AJR 2003; 181:335-340
© American Roentgen Ray Society
A New Pregnancy Policy for a New Era
Georges Y. El-Khoury1,
Mark T. Madsen1,
Meghan E. Blake2,3 and
Jerome Yankowitz4
1 Department of Radiology, The University of Iowa, Roy J. and Lucille A. Carver
College of Medicine, 200 Hawkins Dr., Iowa City, IA 52242.
2 West Suburban Hospital Medical Center, Erie at Austin, Oak Park, IL
60302.
3 Present address: Department of Radiology, Boston Medical Center, 88 E. Newton
St., Boston, MA 02118.
4 Department of Obstetrics and Gynecology, The University of Iowa, Roy J. and
Lucille A. Carver College of Medicine, Iowa City, IA 52242.
Received September 16, 2002;
accepted after revision February 3, 2003.
Address correspondence to G. Y. El-Khoury.
Presented at the annual meeting of the American Roentgen Ray Society,
Atlanta, AprilMay 2002.
Introduction
In a busy radiology practice, encountering pregnant or possibly pregnant
patients who require imaging is fairly common. Mann et al.
[1] reported that 30% of female
patients in a major trauma center were of child-bearing age, and 15% of these
patients were either definitely or possibly pregnant. As a result, irradiation
of the fetus during diagnostic imaging of the mother is a routine occurrence.
Exposing the fetus to ionizing radiation is always an anxiety-provoking
problem to patients and physicians alike. This problem continues to be
exacerbated by the increased use of high-dose procedures such as fluoroscopy
and CT. The number of prolonged interventional procedures performed under
fluoroscopic control over the past 10 years has dramatically increased.
Concern over the radiation dose from these procedures prompted the United
States Food and Drug Administration to issue an advisory warning about the
potential for radiation-induced skin burns after interventional procedures
[2]. An even bigger concern is
multidetector CT, which has become the primary diagnostic tool in the
emergency setting. The radiation dose from CT accounts for 40% of the annual
collective dose to the public from all medical procedures
[3].
Because of the concern over radiation dose to the fetus, radiologists at
our institution have been reluctant to use multidetector CT on pregnant
patients without careful consideration of other diagnostic options. Some
referring physicians have viewed this caution as an infringement on their
rights to treat their patients. These concerns were brought before the
committee that oversees the diagnostic service in our institution. After
exhaustive discussions, it became obvious that establishing a clear policy for
imaging pregnant patients was badly needed. Because it has been the
traditional role of the radiologist to counsel pregnant patients on the
effects of ionizing radiation to the fetus and to advise referring physicians
about alternative imaging modalities that can yield similar diagnostic
information without the use of ionizing radiation, the department of radiology
was charged with the responsibility for developing this policy. Together with
input from the radiation physics and radiation biology faculty and the
obstetrics department, a pregnancy policy was drafted to achieve the following
objectives. First, the policy should protect the mother and fetus, keeping in
mind that the well-being of the fetus depends primarily on the well-being of
the mother. If the mother's life is at risk and clear indications for an
imaging study exist, the examination should not be denied or delayed because
of the pregnancy. Second, the policy should encompass all possible clinical
situations, and finally, the policy should be clear and easy to implement.
The policy that we have developed is given in Appendix 1, and the informed
consent forms that we use are given in Appendixes 2 and 3. In addition, we
provide easy-to-use tables that will enable the radiologist to estimate fetal
dose for common radiographic procedures.
Table 1 gives estimates of
fetal doses for radiographic images and fluoroscopy of the pelvis and abdomen
for a range of patient body thickness. The fetal dose for fluoroscopic
procedures of the abdomen or pelvis with the fetus in the field of view
depends on the entrance skin dose. On new fluoroscopic units, the entrance
skin dose can be obtained from the dosearea product meter by dividing
the measured value by the field size. Fetal dose can be conservatively
estimated as 0.15 times the entrance skin dose.
Table 2 provides estimates of
fetal dose for CT of the abdomen and pelvis.
