Download Multiple Sclerosis Therapeutics, Third Edition by Jeffrey A. Cohen, Richard A. Rudick PDF

By Jeffrey A. Cohen, Richard A. Rudick

Since the booklet of the former version of this quantity, there was significant growth in a couple of components of a number of sclerosis (MS) learn. even if immunosuppressive remedies stay constructed and subtle, extra precise immunomodulatory treatments are surfacing as we examine extra approximately how the immune process works in wellbeing and fitness and disease.

Multiple Sclerosis Therapeutics, 3rd Edition

presents a complete overview of medical trial technique and healing modalities in MS. This version displays present knowing of the pathophysiology of the sickness and contains well known and rising remedies.

Topics include:

  • Biomarkers in MS
  • Pharmacogenomics
  • Emerging healing modalities resembling natalizumab, T-cell-based and B-cell-based remedies, cytokine/chemokine-based treatments, statins, and 4-aminopyridine
  • Neuroprotection
  • The use of OCT and MRI to lead illness therapy

Within the subsequent a number of years, we are going to start to become aware of the application and the restrictions of stem cells within the therapy of MS. it's most probably that the following variation of this text will comprise medical trial info that overview early makes an attempt at apprehensive approach regeneration in MS. until eventually that point happens, this quantity continues to be a necessary source for neurologists and someone interested by the therapy of MS.

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Extra info for Multiple Sclerosis Therapeutics, Third Edition

Sample text

A sizable number of studies support the validity of the MSFC, showing correlation with the EDSS (both cross-sectional correlation at one point in time and longitudinal correlation over time)87,92–95 and with disease stage93. The MSFC has been shown to correlate more strongly with T2-hyperintense lesion burden on cranial MRI and whole brain atrophy96–98 as compared with the EDSS. The clinical relevance of the MSFC was supported by its correlation with patient self-reported MS symptoms and health-related quality of life94,99.

Another 10–20% have benign disease, with mild intermittent neurological symptoms but minimal disease progression and disability, decades after the onset of symptoms. There may be some ‘drift’ in the severity of MS toward a more benign prognosis. Increased awareness of MS, increased recognition of the benefits of early treatment and widespread use of MRI scanning for patients with non-specific symptoms such as fatigue or numbness has undoubtedly led to many patients being diagnosed with MS who may have mild disease8.

E. not a pseudo-relapse). Although seemingly straightforward conceptually, relapses can be difficult to identify accurately in clinical trials. The relapse assessment process is triggered by the patient reporting new symptoms, and this requires contact with the patient, either at scheduled visits and phone calls, or by contact initiated by the patient. The frequency of patient reports will depend on the study visit frequency and the ease of access between visits, and these factors vary significantly between and even within studies.

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