Airway Management of Hypokalaemic Paralysis with Trismus and Bulbar Palsy Due To Conn's Syndrome

Abstract

Hypokalaemic paralysis is an atypical condition of acute muscle weakness caused by a variety of disorders, occurring when plasma potassium ion levels drop below 3.5 mmol/L. This reduction in potassium affects the resting membrane potential of muscle cells, leading to paralysis.¹

Trismus associated with hypokalaemia is rare, with only one documented case.² Trismus is a tonic spasm of the masticatory muscles, particularly the masseter and temporalis, resulting in reduced jaw opening.^{1, 2} In such cases, respiratory arrest and death due to severe arrhythmia have been reported, primarily due to prolonged hypoxaemia and delays in airway management. Thus, urgent care and emergency physicians must ensure adequate oxygenation, ventilation, and, if necessary, perform rapid sequence intubation (RSI).²

This case report examines the clinical evidence on the use of neuromuscular relaxants and RSI in emergency rooms for muscle paralysis due to ionic alterations. The uniqueness of this case lies in the combination of trismus, hypokalaemic paralysis, and Conn's syndrome undergoing surgical intervention.

A 45-year-old male gravedigger with a history of high blood pressure treated with enalapril and hydrochlorothiazide presented with 10 days of paraesthesia in his right hand and fingers of his left hand, along with progressive leg weakness. Over the past 3 days, he experienced difficulty swallowing, dysphasia, dysarthria, and cervical muscle weakness. He denied drug, alcohol, or canned food use.

On arrival, the patient was conscious and oriented, with a heart rate of 95 bpm, blood pressure of 170/110 mmHg, and oxygen saturation of 92%. Neurological examination was normal, but he had difficulty opening his mouth and weakness in bulbar and cervical muscles. Oropharyngeal examination showed uvula swelling, likely due to soft palate paralysis.

The patient exhibited motor weakness with upper extremity strength of 2/5 and lower extremity strength of 1/5. Venous blood gas analysis revealed marked alkalosis and severe hypokalaemia (1.3 mmol/L). ECG showed a sinus rhythm with flattened T waves, consistent with hypokalaemia. Treatment included Hydrocortisone 200 mg and intravenous infusion of 40 mEq of potassium chloride in saline. Although corticosteroid treatment can exacerbate hypokalaemia, Hydrocortisone was administered empirically, due to its rapid anti-inflammatory effect, aimed at managing uvular edema and a potential inflammatory process that could compromise the airway. The priority at that point was to ensure patient stabilization and secure adequate airway access.

During observation, the patient developed respiratory failure with cyanosis, requiring unsuccessful face mask ventilation, dropping saturation to 53%. Cisatracurium 20 mg and Midazolam 15 mg were administered for orotracheal intubation, which was difficult due to trismus. ENT specialists performed an emergency tracheostomy. The patient suffered cardiac arrest but was resuscitated after 1 min of chest compressions and adrenaline boluses.

Post-tracheostomy, ventilation improved saturation to 99%, allowing the patient to be moved to surgery for tracheotomy completion and mechanical ventilation connection. Serum potassium levels slightly improved to 2.1 mmol/L. Vocal cord integrity was assessed using a flexible fibrobronchoscope, ruling out damage.

The patient was transferred to the ICU, where continuous potassium replacement improved respiratory function and muscle strength. Trismus resolved after 24 h, but hypokalaemia persisted (2.3 mmol/L). Mechanical ventilation was removed 4 days later. The patient remained in the ICU for 20 days before being discharged to internal medicine for further study.

The diagnosis of primary hyperaldosteronism was confirmed by the endocrinology department following an extensive diagnostic workup. Endocrinological tests revealed elevated aldosterone levels with very low plasma renin activity, which were confirmed through the saline infusion test, iodocholesterol scan, adrenal vein sampling, and several other differential diagnostic tests. This process ultimately confirmed aldosterone overproduction by a left adrenal adenoma, leading to the final diagnosis of Conn's syndrome.

The treatment consisted of laparoscopic surgery to remove the adrenal adenoma, which was successfully performed. A long-term endocrine follow-up was conducted to monitor for possible recurrences and ensure the complete resolution of hypokalaemia and hyperaldosteronism.

This case emphasizes the need for rapid recognition of severe hypokalaemia to prevent cardiorespiratory failure and highlights a rare instance of quadriparesis with bulbar palsy and trismus due to an aldosterone-producing adenoma. The combination of trismus with hypokalaemia is extremely rare, and emergency physicians must be proficient in airway management and RSI, including the use of rocuronium and sugammadex.

Research Group in Anesthesia, Resuscitation and Perioperative Medicine (GIIS079) of Aragon Health Research Institute (IIS Aragon); University of Zaragoza, Spain.