HIPAA Training: Privacy Review and Audit Survival Guidebenefitexpress
HIPAA Privacy Overview for Employers. Review a helpful checklist of requirements an employer must adopt to stay compliant with HIPAA and to survive an audit by Health and Human Services (HHS).
Health Care delivery system is the skeleton of meeting healthcare needs of enormous population of every country.
In order to have a clear view of community medicine, it is essential to know about different health care systems in order to fulfill learning objectives of students.
Synthesis Report of Health Information Systems in IndiaHFG Project
Resource Type: Report
Authors: Michael P. Rodriguez, Gajinder Pal Singh and Jim Setzer
Published: May 31, 2014
Resource Description:
A highly functioning national health information system (HIS) facilitates transparent and evidence-based decision making that ultimately leads to improvements in the health status of a country’s population.1 Rather than reflecting a single structure through which routine health statistics in a country are reported, most country health information systems are made up of multiple sub-systems that may or may not be well-coordinated, potentially collect some of the same information, and typically place the largest burden for reporting on those at the lowest levels of the health system, the primary health care facility staff. All of these characteristics present risks to the ability of the health system to function efficiently and effectively. The Health Metrics Network (HMN) Framework, published in 2008, provides a useful lens for viewing the efforts of the Republic of India to improve the production and availability of health information at all levels of its health system, from health facility to district, state, national and international levels, and to use that information to improve health outcomes.
The objectives of this report are to use the HMN Framework to examine, organize and summarize some of the publicly available written information on the Indian HIS and to serve as a resource tool for stakeholders throughout the Indian health system pursuing efforts to strengthen the HIS. This report is intended to highlight the progress that has been made to date and to discuss some of the gaps in the Indian HIS using the HMN Framework, which can then form the basis of discussions on HIS strengthening priorities.
HIPAA Training: Privacy Review and Audit Survival Guidebenefitexpress
HIPAA Privacy Overview for Employers. Review a helpful checklist of requirements an employer must adopt to stay compliant with HIPAA and to survive an audit by Health and Human Services (HHS).
Health Care delivery system is the skeleton of meeting healthcare needs of enormous population of every country.
In order to have a clear view of community medicine, it is essential to know about different health care systems in order to fulfill learning objectives of students.
Synthesis Report of Health Information Systems in IndiaHFG Project
Resource Type: Report
Authors: Michael P. Rodriguez, Gajinder Pal Singh and Jim Setzer
Published: May 31, 2014
Resource Description:
A highly functioning national health information system (HIS) facilitates transparent and evidence-based decision making that ultimately leads to improvements in the health status of a country’s population.1 Rather than reflecting a single structure through which routine health statistics in a country are reported, most country health information systems are made up of multiple sub-systems that may or may not be well-coordinated, potentially collect some of the same information, and typically place the largest burden for reporting on those at the lowest levels of the health system, the primary health care facility staff. All of these characteristics present risks to the ability of the health system to function efficiently and effectively. The Health Metrics Network (HMN) Framework, published in 2008, provides a useful lens for viewing the efforts of the Republic of India to improve the production and availability of health information at all levels of its health system, from health facility to district, state, national and international levels, and to use that information to improve health outcomes.
The objectives of this report are to use the HMN Framework to examine, organize and summarize some of the publicly available written information on the Indian HIS and to serve as a resource tool for stakeholders throughout the Indian health system pursuing efforts to strengthen the HIS. This report is intended to highlight the progress that has been made to date and to discuss some of the gaps in the Indian HIS using the HMN Framework, which can then form the basis of discussions on HIS strengthening priorities.
Presentation was given by Jim Anfield to Chicago Technology For Value-Based HealthCare (https://www.meetup.com/Chicago-Technology-For-Value-Based-Healthcare-Meetup/).
Chapter 19National Health Insurance& Managed Care.docxwalterl4
Chapter 19
National Health Insurance
& Managed Care
LEARNING OBJECTIVES
• Discuss the purpose and various titles of the
Patient Protection and Affordable Care Act of
2010 (PPACA).
• Discuss the Supreme Court’s ruling on the
constitutionality of the PPACA.
• Describe the common models of managed care
organizations.
• Explain what can happen if a state fails to comply
with the PPACA.
