Primary spontaneous pneumomediastinum (PSPM) is a self-limited condition that is problematic due to the difficulty in discriminating it from life-threatening processes such as esophageal perforation and mediastinitis. PSPM patients present with mediastinal emphysema and no traumatic or iatrogenic cause. By contrast, secondary pneumomediastinum may be secondary to processes such as esophageal perforation and traumatic injury of the esophagus or tracheobronchial tree. Hamman first described PSPM in 1939 (1). The associated auscultation finding of “crunching” with cardiac contraction is referred to as the “Hamman sign.” Despite its moniker, PSPM can often be associated with processes causing sudden intrathoracic pressure changes. For example, these changes may be associated with coughing or retching. Patients frequently have a history of asthma or smoking (2). Pathophysiologically, the condition is thought to result from pressure changes leading to alveolar rupture followed by tracking of air along the bronchovascular tissue plane, a process known as the Macklin effect (3). Cases have attributed PSPM to other Valsalva events, such as child-birth (4), diabetic ketoacidosis (5), fellatio (6) and cannabinoid hyperemesis syndrome (7). However, PSPM patients may present without any clear inciting event or predisposing factors (8,9).
Patients with PSPM frequently present with chest pain and crepitus, prompting hospital admission and an extensive workup to rule out esophageal perforation. An improved understanding of the typical presentation and history of patients with PSPM may help discriminate these patients from those with more life-threatening conditions.
The aims of this study were to better characterize contemporary diagnosis and management of this condition based on the best clinical evidence available, which is limited to retrospective case series. We undertook a comprehensive review of PSPM case series to evaluate demographics, symptoms, clinical signs, histories, vitals, diagnostic methods, management, treatment and recurrence rates. We present the following article in accordance with the Narrative Review reporting checklist (available at http://dx.doi.org/10.21037/jtd-21-193).
We conducted a PubMed search using the MeSH term “Mediastinal Emphysema”[Mesh], to identify randomized controlled trials, meta-analyses and case series (with 10 or more patients) relevant to the clinical presentation and management of patients with PSPM. This search strategy, conducted in May 2020, yielded 3,547 results. All titles and abstracts were reviewed. There were no relevant randomized controlled trials or meta-analyses. There were multiple small case series. Of these, we selected case series with more than 10 patients and excluded non-English language studies. Fourteen case series met our initial criteria. One series was removed because it included secondary pneumomediastinum cases. Evaluation of the remaining thirteen citations resulted in identification of an additional six case series that were appropriate for inclusion. Clinical variables were abstracted from the texts and included: demographics: age and gender; symptoms: chest pain, dyspnea, and neck pain; clinical signs: subcutaneous emphysema, Hamman sign, and pneumothorax; histories: smoking, cough, asthma, physical exertion, and retching/emesis; vitals: fever, tachycardia, hypotension, tachypnea, and hypoxemia; diagnostic studies: chest X-ray (CXR), chest computed tomography (CT), esophagram, EGD, and bronchoscopy; management/treatment: antibiotics, thoracostomy tubes for concurrent pneumothorax, hospital admission and duration; and recurrence rates.
Nineteen case series were appropriate for inclusion (2,8,9,10-25). Publication dates ranged from 1991 to 2017. On average the studies included a relatively small number (28.2) of patients (Table 1). In total, the combined case series included 535 patients with PSPM. Of the fifteen studies that reported mean ages, the average mean age was 23 years. All but two studies included pediatric patients. There was a clear male predominance (72% male versus 28% female), which has been noted previously (26).
Most of the studies reported on possible inciting or pre-disposing factors in patients presenting with PSPM. Ten of the studies reported smoking history, with an average rate of 29.6% (Table 2). The incidence of cough averaged 27.7% (Table 2). A history of asthma was noted in fifteen of the studies, with an average rate of 25.9% (Table 2). Recent physical exertion was reported in 21.1% (Table 2). Finally, retching/emesis was reported in 13% (Table 2). Taken together, these findings bolster the conclusion that processes involving sudden intrathoracic pressure changes are strongly associated with PSPM.
Symptoms and signs
Chest pain was the most common symptom and was the only symptom reported in each of the nineteen case series (Table 3). Taken together, 70.9% of patients with PSPM presented with chest pain. Dyspnea was the second most reported symptom with an average rate of 43.4% (Table 3). Finally, 32.9% of patients reported neck pain (Table 3). Subcutaneous emphysema was the most common sign with an average rate of 54.2% (Table 4). The average rate of Hamman sign in the eleven studies reporting it was 23.5% (Table 4). Finally, 10.8% of patients presenting with PSPM were also found to have a pneumothorax (Table 4). Taken together, these results present a clearer picture of the common presenting symptoms and signs of patients with PSPM.
