Current through Register Vol. 49, No. 9, September, 2024
SECTION 3.
DEFINITIONS.
Free-Standing Birthing Centers - any facility
which is organized to provide family-centered maternity care in which births
are planned to occur in a home-like atmosphere away from the mother's usual
residence following a low risk pregnancy. The facility shall not provide
operative obstetrics, including use of forceps, vacuum extractions, Caesarean
sections, or tubal ligations. The Free-Standing Birthing Center must be located
within thirty (30) minutes of a hospital (via ambulance) which offers obstetric
and nursery services and which maintains an on-call team to provide emergency
C-sections and stabilization of infants.
Administrator - an individual designated to
provide daily supervision and administration of the Free Standing Birthing
Center.
Certified Nurse Midwife - a trained and licensed
advanced practice nurse in accordance with the Arkansas Nurse Practice Act,
Arkansas Code Annotated §
17-87-314, et seq.
Complications - any condition according to written
risk criteria of the Free-Standing Birthing Center that contraindicates
continued care in the Free-Standing Birthing Center.
Large Free-Standing Birthing Center - a birthing
center comprised of four (4) or more birthing rooms with an exam room.
Low Risk Pregnancy - a normal uncomplicated
pregnancy as determined by a generally accepted course of prenatal care and the
expectation of a normal uncomplicated birth as defined by a reasonable and
generally accepted criteria of maternal and fetal health.
Medical Director - a person licensed to practice
medicine in the state of Arkansas.
Preterm - before the end of the thirty-seventh
(37th) week of gestation.
Professional Review Committee - shall be composed
of at least three (3) members. The members shall include a Physician with
advanced training in Obstetrics, one (1) Certified Nurse Midwife and/or one (1)
Registered Nurse (required for large Free- Standing Birthing Centers).
Qualified Physician - a person licensed to
practice medicine in the State of Arkansas, who has obstetrical privileges at
the licensed hospital.
Small Free-Standing Birthing Center - a birthing
center comprised of three (3) or fewer birthing rooms and occupied by fewer
than four (4) patients, not including newborns, at any time.
Term - at thirty-seven (37) weeks gestation, or
greater.
SECTION 4.
LICENSING.
A. Application for
License. Application for a license or renewal of a license for a Free- Standing
Birthing Center shall be made to the Arkansas Department of Health on forms
provided by the Division of Health Facility Services. The application shall set
forth the complete name and address of the Free-Standing Birthing Center for
which the license is sought and any additional information as required by the
Arkansas Department of Health.
B.
The Free-Standing Birthing Center shall have a written agreement with a local
hospital which has twenty-four (24) hour obstetric services. The Free-Standing
Birthing Center shall be within thirty (30) minutes of the hospital. If the
hospital ceases to provide obstetric services, the Birthing Center shall obtain
a written agreement with another hospital that provides obstetric services and
is within thirty (30) minutes of the Birthing Center. If another written
agreement cannot be obtained, the Birthing Center must cease providing
services, notify the Division of Health Facility Services in the Arkansas
Department of Health, and surrender the license to the Division. The Birthing
Center may reapply for licensure once a new written agreement is
obtained.
C. Fee. In accordance
with Section 5 of Act 891 of 1997, each application for initial licensure of a
Free-Standing Birthing Center shall be accompanied by a fee of one thousand
dollars ($1000). The fee shall be payable to the Arkansas Department of
Health.
D. Renewal of License. A
license, unless revoked, shall be renewable annually upon payment of a fee of
one thousand dollars ($1000) to the Arkansas Department of Health accompanied
by an application for re-licensure. The application for annual license renewal
along with the fee shall be postmarked no later than January 2 of the year for
which the license is issued.
E.
Issuance of License. A license shall be issued only for the premises and person
or persons reflected in the application and shall be posted in a conspicuous
place in the Free-Standing Birthing Center. The license shall be effective on a
calendar year basis and shall expire on December 31 of each calendar year.
The license shall not be transferrable and shall expire if a
change of ownership occurs.
F. Change of Ownership. It shall be the
responsibility of the Free-Standing Birthing Center to notify the Division of
Health Facility Services in writing at least thirty (30) days prior to the
effective date of a change of ownership. The following information shall be
submitted for review and approval:
1. License
application
2. One thousand dollars
($1000) change of ownership fee; and
3. Legal documents, ownership agreements, and
other information to support relicensure requirements.
G. Management Contract. It shall be the
responsibility of the Free-Standing Birthing Center to notify the Division of
Health Facility Services in writing at least thirty (30) days prior to entering
into a management contract or agreement with an organization or firm. A copy of
the contract or agreement shall be submitted for review to assure the
arrangement does not affect the license status.
H. Closure. Once a Free-Standing Birthing
Center closes, it shall no longer be considered licensed. The license issued to
the Free-Standing Birthing Center shall be returned to the Division of Health
Facility Services. To be eligible for re-licensure, the Free-Standing Birthing
Center shall meet requirements for new construction and all the current life
safety and health regulations.
I.
Inspection. Any authorized representative of the Arkansas Department of Health
shall have the right to enter upon or into the premises of any Free-Standing
Birthing Center at any time in order to make whatever inspection it deems
necessary in order to assure minimum standards and regulations are
met.
SECTION 5.
GOVERNING BODY.
A Free-Standing Birthing Center shall have an organized
Governing Body which shall be legally responsible for maintaining patient care,
establishing policies for the facility and shall be legally responsible for the
conduct of the center.
A. Governing
Body Bylaws. The Governing Body shall adopt written bylaws which shall be
available to all members of the Governing Body. The bylaws shall ensure the
following:
1. The Governing Body shall consist
of three (3) or more individuals;
2. Maintenance of professional standards of
practice;
3. Terms,
responsibilities and methods of selecting members and officers;
4. Selection of an Administrator with
responsibility for operation and maintenance of the facility;
5. Methods for establishing Governing Body
committees and the duties of each committee;
6. Coordination of activities and general
policies of the departments;
7.
Liaison between the Governing Body and Professional Review Committee documented
quarterly;
8. Quarterly Governing
Body meetings with maintenance of minutes signed by an officer;
9. Provision for formal approval of the
organization, bylaws, rules, regulations, and protocols of the Free-Standing
Birthing Center staff and their services;
10. Method of credentialing or appointing
members to the professional and other authorized staff;
11. Methods by which Quality Improvement (QI)
is established;
12. Establishment
of a quorum to be met in order to conduct business;
13. Annual approval of the operating budget
by the Governing Body; and
14.
Compliance with federal, state and local laws.
B. Governing Body Minutes. The Governing Body
minutes shall include at least the following information:
1. Review, approval and revision of the
Governing Body bylaws and the Professional Review Committee bylaws, rules,
regulations and protocols;
2.
Election of officers, as indicated in the bylaws;
3. Documentation that the liaison between the
Governing Body and Professional Review Committee is maintained;
4. Appointment and reappointment of the
Professional Review Committee and other credentialed staff as indicated in the
bylaws;
5. Review and approval of
reports received from the Professional Review Committee and
Administration;
6. Review and
approval of the Quality Improvement Plan of the facility, at least annually,
also documentation of the quarterly Quality Improvement summaries.
C. Credential Files. An individual
file shall be maintained for each physician, Certified Nurse Midwife, Advanced
Practice Nurse, and other allied health practitioners practicing in the
FreeStanding Birthing Center and shall include at least the following:
1. Verification of year, and school of
graduation; date of licensure; postgraduate or special training and
experience;
2. Specific delineation
of privileges requested and granted;
3. Detailed application signed by the
applicant, the chairman of the Professional Review Committee and an officer of
the Governing Body;
4.
Documentation of the applicant's agreement to abide by the Free-Standing
Birthing Center bylaws, rules, regulations, and protocols;
5. Verification of current Arkansas license
and certification as applicable;
6.
Verification of each applicant's Drug Enforcement Agency (DEA)
permit;
7. Verification of at least
three (3) professional references;
8. Documentation of all actions taken by the
Professional Review Committee and Governing Body indicating the privileges
granted, approval of appointment/reappointment, and other related data;
and
9. Evaluation of professional
performance at the time of re-appointment.
D. Professional Review Committee Bylaws. The
Professional Review Committee bylaws shall include at least the following
provisions:
1. Responsible to the Governing
Body for the quality of health care provided in the Free-Standing Birthing
Center and for the ethical and professional practices of its members;
2. Requirements for membership;
3. Election of officers, responsibilities and
terms;
4. Functions, frequency of
meetings and composition (quorum) and attendance requirements;
5. Written minutes shall be maintained of all
meetings and shall be signed by the chairman;
6. An appeals process if
appointment/reappointment is not granted by the Governing Body;
7. Delineation of maintaining accurate and
complete medical records; and
8.
Approval of the bylaws and amendments by the Professional Review Committee and
the Governing Body.
E.
Professional Review Committee Minutes. Professional Review Committee minutes
shall include at least the following:
1.
Documentation of review of committee reports including quarterly Quality
Improvement (QI) summaries;
2.
Review, approval and revision of the Professional Review Committee bylaws,
rules, regulations, and protocols;
3. Election of officers as specified by the
bylaws;
4. Documentation of a
practitioner designated as chairman of the committee to direct the services
defined in the bylaws; and
5.
Documentation of appointments, reappointments, and approval of requested
privileges to the Free-Standing Birthing Center staff as specified in the
bylaws, but at least every two (2) years.
F. Quality Improvement (QI) Program.
1. The Free-Standing Birthing Center shall
develop, implement, and maintain a QI program. The QI plan shall be reviewed
and approved annually by the Governing Body. The facility shall appoint a QI
Committee with functions to include:
a.
Quarterly meetings with maintenance of written minutes;
b. Collection of data on the functional
activities identified as priorities in QI and benchmark against past
performance and national or local standards; and
c. Development and implementation of
improvement plans for identified issues, with monitoring, evaluation and
documentation of effectiveness.
2. The scope of the QI Program shall include,
but not be limited to, activities regarding the following:
a. Assessment of processes and outcomes.
Outcome data for morbidity, mortality, maternal and infant transfers and
referrals, complications, Apgar scores, patients delivering outside the center,
and other performance data shall be collected and analyzed on an ongoing
basis;
b. Evaluation of customer
satisfaction (patients, providers, patients= families, employees);
c. Measurement of staff
performance;
d. Complaint
resolution;
e. Utilization data;
and
f.
Organizational/administrative performance.
3. Reporting. QI activities shall be reported
to the Professional Review Committee and the Governing Body on a quarterly
basis and shall be documented in the Governing Body meeting minutes.
4. Policies and Procedures covering all
functions of the QI Program shall be maintained. All policies and procedures
not contained within the QI Plan shall be maintained in a manual. The first
page of the manual shall have the annual review date and signatures of the
persons conducting the review.
SECTION 6.
GENERAL
ADMINISTRATION.
A. Each institution
shall have an Administrator responsible for the management of the institution.
The responsibilities of the Administrator shall include:
1. Keeping the Governing Body fully informed
of the status of the Free-Standing Birthing Center by submitting periodic
written reports or by attending meetings of the Governing Body;
2. Conducting meetings at regular intervals
and maintaining minutes of the meetings; and
3. Preparation of an annual operating budget
to be submitted to the Governing Body for approval.
B. Policies and procedures shall be provided
for the general administration of the facility and for each service. All
policies and procedures shall have evidence of ongoing review and/or revision.
The first page of each manual shall have the annual review date, signature of
the department supervisor and/or person(s) conducting the review.
C. Provisions shall be made for safe storage
of patient's valuables.
D. Each
facility shall develop and maintain a written disaster plan which includes
provisions for complete evacuation of the facility. The plan shall provide for
widespread disasters, as well as for disasters occurring within the local
community and birthing center. The disaster plan shall be rehearsed at least
twice a year, preferably as part of a coordinated drill in which other
community emergency agencies participate. One (1) drill shall simulate a
disaster of internal nature and the other external. Written reports and
evaluation of all drills shall be maintained.
E. There shall be a posted list of names,
telephone numbers, and addresses available for emergency use. The list shall
include center management personnel and staff, the local police department, the
fire department, ambulance service, Red Cross, and other available emergency
units. The list shall be reviewed and updated at least every six (6)
months.
