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Catatonia in the general hospital: a case series wading through diagnostic & management challenges 在综合医院紧张症:涉水通过诊断和管理挑战的案例系列
Pub Date : 2023-02-05 DOI: 10.56310/pjns.v17i03.201
Shireen Najam, Marium Mansoor, M. Hafiz, A. Shafique, Ifrah Hambal, Banafsha Gul, Tania Nadeem
Catatonia is a cluster of affective, behavioral, and motor symptoms. Its causes are multifactorial ranging from severe and untreated psychiatric illnesses to neurological diseases and other general medical conditions. It is estimated that 20% of catatonia causes are due to medical conditions out of which two thirds are due to an underlying neurological condition which might include encephalitis, neural injury, developmental disorders, structural brain pathology, or seizures. Symptoms of catatonia can wax and wane, fluctuating between the retarded and the excited type within hours making it more difficult to identify and diagnose. If left untreated, catatonia can lead to multiple medical complications which can lead to significant long-term morbidity and mortality. The initial complications include dehydration, malnourishment, electrolyte imbalance, deep venous thrombosis, pulmonary embolism, pneumonia, urinary tract infection, and retention. In the long run, patients can have sepsis, rhabdomyolysis, DIC, decubitus ulcers, arrhythmia, renal failure, and liver dysfunction. This article  will describe  three patients (adolescent & adult) that presented to Aga Khan University Hospital (AKUH), Karachi with challenging presentations of catatonia. Their diagnostic and management difficulties will be discussed.
紧张症是一组情感、行为和运动症状。其原因是多方面的,从严重和未经治疗的精神疾病到神经疾病和其他一般医疗条件。据估计,20%的紧张症原因是由于医疗条件,其中三分之二是由于潜在的神经系统疾病,其中可能包括脑炎、神经损伤、发育障碍、结构性脑病理或癫痫发作。紧张症的症状会忽强忽弱,在数小时内在迟钝型和兴奋型之间波动,这使得它更难识别和诊断。如果不及时治疗,紧张症可导致多种医学并发症,从而导致严重的长期发病率和死亡率。最初的并发症包括脱水、营养不良、电解质失衡、深静脉血栓形成、肺栓塞、肺炎、尿路感染和尿潴留。从长期来看,患者可能出现败血症、横纹肌溶解、DIC、褥疮、心律失常、肾功能衰竭和肝功能障碍。这篇文章将描述三个病人(青少年和成人)提出阿迦汗大学医院(AKUH),卡拉奇与紧张症具有挑战性的介绍。我们将讨论其诊断和治疗的困难。
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引用次数: 0
MR textural features (RADIOMICS) for predicting response to treatment in patients with intracranial tuberculoma: A retrospective cross-sectional study 预测颅内结核瘤患者治疗反应的MR结构特征(RADIOMICS):一项回顾性横断面研究
Pub Date : 2023-02-05 DOI: 10.56310/pjns.v17i03.176
A. Muhammad, Shahmeer Khan, Wasay Muhammad, Azeemuddin Muhammad, A. Shoukat, Hamzullah Khan
Background and objective: MR based radiomics can potentially response to treatment in intracranial tuberculoma, but very scarce literature is available in this regard. The purpose of this study was to determine whether MR based radiomic features can be used to predict response to antituberculosis (AT) treatment. Methods: Data of patients with intracranial tuberculomas who underwent MR imaging and AT treatment at our institution during the last 10 years was analyzed. In each case follow-up imaging performed at 6 months post initiation of treatment was reviewed to establish response to treatment. The textural analysis was performed by two consultant neuroradiologists, using open-source software (Lifex) with FLAIR coronal image after contrast administration from pretreatment MRI study radiomic analysis. Results:  Twenty-four patients with mean age 33.8 years were included in the study. Sixteen patients were in the treatment responsive group while eight patients were in the treatment resistant group. Thirty-eight radiomic parameters were extracted for each patient. There was a significant difference in three out of 38 parameters (histogram skewness, GLCM correlation and NGLDM Coarseness) in patients amongst the two groups. Logistic regression model was developed using these parameters which accurately predicted 83.3% of the cases according to the response to the AT treatment (χ2=11.517, p=0.003). ROC curve analysis was performed using histogram skewness which showed acceptable discrimination (p=0.037 and 95% CI =0.577-0.954) for predicting the response to treatment. Conclusion: MR textural parameters (histogram skewness, GLCM correlation and NGLDM Coarseness) may be used as imaging biomarkers to predict response to treatment in patients with intracranial tuberculoma.
