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Handbook of Genetic Counseling/Lupron Exposure
Reference material by Wikibooks contributors. This retains its source identity and is not 411 news reporting.
Lupron Exposure
Contracting
Introductions and small talk
Confirm referring physician
Assess understanding of the reason for the referral to genetics
What concerns or questions do you have that you would like to discuss today?
Outline session agenda
Medical and family history questions
Some of the possible effects that lupron can have on the pregnancy
Options available to you
Discussion of concerns and questions
Elicit Medical History
Confirm LMP: __________
EDC: __________
Today's gestational age: __________
Have you had an ultrasound?
Date of ultrasound: __________
Results of ultrasound: __________
How has the pregnancy been going so far?
When did you first find out you were pregnant
What medications are you taking?
Amount and frequency of each.
When did you start taking each?
Do you have any other medical problems?
Any complications with the pregnancy
Elicit Family History
(3 generations)
Anyone had: multiple SAB, SB, early deaths or babies that required surgery as infants?
Anyone born with birth defects such as cleft lip or palate, spina bifida, or heart problems
MR/LD
Has anyone in family had cancer (dx. <50) or chronic illnesses (heart disease, diabetes)
Anyone with muscle weakness or muscular dystrophy
Anyone with bleeding disorders
Anyone with any other genetic disorders such as cystic fibrosis, PKU, etc.
Discuss possible side effects of taking lupron at time of conceptions
All pregnancies are at a 3-5% risk of birth defects or mental retardation
There may be an increase in risks to the fetus when a woman is on lupron at conception.
HOWEVER, this doesn't mean that the baby will be born with a problem, it just means that we know that based on your special circumstances, your pregnancy may be at an increased risk for miscarriage or maybe even a birth defect
The reasons we believe there might be an increased risk are based on a small number of women who were exposed to lupron during pregnancy as well as animal studies
We can tell you what has been reported, but the numbers are too small to make any real conclusions
125 women who were exposed to lupron at the time of pregnancy have been identified and reported as of Feb 2002
35 of them miscarried (28%), one was terminated for trisomy 18, three were ectopic pregnancies (2.4%)
2 of the 125 infants had congenital anomalies which included bilateral inguinal hernia and other atretic kidney (positive family history for atretic kidney)
14 were still ongoing pregnancies and 71 had babies with no malformations or health problems
6 children (around age 7) who were exposed to lupron or a similar medication (GnRH agonist).
1 had a cleft palate
1 had a seizure disorder
3 had ADHD
HOWEVER this is a very small number of children and is not enough to base any conclusions on
Also, it was unclear how they were defining ADHD because they all had normal psychological tests
Most of the studies regarding the risks that lupron poses for a pregnancy have been done on rabbits and rats.
These studies are often not directly related to effects and risks for humans because these animals are different enough that drugs can have a different effect on them when compared to a human fetus.
Increased fetal mortality and decreased fetal weights in rabbits when given 1/30th and 1/3rd the human dose and for rats at 1/3rd the human dose
Although not all agree with the interpretation, studies on rabbits suggest that there may be an increase in some birth defects, which include hydrocephalus or vertebral anomalies (dose related at 1/300th, 1/30th and 1/3rd the human dose)
Rats showed no increase in birth defects
We therefore don't really have a lot of conclusive information, but the main concern would seem to be an increased risk for pregnancy loss.
This increase in fetal mortality is likely due to alterations in hormonal levels brought about by the drug (estrogen and progestin levels reduced to levels within the menopausal range)
Options
Level II ultrasound -- performed at 18 -20 weeks
Done by an experienced technician
Can detect many birth defects
Developing organs will be looked at in detail
Can often detect abnormalities in the formation of the limbs, spine, heart, and brain
U/S is good to make us suspicious of some birth defects but it can't tell us everything
We won't know if there is mental deficiency by u/s
Also, u/s is dependent upon cooperation of the baby. Sometimes we just can't get a great view and may not be able to see everything we are looking for
But it can usually provide some reassurance to see that organs and body parts have formed properly
Maternal Serum Marker Screening
(Unrelated to any risks due to exposure there is a blood test that is routinely offered to all pregnant women)
MSAFP at about 16-18 weeks
Screening performed on a sample of your blood
Can provide an indication that a fetus may be at a higher or lower risk than the general population to have an ONTD, but it will not tell us for certain if there is a neural tube defect
Detects about 80-90% of ONTD's (so it can miss some)
Will also tell if fetus is at an increased risk above your age-related risk for a chromosome abnormality
Blood test can also look at other markers in the blood and determine if there may be an increased risk for two chromosomal abnormalities (for which you are not at an increased risk for based on your history of seizures and medications)
Discuss CF carrier screening
Psychosocial Considerations
Guilt over doing something that may cause birth defects
Anxiety because we don't know what to expect
Was this a planned pregnancy and is she excited to be pregnant or was this unexpected
Any other health concerns or circumstances that would make this a difficult pregnancy
Assess support system and coping strategies
Follow-up
Questions?
Schedule level II ultrasound
Lupron Facts
GnRH - agonist - mimicks GnRH, but is more potent
Considered category X drug (meaning benefits to women don't outweigh potential risk to fetus and it is contraindicated for women who could potentially get pregnant)
Not known if transfers to human milk, but structure makes this unlikely
No breast feeding data are available
Triggers release of LH and FSH (hormones that stimulate ovary in preparation for ovulation)
First taken then any LH and FSH stored in pituitary is released, but further production and release is blocked
When LH and FSH blocked, ovarian follicle and egg don't grow and less estrogen produced by ovary
Initial release of FSH and LH may cause one last cycle before suppressing ovarian activity
Should therefore use backup protection during the first month of treatment
Lupron is used in preparation for infertility treatments and when it is used in this fashion before conception there has been no increased risk of fetal anomalies reported to be associated with the infertility treatment.
References
Medications and Mother's Milk. 1999. Pharmasoft Medical Publishing.
Briggs, GG, Freeman, RK, and Yaffe, SJ. Drugs in Pregnancy and Lactation (5th edition). 1998. Williams and Wilkins.
Reprotox database
Warning Label that comes with the lupron injection
Stuart, Ira, and Fox. Human Physiology (4th edition). 1993. Wm. C. Brown Publishers.
Notes
The information in this outline was last updated in 2002.