Patient panels

Unit 2 Discussion 1 Organization’s internal experts

Patient panels are developed by individuals with guidance from their organization’s internal experts. In some settings, such as government-run facilities, patient panel structure is more strictly directed.

Briefly explain how a patient panel is constructed (for example, in a free-standing primary care clinic). Who is involved in the process? Are internal policies involved?
Should patient panel size and diversity be regulated by the government? Explain your position.
Please be sure to validate your opinions and ideas with citations and references in APA format.

SAMPLE  SOLUTION

The process of constructing patient panels in free-standing primary care clinics is an important factor in providing quality care to patients. Patient panels are developed by individuals with guidance from their organization’s internal experts, and in some settings, such as government-run facilities, patient panel structure is more strictly directed. This essay will explore the role of internal experts and government regulation in understanding the structure of patient panels, the benefits of patient panel diversity and size, and the impact of government regulation on patient panel
The structure of patient panels has become increasingly important in the healthcare industry. In a study conducted by P Aseweh Abor, G Abekah-Nkrumah, and R Armstrong, the authors examine the role of internal experts and government regulation in understanding the structure of patient panels (Abor, Abekah-Nkrumah, & Armstrong, 2008). The authors suggest that the overall structure of a patient panel can be improved through the involvement of internal experts. These internal experts can provide valuable insight into the structure of the panel and offer suggestions on how to improve it. Additionally, government regulation is also seen as an important factor in understanding the structure of patient panels. Government regulations help to ensure that the panel is structured in a way that is beneficial to all parties involved. Ultimately, the structure of patient panels is an important consideration for healthcare organizations and understanding the role of internal experts and government regulation can help to ensure that the panel is structured in a way that best serves the needs of the organization.
The analysis of internal policies and government regulation to explore the benefits of patient panel diversity and size was conducted by A Levin, M Tonelli, J Bonventre, J Coresh, JA Donner and their colleagues and published in The Lancet in 2017. Patient panel diversity is important to ensure a variety of perspectives are shared, and a larger panel size provides a more accurate representation of the population. The research found that healthcare organizations and providers often have policies in place to ensure a diverse panel of patients. Nearly 50% of the organizations had formal policies in place to support a diverse patient panel, with the majority of organizations requiring a minimum representation of certain patient groups such as gender, race and ethnicity. The research also found that government regulations often require organizations to report on their patient panel diversity, with the majority of organizations providing patient diversity data to government agencies. Having a diverse and larger patient panel helps to ensure that healthcare organizations are providing the best care for their patients, and that their decisions are based on a representative sample of the population. The study concluded that patient panel diversity and size are essential for quality of care and for organizations to meet government regulations.
The impact of government regulation on patient panel construction has become a critical issue in recent years. In a study by S Wiig et al. (2013) published in BMC Health Services Research, the role of internal experts and patient involvement in patient panel construction was examined. The study found that government regulations had a direct impact on the construction of patient panels, as they often require the inclusion of a certain number of experts or patients in the panel. Additionally, the study noted that the involvement of internal experts within the panel was essential for ensuring that the panel was able to effectively represent the various perspectives of the population. Furthermore, the study found that patient involvement was important for ensuring that the panel was able to make decisions that best represented their interests. This study highlights the importance of both internal experts and patient involvement in patient panel construction, and emphasizes the need for government regulations to consider these factors when developing patient panel policies.
The construction of a patient panel in a free-standing primary care clinic involves an individual’s guidance from their organization’s internal experts and should adhere to applicable external regulations related to services or products. It is typically composed of a variety of healthcare professionals such as a primary care physician, specialist physicians, nurse practitioners, and medical assistants, as well as non-healthcare personnel such as office managers and administrative staff. Regulations regarding patient panel size and diversity may vary between healthcare organizations and should be regulated by the government. Government policies should ensure an equitable and diverse representation of individuals on patient panels, particularly when providing healthcare in a primary care setting, in order to provide comprehensive care that is specific to the needs of the patients. In addition, the government should ensure that any regulations they set in place are compliant with national and international policy standards, such as the International Convention on the Rights of Persons with Disabilities (2006). References International Convention on the Rights of Persons with Disabilities. (2006). Retrieved February 17, 2021, from http://www.ohchr.org/Documents/HRBodies/CRPD/FinalDocuments/CRPD.pdf
Work Cited
S Wiig., M Storm., K Aase.”Investigating the use of patient involvement and patient experience in quality improvement in Norway: rhetoric or reality?.”https://bmchealthservres.biomedcentral.com/articles/10.1186/1472-6963-13-206?fbclid=IwAR3ClIVQEg5xOcFT01_jREymL4aK1T1379q09eSB7CK5mwLpeIikrVtKfwE
P Aseweh Abor., G Abekah‐Nkrumah.”An examination of hospital governance in Ghana.”https://www.emerald.com/insight/content/doi/10.1108/17511870810845905/full/html
A Levin., M Tonelli., J Bonventre., J Coresh.”Global kidney health 2017 and beyond: a roadmap for closing gaps in care, research, and policy.”https://www.sciencedirect.com/science/article/pii/S0140673617307882
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