F. There shall be current
reference material available onsite to meet the professional and technical
needs of birthing center personnel including: current books, periodicals, and
other pertinent materials.
G. All
employees shall be required to have annual in-services on safety, fire safety,
back safety, infection control, standard precautions, disaster preparedness and
confidential information.
H.
Procedures shall be developed for the retention and accessibility of the
patients' medical records if the Free-Standing Birthing Center closes. The
medical records shall be stored within the State of Arkansas for the required
retention period and shall be accessible for patient use.
I. Any Free-Standing Birthing Center that
closes shall meet the requirements for new construction in order to be eligible
for re-licensure. Once a facility closes, it is no longer licensed. The license
shall be immediately returned to Health Facility Services. To be eligible for
licensure all the referenced National Fire Codes (NFPA) and health regulations
shall be met.
J. The Free-Standing
Birthing Center Administrator shall develop policies and procedures that, upon
request of the patient, an itemized statement of all services shall be provided
within thirty (30) days after discharge or thirty (30) days after request,
whichever is later. The policy shall include a statement advising the patient
in writing of her right to receive the itemized statement of all
services.
K. A general consent for
medical treatment and care shall be signed by the patient or legal guardian.
Written or verbal consent shall not release the facility or its personnel from
upholding the rights of its patients including but not limited to the right to
privacy, dignity, security, confidentiality, and freedom from abuse or
neglect.
L. The center shall have a
procedure for infant identification at the time of birth which shall be
sufficient to identify the infant(s) with one (1) mother. Large Free-Standing
Birthing Centers shall use waterproof plastic identification bands with tag
inserts written in waterproof ink. These shall be placed on the mother and
infant in the birthing room at the time of delivery and shall remain in place
during the entire stay.
M. A record
book shall be kept up to date and shall contain the following information:
1. Mother's maiden name and father's
name;
2. Baby's sex, date, time and
place of birth; and
3. Physicians',
Certified Nurse Midwife (CNM) and/or Registered Nurses' names.
N. There shall be written policies
and procedures jointly developed by the Medical Director and the professional
staff, which define the care provided at the Birthing Center.
O. There shall be written documentation of
annual review of the policies and procedures, with revision as
indicated.
P. Policies and
procedures shall include but are not limited to:
1. Initial risk assessment;
2. Criteria for maternal transfer to an acute
care facility during the antepartal, intrapartal and postpartum phases;
and
3. Criteria for infant transfer
to an acute care facility;
4.
Admission criteria;
5. Nursing
assessment;
6. Family support and
participation;
7. Medication
administration;
8. Care of the
newborn to include administration of prophylactic medications required by the
Arkansas Department of Health;
9.
Emergency procedures;
10. Fetal
demise;
11. Vital statistics
registration;
12. Infection
control; and
13. Aftercare of the
mother and infant.
Q.
The facility shall report to the Arkansas Department of Health, Division of
Vital Statistics, a patient is transferred from the care of a lay midwife
during the labor and delivery process to the hospital or other licensed
healthcare facility.
SECTION
7.
SERVICES.
Care in Free-Standing Birthing Centers shall be provided by a
Licensed Physician and/or CNM and other qualified professionals and clinical
staff with access to and availability of consulting clinical specialists.
Ancillary personnel shall be available to care for the volume of patients and
programs offered.
A. Services provided
in Free-Standing Birthing Centers may include antepartal, intrapartal,
postpartal care and the care of the newborn infant.
B. Local analgesia/anesthesia for pudendal
block and episiotomy repair shall be permitted.
C. Surgical services shall be limited to
those normally performed during uncomplicated childbirth, such as episiotomy
and repair of lacerations.
D. The
care of the newborn may include a recognized method of circumcision which
limits blood loss to less than one cubic centimeter (1cc).
E. The following shall be prohibited in
Free-Standing Birthing Centers:
1.
Administration of general and conductive analgesia/anesthesia to include spinal
and epidural analgesia/anesthesia;
2. Administration of all types conscious
sedation;
3. Performance of
Caesarean sections and operative obstetrics to include tubal
ligations;
4. I.V. analgesia is
prohibited; and
5. Stimulation or
augmentation with chemical agents, e.g., oxytocics during the first and second
stages of labor.
SECTION
8.
PATIENT CARE SERVICES.
A. Organization.
1. The center shall be organized to ensure
twenty-four (24) hour Registered Nurse coverage as needed.
2. A physician, Certified Nurse Midwife,
and/or Registered Nurse, shall be available and onsite for patient care during
the entire time a patient is in the center.
3. Services during labor and delivery shall
be provided under protocols developed by the clinical staff and approved by the
Governing Body in accordance with accepted standards of care.
4. Authority and responsibilities of all
patient care staff shall be clearly defined in written policies.
5. Services shall be organized to ensure that
management functions are effectively conducted. These functions shall include,
but are not limited to:
a. Development and
implementation of policies and procedures related to patient care;
b. Review of policies and procedures at least
annually to reflect current standards of maternal and newborn care. The first
page of each manual shall have the review date and approval signatures of the
person(s) conducting the review;
c.
Establishment of a mechanism for review and evaluation of care and services
provided at the center;
d.
Orientation and maintenance of qualified staff for provision of care;
e. Provisions for staff development,
including at least twelve (12) in- service education programs for professional
staff annually; and
f. Provisions
for current nursing literature and reference materials.
6. Patients shall have access to twenty-four
(24) hour telephone consultation with either a Registered Nurse or Certified
Nurse Midwife or physician.
B. Qualifications.
1. The Certified Nurse Midwife shall provide
documentation of current licensure, as required by the Arkansas State Board of
Nursing. The documentation shall be maintained as part of the credential file
for that person.
2. Licensed
nursing personnel shall practice in accordance with the Nurse Practice Act of
the State of Arkansas.
3.
Documentation of current licensure shall be maintained for all nursing
personnel who practice in the center.
4. All clinical staff of the center shall be
required to provide documentation of training and continued competence in adult
and Neonatal Resuscitation Program (NRP) or its equivalent.
C. Staffing.
1. A physician, Certified Nurse Midwife, or
Registered Nurse with demonstrated competencies in labor and delivery shall be
required to deliver one to one (1:1) care during labor, delivery and
post-delivery until both mother and newborn are stable.
2. There shall be adequate numbers of
professional and support staff on duty and on call to meet the patient's needs:
for services routinely provided; during periods of high demand or emergency; to
assure patient safety and satisfaction; and to assure that no patient in active
labor is unattended.
3. During the
second stage of labor, two to one (2:1) patient care is required, with one (1)
of the clinical staff being a physician or Certified Nurse Midwife and the
other being a Registered Nurse.
4.
Clinical staff who have demonstrated ability to perform neonatal and adult
resuscitation procedures shall be present during each birth.
SECTION 9.
PROGRAM REQUIREMENTS.
A. The
birthing center shall have written criteria for evaluation of risk status,
admission, transfer, discharge, and complications requiring medical or surgical
intervention. The criteria shall be developed by the clinical staff and
approved by the Governing Body.
1. Criteria
for admission for labor, birth, and postpartum care shall include, but is not
limited to:
a. Low-risk pregnancy with the
expectation of a singleton, vertex, spontaneous vaginal birth at term without
complications;
b. Evidence of
adequate prenatal care which begins no later than twenty-eight (28) weeks
gestation and provides continuous prenatal screening; and
c. Evidence of preparation for
out-of-hospital birth and early discharge.
2. Criteria shall be developed for conditions
of the mother or neonate requiring transfer to an acute care
facility.
3. Criteria for discharge
of the mother and newborn in not more than twenty-four (24) hours from
admission shall be developed and approved by the Governing Body.
B. In no event shall a patient
meeting any of the following criteria be accepted as a candidate for delivery
at a Free-Standing Birthing Center:
1. Females
below fourteen (14) years of age;
2. Documented problems in the maternal
medical history, including:
a. Heart
disease;
b. Pulmonary
embolus;
c. Symptomatic congenital
defects;
d. Moderate to severe
renal disease, including nephritis;
e. Severe mental health problems and/or
current use of drugs related to its management;
f. Epilepsy or seizures after ten (10) years
of age which required use of anticonvulsive medications;
g. Breech presentation;
h. Preterm labor;
i. Insulin-dependent gestational
diabetes;
j. Thyroid disease which
is not maintained in euthyroid state;
k. Bleeding disorder or hemolytic
disease;
l. Other serious medical
problems;
m. Multiple
births;
n. Vaginal birth following
C-section (VBAC);
o.
Preeclampsia;
p. Moderate or severe
asthma;
q. Severe obstructive
pulmonary disease;
r. Severe
systemic disease (e.g., SLE, hyperthyroidism, Marfan's syndrome);
s. Hypercoagulable state (i.e., protein S or
C deficiency, AT III deficiency); or
t. History of intracranial injury.
3. Patients with the following
physical findings:
a. Previous Rh
sensitization;
b. Positive HIV
antibody;
c. Gestation of more than
twenty-eight (28) weeks with no prenatal care;
d. Hematocrit below 28%;
e. S/S (sickling) hemoglobin or abnormal
protein electrophoresis;
f.
Evidence of active tuberculosis; and
g. Chronic hypertension;
h. Known severe fetal abnormality;
i. Severe Polyhydramnios;
j. Severe Oligohydramnios;
k. Placenta previa.
C. Admission to the Program.
Childbearing women prior to twenty-eight (28) weeks gestation seeking care in
the center shall be initially screened by either the physician or Certified
Nurse Midwife or Registered Nurse Practitioner, or Advanced Practice Nurse. The
initial screening shall include at a minimum:
1. Complete social, family, medical,
reproductive, nutritional and behavioral history;
2. Evidence of results of complete physical
examination to include Papanicolaou smear and assessment for sexually
transmitted diseases; and
3.
Prenatal laboratory profile to include a complete blood count, blood type and
Rh antibody screen if necessary, urinalysis or urine culture, tests for
sexually transmitted diseases, mother's Hepatitis C status, and other tests as
medically indicated. The healthcare provider shall record in the medical record
if the pregnant woman declines to be tested for Hepatitis C.
D. Continuing prenatal care shall
include a repeat evaluation of the hemoglobin or hematocrit at twenty-eight
(28) to thirty-six (36) weeks gestation.
E. Free-Standing Birthing Centers shall
comply with Arkansas Statutes (Act 192 of 1967 as amended by Act 481 of 1981,
the same being Ark. Code Ann.
20-15-302 -304), which require
newborn infants to be tested for phenylketonuria, congenital hypothyroidism and
galactosemia.
F. Newborn testing
for critical congenital heart defects shall include the performance of pulse
oximetry testing all newborns before discharge. Ark. Code Ann. §
20-9-103. Performance of a pulse
oximetry test on a newborn is not required if the parent or legal guardian of
the newborn object to the testing on medical, religious, or philosophical
grounds.
G. Newborn testing for
genetic illnesses shall be in accordance with Arkansas Rules Pertaining to
Testing of Newborn Infants and Ark. Code Ann. § 20-15- 302.
H. Newborn testing for early detection of
hearing loss shall be in accordance with Arkansas Rules Pertaining to the
Universal Newborn/Infant Hearing Screening, Tracking and Intervention Program
and Ark. Code Ann.
20-15-1504.
I. Educational Plan for Ante-partum Care.
1. There shall be a written plan which shall
include but not limited to:
a. Anticipated
physiologic, psychologic changes during pregnancy;
b. Fetal development;
c. Normal nutrition;
d. Warning signs of complications of
pregnancy;
e. Self care to include
information of the dangers of smoking, alcohol and substance abuse, the need
for dental care;
f. Stages of
labor;
g. Non-pharmacologic
techniques to promote comfort and relaxation during labor;
h. Delivery process;
i. Immediate care of the newborn;
j. Criteria for and process of transfer to an
acute care facility;
k. Normal
postpartum;
l. Criteria for
discharge from the center;
m.
Breast-feeding;
n. Importance of
immunization;
o. Child safety to
include use of carseats;
p.
Directions for obtaining laboratory tests for newborns required by the Arkansas
Department of Health;
q.
