În concluzie, sintetizând toate aspectele discutate mai sus, prin prisma datelor ştiinţifice actuale privind scleroza multiplă (afecţiune pentru care în mod particular toate normele privind diagnosticul şi tratamentul au un caracter istoric, limitat în timp, datorită multelor aspecte necunoscute încă, dar care vor fi descifrate o dată cu progresul rapid al cunoaşterii ştiinţifice) putem afirma în acest moment următoarele principii de diagnostic şi tratament:
Diagnosticul pozitiv de scleroză multiplă se face în principal pe baza datelor clinice şi a aspectului IRM conform criteriilor stabilite de McDonald şi colab. si revizuite. Celelalte investigaţii paraclinice devin necesare doar dacă pe baza acestor date nu se poate stabili certitudinea de diagnostic şi pentru realizarea diagnosticului diferenţial.
Stabilirea diagnosticului de SM certă implică stabilirea formei clinice şi a gradului de invalidare prin folosirea unor scale de evaluare specifice (EDSS).
Tratamentul puseului de SM (recădere, recidivă) se face de elecţie cu doze mari de glucocorticoizi administrate i.v. pe termen scurt.
Este demonstrat faptul ca initierea cat mai rapida a terapiei imunomodulatoare (in stadiul de CIS) poate reduce dizabilitatea pe termen scurt si lung.
Toate cazurile de SMRR au indicaţie de tratament imunomodulator de lungă durată pe termen nelimitat.
SM este o boală cronică, pe toată durata vieţii şi nu este cunoscută în prezent nici o raţiune de întrerupere a unui astfel de tratament, o dată început; dacă un anumit tip de tratament modificator al evoluţiei nu este tolerat sau eşuează, trebuie să se recurgă la o altă terapie cunoscută din aceeaşi categorie.
Evoluţia pacienţilor trebuie să fie supravegheată clinic şi prin IRM. Modificările sau adăugirile la tratament trebuie începute înainte de pierderea ireversibilă a unei funcţii neurologice.
Cazurile de SMSP necesită tratament agresiv precoce. Tratamentul instituit tardiv la aceşti pacienţi (mai mulţi ani de la virajul formei RR spre SP) aduce beneficii clinice mult mai mici.
Nu este de aşteptat ca formele primar progresive de boală (SMPP) să răspundă semnificativ la un tratament modificator al evoluţiei bolii cunoscut în prezent.
Tratamentul simptomatic şi recuperator este tot atât de important ca şi tratamentul modificator al evoluţiei bolii din perspectiva ameliorării calităţii vieţii zilnice a pacientului şi familiei sale.
BIBLIOGRAFIE
Coyle PK, Hammad MA – Atlas of multiple sclerosis. Science Press, London 2003.
Compston A, Coles A. Multiple sclerosis. Lancet. 2008 372: 1502-1517.
Stamatoiu IC (sub red.) – Scleroză multiplă, Editura Medicală, Bucureşti, 1989.
Victor M, Ropper AH – Adams and Victor’s Principles of Neurology, 9-th edition, McGraw-Hill, New York, 2009.
McDonald WI et al – Recommended diagnostic criteria for multiple sclerosis: guidelines from the international panel on the diagnosis of multiple sclerosis. Ann Neurol, 2001; 50: 121-127.
Polman et al. Diagnostic Criteria for Multiple Sclerosis: 2005 Revisions to the “McDonald” Criteria. AnnNeurol. (2005) 58:840-846.
Barkhof et al. Comparison of MR imaging criteria at first presentation to predict conversion to clinically definite MS. Brain (1997) 120:2059-2069.
Tintoré et al. Isolated demyelinating syndromes: comparison of different imaging criteria to predictconversion to clinically definite MS. Am J Radiology (2000) 21:702-706.a
Miller D et al. Clinically isolated syndromes suggestive of multiple sclerosis, part I: natural history, pathogenesis, diagnosis, and prognosis. Lancet Neurol. 2005;4(5):281-8.
Miller D et al. Clinically isolated syndromes suggestive of multiple sclerosis, part 2: non-conventional MRI,recovery processes, and management. Lancet Neurol. 2005;4(6):341-8.
Korteweg T et al. MRI criteria for dissemination in space in patients with clinically isolated syndromes: a multicentre follow-up study. Lancet Neurol. 2006;5(3):221-7.
