Audio conference on Until The Crystal Ball For 6 Month Prognosis Is Invented, You Have To Document Eligibility by Charlene Ross ? Review the Medicare regulations related eligibility and use of the Local Coverage Determinations (LCD)s.
Hospital Readmission Reduction: How Important are Follow Up Calls? (Hint: Very)SironaHealth
Starting in 2012, the Centers for Medicare and Medicaid Services (CMS) will begin withholding payments for potentially avoidable readmissions. This presentation reviews these new regulations, what causes excessive readmissions, and how hospitals can positively impact patient health by reaching out 24-72 hours after discharge.
Health IT Summit Boston 2014 – Case Study “Beyond MU Stage 2: Maximizing the value of your HER” with Larry Garber, Medical Director of Informatics, Reliant Medical Group
Do States Like Telehealth? – Telehealth Crash Course Webinar SeriesEpstein Becker Green
Telehealth has gone mainstream. As technology becomes more sophisticated and clinicians find innovative ways to provide services, the various applications of telehealth are taking on new dimensions. The trend toward telehealth is being driven by employers, private insurers, clinicians, and technology companies. The trend notwithstanding, serious legal and regulatory issues remain and will be a barrier to the wider adoption of telehealth. With the significant attention that recent litigation and enforcement activities in certain states have received, many view state laws and policies as the biggest impediment to the wider adoption of telehealth.
In the second installment of EBG’s Telehealth Crash Course series, we will discuss recent legal and regulatory developments in the states related to telehealth and the various initiatives underway to facilitate greater adoption of telehealth. Additionally, we will address issues such as multistate provider licensure, scope of practice, prescribing, and recently introduced state telehealth-related bills.
Epstein Becker Green Webinar - Presented by Rene Quashie on 9/15/2015.
http://www.ebglaw.com/ren%C3%A9-y-quashie/events/do-states-like-telehealth-telehealth-crash-course-webinar-series/
These materials have been provided for informational purposes only and are not intended and should not be construed to constitute legal advice. The content of these materials is copyrighted to Epstein Becker & Green, P.C. ATTORNEY ADVERTISING.
Office-Based Surgical Suite (OBSS) Regulation, Registration and AccreditationJeffrey Restuccio
This short presentation discusses how each state regulates the OBSS a little differently. Many don't require registration or accreditation for local anesthesia procedures--but some do! Be sure to check with the latest regulations and a healthcare attorney when setting up an OBSS.
Hospital Readmission Reduction: How Important are Follow Up Calls? (Hint: Very)SironaHealth
Starting in 2012, the Centers for Medicare and Medicaid Services (CMS) will begin withholding payments for potentially avoidable readmissions. This presentation reviews these new regulations, what causes excessive readmissions, and how hospitals can positively impact patient health by reaching out 24-72 hours after discharge.
Health IT Summit Boston 2014 – Case Study “Beyond MU Stage 2: Maximizing the value of your HER” with Larry Garber, Medical Director of Informatics, Reliant Medical Group
Do States Like Telehealth? – Telehealth Crash Course Webinar SeriesEpstein Becker Green
Telehealth has gone mainstream. As technology becomes more sophisticated and clinicians find innovative ways to provide services, the various applications of telehealth are taking on new dimensions. The trend toward telehealth is being driven by employers, private insurers, clinicians, and technology companies. The trend notwithstanding, serious legal and regulatory issues remain and will be a barrier to the wider adoption of telehealth. With the significant attention that recent litigation and enforcement activities in certain states have received, many view state laws and policies as the biggest impediment to the wider adoption of telehealth.
In the second installment of EBG’s Telehealth Crash Course series, we will discuss recent legal and regulatory developments in the states related to telehealth and the various initiatives underway to facilitate greater adoption of telehealth. Additionally, we will address issues such as multistate provider licensure, scope of practice, prescribing, and recently introduced state telehealth-related bills.
