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1.
J Patient Saf ; 15(3): 181-183, 2019 09.
Artículo en Inglés | MEDLINE | ID: mdl-28452918
2.
J Nurs Adm ; 47(11): 537-544, 2017 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-29045356

RESUMEN

OBJECTIVE: The aims of the project are to increase knowledge related to opioids and improve adherence to evidence-based interventions for sedation monitoring and assessment in adult inpatients receiving opioids for pain through delivery of an interprofessional online program. BACKGROUND: Preventable opioid-induced respiratory depression is a patient safety risk in hospitals. Sedation and respiratory assessment and monitoring guidelines and tools are available to improve practice. METHODS: An interprofessional team identified organization-specific drivers of opioid-induced sedation and respiratory depression using process improvement methodology, developed interventions, and evaluated clinician opioid knowledge and documentation practice. RESULTS: Opioid knowledge survey responses improved after the interventions. Audits showing improved appropriate documentation by RNs of the correct sedation scale were performed over 2 separate 3-month periods. CONCLUSIONS: Clinicians demonstrated increased knowledge about newly adopted sedation and monitoring practices targeted to prevent opioid-induced respiratory depression.


Asunto(s)
Analgésicos Opioides/efectos adversos , Conocimientos, Actitudes y Práctica en Salud , Monitoreo Fisiológico/enfermería , Personal de Enfermería en Hospital/educación , Manejo del Dolor/enfermería , Seguridad del Paciente/normas , Insuficiencia Respiratoria/inducido químicamente , Adulto , Analgésicos Opioides/administración & dosificación , Analgésicos Opioides/normas , Humanos , Relaciones Interprofesionales , Monitoreo Fisiológico/métodos , Personal de Enfermería en Hospital/normas , Estudios de Casos Organizacionales , Manejo del Dolor/métodos , Insuficiencia Respiratoria/enfermería , Insuficiencia Respiratoria/prevención & control , Medición de Riesgo/métodos
3.
J Nurs Adm ; 46(2): 75-81, 2016 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-26771475

RESUMEN

OBJECTIVE: The aim of this medication safety pilot program was to increase RN sensitivity to potential error risk, improve behaviors, and reduce observed medication administration errors (MAEs). BACKGROUND: MAEs are common and preventable and may lead to adverse drug events, costing the patient and organization. MAEs are low visibility, rarely intercepted, and underreported. METHODS: An interprofessional team used process improvement methodology to develop a human factors-based medication safety pilot program to address identified issues. An observational time-series design study monitored the effect of the program. RESULTS: After the program, error interception practices during administration increased, and some nurses reported using a mindfulness strategy to gain situational awareness before administration. Process behaviors were performed more consistently, and the risk of MAE decreased. Familiarity and complexity were identified as additional variables affecting MAE outcome. CONCLUSIONS: Strategies to support safe medication administration may reduce error and be of interest to nurse leaders.


Asunto(s)
Enfermedad Crítica/enfermería , Errores de Medicación/prevención & control , Proceso de Enfermería/normas , Administración de la Seguridad , Humanos , Illinois , Evaluación de Resultado en la Atención de Salud , Proyectos Piloto
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