Bill Text: IL SB3734 | 2023-2024 | 103rd General Assembly | Introduced
Bill Title: Amends the Medical Patient Rights Act. Requires the Department of Public Health to develop an expanded informed consent document and expanded informed consent process for all patients scheduled to undergo atherectomy.
Spectrum: Partisan Bill (Democrat 1-0)
Status: (Introduced) 2024-02-09 - Referred to Assignments [SB3734 Detail]
Download: Illinois-2023-SB3734-Introduced.html
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| 1 | AN ACT concerning health.
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| 2 | Be it enacted by the People of the State of Illinois, | |||||||||||||||||||
| 3 | represented in the General Assembly:
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| 4 | Section 5. The Medical Patient Rights Act is amended by | |||||||||||||||||||
| 5 | adding Section 5.3 as follows:
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| 6 | (410 ILCS 50/5.3 new) | |||||||||||||||||||
| 7 | Sec. 5.3. Informed consent for patients undergoing | |||||||||||||||||||
| 8 | atherectomy. | |||||||||||||||||||
| 9 | (a) By October 1, 2024, the Department of Public Health | |||||||||||||||||||
| 10 | shall develop an expanded informed consent document and | |||||||||||||||||||
| 11 | expanded informed consent process for all patients scheduled | |||||||||||||||||||
| 12 | to undergo atherectomy, which is a procedure that involves | |||||||||||||||||||
| 13 | opening arteries blocked by plaque using a long, narrow tube | |||||||||||||||||||
| 14 | with a sharp blade, laser or rotating device on the end to | |||||||||||||||||||
| 15 | scrape away, dissolve, or break up plaque without making a | |||||||||||||||||||
| 16 | large incision. The expanded informed consent document and | |||||||||||||||||||
| 17 | expanded informed consent process shall be completed and shall | |||||||||||||||||||
| 18 | include, at a minimum, all of the following: | |||||||||||||||||||
| 19 | (1) all informed consent questions required by federal | |||||||||||||||||||
| 20 | law, including, but not limited to, questions that | |||||||||||||||||||
| 21 | address: | |||||||||||||||||||
| 22 | (A) the nature of the procedure; | |||||||||||||||||||
| 23 | (B) the risks and benefits of the procedure; | |||||||||||||||||||
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| 1 | (C) reasonable alternatives to the procedure; | ||||||
| 2 | (D) the risks and benefits of alternative | ||||||
| 3 | treatment options; and | ||||||
| 4 | (E) the patient's understanding of the factors | ||||||
| 5 | described in subparagraphs (A) through (D). | ||||||
| 6 | (2) a description of the specific risks and outcomes | ||||||
| 7 | that are associated with atherectomies and that are | ||||||
| 8 | identified by the National Institutes of Health, | ||||||
| 9 | including, but not limited to: | ||||||
| 10 | (A) the impact that smoking has on the patient's | ||||||
| 11 | risk of repeated claudication; | ||||||
| 12 | (B) the impact that smoking will have after | ||||||
| 13 | claudication; | ||||||
| 14 | (C) the increased risk that occurs when 2 or more | ||||||
| 15 | arteries are treated, including, but not limited to, a | ||||||
| 16 | shorter time to repeat claudication, duration between | ||||||
| 17 | procedures, or an increased likelihood that a repeat | ||||||
| 18 | atherectomy or another surgical intervention may be | ||||||
| 19 | needed; | ||||||
| 20 | (D) common complications that may result from | ||||||
| 21 | atherectomy, including, but not limited to, the | ||||||
| 22 | perforation of an artery, and the likelihood of death | ||||||
| 23 | after these complications; | ||||||
| 24 | (E) the impact of atherectomy on long-term health, | ||||||
| 25 | including, but not limited to, the likelihood of a | ||||||
| 26 | major adverse limb event, amputation, and repeated | ||||||
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| 1 | atherectomies; | ||||||
| 2 | (F) the increased likelihood of death, amputation, | ||||||
| 3 | and repeat atherectomies, based on race or ethnicity; | ||||||
| 4 | and | ||||||
| 5 | (G) a description of how Black and hispanic | ||||||
| 6 | patients have a significantly greater risk of death | ||||||
| 7 | after amputation, if the atherectomy results in a | ||||||
| 8 | major amputation. | ||||||
| 9 | (d) The expanded informed consent process shall require: | ||||||
| 10 | (1) the informed consent document to be first read and | ||||||
| 11 | completed directly by the patient; | ||||||
| 12 | (2) after the informed consent document is read and | ||||||
| 13 | completed by the patient, a health provider to read each | ||||||
| 14 | line of the informed consent document to the patient and | ||||||
| 15 | document the patient's answers; | ||||||
| 16 | (3) the provider to record any discrepancies between | ||||||
| 17 | the patient's written answers and the patient's verbal | ||||||
| 18 | answers as documented by the provider; | ||||||
| 19 | (4) the provider and the patient to sign the document; | ||||||
| 20 | (5) the provider to provide copies of the informed | ||||||
| 21 | consent documents to the patient; and | ||||||
| 22 | (6) the provider to retain and store a copy of the | ||||||
| 23 | document in medical records. | ||||||
| 24 | (e) The informed consent document shall minimally include: | ||||||
| 25 | (1) one column for patient answers and one column for | ||||||
| 26 | the provider to record the patient's verbal answers; and | ||||||
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