Sulaiman Raashda A, Alali Abdulaziz, Hosaini Sulaiman, Hussein Maged, Pasha Farooq, Albogami Muneerah, Sheikh Aamir N, AlSayed Moeen, Al-Owain Mohammed
Department of Medical Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
Department of Emergency Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Am J Emerg Med. 2022 May;55:138-142. doi: 10.1016/j.ajem.2022.02.053. Epub 2022 Mar 9.
An increasing number of pediatric patients with inherited metabolic disorders are reaching adulthood. In addition, many patients are diagnosed for the first time in adult life due to improved awareness of these disorders and the availability of advanced diagnostic technology. Knowledge of these inherited metabolic disorders in adults is crucial for the emergency physician to promptly recognize their acute illness and appropriately manage them in the emergency department.
This review provides an overview of various inherited metabolic disorders which present to the emergency department with acute metabolic decompensation.
Acute illness in these patients is often triggered by a catabolic event such as intercurrent illness, fasting, postpartum, or use of certain medication. It may present in a variety of ways related to severe hyperammonemia, metabolic acidosis, leucine encephalopathy or hypoglycemia. In this review, we describe the clinical presentation, evaluation and immediate management of their critical illness in the emergency department.
Acute metabolic decompensation is a life-threatening condition. The emergency physician is usually the first provider to evaluate these patients when they present to the emergency department. Early recognition of their illness and prompt management of these cases improve patient outcomes.
越来越多患有遗传性代谢紊乱的儿科患者已步入成年期。此外,由于对这些疾病的认识提高以及先进诊断技术的应用,许多患者在成年后首次被诊断出患有此类疾病。对于急诊医生而言,了解成人遗传性代谢紊乱的相关知识对于及时识别其急性疾病并在急诊科进行妥善处理至关重要。
本综述概述了因急性代谢失代偿而就诊于急诊科的各种遗传性代谢紊乱。
这些患者的急性疾病通常由分解代谢事件引发,如并发疾病、禁食、产后或使用某些药物。其表现形式多样,与严重高氨血症、代谢性酸中毒、亮氨酸脑病或低血糖有关。在本综述中,我们描述了这些患者在急诊科的临床表现、评估及紧急处理方法。
急性代谢失代偿是一种危及生命的状况。当这些患者前往急诊科就诊时,急诊医生通常是首位对其进行评估的医疗人员。早期识别病情并及时处理这些病例可改善患者预后。