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A Fully Malfunctioning Implantable Cardioverter-Defibrillator Device. 完全失灵的植入式心律转复除颤器设备。
IF 0.8 Q3 Medicine Pub Date : 2023-04-01 DOI: 10.5543/tkda.2022.13701
Serkan Çay, Meryem Kara, Zcan Zeke, Firat Ozcan, Serkan Topaloglu
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引用次数: 0
[Comments on Cardiology]. 【心脏病学评论】。
IF 0.8 Q3 Medicine Pub Date : 2023-03-01 DOI: 10.5543/tkda.2023.24884
Ertan Ural
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引用次数: 0
An Uncorrected Tetralogy of Fallot with a History of 4 Consecutive Pregnancies Presenting with Cardiac Tamponade. 1例未纠正的法洛四联症伴4次连续妊娠,并伴有心脏填塞。
IF 0.8 Q3 Medicine Pub Date : 2023-03-01 DOI: 10.5543/tkda.2022.53563
Cemalettin Akman, Sinem Aydın, Gamze Babür Güler, Enes Arslan, Ahmet Güner
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引用次数: 0
Prognostic Significance of High-Sensitivity Troponin T in Nonischemic Heart Failure with Reduced Ejection Fraction. 高敏肌钙蛋白T在非缺血性心力衰竭伴射血分数降低中的预后意义。
IF 0.8 Q3 Medicine Pub Date : 2023-03-01 DOI: 10.5543/tkda.2023.26900
Gülsüm Meral Yılmaz Öztekin, Ahmet Genç

Objective: Cardiac biomarkers can help diagnose and predict heart failure prognosis. High-sensitivity troponin T has frequently been investigated in ischemic heart failure studies. However, the relation between high-sensitivity troponin T and mortality in nonischemic heart failure and its level indicating poor prognosis remain unclear. This study aimed to show whether high-sensitivity troponin T is a predictor of all-cause mortality and the cut-off value for high-sensitivity troponin T in patients with nonischemic heart failure with reduced ejection fraction.

Methods: We included 249 nonischemic heart failure patients with left ventricular ejection fraction ≤ 40%, age ≥ 18 years, and high-sensitivity troponin T level known.

Results: Of the patients, 59.8% were male, 73.5% were New York Heart Association I or II, and the median age was 64. High-sensitivity troponin T value of the patients was 18 ng/L [inter-quartile range, 10-34]. The cut-off value of high-sensitivity troponin T for all-cause mortality was 21.5 ng/L, with 72.6% sensitivity and 69.9% specificity (area under the curve: 0.760, 95% CI: 0.692-0.828, P < 0.001). Patients were compared according to the 21.5 ng/L high-sensitivity troponin T cut-off value. At 30-month follow-up, all-cause mortality was 29.3%. According to the Kaplan-Meier analysis, the mortality rate was 14% in the high-sensitivity troponin T < 21.5 ng/L group, while the mortality rate was 50% in the high-sensitivity troponin T ≥ 21.5 ng/L group (P < 0.001, log-rank test). Baseline high-sensitivity troponin T was inde-pendently associated with all-cause mortality in nonischemic heart failure with reduced ejection fraction when adjusted for estimated glomerular filtration rate, hemoglobin, N-terminal pro-brain natriuretic peptide, body mass index, and left atrial diameter (hazard ratio: 1.012, 95% confidence interval: 1.003-1.020, P = 0.005).

Conclusion: The high-sensitivity troponin T cut-off value was 21.5 ng/L to predict a worse prognosis in nonischemic heart failure with reduced ejection fraction. There was an independent association between high-sensitivity troponin T and all-cause mortality.

