2005, Number 5
<< Back Next >>
Rev Mex Neuroci 2005; 6 (5)
Landry-Guillain-Barré-Strohl syndrome. A series in a reference hospital
Monroy GJ, Núñez OL
Language: Spanish
References: 84
Page: 372-383
PDF size: 101.98 Kb.
ABSTRACT
Objective. To reflect the experience with Guillain-Barré-Strohl syndrome in the Neurology Service of the Centro Médico Nacional 20 de Noviembre (CMN), in a four years period. We analyzed the general, clinical, paraclinical, therapeutic and prognostic characteristics, as well as the outcome. 25 clinical records of patients with final diagnosis of Guillain Barré attended the last four years in the Service of Neurology of the CMN were reviewed. The hospitalization due to GB represents 1.00-3.71% from the total; 18 (72%) were men and sevent (28%) women, with ages between 15-76 years with average of 44.92 years. There were 13 patients (52%) with antecedents of respiratory infections within the previous 1-8 weeks. The time from the beginning of GB to the arrival to the CMN was an average of 14.40 days with an interval of 3-65 days. Of 15 refered patients, 11 arrived within the therapeutic window (the first two weeks) (73.33%). The average of stay in Intensive Care Unit was 26.57 days with an interval of 7-61, and the stay in the service of Neurology was of 3-40 days with an average of 11.88. The initial symptoms of the patients were distal weakness of lower extremities (28%) and distal weakness in the upper limbs (20%); the main signs were arreflexia (72%) and hyporreflexia (28%), with predominance of a symmetrical upper paresia (27.27%), and affection of facial muscles in 28%. Six patients (24%) needed mechanical ventilation during 10-79 days (average of 32.83). 48% of patients presented dysautonomia, mainly severe arterial hypertension and tachicardia. On the other hand, cerebrospinal fluid analysis showed albuminocytologic dissociation in 80%; the electrophysiologic studies showed a mixed mild axonal damage and moderate demyelization in 28% of the cases. Sequelae after six months were hiporreflexia (51%) and dysestesias (24%). The most utilized treatment were intravenous inmunoglobulin and plasma exchange in 24% and 20% respectively. A linear correlation between the presence of tree or more risk factors and a greater need of hospital stay was found.
REFERENCES
Dana I, et. al. Guillain Barré syndrome. Am Fam Physician 2004; 69: 2405-10.
Pascuzzi RM. Peripheral neuropathies in clinical practice. M Clin N Am 2003; 87: 3.
Ho TW, et al. Guillain Barré syndrome. Curr Opin Neurol 1999; 12(4): 389-94.
Ho TW, et al. Patterns of recovery in the Guillain Barré syndromes. Neurology 1997; 48(3): 695-700.
S. Anne J, et al. Guillain Barré syndrome. Adolesc Med 2002; 13: 487-94.
Bonduelle M. Guillain Barré syndrome. Arch Neurol 1998; 55(11): 1483-4.
Fulgham J. Guillain Barré syndrome. Crit Care Clin 1997; 13(1).
Ropper A. Guillain-Barré Syndrome. FA Davis Company. 1st. Edition; 1991.
Tellería A. Síndrome de Guillain-Barré. Rev Neurol 2002; 34: 954-66.
Winer J. Treatment of Guillain Barré syndrome. QJM 2002; 95(11): 717-21.
Carol A, et al. A review of the management of Guillain Barré syndrome in a regional neurological rehabilitation unit. Int J Reh Res 2003; 16: 297-302.
Jacobs BC, et al. The spectrum of antecedent infections in Guillain Barré syndrome: A case-control study. Neurology 1998; 51: 4.
Emilia-Romagna Study group on clinical and epidemiological problems in neurology. A prospective study on the incidence and prognosis of Guillain-Barré syndrome in Emilia-Romagna region, Italy (1992-1993). Neurology 1997; 48(1).
Hahn A. Guillain Barré syndrome. Lancet 1998; 352: 635-41.
Govoni V. Epidemiology of the Guillain Barré syndrome. Curr Opin Neurol 2001; 14: 606-13.
Chio A, et al. Guillain Barré syndrome. A prospective, population-based incidence and outcome survey. Neurology 2003; 60(7): 1146-50.
Green D, et al. Mild Guillain Barré syndrome. Arch Neurol 2001; 58(7): 1098-1101.
Van Koningsveld R, et al. Infections and course of mild forms of Guillain Barré syndrome. Neurology 2002; 58: 4.
Fletcher D, et al. Long term outcome in patients with Guillain Barré syndrome requiring mechanical ventilation. Neurology 2000; 54(12): 2311-15.
