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Cardiac Device Monitoring

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Director of Cardiac Pacing and Tachyarrhythmia Devices. Cleveland Clinic ... Brian Whitman or Rebecca Kelly at the American College of Cardiology. 202-375-6000 ... – PowerPoint PPT presentation

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Title: Cardiac Device Monitoring


1
Cardiac Device MonitoringCoding Update for
2009PresentersBruce L. Wilkoff MDDirector
of Cardiac Pacing and Tachyarrhythmia
DevicesCleveland ClinicLinda Gates-Striby
CCS-P, ACS-CA  Compliance Manager   The Care
Group, LLC Cathie BigaPresident/CEO
Cardiovascular Management of Illinois
2
ACC/HRS/CMS Consensus
  • Current CPT code selections for CIED Monitoring
  • Do not reflect current practice and technology.
  • Inadequate for reporting
  • Professional
  • Technical
  • Need to modernize
  • Current codes
  • Code descriptions
  • Provide for evolving technology

3
CPT Code Revisions
Desired Outcomes
4
Structure for 2009 Codes
  • Programming CIED Evaluations
  • Interrogation CIED Evaluations
  • Remote
  • In person
  • Trans-telephonic Rhythm Strip Evaluations
  • Peri-procedural Programming Device Evaluations
  • Implantable Cardiac Monitors
  • Implantable Loop Recorders
  • Mobile Cardiovascular Telemetry

5
Overview
6
Programming Device Evaluations
7
Programming Device Evaluation Definition
  • All device functions, including the battery,
    programmable settings and lead(s) when present
    are Interrogated evaluated. Iterative
    adjustments provide information that permits the
    operator to assess and select the most
    appropriate final program parameters to provide
    for consistent delivery of the appropriate
    therapy and to verify the efficiency and function
    of the device.

8
Lead Systems
  • Device, single leadpacing sensing in one
    chamber of the heart (e.g., VVI system)
  • Device, dual leadpacing sensing in two
    chambers of the heart (e.g., DDD system)
  • Device, multiple leadpacing sensing in three
    or more chambers of the heart (e.g.,
    biventricular system)

9
Peri Procedural Programming Evaluation
Definition
  • The device system data are interrogated to
    evaluate the lead(s), sensor(s) and battery along
    with review of stored information including
    patient and system measurements. The device is
    programmed to settings appropriate for the
    surgery, procedure or test. A second evaluation
    and programming are performed after the surgery,
    procedure or test to provide settings appropriate
    to the post procedural situation.

10
Interrogation Device EvaluationIn Person
11
Interrogation Device Evaluation Remote
12
Interrogation Device Evaluation
DefinitionRemote OR In Person
  • Using an office, hospital or emergency room
    instrument, stored and measured information about
    the lead(s) when present, sensor(s) when present,
    battery and the implanted pulse generator
    function, as well as data collected about the
    patients heart rhythm and heart rate is
    retrieved. The retrieved information is evaluated
    to determine the current programming of the
    device and to evaluate certain aspects of the
    device function, such as battery voltage, lead
    impedance, tachycardia detection settings, and
    rhythm treatment settings.

13
Trans Telephonic Rhythm Strip Evaluation
Definition
  • Also called transtelephonic pacemaker monitoring.
    The service is an electrocardiographic rhythm
    strip transmitted over the telephone by the
    patient using a transmitter and recorded by a
    receiving location using a receiver/recorder. The
    electrocardiographic rhythm strip is recorded
    both with and without a magnet applied over the
    pacemaker. The rhythm strip is evaluated for
    heart rate and rhythm, atrial and ventricular
    capture (if observed) and atrial and ventricular
    sensing (if observed). Also the battery status is
    determined by measurement of the paced rate
    during the magnet applied electrocardiographic
    rhythm strip.

14
Implantable Cardiovascular Monitor Definition
  • Used to assist the physician in the management of
    non-rhythm related cardiac conditions such as
    heart failure. The device collects longitudinal
    physiologic cardiovascular data elements from one
    or more internal sensors and/or external sensors
    for patient assessment and management. The
    function of the ICM may be an additional function
    of an implantable cardiac device (CRT-D) or a
    function of a stand-alone device.

