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Research Registration and Billing

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Title: Research Registration and Billing


1
Research Registration and Billing
  • One Institutions Experience
  • Cincinnati Childrens Medical Center
  • Presenter Andrea L. Smith
  • Andrea.smith_at_cchmc.org

2
Research Registration and Billing
  • Overview
  • Old Process
  • New Process
  • Nuts and Bolts Basics
  • Registration Steps
  • The Study Invoice
  • Important Tips to Get Started

3
What Started It All
  • One Case in 2001
  • Insurance Billed In Error
  • Insurance Reimbursed
  • Consequences

4
Overview
  • History
  • Initial meeting September 25, 2001
  • Intra-disciplinary Committee formed
  • Process mapped
  • Process redesign
  • Administration support and buy-in

5
Overview
Functions Represented
  • Laboratory
  • Patient Financial
  • Services
  • Pharmacy
  • Regulatory Affairs
  • Research
  • Administration
  • HIPAA, Legal Offices
  • Accounting
  • Admitting/Registration
  • Clinical Research Center
  • Clinical Trials Office
  • Divisional Reps
  • Health Info Mgmt (HIM)
  • Information Services

6
Overview
  • Objectives
  • To increase research subject safety
  • To comply with accreditation and regulatory
    agencies
  • To develop efficient and standardized
    administrative research processes
  • To serve as a data source

7
Overview
  • Objectives
  • To provide a formal infrastructure for scheduling
    and registration of research subjects
  • To ensure timely and proper billing
  • To establish consistent and standardized charges
    for research procedures

8
Overview
  • The Need for Change
  • The current process is not understood by
    researchers and not documented (tribal legend)
  • Most research outpatients not registered in any
    hospital system under own name.

9
Overview
  • Old Process
  • Obtain patient account number from Hospital
    Laboratory for study.
  • Registrars have to remember to code research
    visits x10 for inpatient or x70 for
    outpatients.
  • No standardized information about how to set up a
    research study or put subjects through
    administrative pipeline available.
  • Bills do not have participant-specific
    information.

10
New Process
11
New Process
  • Obstacles
  • Investigators/Faculty You are telling us how
    to do our research.
  • Study Coordinators You are telling us to do
    more duties on top of all the other things.
  • Finance personnel We are not going to change
    our system for research low volume, going great
    as it is.
  • Older systems for registration, billing built
    for the clinical world.

12
Outpatient Research Subjects
  • A subject enrolled in a research study who is
    physically seen on any CCHMC property, or has a
    test performed on any CCHMC property.
  • Clinical inpatients who are simultaneously
    involved in a research study will also be
    registered as an outpatient for research
    procedures.

13
Overview
  • Roles and responsibilities
  • Principal Investigators
  • Study Coordinators
  • Billing Coordinators
  • Registration Personnel
  • Lead Administrators

14
Research Registration Process
1 2 3 4
Research Study Approved
USF Form Processed
656 Number Assigned
Study Coordinator Schedules Visit
Study Coordinator Pre-Registers Study Subject
Registrar Activates Account
Study Subject Presents for Visit
Study Subject Receives Service
Billing Enters Charges

Charges Electronically Passed to Bill
15
(No Transcript)
16
USF provides important data
  • Funding Source
  • ? Federal/ Non-Profit (Fee schedule 1)
  • ? Industry (Fee schedule 2)
  • Divisional/ Institutional (Fee schedule 2)
  • The funding source determines which fee
    schedule or discount will be used.

17
Scheduling Information
  • Research Registration will not require that you
    change your current scheduling system.
  • Main objective is to ensure scheduling
    information is communicated to the person
    responsible for activating outpatient
    registration.

18
The Basics
  • All research subjects will be registered with a 4
    million patient account number (a unique series)
  • Once the USF form has been completed, a 656
    guarantor number (similar to insurance guarantor
    numbers) will be issued for each funding source.

19
The Basics
  • The hospital service code for all research visits
    will be RSH or RSS for satellite clinics
  • The clinic code for all visits will be the same
    as the clinic code for medical visits (area of
    service)
  • The diagnosis code will be V70.7 for all research
    visits.

20
Registration Steps
  • Pre-registration (Study Coordinator)
  • Account Activation (Clinic or Treatment Center
    personnel)

21
Registration Master Menu Screen
Admit Supervisor Master
Menu 11/26/03 1506

-----------------------------
--------------------------------------------------
-
INQUIRIES
PRINT OPTIONS
! 01 EAD Inquiry
! 20 Print Reports !
02 Numeric Inquiry
! 03 Inhouse Patient
Name Inquiry
! 04 Phonetic Inquiry


CENSUS INQUIRIES

! 10 Nurse Station Census (Occ Beds)
MISCELLANEOUS OPTIONS ! 11 Nurse
Station Census (All Beds) ! 30 Post Bed
Status ! 12 Nurse Stations At A
Glance ! 31 Misc Menu
! 13 Supercensus (1 line)
! 32 Trauma Stat/Alert or Med Resus ! 14
Supercensus (Active File) ! 33
Scheduling ! 15 List Beds
For Nurse Station ! 34 Scheduling
Maintenance ! 16 Care Provider Census
! 35 Insurance Eligibility
! 17 Display Temporary Patients !
36 Message Mailbox
-------------------------------------------------
------------------------------- OPD1 SP06
(LU) Enter
__ Press Enter ! PF11 Signoff

