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Essay on health literacy
Essay on health literacy
Importance of communication in health education
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part to play as well, however it must be integrated with other program areas to achieve the anticipated results.
Strategies for the improvement of health literacy are vital tools of empowerment showing huge potential in the reduction of health inequalities. Take into consideration that people suffering from the condition of limited health literacy have produced the worst health outcomes. Health literacy has larger role to play in affecting the health outcomes among individuals with lower education as compared to those with higher education. Measures and steps to improve health literacy have been revealed to impact various health outcomes such as: disease reduction, making depression more severe, improving availability of health information and bettering health behaviors.
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problem is not fully solved implying further research should be conducted specially to address the following concerns. Further research will assist in determining how improving the health literacy of the culturally diverse and minority groups and bettering the health and social care services can positively impact public health outcomes on a long term. It will assist in determining the most ideal measures to take in order to better health literacy of the vulnerable populations and improve the healthcare quality and public healthcare systems. Additionally, it will play a significant role in determining how cost effective the health literacy initiatives are (In Zerwekh & In Garneau, 2014). The notion of enhancing health literacy to improve health outcomes and promote health equity is rapidly growing. Health literacy plays an important role in shaping the health outcomes among disadvantaged groups such as individuals with lower education levels. A recent review upheld that vulnerable groups stand higher chances of benefitting from shared decision making initiatives than learned groups of people. Increasing health literacy therefore shows great potential to promote health equality (In Zerwekh & In Garneau, 2014). Evidence oriented measures aimed at addressing the issue of health literacy are arising from the grounds of health communication processes, health care and population health. This has seen the simplification and improvement of written material, and usage of other targeted tactics to patient education and bettering patient-healthcare provider communication. Interventions are taking place in various forms and have led to positive outcomes, showing that the issue of health literacy can be addressed effectively. In relation to health information technology and health communication strategies, below is a health literacy action plan that encompasses some proposed solutions to improve health literacy and eventually the quality of health care as well. o Promoting interoperability This relates with the ability to share and reliably apply health information across health care settings, and systems which is a requisite in the attainment of electronically based quality improvement. o Reinforcing privacy and health information security Maintaining public trust is vital; hence individual’s medical information should be protected at whatever costs.
Health care and health care information are turning to become unity and are working together to facilitate improvement of health care quality and equity. Therefore, health providers and other relevant stakeholders must strive to put in place strong measures capable of effecting heightened privacy and security precautions. More transparency must also be ensured when medical care organizations and institutions are handling patient’s medical data.
o Providing support for the National Quality Strategy
Health information technology must be used as the powerful tool it is to attain the ultimate goal of generating improved healthcare quality and public health outcomes. The NQS outlines objectives and concerns for improving health equality and health care quality the same way. It implies that the quality improvement being enabled through health information technology will support the goals envisioned by the NQS (Taylor, 2015).
o Reinforcing the existing health information technology
infrastructure More investments need to be directed towards health information technology to facilitate a wider embracement of certified health IT infrastructure. This should involve bridging the gaps and redesigning the necessary standards for sharing, seizing and applying health care information for quality improvement activities. These encompass, quality assessments and evaluation, public health and new payment frameworks and decision support (In Zerwekh & In Garneau, 2014). o Empowering the quality ecosystem entirely Health information should be collected, shared and used specially for quality improvement. This will match the ideal information with the appropriate individuals and the time they need to use it. Many people will benefit from data availability and accessibility and greater transparency. They encompass, health care providers, patients, researchers, policy makers and payers. New analytical tools can be applied as well as decision support resources purposely for informing the decision making process which, will enable better management of health care systems (Postal & Armstrong, 2013). o Capturing once and replication There should be user centered health information technology systems such that healthcare providers can seize all necessary information in a structured manner during the delivery of healthcare services. Such data is helpful in monitoring the progress of patients and their health needs. Furthermore, this data can also be harnessed, collected, and evaluated to facilitate decision support, quality assessment and reporting, public health management, population health outcomes and research. These efficiencies stand to minimize costs for stakeholders in the healthcare sector. o Supporting all levels of health information technology sophistication Various health care settings may require differing quality improvement to support their functionality. Health care providers with similar health information needs should device ways of working their quality improvements to their advantage. o Increasing flexibility through modularity Due to complexity of the health care systems, there is high resistance to change. This should present choice in case they are subdivided into independent mechanisms capable of being linked together. We should consider the changes occurring to health care delivery and healthcare technologies as time passes, therefore quality ecosystems potential to evolve must be preserved to enable us benefit from the advances in technology and research advancements in healthcare delivery. The purpose of modularity is to stimulate flexibility to create room for innovation and adopting new and more effective approaches without disrupting the entire healthcare system. However, it is our role to ensure that modularity does not present further complications (In Zerwekh & In Garneau, 2014). o Aligning and simplification Many government and private information collections and reporting needs are meant for quality improvement of clinical programs. Persistent efforts towards alignment and simplification of these needs can reduce the burden arising from collecting and reporting while leveraging information replication capabilities of health information technology. This implies that specially focusing on improving data needs is fundamental to promote embracement in the market (Taylor, 2015).
