NEUROPSYCHIATRIC SYSTEMIC LUPUS ERYTHEMATOUS: A DIAGNOSIS OF SUSPICION AND EXCLUSION

IF 8.6 1区 医学 Q1 CRITICAL CARE MEDICINE Chest Pub Date : 2023-10-01 DOI:10.1016/j.chest.2023.07.1943
REENA PATEL, PRIYANKA BATTA, HENA YAGNIK
{"title":"NEUROPSYCHIATRIC SYSTEMIC LUPUS ERYTHEMATOUS: A DIAGNOSIS OF SUSPICION AND EXCLUSION","authors":"REENA PATEL, PRIYANKA BATTA, HENA YAGNIK","doi":"10.1016/j.chest.2023.07.1943","DOIUrl":null,"url":null,"abstract":"SESSION TITLE: Critical Care Case Report Posters 49 SESSION TYPE: Case Report Posters PRESENTED ON: 10/10/2023 09:40 am - 10:25 am INTRODUCTION: Systemic lupus erythematosus (SLE) is a chronic autoimmune process affecting multiple systems within the body. Known as neuropsychiatric SLE (NPSLE), diagnosis may require exclusion of other causes however prompt recognition will aid in appropriate symptomatic management. CASE PRESENTATION: A 48-year-old female with known diagnosis of SLE presented to the ED due to slurred speech and weakness. In the ED, patient was found to be tachycardic, otherwise vitals were stable. Initial labwork was significant for leukocytosis, microcytic anemia, thrombocytosis, AKI, and anion gap metabolic acidosis. Patient underwent CT brain and CTA head and neck which showed no acute abnormalities, no high-grade stenosis, dissection, or occlusion in the vessels of the head or neck. CT abdomen/pelvis and CXR also showed no acute abnormalities. Patient was initially started on broad spectrum antibiotics in setting of suspected sepsis of unknown origin. Patient was also started on a sodium bicarb drip and AKI as well as anion gap metabolic acidosis resolved however patient's slurred speech persisted. Patient also had episodes of hallucinations and delirium as well. MRI brain showed no acute intracranial process; it did show signs of chronic small vessel ischemic changes and moderate to advanced cerebral volume loss most pronounced in the frontal and temporal regions. Urinalysis was notable for proteinuria which was confirmed by two samples of elevated urine protein creatinine ratio. ESR, CRP, ferritin, and D dimer were noted to be elevated. CTA chest confirmed no pulmonary embolism. Rheumatology was consulted due to suspicion of lupus flare. IV antibiotics were discontinued, and patient was placed on Solu-Medrol 1000mg daily for three days and patient's mentation and slurred speech resolved. DISCUSSION: This case demonstrates the importance of clinical suspicion and awareness of NPSLE to allow for treatment in an appropriate timeframe. Many patients with SLE, estimated to be about one-third to one-half of patients, will experience neurologic or psychiatric symptoms throughout their disease course (1). NPSLE symptoms may precede or occur alongside with other manifestations of SLE disease activity (2) For most manifestations of NPSLE, no biomarkers or diagnostic tests are specific enough to attribute a patient's clinical presentation to SLE, however diagnosis should include exclusion of other causes. Identification and treatment is significant as some studies have found an increased risk of mortality in patients with NPSLE compared to SLE patients without NPSLE (3). CONCLUSIONS: In conclusion, clinicians should