Instruction as to clothing/supplies needed at the time of discharge from the
center;
r. Instruction shall be
appropriate to the assessed educational level and within the cultural framework
of the childbearing family; and
s.
The educational plan shall include provisions for material and teaching in
languages other than the dominant language where possible.
t. Informing, counseling and instructing the
pregnant woman, by a physician or healthcare provider, regarding Hepatitis
C.
2. The facility shall
develop instructional programs to orient family members desiring to be present
at the birth.
3. There shall be
written documentation in the patient record of patient/family receipt of
instructions.
4. There shall be
documentation of annual review and revision of the educational plan.
J. Family Participating in The
Birth Process.
5. The number of
individuals/family members present at the time of birth shall be determined by
center policy which takes into account room size and need for infection
control.
6. Individuals/family
members shall abide by the center's infection control policies in regard to
handwashing, apparel, etc.
7. An
adult not involved in the birthing process shall be in charge of the
children.
8. Children shall be
screened for infectious disease by either the physician or CNM or RN prior to
admission to the birthing room. Children with evidence of infectious disease
will not be allowed in the birthing room.
9. Only children who have completed sibling
evaluation or preparation will be allowed in the birthing room.
10. Animals, except for seeing eye dogs,
shall be prohibited in the Free-Standing Birthing Center at any time.
K. Emergency Procedures. The
Free-Standing Birthing Center shall have written procedures for emergency
transfer of mother and/or newborn to an acute care facility.
L. Minimum Equipment for Birthing Rooms. The
birthing room shall be attractively furnished and decorated; furniture, vinyl
wall covering, pictures, radios, television and other amenities may be utilized
so long as the potential medical needs of the mother and newborn are not
compromised. The furniture shall be easily cleanable.
1. Sterile equipment shall be used for the
delivery.
2. Professionals directly
involved in the delivery shall wear clean attire and sterile gloves.
3. Minimum equipment for the birthing room
shall include:
a. Bed with waterproof
pad;
b. A heated newborn crib,
bassinet or newborn examination unit;
c. Sphygmomanometer and stethoscopes - adult
and newborn sizes;
d.
Fetoscope;
e. Oxygen and oxygen
equipment including tubing, nasal prongs, ambu bags, and masks;
f. Suction and suction equipment including
DeLee traps for newborn suction;
g.
Mobile or mounted spotlight or lamp;
h. Maternal and newborn airways;
i. Storage for clothing, linens and
supplies;
j. Wall clock;
k. Newborn scales;
l. Tape measure;
m. Identification supplies - maternal and
newborn;
n. Prophylactic
medications for newborns as required by the Arkansas Department of
Health;
o. Emergency call
system;
p. Apgar chart;
q. Amniotic hook;
r. Bulb syringe;
s. Nitrazine paper; and
t. Emergency drugs, as identified by the
facility.
SECTION 10.
HEALTH INFORMATION
SERVICES.
The Free-Standing Birthing Center shall maintain a system for
the completion and storage of the medical record. The record shall provide a
format for continuity and documentation of legible, uniform, complete and
accurate maternal and infant information readily accessible and maintained in a
system that ensures confidentiality.
A. General Requirements.
1. The Free-Standing Birthing Center shall
adopt a record form for use that contains information required for transfer to
an acute care maternal and newborn service.
2. Record reviews with criteria for
identification of problems and follow-up shall be reported to the QI Committee
quarterly.
3. Responsibility for
the processing of records is assigned to an individual employed by the
Free-Standing Birthing Center.
4.
All medical records shall be retained in either the original, microfilm or
other acceptable methods for ten (10) years after the last discharge.
5. Complete medical records of minors shall
be retained for a period of two (2) years after the age of majority is
reached.
6. The original or a copy
of the original (when the original is not available) of all reports shall be
filed in the medical record.
7. The
record shall be permanent and shall be either typewritten or legibly written in
blue or black ink.
8. All
typewritten reports shall include the date of dictation and the date of
transcription.
9. All dictated
records shall be transcribed within forty-eight (48) hours.
10. Errors shall be corrected by drawing a
single line through the incorrect data, labeling it as "Error," initialing and
dating the entry.
11. Birth
certificates shall be completed according to the Bureau of Vital Records,
Arkansas Department of Health.
12.
Policies and procedures for Health Information Services shall be developed. The
manual shall have evidence of ongoing review and/or revision. The first page of
the manual(s) shall have the annual review date, signature of the department
supervisor and/or person(s) conducting the review.
13. Medical records shall be protected to
ensure confidentiality, prevention of loss, and to ensure availability on a
twenty-four (24) hour basis.
14.
All medical records, whether stored within the facility or away from the
facility shall be protected from destruction by fire, water, vermin, dust,
etc.
15. Medical records shall be
considered confidential. All medical records (including those filed outside the
facility) shall be secured at all times. Records shall be available to
authorized personnel from the Arkansas Department of Health.
16. Written consent of the patient or legal
guardian shall be presented as authority for release of medical information.
There shall be policies and procedures developed concerning all phases of
release of information.
17.
Original medical records shall not be removed from the facility except upon
receipt of a subpoena duces tecum by a court having authority for issuing such
an order.
18. Medical records shall
be complete and contain all required signed documentation no later than thirty
(30) days following the patient's discharge date.
19. Medical records shall be destroyed by
burning or shredding. Medical records shall not be disposed of in landfills or
other refuse collection sites.
20.
Each entry into the medical record shall be authenticated by the individual who
is the source of the information. Entries shall include observations, notes and
other information included in the record.
21. Signatures shall be at least, the first
initial, last name and title. Computerized signatures by code, number,
initials, or the method developed by the facility are acceptable.
22. There shall be policies and procedures
approved by the Arkansas Department of Health for use of computerized medical
records.
B. Record
Content. Each record shall include but not be limited to documentation of:
1. Demographic and patient
information;
2. Orientation to
program and informed consent;
3.
Complete family, medical, social, reproductive, nutrition and behavioral
history;
4. Initial physical
examination, evaluation of risk status and laboratory test result;
5. Appropriate referral of patients who did
not meet the Free-Standing Birthing Center criteria on the initial
screening;
6. Documentation of each
periodic examination and evaluation of risk factors;
7. Instructions, education including changes
in pregnancy, self-care, nutritional counseling, preparation for labor, family
preparation, explanation on examinations and laboratory tests, newborn
assessment and care;
8. Monitoring
of labor progress;
9. Physical
assessment of newborn, e.g., Apgar score;
10. Labor and discharge summaries;
11. Home care, follow-up and referrals;
and
12. Informed consent signed by
the patient.
SECTION
11.
PHARMACEUTICAL SERVICES.
A. Organization.
1. Free-Standing Birthing Centers shall have
provisions for pharmaceutical services regarding the procurement, storage,
distribution and control of all medications. The Free-Standing Birthing Center
shall be in compliance with all state and federal regulations.
2. Pharmaceutical services shall be under the
direction of a licensed pharmacist. A licensed pharmacist means any person
licensed to practice pharmacy by the Arkansas State Board of Pharmacy who
provides pharmaceutical services as defined in the Pharmacy Practice Act. The
pharmacist shall make provisions that shall include but not be limited to:
a. Development and implementation of pharmacy
policies and procedures;
b. Annual
review and revisions of pharmacy policies and procedures, with documentation of
date(s) of review;
c. Maintenance
of medications in the Free-Standing Birthing Center to meet the needs of the
population served;
d. Maintenance
of medications in the Free-Standing Birthing Center to assure accountability;
and
e. Proper storage of
medications.
B. Staffing. Pharmaceutical services shall be
provided by a licensed pharmacist. This service may be provided on a consulting
basis. Onsite consultation by the pharmacist shall be required at least
monthly, if medications other than those in the following categories are stored
in the facility: emergency or eye prophylaxis drugs, oxytocics, and vitamin K.
The storage of controlled substances in any manner shall require monthly onsite
consultation by the pharmacist. When onsite consultation by the pharmacist is
required monthly, documentation of each consult shall be recorded and
maintained at the Free-Standing Birthing Center. Documentation of each
consultation visit shall be recorded and maintained at the Free-Standing
Birthing Center. Documentation of each visit shall include compliance with but
not be limited to:
1. Proper drug
storage;
2. Disposal of medications
no longer needed, discontinued, or outdated;
3. Proof of receipt and administration of
controlled substances and proper storage of such medications;
4. Verification that medications in stock
conform to the specified quantities on posted lists;
5. Proper labeling; and
6. Maintenance of emergency carts or
kits.
C. Policies and
Procedures. There shall be pharmacy policies and procedures to include but not
limited to:
1. Detailed job description of the
licensed pharmacist;
2. Procurement
of medications;
3. Distribution and
storage of medications;
4. A
listing of floor stock medications with minimum and maximum quantities to be
maintained in the Free-Standing Birthing Center;
5. A listing of medications with exact
quantities to be maintained in emergency kits;
6. Destruction of deteriorated, non-sterile,
non-labeled or damaged medications by the pharmacist;
7. Listing controlled substances to be
destroyed on the proper forms and either sending a copy of the form with the
medications to the Arkansas Department of Health by registered mail or
delivering the form and medications in person;
8. Maintenance of all drug records for a
minimum of two (2) years;
9.
Maintenance of medications brought to the Free-Standing Birthing Center by the
patient;
10. Drug
recalls;
11. Reporting of adverse
drug reactions and medication errors to the attending physician and/or CNM and
the Professional Review Committee;
12. Accountability of controlled
substances;
13. Reporting of
suspected drug loss, misuse, or diversion according to state law; and
14. Use of Automatic Medication Dispensing
Devices, if applicable.
D. Drug Storage and Security. Medications
maintained at the Birthing Center shall be properly stored and safeguarded to
ensure:
1. Locked storage of all
medications;
2. Proper lighting and
ventilation as required by manufacturer;
3. Proper temperature controls with daily
temperature documentation of medication refrigerators to assure storage between
thirty-six and forty-six (36-46) degrees Fahrenheit or two and eight (2-8)
degrees Centigrade;
4. Separate
storage of biologicals and medications from food;
5. Accessibility to licensed personnel only;
and
6. Proper use of any Automatic
Medication Dispensing Devices.
E. Controlled Substances. The following shall
be adhered to in the maintenance of controlled substances in the Free-Standing
Birthing Center:
1. Controlled drugs shall be
double-locked;
2. A record of the
procurement and disposition of each controlled substance shall be maintained in
the Free-Standing Birthing Center and readily retrievable. Each entry on the
disposition record shall reflect the actual dosage administered to the patient,
the patient's name, date, time, and signature of the licensed person
administering the medication. The signature shall consist of a first initial,
last name and title. (Licensed personnel who may legally administer controlled
substances shall include only those personnel authorized by their current
Practice Act and licensed by the Arkansas State Medical Board and Arkansas
State Nursing Board.) Any error of entry on the disposition record shall follow
a policy for correction of errors and accurate accountability. If the licensed
person who procures medication from the double-locked security is not the
licensed person who administers the medication, then both persons shall sign
the disposition record;
3. When
breakage or wastage of a controlled substance occurs, the amount given and
amount wasted shall be recorded by the licensed person who wasted the
medication and verified by the signature of a licensed person who witnessed the
wastage. Documentation shall include how the medication was wasted. In addition
to the above referenced licensed personnel, licensed pharmacists shall be
allowed to witness wastage of controlled substances. When a licensed person is
not available to witness wastage, the partial dose shall be sent to the
Arkansas Department of Health, Division of Pharmacy Services and Drug Control
for destruction;
4. There shall be
an audit each shift change of all controlled substances stocked in the
Free-Standing Birthing Center which shall be recorded by an oncoming nurse and
witnessed by an off-going nurse. Exception: If only one (1) licensed nurse is
on duty, an audit shall be conducted by that licensed nurse. When a second
licensed nurse arrives, a second audit shall be conducted by both nurses on
duty. If discrepancies are noted, the Director of Nursing and the Pharmacy
Consultant shall be notified. As with the witnessing of wastage, licensed
pharmacists shall be allowed to witness controlled substance audits;
and
5. Records generated by
Automatic Dispensing Devices shall comply with these requirements.
