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Chronic Mesenteric Ischemia, More Attention is Needed in Cases with Prolonged Abdominal Pain: A Case Report and Brief Review 慢性肠系膜缺血,长时间腹痛需多加注意:1例报告及简要回顾
Pub Date : 2023-07-10 DOI: 10.5812/intjcardiovascpract-136286
Azadeh Tahooni, S. Eftekhari, A. Kabir
Introduction: Symptomatic chronic mesenteric ischemia (CMI) is a rare condition that usually occurs due to mesenteric artery stenosis (MAS) with a common incidence. Although the prevalence of symptomatic CMI is less than 2%, MAS is more common in the elderly. Case Presentation: A 60-year-old woman with prolonged eating-related abdominal pain and weight loss treated as cholelithiasis by endoscopic retrograde cholangiography was readmitted by recurrent epigastric pain. At this time, she was reevaluated by computed tomography angiography (CTA), and CMI was confirmed. She was treated with percutaneous mesenteric artery stenting and was discharged without pain. There were no complications or pain after 3 months of follow-up. Conclusions: The most prevalent causes of CMI are atherosclerotic processes, such as hypertension, hyperlipidemia, overweight, metabolic syndrome, and smoking. The diagnosis of CMI is confirmed by CTA. Recently, endovascular treatment by percutaneous mesenteric artery stenting is more common than the surgical approaches because of lower in- and out-hospital complications.
症状性慢性肠系膜缺血(CMI)是一种罕见的疾病,通常由肠系膜动脉狭窄(MAS)引起,发病率较高。尽管症状性CMI的患病率不到2%,但MAS在老年人中更为常见。病例介绍:一名60岁女性,长期进食相关腹痛和体重减轻,经内镜逆行胆道造影治疗为胆石症,因复发性胃脘痛再次入院。此时,她通过计算机断层血管造影(CTA)重新评估,并确认CMI。经皮肠系膜动脉支架植入术治疗,无疼痛出院。随访3个月,无并发症和疼痛。结论:CMI最常见的原因是动脉粥样硬化过程,如高血压、高脂血症、超重、代谢综合征和吸烟。CMI的诊断经CTA证实。近年来,经皮肠系膜动脉支架植入术比外科手术更常见,因为其院内和院外并发症较低。
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引用次数: 0
Surgical Outcomes of Repairing Ebstein Anomaly: A Single-Center Experience 修复Ebstein畸形的手术结果:单中心经验
Pub Date : 2023-07-10 DOI: 10.5812/intjcardiovascpract-136592
A. Jalali, Aghdas Shadmehr, Mozghan Parsaee, Z. Khajali, Sara Adimi, Ronak Ahmadi, Amir Ghaffari, S. Saedi
Background: Ebstein anomaly (EA) is a rare congenital disorder of the tricuspid valve (TV), accounting for about one percent of congenital heart defects. Considering highly variable anatomy, diverse corrective surgical methods are currently utilized. Cone reconstruction provides a near anatomic tricuspid restoration method that has triggered enthusiasm for early repair over recent years. Objectives: In the current study, we aimed to evaluate the clinical and echocardiographic features and outcomes of patients who underwent surgical correction of EA in our referral center. Methods: In this study, we reviewed the medical records of 35 patients with EA who underwent cone repair or TV replacement and had accessible echocardiographic data before and at least one year following the corrective surgery. The patients were evaluated for residual tricuspid regurgitation (TR) severity, right ventricular (RV) size, RV fractional area change (FAC), left ventricular end-systolic diameter (LVESD), left ventricular end-diastolic diameter (LVEDD), and 2D left ventricular ejection fraction (LVEF) before and after the operation. Results: Mean age of the patients was 29.49 ± 9.13 years, and 54.3% of them were female. Twenty-one (60%) patients underwent cone repair, and 14 were subjected to TV replacement. Seven (20%) patients required reoperation; redo TV repair was conducted in three patients (8.6%); two (5.7%) patients underwent biologic TV replacement; mechanical TV replacement was performed in one patient (2.9%) who had degenerative biologic TVs, and one patient (2.9%) was subjected to redo-operation due to mechanical TV malfunction. Positive changes in the means of RV-FAC and 2D-LVEF were statistically significant in all patients irrespective of the type of surgery (P < 0.001), but changes in the means of RV size (P = 0.38) and LVESD (P = 0.302) were not statistically significant. There was a significant increase in functional RV size in both groups of patients who underwent repair (P = 0.063) or replacement (P = 0.02). Conclusions: The present study revealed satisfactory post-op results for cone TV repair in patients with EA, evidenced by reduced TR severity and improved biventricular functional parameters. Assessing the durability of the outcomes of cone TV repair needs longer-term follow-ups.