目的:心脏生物标志物有助于心衰的诊断和预后预测。高敏感性肌钙蛋白T在缺血性心力衰竭研究中经常被研究。然而,高敏感性肌钙蛋白T与非缺血性心力衰竭死亡率的关系及其预示不良预后的水平仍不清楚。本研究旨在表明高敏感性肌钙蛋白T是否是全因死亡率的预测因子,以及高敏感性肌钙蛋白T在射血分数降低的非缺血性心力衰竭患者中的临界值。方法:我们纳入249例左室射血分数≤40%、年龄≥18岁、已知高敏感肌钙蛋白T水平的非缺血性心力衰竭患者。结果:患者中男性占59.8%,纽约心脏协会I级或II级占73.5%,中位年龄64岁。患者高敏肌钙蛋白T值为18 ng/L[四分位数间距,10-34]。高敏感性肌钙蛋白T对全因死亡率的临界值为21.5 ng/L,敏感性72.6%,特异性69.9%(曲线下面积:0.760,95% CI: 0.692 ~ 0.828, P < 0.001)。根据21.5 ng/L高敏感肌钙蛋白T临界值对患者进行比较。随访30个月,全因死亡率为29.3%。Kaplan-Meier分析显示,高敏感肌钙蛋白T < 21.5 ng/L组死亡率为14%,高敏感肌钙蛋白T≥21.5 ng/L组死亡率为50% (P < 0.001, log-rank检验)。基线高敏感性肌钙蛋白T与射血分数降低的非缺血性心力衰竭患者的全因死亡率独立相关,经肾小球滤过率、血红蛋白、n端前脑利钠肽、体重指数和左心房内径校正(风险比:1.012,95%可信区间:1.003-1.020,P = 0.005)。结论:高敏感性肌钙蛋白T临界值为21.5 ng/L可预测射血分数降低的非缺血性心力衰竭患者预后较差。高敏感性肌钙蛋白T与全因死亡率之间存在独立关联。
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引用次数: 0
Improvement In Adherence To Guidelines For Anticoagulant Therapy Of Atrial Fibrillation: We Can Still Do Better. 房颤抗凝治疗指南依从性的提高:我们仍然可以做得更好。
IF 0.8 Q3 Medicine Pub Date : 2023-03-01 DOI: 10.5543/tkda.2023.88033
Ayhan Erkol
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引用次数: 0
Value of CHADS-VASc Score in Diverse Cardiovascular Conditions. CHADS-VASc评分在不同心血管疾病中的价值
IF 0.8 Q3 Medicine Pub Date : 2023-03-01 DOI: 10.5543/tkda.2023.51706
Burak Turan
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引用次数: 0
Modified Glasgow Prognostıc Score May Be Useful to Predict Major Adverse Cardiac Events in Heart Failure Patients Undergone Cardiac Resynchronization Treatment. 改良格拉斯哥Prognostıc评分可能有助于预测心脏再同步化治疗的心力衰竭患者的主要不良心脏事件。
IF 0.8 Q3 Medicine Pub Date : 2023-03-01 DOI: 10.5543/tkda.2022.99448
Güney Erdogan, Mustafa Yenerçağ, Melisa Uçar, Onur Öztürk, Onur Osman Şeker, Osman Can Yontar, Ender Özgün Çakmak, Ali Karagöz, İrfan Şahin, Uğur Arslan

Objective: Whether modified Glasgow prognostic score predicts prognosis in patients with cardiac resynchronization therapy with defibrillation is unknown. Our aim was to investigate the association of modified Glasgow prognostic score with death and hospitalization in cardiac resynchronization therapy with defibrillation patients.

Methods: A total of 306 heart failure with reduced ejection fraction patients who underwent cardiac resynchronization therapy with defibrillation implantation were categorized into 3 groups based on their modified Glasgow prognostic score categorical levels. C-reactive protein >10 mg/L or albumin <35 g/L was assigned 1 point each and the patients were classified into 0, 1, and 2 points, respectively. Remodeling was determined according to the clinical event and myocardial remodeling criteria. Major adverse cardiac events were defined as mortality and/or hospitalization for heart failure.

Results: Age, New York Heart Association functional class, modified Glasgow prognostic score prior to cardiac resynchronization therapy with defibrillation, sodium levels, and left atrial diameter were higher in the major adverse cardiac events(+) group. Age, left atrial diameter, and higher modified Glasgow prognostic score were found to be predictors of heart failure hospitalization/death in multivariable penalized Cox regression analysis. Besides, patients with lower modified Glasgow prognostic score showed better reverse left ventricular remodeling demonstrated by increase in left ventricle ejection fraction and decline in left ventricle end systolic volume.

