TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.10 PURPOSE (REPEALED)
Section 1010.10 Purpose (Repealed)
(Source: Repealed at 36 Ill.
Reg. 8017, effective May 8, 2012)
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.20 DEFINITIONS
Section 1010.20 Definitions
"Act"
means the Health Finance Reform Act.
"Admission, Discharge and
Transfer (ADT) trigger event" means messages from HL7 standard, triggered
by admission (A01), Register (A04), Update (A08) and Discharge (A03).
"Affirmation statement"
means a document that, when signed by a hospital or ambulatory surgical
treatment center administrator or an authorized representative of a hospital or
ambulatory surgical treatment center submitting data to the Department,
affirms, to the best of the signer's knowledge, that any necessary corrections
to data submitted to the Department have been made and that the data submitted
are complete and accurate.
"Agency for Healthcare
Research and Quality" or "AHRQ" means a federal agency that is a
part of the U.S. Department of Health and Human Services.
"Ambulatory patient
classification" or "APC" means a definition by the Centers for
Medicare and Medicaid Services (CMMS) for the prospective payment system (PPS)
under Medicare for hospital outpatient services. All services paid under the PPS
are classified into groups called APCs. Services in each APC
are similar clinically and in terms of the resources they require. A payment
rate is established for each APC based on the resources involved in treatment.
"Ambulatory surgical
treatment center" means a facility licensed under the Ambulatory Surgical
Treatment Center Act.
"Application" means
technical software tools that provide access and analysis for the syndromic
surveillance data.
"Batch" means a file
that transfers multiple messages together.
"CCYYMMD" means a
calendar date in the format of century, year, month and day of the week, where
1 = Sunday, 2 = Monday, etc.
"CCYYMMDD" means a
calendar date in the format of century, year, month and day, without
separators.
"Chief complaint" means
a patient’s self-reported complaint of reason for visit. It is the most
complete description and may include multiple symptoms as free text summary of
the patient’s own words as well as a drop-down selection of symptoms.
"Claims and encounter"
means either a request to obtain payment,
and necessary accompanying information, from a health care provider to a health
plan, for health care or an inpatient stay or outpatient visit in
which a claim is not generated.
"Cleaned claims data"
means data that have passed validity tests that edit for individual element
content and comparison with related elements for appropriate context within the
time periods and value ranges appropriate for the data file.
"Clinical Classification
Software" or "CCS" means a diagnosis and procedure
categorization scheme developed by the Healthcare Cost and Utilization Project.
"Compliance percentage"
means the value obtained when the number of cleaned and unduplicated claims and
encounters per calendar month is divided by the reported discharge count for
the same calendar month, with the dividend of this calculation multiplied by
100.
"Computed tomographic scan"
or "CT scan" means a computed tomographic
scan of the head and other parts of the human body.
"Consumer Guide to Health
Care" means a comparative health care information report showing
conditions and procedures that demonstrate the widest variation in charges and
quality of care in inpatient and outpatient services provided in hospitals and
ambulatory surgical treatment centers.
"Current Procedural
Terminology" or "CPT" means a listing of descriptive terms and
identifying codes providing a consistent and standardized language for
reporting medical services and procedures performed by physicians. These codes
are maintained and distributed by the American Medical Association (330 N.
Wabash Ave., Suite 39300, Chicago IL 60611-5885).
"Custom dataset" means
requests for specific data elements for particular research or reporting tasks.
This may include specific aggregations or combinations of data values into
categories or groups.
"Data submission manual"
means the Department's Technical Reference for Data Submission document
specifying the details of the record layout, the outpatient surgical procedure
code range, specifications of identification of emergency department and
observation cases and contact information for questions related to data
submission.
"Data submission profile"
means a set of validation and verification reports containing accumulated
statistical summaries of all data submitted to the Department by the facility
for each month of the current collection period. These reports contain
information identifying claims and encounters that fail Departmental edits, as
well as data quality statistics showing data accepted up to and including the
latest submission.
"Data
use agreement" means a written contract between parties that defines the
care and handling of sensitive or restricted use data, including, but not
limited to, the terms of the agreement, ownership of the data, security
measures and access to the data, uses of the data, data confidentiality
procedures, duration of the agreement, disposition of the data at the
completion of the contract, and any penalties for violation of the terms of the
agreement.
"De-identified" means
data that do not contain directly identifiable individual patient health
information as defined in HIPAA privacy regulations (Security and Privacy); or data
that, through analysis by an experienced expert statistician or by the use of
probability software, can be shown to have a low probability of individual
identification.
"Department" or
"DPH" means the Illinois Department of Public Health.
"Diagnosis Related Group"
or "DRG" means a patient classification scheme that provides a means
of categorizing hospital inpatients according to the resources required in
treatment, developed for the Centers for Medicare and Medicaid Services for use
in the Medicare Prospective Payment System.
"Diagnostic" means the
process used to identify or characterize, as accurately as possible, the
details of a medical condition or injury.
"Electronically submit"
means that required data submission will be carried out by the transfer of
appropriate files to the Department's secure web server. Physical media of any
form or type will not be used in the transfer of these data.
"Emergency Department" or
"ED" means the location within hospitals where persons receive
initial treatment by health care professionals for conditions of an immediate
nature caused by injury or illness. The person treated may or may not be
admitted to the hospital as an inpatient. Services furnished to an individual
who has an emergency medical condition are defined in 42 CFR 424.101.
"Emerging technology"
means new approaches to the treatment of medical conditions through the use of
existing machines and equipment in new and different ways or the development of
new machines and equipment for a specific form of medical treatment.
"Ethnicity" means the
classification of a person's ethnic background. Classification categories
collected will follow the Federal Office of Management and Budget (OMB)
Statistical Policy Directive Number 15, "Race and Ethnic Standards for
Federal Statistics and Reporting".
"Facility" means a
hospital, as defined in the Hospital Licensing Act and the University
of Illinois Hospital Act, or an ambulatory surgical treatment center, as
defined in the Ambulatory Surgical Treatment Center Act. For syndromic
surveillance, a facility can also be a site that provides urgent care, and does
not include ambulatory surgical treatment centers.
"Final closing date"
means the final day, 65 days after the end of each calendar quarter, on which
electronically submitted corrections and missing data are accepted for each
quarterly data submission period.
"Federal Information
Processing Standards" or "FIPS" means a standardized set of
numeric or alphabetic codes issued by the National Institute of Standards and
Technology (NIST) to ensure uniform identification of geographic entities
through all federal government agencies.
"Fully populated test data"
means that each field or individual element specified in each record of the
file contains data values. Complete data allow the exercise of all parts of the
computer program used to produce the file. This will provide more robust testing outcomes, reduce the number of test
runs necessary, and improve the quality of data submissions.
"Healthcare Common Procedure
Coding System" or "HCPCS" means a set of health
care procedure codes based on the American Medical Association's Current
Procedural Terminology (CPT). The HCPCS was established to provide a
standardized coding system for describing the specific items and services
provided in the delivery of health care. HIPAA made the HCPCS mandatory for
Medicare and Medicaid billings. HCPCS includes three levels of codes:
Level I consists of
the American Medical Association's Current Procedural Terminology (CPT) and is
numeric.
Level II codes are
alphanumeric and primarily include non-physician services such as ambulance
services and prosthetic devices.
Level III consists
of temporary codes for emerging technologies, services and procedures.
"Healthcare Cost and
Utilization Project" or "HCUP" means a group of health care
databases and software tools and products created by a government and industry
partnership and sponsored by AHRQ.
"Health plan" means an
individual or group plan that provides, or pays the cost of, medical care. Further
explanation can be found in HIPAA privacy regulations.
"HH" means clock time in
hours using 24-hour time from 00 to 23 rounded to the nearest hour.
"Health Insurance Portability
and Accountability Act privacy regulations" or "HIPAA privacy
regulations" means regulations promulgated at 45 CFR 160 and 45 CFR 164,
Subparts A and E, under section 264(c) of the Health Insurance Portability and
Accountability Act of 1996.
"Health Level 7 (HL7)"
means the industry standards organization (www.hl7.org) for healthcare data
exchange. HL7 is a registered trademark of Health Level Seven, Inc. Reg. U.S.
Pat and TM office.
"HL7 version 2.5.1"
means a nationally recognized standard for electronic data exchange between
systems housing health care data. HL7 version 2.5.1 defines syntax, format and
standard vocabulary for HL7 messages.
"Hospital" means any
institution, place, building, or agency, public or private, whether organized
for profit or not for profit, that is subject to licensure by the Illinois
Department of Public Health under the Hospital Licensing Act, and the
University of Illinois Hospital as defined in the University of Illinois
Hospital Act.
"Imaging" means the
technique and process used to create images of the human body or its parts or
functions for clinical purposes seeking to reveal, diagnose or examine disease
or injury.
"Implementation guide"
means a national HL7 standard document that guides the HL7 messages for
syndromic surveillance submissions defining the message and content references
for electronic health record certifications.
