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Electronic early notification of sepsis in hospitalized ward patients: a study protocol for a stepped-wedge cluster randomized controlled trial

BACKGROUND: To evaluate the effect of screening for sepsis using an electronic sepsis alert vs. no alert in hospitalized ward patients on 90-day in-hospital mortality. METHODS: The SCREEN trial is designed as a stepped-wedge cluster randomized controlled trial. Hospital wards (total of 45 wards, con...

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Detalles Bibliográficos
Autores principales: Arabi, Yaseen M., Alsaawi, Abdulmohsen, Al Zahrani, Mohammed, Al Khathaami, Ali M., AlHazme, Raed H., Al Mutrafy, Abdullah, Al Qarni, Ali, Al Shouabi, Ahmed, Al Qasim, Eman, Abdukahil, Sheryl Ann, Al-Rabeah, Fawaz K., Al Ghamdi, Huda, Al Ghamdi, Ebtisam, Alansari, Mariam, Abuelgasim, Khadega A., Alatassi, Abdulaleem, Alchin, John, Al-Dorzi, Hasan M., Ghamdi, Abdulaziz A., Al-Hameed, Fahad, Alharbi, Ahmad, Hussein, Mohamed, Jastaniah, Wasil, AlKatheri, Mufareh Edah, AlMarhabi, Hassan, Mustafa, Hani T., Jones, Joan, Al-Qahtani, Saad, Qahtani, Shaher, Qureshi, Ahmad S., Salih, Salih Bin, Alselaim, Nahar, Tashkandi, Nabiha, Vishwakarma, Ramesh Kumar, AlWafi, Emad, Alyami, Ali H., Alyousef, Zeyad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8503718/
https://www.ncbi.nlm.nih.gov/pubmed/34635151
http://dx.doi.org/10.1186/s13063-021-05562-5
Descripción
Sumario:BACKGROUND: To evaluate the effect of screening for sepsis using an electronic sepsis alert vs. no alert in hospitalized ward patients on 90-day in-hospital mortality. METHODS: The SCREEN trial is designed as a stepped-wedge cluster randomized controlled trial. Hospital wards (total of 45 wards, constituting clusters in this design) are randomized to have active alert vs. masked alert, 5 wards at a time, with each 5 wards constituting a sequence. The study consists of ten 2-month periods with a phased introduction of the intervention. In the first period, all wards have a masked alert for 2 months. Afterwards the intervention (alert system) is implemented in a new sequence every 2-month period until the intervention is implemented in all sequences. The intervention includes the implementation of an electronic alert system developed in the hospital electronic medical records based on the quick sequential organ failure assessment (qSOFA). The alert system sends notifications of “possible sepsis alert” to the bedside nurse, charge nurse, and primary medical team and requires an acknowledgment in the health information system from the bedside nurse and physician. The calculated sample size is 65,250. The primary endpoint is in-hospital mortality by 90 days. DISCUSSION: The trial started on October 1, 2019, and is expected to complete patient follow-up by the end of October 2021. TRIAL REGISTRATION: ClinicalTrials.gov NCT04078594. Registered on September 6, 2019 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13063-021-05562-5.