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[Therapeutic strategies against myasthenia gravis].

Nihon rinsho. Japanese journal of clinical medicine (2013-06-20)
Kimiaki Utsugisawa, Yuriko Nagane
ZUSAMMENFASSUNG

Many patients with myasthenia gravis (MG) still find it difficult to maintain daily activities due to chronic residual fatigability and long-term side effects of oral corticosteroids, since full remission is not common. Our analysis demonstrated that disease severity, oral corticosteroids, and depressive state are the major factors negatively associated with QOL, and that QOL of MM status patients taking < or = 5 mg prednisolne/day is identically good as that seen in CSR and is a target of treatment. In order to achieve early MM or better status with prednisolne < or = 5 mg/day, we advocate the early aggressive treatment strategy that can achieve early improvement by performing an aggressive therapy using combined treatment with plasmapheresis and high-dose intravenous methylprednisolone and then maintain an improved status using low-dose oral corticosteroids and calcineurin inhibitors.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Prednisolon, ≥99%
Supelco
Prednisolon, Pharmaceutical Secondary Standard; Certified Reference Material
Prednisolon für die Peakidentifizierung, European Pharmacopoeia (EP) Reference Standard
Supelco
Prednisolon, VETRANAL®, analytical standard
Prednisolon, European Pharmacopoeia (EP) Reference Standard
Prednisolon für die Systemeignung, European Pharmacopoeia (EP) Reference Standard