We found limited data on the presenting vitals and laboratory values for patients with PSPM. For example, the presence of fever was reported in only six studies, with an average rate of 18.8% (Table S1). The absence of tachycardia was noted by Jougon et al. (13) while Campillo-Soto et al. (15) and Weissberg & Weissberg (8) reported tachycardia in 5.6% and 7% of the patients, respectively (Table S1). Jougon et al. (13) was the only report commenting on hypotension, which was not observed in their case series. One patient with tachypnea was reported in the case series by Campillo-Soto et al. (15) and one patient with hypoxemia was noted in the case series by Mondello et al. (18), respectively (Table S1). Finally, only seven of the studies reported on the presence of leukocytosis, with an average rate of 30.8%, and four studies reported white blood cell count (Table S2). Taken together, data on the typical vitals and basic laboratory values for patients presenting with PSPM is scant.
Which diagnostic studies are typically performed in the evaluation of spontaneous pneumomediastinum? CXR was obtained in 96.9% of patients (Table 5). CT scans were obtained in 65% (Table 5). It was not possible to determine if CT imaging was required for diagnosis of pneumomediastinum or obtained to rule in/out other potential disease processes. In the series reported by Kaneki et al., they obtained CT in all patients to better understand the CT findings of PSPM (11). They concluded that approximately 30% of PSPM cases were poorly detected by CXR alone and that PSPM is likely an underdiagnosed entity. Three of the studies specifically commented on the presence or absence of effusion on imaging. None of the patients (n=104 patients) in these series had an effusion (Table S3). In the case series reported by Bakhos et al., comparison was made with a group of thirteen esophageal perforation patients (24). Notably, the rate of effusion in the esophageal perforation group was 31%. Esophagrams were reported in fifteen studies, with a rate of 35.6% of patients (Table 5). Finally, EGDs were performed in 13% of the patients (Table 5). Bronchoscopy was performed in 14.6% of patients (Table 5). These results show that CXR is the most common diagnostic modality used in the diagnosis of pneumomediastinum, but CT imaging and esophagrams are common diagnostic adjuncts.
Management and treatment
Interventions were rare. Furthermore, they were almost exclusively limited to complications arising from concurrent pneumothorax. Overall, we found scant data regarding management of concurrent pneumothorax, but several case series did report thoracostomy tube placement with a rate of 76% (Table S4). A single patient, out of the entire 535 patients in the nineteen series, underwent an operation for “tension pneumothorax” within several hours of presentation. The patient underwent a thoracotomy with opening of the mediastinal pleura (22). To our knowledge, this is the only patient who underwent an operation and the indication was tension pneumothorax. The only other intervention noted was drainage of subcutaneous emphysema in 10 of the 18 total patients reported in the series of Mondello et al. (18). This may be more reflective of institutional or individual surgeon practice and does not appear to be a common treatment regimen. Taken together, the need for invasive interventions in PSPM patients is rare and almost exclusively undertaken for management of concurrent pneumothorax.
Despite the self-limited nature of PSPM, these patients are frequently admitted to the hospital and treated with antibiotics. Six studies reported on the use of antibiotics with 43% of patients receiving antibiotics (Table 6). Importantly, there are no reported cases of mediastinitis and no prospective studies on the use of antibiotics in PSPM. There were no reported mortalities. Fifteen case series reported rates of PSPM recurrence, with an average rate of 0.98% (Table S5). The follow up periods varied widely, as did the methods of follow up (Table S5). We did not find data regarding the rate of hospital transfers. 86.5% of the patients were admitted to the hospital with a mean length of hospital stay of 4.4 days (Table 6). Due to the retrospective nature of this case series review, the current available data do not have the granularity to determine reasons (e.g., pain management, diagnostic uncertainty, etc.) for admission or length of stay. Together these data show that the vast majority of patients with this benign condition are admitted to the hospital for multiple days and nearly half of them are treated with antibiotics.
PSPM continues to pose a difficult clinical problem because it can be difficult to discriminate from life-threatening conditions with a similar presentation, namely esophageal perforation. While this difficulty is a defining feature encountered by practicing clinicians, the reasons for this difficulty are unclear. We sought to understand the reasons for this diagnostic difficulty. Case series represent the best evidence currently available. Our review of these case series has the expected limitations associated with retrospective studies, including the possibility of selection and publication bias. Other limitations include the potential for variable definitions of clinical parameters on the case series level.
Although the clinical presentation of esophageal perforation is beyond the scope of this review, it is clear that we need to better understand how it differs from that of PSPM. Chest pain, dyspnea and subcutaneous emphysema are common in the presentation of PSPM, but they are also common in the presentation esophageal perforation (27). In their systematic review of 33 case series including 1,452 esophageal perforation patients, Hasimoto et al. found the mean age was 55.2 years (27). Approximately 80% of esophageal perforations have a clear iatrogenic or traumatic/post-surgical etiology in their history. Spontaneous esophageal perforations, i.e., Boerhaave’s syndrome, represented approximately 20 percent of the cases (27). It is this patient population that must be discriminated from PSPM patients. The typical Boerhaave’s patient is a ~55–65 years old male, often with a history of excessive alcohol and/or food consumption following by severe retching/emesis. While age is an important demographic variable that differs between PSPM and esophageal perforation, Boerhaave’s cannot be excluded from the differential diagnosis simply based on patient age.
