Diagnostic Imaging During Pregnancy and Lactation

Today we’re going to review a source of constant consultation and confusion: diagnostic imaging during pregnancy and breastfeeding. ACOG CO 723 is the definitive reading on this subject, and we use it to structure this episode. Critical take home: ACOG states that critical imaging studies should not be withheld from a pregnant patient if needed to make a diagnosis. 

Ultrasound

  • Sonography utilizes sound waves to produce a visible image, and is not a form of ionizing radiation.

    • Thus, it is considered the safest mode of imaging in pregnancy.

    • However, ACOG still recommends sticking to the ALARA principle of exposure in pregnancy (“As Low As Reasonably Achievable”) to minimize any potential untoward effects. 

    • One of these theoretical effects involves color or spectral flow Doppler. Due to its intensity, the theoretical temperature increase surrounding the area being study can be as high as 2deg C, or 3.6deg F. It’s unlikely than any temperature increase would be sustained at any fetal anatomic site to cause harm. However, for this reason, even ultrasound exposure should be used judiciously. 

MRI

  • Allows for visualization of soft-tissue structures like ultrasound

    • However, as MRI is operator-independent, pick up rates for certain pathologies like appendicitis tend to be higher.

    • There are no special contraindications or considerations in pregnancy for non-contrast MRI, other than the usual screening surrounding metal or magnet-sensitive implants, such as pacemakers. 

  • Non-contrast MRI is sufficient for diagnosis; however, some diagnoses or studies may be improved by the use of gadolinium-based contrast, for which there is uncertainty regarding fetal effects.

    • Gadolinium is water-soluble, and thus crosses the placenta into fetal circulation.

    • Free gadolinium is toxic, so it is bound, or chelated, when administered for studies.

      • There is concern that since this bound gadolinium can enter fetal circulation, it can recycle in the fetal circulation. This potentially could sit for long enough that the gadolinium could dissociate and become free; thus become toxic. 

      • Given at least the concern for potential poor outcomes, gadolinium-based contrast should be limited in use to cases where there is an absolute clear benefit to its administration.

    • Gadolinium’s water-solubility makes it an OK contrast agent to use during lactation.

      • Less than 0.04% of a dose of gadolinium will be excreted in breastmilk in the first 24 hours, and less than 1% of this will be absorbed in the infant GI tract. Thus, breastfeeding should not be interrupted after gadolinium contrast studies.

CT, XRAY, and other ionizing radiation studies
Before talking about ionizing radiation studies, it’s important to know some vocabulary and measurements of radiation:

  • Exposure is the number of ions produced by radiation in the form of X-rays or gamma rays per kilogram of air. This is measured in Roentgen units.

  • Dose is the amount of energy deposited per kilogram of tissue. This is the usual consideration when we talk about radiation in pregnancy. This is measured in rads or in Gray units; 100 rad is equivalent to 1 Gray.

  • Relative effective dose is the amount of energy deposited per kilogram of tissue, and normalized for biological effectiveness on the tissue. This is measured in Roentgen equivalent men (rem) or Sievert units.


Again, the dose is what we usually consider and track with respect to radiation in pregnancy.

  • The background dose of radiation a fetus is exposed to during pregnancy is around 1 mGy.

  • From CO 723 — a reference for doses associated with different imaging studies.

ACOG CO 723

ACOG CO 723

The risk of radiation exposure on a developing fetus depends on both the dose of radiation, as well as the gestational age at which the exposure occurs.

  • For instance, if an exposure of 50-100 mGy occurs prior to implantation (0-2 weeks post fertilization), there is generally an all or none effect; that is to say, this usually results in miscarriage, or no consequence at all.

  • During organogenesis, or 2-8 weeks post-fertilization, congenital anomalies or growth restriction can be seen with cumulative doses of 200-250 mGy.

  • The risk of severe intellectual deficit or microcephaly is most prominent around 8-15 weeks, with doses between 60 - 300 mGy.

