首页 > 最新文献

Heart International最新文献

英文 中文
Use of Stent Enhancement Technique During Percutaneous Coronary Intervention - A Case Series. 在经皮冠状动脉介入治疗中使用支架增强技术--一个病例系列。
IF 1.9 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2019-10-11 eCollection Date: 2019-01-01 DOI: 10.17925/HI.2019.13.1.28
Filippo Figini, Yves Louvard, Imad Sheiban

Stent enhancement allows clear visualisation of implanted stents. This method, originally intended to assess stent under-expansion, can prove extremely valuable in several other situations. We present three cases illustrating its potential uses in assessment of stent failure, intraprocedural stent disruption and treatment of aorto-ostial and bifurcation lesions. Whilst stent enhancement cannot replace intravascular imaging, compared to simple angiography it can significantly improve percutaneous coronary intervention outcomes with no additional cost and with minimal procedural time.

支架增强可以清晰地观察植入的支架。这种最初用于评估支架扩张不足的方法在其他一些情况下也极具价值。我们介绍了三个病例,说明了这种方法在评估支架失败、术中支架断裂以及治疗主动脉和分叉病变方面的潜在用途。虽然支架增强不能取代血管内成像,但与简单的血管造影相比,它能显著改善经皮冠状动脉介入治疗的效果,而且无需额外费用,手术时间也最短。
{"title":"Use of Stent Enhancement Technique During Percutaneous Coronary Intervention - A Case Series.","authors":"Filippo Figini, Yves Louvard, Imad Sheiban","doi":"10.17925/HI.2019.13.1.28","DOIUrl":"10.17925/HI.2019.13.1.28","url":null,"abstract":"<p><p>Stent enhancement allows clear visualisation of implanted stents. This method, originally intended to assess stent under-expansion, can prove extremely valuable in several other situations. We present three cases illustrating its potential uses in assessment of stent failure, intraprocedural stent disruption and treatment of aorto-ostial and bifurcation lesions. Whilst stent enhancement cannot replace intravascular imaging, compared to simple angiography it can significantly improve percutaneous coronary intervention outcomes with no additional cost and with minimal procedural time.</p>","PeriodicalId":12836,"journal":{"name":"Heart International","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2019-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524748/pdf/heart-int-13-28.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40664274","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Improved Dosing and Administration of Rivaroxaban when Prescribed by a Cardiologist. 改进利伐沙班的剂量和管理时,由心脏病专家开出。
IF 0.2 Q4 Medicine Pub Date : 2019-10-11 eCollection Date: 2019-01-01 DOI: 10.17925/HI.2019.13.1.24
Madeline R Leiter, Kathleen A Packard, Yongyue Qi, Steven K Krueger

Rivaroxaban is a direct oral anticoagulant (DOAC) indicated to reduce risk of stroke and systemic embolism in patients with non-valvular atrial fibrillation (AF). A discrepancy exists between the recommended dosage and real-world use of DOACs, especially rivaroxaban, thus putting patients at risk of thromboembolic events.

Methods: This retrospective study assessed real-world prescribing and patient adherence to dietary requirements during use of rivaroxaban in 116 patients with AF. Associations between prescriber specialty and the correct dosing and administration were assessed using the Chi-Square test.

Results: Most rivaroxaban prescriptions were ordered by cardiologists (50.9%). Sixty-nine patients (59.5%) were taking the right dose at the correct time with an adequate meal. Of the 47 (40.5%) taking rivaroxaban incorrectly, 39 (33.6%) had not been administered an adequate meal and eight (6.9%) were not prescribed the correct dose. Compared with other prescribers, patients were most likely to be taking the correct dose and administration when prescribed by cardiologists (72.9% versus 45.6%; p=0.003). Patients were least likely to be taking the correct dose and administration when prescribed by primary care providers (44.4% versus 69.0%; p=0.009). This difference was driven by patients who did not take the treatment with an adequate meal.