F. Medications.
1. All verbal or telephone orders for
medications shall be received by a licensed nurse, Certified Nurse Midwife, or
Registered Pharmacist and reduced to writing into the patient's medical record.
Verbal or telephone orders shall be countersigned by the practitioner within
twenty-four (24) hours. Signed facsimile orders are acceptable provided the
facsimile paper is of a permanent nature.
2. The Free-Standing Birthing Center may
procure medications for its patients through community pharmacists, or
medications may be procured through the Free-Standing Birthing Center's
physician or CNM's registration. Clinicians shall administer or shall order
medications to be administered to patients while in the Free-Standing Birthing
Center.
SECTION
12.
INFECTION CONTROL FOR FREE-STANDING BIRTHING
CENTERS.
A. General.
1. The facility shall develop and use a
coordinated process that effectively reduces the risk of endemic and epidemic
nosocomial infections in patients, health care workers and visitors.
2. The facility shall follow standard Centers
for Disease Control and Prevention (CDC) precautions.
3. The Administrator shall designate a
qualified individual (Registered Nurse or Laboratorian) who shall:
a. Coordinate the activities of the Infection
Control Committee;
b. Direct
surveillance activities;
c. Ensure
policies established by the committee are carried out; and
d. Gather and report data regarding the
facility-s nosocomial infections.
4. There shall be policies and procedures
establishing and defining the Infection Control program including:
a. Definition of nosocomial infections which
conforms to the current CDC definition;
b. Measures to identify infections up to
thirty (30) days postpartum, investigate and report nosocomial infections and a
system of evaluating and maintaining records of infection among both patients
and health care workers;
c. Methods
for obtaining reports of infections in patients and health care workers in a
manner and time sufficient to limit the spread of infections;
d. Measures for assessing and identifying
patients and healthcare workers at risk for nosocomial infections and
communicable diseases;
e. Measures
for prevention of infections;
f.
Provisions for education of patients and their families concerning
infections;
g. A plan for
monitoring and evaluating all aseptic and sanitation techniques employed within
the facility to ensure approved infection control procedures are
followed;
h. Techniques for:
1) Handwashing;
2) Scrub techniques;
3) Asepsis;
4) Sterilization;
5) Disinfection;
6) Housekeeping;
7) Linen care;
8) Liquid and solid waste disposal of both
infectious and regular waste. Disposal of infectious waste shall conform to the
latest edition of the Rules and Regulations Pertaining to the Management of
Medical Waste from Generators and Health Care Related Facilities;
9) Disposal of placenta;
10) Sharps and needle disposal;
11) Separation of clean from dirty process;
and
12) Other means of limiting the
spread of contagion.
i.
A requirement that disinfectants, antiseptics and germicides be used in
accordance with the manufacturer's directions;
j. Employee health;
k. Visitation Rules. All children under the
age of twelve (12) years shall be screened for communicable disease and shall
not be admitted into the facility if they are obviously ill; and
l. Guide dogs. No animals except certified
dogs for the seeing impaired will be allowed into the facility.
5. There shall be an orientation
program for all new health care workers concerning the importance of infection
control and each health care worker's responsibility in the facility's
infection control program.
6. There
shall be a plan for each employee to receive annual in-services and educational
programs as indicated based on assessment of the infection control
process.
7. The infection control
officer shall maintain a log of infectious diseases.
8. No item shall be used past the expiration
date.
9. One (1) time patient care
items shall not be reused.
10. If
sterilization facilities are present, the Association for the Advancement of
Medical Instrumentation (AAMI) standards or the Center for Disease Control
(CDC) recommended practices for sterilization in health care facilities shall
be followed.
B.
Infection Control Committee.
1. There shall be
a Professional Review Committee appointed by the Governing Body to monitor and
provide direction for the Infection Control program:
a. Administration;
b. Housekeeping;
c. Laboratory; and
d. Nursing.
2. The Governing Body shall appoint a
qualified individual to serve as chairperson of the Infection Control
Committee.
3. The Infection Control
Committee shall meet at least every two (2) months. Minutes of the meetings
shall reflect the Committee's actions in monitoring and directing the
facility's Infection Control program.
4. The Committee shall fulfill the following
responsibilities:
a. Assist in the development
of and approval of all infection control policies and procedures within the
facility;
b. Annually review and
approve all infection control policies and procedures within the
facility;
c. Direct all purchases
of equipment and/or supplies used for disinfection, decontamination, sanitation
and/or sterilization;
d. Annually
review and approve all products used throughout the facility related to
disinfection, decontamination, sanitation and/or sterilization and approve all
interim changes;
e. At each meeting
review the results of the biological spore tests on the facility's
autoclaves;
f. Monitor any
contractual services relative to infection control (e.g., waste management and
laundry) to ensure compliance with all applicable regulations; and,
g. Review any special infection control
studies conducted within the facility.
C. Employee Health.
1. There shall be policies and procedures for
screening health care workers for communicable diseases and monitoring health
care workers exposed to patients with any communicable diseases.
2. There shall be policies regarding health
care workers with infectious diseases or carrier states. The policies shall
clearly state when health care workers shall not render direct patient care.
NOTE: Health care workers employed by the facility, while
affected with any disease in a communicable stage or while a carrier of such
diseases, or while afflicted with boils, jaundice, infected wounds, diarrhea or
acute respiratory infections, shall not work in any area in any capacity in
which there is a likelihood of such person contaminating food, food contact
surfaces, supplies, or any surface with pathogenic organisms or transmitting
disease to patients, facility personnel or other individuals within the
facility.
3. There shall be
a plan for ensuring that each health care worker has measures for prevention of
communicable disease outbreaks, especially Mycobacterium tuberculosis (TB). All
plans for the prevention of transmission of TB shall conform to the most
current CDC Guidelines for Preventing the Transmission of Mycobacterium
Tuberculosis in Health Care Facilities.
4. There shall be a plan for ensuring that
all health care workers who are frequently exposed to blood and other
potentially infectious body fluids are offered immunizations for Hepatitis
B.
SECTION
13.
NUTRITION SERVICES.
A. Free-Standing Birthing Centers shall
develop policies and procedures for the provision of food and nourishments for
patient consumption. Food and nourishments may be brought to the center by
patients or their families, if allowed by facility policy.
B. If meals and nourishments are provided for
patients by the center, the following conditions shall exist:
1. Food shall come from an approved
commercial source;
2. Only
prepackaged complete meals, food items (to include condiments) or snacks shall
be served;
3. There shall be
sufficient space provided for cold and dry storage of food items. Sufficient
space shall be defined by the facility's established stock level;
4. Only disposable dishware and eating
utensils shall be permitted;
5.
There shall be designated space provided for the assembly and service of meals.
It shall contain at least the following items:
a. Refrigerator and freezer;
b. Microwave;
c. Two (2) compartment sink with
drainboard;
d. Cabinet, drawer, and
counter space;
e. Can
opener;
f. Small
utensils;
g. Self-dispensing ice
machine;
h. Trash
receptacle;
i. Handwashing
facilities or equivalent; and
j.
Non-commercial under counter dishwasher.
6. Policies and procedures shall be
established for the cleaning and maintenance of all equipment, storage and
workspace;
7. Temperatures for
refrigeration equipment shall be maintained between thirty- six to forty
(36-40) degrees Fahrenheit. A hermetically sealed indicating thermometer
accurate to plus or minus three (3) degrees Fahrenheit shall be located to
measure the air temperature in the warmest part of the storage unit.
Temperatures shall be monitored and recorded at least three (3) times daily.
Small Free-Standing Birthing Centers not providing meals or hazardous foods
shall monitor and record temperatures on each day the facility is
open;
8. Freezers containing foods
to be stored for ten (10) days or less shall maintain zero (0) degrees
Fahrenheit plus or minus ten (10) degrees Fahrenheit. Frozen foods stored for
longer than ten (10) days shall be maintained at a temperature of zero (0)
degrees Fahrenheit or below. A hermetically sealed indicating thermometer
accurate to plus or minus three (3) degrees Fahrenheit shall be located to
measure the air temperature in the warmest part of the storage unit.
Temperatures shall be monitored and recorded at least three (3) times daily.
Small Free- Standing Birthing Centers not providing meals or hazardous foods
shall monitor and record temperatures on each day the facility is
open;
9. Policies and procedures
shall be established for the storage, dating and rotation of all food items.
Policies must be in place to assure that food stored during periods the
facility is not in operation maintains proper temperatures;
10. Employee food shall be labeled and
separated from patient food in refrigerators and freezers; and
11. Signs should be visible to warn persons
with pacemakers of the presence of a microwave oven, if applicable.
SECTION 14.
PHYSICAL ENVIRONMENT FREE-STANDING BIRTHING CENTER.
A. Building and Grounds.
1. The building and equipment shall be
maintained in a state of good repair at all times.
2. Facility premises shall be kept clean,
neat and free of litter and rubbish.
3. All openings to attics and to spaces
between ceilings and roof decks shall be kept closed at all times.
4. Rooms containing gas fired equipment shall
not be used for storage except for noncombustible materials.
5. Corridors, attics, and passageways shall
be free of storage. Exits shall not be blocked by storage of furniture or
equipment at any time.
6. Emergency
wireless communication shall be provided and maintained in a state of good
repair.
7. Each Free-Standing
Birthing Center shall develop a written preventive maintenance plan. This plan
shall be available to the Department for review at any time. Such plans shall
provide for maintenance as recommended by manufacturer, applicable codes, or
designer.
8. All handwashing
facilities shall be equipped with hands-free handles, disposable soap
dispenser, paper towel dispenser and trash receptacle.
9. Vertical and horizontal transport systems
shall be operated and maintained in a manner to provide for safe
transport.
10. Hazardous cleaning
solutions, compounds, and substances shall be labeled and kept in an enclosed
storage area or approved cabinet separate from other cleaning
materials.
11. Doors located on
exit access corridors and those for entry to patient care areas shall be
labeled as to their intended use for convenience and emergency purposes. All
patient rooms shall be labeled and hazardous rooms labeled as to
classification.
12. Fire safety and
other safety systems shall be operated and maintained in a manner to protect
patients, personnel, visitors, and property from fire and the products of
combustion.
13. A supply of hot
water for patient use shall be available at all times, in accordance with CDC
guidelines. A month log shall be maintained as to presence/absence of hot
water.
14. Heating, ventilating and
air-conditioning (HVAC) systems shall be operated, and maintained in a manner
to provide a comfortable and safe environment for patients, personnel, and
visitors. In large Free-Standing Birthing Centers, an air filter change out log
shall be maintained.
15. Plumbing
systems, including equipment and systems for the supply and distribution of
potable, non-potable, and/or high purity (such as deionized and sterilized)
water, and equipment and systems for the complete and safe removal or
dispersion of storm water and waste water, shall be operated and maintained in
a manner to be adequate, safe and reliable for all required facility
operations.
16. Boiler systems and
hot water delivery systems shall be operated, and maintained in a manner to
provide a safe supply of steam and/or hot water for all required facility
operations.
17. If provided,
medical gas and vacuum systems shall be operated and maintained in accordance
with NFPA 99, Standard for Health Care Facilities, in a manner to provide an
adequate and safe supply for all required activities.
18. Exit lights shall be illuminated at all
times in accordance with NFPA 101, Life Safety Code.
19. Facilities shall have lighting levels
that are conducive to efficient work, safety, and patient comfort.
20. In large Free-Standing Birthing Centers,
the required emergency power generator shall be exercised weekly for thirty
(30) minutes and exercised under load conditions monthly for thirty (30)
minutes. An equipment log shall be maintained of all tests, malfunctions and
the immediate corrective actions. Preventive maintenance work or repairs shall
be noted.
21. Communication
systems, including telephone, nurse call, and internal/external paging shall
operate effectively and reliably at all times.
22. The electrical distribution system shall
be operated and maintained in a manner to provide safe electrical power for all
required activities.
B.
Maintenance and Engineering.
1. The physical
plant and equipment maintenance programs shall be under the direction of a
person qualified by training and/or experience and licensed where
required.
2.
