Aktuelle Neurologie 2014; 41(08): 447-453
DOI: 10.1055/s-0034-1387786
Übersicht
© Georg Thieme Verlag KG Stuttgart · New York

Myasthenia gravis und Schwangerschaft

Myasthenia gravis and Pregnancy
J. Klehmet
1   Klinik für Neurologie, Charité – Universitätsmedizin Berlin
2   NeuroCure Clinical Research Center, Charité – Universitätsmedizin Berlin
,
S. Ohlraun
2   NeuroCure Clinical Research Center, Charité – Universitätsmedizin Berlin
,
A. Meisel
1   Klinik für Neurologie, Charité – Universitätsmedizin Berlin
2   NeuroCure Clinical Research Center, Charité – Universitätsmedizin Berlin
› Author Affiliations
Further Information

Publication History

Publication Date:
14 October 2014 (online)

Zusammenfassung

Fragen zur Familienplanung und Schwangerschaft sind von großer praktischer Bedeutung in der Behandlung von Myasthenie-Patientinnen, da die Erstmanifestation häufig in die entscheidende Lebensphase der Familienplanung fällt. Schwangerschaft, Geburt und Stillen sind zwar mit einigen Besonderheiten verbunden, stellen unter Beachtung entsprechender Vorsichtsmaßnahmen in der Regel aber kein nennenswert erhöhtes Risiko im Vergleich zur Normalpopulation dar. Im Idealfall sollte die Schwangerschaft bei Myasthenie-Patientinnen nach Absprache mit dem behandelnden Neurologen bzw. der behandelnden Neurologin erfolgen, sodass eine Remission vor Eintritt der Schwangerschaft erreicht werden kann. Pyridostigmin und Glukokortikosteroide (Prednison, Prednisolon, Methylprednisolon) sind sicher einsetzbare Standard-Therapeutika in der Schwangerschaft. Es wird angestrebt, eine bestehende Therapie mit Azathioprin vor einer Schwangerschaft umzustellen. Bei ungeplanter Schwangerschaft kann nach dem gegenwärtigen Kenntnisstand die Therapie mit Azathioprin und Cyclosporin A fortgeführt werden. Schwangerschaften unter Mycophenolat Mofetil, Methotrexat, sowie Tacrolimus müssen konsequent vermieden werden. Gegebenenfalls sollte eine Umstellung auf Glukokortikosteroide oder intravenöse Immunglobuline erfolgen. Intravenöse Immunglobuline oder Plasmapheresen werden bei Exazerbationen bzw. myasthener Krise auch in der Schwangerschaft eingesetzt. Fetale Missbildungen wie Arthrogryposis multiplex congenita oder das fetale Acetylcholin Rezeptor-Inaktivierungssyndrom (FARIS-Syndrom) sind sehr selten und können durch hochauflösende Ultraschalluntersuchungen frühzeitig erkannt werden. Die Myasthenia gravis an sich stellt keine Indikation für eine Sectio caesarea dar. Die Entbindung sollte jedoch in einem Zentrum mit kooperierender Geburtshilfe, Neonatologie und Neurologie durchgeführt werden, da das peripartale und perinatale Risiko erhöht und nicht vorhersagbar ist. Die neonatale Myasthenie kann bei einem Fünftel der Neugeborenen myasthener Mütter auftreten und wird mit Pyridostigmin oder bei schweren Verläufen mittels Plasmapherese behandelt. Beispielhaft werden typische Fallkonstellationen für die individuelle Beratung und Betreuung von Myasthenie-Patientinnen mit Kinderwunsch oder bereits eingetretener Schwangerschaft präsentiert.

Abstract

Family planning issues and pregnancy are frequent concerns in the medical care of patients with myasthenia gravis since disease onset often coincides with this time period on life. Pregnancy, delivery and breastfeeding represent in fact special situations in this group of patients; however, they are not associated with higher risks of complications compared to normal population. Pregnancy should be planned in consultation with the treating neurologist so that disease remission can be achieved before the patient gets pregnant. During pregnancy, pyridostigmine and glucocorticosteroids may be used. Treatment with azathioprine, methotrexate, mycophenolate mofetil, cyclosporine A as well as tacrolimus should be terminated and if necessary changed to glucocorticosteroids or intravenous immunoglobulins. Under certain circumstances, azathioprine as well as cyclosporine A may be continued. Severe exacerbations can be treated with intravenous immunoglobulins and plasma exchange. Fetal deformities such as arthrogryposis multiplex congenita or the fetal acetylcholine receptor inactivation syndrome (FARIS) are very rare conditions and can be recognized in early pregnancy by high-definition ultrasound. Myasthenia gravis is no indication for cesarean section. However, delivery should be accomplished in a centre with collaborating obstetrics, neonatology and neurology. Approximately 20% of infants born to myasthenic mothers develop neonatal myasthenia and will be treated with pyridostigmine and in severe cases with plasma exchange. Here we discuss typical case constellations providing a basis for medical care and individual counseling of myasthenia gravis patients, either already pregnant or presenting with questions related to family planning.