keep NPSLE in mind for patients with neurological or psychiatric symptoms specially when other causes have been ruled out. REFERENCE #1: Hanly JG;Urowitz MB;Su L;Bae SC;Gordon C;Wallace DJ;Clarke A;Bernatsky S;Isenberg D;Rahman A;Alarcón GS;Gladman DD;Fortin PR;Sanchez-Guerrero J;Romero-Diaz J;Merrill JT;Ginzler E;Bruce IN;Steinsson K;Khamashta M;Petri M;Manzi S;Dooley MA;Ramsey-Goldman R; Prospective analysis of neuropsychiatric events in an international disease inception cohort of patients with systemic lupus erythematosus. Annals of the rheumatic diseases. https://pubmed.ncbi.nlm.nih.gov/19359262/. Accessed March 31, 2023. REFERENCE #2: Hanly JG;Urowitz MB;Gordon C;Bae SC;Romero-Diaz J;Sanchez-Guerrero J;Bernatsky S;Clarke AE;Wallace DJ;Isenberg DA;Rahman A;Merrill JT;Fortin PR;Gladman DD;Bruce IN;Petri M;Ginzler EM;Dooley MA;Ramsey-Goldman R;Manzi S;Jönsen A;Alarcón GS;van Vollenhoven R. Neuropsychiatric events in systemic lupus erythematosus: A longitudinal analysis of outcomes in an international inception cohort using a multistate model approach. Annals of the rheumatic diseases. https://pubmed.ncbi.nlm.nih.gov/31915121/. Accessed March 31, 2023. REFERENCE #3: Ahn GY;Kim D;Won S;Song ST;Jeong HJ;Sohn IW;Lee S;Joo YB;Bae SC; Prevalence, risk factors, and impact on mortality of neuropsychiatric lupus: A prospective, single-center study. Lupus. https://pubmed.ncbi.nlm.nih.gov/29688144/. Accessed March 31, 2023. DISCLOSURES: No relevant relationships by Priyanka Batta No relevant relationships by Reena Patel No relevant relationships by Hena Yagnik","PeriodicalId":9782,"journal":{"name":"Chest","volume":"45 1","pages":"0"},"PeriodicalIF":8.6000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chest","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.chest.2023.07.1943","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CRITICAL CARE MEDICINE","Score":null,"Total":0}
引用次数: 0

Abstract

SESSION TITLE: Critical Care Case Report Posters 49 SESSION TYPE: Case Report Posters PRESENTED ON: 10/10/2023 09:40 am - 10:25 am INTRODUCTION: Systemic lupus erythematosus (SLE) is a chronic autoimmune process affecting multiple systems within the body. Known as neuropsychiatric SLE (NPSLE), diagnosis may require exclusion of other causes however prompt recognition will aid in appropriate symptomatic management. CASE PRESENTATION: A 48-year-old female with known diagnosis of SLE presented to the ED due to slurred speech and weakness. In the ED, patient was found to be tachycardic, otherwise vitals were stable. Initial labwork was significant for leukocytosis, microcytic anemia, thrombocytosis, AKI, and anion gap metabolic acidosis. Patient underwent CT brain and CTA head and neck which showed no acute abnormalities, no high-grade stenosis, dissection, or occlusion in the vessels of the head or neck. CT abdomen/pelvis and CXR also showed no acute abnormalities. Patient was initially started on broad spectrum antibiotics in setting of suspected sepsis of unknown origin. Patient was also started on a sodium bicarb drip and AKI as well as anion gap metabolic acidosis resolved however patient's slurred speech persisted. Patient also had episodes of hallucinations and delirium