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Explore this issue:January 2019
Facial nerve paralysis (FNP) is a potential complication following parotid surgery. Despite meticulous dissection, identification of key landmarks, and gross preservation of neural tissue, the incidence of transient FNP following parotidectomy varies from 12% to 40%. Although independent tumor and patient risk factors (tumor size, pathology, recurrent disease, deep lobe location, nerve involvement, revision surgery, radiation therapy) may alter prognosis, attempts to improve facial nerve outcomes are based on literature supporting anti-inflammatory modalities such as corticosteroids.
The use of corticosteroids has been shown to improve outcomes in spontaneous idiopathic facial nerve (Bell) palsy, the etiology of which is rooted in an inflammatory pathway, leading to edema and ischemia to portions of the facial nerve. Although corticosteroids are frequently successful for treating FNP due to primary inflammatory and idiopathic etiologies, postoperative FNP is also subject to iatrogenic mechanical forces during dissection, with potential for microvascular or microstructural neural injury. Because the effects of FNP alter patient physical and social well-being, attempts to prevent or mitigate nerve impairment following dissection are paramount. Therefore, we sought to investigate the literature for evidence detailing the impact of perioperative corticosteroids on facial nerve outcomes following parotid surgery.
There is insufficient evidence to support the use of perioperative steroids in patients undergoing parotid surgery. To date, no investigation has demonstrated a positive correlation of corticosteroids on improved facial nerve function, both on immediate postoperative outcomes and on the rate of recovery in long-term follow-up. Unfortunately, evidence overall is limited. Future research should focus on well-designed trials assessing corticosteroid use tailored to preoperative and intraoperative factors linked to increased risk of permanent FN paralysis after parotid surgery (Laryngoscope. 2018;128: 2433-2434).