View CLG: Tardive Dyskinesia

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Q: 什么是迟发性运动障碍疾病? 它有哪些类型?
迟发性运动障碍(TD)是一种神经系统疾病,其特征是面部、四肢或躯干的不自主、重复运动。这种情况通常是由于长期使用某些药物,特别是用于治疗精神健康障碍的抗精神病药物。这些运动可能包括做鬼脸、舌头突出、嘴唇啜动、撅嘴和快速眨眼。它也可以影响肢体,如脚趾轻弹、脚踏或四肢不受控制的运动。

迟发性运动障碍有几种类型,包括:
1. 迟发性肌张力障碍 - 以缓慢、持续的肌肉收缩为特征,导致扭曲、重复的运动或异常姿势。
2. 迟发性静坐不能 - 涉及内心的不安感和不断运动的冲动,通常伴有重复运动。
3. 迟发性抽动秽语综合征 - 类似于抽动秽语综合征,伴有不自主的发声和运动。
4. 迟发性肌阵挛 - 涉及短暂、突然的抽动,通常涉及身体中部或四肢。
5. 迟发性震颤 - 表现为节律性、振荡性运动,可能类似于帕金森病震颤,但由使用神经安定剂引起。

这种情况可能令人痛苦,并且显著影响人的生活质量。早期识别和管理对于可能逆转或管理症状至关重要。
Q: 鉴别诊断迟发性运动障碍需要什么患者数据?包括症状、病史、体查、诊断检查等。
为了鉴别诊断迟发性运动障碍(TD),需要收集一系列病人信息和检查结果,包括:
1. 症状: TD通常表现为不自主、重复的身体动作,如面部扭曲、舌头动作、咂嘴、抿嘴和眼睛快速眨动。观察这些症状的持续时间和任何进展非常重要。
2. 病史: 包括患者使用神经阻滞剂(抗精神病药物)的持续时间和类型,因为TD通常与这些药物的长期使用有关。其他可能引起类似症状的药物信息、精神病史和任何以前的运动障碍诊断也至关重要。
3. 体格检查: 需要进行全面的神经系统检查,以评估运动和感觉功能,检查反射,并观察任何不自主运动。
4. 诊断测试: 虽然没有专门针对TD的测试,但可以进行测试以排除其他条件。这可能包括:
• 血液测试以排除代谢原因。
• 像MRI或CT扫描这样的影像学研究,以排除大脑结构异常。
• 脑电图(EEG)排除癫痫疾病。
5. 药物使用的持续时间: 记录患者使用抗精神病药物或其他神经阻滞剂的时间长度,因为TD的风险随着使用时间的增长而增加。
6. 对药物变化的反应: 观察在改变致病药物的剂量或停用这些药物时症状的变化情况。

通过收集这些全面的资料,医疗提供者可以更准确地将TD与帕金森病、亨廷顿病和肌张力障碍等其他运动障碍区分开来。
Q: 运动迟缓性病变患者有什么典型的病情、具体的体查结果和诊断检查结果?
运动迟缓性病变(TD)是一种神经系统疾病,其特征是面部、四肢或躯干的不自主、重复性动作。它通常由长期使用某些精神科药物引起,尤其是抗精神病药。以下是诊断过程中可能出现的具体结果:
1. 病史采集:
• 用药历史: 医生会询问当前和过去的用药情况,特别是使用抗精神病药或其他多巴胺拮抗剂的情况,因为这些药物与TD有很大关联。
• 症状起始和持续时间: 了解症状开始的时间及其进展情况至关重要。
• 既往健康问题: 任何神经系统疾病或其他相关健康问题的历史也会被考虑在内。
2. 体格检查:
• 观察动作: 医生将寻找不自主的动作,如扭曲、眨眼、咂嘴或其他典型的TD重复动作。
• 神经系统检查: 评估动作的严重程度和分布情况,排除其他神经系统状况。
3. 诊断测试:
• 没有特定的实验室测试可以确认TD,但可能进行测试以排除其他状况。
• 影像检查: 脑部影像(如MRI或CT扫描)可能用于排除其他神经系统疾病。
• 视频记录: 有时候,会录制动作视频,以供专家更详细地分析。