"Initial closing date"
means the date, 60 days after the end of each calendar quarter, established for
all hospitals and ambulatory surgical treatment centers to electronically
submit inpatient and outpatient claims and encounter data to the Department.
"Invasive" means a medical
procedure that penetrates or breaks the skin or a body cavity by means of a
perforation, incision, catheterization or other methods into a patient's body.
"Limited datasets" means
data containing protected health information (PHI) that excludes certain direct
identifiers of the individual or of relatives, employers or household members
of the individual, as defined in HIPAA privacy regulations.
"Magnetic resonance imaging"
or "MRI" means a technology used to visualize internal body
structures by using strong magnet fields in conjunction with radio frequency
fields to analyze deep soft tissue without the use of harmful radiation.
"Major Diagnostic Category"
or "MDC" means a collection of DRGs for categorizing specifically
defined interventions and illnesses related to an organ or a body system, not to the cause of an illness or injury.
"Mammography" means the
process of utilizing low-dose X-rays to examine the human breast as a
diagnostic and screening tool for the detection of cancer.
"Meaningful Use" is the
original term in the Health Information Technology for Economic and Clinical
Health (HITECH) Act for the exchange of health care data across systems to
promote meaningful use of health information technology to improve the quality
and value of American health care. Meaningful Use is the criteria cited to
satisfy the CMMS final rule of the federal HITECH Act of 2009 (78 FR 5565,
January 25, 2013). Meaningful Use program was later termed Promoting
Interoperability.
"Minimally invasive"
means a medical procedure carried out by entering the body
through the skin or through a body cavity or anatomical opening, but with the
smallest disturbance possible to these structures. Special medical equipment
may be used, such as fiber optic cables, miniature video cameras and special
surgical instruments handled via tubes inserted into the body through small
openings in its surface.
"National Provider Identifier"
or "NPI" means a unique identification number assigned to all health
care providers to be used by all health plans. The NPI will be issued and
maintained by the National Provider System.
"National Uniform Billing
Committee" or "NUBC" means the group including all major
national provider and payer organizations formed to develop and maintain the
national standard health care uniform bill.
"Near real-time" means
the timeliness of the data submitted for syndromic surveillance. Near real-time
is defined in the implementation guide as data that must be submitted at least
within 24 hours of the date and time of the patient’s initial encounter.
Updates to a patient record must also be submitted within 24 hours of the
information being added to the record. Real time data transmission, or very
frequent batch data transmission, is at least hourly or <15 minutes from
entry in the hospital record.
"National Institute of
Standards and Technology (NIST)" means the government agency that
developed the syndromic surveillance message certification tool.
"Non-invasive surgery"
means a medical procedure using highly focused beams of radiation when the
nature or location of the condition is not amenable to mechanical intervention.
"Observation
care" or "OC" means services furnished to a person by a hospital
on the hospital's premises, including use of a bed and at least periodic
monitoring by a hospital's nursing or other staff, which are reasonable and
necessary to evaluate an outpatient's condition or to determine the need for a
possible admission to the hospital as an inpatient. In general, the duration of
observation care services is less than 24 hours, although, in some
circumstances, patients may require a second day.
"Office of the National
Coordinator (ONC)" means the national agency that establishes the standard
used for syndromic surveillance in the CMMS final rule of the HITECH Act of
2009.
"On-boarding" means the
process for a hospital or facility to connect to DPH to test and submit
syndromic surveillance messages.
"Organizational Identifier
(OID)" means the registration of a facility obtained at HL7.org. This is
an alternative Facility ID to the NPI for syndromic surveillance.
"Outpatient" means any
health care service provided in a hospital to a patient who is not admitted to
the hospital as an inpatient, or any health care service provided to a patient
in a licensed ambulatory surgical treatment center. For syndromic surveillance,
Emergency Department services are uniquely identified as separate from other
outpatient visits.
"Outpatient surgery" means
specific procedures performed on an outpatient basis in a hospital or licensed
ambulatory surgical treatment center. Specific ranges of required procedure
codes can be found in the Department's data submission manual.
"Patient class" means
patient classification within a facility, including for example Emergency,
Inpatient or Observation.
"Personal health information"
or "PHI" means the information defined in HIPAA privacy regulations.
"Public Health Information
Network" or "PHIN" means the Center for Disease Control's (CDC)
national initiative to increase capacity of public health agencies to
electronically exchange data and information across organizations and
jurisdictions. The PHIN Vocabulary Access and Distribution System (VADS)
standard code set values are available at https://www.cdc.gov/phin/resources
/vocabulary/index.html.
"Positron emission tomography
scan" or "PET scan" means a nuclear medicine imaging technology
that creates a three dimensional view of functional body processes.
"Public use data" means
any form of data from the Department's comprehensive discharge database or
facility-level database that contains de-identified data.
"Race" means the
classification of a person's racial background. Classification categories
collected will follow the Federal Office of Management and Budget (OMB)
Statistical Policy Directive Number 15, "Race and Ethnic Standards for
Federal Statistics and Reporting".
"Raw data" means any
file, individual record, or any subset thereof that contains information about
an individual health care service provided to a single patient and is released
by the Department in data products or custom data files.
"Reciprocal data availability"
means that, if a data requester controls the discharge data or syndromic
surveillance of another state, release of Illinois discharge data or syndromic
surveillance to that state entity would be contingent on the availability of
discharge data or syndromic surveillance from that state of comparable
quantity, quality and content at a similar price point.
"Research" means a systematic investigation,
including development, testing and evaluation, designed to develop or
contribute to generalizable knowledge. Activities that meet this definition
constitute research, whether or not they are conducted or supported under a
program that is considered research for other purposes. For example, some
demonstration and service programs may include research activities.
"Secure
file transfer protocol (SFTP)" means a network protocol for sending files
securely in a protected shell for data submissions.
"Small number" means any
number that is small enough to be useful in an attempt to determine the
identity of a specific individual patient when used in conjunction with other
elements in the data file or when the data file is linked with information from
other sources. The Department considers a small number to be any cell size
fewer than 10.
"Sonography" and "Ultrasonography"
mean the use of sound waves at frequencies above the audible range of human
hearing as a diagnostic tool for visualizing internal body structures,
including tendons, muscles, joints, organs and other internal masses.
"Standard" means
technical specifications for data exchange.
"Surgery" means treatment of diseases or injuries by manual and/or instrumental
methods. The methods may include invasive, minimally invasive, or non-invasive
procedures, depending on the condition treated and the nature of the
instruments and technology used.
"Syndromic
Surveillance" means a data collection process that regularly and
systematically uses health-related data in near real-time to make information
available on the health of a community. The information provides disease trends
and detection of emerging events for surveillance.
"Therapeutic" means
medical activities designed to treat or cure a disease, condition or injury.
"Uniform" means related
unique data values that are combined into a smaller number of common
categories.
"Uniform bill" means the
uniform electronic billing form pursuant to the Health Insurance Portability
and Accountability Act, which is developed as a standard instrument
for use by institutions and payers in the handling of health care claims.
(Section 4-2(d)(1) of the Act)
"Unique Physician
Identification Number" or "UPIN" means a unique identification
number assigned to all Medicare providers. The UPIN Registry is maintained by
the National Heritage Insurance Company under contract from the Centers for
Medicare and Medicaid Services.
"Urgent Care Services"
means services defined in 42 CFR 405.400 that are furnished within 12 hours in
order to avoid onset of an emergency medical condition. Urgent Care Services
differs from services provided in response to an emergency medical condition
because immediate care is not needed to avoid placing the health of the
individual in serious jeopardy or to avoid serious impairment or dysfunction.
"Validation" means the
process for healthcare systems to test and certify the syndromic messages to be
correctly formatted with complete information.
(Source: Amended at 47 Ill.
