Sentence examples for a valid registry from inspiring English sources

It is often difficult to determine which items correspond to which applications, and by attempting to remove items yourself, you might accidentally remove a valid registry item, causing software crashes and errors.

A pilot test in 17 primary care and specialty centres, shows that it is feasible to implement a valid registry for these patients within the SNHS [ 75].

This study encompassed the entire population of consecutive, newly diagnosed lung cancer patients in Denmark identified through a valid hospital registry.

Of the 54 449 infertile women, all but 87 had a valid civil registry number, leaving 54 362 women in the cohort for analysis.

Furthermore, only patients with a valid civil registry number (a unique personal identification number issued to all Danish citizens that allows unambiguous linkage between public registries) were included in the study.

61 Valid registries will be required to meet a number of pre-established criteria, including ≥80% successful SBP and DBP recordings during the daytime and night-time periods, 24 h duration and ≥1 BP measurement/h.

The main strengths of our study are its comparatively large size, yielding precise risk estimates, and the use of independent population-based and highly valid registries for assessing PPI use and comorbidity, minimizing the possibility of recall and investigator bias as compared with other studies.

Although this identifier is complete both in the hospital discharge data and population registry, only 70% of the records in the Vital Statistics registry had a valid PHN, because it was not a mandatory variable.

The registry is a valid source of data on anemia caused by bleeding for various purposes including research and monitoring health care.

We found that for children with ALL, a risk stratification system based on treatment protocol as recorded in a population-based pediatric cancer registry was a valid proxy of disease risk as compared to biology-based risk algorithms.

With increasing recognition that patient registries represent a valid, effective and important methodology for the collection of prospective observational data and the continued emergence of new patient registries for neurological conditions, it is essential to consider the perspectives of all relevant stakeholders.