背景:Ebstein异常(EA)是一种罕见的先天性三尖瓣疾病,约占先天性心脏缺陷的1%。考虑到高度多变的解剖结构,目前采用多种矫正手术方法。椎体重建提供了一种接近解剖结构的三尖瓣修复方法,近年来引发了对早期修复的热情。目的:在本研究中,我们旨在评估在我们转诊中心接受手术矫正EA患者的临床和超声心动图特征和结果。方法:在本研究中,我们回顾了35例接受锥体修复或电视更换的EA患者的医疗记录,并在矫正手术前和术后至少一年可获得超声心动图数据。评估患者术前、术后残余三尖瓣返流(TR)严重程度、右心室(RV)大小、右心室分数面积变化(FAC)、左心室收缩末内径(LVESD)、左心室舒张末内径(LVEDD)、左心室2D射血分数(LVEF)。结果:患者平均年龄29.49±9.13岁,女性占54.3%。21例(60%)患者接受视锥修复,14例接受电视更换。7例(20%)患者需要再手术;重做电视修复3例(8.6%);2例(5.7%)患者行生物电视置换术;1例(2.9%)退行性生物电视患者行机械电视置换,1例(2.9%)因机械电视故障行再手术。不论手术类型,所有患者RV- fac和2D-LVEF均数的阳性变化均有统计学意义(P < 0.001),但RV大小(P = 0.38)和LVESD均数的变化无统计学意义(P = 0.302)。两组接受修复(P = 0.063)或置换(P = 0.02)的患者功能性右心室大小均显著增加。结论:本研究显示锥体电视修复术对EA患者的术后效果满意,表现为TR严重程度的降低和双心室功能参数的改善。评估锥形电视修复效果的持久性需要更长期的随访。
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引用次数: 0
Association of rs505080 Single Nucleotide Polymorphism in Lamin-A Gene with Familial Dilated Cardiomyopathy in Iranian Population; A Case-Control Study 伊朗人群Lamin-A基因rs505080单核苷酸多态性与家族性扩张型心肌病的相关性研究病例对照研究
Pub Date : 2023-06-12 DOI: 10.5812/intjcardiovascpract-133637
Saiedeh Erfanian, Zahra Hooshanginezhad, A. Hassani, M. Ghabouli, M. Shojaie
Background: Dilated cardiomyopathy (DCM) is among the most prevalent causes of heart failure and sudden cardiac death worldwide. Nuclear lamin protein coding genes are believed to have a definitive role in the DCM phenotype. The rs505058 thymine (T) to cytosine (C) polymorphism in the lamin-A gene is one of the most common mutations reported in familial DCM in previous studies. Objectives: We aimed to demonstrate the possible role of this SNP in the lamin A and C (LMNA) gene in the incidence of DCM among the south of Iran population. Methods: This case-control study included 65 patients with familial DCM and 70 healthy participants in south Iran. DNA was extracted from nucleated blood cells, and polymerase chain reaction (PCR) was performed. First, the sequence of the LMNA gene was investigated. Then the frequency of alleles C (mutated allele) and T (normal) of the LMNA gene (rs505058) was compared between the case and controls. Results: No notable differences were seen in gender and age between the case and controls. The genotype frequencies of the LMNA rs505058 T/C polymorphism were 6% (CC), 31% (CT), and 63% (TT) amongst cases, and 1% (CC), 13% (CT) and 86% (TT) in controls. For allele level comparison, the LMNA rs505058 C allele has been shown to have a statistically significant association with an enhancement in the risk of dilated cardiomyopathy (OR = 2.92; 95% CI = 1.05 to 8.15, P-value = 0.034) Conclusions: The results indicated that the rs505058 T/C SNP of the LMNA gene is associated with familial DCM patients in the Iranian population.