Reg. 4017, effective March 10, 2023)
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.30 INCORPORATED AND REFERENCED MATERIALS
Section 1010.30 Incorporated and Referenced Materials
The following materials are incorporated or referenced in
this Part:
a) Federal Regulations
1) Prospective
Payment Systems for Inpatient Hospital Services (42 CFR 412), October 1, 2005
2) Medical
Facility Construction and Modernization (42 CFR 124), October 1, 2005
3) Security
and Privacy (45 CFR 164), October 1, 2005
4) Medicare
and Medicaid Programs; Electronic Health Record Incentive Program, Final Rule (75
FR 44313, July 28, 2010) available at:
https://www.federalregister.gov/documents/2010/07/28/2010-17207/medicare-and-medicaid-programs-electronic-health-record-incentive-program
5) Medicare
and Medicaid Programs; Electronic Health Record Incentive Program - Stage 2,
(See Meaningful Use), Final Rule (77 FR 53967, September 4, 2012) available
at: https://www.federalregister.gov/documents/
2012/09/04/2012-21050/medicare-and-medicaid-programs-electronic-health-record-incentive-program-stage-2
6) Medicare
and Medicaid Programs; Patient Protection and Affordable Care Act;
Interoperability and Patient Access for Medicare Advantage Organization and
Medicaid Managed Care Plans, State Medicaid Agencies, CHIP Agencies and CHIP
Managed Care Entities, Issuers of Qualified Health Plans on the
Federally-Facilitated Exchanges, and Health Care Providers (See CMMS
Interoperability rule; Admission, Discharge, and Transfer (ADT) at
25586-25603), Final Rule (85 FR 25510, May 1, 2020) available at: https://www.federalregister.gov/documents/2020/05/01/
2020-05050/medicare-and-medicaid-programs-patient-protection-and-affordable-care-act-interoperability-and
7) Health
Information Technology: Initial Set of Standards, Implementation
Specifications, and Certification Criteria for Electronic Health Record
Technology, Final Rule (75 FR 44589, July 28, 2010) available at: https://www.federalregister.gov/documents/2010/07/28/2010-17210/health-information-technology-initial-set-of-standards-implementation-specifications-and
8) 2014
Edition Release 2 Electronic Health Record (EHR) Certification Criteria and the
ONC HIT Certification Program; Regulatory Flexibilities, Improvements, and
Enhanced Health Information Exchange, Final Rule (79 FR 54429, September 11,
2014) available at: https://www.federalregister.gov/documents/2014/09/11/2014-21633/2014-edition-release-2-electronic-health-record-ehr-certification-criteria-and-the-onc-hit
b) Federal Guidelines
1) "Race
and Ethnic Standards for Federal Statistics and Reporting", Statistical
Policy Directive Number 15, Federal Office of Management and Budget (OMB),
October 30, 1997
2) HL7
version 2.5.1. Implementation Guide: Syndromic Surveillance Release 1-US Realm,
Standard for Trial Use, July 2019. (http://www.hl7.org/)
3) Data
Modernization Initiative available at: https://www.cdc.gov/ surveillance
/data-modernization/index.html?CDC_AA_refVal=https
%3A%2F%2Fwww.cdc.gov%2Fsurveillance%2Fsurveillance-data-strategies%2Fdata-IT-transformation.html
4) NIST
2015 Edition ONC HealthIT Certification Test Tools available at:
https://www.nist.gov/itl/ssd/systems-interoperability-group/nist-2015-edition-onc-healthit-certification-test-tools
c) Federal Statutes
1) Gramm-Leach-Bliley
Act (12 U.S.C. 1811)
2) Social
Security Act (42 U.S.C. 1320)
3) Health
Insurance Portability and Accountability Act of 1996 (110 U.S.C. 1936)
4) Health
Information Technology for Economic and Clinical Health (HITECH) Act, Title
XIII of Division A and Title IV of Division B of the American Recovery and
Reinvestment Act of 2009 (ARRA), 42 U.S.C. Section 300jj et seq.;
Section 17901 et seq.
5) Public
Health Security and Bioterrorism Preparedness and Response Act of 2002, 42
U.S.C. 262a
d) State Statutes
1) Illinois Health Finance Reform Act [20 ILCS 2215]
2) Department
of Public Health Powers and Duties Law of the Civil Administrative Code of Illinois [20 ILCS 2310]
3) University of Illinois Hospital Act [110 ILCS 330]
4) Ambulatory
Surgical Treatment Center Act [210 ILCS 5]
5) Hospital
Licensing Act [210 ILCS 85]
6) Communicable
Disease Reporting Act [745 ILCS 45]
7) Illinois
Health Statistics Act [410 ILCS 520]
8) Department
of Public Health Act [20 ILCS 2305]
e) State of Illinois Rules
Control of
Communicable Diseases Code (77 Ill. Admin. Code 690)
f) Federal
regulations and guidelines incorporated by reference in this Part are
incorporated on the date specified and do not include any later amendments or
editions.
(Source:
Amended at 47 Ill. Reg. 4017, effective March 10, 2023)
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.40 DATA SUBMISSION REQUIREMENTS
Section 1010.40 Data Submission Requirements
a) Inpatient and Outpatient
Claims and Encounter Data
1) Hospitals
and ambulatory surgical treatment centers shall electronically submit patient
claims and encounter data, as outlined in this subsection (a), to the
Department no later than the initial closing date, 60 calendar days after the
last day of each calendar quarter. Calendar quarters shall begin on January 1,
April 1, July 1, and October 1 and shall end on March 31, June 30, September
30, and December 31. Beginning no later than 45 days after the last day of
each calendar quarter, hospitals and ambulatory surgical treatment centers
shall begin an internal review of all quarterly data accepted by the Department.
The quarterly review shall involve detailed evaluation of data quality feedback
reports by facility staff with sufficient general knowledge of patient mix and
services provided to allow identification of unreasonable or incomplete
submission statistics.
A) Hospitals shall submit
to the Department:
i) Claims
and encounter data pertaining to each inpatient discharged. Production and
test data shall be submitted as specified in Appendix A;
ii) Claims
and encounter data pertaining to case data for each emergency department (ED)
visit (wherever care is administered) and each observation case (OC) in the
outpatient format specified in Appendix C; and
iii) Claims
and encounter data related to diagnostic or therapeutic imaging conducted
during or related to an inpatient stay that may include, but are not limited
to, techniques described in Appendix K. These data may include, but are not
limited to, events occurring during a visit for surgery or scheduled imaging
for purposes of evaluating the need for treatment, determining the nature or
extent of necessary treatment, or evaluating the outcomes of treatment. Data
elements for these cases, specified in Appendix C, shall
begin with the cases for patients discharged on October 1, 2012.
B) Hospitals
and ambulatory surgical treatment centers shall report to the Department:
i) Information
relating to any patient treated with an ambulatory surgical procedure within
any of the general types of surgeries as specified in Appendix B;
ii) Claims
and encounter data for each surgical or invasive procedure outlined in
subsection (a)(1)(B)(i), as specified in Appendix C;
iii) Claims
and encounter data related to diagnostic or therapeutic imaging that may include,
but are not limited to, techniques described in Appendix K. These data may
include, but are not limited to, events occurring during a visit for surgery or
scheduled imaging for purposes of evaluating the need for treatment,
determining the nature or extent of necessary treatment, or evaluating the
outcomes of treatment. Data elements for these cases, specified in Appendix C,
shall begin with the cases for patients discharged on October 1, 2012.
C) Only
data consisting of the elements listed in Appendices A and C in the expanded
format, as detailed in the Department's data submission manual, will be
accepted.
2) Each
hospital and ambulatory surgical treatment center shall electronically submit
to the Department all patient claims and encounter data pursuant to this
subsection (a). These submissions shall be in accordance with the uniform
electronic transaction standards and code set standards adopted by the
Secretary of Health and Human Services under the Social Security Act and the
physical specifications, format and record layout specified in the Department's
data submission manual.
3) To be
considered compliant with this Section, a hospital's or ambulatory surgical
treatment center's data submission shall:
A) Be
submitted to the Department electronically, as specified in the data submission
manual;
B) Consist
of an individual facility data file; and
C) Meet
the Department's minimum level of data submission compliance on or before the
data submission due date. Hospitals and ambulatory surgical treatment centers shall
maintain a compliance percentage of no less than 98% for each calendar month.
4) Failure
to comply with this Section may subject the facility to penalties as provided
in the Ambulatory Surgical Treatment Center Act and the Hospital Licensing Act.
b) Inpatient
and Outpatient Report of Monthly Discharge and Outpatient Surgery Counts
1) Each
hospital shall, within 30 calendar days following the last day of each calendar
month, submit:
A) The
actual total number of hospital inpatient discharges for that calendar month. In
the case of multiple births, each child is counted as a discharge. This number
shall include those inpatient cases receiving diagnostic or therapeutic imaging
as defined in subsection (a)(1)(A)(iii); and
B) The
actual number of hospital outpatient cases with a surgical procedure as defined
in this Part for that calendar month.
2) Each
hospital shall, within 30 calendar days following the last day of each calendar
month, submit for each category the actual number of hospital outpatient cases
with an emergency department visit, observation stay, or surgery, as defined in
this Part for that calendar month. Beginning with patients discharged on
October 1, 2012, each hospital shall submit the actual number of cases with an
outpatient visit for diagnostic or therapeutic imaging as defined in subsection
(a)(1)(B)(iii). Each patient shall be counted only once, except that
imaging-only visits shall be counted separately. Outpatient surgical cases,
regardless of other services, shall be counted as surgical cases. Non-surgical
cases, excluding imaging-only visits, shall be counted separately as ED or OC,
based on the last service received.
3) Each
ambulatory surgical treatment center shall, within 30 calendar days following
the last day of each calendar month, submit the actual total number of licensed
ambulatory surgical treatment center outpatient cases with surgery for that
calendar month as defined in this Part. Beginning with patients discharged on
October 1, 2012, this count shall include the actual number of cases with a
visit for diagnostic or therapeutic imaging as defined in subsection
(a)(1)(B)(iii).
4) All
filings required in this Section shall be reported using the Department's
electronic submission systems.
