Natasa Nejković, Snezana Protić, Nemanja Zarić, Zoran Krivokapić, Durasić Ljubomir
Center for anesthesiology and reanimatology, Clinical Center of Serbia.
Acta Chir Iugosl. 2012;59(2):121-3.
Malignant hyperthermia (MH) is a form of myopathy that is usually triggered by volatile anaesthetics such as halothane, sevoflurane and desflurane and depolarising muscle relaxants such as succinylcholine. Pathologic response in MH include increase in oxygen consumption, increase in endtidal CO2, tachycardia, hyperthermia, hyperkalemia and muscle rigidity. Immediate recognition and treatment are crucial to avoid lethal outcome. Molecular genetic studies have confirmed that ryanodine muscle receptors are responsible for MH. We present a case of leptosuccin induced MH with masseter muscle rigidity, mild pCO2 increase (6.3 kPa), elevated body temperature measured with esophageal temperature probe (39.5 degrees C), tachycardia (115 beats/min) and respiratory and metabolic acidosis (pH was 7,23) in a patient who underwent low anterior resection of the rectum for gastrointestinal stromal tumor (GIST) of the rectum.
恶性高热(MH)是一种肌病形式,通常由氟烷、七氟烷和地氟烷等挥发性麻醉剂以及琥珀酰胆碱等去极化肌肉松弛剂引发。MH的病理反应包括耗氧量增加、呼气末二氧化碳增加、心动过速、高热、高钾血症和肌肉强直。立即识别和治疗对于避免致命后果至关重要。分子遗传学研究已证实,兰尼碱肌肉受体是导致MH的原因。我们报告一例在因直肠胃肠道间质瘤(GIST)接受直肠前切除术的患者中,由左旋琥珀酰明胶诱发的MH病例,该患者出现咬肌强直、轻度pCO₂升高(6.3kPa)、经食管温度探头测量体温升高(39.5℃)、心动过速(115次/分钟)以及呼吸性和代谢性酸中毒(pH为7.23)。