 
  • Literatur

  • 1 Klehmet J, Dudenhausen J, Meisel A. Course and treatment of myasthenia gravis during pregnancy. Nervenarzt 2010; 81: 956-962
  • 2 Batocchi AP, Majolini L, Evoli A et al. Course and treatment of myasthenia gravis during pregnancy. Neurology 1999; 52: 447-452
  • 3 Plauche WC. Myasthenia gravis in mothers and their newborns. Clin Obstet Gynecol 1991; 34: 82-99
  • 4 Djelmis J, Sostarko M, Mayer D et al. Myasthenia gravis in pregnancy: report on 69 cases. Eur J Obstet Gynecol Reprod Biol 2002; 104: 21-25
  • 5 Schroder A, Ellrichmann G, Chehab G et al. Rituximab in treatment for neuroimmunological disease. Nervenarzt 2009; 80: 155-160
  • 6 Hoff JM, Daltveit AK, Gilhus NE. Myasthenia gravis: consequences for pregnancy, delivery, and the newborn. Neurology 2003; 61: 1362-1366
  • 7 Niks EH, Verrips A, Semmekrot BA et al. A transient neonatal myasthenic syndrome with anti-musk antibodies. Neurology 2008; 70: 1215-1216
  • 8 O’carroll P, Bertorini TE, Jacob G et al. Transient neonatal myasthenia gravis in a baby born to a mother with new onset anti-Musk mediated myasthenia gravis. J Clin Neuromuscul Dis 2009; 11: 69-71
  • 9 Powell HR, Ekert H. Methotrexate-induced congenital malformations. Med J Aust 1971; 2: 1076-1077
  • 10 Barnes PR, Kanabar DJ, Brueton L et al. Recurrent congenital arthrogryposis leading to a diagnosis of myasthenia gravis in an initially asymptomatic mother. Neuromuscul Disord 1995; 5: 59-65
  • 11 Hall JG, Reed SD. Teratogens associated with congenital contractures in humans and in animals. Teratology 1982; 25: 173-191
  • 12 Moutard-Codou ML, Delleur MM, Dulac O et al. Severe neonatal myasthenia with arthrogryposis. Presse Med 1987; 16: 615-618
  • 13 Brueton LA, Huson SM, Cox PM et al. Asymptomatic maternal myasthenia as a cause of the Pena-Shokeir phenotype. Am J Med Genet 2000; 92: 1-6
  • 14 Riemersma S, Vincent A, Beeson D et al. Association of arthrogryposis multiplex congenita with maternal antibodies inhibiting fetal acetylcholine receptor function. J Clin Invest 1996; 98: 2358-2363
  • 15 Vincent A, Newland C, Brueton L et al. Arthrogryposis multiplex congenita with maternal autoantibodies specific for a fetal antigen. Lancet 1995; 346: 24-25
  • 16 Oskoui M, Jacobson L, Chung WK et al. Fetal acetylcholine receptor inactivation syndrome and maternal myasthenia gravis. Neurology 2008; 71: 2010-2012
  • 17 Licht C, Model P, Kribs A et al. Transient neonatal myasthenia gravis. Nervenarzt 2002; 73: 774-778
  • 18 Hoff JM, Daltveit AK, Gilhus NE. Myasthenia gravis in pregnancy and birth: identifying risk factors, optimising care. Eur J Neurol 2007; 14: 38-43
  • 19 Gurjar M, Jagia M. Successful management of pregnancy-aggravated myasthenic crisis after complete remission of the disease. Aust N Z J Obstet Gynaecol 2005; 45: 331-332
  • 20 Moskovitz DN, Bodian C, Chapman ML et al. The effect on the fetus of medications used to treat pregnant inflammatory bowel-disease patients. Am J Gastroenterol 2004; 99: 656-661
  • 21 Armenti VT, Radomski JS, Moritz MJ et al. Report from the National Transplantation Pregnancy Registry (NTPR): outcomes of pregnancy after transplantation. Clin Transpl 2002; 121-130
  • 22 Lamarque V, Leleu MF, Monka C et al. Analysis of 629 pregnancy outcomes in transplant recipients treated with Sandimmun. Transplant Proc 1997; 29: 2480
  • 23 Le RC, Coulomb A, Elefant E et al. Mycophenolate mofetil in pregnancy after renal transplantation: a case of major fetal malformations. Obstet Gynecol 2004; 103: 1091-1094
  • 24 Milunsky A, Graef JW, Gaynor Jr MF. Methotrexate-induced congenital malformations. J Pediatr 1968; 72: 790-795
  • 25 Paskulin GA, Gazzola Zen PR, de Camargo Pinto LL et al. Combined chemotherapy and teratogenicity. Birth Defects Res A Clin Mol Teratol 2005; 73: 634-637