5) Effective
60 days after the end of each calendar quarter, monthly reported discharge
count acceptance for that calendar quarter will end. If any facility finds it
necessary to change monthly reported counts after the initial closing date and
before the final closing date, the facility administrator shall submit the
revised monthly count with a written justification.
c) Syndromic
Surveillance
Hospitals are facilities that are
mandated to report and urgent care centers and other facilities providing
urgent care services are recommended to report the following:
1) Facilities
shall electronically submit all patient clinical encounter data, as outlined in
this subsection (c), to the Department in near real-time, no later than 24
hours from the initial patient date and time of visit, and preferably within 1
hour of the encounter. Updates to the patient record shall also be submitted
within these timeframes. Facilities shall submit to the Department:
A) Clinical
encounter data pertaining to each Emergency Department (ED) visit. Message
types for Registration, Admissions, Discharge and Update to be submitted.
Production data elements are specified in Appendix L;
B) Clinical
encounter data pertaining to all inpatient visits. Message types for Admission,
Updates and Discharge to be submitted. Production data elements are specified
in Appendix L;
C) Clinical
encounter data pertaining to observation visits which may occur as a result of
an ED visits or precede an inpatient admission. Production data elements are
specified in Appendix L; and
D) Clinical
encounter data pertaining to urgent care visits as defined in Section 1010.20.
2) Each
facility shall electronically submit to the Department all patient clinical
encounter data pursuant to this subsection (c). These submissions shall be in
accordance with the uniform electronic transaction standards and code set
standards adopted by the Office of the National Coordinator and the CMMS in
accordance with the HITECH Act of 2009 and the HL7 specifications, format and
record layout specified in the HL7 syndromic surveillance implementation guide
version 2.0 or later as adopted by the HL7 organization.
3) To be
considered compliant with this Section, a facility's data submission shall:
A) Be
submitted to the Department electronically, in near real-time no later than
within 24 hours of the date and time of visit.
B) Consist
of batched HL7 version 2.5.1 messages.
C) Meet
the Department's minimum level of data submission compliance for data quality
standards for completion of elements outlined in Appendix L.
D) Be
submitted for every calendar day. Any outages of data submission will need to
be backfilled once issues are resolved.
E) Facilities
shall provide notice one week in advance of the reporting system being offline
for 24 hours or more for any reason such as system upgrade or vendor
transition, if the event was planned. In the event of an unplanned system
outage, hospitals shall make all possible attempts to bring the system online
in a timely manner.
F) Any facility
that falls out of compliance for more than seven days shall submit a resolution
plan to the Department with a correction timeline of 30 days.
G) Facilities
may submit data directly to the Department or through a third party acting as
their agent. Providers selecting this option are responsible for ensuring that
all data specifications conform to the requirements of this Part.
4) Failure
to comply with this Section may subject the facility to penalties as provided
in the Ambulatory Surgical Treatment Center Act and the Hospital Licensing Act.
(Source: Amended at 47 Ill.
Reg. 4017, effective March 10, 2023)
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.50 COMMON DATA VERIFICATION, REVIEW, AND COMMENT PROCEDURES
Section 1010.50 Common Data Verification, Review, and
Comment Procedures
a) Each
facility shall review its patient discharge data for accuracy and completeness
before submitting the data specified in this Part to the Department.
b) The
Department will edit each data submission for proper file formatting; content
and context edits will be applied to each data element as appropriate; the file
will be checked for duplicate records; and the database transactions will
result in a data submission profile that will be available in electronic format
on the Department's data submission web site.
c) The
submitting facility shall obtain and review the data submission profile as
specified in subsection (b) of this Section from each data submission to verify
that data received and accepted by the Department are in fact a complete and
accurate representation of the services provided by the facility during the
stated time frames. If a facility or the Department determines that any data
are in fact incomplete or inaccurate, it is the facility's responsibility to
submit corrected data prior to the final closing date of the affected data
collection period.
d) If
the Department determines that data submitted by a facility are questionable,
inaccurate or incomplete during or after the close of a quarterly submission
period, the Department shall conduct an on-site review of the facility's data
submission practices. Upon notification of the need for such a review by the
Department, any hospital or ambulatory surgical treatment center affected
shall, within 2 calendar weeks or 10 working days, whichever is the longer,
gather information related to the review process. The facility shall provide
suitable workspace and access to all required information from the medical
records and patient claims and encounter data underlying and documenting the
inpatient or outpatient data under review. Facilities shall provide access to
other related documentation deemed necessary to conduct a successful desk audit
of inpatient and outpatient data submitted. The on-site review shall be
carried out by Department staff over a minimum of one working day and extend
for no more than three working days. The facility under review shall ensure
the availability of persons knowledgeable of the internal organizational
processes and information processing systems with the ability to identify
inaccurate and unreasonable data characteristics based on the patient mix and
services provided by the facility. Facility staff shall produce a summary
document within 30 days identifying the findings of the on-site review and
detailing the corrective action necessary to correct the deficiencies
discovered. The facility shall closely monitor future data submissions to
ensure that submissions accurately reflect actual patient mix and health care
services provided. It is the responsibility of each facility to review the
results of each data submission for erroneous, inaccurate, incomplete or
unreasonable information in data accepted by the Department and to resubmit
accurate data prior to the end of the submission period.
e) Final
edited data shall be received prior to the final closing date, 20 calendar days
after the start date for internal data review as specified in Section
1010.40(a)(1) of this Part. Five calendar days are specified between the
initial and final closing dates to correct errors in claims and encounter data
that were rejected on the last day of submission. There shall be no correction
period for erroneous data received during this five-day period. To meet these
requirements, the facility shall do all of the following:
1) Correct
and re-submit all data rejected throughout the quarterly submission period
because of errors revealed by the Department edit checks performed under
subsection (b) of this Section, and submit any missing claims and encounter
data;
2) Review
the resultant data profile for accuracy and completeness; and
3) Supply
the Department with an affirmation statement, signed by the chief executive
officer or designee, indicating that the facility's data are accurate and
complete.
f) Failure
to comply with subsections (d) and (e) of this Section shall result in the
facility's being noncompliant with this Section, and the facility may be
subject to penalties as provided in the Ambulatory Surgical Treatment Center
Act and the Hospital Licensing Act.
g) After
the facility has made any revisions under subsection (e) of this Section in the
data for a particular time period, a data submission profile will be available
for the submitting facility's review.
h) If
the Department discovers data errors after releasing the data, or if a facility
representative notifies the Department of data errors after the Department
releases the data, the Department will note the data errors as caveats to the
completed datasets. No revisions or additions to discharge data, case data, or
monthly counts will be accepted after the final closing date of each quarterly
data collection period. If the Department makes an error in the preparation,
presentation or reporting of collected data, the error will be corrected.
i) The
Department will reply to the submitting facility acknowledging receipt of the
signed affirmation statement required in subsection (e)(3).
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.55 SYNDROMIC DATA VERIFICATION, REVIEW, AND COMMENT PROCEDURES
Section 1010.55 Syndromic Data Verification, Review, and
Comment Procedures
a) The
facility will participate in on-boarding and validation by submitting test
messages to the Department in HL7 version 2.5.1 format.
b) Validation
will include Department review of test messages demonstrating the ability to
send all data elements listed in Appendix L. Upon Department approval,
facilities will begin sending continuous live data as a production feed,
post-testing. The Department will review the first 30-days of messages in
production for completion and accuracy with code sets as a second step in
validation. The Department will confirm whether the submission is valid.
c) The
Department will process data from the HL7 message, extracting the data and
storing it in Department technology infrastructure.
d) The
Department will send modified messages to the Centers for Disease Control and
Prevention for additional processing into analytical applications for use by
public health authorities as identified in the Control of Communicable Diseases
Code.
e) The facility
will send messages from an ONC NIST-certified interface.
f) The facility
technical contact information will be provided to the Department and kept
up-to-date for the Department to utilize in the event data submission issues
arise. This will include a facility point of contact and can also include an
Electronic Medical Record vendor at the discretion of the facility.
g) The facility
will complete a re-validation process, when there is a major upgrade, long
outage or vendor change to the facility’s Electronic Medical Record.
Notification shall be made to the Department at least 30 days prior to a change
that requires a need for re-validation.
h) The facility
will respond within 15 days to any Department identified errors or needs for
improvements and corrections of data quality. This may include review of chief
complaint content for free text content improvements, incomplete information or
non-standardized coded data.
i) The
facility may be asked for independent confirmation of counts of total visits,
visit types or specific causes (such as overdose counts) to confirm accuracy
and validity of the syndromic surveillance data.
j) The Department
will supply annual documentation that the facility is compliant with Promoting
Interoperability standards for Federal CMS reimbursement.
(Source: Added
at 47 Ill. Reg. 4017, effective March 10, 2023)
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.60 DATA DISSEMINATION
Section 1010.60 Data Dissemination
a) The
Department will provide facilities the opportunity to review the Consumer Guide
to Health Care (Guide) prior to public release. The entire report will be made
available to each facility on the Department's secure web server for review
before publication. This review period will end 15 working days after the
availability date of the review material. During the review period, each
facility may submit written comments concerning its report content to the
Department. Comments shall be submitted on facility letterhead and shall be
signed by the administrator or designee. All comments received by the
Department will be kept on file. No comments will be accepted after the end of
the review period and no changes to the content of the Guide will be accepted. If
any facility or the Department finds erroneous or incomplete data in the Guide,
these data will be identified and footnoted prior to publication. If the
Department makes an error in the preparation or presentation of the Guide, the
error will be corrected.
b) Limited
Data Product and Report requests approved by the Department shall result in the
creation of the minimum necessary data set from the population of data elements
available to the requester and accompanying data use agreement covering access,
usage, distribution and confidentiality of the data.
