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Eur J Cardiothorac Surg 2004;25:852-855
© 2004 Elsevier Science NL
a Section of Cardiothoracic Surgery, Yale-New Haven Hospital, Yale University School of Medicine, New Haven, CT, USA
b St Mary's Hospital, Yale University School of Medicine, New Haven, CT, USA
Received 22 December 2003; received in revised form 24 January 2004; accepted 28 January 2004.
* Corresponding author. Address: 22 Socratous Str, 1st Floor, Kifissia 14561, Athens, Greece. Tel.: +30-210-8083743/6937-307272; fax: +30-210-8012-689
e-mail: dkorkolis_2000{at}yahoo.com
| Abstract |
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Key Words: Pneumomediastinum Spontaneous pneumomediastinum Mediastinal emphysema
| 1. Introduction |
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The purpose of this study was to review a single institution's clinical experience with SPM and to detail a reasonable course of evaluation and treatment.
| 2. Materials and methods |
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All SPM case records were carefully reviewed in respect to the demographic data, symptoms, clinical findings at presentation, precipitating factors, diagnostic workup performed, offered treatment, length of hospital stay, as well as natural course and outcome. Precipitating factors reviewed included a recent or remote history of drug abuse, the performance of a Valsalva-type maneuver and a recent history of physical activity. In addition, cigarette smoking and other pulmonary-related medical problems were recorded. Charts were specifically reviewed for the presence or absence of subcutaneous emphysema or bronchospasm in the clinical evaluation. Chest radiograph and computerized tomography (CT) scan results were analyzed, whereas the use of additional diagnostic tests, such as esophagogram and flexible bronchoscopy, were justified and recorded. Reasons for admission, possible complications, length of hospital stay and course of the disease were taken under consideration.
| 3. Results |
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At the time of initial evaluation, all patients had one or more symptoms that could be related to the presence of a pneumomediastinum. Acute onset retrosternal chest pain was the predominant symptom seen in 66.6% of cases. Persistent cough was apparent in 41.6% and discomfort related to their neck or throat (e.g. sore throat, dysphagia) was described in 33.3% of patients. Only two patients (8.3%) were complaining of dyspnea or shortness of breath, on presentation (Table 1).
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After careful investigation, predisposing agents for the development of SPM could be identified in most patients. The most frequent precipitating factor was a history of illegal drug abuse (cocaine and heroin), which was noted in six patients (25%). Other factors included acute bronchial asthma in four patients (16.6%), non-contact physical activity (tennis, weightlifting) in four (16.6%), violent coughing (including a case of idiopathic pulmonary fibrosis) in four (16.6%), recent performance of contact-sports (football, wrestling) in two (8.3%) and a vigorous vomiting episode in two patients (8.3%). In the remaining two patients (8.3%) no predisposing factor was found and SPM developed entirely at rest (Table 2).
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All patients had antibiotic prophylaxis given for the prevention of mediastinitis. This consisted of a third-generation cephalosporin, such as ceftriaxone. Broader coverage with the addition of clindamycin was used when the possibility of splanchnic perforation was high and when the presentation was accompanied by fever or leukocytosis, in a delayed and suspicious setting. Nevertheless, these agents were discontinued shortly, thereafter.
Half of our patients were admitted to the hospital, whereas the remaining were released and followed-up in an outpatient basis. Reasons for admission included control of bronchospasm and cough in four patients (33.3%), treatment of associated infection in four (33.3%), management of concurrent pneumothorax in two (16.6%) and evaluation of suspected tuberculosis in two patients (16.6%).
All patients were managed with bed rest, pain control, follow-up chest X-ray, work-up for asthma and oxygen therapy. Oxygen therapy helped with the absorbance of mediastinal air and led to rapid resolution of SPM. One patient with pneumothorax had a temporary Heimlich valve placed, whereas the diagnosis of tuberculosis in the other two was excluded.
