Sentence examples for source registries from inspiring English sources

All three source registries contain nationwide data with good quality and coverage.

These secondary outcomes were selected both based on the quality and accuracy of these outcomes in the source registries, and in order to cover a clinically representative range of adverse short-term and long-term events after transfusion (mortality, cardiovascular, oncology, mortality, infections, renal).

* CKAN - an open source registry of open data, currently used to power data.gov.uk.

The ICTRP publishes a hyperlink to the record in the source registry (i.e. the registry that provided the data) so users can view additional information, if required.

Descriptive information on study phase, study design, randomization status and inclusion criteria for gender and age of participants was extracted manually from the complete registered record in the source registry.

The ICTRP publishes a hyperlink to the record in the source registry (ie, the registry that provided the data) so users can view additional information, if required.

This library is used by the project Open Source Registry System for Rare Diseases in the EU (OSSE) for seamlessly integrating two data pools [ 84, 85].

Other TAVI series included up to 60% of patients with a logistic EuroScore <20% [ 18], and our own cohort compares favourably to the Source Registry [ 16] which consists to one-third of such patients.

First, the recent publication of the survival results from the SOURCE registry 22 allow us to compare the death rates at 1 year between the population included in our meta-analysis (3496 patients; 1-year mortality=23.2%) and the large patient series included in this registry (3195 patients; 1-year mortality=24.0%).

While it should be stressed that the population enrolled in the SOURCE registry could not be included in our analysis due to the lack of survival data after 1 year, these nearly identical results at 1 year suggest a good representativeness of the patients of our meta-analysis.

We therefore extended an open-source registry platform, the Rare Disease Registry Framework (RDRF) to establish an Independent Rare Disease Registry (IRDR).