Two Cases of Cerebral Air Embolism That Occurred during Esophageal Ballooning and Endoscopic Retrograde Cholangiopancreatography
Article information
Abstract
Cerebral air embolism is an extremely rare complication of endoscopic procedure and often life threatening. We present two cases of cerebral infarction due to air embolization caused by an endoscopic intervention. The first case occurred during esophageal balloon dilatation for the treatment of a stricture of an anastomosis site in a 59-year-old man and the second case occurred during endoscopic papillary balloon dilatation in a 69-year-old man who had distal common bile duct stones. After the procedure, cardiopulmonary instability and altered mental status were observed in both patients, and cerebral air embolism was diagnosed in both cases. Hyperbaric oxygen therapy was started in the first case, and high FiO2 therapy was applied in the second case. Although this complication is rare, patient outcomes can be improved if physicians are aware of this potential complication, and immediately begin proper management.
INTRODUCTION
Gastrointestinal endoscopy has become a routine medical procedure for diagnostic and therapeutic purposes in many diseases. As the number of cases needing an endoscopic procedure has increased, the incidence of various complications have also increased, making their proper management more important [1-4].
Air embolism is a very rare endoscopic complication that manifests with cardiopulmonary instability and neurologic symptoms. However, because of similar symptoms, it is difficult to distinguish cerebral infarction from sedative-related complications and, owing to its rarity and the unexplained mechanism involved, physicians rarely suspect brain damage induced by air embolism [5].
We here report our experiences with two adult cases of cerebral air embolism after endoscopic procedures—esophageal balloon dilatation and endoscopic papillary balloon dilatation (EPBD)—and their clinical outcomes.
CASE REPORTS
Case 1
A 59-year-old man presented with a 4-week history of progressive dysphagia. He had undergone a total gastrectomy with D2 dissection 2 years previously for gastric cancer, and the pathologic stage was T3N0M0. Two months after the operation, bone metastasis was found and chemotherapy was applied with S-1 (an oral fluorouracil chemotherapeutic agent). On admission, he had an Eastern Cooperative Oncology Group performance status of 3 and was restricted to a liquid diet. An esophagogastroduodenoscopy revealed a benign esophageal stricture at the esophagojejunostomy anastomotic ring (Fig. 1A). Endoscopic balloon dilatation was chosen to achieve proper nutritional support.
This procedure was performed under sedation with intravenous midazolam (2 mg) and with constant vital sign monitoring. His vital signs were stable during the procedure, and through-the-scope ballooning was performed with a Cover-Edge wire-guided balloon dilatation catheter (Boston Scientific, Cork, Ireland) under the following conditions: to 8 mm for 30 seconds with 3 atmospheric pressure, 9 mm for 60 seconds with 4 atmospheric pressure, and 10 mm for 60 seconds with 9 atmospheric pressure (Fig. 1B). After the procedure was completed, he became unresponsive (Glasgow coma scale, 3/15), hypotensive (systolic blood pressure/diastolic blood pressure, 66/41 mm Hg), and hypopneic (respiratory rate, 10 breaths per minute).
His vital signs stabilized after O2 was supplied through a venture mask (FiO2 50%), and after fluid resuscitation and flumazenil injection. However, his altered mental status was not reversed after flumazenil injection.
To determine the cause of the mental change, magnetic resonance imaging (MRI) and brain computed tomography (CT) were performed (Fig. 2), and multiple cerebral infarctions due to air embolism were found. Intubation was performed to increase the O2 supply. Three hours after the procedure, hyperbaric therapy was applied. The therapy was instituted at 3 atmospheric pressure for 2 hours 45 minutes, and gradual decompressed was performed for 1 hour 5 minutes. After hyperbaric therapy, the embolism had nearly disappeared in the follow-up MRI and the vital signs had stabilized. Extubation was performed 4 days after the event, and left-sided weakness remained. Twelve months after the event, he still undergoes rehabilitation treatment for left-sided hemiparesis; however, he can ambulate with minimal assistance.
Case 2
A 69-year-old man was admitted to our hospital with persistent right upper quadrant pain since 2 weeks. Abdominal CT showed distal common bile duct stones, and he underwent therapeutic endoscopic retrograde cholangiopancreatography (ERCP) under sedation with intravenous midazolam (2 mg). His vital signs were stable during the procedure. Multiple filling defects were found, and EPBD was performed to avoid bleeding due to pericholedochal varices. Multiple stones were removed with a hurricane balloon dilatation catheter (Boston Scientific) (Fig. 1C, D), and a fully covered metal stent was inserted to compress the varices.
