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Regression Discontinuity Designs in Health

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 24 June 2021 Photo: Pixabay / geralt This systematic review demonstrates that regression discontinuity designs have been widely applied in health research and could be used more widely still. Shortcomings in study quality and reporting suggest that the potential benefits of this method have not yet been fully realized. Read th

https://www.lupop.lu.se/article/regression-discontinuity-designs-health - 2025-01-10

Is Cohort Representativeness Passé? Poststratified Associations of Lifestyle Risk Factors with Mortality in the UK Biobank

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 25 June 2021 Lack of representativeness may distort the associations of alcohol with CVD mortality, and may underestimate health hazards among those with cumulatively the least healthy lifestyles. Read the paper at https://journals.lww.com/epidem/Fulltext/2021/03000/Is_Cohort_Represent…

https://www.lupop.lu.se/article/cohort-representativeness-passe-poststratified-associations-lifestyle-risk-factors-mortality-uk - 2025-01-10

To Adjust or Not to Adjust? When a “Confounder” Is Only Measured After Exposure

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 26 June 2021 Foto från snd.gu.se Advice regarding the analysis of observational studies of exposure effects usually is against adjustment for factors that occur after the exposure, as they may be caused by the exposure (or mediate the effect of exposure on outcome), so potentially leading to collider stratification bias. Howev

https://www.lupop.lu.se/article/adjust-or-not-adjust-when-confounder-only-measured-after-exposure - 2025-01-10

Causal Organic Indirect and Direct Effects: Closer to the Original Approach to Mediation Analysis, with a Product Method for Binary Mediators

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 27 June 2021 Mediation analysis, which started in the mid-1980s, is used extensively by applied researchers. Indirect and direct effects are the part of a treatment effect that is mediated by a covariate and the part that is not. Subsequent work on natural indirect and direct effects provides a formal causal interpretation, ba

https://www.lupop.lu.se/article/causal-organic-indirect-and-direct-effects-closer-original-approach-mediation-analysis-product - 2025-01-10

Recent Trends in Patient Registries for Health Services Research

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 28 June 2021 Patient registries are an established methodology in health services research. Since more than 150 years, registries collect information concerning groups of similar patients to answer research questions. Elaborated recommendations about an appropriate development and an efficient operation of registries are avail

https://www.lupop.lu.se/article/recent-trends-patient-registries-health-services-research - 2025-01-10

Open Science—A Question of Trust

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 29 June 2021 Collaboration and the sharing of knowledge is at the heart of Open Science (OS). However, we need to know that the knowledge we find and share is really what it purports to be; and we need to know that the authors we hope to collaborate with are really the people they claim to be. Read the paper at https://direct.

https://www.lupop.lu.se/article/open-science-question-trust - 2025-01-10

The MSBase pregnancy, neonatal outcomes, and women’s health registry

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 30 June 2021 Photo: Pixabay / Free-photos Here, we describe the new MSBase pregnancy, neonatal outcomes and women’s health registry. We provide the rationale for, and detailed description of, the variables collected within the registry, together with data acquisition details. Read the paper at https://journals.sagepub.com/doi/

https://www.lupop.lu.se/article/msbase-pregnancy-neonatal-outcomes-and-womens-health-registry - 2025-01-10

Generalizability of Subgroup Effects

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 1 July 2021 Generalizability methods are increasingly used to make inferences about the effect of interventions in target populations using a study sample. Most existing methods to generalize effects from sample to population rely on the assumption that subgroup-specific effects generalize directly. However, researchers may be

https://www.lupop.lu.se/article/generalizability-subgroup-effects - 2025-01-10

Pregnancy intention data completeness, quality and utility in population-based surveys

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 2 July 2021 From Wikimedia Commons An estimated 40% of pregnancies globally are unintended. Measurement of pregnancy intention in low- and middle-income countries relies heavily on surveys, notably Demographic and Health Surveys (DHS), yet few studies have evaluated survey questions. Read the paper at https://pophealthmetrics.

https://www.lupop.lu.se/article/pregnancy-intention-data-completeness-quality-and-utility-population-based-surveys - 2025-01-10

Redesign of the Australian Cystic Fibrosis Data Registry: A multidisciplinary collaboration

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 3 July 2021 Clinical registries that monitor and review outcomes for patients with cystic fibrosis have existed internationally for many decades. However, their purpose continues to evolve and now includes the capability to support clinical effectiveness research, clinical trials and Phase IV studies, and international data co

https://www.lupop.lu.se/article/redesign-australian-cystic-fibrosis-data-registry-multidisciplinary-collaboration - 2025-01-10

The European Paediatric Rare Tumours Network - European Registry (PARTNER) project for very rare tumors in children