...). Privacy and Health Information Technology. Journal of Law Medicine, 37(2), 121-149. Retrieved January 28, 2011 from CINAHL database
The reporting party (RP) stated her son Michael Girard DOB: 2/13/68 is a resident living in the facility. The RP disclosed the facility does not provide meals that meet the recommended dietary allowance. An example of breakfast would be two donuts and a glass of milk; one hard-boiled egg. The residents were served hot dogs and can soup. The residents are not provided fresh fruits or vegetables. The residents are sent to their rooms at 6PM and receive cookies and soda as a snack. According to the RP the residents don't have access to the food. All the food is locked up and a resident named Dale has the only key. The residents do not have access to the microwave oven to warm their food. Additionally the residents have no access to the television and are forced to watch CNN or programs preferred by the caregivers.
The safety department for the company advertises the slogan “SAFTEY FIRST, EVERY TASK, EVERY DAY” to promote a safe work environment.
I will be sentencing Andrew Medina as a youth. The Charges I will be giving Andrew Medina is Intensive Rehabilitation Custody and Supervision for 3 years, Intensive Support and Supervision Program for 3 years, Probation for 1 year and 100 hours of community service within one year. I believe after he finishes these charges he will be reintegrate and rehabilitated. During Andrews time at Intensive Rehabilitation Custody and Supervision he will be taking regular classes as if he is a normal child to help him rehabilitate. After he is done his time in Custody he will go on to do Intensive Support and Supervision Program for 3 years to help him. He will talk to his Supervisor every other day for a month and then get less and less time with him
. HIPAA privacy rules are complicated and extensive, and set forth guidelines to be followed by health care providers and other covered entities such as insurance carriers and by consumers. HIPAA is very specific in its requirements regarding the release of information, but is not as specific when it comes to the manner in which training and policies are developed and delivered within the health care industry. This paper will discuss how HIPAA affects a patient's access to their medical records, how and under what circumstances personal health information can be released to other entities for purposes not related to health care, the requirements regarding written privacy policies for covered entities, the training requirements for medical office employees and the consequences for not following the policy.
The guidance explains and clarifies key provisions of the medical privacy regulation, which was published last December (HIPAA, 1996). Guaranteeing the accuracy, security, and protection of the privacy of all medical information is crucial and an ongoing challenge for many organizations. References American Medical Association (2005). Retrieved December 7, 2008, from http://www.ad http://www.ama-assn.org/.
Many new technologies are being used in health organizations across the nations, which are being utilized to help improve the quality of health care. Electronic Health Records (EHRs) play a critical role in improving access, quality and efficiency of healthcare ("Electronic health records," 2014). In order to assist in expanding the use of EHR’s, in 2011 The Centers for Medicaid and Medicare Services (CMS), instituted a EHR incentive program called the Meaningful use Program. This program was instituted to encourage and expand the use of the HER, by providing health professional and health organizations yearly incentive payments when they demonstrate meaningful use of the EHR ("Medicare and medicaid," 2014). The Meaningful use program will be explored including its’ implications for nurses, nursing, national policy, how the population health data relates to Meaningful use data collection in various stages and finally recommendations for beneficial improvement for patient outcomes and population health and more.