Conclusion: Modified Glasgow prognostic score prior to cardiac resynchronization therapy with defibrillation can be used as a predictor of long-term heart failure hospitalization and death in addition to age and left atrial diameter. These results can guide the patient selection for cardiac resynchronization therapy with defibrillation therapy and highlight the importance of nutritional status.

目的:改良格拉斯哥预后评分是否能预测心脏再同步化除颤治疗患者的预后尚不清楚。我们的目的是调查改良格拉斯哥预后评分与心脏再同步化治疗除颤患者死亡和住院的关系。方法:306例接受心脏再同步化治疗合并除颤植入的心力衰竭患者,根据其改良格拉斯哥预后评分分类水平将其分为3组。结果:年龄、纽约心脏协会功能分级、心脏再同步化除颤治疗前的改良格拉斯哥预后评分、钠水平和左房内径在主要心脏不良事件(+)组中较高。在多变量惩罚Cox回归分析中发现,年龄、左房径和较高的修正格拉斯哥预后评分是心力衰竭住院/死亡的预测因子。此外,改良格拉斯哥预后评分较低的患者表现出更好的左心室反向重构,表现为左心室射血分数升高和左心室收缩末期容积下降。结论:除年龄和左心房直径外,心脏再同步化除颤治疗前的改良格拉斯哥预后评分可作为长期心力衰竭住院和死亡的预测指标。这些结果可以指导患者选择心脏再同步化治疗与除颤治疗,并强调营养状况的重要性。
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引用次数: 1
Paradoxical Computed Tomography-Derived Fractional Flow Reserve Changes Due to Vessel Morphology and Constituents. 由于血管形态和成分,矛盾的计算机断层成像衍生的分流储备变化。
IF 0.8 Q3 Medicine Pub Date : 2023-03-01 DOI: 10.5543/tkda.2022.02281
Toshimitsu Tsugu, Kaoru Tanaka, Yuji Nagatomo, Michel De Maeseneer, Johan de Mey

Computed tomography-derived fractional flow reserve decreases from the proximal to the distal with coronary stenosis. According to the principles of fluid dynamics, paradoxical computed tomography-derived fractional flow reserve changes require an unconventional vessel mor-phology and specific site of the vessels with a high driving force. Therefore, only a few articles have reported a paradoxical increase of computed tomography-derived fractional flow reserve. We present a case report of marked computed tomography-derived fractional flow reserve elevation in the middle left anterior descending artery with a severe coronary stenosis. Computed tomography-derived fractional flow reserve was 0.94 just proximal to the stenotic lesion and decreased to 0.65 at the maximum stenosis area but recovered to 0.80 in the distal segment. We speculated that the vessel morphology could have caused a pressure recovery phenomenon, resulting in paradoxical computed tomography-derived fractional flow reserve changes.

在冠状动脉狭窄时,ct显示血流储备从近端到远端逐渐减少。根据流体动力学原理,矛盾的计算机层析成像衍生的分流储量变化需要非常规的血管形态和高驱动力的特定血管位置。因此,只有少数文章报道了计算机层析成像衍生的分流储备的矛盾增加。我们提出一个病例报告,在严重冠状动脉狭窄的左前降支中,有明显的计算机断层扫描衍生的分数血流储备升高。计算机断层扫描得出的血流储备分数在狭窄病变近端为0.94,在最大狭窄区域降至0.65,但在远端恢复到0.80。我们推测,血管形态可能导致压力恢复现象,导致计算机断层扫描得出的流量储量变化的矛盾。
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引用次数: 0
Bone Marrow Transplantation as a Rare Cause of Pulmonary Arterial Hypertension. 骨髓移植是肺动脉高压的罕见病因。
IF 0.8 Q3 Medicine Pub Date : 2023-03-01 DOI: 10.5543/tkda.2023.13944
Zeynep Ulutaş, Hilal Ermiş, Necip Ermiş, Ilhami Berber, Şıho Hidayet