背景:扩张型心肌病(DCM)是世界范围内导致心力衰竭和心源性猝死的最常见原因之一。核层蛋白编码基因被认为在DCM表型中起决定性作用。lamin-A基因的rs505058胸腺嘧啶(T)到胞嘧啶(C)多态性是以往研究中报道的家族性DCM中最常见的突变之一。目的:我们旨在证明在伊朗南部人群中,层状蛋白A和C (LMNA)基因中的这种SNP在DCM发病率中的可能作用。方法:本病例对照研究包括伊朗南部65例家族性DCM患者和70名健康参与者。从有核血细胞中提取DNA,进行聚合酶链反应(PCR)。首先,研究了LMNA基因的序列。然后比较病例与对照组LMNA基因(rs505058)等位基因C(突变等位基因)和T(正常等位基因)的频率。结果:病例与对照组在性别和年龄上无显著差异。病例中LMNA rs505058 T/C多态性基因型频率分别为6% (CC)、31% (CT)和63% (TT),对照组为1% (CC)、13% (CT)和86% (TT)。对于等位基因水平的比较,LMNA rs505058 C等位基因与扩张性心肌病风险的增加具有统计学意义(OR = 2.92;(95% CI = 1.05 ~ 8.15, p值= 0.034)结论:伊朗人群中LMNA基因rs505058 T/C SNP与家族性DCM患者相关。
{"title":"Association of rs505080 Single Nucleotide Polymorphism in Lamin-A Gene with Familial Dilated Cardiomyopathy in Iranian Population; A Case-Control Study","authors":"Saiedeh Erfanian, Zahra Hooshanginezhad, A. Hassani, M. Ghabouli, M. Shojaie","doi":"10.5812/intjcardiovascpract-133637","DOIUrl":"https://doi.org/10.5812/intjcardiovascpract-133637","url":null,"abstract":"Background: Dilated cardiomyopathy (DCM) is among the most prevalent causes of heart failure and sudden cardiac death worldwide. Nuclear lamin protein coding genes are believed to have a definitive role in the DCM phenotype. The rs505058 thymine (T) to cytosine (C) polymorphism in the lamin-A gene is one of the most common mutations reported in familial DCM in previous studies. Objectives: We aimed to demonstrate the possible role of this SNP in the lamin A and C (LMNA) gene in the incidence of DCM among the south of Iran population. Methods: This case-control study included 65 patients with familial DCM and 70 healthy participants in south Iran. DNA was extracted from nucleated blood cells, and polymerase chain reaction (PCR) was performed. First, the sequence of the LMNA gene was investigated. Then the frequency of alleles C (mutated allele) and T (normal) of the LMNA gene (rs505058) was compared between the case and controls. Results: No notable differences were seen in gender and age between the case and controls. The genotype frequencies of the LMNA rs505058 T/C polymorphism were 6% (CC), 31% (CT), and 63% (TT) amongst cases, and 1% (CC), 13% (CT) and 86% (TT) in controls. For allele level comparison, the LMNA rs505058 C allele has been shown to have a statistically significant association with an enhancement in the risk of dilated cardiomyopathy (OR = 2.92; 95% CI = 1.05 to 8.15, P-value = 0.034) Conclusions: The results indicated that the rs505058 T/C SNP of the LMNA gene is associated with familial DCM patients in the Iranian population.","PeriodicalId":31436,"journal":{"name":"International Journal of Cardiovascular Practice","volume":"10 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77857853","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Eosinophilic Myocarditis: A Case Report and Literature Review 嗜酸性心肌炎1例报告并文献复习
Pub Date : 2023-02-24 DOI: 10.5812/intjcardiovascpract-134163
Sepideh Jafari Naeini, H. Pouraliakbar, S. M. Mirhosseini, A. Bagheri
: Eosinophilic myocarditis (EM) is a rare type of myocarditis usually diagnosed by endomyocardial biopsy; however, it can also be diagnosed by cardiac magnetic resonance imaging. Different presentations cause some problems in the diagnosis and treatment. Herein, we present a middle-aged female case with eosinophilia and EM.
