liver adenoma
Conditions
Interventions
None listed
Sponsors
Erasmus MC, Universitair Medisch Centrum Rotterdam
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Study groep: Properly Dutch speaking, pregnant patients, 18 years of age or older with a radiologically and/or histologically proven diagnosis of hepatocellular adenoma can be included in the study. Radiological diagnosis of HCA will be based on contrast enhanced magnetic resonance imaging (pre- or postpartum). Lesions must not exceed 5 cm. Informed consent must be signed.
Exclusion criteria
Exclusion criteria: Dementia or impaired mental function that would counter the understanding of giving informed consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| *To investigate the proportion of patients in which HCA growth during pregnancy occurs | — |
Secondary
| Measure | Time frame |
|---|---|
| *To investigate in which trimester of pregnancy growth of HCA occurs; *To investigate the degree of growth of HCA during pregnancy; *To investigate whether there is regression of HCA postpartum; *To investigate the HCA-related interventions during pregnancy; *To investigate the incidence of bleeding of HCA during pregnancy; *To investigate liver-related clinical signs during pregnancy; *To investigate elevated liver enzymes during pregnancy; *To evaluate the quality of life of pregnant patients with HCA; *To investigate whether there is a difference between quality of life of pregnant patients with HCA and pregnant patients with other comorbidity that have an indication for pregnancy care at the obstetrician in secondary care and healthy pregnant patients. | — |
Countries
Netherlands
Outcome results
None listed