Epstein Becker Green Webinar - Presented by Rene Quashie on 9/15/2015.
http://www.ebglaw.com/ren%C3%A9-y-quashie/events/do-states-like-telehealth-telehealth-crash-course-webinar-series/
These materials have been provided for informational purposes only and are not intended and should not be construed to constitute legal advice. The content of these materials is copyrighted to Epstein Becker & Green, P.C. ATTORNEY ADVERTISING.
Office-Based Surgical Suite (OBSS) Regulation, Registration and AccreditationJeffrey Restuccio
This short presentation discusses how each state regulates the OBSS a little differently. Many don't require registration or accreditation for local anesthesia procedures--but some do! Be sure to check with the latest regulations and a healthcare attorney when setting up an OBSS.
It has been a longstanding challenge to integrate patient data from EMRs (Electronic Medical Record systems) with EDC (Electronic Data Capture) systems for clinical studies and trials.
The challenges include:
Low adoption rates of EMRs in physician practices
Lack of interoperability tools provided by vendors to extract data from EMRs
Lack of standardized payload (content) and method of delivering (transport) from different EMRs to the EDC systems
All subjects of clinical studies not being part of the same health system and therefore same EMR
Lack of automated methods for identifying the same patient between EMRs and EDC systems
Inability to map and translate the EMR data into CRFs (case report forms) of the EDC systems
These hurdles have been so high that the task has rarely been attempted in earnest, let alone accomplished in any significant way. That is until recently. How are these challenges being overcome today? What changes have allowed this integration to be to considered and implement today? The answer is: lots!
DIA 2015 - EMR/EHR Clinical Data Intergration with EDC SystemsClinCapture
It has been a longstanding challenge to integrate patient data from EMRs (Electronic Medical Record systems) with EDC (Electronic Data Capture) systems for clinical studies and trials.
Integration between disparate systems can be done in many ways. Any two systems can be integrated given enough time and money. However, if there is to be wide-scale integration between applications used by clinicians at their practice or in the hospital, it requires the formation and use of standards for the structure and content of data as well as the transport of data between two systems.
A historic problem has been the lack of EMR adoption, particularly in physician offices. Thankfully, this is improving dramatically, something I will touch on later.
There is also a historic problem that Case Report Forms and the databases that contain them in EDC systems are routinely not designed from the start with standardized labels, content or structure. More adoption of the CDISC standards, such as C-DASH (clinical data acquisition standards harmonization) which dictates structure and content, and ODM (operational data model) which is an XML rendering of the CDASH CRFs.. If you take anything away from this talk, please ensure any data capture you do within an EDC system going forward meets the ODM model.
Patient matching between systems is important. There is a whole industry for Community and Master Patient Indexes to link records in disparate systems to the same patient. This gets even more complex when the patients are to be kept anonymous or the studies are blinded.
Lastly, moving data across systems is a challenge. There are two primary methods – 1) asynchronous file transfer in conjunction with an ETL, or 2) APIs where one system is inquiring in real time into another application for data. The latter is usually regarded as a more robust integration, but without standard APIs these are one off solutions. The former, using ETL, requires the sending and receiving applications be able to communicate
Dealing With Payers With Physician Driven Cost AndWilliam Cockrell
This is a presentation I just did for MGMA Alabama on how providers should develop their own cost and quality data. Thanks to RealTime Medical Data for their support.
Enhancing Access, Quality, and Equity for Persons With Advanced IllnessVITASAuthor
This diverse panel examined various facets of healthcare access, equity, and inclusion as it
relates to individuals in underserved communities who are coping with advanced illness. Based on their
decades of experience in end-of-life care, as well as evidence-based data and a compelling case study
of a Filipino-American US Navy Veteran, panel members shared strategies on how to mitigate
current barriers, including ensuring patients are granted timely access to hospice and palliative
services and that appropriate levels of care are provided.
Implementation of Timely and Effective Transitional Care Management ProcessesCHC Connecticut
Join us to discuss best practices for integrating daily follow-ups for patients recently hospitalized for health emergencies. Effectively following up with patients is a critical responsibility for integrated care teams.
