Hostname: page-component-586b7cd67f-g8jcs Total loading time: 0 Render date: 2024-11-26T02:24:22.910Z Has data issue: false hasContentIssue false

IGIV in Neurology — Evidence and Recommendations

Published online by Cambridge University Press:  05 August 2019

Vera Bril*
Affiliation:
Division of Neurology, The Toronto Hospital
Kent Allenby
Affiliation:
Bayer Corporation Westhaven USA
Gyl Midroni
Affiliation:
Division of Neurology, St Michael's Hospital, University of Toronto
Paul W. O'Connor
Affiliation:
Division of Neurology, St Michael's Hospital, University of Toronto
Jiri Vajsar
Affiliation:
Division of Neurology, HSC Research Institute, Hospital for Sick Children, Toronto, University of Toronto
*
Reprint requests to: Dr. Vera Bril, EN 11-209, General division, The Toronto Hospital, 200 Elizabeth Street, Toronto, Ontario, Canada M5G 2C4
Rights & Permissions [Opens in a new window]

Abstract:

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Objective:

To summarize the evidence for neurologic uses of immunoglobulin, intravenous (IGIV) in light of present-day clinical usage. This summary guided the development of practice recommendations for the effective and efficient use of IGIV in Neurology.

Methods:

MEDLINE was searched to identify pertinent English-language review articles and original reports (n = 231) on the use of IGIV in neurology (excluding editorials, letters, and comments) published before March 1998. Evidence on alternative therapies was only included as compared to IGIV. The relevant original reports and review articles and older classic studies (n = 92) were synthesized into an information foundation. Extracted data included laboratory and clinical findings, objective measures, and clinical impressions. Clinical recommendations were based on evidence quality, graded by study design, clinical experiences of IGIV in Neurology Advisory Board members, and the conditions of IGIV use in therapy.

Results and Conclusions:

In neurology, many disorders are poorly understood, and the mechanisms behind beneficial regimens even less so. As a result, it is fairly common for best-practice decisions to rest on weaker evidence. The usefulness of IGIV in neurology can be described by a “combined score” based on evidence quality and strength of impact. Combined scores ranged from A+ (strongly recommended) to C (recommended as a last resort). The following clinical recommendations are made: IGIV is: strongly recommended for the treatment of Guillain-Barré syndrome (A+); favorably recommended for the treatment of chronic inflammatory demyelinating polyradiculoneuropathy, dermatomyositis, and multifocal motor neuropathy (A); recommended as a second resort for the treatment of multiple scerosis and myasthenia gravis (B); and recommended as a last resort for the treatment of polymyositis, inclusion-body myositis, intractable epilepsies, and stiff-man syndrome (C).

Résumé:

Résumé:But:

Nous faisons un sommaire des données en faveur de l'utilisation d'immunoglobuline intraveineuse (IGIV) en neurologie à la lumière de son utilisation actuelle en clinique. Ce sommaire a inspiré le développement de recommandations pour l'utilisation efficace de l'IGIV en neurologie.

Méthodes:

Nous avons procédé à une recherche dans MEDLINE pour identifier les articles de revue pertinents en langue anglaise et les présentations originales (n = 231) sur l'utilisation de l'IGIV en neurologie (à l'exclusion des éditoriaux, des lettres à l'éditeur et des commentaires) publiés avant mars 1998. Les données sur les traitements alternatifs ont été incluses seulement pour les comparer à l'IGIV. Les présentations originales pertinentes, les articles de revue et les études classiques plus anciennes (n = 92) ont été résumés en une fiche d'information. Les données ainsi extraites incluaient des observations cliniques et biochimiques, des mesures objectives et des impressions cliniques. Les recommandations cliniques étaient basées sur la qualité des observations, classées par plan d'étude, les expériences cliniques des membres du conseil aviseur sur l'IGIV en neurologie et les conditions d'utilisation de l'IGIV en clinique.

Résultats et conclusions:

En neurologie, plusieurs pathologies sont mal comprises et les mécanismes par lesquels certaines thérapies procurent un bénéfice le sont encore moins. Il est donc assez fréquent que la meilleure décision clinique repose sur des données faibles. L'utilité de l'IGIV en neurologie peut être présentée sous la forme d'une "cote combinée" basée sur la qualité des observations et la force de l'impact. Les cotes combinées variaient de A= (fortement recommandée) à C (recommandée en dernier recours). Nous faisons les recommandations suivantes: l'IVIG est recommandée dans le traitement de la polyradiculoneuropathie démyélinisante inflammatoire chronique, la dermatomyosite et la neuropathie motrice multifocale (A); recommandée en deuxième recours pour le traitement de la sclérose en plaques et la myasthénie grave (B); et recommandée en dernier recours pour le traitement de la polymyosite, la myosite à corps d'inclusion, les épilepsies résistantes au traitement et le syndrome de l'homme raide (C).

