Diko : en:perinatal incident that affected a neonate:find:pt:^event:ord:ahrq

en:perinatal incident that affected a neonate:find:pt:^event:ord:ahrq

Catégories

Nom

Informations lexicales

Langue:anglais

Liens externes

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umls:C3847464

Associations d'idées

[F]

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en:ingredient - rxnorm rxcui:id:pt:medication:nom

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en:family or guardian was notified:find:pt:^patient:ord:ahrq

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en:vendor model number:id:pt:{device}:nom

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en:reporter of adverse event or unsafe condition:pn:pt:^event:nom

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en:actual route of administration - attempted or completed:find:pt:^patient:nom:ahrq

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en:incorrect action:type:pt:^patient:nom:ahrq

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en:other unique product identifier:id:pt:{device}:nom

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en:electronic health record system component:type:pt:electronic health record:nom:ahrq

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en:problem that resulted from the equipment or device function problem:type:pt:{device}:nom:ahrq

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en:event was associated with a handover:find:pt:^event:ord:ahrq

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en:extent of harm to the patient:find:pt:^patient:nom:ahrq

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en:health information technology device was involved:find:pt:^event:ord:ahrq

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en:location of patient safety event or unsafe condition:find:pt:^event:nar:ahrq

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en:sex:type:pt:^patient:nom:ahrq

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en:reporter phone number:tele:pt:^event:nom

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en:documented rescue interventions:type:pt:^patient:nom:ahrq

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en:ingredients for compounded preparations:find:pt:medication:nom

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en:medication:type:pt:medication:nom:ahrq

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en:stage in the process that the event originated, regardless of the stage at which it was discovered:find:pt:^patient:nom:ahrq

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en:perinatal incident that affected a neonate

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en:best characterization of health information technology device:find:pt:{device}:nom:ahrq

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en:best description for incorrect strength or concentration:find:pt:^patient:ord:ahrq

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en:best description of the event or unsafe condition:find:pt:^event:nom:ahrq

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en:categories associated with patient safety event or unsafe condition:find:pt:^event:nom:ahrq

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en:type of nutritional product:type:pt:^patient:nom:ahrq

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en:agency for healthcare research and quality (ahrq) survey

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en:device intended for single use was involved in the event or unsafe condition:find:pt:^event:ord:ahrq

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en:manufacturer name:id:pt:medication:nom

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en:yes

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en:no

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en:additional details of event or unsafe condition:find:pt:^event:nar:ahrq

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en:medication or substance was prescribed:find:pt:^patient:ord:ahrq

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en:contributing factors for event were known:find:pt:^event:ord:ahrq

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en:device intended for single use was reused in the event or unsafe condition:find:pt:^event:ord:ahrq

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en:medication strength:dosage:point in time:medication:quantitative

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en:action that prevented the near miss incident from reaching the patient:find:pt:^patient:nom:ahrq

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en:anticipated duration of harm to the patient:find:pt:^patient:ord:ahrq

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en:race:type:pt:^patient:nom:ahrq

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en:rate all your health care in the last 12 months:score:12mo:^patient:ord:ahrq

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en:best description for the incorrect rate:find:pt:^patient:ord:ahrq

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en:event resulted in the device being removed:find:pt:^event:ord:ahrq

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en:circumstances involving the health information technology device in the event or unsafe condition:type:pt:{device}:nom:ahrq

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en:other unique product identifier:type:pt:{device}:nom

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en:expiration date:date:pt:medication:qn:ahrq

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en:location of patient safety event or unsafe condition:type:pt:^event:nom:ahrq

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en:reporter job or position:type:pt:^event:nom

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en:rescue intervention was attempted:find:pt:^patient:ord:ahrq

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en:healthcare professional:type:pt:^event:nom:ahrq

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en:national quality forum (nqf) serious reportable event:type:pt:^event:nom:ahrq

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en:administrative or billing system component:type:pt:administrative or billing system:nom:ahrq

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en:clinical drug component - rxnorm rxcui:id:pt:medication:nom

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en:expiration date:date:point in time:{device}:quantitative

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en:event was a national quality forum (nqf) serious reportable event:find:pt:^event:ord:ahrq

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en:description of patient safety event or unsafe condition:find:pt:^event:nar:ahrq

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en:history of allergies or sensitivities to the medication or substance administered was documented:find:pt:^patient:ord:ahrq

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en:medication or substance contraindication - potential or actual interaction:find:pt:^patient:nom:ahrq

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en:patient safety event:id:pt:^event:nom:ahrq

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en:vendor serial number:id:pt:{device}:nom

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en:incident preventability:find:pt:^event:nom:ahrq

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en:device name:id:pt:{device}:nom

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en:dose form:type:pt:medication:nom