Equipment
Management Program (EMP). There shall be a preventive maintenance
program designed to assure the electrically powered patient care equipment used
to monitor or diagnose performs properly and safely. This program shall be
administered by individuals qualified through training and/or experience or by
procuring a contractual maintenance agreement. The following are minimum
program elements:
a. A list of electrically
powered patient care equipment shall be maintained regardless of location or
ownership;
b. Each device, or
identical group of devices, shall have a procedure establishing minimum
criteria against which performance and safety are measured. The elements of
these procedures shall be based on NFPA 99, Standard for Health Care
Facilities, and the manufacturer's directions;
c. Each device shall be tested at intervals
of not more than six (6) months unless there is documented evidence that less
frequent testing is justified;
d.
Historical records documenting acceptable performance as established by the
procedures shall be maintained;
e.
A program to identify and repair equipment failures shall be
maintained;
f. In large
Free-Standing Birthing Centers, user or owner departments shall be notified of
the status of their equipment when it will be out of service more than
twenty-four (24) hours;
g. There
shall be operator and maintenance instructions for each device on the
electrically powered patient care equipment list; and
h. Individuals shall be trained to operate
and maintain equipment used in the performance of their duties. This training
shall be documented.
3.
Utilities Management Program (UMP). There shall be a
preventive maintenance program designed to assure that the physical plant
equipment and building systems perform properly and safely. This program shall
be administered by individuals qualified through training and/or experience or
by procuring a contractual agreement. This program shall consist of at least
the following minimum elements:
a. A list of
physical plant equipment and building systems shall be maintained regardless of
location or ownership;
b. Equipment
and building system shall have a procedure establishing minimum criteria
against which performance and safety are measured. The elements of these
procedures shall be based on NFPA 99, Standard for Health Care Facilities, and
the manufacturer's directions and the experience of the repair technician or
operator;
c. Equipment and building
system, shall be tested, serviced, or inspected at intervals of not more than
twelve (12) months unless there is documented evidence that less frequent
service is justified;
d. Historical
records documenting acceptable performance as established by the procedures
shall be maintained;
e. A program
to identify and repair equipment failures shall be maintained;
f. In large Free-Standing Birthing Centers,
user or owner departments shall be notified of the status of their equipment or
system when it will be out of service for more than twenty-four (24)
hours;
g. There shall be operator
and/or maintenance instructions for each piece of equipment or building system
on the list; and
h. Individuals
shall be trained to operate and maintain physical plant equipment and/or
building systems. This training shall be documented.
4.
Life Safety Management
Program. There shall be a preventive maintenance program designed
to assure that all circuits of fire alarm and detection systems are tested on a
quarterly basis and all components receive annual preventive maintenance.
Analog detection devices that provide automatic self testing are exempt from
the quarterly testing requirement. This program shall be administered by
individuals qualified through training and/or experience or by procuring a
contractual maintenance agreement. This program shall consist of the following
minimum elements:
a. A list of all fire
protection equipment or component groups shall be maintained;
b. Each piece of equipment and/or component
groups, shall have a procedure establishing minimum criteria against which
performance and safety are measured. The elements of these procedures shall be
based on the NFPA 72, National Fire Alarm Code, the manufacturer's
recommendations and the experience of the repair technician or
operator;
c. Fans or dampers in air
handling and smoke management systems shall be reliable and functional at all
times;
d. Automatic fire
extinguishing systems shall be inspected and tested annually in accordance with
NFPA 13, Standard for the Installation of Sprinkler Systems, and NFPA 96,
Standard for Ventilation Control and Fire Protection of Commercial Cooking
Operations. Actual discharge of the fire extinguishing system shall not be
required. Records documenting acceptable performance as established by the
procedures shall be maintained;
e.
A program to identify and repair equipment and/or component group failures
shall be maintained;
f. Systems for
transmitting fire alarms to the local fire department shall be reliable and
functional at all times;
g. There
shall be operator and maintenance instructions for each piece of equipment
and/or component group on the list;
h. Individuals shall be trained to operate
and maintain all equipment and/or component group on the list; and
i. Portable fire extinguishers shall be
clearly identified. (Refer to Section 14, Safety Services.)
5.
Emergency
Procedures Program (EPP). There shall be written emergency
procedures or a disaster management plan for utility system disruptions or
failures which address the specific and concise procedures to follow in the
event of a utility system malfunction or failure of the water supply, hot water
system, medical gas system, sewer system, bulk waste disposal system, natural
gas system, commercial power system, communication system and boiler or steam
delivery system. These procedures shall contain but are not limited to the
following information:
a. A method of
obtaining alternative sources of essential utilities;
b. A method of shutoff and location of valves
for malfunctioning systems;
c. A
method of notification of facility staff in affected areas; and
d. A method of obtaining repair
services.
6. There shall
be sufficient supervisory and support personnel to provide maintenance services
in relation to the size and complexity of the facility and the services that
are provided.
7. In large
Free-Standing Birthing Centers, a liaison with the QI, Infection Control and
Safety Committees shall be maintained.
C. Environmental Services.
1. The environmental services shall be under
the direction of a person qualified by training and/or experience and licensed
where required.
2. In large
Free-Standing Birthing Centers, a designee from this department shall be a
member of the Infection Control Committee.
3. Dry, or untreated dusting, sweeping, or
mopping, except vacuum type cleaning shall be prohibited within the
facility.
D. Laundry
Services.
1. Laundry may be done on- or
off-site. If onsite, an area for laundry equipment with counter and storage
space shelving shall be provided. Depending on size and occupancy of center,
ordinary household laundry equipment may be provided. (Soiled laundry shall be
held in the soiled holding area until deposited in the washer.)
2. Hot water supplied to laundry areas shall
be a minimum of 110 Fahrenheit. Chlorine bleach and other laundry chemicals
shall be used at effective concentrations that disinfect for the laundry size,
cycle time and water temperature, as recommended by the chemical
manufacturer(s).
3. Clean laundry
shall be mechanically dried only.
4. Separate containers for the disposal of
infectious waste and sharps shall be located in the soiled linen
area.
E. Safety
Services.
1. There shall be an effective
program to enhance safety within the facility and grounds. In large
Free-Standing Birthing Centers, the program shall be established and monitored
by a Safety Committee appointed by the Administrator. Committee members shall
be selected from Administration, Nursing, Maintenance, Housekeeping, the
Medical Staff and others as appropriate.
2. In large Free-Standing Birthing Centers,
the Safety Committee shall meet a minimum of once every three (3) months to
fulfill safety objectives. Minutes of each meeting shall be recorded and kept
in the facility.
3. The
Administrator shall designate a specific individual to carry out policies
established by the safety program.
4. The orientation program for the facility
personnel shall include the importance of general safety, fire safety and the
responsibility of each individual to the program.
5. The Safety Committee of large
Free-Standing Birthing Centers and designated individual of small Free-Standing
Birthing Centers shall have the following functions:
a. Investigation and evaluation of each
accident, injury or safety hazard report;
b. Provision for safety-related information
to use in orientation and education programs;
c. Monitoring the results of the safety
program and analyzing the effectiveness of the program annually;
d. Conducting fire drills and disaster drills
at required intervals;
e. Reporting
conclusions, recommendations, and actions of Committee at least quarterly to
Administration; and
f. Ensuring
each department or service shall have a safety policy and procedure manual
within their own area that is a part of the overall facility safety manual and
establishes safety policies and procedures specific to each area.
6. Fire extinguishers shall be
provided in adequate numbers, of the correct type, and shall be properly
located and installed in accordance with NFPA 10, Standard for Portable Fire
Extinguishers. Personnel shall be trained in the proper use of fire
extinguishers and equipment. Personnel shall follow procedures in fire
containment and evacuating patients in case of fire or explosion. There shall
be an annual check of all fire extinguishers by qualified persons in accordance
with NFPA 10, Standard for Portable Fire Extinguishers. The date the check was
made and the initials of the inspector shall be recorded on the fire
extinguisher or on a tag attached to the extinguisher.
7. A plan shall be available for the
protection of patients, visitors, and employees for evacuation in the event of
an emergency. Any fire or disaster event at the facility shall be reported
immediately to the Arkansas Department of Health by telephone 661-2201 during
regular working hours or to 1-800-554 -5738 or 661- 2136 after normal working
hours, holidays and weekends.
8.
There shall be policies and procedures to address usage of tobacco. "No
Smoking" signs or international symbol for no smoking shall be posted in any
room or compartment where flammable liquids, combustible gases, or oxygen is
used or stored, and in any other hazardous locations.
9. There shall be rules and regulations
governing the routine methods of handling and storing flammable and explosive
agents.
10. There shall be keys
available to assure prompt access to all locked areas. All doors shall be
devised so they can be opened from the inside of the locked area. Special door
locking devices are acceptable in limited areas. Usage is subject to all codes
and regulations.
11. All required
exit doors shall remain unlocked in accordance with NFPA 101, Life Safety
Code.
12. A list of Material Safety
Data Sheets (MSDS) for solutions, cleaning compounds, disinfectants, vermin
control chemicals, and other potentially hazardous substances used in
connection with the facility shall be readily available onsite.
SECTION 15.
PHYSICAL FACILITIES, FREE-STANDING BIRTHING CENTERS.
A. Definitions.
1. Accessible - having access to but which
first may require the removal of a panel, door or similar covering of the item
described.
2. Addition - an
extension or increase in floor area, height of a building, or
structure.
3. Alter or Alteration -
any change(s) or modification in construction or occupancy or the installation
or the assembly of any new structural components, or any change(s) to the
existing structural component, in a system, building, and structure.
4. And/Or (in a choice of two (2) code
provisions) - signifies that use of both provisions shall satisfy the code
requirements and use of either provision is acceptable, also. The most
restrictive provision shall govern. Where there is a conflict between a general
requirement and a specific requirement the specific or restrictive requirement
shall be applicable.
5. Architect -
a duly registered architect and licensed by the State of Arkansas.
6. Corridor - a passage way into which
compartments or rooms open and which is enclosed by partitions and/or walls and
a ceiling, or a floor/roof deck above.
7. Dead end - a hallway, corridor or space
open to a corridor so arranged that it can be entered, from an exit access
corridor without passage through a door, but does not lead to an
exit.
8. Engineer - a duly
registered engineer and licensed by the State of Arkansas.
9. Licensing agency - Arkansas Department of
Health, Division of Health Facility Services or current name.
10. Listed - equipment or materials included
in a list published by a nationally recognized testing laboratory, inspection
agency or other organization concerned with products evaluation that maintains
periodic inspection of production of listed equipment or materials, and whose
listing states either that the equipment or materials meets nationally
recognized standards or has been tested and found suitable for use in a
specific manner.
11. Narrative
program - the narrative program describes the functional and utilizational
information related to fulfillment of the Free-Standing Birthing Center's
objectives. The description reflects those services necessary for complete
operation of the facility. Some common elements which shall be included address
policies and procedures; intent or purpose; space requirements; staff patterns,
quantities, and credentials.
12.
New construction - these rules establish health, safety and welfare
requirements for the design of all new Free-Standing Birthing Centers and
related institutions. Where new work is done within the state, all portions of
the work shall comply with applicable sections of these rules.
13. Partition - an interior wall, other than
folding or portable, that subdivides spaces within any story, attic or basement
of a building.
14. Patient care
area - any portion of a Free-Standing Birthing Center wherein patients are
intended to be examined or treated.
15. Plenum - an air compartment or chamber to
which one (1) or more ducts are connected and which forms part of air
distribution system.
16. Readily
assessable - having direct access without the need of removing any panel, door
or similar covering of the item described, and without requiring the use of
portable ladders, chairs, etc.
17.
Renovation - construction performed within an existing facility.
18. Repair - the reconstruction or renewal of
any part of an existing building for the purpose of maintenance.
19. Room - a separate, enclosed space, with
doorway(s), for one (1) named function.
20. Through Penetration Protection - a system
installed to resist, for a prescribed time period, the passage of flame, heat,
and hot gases through openings which penetrate an entire fire resistant
assembly in order to accommodate cables, cable trays, conduits, tubing, pipes,
ductwork or similar terms.
21.
Toilet - A room designated exclusively for a water closet, lavatory, and tub or
shower.
B. General
Considerations.