After ERCP, he became unresponsive (Glasgow coma scale, 3/15) and hypoxic (SpO2, 80%). He subsequently became hypotensive and bradycardic, and finally progressed into pulseless electrical cardiac arrest. Cardiopulmonary resuscitation was carried out for 7 minutes before spontaneous circulation was recovered. An imaging evaluation was then performed to determine the cause of the event. Brain MRI and brain CT showed multiple cerebral infarctions (right middle, left anterior, and left posterior cerebral artery territories); however, the images could not distinguish air embolism from other causes. Cholangiography taken during the procedure showed air within the portal veins (Fig. 3), and air embolism could be diagnosed clinically. High FiO2 therapy was provided, and low-molecular-weight heparin was used because other infarction causes could not be ruled out.
After 4 days, the patient’s mental status was restored and he was extubated. He underwent rehabilitation treatment for left-sided weakness, and the neurologic deficit improved considerably. Recently, at 2 months after the event, he is able to perform normal activities of daily living.
DISCUSSION
We here present two cases of cerebral air embolism as a rare complication of therapeutic endoscopy. Rapid diagnoses and prompt treatments were performed in both patients, who both survived. However, the first patient now has a persistent left-sided hemiparesis. In our experience, early suspicion and proper management of air embolism can improve clinical outcomes, although cerebral infarction due to air embolism is an extremely rare and unexpected complication that cannot be completely explained and typically has a poor prognosis.
The mechanism of cerebral air embolization during therapeutic endoscopy is unclear. In theory, the volume of air and rate of accumulation is important in determining the morbidity and mortality after a vascular air embolism develops. A large volume (~5 mL/kg) or rapid entry of gas migrating to the pulmonary circulation places strain on the right ventricle. As the pulmonary arterial pressure increases, the left ventricular preload decreases. This situation results in diminished cardiac output that leads to cardiovascular collapse and cerebral hypoperfusion. Venous gas embolism may migrate to the systemic circulation through a shunt such as a patent foramen ovale. However, it has been reported that a large volume of venous gas can enter the arterial circulation through transpulmonary passage of air, without cardiac defects or shunt. The air of the venous circulation enters the arterial systemic circulation and obstructs the end artery, which is a paradoxical embolism [6]. This mechanism can explain the presentation of our two current patients: the air around the balloon entered through the anastomosis site or biliary tract, and the venous embolism entered the arterial circulation through a transient patent foramen ovale or transpulmonary passage.
To our knowledge, there have been 21 reported cases to date of cerebral embolism complications after an endoscopic procedure, including our current cases (Table 1) [7-24]. The cerebral embolism occurred during or after ERCP in 11 of these cases, and was found during or after another therapeutic esophagogastroduodenoscopy in the remaining 10 cases. Six of the 21 reported patients had undergone major surgery, such as Billroth II operation, total gastrectomy, or Whipple’s operation. In addition, the presence of a shunt was evaluated in 17 of these patients, of whom seven did not have a shunt, such as a patent foramen ovale or arteriovenous malformation, including our two present patients.
There are no standard treatments for cerebral air embolisms that occur during or after an endoscopic procedure, and some previous reports [12,13] have shown that early hyperbaric oxygen therapy has a beneficial effect. Hyperbaric oxygenation therapy may reduce air bubble size, accelerate nitrogen reabsorption, and increase the oxygen content of arterial blood, potentially reducing the ischemia. However, the delay to treatment application has been reported to range from 3 to 48 hours [25].
Among the five previously reported patients who underwent hyperbaric oxygen therapy, two, including our first case herein, showed full or partial neurologic recovery. The other three patients had poor outcomes, including death or severe neurologic deficit. The remaining 15 patients received high FiO2 therapy or conservative management without hyperbaric oxygen therapy. Of these, six patients died and nine patients survived with or without a neurologic deficit.
In conclusion, we here report two cases of cerebral air embolism as a rare complication of therapeutic endoscopy. Although it is difficult to make this diagnosis because it can be confused with a sedative-related problem, our patients underwent appropriate early management and achieved good outcomes. Physicians should therefore be aware of the risk of cerebral air embolism during or after endoscopic procedures in patients who show cardiopulmonary instability and neurologic symptoms.
Notes
Conflicts of Interest: The authors have no financial conflicts of interest.