Patient-Patient Centered Outcomes Research

Papers
(The H4-Index of Patient-Patient Centered Outcomes Research is 15. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-05-01 to 2025-05-01.)
ArticleCitations
Dealing with Discontinuity in Cancer Care Trajectories: Patients’ Solutions87
Prosocial Behaviour and Antibiotic Resistance: Evidence from a Discrete Choice Experiment51
Exploring the Preferences of the Australian Public for Antibiotic Treatments: A Discrete Choice Experiment30
Development of Patient and Caregiver Conceptual Models Investigating the Health-Related Quality of Life Impacts of Malignant Pleural Mesothelioma24
Fighting to Breathe and Fighting for Health-Related Quality of Life: Measuring the Impact of Being Dependent on Technology for Breathing on the Child and Their Caregiver22
Preferences of Patients with Amyotrophic Lateral Sclerosis for Intrathecal Drug Delivery: Choosing between an Implanted Drug-Delivery Device and Therapeutic Lumbar Puncture22
Patient-Reported Experience and Outcome Measures in People Living with Diabetes: A Scoping Review of Instruments22
Perspectives of Pediatric Rheumatologists on Initiating and Tapering Biologics in Patients with Juvenile Idiopathic Arthritis: A Formative Qualitative Study22
Acknowledgement to Referees21
Developing a Conceptual Framework for Socioeconomic Impact Research in European Cancer Patients: A ‘Best-Fit’ Framework Synthesis18
15th Meeting of the International Academy of Health Preference Research18
Gauging Incentive Values and Expectations (G.I.V.E.) among Blood Donors for Nonmonetary Incentives: Developing a Preference Elicitation Instrument through Qualitative Approaches in Shandong, China17
Adaptation of a Shared Decision-Making Tool for Early Rheumatoid Arthritis Treatment Decisions with Indigenous Patients17
A Standard Set of Value-Based Patient-Centered Outcomes and Measures of Overall Health in Adults16
Adverse Event Reporting in Cancer Clinical Trials: Incorporating Patient-Reported Methods. A Systematic Scoping Review16
Designing HIV Testing and Self-Testing Services for Young People in Nigeria: A Discrete Choice Experiment15
Patient and Public Preferences for Coordinated Care in Switzerland: Development of a Discrete Choice Experiment15
What Matters for Evaluating the Quality of Mental Healthcare? Identifying Important Aspects in Qualitative Focus Groups with Service Users and Frontline Mental Health Professionals15
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