Type
Neurological Practice
Copyright
Copyright © The Canadian Journal of Neurological 1999

References

1. Pirofsky, B, Kinzey, DM. Intravenous immune globulins: a review of their uses in selected immunodeficiency and autoimmune disease. Drugs 1992; 43: 614.Google Scholar
2. Infectious Diseases and Immunization Committee, Ottawa, Ontario, Canada. Intravenous immune globulin use in children. Can Med Assoc J 1992; 146: 121124.Google Scholar
3. Rivet, C. Canadian Blood Agency/Agence Canadienne du sang: Utilization management of albumin and intravenous immune globulin. Canadian Apheresis Group Bulletin 1995: 78.Google Scholar
4. Van der Meché, FG, Schmitz, PI, for the Dutch Guillain-Barré Study Group. A randomized trial comparing intravenous immune globulin and plasma exchange in Guillain-Barré syndrome. N Engl J Med 1992; 326: 11231129.Google Scholar
5. Ropper, AH. The Guillain-Barré syndrome. N Engl J Med 1992; 326: 11301136.Google Scholar
6. Van der Meché, FG. The Guillain-Barré syndrome. In: McLeod, JG, ed. Inflammatory Neuropathies. BailliPre’s Clin Neurol 1994; 3: 7394.Google Scholar
7. Bril, V, Ilse, WK, Pearce, R, et al. Pilot trial of immunoglobulin versus plasma exchange in patients with Guillain-Barré syndrome. Neurology 1996; 46: 100103.Google Scholar
8. Plasma Exchange/Sandoglobulin Guillain-Barré Syndrome Trial Group. Randomized trial of plasma exchange, intravenous immunoglobulin, and combined treatments in Guillain-Barré syndrome Lancet 1997; 349(9047): 225230.Google Scholar
9. Corbanese, U, Martinuzzi, A, Possamai, C, et al. Guillain-Barré syndrome with associated thrombocytopenia: prompt response to combined corticosteroid and immunoglobulin treatment. Neuromuscul Disord 1998; 8: 5052.Google Scholar
10. Imai, N, Miyata, K, Terayama, Y, Ishihara, N. [A case of Guillain Barré syndrome treated with plasma exchange and intravenous high-dose immune globulin]. Rinsho Shinkeigaku 1997; 37: 520522.Google Scholar
11. Enders, U, Toyka, KV, Hartung, HP, Gold, R. Failure of intravenous immunoglobulin (IVIg) therapy in experimental autoimmune neuritis (EAN) of the Lewis rat. J Neuroimmunol 1997; 76: 112116.Google Scholar
12. Reisin, RC, Pociecha, J, Rodriguez, E, et al. Severe Guillain-Barré syndrome in childhood treated with human immune globulin. Pediatr Neurol 1996 May; 14: 308312.Google Scholar
13. Shahar, E, Shorer, Z, Roifman, CM, et al. Immune globulins are effective in severe pediatric Guillain-Barré syndrome. Pediatr Neurol 1997; 16: 3236.Google Scholar
14. Zafeiriou, DI, Kontopoulos, EE, Katzos, GS, Gombakis, NP, Kanakoudi, FG. Single dose immunoglobulin therapy for childhood Guillain-Barré syndrome. Brain Dev 1997; 19: 323325.Google Scholar
15. Kanra, G, Ozon, A, Vajsar, J, et al. Intravenous immunoglobulin treatment in children with Guillain-Barré syndrome. Eur J Pediatr 1997; 1: 712.Google Scholar
16. Van Doorn, PA, Vermeulen, M, Brand, A, Mulder, PG, Busch, HF. Intravenous immunoglobulin treatment in patients with chronic inflammatory demyelinating polyneuropathy. Clinical and laboratory characteristics associated with improvement. Arch Neurol 1991; 48: 217220.Google Scholar
17. Van Doorn, PA, Brand, A, Strengers, PF, Meulstee, J, Vermeulen, M. High-dose intravenous immunoglobulin treatment in chronic inflammatory demyelinating polyneuropathy. A double-blind placebo controlled cross-over study. Neurology 1990; 40: 209212.Google Scholar
18. Vermeulen, M, Van Doorn, PA, Brand, A, et al. Intravenous immunoglobulin treatment in patients with chronic inflammatory demyelinating polyneuropathy: a double blind, placebo controlled study. J Neurol Neurosurg Psychiatry 1993; 56: 3639.Google Scholar