背景和目的:基于MR的放射组学对颅内结核瘤的治疗有潜在的应答,但这方面的文献很少。本研究的目的是确定基于MR的放射学特征是否可以用来预测抗结核(AT)治疗的反应。方法:分析我院近10年来接受磁共振成像和AT治疗的颅内结核瘤患者的资料。在每个病例中,在治疗开始后6个月进行随访影像学检查,以确定对治疗的反应。纹理分析由两名神经放射学顾问使用开源软件(Lifex)对MRI研究放射学分析前对比剂给药后的FLAIR冠状图像进行。结果:24例患者纳入研究,平均年龄33.8岁。16例患者为治疗反应组,8例患者为治疗抵抗组。为每位患者提取38个放射学参数。两组患者的38个参数(直方图偏度、GLCM相关性和NGLDM粗度)中有3个存在显著差异。利用这些参数建立Logistic回归模型,根据AT治疗的反应准确预测83.3%的病例(χ2=11.517, p=0.003)。采用直方图偏度进行ROC曲线分析,可接受判别(p=0.037, 95% CI =0.577 ~ 0.954)预测治疗反应。结论:MR结构参数(直方图偏度、GLCM相关性和NGLDM粗度)可作为预测颅内结核瘤患者治疗反应的成像生物标志物。
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引用次数: 0
Anti-NMDA Receptor Encephalitis presenting with severe episodic hypertension: a case report 以严重发作性高血压为表现的抗nmda受体脑炎1例
Pub Date : 2023-02-05 DOI: 10.56310/pjns.v17i03.202
T. Arshad, M. Hussain, A. Yousafzai, Arsalan Ahmad
Anti-N-methyl-D-aspartate receptor (Anti-NMDAR) encephalitis is one of the most commonly emerging autoimmune encephalitis in children and young adults in recent years. Clinical manifestations range from prodromal symptoms to seizures, movement disorder, psychiatric manifestations, cognitive/speech impairment, and autonomic dysfunction. Our case presented with initial symptoms of severe episodic hypertension, sweating, agitation, and tachycardia. She received early care for pheochromocytoma and panic disorder in Qatar, but there was no relief. Three weeks later, she presented in our emergency room with seizures, cognitive/speech impairment, and orofacial dyskinesia. Electroencephalography EEG revealed right hemispheric delta activity and cerebrospinal fluid CSF anti-NMDA Receptor IgG was positive. Magnetic resonance imaging MRI brain and CSF studies were normal. She was treated symptomatically for hypertension and psychiatric manifestations. She received high dosage pulse intravenous methylprednisolone, followed by intravenous immunoglobulin, which significantly alleviated her cognitive, neuropsychiatric, and autonomic features. Severe Hypertension is an uncommon presentation of Anti- NMDAR encephalitis.  Early recognition and prompt management improves prognosis and long term sequelae.