Lawn N, et al. Fatal Guillain Barré syndrome. Neurology 1998; 50(4): A242.
Lawn N, et al. Fatal Guillain Barré syndrome. Neurology 1999; 52(3): 635-8.
Low P. Autonomic neurophaties. Curr Opin Neurol 1998; 11(5): 531-7.
Low P. Autonomic neuropathies. Curr Opin Neurol 2002; 15: 606-9.
Abutaher Y, et al. Cardiac arrhythmias in patients with severe Guillain Barré syndrome. Neurology 1999; 52(6) Supp 2.
Hartug HP, et al. Drains the roots: a new treatment for Guillain Barré syndrome? Neurology 2001; 57(5).
Sulton L. A multidisciplinary care approach to Guillain Barré syndrome. Dim Crit Care Nursing 2001; 20(1): 16-22.
Visser LH, et al. Prognostic factors of Guillain Barré syndrome after immunoglobulin or plasma exchange. Neurology 1999; 53(3): 598-604.
Yuki N, et al. Minimal number of plasma exchanges need to reduce immunoglobulin in Guillain Barré syndrome. Neurology 1998; 51(3): 875-7.
Tsang R. The relationship of Campylobacter jejuni infection and the development of Guillain Barré syndrome. Curr Opin Inf Dis 2002; 15: 221-8.
Van Doorn PA, et al. Treatment of inmune neuropathies. Curr Opin Neurol 2002; 15: 623-31.
Van Doorn PA. Immunotherapy for Guillain Barré syndrome. Lanc Neur 2004; 3(2).
Berciano J. Acute motor conduction block neuropathy: another Guillain Barré syndrome variant. Neurology 2004; 62(6).
Bernsen RAJAM, et al. Residual physical outcome and daily living 3 to 6 years after Guillain Barré syndrome. Neurology 1999; 53(2).
Bril V, et al. Pilot trial of immunoglobulin versus plasma exchange in patients with Guillain Barré syndrome. Neurology 1996; 46(1): 100-3.
Chandra P, et al. Gabapentin for the treatment of pain in Guillain Barré syndrome: a double bild, placebo-controlled, crossover study. Anest Analg 2002; 95(6): 1719-23.
Chio A, et al. A prospective, population-based study of long term outcome of Guillain Barré syndrome in Piemonte and Valle d’Aosta, Italy. Neurology 1999; 56(6): A130-A131.
Combarros O, et al. Taste loss as an initial symptom of Guillain Barré syndrome. Neurology 1996; 47(6): 1604-5.
Delaney Y, et al. Bilateral crocodile tears in a patient with Guillain Barré syndrome. J Neuro-Opftalmol 2002; 22: 113-15.
Donofrio P. Autonomic disorders. Neurologist 2001; 7: 220-33.
Flachenecker P, et al. Eyeball pressure testing in the evaluation of serious bradyarrithmias in Guillain Barré syndrome. Neurology 1996; 47(1): 102-8.
Gordon P, et al. Early electrodiagnostic findings in Guillain Barré syndrome. Arch Neurol 2001; 58: 913-17.
Hadden RDM. Preceding infections, immune factors, and outcome in Guillain Barré syndrome. Neurology 2001; 56(6).
Hahn A. Intravenous immunoglobulin treatment in peripheral nerve disorders-indications, mechanisms of action and side effects. Curr Opin Neurol 2000; 13: 575-82.
Hahn A. The challenge of respiratory dysfunction in Guillain Barré syndrome. Arch Neurol 2001; 58(6): 871-2.
Haider NR, et al. Rehabilitation in Miller Fisher variant of Guillain Barré syndrome. Phys Med Reh 1998; 77(2): 177-8.
Hartung HP, et al. Acute immunoinflamatory neuropathy: update on Guillain Barré syndrome. Curr Opin Neurol 2002; 13: 371-7.
Henderson RD, et al. The morbidity of Guillain Barré syndrome admitted to the intensive care unit. Neurology 2003; 60(1): 17-21.
Hoffman O, et al. SIADH as the first symptom of Guillain Barré syndrome. Neurology 1999; 53(6): 1365.
Hughes RAC, et al. Practice parameter: immunotherapy for Guillain Barré syndrome: report of the quality standars subcommitte of the american academy of neurology. Neurology 2003; 61(6).
Hughes R, et al. Systematic review of corticosteroid treatment for Guillain Barré syndrome. Neurology 1999; 52(2): A127-A128.
Kuwabara S, et al. Two patterns of clinical recovery in Guillain Barré syndrome with IgG anti-GM1 antibody. Neurology 1998; 51(6): 1656-60.
