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Chryseobacterium Indologenes Sepsis and Acute Renal Failure Secondary to Abdominal Compartment Syndrome in a Confirmed COVID-19 Patient 一例确诊的新冠肺炎患者因腹腔隔室综合征继发的Indologenes Chryseobacterium Sepsis和急性肾衰竭
Q3 Medicine Pub Date : 2022-04-14 DOI: 10.1155/2022/7946158
A. J. Quiroz Alfaro, I. J. Rodríguez Acosta, Mayumi Tanaka Takegami, Liliana Michelle Bracho Maya, Roberto Eduardo Quiroz Simanca
Sepsis due to nosocomial pathogens markedly increases morbidity and mortality in the critically ill patient. The SARS-CoV-2 (COVID-19) pandemic has increased the number of patients requiring intensive care unit (ICU) in-patient management. Chryseobacterium indologenes (C. indologenes) is a group of multiresistant gram-negative bacteria associated with in-hospital environment and catheter-associated infections of increasing importance in the ICU. SARS-CoV-2 severe infection in the critically ill patient increases the risk of abdominal compartment syndrome (ACS) and acute kidney injury (AKI). We hereby report a case of a patient with SARS-CoV-2 severe infection, C. indologenes sepsis, abdominal compartment syndrome, and secondary renal failure.
院内病原菌引起的脓毒症显著增加危重病人的发病率和死亡率。SARS-CoV-2 (COVID-19)大流行增加了需要重症监护病房(ICU)住院管理的患者数量。吲哚黄杆菌(C. indologenes)是一组多重耐药革兰氏阴性菌,与院内环境和导管相关感染有关,在ICU中日益重要。危重患者严重感染SARS-CoV-2可增加腹腔隔室综合征(ACS)和急性肾损伤(AKI)的风险。我们在此报告一例SARS-CoV-2严重感染,吲哚原体脓毒症,腹腔隔室综合征和继发性肾衰竭的患者。
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引用次数: 2
A Rare Cause of a Rare Disorder: E. coli-Induced Purpura Fulminans Secondary to Urinary Tract Infection 一种罕见疾病的罕见原因:大肠杆菌引起的继发于尿路感染的暴发性紫癜
Q3 Medicine Pub Date : 2022-04-06 DOI: 10.1155/2022/9291424
J. Lowry, E. Noel
Purpura fulminans is a devastating thrombotic disorder infrequently encountered in medical practice and amongst the medical literature. It is a hematologic emergency in which prompt recognition and initiation of treatment are critical to mitigate its significant morbidity and mortality. Surgical evaluation is commonly required, since the debilitating skin and soft tissue necrosis often degenerate into necrotizing fasciitis, critical limb ischemia, warranting surgical interventions in either a staged or single-step approach. Purpura fulminans can be neonatal, infectious, or idiopathic. Infection-induced purpura fulminans is less common, and only a few microorganisms have been associated with this condition: Meningococcus spp., Pneumococcus spp., or Staphylococcus spp. This report presents a rare case of Escherichia coli-induced purpura fulminans. Apart from the unfortunate partial amputation of all left-hand five digits, our patient made a full recovery following effective infectious source control, supportive care with volume resuscitation, anticoagulation, and wound care.