PPACA Purpose
• Increase # of Americans covered by health
insurance
• Decrease cost of insurance
– Make more affordable through shared
responsibility
• Eliminate discriminatory acts
– Exclusion due to pre-existing conditions,
health status, & gender.
PPACA Reforms Health Care – I
• Eliminate lifetime & unreasonable annual limits on
benefits
• Prohibit recessions of health insurance policies
• Assistance for uninsured due to pre-existing
conditions
• Require coverage: preventative services &
immunizations
• Extend dependent coverage up to age 26
PPACA Reforms Health Care - II
• Develop uniform coverage documents so consumers
can make equal insurance comparisons
• Cap insurance company
– nonmedical & administrative expenditures
• Ensure consumers have access to an effective
appeals process
– provide a place to turn for help
• navigating the appeals process & assessing
coverage
Supreme Court 6/28/12
• Agreed that the requirement for nearly all
Americans to buy health insurance.
• Court excised part of law requiring states to
expand their Medicaid coverage in a joint
federal–state effort, to families with incomes
up to 133% of the Federal Poverty Level (FPL).
PPACA Titles
Title I. Quality Affordable Health Care for All
Americans
Title II. The Role of Public Programs
Title III. Improving the Quality and Efficiency of
Health Care
Title IV. Prevention of Chronic Disease and
Improving Public Health
Title V. Health Care Workforce
PPACA Titles – II
Title VI. Transparency and Program Integrity
Title VII. Improving Access to Innovative Medical
Therapies
Title VIII. CLASS Act
Title IX. Revenue Provisions
Title IX. Strengthening Quality, Affordable
Health Care for All Americans
Models of Managed Care
Organizations (MCO’s)
• Health Maintenance Organizations
• Preferred Provider Organizations
• Exclusive Provider Organizations
• Point of Service Plans
• Experience-Rated HMOs
• Specialty HMO’s
• Independent Practice Associations
• Physician Group Practice
Models of MCOs – II
• Group Practice without Walls
• Physician-Hospital Organizations
• Medical Foundations
• Managed Service Organizations
• Vertically Integrated Delivery System
• Horizontal Consolidations
• Federally Qualified
Federally Qualified MCOs
• Strictly Voluntary
• Must Meet Federal Standards
• Less flexibility in
– benefits packages
– setting premium rates
• Must Provide Basic Package of Health Services
State HMO Laws – I
• Specify what types on entities may operate an
MCO.
• Require the provisio.
HIPAA Compliance Made Easy: Conducting a Risk AssessmentConference Panel
Conducting a HIPAA risk assessment is a legal requirement, and this webinar will equip healthcare organizations with the knowledge and tools necessary to fulfill this obligation. By understanding the risks that threaten the confidentiality, integrity, and availability of protected health information, organizations can take proactive measures to mitigate these risks and establish a robust compliance framework.
Attending the "How to Conduct a HIPAA Risk Assessment Webinar" will empower healthcare organizations to embark on a continuous risk assessment process, enabling them to stay informed about evolving threats and ensure ongoing compliance with HIPAA standards and implementation specifications. By embracing the insights and best practices shared in the webinar, organizations can strengthen their security posture and safeguard patient information effectively.
Register,
https://conferencepanel.com/conference/how-to-conduct-a-hipaa-risk-assessment-and-the-surprising-danger-of-not-doing-one
SROA Presentation - Clinical Results of a Medical Error Reduction/Compliance ...edbkline
Clinical results from application of paper-based medical error reduction/compliance program vs software-based MERP program implenented at 30 free-standing radiation oncology centers.
What quality measures does the MCO have in placeSolutionManag.pdfformicreation
What quality measures does the MCO have in place?
Solution
Managed care organizations (MCOs) are responsible for ensuring that persons enrolled in their
plans receive quality health care. In addition, MCOs publicly funded through the Medicare and
Medicaid programs are required by State and Federal governments to meet certain quality
standards.
To fulfill their responsibilities, MCOs need ready access to a comprehensive array of evidence-
based clinical information and other clinical performance measures to enable them to evaluate
their providers\' performance and identify areas where improvement is needed. They also need to
know how their members feel about the care they receive and the way they are treated. Finally,
they need to ensure that both their providers and members are aware of the most recent
preventive care recommendations.
