
scenario is more complicated when we consider the medical
act and the principle of beneficence of seeking the patient
well-being. There is the fear of medical legal consequences
in this case, by action or omission, which in practice leads
to considering that nothing could be pharmacologically
prescribed in this clinical context. There is also the
neurophobia by the fear of a secondary headache, added
to the logical fear of potential harm to the fetus. This is
associated with the existence of few safe drugs or medicines
which safety is known but studies cannot be performed,
thus tables are based on case reports.
Also, we must remember that 2 to 7% of migraines in
pregnancy are "de novo" and it is necessary to think of
secondary headaches, and that 35% of pregnant patients
in the doctor's waiting room have secondary headache.
Neuroimaging procedures are essential in the ancillary
investigation of those patients, and tomography and
magnetic resonance bring a minimal risk for both pregnant
women and fetus – as long as an intravenous contrast
enhancement is not used.
Secondary headaches to be considered in pregnancy
are hypertensive syndromes associated with pregnancy:
eclampsia and preeclampsia; posterior reversible
encephalopathy; hemolysis, increased liver enzymes, and
low platelets syndrome (HELLP); reversible cerebral
vasoconstriction syndrome; pituitary apoplexy; venous
thrombosis; brain hemorrhage: aneurysmal or AVM; artery
dissection; idiopathic intracranial hypertension; and
meningitis.
And then, the authors described the treatment of
migraines in pregnancy, giving emphasis to non-
pharmacological management. As for drugs, in acute pain
not every medication can be taken, and this should be
taken into account by migraineurs before becoming
pregnant.
Further, the paper elegantly addresses the need to
prevent migraine chronification, and discusses that among
the modifiable factors are overweight, snoring, sleep apnea
and insomnia, excessive consumption of caffeine, high
frequency of headaches, frequent use of analgesics, other
associated pains, neck trauma, emotional disturbances, and
social, labour or affective changes.
In this review, products such as riboflavin and
magnesium are emphasized with level of evidence B. Topical
products like capsaicin with mint prepared with ethyl alcohol
solution and topic acetaminophen are interesting to be
prescribed to pregnant women. And here this review brought
a novelty to the physicians who treat their pregnant
migraineur patients.
The paper defines teratogenicity which is the structural
or functional defect in organogenesis, involving from 3rd
to 8th gestational weeks. The teratogenic action produced
by medicines varies along the timeline related to the different
periods of susceptibility to the injury. The risk of teratogenicity
is not known in more than 90 % of the drugs approved by
the FDA.
The prescription should balance or consider aspects
which are very easy to be considered, even though difficult
to be performed or to act. This is because no controlled
studies are available, and the use of drugs would not be
recommended.
Considering the risk and benefit includes to evaluate
the gestational age and teratogenic risk at this stage, the
effectiveness of the medication, the risk categories of this
drug, and the will of the pregnant to use medication, to
decide to bear the pain (which I do not agree particularly),
to take the risk of the drug, to face the possibility of the
route of administration, and to take the effects of pain on
the body and on pregnancy, and the adverse effects of the
available medicines.
There is not enough evidence to recommend a
specific protocol in the treatment of acute migraine in
any given situation. This absence obliges the physician
to make a decision in each case where the indication
does not necessarily correlate to the prescription (in this
situation I name it as the 'art of medicine with little
evidence').
Yet, the paper describes the options in acute migraine
during pregnancy considering the principles of beneficence
and nonmaleficence.
Acetaminophen - no established risk, mothers often
use in pregnancy.
Anti-inflammatories - can be used diclofenac (50
mg), ibuprofen (400mg), naproxen (500 - 1,000 mg),
piroxicam and indomethacin, which are categorized as risk
B. Aspirin in doses of 900 - 1,000 mg shown efficacy in
relief from migraine, and the risk is C. Avoid in the first
quarter and in the woman who plans to become pregnant
due to the possibility to prevent ovulation, implantation of
the egg, or abortion. It is not recommended to use cyclo-
oxygenase-2 inhibitors.
Triptans - a recent meta-analysis study concluded
that the use of sumatriptan in pregnancy does not show
increased risk of prematurity or birth malformations, and
this sporadic use in pregnancy is acceptable because of
low-risk.
Opioids - the risk is C, as the triptans, but opioids are
associated with numerous complications in both the fetus
MELHADO EM
72 Headache Medicine, v.7, n.3, p.71-73, Jul./Aug./Sep. 2016