二次性低血性的临床特征和恢复模式
Akiyuki Hiraga1, Kazuho Kojima2, Satoshi Kuwabara3
1Department of Neurology, Chiba Rosai Hospital, 2-16 Tatsumidai-Higashi, Ichihara-shi, Chiba, 290-0003, Japan. hiragaa@yahoo.co.jp.
Journal of neurology
|August 4, 2023
概括
二次性低性 (HP) 通常源于生活方式因素,并表现为异常症状. 反弹性低血和延迟性高血是常见的,即使在补充后,也需要仔细监测.
科学领域:
- 神经学 神经学
- 内分泌学 在内分泌学.
- 内部医学 内部医学
背景情况:
- 二次性低性 (HP) 是一种关于其频率,神经症状和恢复模式的有限记录信息的疾病.
- 了解二次性HP的特征对于及时诊断和管理至关重要.
研究的目的:
- 分析被诊断患有二次低性的患者的频率,病因,临床特征和恢复模式.
- 提供关于二级HP的呈现和进展的见解.
主要方法:
- 2011年4月至2022年3月期间入院的18名二次HP成年患者的临床和实验室记录的回顾性审查.
- 排除患有遗传性低性周期性的患者.
主要成果:
- 常见的病因包括慢性酒,腹和不均衡的饮食 (16/18患者).
- 不典型的症状,如疲劳是常见的;不对称的或上肢的弱点发生在一些患者.
- 复发性高血症 (56%) 和延迟性高血症 (67%) 是常见的,低与复发性高血症相关.
结论:
- 二次性HP主要与生活方式因素有关,并且经常呈现非特异性,非典型的症状.
- 反弹性低血和延迟性高血是常见的并发症,需要在治疗后进行警监测.
- 连续监控对于有效管理二级HP至关重要.
相关概念视频
Acute Kidney Injury III: Clinical Manifestations
32
Acute Kidney Injury (AKI) progresses through distinct clinical phases: the oliguric, diuretic, and recovery phases, each marked by unique manifestations and challenges.Oliguric Phase:The oliguric phase is the initial stage of AKI, typically lasting 10 to 14 days. This phase is marked by a significant reduction in urine output, usually less than 400 mL per day, indicating decreased kidney function. Fluid retention is a prominent feature, leading to symptoms such as edema, hypertension, and...
32
Depolarizing Blockers: Mechanism of Action
1.6K
Depolarizing blockers act on skeletal muscle fibers' membranes and induce their depolarization. Most depolarizing blockers have two quaternary N+ atoms that bind the nicotinic acetylcholine receptors and cause neuromuscular blockade within minutes.
Succinylcholine is the most commonly used depolarizing blocker. Chemically, it constitutes two molecules of acetylcholine joined together by an acetate methyl group. They act on the receptors in the same way as acetylcholine. Because...
Succinylcholine is the most commonly used depolarizing blocker. Chemically, it constitutes two molecules of acetylcholine joined together by an acetate methyl group. They act on the receptors in the same way as acetylcholine. Because...
1.6K
Peripheral Arterial Disease II: Clinical Manifestations and Diagnostic Evaluation
17
Clinical manifestationsPeripheral Arterial Disease (PAD) manifests through a range of symptoms, from the characteristic intermittent claudication to atypical presentations and severe complications in advanced stages. Intermittent claudication, a hallmark symptom of PAD, presents as exercise-induced muscle pain that typically resolves within minutes of rest. This pain is reproducible and stems from inadequate blood flow, leading to the accumulation of lactic acid produced during anaerobic...
17
Chronic Kidney Disease II: Clinical Manifestations
30
Chronic Kidney Disease (CKD) progressively impairs multiple body systems due to the accumulation of uremic toxins, which disrupt cellular functions across various organs.Neurologic symptomsNeurologic symptoms often arise early in CKD, as uremic toxin buildup drives changes in cognitive and motor functions. Patients frequently experience fatigue, headache, confusion, difficulty concentrating, and, in severe cases, seizures. Peripheral neuropathy commonly manifests as burning sensations in the...
30
Parkinson's Disease: Overview
598
Neurodegenerative disorders are progressive diseases that cause irreversible damage and loss to neurons in specific brain areas. Examples of these disorders include Parkinson's disease, Alzheimer's disease, Multiple Sclerosis (MS), and Amyotrophic Lateral Sclerosis (ALS). These disorders share characteristics such as proteinopathies, selective neuronal vulnerability, and a complex interplay between genetic and environmental factors. The primary therapeutic goal for these conditions is...
598
Depolarizing Blockers: Pharmocokinetics
353
Depolarizing blockers are administered through intravenous injection. Succinylcholine is the most common choice of depolarizing blockers in emergency clinical practices. Although they have a rapid onset, they readily diffuse away from the motor end plate into the extracellular fluid. They are metabolized by enzymes such as liver butyrylcholinesterase and plasma pseudocholinesterases. This produces a short duration of action, typically 5-10 minutes long, unlike nondepolarizing blockers, which...
353