Our review reveals a very limited understanding of the vitals and basic laboratory values of patients presenting with PSPM. Indeed, there is insufficient data to make any meaningful conclusions regarding the rates of tachycardia, hypotension, tachypnea or hypoxemia in this patient population. We suspect that the presence of fever and leukocytosis in this patient population, coupled with minimal understanding of other vitals and labs, likely contributes to concern for esophageal perforation. A better understanding of these basic clinical variables may improve our ability to discriminate between patients with PSPM and patients with esophageal perforation.
CT imaging is typically inadequate to discern between PSPM and esophageal perforation. To date, there is scant radiologic data specifically comparing non-contrast CT findings between patients with PSPM and esophageal perforation. Notably, while pleural effusions are apparent in ~10–30% of esophageal perforations, zero effusions were reported in our review of these PSPM case series. We anticipate that further radiologic studies comparing PSPM and esophageal perforation cases could significantly improve our ability to discriminate between these two diagnoses.
Since CXR and non-contrast CT imaging is currently insufficient to discriminate between PSPM and esophageal perforation two key questions arise: (I) which patients need studies beyond CXR or CT and (II) which study is needed? Fluoroscopic contrast esophagram has traditionally been regarded as the gold-standard for identification of esophageal perforation (28). In our experience, many referring centers do not have fluoroscopic esophagram capabilities and patients are frequently transferred solely due to lack of this resource. An important development in this area is the growing body of evidence suggesting that contrast computed tomography esophagram has a sensitivity and negative predict value for esophageal perforation that is equivalent to traditional fluoroscopic contrast esophagram (29). Because CT esophagram can be performed at essentially any center with CT imaging capabilities, it has the potential to significantly decrease the inter-facility transfers and diagnostic delays. Either fluoroscopic contrast esophagram or contrast CT esophagram can be used when evaluation for esophageal perforation is indicated. We use the term “contrast esophagram” to refer to either of these modalities. While there is clearly a role for contrast esophagram in the workup of select patients presenting with pneumomediastinum, currently there is no consensus regarding which pneumomediastinum patients should undergo a study. The current PSPM literature does not address this issue. Taken together, these findings suggest that a high index of suspicion, with case by case physician judgement, including communication between Emergency Medicine physicians and Thoracic Surgeons, remains important. Finally, if diagnostic uncertainty regarding possible esophageal perforation remains, contrast esophagram is indicated.
Even when the diagnosis of PSPM is clearly established, questions remain regarding optimal management. Because small concurrent pneumothoraces are present in approximately ten percent of these patients, and may be occult, thoracic CT is a valuable adjunct in these patients. Given the potential for tension physiology, we suggest that concurrent pneumothorax should be managed in a manner similar to primary spontaneous pneumothorax patients. We propose that when the diagnosis of PSPM without concurrent pneumothorax is made with confidence, no additional testing, work-up or treatment is indicated. While admission may be indicated for management of pain, nausea/emesis, or other reasons, it is likely unnecessary for stable patients who meet disposition criteria. A brief period of observation to confirm clinical stability is reasonable. Patients should be educated about the small, approximately 1%, chance of recurrence. Finally, there is no evidence supporting the use of antibiotics in isolated PSPM and they are not indicated unless there is diagnostic uncertainty with concern for other etiologies, such as Boerhaave’s, esophageal necrosis, or mediastinitis.
- PSPM is often difficult to discriminate from esophageal perforation due to a shared constellation of clinical signs and symptoms.
- PSPM patients typically healthy and present in their 20s whereas esophageal perforation patients typically present in their 50-60s.
- We have a very limited understanding of PSPM vitals and labs. This likely contributes to the diagnostic uncertainty.
- Imaging by CXR and CT is typically not able to discriminate between PSPM and esophageal perforation, but pleural effusion should raise concern for perforation.
- Fluoroscopic esophagrams or CT contrast esophagrams are the best tests to identify esophageal perforations, but further research is needed to determine which patients need these studies.
- Approximately 10% of PSPM patients present with concurrent pneumothorax, which should be managed by standard spontaneous pneumothorax algorithms due to the possibility of tension pneumothorax.
- An improved understanding of the above issues may significantly improve our ability to efficiently arrive at the correct diagnosis and management for these patients.
The authors thank Dr. Erik Lewis for critical reading of the manuscript.
Reporting Checklist: The authors have completed the Narrative Review reporting checklist. Available at http://dx.doi.org/10.21037/jtd-21-193
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/jtd-21-193). The authors have no conflicts of interest to declare.
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