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Consultant for Pediatricians. Vol. 5 No. 9
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Case In Point: Spontaneous Pneumothorax in a Teenage Boy

By CURT STANKOVIC, MD and PRASHANT MAHAJAN, MD, MPH, MBA | September 1, 2006
Dr Stankovic is a pediatric emergency medicine fellow at the Carman and Ann Adams Department of Pediatrics, Children's Hospital of Michigan in Detroit. Dr Mahajan is associate professor of pediatrics and emergency medicine at Wayne State University; he is also research director in pediatric emergency medicine at the Carman and Ann Adams Department of Pediatrics at Children's Hospital.

DIAGNOSIS AND MANAGEMENT

The diagnosis usually can be made after a detailed history and physical examination. Chest radiographs can confirm the diagnosis and determine the size of the pneumothorax. A recent randomized controlled trial found no advantage for inspiratory/expiratory films.4

The objectives of management are to eliminate the intrapleural air collection, to facilitate pleural healing, and to prevent recurrence. The treatment of SP is multifactorial and depends on its size, course, and classification. A small pneumotho-rax may resolve spontaneously. Needle decompression or chest tube placement may be needed to facilitate reexpansion when air accumulation is relatively large. Strong- ly consider therapeutic interventions for patients with recurrent pneumo- thorax.

While the treatment options for PSP and SSP are the same, the conditions are managed differently. In asymptomatic patients with PSP who have less than 15% air accumulation, simple observation and administration of 100% oxygen have been successfully used as a treatment option.1 Oxygen increases the resorption rate of the pneumothorax 3-fold to 4-fold; the greatest increases occur in patients with larger pneumothoraces. The application of oxygen creates a gas pressure gradient between the pleural space and the tissue capillaries that surround the pleural space. This enhances the absorption of nitrogen and other gases within this space.5

If the pneumothorax is smaller than 15% and if the patient is symptomatic but hemodynamically stable, needle aspiration is considered the treatment of choice. Advantages include its relative simplicity and lack of invasiveness.6

SSP, on the other hand, can be life-threatening. Most patients are treated with a chest tube. Tube thoracostomy has been advocated for patients with PSP in whom simple aspiration fails--and for most patients with SSP.1,6 Other more invasive management options include pleural sclerosis (pleurodesis) and video-assisted thoracic surgery (VATS).

RECURRENCE

Recurrence rates can be high, espeically if SP is untreated. Recurrence rates as high as 30% at 6 months and 50% at 2 years have been reported.1 More specifically, recurrence rates have been reported at 28% for PSP and 53% for SSP.1 There is a 15% rate of recurrence on the contralateral side in patients with PSP. Recurrence is more likely in patients who are tall and thin and who smoke; however, there is no relationship with the number or size of apical blebs on CT. Once a recurrence has occurred, the risk for repeated pneumothoraces exceeds 50%.7

Chest tube insertion helps relieve the pneumothorax and improve symptoms. However, it does not reduce the risk of recurrence as significantly as VATS or pleurodesis. One randomized trial compared simple needle aspiration with tube thoracostomy in the management of first-time PSP.8 Recurrence rates were measured at 1 week (11% vs 12%), at 3 months (15% vs 8%), at 1 year (22% vs 42%), and at 2 years (31% vs 25%). There were no statistically significant differences between the 2 treatment modalities.

LONG-TERM CARE

Patients who have had SP need to stop smoking and to avoid high altitudes, scuba diving, or flying in an unpressurized aircraft in attempt to limit the risk of a recurrent pneumothorax.

TAKE-HOME MESSAGE

Cardiac causes of pediatric chest pain are uncommon. If the pain is associated with shortness of breath, especially in a thin adolescent who smokes, consider spontaneous pneumothorax (SP). When SP is diagnosed, it is important to differentiate between a primary and secondary cause because management differs.

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REFERENCES:
1. Light RW. Pneumothorax. In: Murray JF, Nadel JA, eds. Textbook of Respiratory Medicine. Philadelphia: WB Saunders; 1994:2193-2210.
2. Melton LJ 3rd, Hepper NG, Offord KP. Incidence of spontaneous pneumothorax in Olmsted County, Minnesota: 1950-1974. Am Rev Respir Dis. 1979;20: 1379-1382.
3. Wilson WG, Aylsworth AS. Familial spontaneous pneumothorax. Pediatrics. 1979,64:172-175.
4. Seow A, Kazerooni EA, Pernicano PG, Neary M. Comparison of upright inspiratory and expiratory chest radiographs for detecting pneumothoraces. AJR. 1996;166:313-316.
5. Chada TS, Cohn MA. Noninvasive treatment of pneumothorax with oxygen inhalation. Respiration. 1983;44:147-152.
6. Light RW. Spontaneous Pneumothorax. In: Pleural Diseases. 3rd ed. Baltimore: Williams & Wilkins; 1995;24.
7. Mason RJ.Pneumothorax, chylothorax, hemothorax, and fibrothorax. In: Murray and Nadel's Textbook of Respiratory Medicine.3rd ed. Philadelphia: Elsevier; 2005:1964.
8. Ayed AK, Chandrasekaran C, Sukumar M. Aspiration versus tube drainage in primary spontaneous pneumothorax: a randomized study. Eur Respir J. 2006;27:477-482.


 
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