15
Implantable Loop Recorder Definition
  • An implantable device that continuously records
    the electrocardiographic rhythm triggered
    automatically by rapid and slow heart rates or by
    the patient during a symptomatic episode. The ILR
    function may be the only function of the device
    or it may be part of a pacemaker or ICD.

16
Mobile Cardiovascular Telemetry
  • A wearable device that continuously records the
    electrocardiographic rhythm from external
    electrodes. Segments of the ECG data are
    automatically (without patient intervention)
    transmitted to a remote surveillance location by
    cellular or landline telephone signal. There is
    continuous real time data analysis by
    preprogrammed algorithms in a device and attended
    surveillance of the transmitted rhythm segments
    by a surveillance center. The surveillance
    center technician reviews the data and notifies
    the physician depending upon the prescribed
    criteria.

17
Action Plan For Implementation
  • Successful implementation requires planning and
    multiple steps
  • 2009 brings changes not only to the device codes
    but to echo and stress echo, as well as others
    (i.e. injections and infusion codes)

18
Education and Awareness
  • Identify your implementation team
  • - include a physician representative
  • - device clinic staff
  • - holter/event monitoring representative
  • - coders and billers
  • - consider CHF clinic and scheduling staff

19
Identify Your Services
  • Are you performing or planning to perform remote
    checks?
  • If providing remote services, are you performing
    the technical side as well?
  • Do you have patients with devices that would
    qualify as an ICM? Is anyone using that data?
  • Are you performing or planning to perform MCOT?

20
Review The Billing Process
  • How are charges being submitted now?
  • How will you handle so many 90 and 30 day
    services?
  • What changes will be needed for your billing
    forms/fee tickets?
  • Are there EMR implications?
  • Will you want to track the number of services
    actually rendered in a 90 day period?
  • How will you ensure all billable services have
    been captured?

21
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23
Documentation Review
  • Where do you keep your device check reports?
  • Can you distinguish a remote service from an
    in-person interrogation?
  • Review your reports for the key components of a
    programming evaluation versus an interrogation
    evaluation.
  • Will you need to make any changes in your
    documentation?
  • Are there implications to software that you may
    be using for device checks?

24
Additional Factors To Consider
  • Review supervision requirements
  • Watch for CCI changes
  • Watch for changes in local and National medical
    policies
  • We know CMS is covering the services, but what
    about commercial payors?

25
Areas To Watch
  • Reprogramming is not the determining factor for
    choosing the correct code
  • Interrogation codes same code for a single,
    dual and multi lead device
  • Programming codes codes change for single, dual
    and multi lead
  • Dont forget to bill for the technical side of
    remote services if you are performing that
    service
  • How do we fit the new codes into existing medical
    policies?
  • Watch for inappropriate denials chances are we
    understand the rules better than the payors

26
Administrative Concerns
  • Setting your fee
  • - Consider implications of 30 or 90 day codes
  • - Keep in mind CMS did not accept the full AMA
    recommended RVU on all codes
  • - We cant tell you how to set your fee or what
    your fee should be, only issues to consider

27
Contracted Rate Implications
  • Identify your top commercial payors and evaluate
    for contract implications
  • Do you have contracts that were negotiated per
    CPT code?
  • Do you have contracts that locked in to a
    previous year of Medicare reimbursement?

28
Budget Process
  • Understand that the codes do not have a direct
    crosswalk
  • Determine how you will conduct your financial
    analysis
  • 2009 is a complicated year on its own how deep
    will you really need to go into the new device
    codes?
  • 2009 echo codes are a bit easier to estimate

29
Compensation Models
  • Will your compensation model require that you
    track all services rendered?
  • Example The physician doing the first read of
    a 90 day service will probably be your billing
    provider. Do you need to credit the physician
    who may read other services in that 90 day
    period?

30
Additional Upcoming Presentations
  • Heart Rhythm Society
  • December 17, 2008
  • January 12, 2008
  • MedAxiom
  • December 4, 2008

31
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32
2009 New Code Overview
33
2009 New Code Overview
34
2009 New Code Overview
35
Thank You!
  • If you should have any additional questions,
    please feel free to contact
  • Brian Whitman or Rebecca Kelly at the American
    College of Cardiology
  • 202-375-6000

35
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