The Patient - Patient-Centered Outcomes Research

Title Publication Date Language Citations
Patient Perspectives of Dabigatran: Analysis of Online Discussion Forums2013/09/13English32
Factors Affecting Patients’ Perception On, and Adherence To, Anticoagulant Therapy: Anticipating the Role of Direct Oral Anticoagulants2016/07/20English32
Development of a Patient-Reported Outcome Measure for Non-Alcoholic Steatohepatitis (NASH-CHECK): Results of a Qualitative Study2020/12/18English32
Self-Care of People with Chronic Obstructive Pulmonary Disease: A Meta-Synthesis2017/02/14English32
What Outcomes are Important for Gout Patients? In-Depth Qualitative Research into the Gout Patient Experience to Determine Optimal Endpoints for Evaluating Therapeutic Interventions2016/07/06English32
Patient Perceptions of Generic Medicines: A Mixed-Methods Study2014/01/03English32
Great Expectations2011/06/01English32
The Patient Experience with Soft Tissue Sarcoma: A Systematic Review of the Literature2016/10/15English31
Analysis of Health-Related Quality-of-Life Instruments Measuring the Impact of Bariatric Surgery2011/06/01English31
Painful Diabetic Peripheral Neuropathy: Results of a Survey Characterizing the Perspectives and Misperceptions of Patients and Healthcare Practitioners2013/11/22English31
Parent Empowerment in Pediatric Healthcare Settings: A Systematic Review of Observational Studies2018/10/17English31
Trust and Safe Spaces: Mental Health Consumers’ and Carers’ Relationships with Community Pharmacy Staff2013/10/30English30
Factors in Patient Empowerment: A Survey of an Online Patient Research Network2016/05/07English30
Validity and Reliability of a Novel Multimodal Questionnaire for the Assessment of Abdominal Symptoms in People with Cystic Fibrosis (CFAbd-Score)2019/03/18English30
Novel Statistical Approach to Determine Inflammatory Bowel Disease: Patients’ Perspectives on Shared Decision Making2015/05/12English29
A Systematic Review of Discrete-Choice Experiments and Conjoint Analysis Studies in People with Multiple Sclerosis2018/01/08English29
Patient and Family Advisory Councils (PFACs): Identifying Challenges and Solutions to Support Engagement in Research2018/02/01English29
Eliciting Preferences for HIV Prevention Technologies: A Systematic Review2020/12/15English29
The Use of Patient-Reported Outcome Measures in Rare Diseases and Implications for Health Technology Assessment2021/01/19English29
How Much Time Do Patients Spend on Outpatient Visits?2008/07/01English29
Psychometric Evaluation of the Cushing’s Quality-of-Life Questionnaire2013/04/11English29
Public and Patient Involvement at the UK National Institute for Health and Clinical Excellence2011/01/01English29
Towards Patient-Centered Care for Depression2010/09/01English29
Patient Preferences for Injectable Treatments for Multiple Sclerosis in the United States: A Discrete-Choice Experiment2015/08/11English29
Walking Speed and Health‐Related Quality of Life in Multiple Sclerosis2013/09/28English28
A Head-to-Head Comparison of the EQ-5D-5L and AQoL-8D Multi-Attribute Utility Instruments in Patients Who Have Previously Undergone Bariatric Surgery2016/02/03English28
The Shared Decision-Making Process in the Pharmacological Management of Depression2019/09/23English28
A Qualitative Research for Defining Meaningful Attributes for the Treatment of Inflammatory Bowel Disease from the Patient Perspective2020/01/30English28
Measuring Preferences for Colorectal Cancer Screening2010/06/01English28
Is Shared Decision Making a Utopian Dream or an Achievable Goal?2015/02/14English28