Current through Register Vol. 42, No. 11, August 30, 2024
(1) Governing
Authority.
(a) Responsibility. The governing
authority or the owner or the person or persons designated by the owner as the
governing authority shall be the supreme authority of the facility, responsible
for the management, control, and operation of the facility, including the
appointment of a qualified medical staff (or in the absence of an organized
medical staff) a medical director.
(b) Organization. The governing authority
shall be formally organized in accordance with a written constitution and/or
bylaws. In the event the governing authority consists of one person, this
requirement must still be met. Such constitution and/or bylaws shall include:
1. Identification of the facility.
2. The purpose for which the facility is
organized.
3. Length of tenure and
mechanism for appointment of members of the governing body.
4. Appointments and duties of the chief
executive officer.
5. Requirement
that the medical staff (if such exists) be organized in accordance with bylaws
approved by the governing authority.
6. Mechanism for appointment of medical staff
members and a medical director.
7.
Mechanism for approval of medical staff bylaws and policies governing
activities of the medical director if an organized medical staff does not
exist.
(c) Meetings. The
governing authority shall meet regularly. A copy of the minutes of these
meetings shall be kept as a permanent record of the facility.
(d) Notification of Chief Executive Officer.
The State Board of Health shall be advised of the chief executive officer's
name within 15 days of his appointment.
(2) The Chief Executive Officer.
(a) Responsibility. There shall be a
competent, well-trained chief executive officer who shall have executive
authority and be responsible for directing, coordinating, and supervising the
overall activities of the facility. The chief executive officer and the medical
director or other qualified employee of the facility may be one and the same
person.
(b) Enforcement of Medical
Staff Regulations. As the authorized representative of the governing authority,
the chief executive officer shall have the authority to enforce medical staff
rules and regulations with regard to patient care, after consultation with
appropriate members of the medical staff.
(c) Policies and Procedures. The chief
executive officer shall be responsible for assuring, either directly or through
delegation of authority, that policies promulgated by the governing authority
are carried out. Appropriate procedures to enforce these policies, assure
proper patient care and safety, and meet requirements of these Rules, shall be
developed in writing. Policies and procedures shall be developed to include the
following areas:
1. Patient admission and
discharge. These shall be for both in-facility care and self-care or home
care.
2. Requirement for a complete
history and physical examination on admission and at least annually.
3. Required diagnostic procedures.
4. Patients waiting for renal transplant must
be typed initially for Human Leukocytes Antigens (HLA) and screened for
antibodies to HLA. The facility must complete an Agreement or Arrangement with
a State licensed and/or CLIA licensed Histocompatibility Laboratory which
contains the provision for HLA typing and antibody screening, including the
frequency of antibody screening.
(3) Self-Care Dialysis. Self-Care Dialysis
Training Program. If the facility offers self-care dialysis training, a
qualified registered nurse is in charge of the training. Appropriate records of
this training shall be maintained in the patient's record.
(4) Use of Outside Resources. Contractual
Service Agreements. There are written contractual agreements and arrangements
for services which the facility or its employees do not provide directly. The
agreement or arrangement delineates the responsibilities, functions,
objectives, and services provided by the outside resource and is signed and
dated by an authorized representative of the facility and the person or agency
providing the service.
(5) Fire
Evacuation Plan.
(a) Written Evacuation Plan.
A written fire control and evacuation plan shall be maintained by each
facility. In addition, necessary instruction and fire evacuation routes shall
be posted in conspicuous places in the facility and shall be kept
current.
(b) Fire Drills. Fire
drills shall be conducted at least quarterly and written observations of the
effectiveness of these rehearsals shall be filed and kept for at least three
years.
(6) Communication
Facilities.
(a) Personnel Paging Systems.
Arrangements shall be provided within the facility to summon additional
personnel or help when, or if needed, in the event of emergency conditions. In
general, if all personnel (or occupants) are within hearing distance of any
area of the facility, this would be deemed sufficient. Otherwise, there shall
be a call system to all portions of the building normally occupied by personnel
of the facility.
(b) Telephones.
There shall be an adequate number of telephones to summon help in case of fire
or other emergency, and these shall be located so as to be quickly accessible
from all parts of the building.
(7) Records.
(a) Responsibility for Medical Records. There
is a qualified member of the facility's staff designated to serve as supervisor
of medical records.
(b) Maintenance
and Content of Medical Records.
1. The
facility maintains complete medical records on all patients, including those
receiving care within the facility and those self-care or home dialysis
patients for whom the facility has assumed responsibility. These medical
records shall be maintained in accordance with acceptable professional
standards and practices.
2. Each
patient's record shall contain sufficient information to identify the patient
clearly, to justify the diagnosis and treatment and to accurately document the
rendition and results of treatment.
3. The medical record shall contain
physicians' orders for all medications to be administered, treatments to be
given and services to be rendered.
4. Nurses' notes records shall be maintained
for each patient in the facility. In addition to regular entries concerning
special diets and medications administered, personal services rendered and
observations made, other notes, which may be of importance to the attending
physician or other nursing personnel shall be annotated.