Discussion
All diagnostic procedures involving the use of ionizing radiation require a
balance between the risk and benefits. Although the risk associated with
diagnostic radiation doses to the fetus is low, it is significantly larger
than that for the adult. The developing fetus is more sensitive to ionizing
radiation, and the time available for the detriment to be expressed is much
longer. High radiation doses to the fetus are associated with abortion, body
size reduction, mental retardation, and increased incidence of future cancers
[4,
5]. However, there are
insufficient data on humans to precisely quantify harmful effects on the fetus
at doses below 50 mSv (5 rem). Somatic effects such as body size and mental
retardation appear to have dose thresholds in the range of 50100 mSv
(510 rem)
[57].
The excess risk for childhood cancer is estimated as 0.06% / 10 mSv (0.06% / 1
rem)
[810].
Most radiographic imaging studies on pregnant patients have until recently
been associated with fetal doses well below 50 mSv (5 rem), leading to the
conclusion that the risk of fetal detriment is small. However, there continues
to be ongoing investigations into the biologic effects of low-dose irradiation
and its safety, especially to the fetus. The potential risk of low-dose
radiation in humans cannot be measured directly and is often estimated from
linear or linearquadratic extrapolation from higher doses
[11]. Experimental work has
recently emerged showing a linear response for the induction of mutations in
human cells by X-ray exposures below 100 mSv (10 rem)
[12]. New reports on the
atomic bomb survivors who were exposed to low-dose radiation (5100 mSv)
have shown an increased incidence of cancer later in life
[7,
10]. The Committee on
Biological Effects of Ionizing Radiation estimates a 1.21.5% increase
in cancers for 5-year-old children who received a uniform body dose of 100 mSv
(10 rem) [13]. There is also
evidence that delivering a dose of 10 mSv (1 rem) to the breast of women less
than 35 years old increases their risk of breast cancer by approximately 14%
over the spontaneous rate in the general population
[14]. Although the
identifiable radiation risks are still small, this ongoing work focuses public
attention on fetal radiation and adds to the concerns that are raised whenever
a fetus is irradiated.
The goal of our policy is to expedite imaging studies when pregnant
patients are involved, while limiting fetal radiation dose. Although avoiding
radiation exposure to the fetus is desirable, failure to correctly diagnose
the medical problems of the mother more often poses a much greater risk to the
fetus. Thus, when faced with a pregnant patient, all involved personnel should
be prepared with a plan of action that will best address the medical needs of
the mother, while minimizing the radiation exposure to the fetus. The
implementation of this policy in our radiology department after 1 year has
resulted in a significant improvement in the workflow and has established
better cooperation between the radiologists and the referring physicians.
Conclusion
It is important to have a clear policy for handling requests for imaging
procedures involving pregnant women. A workable policy should address the
concerns of referring physicians, radiologists, and patients. The policy
presented in this article attempts to satisfy these needs. With low levels of
fetal exposure, the policy allows the examination to proceed without delay.
With higher radiation levels, the policy seeks to involve the radiologist,
referring physician, and patient to make informed decisions to protect the
health of the mother and the fetus. The key elements for making this policy
work are education and communication. The radiologist should be aware of the
level of fetal radiation doses for radiologic procedures and the magnitude of
the associated risks to initiate effective communication with both the
referring clinician and the patient.
APPENDIX 1. The Pregnancy Policy
A. Useful Background Information
The radiation dose to the fetus from conventional diagnostic procedures
when the fetus is not in the X-ray beam is approximately the same as the daily
background radiation dose received by the average American (
10 mSv or 1
mrem). The fetal dose from CT or fluoroscopy when the fetus is not in the
X-ray beam is typically less than 5 mSv (500 mrem).
Imaging studies such as abdominal radiography, lumbosacral spine
examination, and limited excretory urography typically deliver less than 10
mSv (1 rem) to the fetus [5]
(Table 1). Examinations in
which the fetus usually receives a radiation dose greater than 10 mSv (1 rem)
include barium enema, CT of the abdomen and pelvis, and interventional
procedures involving lengthy fluoroscopy
[5] (Tables
1 and
2).