抗n -甲基- d -天冬氨酸受体(Anti-NMDAR)脑炎是近年来儿童和青少年中最常见的自身免疫性脑炎之一。临床表现包括前驱症状、癫痫发作、运动障碍、精神表现、认知/语言障碍和自主神经功能障碍。我们的病例最初表现为严重的发作性高血压、出汗、躁动和心动过速。她在卡塔尔接受了嗜铬细胞瘤和恐慌症的早期治疗,但没有得到缓解。三周后,她因癫痫发作、认知/语言障碍和口面部运动障碍出现在我们的急诊室。脑电图显示右半球δ活动,脑脊液CSF抗nmda受体IgG阳性。脑核磁共振及脑脊液检查正常。她以高血压和精神症状对症治疗。她接受大剂量脉搏静脉注射甲基强的松龙,随后静脉注射免疫球蛋白,这显著缓解了她的认知、神经精神和自主神经特征。严重高血压是抗NMDAR脑炎的罕见表现。早期识别和及时处理可改善预后和长期后遗症。
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引用次数: 1
Experience with anti NMDA receptor antibody encephalitis in a tertiary care hospital in Pakistan 抗NMDA受体抗体脑炎在巴基斯坦三级医院的经验
Pub Date : 2023-02-05 DOI: 10.56310/pjns.v17i03.189
H. Rajput, Zaid Waqar, Muhammad Hassan, Neelma Naz Khattak, Umair Hassan, Iqra Athar, Mazhar Badshah
Background and objective: Anti NMDA receptor (Anti-NMDAR) antibody encephalitis is an increasingly recognized form of auto immune encephalitis. The objective of this study was to determine the demographic, clinical and laboratory factors associated with this syndrome.   Methods: All cases presenting to neurology, Pakistan institute of medical sciences, Islamabad, from June 2017 till January 2020 were reviewed retrospectively. Patients fulfilling the diagnostic criteria for Anti NMDA receptor (Anti-NMDAR) antibody encephalitis were included. All patients were evaluated with cerebrospinal fluid (CSF)routine examination, MRI brain, autoimmune encephalitis profile and for presence of oligoclonal bands (OCB) in CSF. Statistical analysis was done using SPSS version 23.0. Results: A total of 7 patients were diagnosed as having Anti-NMDARantibody encephalitis. Five patients were female and two were male. Four patients had some type of psychiatric disturbances upon presentation of these behavioral abnormalities and irritability were found in all four. Orofacial abnormal movements were found in four patients while one patient had myoclonic seizures. Conclusion: Anti-NMDARreceptor encephalitis is a common cause of encephalitis associated with neurological and psychiatric symptoms. Delay in diagnosis can occur due to non-specific symptoms and signs present in early stages of illness,this can lead to long term neurological disability.
背景与目的:抗NMDA受体(Anti- nmdar)抗体脑炎是一种越来越被认识的自身免疫性脑炎。本研究的目的是确定与该综合征相关的人口学、临床和实验室因素。方法:回顾性分析2017年6月至2020年1月在伊斯兰堡巴基斯坦医学研究所神经内科就诊的所有病例。纳入符合抗NMDA受体(Anti- nmdar)抗体脑炎诊断标准的患者。所有患者均通过脑脊液(CSF)常规检查、脑MRI、自身免疫性脑炎概况和脑脊液中是否存在寡克隆带(OCB)进行评估。采用SPSS 23.0进行统计分析。结果:7例患者诊断为抗nmdarantibody脑炎。其中女性5例,男性2例。4例患者在表现出这些行为异常时出现了某种类型的精神障碍,并且在所有4例患者中都发现了烦躁。4例患者出现口面部异常运动,1例患者出现肌阵挛性发作。结论:抗nmdar受体脑炎是脑炎伴神经和精神症状的常见原因。由于疾病早期阶段出现的非特异性症状和体征可能导致诊断延误,这可能导致长期的神经功能障碍。
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引用次数: 0
Predictors of early seizures after first acute stroke 首次急性中风后早期癫痫发作的预测因素
Pub Date : 2023-02-05 DOI: 10.56310/pjns.v17i03.196
Malik Muhammad Adil, Sumaira Nabi, Maryam Khalil, Zeeshan Munawar, Nayab Aslam, Zaid Waqar
Background and objective: There is a lack of local data regarding the frequency and predictors of early seizures after stroke. The objective of this study was to determine the frequency of early seizures after stroke and identify the predictors which lead to them after first acute stroke. Methods: This cross-sectional observational study was conducted in the Department of Neurology, Pakistan Institute of Medical Sciences, Islamabad from October 2021 to June 2022.  A total of 310 consecutive eligible patients of acute stroke were recruited. Key inclusion criteria included any patient of >20 years of age with confirmed diagnosis of stroke on imaging, non-traumatic, with no history of seizures in past. Data was analyzed by SPSS version 23.0. Results: The mean age of patients in the seizures group was 48.40 ± 20.9 years. Hypertension was the most common co-morbid present in 225 (76.5%) patients. Early seizures were found in 52 (16.8%) patients with 42 (80.76%) having seizures in first 24 hours of stroke (p value 0.001). On National Institute of Health Sciences Scale (NIHSS) score most patients 125 (40.3%) had moderate severity score i.e. score in between 7 to 25 (p value 0.05). Ischemic stroke was identified as the stroke variety with most of the early seizures i.e. 16 (30.76%) (p value 0.003). Conclusion: Early seizures were not infrequent after acute stroke (16.77%) in our study. Early seizures were associated with younger age, cortical region lesion, ischemic stroke, followed by cerebral venous thrombosis. Higher NIHSS score and greater disability was associated with increased incidence of early seizures.  