1) The
Department, in accordance with Section 2310-33 of the Department of Public
Health Powers and Duties Law of the Civil Administrative Code of Illinois, will
charge fees to the requesting entity for providing access to data files or
producing studies, data products or analyses of data. A schedule of fees for
standard and custom datasets and products according to category of purchaser is
presented in Section 1010.70 of this Part. In determining fees, the Department
will consider all of the following:
A) Type
of data and specified usage;
B) Record
count and computer time required;
C) Access
fees for computer time;
D) Staff
time expended to process the request; and
E) Handling
and shipping charges.
2) All
requests for data files, data products, aggregations or reports containing
limited data elements shall be made in writing to the Department using Department
forms available at
https://dph.illinois.gov/content/dam/soi/en/web/idph/files/forms/formsoppsdischarge-data-request-form.pdf.
All data obtained from the Department shall be used solely for the purpose
identified by the requesting entity and for use by the requesting entity. The
scope and term of this usage will be detailed in a data use agreement specific
to each request. Use of the data for any other
purpose shall require a separate and specific written request, approval, and
data use agreement.
3) When the
Department prepares facility-specific data, reports or comparative analyses for
public release, affected facilities will be given the opportunity to review and
comment on the data, studies or reports and their content prior to release to
the public. Facilities will be provided access to the entire report on the
Department's secure web server for review prior to publication. The review
period will end 15 working days after the availability date of the review
material. While no changes to previously submitted data will be accepted, the
Department will accept written comments and explanations from facilities during
the review period. The Department will keep these comments and explanations on
file and, as appropriate and reasonable, will incorporate them into the text
description of the published report, study or analysis. If a Department error
is found in the publication, the error will be corrected.
c) De-identified
Data Files and Reports
1) Public
use data files, reports and studies based on information submitted by hospitals
and ambulatory surgical treatment centers shall contain de-identified data and
shall comply with State and federal law, including, but not limited to, the
Gramm-Leach-Bliley Act and the HIPAA privacy regulations.
2) All
requests for public use files or special compilations, reports, studies or
analyses derived from public use files shall be made in writing to the
Department, with forms available at
https://dph.illinois.gov/content/dam/soi/en/web/idph/files/forms/formsoppsdischarge-data-request-form.pdf.
The release of data related to an approved public use data request shall not
require a detailed data request form or comprehensive data use agreement. However,
each request will be evaluated and, if necessary, will require a signed data
use agreement appropriate to the content of the data requested. The data use agreement
will include, but not be limited to, restrictions on patient identification and
sale or release of the data to third parties.
3) Facility
syndromic surveillance data submitted to the Department may be used for
epidemiological investigation or other disease intervention activities of the
Department or local health department. Investigation shall include obtaining
laboratory and clinical data necessary for case ascertainment. Findings of the
investigation shall be used to institute control measures to minimize or reduce
the risk of disease spread or to reduce exposures in a public health emergency
event recognized or declared by local, State, or federal authorities.
4) Syndromic
surveillance data will be released for local health departments and the Centers
for Disease Control and Prevention, consistent with the Department of Public
Health Act and the Control of Communicable Diseases Code and used for monitoring
public health. Release will be through secure transfer of data and accessed by
approved software tools for data analysis.
5) Release
of aggregate, de-identified syndromic surveillance data is permitted only by
the Department or local health department of the jurisdiction that the data
describes.
6) Release
of syndromic surveillance data to individuals or entities other than the public
health agencies identified requires a data use agreement. A data request form
to initiate the process will be made available publicly at
https://redcap.dph.illinois.gov/surveys/?s=MAPECL9E73. Any release of syndromic
surveillance data must be consistent with the Department of Public Health Act
and Health Statistics Act. Only the Department can review and approve the
release of visit-level syndromic surveillance data to a third party.
7) Facility
user access is permitted only for data specific to the user's facility or
health care system. Any sharing of data across facilities will require an
agreement between the facilities and provided to the Department or due to provisions
in applicable administrative rules (such as for extensively drug-resistant
organism (XDRO) data or data for the Prescription Monitoring Program (PMP)).
Aggregate data at the State level may be shared with facility users, but
aggregate level of visits to facilities at the county level may not be shared
with facility users.
8) The
Department will not release any syndromic data or information obtained
pursuant to this Part to any individuals or entities for purposes other
than the protection of the public health. Release will be through secure transfer
of data and accessed by approved software tools for data analysis.
A) All
access to data by the Department, reports made to the Department, the identity
of or facts that would tend to lead to the identity of the individual who is
the subject of the report, and the identity of or facts that would tend to lead
to the identity of the author of the report, the author being an individual or
the reporting facility, in the case of syndromic surveillance, shall be
strictly confidential, are not subject to inspection or dissemination, and
shall be used only for public health purposes by the Department, local public
health authorities, or the Centers for Disease Control and Prevention.
B) Entities
or individuals submitting reports or providing access to the Department shall
not be held liable for the release of information or confidential data to the
Department in accordance with this subsection. (Section 2(h)(i)(C) of the
Department of Public Health Act) [20 ILCS 2305/2(h)(i)(C)]
d) Patient
Confidentiality and Data Security
1) Patient
name, address, any part of the Social Security number, unique
patient identifier based on the last four digits of the patient's Social
Security number, or any other data that the Department
believes could be used to determine the identity of an individual patient shall
be stored and processed in the most secure manner possible. (Section 4-2(d)(4)
of the Act) Only authorized staff will have access to these data, with all
computers and databases secured by password. Only computers located in
controlled Department work sites will allow access to these data.
2) Patient
name, address, and any part of the Social Security number will not be released
publicly. These data may be used to link discharge data or syndromic
surveillance with other data sets internal or external to the Department, with
linkage results released under guidelines of appropriate Department controls.
The patient name, address, and any part of the Social Security number will not
be released as part of these linkage results. The Department will evaluate any
request for access to any or all of these three specific identifiers by
authorized staff of other Illinois State agencies, local health departments, or
approved research project participants individually. Evaluation criteria
include need and security of patient confidentiality. The unique patient
identifier may be released to State agencies, local health departments and
approved data requesters using appropriate guidelines.
(Source: Amended at 47 Ill.
Reg. 4017, effective March 10, 2023)
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.70 DATA CUSTOMER CATEGORIES AND DATA PRODUCT FEE SCHEDULE
Section 1010.70 Data Customer Categories and Data
Product Fee Schedule
This Section establishes customer categories, data product
descriptions, and data product fees. The release of any patient level or small
number data by the Department shall be contingent on the approval of the
request and execution of an appropriate data use agreement.
a) Customer
categories are established as follows:
1) Category I: Resellers
A) Any
corporation, association, coalition, person, entity or individual that
redistributes in any form any of the data or products (or any subset of the
data or products) obtained from the Department for any revenue is engaged in
reselling of the data or products and shall pay for the data or products at the
reseller rate.
B) All
redistribution shall be restricted to de-identified data as defined by HIPAA
privacy regulations.
2) Category
II: Commercial, Private, For-Profit Organizations and Non-Illinois State
and Local Government Entities
A) Any
corporation, association, coalition, person, entity or individual that
functions in whole or in part for the benefit of the owners, members, or
sponsors of the corporation or organization seeking to obtain data or products
(or any subset thereof) from the Department is presumed to be acquiring the
data or products for a commercial use;
B) Any
non-profit organization that purchases data materials on behalf of, either in
whole or in part, or receives payment from, for-profit organizations for work
done is presumed to be acquiring the data or products for a commercial use;
C) Non-Illinois
state and local government data release will be contingent on reciprocal data
availability; and
D) The
Department will waive established data fees to non-Illinois government entities
when entering into data sharing agreements for exchange of data of similar
content. Discharge data received from non-Illinois data sources will be
accepted in lieu of the fees shown in Appendix I. This waiver of fees will be
contingent upon the non-Illinois entity waiving any fees charged, with
acceptance of Illinois data in lieu of payment.
3) Category
III: Federal government, educational institutions, all non-profit organizations,
and college students enrolled in non-Illinois educational institutions,
including:
A) The
federal government;
B) Other
non-state or local political subdivisions outside of the State of Illinois that are not covered under Category II; and
C) All
educational institutions (Illinois and non-Illinois), all non-profit
organizations, and all college students enrolled in non-Illinois educational
institutions.
4) Category
IV: Illinois General Assembly, Executive Office of the Governor, State of Illinois Constitutional Officers, Agencies of Illinois State Government, Illinois county
and local government, and college students enrolled in Illinois educational
institutions.
b) The following data
products are available at rates established by the Department:
1) Standard
datasets are defined sets of data elements consisting of the minimum necessary
group of elements for a specific request identified from the list of elements
available to each category of requester.
