2019
DOI: 10.1016/j.ncl.2018.09.003
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Management of Myasthenia Gravis in Pregnancy

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Cited by 22 publications
(54 citation statements)
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“…Corticosteroid treatment is very effective in most MG patients and can be an option for treatment in pregnant women where immunosuppression therapy is needed to treat MG that is getting worse during pregnancy. The use of high doses of corticosteroids may be associated with premature rupture of membranes (Waters, 2019). The drug commonly used is prednisone at a dose of 1 mg / kg per day, given as a one-time dose (Chaudhry, Vignarajah, & Koren, 2012).…”
Section: Abstrakmentioning
confidence: 99%
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“…Corticosteroid treatment is very effective in most MG patients and can be an option for treatment in pregnant women where immunosuppression therapy is needed to treat MG that is getting worse during pregnancy. The use of high doses of corticosteroids may be associated with premature rupture of membranes (Waters, 2019). The drug commonly used is prednisone at a dose of 1 mg / kg per day, given as a one-time dose (Chaudhry, Vignarajah, & Koren, 2012).…”
Section: Abstrakmentioning
confidence: 99%
“…Because of the serious side effects of longterm use of corticosteroids, steroid-sparing immunosuppression drugs have been developed, including azathioprine, cyclophosphamide, cyclosporine, methotrexated and and new mycophenolate mofetil (Chaudhry et al, 2012). The use of immunosuppressants should be avoided during pregnancy because of its teratogenic effects (Waters, 2019). Safety of the use of intravenous immunoglobulin in MG patients who are pregnant until now there has been no report.…”
Section: Abstrakmentioning
confidence: 99%
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“…MG occurs twice as frequently in women than men and typically affects women of child-bearing age [3]. MG does not affect fertility, and pregnancy does not appear to have a long-term adverse impact on the course of the disease; therefore, pregnancy can be expected in women with gMG.…”
Section: Introductionmentioning
confidence: 99%
“…43, 4, 5]. С другой -плод также является объектом аутоиммунной агрессии со стороны организма матери вследствие трансплацентарной передачи материнских АТ с риском развития транзиторной неонатальной миастении (ТНМ) у 10-35% новорожденных [6][7][8][9][10]. Показано, что пассаж материнских АТ через фетоплацентарный барьер происходит во всех случаях и их титр в крови новорожденного сопоставим с титром материнских АТ [11].…”
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