5. Nurses' notes and physician orders shall
be kept at the nurses' station while current and shall be placed in the
patient's file folder when completed.
6. All entries on all records and reports
shall be legibly written in ink or typewritten.
7. A physician may use a rubber stamp
signature to sign records and reports, if that physician has submitted a
letter, kept on file in the facility, indicating that the rubber stamp is for
his own use and will not be used by any other personnel within the
facility.
(c) Completion
and Organization of the Record.
1. Current
medical records and those of discharged patients are completed promptly (not to
exceed 15 days after discharge or death) and all clinical information
pertaining to a patient is centralized in the patient's medical
record.
2. The medical record shall
be organized in such a manner as to retrieve information readily. If numerical
indexing is used, an alphabetical cross-reference is utilized to facilitate
retrieval.
(d)
Confidentiality of Medical Records. When an individual enters an End Stage
Renal Disease Treatment or Transplant Center, records and information regarding
him are confidential. Information shall not be shared with visitors, other
patients, or anyone not having responsibility for his care. Access to these
records shall be limited to designated staff members, physicians and others
having professional responsibility, and to representatives of the State Board
of Health.
(e) Storage and
Protection of Medical Records.
1. The
facility maintains adequate facilities, equipment, and space conveniently
located to provide efficient processing of medical records and other medical
information.
2. The medical record
shall be protected against loss, destruction (from water and fire damage) or
unauthorized use. The facility has written policies and procedures which govern
the use and release of information contained in the medical record. A medical
record shall be maintained for six years after discharge of patient, or six
years after patient reaches majority under State law, whichever is
longer.
(f) Transfer of
Medical Information. The facility provides for the interchange of medical and
other information necessary or useful in the care and treatment of patients
transferred between treating facilities.
(g) Personnel Records. A personnel record
shall be maintained for each employee. The personnel record shall include
application for employment, which contains information regarding education,
training, experience, and if applicable, registration and/or licensure
information of the applicant, and record of physical examinations. The names
and qualification of all professional employees shall be kept on file for
inspection by the State Board of Health.
(h) Disposition of Medical Records. When an
End Stage Renal Disease Treatment or Transplant Center ceases to operate,
either voluntarily or by revocation of its license, the governing body
(licensee), at or prior to such action, shall develop a proposed plan for the
disposition of its medical records. Such plans shall be submitted to the
Alabama Department of Public Health for approval and shall contain provisions
for the proper storage safeguarding and confidentiality, transfer and/or
disposal of patient's medical records and x-ray files. Any center that fails to
develop such plans of disposition of its records acceptable to the Alabama
Department of Public Health shall dispose of its records as directed by a court
of appropriate jurisdiction.
(8) Housekeeping Services.
(a) Personnel. Sufficient personnel are
employed to maintain the facility clean and orderly. Personnel utilized in
nursing and other activities may be utilized to perform routine housekeeping
chores, however, specific written instructions to eliminate possible sources of
cross-contamination must be developed. Primary patient care personnel shall not
perform general decontamination and housekeeping chores during periods in which
they are caring for patients.
(b)
Techniques. Written procedures outlining techniques to be followed in routine
housekeeping and decontamination are developed and maintained. Procedure rooms
and areas must be cleaned, using appropriate disinfectants, between each
procedure.
(c) Premises. The
premises shall be kept neat and clean, and free of accumulation of rubbish,
weeds, ponded water, or other conditions of similar nature which would have a
tendency to create a health hazard.
(d) Control of Insects, Rodents, etc. The
facility shall be kept free of ants, flies, roaches, rodents and other vermin.
Proper methods of their eradication or control shall be utilized.
(e) Toilet Room Cleanliness. Floors, walls,
ceilings, and fixtures of all toilet rooms shall be kept clean and free of
objectionable odors. These rooms shall be kept free from an accumulation of
rubbish, cleaning supplies, toilet articles, etc.
(f) Housekeeping Facilities and Services.
Housekeeping facilities and services are required to be such that comfortable
and sanitary conditions for patients and employees are constantly
maintained.
(g) Equipment and
Supplies. The facility shall maintain an adequate quantity of housekeeping and
maintenance equipment and supplies.
(9) Infection Control.
(a) Policies and Procedures. There are
written policies and procedures in effect for preventing and controlling
hepatitis and other infections. The policies and procedures support sound
patient care and promote good personal practices and include appropriate
aseptic and isolation techniques to be used.
(b) Sterilization. Definitive written
procedures governing sterilization techniques shall be developed. Pressurized
steam sterilization is the preferred method; however, gas sterilization and
soaking of some types of equipment or instruments in a bacteriocidal solution
of approved efficacy may be permitted. Procedures are to include:
1. Technique to be used for a particular
instrument or group of instruments.
2. Length of time to accomplish
sterilization.
3. Prohibition
against reuse of one-time use (disposable) items with the exception of renal
dialyzers and dialyzer lines provided a written processing protocol for reuse
is submitted to the Alabama Department of Public Health.
