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Rep. Mary E. Flowers
Filed: 3/2/2012
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1 | | AMENDMENT TO HOUSE BILL 3772
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2 | | AMENDMENT NO. ______. Amend House Bill 3772 on page 1, line |
3 | | 5, by replacing "10-20" with "10-15, 10-20,"; and |
4 | | on page 1, immediately below line 6, by inserting the |
5 | | following:
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6 | | "(410 ILCS 522/10-15)
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7 | | Sec. 10-15. Health care facility requirements to report, |
8 | | analyze, and correct. |
9 | | (a) Reports of adverse health care events required. Each |
10 | | health care facility shall report to the Department the |
11 | | occurrence of any of the adverse health care events described |
12 | | in subsections (b) through (g) no later than 30 days after |
13 | | discovery of the event. The report shall be filed in a format |
14 | | specified by the Department and shall identify the health care |
15 | | facility, but shall not include any information identifying or |
16 | | that tends to identify any of the health care professionals, |
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1 | | employees, or patients involved. |
2 | | (a-5) Revisions of the listing of events. The Department |
3 | | may by rule revise the listing of events reportable under this |
4 | | Act to conform with the latest National Quality Forum |
5 | | guidelines. |
6 | | (b) Surgical events. Events reportable under this |
7 | | subsection are: |
8 | | (1) Surgery performed on a wrong body part that is not |
9 | | consistent with the documented informed consent for that |
10 | | patient. Reportable events under this clause do not include |
11 | | situations requiring prompt action that occur in the course |
12 | | of surgery or situations whose urgency precludes obtaining |
13 | | informed consent. |
14 | | (2) Surgery performed on the wrong patient. |
15 | | (3) The wrong surgical procedure performed on a patient |
16 | | that is not consistent with the documented informed consent |
17 | | for that patient. Reportable events under this clause do |
18 | | not include situations requiring prompt action that occur |
19 | | in the course of surgery or situations whose urgency |
20 | | precludes obtaining informed consent. |
21 | | (4) Retention of a foreign object in a patient after |
22 | | surgery or other procedure, excluding objects |
23 | | intentionally implanted as part of a planned intervention |
24 | | and objects present prior to surgery that are intentionally |
25 | | retained. |
26 | | (5) Death during or immediately after surgery of a |
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1 | | normal, healthy patient who has no organic, physiologic, |
2 | | biochemical, or psychiatric disturbance and for whom the |
3 | | pathologic processes for which the operation is to be |
4 | | performed are localized and do not entail a systemic |
5 | | disturbance. |
6 | | (c) Product or device events. Events reportable under this |
7 | | subsection are: |
8 | | (1) Patient death or serious disability associated |
9 | | with the use of contaminated drugs, devices, or biologics |
10 | | provided by the health care facility when the contamination |
11 | | is the result of generally detectable contaminants in |
12 | | drugs, devices, or biologics regardless of the source of |
13 | | the contamination or the product. |
14 | | (2) Patient death or serious disability associated |
15 | | with the use or function of a device in patient care in |
16 | | which the device is used or functions other than as |
17 | | intended. "Device" includes, but is not limited to, |
18 | | catheters, drains, and other specialized tubes, infusion |
19 | | pumps, and ventilators. |
20 | | (3) Patient death or serious disability associated |
21 | | with intravascular air embolism that occurs while being |
22 | | cared for in a health care facility, excluding deaths |
23 | | associated with neurosurgical procedures known to present |
24 | | a high risk of intravascular air embolism. |
25 | | (d) Patient protection events. Events reportable under |
26 | | this subsection are: |
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1 | | (1) An infant discharged to the wrong person. |
2 | | (2) Patient death or serious disability associated |
3 | | with patient disappearance for more than 4 hours, excluding |
4 | | events involving adults who have decision-making capacity. |
5 | | (3) Patient suicide or attempted suicide resulting in |
6 | | serious disability while being cared for in a health care |
7 | | facility due to patient actions after admission to the |
8 | | health care facility, excluding deaths resulting from |
9 | | self-inflicted injuries that were the reason for admission |
10 | | to the health care facility. |
11 | | (e) Care management events. Events reportable under this |
12 | | subsection are: |
13 | | (1) Patient death or serious disability associated |
14 | | with a medication error, including, but not limited to, |
15 | | errors involving the wrong drug, the wrong dose, the wrong |
16 | | patient, the wrong time, the wrong rate, the wrong |
17 | | preparation, or the wrong route of administration, |
18 | | excluding reasonable differences in clinical judgment on |
19 | | drug selection and dose. |
20 | | (2) Patient death or serious disability associated |
21 | | with a hemolytic reaction due to the administration of |
22 | | ABO-incompatible blood or blood products. |
23 | | (3) Maternal death or serious disability associated |
24 | | with labor or delivery in a low-risk pregnancy while being |
25 | | cared for in a health care facility, excluding deaths from |
26 | | pulmonary or amniotic fluid embolism, acute fatty liver of |
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1 | | pregnancy, or cardiomyopathy. |
2 | | (4) Patient death or serious disability directly |
3 | | related to hypoglycemia, the onset of which occurs while |
4 | | the patient is being cared for in a health care facility |
5 | | for a condition unrelated to hypoglycemia. |
6 | | (f) Environmental events. Events reportable under this |
7 | | subsection are: |
8 | | (1) Patient death or serious disability associated |
9 | | with an electric shock while being cared for in a health |
10 | | care facility, excluding events involving planned |
11 | | treatments such as electric countershock.
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12 | | (2) Any incident in which a line designated for oxygen |
13 | | or other gas to be delivered to a patient contains the |
14 | | wrong gas or is contaminated by toxic substances.
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15 | | (3) Patient death or serious disability associated |
16 | | with a burn incurred from any source while being cared for |
17 | | in a health care facility that is not consistent with the |
18 | | documented informed consent for that patient. Reportable |
19 | | events under this clause do not include situations |
20 | | requiring prompt action that occur in the course of surgery |
21 | | or situations whose urgency precludes obtaining informed |
22 | | consent.
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23 | | (4) Patient death associated with a fall while being |
24 | | cared for in a health care facility.
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25 | | (5) Patient death or serious disability associated |
26 | | with the use of restraints or bedrails while being cared |
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1 | | for in a health care facility. |
2 | | (g) Physical security events. Events reportable under this |
3 | | subsection are: |
4 | | (1) Any instance of care ordered by or provided by |
5 | | someone impersonating a physician, nurse, pharmacist, or |
6 | | other licensed health care provider. |
7 | | (2) Abduction of a patient of any age. |
8 | | (3) Sexual assault on a patient within or on the |
9 | | grounds of a health care facility. |
10 | | (4) Death or significant injury of a patient or staff |
11 | | member resulting from a physical assault that occurs within |
12 | | or on the grounds of a health care facility. |
13 | | (h) Definitions. As used in this Section 10-15: |
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"Death" means patient death related to an adverse event |
15 | | and not related solely to the natural course of the patient's |
16 | | illness or underlying condition. Events otherwise reportable |
17 | | under this Section 10-15 shall be reported even if the death |
18 | | might have otherwise occurred as the natural course of the |
19 | | patient's illness or underlying condition. |
20 | | "Serious disability" means a physical or mental |
21 | | impairment, including loss of a body part, related to an |
22 | | adverse event and not related solely to the natural course of |
23 | | the patient's illness or underlying condition, that |
24 | | substantially limits one or more of the major life activities |
25 | | of an individual or a loss of bodily function, if the |
26 | | impairment or loss lasts more than 7 days prior to discharge or |