Severe bronchospasm and desaturation in a child associated with rapacuronium.

The patient was a 10-yr-old girl who was brought to the operating room to undergo appendectomy. Except for 1 week of abdominal pain and mild nausea but no vomiting, her history was negative. There were no previous anesthetics, environmental or drug allergies, recent upper respiratory infection, or reactive airway disease. No one in her household smoked. She weighed 62 kg and was 138 cm tall. Except for findings related to her surgical problem, her physical examination was unremarkable, and her chest was clear. While the patient was preoxygenated for 3 min using a 6-l/min flow of O2, the usual monitors were applied. Then, 1 mg midazolam and 50 mg fentanyl were administered intravenously. After an additional 2 min of oxygen administration, a rapid sequence induction was performed with 150 mg propofol, immediately followed by 100 mg intravenous rapacuronium (approximately 1.6 mg/kg). After 30 s, O2 saturation was noted to decrease from 100% to approximately 95%. We elected to administer ventilation by mask for an additional 45 s with 100% O2 while applying cricoid pressure. Her chest rose, but O2 saturation improved only slightly to 96%. A cuffed No. 6.5 endotracheal tube was placed in her trachea with apparent ease, followed by an immediate attempt at manual ventilation. Despite ventilating pressures of up to 30 cm H2O, breath sounds, chest movement, endotracheal tube fogging, end-tidal carbon dioxide, or gastric sounds could not be detected. The anesthesia circuit was rechecked quickly and was observed to be patent. While maintaining cricoid pressure, the endotracheal tube was removed and noted to be unobstructed, and an attempt was made at bag and mask ventilation. Unlike with the preintubation mask ventilation, this time, there were no chest movements, breath sounds, or end-tidal carbon dioxide. The patient was reintubated easily, but ventilation remained impossible. Approximately 2 min had elapsed since her initial intubation. At this point, she also was noted to have truncal erythema and an O2 saturation of 70%. She was given four doses of 100 mg albuterol aerosol via the endotracheal tube, and ventilation was attempted again with 8% sevoflurane in O2. During the next minute, it became possible to ventilate with small tidal volumes and ventilating pressures between 20 and 30 cm H2O. O2 saturations began to increase, and wheezing breath sounds could now be heard. A treatment of 2.5 mg nebulized albuterol was administered via the endotracheal tube, and 50 mg benadryl was administered intravenously. During the ensuing 5 min, manual ventilation became progressively easier with tidal volumes increasing to 350–450 ml at pressures of 15–20 cm H2O. The patient’s O2 saturation increased to 100%, breath sounds returned to normal, and the erythema dissipated. During this event, her blood pressure had ranged between 90/60 and 110/50 mmHg, and her pulse had ranged between 90 and 115 beats/min. Anesthesia was continued with 2–4% sevoflurane, 2 l/min O2, and 2 l/min N2O. Rocuronium, 10 mg, was required to assist with relaxation. Surgery proceeded uneventfully with the removal of an inflamed retrocecal appendix. Muscle relaxation was reversed with 1 mg neostigmine and 0.2 mg glycopyrrolate. With the patient spontaneously breathing, volumes of 250–400 ml at a respiratory rate of 20 breaths/min, and an equal train-of-four, nitrous oxide was discontinued. We elected to extubate the patient deeply, so after 5 min of 4% sevoflurane in O2, the stomach and oropharynx were thoroughly suctioned, and the endotracheal tube was removed. She continued to breathe 100% O2 spontaneously, awoke, and was transferred to the postanesthesia care unit, where her O2 saturation with room air was 99–100% and her chest was clear. Chest radiography results were negative. She was transferred to the pediatric unit and was discharged on the second postoperative day.