Hyperemesis gravidarum
Conditions
Interventions
None listed
Sponsors
The University of Tokyo
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: All mothers who were admitted to obstetric clinics or hospitals for delivery from January 2005 to December 2016 and on their newborns.
Exclusion criteria
Exclusion criteria: We excluded mothers aged under 19 years.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Safety outcomes included newborns' congenital anomalies, low birthweight (ICD-10, P070 or P071), and preterm birth (P072 or P073). Congenital anomalies were defined according to the criteria of the Congenital Anomaly Register for Oxfordshire, Berkshire and Buckinghamshire. | — |
Secondary
| Measure | Time frame |
|---|---|
| For mothers with hyperemesis gravidarum, we defined effectiveness outcomes as unplanned hospital admission for treating hyperemesis gravidarum and total medical costs during pregnancy within 20 weeks of gestation. | — |
Countries
Japan
Contacts
Public ContactNobuaki Michihata
The University of Tokyo Department of Health Services Research, Graduate School of Medicine
Outcome results
None listed