背景和目的:缺乏关于中风后早期癫痫发作的频率和预测因素的本地数据。本研究的目的是确定中风后早期癫痫发作的频率,并确定导致首次急性中风后癫痫发作的预测因素。方法:本横断面观察性研究于2021年10月至2022年6月在伊斯兰堡巴基斯坦医学科学研究所神经内科进行。共招募了310例连续的急性卒中患者。主要纳入标准包括任何年龄>20岁、影像学确诊为卒中、非创伤性、既往无癫痫发作史的患者。数据分析采用SPSS 23.0版本。结果:癫痫发作组患者平均年龄48.40±20.9岁。高血压是225例(76.5%)患者中最常见的合并症。52例(16.8%)患者出现早期癫痫发作,42例(80.76%)患者在卒中后24小时出现癫痫发作(p值0.001)。在美国国立卫生科学研究所量表(NIHSS)评分中,大多数125例(40.3%)患者为中度严重程度评分,即评分在7 ~ 25之间(p值0.05)。缺血性卒中为卒中类型,早期癫痫发作最多,16例(30.76%)(p值0.003)。结论:急性脑卒中后早期癫痫发作并不少见(16.77%)。早期癫痫发作与年龄小、皮质区病变、缺血性脑卒中、脑静脉血栓形成相关。较高的NIHSS评分和更大的残疾与早期癫痫发作的发生率增加有关。
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引用次数: 0
Pediatric stroke: a review 儿科中风:综述
Pub Date : 2023-02-05 DOI: 10.56310/pjns.v17i03.215
T. Sultan
Background & Objectives: Pediatric stroke is a focal neurological deficit lasting more than 24 hours because of stenosis, occlusion or rupture of cerebral blood vessels. Variable etiological factors are involved ranging from cardiac, haematological, infectious, immune mediated to arteriopathies which is emerging as most important cause of arterial ischemic stroke in children. In this review article we will discuss paediatric stroke with its epidemiology, etiological factors in particular arteriopathies, diagnostic modalities, management protocols and outcome. Methods: We searched stroke in Pubmed and found 15315 articles, narrowed down to stroke in children (3814) and selected 45 articles for review. Review: Stroke in children is defined as a focal neurological deficit that persists for more than 24 hours and is caused by stenosis, occlusion or rupture of cerebral blood vessels. Stroke may be arterial, venous or because of occlusion of venous sinuses. Arterial strokes may be ischemic, haemorrhagic or ischemic-haemorrhagic. About half of strokes in children are of arterial ischemic strokes in contrast to adults where about 80-85% strokes are of arterial ischemic strokes. Stroke in children is comparable to brain tumors and is one of top ten common causes of death in children. Arterial ischemic stroke in children has significant risk of mortality and morbidity leading to functional disability of patient along with financial burden over family and society. In one study it was estimated that 10-25% of children with stroke die, 25% have recurrence and about 66% of children have neurological deficit after recovery from acute illness or have future epilepsy, behaviour disorder or learning disabilities. Early recognition and prompt treatment of paediatric stroke can reduce mortality, morbidity and in return can reduce both social and financial burden over society. Conclusion: In this review article we will discuss paediatric strokes, epidemiology, risk factors, differential diagnosis, investigations, management protocols, preventive measures and outcome.