19. Dyck, PJ, Litchy, WJ, Kratz, KM, et al. A plasma exchange versus immune globulin infusion trial in chronic inflammatory demyeli-nating polyradiculoneuropathy. Arm Neurol 1994; 36: 838845.Google Scholar
20. Hahn, AF, Bolton, CF, Zochodne, D, Feasby, TE. Intravenous immunoglobulin treatment in chronic inflammatory demyelinat-ing polyneuropathy: a double-blind, placebo-controled, crossover study. Brain 1996; 119(Pt 4): 10671077.Google Scholar
21. Van Dijk, GW, Notermans, NC, Franssen, H, Oey, PL, Wokke, JH. Response to intravenous immunoglobulin treatment in chronic inflammatory demyelinating polyneuropathy with only sensory symptoms. J Neurol 1996; 243: 318322.Google Scholar
22. Simmons, Z, Wald, JJ, Albers, JW. Chronic inflammatory demyelinating polyradiculoneuropathy in children: II. Long-term follow-up, with comparison to adults. Muscle Nerve 1997; 20: 15691575.Google Scholar
23. Simmons, Z, Wald, JJ, Albers, JW. Chronic inflammatory demyelinating polyradiculoneuropathy in children: I. Presentation, elec-trodiagnostic studies, and initial clinical course, with comparison to adults. Muscle Nerve 1997; 20: 10081015.Google Scholar
24. Thomas, PK, Claus, D, Jaspert, A, et al. Focal upper limb demyelinating neuropathy. Brain 1996; 119(Pt 3): 765774.Google Scholar
25. Choudhary, PP, Hughes, RA. Long-term treatment of chronic inflammatory demyelinating polyradiculoneuropathy with plasma exchange or intravenous immunoglobulin. QJM 1995; 88: 493502.Google Scholar
26. Grehl, H, Jaspert, A, Claus, D, Neundorfer, B. Immunglobulintherapie chronisch-entzundlicher Neuropathien [Immunoglobulin therapy of chronic inflammatory neuropathies]. Nervenarzt 1996; 67: 10031010.Google Scholar
27. Mariette, X, Chastang, C, Clavelou, P, et al., for The IgM-associated Polyneuropathy Study Group. A randomized clinical trial comparing interferon-alpha and intravenous immunoglobulin in polyneuropathy associated with monoclonal IgM. J Neurol Neurosurg Psychiatry 1997; 63: 2834.Google Scholar
28. Gorson, KC, Allam, G, Ropper, AH. Chronic inflammatory demyelinating polyneuropathy: clinical features and response to treatment in 67 consecutive patients with and without a monoclonal gammopathy. Neurology 1997; 48: 321328.Google Scholar
29. Chaudhry, V, Corse, AM, Cornblath, DR, et al. Multifocal motor neuropathy: response to human immune globulin [see comments]. Ann Neurol 1993; 33: 237242.Google Scholar
30. Azulay, JP, Blin, O, Pouget, J, et al. Intravenous immunoglobulin treatment in patients with motor neuron syndromes associated with anti-GM1antibodies: a double-blind, placebo-controlled study. Neurology 1994; 44(3Pt1): 429432.Google Scholar
31. Comi, G, Nemni, R, Amadio, S, Galardi, G, Leocani, L. Intravenous immunoglobulin treatment in multifocal motor neuropathy and other chronic immune-mediated neuropathies. Mult Scler 1997; 3: 9397.Google Scholar
32. Stangel, M, Hartung, HP, Marx, P, Gold, R. Intravenous immunoglobulin treatment of neurological autoimmune diseases. J Neurol Sci 1998; 153: 203214.Google Scholar
33. Dalakas, MC. Intravenous immune globulin therapy for neurologic diseases. Ann Intern Med 1997; 126: 721730.Google Scholar
34. Azulay, JP, Rihet, P, Pouget, J, et al. Long term follow up of multifocal motor neuropathy with conduction block under treatment. J Neurol Neurosurg Psychiatry 1997; 62: 391394.Google Scholar
35. Van den Berg, LH, Franssen, H, Wokke, JH. The long-term effect of intravenous immunoglobulin treatment in multifocal motor neuropathy. Brain 1998; 121( Pt 3): 421428.Google Scholar