A) Research
Oriented Dataset (RODS) containing data elements listed in Appendix D of this
Part.
B) Universal
Dataset (UDS) containing data elements listed in Appendix E of this Part.
C) State
Inpatient Dataset (SIDS) containing elements derived for the purposes of the
HCUP, Appendix F of this Part.
D) State
Ambulatory Surgery Dataset (SASDS) containing elements derived for the purposes
of the HCUP, Appendix G of this Part.
E) Revenue
Code Dataset (RCDS), a supplement to datasets A through D containing data
elements listed in Appendix H of this Part.
2) The
Department will evaluate requests for custom datasets and make the
determination of complex or simple based on details of the request.
A) Complex
dataset: a subset of RODS, UDS, SIDS or SASDS (with or without RCDS) that
contains the majority of significant data elements, or an intricate aggregation
or report that includes many significant data elements and compound
relationships.
B) Simple
dataset: a subset of RODS, UDS, SIDS or SASDS (without RCDS) that contains a
small number of significant data elements, or a straightforward aggregation or
report that includes few significant data elements and no, or a single,
relationship.
c) Standard
data product fees by category are set forth in Appendix I of this Part. In
addition to standard data product fees, the Department will assess data request
processing and data product preparation fees as follows:
1) The
Department will assess a non-refundable data request application fee of $100. The
application fee shall be applied to the final cost of approved and completed
data products.
2) The
Department will assess fees for the costs of preparing requested data products,
including, but not limited to, programming, research, administrative, media and
shipping as described in Appendix J of this Part. The minimum charge will be
one unit per resource factor, with additional units as necessary for more
complicated requests.
(Source: Amended at 36 Ill.
Reg. 8017, effective May 8, 2012)
Section 1010.APPENDIX A Uniform Inpatient Discharge Data
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.APPENDIX A UNIFORM INPATIENT DISCHARGE DATA
Section 1010.APPENDIX A Uniform Inpatient Discharge
Data
Data elements affected by
implementation of the ICD-10 coding scheme on October
1, 2013 (or as stipulated by CMMS) are noted when necessary and appropriate.
Detail Data
1. Hospital identifier
(federal tax identification number/Department assigned/NPI)
2. Patient account number
3. Discharge time (HH)
4. Patient zip code and
Plus 4
5. Patient birth date
(MMDDCCYY)
6. Patient sex
7. Admission date (MMDDYY)
and time (HH)
8. Type of admission
9. Source of admission
10. Patient discharge
status
11. Type
of bill
12. Total
patient charges and components of charges (by revenue code, units of service
and charges)
13. Primary payer ID and
health plan name
14. Secondary and tertiary
payer ID and health plan name (required when present)
15. Principal
and secondary diagnosis codes, when present (up to 25 per data record and up
to 50 with record pagination when necessary)
ICD-9 codes
required: current discharges through discharges of September
30, 2013 (or last date of CMMS acceptance of ICD-9 codes)
ICD-10 codes
required: discharges on and after October
1, 2013 (or first date of CMMS acceptance of ICD-10 codes)
16. Principal
and secondary procedure codes and dates (MMDDYY), when present (up to 25 per
data record and up to 50 with record pagination when necessary)
ICD-9 codes
required: current discharges through discharges of September
30, 2013 (or last date of CMMS acceptance of ICD-9 codes)
ICD-10 codes
required: discharges on and after October
1, 2013 (or first date of CMMS acceptance of ICD-10 codes)
17. Attending clinician ID
number/NPI
18. Other clinician ID
number/NPI (up to two required when present)
19. Patient race (according
to OMB guidelines)
20. Patient ethnicity
(according to OMB guidelines)
21. Patient
county code (five digits: state and county codes for Illinois and border state
residents (FIPS code))
22. Diagnosis present at
admission for each diagnosis
23. External cause of
injury codes (required when present)
ICD-9 Ecodes:
three required if available: current discharges through discharges of September 30, 2013 (or last date of CMMS acceptance of ICD-9 codes)
ICD-10 Ecodes:
eight required if available: discharges on and after October
1, 2013 (or first date of CMMS acceptance of ICD-10 codes)
24. Newborn birth weight
value code and birth weight in grams
25. Admitting diagnosis
code
ICD-9 code
required: current discharges through discharges of September
30, 2013 (or last date of CMMS acceptance of ICD-9 codes)
ICD-10 code
required: discharges on and after October
1, 2013 (or first date of CMMS acceptance of ICD-10 codes)
26. Do not resuscitate
indicator (entered in first 24 hours of stay)
27. Prior
stay occurrence code and prior stay from and through dates (required when
present)
28. Operating
clinician ID number/NPI (required when surgical procedures present as a
component of treatment)
29. Accident state
abbreviation (required when present)
30. Condition employment
related (required when present)
31. Accident
employment related occurrence code and date of accident (required when present)
32. Crime victim occurrence
code and date of crime (required when present)
33. Statement covers period
(from and through [discharge date] dates)
34. Insurance group numbers
(up to three required when present)
35. Page number and total
number of pages
36. Diagnoses code version
qualifier
ICD-9 indicator
required = 9: current discharges through discharges of September
30, 2013 (or last date of CMMS acceptance of ICD-9 codes)
ICD-10 indicator
required = 0: discharges on and after October
1, 2013 (or first date of CMMS acceptance of ICD-10 codes)
37. Condition
code indicating patient admitted directly from this facility's emergency
room/department
38. Patient name (first,
middle, last, suffix)
39. Patient
address (PO Box or street address, apartment number, city and state)
40. Unique
patient identifier based on the last four digits of patient Social Security
number
41. Primary
insured's unique identifier (beneficiary/policy #)
42. Any
element or service adopted for use by the the National Uniform Billing
Committee pursuant to Section 4-2(d)(14) of the Act. Elements or services
would be added as a submission requirement accompanied by sufficient
notification to all submitting facilities and health care systems. Notice
would be provided no less than 90 days in advance of the submission
requirement.
(Source: Amended at 36 Ill.
Reg. 8017, effective May 8, 2012)
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.APPENDIX B AMBULATORY CATEGORIES
Section 1010.APPENDIX B Ambulatory Categories
1. Surgeries on the
integumentary system
2. Surgeries on the
musculoskeletal system
3. Surgeries on the
respiratory system
4. Surgeries on the
cardiovascular system
5. Surgeries on the hemic
and lymphatic systems
6. Surgeries on the
mediastinum and diaphragm
7. Surgeries on the
digestive system
8. Surgeries on the urinary
system
9. Surgeries on the male
genital system
10. Intersex surgery
11. Surgeries on the female
genital system
12. Surgeries on the female
reproductive system
13. Surgeries on the
endocrine system
14. Surgeries on the
nervous system
15. Surgeries on the eye
and ocular adnexa
16. Surgeries on the
auditory system
17. Emergency department
visits
18. Diagnostic imaging
(Source: Amended at 36 Ill.
Reg. 8017, effective May 8, 2012)
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.APPENDIX C AMBULATORY SURGICAL DATA ELEMENTS
Section 1010.APPENDIX C Ambulatory Surgical Data
Elements
Data elements affected by implementation of ICD-10 coding
scheme October 1, 2013 (or as stipulated by CMMS) are noted when necessary and
appropriate.
Detail Data
1. Facility identifier
(Federal tax identification number/Department assigned/NPI)
2. Surgical site identifier
(Department assigned)
3. Patient account number
4. Patient zip code and
Plus 4
5. Patient birth date
(MMDDCCYY)
6. Patient sex
7. Date (MMDDYY) and time (HH)
of visit
8. Time (HH) of discharge
9. Type of admission/visit
10. Source of
admission/visit
11. Patient discharge
status
12. Type of bill
13. Total
patient charges and components of those charges (revenue codes, HCPCS codes
with modifiers, date of service, units of service and charges)
14. Primary payer ID and
health plan name
15. Secondary and tertiary
payer ID and health plan name (required when present)
16. Principal
and secondary diagnosis codes, when present (up to 25 per data record and up to
50 with record pagination when necessary)
ICD-9 codes
required: current discharges through discharges of September
30, 2013 (or last date of CMMS acceptance of ICD-9 codes)
ICD-10 codes
required: discharges on and after October
1, 2013 (or first date of revised CMMS acceptance of ICD-10 codes)
17. Principal
and secondary procedure codes and dates (MMDDYY), when present (up to 25 per
data record and up to 50 with record pagination when necessary); only the
values of the CPT coding scheme will be accepted as procedure codes for
outpatient data submissions
18. Attending clinician ID
number/NPI
19. Operating clinician ID
number/NPI
20. Other clinician ID
number/NPI (up to 2 required when present)
21. Patient race (according
to OMB guidelines)
22. Patient ethnicity
(according to OMB guidelines)
23. External cause of
injury codes (required when present)
ICD-9 Ecodes:
three required if available: current discharges through discharges of September 30, 2013 (or last date of CMMS acceptance of ICD-9 codes)
ICD-10 Ecodes:
eight required if available: discharges on and after October
1, 2013 (or first date of CMMS acceptance of ICD-10 codes)
24. Patient
county code (5 digits: state and county codes for Illinois and border state
residents (FIPS code))
25. Patient reason for
visit (diagnosis codes up to three required when present)
26. Accident state
abbreviation (required when present)
27. Condition employment
related (required when present)
28. Accident
employment related occurrence code and date of accident (required when present)
29. Crime victim occurrence
code and date of crime (required when present)
30. Page number and total
number of pages of this claim
31. Insurance group number
(up to three required when present)
32. Diagnoses code version
qualifier
ICD-9 indicator
required = 9: current discharges through discharges of September
30, 2013 (or last date of CMMS acceptance of ICD-9 codes)
ICD-10 indicator
required = 0: discharges on and after October
1, 2013 (or first date of CMMS acceptance of ICD-10 codes)
33. Statement covers period
(from and through [discharge date] dates)
34. Patient name (first,
middle, last, suffix)
35. Patient
address (PO Box or street address, apartment number, city and state)
36. Unique
patient identifier based on the last four digits of patient Social Security number
37. Primary
insured's unique identifier (beneficiary/policy #)
38. Any
element or service adopted for use by the National Uniform Billing Committee
pursuant to Section 4-2(d)(14) of the Act. Elements or services would be added
as a submission requirement accompanied by sufficient notification to all
submitting facilities and health care systems. Notice would be provided no
less than 90 days in advance of the submission requirement.
