Skip to main content

Clinical Documentation for Risk Adjusted Contracts in a changing Environment


Overview
This session with explain the Medicare Advantage Program of Risk Adjustment and how ICD-10 codes map to HCC Categories. We will discuss Types of Risk Adjustment Models, HCC Concepts and how HCC works. Documentation requirements will be explained, as well as qualifying Provider Types and appropriate sources for documentation.
Objectives include an explanation of the history of HCC Coding, how it works, calculation of RAF Scores, Coding & financial impact.
Examples of HCC Categories and the ICD-10 codes mapping to them will be illustrated with a sample note. The speaker will review risks by pointing out Common Coding and Documentation Errors found during RADV Audits. The attendees will receive coding and documentation tips to improve their RAF scores.
Why should you attend this webinar?
To learn about future reimbursement models and improve risk adjustment bonus scores.
Areas Covered in the Session:
Topics which will be covered in the session (bulleted point)
  •  Background of HCC Coding 
  •  How Dignosis Codes link to HCC categories
  •  How HCC categories affect a patient's Risk Score
  •  RADV Audits and Common Errors
Who can Benefit:
Physician Leaders, Financial officers, coders and billers.
Compliance Key INC
717-208-8666

Comments

Popular posts from this blog

Essentials of Affirmative Action and OFCCP Compliance

Compliance Key INC  -  Human Resource Training Online                                                                  Janette Levey Frisch Janette Levey Frisch is Keynote Speaker at Compliance key Inc. She is founder of  The EmpLAWyerologist Firm, has over 20 years of legal experience, more than 10 of which she has spent in Employment Law. It was during her tenure as sole in-house counsel for a mid-size staffing company headquartered in Central New Jersey, with operations all over the continental US, that she truly developed her passion for Employment Law.   Webinar Id:   CICJE001  10.00 AM PT | 01.00 PM ET   01/09/2018  Duration: 90 mins  Overview If you are a federal contractor, having a firm grasp on the essentials ...

Understanding Design Controls

Compliance Key INC  -  Medical Device Training Overview Design Controls are the processes used to design, develop, and manage medical devices that you manufacture. They are mandated by federal regulation, however, the regulations concerning design controls are vague in terms of the specific process steps required and the approaches that should be taken to achieve compliance should be developed. Knowing how the FDA both views and examines design controls is crucial to achieving compliance throughout the life of the medical devices you manufacture and is one of the most valuable compliance subject areas to explore. Noncompliance in design controls, which are consistently uncovered by the FDA during inspections and examinations, are concerned with the design control process that has been designed and applied and the documentation required to support each design control step. The specific sections of the regulations that apply to design controls include CFR 21 Part 820 Qua...

Building a Compliance Program

Compliance Key INC  -  Compliance Training Webinar                                   Lisa M. Marsden Lisa M. Marsden, IACCP, is Keynote speaker at Compliance Key, Inc. She is the president and founder of Coulter Strategic Services. Coulter Strategic Services provides financial advisors and consulting firms with compliance and project management services. Prior to that, Ms. Marsden was the chief operating officer/chief compliance officer of Financial Trust Asset Management, Boca Raton, Florida.  Webinar Id:  CICLB005  10:30 AM PT | 01:00 PM ET  05/15/2018  Duration 60 mins  Overview Whether you are creating a new compliance program as a new CCO or a new firm or if you are updating an existing program this webinar will guide you through the process. Why should you attend this webinar? Rule 17j-1. Effective Date: A...