暴发性紫癜是一种破坏性的血栓性疾病,在医学实践和医学文献中很少遇到。这是一种血液学紧急情况,及时识别和开始治疗对于减轻其显著的发病率和死亡率至关重要。通常需要手术评估,因为衰弱的皮肤和软组织坏死经常退化为坏死性筋膜炎,严重的肢体缺血,需要分阶段或单步手术干预。暴发性紫癜可为新生儿、传染性或特发性。感染引起的暴发性紫癜不太常见,只有少数微生物与此病有关:脑膜炎球菌、肺炎球菌或葡萄球菌。本文报告一例罕见的大肠杆菌引起的暴发性紫癜。除了不幸的左手五指部分截肢外,我们的患者在有效的传染源控制、容积复苏、抗凝和伤口护理等支持性护理后完全康复。
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引用次数: 1
Methamphetamine-Induced Bowel Ischemia in a 50-Year-Old Male 甲基苯丙胺致50岁男性肠道缺血
Q3 Medicine Pub Date : 2022-04-05 DOI: 10.1155/2022/9690034
Brian Kurtz, Abdalhai Alshoubi, K. Nguyen, Eric Gehres
Methamphetamine intoxication is a known risk factor for nonocclusive mesenteric ischemia (NOMI). We describe a case of a 50-year-old male with a history of polysubstance abuse who presented to the Emergency Department with severe abdominal pain and coffee-ground emesis. Computed tomographic (CT) imaging demonstrated portal venous gas and diffuse colonic wall thickening concerning for ischemic colitis. The patient underwent exploratory laparotomy with resection of the ascending colon as well as a necrotic section of the jejunum. Further embolic workup was negative with a subjective history of amphetamine use prior to presentation. NOMI has a high fatality rate, and we recommend providers include drug-induced bowel infarction on their differential when presented with findings of ischemic bowel of unclear etiology.
甲基苯丙胺中毒是非闭塞性肠系膜缺血(NOMI)的一个已知危险因素。我们描述了一例50岁男性,有多物质滥用史,因严重腹痛和咖啡地呕吐到急诊科就诊。计算机断层扫描(CT)显示门静脉气体和弥漫性结肠壁增厚与缺血性结肠炎有关。患者接受了剖腹探查术,切除了升结肠和坏死的空肠。进一步的栓塞检查是阴性的,在出现之前有苯丙胺使用的主观病史。NOMI的病死率很高,当发现病因不明的缺血性肠时,我们建议提供者将药物诱导的肠梗死纳入其鉴别标准。
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引用次数: 1
Multiple Electroencephalogram Recordings for Monitoring the Evolution of Neurological Complications during Baclofen Withdrawal Syndrome 多种脑电图记录监测巴氯芬戒断综合征期间神经系统并发症的演变
Q3 Medicine Pub Date : 2022-03-07 DOI: 10.1155/2022/4245667
M. Scarpino, G. Lanzo, C. Chelazzi, Antonio Maiorelli, V. Bessi, M. Focardi, F. Lolli, A. Grippo
Baclofen withdrawal syndrome represents a clinical emergency that can lead to life-threatening complications. It is often a diagnostic challenge because of its nonspecific nature of presentation and degree of symptom overlap with other clinical diseases. Electroencephalography (EEG) might provide important supporting evidence when neurological complications are involved. We present the case of a 55-year-old woman with sudden onset of motor manifestations at the limbs and an altered mental status 24 hours after cessation of intrathecal baclofen administration, following the removal of the pump due to infection, in whom a computed tomography did not show any acute-onset brain injuries, and multiple EEG recordings were performed. The first EEG showed the presence of bilateral sharply contoured waves, in the absence of epileptic discharges and seizures. No correlation between motor manifestations and EEG changes were detected. This EEG pattern was considered to be the expression of an overexcitation of the central nervous system (CNS) due to the loss of baclofen inhibitory effects, excluding an epileptic origin of motor manifestations. Another EEG, performed 24 hours later, showed the presence of triphasic waves with severe generalised slowing, suggesting the presence of encephalopathy. The last EEG, performed 48 hours after the previous recording, when a recovered state of consciousness was already present, showed regression of the triphasic waves and a reorganisation of the background activity. In our case, repeated EEG evaluation allowed monitoring the evolution of acute encephalopathy developed during baclofen withdrawal syndrome, from the initial phase of CNS hyperexcitability, through the phase of metabolic encephalopathy, and to its resolution. This modality allowed for optimising the diagnostic-therapeutic management of the patient during her stay in the intensive care unit.