Valid, reliable, and cost-effective measurement tools must be available to make such
determinations, but these tools have not always been available. Furthermore, because the science
of performance measurement is relatively new, additional measures need to be developed and
those that have been developed can be improved. Therefore, to ensure that their enrollees in
MCOs receive high-quality care, MCOs need a reliable source to provide the most current and
scientifically sound tools.
In response to this need, the Agency for Healthcare Research and Quality (AHRQ) has funded
research to compile a database of evidence-based clinical guidelines and to develop clinical
performance measures, member satisfaction surveys, and preventive care recommendations that
can help MCOs meet their responsibilities. Additionally, AHRQ funds research and develops
performance measures and guidelines that MCOs, insurers, providers, and consumers can trust.
This report describes these tools and how they have been used and provides information on
where to learn more about them.
Background
Around one-half of insured Americans are enrolled in some form of managed care. However, as
the number of persons enrolled in MCOs increased in the 1990s, health care purchasers,
policymakers, and other stakeholders became concerned about the potential for health care
quality to diminish. In their view, the policies and practices imposed by MCOs to reduce what
MCOs define as unnecessary care might result in patients not receiving needed care. Therefore,
MCOs faced accreditation systems and other requirements to ensure that patients were receiving
the most appropriate care.
More recently, MCOs have had to address other emerging concerns such as: Rapid introduction
of new technologies, Data showing unexplained variations in the provision of care, Severe cost
pressures.
These factors have provided additional motivation to MCOs to develop systematic ways of
preserving and enhancing health care quality and cost-effectiveness.
Evidence-based practice guidelines and performance measures were developed to help ensure
that patients always receive the most appropri.
India Clinical Trials Market: Industry Size and Growth Trends [2030] Analyzed...Kumar Satyam
According to TechSci Research report, "India Clinical Trials Market- By Region, Competition, Forecast & Opportunities, 2030F," the India Clinical Trials Market was valued at USD 2.05 billion in 2024 and is projected to grow at a compound annual growth rate (CAGR) of 8.64% through 2030. The market is driven by a variety of factors, making India an attractive destination for pharmaceutical companies and researchers. India's vast and diverse patient population, cost-effective operational environment, and a large pool of skilled medical professionals contribute significantly to the market's growth. Additionally, increasing government support in streamlining regulations and the growing prevalence of lifestyle diseases further propel the clinical trials market.
Growing Prevalence of Lifestyle Diseases
The rising incidence of lifestyle diseases such as diabetes, cardiovascular diseases, and cancer is a major trend driving the clinical trials market in India. These conditions necessitate the development and testing of new treatment methods, creating a robust demand for clinical trials. The increasing burden of these diseases highlights the need for innovative therapies and underscores the importance of India as a key player in global clinical research.
One of the most developed cities of India, the city of Chennai is the capital of Tamilnadu and many people from different parts of India come here to earn their bread and butter. Being a metropolitan, the city is filled with towering building and beaches but the sad part as with almost every Indian city
Telehealth Psychology Building Trust with Clients.pptxThe Harvest Clinic
Telehealth psychology is a digital approach that offers psychological services and mental health care to clients remotely, using technologies like video conferencing, phone calls, text messaging, and mobile apps for communication.
Welcome to Secret Tantric, London’s finest VIP Massage agency. Since we first opened our doors, we have provided the ultimate erotic massage experience to innumerable clients, each one searching for the very best sensual massage in London. We come by this reputation honestly with a dynamic team of the city’s most beautiful masseuses.
CRISPR-Cas9, a revolutionary gene-editing tool, holds immense potential to reshape medicine, agriculture, and our understanding of life. But like any powerful tool, it comes with ethical considerations.
Unveiling CRISPR: This naturally occurring bacterial defense system (crRNA & Cas9 protein) fights viruses. Scientists repurposed it for precise gene editing (correction, deletion, insertion) by targeting specific DNA sequences.
The Promise: CRISPR offers exciting possibilities:
Gene Therapy: Correcting genetic diseases like cystic fibrosis.
Agriculture: Engineering crops resistant to pests and harsh environments.
Research: Studying gene function to unlock new knowledge.
The Peril: Ethical concerns demand attention:
Off-target Effects: Unintended DNA edits can have unforeseen consequences.
Eugenics: Misusing CRISPR for designer babies raises social and ethical questions.
Equity: High costs could limit access to this potentially life-saving technology.