Experts will share how their teams respond to patients to identify care gaps and support the transition of care. Workflow descriptions will provide participants with the tools to support their work to adapt specific steps into their model of team-based care.
Panelists:
• Mary Blankson, DNP, APRN, FNP-C, FAAN, Chief Nursing Officer, Community Health Center, Inc.
• Veena Channamsetty, MD, FAAFP, Chief Medical Officer, Community Health Center, Inc.
• Bibian Ladino-Davis, Behavioral Health Coordinator, Weitzman Institute
The Value Proposition of Hospice | VITASVITASAuthor
The goal of this webinar was to help hospice and healthcare professionals discover the evidence-based benefits of hospice care, while gaining key insights on hospice eligibility guidelines, how hospice differs from other types of care, and how the Medicare Hospice Benefit helps patients facing advanced illness.
Addressing Medical Necessity Denials and RecoupmentsPYA, P.C.
With increased denials and recoupments related to medical necessity at the forefront of discussions at this year’s American Health Lawyers Association Institute on Medicare and Medicaid Payment Issues, PYA was prepared to inform and assist providers instituting best practices to address medical necessity denials. PYA Principal Denise Hall-Gaulin co-presented “Medical Status-Current Status/Key Best Practices in Prevention of Medical Necessity Denials and Recoupments” with Michael Spake, VP of External Affairs and Chief Compliance and Integrity Officer at Lakeland Regional Health.
The presentation included:
A discussion of medical necessity—what it means and what it affects
Information regarding medical necessity determinations and criteria for determination
Definitions for categorically excluded services
Criteria for admission (skilled nursing facilities and inpatient rehabilitation facilities included)
Determining Prognosis in Cancer and Non-cancer DiagnosisVITAS Healthcare
This helps physicians, nurses, case managers and social workers understand the trajectories of dying from cancer and non-cancer diagnoses, including heart, lung, kidney and liver disease, stroke, HIV/AIDS, dementia and neurodegenerative diseases. Aided by a better grasp of the decline-related domains involved in poor prognosis, disease progression and disease end stages, attendees will be better positioned to identify patients and residents who are appropriate for hospice care.
Controlled Substance Prescribing: What to Do?RIAPA
Dr. James MacDonald, Chief Administrative Officer or the RI Board of Medical Licensure and Discipline presents to the RIAPA on controlled substance prescribing in RI.
Continuity of care at the primary health care level narrative reviewDr. Anees Alyafei
A narrative review on continuity of care at the level of primary health care, definition, types, how it could be measured, and the expected effects on the patients, health care providers, and health institutes.
It has been a longstanding challenge to integrate patient data from EMRs (Electronic Medical Record systems) with EDC (Electronic Data Capture) systems for clinical studies and trials.
The challenges include:
Low adoption rates of EMRs in physician practices
Lack of interoperability tools provided by vendors to extract data from EMRs
Lack of standardized payload (content) and method of delivering (transport) from different EMRs to the EDC systems
All subjects of clinical studies not being part of the same health system and therefore same EMR
Lack of automated methods for identifying the same patient between EMRs and EDC systems
Inability to map and translate the EMR data into CRFs (case report forms) of the EDC systems
These hurdles have been so high that the task has rarely been attempted in earnest, let alone accomplished in any significant way. That is until recently. How are these challenges being overcome today? What changes have allowed this integration to be to considered and implement today? The answer is: lots!
DIA 2015 - EMR/EHR Clinical Data Intergration with EDC SystemsClinCapture
It has been a longstanding challenge to integrate patient data from EMRs (Electronic Medical Record systems) with EDC (Electronic Data Capture) systems for clinical studies and trials.
Integration between disparate systems can be done in many ways. Any two systems can be integrated given enough time and money. However, if there is to be wide-scale integration between applications used by clinicians at their practice or in the hospital, it requires the formation and use of standards for the structure and content of data as well as the transport of data between two systems.
A historic problem has been the lack of EMR adoption, particularly in physician offices. Thankfully, this is improving dramatically, something I will touch on later.