1. The requirements set forth
herein have been established by the Department and constitute minimum
requirements for new construction, new addition(s), and/or major renovations in
facilities requiring licensure under these rules. These requirements are
considered necessary to ensure properly planned and well constructed
Free-Standing Birthing Centers which can be efficiently maintained and operated
to furnish adequate services. In many instances, these minimum requirements
shall need to be exceeded for the facility to function as programmed.
2. Facilities shall be accessible to the
public, staff, and patients with physical disabilities. Minimum barrier free
requirements shall be those set forth by the Arkansas State Building Services,
Minimum Standards and Criteria - Accessibility for the Physically Disabled
Standards.
3. Projects involving
renovation, and additions to existing facilities shall be programmed and phased
to minimize disruption of the existing functions. Access, exits and fire
protection shall be maintained for the occupant's and the facility's
safety.
4. Codes and Standards.
Nothing stated herein shall relieve the owner from compliance with building
codes, ordinances, and regulations which are enforced by city, county, or other
State jurisdictions. Where such codes, ordinances, and regulations are not in
effect, the owner shall consult the state building codes for all components of
the building type which are not specifically covered by these minimum
requirements. In location where there is a history of tornadoes, floods,
earthquakes or other regional disasters, planning and design shall consider the
need to protect the occupants and the facility.
5. No new mechanical, electrical, plumbing,
fire protection, or medical gases system shall be installed, nor any such
existing system materially altered or extended, until complete plans and
specifications for installation, alteration, or extensions have been submitted
to the licensing agency for review and approval.
C. Plan Review. The following list
illustrates the process flow which shall be used for all new construction,
remodeling, and/or alterations and shall include:
1. Narrative program;
2. Site location;
3. Preliminary drawings;
4. Submission of plan review fee;
5. Final construction documents;
6. Letter of approval for construction
documents;
7. Site observations
during construction; and
8. Final
site observation.
D.
Narrative Program.
1. The facility shall
supply for each project (whether new construction, addition, modernization, and
renovation) a narrative program that describes the purpose of the project, the
projected demand or utilization, staffing patterns, departmental relationships,
space requirements, and other basic information relating to the fulfillment of
the institution's objectives.
2.
The facility's narrative program and/or construction documents shall be
approved by all applicable Departments prior to starting
construction.
E. Site
Location.
1. Location.
a. The site of any Birthing Center shall be
easily accessible to the community and to service vehicles such as fire
protection apparatus.
b. Facilities
shall be located with due regard to the accessibility by public transportation
for patients, staff, and visitors, and availability of competent medical and
surgical consultation.
c. The
facility shall have security measures for patients, personnel, and the public
consistent with the conditions and risks inherent in the location of the
facility.
d. The facility shall be
located to provide reliable utilities (water, natural gas, sewer and
electricity). The water supply shall have the capacity to provide normal usage
plus firefighting requirements. The electricity shall be of stable voltage and
frequency.
e. The site shall afford
good drainage and shall not be subject to flooding, located near insect
breeding areas, noise, or other nuisance producing locations.
2. Roads and Parking.
a. Paved roads and walks shall be provided
within the lot lines to provide access to the main entrance and service
entrance, including loading and unloading areas for delivery trucks.
b. Each facility shall have parking spaces to
satisfy the minimum needs of patients, employees, staff, and visitors. Space
shall be provided for emergency and delivery vehicles.
3. Subsoil Investigation. Subsoil
investigation shall be made to determine the subsurface soil and water
conditions. The investigation shall include a sufficient number of test pits or
test borings to determine, in the judgment of the architect and the structural
engineer, the true subsurface conditions. Results of the investigation shall be
available in the form of a soil investigation report or a foundation
engineering report. The investigation shall be made in close cooperation with
the architect and structural engineer and shall contain detailed
recommendations for foundation design and gradings. The following is a general
outline of the suggested scope of soil investigation:
a. The borings or test pits shall extend into
stable soils well below the bottom of any proposed foundations. A field log of
the borings shall be made and the thickness, consistency, and character of each
layer recorded;
b. The amount and
elevation of groundwater encountered in each pit or boring and its probable
variation with the seasons and effect on the subsoil shall be determined. High
or low water levels of nearby bodies of water affecting the ground level shall
also be determined;
c. Laboratory
tests shall be performed to determine the safe bearing value and
compressibility characteristics of the various strata encountered in each pit
or boring;
d. Maximum depth of
frost penetration below surface of the ground shall be recorded; and
e. Tests shall be made to determine whether
the soil contains alkali in sufficient quantities to affect concrete
foundations.
4.
Approval. The new building site shall be observed and approved by the
Department before construction begins.
F. Preliminary Drawings. Schematic drawings
shall be submitted to the Department for the proposed facility. Schematic
drawings shall illustrate a basic understanding of the architectural,
mechanical, electrical and plumbing systems. The drawings shall include
schematic plans, building sections, exterior elevations (all sides),
preliminary finish schedule, and general notes. Code criteria shall be
submitted that is specific to the proposed facility and exhibits a knowledge of
the building and fire code requirements including but not limited to
construction type, fire protection ratings, means of egress and smoke
compartmentalization. Drawings shall be at a scale to clearly represent the
intent. A graphic and/or written scale and directional arrow shall be on each
drawing.
G. Submission of Plan
Review Fee. A plan review fee in the amount of one (1) percent of the total
cost of construction or five hundred dollars ($500.00), whichever is less,
shall be paid for the review of drawings and specifications (contract
documents). The plan review fee check shall be made payable to the Division of
Accounting, Arkansas Department of Health. A cost estimate shall accompany the
drawings and specifications unless the maximum fee of five-hundred dollars
($500.00) is submitted. The Division of Health Facility Services (DHFS) will
coordinate the review of drawings and specifications for all Arkansas
Department of Health offices.
H.
Final Construction Documents.
1. Requirements
for drawings and specifications shall be prepared by an architect and/or
engineer licensed by the State of Arkansas. The Architect and/or Engineer shall
prepare and submit construction documents with the respective seals for each
professional discipline. Architectural construction documents shall be prepared
by an Architect and engineering (mechanical, electrical, civil and structural)
construction documents shall be prepared by an (mechanical, electrical, civil
and structural) Engineer.
2.
Working drawings and specifications shall be prepared in a manner that clearly
defines the scope of the work and is consistent with the professional standard
of practice for architects and engineers. Working drawings and specifications
shall be complete for contract purposes. Working drawings and specifications
for each of the following disciplines of work: civil, architectural, life
safety and fire protection, structural, mechanical, and electrical may include,
but are not limited to, the following:
a.
Civil.
1) Site survey including a legal
description of the property.
2)
Site plans including demolition, grading, utility and building/dimension
types.
3) Sections, details,
schedules, notes and legends for site plans.
b. Architectural.
1) Plans including demolition, reference,
dimension, life safety, reflected ceiling, enlarged, millwork, equipment and
furnishing types.
2) Sections
including building, partition and detail types.
3) Elevations including interior and exterior
types.
4) Details including plan
and section types.
5) Schedules
including drawing sheets finish, door and window types.
6) Notes including general and specific as
required to clearly define the scope of work.
7) Legends including abbreviation and symbol
types.
c. Life Safety
and Fire Protection.
1) Limits of each smoke
compartment.
2) Location of each
smoke barrier wall.
3) Dimensions
and gross areas of each smoke compartment.
4) Location of each fire rated wall or
partition, fire separation wall and horizontal exit.
5) Location of each exit sign, fire pull
station, and extinguisher cabinet and extinguisher.
6) Travel distance(s) from the most remote
location(s) in the building to an exit as defined by NFPA 101 (i.e., horizontal
exit, exit passageway, enclosed exit stair, exterior exit door).
d. Structural.
1) Plans including demolition, foundation,
floor framing, roof framing, reference and dimension types.
2) Sections including partial building and
detail types.
3) Details including
plan and section types.
4)
Schedules including pier, footing, beam, girder, column and reinforcing
types.
5) Notes including general
and specific as required to clearly define the scope of the work.
6) Legends including abbreviation and symbol
types.
e. Mechanical.
1) Heating, piping, and air-conditioning
systems:
a) Steam heated equipment, such as
sterilizers, warmers, and steam tables;
b) Heating and steam mains and branches with
pipe sizes;
c) Diagram of heating
and steam risers with pipe sizes;
d) Sizes, types, and heating surfaces of
boilers and oil burners, if any;
e)
Pumps, tanks, boiler breeching and piping, and boiler room
accessories;
f) Air-conditioning
systems with required equipment, water refrigerant piping, and ductwork showing
required fire smoke/dampers;
g)
Exhaust, return, and supply ventilating systems with piping and required
fire/smoke dampers;
h) Air
quantities for all room supply, return, and exhaust ventilating duct
openings;
i) A ventilation schedule
specifying the following information: room number, room name, room volume
(ft3), required room air changes, required outside air changes, required air
movement relative to adjacent area, required air filtration (% efficiency),
required room total supply air quantity (cubic feet per minute (CFM), required
outside air quantity (CFM), required room exhaust air quantity (CFM), design
room total supply air quantity (CFM), design room return air quantity (CFM),
design outside air quantity (CFM), design room exhaust air quantity (CFM),
design room air filtration (% efficiency), room design summer (F) dry bulb/wet
bulb (DB/WB), room design winter ( F) DB/WB, outside air design summer ( F)
DB/WB, and outside air design winter (F) DB/WB; and
j) Air filter design pressure drop both clean
and dirty.
2) Plumbing,
drainage, and standpipe systems:
a) Size and
elevation of street sewer, house sewer, house drains, and street water
main;
b) Locations and size of
soil, waste, and vent stacks with connections to house drains, clean outs,
fixtures and equipment;
c) Size and
location of hot and cold circulating mains, branches, and risers from the
service entrance and tanks;
d)
Riser diagram to show all plumbing stacks with vents, water risers, and fixture
connections;
e) Gas, oxygen, and
special connections;
f) Standpipe
and sprinkler systems; and
g)
Plumbing fixtures and equipment which require water and drain
connections.
3)
Elevators and dumbwaiters: Details and dimensions of shaft, pit and machine
room, sizes of car platform and doors.
4) Kitchens, laundry, refrigeration, and
laboratories detailed at a satisfactory scale (1/4 inch scale) to show the
location, size, and connection of all fixed and moveable equipment.
f. Electrical.
1) All electrical wiring, outlets, smoke
detectors, and equipment which require electrical connections.
2) Electrical service entrance with switches,
and feeders to the public service feeders, characteristics of the light and
power current and transformers and their connections, if located in the
building.
3) Plan and diagram
showing main switchboard power panels, light panels and equipment. Diagram of
feeder and conduit sizes with a schedule of feeder breakers or
switches.
4) Light outlets,
receptacles, switches, power outlets, and circuits.
5) Telephone layout showing service entrance,
telephone switchboard, terminal boxes, and telephone outlets.
6) Nurses' call system with outlets for beds,
duty stations, door signal lights, annunciators, and wiring diagrams.
7) Staff paging and doctors in-and-out
registry system with all equipment wiring, if provided.
8) Fire alarm system with stations, signal
devices, control board, and wiring diagrams.
9) Emergency electrical system with outlets,
transfer switch, source of supply, feeders, and circuits.
10) Medical gas alarm system.
11) All other electrically operated systems
and equipment.
g.
Specifications.
1) Specifications shall
supplement the drawings to fully describe types, sizes, capacities,
workmanship, finishes, and other characteristics of all materials and equipment
and shall include the following:
a) Cover or
title sheet with architect and/or engineer seal;
b) Index;
c) General conditions;
d) General requirements; and
e) Sections describing material and
workmanship in detail for each class of work.
h. All construction documents and
specifications shall be approved by the Department prior to the beginning of
construction and a letter shall be issued from the licensing agency granting
approval to commence with construction. The Department shall have a minimum of
six (6) weeks to review construction documents and specifications. The Division
of Health Facility Services shall coordinate the plan review with other
Divisions in the Department.
I. Site Observation During Construction. The
new building site shall be observed and approved by the Department before
construction begins. The construction of the new building and/or addition shall
be observed during the construction phases and before occupying the building
and/or addition.
1. This Department is to be
notified when construction begins and a construction schedule shall be
submitted to determine inspection dates.
