Up to 60% - 70% of women with preexisting migraine report improvement or cessation of migraine during pregnancy, particularly women with a history of menstrual migraine. If no improvement is seen towards the end of the first trimester, migraine is likely to continue throughout pregnancy and postpartum (
5). In addition, a large majority of pregnant women experience hyperemesis gravidarum, defined as vomiting in pregnancy that may lead to weight loss, dehydration, acidosis from starvation, alkalosis from loss of hydrochloric acid in vomitus, and hypokalemia (
6,
7). Migraine and hyperemesis gravidarum have a similar predisposition so the sufferer might have the comorbid risk (
6). Although our case had a history of migrainous headaches, only migrainous features of photophobia and phonophobia had occurred in each vertiginous attack. Because nausea and vomiting had persisted for only half a day, hyperemesis gravidarum was unlikely.
In a Taiwanese case-series study, vertigo was prone to occur in pregnant women with advanced maternal age (over 34 years old) and primipara, during the third trimester of pregnancy, and 33% of these vertigos were attributable to basilar-type migraine; however, acoustic neuroma was also possible (
8). In our patient, during the second vertiginous attack, she experienced nausea, vomiting, phonophobia and photophobia rather than headache or other neurological focal signs. The rightward horizontal beating gaze nystagmus implicated predominance of right vestibular function. Normal head thrust test and normal pure tone audiometry excluded vestibular neuritis, sudden deafness or Ménière’s disease; hence, central vertigo was highly suspected. However, brain magnetic resonance imaging/angiography demonstrated unremarkable findings, thus acute infarction, neoplasm or other demyelization changes were excluded. Our patient, had a history of migraines. So far, she has experienced vertiginous attacks eight times. During each vertiginous attack, migrainous features of photophobia and phonophobia occurred at the same time, which matched the diagnostic criteria (i), (ii), (iii)-(b) and (iv). Hence, she was diagnosed with vestibular migraine.
Although vestibular migraine is self-limited, teratogenic risk should be avoided when we treat vertigo in pregnant women. Our patient had been treated with diphenhydramine, diphenidol, betahistine, methylcobalamin and prochlorperazine maleate before becoming aware of her pregnancy. Her pregnancy was indeed an accident. The class of antihistamine diphenhydramine was B, and those of antiemetic prochlorperazine and antivertigo diphenidol were C; yet that of betahistine was not available; fortunately, class D or X drugs were not prescribed for the attack, and no teratogenic effect was found. In fact, most drugs are not licensed for use during pregnancy and breastfeeding and should only be considered if the potential benefits to the woman and fetus outweigh the potential risks. Thus, our patient did not take any medications for the third attack because of lactation.
Pregnancy is expected to occur together with vertigo in females of the childbearing age. Pregnancy test is recommended when menses is out of schedule; even if sterility has been confirmed. Any anti-vertiginous medication with teratogenic risk should be avoided if pregnancy is not completely excluded; antihistamine diphenhydramine (FDA class B) are recommended first for symptomatic control. Antiemetic prochlorperazine (FDA class C) or antivertiginous diphenidol (FDA class C) was considered only after the FDA class B drug fails to control the symptom. Furthermore, if such patients present migrainous headaches, FDA class B drugs including acetaminophen, diclofenac, ibuprofen, naproxen, meperidine and metoclopramide are recommended, yet class X drugs including ergotamine and dihydroergotamine should be avoided (
5).