Department of Anesthesiology H187, The North American Malignant Hyperthermia Registry of MHAUS, Penn State College of Medicine, Hershey, Pennsylvania 17033, USA.
Anesth Analg. 2010 Feb 1;110(2):498-507. doi: 10.1213/ANE.0b013e3181c6b9b2.
We analyzed cases of malignant hyperthermia (MH) reported to the North American MH Registry for clinical characteristics, treatment, and complications.
Our inclusion criteria were as follows: AMRA (adverse metabolic/musculoskeletal reaction to anesthesia) reports between January 1, 1987 and December 31, 2006; "very likely" or "almost certain" MH as ranked by the clinical grading scale; United States or Canadian location; and more than one anesthetic drug given. An exclusion criterion was pathology other than MH; for complication analysis, patients with unknown status or minor complications attributable to dantrolene were excluded. Wilcoxon rank sum and Pearson exact chi(2) tests were applied. A multivariable model of the risk of complications from MH was created through stepwise selection with fit judged by the Hosmer-Lemeshow statistic.
Young males (74.8%) dominated in 286 episodes. A total of 6.5% had an MH family history; 77 of 152 patients with MH reported >or=2 prior unremarkable general anesthetics. In 10 cases, skin liquid crystal temperature did not trend. Frequent initial MH signs were hypercarbia, sinus tachycardia, or masseter spasm. In 63.5%, temperature abnormality (median maximum, 39.1 degrees C) was the first to third sign. Whereas 78.6% presented with both muscular abnormalities and respiratory acidosis, only 26.0% had metabolic acidosis. The median total dantrolene dose was 5.9 mg/kg (first quartile, 3.0 mg/kg; third quartile, 10.0 mg/kg), although 22 patients received no dantrolene and survived. A total of 53.9% received bicarbonate therapy. Complications not including recrudescence, cardiac arrest, or death occurred in 63 of 181 patients (34.8%) with MH. Twenty-one experienced hematologic and/or neurologic complications with a temperature <41.6 degrees C (human critical thermal maximum). The likelihood of any complication increased 2.9 times per 2 degrees C increase in maximum temperature and 1.6 times per 30-minute delay in dantrolene use.
Elevated temperature may be an early MH sign. Although increased temperature occurs frequently, metabolic acidosis occurs one-third as often. Accurate temperature monitoring during general anesthetics and early dantrolene administration may decrease the 35% MH morbidity rate.
我们分析了北美恶性高热登记处报告的恶性高热病例,以了解其临床特征、治疗和并发症。
我们的纳入标准如下:1987 年 1 月 1 日至 2006 年 12 月 31 日之间的 AMRA(麻醉不良代谢/肌肉骨骼反应)报告;临床分级量表评为“极可能”或“几乎肯定”的恶性高热;美国或加拿大的地理位置;使用了不止一种麻醉药物。排除标准为病理学以外的恶性高热;在并发症分析中,排除了因丹曲林而出现未知状态或轻微并发症的患者。应用 Wilcoxon 秩和检验和 Pearson 确切卡方检验。通过逐步选择建立恶性高热并发症风险的多变量模型,通过 Hosmer-Lemeshow 统计量判断拟合度。
286 个发作中,年轻男性(74.8%)占主导地位。6.5%有恶性高热家族史;152 例恶性高热患者中有 77 例报告了>或=2 次无明显异常的全身麻醉。在 10 例中,皮肤液晶温度没有趋势。最初常见的恶性高热体征是高碳酸血症、窦性心动过速或咀嚼肌痉挛。63.5%的患者体温异常(中位数最高,39.1°C)是第一个至第三个体征。尽管 78.6%的患者既有肌肉异常又有呼吸性酸中毒,但只有 26.0%的患者有代谢性酸中毒。丹曲林的总剂量中位数为 5.9mg/kg(第 1 四分位数,3.0mg/kg;第 3 四分位数,10.0mg/kg),尽管有 22 例患者未接受丹曲林治疗且存活下来。共有 53.9%的患者接受了碳酸氢盐治疗。在 181 例恶性高热患者中(63.9%)发生了不包括复发、心脏骤停或死亡的并发症。21 例患者出现了体温<41.6°C(人类临界热最大值)的血液和/或神经系统并发症。体温每升高 2°C,并发症发生的可能性增加 2.9 倍,丹曲林使用每延迟 30 分钟,可能性增加 1.6 倍。
体温升高可能是恶性高热的早期体征。尽管体温升高很常见,但代谢性酸中毒的发生率仅为其三分之一。在全身麻醉期间进行准确的体温监测和早期使用丹曲林可能会降低 35%的恶性高热发病率。