(Source: Amended at 36 Ill.
Reg. 8017, effective May 8, 2012)
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.APPENDIX D RESEARCH ORIENTED DATASET (RODS) DATA ELEMENTS
Section 1010.APPENDIX D Research Oriented
Dataset (RODS) Data Elements
1. Facility identifier (federal
tax identification number/Department assigned/NPI)
2. Patient sex
3. Admission/visit type
4. Admission/visit source
5. Length
of stay (in whole days; inpatient only)
6. Patient discharge status
7. Principal diagnosis code
and up to 24 secondary codes
8. Principal procedure code
and up to 24 secondary codes
9. DRG
(or successor category grouping) code inpatient/APC outpatient
10. MDC (or successor) code
inpatient/body system outpatient
11. Total charges
12. Room/board charges
(inpatient only)
13. Ancillary charges
14. Anesthesiology
charges
15. Pharmacy charges
16. Radiology charges
17. Clinical lab charges
18. Labor/delivery
charges (inpatient only)
19. Operating room
charges
20. Oncology charges
21. Other charges
22. Combined bill
indicator (inpatient only)
23. Patient county
24. Patient planning area
25. Patient Health
Service Area
26. Hospital Health
Service Area
27. Patient date of birth
(CCYYMMDD)
28. Admission date
(CCYYMMDD) and time (HH)
29. Discharge Date
(CCYYMMDD) and time (HH)
30. Primary, secondary
and tertiary payer IDs and health plan names (when available)
31. Patient zip code in every
record
32. Primary surgical
procedure date (if present)
33. Patient race
34. Patient ethnicity
35. Newborn birth weight
in grams
36. Do Not Resuscitate
(DNR) (inpatient only)
37. Condition employment
related
38. Accident employment related
39. Crime victim
40. Admitting diagnosis
code/reason for visit code
41. Diagnosis present at
admission for each diagnosis code (inpatient only)
42. Ecodes (when present)
43. Row ID (when
necessary: provides linkage to Revenue Code Dataset)
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.APPENDIX E UNIVERSAL DATASET (UDS) DATA ELEMENTS
Section 1010.APPENDIX E Universal Dataset (UDS)
Data Elements
1. Facility identifier (federal
tax identification number/Department assigned/NPI)
2. Patient sex
3. Admission/visit type
4. Admission/visit source
5. Length of stay (in whole
days) (inpatient only)
6. Patient discharge status
7. Principal diagnosis code
and up to 14 secondary codes
8. Principal procedure code
and up to 9 secondary codes
9. DRG (or successor
category grouping) code inpatient/APC outpatient
10. MDC (or successor) code
inpatient/body system outpatient
11. Total charges
12. Room/board charges
(inpatient only)
13. Ancillary charges
14. Anesthesiology
charges
15. Pharmacy charges
16. Radiology charges
17. Clinical lab charges
18. Labor/delivery
charges (inpatient only)
19. Operating room
charges
20. Oncology charges
21. Other charges
22. Combined bill
indicator (inpatient only)
23. Primary health plan
type
24. Secondary health plan
type
25. Tertiary health plan
type
26. Patient county
27. Patient planning area
28. Patient Health
Service Area
29. Hospital Health
Service Area
30. Patient age (in whole
years or days if less than one year)
31. Admission date
(CCYYMMD)
32. Patient zip code (zip
may be masked when hospital/zip cell size less than 10)
33. Newborn birth weight
in grams
34. Do Not Resuscitate
(DNR) (inpatient only)
35. Hospitalization
employment related
36. Admitting diagnosis
code
37. Diagnosis present at
admission for each diagnosis code (inpatient only)
38. Ecodes (when present)
39. Number of days
between admission and primary procedure (inpatient only)
(if present)
40. Row ID (when
necessary: provides linkage to Revenue Code Dataset)
(Source: Amended at 36 Ill.
Reg. 8017, effective May 8, 2012)
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.APPENDIX F STATE INPATIENT DATASET (SIDS) DATA ELEMENTS
Section 1010.APPENDIX F State Inpatient Dataset
(SIDS) Data Elements
1. Age in years at
admission
2. Age in days (when age
< 1 year)
3. Age in months (when age
< 11 years)
4. Admission month
5. Admission source
(uniform)
6. Admission type
7. Admission day is a
weekend
8. Room and board charges
9. Ancillary charges
10. Anesthesiology
charges
11. Pharmacy charges
12. Radiology charges
13. Clinical lab charges
14. Labor-delivery
charges
15. Operating room
charges
16. Oncology charges
17. Other charges
18. Died during
hospitalization
19. Disposition of
patient (uniform)
20. Discharge quarter
21. DRG (or successor
category grouping) code in effect on discharge date
22. Data source hospital
identifier
23. Principal diagnosis
24. Up to 14 secondary
diagnoses
25. CCS: principal
diagnosis
26. CCS: up to 14
secondary diagnoses
27. Indicator of sex
28. Length of stay (as
received from source)
29. MDC (or successor)
code in effect on discharge date
30. Number of diagnoses
on this record
31. Number of procedures
on this record
32. Primary expected
health plan identifier (uniform)
33. Secondary expected
health plan identifier (uniform)
34. Principal procedure
code (if present)
35. Up to 9 secondary
procedure codes (if present)
36. CCS: principal
procedure (if present)
37. CCS: up to 9
secondary procedures (if present)
38. Total charges (as
received from source)
39. Calendar year of
discharge
40. Patient zip code
(uniform)
41. Patient county code
(uniform)
42. Newborn birth weight
in grams
43. Do Not Resuscitate
(DNR)
44. Hospitalization
employment related
45. Admitting diagnosis
code
46. Diagnosis present at
admission for each diagnosis code
47. Ecodes (when present)
48. Number of days
between admission and primary procedure (if present)
49. Row ID (when
necessary: provides linkage to Revenue Code Dataset)
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.APPENDIX G STATE AMBULATORY SURGERY DATASET (SASDS) DATA ELEMENTS
Section 1010.APPENDIX G State Ambulatory Surgery Dataset
(SASDS) Data Elements
1. Age in years at
admission/visit
2. Age in days (when age
< 1 year)
3. Age in months (when age
< 11 years)
4. Admission/visit month
5. Admission/visit source
(uniform)
6. Admission/visit type
7. Admission/visit day is a
weekend
8. Anesthesiology charges
9. Pharmacy charges
10. Radiology
charges
11. Clinical
lab charges
12. Operating
room/surgical suite charges
13. Oncology
charges
14. Other charges
15. Disposition
of patient (uniform)
16. Discharge
quarter
17. Data
source hospital identifier
18. Principal
diagnosis
19. Up
to 14 secondary diagnoses
20. CCS:
principal diagnosis
21. CCS:
up to 14 secondary diagnoses
22. Indicator
of sex
23. APC code
24. Body system affected
by condition/injury
25. Number of diagnoses
on this record
26. Number of procedures
on this record
27. Primary expected
health plan identifier (uniform)
28. Secondary expected
health plan identifier (uniform)
29. Principal procedure
code (if present)
30. Up to 9 secondary
procedure codes (if present)
31. CCS: principal
procedure (if present)
32. CCS: up to 9
secondary procedures (if present)
33. Total charges (as
received from source)
34. Calendar year of
discharge
35. Patient zip code
(uniform)
36. Patient county code
(uniform)
37. Race
38. Ethnicity
39. Hospitalization
employment related
40. State of accident
41. Reason for visit
42. Ecodes (when present)
43. Row ID (when
necessary: provides linkage to Revenue Code Dataset)
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.APPENDIX H REVENUE CODE DATASET (RCDS) DATA ELEMENTS
Section 1010.APPENDIX H Revenue
Code Dataset (RCDS) Data Elements
1.
