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. 2014 Jul;21(7):948-55.
doi: 10.1111/ene.12439. Epub 2014 Apr 9.

Total drug treatment and comorbidity in myasthenia gravis: a population-based cohort study

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Total drug treatment and comorbidity in myasthenia gravis: a population-based cohort study

J B Andersen et al. Eur J Neurol. 2014 Jul.

Abstract

Background and purpose: Comorbidity in myasthenia gravis (MG) is important for diagnosis, treatment and prognosis. Disease complexity was assessed by examining total drug treatment, immune therapy and comorbidity in a complete national MG cohort.

Methods: All recipients of the MG-specific drug pyridostigmine 2004-2010 registered in the compulsory Norwegian Prescription Database who met the inclusion criteria were included. The pyridostigmine group was compared with the general Norwegian population.

Results: Myasthenia gravis patients received co-medication more often than the controls for nearly all groups of medication, including insulins (95% confidence interval 2.0-3.7), thyroid therapy (1.7-2.5), antidepressants (1.3-1.7), anti-infectives (1.2-1.4), lipid-modifying agents (1.1-1.4) and immunomodulating agents (6.8-8.8).

Conclusions: Myasthenia gravis patients are more often treated with non-MG prescription drugs than controls, reflecting frequent co-medication and comorbidity.

Keywords: comorbidity; drug therapy; myasthenia gravis.

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Figures

Figure 1
Figure 1
Selection of the MG study cohort. *Recipients of pyridostigmine who did not meet the inclusion criteria during the study period.
Figure 2
Figure 2
(a) Mean number of new groups of immunomodulating agents used in MG patients (%) below and above 50 years of age after MG diagnosis per year, 2004–2010. Open bars, patients <50 years; hatched bars, patients ≥50 years. (b) Mean number of new groups of immunomodulating agents used in MG men and women (%) after MG diagnosis per year, 2004–2010. Open bars, men; hatched bars, women.

References

    1. Querol L, Illa I. Myasthenia gravis and the neuromuscular junction. Curr Opin Neurol. 2013;26:459–465. - PubMed
    1. Owe JF, Daltveit AK, Gilhus NE. Causes of death among patients with myasthenia gravis in Norway between 1951 and 2001. J Neurol Neurosurg Psychiatry. 2006;77:203–207. - PMC - PubMed
    1. Gilhus NE, Owe JF, Hoff JM, et al. Myasthenia gravis: a review of available treatment approaches. Autoimmune Dis. 2011;2011:847393. - PMC - PubMed
    1. WHO Collaborating Centre for Drug Statistics Methodology. Oslo, Norway: 2005. Norwegian Institute of Public Health Guidelines for ATC classification and DDD assignment.
    1. Skeie GO, Apostolski S, Evoli A, et al. Guidelines for treatment of autoimmune neuromuscular transmission disorders. Eur J Neurol. 2010;17:893–902. - PubMed

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