The mean hospital stay was 2 days (range between 1 and 5 days). No complications were seen. Patients were discharged when fully evaluated and asymptomatic, even with some residual radiographic findings of pneumomediastinum. In a follow-up period of 310 years, no recurrence of SPM was noted and no re-admission for the same reason was recorded.
| 4. Discussion |
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In the international literature, SPM has been linked to many causes such as bronchial asthma [8], diabetic ketoacidosis [9], forceful straining during exercise [10], inhalation of drugs [11], childbirth [12], severe cough or vomiting [13], as well as other activities associated with the Valsalva maneuver [14].
Miller and colleagues [15] were the first to report SPM in the setting of inhalation of an illicit drug (i.e. marijuana). Mattox [16] subsequently reported a series of patients with SPM who were frequent users of marijuana and heroin. More recently, SPM has been reported in association with inhaling nitrous oxide [17], smoking free-base [18] or crack-cocaine [19] and ecstasy abuse [20]. There are still questions as to whether SPM seen with inhalation drug used is caused by the same barotrauma-related mechanism or whether it is caused by the direct toxic action of heat and the strong vasoconstrictive action of the inhaled substances [14]. Valsalva-type manipulations are quite common among users of cocaine or marijuana when they routinely perform a forceful breath-holding type maneuver during inhalation of the respective substance. In our series of 24 patients with SPM, recent or remote history of illegal drug abuse was the most frequent predisposing factor, accounting for 25% of cases. It is, therefore, thought that the current incidence of SPM is considerably more common than was previously believed. In addition, there is a reason to expect that, in the era of inhalation drug use, cases of SPM will most likely increase in frequency, particularly in younger individuals. The disturbing young age of these patients has been shown in our series as well as in others [21,22]. In contrast, no correlation with a particular somatotype, as in the case of spontaneous pneumothorax, was observed.
The clinical presentation of SPM can often be subtle and the diagnosis sometimes missed or delayed [13]. Every patient in our series presented with one or more symptoms that could be directly or indirectly related to the presence of a pneumomediastinum. A high-index of suspicion is, therefore, necessary for its prompt diagnosis. Chest pain has been usually found to be the predominant symptom [13,22]. Symptoms such as cough, dyspnea or dysphagia have been also reported [13,22,23].
Subcutaneous emphysema, either in the neck or chest, although characteristic for SPM, has only been noted in half of our patients, even after radiologic documentation. The presence of subcutaneous emphysema in SPM is not stable and varies from 40 to 100%, in different reports [14,21,22].
The initial differential diagnosis of SPM assessed by a thoracic surgeon should be broad and includes cardiac, pulmonary, musculoskeletal and esophageal causes (Table 3). The majority of these causes can be safely excluded with a thorough history, detailed physical examination, electrocardiographic evaluation, as well as radiographic or endoscopic assessment, as indicated.
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The issue of prophylactic antibiotic coverage in SPM is contradictory. All patients in our study received at least one dose of a third-generation cephalosporin. That seems reasonable, particularly in highly suspicious cases and until any additional workup is completed. Although recent reports from smaller series [13,21,22] advocate immediate admission or expedite diagnostic approach, we found that SPM does not usually require aggressive intervention or hospitalization. Patients who were admitted developed no complications, such as tension pneumomediastinum, delayed pneumothorax or airway compromise, and were safely discharged within a few days. In addition, none of those treated in an outpatient basis showed exacerbation or future recurrence. With the increase in the incidence of SPM, the financial savings of avoiding hospitalization for these patients should be appreciated. Taking into consideration the benign nature of this entity, only cases, where the diagnosis is in question, the underlying disease needs specific treatment or the possibility of an organ perforation cannot be ruled out, should be considered for further diagnostic workup and admission.
In conclusion, SPM is an uncommon and self-limited clinical entity. It follows alveolar rupture into the pulmonary interstitium and is produced by an acute episode of high-intrathoracic pressure. It usually occurs in young adults with a rising frequency in illegal drug users. Although chest pain is the predominant symptom, SPM shows a wide range of clinical features, necessitating a thorough differential diagnosis and a high-index of suspicion. Chest radiography may not always be sufficient, whereas CT scan, with its decreasing cost and increasing availability, offers both the confirmation of the diagnosis and the assessment of any associated causes or abnormalities, and should be used. Hospitalization and aggressive approach should be limited and individualized. SPM has a benign natural course and responds well to conservative treatment.
| References |
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