Freedman MS et al – International consensus statement on the use of disease-modifying agents in multiple sclerosis. Multiple Sclerosis, 2002; 8; 19-23.
Goodin DS et al – Disease modifying therapies in multiple sclerosis. Report of the Therapeutics and Technology Assessment Subcommitee of the American Academy of Neurology and the MS Council for Clinical Practice Guidelines. Neurology, 2002; 58: 169-178.
National Multiple Sclerosis Society (NMSS)– Disease management consensus statement, Treatments > Medications Used in MS, site accesibil pe Internet la www.nmss.org
Panitch H et al – Randomized, comparative study of interferon beta-1a treatment regimens in MS. The EVIDENCE Trial, Neurology, 2002; 59: 1496-1506.
PRISMS Study Group – Randomized double-blind placebocontroled study of interferon b-1a in relapsing-remitting multiple sclerosis. Lancet, 1998; 352: 1498-1504.
Samuels MA (edit.)– Manual of neurologic therapeutics, 7-th edition, Lippincott Williams & Wilkins, Philadelphia 2004.
Sharief MK – Dose and frequency of administration of interferon-b affect its efficacy in multiple sclerosis. Clin Drug Invest 2003; 23: 551-559.
Goodin DS et al. Assessment: The use of natalizumab (Tysabri) for the treatment of multiplesclerosis (an evidence-based review): Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. Neurology 2008;71;766-773
NICE technology appraisal guidance 127: Natalizumab for the treatment of adults with highly active relapsing–remitting multiple sclerosis. 2007
Multiple Sclerosis Therapy Consensus Group: Escalating immunotherapy of multiple sclerosis. New aspects and practical application. J Neurol (2004) 251 : 1329–1339
Multiple Sclerosis Therapy Consensus Group (MSTCG):Basic and escalating immunomodulatory treatments in multiple sclerosis: Current therapeutic recommendations. J Neurol (2008) 255:1449–1463
EMSP - European MS Platform 2003, 2005, 2008 - Basic and escalating immunomodulatory treatments in Multiple Sclerosis. Current therapeutic recommendations.
Comi G et al. Effect of glatiramer acetate on conversion to clinically definite multiple sclerosis in patients with clinically isolated syndrome (PreCISe study): a randomised, double-blind, placebo-controlled trial. Lancet. 2009;31;374(9700):1503-11.
Burks JS et al. Guidelines on use of anti-IFN-B antibody measurements in multiple sclerosis: report of an EFNS Task Force on IFN-B antibodies in multiple sclerosis. Eur J Neurol. 2007;14(6):e8-9
Rudick RA, Polman CH. Current approaches to the identification and management of breakthrough disease in patients with multiple sclerosis. Lancet Neurol. 2009;8(6):545-59
Centonze D et al. Early relapses after the first dose of natalizumab in active multiple sclerosis patients. Mult Scler. 2008.14(8):1137-8
Rinaldi F et al. Severe relapses after the first infusion of natalizumab in active relapsing-remitting multiple sclerosis. Mult Scler. 2009 Oct 15. [Epub ahead of print]
Iacobaeus E et al.Analysis of cerebrospinal fluid and cerebrospinal fluid cells from patients with multiple sclerosis for detection of JC virus DNA. Mult Scler. 2009;15(1):28-35
Chen Y et al.Asymptomatic reactivation of JC virus in patients treated with natalizumab. N Engl J Med. 2009;10;361(11):1067-74
Lindå H et al. Progressive multifocal leukoencephalopathy after natalizumab monotherapy. N Engl J Med. 2009;10;361(11):1081-7
Wenning W et al. Treatment of progressive multifocal leukoencephalopathy associated with natalizumab. N Engl J Med. 2009;10;361(11):1075-80
Boster Aet al. Intense immunosuppression in patients with rapidly worsening multiple sclerosis: treatment guidelines for the clinician. Lancet Neurol. 2008;7(2):173-83
L Kappos et al. Natalizumab treatment for multiple sclerosis: recommendations for patient selection and monitoring, Lancet Neurol2007;6,431–441
EMSP - European-wide Recommendations on Rehabilitation for People affected by Multiple Sclerosis. 2004. R.I.M.S. - Rehabilitation in Multiple Sclerosis