LaGanke C, et al. Does sensory Guillain Barré syndrome exist? Neurology 1998; 50(4): A142-A143.
Lawn N, et al. Anticipating mechanical ventilation in Guillain Barré syndrome. Neurology 1999; 52(6): A512-A513.
Lawn N, et al. Anticipating mechanical ventilation in Guillain Barré syndrome. Arch Neurol 2001; 58(6): 893-8.
Levin K. Variants and mimics of Guillain Barré syndrome. Neurologist 2004; 10: 61-74.
Linenbaum Y. Treatment approaches for Guillain Barré syndrome and chronic inflammatory demyelinating polyrradiculoneuropathy. N Clin 2001; 19(1).
Lisak R. Liver function in Guillain Barré syndrome. Neurology 1996; 47(6): 1606.
Meythaler J. Rehabilitation outcomes of patients who developed Guillain Barré syndrome. Phys Med Reh 1997; 76(5): 411-19.
Mori M. Clinical features and prognosis of Miller Fisher syndrome. Neurology 2001; 56(8).
Mori M. Chronic inflammatory demyelinating polyneuropathy presenting with features of GBS. Neurology 2002; 58(6).
Moulin DE, et al. Pain in Guillain Barré syndrome. Neurology 1997; 48(7): 328-31.
Mukesh T, et al. Carbamazepine for pain management in Guillain Barré syndrome patients in the intensive care unit. Crit Care Med 2000; 28(3): 655-8.
Nagaoka U, et al. Cranial nerve enhancement on three-dimensional MRI in Miller Fisher syndrome. Neurology 1996; 47(6): 1601-2.
Nishino S, et al. CSF hypocretin levels in Guillain Barré syndrome and other inflammatory neuropathies. Neurology 2003; 61(6).
Oh S, et al. Sensory Guillain Barré syndrome. Neurology 2001; 56(1).
Oomes PG, et al. Liver function disturbances in Guillain Barré syndrome: a prospective longitudinal study in 100 patients. Neurology 1996; 46(1): 96-100.
Pritchard BM, et al. A randomized controlled trial of recombinant interferon-beta 1a in Guillain Barré syndrome. Neurology 2003; 61: 1282-4.
Rana S, et al. Intravenous immunoglobulins versus plasmapheresis in older patients with Guillain Barré syndrome. J Am Ger Soc 1999; 47(11).
Samdani A, et al. Bilateral facial paralysis. Physical Med Reh 1997; 76(2): 170.
Sanders G. A case of Guillain Barré syndrome presenting as ataxia. Am J Em Med 2004; 22(2).
Sater R. The use of intravenous immunoglobulin for neurologic diseases. Neurology 1998; 51(6).
Sater R, et al. Treatment of Guillain Barré syndrome with intravenous immunoglobulin. Neurology 1998; 51(1): S9-S15.
Shahar E. Outcome of severe Guillain Barré syndrome in children: comparison between untreated cases versus gamma globulin therapy. Clin Neurophar 2003; 26(2): 84-7.
Sharief M, et al. IV immunoglobulin reduces circulating proinflammatory cytokines in Guillain Barré syndrome. Neurology 1999; 52(9): 1833-8.
Sharshar T, et al. Early predictors of mechanical ventilation in Guillain Barré syndrome. Crit Care Med 2003; 31: 278-83.
Society of critical care medicine. Predicting the duration of mechanical ventilation in Guillain Barré syndrome: a new index based on respiratory function tests. Crit Care Med 1999; 27(1S): 158A.
Sususki K, et al. Acute faciel diplegia and hyperreflexia: A Guillain Barré syndrome variant. Neurology 2004; 62(5).
Van Koningsveld R, et al. Changes in referral pattern and its effect on outcome in patients with Guillain Barré syndrome. Neurology 2001; 56: 564-6.
Wollinsky K, et al. CSF filtration is an effective treatment of Guillain Barré syndrome. Neurology 2001; 57(5).
Yee T, et al. Acute sensory neuropathy: A sensory form of Guillain Barré Syndrome? J Clin Neuromusc Dis 2001; 2: 135-8.
Yuki N, et al. Ataxic Guillain Barré syndrome with anti-GQ1b antibody: relation to Miller Fisher Syndrome. Neurology 2000; 54(9): 1851-3.
Yuki N. Axonal Guillain Barré syndrome subtypes: do we need more splinting? Neurology 2003; 61(5).
Yuki N, et al. Guillain Barré syndrome presenting with loss of taste. Neurology 2002; 58(9).
Yuki N. Infectious origins of, and molecular mimicry in Guillain Barré and Fisher syndromes. Lan Inf Dis 2001; 1(1).