2019
DOI: 10.1136/bmjopen-2018-025117
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Electronic Alerts for Acute Kidney Injury Amelioration (ELAIA-1): a completely electronic, multicentre, randomised controlled trial: design and rationale

Abstract: IntroductionAcute kidney injury (AKI) is common among hospitalised patients and under-recognised by providers and yet carries a significant risk of morbidity and mortality. Electronic alerts for AKI have become more common despite a lack of strong evidence of their benefits. We designed a multicentre, randomised, controlled trial to evaluate the effectiveness of AKI alerts. Our aim is to highlight several challenges faced in the design of this trial, which uses electronic screening, enrolment, randomisation, i… Show more

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Cited by 18 publications
(16 citation statements)
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References 28 publications
(17 reference statements)
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“…A detailed description of the trial design and rationale has been previously published 15. Briefly, we conducted a patient level, parallel group, randomized controlled trial of health record electronic alerts versus usual care in adults with acute kidney injury at six hospitals in the Yale New Haven Health System in Connecticut and Rhode Island, US.…”
Section: Methodsmentioning
confidence: 99%
“…A detailed description of the trial design and rationale has been previously published 15. Briefly, we conducted a patient level, parallel group, randomized controlled trial of health record electronic alerts versus usual care in adults with acute kidney injury at six hospitals in the Yale New Haven Health System in Connecticut and Rhode Island, US.…”
Section: Methodsmentioning
confidence: 99%
“…YNHHS includes six hospitals in southern Connecticut and Rhode Island with a mix of teaching and nonteaching, urban and sub-urban, as well as university and community hospitals. 20,21 We excluded patients <18 years of age, those with International Classification of Diseases (ICD)-10 for end-stage kidney disease (N18.6) or kidney transplant (Z94) on a prior encounter or with first encounter creatinine ≥4 mg/dl. We only included the first hospital encounter during observation period.…”
Section: Patients and Settingsmentioning
confidence: 99%
“…This was operationalized by leveraging an existing AKI detection algorithm we had in use for a different study. 20 For the current analysis, we additionally excluded individuals with a history of kidney transplant (based on International Classification of Diseases, Tenth Revision code Z94.0) or who had a prior hospitalization that generated a pre-AKI alert (to avoid interdependence of observations). Enrollment in this prospective study operated under a waiver of informed consent because data were extracted through electronic chart review and deidentified after outcome assessment.…”
Section: Patientsmentioning
confidence: 99%