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Antiparkinsonian treatment in pregnancy
Author(s) -
De Mari Michele,
Zenzola Angelo,
Lamberti Paolo
Publication year - 2002
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.10040
Subject(s) - citation , library science , humanities , medicine , art , computer science
We read with interest the article by Shulman and colleagues in a 2000 issue of MovementDisorders. 1 In that article, one case of pregnancy in a patient with Parkinson’s disease (PD) on levodopa therapy was reported. After prospective and quantitative neurological examination of the patient, the authors concluded that pregnancy exacerbates PD and could have a longterm negative impact on the course of the illness. A few cases of pregnancy in parkinsonian women have been described; all of these patients were treated with levodopa but none demonstrated major drug teratogenity. 1–4 Moreover, dopamine agonist treatment during pregnancy of PD patients has been reported by Benito-Leon and associates 3 as a bromocriptine monotherapy; another patient described by Hagell and coworkers discontinued bromocriptine after 2 months of pregnancy. In neither case did bromocriptine treatment result in any teratogenity. Pergolide administration in parkinsonian women during pregnancy has not been reported previously. We describe a woman with PD treated with combined pergolide and levodopa therapy during pregnancy. A 36-year-old woman developed PD with progressive motor slowness in the left limbs at age 32 years in 1996. At the first examination, she presented a slight rigidity and bradykinesia to the left arm and leg and a mild hypomimia. There was no evidence of resting tremor. Hoehn and Yahr rating was 2. Evaluation for other causes of parkinsonism revealed no significant abnormalities. Family history for PD was not reported. Treatment with pergolide up to a dose of 1 mg three times daily resulted in partial improvement, and after 6 months levodopa was added at a dose of 200 mg per day, resulting in optimal control of her symptoms. After 2 years the patient complained of a predictable wearing-off period in the afternoon, demonstrated as slight bradykinesia, mild rigidity in lower limbs, and gait disturbances such as short steps and shuffling, mainly in her left leg. When the patient became pregnant at age 35 years, the dosage of pergolide and levodopa was continued throughout the pregnancy. During the pregnancy, all wearing-off phenomena disappeared and she had optimal control of motor symptoms throughout the day. She gave birth to a normal-term infant in July 2000 with Apgar scores of 9, by cesarean section, because of a podalic presentation. The child shows no evidence of congenital malformation and remains healthy at this time, 13 months of age, with normal development. During the puerperal period the end-of-dose wearing-off symptom reappeared and reached the same level as before pregnancy. To our knowledge, this is the first description of combined pergolide and levodopa treatment during pregnancy in a woman with PD. Except for one case of osteomalacia and another of spontaneous abortion, for which the cause is not well established, no major complications of pregnancy, nor any adverse effects on the fetus that could primarily be related to levodopa plus carbidopa or benserazide have been reported in the literature. 1–7 Studies of carbidopa–levodopa in laboratory animals demonstrated some increase in skeletal malformation but only with high doses, greater than 500 mg/kg/day. 6

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