The Path Forward: Responsible development is crucial:
International Collaboration: Clear guidelines are needed for research and human trials.
Public Education: Open discussions ensure informed decisions about CRISPR.
Prioritize Safety and Ethics: Safety and ethical principles must be paramount.
CRISPR offers a powerful tool for a better future, but responsible development and addressing ethical concerns are essential. By prioritizing safety, fostering open dialogue, and ensuring equitable access, we can harness CRISPR's power for the benefit of all. (2998 characters)
CHAPTER 1 SEMESTER V PREVENTIVE-PEDIATRICS.pdfSachin Sharma
This content provides an overview of preventive pediatrics. It defines preventive pediatrics as preventing disease and promoting children's physical, mental, and social well-being to achieve positive health. It discusses antenatal, postnatal, and social preventive pediatrics. It also covers various child health programs like immunization, breastfeeding, ICDS, and the roles of organizations like WHO, UNICEF, and nurses in preventive pediatrics.
Antibiotic Stewardship by Anushri Srivastava.pptxAnushriSrivastav
Stewardship is the act of taking good care of something.
Antimicrobial stewardship is a coordinated program that promotes the appropriate use of antimicrobials (including antibiotics), improves patient outcomes, reduces microbial resistance, and decreases the spread of infections caused by multidrug-resistant organisms.
WHO launched the Global Antimicrobial Resistance and Use Surveillance System (GLASS) in 2015 to fill knowledge gaps and inform strategies at all levels.
ACCORDING TO apic.org,
Antimicrobial stewardship is a coordinated program that promotes the appropriate use of antimicrobials (including antibiotics), improves patient outcomes, reduces microbial resistance, and decreases the spread of infections caused by multidrug-resistant organisms.
ACCORDING TO pewtrusts.org,
Antibiotic stewardship refers to efforts in doctors’ offices, hospitals, long term care facilities, and other health care settings to ensure that antibiotics are used only when necessary and appropriate
According to WHO,
Antimicrobial stewardship is a systematic approach to educate and support health care professionals to follow evidence-based guidelines for prescribing and administering antimicrobials
In 1996, John McGowan and Dale Gerding first applied the term antimicrobial stewardship, where they suggested a causal association between antimicrobial agent use and resistance. They also focused on the urgency of large-scale controlled trials of antimicrobial-use regulation employing sophisticated epidemiologic methods, molecular typing, and precise resistance mechanism analysis.
Antimicrobial Stewardship(AMS) refers to the optimal selection, dosing, and duration of antimicrobial treatment resulting in the best clinical outcome with minimal side effects to the patients and minimal impact on subsequent resistance.
According to the 2019 report, in the US, more than 2.8 million antibiotic-resistant infections occur each year, and more than 35000 people die. In addition to this, it also mentioned that 223,900 cases of Clostridoides difficile occurred in 2017, of which 12800 people died. The report did not include viruses or parasites
VISION
Being proactive
Supporting optimal animal and human health
Exploring ways to reduce overall use of antimicrobials
Using the drugs that prevent and treat disease by killing microscopic organisms in a responsible way
GOAL
to prevent the generation and spread of antimicrobial resistance (AMR). Doing so will preserve the effectiveness of these drugs in animals and humans for years to come.
being to preserve human and animal health and the effectiveness of antimicrobial medications.
to implement a multidisciplinary approach in assembling a stewardship team to include an infectious disease physician, a clinical pharmacist with infectious diseases training, infection preventionist, and a close collaboration with the staff in the clinical microbiology laboratory
to prevent antimicrobial overuse, misuse and abuse.
to minimize the developme
Global launch of the Healthy Ageing and Prevention Index 2nd wave – alongside...ILC- UK
The Healthy Ageing and Prevention Index is an online tool created by ILC that ranks countries on six metrics including, life span, health span, work span, income, environmental performance, and happiness. The Index helps us understand how well countries have adapted to longevity and inform decision makers on what must be done to maximise the economic benefits that comes with living well for longer.
Alongside the 77th World Health Assembly in Geneva on 28 May 2024, we launched the second version of our Index, allowing us to track progress and give new insights into what needs to be done to keep populations healthier for longer.
