None listed
Conditions
Interventions
Experimental group:Nurses use the clinical decision support system for medication administration of high-alert medication
Control group:Medication administration as usual, with no clinical decision support system
Sponsors
School of Nursing, Fudan University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Nurses who administer high-alert drugs intravenously have the following inclusion criteria: (1) Nurses employed at the study site; (2) Currently engaged in clinical work directly related to intravenous administration of high-alert drugs in children; (3) Informed consent to participate in the study. 2. For children and their parents receiving intravenous administration of high-alert drugs, the inclusion criteria are: (1) Children hospitalized at the study site during the study period; (2) 1 month <= correction month age < 18 years; (3) Receiving intravenous administration of high-alert drugs in children according to the doctor's advice; (4) Informed consent.
Exclusion criteria
Exclusion criteria: 1. The exclusion criteria for nurses who administered high-alert drugs intravenously were: they were not on duty during the study period; 2. For children and their parents receiving intravenous administration of high-warning drugs, the exclusion criteria are: failure to complete the questionnaire due to critical condition and other reasons.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Medication administration error of intravenous high-alert medication;Adverse event of intravenous high-alert medication;Compliance of nurses on high-alert medication administration;Mental workload of nurses on high-alert medication administration; | — |
Secondary
| Measure | Time frame |
|---|---|
| Knowledge of patients' family;Satisfaction of patients' family;Knowledge of nurses; | — |
Countries
China
Contacts
Public ContactHu Yan
Outcome results
None listed