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en:ethnicity:type:pt:^patient:nom:ahrq

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en:vendor firmware version:id:pt:{device}:nom

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en:unique device identifier:identifier:point in time:{device}:nominal

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en:biological product:type:pt:medication:nom:ahrq

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en:dose form - rxnorm rxcui:id:pt:medication:nom

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en:event:type:pt:^event:nom:ahrq

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en:medication or other substance was involved:find:pt:^event:ord:ahrq

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en:patient safety event report - hospital - healthcare event reporting form - version 1.2:-:pt:^patient:-:ahrq

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en:asset tag number:identifier:point in time:{device}:nominal

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en:brand name:id:pt:medication:nom

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en:generic or investigational drug name:id:pt:medication:nom

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en:manufacturer name:id:pt:{device}:nom

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en:reporter of adverse event or unsafe condition:type:pt:^event:nom:ahrq

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en:medication or substance involved:type:pt:^patient:nom:ahrq

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en:rate all your child's health care in the last 12 mos:score:12mo:^patient:qn:ahrq

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en:age at time of event:find:pt:^patient:nom:ahrq

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en:best characterization of medication or other substance event:find:pt:^event:nom:ahrq

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en:best description for the incorrect timing:find:pt:^patient:ord:ahrq

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en:contributing factors for event:find:pt:^event:nom:ahrq

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en:anonymous reporter:find:pt:^event:ord:ahrq

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en:device identifier:type:pt:{device}:nom:ahrq

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en:lot or batch number:identifier:point in time:{device}:nominal

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en:at the time of the event, the device was placed within the patient's tissue:find:pt:^patient:ord:ahrq

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en:best description for the incorrect dose:find:pt:^patient:nom:ahrq

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en:brand name - rxnorm rxcui:id:pt:medication:nom

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en:medication or substance was given:find:pt:^patient:ord:ahrq

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en:intended route of administration:find:pt:^patient:nom:ahrq

•

en:device involved in patient safety event or unsafe condition:type:pt:{device}:nom:ahrq

•

en:timing of harm assessment:find:pt:^patient:ord:ahrq

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en:reporter email:e-mail address:point in time:^event:nominal

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en:increased length of stay due to incident:find:pt:^patient:ord:ahrq

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‹

100

en:medication strength:dosage:point in time:medication:quantitative

•

en:manufacturer name:id:pt:medication:nom

•

en:age at time of event:find:pt:^patient:nom:ahrq

•

en:ingredient - rxnorm rxcui:id:pt:medication:nom

•

en:unique device identifier:identifier:point in time:{device}:nominal

•

en:circumstances involving the health information technology device in the event or unsafe condition:type:pt:{device}:nom:ahrq

•

en:contributing factors for event were known:find:pt:^event:ord:ahrq

•

en:increased length of stay due to incident:find:pt:^patient:ord:ahrq

•

en:vendor firmware version:id:pt:{device}:nom

•

en:vendor serial number:id:pt:{device}:nom

•

en:rate all your health care in the last 12 months:score:12mo:^patient:ord:ahrq

•

en:brand name:id:pt:medication:nom

•

en:reporter of adverse event or unsafe condition:type:pt:^event:nom:ahrq

•

en:type of nutritional product:type:pt:^patient:nom:ahrq

•

en:best characterization of medication or other substance event:find:pt:^event:nom:ahrq

•

en:patient safety event:id:pt:^event:nom:ahrq

•

en:ingredients for compounded preparations:find:pt:medication:nom

•

en:best description for the incorrect rate:find:pt:^patient:ord:ahrq

•

en:health information technology device was involved:find:pt:^event:ord:ahrq

•

en:medication or substance was prescribed:find:pt:^patient:ord:ahrq

•

en:rescue intervention was attempted:find:pt:^patient:ord:ahrq

•

en:dose form - rxnorm rxcui:id:pt:medication:nom

•

en:contributing factors for event:find:pt:^event:nom:ahrq

•

en:documented rescue interventions:type:pt:^patient:nom:ahrq

•

en:perinatal incident that affected a neonate

•

en:family or guardian was notified:find:pt:^patient:ord:ahrq

•

en:reporter email:e-mail address:point in time:^event:nominal

•

en:patient safety event report - hospital - healthcare event reporting form - version 1.2:-:pt:^patient:-:ahrq

•

en:reporter of adverse event or unsafe condition:pn:pt:^event:nom

•

en:event:type:pt:^event:nom:ahrq

•

en:biological product:type:pt:medication:nom:ahrq

•

en:intended route of administration:find:pt:^patient:nom:ahrq

•

en:history of allergies or sensitivities to the medication or substance administered was documented:find:pt:^patient:ord:ahrq