TD的管理包括修改用药方案,可能在医学监督下减少或停用抗精神病药物,并考虑可能有助于缓解症状的药物。
Q: 请提供一个迟发性运动障碍患者的电子病历示例?包括病情、体查、各种鉴别诊断检查结果。
病人姓名: 约翰·多伊
年龄: 58岁
性别: 男
日期: 2024年5月3日

症状:
• 持续的非自主运动,特别是面部扭曲和舌头运动
• 类似弹钢琴的手指动作
• 偶尔非自主的脚趾动作
• 运动不伴随疼痛
病史:
• 20年前被诊断为精神分裂症
• 长期使用抗精神病药物(氟哌啶醇)达15年
• 家族中无神经系统疾病史
• 不吸烟,偶尔饮酒
体格检查:
• 生命体征稳定(血压120/80,心率72次/分钟,体温98.6华氏度)
• 神经系统检查:面部和四肢出现异常非自主动作,步态和感觉功能无异常。
诊断测试:
• 血液测试: 完全血细胞计数、肝功能测试和甲状腺功能测试均在正常范围内
• 头部MRI: 未检测到异常
• 脑电图(EEG): 正常
初步鉴别诊断:
• 迟发性运动障碍,可能由长期使用抗精神病药物引起
• 帕金森病:考虑到年龄可能性存在但通过运动类型较不可能
• 亨廷顿病:由于没有家族史和正常的MRI,可能性不大

这份记录作为进一步调查和咨询的基础,主要关注由长期使用抗精神病药物可能引发的迟发性运动障碍的管理。
Q: 请提供一个迟发性运动障碍患者的一段话简明病历示例?
迟发性运动障碍是一种神经系统疾病,其特征是身体不自主、重复的动作。这种状况通常是长期使用或高剂量使用抗精神病药物的副作用,尤其是旧型药物。一个典型的病例可能涉及一个55岁的患者,他因精神分裂症已经接受抗精神病治疗20年。最近,他们经历了持续的不自主动作,如眨眼、咀嚼或扭曲面部,这些不仅令人痛苦,还干扰日常活动。尽管精神症状有所减轻,但这些运动障碍显著影响了患者的生活质量。
Q: 为鉴别诊断迟发性运动障碍,需要排除哪些疾病?请逐一列出,简单说明。
迟发性运动障碍(TD)的特征是面部、颈部和肢体的非自主重复运动。诊断TD时,必须排除可能出现类似症状的其他疾病。在鉴别诊断中主要应考虑的疾病包括:
1. 药物诱导的帕金森病 - 可以表现为类似的运动症状,但通常涉及到僵硬和运动迟缓,与TD中的运动不同。
2. 亨廷顿病 - 一种遗传性疾病,可能引起舞蹈症和其他运动障碍,这可能与TD混淆。
3. 威尔森病 - 一种罕见的遗传性疾病,导致铜积累,可以引起精神或神经系统症状,包括运动障碍。
4. 神经性恶性综合症(NMS) - 虽然NMS通常表现为肌肉僵硬、发热和自主神经不稳,但其与神经性药物的关联可能会混淆诊断。
5. 图雷特综合症 - 以抽动为特征,可能模仿TD的运动。
6. 风湿性舞蹈症(Sydenham舞蹈症) - 在链球菌感染后出现非自主运动,可能类似TD。
还应考虑患者的用药历史,因为许多TD病例与长期使用神经性药物有关。

Bilingual Comparison

Q: What is Tardive Dyskinesia? Its types?
Tardive dyskinesia (TD) is a neurological disorder characterized by involuntary, repetitive movements of the face, limbs, or trunk. It often results from long-term use of certain medications, particularly antipsychotics used to treat mental health disorders. These movements may include grimacing, tongue protrusion, lip smacking, puckering, and rapid eye blinking. It can also affect the limbs with movements like toe tapping, foot stamping, or uncontrollable movements of the arms and legs.