There is also a historic problem that Case Report Forms and the databases that contain them in EDC systems are routinely not designed from the start with standardized labels, content or structure. More adoption of the CDISC standards, such as C-DASH (clinical data acquisition standards harmonization) which dictates structure and content, and ODM (operational data model) which is an XML rendering of the CDASH CRFs.. If you take anything away from this talk, please ensure any data capture you do within an EDC system going forward meets the ODM model.
Patient matching between systems is important. There is a whole industry for Community and Master Patient Indexes to link records in disparate systems to the same patient. This gets even more complex when the patients are to be kept anonymous or the studies are blinded.
Lastly, moving data across systems is a challenge. There are two primary methods – 1) asynchronous file transfer in conjunction with an ETL, or 2) APIs where one system is inquiring in real time into another application for data. The latter is usually regarded as a more robust integration, but without standard APIs these are one off solutions. The former, using ETL, requires the sending and receiving applications be able to communicate
Dealing With Payers With Physician Driven Cost AndWilliam Cockrell
This is a presentation I just did for MGMA Alabama on how providers should develop their own cost and quality data. Thanks to RealTime Medical Data for their support.
Enhancing Access, Quality, and Equity for Persons With Advanced IllnessVITASAuthor
This diverse panel examined various facets of healthcare access, equity, and inclusion as it
relates to individuals in underserved communities who are coping with advanced illness. Based on their
decades of experience in end-of-life care, as well as evidence-based data and a compelling case study
of a Filipino-American US Navy Veteran, panel members shared strategies on how to mitigate
current barriers, including ensuring patients are granted timely access to hospice and palliative
services and that appropriate levels of care are provided.
Implementation of Timely and Effective Transitional Care Management ProcessesCHC Connecticut
Join us to discuss best practices for integrating daily follow-ups for patients recently hospitalized for health emergencies. Effectively following up with patients is a critical responsibility for integrated care teams.
Experts will share how their teams respond to patients to identify care gaps and support the transition of care. Workflow descriptions will provide participants with the tools to support their work to adapt specific steps into their model of team-based care.
Panelists:
• Mary Blankson, DNP, APRN, FNP-C, FAAN, Chief Nursing Officer, Community Health Center, Inc.
• Veena Channamsetty, MD, FAAFP, Chief Medical Officer, Community Health Center, Inc.
• Bibian Ladino-Davis, Behavioral Health Coordinator, Weitzman Institute
The Value Proposition of Hospice | VITASVITASAuthor
The goal of this webinar was to help hospice and healthcare professionals discover the evidence-based benefits of hospice care, while gaining key insights on hospice eligibility guidelines, how hospice differs from other types of care, and how the Medicare Hospice Benefit helps patients facing advanced illness.
Addressing Medical Necessity Denials and RecoupmentsPYA, P.C.
With increased denials and recoupments related to medical necessity at the forefront of discussions at this year’s American Health Lawyers Association Institute on Medicare and Medicaid Payment Issues, PYA was prepared to inform and assist providers instituting best practices to address medical necessity denials. PYA Principal Denise Hall-Gaulin co-presented “Medical Status-Current Status/Key Best Practices in Prevention of Medical Necessity Denials and Recoupments” with Michael Spake, VP of External Affairs and Chief Compliance and Integrity Officer at Lakeland Regional Health.
The presentation included:
A discussion of medical necessity—what it means and what it affects
Information regarding medical necessity determinations and criteria for determination
Definitions for categorically excluded services
Criteria for admission (skilled nursing facilities and inpatient rehabilitation facilities included)
Determining Prognosis in Cancer and Non-cancer DiagnosisVITAS Healthcare
This helps physicians, nurses, case managers and social workers understand the trajectories of dying from cancer and non-cancer diagnoses, including heart, lung, kidney and liver disease, stroke, HIV/AIDS, dementia and neurodegenerative diseases. Aided by a better grasp of the decline-related domains involved in poor prognosis, disease progression and disease end stages, attendees will be better positioned to identify patients and residents who are appropriate for hospice care.