The speakers included:
Professor Orazio Schillaci, Minister of Health, Italy
Dr Hans Groth, Chairman of the Board, World Demographic & Ageing Forum
Professor Ilona Kickbusch, Founder and Chair, Global Health Centre, Geneva Graduate Institute and co-chair, World Health Summit Council
Dr Natasha Azzopardi Muscat, Director, Country Health Policies and Systems Division, World Health Organisation EURO
Dr Marta Lomazzi, Executive Manager, World Federation of Public Health Associations
Dr Shyam Bishen, Head, Centre for Health and Healthcare and Member of the Executive Committee, World Economic Forum
Dr Karin Tegmark Wisell, Director General, Public Health Agency of Sweden
Artificial Intelligence to Optimize Cardiovascular Therapy
Regulating Healthcare - Lecture E
1. Introduction to Health Care
and Public Health in the U.S.
Regulating Health Care
Lecture e
This material (Comp 1 Unit 6) was developed by Oregon Health & Science University, funded by the Department
of Health and Human Services, Office of the National Coordinator for Health Information Technology under
Award Number 90WT0001.
This work is licensed under the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International
License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/.
2. Regulating Health Care
Learning Objectives - 1
• Describe the role of accreditation,
regulatory bodies, and professional
associations in health care in the U.S.
(Lecture a)
• Describe the basic concepts of law in the
United States: the legal system, sources of
law, classification of laws, the court
system, and the trial process. (Lecture b)
2
3. Regulating Health Care
Learning Objectives - 2
• Describe legal aspects of medicine
involving the Affordable Care Act,
professional standards in health care,
medical malpractice, Tort reform, and
Medicare and Medicaid Fraud and Abuse
(Lecture c)
3
4. Regulating Health Care
Learning Objectives - 3
• Describe key components of the Health
Insurance Portability and Accountability Act
(HIPAA) and describe efforts to promote patient
safety in the U.S. (Lecture d)
• Discuss the need for quality clinical
documentation for the use of the health record
as a legal document, communication tool and a
key to prove compliance for health care
organizations. (Lecture e)
4
5. The Health Record
• Summarizes a patient’s health conditions
and care activities
• Historically existed on paper but have
become increasingly digitized
• Serves as a
– Communication and quality enhancement tool
– Legal record of the care provided
5
6. The Health Record as
Tool for Patient Safety
• Providing care based on a full
understanding of a patient’s current and
past conditions is a key element of safe
care
• Information in the health record is
monitored for accuracy and completeness
• The health record is used to manage risk
and improve care
6
7. The Health Record
as a Legal Record
• Considered the business record for a
health care organization
• Also a legal record
– Admissible in a court of law
– Substantiates quality of care provided
7
8. Governance of Health Record
• Federal and State Laws, Regulations, and
Rules
• The Joint Commission and other voluntary
accreditation
• Medical staff bylaws
8
9. Quality Clinical Documentation
for Legal Purposes
• Hand-written documentation
– Illegibility introduces malpractice risk
• Electronic documentation
– Mistakes can be made, but the legibility of
health record content is improved
– More detailed notes
• “What isn’t documented isn’t done”
9
10. Quality Clinical Documentation to
Avoid Fraud and Abuse Accusations
• Clinical documentation improvement
programs support high-quality
documentation
– Train providers
• High-quality documentation supports
accurate coding and reimbursement
• Accurate coding is needed to avert
accusations of fraud and abuse
10
11. OIG Compliance Program Tips - 1
• The Seven Fundamental Elements of an
Effective Compliance Program
1. Implementing written policies, procedures and
standards of conduct
2. Designating a compliance officer and
compliance committee
3. Conducting effective training and education.
4. Developing effective lines of communication
11
12. OIG Compliance Program Tips - 2
• The Seven Fundamental Elements of an
Effective Compliance Program
5. Conducting internal monitoring and auditing
6. Enforcing standards through well-publicized
disciplinary guidelines
7. Responding promptly to detected offenses and
undertaking corrective action
• OIG compliance education videos:
http://oig.hhs.gov/newsroom/video/2011/heat_modules.asp
12
13. Corporate Integrity Agreements - 1
• A comprehensive CIA includes
requirements to:
– Hire a compliance officer/appoint a
compliance committee
– Develop written standards and policies
– Implement a comprehensive employee
training program
– Retain an independent review organization to
conduct annual reviews
13
14. Corporate Integrity Agreements - 2
• A comprehensive CIA includes
requirements to:
– Establish a confidential disclosure program
– Restrict employment of ineligible persons
– Report overpayments, reportable events, and
ongoing investigations/legal proceedings
– Provide an implementation report and annual
reports to OIG on the status of the entity's
compliance activities
14
15. Compliance Beyond
Fraud and Abuse
• HIPAA Privacy and Security Rules
– What is the plan for appropriate release of
PHI?
