Current through Register Vol. 48, No. 9, September 27, 2024
(1) Limitation of
Services Offered by Birthing Center: (I)
In order to be delivered in a birthing center, the woman and/or
her infant shall exhibit no evidence of:
(a) severe anemia;
(b) diabetes mellitus;
(c) symptomatic heart disease;
(d) severe hypertension or
preeclampsia;
(e) renal
disease;
(f)
thrombophlebitis;
(g) multiple
gestation;
(h) active herpes
(within one week of delivery), syphilis, or HIV positive;
(i) placental abnormalities;
(j) premature labor;
(k) intrauterine growth
retardation;
(l) fetal
disease;
(m) previous caesarean
delivery with classical incision;
(n) desire for transfer;
(o) anticipated macrosomia;
(p) breech birth;
(q) six or more (nonmiscarriage or
nonabortion) pregnancies;
(r)
polyhydramnios or oligohydramnios, or chorionitis;
(s) malformed fetus;
(t) any other high risk condition.
(2) Birthing Center Policies and
Procedures: The facility shall formulate written policies and procedures which
shall include, but not be limited to: (II)
(a) Informed consent which shall be obtained
prior to the onset of labor and shall include evidence of an explanation by
personnel of the birthing service offered and potential risks. Documentation of
the informed consent must be filed in the patient's chart.
(b) Registration of birth and fetal death or
death certificates.
(c) Infection
control committee duties and responsibilities shall include the development and
implementation of specific patient care and administrative policies aimed at
investigating, controlling and preventing infections in the facility.
(d) Arrangements shall be made for all
mothers to be screened for blood type and Rh factor. Those determined to be Rh
negative shall have provision for appropriate follow-up studies both prenatally
and at time of delivery in order to determine the need for Anti D Immune
Globulin (Human) to prevent sensitization by the post partum mother. There
shall be evidence of a plan for the appropriate use of Rh immune
globulin.
(e) The physician or
midwife shall, upon the birth of a child, instill or cause to be instilled in
each eye of such newborn antibiotics of currently proven efficacy in preventing
development of ophthalmia neonatorum. A maximum delay of one hour shall be
allowed between the time of birth and the administration of an approved
prophylactic agent.
(3)
Pharmaceutical Services: (I)
(a) Written
policies shall be established addressing the type and intended use of any drug
to be used within the facility.
(b)
There shall be policies and procedures addressing the receiving, transcribing,
and implementing of orders for administration of drugs.
(c) There shall be written prescriptions or
orders signed by a practitioner legally authorized to prescribe in South
Carolina for all drugs administered to mother and infant within the birthing
center.
(d) Drugs shall be
administered by personnel or clinical staff currently licensed in South
Carolina to administer drugs.
(e)
Drugs, medications, and chemicals kept anywhere in the center shall be clearly
labeled with drug name, strength, and expiration date.
(f) Drugs, medications, and chemicals shall
be stored and secured in specifically designated cabinets, closets, drawers, or
storerooms and made accessible only to authorized persons.
(g) Drugs requiring refrigeration shall be
kept secure in a refrigerator under proper temperature. Each refrigerator shall
be provided with a thermometer.
(4) Laboratory Services:
The center shall enter into a signed written agreement with a
certified clinical laboratory to ensure accessibility to a full range of
clinical laboratory testing, as may be required.
(5) Birthing Center Equipment and Supplies:
There shall be appropriate equipment and supplies maintained
for the mother and the newborn to include but not limited to: (II)
(a) A bed suitable for labor, birth, and
recovery;
(b) Oxygen with flow
meters and masks or equivalent;
(c)
Mechanical suction and bulb suction (immediately available);
(d) Resuscitation equipment to include
resuscitation bags, endotracheal tubes and oral airways for the mother and
newborn;
(e) Firm surfaces suitable
for resuscitation;
(f) Emergency
medications, intravenous fluids, and related supplies and equipment for both
mother and newborn;
(g) Fetal
monitoring equipment;
(h) A means
of monitoring and maintaining the optimum body temperature of the
newborn;
(i) A clock with a sweep
second hand;
(j) Sterile suturing
equipment and supplies;
(k)
Adjustable examination light;
(l)
Containers for soiled linen and waste materials which shall be
closed;
(m) Refrigeration unit or
units;
(n) Matching identification
for the baby to the mother shall be provided.