嗜酸性心肌炎(EM)是一种罕见的心肌炎,通常通过心肌内膜活检诊断;然而,它也可以通过心脏磁共振成像来诊断。不同的表现形式给诊断和治疗带来了一些问题。在此,我们报告一例中年女性嗜酸性粒细胞增多和EM。
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引用次数: 0
Association of Left Ventricular Systolic Function with Diagonal Branch Flow in Patients with First Anterior ST-Elevation Myocardial Infarction Treated with Primary Angioplasty 原发性血管成形术治疗首次st段抬高型心肌梗死患者左心室收缩功能与斜支血流的关系
Pub Date : 2023-02-22 DOI: 10.5812/intjcardiovascpract-129928
Mehrdad Raadi, Elnaz Javanshir, Rezvaniyeh Salehi, A. Separham
Background: There are few studies about the impact of diagonal branch blood flow on echocardiographic findings in patients with first acute anterior myocardial infarction undergoing primary angioplasty. Objectives: We aimed to compare left ventricular systolic function measures in patients with first acute anterior ST-segment elevation myocardial infarction (STEMI) treated with primary angioplasty based on diagonal branch blood flow after the procedure. Methods: This study was a single-center study that enrolled patients with their first acute anterior STEMI treated with primary angioplasty in our center between October 2020 and March 2021. Patients were divided into two groups: The patients with final thrombolysis in myocardial infarction (TIMI) flow III in diagonal (sufficient diagonal flow) and patients with final TIMI flow less than III in diagonal (insufficient diagonal flow) after the procedure. The left ventricular Wall-Motion Score Index (WMSI) and left ventricular ejection fraction (LVEF) were compared between the two groups. Results: A total of 107 patients with first anterior STEMI treated with primary PCI were enrolled in the present study, of which 13 patients (12.1%) had insufficient diagonal flow after primary coronary angioplasty. The LVEF was lower in patients with insufficient diagonal flow (32.92 ± 7.29% vs. 39 ± 8.68%, P = 0.018). Also, this group had higher LV WMSI (1.68 ± 0.28 vs. 1.49 ± 0.26, P = 0.029). Conclusions: The present study showed that in patients with first acute anterior STEMI undergoing primary angioplasty, insufficient diagonal branch flow after the procedure was associated with worse left ventricular systolic function and higher LV WMSI.
