This article concerns the potential benefits of clinical disease registers, but points to the problems inherent in maintaining high quality reliable datasets. It comments on a recent (accompanying) paper from the West of Scotland that extracted data from existing administrative and clinical datasets to produce a meaningful registry
Traditional cancer registries have often been siloed efforts, established by single groups with limi...
Background: Clinical outcome registries are an increasingly vital component of ensuring quality and ...
BackgroundClinical registry participation is a measure of healthcare quality. Limited knowledge exis...
International audienceIdeally, collection of clinical data should be an integral part of healthcare ...
AbstractMedical registries are useful to summarize retrospective or prospective data in a fashion th...
Large scale collection and analysis of data on patients’ experiences and outcomes have become staple...
Background: Clinical quality registries (CQRs) are playing an increasingly important role in improvi...
Clinical quality registries (CQRs) are playing an increasingly important role in improving health ou...
The origin of cancer registries was to create clinical surveys and perform patient follow-up, the ob...
BACKGROUND: Clinical trials generally each collect their own data despite routinely collected health...
Disease registries have the invaluable potential to provide an insight into the natural history of t...
– Clinical registries are health information systems, which have the mission to collect multidimensi...
Within the 21 APEC economies alone, there are an estimated 200 million individuals living with a rar...
Contains fulltext : 137052.pdf (publisher's version ) (Open Access)INTRODUCTION: T...
BACKGROUND: Clinical trials generally each collect their own data despite routinely collected health...
Traditional cancer registries have often been siloed efforts, established by single groups with limi...
Background: Clinical outcome registries are an increasingly vital component of ensuring quality and ...
BackgroundClinical registry participation is a measure of healthcare quality. Limited knowledge exis...
International audienceIdeally, collection of clinical data should be an integral part of healthcare ...
AbstractMedical registries are useful to summarize retrospective or prospective data in a fashion th...
Large scale collection and analysis of data on patients’ experiences and outcomes have become staple...
Background: Clinical quality registries (CQRs) are playing an increasingly important role in improvi...
Clinical quality registries (CQRs) are playing an increasingly important role in improving health ou...
The origin of cancer registries was to create clinical surveys and perform patient follow-up, the ob...
BACKGROUND: Clinical trials generally each collect their own data despite routinely collected health...
Disease registries have the invaluable potential to provide an insight into the natural history of t...
– Clinical registries are health information systems, which have the mission to collect multidimensi...
Within the 21 APEC economies alone, there are an estimated 200 million individuals living with a rar...
Contains fulltext : 137052.pdf (publisher's version ) (Open Access)INTRODUCTION: T...
BACKGROUND: Clinical trials generally each collect their own data despite routinely collected health...
Traditional cancer registries have often been siloed efforts, established by single groups with limi...
Background: Clinical outcome registries are an increasingly vital component of ensuring quality and ...
BackgroundClinical registry participation is a measure of healthcare quality. Limited knowledge exis...