Ill. Admin. Code tit. 68, § 1345.65 - Adverse Occurrences
a)
"Adverse occurrence" shall be defined for the purposes of this Section as:
1) The death of a neonate under the
licensee's care within 48 hours after delivery or attempted delivery, not
including a stillbirth or miscarriage;
2) The death after a pregnant or postpartum
patient under the licensee's care within 48 hours after delivery or attempted
delivery;
3) The in-patient
emergency hospitalization of a neonate under the licensee's care within 48
hours after delivery or attempted delivery; or
4) The in-patient emergency hospitalization
of a patient under the licensee's care within 48 hours after delivery or
attempted delivery.
b)
"Emergency hospitalization" shall be defined for the purposes of this Section
as a hospitalization of a neonate or patient suffering an acute injury or
illness that poses an immediate risk to life or long-term health requiring
immediate medical attention and that is related to delivery or attempted
delivery.
c) Maternal emergency
hospitalization events reportable under this Section include:
1) Acute myocardial infarction;
2) Aneurysm;
3) Acute renal failure;
4) Adult respiratory distress
syndrome;
5) Amniotic fluid
embolism;
6) Cardiac
arrest/ventricular fibrillation;
7)
Conversion of cardiac rhythm;
8)
Disseminated intravascular coagulation;
9) Eclampsia;
10) Heart failure/arrest;
11) Puerperal cerebrovascular
disorders;
12) Pulmonary
edema/acute heart failure;
13)
Severe anesthesia complications;
14) Sepsis;
15) Shock;
16) Sickle cell disease with
crisis;
17) Air and thrombotic
embolism;
18) Blood products
transfusion;
19)
Hysterectomy;
20) Temporary
tracheostomy;
21)
Ventilation;
22) Hemorrhage or
excessive laceration bleeding requiring repair;
23) Retained placenta;
24) Cord prolapse; or
25) Other adverse conditions or occurrences
equivalent to those listed above.
d) Neonatal emergency hospitalization events
reportable under this Section include:
1)
Severe birth trauma;
2) Severe
hypoxia/asphyxia;
3) Severe shock
and resuscitation;
4) Neonatal
severe respiratory complications;
5) Neonatal severe infection;
6) Neonatal severe neurological
complications;
7) Severe shock and
resuscitation procedures;
8)
Neonatal severe respiratory procedures;
9) Neonatal severe neurological
procedures;
10) Sepsis;
or
11) Other adverse conditions or
occurrences equivalent to those listed above.
e) A licensee shall report to the Division
within 24 hours after each adverse occurrence that involves the death of a
neonate or patient. The report shall be submitted to the Division on a form
provided by the Division and mailed to the Division or submitted
electronically.
f) A licensee shall
report to the Division within 14 days after each adverse occurrence that
involves the in-patient emergency hospitalization of a neonate or patient. The
report shall be submitted to the Division on a form provided by the Division
and mailed to the Division or submitted electronically.
g) The adverse occurrence report shall be in
writing and shall include:
1) The licensee's
name and license number;
2) The
date and time of the occurrence;
3)
The location of the occurrence, including the name and address of the birth
center, if applicable;
4) The name
of the patient;
5) The name of the
hospital involved in the occurrence, if any; and
6) The circumstances involved in such
occurrence.
h) The
adverse occurrence report is required by the Division to assist in its mission
of protecting the public. The filing of such report by a licensee shall not
constitute an admission by the licensee of any wrongdoing, malpractice, error
or omission in treatment, or even that the death or in-patient emergency
hospitalization is related to the licensee's care. A licensee shall be
responsible for filing an adverse occurrence report only for those adverse
occurrences of which the licensee has knowledge or should reasonably have been
expected to have knowledge. In the event that a licensee does not have
knowledge or cannot reasonably be expected to have knowledge, but subsequently
obtains actual knowledge of an adverse occurrence, then such licensee shall
file an adverse occurrence report within 24 hours after obtaining knowledge of
the death of a neonate or patient or within 14 days after obtaining knowledge
of the in-patient emergency hospitalization of a neonate or patient. An adverse
occurrence report is an investigatory record and is confidential under Section
180 of the Act.
i) Failure to
provide such a report to the Division shall be grounds for discipline (see
Section 100(a)(8) of the Act and Section
1345.70).
j) A licensed certified professional midwife
shall be deemed to be in compliance with the reporting requirements of this
Section if the licensed certified professional midwife is employed by or is
practicing at a birth center and the birth center submits the report required
by this Section.
Notes
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