    • There is an estimated 25 point IQ loss per 1000 mGy exposure during this time period. 

    • A lower risk of severe intellectual disability may persist through 25 weeks gestation, though again with exposures of 250mGy or more.

  • Other risks include childhood cancer. With respect to leukemia, it is estimated the risk of childhood leukemia increases 1.5-2 fold with a 10-20mGy dose, over a background leukemia risk of 1 in 3000.

  • Radiologists and radiation physicists can help to calculate doses for patients exposed to multiple studies or with occupational hazards. 

With respect to contrast:

  • Oral contrast poses no real or theoretical harm to pregnant or lactating mothers and their infants.

  • IV contrast tends to be iodinated, but is also water-soluble.

    • So similarly to gadolinium, in pregnant patients this crosses the placenta.

    • Animal studies have demonstrated no teratogenic effects from its use, but it is recommended to limit use of iodinated contrast unless necessary.

    • Also similarly to gadolinium, because of this water solubility, iodinated contrast is excreted minimally in breastmilk, and breastfeeding should be continued without interruption.

Nuclear medicine studies

Radioisotopes for nuclear medicine studies, such as VQ scans, thyroid scans, and bone scans, are variable in their potential effects on the fetus.

  • Technetium-99 is one of the most common radioisotopes used for these studies, and given its short half life of 6 hours as well as its pure gamma ray emission, is generally accepted as safe to use when indicated in pregnancy.

  • Radioactive iodine (I-131), by contrast (punny!), readily crosses the placenta and has a half-life of 8 days, and has known adverse effects on the fetal thyroid. Thus, it is contraindicated for use in pregnancy, and is also recommended against use in breastfeeding mothers until breast milk has been cleared of the radioisotope. 


Abnormal Uterine Bleeding: The Basics

Today we talk through the varied etiologies and a basic workup for a common GYN complaint: abnormal uterine bleeding. ACOG PB 128 makes for good companion reading for women of reproductive age.

The terminology of AUB has changed quite a bit, and you may still hear older terms being used. “Dysfunctional uterine bleeding” or DUB has fallen out of favor, as have terms such as metrorrhagia or menorrhagia, yielding instead to simpler terminology such as prolonged menstrual bleeding and heavy menstrual bleeding, respectively. The terms such as oligomenorrhea (bleeding cycles > 35 days apart) and polymenorrhea (cycles < 21 days apart) are also in use to some degree.

Heavy bleeding is difficult to discern, but for research purposes has been described as >80cc blood loss per cycle. In clinical practice, this is obviously impractical, so we rely on subjective descriptions of heavy bleeding to guide care.

The biggest takeaways from this episode include the PALM-COIEN classification of bleeding by FIGO, as well as the common culprits of bleeding by age group. Remember also the criteria for working up for disorders of coagulation, which we’ve put here (though contained in the practice bulletin).

Stay tuned for future episodes about the treatments of these various etiologies, or check out our friends at The OBG Project for excellent summaries of guidelines and new literature!

ACOG PB 128

ACOG PB 128

ACOG PB 128

Care of the Transgender Patient

Today we sit down with Dr. Beth Cronin, clinical associate professor and assistant program director at Brown / Women and Infants of Rhode Island. Dr. Cronin has become a national expert in the care of LGBTQ patients, and is a fixture at ACOG and other venues, and we are lucky enough today to have her break down the need-to-know essentials for the OB/Gyn.

Definitions are an excellent place to start, and set the stage for this conversation:

  • Sex is what we do in the delivery room - defining “male” or “female” based on the presence of external genitalia.

  • Gender is a social construct, comprising attitudes, feelings, or behaviors associated to “male” or “female” by a culture.

  • Gender identity is a person’s internal sense of their gender:

    • Cisgender the biological sex and gender identity align

    • Transgender the biological sex and gender identity are opposite:

      • Transgender woman biological sex male, identity female

      • Transgender man biological sex female, identify male

    • Gender should be viewed along a spectrum, with varying definitions for terms such as gender fluid, gender queer, or nonbinary.