(6) Clinical Staff:
(a) All clinical staff who practice in a
facility shall be organized as a clinical staff with appropriate bylaws
approved by the governing body. The clinical staff shall meet at least
quarterly and minutes shall be maintained of such meetings.
(1) A physician must be on call and available
to provide medical assistance at the birthing center at all times that it is
serving the public. (I)
(2) A
physician shall make a written determination that the planned birth is low
risk. (I)
(3) The center shall
enter into a signed written agreement with an obstetrician(s) and a
pediatrician(s) to ensure their availability to the staff and mother at all
times that it is serving the public. (I)
(b) The facility shall have an organized
midwifery department under the supervision of a Director of Midwifery. (II)
(1) The Director of Midwifery shall be a
certified nurse-midwife and be responsible and accountable for all midwifery
service to include:
(a) delivery of midwifery
services to patients;
(b)
development and maintenance of midwifery service objectives, standards of
midwifery practice, midwifery policy and procedure manuals (reviewed annually),
written job descriptions for each type of midwifery personnel;
(c) coordination of midwifery services with
other patient services;
(d)
establishment of a means of assessing the midwifery care needs of patients and
staffing to meet those needs;
(e)
staff development.
(c) An adequate number of licensed and
ancillary midwifery personnel shall be on duty to meet the total midwifery
needs of patients. Midwifery personnel shall be assigned to duties consistent
with their training and experience. (I)
(d) At least one member of the clinical staff
or a registered nurse shall be in the facility when a patient is present; and
up to at least one hour after each mother's delivery. Two members of the
clinical staff or one member of the clinical staff and a registered nurse shall
be present during the mother's delivery. (I)
(7) Medical Records: An accurate complete
medical record shall be maintained for each patient.
(a) A legible medical record in ink shall
include at least the following:
(1) admitting
identification data including patient history and physical
examination;
(2) signed
consent;
(3) orders of physician or
certified practitioner;
(4)
laboratory tests;
(5) prenatal care
record containing at least prenatal blood serology, Rh factor determination and
obstetrical history and physical examination;
(6) labor and delivery record;
(7) records of anesthesia and analgesia and
medication given in the course of labor, delivery and post partum;
(8) recovery and other progress
notes;
(9) record of all
medications and treatments ordered and administered;
(10) condition and referral on
discharge.
(b) Records
of newborn infants shall include in addition to the requirements for medical
records the following information:
(1) date
and hour of birth, birth weight and length, period of gestation, sex, condition
of infant on delivery and APGAR rating;
(2) mother's name and patient number, and/or
similar identification;
(3) record
of opthalmic prophylaxis;
(4)
record of administration of Rh immune globulin if any;
(5) appropriate physical examination at birth
and at discharge;
(6) Test results
and date specimen was collected for PKU and hypothyroid newborn screening test.
(Exempt only when parents object because of religious convictions; then file
copy of executed "Statement of Religious Objection Form," DHEC #1804 with
newborn record.)
(c)
Provisions shall be made by the facility for the storage of medical records in
an environment which will prevent unauthorized access and deterioration. The
records shall be treated as confidential and shall not be disposed of under 10
years. Records may be destroyed after 10 years provided that:
(1) Records of minors must be retained until
after the expiration of the period of election following achievement of
majority as prescribed by statute.
(2) The facility retains an index, register,
or summary cards providing such basic information as dates of admission and
discharge, name of responsible clinical staff, and record of diagnoses for all
records so destroyed.
(d) Facilities that microfilm before 10 years
have expired must film the entire record.
(e) In the event of change of ownership, all
medical records shall be transferred to the new owners.
(f) Prior to the closing of a facility for
any reason, the facility shall arrange for preservation of records to insure
compliance with these regulations. The facility shall notify the Department, in
writing, describing these arrangements.
(g) Information to be Provided to Other
Health Care Providers. In order to contribute to the continuity of quality of
care, procedures must be established and implemented to provide discharge
summaries and/or other appropriate information to health care providers to whom
patients are discharged, transferred or referred.