背景:对于首次急性前壁心肌梗死行初级血管成形术的患者,斜支血流对超声心动图表现的影响研究较少。目的:我们的目的是比较首次急性st段前抬高型心肌梗死(STEMI)患者在手术后基于斜支血流的初级血管成形术中左心室收缩功能的测量。方法:本研究是一项单中心研究,纳入了2020年10月至2021年3月期间在我们中心接受初级血管成形术治疗的首次急性前路STEMI患者。将患者分为两组:术后最终溶栓心肌梗死(TIMI)血流呈对角线III级(充分对角线血流)和最终TIMI血流小于对角线III级(不足对角线血流)的患者。比较两组患者左室壁运动评分指数(WMSI)和左室射血分数(LVEF)。结果:本研究共纳入107例经PCI治疗的首次前路STEMI患者,其中13例(12.1%)患者在初次冠状动脉成形术后出现对角血流不足。斜流不足组LVEF较低(32.92±7.29% vs. 39±8.68%,P = 0.018)。此外,该组lvwmsi较高(1.68±0.28∶1.49±0.26,P = 0.029)。结论:本研究表明,在首次急性前路STEMI患者行初级血管成形术后,斜支血流不足与左室收缩功能恶化和左室WMSI升高有关。
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引用次数: 1
Fulminant Myocarditis Complicated with Immune Checkpoint Inhibitor in Patients with Thymoma: Report of Three Cases 胸腺瘤患者暴发性心肌炎合并免疫检查点抑制剂3例报告
Pub Date : 2023-01-22 DOI: 10.5812/intjcardiovascpract-130990
Daozheng Huang, Feier Song, Weidai Zhang, Huan Ma, Xingtao Lin, Tiehe Qin, Shouhong Wang
: Immune checkpoint inhibitors (ICIs) prevent the immune escape of tumor cells, which helps immune cells such as T lymphocytes to continuously monitor and kill tumor cells, and play powerful anti-tumor role. Immune checkpoint inhibitor-associated myocarditis has been rarely reported; however, its latent, rapidly developed, and lethal onset has gradually attracted the attention of clinicians. This study aimed to report cases of fulminant myocarditis in three patients with thymoma who were treated with pembrolizumab, one of the programmed cell death protein 1 inhibitors (PD-1 inhibitors).
:免疫检查点抑制剂(Immune checkpoint inhibitors, ICIs)能够阻止肿瘤细胞的免疫逃逸,帮助T淋巴细胞等免疫细胞持续监测和杀伤肿瘤细胞,发挥强大的抗肿瘤作用。免疫检查点抑制剂相关的心肌炎很少报道;但其潜伏性、发展迅速、致死性等特点逐渐引起临床医生的重视。本研究旨在报道3例胸腺瘤患者的暴发性心肌炎,这些患者接受了pembrolizumab治疗,pembrolizumab是程序性细胞死亡蛋白1抑制剂(PD-1抑制剂)之一。
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引用次数: 0
Venous Thromboembolism in COVID-19 Patients: A Single-Center Case Series COVID-19患者静脉血栓栓塞:单中心病例系列
Pub Date : 2023-01-16 DOI: 10.5812/intjcardiovascpract-133219
Z. Ahmadi, M. Keshmiri, B. Sharif kashani, Sima Noorali, Somayeh Lookzadeh, Sina Aghdasi, Mahsa Riahi, Aylar Fazlzadeh, A. Mohamadifar, A. Serati, S. Shafaghi
: Since thrombosis occurrence among coronavirus disease 2019 (COVID-19) patients is a critical complication, this study aimed to describe the clinical characteristics and outcomes of COVID-19-associated pulmonary thromboembolism (PTE). This case series of 39 venous thromboembolism (VTE) patients represents clinical characteristics, laboratory data, imaging data, and outcomes. The mean age of the patients was 55 ± 15 years. Moreover, 25 patients (64.10%) were male. The most frequent COVID-19 clinical presentations were dyspnea and cough in 22 (56.41%) and 19 (48.71%) patients, respectively. Additionally, the most frequent PTE clinical presentations were palpitation and anxiety in 28 (71.79%) and dyspnea in 24 (61.53%) patients. Additionally, eight patients (20.51%) showed deep vein thrombosis in color Doppler ultrasound. The mean measures of D-dimer, erythrocyte sedimentation rate and C-reactive protein were 3680 ng/mL, 53 mm/hour, and 44 mg/L, respectively. Supplemental oxygen and a ventilator were required in 29 (74.35%) and 2 (5.12%) patients, respectively. One patient died from PTE complications, and others improved without any complications. The VTE is a potentially life-threatening complication that frequently occurs in patients with COVID-19. Therapeutic doses of anticoagulants, extended thromboprophylaxis, meticulous assessments, follow-up, and high clinical suspicion to the early detection of PTE are necessary in this regard.
