Oklahoma 2025 2025 Regular Session

Oklahoma House Bill HB1600 Comm Sub / Bill

Filed 03/05/2025

                     
 
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STATE OF OKLAHOMA 
 
1st Session of the 60th Legislature (2025) 
 
COMMITTEE SUBSTITUTE 
FOR 
HOUSE BILL NO. 1600 	By: Gise and Williams 
 
 
 
 
 
COMMITTEE SUBSTITUTE 
 
An Act relating to health care; enacting the Lori 
Brand Patient Bill of Rights Act of 2025 ; creating a 
list of rights for a patient seeking treatment; 
specifying certain responsibilities of patients 
seeking treatment; creating certain rights for minor 
patients seeking treatment; specifying certain 
responsibilities of parents of minor patients s eeking 
treatment in this state; providing for codification; 
and providing an effective date. 
 
 
 
 
 
BE IT ENACTED BY THE PEOPLE OF THE STATE OF OKLAHOMA: 
SECTION 1.     NEW LAW     A new section of law to be codified 
in the Oklahoma Statutes as Section 3401 of Title 63, unless there 
is created a duplication in numbering, reads as follows: 
This act shall be known and may be cited as the "Lori Brand 
Patient Bill of Rights Act of 2025 ". 
SECTION 2.     NEW LAW     A new sect ion of law to be codified 
in the Oklahoma Statutes as Section 3401.1 of Title 63, unless there 
is created a duplication in numbering, reads as follows:   
 
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A.  Each patient treated in this state shall have the following 
rights when being treated: 
1.  The right to considerate and respectful care, provided in a 
safe environment, free from all forms of abuse, neglect, harassment, 
and exploitation; 
2.  To receive information in a manner that he or she 
understands.  Communications with the patient shall be effective and 
provided in a manner that facilitates understanding by the patient. 
Written information provided will be appropriate to the age, 
understanding, and, as appropriate, the language of the patient.  As 
appropriate, communications specific to the vision -, speech-, 
hearing-, cognitive-, and language-impaired patient will be 
provided.  The hospital shall meet the requirements of federal 
regulations that require program and facility accessibility; 
3.  To receive as much information about any proposed treatment 
or procedure as he or she may need in order to give informed consent 
or to refuse the course of treatment.  Except in emergencies, this 
shall include a description of the procedure or treatment, the 
medically significant risks involved in the procedure or treatment, 
alternate courses of treatment or nontreatment and the risks 
involved in each, and the name of the person who will carry out the 
procedure or treatment; 
4. To have an advance directive attorney for health care 
concerning treatment or to design ate a surrogate decision-maker with   
 
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the expectation that the hospital will honor the intent of that 
directive to the extent allowed by law and hospital policy.  The 
health care provider must advise a patient of his or her rights 
under state law and hospita l policy to make informed medical 
decisions, ask if the patient has an advance directive, and include 
that information in patient records.  The patient has the right to 
timely information about hospital policy that may limit its ability 
to implement a legally valid advance directive; 
5. To participate in the development and implementation of his 
or her plan of care and actively participate in decisions regarding 
his or her medical care; 
6.  To accept medical care or to refuse treatment, to the extent 
permitted by law, and to be informed of the consequences of such 
refusal; 
7.  To become informed of his or her rights as a patient in 
advance of, or when discontinuing, the provision of care.  The 
patient may appoint a representative to receive this information 
should he or she so desire; 
8.  To have a family member or representative of his or her 
choice notified promptly of his or her admission to the hospital; 
9.  To request that no information regarding his or her 
admittance, diagnosis, or treatment be releas ed; 
10.  To review the records and obtain a copy of the medical 
records pertaining to his or her medical care and to have the   
 
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information explained or interpreted as necessary, except when 
restricted by law; 
11.  To reasonable continuity of care, when appr opriate, and to 
be informed by the doctor and other caregivers of available and 
realistic patient care options when hospital care is no longer 
appropriate; 
12. To confidential treatment of all communications and records 
pertaining to his or her care and s tay at the hospital; 
13.  To expect that, within its capability, capacity, and 
policies, the hospital will make a reasonable response to the 
request of a patient for appropriate and medically directed care and 
services.  The hospital must provide evaluatio n, service, and a 
referral as indicated by the urgency of the case.  When medically 
appropriate and legally permissible, or when a patient has requested 
a transfer, that patient may be transferred to another facility.  
That facility must have first accepte d the patient for transfer.  
The patient must also have the benefit of the complete information 
and explanation concerning the need for, risks and benefits of, and 
alternatives to such a transfer; 
14.  The patient or patient 's representative has the right to 
participate in the consideration of ethical issues that might arise 
in the care of the patient.  The hospital shall have a mechanism for 
the consideration of ethical issues arising in the care of patients   
 