背景与目的:小儿卒中是由于脑血管狭窄、闭塞或破裂引起的持续24小时以上的局灶性神经功能缺损。各种病因因素涉及心脏、血液、感染、免疫介导的动脉病变,动脉病变正在成为儿童动脉缺血性中风的最重要原因。在这篇综述文章中,我们将讨论小儿中风的流行病学,病因,特别是动脉病变,诊断方式,管理方案和结果。方法:我们在Pubmed中检索中风,共找到15315篇文章,将范围缩小到儿童中风(3814篇),并选择45篇文章进行综述。回顾:儿童卒中被定义为持续24小时以上的局灶性神经功能缺损,由脑血管狭窄、闭塞或破裂引起。中风可能是动脉性、静脉性或因静脉窦闭塞所致。动脉性中风可为缺血性、出血性或缺血性-出血性。大约一半的儿童中风是由动脉缺血性中风引起的而成人中风是由动脉缺血性中风引起的大约80-85%。儿童中风与脑肿瘤相当,是儿童十大常见死亡原因之一。儿童动脉缺血性脑卒中具有显著的死亡率和发病率风险,导致患者功能残疾,并给家庭和社会带来经济负担。据一项研究估计,10-25%的中风儿童死亡,25%复发,约66%的儿童在急性疾病康复后出现神经功能障碍,或未来有癫痫、行为障碍或学习障碍。早期发现和及时治疗小儿中风可降低死亡率和发病率,反过来可减轻社会和经济负担。结论:在这篇综述文章中,我们将讨论儿科中风,流行病学,危险因素,鉴别诊断,调查,管理方案,预防措施和结果。
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引用次数: 0
Post COVID-19 vaccine Guillain Barre Syndrome COVID-19疫苗后格林-巴利综合征
Pub Date : 2022-12-04 DOI: 10.56310/pjns.v17i02.174
Soban Khan, M. Khalil, Zaid Waqar, Sajid Khan, Zakir Jan
The Guillain Barre Syndrome (GBS) is an acute immune mediated progressive polyneuropathy having an acute monophasic illness leading to paralysis. The clinical features are progressive ascending symmetrical muscle weakness that may lead to respiratory failure. Diagnosis is based upon clinical presentation and is supported by a lumbar puncture with CSF analysis demonstrating albumin cytological dissociation and electrophysiological studies. Our patient presented to us with progressive ascending paralysis after receiving COVID 19 vaccine.
格林-巴利综合征(GBS)是一种急性免疫介导的进行性多神经病变,伴有急性单相疾病,可导致瘫痪。临床特征为进行性上升对称肌无力,可导致呼吸衰竭。诊断是基于临床表现,并由腰椎穿刺脑脊液分析证实白蛋白细胞学分离和电生理研究支持。我们的患者在接受COVID - 19疫苗后出现进行性上升性麻痹。
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引用次数: 0
Succinic semialdehyde dehydrogenase deficiency – a rare cause of metabolic stroke 琥珀半醛脱氢酶缺乏症——代谢性中风的罕见病因
Pub Date : 2022-12-04 DOI: 10.56310/pjns.v17i02.180
A. Wasim, Javeria Alvi, T. Sultan
Succinic semialdehyde dehydrogenase (SSADH) deficiency is a rare neurometabolic disorder characterized by defective degradation of gamma-aminobutyric acid (GABA), a major inhibitory neurotransmitter of the brain. Children with SSADH deficiency present with motor mental delay, intractable seizures, infantile onset hypotonia, speech disturbances, extrapyramidal symptoms and ataxia. This wide spectrum results from increased accumulation of 4hydroxy butyric acid (4HBA) leading to down regulation of GABA receptors, which likely explain epileptogenesis but the pathophysiology of stroke in SSADH deficiency is not much elucidated. Here, we report an infant aged 11 months, product of consanguineous marriage with significant family history of motor delay and intellectual disability, presented with sudden onset focal neurological deficit preceded by diarrheal illness. Examination revealed an infant with age-appropriate milestones having left uncrossed hemiplegia along with neuroradiological evidence of right globus pallidus ischemic infarct. Urinary organic acid profile by chromatography was suggestive of 4 hydroxybutyric aciduria.