4. Temperature, time, and pressure for steam
sterilization.
5. Proper methods of
preparation of items for sterilization (cleaning, wrapping and
dating).
6. Shelf storage time for
sterile items.
7. Use of sterilizer
indicators.
8. Methods of disposal
of contaminated items such as needles, syringes, catheters, gloves,
etc.
9. Use of routine (at least
monthly) sterilizer culture controls.
(c) Investigation of Infections. Reports of
infections such as abscesses, septicemia, hepatitis, or other communicable
diseases observed during admission or follow-up (or return) visit of the
patient shall be made and kept as a part of the administrative files. Efforts
shall be made to determine the origin of any such infection and if the
procedure was found to be related to acquiring the infection, remedial action
shall be taken to prevent recurrence.
(d) Hepatitis Surveillance.
1. Routine surveillance of patients and staff
for HBV infection is essential to determine if transmission is occurring in the
unit. The HBsAg (anti-HBs) status of all patients and staff shall be known to
identify those individuals who are;
(1)
HBsAg-positive and therefore potential sources of infection to others;
(2) anti-HBs-positive and
therefore, immune; and
(3)
HBV-seronegative and therefore susceptible to HBV.
2. Patients for dialysis and new employees
must be screened for HBsAg and anti-HBs before or at the time they enter the
unit in order to determine their serologic status for surveillance purposes.
HBsAg positivity in staff does not necessarily preclude employment in the
dialysis center; these persons may be managed in the same manner as employees
who seroconvert to HBsAg-positive status while working in the unit.
3. The HBsAg status of visiting and home
patients must be known, if possible, at the time of admission to determine if
they are potential sources of infection.
4. The most sensitive test methods available
for HBsAg and anti-HBs detection must be employed.
5. Patients who are seronegative (HBsAg- and
anti-HBs-negative) must be tested once a month for HBsAg, serum glutamic
oxalacetic transaminase (SGOT), and/or serum glutamic pyruvic transaminase
(SGPT) and at least once every three months for anti-HBs. Seronegative staff
members must be tested at least once every six months for HBsAg and
anti-HBs.
6. Patients and staff who
have had hepatitis B as demonstrated by:
(1)
a documented history of hepatitis B;
(2) HBsAg-positivity demonstrated on two
occasions; or
(3) a positive HBsAb
test in the absence of an injection of hepatitis B immune globin, need have
only further HBsAb determinations on an annual basis for hepatitis surveillance
purposes.
7. Patients
and staff who have received a full course (3 injections over a six-month
period) of Heptavax vaccine and have a positive HBsAb test need only further
HBsAb determinations on an annual basis for hepatitis surveillance
purposes.
(e)
Cross-Contamination Prevention.
1. The
facility must employ appropriate techniques to prevent cross-contamination
between the dialysis unit and adjacent hospital or public areas.
2. There must be some type of protective
covering, either plastic, disposable, or launderable, during the time when
blood lines are opened or needles inserted or withdrawn in order to prevent the
patient's street clothing from becoming contaminated.
3. All equipment utilized in dialysis must be
changed or cleaned after each use.
4. Appropriate precautionary measures must be
implemented to prevent facility personnel from contaminating shoes and clothing
that will be worn outside the dialysis unit.
(f) Disposal of Infectious Material and
Waste. Policies and procedures must be developed for the proper handling,
cleaning and disposal of all infectious material and waste products. All
dialysis waste must be contained in a closed sewage drain system.
(g) Isolation Facilities.
1. An isolation dialysis room must be
provided for all Hepatitis B Antigen Positive Dialysis Patients; the room must
be partitioned from treatment areas for Hepatitis B Antigen Negative Patients
and provide separate facilities from toilet, handwashing, janitorial, drug
storage, blood (Hematocrit and clotting time) handling and waste storage and
disposal.
2. Facilities not
equipped with a Hepatitis B Isolation Section as defined above may not accept
for treatment any Hepatitis B Antigen Positive Patients but must complete an
Agreement to transfer any Positive Patients to a facility so
equipped.
(h) Infection
Control Committee. A committee must be established and made up of at least a
physician and the Director of Nurses to evaluate or monitor staff performance,
review all policies and procedures at least annually, and review infectious
cases. This committee shall meet at least monthly.
(i) Linens.
1. All reusable linens, including those used
as sterilizing wrappers, must be laundered before reuse.
2. Linens are handled, stored, processed, and
transported in such a manner as to prevent the spread of infection.
3. The facility has available at all times a
quantity of linen essential for proper care and comfort of patients.
(j) Water Treatment. Water used
for dialysis purposes must be analyzed at least monthly for bacteria and at
least six months for chemicals. The water must be treated as necessary to
maintain a continuous water supply that is biologically and chemically
compatible with acceptable dialysis techniques. Records of test results and
equipment maintenance are maintained at the facility.
Authors: Tigner Zorn, Carol Nason, Jim Prince,
Rick Harris
Statutory Authority:
Code of Ala.
1975, §§
22-21-20,
et
seq.