77 Ill. Adm. Code 840.305
Information Required to be Reported
Section 840
Section 840.305Â Information
Required to be Reported
a)Â Â Â Â Â Â Â Â The Occupational Disease Registry shall consist of information
on the following occupational disease incidences:
1)Â Â Â Â Â Â Â Â Elevated blood lead levels (lead poisoning);
2)Â Â Â Â Â Â Â Â Workplace fatalities;
3)Â Â Â Â Â Â Â Â Workplace nonfatal injuries and illnesses; and
4)Â Â Â Â Â Â Â Â Other specific illnesses such as asbestosis, silicosis and
coal worker's pneumoconiosis.
b)Â Â Â Â Â Â Â Â Information on the occupational disease incidences shall be
collected in four ways.
1)Â Â Â Â Â Â Â Â Information concerning elevated blood lead levels (lead
poisoning) shall be reported to the Department by the facilities specified in
Section 840.300 of this Part.
A)Â Â Â Â Â Â Â The Department will follow up with attending physicians or
patients/cases or will contract with the local health authorities that agree to
conduct interviews with patients/cases, or attending physicians as needed, to
assure the accuracy and completeness of reports. The Department or contracted
local health authority will perform the activities or case follow-up for
elevated blood lead levels equal to or in excess of 10 mcg/dl set forth in
subsection (b)(1)(B).
B)Â Â Â Â Â Â Â The agreement with local health authorities will contain
requirements for the performance of the following activities or patient
follow-up:
i)Â Â Â Â Â Â Â Â Â Trace the patient or case;
ii)Â Â Â Â Â Â Â Â Counsel the patient or case;
iii)Â Â Â Â Â Â Â Educate the patient or case;
iv)Â Â Â Â Â Â Â Interview the patient or case for purposes of collecting,
verifying or completing the information identified in subsection (b)(1) of this
Section; and
v)Â Â Â Â Â Â Â Â Submit completed reports to the Department within 30 business
days after receipt of the laboratory report for adult elevated blood lead
analysis.
2)Â Â Â Â Â Â Â Â Information concerning fatal occupational injuries and
illnesses shall be collected from various reporting sources, including, but not
limited to, death certificates, newspaper clipping services, OSHA reports and
coroner's reports.
3)Â Â Â Â Â Â Â Â Information concerning nonfatal occupational injuries and
illnesses shall be collected using the U.S. Department of Labor, Bureau of
Labor Statistics' Survey of Occupational Injuries and Illnesses, an annual
sample survey of Illinois companies and governmental units.
4)Â Â Â Â Â Â Â Â Information concerning specific illnesses shall be collected
from existing data sources such as the hospital discharge database or medical
records.
c)Â Â Â Â Â Â Â Â Reports of elevated blood lead levels shall be reported by
facilities to the Department by manual submission (paper) or by electronic
submission.
d)Â Â Â Â Â Â Â Â All completed elevated blood lead level submissions are to be
mailed to the Illinois Department of Public Health, Division of Epidemiologic
Studies, Occupational Disease Registry, 535 West Jefferson Street, 3
rd
floor, Springfield, Illinois 62761 or submitted electronically.
e)Â Â Â Â Â Â Â Â Each case's elevated blood lead level incidence report shall
be sent/submitted to the Department within seven days after the date of
laboratory results. A local health authority or other facility shall submit
all data received from a registered, permitted or licensed clinical laboratory
or hospital laboratory to the Department within three business days after the
date the data are received.
f)Â Â Â Â Â Â Â Â Every hospital, clinical or hospital laboratory, or other
facility shall provide representatives of the Department with access to
information including specified occupational disease cases or other cases
specified for research studies related to occupational disease prevention and
control. The Department will conduct studies of all medical, pathological, or
other pertinent records and logs related to occupational disease incidence.
g)Â Â Â Â Â Â Â Â Every hospital, clinical or hospital laboratory, or other
facility shall provide the Department representatives with the patient's name
and attending physician's name for the purpose of follow-up on all laboratory
and existing data base reports received by the Department.
h)Â Â Â Â Â Â Â Â The mode of access and the time during which this access will
be provided shall be by mutual agreement between the hospital, other reporting
facilities and the Department. The Department will not require hospitals and
other reporting facilities to provide information on cases that are dated more
than two years before the Department's request for further information.