The development of pulmonary arterial hypertension after bone marrow transplantation (BMT) is a rare but serious complication. In this case report, we presented the development of pulmonary arterial hypertension in a 22-year-old woman who underwent BMT due to aplastic anemia. Her symptoms on admission included shortness of breath, palpitations and fatigue. Pulmonary hypertension was classified with right heart catheterization as pul monary arterial hypertension. The patient's laboratory, echocardiographic and hemodynamic findings improved with pulmonary arterial hypertension-specific treatment. Pul monary arterial hypertension should be considered in the differ ential diagnosis of BMT patients with 'unexplained' hypoxemia or respiratory distress.

骨髓移植术后肺动脉高压是一种罕见但严重的并发症。在这个病例报告中,我们报告了一位22岁的女性因再生障碍性贫血而接受BMT的肺动脉高压的发展。她入院时的症状包括呼吸急促、心悸和疲劳。肺动脉高压与右心导管被归类为肺动脉高压。患者的实验室,超声心动图和血流动力学结果改善肺动脉高压特异性治疗。对于伴有“不明原因”低氧血症或呼吸窘迫的BMT患者,在鉴别诊断时应考虑肺动脉高压。
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引用次数: 0
A Rare Case of Undifferentiated Pleomorphic Sarcoma with Central Necrosis in the Right Atrium. 罕见的右心房未分化多形性肉瘤合并中央坏死1例。
IF 0.8 Q3 Medicine Pub Date : 2023-03-01 DOI: 10.5543/tkda.2022.97918
Zorica Mladenovic, Slobodan Obradovic, Sasa Ristic, Ljubinko Djenic, Edin Begic

Primary cardiac tumors, which are uncommon types of tumors, can be presented with a variety of clinical signs and symptoms, depending on their location. We present a case of a 57-year-old female patient with a severe right-sided heart failure. Examination using 2-dimensional transthoracic and 3-dimensional transoesophageal echocardiography detected a large, oval, tumor-like formation within the right atrium, which compromised the blood flow from the superior and inferior vena cava. It appeared to have an irregular echo-free space in its central part, probably due to necrosis. Thoracic multislice computed tomography revealed a heterogeneous, expansive, tumor-like mass in the right atrium, with signs of bleeding in its center. Although there were no signs of metastatic dissemination, it could not be excluded that the tumor-like mass originated outside of the heart. The patient underwent surgical resection of the tumor. The surgery was accompanied with bleeding complications that developed due to the central necrosis with local infiltration. During the postoperative period, severe systemic inflammatory response syndrome developed and the patient died. Pathologists diagnosed undifferentiated pleomorphic cardiac sarcoma for which the prognosis is usually poor. The median survival of patients with this type of diagnosis is less than 1 year, even with surgical resection and further adjuvant therapy.

原发性心脏肿瘤是一种罕见的肿瘤类型,根据其位置的不同,可以表现出多种临床体征和症状。我们提出一个病例的57岁的女性患者与严重的右侧心力衰竭。通过二维经胸和三维经食管超声心动图检查,发现右心房内有一个巨大的椭圆形肿瘤样物,妨碍了上下腔静脉的血液流动。它的中心部分似乎有一个不规则的无回声空间,可能是由于坏死。胸部多层计算机断层扫描显示右心房一异质、膨胀性肿瘤样肿块,中心有出血征象。虽然没有转移扩散的迹象,但不能排除肿瘤样肿块起源于心脏外。病人接受了手术切除肿瘤。手术伴有出血并发症,这是由于中央坏死和局部浸润引起的。术后出现严重的全身炎症反应综合征,患者死亡。病理诊断为未分化多形性心脏肉瘤,其预后通常较差。这种诊断的患者的中位生存期不到1年,即使手术切除和进一步的辅助治疗。
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引用次数: 0
期刊
Turk Kardiyoloji Dernegi Arsivi-Archives of the Turkish Society of Cardiology
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