– How is the tracking of release occurring?
– Who is responsible for breach notification?
– What training is being done?
– Is there a team reviewing policies and
procedures?
15
16. Regulating Health Care
Summary – 1 – Lecture e
• The health record is the business and
legal record for a health care organization
• The health record is the communication
tool for the health care team
• Clinical documentation is used to assure
high quality care of the patient, as well as
to provide information for decision-making,
reimbursement and medical coding
16
17. Regulating Health Care
Summary – 2 – Lecture e
• Thorough and complete clinical documentation
protects health care organization from the risk of
fraud, abuse, and malpractice claims
• Compliance programs are important to assure
correct procedures to follow related to
regulations, rules, laws, accreditation, and
internal policies
• HIPAA privacy and security rules need to be
included in compliance plans
17
18. Regulating Health Care
Summary - 1
• Health Care accrediting and certification
organizations
• The U.S. legal system
• Laws governing health care privacy and
security rules
18
19. Regulating Health Care
Summary - 2
• The clinical documentation in the health
record supports quality health care,
administrative and business operations of
the organization, and provides the basis
for legal proof of care that assures
compliance with laws, rules, and
regulations as well as professional
standards of care
19
20. Regulating Health Care
References – 1 – Lecture e
References
American Health Information Management Association. http://www.ahima.org/topics/ehr.
Accessed January 30, 2017.
American Health Information Management Association. http://www.ahima.org/topics/cdi.
Accessed January 30, 2017.
American Health Information Management Association. http://www.ahima.org/topics/psc.
Accessed January 30, 2017.
Bayes, N., Newby, J, Seggern, J, Valerius J. Medical Insurance An integrated claims
process approach 5th edition, 2012. McGraw Hill Companies: New York
Davis, N. Revenue Cycle Management Best Practices, 2011, AHIMA Press: Chicago
Health Care Compliance Program Tips http://oig.hhs.gov/compliance/provider-
compliance-training/index.asp. Accessed January 30, 2017.
LaTour & Eichenwald, Health Information Management, concepts, Principles, and
Practice, Third Edition, 2010 AHIMA Press: Chicago
20
21. Regulating Health Care
References – 2 – Lecture e
References
Office of the Inspector General.
http://oig.hhs.gov/newsroom/video/2011/heat_modules.asp. Accessed January 30,
2017.
Office of Inspector General. A Roadmap for New Physicians: Avoiding Medicare and
Medicaid Fraud and Abuse. http://oig.hhs.gov/fraud/PhysicianEducation. Accessed
January 30, 2017.
Centers for Medicare and Medicaid. http://www.cms.gov/default.asp. Accessed January
30, 2017.
Corporate integrity agreements. http://oig.hhs.gov/compliance/corporate-integrity-
agreements/index.asp. Accessed January 30, 2017.
21
22. Introduction to Health Care
and Public Health in the U.S.
Regulating Health Care
Lecture e
This material was developed by Oregon
Health & Science University, funded by the
Department of Health and Human Services,
Office of the National Coordinator for Health
Information Technology under Award
Number 90WT0001.
22
Editor's Notes
Welcome to Introduction to Health Care and Public Health in the U.S.: Regulating Health Care. This is lecture e.
The component, Introduction to Health Care and Public Health in the U.S., is a survey of how health care and public health are organized and how services are delivered in the U.S. It covers public policy, relevant organizations and their interrelationships, professional roles, legal and regulatory issues, and payment systems. It also addresses health reform initiatives in the U.S.
The Objectives for Regulating Health Care are to:
Describe the role of accreditation, regulatory bodies, and professional associations in health care in the U.S.
Describe the basic concepts of law in the U.S.: the legal system, sources of law, classification of laws, the court system, and the trial process.
Describe legal aspects of medicine involving the Affordable Care Act, professional standards in health care, medical malpractice, tort reform, and Medicare and Medicaid fraud and abuse.