There are several types of tardive dyskinesia, which include:
1. Tardive Dystonia - Characterized by slow, sustained muscle contractions that result in twisting, repetitive movements or abnormal postures.
2. Tardive Akathisia - Involves feelings of inner restlessness and an urge to move constantly, often accompanied by repetitive movements.
3. Tardive Tourettism - Resembles Tourette syndrome with involuntary vocalizations and motor movements.
4. Tardive Myoclonus - Involves brief, sudden jerks typically involving the central part of the body or the limbs.
5. Tardive Tremor - Presents as rhythmic, oscillatory movements which can be similar to Parkinsonian tremors but are caused by the use of neuroleptics.

This condition can be distressing and significantly impact a person's quality of life. Early recognition and management are crucial to potentially reversing or managing the symptoms.
Q: What patient information and test results, including symptoms, medical history, physical exams, and diagnostic tests, are required to differentially diagnose Tardive Dyskinesia?
To differentially diagnose Tardive Dyskinesia (TD), a range of patient information and test results are crucial, including:
1. Symptoms: TD typically manifests as involuntary, repetitive body movements such as grimacing, tongue movements, lip smacking, puckering, and rapid eye blinking. Observations of these symptoms, their duration, and any progression are important.
2. Medical History: Important aspects include the duration and types of neuroleptic (antipsychotic) medications the patient has taken, as TD is often associated with long-term use of these drugs. Information on other medications that may cause similar symptoms, psychiatric history, and any previous diagnoses of movement disorders are also vital.
3. Physical Exam: A comprehensive neurological examination is needed to assess motor and sensory functions, evaluate reflexes, and observe for any involuntary movements.
4. Diagnostic Tests: While there are no specific tests for TD, tests can be conducted to rule out other conditions. These might include:
• Blood tests to rule out metabolic causes.
• Imaging studies like MRI or CT scans to rule out structural abnormalities in the brain.
• Electroencephalogram (EEG) to exclude seizure disorders.
5. Duration of Medication Use: Documentation of how long the patient has been on antipsychotic medication or other neuroleptics, as TD risk increases with prolonged use.
6. Response to Medication Changes: Observations on how symptoms change when the dosage of causative medications is altered or when these medications are discontinued.

By gathering this comprehensive profile, healthcare providers can more accurately differentiate TD from other movement disorders like Parkinson's disease, Huntington’s disease, and dystonia.
Q: What are the specific results from medical history taking, physical examinations, and diagnostic tests for a patient with Tardive Dyskinesia?
Tardive Dyskinesia (TD) is a neurological disorder characterized by involuntary, repetitive movements of the face, limbs, or trunk. It is most often caused by long-term use of certain psychiatric medications, particularly antipsychotics. Here’s how a diagnosis might unfold:
1. Medical History Taking:
• Medication History: The doctor will inquire about current and past medications, especially the use of antipsychotics or other dopamine antagonists, as these are commonly associated with TD.
• Symptom Onset and Duration: Information about when the symptoms started and their progression is crucial.
• Previous Health Issues: Any history of neurological disorders or other relevant health issues will be considered.
2. Physical Examination:
• Observation of Movements: The doctor will look for involuntary movements, such as grimacing, blinking, lip smacking, or other repetitive movements that are typical of TD.
• Neurological Examination: To assess the severity and distribution of the movements and to rule out other neurological conditions.
3. Diagnostic Tests:
• No specific laboratory tests confirm TD, but tests may be conducted to rule out other conditions.
• Imaging Tests: Brain imaging (like MRI or CT scans) might be used to rule out other neurological disorders.
• Video Recording: Sometimes, movements are recorded for more detailed analysis by a specialist.

