of parenteral nutrition bags is described to verify the correct composition of critical compounds before its administration, as well as its impact on safety after two years since its implantation in a population of premature infants.
Method: For the validation of the technique, 35 samples of parenteral nutrition without lipids were processed by the emergency laboratory, following the routine procedures used to measure the concentrations of glucose and electrolytes in plasma and urine. To analyze its impact on safety, pre-implantation and post- implantation risk analysis was carried out using failure mode, effects and criticality analysis (FMECA). Likewise, all out-of-range results and their potential repercussions on patient safety were evaluated.
Results: Regression analysis showed no systematic measurement error for glucose, calcium and potassium; however, there is a constant systematic error for sodium and magnesium, thus both were discarded for routine analysis. Failure mode, effects and criticality analysis results showed a decrease in the risk of the process of 11% for the biochemical test. We tested 1,734 parenteral nutritions from 218 premature neonates; 58 (3.3%) results were out of the acceptance range, and 7 were considered to be potentially dangerous compounding errors.
Conclusions: The biochemical test of glucose and electrolytes is an efficient and reproducible method that prevents possible compounding errors from reaching the patient.
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topic |
Chemical analysis healthcare failure mode effect and criticality analysis Infant Parenteral nutrition Quality control Premature Safety |
url |
http://www.aulamedica.es/fh/pdf/11004.pdf |
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