琥珀半醛脱氢酶(SSADH)缺乏症是一种罕见的神经代谢性疾病,其特征是γ -氨基丁酸(GABA)的降解缺陷,GABA是大脑的主要抑制性神经递质。SSADH缺乏症患儿表现为运动智力迟缓、顽固性癫痫发作、婴儿期低张力、言语障碍、锥体外系症状和共济失调。这种广谱是由于4羟基丁酸(4HBA)的积累增加导致GABA受体的下调,这可能解释了癫痫的发生,但SSADH缺乏导致中风的病理生理机制尚不清楚。在这里,我们报告了一个11个月大的婴儿,近亲婚姻的产物,有明显的运动迟缓和智力残疾的家族史,表现为突发性局灶性神经功能障碍,并伴有腹泻疾病。检查显示一个婴儿与年龄相适应的里程碑有左未交叉偏瘫和神经影像学证据的右侧苍白球缺血性梗死。尿有机酸色谱分析提示4 -羟基丁酸尿。
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引用次数: 0
Iranian stroke model-how to involve health policymakers 伊朗中风模式——如何让卫生政策制定者参与进来
Pub Date : 2022-12-04 DOI: 10.56310/pjns.v17i02.178
M. Farhoudi, E. Sharifipour
Stroke in Iran, with more than 83 million population, is a leading cause of disability and mortality in adults. Stroke has higher incidence in Iran comparing the global situation and unfortunately the onset age of first ever stroke is dropping about 10 years (1). Intravenous thrombolysis, as an approved treatment in ischemic stroke, has been used only in some university or private hospitals in Iran since 2008 (2). The main limit for this therapy in Iran was the lack of coverage by health insurance companies for tPA. A project for situation analysis of stroke cases entering to Imam Reza Hospital, a tertiary university hospital in North-West of Iran, was performed in 2010 by Neurosciences Research Center and the percentage of cases referring on time and are eligible for thrombolysis, barriers, pitfalls and delay gaps in the hospital were detected (3). After analyzing and involving all the related authorities & departments of the Tabriz University of Medical Sciences University and performing a maneuver, thrombolysis in all eligible stroke cases was systematically started as pilot in the hospital since 2010. Other centers such as Firoozgar Hospital in Tehran, Ghaem Hospital in Mashhad, Namazi Hospital in Shiraz, and Alzahra Hospital in Isfahan were active in thrombolysis but non-systematically.    After the first International and the sixth National Iranian Stroke Congress-2013, a WSO endorsed meeting and report of pilot center results, a statement was distributed to offer more motivation and assistance to stroke programs by health policy makers (4). Finally by Iranian stroke association and Iranian Neurological Society follow up, Ministry of health detected stroke as a main health crisis and decided to design and run a program for improving the stroke care in Iran. National stroke committee was organized in 2014 by inviting stroke experts throughout the country. A road map and national strategy were planned to arrange stroke treatment network in Iran reflecting national needs (5). “724” hospitals (means active hospitals for stroke service every 7 days of week and 24 hours a day) were defined for those covering at least 300,000 population around it with basic requirements for