000 nab a22 7a 4500
999 _c16404
_d16404
003 PC16404
005 20210615124555.0
008 210518b xxu||||| |||| 00| 0 eng d
040 _cH12O
041 _aspa
100 _92830
_aParés Pollán, Laura
_eBioquímica clínica
100 _92831
_aGonzález Quintana, Adrián
_eBioquímica clínica
100 _92832
_aDocampo Cordeiro, Jorge
_eBioquímica clínica
100 _9822
_aVargas Gallego, Carmela
_eBioquímica Clínica
100 _92833
_aGarcía Alvárez, G
_eDirección Médica de Continuidad Asistencial
100 _92834
_aRamos Rodríguez, V
_eSubdirección Médica de Servicios Centrales
100 _92835
_aDíaz Rubio-Garcia, M. P.
_eBioquímica Clínica
245 0 0 _aUtilidad del análisis modal de fallos y efectos para la detección de errores en el transporte de muestras al laboratorio clínico.
_h[artículo]
260 _bRevista de calidad asistencial : órgano de la Sociedad Española de Calidad Asistencial,
_c2014
300 _a29(4):197-203.
500 _aFormato Vancouver: Parés-Pollán L, González-Quintana A, Docampo-Cordeiro J, Vargas-Gallego C, García-Álvárez G, Ramos-Rodríguez V et al. Utilidad del análisis modal de fallos y efectos para la detección de errores en el transporte de muestras al laboratorio clínico. Rev Calid Asist. 2014 Jul-Aug;29(4):197-203.
501 _aPMID: 24725518
504 _aContiene 17 referencias
520 _aObjective: Owing to the decrease in values of biochemical glucose parameter in some samples from external extraction centres, and the risk this implies to patient safety; it was decided to apply an adaptation of the «Health Services Failure Mode and Effects Analysis» (HFMEA) to manage risk during the pre-analytical phase of sample transportation from external centres to clinical laboratories. Materials and methods: A retrospective study of glucose parameter was conducted during two consecutive months. The analysis was performed in its different phases: to define the HFMEA topic, assemble the team, graphically describe the process, conduct a hazard analysis, design the intervention and indicators, and identify a person to be responsible for ensuring completion of each action. Results: The results of glucose parameter in one of the transport routes, were significantly lower (P=.006). The errors and potential causes of this problem were analysed, and criteria of criticality and detectability were applied (score≥8) in the decision tree. It was decided to: develop a document management system; reorganise extractions and transport routes in some centres; quality control of the sample container ice-packs, and the time and temperature during transportation. Conclusions: This work proposes quality indicators for controlling time and temperature of transported samples in the pre-analytical phase. Periodic review of certain laboratory parameters can help to detect problems in transporting samples. The HFMEA technique is useful for the clinical laboratory.
710 _9317
_aServicio de Bioquímica Clínica
710 _91803
_aDirección-Gerencia
856 _uhttp://pc-h12o-es.m-hdoct.a17.csinet.es/pdf/pc/1/pc16404.pdf
_ySolicitar documento
942 _2ddc
_cART
_n0