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

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

Overview

This project focuses on a health care information review for patients living with HIV to improve their patient outcomes and fight stigmatization (Villanueva Baselga, 2020). nutritionist notes, the notes from nurses providing care, the patient surveys, discharge data, the referral information, medication list, and the laboratory results. The labs will be particularly important in assessing the immunologic and virologic efficacy of antiretroviral therapy. In addition, the lab data will be key in monitoring any abnormalities connected with the antiretroviral drugs. The patient survey data will be key in knowing the patient’s opinions and attitudes as the care team continues to modify and align the care activities to suit the individual and community needs. These data will be used to improve the quality of care delivered to HIV patients by making individual plans depending on how the patients respond to the medication. Opinions and attitudes will be key in helping the organizations come up with education material and content to educate the patients on overcoming issues such as stigma.

Key Study Components

• 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.