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 4 July 2021 Photo from Manchester Metropolitan University The PARTNER project (Paediatric Rare Tumours Network - European Registry) was launched in 2016. PARTNER aims to create a European Registry dedicated to children and adolescents with very rare tumors (VRT). It links existing national registries and provides a registry fo

https://www.lupop.lu.se/article/european-paediatric-rare-tumours-network-european-registry-partner-project-very-rare-tumors-children - 2025-01-10

Complex systems models for causal inference in social epidemiology

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 5 July 2021 Photo: Pixabay / Gerd Altmann Systems models, which by design aim to capture multi-level complexity, are a natural choice of tool for bridging the divide between social epidemiology and causal inference. In this commentary, we discuss the potential uses of complex systems models for improving our understanding of q

https://www.lupop.lu.se/article/complex-systems-models-causal-inference-social-epidemiology - 2025-01-10

Estimating the hazard rate difference from case-cohort studies

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 6 July 2021 In this paper, we describe a newly developed estimation method that fits the additive hazards models to general two-phase sampling studies along with the R package addhazard that implements it. Read the paper at https://link.springer.com/article/10.1007/s10654-021-00739-3

https://www.lupop.lu.se/article/estimating-hazard-rate-difference-case-cohort-studies - 2025-01-10

Assessing knowledge, attitudes, and practices towards causal directed acyclic graphs: a qualitative research project

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 7 July 2021 We sought to understand why researchers do or do not regularly use DAGs by surveying practicing epidemiologists and medical researchers on their knowledge, level of interest, attitudes, and practices towards the use of causal graphs in applied epidemiology and health research. Read the paper at https://link.springe

https://www.lupop.lu.se/article/assessing-knowledge-attitudes-and-practices-towards-causal-directed-acyclic-graphs-qualitative - 2025-01-10

A Hierarchical Approach Using Marginal Summary Statistics for Multiple Intermediates in a Mendelian Randomization or Transcriptome Analysis

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 8 July 2021 Photo: Pixabay / Arek Socha We propose to extend our previous approach for the joint analysis of marginal summary statistics to incorporate prior information via a hierarchical model (hJAM). Read the paper at https://doi.org/10.1093/aje/kwaa287

https://www.lupop.lu.se/article/hierarchical-approach-using-marginal-summary-statistics-multiple-intermediates-mendelian - 2025-01-10

Assessing the external validity of the VALIDATE-SWEDEHEART trial

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 9 July 2021 Photo: Pixabay / Ben Kerckx The VALIDATE-SWEDEHEART trial was a registry-based randomized trial comparing bivalirudin and heparin in patients with acute myocardial infarction undergoing percutaneous coronary intervention. It showed no differences in mortality at 30 or 180 days. This study examines how well the tria

https://www.lupop.lu.se/article/assessing-external-validity-validate-swedeheart-trial - 2025-01-10

Estimating perceived parental substance use disorder: Using register data to adjust for non-participation in survey research

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 10 July 2021 Photo: Pixabay / Ralf Kunze Aims: To estimate the prevalence of parental substance use disorder (PSUD) in the general population based on young adults' reports adjusted for non-participation using register-based indicators of PSUD. Read the paper at https://europepmc.org/article/med/33878599

https://www.lupop.lu.se/article/estimating-perceived-parental-substance-use-disorder-using-register-data-adjust-non-participation - 2025-01-10

Integrating data from multiple Finnish biobanks and national health-care registers for retrospective studies: Practical experiences

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 11 July 2021 A large cohort, consisting of versatile individual-level phenotype and genotype data, can be constructed by integrating data from several biobanks and health data registers in Finland. Co-operation with biobanks is straightforward. However, long time periods need to be reserved when biobank resources are linked wi

https://www.lupop.lu.se/article/integrating-data-multiple-finnish-biobanks-and-national-health-care-registers-retrospective-studies - 2025-01-10

How to design a registry for undiagnosed patients in the framework of rare disease diagnosis: suggestions on software, data set and coding system

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 12 July 2021 Photo: flickr / agilemktg1 About 30 million people in the EU and USA, respectively, suffer from a rare disease. Driven by European legislative requirements, national strategies for the improvement of care in rare diseases are being developed. Read the paper at https://ojrd.biomedcentral.com/articles/10.1186/s13023

https://www.lupop.lu.se/article/how-design-registry-undiagnosed-patients-framework-rare-disease-diagnosis-suggestions-software-data - 2025-01-10

A Canadian Prospective Study of Linkage of Randomized Clinical Trial to Cancer and Mortality Registry Data

By anna [dot] axmon [at] med [dot] lu [dot] se (Anna Axmon) - published 13 July 2021 Photo: Pixabay / Colin Behrens In a prospective study, we sought to determine acceptability of linkage of administrative and clinical trial data among Canadian patients and Research Ethics Boards (REBs). The goal is to develop a more harmonized approach to data, with potential to improve clinical trial conduct thr

https://www.lupop.lu.se/article/canadian-prospective-study-linkage-randomized-clinical-trial-cancer-and-mortality-registry-data - 2025-01-10