Controlled Substance Prescribing: What to Do?RIAPA
Dr. James MacDonald, Chief Administrative Officer or the RI Board of Medical Licensure and Discipline presents to the RIAPA on controlled substance prescribing in RI.
Continuity of care at the primary health care level narrative reviewDr. Anees Alyafei
A narrative review on continuity of care at the level of primary health care, definition, types, how it could be measured, and the expected effects on the patients, health care providers, and health institutes.
Federally Qualified Health Centers must provide all required primary, preventive and enabling health services, in addition to additional health services, as appropriate and necessary. This can be managed either directly through health center employees and volunteers, or through formal written contracts and formal written referral arrangements.
It is important for health centers to understand that contracts and formal written referral arrangements are not just a piece of paper and not only come with requirements, but also responsibilities on the part of both the health center and the contracted/referral provider(s).
This webinar will address the following:
• HRSA required clinical language for Column II contracts and Column III formal written referral arrangements
• The responsibilities of the health center and the contracted/referral provider
• A high-level review of the clinical chapters associated with Column II and Column III contracts
• Case studies demonstrating gaps in care creating areas of significant risk
• Best Practices to ensure appropriate continuity and quality of care
Are you a new FQHC? Or new to an FQHC? Wondering what FTCA coverage is all about? How do you prepare to be ready to apply for coverage?
Get answers to these questions and more in this introductory webinar that will benefit everyone
Connecting the Dots for Fast-Track Approval for Rare Disease and Orphan DrugMedpace
Managing a rare disease or orphan drug clinical trial has several challenges. Be prepared to understand and take away real world tactical lessons to expedite these studies:
•What are the new promising techniques in clinical studies for Rare Disease research? How are the innovative areas of adaptive strategies and translational medicine being employed?
• How do patient registries and natural history studies provide insights and patients for these studies?
• What quality of life issues play into patient retention in these studies?
• How can regulatory challenges from submissions to drug approvals be met using integrated global knowledge and systems to keep a project on track?
Some diseases have a fairly standard progression. For instance, patients with more advanced Alzheimer’s disease may experience changes in their ability to ambulate, to speak, or to swallow. Other illnesses, however, have less well-documented stages. Additionally, sometimes a patient’s diagnosis is not clear-cut.
Similar to Until The Hospice Crystal Ball for 6 Month Prognosis Is Invented, You Have To Document Eligibility (20)
This year (2016) has seen some reasonably good news for most physicians! More than 19,500 physicians in 25 specialties responded to various surveys and describing their compensation, number of hours worked, practice changes resulting from healthcare reform, and how they have adapted to the new healthcare environment.
For more information - http://blog.audioeducator.com/physician-compensation-report-2016/
MACRA – 3 Important Medicare Payment Changes InfographicAudioEducator
The Medicare Access and CHIP Reauthorization Act of 2015 (MACRA), the much awaited change in healthcare—which totally revamps Medicare (Part B) clinician payments from a fee-for-service to a value-based system is finally here.
For more information - http://blog.audioeducator.com/macra-3-important-medicare-payment-changes-infographic/
2016 healthcare predictions - 2015 was a year of changes for the healthcare industry, most notable of which was the implementation of ICD-10 coding guidelines, but it’s not over yet!
For more information - http://blog.audioeducator.com/healthcare-predictions-2016/
Live audio conference on write, organize and maintain Standard Operating Procedures and teach personnel the methods that will ensure FDA compliance in a manner that will be reproducible, concise and easy to follow.
US, EU & Japan GMP Requirements: Practical ICH Area Differences & Healthcare ...AudioEducator
Live Audio Conference on US, EU & Japan GMP Requirements: Practical ICH Area Differences & Healthcare Inspection Focus – Learn how to focus your internal audits to a US, EU and Japan compliance system.
