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Mediastinal masses may arise from structures normally located in the mediastinum, from those that pass through the mediastinum during development, or from metastatic disease that arises from tumors elsewhere in the body. In children, mediastinal masses tend to be more prevalent in males than in females. , The majority are caused by lymphomas, followed by bronchial cysts, teratomas, vascular malformations, and neurogenic tumors.
Mediastinal masses may present with nonspecific respiratory or cardiovascular symptoms, such as coughing, or present with more severe symptoms, such as superior vena cava syndrome, pulmonary artery obstruction, or culminate in superior mediastinal syndrome (airway compression/tracheal obstruction, vascular compression).
The presence of an anterior mediastinal mass should be regarded as a clinical emergency. Early diagnosis and management are crucial for providing the best chance for a favorable outcome. The latter undoubtedly adds to the challenge of the anesthetic management of these patients, since symptoms such as respiratory or cardiovascular compromise may not be optimized before anesthesia.
General anesthesia confers considerable risk, since the effects of mediastinal masses on airway and vascular structures can impede gas exchange or reduce cardiac output. The symptoms at presentation are essential to developing an anesthetic plan and have been shown to be predictive of anesthetic-related morbidity. In a retrospective review of 118 pediatric patients who presented with mediastinal masses, four preoperative features were significantly associated with anesthetic complications: main‐stem bronchus compression, great vessel compression, orthopnea, and upper body edema. The presence of pleural or pericardial effusions, ventricular dysfunction, tracheal compression (cross-sectional area <50%), and stridor are also associated with anesthetic related morbidity.
The anesthetic management begins with a careful review of the child’s history, symptoms, clinical signs, and radiographic images (computed tomography and/or chest x-ray). In general, patients without orthopnea or cardiovascular symptoms and minimal radiographic evidence of airway obstruction may likely be anesthetized safely. However, physical signs and radiographic evidence have not been consistently shown to be predictive of potential complications; therefore general anesthesia or deep sedation should be avoided whenever possible, and when required, it is essential that the anesthesiologist establishes communication with the surgeon, has a set plan for sedation or anesthesia, and has a plan for rescue in the event of cardiopulmonary compromise. These include repositioning the patient (lateral or prone), the ability to perform rigid bronchoscopy to relieve tracheal compression, and the ability to perform a sternotomy and provide cardiopulmonary bypass or extracorporeal membrane oxygenation (ECMO).
Patients with signs of orthopnea, stridor, dyspnea at rest, and/or a >70% reduction in tracheal cross-sectional area are deemed high-risk, and general anesthesia should be avoided unless absolutely necessary. In older children, tissue diagnosis under local anesthesia has been associated with lower risk of anesthetic complications and has been successfully accomplished in several series. , Distraction techniques such as counting, listening to music, and nonprocedure-related talk have been shown to be effective. However, younger children and those undergoing surgical resection of large mediastinal masses may require a general anesthetic. In this instance, an anesthetic plan that ensures spontaneous respiration is generally preferable. Spontaneous ventilation typically preserves the patency of the intrathoracic airways. On the other hand, positive pressure ventilation may worsen airway compression (e.g., through neuromuscular blockade and/or deep anesthesia reducing support of the surrounding tracheobronchial musculature) and also reduce cardiac output by reducing venous return.
The airway may be managed by mask ventilation only, with a laryngeal mask airway, or with endotracheal intubation. Several methods have been described for the maintenance of anesthesia, including a mixture of sevoflurane in oxygen and halothane in heliox, and low-dose infusions of propofol, dexmedetomidine, and ketamine. The ability of dexmedetomidine and ketamine to provide sedation with minimal respiratory depression has proven beneficial in anesthetizing children with anterior mediastinal masses.
It is noteworthy that several authors have reported cases where intubation has been successfully performed in children with mediastinal masses. , In the event that an endotracheal intubation is necessary, advancement of the endotracheal tube past the segment of obstruction, typically through external compression, may have to be performed. Regardless of the choice of airway management, neuromuscular blockade is generally not recommended because the relaxation of supporting tracheobronchial musculature may contribute to further worsening of airway compromise. However, if neuromuscular blockade is deemed necessary, it is imperative to establish the ability to adequately ventilate the patient before administering muscle relaxants.
The management of the child with an anterior mediastinal mass poses a significant challenge to anesthesiologists. Potential respiratory and cardiovascular complications may be exacerbated under anesthesia, and plans to manage potential complications should be communicated to the entire team before initiation of care. Where possible, diagnostic procedures are best performed with local anesthesia with minimal-to-no sedation. Where deep sedation or general anesthesia is required, maintenance of spontaneous ventilation with or without an endotracheal tube is preferable. Neuromuscular blockade should be avoided whenever possible.
Unlike adults and older children, most children under 2 years of age require anesthesia or sedation for the successful completion of a course of radiotherapy treatments. This is mainly because complete immobilization, which is required for safe and effective radiotherapy, cannot be reliably accomplished in very young children without sedation or anesthesia.
This, in and of itself, presents several challenges. Perhaps most concerning is the fact that younger children may have to be exposed to multiple anesthetics over a relatively short period of time. The inherent risks associated with anesthetizing a very young child and the exposure to the side effects of anesthetic agents used are therefore amplified. In this regard, the safety profile of the chosen anesthetic technique gains further significance. Furthermore, to ensure that there is no interference with the radiotherapy plan from changes in airway management or patient positioning, it is important that the chosen method of anesthesia remains unchanged over the period of treatment and that it is easily replicable. Other challenges include choosing an anesthetic that may facilitate rapid awakening and rapid discharge, since most radiotherapy facilities treat multiple patients or may not have a designated postoperative recovery area.
Several studies have demonstrated that anesthesia in children undergoing radiation therapy may be safely performed by spontaneous ventilation and an unprotected airway. In a large series of 340 children who had undergone 9328 radiotherapy procedures under anesthesia, supplemental oxygen was provided with a face mask or nasal cannula. In another large series describing the anesthetic management of 177 children who had undergone 3833 radiotherapy procedures, supplemental oxygen was provided by face mask in both the supine and prone positions. The placement of an oral airway or laryngeal mask airway was required in rare cases.
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