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and to provide education to caregivers and patie nts on ethical 
issues in health care; 
15.  To be advised of the hospital 's complaint or grievance 
process should the patient wish to communicate a concern regarding 
the quality of care he or she receives.  This includes whom to 
contact to file a complaint.  The patient will be provided with a 
written notice of the complaint determination that contains the name 
of the hospital's contact person, the steps taken on his or her 
behalf to investigate the complaint, the results of the complaint 
and, when possible, the resolution of the complaint concerning the 
quality of care; 
16. To examine and receive an explanation of his or her bill 
regardless of source of payment; 
17.  To remain free from restraints or seclusion in any forms 
that are not medically necessary o r are used as a means of coercion, 
discipline, convenience, or retaliation by staff; 
18.  To receive the visitors whom he or she designates, 
including, but not limited to, a spouse, a domestic partner, 
including a same-sex domestic partner, another family member, or a 
friend.  The patient has the right to withdraw or deny consent at 
any time.  Visitation will not be restricted, limited, or otherwise 
denied on the basis of race, color, national origin, religion, sex, 
or disability; and   
 
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19.  Through use of th e hospital-issued notice of noncoverage, 
Medicare beneficiaries have the right to be informed in advance of 
procedures or treatment for which Medicare may deny payment, and 
that the beneficiary may be personally responsible for full payment 
if Medicare denies payment. 
B.  A patient, guardian of a patient, or legally authorized 
representative of a patient shall have the following 
responsibilities: 
1.  To provide accurate and complete information concerning the 
patient's present complaints, past illnesses, ho spitalizations, 
medications, and other matters relating to his or her health; 
2.  To report perceived risks in the patient 's care and 
unexpected changes in his or her condition to the responsible health 
care provider; 
3.  For the patient's actions should he or she refuse treatment 
or not follow his or her doctor 's orders; 
4.  To ask questions when the patient does not understand what 
he or she has been told about the patient 's care or what he or she 
is expected to do; 
5.  To be considerate of the rights of other patients and 
hospital personnel; 
6.  To participate in educational and discharge planning 
activities necessary to ensure that he or she has adequate knowledge   
 
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and support services to provide him or her with a safe environment 
upon discharge from the hospital; 
7.  To ask the doctor or nurse what to expect regarding pain 
management, to discuss pain relief options with doctors and nurses 
and to help develop a pain management plan, to ask for pain relief 
when pain first begins, to help doctors and nurses assess the 
patient's pain, to tell the doctors and nurses if his or her pain is 
not relieved, and to tell doctors and nurses about any concerns 
about taking pain medication; 
8.  For keeping appointments and for notifying the hospital or 
doctor when he or she is unable to do so; 
9.  Being respectful of his or her personal property and that of 
other patients in the hospital; 
10.  Following hospital procedures; and 
11.  Assuring that the financial obligations of his or her care 
is fulfilled as promptly as poss ible. 
C.  Any minor patient has the following rights when being 
treated in this state: 
1.  To be treated with respect in regards to: 
a. each child and adolescent as a unique individual, and 
b. the caretaking role and individual response of the 
parent and legal guardian;   
 
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2.  To provisions for normal physical and physiological needs of 
a growing child including nutrition, rest, sleep, warmth, activity, 
and freedom to move and explore.  Minors shall have the right to: 
a. appropriate treatment in the least rest rictive 
setting, 
b. not receive unnecessary or excessive medication, 
c. an individualized treatment plan and the right to 
participate in the plan, 
d. a humane treatment environment that provides 
reasonable protection from harm and appropriate 
privacy for personal needs, 
e. separation from adult patients when possible, and 
f. regular communication between the minor patient and  
the patient's family or legal guardian; 
3.  To consistent, supportive, and nurturing care which: 
a. meets the emotional and psychoso cial needs of the 
minor, and 
b. fosters open communication; 
4.  To provisions for self -esteem needs which will be met by 
attempts to give the minor: 
a. the reassuring presence of a caring person, especially 
a parent, 
b. freedom to express feelings or fears with appropriate 
reactions,   
 
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c. as much control as possible over both self and 
situation, 
d. opportunities to work through experiences before and 
after they occur, verbally, in play, or in other 
appropriate ways, and 
e. recognition for coping well during d ifficult 
situations; 
5.  To provisions for varied and normal stimuli of life which 
contributes to cognitive, social, emotional, and physical 
developmental needs such as play, educational, and social activities 
essential to all children and adolescents; 
6.  To information about what to expect prior to, during, and 
following a procedure or experience and support in coping with it; 
7.  To participate in decisions affecting his or her own medical 
treatment; and 
8.  To the minimization of stay duration by recogn izing 
discharge planning needs. 
D.  All parents and legal guardians of minor patients in this 
state shall have the following responsibilities: 
1.  To continue in his or her parenting role to the extent of 
his or her ability; and 
2.  To be available to part icipate in decision-making and 
provide staff with knowledge of other parent or family whereabouts. 
   
 
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SECTION 3.  This act shall become effective November 1, 2025. 
 
60-1-13183 TJ 03/05/25