Managing Disease-Modifying Therapies and Breakthrough Activity in Multiple Sclerosis Patients During the COVID-19

Sherif M Hamdy1, Maged Abdel-Naseer1, Hatem S Shehata1

  • 1Neurology Department, Faculty of Medicine, Cairo University, Cairo, Egypt.

Insights

Managing multiple sclerosis (MS) during the COVID-19 pandemic is challenging due to increased infection risks from disease-modifying therapies (DMTs). This review offers an evidence-based algorithm to balance DMT use against infection risks and potential MS disease activity.

Area of Science:

  • Neurology
  • Infectious Diseases
  • Immunology

Background:

  • The COVID-19 pandemic presents unique challenges for managing complex neurological disorders like multiple sclerosis (MS).
  • Patients with MS have a higher risk of infections due to immune system impairment and treatments like disease-modifying therapies (DMTs).
  • Current management strategies for MS during the pandemic lack consensus, particularly regarding the use of DMTs.

Purpose of the Study:

  • To review the evidence for using DMTs in MS patients during the COVID-19 pandemic.
  • To provide an algorithmic approach for managing MS patients, balancing DMT benefits against infection risks.
  • To outline strategies for managing MS breakthrough activity during the pandemic.

Main Methods:

  • Literature review analyzing evidence on DMT use in MS during the COVID-19 pandemic.
  • Development of an algorithmic approach for clinical decision-making regarding DMT continuation or cessation.
  • Guideline formulation for managing MS exacerbations and infections.

Main Results:

  • DMTs modulate the immune response, increasing susceptibility to infections, a critical concern during the COVID-19 pandemic.
  • An algorithmic approach helps optimize patient care by weighing the risks of infection against the potential for MS disease activation.
  • Strategies are proposed to manage breakthrough MS activity while considering the pandemic context.

Conclusions:

  • Careful consideration of DMTs is crucial for MS patients during the COVID-19 pandemic.
  • An algorithmic approach can guide clinicians in managing MS treatment amidst infection risks.
  • Proactive management of MS and infections is essential for patient well-being during global health crises.

Related Concept Videos

Chronic Obstructive Pulmonary Disease-V: Management01:29

Chronic Obstructive Pulmonary Disease-V: Management

Managing Chronic Obstructive Pulmonary Disease (COPD) involves a multifaceted approach to reduce symptoms, prevent exacerbations, improve overall health status, and slow disease progression. Key strategies include lifestyle modifications, pharmacotherapy, supportive therapies, and, in some cases, surgery. Here is an overview of the primary COPD management strategies:
Smoking Cessation
2.9K
Rheumatic Heart Disease III: Medical Management01:21

Rheumatic Heart Disease III: Medical Management

Rheumatic heart disease (RHD) management can be divided into two main strategies: prevention and long-term management.Primary PreventionPrimary prevention focuses on timely diagnosis and management of group A streptococcal pharyngitis to prevent acute rheumatic fever. The most widely used antibiotic for treating this condition is intramuscular benzathine penicillin G.Acute Rheumatic Fever TreatmentThe primary treatment goal for a patient diagnosed with acute rheumatic fever is to suppress the...
166
Therapeutic Drug Monitoring: Affecting Factors01:29

Therapeutic Drug Monitoring: Affecting Factors

Therapeutic Drug Monitoring (TDM) is the clinical practice of measuring specific drug levels in a patient's blood or body tissues to manage and optimize therapy. TDM is crucial for drugs with narrow therapeutic windows, like warfarin and phenytoin, where incorrect doses can lead to treatment failure or severe side effects. This monitoring ensures the dosage administered is within a safe and effective range. The factors affecting therapeutic drug monitoring include:Patient-Specific Factors:a.
107
Myasthenia Gravis: Overview and Treatment01:20

Myasthenia Gravis: Overview and Treatment

Myasthenia gravis is a neuromuscular transmission disorder characterized by weakness and increased fatigability of skeletal muscles. It is an autoimmune disease affecting approximately one in 2000 people, where antibodies against the α1 subunit of nicotinic acetylcholine receptors are produced.
These antibodies interfere with the function of the nicotinic receptors in three ways: by binding to the receptor and disrupting acetylcholine binding; by causing cross-linking of receptors which...
2.5K
Cystic Fibrosis: Management01:24

Cystic Fibrosis: Management

Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
Sinus disease and chronic...
335