With today's use of electronic medical records software, information discussed in confidence with your doctor(s) will be recorded into electronic data files. The obvious concern is the potential for your records to be seen by hundreds of strangers who work in health care, the insurance industry, and a host of businesses associated with medical organizations. Fortunately, this catastrophic scenario will likely be avoided. Congress addressed growing public concern about privacy and security of personal health data, and in 1996 passed “The Health Insurance Portability and Accountability Act” (HIPAA). HIPAA sets the national standard for electronic transfers of health data.
1. Download the Occupational Health and Safety Act 2004 via the BlackBoard. Read the sections, and briefly explain what each of the following parts of the act refer to:
J&J understands that community is important due to the 60 countries in which it conducts business. J&J has a corporate social responsibility to protect all individuals and must strive to be actively involved in the community. In J&J’s Credo they state, “We are responsible to the communities in which we live and work and to the world community as well. We must encourage civic improvements and better health and education” (2014 Citizenship & Sustainability Report 121). J&J strives to meet this goal through research and testing of their products and through programs such as Social Impact through Procurement, Bridge to Employment, Sight for Kids, Volunteer Support, Stop Hunger Now and Safe Kids.
Hernandez, Lyla M. “Health Literacy, eHealth, and Communication: Putting the Consumer First: Workshop Summary.” Washington, D.C. : National Academies Press, 2009. ebrary. Web. 27 October 2011.
1.2. Compare Buyer behavior and decision making process in different situation (P 1.2) ......... 4
However, health literacy is more than just read and write; it is the ability to understand and able to use health information to make choices about their health (Benyon, 2014). Low health literacy can have detrimental effect on the health of the client because it may cause misunderstand of the medical label or health information. According to McMurray & Clendon (2015), health literacy divided into three different levels which are functional, interactive/communicative and critical health literacy. As for functional levels, it is the most general and fundamental level for the general public because individuals need to receive and understand the information of health such as risk of health decision, consent forms, health instruction or medicine labels. (McMurray & Clendo , 2015) Turning to the next level, interactive/communicative health literacy, mainly involved personal skills to spread health knowledge to the community, and also , people are able to influence social norm and help others individuals to develop their personal health capacity. Because of this, understanding of how organization work and resounding communication skill which can help to support others and knowing how to get different health services other individuals need (McMurray & Clendo , 2015). The third level is critical health literacy, mainly divided to
Health literacy is a term not widely understood by the general population. It is defined as “the degree to which individuals have the capacity to obtain, process and understand basic health information needed to make appropriate health decisions and services needed to prevent or treat illness,” (About health literacy, 2014). A person’s level of health literacy is based on their age, education level, socioeconomic standing, and cultural background. Patients with low health literacy have a more difficult time navigating the health care system. According to the U.S. Department of Health and Human Services, this group of patients may find it harder to find medical services and health care providers, fill out health forms, provide their complete medical history with their providers, seek preventative care, understand the health risks associated with some behaviors, taking care of chronic health conditions, and understanding how to take prescribed medications (About health literacy, 2014). It is to a certain extent the patient’s responsibility to increase their own health literacy knowledge. But to what extent can they learn on their own? Those working in the health field have been trained to navigate the health system and understand the medical terms. They have the knowledge and capability to pass on that understanding to their patients. Health care professionals have a shared responsibility to help improve patients’ health literacy.
The Health Insurance Portability and Accountability Act (HIPAA), Patient Safety and Quality Improvement Act (PSQIA), Confidential Information and Statistical Efficiency Act (CIPSEA), and the Freedom of Information Act all provide legal protection under many laws. It also involves ethical protection. The patient must be able to completely trust the healthcare provider by having confidence that their information is kept safe and not disclosed without their consent. Disclosing any information to the public could be humiliating for them. Patient information that is protected includes all medical and personal information related to their medical records, medical treatments, payment records, date of birth, gender, and