Proportion of Patients From Whom Information Was Collected From Relatives
Identifying Attributes
Care Settings
Country
Publishing Organisation
Type of Quality Indicator
IOM Quality Dimension
Domain
Defining Attributes
Definition
Proportion of patients from whom information was collected from relatives.
Numerator
Number of patients from whom information was collected from relatives.
Denominator
Number of patients.
Exclusions
Use of Risk Adjustment
Risk Adjustments
Stratifications
Service.
Data Attributes
Type of Data Collection
Data Collection Methods
Participating services enter data into a secure online data platform.
Frequency of Data Collection
Frequency of Data Collection in Days
Reporting Methods
Online from www.skde.no/kvalitetsregistre/norkog/sykehus/, also Public annual report, downloadable from web.archive.org/web/20241115012438/https://www.kvalitetsregistre.no/register/nervesystemet/norsk-register-personer-som-utredes-kognitive-symptomer-I.
Reporting Frequency
Reporting Frequency in Days
Indicator Has Recommended Targets
Source and Reference Attributes
Evidence Source
Nåvik, M., Bøhn, B. H., Persson, K., Grasbekk, K., Kirkevold, E., & Selbæk, G. (2023). The Norwegian registry of persons assessed for cognitive symptoms (NorCog) 2022 Annual Report. Retrieved from web.archive.org/web/20241115012438/https://www.kvalitetsregistre.no/register/nervesystemet/norsk-register-personer-som-utredes-kognitive-symptomer-i