鉴于2019冠状病毒病(COVID-19)患者血栓形成是一种重要的并发症,本研究旨在描述COVID-19相关肺血栓栓塞(PTE)的临床特征和结局。本病例系列包括39例静脉血栓栓塞(VTE)患者的临床特征、实验室数据、影像学数据和结果。患者平均年龄55±15岁。男性25例,占64.10%。临床表现以呼吸困难和咳嗽为主,分别为22例(56.41%)和19例(48.71%)。此外,最常见的PTE临床表现为28例(71.79%)患者心悸和焦虑,24例(61.53%)患者呼吸困难。彩色多普勒超声显示深静脉血栓8例(20.51%)。d -二聚体、红细胞沉降率和c反应蛋白的平均值分别为3680 ng/mL、53 mm/h和44 mg/L。29例(74.35%)和2例(5.12%)患者需要补充氧气和呼吸机。一名患者死于PTE并发症,其他患者病情好转,无任何并发症。静脉血栓栓塞是一种可能危及生命的并发症,经常发生在COVID-19患者中。在这方面,治疗剂量的抗凝剂、扩大血栓预防、细致的评估、随访和对PTE早期发现的高度临床怀疑是必要的。
{"title":"Venous Thromboembolism in COVID-19 Patients: A Single-Center Case Series","authors":"Z. Ahmadi, M. Keshmiri, B. Sharif kashani, Sima Noorali, Somayeh Lookzadeh, Sina Aghdasi, Mahsa Riahi, Aylar Fazlzadeh, A. Mohamadifar, A. Serati, S. Shafaghi","doi":"10.5812/intjcardiovascpract-133219","DOIUrl":"https://doi.org/10.5812/intjcardiovascpract-133219","url":null,"abstract":": Since thrombosis occurrence among coronavirus disease 2019 (COVID-19) patients is a critical complication, this study aimed to describe the clinical characteristics and outcomes of COVID-19-associated pulmonary thromboembolism (PTE). This case series of 39 venous thromboembolism (VTE) patients represents clinical characteristics, laboratory data, imaging data, and outcomes. The mean age of the patients was 55 ± 15 years. Moreover, 25 patients (64.10%) were male. The most frequent COVID-19 clinical presentations were dyspnea and cough in 22 (56.41%) and 19 (48.71%) patients, respectively. Additionally, the most frequent PTE clinical presentations were palpitation and anxiety in 28 (71.79%) and dyspnea in 24 (61.53%) patients. Additionally, eight patients (20.51%) showed deep vein thrombosis in color Doppler ultrasound. The mean measures of D-dimer, erythrocyte sedimentation rate and C-reactive protein were 3680 ng/mL, 53 mm/hour, and 44 mg/L, respectively. Supplemental oxygen and a ventilator were required in 29 (74.35%) and 2 (5.12%) patients, respectively. One patient died from PTE complications, and others improved without any complications. The VTE is a potentially life-threatening complication that frequently occurs in patients with COVID-19. Therapeutic doses of anticoagulants, extended thromboprophylaxis, meticulous assessments, follow-up, and high clinical suspicion to the early detection of PTE are necessary in this regard.","PeriodicalId":31436,"journal":{"name":"International Journal of Cardiovascular Practice","volume":"71 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90342195","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Effect of Balloon Mitral Valvuplasty on BNP Plasma Level in Mitral Stenosis 球囊二尖瓣成形术对二尖瓣狭窄患者血浆BNP水平的影响
Pub Date : 2023-01-13 DOI: 10.5812/intjcardiovascpract-131154
M. Mahjoob, Roxana Sadeghi, Mohammad Haji Aghajani, Naser Kachoueian, Pardis Jolfaei, M. Nosrati, Mahshid Haghi