36. Meucci, N, Cappellari, A, Barbieri, S, Scarlato, G, Nobile-Orazio, E. Long term effect of intravenous immunoglobulins and oral cyclophosphamide in multifocal motor neuropathy. J Neurol Neurosurg Psychiatry 1997; 63: 765769.Google Scholar
37. Ferrero, B, Durelli, L, Cavallo, R, et al. The mechanism of action of high-dose immunoglobulin G. Ann NY Acad Sci 1993; 681: 563566.Google Scholar
38. Arsura, EL. Experience with intravenous immunoglobulin in myasthenia gravis. Clin Immunol Immunopathol 1989; 53: S170–SI79.Google Scholar
39. Edan, G, Landgraf, F. Experience with intravenous immunoglobulin in myasthenia gravis: a review. J Neurol Neurosurg Psychiatry 1994; 57: 5556.Google Scholar
40. Uchiyama, M, Yukinovu, 1, Takaya, N, et al. High-dose gammaglobulin therapy of generalized myasthenia gravis. Ann NY Acad Sci 1987; 505: 868871.Google Scholar
41. Grob, D, Arsura, EL, Brunner, NG, Namba, T. The course of myasthenia gravis and therapies affecting outcome. Arm NY Acad Sci 1987; 505: 472499.Google Scholar
42. Jongen, JL, Van Doorn, PA, Van der Meché, FG. High-dose intravenous immunoglobulin therapy for myasthenia gravis. J Neurol 1998; 245: 2631.Google Scholar
43. Van der Meché, FG, Van Doorn, PA. The current place of high-dose immunoglobulins in the treatment of neuromuscular disorders. Muscle Nerve 1997; 20: 136147.Google Scholar
44. Tatay, J, Diez-Tejedor, E, Frank, A, et al. [Association of plasma-pheresis and high doses of intravenous immunoglobulins in the treatment of myasthenia gravis]. Rev Neurol 1997; 25: 14021406.Google Scholar
45. Gajdos, P, Chevret, S, Clair, B, Tranchant, C, Chastang, C, for the Myasthenia Gravis Clinical Study Group. Clinical trial of plasma exchange and high-dose intravenous immunoglobulin in myas- thenia gravis. Ann Neurol 1997; 41: 789796.Google Scholar
46. Bassan, H, Muhlbaur, B, Tomer, A, Spirer, Z. High-dose intravenous immunoglobulin in transient neonatal myasthenia gravis. Pediatr Neurol 1998; 18: 181183.Google Scholar
47. Herrmann, DN, Carney, PR, Wald, JJ. Juvenile myasthenia gravis: treatment with immune globulin and thymectomy. Pediatr Neurol 1998; 18: 6366.Google Scholar
48. Amato, AA, Cornman, EW, Kissel, JT. Treatment of stiff-person syndrome with intravenous immunoglobulin. Neurology 1994; 44: 16521654.Google Scholar
49. Karlson, EW, Sudarsky, L, Ruderman, E, et al. Treatment of stiff-person syndrome with intravenous immune globulin. Arthritis Rheum 1994; 37: 915918.Google Scholar
50. Barker, RA, Marsden, CD. Successful treatment of stiff-person syndrome with intravenous immunoglobulin. J Neurol Neurosurg Psychiatry 1997; 62(letter): 426427.Google Scholar
51. Lepidi, H, Frances, V, Figarella-Branger, D, et al. Local expression of cytokines in neuropathology. Appl Neurobiol 1998; 24: 7379.Google Scholar
52. Jolles, S, Hughes, J, Whittaker, S. Dermatological uses of high-dose intravenous immunoglobulin. Arch Dermatol 1998; 134: 8086.Google Scholar
53. Heckmatt, J, Saunders, C, Peters, AM, et al. Cyclosporin in juvenile dermatomyositis. Lancet 1989; 1(8646): 10631066.Google Scholar
54. Lueck, CJ, Trend, P, Swash, M. Cyclosporin in the management of polymyositis and dermatomyositis. J Neurol 1991; 54: 10071008.Google Scholar
55. Miller, LC, Sisson, BA, Tucker, LB, Denardo, BA, Schaller, JG. Methotrexate treatment of recalcitrant childhood dermatomyositis. Arthritis Rheum 1992; 35: 11431149.Google Scholar
56. Miller, FW, Leitman, SF, Cronin, ME, et al. Controlled trial of plasma exchange and leukpaheresis in polymyositis and dermatomyositis. N Engl J Med 1992; 326: 13801384.Google Scholar