Row ID (provides linkage to primary file)
2.
Revenue Code
3.
HCPCS Code (when available: outpatient only)
4.
Date of Service (when available: outpatient only)
5.
Units of Service
6.
Charge
7.
Revenue Type
8.
Revenue Category
9.
Submission Type (Inpatient or Outpatient)
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.APPENDIX I DATA PRODUCT PRICE LIST
Section 1010.APPENDIX I Data Product Price List
Data Product Price List
|
|
Inpatient Data
1987-Ongoing
[New data
elements will be available beginning with 2009 discharges]
|
Outpatient Data
[Available
only to researchers, Illinois educational institutions, and Illinois
governmental entities]
2002-2008
| 20091 - Ongoing [Available to all approved requesters]
|
|
Product
|
Per Quarter
|
Per Year
|
Per Quarter
|
Per Year
|
|
Category I: Resellers (Customers
for Resale or Redistribution)
|
|
Universal Dataset
|
$8,000
|
$24,000
|
n/a | $8,000
|
n/a | $24,000
|
|
State Inpatient Dataset (SIDS)
|
$8,000
|
$24,000
|
n/a
|
n/a
|
|
State Ambulatory Surgery Dataset
(SASDS)
|
n/a
|
n/a
|
n/a | $8,000
|
n/a | $24,000
|
|
Custom Dataset (Complex)
|
$8,000
|
$24,000
|
n/a | $8,000
|
n/a | $24, 000
|
|
Custom Dataset (Simple)
[Price + app fee + costs]
|
$1,000
|
$3,000
|
n/a | $1,000
|
n/a | $3,000
|
|
Revenue Code
Dataset
Inpatient: 1993-Ongoing
[not available
separetely]
|
$3,000
|
$8,000
|
n/a
|
n/a
|
|
Revenue Code Dataset
(RCDS)
Outpatient:
2002-2008 | 2009-Ongoing
[Not available
separately]
|
n/a
|
n/a
|
n/a | $3,000
|
n/a | $8,000
|
|
HCUP/AHRQ
|
|
$24,000
|
|
n/a | $24,000
|
|
Category II: Commercial/Private/Non-IL Govt/For-Profit
Customers with No Resale or Redistribution
|
|
Universal Dataset
|
$4,000
|
$12,000
|
n/a | $4,000
|
n/a | $12, 000
|
|
State Inpatient Dataset (SIDS)
|
$4,000
|
$12,000
|
n/a
|
n/a
|
|
State Ambulatory Surgery Dataset
(SASDS)
|
n/a
|
n/a
|
n/a | $4,000
|
n/a | $12, 000
|
|
Custom Dataset (Complex)
|
$4,000
|
$12,000
|
n/a | $4,000
|
n/a | $12, 000
|
|
Custom Dataset (Simple)
[Price + app fee + costs]
|
$500
|
$1,500
|
n/a | $500
|
n/a | $1,500
|
|
Revenue Code Dataset (RCDS)
Inpatient: 1993-Ongoing
[Not available separately]
|
$1,500
|
$4,000
|
n/a
|
n/a
|
|
Revenue Code
Dataset Outpatient: 2002-2008 | 2009-Ongoing
[Not available
separately]
|
n/a
|
n/a
|
n/a | $1,500
|
n/a | $4,000
|
|
Category III: Non-Profit/Educational Institution/College
Student Non-IL Institution Customers with No Resale or Redistribution
|
|
Research Oriented Dataset
|
$1,500
|
$4,500
|
$1,000
|
$3,000
|
|
Universal Dataset
|
$1,500
|
$4,500
|
$1,000
|
$3,000
|
|
State Inpatient Dataset (SIDS)
|
$1,500
|
$4,500
|
n/a
|
n/a
|
|
State Ambulatory Surgery Dataset (SASDS)
|
n/a
|
n/a
|
$1,000
|
$3,000
|
|
Custom Dataset (Complex)
|
$1,500
|
$4,500
|
$1,000
|
$3,000
|
|
Custom Dataset (Simple)
[Price + app fee + costs]
|
$100
|
$300
|
$100
|
$300
|
|
Revenue Code Dataset
Inpatient: 1993-Ongoing
Outpatient: 2004-Ongoing
[Not available separately]
|
$500
|
$1,500
|
$300
|
$1,000
|
|
Category IV: IL Gen Assembly/IL Executive Officers/IL
Const Officers/IL and Local Govt/College Student IL Inst Customers with No
Resale or Redistribution
|
|
UDS, SIDS, SASDS, RCDS and Custom Dataset
|
No Fee
|
No Fee
|
No Fee
|
No Fee
|
|
|
|
|
|
|
|
|
|
|
1Outpatient
data may be released earlier if the Department determines that quantity and
quality of data from all facilities has reached a satisfactory level of
comparability.
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.APPENDIX J DATA PRODUCT PREPARATION COST TABLE
Section 1010.APPENDIX J Data Product Preparation Cost
Table
|
Resource
|
|
Hours/Units
|
|
Cost Per Unit
|
|
Programming
|
|
1+
|
|
$100
|
|
Research
|
|
1+
|
|
$65
|
|
Administration
|
|
2
|
|
$25
|
|
Media
(cd-rom/dvd-rom)
|
|
1+
|
|
$5
|
|
Shipping
|
|
1
|
|
Shipper listed cost
|
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.APPENDIX K DIAGNOSTIC AND THERAPEUTIC IMAGING CATEGORIES
Section 1010.APPENDIX K Diagnostic and Therapeutic
Imaging Categories
1. X-Ray
2. CT
Scan
3. Mammography
(diagnostic or screening)
4. Sonography
5. Ultrasonography
6. PET
Scans
7. MRI
(with and without contrast)
8. Nuclear
Medicine
(Source: Added at 36 Ill.
Reg. 8017, effective May 8, 2012)
 | TITLE 77: PUBLIC HEALTH
CHAPTER I: DEPARTMENT OF PUBLIC HEALTH SUBCHAPTER x: HEALTH STATISTICS PART 1010
HEALTH CARE DATA COLLECTION AND SUBMISSION CODE
SECTION 1010.APPENDIX L SYNDROMIC SURVEILLANCE DATA
Section 1010.APPENDIX L Syndromic Surveillance Data
Data elements are to be submitted by messages in HL7
standard format. Data elements are R (Required), RE (Required but may be empty
in messages where the information has not been recorded in the Electronic
Medical Record (EMR)) or O (Optional data elements that should be sent if they
are available in the EMR).
Detail Data
1. Facility
identifier (NPI or ODI) Must be unique for each Facility address)
2. Visit
Identifier
3. Admission
date and time (MMDDCCYYHHMMSS) Only one value (earliest) can be provided per
visit.
4. Patient
Class
5. Patient
birth date (MMDDCCYY) and Age
6. Patient
sex
7. Patient
Race
8. Patient
Ethnicity
9. Patient
ZIP
10. Discharge
Disposition
11. Discharge
date and time (MMDDCCYYHHMMSS)
12. Facility
Name
13. Facility
Address
14. Unique
Patient Identifier (Medical Record Number)
15. Chief
Complaint. This must be in an OBX HL7 segment and sent with every message as
soon as it is available in the EMR. It should be the free text of the patient’s
self-reported reason for visit. If the complaint is captured as from a pick
list, all complaints shall be sent. If both free-text and pick list chief
complaints are captured in the EMR, both shall be sent to the Department.
16. Diagnosis
codes -Admitting, Working or Final. (ICD-10 codes only; as many as available)
17. Triage
Note
18. Clinical
Impression
19. Discharge
date and time (MMDDCCYYHHMMSS)
20. Pregnancy
Status
21. Death
Data and Time
22. Smoking
Status
23. Procedure
Codes
24. Patient
Country
25. Date
of Onset
26. Insurance
Type
27. Initial
Temperature
28. Initial
Pulse Oximetry
29. Initial
Blood Pressure
30. International
Travel History (Country and dates)
31. Problem
List
32. Body
Mass Index (or Weight and Height)
33. Patient
Assigned Location
34. Hospital
Unit
35. Event
Date and Time (MMDDCCYYHHMMSS)
36. Message
Date and Time (MMDDCCYYHHMMSS)
37. Initial
Acuity
38. Patient
name (first, middle, last, suffix)
39. Patient
address (PO Box or street address, apartment number, city, state, and zip code)
40. Medications
Prescribed
41. Attending
Physician (National Provider Index)
42. Facility
Visit Type
43. Event
data and time (MMDDCCYYHHMMSS) and
44. Any
element adopted for use by CDC’s PHIN or HL7 standards organization in Version
2.5.1 of the Syndromic Surveillance Messaging Guide on HL7.org (July 26, 2019).
Elements supported by the Department will be added as a submission requirement
accompanied by sufficient notification to all submitting facilities and health
care systems. Notice will be provided no less than 90 days in advance of the
submission requirement.
(Source: Added
at 47 Ill. Reg. 4017, effective March 10, 2023)
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