Background: Mitral valve stenosis (MS), which could be progressive, is one of the most important valvular disorders in developing countries. Percutaneous transvenous mitral commissurotomy (PTMC) is a well-accepted treatment option for dealing with symptomatic MS. Brain natriuretic peptide (BNP) has been used as a prognostic marker for clinical outcomes in patients with heart failure and acute coronary syndrome routinely. Objectives: This study aimed to determine the relationship between BNP levels and hemodynamic parameters in patients with MS who underwent PTMC. Methods: In this case-control study, 90 patients with severe isolated rheumatic mitral stenosis and undergoing PTMC were enrolled. In the study group, BNP levels were measured by performing radioimmunoassay on all participants 30 minutes before PTMC and 24 hours after PTMC. Data were analyzed using SPSS, and P-value < 0.05 was considered significant. Results: Fifty patients with MS who underwent PTMC were included in this study. The level of BNP before PTMC was 473.78 ± 66.95 pg/dL in patients with MS. The level of BNP in patients after PTMC reached 341.54 ± 48.3 pg/dL, which was indicative of a significant reduction in the level of BNP after PTMC (P-value = 0.006). Conclusions: A considerable decline was observed in the serum level of BNP following a successful PTMC, which was indicative of an improvement in clinical and hemodynamic status; hence, it was reasonably suggested that the serum level of BNP was effective in evaluating the response from patient with severe MS to PTMC.
背景:二尖瓣狭窄(MS)是发展中国家最重要的瓣膜疾病之一,可能是进行性的。经皮经静脉二尖瓣合舒术(PTMC)是治疗症状性多发性硬化症(ms)的一种广为接受的治疗选择。脑钠肽(BNP)已被常规用作心衰和急性冠状动脉综合征患者临床结局的预后指标。目的:本研究旨在确定接受PTMC的MS患者BNP水平与血流动力学参数的关系。方法:在本病例对照研究中,纳入90例重度孤立性风湿性二尖瓣狭窄并行PTMC的患者。在研究组中,通过对所有参与者在PTMC前30分钟和PTMC后24小时进行放射免疫测定来测量BNP水平。数据采用SPSS分析,p值< 0.05为差异有统计学意义。结果:50例MS患者行PTMC纳入本研究。ms患者PTMC治疗前BNP水平为473.78±66.95 pg/dL, PTMC治疗后BNP水平为341.54±48.3 pg/dL,提示PTMC治疗后BNP水平明显降低(p值= 0.006)。结论:PTMC成功后血清BNP水平明显下降,这表明临床和血流动力学状况有所改善;因此,有理由认为血清BNP水平是评价重度MS患者PTMC疗效的有效指标。
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引用次数: 0
Ascending Aortic Pseudoaneurysm Following Aortic Valve Replacement: A Case Report and Literature Review 主动脉瓣置换术后升主动脉假性动脉瘤1例报告及文献复习
Pub Date : 2022-12-25 DOI: 10.5812/intjcardiovascpract-133752
Ehsan Razeghi1, Mohammadhosein Akhlaghpasand, Ashkan Majidi, Setayesh Farahani, Sam Zeraatian Nejad, F. Eghbali
Introduction: Ascending aortic pseudoaneurysm (AAP) rupture is a surgical emergency that needs immediate medical and surgical attention and treatment. This rupture can be caused by a variety of risk factors. Prior cardiovascular surgery is a common cause, and prior aortic valve operation is a rare cause. Case Presentation: In this case report, we describe a 47-year-old male with AAP who had a history of aortic valve replacement because of aortic stenosis.
