Neonatal care prescribing practices
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Referral-level hospitals with: (1) high quality gentamicin prescription baseline clinical data for neonatal inpatient care and, (2) a standardised A&F routine clinical improvement cycle to track prescribing practices in neonatal inpatient care are eligible for inclusion in this study. All neonates admitted to the newborn units in these hospitals with a gentamicin prescription at admission will be included in the study.
Exclusion criteria
Exclusion criteria: Referral-level hospitals without 12 months worth of high quality gentamicin prescription baseline clinical data for neonatal inpatient care and without a standardised A&F routine clinical improvement cycle to track prescribing practices in neonatal inpatient care are not eligible for inclusion in this study. All neonates admitted to the newborn units in these hospitals with missing data on gentamicin prescription at admission will be excluded from this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of this study being measured is the proportion of patients in newborn units receiving an inaccurate Gentamicin prescription over time (i.e., incidence rate ratio) | — |
Secondary
| Measure | Time frame |
|---|---|
| Relative difference in the proportion of patients in newborn units receiving an inaccurate Gentamicin prescription over time (i.e., incidence rate ratio) due to Audit and Feedback package received. | — |
Countries
Kenya
Contacts
Study Project Coordinator