2. Representatives from the Department shall
have access to the construction premises and the construction project for
purposes of making whatever observations deemed necessary throughout the course
of construction.
3. Periodic
observations of construction shall be provided and documented by each design
professional to assure construction is in compliance with the contract
documents. The number and interval of periodic observations shall be approved
by DHFS prior to beginning construction. Documentation of each periodic
observation shall be submitted to DHFS.
4. Any deviation from the accepted
construction documents shall not be permitted during construction, until the
written request for change(s) in the construction is approved by this
Department.
J. Final Site
Observation.
1. Upon completion of
construction and prior to the approval by the Department to occupy and use the
facility, the owner shall be furnished a minimum of one (1) complete set of
reproducible drawings and specifications, and one (1) complete legible set of
as built drawings and specifications showing all construction, fixed equipment,
and mechanical and electrical systems as installed and built. The Department
shall also be provided one (1) complete set of as built drawings and
specifications. In addition, the owner shall be furnished a complete set of
installation, operation, and maintenance manuals and parts lists for the
installed equipment at the time as built prints are provided.
2. No facility shall occupy any new structure
or major addition or renovation space until the appropriate approval has been
received from the local building and fire authorities and licensing
agency.
K. List of
Referenced Publications. Codes and standards which have been referenced in
whole or in part in the various sections of this document are listed below. The
most current codes and standards adopted at the time of this publication are
used. Later issues will normally be acceptable where requirements for function
and safety are not reduced; however, editions of different dates may have
portions renumbered or retitled. Care shall be taken to ensure that appropriate
sections are used. Names and addresses of originators are also included for
information.
1. American National Standards
Institute (ANSI) Standard A17.1, "American National Standard Safety Code for
Elevators, Dumbwaiters, Escalators and Moving Stairs."
2. American Society of Civil Engineers,
(ASCE), "Minimum Design Loads for Buildings and Other Structures."
3. American Society of Heating, Refrigerating
and Air Conditioning Engineers (ASHRAE), "Handbook of Fundamentals" and
"Handbook of Applications."
4.
American Society of Heating, Refrigerating and Air Conditioning Engineers
(ASHRAE), Standard 52, "Method of Testing Air Cleaning Devices Used in General
Ventilation for Removing Particulate Matter."
5. Arkansas State Building Services, Minimum
Standards and Criteria - Accessibility for the Physically Disabled
Standards.
6. Arkansas Fire
Prevention Code, Volume I - Fire Prevention (Standard Fire Prevention Code with
Arkansas Amendments) and Volume II - Building Construction (Standard Building
Code with Arkansas Amendments).
7.
Arkansas State Mechanical Code, Arkansas Department of Health.
8. Arkansas State Plumbing Code, Arkansas
Department of Health.
9. DOP
Penetration Test Method, MIL STD No. 282, "Filter Units, Protective Clothing,
Gas Mask Components and Related Products: Performance Test Methods."
10. Illuminating Engineering Society of North
America, IESNA Publication CP29, "Lighting for Health Care
Facilities."
11. Laws, Rules, and
Regulations Governing Boiler Inspection, Arkansas Department of
Labor.
12. National Council on
Radiation Protection (NCRP), Report No. 33,"Medical X- ray and Gamma Ray
Protection for Energies Up to 10 MeV Equipment Design and Use, 1986."
13. National Council on Radiation Protection
(NCRP), Report No. 49,"Medical X- ray and Gamma Ray Protection for Energies up
to 10 MeV Structural Shielding Design and Evaluation, 1976."
14. National Council on Radiation Protection
(NCRP), Radiation Protection Design Guidelines for 0.1pi29100, MeV Particle
Accelerator Facilities.
15.
National Fire Codes - 1998.
16.
Rules Pertaining to the Management of Regulated Waste from Health Care Related
Facilities, Arkansas Department of Health.
17. Rules Pertaining to Swimming Pools and
Other Related Facilities - Arkansas Department of Health.
L. Availability of Codes and Standards. The
codes and standards referenced in various Sections throughout this document can
be ordered, if they are Government publications, from the Superintendent of
Documents, U.S. Government Printing Office (GPO), Washington, DC 20402. Copies
of non-government publications can be obtained at the addresses listed below.
1. Air Conditioning and Refrigeration
Institute, 1501 Wilson Boulevard, Arlington, VA 22209.
2. American National Standards Institute,
1430 Broadway, New York, NY 10018.
3. American Society of Civil Engineers, 345
East 47th Street, New York, NY 10017.
4. American Society for Testing and
Materials, 1916 Race Street, Philadelphia, PA 19103.
5. American Society of Heating,
Refrigerating, and Air Conditioning, 1741 Tullie Circle, NE, Atlanta GA
30329.
6. Arkansas State Building
Services, 1515 West 7th Street, Suite 700, Little Rock, AR 72201.
7. Arkansas Department of Labor, 10421 West
Markham, Little Rock, AR 72205.
8.
Illuminating Engineering Society of North America (IESNA), 120Wall Street, 17th
Floor, New York, NY 10005.
9.
National Council on Radiation Protection and Measurement, 7910 Woodmont Avenue,
Suite 1016, Bethesda, MD 20814.
10.
National Fire Protection Association, 1 Batterymarch Park, Post Office Box
9101, Quincy, MA 02269-9101.
11.
National Technical Information System (NTIS), 5285 Port Royal Road,
Springfield, VA 22161.
12. Defense
Printing Service, 700 Robbins Avenue, Building 4D, Philadelphia, PA 19111 (for
DOP Penetration Test Method).
13.
Southern Building Code Congress International, Inc., 900 Montclair Road,
Birmingham, AL 35213.
14.
Underwriters' Laboratories, Inc. 333 Princeton Road, Northbrook, IL
60062.
SECTION
16.
CLINICAL FACILITIES, FREE-STANDING BIRTHING
CENTERS.
The extent (number and types) of the administrative, clinical
and diagnostic facilities to be provided shall be determined by the services
contemplated and the estimated patient load as described in the approved
narrative program. The planning of Free-Standing Birthing Center shall provide
for the privacy and dignity of the patient during interview, examination, and
treatment.
A. General. Each element
provided in the Free-Standing Birthing Center shall meet the requirements
outlined herein as a minimum, with the understanding that the elements shall be
expanded where needed.
B. Birthing
Room(s). Birthing rooms shall be adjacent to a toilet room and shall have
storage space sufficient to accommodate the belongings of occupants, bedding,
equipment, and supplies. In addition, the following shall be provided:
1. Birthing rooms shall be adequate in size
to accommodate one (1) patient, her family, and attending staff. Each birthing
room shall have a minimum floor area of one hundred sixty (160) square feet,
excluding vestibule toilets;
2. An
area for equipment and supplies for routine and remedial newborn care, separate
from the equipment supplies for maternal care, shall be provided in each
birthing room in built-in cabinets, closets, or furniture;
3. Medications, syringes, specimen
containers, and instrument packs shall be contained in storage areas not
accessible to children; and
4. The
plan for the birthing room shall be such that it will permit the need for
emergency transfer by stretcher unimpeded.
C. Nurses' Station(s). Facilities for
charting, clinical records, work counter, communication system, space for
supplies and convenient access to handwashing facilities shall be
provided.
D. Medication
Distribution. This may be a medication preparation room or unit, a self-
contained medication dispensing unit, or another approved system. A medication
dispensing unit may be located at the nursing station, in the clean workroom,
or in an alcove or other space under direct control of the nursing or pharmacy
staff.
E. Clean Workroom or Clean
Holding Room. The clean workroom shall contain a work counter and handwashing
and storage facilities. A clean holding room shall be part of a system for
storage and distribution of clean supply materials and shall be similar to
clean workroom except that the work counter and handwashing facilities may be
omitted.
F. Soiled Workroom or
Soiled Holding Room. The soiled workroom shall contain a clinical sink or
equivalent flushing rim fixture, sink equipped for handwashing, work counter,
waste receptacle. A soiled holding room shall be part of a system for
collection and disposal of soiled materials and shall be similar to the soiled
workroom except that the clinical sink and the work counter may be
omitted.
G. If a stretcher is
provided, stretcher storage space shall be out of the direct line of
traffic.
SECTION 17.
PHYSICAL FACILITIES, DETAILS AND FINISHES.
A. Details.
1. Small Free-Standing Birthing Centers shall
meet minimum construction requirements as described by NFPA 101, Life Safety
Code, Chapter 26 with the exceptions noted herein.
2. Renovation in small Free-Standing Birthing
Centers shall meet minimum construction requirements as described by NFPA 101,
Life Safety Code, Chapter 27 with the exceptions noted herein.
3. Large Free-Standing Birthing Centers shall
meet minimum construction requirements as described by NFPA 101, Life Safety
Code, Chapter 12, Section 6 with the exceptions noted herein.
4. Renovation in large Free-Standing Birthing
Centers shall meet minimum construction requirements as described by NFPA 101,
Life Safety Code, Chapter 13, Section 6 with the exceptions noted
herein.
5. Renovations, including
new additions, shall not diminish the level of safety that existed prior to the
start of the work; however, safety in excess of that required for new
facilities is not required.
6. In
large Free-Standing Birthing Centers, the minimum corridor width shall be six
(6) feet. Work corridors less than six (6) feet long may be four (4) feet wide.
In small FreeStanding Birthing Centers, the minimum corridor width shall be
forty-four (44) inches.
7. Items
such as drinking fountains, fold-down writing surfaces, telephone booths,
vending machines, etc., shall not restrict corridor traffic or reduce the
corridor width below the required minimum.
8. The minimum door width for patient use
shall be two (2) feet ten (10) inches. If the facility services patients
transported in beds, the minimum door width shall be three (3) feet eight (8)
inches.
9. Rooms containing
bathtubs, sitz baths, showers, and water closets, subject to occupancy by
patients, shall be equipped with doors and hardware which shall permit access
from the outside in any emergency. When such rooms have only one (1) opening or
are small, the doors shall be capable of opening outwards or be otherwise
designed to be opened without need to push against a patient who may have
collapsed within the room.
10.
Doors, sidelights, borrowed lights, and windows located within eighteen (18)
inches of the floor shall be glazed with safety glass, wire glass, or plastic
glazing material that shall resist breaking and shall not create dangerous
cutting edges when broken. Safety glass or plastic glazing materials shall be
used for shower doors and bath enclosures.
11. Thresholds and expansion joint covers
shall be flush with the floor surface to facilitate use of wheelchairs and
carts.
12. Location and arrangement
of handwashing facilities shall permit proper use and operation.
13. Lavatories and handwashing facilities
shall be securely anchored to withstand an applied downward vertical load of
not less than two hundred fifty (250) pounds on the front of the
fixture.
14. Ceiling heights shall
be as follows:
a. Boiler rooms shall have
ceiling clearances not less than two (2) feet six (6) inches above the main
boiler heater and connecting piping;
b. Rooms containing ceiling-mounted equipment
or ceiling-mounted surgical light fixtures shall have height required to
accommodate the equipment or fixtures, with a minimum height of nine (9) feet
in new construction; and
c. All
other rooms shall not have less than seven (7) feet eight (8) inches. Suspended
tracks, rails, and pipes located in the path of normal traffic shall be not
less than seven (7) feet above the floor and clearances in other areas may be
six (6) feet eight (8) inches above the floor.
15. Rooms containing heat-producing equipment
(such as boiler or heater rooms and laundries) shall be insulated and
ventilated to prevent any adjacent partition surface from exceeding a
temperature of ten degrees (10) Fahrenheit above ambient room
temperature.
16. Approved fire
extinguishers shall be provided in locations throughout the building in
accordance with NFPA Standard No. 10. Extinguishers located in exit corridors
shall be recessed.
17. Rooms for
patient medical records and archived patient medical records that remain on
site shall be kept in a one (1) hour fire rated enclosure and protected by a
smoke detection system. Circulating records at nurse's station or in active
working areas are excluded from this requirement. Offsite buildings or
freestanding buildings used for storage of archived patient medical records
shall be built of noncombustible materials and provide security and smoke
detection systems. Both onsite and offsite records shall be arranged in an
accessible manner and stored at least six (6) inches above the floor and
protected against undue destruction from dust, vermin, water, etc.
