Introduction: The Disease Registry records and maintains the necessary data for each individual patient according to the purpose for which it was designed. These data are widely used to calculate statistical indicators, resource management, resource allocation, and clinical research. One of the main challenges in using disease registries is their low quality data. Incompleteness, inaccuracy and untimeliness are some of the problems with the quality of the data in the disease registries. In this study, the researchers reviewed the views of some medical specialists on ways to improve the quality of data in the diseases registries. In this study, researchers looked at the views of some medical specialist who were in charge of maintaining a dis...
Registries are indispensable in medical studies and provide the basis for reliable study results for...
Contains fulltext : 137052.pdf (publisher's version ) (Open Access)INTRODUCTION: T...
Background: Although cancer treatment information has been collected through the Cancer Registry sys...
Over the past years the number of medical registries has increased sharply. Their value strongly dep...
In the field of rare diseases, registries are considered power tool to develop clinical research, to...
Background: Clinical research registries are rarely driven by data quality assurance. However, quali...
AbstractMedical registries are useful to summarize retrospective or prospective data in a fashion th...
Information technology (IT) is increasingly used in medicine, mainly for processing medical data. Un...
BackgroundDecision-making and strategies to improve service delivery must be supported by reliable h...
Introduction: Rare Diseases Registries (RDRs) are important epidemiological tools for health policy ...
Background: Publically-available databases were established with the purpose of making a large amoun...
Currently medical outcomes research has generally been conducted with 3 sources of data: randomized ...
The transferring of medical records into huge electronic databases has opened up opportunities for r...
The origin of cancer registries was to create clinical surveys and perform patient follow-up, the ob...
Purpose: Data quality is a core value of cancer registries, which bring about greater understanding ...
Registries are indispensable in medical studies and provide the basis for reliable study results for...
Contains fulltext : 137052.pdf (publisher's version ) (Open Access)INTRODUCTION: T...
Background: Although cancer treatment information has been collected through the Cancer Registry sys...
Over the past years the number of medical registries has increased sharply. Their value strongly dep...
In the field of rare diseases, registries are considered power tool to develop clinical research, to...
Background: Clinical research registries are rarely driven by data quality assurance. However, quali...
AbstractMedical registries are useful to summarize retrospective or prospective data in a fashion th...
Information technology (IT) is increasingly used in medicine, mainly for processing medical data. Un...
BackgroundDecision-making and strategies to improve service delivery must be supported by reliable h...
Introduction: Rare Diseases Registries (RDRs) are important epidemiological tools for health policy ...
Background: Publically-available databases were established with the purpose of making a large amoun...
Currently medical outcomes research has generally been conducted with 3 sources of data: randomized ...
The transferring of medical records into huge electronic databases has opened up opportunities for r...
The origin of cancer registries was to create clinical surveys and perform patient follow-up, the ob...
Purpose: Data quality is a core value of cancer registries, which bring about greater understanding ...
Registries are indispensable in medical studies and provide the basis for reliable study results for...
Contains fulltext : 137052.pdf (publisher's version ) (Open Access)INTRODUCTION: T...
Background: Although cancer treatment information has been collected through the Cancer Registry sys...