Describe key components of the Health Insurance Portability and Accountability Act, or HIPAA, and current issues concerning privacy and patient safety in the U.S.
And, discuss the need for quality clinical documentation for use of the health record as a legal document, communication tool, and a key to prove compliance for health care organizations.
This lecture discusses the health record as a communication tool and legal document to demonstrate compliance with laws, rules, regulations, accreditation, and internal policies.
Health records are documents that summarize a patient’s health conditions and care activities. Historically, health records were recorded on paper, but over the past few decades, health records have become increasingly digitized. The terms “electronic medical record” and “electronic health record” are largely synonymous, however, the use of the term “electronic health record” is frequently used to denote that the health record is multi-disciplinary in nature.
The health record is, first and foremost, a tool for communication among members of the health care team. It is important that documentation in the health record be complete and accurate. When all components of the health record are used, such as clinical documentation, lab reports, x-rays, surgical reports, and consult reports, the patient has the best chance of receiving high-quality health care.
Safe patient care necessitates that all care providers have a complete and accurate picture of the patient’s current and past medical conditions. From admission to discharge, whether in an acute care facility, outpatient setting, long-term care, or any other health care system, the information that is documented in the health record is carefully monitored for accuracy and completeness.
After the patient leaves a health care system, the health information management department, or HIMD, continues to assess the completeness of the electronic record. In an electronic health record that includes scanned paper documents, the quality of the scanning process and filing of the documents in the correct area of the record will affect future use of the scanned information.
When an error or incident occurs, an incident report is generated and the risk management department reviews and addresses the incident.
Health care organizations provide ongoing education to care providers regarding best practices in clinical documentation. Education is also provided regarding areas of identified clinical documentation deficiencies or inaccuracies so that they can be avoided. With improved documentation quality, patient safety and health care quality also improve.
In any health care organization, the health record is considered the business record for the organization. As the business record of the organization, the health record holds key information for decision making, both administrative and clinical. The health record will be used for many purposes, such as analyzing the quality of care given a patient, processing claims for reimbursement, conducting research, and planning of resource needs.
As such, it is also the legal record. Information documented in the health record can be used in a court of law as evidence to substantiate the quality of the treatment given to the patient. Therefore, health care organizations must consider the importance of clinical documentation as it relates to the legal health record.
The components of the health record are governed by many different external agencies. These may include federal and state laws, regulations, and administrative rules. Voluntary accreditation, such as by The Joint Commission, introduces requirements for documentation in the health record. At the health care facility level, medical staff bylaws also provide direction for completion and maintenance of documentation in the health record.
It is difficult to keep abreast of all the changes occurring in health record policies. Facilities must develop compliance plans to make sure that external and internal rules are followed. The director of a health information management department must stay up to date on legislative and accreditation changes that affect requirements for documentation in the health record. Key areas of focus include medical coding, reimbursement laws and regulations, and privacy of patients’ health information.
Clinical departments within a health care organization must monitor new laws and regulations for their respective areas. In addition, each facility should also have an oversight committee, department, and/or director to ensure overall compliance with documentation requirements.
Hand-written documentation may be illegible, and mistakes can be made when interpreting the provider’s intentions about treatment. When mistakes occur because of illegible handwriting, the health care facility is at risk for malpractice claims in a court of law. Although mistakes can still be made in an electronic documentation system, illegibility of handwriting will not occur.
Clinical documentation will not protect a health care organization from litigation unless the content is thorough enough to communicate with the members of the health care team about the treatment. Therefore, the health record must provide clear and honest reflections of the care needed or given to patients.
There is an old adage, “What isn’t documented isn’t done.” If the health record does not indicate what is actually done for the patient, the health record as a legal document does not hold up in court.
No legitimate individual provider or health care organization wants to be accused of fraud or abuse. Examples of fraud or abuse include billing for a higher level of service than was provided, or billing for a service that was not provided. Ethical standards must be upheld for reporting claims for reimbursement at all levels of health care. This is best done by developing clinical documentation improvement programs, in which providers are trained to provide high-quality documentation in the health record.
Reimbursement of claims is based on documentation in the health record. A “coding specialist” reviews the health record and provides code numbers that are then linked to a payment system for the payer responsible for the claim.