•

en:expiration date:date:pt:medication:qn:ahrq

•

en:stage in the process that the event originated, regardless of the stage at which it was discovered:find:pt:^patient:nom:ahrq

•

en:problem that resulted from the equipment or device function problem:type:pt:{device}:nom:ahrq

•

en:lot or batch number:identifier:point in time:{device}:nominal

•

en:device identifier:type:pt:{device}:nom:ahrq

•

en:clinical drug component - rxnorm rxcui:id:pt:medication:nom

•

en:actual route of administration - attempted or completed:find:pt:^patient:nom:ahrq

•

en:event was a national quality forum (nqf) serious reportable event:find:pt:^event:ord:ahrq

•

en:device intended for single use was involved in the event or unsafe condition:find:pt:^event:ord:ahrq

•

en:description of patient safety event or unsafe condition:find:pt:^event:nar:ahrq

•

en:national quality forum (nqf) serious reportable event:type:pt:^event:nom:ahrq

•

en:brand name - rxnorm rxcui:id:pt:medication:nom

•

en:location of patient safety event or unsafe condition:find:pt:^event:nar:ahrq

•

en:other unique product identifier:type:pt:{device}:nom

•

en:best description for the incorrect timing:find:pt:^patient:ord:ahrq

•

en:additional details of event or unsafe condition:find:pt:^event:nar:ahrq

•

en:action that prevented the near miss incident from reaching the patient:find:pt:^patient:nom:ahrq

•

en:incident preventability:find:pt:^event:nom:ahrq

•

en:rate all your child's health care in the last 12 mos:score:12mo:^patient:qn:ahrq

•

en:best description of the event or unsafe condition:find:pt:^event:nom:ahrq

•

en:ethnicity:type:pt:^patient:nom:ahrq

•

en:device intended for single use was reused in the event or unsafe condition:find:pt:^event:ord:ahrq

•

en:best characterization of health information technology device:find:pt:{device}:nom:ahrq

•

en:reporter phone number:tele:pt:^event:nom

•

en:medication or substance contraindication - potential or actual interaction:find:pt:^patient:nom:ahrq

•

en:electronic health record system component:type:pt:electronic health record:nom:ahrq

•

en:administrative or billing system component:type:pt:administrative or billing system:nom:ahrq

•

en:anonymous reporter:find:pt:^event:ord:ahrq

•

en:expiration date:date:point in time:{device}:quantitative

•

en:other unique product identifier:id:pt:{device}:nom

•

en:yes

•

en:agency for healthcare research and quality (ahrq) survey

•

en:reporter job or position:type:pt:^event:nom

•

en:anticipated duration of harm to the patient:find:pt:^patient:ord:ahrq

•

en:manufacturer name:id:pt:{device}:nom

•

en:device name:id:pt:{device}:nom

•

en:at the time of the event, the device was placed within the patient's tissue:find:pt:^patient:ord:ahrq

•

en:best description for the incorrect dose:find:pt:^patient:nom:ahrq

•

en:event resulted in the device being removed:find:pt:^event:ord:ahrq

•

en:extent of harm to the patient:find:pt:^patient:nom:ahrq

•

en:medication or substance was given:find:pt:^patient:ord:ahrq

•

en:medication:type:pt:medication:nom:ahrq

•

en:location of patient safety event or unsafe condition:type:pt:^event:nom:ahrq

•

en:vendor model number:id:pt:{device}:nom

•

en:healthcare professional:type:pt:^event:nom:ahrq

•

en:timing of harm assessment:find:pt:^patient:ord:ahrq

•

en:sex:type:pt:^patient:nom:ahrq

•

en:generic or investigational drug name:id:pt:medication:nom

•

en:best description for incorrect strength or concentration:find:pt:^patient:ord:ahrq

•

en:dose form:type:pt:medication:nom

•

en:medication or other substance was involved:find:pt:^event:ord:ahrq

•

en:incorrect action:type:pt:^patient:nom:ahrq

•

en:race:type:pt:^patient:nom:ahrq

•

en:no

•

en:device involved in patient safety event or unsafe condition:type:pt:{device}:nom:ahrq

•

en:event was associated with a handover:find:pt:^event:ord:ahrq

•

en:medication or substance involved:type:pt:^patient:nom:ahrq

•

en:categories associated with patient safety event or unsafe condition:find:pt:^event:nom:ahrq

•

en:asset tag number:identifier:point in time:{device}:nominal

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si tu veux

•

indéniablement

•

aucune

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il n'en est pas question

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sûrement pas

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ou plutôt

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justement non

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ben oui

◀

• Mathieu Lafourcade • LIRMM (données libres en Creative Commons - C0 domaine public) •

• This page link : https://www.jeuxdemots.org/diko.php?gotermid=7976548 • caches: c1=6 c2=102 c3=101

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