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| Pneumothorax in dysferlin myopathy associated with mechanical ventilation | ||||||
| Martín Hunter1, Patricia Karina Aruj2 | ||||||
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1MD, Resident, Department of Internal Medicine, Instituto de Investigaciones Médicas Alfredo Lanari, Buenos Aires, Argentina.
2MD, Pulmonary Physician, Instituto de Investigaciones Médicas Alfredo Lanari, Buenos Aires, Argentina. | ||||||
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| How to cite this article |
| Hunter M, Aruj PK. Pneumothorax in dysferlin myopathy associated with mechanical ventilation. Int J Case Rep Images 2015;6(4):245–247. |
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Case Report
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A 38-year-old female with dysferlin myopathy (and domiciliary use of nocturnal non-invasive positive pressure ventilation and mechanical insufflation-exsufflation respiratory aid) presented with progressive right upper quadrant abdominal discomfort. The vital signs at presentation were: temperature 36.6°C, heart rate 100 beats per minute, blood pressure 140/80 mmHg, respiratory rate 30 breaths per minute, oxygen saturation 96% while breathing ambient air. On examination, breath sounds were absent on the right side. An anteroposterior chest radiograph showed a large collection of gas in the right hemithorax with inversion of the right hemidiaphragm (Figure 1A). Computed tomography (CT) scan of the chest confirmed the diagnosis of large right-sided pneumothorax, with cardiomediastinal shift to the left (Figure 1B). Despite the size of the pneumothorax, the patient was hemodynamically stable and, surprisingly, she did not develop hypoxemia. Pneumothorax was managed with tube thoracostomy. However, since lung expansion was not successfully achieved, a Heimlich valve was placed. After discharge, a new CT scan showed resolution of the pneumothorax with adequate right lung expansion. The patient is still using mechanical ventilation through a tracheostomy at home without further complications. | ||||||
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Discussion
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Mechanical insufflation-exsufflation (MI-E) is a respiratory aid used by patients with weak respiratory muscles to improve cough effectiveness. Machine pressures can range from +60 cm H2O of insufflation to –60 cm H2O of exsufflation[1]. A few limb-girdle muscular dystrophies are associated with weakness of respiratory or oropharyngeal muscles and an increased risk of respiratory failure with disease progression [2]. This patient had a severe restrictive pattern in pulmonary function tests and diminished cough peak flows from inspiratory and expiratory muscle weakness. The cause of pneumothorax was probably due to barotrauma related to high insufflation pressures. | ||||||
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Conclusion
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Although the use of mechanical insufflation-exsufflation (MI-E) alone may or may not increase the risk of barotrauma, clinicians should be aware that the use of MI-E may add to other risk factors to increase the risk of pneumothorax. Although rare, pneumothorax associated with mechanical ventilation has been reported previously in this patient population. | ||||||
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Author Contributions
Martín Hunter – Substantial contributions to conception and designn, Acquisition of data, Analysis and interpretation of data, Drafting the article, Revising it critically for important intellectual content, Final approval of the version to be published Patricia Karina Aruj – Analysis and interpretation of data, Drafting the article, Revising it critically for important intellectual content, Final approval of the version to be published |
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Guarantor of submission
The corresponding author is the guarantor of submission. |
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Source of support
None |
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Conflict of interest
Authors declare no conflict of interest. |
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Copyright
© 2015 Martín Hunter et al. This article is distributed under the terms of Creative Commons Attribution License which permits unrestricted use, distribution and reproduction in any medium provided the original author(s) and original publisher are properly credited. Please see the copyright policy on the journal website for more information. |
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