22
Registration Process
Admit Supervisor Register/Admit
Options 11/26/03 1451
F / Pt
Atn Dr
Adm Dt
Isol
Mr -----------------------------
--------------------------------------------------
- INPATIENT OPTIONS
OUTPATIENT OPTIONS ! 01 Admit
Patient ! 20
Register Outpatient ! 02 Preadmit
Patient ! 21 Preregister
Outpatient ! 03 Admit Preadmitted
Patient ! 22 Enter Temporary
Patient ! 04 Admit Temporary Patient
! 23 Register Insurance Ref Pt
! 05 Quick Admit
! 26 Register Preregistered Patient
! 27 Verify
Temporary Patient
EMERGENCY OPTIONS
MISCELLANEOUS
! 30 Enter Emergency Patient ! 10
SEND REG TO PBS ! 31
Quick ER

! 11 Research Registration Options
! 32 Verify Emergency Patient

---------------------------
--------------------------------------------------
--- ! PF13 Master Menu
Enter __ Press Enter ! PF14
Submenu
! PF11 Signoff
23
Registration Process
Research Coordinator Submenu
11/26/03 1516 BLACKSHEEP ,BABA
F 2 / RSH Pt
400001590 Atn Dr GRUPPO, RALPH A.,
Adm Dt
11/26/03 OA Isol
Mr 1002874 --------------------------
--------------------------------------------------
--- RESEARCH REGISTRATION ONLY
PT LOCATION OPTIONS
INPATIENT/EXTENDED STAY ! 30
Transfer Patient ! 01 Research
Preadmit ! 31 Outpatient Bed Menu
! 02 Upgrade Preadmit
! 32 Discharge Patient
! 03 Research Admit
! 33 Census History




RESEARCH
OUTPATIENT
! 10 Research OP Prereg
MISCELLANEOUS OPTIONS
! 11 Research Upgrade Prereg
! 40 Review Patient Information !
12 Research OP Registration
! 41 Regenerate Documents
! 42 Research Charges




24
Research Registration Process
11/26/03 0809 RESEARCH
REGISTRATIONS-----OUTPATIENT ONLY


PATIENT NAME
MEDICAL RECORD NUMBER
-------------------------------
-----------------------------------------------
LAST NAME BLACKSHEEP FIRST NAME
BABA MI _ ADDRESS
______________________ ZIP _____- ____
COUNTY ___
______________________ CITY
_________________ ST __
GUAR/STUDY ________ GUAR NAME
_____________________ SEX/MAR ST
F _ BIRTHDATE __/__ /____
REG DATE __ /__ /__ REG TIME __
/__ HOSP SERV RSH
PT RACE _ CLINIC CODE ___
PRIMARY INVESTIGATOR ______
PI NAME __________________
HPAA _ DIRECTORY _ HOME PHONE ___
- ___ -____ DX V70.7__

MEDICAL RECORD NUMBER
________ LEAVE FIELD BLANK FOR AUTO ASSIGN
PATIENT NUMBER ____________

COMMENTS ______________________
__________________________
--------------------------------------------------
--------------------------
25
Combined Clinic and Research Visits
  • Subjects may be seen in a Clinic for two
    purposes Clinical (ENT regular follow up visit)
    and as part of a research protocol (in ENT or
    another clinic).
  • For these patients/subjects two types of records
    will be generated. One record for the regular
    clinic visit and a second record for the research
    protocol. Each must be labeled correctly and
    forwarded to the appropriate location (clinic
    visit to HIM and research visit to the PI).

26
Where Will Outpatient Research Records be Stored?
  • Records for research subjects seen at any CCHMC
    property in an outpatient setting (Clinic,
    Radiology, Lab, etc.) will be stored in the
    Outpatient Research Record in the Principal
    Investigators office.

27
Outpatient Research Identification
  • When the research subject registers, a set of
    labels will be generated (or an addressograph
    plate will generate). The first line will
    identify the patient as a Research Subject
  • RESEARCH OUTPT
    RESEARCH OAK
  • DOO ,SCOOBY X
    DOO,SCOOBY X
  • 13Y 9 M RSH 04/12/90
    13Y 9M RSO 041290
  • 400001764 M 99999999
    400001764 M 99999999
  • CIAMBARELLA, E 000111
    CIAMBARELLA, E 00011
  • 011204
    011204
  • Documentation labeled as such must be forwarded
    to the principal investigator listed on the
    addressograph/label.

28
Sensitive Research
  • In the case of research subjects enrolled in
    sensitive research, the Sensitive Research form
    will be forwarded to the HIM Department in lieu
    of the copy of the signed informed consent.

29
HIM (Medical Records) Department Responsibility
  • Based on information received on the USF form,
    the HIM Department will maintain a list of PIs,
    along with primary and secondary contacts for
    each Research Study.
  • In the event an Outpatient Research Record is
    required for patient care, the HIM Department
    will contact the PI.

30
What Reports will be Available?
  • Total visits
  • Total pre-registrations that are not activated
  • Summarized by
  • Study
  • Location (Research Main and Research Oak)
  • Clinic Code
  • These are monthly reports.

31
Audit Information
  • Lead Administrators are responsible for
    designating a person (recommend this be the study
    coordinator) to complete the daily audit log to
    ensure research subjects pre-registered are
    consistent with research subjects registered.

32
Audit Information
  • The purpose of completing the daily audit log is
    to ensure accurate registration and APPROPRIATE
    billing.
  • Incorrect billing may occur when
  • Subjects are registered incorrectly as clinical
    patients
  • Subjects that were seen for a research visit were
    not registered

33
Billing
  • Fee schedule tables in Patient Financial system
    discount the charges to the correct amount
  • Bill (invoice created)

34
The Study Bill
35
Billing
  • Ability to pull billing information which resides
    on Finance server into your Access database
  • Monitor expenses by comparing what was approved
    vs. what was billed.
  • Query data and produce reports.

36
Important Tips
  • Pull together institutional representatives to
    discuss issues
  • Get buy-in from faculty, senior management
  • Map out current process
  • Build case for changes (particularly those
    involving expense to institution)

37
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