THE PREGNANT PATIENT'S BILL OF RIGHTS
Most pregnant women are not fully aware of their rights to informed consent
or the obstetrician's legal obligation to obtain informed consent to treatment.
More than twenty years ago, the American College of Obstetricians and
Gynecologists acknowledged the pregnant patient's right of informed consent in
the following excerpt from its 1974 Standards for Obstetric- Gynecologic
Services (pg 66,67).
"It is important to note the distinction between 'consent' and 'informed
consent'.
Many physicians, because they do not realize there is a difference, believe
they are free from liability if the patient consents to treatment. This is not
true. The physician may still be liable if the patient's consent was not
informed. In addition, the usual consent obtained by a hospital does not in any
way release the physician from his legal duty of obtaining an informed consent
from his patient.
"Most courts consider that the patient is 'informed' if the following
information is given:
· The processes contemplated by the physician as treatment, including
whether the treatment is new or unusual.
· The risks and hazards of the treatment,
· The chances for recovery after treatment.
· The necessity of the treatment.
· The feasibility of alternative methods of treatment.
"One point on which courts do agree is that explanations must be given
in such a way that the patient understands them. A physician cannot claim as a
defense that he explained the procedure to the patient when he knew the patient
did not understand. The physician has a duty to act with due care under the
circumstances; this means he must be sure the patient understands what she is
told."
"It should be emphasized that the following reasons are not sufficient
to justify failure to inform:
1. That the patient may prefer not to be told the unpleasant possibilities
regarding the treatment.
2. That full disclosure might suggest infinite dangers to a patient with an
active imagination, thereby causing her to refuse treatment.
3. That the patient, on learning the risks involved, might rationally decline
treatment. The right to decline is the specific fundamental right protected by
the informed consent doctrine."
American parents are becoming increasingly aware that well-intentioned health
professionals do not always have scientific data to support common American
obstetrical practices and that many of these practices are carried out primarily
because they are part of medical and hospital tradition. In the last forty
years, many artificial practices have been introduced which have changed
childbirth from a physiological event to a very complicated medical procedure in
which all kinds of drugs are used and procedures carried out, sometimes
unnecessarily, and many of them potentially damaging for the baby and even for
the mother. A growing body of research makes it alarmingly clear that every
aspect of traditional American hospital care during labor and delivery must now
be questioned as to its possible effect on the future well-being of both the
obstetric patient and her unborn child.
One in every 35 children born in the United States today will eventually be
diagnosed as retarded; in 75% of these cases there is no familial or genetic
predisposing factor. One in every 10 to 17 children has been found to have some
form of brain dysfunction or learning disability requiring special treatment.
Such statistics are not confined to the lower socioeconomic group but cut across
all segments of American society.
New concerns are being raised by childbearing women because no one knows what
degree of oxygen depletion, head compression, or traction by forceps the unborn
or newborn infant can tolerate before that child sustains permanent brain damage
or dysfunction. The findings regarding the cancer-related drug
diethylstilbestrol have alerted the public to the fact that neither the approval
of a drug by the U.S. Food and Drug Administration nor the fact that a drug is
prescribed by a physician serves as a guarantee that a drug or medication is
safe for the mother or her unborn child. In fact, the American Academy of
Pediatrics' Committee on Drugs has stated that there is no drug, whether
prescription or over-the-counter remedy, which has been proven safe for the
unborn child.
The Pregnant Patient has the right to participate in decisions involving her
well-being and that of her unborn child, unless there is a clearcut medical
emergency that prevents her participation. In addition to the rights set forth
in the American Hospital Association's "Patient's Bill of Rights," the
Pregnant Patient, because she represents TWO patients rather than one, should be
recognized as having the additional rights listed below.
1. The Pregnant Patient has the right, prior to the administration of any
drug or procedure, to be informed by the health professional caring for her of
any potential direct or indirect effects, risks or hazards to herself or her
unborn or newborn infant which may result from the use of a drug or procedure
prescribed for or administered to her during pregnancy, labor, birth or
lactation.
