Scope and range—Accessibility |
Allow reporting in real time and after the event, including after an extended period of time. Allow access to system at multiple points so that reporters can update their account of the event. |
Facilitate access for diverse reporters (e.g., lower literacy, non-English speakers) and allow patient, family members, caregivers, and others who witness an event to report. |
Scope and range—Anonymity and confidentiality |
Mixed opinions about allowing anonymous reporting. Anonymity allows reporter to feel safer but precludes follow-up and investigation. |
Acceptability of anonymous reporting is linked to goals of system; anonymous reporting acceptable if goal is to accumulate data for future action but not workable if goal is to take action. |
System should protect the identity of users and assure them of confidentiality. |
Scope and range—Voluntary vs. mandatory reporting |
System should be voluntary. |
Levels of Operation |
Most stakeholders favor a multilevel system in which reports "roll up" from the local level to State, regional, or national levels. |
Opinions about levels of operation linked to goals of system. Local-level reporting important to provide immediate feedback to health care facility and institute rapid change. Higher-level reporting important for accountability and system-wide learning. |
Consumer advocates favored a reporting system outside the health care institutions, where consumers feel safe. |
Some stakeholders suggested the reporting system be implemented in stages or tested in pilot programs. |
Organizations suitable to operate consumer reporting systems |
Many stakeholders favored Federal government agencies and private/independent/nonprofit organizations. Advantages of government are neutrality and authority; disadvantages are potential to become politicized and government inefficiency. |
Mixed views about hospitals and health care institutions; have experience collecting patient safety data and will be more readily accepted by providers; consumer advocates opposed because not a safe place for consumers to report, and institutions can skew data. |
Little support for consumer advocacy organizations because would be challenging to get buy-in from health care professionals. |
Primary factors to consider: independence/neutrality/transparency, consumer involvement, authority, and ability to investigate. |
Operational approach |
Staff needed to serve as patient advocates, aid in reporting, triage reports, and conduct investigations; skilled analytic staff also needed. |
Divided opinions about whether system should be federally funded or funded by health care organizations. |
Some stakeholders suggested implementing the reporting system in stages or testing it in pilot programs. |
System Infrastructure and design |
Offer multiple reporting modalities and allow both structured and unstructured reports. |
Provide meaningful and timely feedback to reporters. |
Purpose and goals |
Primary goals are organizational-level and system-wide learning and improving quality of care/patient safety (closely linked); also support for consumer empowerment. |
Less support for accountability as goal, which would duplicate existing organizations and mechanisms; also focus on punishment could undermine trust and partnership needed for effective system. |
Linkages to quality improvement |
Stakeholders generally supported linking to existing efforts to improve quality and patient safety. They did not suggest linking to programs that offer financial incentives for quality (pay-for-performance models) or providing feedback to health care facilities or providers. |
Maximizing reporting |
Communication efforts needed in health care institutions (e.g., at intake) and public information campaigns; also work through trusted community organizations and employers. |
Communication about system should convey importance of consumer reporting to improve patient safety. |
Data
- Data Infographics
- Data Visualizations
- Data Tools
- Data Innovations
- All-Payer Claims Database
- Healthcare Cost and Utilization Project (HCUP)
- Medical Expenditure Panel Survey (MEPS)
- AHRQ Quality Indicator Tools for Data Analytics
- MONAHRQ
- State Snapshots
- United States Health Information Knowledgebase (USHIK)
- Data Sources Available from AHRQ
Patient Safety
- Patient Safety Research Summaries
- Patient Safety Resources by Setting
- Quality Measures
-
Reports
- Advances in Patient Safety: From Research to Implementation
- Advances in Patient Safety: New Directions and Alternative Approaches
- Advancing Patient Safety: A Decade of Evidence, Design, and Implementation
- AHRQ-Funded Patient Safety Research Featured in Health Affairs
- Health Care Safety Hotline
- Medical Liability
- National Academy of Medicine Reports
- National Action Plans
- Papers on Diagnostic Safety Topics
- PSNet
- Engaging Patients and Families
- About AHRQ's Quality & Patient Safety Work
- Patient Safety News and Events
- Education & Training
- Resources
Designing Consumer Reporting Systems for Patient Safety Events
Table 2. Key features of ideal consumer reporting systems from stakeholder interviews
Table of Contents
- Designing Consumer Reporting Systems for Patient Safety Events
- Executive Summary
- Chapter 1. Background
- Chapter 2. Conceptual Framework and Design
- Chapter 3. Description of Methods
- Chapter 4. Results and Key Findings
- Chapter 5
- Chapter 6. Discussion and Policy Implications
- Chapter 7. References
- Appendix A. Members of the Technical Expert Panel
- Appendix B. Peer Reviewers
- List of Tables and Exhibits
Publication: 11-0060-EF
Page last reviewed August 2022
Page originally created September 2012
Internet Citation: Table 2. Key features of ideal consumer reporting systems from stakeholder interviews. Content last reviewed August 2022. Agency for Healthcare Research and Quality, Rockville, MD.
https://www.ahrq.gov/patient-safety/patients-families/consumer-exp/reporting/table2.html