as well. MRI brain showed no acute intracranial process; it did show signs of chronic small vessel ischemic changes and moderate to advanced cerebral volume loss most pronounced in the frontal and temporal regions. Urinalysis was notable for proteinuria which was confirmed by two samples of elevated urine protein creatinine ratio. ESR, CRP, ferritin, and D dimer were noted to be elevated. CTA chest confirmed no pulmonary embolism. Rheumatology was consulted due to suspicion of lupus flare. IV antibiotics were discontinued, and patient was placed on Solu-Medrol 1000mg daily for three days and patient's mentation and slurred speech resolved. DISCUSSION: This case demonstrates the importance of clinical suspicion and awareness of NPSLE to allow for treatment in an appropriate timeframe. Many patients with SLE, estimated to be about one-third to one-half of patients, will experience neurologic or psychiatric symptoms throughout their disease course (1). NPSLE symptoms may precede or occur alongside with other manifestations of SLE disease activity (2) For most manifestations of NPSLE, no biomarkers or diagnostic tests are specific enough to attribute a patient's clinical presentation to SLE, however diagnosis should include exclusion of other causes. Identification and treatment is significant as some studies have found an increased risk of mortality in patients with NPSLE compared to SLE patients without NPSLE (3). CONCLUSIONS: In conclusion, clinicians should keep NPSLE in mind for patients with neurological or psychiatric symptoms specially when other causes have been ruled out. REFERENCE #1: Hanly JG;Urowitz MB;Su L;Bae SC;Gordon C;Wallace DJ;Clarke A;Bernatsky S;Isenberg D;Rahman A;Alarcón GS;Gladman DD;Fortin PR;Sanchez-Guerrero J;Romero-Diaz J;Merrill JT;Ginzler E;Bruce IN;Steinsson K;Khamashta M;Petri M;Manzi S;Dooley MA;Ramsey-Goldman R; Prospective analysis of neuropsychiatric events in an international disease inception cohort of patients with systemic lupus erythematosus. Annals of the rheumatic diseases. https://pubmed.ncbi.nlm.nih.gov/19359262/. Accessed March 31, 2023. REFERENCE #2: Hanly JG;Urowitz MB;Gordon C;Bae SC;Romero-Diaz J;Sanchez-Guerrero J;Bernatsky S;Clarke AE;Wallace DJ;Isenberg DA;Rahman A;Merrill JT;Fortin PR;Gladman DD;Bruce IN;Petri M;Ginzler EM;Dooley MA;Ramsey-Goldman R;Manzi S;Jönsen A;Alarcón GS;van Vollenhoven R. Neuropsychiatric events in systemic lupus erythematosus: A longitudinal analysis of outcomes in an international inception cohort using a multistate model approach. Annals of the rheumatic diseases. https://pubmed.ncbi.nlm.nih.gov/31915121/. Accessed March 31, 2023. REFERENCE #3: Ahn GY;Kim D;Won S;Song ST;Jeong HJ;Sohn IW;Lee S;Joo YB;Bae SC; Prevalence, risk factors, and impact on mortality of neuropsychiatric lupus: A prospective, single-center study. Lupus. https://pubmed.ncbi.nlm.nih.gov/29688144/. Accessed March 31, 2023. DISCLOSURES: No relevant relationships by Priyanka Batta No relevant relationships by Reena Patel No relevant relationships by Hena Yagnik
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
神经精神系统红斑狼疮:一个怀疑和排除的诊断
