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Volume 39, Issue 5, Pages 681-684 (May 2004)


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Spontaneous pneumomediastinum: are we overinvestigating?

Presented at the 35th Annual Meeting of the Canadian Association of Paediatric Surgeons, Niagara-on-the-Lake, Ontario, Canada, September 18–21, 2003.

Joyaube Chapdelainea, Mona Beaunoyera, Patrick Daigneaultb, Denis Bérubéb, Andreana Büttera, Alain Ouimeta, Dickens St-VilaCorresponding Author Information

Abstract 

Background

Spontaneous pneumomediastinum (SPM) is uncommon in pediatrics. Because of the growing concern about the risks of radiation in children, the authors analyzed whether an extensive radiologic workup influences management and outcome.

Methods

In a retrospective study from 1991 to 2003, 53 patients were diagnosed with SPM. Charts were reviewed for demographics, predisposing factors, presentation, investigation, and evolution. Pneumomediastinum occurring in the neonatal period or related to either pneumothorax, barotrauma, or trauma were excluded.

Results

Of 53 cases, 26 (49%) were bronchospasm related, 11 (21%) had respiratory tract infections, and 8 (15%) were idiopathic. Four (7.5%) were caused by inhaled foreign bodies while other causes accounted for the remaining 7.5%. No esophageal perforations were identified. Presentations included dyspnea (64%), subcutaneous emphysema (60%), cough (45%), cervical or chest pain (42%), and Hamman’s sign (19%). Postero-anterior chest x-rays (CXR) were diagnostic in all cases except one. Mean number of CXR per hospitalization was 3. Only 3 patients subsequently had pneumothorax, and none required pleural drainage. Of the 8 patients with idiopathic SPM, 5 underwent a barium swallow, and 2 had a chest CT scan; results of all were normal.

Conclusions

More than 70% of SPMs were related to bronchospasm or respiratory tract infections. Idiopathic SPMs deserve more attention because of the concern about esophageal perforation, although most investigations will be negative. SPM usually is a self-limited condition, and prognosis is related to the underlying disorder. Consequently, with clinical improvement, aggressive investigation and follow-up x-ray rarely is warranted.

a Division of General Surgery, Ste-Justine Hospital, Montreal, Quebec, Canada

b Division of Pneumology, Ste-Justine Hospital, Montreal, Quebec, Canada

Corresponding Author InformationAddress reprint requests to Dickens St-Vil, MD, Hôpital Sainte-Justine, 3175 Ste. Catherine Rd, Montreal, Quebec, H3T 1C5 Canada

PII: S0022-3468(04)00063-6

doi:10.1016/j.jpedsurg.2004.01.045


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