Compliance programs have been a focus of health care organizations since the late 1990s, when the U.S. Office of the Inspector General, or OIG, began a campaign against fraud and abuse in health care for the Medicare and Medicaid programs. The fight against fraud and abuse has escalated in the past few years. Those who report fraudulent practices, called “whistleblowers,” are protected.
The issues of fraud and abuse are complicated. Compliance programs within health care organizations broadly focus on all external rules, regulations, laws, accreditation guidelines, internal medical staff bylaws, and department compliance responsibilities. The location of the compliance program depends on the organization. For example, it may operate under a separate department, within risk management, or in the quality department.
The Office of the Inspector General provides training on compliance issues. There are seven fundamental elements of an effective compliance program. Four are shown here and there are three on the next slide.
Conducting internal audits is an important aspect of compliance monitoring. Staff should be made aware of applicable disciplinary actions through well-published guidelines, and when an offense is noted, organizations must respond promptly to take corrective action.
The issues of compliance are broad, deep, and rooted in the quality of health care. The OIG Health Care Fraud Prevention and Enforcement Action Team, or "HEAT“, provides helpful training videos that include a thorough discussion of compliance.
Corporate Integrity Agreements incorporate the principles of a corporate compliance program. These agreements are voluntary unless the organization is found to have issues of fraud or abuse. When that happens, the OIG will require a comprehensive Corporate Integrity Agreement. The comprehensive agreement is outlined on this slide and the next slide.
Examples of Corporate Integrity Agreements can be found on the OIG website, which is listed in the References section of this presentation.
Compliance programs, when broadly applied to a health care organization, are concerned with more than just fraud and abuse. A comprehensive compliance program takes into consideration all rules, regulations, and laws. For example, organizations must follow the policies and procedures of HIPAA pertaining to the release of personal health information, or PHI and the security of data.
The health information management department manages requests for PHI after the patient leaves the facility. Requests may come from patients, lawyers, other health care providers, and other entities. Department personnel are trained in the most up-to-date rules relating to the release of information.
The business office releases health information when needed for claim payment. Sometimes nursing stations release information upon discharge to an extended-care facility. Therefore, several departments may be releasing PHI and need to be well trained about HIPAA policies.
Tracking the release of personal health information must be systematic and transparent. Breaches in security need to be tracked as well. Humans make mistakes, and information may be sent to the wrong patient or third party. When a facility knows this has happened, it must follow relevant policies and procedures as established in the corporate compliance plan.
Likewise, large breaches of data must be reported to the Department of Health and Human Services. For example, a large data breach includes loss of a laptop containing the PHI of 500 or more patients. There are policies and procedures for notifying individual patients when privacy is breached.
All department managers and key personnel must review policies and procedures to address any issues related to the release of information. Although general HIPAA training is mandated for all personnel, additional in-depth training is needed in high-risk areas where breaches could occur. Those areas of risk must be identified and training must be ongoing to ensure compliance.
This concludes lecture e of Regulating Health Care.
The following are the key concepts to remember about this lecture:
The health record is the business and legal record for a health care organization
The health record is the communication tool for the health care team
Clinical documentation is used to assure high quality care of the patient, as well as to provide information for decision-making, reimbursement and medical coding
Thorough and complete clinical documentation protects health care organization from the risk of fraud, abuse, and malpractice claims.
Compliance programs are important to assure the correct procedures are followed related to regulations, rules, laws, accreditation, and internal policies
HIPAA privacy and security rules need to be included in compliance plans
This also concludes the unit Regulating Health Care. In summary, this unit discussed the following:
Organizations such as The Joint Commission accredit and/or certify health care organizations. Regulatory agencies under the authority of Congress issue rules that protect the public. Organizations including The Joint Commission and the Agency for Health Care Research and Quality provide initiatives and resources for patient safety and quality improvement.
The legal system in the U.S. is made up of many courts, where a neutral arena is used for parties to dispute issues.
The laws governing health care are complicated and ever changing. Health Care providers are responsible for following standards of care, obtaining informed consent from patients, and avoiding fraud, waste and abuse.
Compliance with HIPAA privacy and security rules are high priority in health care delivery.
The clinical documentation in the health record supports quality health care, administrative and business operations of the organization, and provides the basis for legal proof of care that assures compliance with laws, rules, and regulations as well as professional standards of care.