Risk perception in natalizumab-treated multiple sclerosis patients and their neurologists

Mult Scler. 2010 Dec;16(12):1507-12. doi: 10.1177/1352458510379819. Epub 2010 Sep 8.

Abstract

Background: Natalizumab is associated with the potentially life-threatening side-effect progressive multifocal leukoencephalopathy (PML). Little is known about patients' and physicians' risk estimates and attitudes towards natalizumab treatment.

Methods: Consecutive natalizumab-treated patients (n = 69) and neurologists (n = 66) in two centres and cooperating private practices received an evidence-based three-page information leaflet about natalizumab-associated PML and an evaluation sheet.

Results: After reading the information, patients were significantly more likely than physicians to intend continuation of natalizumab treatment and willing to accept higher risks of PML: 49% of physicians would stop treatment at a PML risk of 2:10,000 or lower, while only 17% of patients would do so (p < 0.001). This difference could not be explained by risk calculation abilities or lack of understanding. Both groups overestimated natalizumab treatment effects.

Conclusion: Patients had a significantly worse perception of multiple sclerosis as a malignant disease. We conclude that patients were willing to accept a higher risk of PML than neurologists. Coherent with their perception of risks and benefits, patients were also more willing to continue treatment. Open information about treatment-related risks is appreciated and might support shared decision making.

MeSH terms

  • Adult
  • Antibodies, Monoclonal / adverse effects*
  • Antibodies, Monoclonal, Humanized
  • Female
  • Health Knowledge, Attitudes, Practice*
  • Humans
  • Immunologic Factors / adverse effects*
  • Leukoencephalopathy, Progressive Multifocal / chemically induced
  • Male
  • Middle Aged
  • Multiple Sclerosis / drug therapy*
  • Natalizumab
  • Patients*
  • Perception
  • Physician-Patient Relations
  • Physicians*
  • Risk

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Immunologic Factors
  • Natalizumab