BHA-FPX4106 Assessment 4: Summary Report: Health Care information Review Overview

• Data Collection Plan— Data will be obtained from the electronic health records and AHRQ. The staff collecting data must have minimum qualifications, such as a minimum of an undergraduate degree in nursing and two-year clinical experience.
• Data Security Plan—Data collection is to be carried out by trustworthy individuals and with high integrity. Informed consent will be obtained before using the data. The data will be encrypted, and only authorized individuals will have access and passwords to decrypt.
• Benchmarking Plan— Data will only be collected by qualified individuals to meet the requirements. Automation will be done to help meet the standards of interoperability with HIE.
• Quality and Change Management Strategies—Evidence-based strategies of change and quality management will be applied. These methods are to be obtained from the literature.

Conclusion

 This project aims to benefit patients living with HIV. It has been evident that patients living with HIV face stigmatization and  have issues with medication adherence. All of these result in poor outcomes. Therefore, through this comprehensive data retrieval and review, the proposed study will come up with appropriate strategies for reducing stigmatization and improving medication adherence to improve patient outcomes. As such, the quality of patient care delivered by the physician groups will improve through the integration of various educational efforts and patient individualized care plans.

References

Villanueva Baselga, S. (2020). Interactive documentaries and health: Combating HIV-related stigma and cultural trauma. Catalan Journal of Communication & Cultural Studies, 12(2), 273-285. https://doi.org/10.1386/cjcs_00032_1.