About 1.4 million adults and 150,000 youth aged 13-17 are estimated to identify as transgender or gender non-binary in the United States. This population has much higher risks of experiencing discrimination, violence, and sexual assault. Additionally, these patients are likely to have poor experiences in healthcare settings. These patients really need access to care, and OB/Gyns are in perfect position to be safe and welcoming environments for the transgender/gender non-binary community.

For your office and daily practice, it is important to be inclusive, and there are myriad resources to get this started. Staff training and education to promote inclusivity is also important. Inclusive forms and medical record systems that elicit gender identity are important to make available, including documentation of preferred pronouns.

Dr. Cronin also took time today to discuss some clinical care aspects. UCSF and WPATH each have excellent protocols and guidelines for clinical care, including for initiating or maintaining transition care. Modifications of usual care, and care in the midst of hormonal transition, is discussed in great detail at these resources. ACOG also has excellent online modules for OB/Gyns for transgender healthcare, in addition to more primary reading at CO 512, CO 685, and additional ACOG-approved resources for clinicians.

Dr. Cronin easily explains it as “screen the parts that are present” per usual care guidelines, including with respect to things such as breast and cervical cancer screening, contraceptive methods, and pregnancy and abortion care.

Preterm Labor and PPROM

Today we talk about the routine management of PPROM and PTL. We’ve prepared a little chart that we hope is handy for both teaching and learning! Be sure to also check out ACOB PB 171 and PB 188. For some primary literature, check out the BEAM trial on magnesium sulfate, the most recent Cochrane review on steroid administration, the ALPS trial for Antenatal Late Preterm Steroid administration, and the RCT demonstrating benefit to latency antibiotics in PPROM.

(c) CREOGS over Coffee, 2019

We also use the podcast to highlight a number of controversies, differing practice patterns, or areas of new and active research in these clinical topics (with help from our friends at the ObG Project!)

  • Delivery timing: A 2017 Cochrane review suggested better neonatal outcomes with expectant management of PPROM to 37 weeks, convincing enough to have the Royal College of Obstetrics and Gynecology to change their clinical practice guideline to allow expectant management to 37’0.

  • Administration of Corticosteroids: The ObG Project gives a great summary on when to administer betamethasone. In summary:

    • Between 24-34 weeks in all cases of PPROM and in PTL if delivery is expected within 7 days.

    • A single rescue course should be administered if it has been > 14 days since the last course, and delivery is again expected within the subsequent 7 days.

    • Between 34-36’6 weeks if PPROM or PTL occurs, no prior steroids have been administered, and delivery is expected within the subsequent 7 days.

  • Periviability: The management of periviable PPROM is managed very differently by institution, as resources and optimal management strategies remain to be identified. Protocols and policies should be arranged in accordance with the individual obstetrics and neonatology departments. Ideally, counseling for patients experiencing periviable PTL and PPROM should be performed in an interdisciplinary fashion.

  • Outpatient Management of PPROM: There have a few retrospective studies, the most recent of which came from a large series out of France and received some press attention, suggesting that outpatient management may be appropriate in select candidates. That said, this is definitely NOT the standard of care at this time; inpatient management of PPROM is still the standard set forth by ACOG in the absence of larger, prospective studies.

Intimate Partner Violence and Gun Violence

Today we are spending some time on IPV/DV and gun violence. These are topics every OB/GYN should be familiar with; IPV accounts for 250,000 hospital visits, 2,000 deaths, and $8 billion in direct care costs annually on a conservative estimate. 1 in 3 American women is victimized by IPV during their lifetimes, and 1 in 5 report being the victim of sexual assault.

ACOG CO 518 serves as essential reading for our conversation today. Important points from the reading and today’s episode include:

Finally, check out ACOG’s stance and legislative priority list surrounding gun violence. Be active and get involved today — this is our lane!