acute stroke services including thrombolysis. The plan implemented in 2016 in fifty four hospitals in the early phase. The requirements, characteristics and protocols for primary and comprehensive stroke care units were defined for “724” hospitals. Meanwhile a plan for prehospital emergency system education to increase their knowledge about stroke and upgrade the system to transfer the stroke cases to “724” hospitals was activated. This new stroke plan was presented in 10th World Stroke Congress, 2016. (6). An especial national document for acute stroke treatment was published by Ministry of Health. This plan led to coverage of tPA for eligible stroke cases by insurances companies and finally the decrease of its cost. The main components of Iranian Stroke Program “724” are as
在拥有8300多万人口的伊朗,中风是导致成年人残疾和死亡的主要原因。与全球相比,中风在伊朗的发病率更高,不幸的是,首次中风的发病年龄正在下降约10年(1)。静脉溶栓作为一种被批准的缺血性中风治疗方法,自2008年以来仅在伊朗的一些大学或私立医院使用(2)。该疗法在伊朗的主要限制是缺乏医疗保险公司对tPA的覆盖。2010年,神经科学研究中心开展了一项伊朗西北部三级大学医院伊玛目礼萨医院中风病例情况分析项目,发现了医院按时转诊并符合溶栓条件的病例百分比、障碍、陷阱和延迟差距(3)。在分析并让大不里斯医科大学所有相关部门参与并实施了一项策略后,自2010年起,在所有符合条件的脑卒中病例中系统地开展了溶栓试验。德黑兰的Firoozgar医院、马什哈德的Ghaem医院、设拉子的Namazi医院和伊斯法罕的Alzahra医院等其他中心在溶栓方面也很活跃,但不是系统的。在第一届国际和第六届伊朗中风大会(2013)之后,WSO批准了一次会议,并报告了试点中心的结果,发布了一份声明,为卫生政策制定者对中风项目提供更多的动力和帮助(4)。最后,在伊朗中风协会和伊朗神经学会的跟进下,卫生部发现中风是一个主要的健康危机,并决定设计和运行一个项目,以改善伊朗的中风护理。全国中风委员会于2014年成立,由全国各地的中风专家组成。计划制定一项路线图和国家战略,在伊朗安排反映国家需求的中风治疗网络(5)。确定了" 724 "医院(指每周7天、每天24小时提供中风服务的活跃医院),覆盖至少30万周边人口,提供包括溶栓在内的急性中风服务的基本需求。该计划于2016年在54家医院实施,处于早期阶段。为“724”医院确定了初级和综合卒中护理单位的要求、特点和方案。同时,启动院前急救系统教育计划,以增加他们对中风的认识,并升级系统,将中风病例转移到“724”医院。这项新的中风计划在2016年第十届世界中风大会上提出。(6)卫生部发布急性脑卒中治疗国家专项文件。这一计划使得保险公司将tPA纳入符合条件的中风病例,并最终降低了其成本。伊朗卒中项目“724”的主要组成部分如下:(5)公众意识:公众教育考虑到卒中各方面的信息,包括主要预警信号(FAST)、卒中危险因素、生活方式改善和初级预防,第一阶段的重点是FAST。我们通过媒体、网络空间、中风运动、新闻组织和健康中心等不同的方式来传播这些信息,以提高社区意识。在全国范围内开展了世界中风日庆祝活动、全国健康周仪式、公众讲座、专家问答等专题活动。为了传递知识,我们使用了一些动画、海报、横幅、短片和一些特别名人的小册子。卒中团队培训:所有参与急性卒中患者治疗及相关科室和系统的人员、中高层管理人员、急诊人员、神经科医师(“724”计划引入的个体)、急诊医学专家、“724”医院管理人员;护理、急诊科、血库、影像科工作人员;选定的康复中心接受了协议培训,以实施该计划。在参与医院任命了一名联络员,负责监测并向国家中心报告。卒中患者快速转移系统之间的协调:“724”计划中定义了卒中预先通知代码SAMA,用于急诊、医院和大学根据FAST检查怀疑发生卒中时。一旦有疑似急性中风症状的患者在发病后4.5小时内致电调度中心,SAMA代码就会被激活,并向所有相关部门(724医院的急救服务和中风科工作人员)宣布,以便准备紧急入院、成像和其他流程。 急性中风护理病房(SCU)的建立:在所有“724”医院中定义并启动了急性中风护理病房,并由接受过中风培训的神经科医生管理。单位应配备连续心电图和血压监测设施和卒中管理所需的药物。为所有符合条件的中风患者提供溶栓治疗的公共保险。对重要的时间,特别是“从门到针”的时间进行了监控,并试图将其控制在60分钟以内。对scu实施并发症的预防措施,包括吞咽试验、深静脉血栓预防和卒中综合康复小组(职业治疗师、物理治疗师和语言病理学家)。全国“724”卒中登记:设计了一个简短的全国系统,用于登记“724”医院的患者信息。医院数量从2016年的54个中心增加到2022年的120个中心,并继续增加。该数据库显示,在“724”计划的前6年,登记和治疗的急性卒中患者超过6.6万例。其中静脉溶栓13148例,血管内取栓400余例。数据监测显示,从门到针的时间将逐年减少(从2016年的平均69分钟减少到2022年的不到50分钟),接受tPA的患者数量将逐年增加(从2016年的784人增加到2022年的>13000人)。希望伊朗能够在卒中管理和急性缺血性卒中溶栓治疗方面取得重大进展,以覆盖更多符合条件的病例。幸运的是,根据WSO-WHO最近的调查,伊朗在急性卒中服务方面的情况非常好(7)。然而,我们需要取得更多进展,以覆盖更多的患者,实施更多新的先进治疗方法,并促进卒中患者管理的其他方面。
