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Published 4 July 2019 A registry actively documents and standardizes patient data on pre-defined questions. The term "register" emphasizes the data-holding aspect with the aim of describing epidemiological relationships and differences, supporting quality assurance and improvement, as well as clinical research. New publication in Europe PMC.Read more here.
https://www.lupop.lu.se/article/evaluation-multicenter-registry-data - 2025-01-08
Published 5 July 2019 As publications using data from huge registries bcome more popular, so does the belief that the strength of recommendation that can be made from the results is greater than from smaller cohorts. New publication in ESVS Journal.Read more here.
https://www.lupop.lu.se/article/bigger-actually-better-strengths-and-limitations-large-registry-data - 2025-01-08
Published 8 July 2019 Spasticity is often regarded as a major cause of functional limitation in children with cerebral palsy (CP). We analyzed the spasticity development with age in the gastrosoleus muscle in children with CP. New publication in Acta Prthopaedica.Read more here.
Published 26 June 2019 The Department of Public Health, Faculty of Health at Aarhus University, Denmark invites applications for one or more positions as professor in the fields of General Practice, Biostatistics, Nursing, Public Health and Sport Biological Research. Read more here.
https://www.lupop.lu.se/article/position-professor-aarhus-university - 2025-01-08
Published 10 July 2019 The history of the Erlangen Glaucoma Registry goes back 26 years. In this study, we present retrospective demographic and perimetric data on the initial visit of patients with ocular hypertension (OHT), pre-perimetric (prePOAG) and perimetric primary open-angle glaucoma (POAG), normal tension glaucoma (NTG) and secondary open-angle glaucoma (SOAG) and correlate these results
Published 11 July 2019 New publication from Lund University. New publication in Psychiatry Research.Read more here.
https://www.lupop.lu.se/article/sexual-orientation-suicide-ideation-and-suicide-attempt-population-based-study - 2025-01-08
Published 15 July 2019 The aim of DANARREST is to collect data on processes of care and outcomes for patients with in-hospital cardiac arrest in Denmark, and thereby facilitate and monitor quality and quality improvement initiatives. New publication in DovePress.Read more here.
https://www.lupop.lu.se/article/danish-hospital-cardiac-arrest-registry-danarrest - 2025-01-08
Published 16 July 2019 Large registry studies are powerful because of inclusion of large numbers of patients. Knee anterior cruciate ligament repeat revision surgery is rare (<10% at 8 years). The reasons require additional investigation. Patients may be counseled that, based on demographic factors, it is difficult to predict who will need re-revision. New publication in Arthroscopy.Read more here
Published 17 July 2019 Maintained study-based registers (SBRs) have, at their core, study records linked to, potentially, multiple other records such as references, data sets, standard texts and full-text reports. Such registers can minimise and refine searching, de-duplicating, screening and acquisition of full texts. SBRs can facilitate new review titles/updates and, within seconds, inform the t
https://www.lupop.lu.se/article/study-based-registers-reduce-waste-systematic-reviewing-discussion-and-case-report - 2025-01-08
Published 18 July 2019 The National Joint Registry (NJR) was established in 2002 as the result of an unexpectedly high failure rate of a cemented total hip replacement. New publication in Bone & Joint.Read more here.
https://www.lupop.lu.se/article/orthopaedic-registries-uk-view-national-joint-registry-impact-practice - 2025-01-08
Published 19 July 2019 o investigate use of data from a clinical quality registry for cardiac rehabilitation in Denmark, considering the extent to which data are used for local quality improvement and what facilitates the use of these data, with a particular focus on whether there are differences between frontline staff and managers. New publication in BMJ Open.Read more here.
Published 22 July 2019 Total hip arthroplasty (THA) registers are established in several countries to collect data aiming to improve the results after THA. Monitoring of adverse outcomes after THA has focused mainly on revision surgery, but patient-reported outcomes have also been investigated. New publication in Bone & Joint.Read more here.
https://www.lupop.lu.se/article/impact-hip-arthroplasty-registers-orthopaedic-practice-and-perspectives-future - 2025-01-08
Published 23 July 2019 New publication from Lund University New publication in BMC Psychiatry.Read more here.
Published 24 July 2019 National joint registries are gaining more and more importance in the fields of implant monitoring/outlier detection and quality of care. New publication in Bone & Joint.Read more here.
https://www.lupop.lu.se/article/orthopaedic-registries-german-experience - 2025-01-08
Published 25 July 2019 Most data on the epidemiology of cardiogenic shock (CS) have come from patients with acute myocardial infarction admitted to intensive cardiac care units (ICCUs). However, CS can have other aetiologies, and could be managed in intensive care units (ICUs), especially the most severe forms of CS. New publication in Archives of Cardiovascular Diseases.Read more here.
Published 26 July 2019 Hip fracture registries have helped improve quality of care and reduce variability, and several audits exist worldwide. The results of the Spanish National Hip Fracture Registry are presented and compared with 13 other national registries, highlighting similarities and differences to define areas of improvement, particularly surgical delay and early mobilization. New publica
Published 29 July 2019 Clinical registries are health information systems, which have the mission to collect multidimensional real-world data over the long term, and to generate relevant information and actionable knowledge to address current serious healthcare problems. New publication in Bone & Joint.Read more here.
https://www.lupop.lu.se/article/registry-stakeholders - 2025-01-08
Published 30 July 2019 The Nordic Arthroplasty Register Association (NARA) was established in 2007 by arthroplasty register representatives from Sweden, Norway and Denmark with the overall aim to improve the quality of research and thereby enhance the possibility for quality improvement with arthroplasty surgery. Finland joined the NARA collaboration in 2010. New publication in Bone& Joint.Read mo
https://www.lupop.lu.se/article/benefits-collaboration-nordic-arthroplasty-register-association - 2025-01-08
Published 31 July 2019 Establishment of orthopaedic registers started in 1975 and many registers have been initiated since. The main purpose of registers is to collect information on patients, implants and procedures in order to monitor and improve the outcome of the specific procedure. New publication in Bone & Joint.Read more here.
https://www.lupop.lu.se/article/what-when-and-how-orthopaedic-registers-introduction-register-based-research - 2025-01-08
Published 29 July 2019 The newly established Centre for International Health Protection (ZIG) consolidates the international work of the RKI. It contains four units (Public Health Intelligence, Evidence Based Public Health, Preparedness and Operations Support; Public Health Laboratory Support) and a Programme Office hosting specific projects. The jobholder will report directly to the President of
https://www.lupop.lu.se/article/head-department-robert-koch-institut - 2025-01-08