巴氯芬戒断综合征是一种临床紧急情况,可导致危及生命的并发症。由于其表现的非特异性和症状与其他临床疾病重叠的程度,它通常是一个诊断挑战。当涉及神经系统并发症时,脑电图(EEG)可能提供重要的支持证据。我们报告了一名55岁的女性,由于感染而取下泵,在鞘内巴氯芬给药停止24小时后,四肢突然出现运动表现,精神状态改变,计算机断层扫描未显示任何急性脑损伤,并进行了多次脑电图记录。第一次脑电图显示在没有癫痫放电和癫痫发作的情况下,存在双侧尖锐轮廓波。运动表现与脑电图变化无相关性。这种脑电图模式被认为是由于巴氯芬抑制作用的丧失而导致中枢神经系统(CNS)过度兴奋的表达,排除了运动表现的癫痫起源。24小时后进行的另一次脑电图显示存在严重的广泛性减慢的三相波,提示存在脑病。最后一次脑电图是在前一次记录的48小时后进行的,当时已经出现了恢复的意识状态,显示了三相波的消退和背景活动的重组。在我们的病例中,反复的脑电图评估可以监测巴氯芬戒断综合征期间发生的急性脑病的演变,从中枢神经系统高兴奋性的初始阶段,到代谢性脑病的阶段,再到其消退。这种模式允许优化患者在重症监护病房期间的诊断治疗管理。
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引用次数: 1
Widespread Arterial Thrombosis after ChAdOx1 nCov-19 Vaccination 接种ChAdOx1 nCov-19后广泛的动脉血栓形成
Q3 Medicine Pub Date : 2022-02-16 DOI: 10.1155/2022/6804456
G. Berlot, A. Tomasini, Cristina La Fata, S. Pintacuda, Sara Rigutti, A. Falanga
Vaccine-induced thrombotic thrombocytopenia is an uncommon complication of COVID-19 vaccines using adenovirus mRNA carriers and has been associated with thrombosis of the cerebral venous sinuses and portal system. We report a case of a 69-year-old woman admitted to the intensive care unit due to stroke caused by thrombosis of the right carotid artery 9 days after receiving the ChAdOx1 nCov-19 vaccine. Further investigations demonstrated multiple thrombi in the arterial tree in the absence of any venous involvement. The clinical course and the treatment are described and discussed.
疫苗诱导的血栓性血小板减少症是使用腺病毒mRNA载体的COVID-19疫苗的一种罕见并发症,与脑静脉窦和门静脉系统血栓形成有关。我们报告一例69岁妇女,在接种ChAdOx1 nCov-19疫苗9天后,因右颈动脉血栓形成引起的中风而住进重症监护室。进一步的调查显示,在没有任何静脉受累的情况下,动脉树有多个血栓。对临床过程和治疗方法进行了描述和讨论。
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引用次数: 3
Risen Alive: The Lazarus Phenomenon. 复活:拉撒路现象。
Q3 Medicine Pub Date : 2022-02-15 eCollection Date: 2022-01-01 DOI: 10.1155/2022/3322056
Waqar Haider Gaba, Shahad Abobakar El Hag, Shaima Mustafa Bashir

The Lazarus phenomenon described as delayed return of spontaneous circulation (ROSC) after cessation of CPR is rare, though underreported. We present the case of a 25-year-old woman who visited our hospital for persistent vomiting and weight loss for the last six months following bariatric surgery. On the 16th day of admission, the patient experienced cardiac arrest (code blue). The patient underwent 73 min of continuous cardiopulmonary resuscitation (CPR); however, no responses were observed, which led to an announcement of death. Fifty minutes later, the family members noticed subtle eye movements that necessitated resumption of the advanced cardiac life support protocol and resuscitation. The patient survived; however, she developed significant neurological deficits secondary to prolonged anoxic brain injury. She was discharged after a ten-week stay in the hospital but did not achieve full neurologic, cognitive, and motor recovery. Patients should be observed and monitored after the cessation of CPR before confirming death.

