SIRAD: Secure Infrastructure for Research with Administrative Data

2022 ◽  
Author(s):  
Mark Howison ◽  
Marcelle Goggins
Keyword(s):  
Administrative Data

Decision Support Systems and Informatics for Child Welfare Administrative Data to Inform Practice and Policy

2012 ◽  
Author(s):  
Hye-Chung Kum ◽  
Joy Stewart ◽  
Terry Moore ◽  
Michael Dineen
Keyword(s):  
Decision Support ◽  
Child Welfare ◽  
Decision Support Systems ◽  
Administrative Data ◽  
Support Systems

Administrative data use in colon and rectal surgery

2003 ◽  
Vol 14 (1) ◽  
pp. 26-32 ◽  
Author(s):  
Arden M. Morris
Keyword(s):  
Administrative Data ◽  
Data Use ◽  
Rectal Surgery ◽  
Colon And Rectal Surgery

Reconciling Trends in Volatility: Evidence from the SIPP Survey and Administrative Data

2020 ◽  
Author(s):  
Michael Carr ◽  
Robert Moffitt ◽  
Emily Wiemers
Keyword(s):  
Administrative Data

Epidemiology of pheochromocytoma and paraganglioma: population-based cohort study

2021 ◽  
Vol 184 (1) ◽  
pp. 19-28
Author(s):  
Alexander A Leung ◽  
Janice L Pasieka ◽  
Martin D Hyrcza ◽  
Danièle Pacaud ◽  
Yuan Dong ◽  
...  
Keyword(s):  
Cohort Study ◽  
Administrative Data ◽  
Laboratory Data ◽  
Population Based ◽  
Incidence Rates ◽  
Primary Objective ◽  
Administrative Databases ◽  
Secondary Objective ◽  
True Frequency ◽  
Clinical Records

Objective Despite the significant morbidity and mortality associated with pheochromocytoma and paraganglioma, little is known about their epidemiology. The primary objective was to determine the incidence of pheochromocytoma and paraganglioma in an ethnically diverse population. A secondary objective was to develop and validate algorithms for case detection using laboratory and administrative data. Design Population-based cohort study in Alberta, Canada from 2012 to 2019. Methods Patients with pheochromocytoma or paraganglioma were identified using linked administrative databases and clinical records. Annual incidence rates per 100 000 people were calculated and stratified according to age and sex. Algorithms to identify pheochromocytoma and paraganglioma, based on laboratory and administrative data, were evaluated. Results A total of 239 patients with pheochromocytoma or paraganglioma (collectively with 251 tumors) were identified from a population of 5 196 368 people over a period of 7 years. The overall incidence of pheochromocytoma or paraganglioma was 0.66 cases per 100 000 people per year. The frequency of pheochromocytoma and paraganglioma increased with age and was highest in individuals aged 60–79 years (8.85 and 14.68 cases per 100 000 people per year for males and females, respectively). An algorithm based on laboratory data (metanephrine >two-fold or normetanephrine >three-fold higher than the upper limit of normal) closely approximated the true frequency of pheochromocytoma and paraganglioma with an estimated incidence of 0.54 cases per 100 000 people per year. Conslusion The incidence of pheochromocytoma and paraganglioma in an unselected population of western Canada was unexpectedly higher than rates reported from other areas of the world.

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