Asymptomatic hemilateral pneumothorax and pneumomediastinum following surgical tracheostomy in a patient with hyponatremia and zolpidem withdrawal delirium

Pneumothorax following tracheostomy is a rare complication, with a reported incidence of approximately 1% following both open surgical and percutaneous tracheostomy [1, 2], but potentially life-threatening complication. Post-tracheostomy pneumothorax can usually be diagnosed by clinical signs and symptoms even before a postoperative chest film is obtained. We report a case of asymptomatic pneumothorax and pneumomediastinum following tracheostomy in an adult patient with delirium, but was diagnosed by radiographic examinations of the next day.

A 59-year-old man was admitted to our acute care unit due to persistent intraoral bleeding following extraction of a wisdom tooth. The patient habitually took 20 mg/day of zolpidem, imidazopyridine class of γ-aminobutyric acid A (GABA_A) receptor agonist, often taking more than 50 mg/day. Laboratory tests indicated hyponatremia (Na 123 mEq/L, serum osmolality 256 mOsm/L) secondary to the syndrome of inappropriate secretion of antidiuretic hormone (SIADH) (ADH 45.3 pg/mL). At the time of admission, he mumbled in delirium and developed generalized tonic seizures twice.

At 11 h after his admission, he vomited approximately 200 mL of clot and blood, and SpO₂ decreased to 80%; since aspiration due to intraoral bleeding was suspected, emergency hemostasis and tracheostomy for postoperative respiratory management were performed. Two hours later, SpO₂ was 100% with 5 L/min oxygen through the tracheostomy mask. We continuously infused 3% hypertonic saline and administered fosphenytoin and diazepam for treatment of hyponatremia and generalized tonic seizures, respectively. With this treatment, hyponatremia improved and generalized tonic seizures were relieved, while delirium and confusion lasted.

On the second hospital day, he complained of pain in his head and neck together with mild dyspnea (SpO₂ 95–96% with 2 L/min oxygen). Hemilateral pneumothorax, pneumomediastinum, and subcutaneous emphysema were diagnosed by chest X-ray and CT images of the thorax and neck, for which a chest tube was inserted (Fig. 1). On the seventh hospital day, CT images indicated disappearance of the pneumothorax and remission of subcutaneous emphysema and pneumomediastinum, and the chest tube was removed. On the ninth hospital day, his consciousness and communication normalized and he was discharged on the twelfth hospital day.

CT images of the neck and thorax on the day following tracheostomy. CT images revealed emphysema of the chest, neck and mediastinum, and pneumothorax of the right lung

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The diagnosis of post-tracheostomy pneumothorax is usually based on clinical signs and symptoms, such as sudden and acute chest pain, dyspnea, tachycardia, decreased breath sounds and oxygen desaturation, and routine use of post-tracheostomy chest radiography has currently been reported as unnecessary in adults [3,4,5]. In this case, when tension pneumothorax and pneumomediastinum were diagnosed by chest X-ray and CT examinations, the patient did not have any of the usual features of both pneumothorax and pneumomediastinum; he only complained of pain in his head and neck, and his SpO₂ was 95–96% while breathing 2 L/min oxygen. Symptoms of hyponatremia and zolpidem withdrawal include delirium, confusion, disorientation, and seizures [6, 7]. Patients with delirium exhibit symptoms of disturbances in consciousness, orientation, memory, perception, and behavior: tactile hallucinations in patients with delirium may involve paresthesia and pain [8]. We assumed that our patient’s sensory disturbance associated with the delirium may have resulted in the absence of clinical signs of tension pneumothorax.

The current case suggests that postoperative radiographic examinations may have a role to play in the early diagnosis of pneumothorax and pneumomediastinum in patients with delirium.

ADH:

Antidiuretic hormone

CT:

Computed tomography

GABA_A :

γ-Aminobutyric acid A

SIADH:

Syndrome of inappropriate secretion of antidiuretic hormone

SpO₂ :

Percutaneous oxygen saturation

Not applicable.

Funding

None.

Availability of data and materials

Not applicable.

Affiliations

1. Department of Anesthesiology, Kindai University Faculty of Medicine, 377-2 Ohno-higashi, Osaka-sayama, Osaka, 589-8511, Japan

   • Yoshihiro Takasugi
   • , Risa Aoki
   •  & Shota Tsukimoto

Contributions

YT wrote the manuscript as the corresponding author. YT and RA conducted anesthetic management to the patient. ST and RA participated in laboratory data collection and drafted the article. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Yoshihiro Takasugi.

Ethics approval and consent to participate

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Consent for publication

Written informed consent was obtained from the patient for publication of this case report and any accompanying images.

Competing interests

The authors declare that they have no competing interests.

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