Because health risks associated with radiation to the fetus are cumulative,
previous exposures to radiation must be considered before new procedures are
initiated.
B. Identifying the Pregnant Patient
The radiology department should be notified when a patient is known or
thought to be pregnant. This information should be stated on the X-ray
requisition or entered electronically on the order entry screen.
Before every imaging study or interventional procedure, the technologist
should inquire from all female patients of child-bearing age (age range,
1255 years) whether she is, or may possibly be, pregnant. The
radiologist in charge should be notified about any pregnant or possibly
pregnant patients referred for imaging. If the patient is too sick to answer
questions, the technologist should ask the family or treating physician. If a
definitive answer about the patient's pregnancy status cannot be obtained and
the patient's condition permits, a pregnancy test should be performed.
C. Clinical Scenarios
- For examinations of body parts above the diaphragm or below the hips, the
patient should be assured that there is no scientific evidence that the
examination will result in any detectable harm to the fetus. Shielding of the
abdomen and pelvis with lead aprons can be used if feasible, but it is not
essential.
- For examinations in which the fetus is in the direct x-ray beam and the
estimated dose as determined from Tables
1 and
2 is less than 10 mSv (1 rem),
the radiologist should discuss the benefits versus the risks of the procedure
with the referring physician. Imaging techniques not involving ionizing
radiation such as sonography and MR imaging should be considered. If the
examination is judged to be appropriate and necessary, the clinician
responsible for the care of the patient should document in the medical record
that the imaging study is indicated for the patient management. The
radiologist will explain the procedure to the patient and assure her that the
risk to the fetus is small. The radiation dose should be kept as low as
possible consistent with obtaining the required diagnostic information.
- For examinations in which the fetus is in the direct beam and the estimated
dose as determined from Tables
1 and
2 is more than 10 mSv (1 rem)
but less than 50 mSv (5 rem), the radiologist and referring physician should
discuss other options such as sonography or MR imaging that can provide the
needed information without the use of ionizing radiation. If the imaging
procedure is deemed appropriate, the patient should be involved in the
decision to proceed with the examination. The patient should be informed by
the radiologist of the risks and benefits of the diagnostic test or
interventional procedure. The patient will be required to sign an informed
consent form (Appendix 2). The clinician responsible for the care of the
patient should document in the medical record that the test is indicated for
the management of the patient.
- For the rare occasion in which the estimated dose to the fetus exceeds 50
mSv (5 rem), a formal calculation of the dose will be conducted by a radiation
physicist or equally qualified individual. The patient should be counseled
about the risks to the fetus. The referring physician and the radiologist
should document in the patient's medical record explaining the circumstances
and medical justification for the examination or procedure. The patient will
be required to sign an informed consent form (Appendix 3).
- Technical principles to be followed in every pregnant patient:
- Limit exposures to those that are absolutely essential for the
diagnosis.
- Every effort must be made to eliminate repeated exposures resulting from
technical errors. Repeated exposures should not be performed without
consulting the radiologist in charge.
- Precise collimation and pelvic shielding should be used whenever
possible.
- Fluoroscopy should be limited to short bursts as needed. All fluoroscopy
procedures must be timed, and a record of the fluoroscopy time, kilovoltage,
and milliampere-second must be kept. Newly installed fluoroscopy units have a
dosearea product meter that will provide this information. The last
image hold and electronic collimation features should be used during
fluoroscopy.
- For CT of the abdomen and pelvis, the radiologist should consider parameter
settings that will minimize the fetal dose while yielding useful diagnostic
information. Factors that affect the dose include kilovoltage,
milliampere-second, acquisition slice thickness, and pitch. Increasing the
acquisition slice thickness and pitch and decreasing the milliampere-second
and kilovoltage are associated with a significant lowering of the radiation
dose (
50% [15]).
- As recommended by the International Radiation Protection Association
policy, elective MR imaging should be postponed until after the first
trimester [16].
- All contrast media should be used with caution in pregnant women
[17].
APPENDIX 2. Consent Form
APPENDIX 3. Consent Form
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