简介:升主动脉假性动脉瘤(AAP)破裂是一种外科急诊,需要立即进行医学和外科治疗。这种破裂可由多种危险因素引起。先前的心血管手术是常见的原因,而先前的主动脉瓣手术是一个罕见的原因。病例介绍:在这个病例报告中,我们描述了一个47岁的男性AAP,他有主动脉瓣置换术的历史,因为主动脉狭窄。
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引用次数: 0
Prevalence and Hemodynamic Consequences of Mitral Valve Abnormalities in Atrial Septal Defect 房间隔缺损二尖瓣异常的患病率及血流动力学后果
Pub Date : 2022-11-12 DOI: 10.5812/intjcardiovascpract-131707
M. Shojaeifard, S. Keshavari, Saideh Jamshidi, H. Bakhshandeh, Mohammad Ali Ghaznavai, Hossein Dehghani Mohammad Abadi, S. Erami
Background: Atrial septal defect (ASD) is a common congenital heart disease in adults. Concomitant mitral valve disease in patients with ASD could have significant hemodynamic effects whit a great impact on managing this congenital defect. Objectives: This study evaluated the prevalence of mitral valve abnormalities and the hemodynamic burden associated with different types of ASD. Methods: This retrospective study reanalyzed 1,006 consecutive patients referred to Rajaie Heart Center in Tehran from March 2019 to February 2022. We evaluated adult patients with the diagnosis of a shunt at the atrial level. Diagnoses were made with 2D and 3D transthoracic echocardiography (TTE) and transesophageal echocardiography (TEE). 3D analysis was performed with 3D zoom, mitral valve navigation (MVN), and full-volume and multi-planar reconstruction (MPR) modalities. We performed statistical analysis by SPSS version 22.0. The qualitative data were expressed as frequency and percentage. Data were compared between subgroups via Mann-Whitney U/Kruskal-Wallis tests for the interval variables, Pearson's chi-square test for nominal variables, and chi-square for trends test for ordinal variables. Results: The distribution of different ASD types was ostium secundum in 88.8% of cases, primum ASD in 0.9%, SVC-type sinus venosus ASD in 9%, IVC-type sinus venosus in 0.4%, and unroofed coronary sinus in 0.9%. We found mitral valve abnormalities in 21.1% of cases, and the most common mitral valve abnormality were prolaptic lesions (17.4%). Conclusions: Age, ASD size, estimated Systolic Pulmonary Artery Pressure (SPAP), and severity of mitral regurgitation (MR) were markedly higher were markedly higher among patients with MV anomalies, more over left ventricular ejection fraction (LVEF) was significantly lower among this group (P-value < 0.05).
背景:房间隔缺损(ASD)是成人常见的先天性心脏病。ASD患者合并二尖瓣病变可能会对血流动力学产生显著影响,对治疗这种先天性缺陷有很大影响。目的:本研究评估与不同类型ASD相关的二尖瓣异常的患病率和血流动力学负担。方法:本回顾性研究重新分析了2019年3月至2022年2月在德黑兰Rajaie心脏中心连续转诊的1006例患者。我们评估了诊断为心房水平分流的成年患者。通过二维和三维经胸超声心动图(TTE)和经食管超声心动图(TEE)进行诊断。采用三维变焦、二尖瓣导航(MVN)、全容积和多平面重建(MPR)方式进行三维分析。采用SPSS 22.0进行统计分析。定性数据用频率和百分比表示。对区间变量采用Mann-Whitney U/Kruskal-Wallis检验,对标称变量采用Pearson卡方检验,对有序变量采用趋势卡方检验。结果:不同类型ASD的分布为:第二口占88.8%,原发型占0.9%,svc型静脉窦占9%,ivc型静脉窦占0.4%,无顶冠状窦占0.9%。我们在21.1%的病例中发现二尖瓣异常,最常见的二尖瓣异常是脱垂病变(17.4%)。结论:年龄、ASD大小、估计收缩压(SPAP)、二尖瓣返流严重程度(MR)均显著高于MV异常组,高于左室射血分数(LVEF)组显著低于MV异常组(p值< 0.05)。
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引用次数: 0
期刊
International Journal of Cardiovascular Practice
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