会议名称:重症病例报告海报会议类型:病例报告海报提交时间:2023年10月10日上午09:40 - 10:25介绍:系统性红斑狼疮(SLE)是一种影响体内多个系统的慢性自身免疫过程。被称为神经精神性SLE (NPSLE),诊断可能需要排除其他原因,但及时识别将有助于适当的症状管理。病例介绍:一名48岁女性,已知SLE诊断,因言语不清和虚弱而到急诊科就诊。在急诊科,发现病人心动过速,其他生命体征稳定。最初的实验室检查对白细胞增多、小细胞性贫血、血小板增多、AKI和阴离子间隙代谢性酸中毒有重要意义。患者行颅脑CT及头颈部CTA检查,未见急性异常,头颈部血管无高度狭窄、夹层、闭塞。腹部/骨盆CT及CXR均未见急性异常。患者最初开始使用广谱抗生素,以怀疑不明原因的败血症。患者也开始滴注碳酸氢钠,AKI和阴离子间隙代谢性酸中毒得到解决,但患者的言语不清仍然存在。病人也有幻觉和谵妄发作。脑MRI未见急性颅内病变;确实显示出慢性小血管缺血改变和中度至晚期脑容量减少的迹象,最明显的是额叶和颞叶区域。两例尿样中尿蛋白肌酐比值升高证实了蛋白尿。ESR、CRP、铁蛋白和D二聚体均升高。胸部CTA证实无肺栓塞。因怀疑狼疮发作而咨询风湿病学。停用静脉抗生素,给予舒美罗1000mg / d,连用3天,患者精神状态、言语不清消失。讨论:该病例证明了临床怀疑和对NPSLE的认识对于在适当的时间内进行治疗的重要性。许多SLE患者,估计约占患者的1 / 3至1 / 2,在整个病程中都会出现神经系统或精神症状(1)。NPSLE症状可能先于或与SLE疾病活动的其他表现一起发生(2)对于大多数NPSLE的表现,没有足够的生物标志物或诊断测试特异性地将患者的临床表现归因于SLE,但诊断应排除其他原因。一些研究发现,与无NPSLE的SLE患者相比,NPSLE患者的死亡风险增加,因此识别和治疗NPSLE具有重要意义(3)。结论:临床医生在排除其他原因后,对于有神经或精神症状的患者应注意NPSLE。参考文献1:Hanly JG, Urowitz MB, Su L, Bae SC, Gordon C, Wallace DJ, Clarke A, Bernatsky S, Isenberg D, Rahman A, Alarcón GS, Gladman DD, Fortin PR, Sanchez-Guerrero J, Romero-Diaz J, Merrill JT, Ginzler E, Bruce IN, Steinsson K, hamashta M, Petri M, Manzi S, Dooley MA, Ramsey-Goldman R, Ramsey-Goldman R系统性红斑狼疮患者国际疾病初始队列神经精神事件的前瞻性分析。风湿病编年史。https://pubmed.ncbi.nlm.nih.gov/19359262/。2023年3月31日访问。文献#2:Hanly JG, Urowitz MB, Gordon C, Bae SC, Romero-Diaz J, Sanchez-Guerrero J, Bernatsky S, Clarke AE, Wallace DJ, Isenberg DA, Rahman A, Merrill JT, Fortin PR, Gladman DD, Bruce IN, Petri M, Ginzler EM, Dooley MA, Ramsey-Goldman R, Manzi S, Jönsen A, Alarcón GS, van Vollenhoven R.系统性红斑狼疮的神经精神事件:采用多状态模型方法的回顾性分析。风湿病编年史。https://pubmed.ncbi.nlm.nih.gov/31915121/。2023年3月31日访问。参考文献#3:Ahn GY, Kim D, Won S, Song ST, Jeong HJ, Sohn IW, Lee S, Joo YB, Bae SC,神经精神性狼疮的患病率、危险因素和对死亡率的影响:一项前瞻性、单中心研究。红斑狼疮。https://pubmed.ncbi.nlm.nih.gov/29688144/。2023年3月31日访问。披露:Priyanka Batta没有相关关系Reena Patel没有相关关系Hena Yagnik没有相关关系
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Chest
Chest 医学-呼吸系统
CiteScore
13.70
自引率
3.10%
发文量
3369
审稿时长
15 days
期刊介绍: At CHEST, our mission is to revolutionize patient care through the collaboration of multidisciplinary clinicians in the fields of pulmonary, critical care, and sleep medicine. We achieve this by publishing cutting-edge clinical research that addresses current challenges and brings forth future advancements. To enhance understanding in a rapidly evolving field, CHEST also features review articles, commentaries, and facilitates discussions on emerging controversies. We place great emphasis on scientific rigor, employing a rigorous peer review process, and ensuring all accepted content is published online within two weeks.
期刊最新文献
Win Ratio Analysis to Clarify Clinical Benefits: A Post Hoc Analysis of Phase 3 BOREAS and NOTUS. Association of High Cardiovascular Disease Risk Obstructive Sleep Apnea with Incident Atrial Fibrillation: the Multi-Ethnic Study of Atherosclerosis. Demographic and physiologic differences between fibrotic and non-fibrotic CT subtypes of sarcoidosis. Evaluating the Association Between Patient Priorities and ICU Care Delivery in Adults Receiving Mechanical Ventilation. Effects of a Novel Dual Phosphodiesterase 3 and 4 Inhibitor TQC3721 in Patients with COPD in China (PACER-II): a phase 2, multicentre, randomised, double-blind, placebo-controlled trial
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1