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Myositis in H1N1 Infection Compounds to Myasthenic Crisis
Jayantee Kalita1, Sarvesh K Chaudhary1, Prakash C Pandey1
1Department of Neurology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Abstract:
Infection is an important trigger of myasthenic crisis (MC), and those infections manifest with pneumonia and muscle involvement may result in more frequent MC. We report two myasthenia gravis (MG) patients with H1N1 infection, and highlight the reasons for deterioration. Two patients with MG had H1N1 infection. The diagnosis of MG was confirmed by neostigmine, repetitive nerve stimulation, and anti-acetylcholine receptor antibody tests. H1N1 was confirmed by nucleic acid detection study, and myositis by creatinine kinase. The patient with pneumonia and myositis had MC needing mechanical ventilation for 10 days, and the other patient without myositis did not have MC. They were treated with oseltamivir 75 mg twice daily for 5 days, and the patients with MC received ceftriaxone intravenously. Both the patients were on prednisolone and azathioprine, and none received prior H1N1 vaccination. The lady with MC with myositis was discharged on day 27 in wheelchair bound state, and the other one patient without myositis or MC was discharged on 6th day with full recovery. These patients highlight the need for evaluation for myositis along with pneumonia in the MG patients with H1N1 infection. Vaccination in MG patients on immunosuppression may be useful.
Insights
Infections like H1N1 can trigger myasthenic crisis (MC) in myasthenia gravis (MG) patients, especially with pneumonia and myositis. Prompt evaluation for muscle involvement is crucial for managing MG patients during H1N1 infection.
Area of Science:
- Neurology
- Infectious Diseases
- Immunology
Background:
- Infection is a known precipitant of myasthenic crisis (MC) in myasthenia gravis (MG).
- Pneumonia and concurrent muscle involvement may exacerbate MC frequency and severity in MG patients.
- Influenza A (H1N1) infection presents a significant risk for MG patients, particularly those on immunosuppressive therapy.
Purpose of the Study:
- To report two cases of myasthenia gravis (MG) patients experiencing H1N1 infection.
- To identify key factors contributing to the deterioration and myasthenic crisis (MC) in these patients.
- To emphasize the importance of evaluating for myositis in MG patients with H1N1-associated pneumonia.
Main Methods:
- Case report of two myasthenia gravis (MG) patients diagnosed with H1N1 infection.
- Diagnostic confirmation of MG via neostigmine test, repetitive nerve stimulation, and anti-acetylcholine receptor antibody assays.
- H1N1 infection confirmed by nucleic acid detection; myositis assessed by creatinine kinase levels.
Main Results:
- One MG patient with H1N1, pneumonia, and myositis developed a severe myasthenic crisis (MC) requiring 10 days of mechanical ventilation.
- The second MG patient with H1N1 but without myositis did not experience MC and recovered fully within 6 days.
- Both patients were on prednisolone and azathioprine and had not received prior H1N1 vaccination.
Conclusions:
- Myositis, in addition to pneumonia, significantly increases the risk of myasthenic crisis (MC) in MG patients with H1N1 infection.
- Early detection and management of myositis are critical for improving outcomes in MG patients with H1N1.
- H1N1 vaccination may be beneficial for MG patients, especially those on immunosuppressive treatments.
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