  • 26 Paladini D, Vassallo M, D’Armiento MR et al. Prenatal detection of multiple fetal anomalies following inadvertent exposure to cyclophosphamide in the first trimester of pregnancy. Birth Defects Res A Clin Mol Teratol 2004; 70: 99-100
  • 27 Klink DT, van Elburg RM, Schreurs MW et al. Rituximab administration in third trimester of pregnancy suppresses neonatal B-cell development. Clin Dev Immunol 2008; 2008; 1-6
  • 28 Friedman DM, Llanos C, Izmirly PM et al. Evaluation of fetuses in a study of intravenous immunoglobulin as preventive therapy for congenital heart block: Results of a multicenter, prospective, open-label clinical trial. Arthritis Rheum 2010; 62: 1138-1146
  • 29 Lefvert AK, Osterman PO. Newborn infants to myasthenic mothers: a clinical study and an investigation of acetylcholine receptor antibodies in 17 children. Neurology 1983; 33: 133-138
  • 30 Rodriguez-Pinilla E, Martinez-Frias ML. Corticosteroids during pregnancy and oral clefts: a case-control study. Teratology 1998; 58: 2-5
  • 31 Gaudier FL, Santiago-Delpin E, Rivera J et al. Pregnancy after renal transplantation. Surg Gynecol Obstet 1988; 167: 533-543
  • 32 Alexander N, Rosenlöcher F, Stalder T et al. Impact of antenatal glucocorticoid exposure on endocrine stress reactivity in term-born children. J Clin Endocrinol Metab 2012; 97: 3538-3544
  • 33 Ostensen M, Brucato A, Carp H et al. Pregnancy and reproduction in autoimmune rheumatic diseases. Rheumatology (Oxford) 2011; 50: 657-664
  • 34 Janssen NM, Genta MS. The effects of immunosuppressive and anti-inflammatory medications on fertility, pregnancy, and lactation. Arch Intern Med 2000; 160: 610-619
  • 35 Bar OB, Hackman R, Einarson T et al. Pregnancy outcome after cyclosporine therapy during pregnancy: a meta-analysis. Transplantation 2001; 71: 1051-1055
  • 36 Armenti VT, Ahlswede KM, Ahlswede BA et al. National transplantation Pregnancy Registry-outcomes of 154 pregnancies in cyclosporine-treated female kidney transplant recipients. Transplantation 1994; 57: 502-506
  • 37 Kainz A, Harabacz I, Cowlrick IS et al. Analysis of 100 pregnancy outcomes in women treated systemically with tacrolimus. Transpl Int 2000; 13 (Suppl. 01) S299-S300
  • 38 Buckley LM, Bullaboy CA, Leichtman L et al. Multiple congenital anomalies associated with weekly low-dose methotrexate treatment of the mother. Arthritis Rheum 1997; 40: 971-973
  • 39 Donnenfeld AE, Pastuszak A, Noah JS et al. Methotrexate exposure prior to and during pregnancy. Teratology 1994; 49: 79-81
  • 40 Pergola PE, Kancharla A, Riley DJ. Kidney transplantation during the first trimester of pregnancy: immunosuppression with mycophenolate mofetil, tacrolimus, and prednisone. Transplantation 2001; 71: 994-997
  • 41 Schaefer C, Spielmann H, Vetter K. Immunmodulatoren und Therapie rheumatischer Erkrankungen. In: Schaefer C, Spielmann H, Vetter K. Hrsg Arzneiverordnung in Schwangerschaft und Stillzeit. 2006. Urban und Fischer; München Jena: 679
  • 42 Watson WJ, Katz VL, Bowes Jr WA. Plasmapheresis during pregnancy. Obstet Gynecol 1990; 76: 451-457
  • 43 Kaaja R, Julkunen H, Ammala P et al. Intravenous immunoglobulin treatment of pregnant patients with recurrent pregnancy losses associated with antiphospholipid antibodies. Acta Obstet Gynecol Scand 1993; 72: 63-66
  • 44 Polilli E, Parruti G, D’Arcangelo F et al. Preliminary evaluation of the safety and efficacy of standard intravenous immunoglobulins in pregnant women with primary cytomegalovirus infection. Clin Vaccine Immunol 2012; 19: 1991-1993
  • 45 Cohen BA, London RS, Goldstein PJ. Myasthenia gravis and preeclampsia. Obstet Gynecol 1976; 48 (Suppl. 01) 35S-37S
  • 46 Fraser D, Turner JW. Myasthenia Gravis and Pregnancy. Proc R Soc Med 1963; 56: 379-381
  • 47 Notarianni LJ, Oliver SE, Dobrocky P et al. Caffeine as a metabolic probe: a comparison of the metabolic ratios used to assess CYP1A2 activity. Br J Clin Pharmacol 1995; 39: 65-69