77 Ill. Adm. Code 640.90
State Perinatal Reporting System
Section 640
Section 640.90Â State Perinatal
Reporting System
a)Â Â Â Â Â Â Â Â Purpose
The Department
will maintain a State Perinatal Reporting System to follow selected high-risk
perinatal patients to ensure that those patients are assessed at appropriate
intervals, receive intervention as needed, and are referred for needed support
services.
b)Â Â Â Â Â Â Â Â Identification and Referral of High-Risk Maternal Patients
1)Â Â Â Â Â Â Â Â Each designated APC and Level III hospital that provides
obstetrical care shall establish criteria and procedures for identifying
high-risk pregnant and postpartum patients. A statement describing the criteria
and procedures shall be on file and shall be provided to the Department on
request.
2)Â Â Â Â Â Â Â Â The hospital's Perinatal Review Committee, or other committee
established for the purpose of internal quality control or medical study for
the purpose of reducing morbidity or mortality or improving patient care, shall
collect and submit the information required in subsection (b)(1) to the
Department. These data will be considered confidential under Section 8-2101 of
the Code of Civil Procedure.
c)Â Â Â Â Â Â Â Â Identification of Perinatal Patients
1)Â Â Â Â Â Â Â Â All Illinois hospitals licensed to provide obstetrical and
newborn services shall report information on all perinatal patients. The
Department requests, but does not require, reports on perinatal patients from
hospitals outside Illinois.(The Department does request reports from the St.
Louis APCs or hospitals maintained by the federal government or other
governmental agencies within the United States.)
2)Â Â Â Â Â Â Â Â Each hospital shall prepare a Perinatal Report record (see
Appendix I), to be provided by the Department, for patients meeting one of the
following conditions:
A)Â Â Â Â Â Â Â Live-birth; or
B)Â Â Â Â Â Â Â Diagnosed prior to discharge from newborn hospitalization as a
perinatal or neonatal death.
3)Â Â Â Â Â Â Â Â Women who present with spontaneous abortion, ectopic pregnancy
or hydatidiform mole are perinatal patients and shall be reported. The products
of induced abortions shall not be reported to the State Perinatal Reporting
System.
4)Â Â Â Â Â Â Â Â Fetal death (gestation greater than 20 weeks) is considered a
reportable perinatal outcome. These fetal deaths do not have to be reported
through the State Perinatal Reporting System, because they are already reported
and compiled in the Department's  Vital Records database.
5)Â Â Â Â Â Â Â Â Every hospital shall provide representatives of the Department
with access to information from all medical, pathological, and other records
and logs related to reportable registry information. The mode of access and the
time during which this access will be provided shall be by mutual agreement
between the hospital and the Department.
6)Â Â Â Â Â Â Â Â The State Perinatal Reporting System also will be complemented
with information from the Department's Vital Records live birth database under
the Vital Records Act, the Adverse Pregnancy Outcomes Reporting System under
the Illinois Health and Hazardous Substances Registry Act and other Maternal
and Child Health Reports and submissions.
7)Â Â Â Â Â Â Â Â The State Perinatal Reporting System consists of two forms of
reporting. This reporting shall be on the forms provided by the Department or
through electronic means that meets the exact specifications of the
Department's data processing system. Complete perinatal reporting information shall
be reported to the Department within 14 days after infant discharge, regardless
of the method of reporting.
d)Â Â Â Â Â Â Â Â Availability of Information
1)Â Â Â Â Â Â Â Â The patient and hospital-identifying information submitted to
the Department or certified local health department under the Act and this Part
shall be privileged and confidential and shall not be available for disclosure,
inspection or copying under the Freedom of Information Act or the State Records
Act, except as described in this Section. These data shall also be considered
confidential under Section 8-2101 of the Code of Civil Procedure.
2)Â Â Â Â Â Â Â Â Aggregate summaries and reports of follow-up activities may be
provided upon request to hospitals, to APCs, and to the certified local health department
designated by the Department to provide follow-up services to the patients. These
reports may contain information provided by the referring hospital and
information provided by the follow-up certified local health department.
Patient or hospital specific data provided to the appropriate designee under
this Section are confidential and shall be handled in accordance with the
Illinois Health Statistics Act and Section 9 of the Hospital Licensing Act.
These data shall also be considered confidential under Section 8-2101 of the
Code of Civil Procedure.
3)Â Â Â Â Â Â Â Â All reports issued by the Department in which the data are
aggregated so that no patient or reporting hospital may be identified shall be
available to the public pursuant to Access to Public Records of the Department
of Public Health and the Freedom of Information Act.
e)Â Â Â Â Â Â Â Â Quality Assurance and Continuous Quality Improvement
1)Â Â Â Â Â Â Â Â Reporting entities (i.e., hospitals, certified local health
departments and managed care entities (MCEs) shall be subject to review by the
Department to assess the timeliness, correctness and completeness of the
reports submitted by the entity.
2)Â Â Â Â Â Â Â Â Reporting entities (i.e., hospitals, certified local health
departments and MCEs shall supply additional information to the Department at
the Department's request when additional information is needed to confirm the
accuracy of reports previously submitted, or to clarify information previously
submitted. The Department will not request data that are more than two years
old.