Prognostic data after ICH associated with non-vitamin K antagonist oral anticoagulants (NOAC) compared to vitamin K antagonists (VKA) are sparse. We compared 90-day survival and functional outcome following NOAC-ICH versus VKA-ICH using data from the Swedish Stroke Register (Riksstroke).

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Riksstroke also undergoes extensive internal data validation, with no indications of systematic differences in data quality between hospitals . The rate of missing data was also low; this, along with the prospective nature of data collection in Riksstroke, vouches for better data quality than that obtained by using sources that accumulate data Data Sources Riksstroke was established in 1994 to monitor, support, and improve the quality of Swedish stroke care.20 The register is estimated to cover 94% of all stroke patients treated in Swedish hospitals, and all hospitals admitting acute stroke patients participate (72 hospitals Methods: Patients with a first-ever ICH in the Swedish Stroke Register (Riksstroke) 2005 to 2012 who survived hospital discharge were included. Riksstroke data were individually linked with other national registers to determine comorbid conditions and dispensed prescriptions of antithrombotic agents. Data and variable definitions. Patients included in the study were registered in Riksstroke with intracerebral hemorrhage, ICH (ICD-10 code I61) or ischemic stroke, IS (ICD-10 code I63) between January 1, 2009 and October 1, 2012. Riksstroke is the Swedish quality register for stroke care and has an estimated coverage of >90% of stroke patients admitted to hospital.

Den första studien av T Andersson · 2020 — Two methods for treating datasets with missing data were used, complete case analysis and multiple imputation by chained equations (MICE). They were The Stroke policy and quality register research group has several ongoing projects based on data from Riksstroke, and in many studies also using data record Riksstroke. Riksstroke är nationellt kvalitetsregister för stroke. Stroke är ett samlingsnamn för hjärnskador som orsakas av en blodpropp eller blödning i hjärnan.

Tillgång till data för uppföljning är en viktig del i utvecklingen av en jämlik, effektiv och genom det nationella kvalitetsregistret Riksstroke.

Det är därför en av de viktigaste parametrarna i Riksstroke, säger bra överens med vad vi ser i våra data över ADL-beroende, säger han. Riksstrokes senaste årsrapport1 visar att andelen patienter som uppger att Data från Riksstroke visar att 16 procent av de patienter som var Avhandlingen är baserad på data från det nationella kvalitetsregistret för strokesjukvård, Riksstroke, berikat med data över beläggningsgrad. Projektet bygger på data från Riksstroke, det svenska kvalitetsregistret för strokesjukvård, och mer specifikt en långtidsuppföljning som 2019Pressmeddelande från Riksstroke – Årets Strokeenhet är utsedd!

Men data från Riksstroke visar att det är stora skillnader i behov av kommunal omsorg efter stroke, säger Jesper Petersson, verksamhetschef

The data set comprises linked information from Riksstroke, Statistics Sweden and the National Board of Health and Welfare and cannot be made publically available due to Swedish legislation.

Demographics, risk factors, type of care and length of stay • Slightly more men than women were registered.
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Kostnaden för Projektmålet är att validera databasen RIKSSTROKE-TIA för att kunna utnyttja data från registret. Två oberoende granskare granskar avidentifierade journaler av I flera projekt har data lagts samman med andra register, tex det nationella kvalitetsregistret Riksstroke. Publicerade studier.
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Riksstroke also undergoes extensive internal data validation, with no indications of systematic differences in data quality between hospitals . The rate of missing data was also low; this, along with the prospective nature of data collection in Riksstroke, vouches for better data quality than that obtained by using sources that accumulate data

Bortfall ger Publications with data from Riksstroke. Also available in Svenska.

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Enligt data från Riksstroke är den årliga totala kostnaden 18,3 miljarder exklusive anhörigas vårdinsatser.2. Den akuta behandlingen av akut ischemisk stroke är

Därefter sker randomisering i Riksstrokes inmatningsfönster. Under studien Det nationella kvalitetsregistret Riksstroke har funnits under många år och har inneburit ett viktigt stöd för utveckling och kvalitetssäkring av den akuta strokevården på sjukhus.

The Riksstroke database has permitted more detailed analyses than in studies based solely on routine administrative data. Our findings might be limited by the use of administrative registers to study outcome because suicide diagnoses have not been systematically validated in the Swedish Inpatient Register and the Cause of Death Register.

It is important that this data come from credible sources, as the validity of the research is determined by where it comes from.

The rate of missing data was also low; this, along with the prospective nature of data collection in Riksstroke, vouches for better data quality than that obtained by using sources that accumulate data Data Sources Riksstroke was established in 1994 to monitor, support, and improve the quality of Swedish stroke care.20 The register is estimated to cover 94% of all stroke patients treated in Swedish hospitals, and all hospitals admitting acute stroke patients participate (72 hospitals Methods: Patients with a first-ever ICH in the Swedish Stroke Register (Riksstroke) 2005 to 2012 who survived hospital discharge were included. Riksstroke data were individually linked with other national registers to determine comorbid conditions and dispensed prescriptions of antithrombotic agents. Data and variable definitions. Patients included in the study were registered in Riksstroke with intracerebral hemorrhage, ICH (ICD-10 code I61) or ischemic stroke, IS (ICD-10 code I63) between January 1, 2009 and October 1, 2012. Riksstroke is the Swedish quality register for stroke care and has an estimated coverage of >90% of stroke patients admitted to hospital. 16,17 The register includes data collected during admission, as well as survey data from paper-based follow-up questionnaires distributed to all registered patients at 3- and 12-month post-stroke (and additionally at three or five years for selected cohorts).