18. Fluorescent light fixtures shall be
provided with protective covers if used in food preparation and serving areas
and patient care and treatment spaces.
19. No operable fireplace shall be permitted
in the facility. Inoperable fireplace(s) shall be sealed at the upper and lower
portions of the flue.
B.
Finishes.
1. Cubicle curtains and draperies
shall be noncombustible or flame retardant and shall pass both the large and
small scale tests of NFPA Standard 701.
2. Interior wall, ceiling and floor finish
classifications shall be in accordance with NFPA 101, 26-3.3.
3. Floor materials shall be easily cleanable
and appropriately wear resistant. Floors in areas used for food preparation or
food assembly shall be water resistant and grease-proof. Joints in tile and
similar material in such areas shall be resistant to food acids. In all areas
frequently subject to wet cleaning methods, floor-materials shall not be
physically affected by germicidal and cleaning solutions. Floors that are
subject to traffic while wet (such as shower and bath areas) shall have a
non-slip surface.
4. Floors and
wall bases in birthing rooms shall be coved with the floor, tightly sealed
within the wall, and constructed without voids.
5. Wall finishes shall be washable and, in
the vicinity of plumbing fixtures, shall be smooth and water
resistant.
6. Floors and walls
penetrated by pipes, ducts, and conduits shall be tightly sealed to minimize
entry of rodents and insects.
7.
Ceilings in birthing rooms and soiled/clean utility rooms shall be washable,
waterproof, lay-in vinyl coated gypsum board, gypsum board, plaster or
equivalent.
8. Ceilings shall have
access panels a minimum of two (2) feet by two (2) feet provided where
mechanical or electrical maintenance or repair to the facilities above the
ceiling shall include, but not be limited to, cut-off valves, air filters,
clean out plugs, etc.
SECTION 18.
PHYSICAL FACILITIES,
MECHANICAL REQUIREMENTS.
A. General.
1. Prior to completion and acceptance of the
facility, all mechanical systems shall be tested, balanced, and operated to
demonstrate to the owner or his representative that the installation and
performance of these systems conform to the requirements of the plans and
specifications. The test and balance report shall be based on ASHRAE Systems
Guide Standards, and a copy of the final report shall be on file at the
facility.
2. Upon completion of the
contract, the owner shall be furnished with a complete set of manufacturers'
operating, maintenance instructions, and parts list with numbers and
description of each piece of equipment. He shall also be provided with
instructions in the operational use of systems and equipment as
required.
B. Thermal and
Acoustical Insulation.
1. Insulation shall be
provided for the following within the building:
a. Boilers, smoke breeching, and
stacks;
b. Steam supply and
condensate return piping;
c. Hot
water piping above 110 F and all hot water heaters, generators, and
convertors;
d. Chilled water,
refrigerant, and other process piping and equipment operating with fluid
temperature below ambient dewpoint;
e. Water supply and drain piping on which
condensation may occur;
f. Air
ducts and casing with outside surface temperature below ambient dew point;
and
g. Other piping, ducts, and
equipment as necessary to maintain the efficiency of the system.
2. Insulation on cold surfaces
shall include an exterior vapor barrier.
3. Insulation, including finishes on the
exterior surfaces of ducts, pipes, and equipment, shall have a flame spread
rating of twenty-five (25) or less and a smoke developed rating of fifty (50)
or less as determined by an independent testing laboratory in accordance with
NFPA 255. The smoke development rating for pipe insulation shall not exceed one
hundred fifty (150).
4. Interior
duct lining is a potential health hazard and shall not be permitted.
C. Steam and Hot Water Systems and
Pressure Vessels.
1. All pressure vessels
shall have the ASME seal and shall meet the requirements of the Arkansas Boiler
Inspector, Arkansas Department of Labor.
2. Boilers shall have the capacity, based
upon the net ratings published by the Hydronics Institute or another acceptable
national standard, to supply the normal requirements of all systems and
equipment.
3. Supply and return
mains and risers of cooling, heating, and process steam systems shall be valved
to isolate the various sections of each system. Each piece of equipment shall
be valved at the supply and return ends.
D. Air Conditioning, Heating and Ventilating
Systems.
1. For laundries a maximum average
design temperature of 83-85 F at summer design conditions shall be assumed,
with higher temperatures permitted adjacent to heat producing equipment such as
ironers. For all other occupied areas a design temperature of 72 F for cooling
and heating design conditions shall be assumed.
2. All air-supply and air-exhaust systems
shall be mechanically operated.
3.
Outdoor intakes shall be located as far as practical but not less than twenty-
five (25) feet in large Free-Standing Birthing Centers and ten (10) feet in all
other Free-Standing Birthing Centers from exhaust outlets of ventilating
systems, combustion equipment stacks, medical/surgical vacuum systems, plumbing
vents stacks, or areas which may collect vehicular exhaust and other noxious
fumes. The bottom of outdoor air intakes serving central systems shall be
located as high as practical but not less than six (6) feet above the ground
level, or if installed above the roof, three (3) feet above the roof level.
Exhaust outlets from areas that may be contaminated shall be above roof level
and arranged to minimize recirculation of exhaust air into the
building.
4. It shall be prohibited
to use exit access corridors, separated from building use areas by fire-rated
partitions and providing access to exit, for return or exhaust from adjoining
air-conditioned spaces through louvers or other devices mounted in corridor
doors, partitions, or ceilings.
5.
The space above ceilings shall not be used as plenum space to supply to, return
air from, or to exhaust air from any patient care area in large Free- Standing
Birthing Centers.
6. In large
Free-Standing Birthing Centers, all central air conditioning systems shall be
equipped with two (2) filters. Filter bed number one (1) shall be located
upstream of the air conditioning equipment and have an efficiency of no less
than thirty (30) percent. Filter bed number two (2) shall be located downstream
of any fan or blowers and have an efficiency of no less than ninety (90)
percent. Filtration efficiency ratings shall be based on dust spot efficiency
per ASHRAE 52-76.
7. Non-central
air handling systems, i.e., individual room units that are used for heating and
cooling purposes (fan-coil units, heat pump units, etc.), shall be equipped
with permanent (cleanable) or replaceable filters. The filters shall have a
minimum efficiency of 68 percent weight arrestance. These units may be used as
recirculating units only. All outdoor air requirements shall be met by a
separate central air handling system with the proper filtration.
8. Direct gas-fired space heating equipment
(i.e. products of combustion are not separated from the air stream) shall not
be used in patient care areas.
9.
Duct humidifiers, when located upstream of final filters, shall be located a
minimum of fifteen (15) feet upstream of final filters or shall be fitted with
water removal devices which do not allow any water droplets to reach the
filter. Humidifiers shall be connected to air flow proving switches that
prevent humidification unless the required volume of air flow is present or
high limit humidistats are provided. All duct takeoffs shall be sufficiently
downstream of the humidifier to ensure complete moisture dissemination.
Humidifiers that utilize direct contact of water with the air stream shall not
be used.
10. Air handling duct
systems shall meet the requirements of NFPA 90A and those contained herein.
When approved for use, flexible duct lengths shall be limited to a maximum of
fourteen (14) feet.
11.
Penetrations in barriers that have been designed to provide radiation shielding
shall not compromise the effectiveness of the shielding.
12. Fire, smoke dampers, and smoke detectors
shall be constructed, located, and installed in accordance with the
requirements of NFPA 101.
13.
Boiler rooms shall be provided with sufficient outdoor air to maintain maximum
combustion rates of equipment and to limit temperatures in working stations to
10 F above design temperature.
SECTION 19.
PHYSICAL FACILITIES,
PLUMBING AND OTHER PIPING SYSTEMS.
All plumbing systems shall be designed and installed in
accordance with the requirements of the latest edition of the Arkansas State
Plumbing Code. Only metal piping or piping material of a type approved by the
Arkansas Department of Health for corrosive wastes, etc., shall be
permitted.
A. Plumbing Fixtures.
1. The material used for plumbing fixtures
shall be nonabsorbent acid-resistant material.
2. All fixtures used by the staff and all
lavatories used by patients and food handlers shall be trimmed with valves
which can be operated without the use of hands.
3. Clinical sinks shall have an integral trap
in which the upper portion of the water trap provides a visible seal.
B. Water Supply Systems.
1. Systems shall be designed to supply water
at sufficient pressure to operate all fixtures and equipment during maximum
demand periods.
2. Each water
service main, branch main, riser, and branch to a group of fixtures shall be
valved. Stop valves shall be provided at each fixture. Appropriate panels for
access shall be provided at all valves where required.
3. Backflow preventers (vacuum breakers)
shall be installed on hose bibs, laboratory sinks, janitors' sinks, and on all
other fixtures to which hoses or tubing can be attached.
4. Water distribution systems shall be
arranged to provide hot water at each hot water outlet at all times. Hot water
at shower, bathing, and handwashing facilities shall not exceed 110 degrees
F.
5. The hot water heating
equipment and storage tank(s) shall be fabricated of corrosion resistant metal
or lined with noncorrosive material.
C. Drainage Systems.
1. Drain lines from sinks in which acid
wastes may be poured shall be fabricated from an acid-resistant
material.
2. Building sewers shall
discharge into a community sewage system. Where such a system is not available,
a facility providing sewage treatment shall conform to applicable local and
state regulations.
D.
All piping, except control line tubing, shall be identified as to content. All
valves shall be tagged, and a valve schedule shall be maintained at the
facility for permanent record.
E.
Gas and Vacuum Systems.
1. Gas and vacuum
systems if installed shall be in accordance with NFPA 99, Chapter 4. In large
Free-Standing Birthing Centers, a piped medical gas system shall be required
and shall be installed in accordance with NFPA 99, Chapter 4.
SECTION 20.
PHYSICAL FACILITIES, ELECTRICAL REQUIREMENTS.
All material and equipment, including conductors, controls, and
signaling devices shall be installed to provide a complete electrical system
with the necessary characteristics and capacity to supply the electrical
facilities shown in the specifications or indicated on the plans.
Compliance shall be in accordance with applicable Sections of
NFPA 70 and NFPA 99. All materials shall be listed as complying with available
standards of Underwriters' Laboratories, Inc., or other similarly established
standards.
A. Performance Tests. All
electrical installations, including alarm, nurses call and communication
systems shall be tested to demonstrate that equipment is installed and operates
as planned and specified. A written record of performance tests on special
electrical systems and equipment shall be supplied to the owner.
B. Lighting. All spaces occupied by people,
machinery, and equipment within buildings, approaches to buildings, and parking
lots shall have lighting. Lighting levels shall be in accordance with IES
Lighting Handbook (1987, Volume II, Applications) and Lighting for Health Care
Facilities (1985).
C. Equipment
Installation in Special Areas. Ground fault circuit interrupters shall comply
with NFPA 70. When ground fault circuit interrupters (GFCI) are used in
critical areas, provisions shall be made to insure that other essential
equipment is not affected by activation of one (1) interrupter.
D. Nurses' Call System. In large
Free-Standing Birthing Centers, a nurses emergency call system shall be
provided for patients' use at each patient's toilet, bath, sitz bath, and
shower room. This system shall be accessible to a collapsed patient lying on
the floor. Inclusion of a pull cord shall satisfy this standard. The emergency
call signal (i.e., visible and audible) shall be distinguishable from the
normal nurse call signal, and the call light shall be cancelable only at the
station of origin. The signal shall activate an enumerator panel at the nurse
station, a visible signal in the corridor at the patient's door, and at other
areas defined by the functional program. Provisions for emergency call shall
also be needed in outpatient and treatment areas where patients may be subject
to incapacitation.
E. Fire Alarm
System. A protected premises fire alarm system as defined in Chapter 3 of NFPA
72, National Fire Alarm Code shall be required. In large Free-Standing Birthing
Centers, fire alarm systems shall conform to NFPA 101, Life Safety Code,
12-6.3.4.
F. Emergency Electrical
Service. Emergency egress lighting (battery back-up) and delivery rooms
lighting (battery back-up) shall be provided. In large Free- Standing Birthing
Centers, emergency lighting and power shall be provided in accordance with NFPA
99, NFPA 101, and NFPA 110 with eight (8) hours of onsite fuel.