57. Olson, NY, Lindsley, CB. Adjunctive use of hydroxychloroquine in childhood dermatomyositis. J Rheumatol 1989; 16: 15451547.Google Scholar
58. Roifman, CM, Schaffer, FM, Wachsmuth, SE, Murphy, G, Gelfand, EW. Reversal of chronic polymyositis following intravenous immune serum globulin therapy. JAMA 1987; 258: 513515.Google Scholar
59. Cherin, P, Herson, S, Wechsler, B, et al. Efficacy of intravenous gammaglobulin therapy in chronic refractory polymyositis and der-matomyositis: an open study with 20 adult patients. Am J Med 1991; 91: 162168.Google Scholar
60. Cherin, P, Piette, JC, Wechsler, B, et al. Intravenous gamma globulin as first line therapy in polymyositis and dermatomyositis: an open study in 11 adult patients. J Rheum 1994; 21: 10921097.Google Scholar
61. Barohn, RJ. The therapeutic dilemma of inclusion body myositis. Neurology 1997; 48: 567568.Google Scholar
62. Van der Meulen, MF, Hoogendijk, JE, Jansen, GH, Veldman, H, Wokke, JH. Absence of characteristic features in two patients with inclusion body myositis. J Neurol Neurosurg Psychiatry 1998; 64(3): 396398.Google Scholar
63. Horvath, R, Fu, K, Johns, T, et al. Characterization of the mitochondrial DNA abnormalities in the skeletal muscle of patients with inclusion body myositis. J Neuropathol Exp Neurol 1998; 57(5): 396403.Google Scholar
64. Sussman, GL, Pruzanski, W. The role of intravenous infusions of gamma globulin in the therapy of polymyositis and dermato-myositis. J Rheum 1994; 21: 990992.Google Scholar
65. Dalakas, MC, Illia, I, Dambrosia, J, et al. A controlled trial of high dose intravenous immune globulin infusions as treatment for der-matomyositis. N Engl J Med 1993; 329: 19932000.Google Scholar
66. Lang, BA, Laxer, RM, Murphy, G, Silverman, ED, Roifman, CM. Treatment of dermatomyositis with intravenous gammaglobulin. Am J Med 1991; 91: 169172.Google Scholar
67. Collet, E, Dalac, S, Maerens, B, et al. Juvenile dermatomyositis: treatment with intravenous gammaglobulin. Br J Dermatol 1994; 130: 231234.Google Scholar
68. Sansome, A, Dubowitz, V. Intravenous immunoglobulin in juvenile dermatomyositis-four year review of nine cases. Arch Dis Child 1995; 72: 2528.Google Scholar
69. Tsai, MJ, Lai, CC, Lin, SC, et al. Intravenous immunoglobulin therapy in juvenile dermatomyositis. Chung Hua Min Kuo Hsiao Erh Ko I Hsueh Hui Tsa Chih 1997; 38: 111115.Google Scholar
70. Dalakas, MC, Sonies, B, Dambrosia, J, et al. Treatment of inclusion body myositis with IVIg: a double-blind, placebo-controlled study. Neurology 1997; 48: 712716.Google Scholar
71. Rotherfelder, U, Neu, I, Pelka, R. Therapy for multiple sclerosis with immunoglobulin G. Munch Med Wochenschr 1982; 124: 7478.Google Scholar
72. Soukop, W, Tschabitscher, H. Gamma globulin therapy in multiple sclerosis. Theoretical considerations and initial clinical experience with 7S immunoglobulins in MS therapy. Wien Med Wochenschr 1986; 136: 477480.Google Scholar
73. Schuller, E, Govaerts, A. First results of immunotherapy with immunoglobulin G in multiple sclerosis patients. Eur Neurol 1983; 22: 205212.Google Scholar
74. Van Engelen, BG, Hommes, OR, Pinckers, A, et al. Improved vision after intravenous immunoglobulin in stable demyelinating optic neuritis. Arm Neurol 1992; 32: 834835.Google Scholar
75. Noseworthy, JH, Rodriguez, M, An, KN, et al. IVIG treatment in multiple sclerosis: pilot study results and design of placebo-controlled, double-blind clinical trial. Arm Neurol 1994; A(abstr): 325(P266).Google Scholar
76. Achiron, A, Pras, E, Gilad, R, et al. Open controlled therapeutic trial of high-dose intravenous immunoglobulins in relapsing-remitting multiple sclerosis. Arch Neurol 1992; 49: 12331236.Google Scholar