拉撒路现象被描述为停止心肺复苏术后自发循环的延迟恢复(ROSC)是罕见的,尽管报道不足。我们提出的情况下,25岁的妇女谁到我们医院持续呕吐和体重下降,在减肥手术后的最后六个月。入院第16天,患者出现心脏骤停(蓝色代码)。患者接受了73分钟的持续心肺复苏(CPR);然而,没有观察到任何反应,这导致宣布死亡。50分钟后,家属注意到患者的眼球有细微的运动,需要恢复先进的心脏生命支持程序和复苏。病人活了下来;然而,她出现了继发于长期缺氧脑损伤的显著神经功能缺损。她在住院十周后出院,但没有达到完全的神经、认知和运动恢复。应在心肺复苏术停止后对患者进行观察和监测,然后再确认死亡。
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引用次数: 1
COVID-19-Induced Fatal Thrombotic Thrombocytopenic Purpura in a Healthy Young Patient. 2019冠状病毒病致致命性血栓性血小板减少性紫癜的研究
Q3 Medicine Pub Date : 2022-01-01 DOI: 10.1155/2022/2934171
Mariana Codevila Buere Pereira, Bruna Ruschel, Bruna Schneider, Vitor Salomão Gonçalves Melo de Melgar, Tatiana Helena Rech

Since the global coronavirus disease 2019 (COVID-19) pandemic began, findings indicate that severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) might induce autoimmune disorders. Thrombotic thrombocytopenic purpura (TTP) is a devastating disease if not emergently treated. It presents with severe thrombocytopenia, microangiopathic hemolytic anemia, and neurologic findings with or without renal insufficiency. The antibody-mediated reduced activity of the disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS13) induces the accumulation of ultrahigh-molecular-weight multimers of von Willebrand factor, leading to platelet aggregation and thrombosis. TTP can be an unusual presentation of COVID-19 disease mediated by the virus-induced immune response. We report a case of a healthy young patient presenting with the classic TTP pentad a few days after a diagnosis of COVID-19 confirmed by a positive SARS-CoV-2 RT-PCR test. The patient was initially treated with high-dose methylprednisolone and fresh frozen plasma until she was transferred to a tertiary care facility and plasma exchange was available. She evolved with a malignant ischemic vascular accident and was declared brain-dead 24 hours after the first plasma exchange section.

自2019年全球冠状病毒病(COVID-19)大流行开始以来,研究结果表明,严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)可能诱发自身免疫性疾病。血栓性血小板减少性紫癜(TTP)是一种毁灭性的疾病,如果不紧急治疗。它表现为严重的血小板减少症、微血管病性溶血性贫血和伴有或不伴有肾功能不全的神经学表现。抗体介导的具有血小板反应蛋白1型基元的崩解素和金属蛋白酶13 (ADAMTS13)的活性降低诱导血管性血友病因子超高分子量多聚体的积累,导致血小板聚集和血栓形成。TTP可能是由病毒诱导的免疫反应介导的COVID-19疾病的一种不寻常表现。我们报告一例健康的年轻患者,在经SARS-CoV-2 RT-PCR检测阳性的COVID-19诊断后几天出现经典的TTP pentad。患者最初接受大剂量甲基强的松龙和新鲜冷冻血浆治疗,直到她被转移到三级医疗机构并进行血浆交换。她发展为恶性缺血性血管意外,并在第一次血浆交换后24小时被宣布脑死亡。
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引用次数: 2
Response to: Comment on "Acetazolamide Intoxication in an Elderly Patient with Diabetes and Chronic Renal Failure after Cataract Surgery". 对“老年糖尿病合并白内障术后慢性肾功能衰竭患者乙酰唑胺中毒”的评论。
Q3 Medicine Pub Date : 2021-12-29 eCollection Date: 2021-01-01 DOI: 10.1155/2021/9892830
Juliana Maria Kerber, Juliana Dias de Mello, Karolinny Borinelli de Aquino Moura, Gustavo Cardoso da Silva, Iuri Christmann Wawrzeniak, Tatiana Helena Rech
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引用次数: 0
Diagnostic Pitfalls in Papillary Muscle Rupture-Associated Acute Mitral Regurgitation after Acute Myocardial Infarction. 急性心肌梗死后乳头肌破裂相关急性二尖瓣反流的诊断缺陷。
Q3 Medicine Pub Date : 2021-12-21 eCollection Date: 2021-01-01 DOI: 10.1155/2021/1396194
Akiko Kameyama, Hiroshi Imamura, Hiroshi Kamijo, Kanako Takeshige, Katsunori Mochizuki, Kenichi Nitta

Papillary muscle rupture (PMR) is a rare and fatal complication of acute myocardial infarction (AMI). We report a case of acute mitral regurgitation (MR) due to PMR with pulmonary edema and cardiogenic shock following AMI with small myocardial necrosis. An 88-year-old woman was brought to our emergency department in acute respiratory distress, shock, and coma. She had no systolic murmur, and transthoracic echocardiography was inconclusive. Coronary angiography showed obstruction of the posterior descending branch of the right coronary artery. Although the infarction was small, the hemodynamics did not improve. Transesophageal echocardiography established papillary muscle rupture with severe mitral regurgitation 5 days after admission. Thereafter, the patient and her family did not consent to heart surgery, and she eventually died of progressive heart failure. Physicians should be aware of papillary muscle rupture with acute mitral regurgitation following AMI in patients with unstable hemodynamics, no systolic murmur, and no abnormalities revealed on transthoracic echocardiography.