Management of TD includes modifying the medication regimen, possibly reducing or discontinuing the use of antipsychotic drugs under medical supervision, and considering medications that might help alleviate the symptoms.
Q: Please provide an example medical record containing symptoms, medical history, physical examination, and results of diagnostic tests, which is required for a differential diagnosis for a patient with Tardive Dyskinesia?
Patient Name: John Doe
Age: 58 years
Sex: Male
Date: May 3, 2024

Symptoms:
• Persistent involuntary movements, particularly grimacing and tongue movements
• Finger movements resembling piano playing
• Occasional involuntary movements of the toes
• No pain associated with the movements
Medical History:
• Diagnosed with schizophrenia 20 years ago
• Long-term use of antipsychotic medication (Haloperidol) for 15 years
• No history of neurological disorders in the family
• Non-smoker and occasional alcohol user
Physical Examination:
• Vital Signs: Stable (BP 120/80, HR 72 bpm, Temp 98.6°F)
• Neurological Examination: Abnormal involuntary movements noted, especially in the facial area and extremities. No issues with gait or sensory functions.
Diagnostic Tests:
• Blood Tests: CBC, liver function tests, and thyroid function tests—all within normal limits
• MRI of the Brain: No abnormalities detected
• Electroencephalogram (EEG): Normal
Preliminary Differential Diagnosis:
• Tardive Dyskinesia due to long-term antipsychotic use
• Parkinson's Disease: considered due to age but less likely given the type of movements
• Huntington’s Disease: unlikely due to no family history and normal MRI

This record serves as a base for further investigations and consultations, primarily focusing on the management of Tardive Dyskinesia potentially induced by prolonged antipsychotic medication usage.
Q: Please provide a one-paragraph patient case example of Tardive Dyskinesia?
Tardive dyskinesia is a neurological disorder characterized by involuntary, repetitive body movements. This condition often arises as a side effect of long-term or high-dosage use of antipsychotic medications, particularly older ones. A typical patient case might involve a 55-year-old individual who has been on antipsychotic treatment for schizophrenia over the last 20 years. Recently, they've experienced persistent involuntary movements such as blinking, chewing, or grimacing, which are not only distressing but also interfere with daily activities. Despite the reduction in psychotic symptoms, the patient's quality of life is significantly affected by these motor disturbances.
Q: Briefly describe the diseases that should be ruled out in differential diagnosis of Tardive Dyskinesia?
Tardive dyskinesia (TD) is characterized by involuntary, repetitive movements, typically of the face, neck, and limbs. When diagnosing TD, it's essential to rule out other conditions that may present with similar symptoms. The main diseases to consider in the differential diagnosis include:
1. Drug-induced Parkinsonism - This can present with similar motor symptoms but typically involves rigidity and bradykinesia, unlike the movements seen in TD.
2. Huntington's Disease - A genetic disorder that can cause chorea and other movement disorders, which could be mistaken for TD.
3. Wilson’s Disease - A rare genetic disorder leading to copper accumulation, which can cause psychiatric or neurological symptoms including movement disorders.
4. Neuroleptic Malignant Syndrome (NMS) - Although NMS typically presents with muscle rigidity, fever, and autonomic instability, its association with neuroleptic drugs can confuse the diagnosis.
5. Tourette Syndrome - Characterized by tics, which can mimic the movements of TD.
6. Rheumatic Chorea (Sydenham's chorea) - Presents with involuntary movements following a streptococcal infection, potentially resembling TD.
It is also important to consider the patient's medication history, as many cases of TD are associated with prolonged use of neuroleptic drugs.


ID: g9443403
Type: aiknowledge
UMLS CUI: C0686347
Status: shared
Created: 2024-06-02
By: aj_elhsi_org
Updated: 2024-10-17
By: aj_elhsi_org


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