77. Achiron, A, Gilad, R, Margalit, R, et al. Intravenous gammaglobulin treatment in multiple sclerosis and experimental autoimmune diseases: delineation of usage and mode of action. J Neurol Neurosurg Psychiatry 1994; 57(Suppl.): 5761.Google Scholar
78. Fazekas, F, Deisenhammer, F, Strasser-Fuchs, S, Nahler, G, Mamoli, B, for the Austrian Immunoglobulin in Multiple Sclerosis Study Group. Randomized placebo-controlled trial of monthly intravenous immunoglobulin therapy in relapsing-remitting multiple sclerosis. Lancet 1997; 349(9052): 589593.Google Scholar
79. Fazekas, F, Deisenhammer, F, Strasser-Fuchs, S, Nahler, G, Mamoli, B. Treatment effects of monthly intravenous immunoglobulin on patients with relapsing-remitting multiple sclerosis: further analyses of the Austrian Immunoglobulin in MS study. Mult Scler 1997; 3: 137141.Google Scholar
80. Sorensen, PS, Wanscher, B, Schreiber, K, et al. A double-blind, cross-over trial of intravenous immunoglobulin G in multiple sclerosis: preliminary results. Mult Scler 1997; 3: 145148.Google Scholar
81. Achiron, A, Gabbay, U, Gilad, R, et al. Intravenous immunoglobulin treatment in multiple sclerosis. Effect on relapses. Neurology 1998; 50: 398402.Google Scholar
82. Paty, DW, Li, DKB, for the UBC MS/MRI Study Group and IFNB Multiple Sclerosis Study Group. Interferon beta-Ib is effective in relapsing-remitting multiple sclerosis. II. MRI analysis results of a multicenter, randomized, double-blind, placebo-controlled trial. Neurology 1993; 43: 662667.Google Scholar
83. Achiron, A, Barak, Y, Goren, M, et al. Intravenous immunoglobulin in multiple sclerosis: clinical and neuroradiologic results and implications for possible mechanisms of action. Clin Exp Immunol 1996; 104(Suppl.-1): 6770.Google Scholar
84. Francis, GS, Freedman, MS, Antel, JP. Failure of intravenous immunoglobulin to arrest progression of multiple sclerosis: a clinical and MRI based study. Mult Scler 1997; 3: 370376.Google Scholar
85. Sorensen, PS, Wanscher, B, Jensen, CV, et al. Intravenous immunoglobulin G reduces MRI activity in relapsing multiple sclerosis. Neurology 1998; 50(5): 12731281.Google Scholar
86. Van Engelen, BG, Renier, WO, Weemaes, CM, Gabreels, FJ, Meinardi, H. Immunoglobulin treatment in epilepsy, a review of the literature. Epilepsy Res 1994; 19: 181190.Google Scholar
87. Van Engelen, BG, Renier, WO, Weemaes, CM, et al. High-dose intravenous immunoglobulin treatment in cryptogenic West and Lennox-Gastaut syndrome; an add-on study. Eur J Pediatr 1994; 153: 762769.Google Scholar
88. Van Rijckevorsel-Harmant, K, Delire, M, Schmitz-Moorman, W, Wieser, HG. Treatment of refractory epilepsy with intravenous immunoglobulins. Results of the first double-blind/dose finding clinical study. Int J Clin Lab Res 1994; 24: 162166.Google Scholar
89. Hart, YM, Cortez, M, Andermann, F, et al. Medical treatment of Rasmussen’s syndrome (chronic encephalitis and epilepsy): effect of high-dose steroids or immunoglobulins in 19 patients [see comments]. Neurology 1994; 44: 10301036.Google Scholar
90. Fayad, MN, Choueiri, R, Mikati, M. Landau-Kleffner syndrome: consistent response to repeated intravenous gamma-globulin doses: a case report. Epilepsia 1997; 38: 489494.Google Scholar
91. Lagae, LG, Silberstein, J, Gillis, PL, Casaer, PJ. Successful use of intravenous immunoglobulins in Landau-Kleffner syndrome. Pediatr Neurol 1998; 18: 165168.Google Scholar
92. Roifman, C (chair), Balter, M, Blanchette, V, et al., for The Consensus Working Group. Present and future uses of IVIG. McLean Hunter Healthcare (newsletter) 1997.Google Scholar