Prevention of medical errors in newborns Pregnancy and Childbirth
Conditions
Interventions
During the randomised phase, patients were assigned to the intervention or the control group at admission according to a simple randomisation using a web-based system (www.dcode.fr). Pharmaceutical va
Sponsors
Hospital Universitario 12 De Octubre
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All patients born during the study period who were admitted to the NICU and stayed for at least 24 hours and with active pharmacological treatment
Exclusion criteria
Exclusion criteria: Patients admitted without pharmacological treatment or less than 24h.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of prescription errors detected by a clinical pharmacist in e-prescribing measured at the end of the study | — |
Secondary
| Measure | Time frame |
|---|---|
| Percentage of prescribing errors reaching the patient according to the nursing administration record measured at the end of the study | — |
Countries
Spain
Contacts
Public ContactMaria Dolores Canales
Outcome results
None listed