Revenue Cycle: Tracking Reimbursement for DRGs, APCs and MPFSAudioEducator
Review the reimbursement tracking as part of the revenue cycle, and understand the basics of DRGs, APCs and MPFS in this audio session with Duane Abbey.
Recipe for Success: How to Effectively Manage an Allergen ProgramAudioEducator
Audio conference on Recipe for Success: How To Effectively Manage an Allergen Program by Valerie Scheidt – Learn steps to execute allergen procedures in daily activities.
Pediatric coding and documentation challengesAudioEducator
Understand the Various Coding and Documentation Challenges you Face for Pediatric Medical Care by Kim Garner-Huey. Webinar will update you on Pediatric CPT codes along with ICD 10 codes.
Medical Necessity and Recent Government Scrutiny and Theories of EnforcementAudioEducator
Know the basics of how ‘medically necessary’ services are defined by government health plans; and which often are followed by private payors in this audio session.
The dimensions of healthcare quality refer to various attributes or aspects that define the standard of healthcare services. These dimensions are used to evaluate, measure, and improve the quality of care provided to patients. A comprehensive understanding of these dimensions ensures that healthcare systems can address various aspects of patient care effectively and holistically. Dimensions of Healthcare Quality and Performance of care include the following; Appropriateness, Availability, Competence, Continuity, Effectiveness, Efficiency, Efficacy, Prevention, Respect and Care, Safety as well as Timeliness.
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.
How many patients does case series should have In comparison to case reports.pdfpubrica101
Pubrica’s team of researchers and writers create scientific and medical research articles, which may be important resources for authors and practitioners. Pubrica medical writers assist you in creating and revising the introduction by alerting the reader to gaps in the chosen study subject. Our professionals understand the order in which the hypothesis topic is followed by the broad subject, the issue, and the backdrop.
https://pubrica.com/academy/case-study-or-series/how-many-patients-does-case-series-should-have-in-comparison-to-case-reports/
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
COVID-19 PCR tests remain a critical component of safe and responsible travel in 2024. They ensure compliance with international travel regulations, help detect and control the spread of new variants, protect vulnerable populations, and provide peace of mind. As we continue to navigate the complexities of global travel during the pandemic, PCR testing stands as a key measure to keep everyone safe and healthy. Whether you are planning a business trip, a family vacation, or an international adventure, incorporating PCR testing into your travel plans is a prudent and necessary step. Visit us at https://www.globaltravelclinics.com/
ICH Guidelines for Pharmacovigilance.pdfNEHA GUPTA
The "ICH Guidelines for Pharmacovigilance" PDF provides a comprehensive overview of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines related to pharmacovigilance. These guidelines aim to ensure that drugs are safe and effective for patients by monitoring and assessing adverse effects, ensuring proper reporting systems, and improving risk management practices. The document is essential for professionals in the pharmaceutical industry, regulatory authorities, and healthcare providers, offering detailed procedures and standards for pharmacovigilance activities to enhance drug safety and protect public health.
TOP AND BEST GLUTE BUILDER A 606 | Fitking FitnessFitking Fitness
"Feature:
• Intelligent Ergonomically Design Glute Builder Is A Must Have For Those Looking To Target Their Gluteal Muscles And Hamstrings With Precision.
• The Ability To Adjust The Starting Position, This Machine Allows For A More Targeted Workout That Is Tailored To Your Specific Needs.
• Spacious And Supportive Cushioned Seat Provide Added Comfort And Stability During Your Workout."
Get more information visit on:- www.fitking.in
Our mail I.D:-care@fitking.in, fitking.in@gmail.com
Call us at :- 9958880790, 9870336406, 8800695917
4. Hospice Eligibility Clarification
“The certification regarding terminal illness of an
individual shall be based on the physician’s or medical
director’s clinical judgment regarding the normal
course of the individual’s illness.”
CMS Program Memorandum
Transmittal AB-03-040 (CR 2570)
March 28, 2003
Over the years CMS has stated in different venues
and at different times that the physician does not
need to know if the specific individual will die in 6
months, but rather that individuals who present in the
same way generally die in 6 months.
4