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引用次数: 1
Risk factors of intracerebral hemorrhage- a cross sectional study 脑出血的危险因素-横断面研究
Pub Date : 2022-12-04 DOI: 10.56310/pjns.v17i02.142
Mir Jalal-ud-din, Raheel Jehangir Jadoon, Samia Wazir Khawaja, Rashid Ali, Syed Affan Ali, Ibtisam
BACKGROUND: Stroke is the most common cause of disability and a leading cause of mortality worldwide. Though the incidence is falling in West but probably rising in Asia. The burden of stroke risk factors in Pakistan is enormous. Data on stroke incidence and prevalence from Pakistan is scarce; however, there are several reported case series in literature highlighting significant differences in terms of stroke epidemiology, risk factors and stroke subtypes/patterns. METHODS: This descriptive cross sectional study was conducted from August 2019 to February 2020, on 109 patients from medical units of DHQ Teaching Hospital Abbottabad. Diagnosis of cerebrovascular accidents was made on focal neurological deficit lasting more than 24 hours. CT scan brain was done in all patients to detect intra cerebral bleed. Detailed history and medical records were carefully scrutinized in the patients of intracerebral bleed to detect factors leading to it like uncontrolled hypertension. Fasting blood glucose, fasting serum cholesterol and fasting triglycerides were done to detect uncontrolled diabetes and hyperlipidemia. Data was collected on a structured proforma and analysed using SPSS 20. RESULTS: Majority of the patients were 39.81%(n=41) >70 years of age, 71 (68.93%) were male and 32 (31.07%) female, frequency of intracerebral bleed among patients presenting with acute cerebrovascular accidents was recorded in 8.74%(n=9), among them 66.67%(n=6) had history of uncontrolled hypertension, 44.44%(n=4) had diabetes and 33.33%(n=3) had hyperlipidemia. CONCLUSIONS: Frequency of intracerebral bleed is higher among patients presenting with cerebrovascular accidents, hypertension is recorded the most common risk factor for this complication.
背景:中风是最常见的致残原因,也是世界范围内死亡的主要原因。虽然发病率在西方正在下降,但在亚洲可能正在上升。在巴基斯坦,中风风险因素的负担是巨大的。巴基斯坦关于中风发病率和流行率的数据很少;然而,文献中有几个报道的病例系列强调了卒中流行病学,危险因素和卒中亚型/模式方面的显着差异。方法:本描述性横断面研究于2019年8月至2020年2月对阿伯塔巴德DHQ教学医院医疗单位的109名患者进行。当局灶性神经缺损持续24小时以上时,诊断为脑血管意外。所有患者均行颅脑CT扫描,检查颅内出血。仔细检查脑出血患者的详细病史和医疗记录,以发现导致脑出血的因素,如未控制的高血压。空腹血糖、空腹血清胆固醇和空腹甘油三酯检测未控制的糖尿病和高脂血症。数据以结构化形式收集,并使用SPSS 20进行分析。结果:年龄>70岁的患者占39.81%(n=41),男性71例(68.93%),女性32例(31.07%),急性脑血管意外患者中脑出血发生率为8.74%(n=9),其中66.67%(n=6)有高血压未控制史,44.44%(n=4)有糖尿病,33.33%(n=3)有高脂血症。结论:脑血管意外患者发生脑出血的频率较高,高血压是该并发症最常见的危险因素。
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引用次数: 1
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Pakistan Journal of Neurological Sciences
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