Argumentative Essay On Hippa

HIPPA is the law to protect health information communicated in any manner. It states the privacy and security regulations on the rights and standards of the patient. It also defined the penalties for those who fail to protect the individual’s identifiable health information. The information on patient’s name, diagnosis, important activities for the shift and room number are all included in the HIPPA privacy rule. HIPPA privacy rule part § 162.1002 Medical data code sets. (i) Prevention. (ii) Diagnosis. (iii) Treatment. (iv)

The Health Insurance Portability and Accountability Act (HIPAA) is a set of national standards created for the protection of health information; it is also known as a “Privacy Rule”. This rule was employed in 1996 by the US Department of Health and Human Services (DHHS) to address the use and disclosure of an individual’s health information as well as the standards for the individual’s privacy rights to understand and control the manner in which their information is used.

In 1996, the HIPPA act was passed. Health Insurance Portability and Accountability Act (HIPAA), which was directed to improve the areas in the health field. For instance, lowering the number of errors and mistreatment, for individuals to have the access to transfer health coverage according to their present situation, and most importantly it monitors security and confidentiality information to ensure its being controlled in an accurate manner. This act gives congress ability to govern financial matter such as, federal level funding processes pertaining to different health documentation. Providing quality care while protecting patient’s information is a priority controlled under HIPAA, which accepts collaboration with all state and federal

When you go to the hospital you always fill some papers at firs and this is related to HIPAA.

What are HIPAA rights? Knowing your rights can be useful. It’s important to know them so that if you ever feel like something isn’t correct, you know how you can act on it. One of your rights as a healthcare consumer is that you can ask to request or see a copy of your medical records or any other health information at any time (hhs.gov/cosumer rights). You are also allowed to change or correct any information in your files that you believe are wrong. This means that if there is something in your file, like a test result that you disagree on, even if the hospital doesn’t, they have to make note of that in your file. You can also see who has accessed and seen your health information. It is your right to ask for your information to not to be shared with certain doctors, nurses, or certain individuals or organizations (hhs.gov/cosumer rights). HIPAA also allows you to allow someone to speak on your behalf. If

HIPPA is a rule that helps protects a patient’s privacy when it comes to their health or medical information. It is also known as a security rule that helps in protecting electronic health information as well. As in the health care patient safety and confidentiality is an important rule to follow at all times. A standard of HIPPA is privacy. When it comes to privacy it is meant by protecting a patient’s medical information in any form needs to be controlled at all times. It is a rule that is balanced and used to protect the disclosure of the patient’s health information that is needed for patient care and treatment. It is important that any person working in the health care setting is aware of this rule as it is important to follow when

Consent and authorization are treated differently when it comes to the privacy rule. Consent gives doctors who directly care for the patient permission to use and disclose protected health information (PHI), for the purposes of treating the patient. Authorization on the other hand, is more specific to the procedure or treatment being performed at the time and has an expiration date. An authorization is needed to disclose PHI to employers for employment decisions or to insurance companies to determine eligibility for life insurance. So, giving consent for treatment does not give a health care entity permission to disclose PHI to unauthorized third parties.

The basic purpose of HIPAA is maintaining the privacy of a patience’s information and a protection of their rights. Keep in mind that doctors gain a great deal of knowledge about their patience that they could openly share, rather unethically, for research purposes, gossip, and other unkind reasons. HIPAA made it illegal to do that which was a practice for many years. With the proliferation of copiers, medical personal would copy patient information and let it sit around the office. Also, the information would be copied and given to other interested parties preventing people to get jobs or other benefits. A key point in all of this is health insurance.

HIPAA also known as the Health Insurance Portability and Accountability Act was passed by congress and signed by President Bill Clinton on August 21, 1966. HIPAA includes several provisions and is the United States legislation that protects the privacy and security of patients’ medical health information and records. This Act contains five different sections that addressed different aspects of healthcare. Section one protects individuals’ healthcare coverage that have lost or changed jobs, as well as prohibiting discrimination due to pre-existing conditions. Section two was anticipated to combat fraud, waste and abuse by establishing national standards that remained in compliance with privacy regulations. Section three includes making sure that the Internal Revenue Code (IRC) provides tax

In this paper, I will discuss the principles that permit disclosure of protected health information with or without the patient’s consent for each of the four categories, government agencies, legal agencies or representatives and research groups. I will also state whether I feel privacy safeguards are adequate to support those principles.

But when those involved in these legitimate activities make demands that seem inappropriate, the records must be protected. Disclosure of personal medical information should also be subject to patients’ or families’ consent (Richmond et al. 2009).

Health Insurance Portability and Accountability Act or HIPAA is a statute endorsed by the U.S. Congress in 1996. It offers protections for many American workers which improves portability and continuity of health insurance coverage. The seven titles of the final law are Title I - Health care Access , Portability, Title II - Preventing Health Care Fraud and Abuse; administrative simplification; Medical Liability Reform; Title III – Tax-related Health Provisions; Title IV – Application and

Using the Foundation of Knowledge Model, I would explain to the vice-president that knowledge acquisition, which occurs through education and research, occurred in our department during a morning huddle, where HIPPA standards were first introduced to members of our department (McGonigle & Mastrian, 2012). Through an introduction of what HIPPA meant for healthcare providers, staff learned that HIPPA meant confidentiality of protected health information (“Health insurance,” 2013). This meant staff were to only access patient information for patients they were taking care of and they needed to be cautious with whom and where patient information was discussed. All staff were required to complete a learning module and pass the module and

HIPAA as we have all learned by now stands for the Health Insurance Portability and Accountability Act. HIPAA mandates providers and contractors to use approved standardized code sets so as to ensure the ebb and flow of our health care system can continue to improve and become more efficient. Let's look at it another way. You have hundreds of thousands of medical facilities all coding their bills. Imagine if they all did things differently and all used different code sets how much harder it would be for insurance companies to pay out in a timely manner.

Knowing the difference between privacy and confidentiality can be confusing. Privacy is the right of individuals to keep information about themselves from being disclosed; that is, people (our patients) are in control of others access to themselves or information about themselves. Patients decide who, when, and where to