Myasthenia gravis medical therapy: Difference between revisions
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# Azathioprine: [[Azathioprine]], a [[purine]] analogue which inhibits the [[Nucleic acid|nucleic acids]] synthesis, can cause improvement in about 90 percent of myasthenia gravis patients but the onset of this effect takes at least 6 to 12 month.(13-14-15-16 chronic) [[Azathioprine]] can cause [[macrocytosis]] (increased [[MCV]]) and [[Malignancy|malignancies]] such as [[Non hodgkin lymphoma|non-hodgkin lymphoma]]. (19-20 chronic) | # Azathioprine: [[Azathioprine]], a [[purine]] analogue which inhibits the [[Nucleic acid|nucleic acids]] synthesis, can cause improvement in about 90 percent of myasthenia gravis patients but the onset of this effect takes at least 6 to 12 month.(13-14-15-16 chronic) [[Azathioprine]] can cause [[macrocytosis]] (increased [[MCV]]) and [[Malignancy|malignancies]] such as [[Non hodgkin lymphoma|non-hodgkin lymphoma]]. (19-20 chronic) | ||
# Mycophenolate: [[Mycophenolate]] mofetil, a [[purine]] synthesis blocker in [[Lymphocyte|lymphocytes]], is proven to be effective in reducing the [[Symptom|symptoms]] of [[Myasthenia gravis|MG]] patients and their need to [[glucocorticoids]].(25-26) | # Mycophenolate: [[Mycophenolate]] mofetil, a [[purine]] synthesis blocker in [[Lymphocyte|lymphocytes]], is proven to be effective in reducing the [[Symptom|symptoms]] of [[Myasthenia gravis|MG]] patients and their need to [[glucocorticoids]].(25-26) | ||
# Cyclosporine: [[Cyclosporine]], an immunomodulatory agent which blocks the production of [[Interleukin 2|interleukin-2]] and inhibits the function of [[T helper cell|T helper cells]], can cause improvement in about 90 percent of [[Myasthenia gravis|MG]] patients after 1 to 2 months of start but the maximum effect will appear after 7 months.(32-33-34 chronic) This drug can cause [[tremor]], [[nausea]], [[Myalgia|myalgias]], [[gingival hyperplasia]], [[hypertrichosis]] and [[Malignancy|malignancies]] such as [[squamous cell skin cancer]] and [[lymphoma]].(34) | # Cyclosporine: [[Cyclosporine]], an immunomodulatory agent which blocks the production of [[Interleukin 2|interleukin-2]] and inhibits the function of [[T helper cell|T helper cells]], can cause improvement in about 90 percent of [[Myasthenia gravis|MG]] patients after 1 to 2 months of start but the maximum effect will appear after 7 months.(32-33-34 chronic) This drug can cause [[nephrotoxicity]] (37), [[tremor]], [[nausea]], [[Myalgia|myalgias]], [[gingival hyperplasia]], [[hypertrichosis]] and [[Malignancy|malignancies]] such as [[squamous cell skin cancer]] and [[lymphoma]].(34) | ||
# Tacrolimus | # Tacrolimus: [[Tacrolimus]], an immunosuppressive macrolid can significantly reduce the requirement to [[prednisolone]] and [[Myasthenia gravis|MG]] [[Symptom|symptoms]] in almost 67 to 87 percent of patients with less [[nephrotoxicity]] than [[cyclosporine]].(37-38-40 ta44 chronic) the side effects of this drug include [[hyperglycemia]], [[hypomagnesemia]], [[Paresthesia|paresthesias]] and [[tremor]].(45) | ||
# Rituximab | # Rituximab: [[Rituximab]], a [[Monoclonal antibodies|monoclonal antibody]] against [[B cell]] membrane marker [[CD20]] can be used in refractory myasthenia gravis. This drug is also effective in patients with anti [[MuSK]] antibody.(46-47-48-49-50 chronic) | ||
# Methotrexate | # Methotrexate: [[Methotrexate]] is an [[Immunosuppressive drug|immunosuppressant]] agent which suggested to be effective as a second line [[Immunosuppressive drug|immunosuppressant]] for [[Myasthenia gravis|MG]] patients.(51-52) | ||
# Etanercept | # Etanercept: | ||
# Cyclophosphamide | # Cyclophosphamide | ||
Revision as of 14:35, 21 June 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Medical Therapy
The mainstays of medical therapy for myasthenia gravis are:
Symptomatic treatments
An oral anticholinesterase like pyridostigmine is usually the first drug in MG patients.(5) these drugs can reduce the degradation of Ach in the synaptic cleft.(7) limbs and bulbar muscles respond very well to these drugs but ocular symptoms including diplopia are resistance to these medications.(8) (manabe az treatment)
Chronic immunomodulating treatments
- glucocorticoids: There are many studies supporting the beneficial effect of glucocorticoids like oral prednisone and pulsed intravenous (IV) methylprednisolone in MG patients. This group of drugs can improve the symptoms in almost 50 percent of patients.(6,7,8,11 chronic) the side effects of these drug are: Skin thinning and purpura(13), Cushingoid appearance and weight gain(4), cataracts and glaucoma(7), ischemic heart disease and heart failure(31), gastritis, ulcer formation, and gastrointestinal bleeding(48-49), menstrual irregularities in women and low fertility in both men and women(66-67) and psychiatric and cognitive symptoms(71).(manabe az avareze korton)
- immunosuppressive drugs
- Azathioprine: Azathioprine, a purine analogue which inhibits the nucleic acids synthesis, can cause improvement in about 90 percent of myasthenia gravis patients but the onset of this effect takes at least 6 to 12 month.(13-14-15-16 chronic) Azathioprine can cause macrocytosis (increased MCV) and malignancies such as non-hodgkin lymphoma. (19-20 chronic)
- Mycophenolate: Mycophenolate mofetil, a purine synthesis blocker in lymphocytes, is proven to be effective in reducing the symptoms of MG patients and their need to glucocorticoids.(25-26)
- Cyclosporine: Cyclosporine, an immunomodulatory agent which blocks the production of interleukin-2 and inhibits the function of T helper cells, can cause improvement in about 90 percent of MG patients after 1 to 2 months of start but the maximum effect will appear after 7 months.(32-33-34 chronic) This drug can cause nephrotoxicity (37), tremor, nausea, myalgias, gingival hyperplasia, hypertrichosis and malignancies such as squamous cell skin cancer and lymphoma.(34)
- Tacrolimus: Tacrolimus, an immunosuppressive macrolid can significantly reduce the requirement to prednisolone and MG symptoms in almost 67 to 87 percent of patients with less nephrotoxicity than cyclosporine.(37-38-40 ta44 chronic) the side effects of this drug include hyperglycemia, hypomagnesemia, paresthesias and tremor.(45)
- Rituximab: Rituximab, a monoclonal antibody against B cell membrane marker CD20 can be used in refractory myasthenia gravis. This drug is also effective in patients with anti MuSK antibody.(46-47-48-49-50 chronic)
- Methotrexate: Methotrexate is an immunosuppressant agent which suggested to be effective as a second line immunosuppressant for MG patients.(51-52)
- Etanercept:
- Cyclophosphamide
Rapid immunomodulating treatments
- plasmapheresis
- intravenous immune globulin