Allen G C, Larach M G, Kunselman A R
The North American Malignant Hyperthermia Registry, Department of Anesthesia, College of Medicine, The Pennsylvania State University, Hershey 17033-0850, USA.
Anesthesiology. 1998 Mar;88(3):579-88. doi: 10.1097/00000542-199803000-00006.
The caffeine-halothane contracture test (CHCT) is the only recognized laboratory test to diagnose malignant hyperthermia (MH). The authors report the results of their analysis of pooled data from the North American Malignant Hyperthermia Registry database to determine the sensitivity and specificity of the CHCT.
The MH Clinical Grading Scale was used to identify 32 case subjects who were "almost certain" to be MH susceptible based on clinical criteria alone. Their CHCT results were compared with those of a group of 120 control subjects considered to be at low risk for MH. Diagnostic thresholds of the CHCT were adjusted, and its component tests were combined to generate receiver operating characteristic curves. The maximal Youden index for each component test was chosen as the diagnostic threshold indicative of MH susceptibility.
The highest sensitivity (97%; 95% CI, 84-100%) was achieved with a two-component test with thresholds of > or = 0.5 g contracture for 3% halothane, > or = 0.3 g contracture at 2 mM caffeine, or both, considered positive for MH. The test specificity was 78% (95% CI, 69-85%). The addition of other CHCT component tests did not improve CHCT sensitivity or specificity.
The CHCT achieves high sensitivity and acceptable specificity as a clinical laboratory diagnostic test when it is performed according to published standards. However, it cannot be used as a screening test because of the low prevalence of MH in the general population.
咖啡因-氟烷挛缩试验(CHCT)是诊断恶性高热(MH)唯一被认可的实验室检查。作者报告了他们对北美恶性高热注册数据库汇总数据的分析结果,以确定CHCT的敏感性和特异性。
使用MH临床分级量表,仅根据临床标准确定32例“几乎肯定”对MH易感的病例受试者。将他们的CHCT结果与一组被认为MH风险较低的120名对照受试者的结果进行比较。调整CHCT的诊断阈值,并将其组成试验合并以生成受试者工作特征曲线。选择每个组成试验的最大约登指数作为指示MH易感性的诊断阈值。
采用双组分试验,对于3%氟烷挛缩阈值≥0.5 g、2 mM咖啡因挛缩阈值≥0.3 g或两者均有此情况时判定为MH阳性,此时敏感性最高(97%;95%CI,84-100%)。试验特异性为78%(95%CI,69-85%)。添加其他CHCT组成试验并未提高CHCT的敏感性或特异性。
按照已发表的标准进行CHCT时,作为一项临床实验室诊断试验,其具有较高的敏感性和可接受的特异性。然而,由于一般人群中MH的患病率较低,它不能用作筛查试验。