Phenotyping Healthcare Use 2–3 Decades Before the First Multiple Sclerosis Demyelinating Event
ABSTRACT Objective Phenotype hospital, physician, and emergency department (ED) visits by diagnoses and specialty up to 29 years pre‐multiple sclerosis (MS) onset versus a matched population without MS. Methods We identified people with MS (PwMS) using population‐based administrative data from Ontario, Canada (1991–2020).
Helen Tremlett+8 more
wiley +1 more source
Shared decision making and chronic diseases
Desroches Sophie
doaj +1 more source
From Idealist to Realist-Designing and Implementing Shared Decision-Making Interventions in the Choice of Antipsychotic Prescription in People Living with Psychosis (SHAPE): A Realist Review. [PDF]
Fitzgerald I+9 more
europepmc +1 more source
Using patient and physician perspectives to develop a shared decision-making framework for colorectal cancer [PDF]
Marisa Leon-Carlyle+5 more
openalex +1 more source
Genetic Profile and Symptom Pattern Explain Variability of Deep Brain Stimulation Effect in Dystonia
ABSTRACT Objective Bilateral globus pallidus pars interna deep brain stimulation (GPi‐DBS) is a recognized and effective treatment option for drug‐resistant dystonia patients. However, the clinical GPi‐DBS outcomes vary significantly. Herein, we explored the pre‐implant factors affecting GPi‐DBS effectiveness.
Mahboubeh Ahmadipour+6 more
wiley +1 more source
Stakeholders\u27 perspectives on postmastectomy breast reconstruction: Recognizing ways to improve shared decision making [PDF]
Adams+26 more
core +2 more sources
The Effects of Patients' Health Information Behaviors on Shared Decision-Making: Evaluating the Role of Patients' Trust in Physicians. [PDF]
Song M+5 more
europepmc +1 more source
Physicians' Shared Decision-Making Behaviors in Depression Care
Henry N. Young
openalex +2 more sources
Genetic Diversity and Expanded Phenotypes in Dystonia: Insights From Large‐Scale Exome Sequencing
ABSTRACT Objective Dystonia is one of the most prevalent movement disorders, characterized by significant clinical and etiological heterogeneity. Despite considerable heritability (~25%), the etiology in most patients remains elusive. Moreover, understanding correlations between clinical manifestations and genetic variants has become increasingly ...
Mirja Thomsen+47 more
wiley +1 more source