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Implementation of early warning system in the clinical teaching unit to reduce unexpected deaths.
Swami, Tara; Shams, Ali; Mittelstadt, Matthew; Guenther, Catherine; Tse, Tiffanie; Noor, Hifsa; Shahid, Rabia.
Afiliação
  • Swami T; University of Saskatchewan College of Medicine, Saskatoon, Saskatchewan, Canada.
  • Shams A; University of Saskatchewan College of Medicine, Saskatoon, Saskatchewan, Canada.
  • Mittelstadt M; University of Saskatchewan College of Medicine, Saskatoon, Saskatchewan, Canada.
  • Guenther C; University of Saskatchewan College of Medicine, Saskatoon, Saskatchewan, Canada.
  • Tse T; University of Saskatchewan College of Medicine, Saskatoon, Saskatchewan, Canada.
  • Noor H; University of Saskatchewan College of Medicine, Saskatoon, Saskatchewan, Canada.
  • Shahid R; Department of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada rks032@mail.usask.ca.
BMJ Open Qual ; 12(2)2023 06.
Article em En | MEDLINE | ID: mdl-37263736
BACKGROUND: Early detection of patients with clinical deterioration admitted to the hospital is critical. The early warning system (EWS) is developed to identify early clinical deterioration. Using individual patient's vital sign records, this bedside score can identify early clinical deterioration, triggering a communication algorithm between nurses and physicians, thereby facilitating early patient intervention. Although various models have been developed and implemented in emergency rooms and paediatric units, data remain sparse on the utility of the EWS in patients admitted to general internal medicine wards and the processes and challenges encountered during the implementation. LOCAL PROBLEM: There is a lack of standardised tools to recognise early deterioration of patient condition. METHODS: This was a quality improvement project piloted in the clinical teaching unit of a tertiary care hospital. Data were collected 24 weeks pre-EWS and 55 weeks post-EWS implementation. A series of Plan, Do, Study, Act cycles were conducted to identify the root cause, develop a driver diagram to understand the drivers of unexpected deaths, run a sham test trial run of the EWS, educate and obtained feedback of clinical care teams involved, assess adherence to the EWS during the pilot project (6 weeks pre-EWS and 6 weeks post-EWS implementation), evaluate outcomes by extending the duration to 24 weeks pre-EWS and 55 weeks post-EWS implementation, and retrospectively review the uptake of the EWS. INTERVENTIONS: Implementation of a standardised protocol to detect deterioration in patient condition. RESULTS: During the pre-EWS implementation phase (24 weeks), there were 4.4 events per week (1.2 septic workups, 1.9 observation unit transfers, 0.7 critical care transfers, 0.13 cardiac arrests and 0.46 per week unexpected deaths). In the post-EWS implementation phase (55 weeks), there were 4.2 events per week (1.0 septic workup, 1.9 observation unit transfers, 0.82 critical care transfers, 0.25 cardiac arrests and 0.25 unexpected deaths). CONCLUSION: The EWS can improve patient care; however, more engagement of stakeholders and electronic vital sign documentation may improve the uptake of the system.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 2_ODS3 / 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Deterioração Clínica / Parada Cardíaca Tipo de estudo: Guideline / Observational_studies / Prognostic_studies / Screening_studies Limite: Child / Humans Idioma: En Revista: BMJ Open Qual Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 2_ODS3 / 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Deterioração Clínica / Parada Cardíaca Tipo de estudo: Guideline / Observational_studies / Prognostic_studies / Screening_studies Limite: Child / Humans Idioma: En Revista: BMJ Open Qual Ano de publicação: 2023 Tipo de documento: Article