乳头状肌破裂是急性心肌梗死(AMI)的一种罕见且致命的并发症。我们报告一例急性二尖瓣反流(MR)由于PMR肺水肿和心源性休克后AMI小心肌坏死。一位88岁的妇女因急性呼吸窘迫、休克和昏迷被送到急诊科。她没有收缩期杂音,经胸超声心动图无结论。冠状动脉造影显示右冠状动脉后降支梗阻。梗死虽小,但血流动力学未见改善。入院后5天经食管超声心动图证实乳头肌破裂伴严重二尖瓣反流。此后,患者及其家属不同意进行心脏手术,最终死于进行性心力衰竭。对于血流动力学不稳定、无收缩期杂音、经胸超声心动图未发现异常的AMI患者,医生应注意乳头肌破裂合并急性二尖瓣反流。
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引用次数: 1
Combined Hyperglycemic Hyperosmolar Syndrome and Diabetic Ketoacidosis Associated with COVID-19 in a Pediatric Patient. 新冠肺炎合并高血糖高渗综合征和糖尿病酮症酸中毒1例
Q3 Medicine Pub Date : 2021-11-27 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6429710
Yu Shan Tseng, Bradley Tilford, Usha Sethuraman, Katherine Cashen

Although most children with coronavirus disease 2019 (COVID-19) are asymptomatic or only with mild symptoms, many symptomatic children still require admission to the intensive care unit. Multiple cases of diabetic ketoacidosis (DKA) and hyperosmolar hyperglycemic syndrome (HHS) associated with COVID-19 have been reported in adults. However, to our knowledge, only few similar cases have been published in the pediatric population. We report one of the first few severe cases of mixed HHS with DKA associated with COVID-19 in an adolescent. Our patient was successfully treated with intravenous immunoglobulin, Remdesivir, and methylprednisolone. As the pandemic continues, clinicians should be aware of this syndrome and consider early use of Remdesivir and corticosteroids. Further studies are required to understand the pathophysiology of this syndrome occurring with COVID-19.

尽管大多数2019冠状病毒病(新冠肺炎)儿童无症状或症状轻微,但许多有症状的儿童仍需要入住重症监护室。据报道,成人中出现多例与新冠肺炎相关的糖尿病酮酸中毒(DKA)和高渗性高血糖综合征(HHS)。然而,据我们所知,只有少数类似的病例在儿科人群中发表。我们报告了青少年中为数不多的与新冠肺炎相关的混合HHS和DKA重症病例之一。我们的患者成功地接受了静脉注射免疫球蛋白、瑞德西韦和甲基强的松龙的治疗。随着疫情的持续,临床医生应该意识到这种综合征,并考虑尽早使用瑞德西韦和皮质类固醇。需要进一步的研究来了解新冠肺炎引起的这种综合征的病理生理学。
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引用次数: 0
期刊
Case Reports in Critical Care
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