2. The Pregnant Patient has the right, prior to the proposed therapy, to be
informed, not only of the benefits, risks and hazards of the proposed therapy
but also of known alternative therapy, such as available childbirth education
classes which could help to prepare the Pregnant Patient physically and mentally
to cope with the discomfort or stress of pregnancy and the experience of
childbirth, thereby reducing or eliminating her need for drugs and obstetric
intervention. She should be offered such information early in her pregnancy in
order that she may make a reasoned decision.
3. The Pregnant Patient has the right, prior to the administration of any
drug, to be informed by the health professional who is prescribing or
administering the drug to her that any drug which she receives during pregnancy,
labor and birth, no matter how or when the drug is taken or administered, may
adversely affect her unborn baby, directly or indirectly, and that there is no
drug or chemical which has been proven safe for the unborn child.
4. The Pregnant Patient has the right if Cesarean birth is anticipated, to be
informed prior to the administration of any drug, and preferably prior to her
hospitalization, that minimizing her and, in turn, her unborn baby's intake of
nonessential pre-operative medicine will benefit her baby.
5. The Pregnant Patient has the right, prior to the administration of a drug
or procedure, to be informed of the areas of uncertainty if there is NO properly
controlled follow-up research which has established the safety of the drug or
procedure with regard to its direct and/or indirect effects on the
physiological, mental and neurological development of the child exposed, via the
mother, to the drug or procedure during pregnancy, labor, birth or lactation--
(this would apply to virtually all drugs and the vast majority of obstetric
procedures).
6. The Pregnant Patient has the right, prior to the administration of any
drug, to be informed of the brand name and generic name of the drug in order
that she may advise the health professional of any past adverse reaction to the
drug.
7. The Pregnant Patient has the right to determine for herself, without
pressure from her attendant, whether she will accept the risks inherent in the
proposed therapy or refuse a drug or procedure.
8. The Pregnant Patient has the right to know the name and qualifications of
the individual administering a medication or procedure to her during labor or
birth.
9. The Pregnant Patient has the right to be informed, prior to the
administration of any procedure, whether that procedure is being administered to
her for her or her baby's benefit (medically indicated) or as an elective
procedure (for convenience, teaching purposes or research).
10. The Pregnant Patient has the right to be accompanied during the stress of
labor and birth by someone she cares for, and to whom she looks for emotional
comfort and encouragement.
11. The Pregnant Patient has the right after appropriate medical consultation
to choose a position for labor and for birth which is least stressful to her
baby and to herself.
12. The Obstetric Patient has the right to have her baby cared for at her
bedside if her baby is normal, and to feed her baby according to her baby's
needs rather than according to the hospital regimen.
13. The Obstetric Patient has the right to be informed in writing of the name
of the person who actually delivered her baby and the professional
qualifications of that person. This information should also be on the birth
certificate.
14. The Obstetric Patient has the right to be informed if there is any known
or indicated aspect of her or her baby's care or condition which may cause her
or her baby later difficulty or problems.
15. The Obstetric Patient has the right to have her and her baby's hospital
medical records complete, accurate and legible and to have their records,
including Nurses' Notes, retained by the hospital until the child reaches at
least the age of majority, or, alternatively, to have the records offered to her
before they are destroyed.
16. The Obstetric Patient, both during and after her hospital stay, has the
right to have access to her complete hospital medical records, including Nursing
Notes, and to receive a copy upon payment of a reasonable fee and without
incurring the expense of retaining an attorney.
It is the obstetric patient and her baby, not the health professional, who
must sustain any trauma or injury resulting from the use of a drug or obstetric
procedure. The observation of the rights listed above will not only permit the
obstetric patient to participate in the decisions involving her and her baby's
health care, but will help to protect the health professional and the hospital
against litigation arising from resentment or misunderstanding on the part of
the mother.
© Doris Haire
American Foundation for Maternal and Child Health