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A Case Report of Suspected Malignant Hyperthermia: How Will the Diagnosis Affect a Patients Insurability?

机译:疑似恶性高热的病例报告:诊断将如何影响患者的可保性?

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摘要

The purpose of this case report is to increase awareness that a diagnosis of malignant hyperthermia may have long-lasting or permanent effects on a patient's insurance eligibility or premiums despite legislation providing varying levels of protection from preexisting conditions or genetic discrimination. We present a case of severe rigors, unexplained severe metabolic acidosis, and severe hyperthermia in a patient after general anesthesia for extensive head and neck surgery. The patient was treated for malignant hyperthermia and demonstrated a significant clinical improvement with the administration of dantrolene. Even with an “almost certain” diagnosis of malignant hyperthermia by clinical presentation, genetic testing was negative and the gold-standard caffeine-halothane contracture test has yet to be performed. Laboratory results, clinical grading scales, and genetic testing support a diagnosis of malignant hyperthermia but the gold standard is a live muscle biopsy and caffeine-halothane contracture test. A clinical diagnosis of MH or a positive caffeine-halothane contracture test could result in exclusion from genetic discrimination legislature due to the fact that diagnosis can be confirmed without genetic testing. The fate of the Affordable Care Act may also affect how insurance companies scrutinize this disease. Improving accuracy of MH diagnosis in hospital discharge records will be crucial.
机译:本案例报告的目的是提高人们的认识,尽管立法提供了针对既有疾病或遗传歧视的不同程度的保护措施,但对恶性高热的诊断可能会对患者的保险资格或保费产生长期或永久性影响。我们提出了在全身麻醉后进行广泛的头颈部手术的患者中,严重严峻,无法解释的严重代谢性酸中毒和严重体温过高的情况。该患者接受了恶性高热治疗,并在服用丹特罗烯后表现出明显的临床改善。即使通过临床表现“几乎可以肯定”地诊断出恶性高热,基因检测还是阴性的,尚无金标准的咖啡因-氟烷挛缩试验。实验室结果,临床分级量表和基因检测支持对恶性高热的诊断,但金标准是活肌活检和咖啡因-氟烷挛缩试验。 MH的临床诊断或咖啡因-氟烷挛缩试验阳性可能会导致排除遗传歧视立法机构的影响,因为无需进行基因检测即可确诊。 《平价医疗法案》的命运也可能会影响保险公司对这种疾病的审查方式。提高出院记录中MH诊断的准确性至关重要。

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