Conclusion: Inappropriate prescribing, administration and non-adherence to DOACs can have devastating consequences. This highlights the importance of formal systematic education of patients prescribed DOACs across the whole health system. Future studies are warranted to explore the impact of non-adherence to rivaroxaban dietary requirements on clinical outcomes.

利伐沙班是一种直接口服抗凝剂(DOAC),用于降低非瓣膜性心房颤动(AF)患者中风和全身栓塞的风险。DOACs的推荐剂量与实际使用存在差异,特别是利伐沙班,从而使患者面临血栓栓塞事件的风险。方法:本回顾性研究评估了116例房颤患者在使用利伐沙班期间的真实处方和患者对饮食要求的依从性。使用卡方检验评估处方医师专业与正确给药和给药之间的关系。结果:利伐沙班处方多数由心内科医师开具(50.9%)。69例患者(59.5%)在正确的时间和适当的膳食中服用了正确的剂量。在47例(40.5%)错误服用利伐沙班的患者中,39例(33.6%)未给予足够的膳食,8例(6.9%)未给予正确的剂量。与其他开处方者相比,患者最有可能在心脏病专家开处方时服用正确的剂量和给药(72.9%对45.6%;p = 0.003)。当初级保健提供者开出处方时,患者最不可能服用正确的剂量和给药(44.4%对69.0%;p = 0.009)。造成这种差异的原因是患者在接受治疗时没有吃足够的饭。结论:不适当的处方、给药和不遵守DOACs可造成毁灭性的后果。这突出了在整个卫生系统中对患者进行正式系统的doac处方教育的重要性。未来的研究有必要探讨不遵守利伐沙班饮食要求对临床结果的影响。
{"title":"Improved Dosing and Administration of Rivaroxaban when Prescribed by a Cardiologist.","authors":"Madeline R Leiter,&nbsp;Kathleen A Packard,&nbsp;Yongyue Qi,&nbsp;Steven K Krueger","doi":"10.17925/HI.2019.13.1.24","DOIUrl":"https://doi.org/10.17925/HI.2019.13.1.24","url":null,"abstract":"<p><p>Rivaroxaban is a direct oral anticoagulant (DOAC) indicated to reduce risk of stroke and systemic embolism in patients with non-valvular atrial fibrillation (AF). A discrepancy exists between the recommended dosage and real-world use of DOACs, especially rivaroxaban, thus putting patients at risk of thromboembolic events.</p><p><strong>Methods: </strong>This retrospective study assessed real-world prescribing and patient adherence to dietary requirements during use of rivaroxaban in 116 patients with AF. Associations between prescriber specialty and the correct dosing and administration were assessed using the Chi-Square test.</p><p><strong>Results: </strong>Most rivaroxaban prescriptions were ordered by cardiologists (50.9%). Sixty-nine patients (59.5%) were taking the right dose at the correct time with an adequate meal. Of the 47 (40.5%) taking rivaroxaban incorrectly, 39 (33.6%) had not been administered an adequate meal and eight (6.9%) were not prescribed the correct dose. Compared with other prescribers, patients were most likely to be taking the correct dose and administration when prescribed by cardiologists (72.9% versus 45.6%; p=0.003). Patients were least likely to be taking the correct dose and administration when prescribed by primary care providers (44.4% versus 69.0%; p=0.009). This difference was driven by patients who did not take the treatment with an adequate meal.</p><p><strong>Conclusion: </strong>Inappropriate prescribing, administration and non-adherence to DOACs can have devastating consequences. This highlights the importance of formal systematic education of patients prescribed DOACs across the whole health system. Future studies are warranted to explore the impact of non-adherence to rivaroxaban dietary requirements on clinical outcomes.</p>","PeriodicalId":12836,"journal":{"name":"Heart International","volume":null,"pages":null},"PeriodicalIF":0.2,"publicationDate":"2019-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562422/pdf/heart-int-13-24.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40664275","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
What are the Pathological Concerns and Limitations of Current Drug-coated Balloon Technology? 目前的药物涂层球囊技术存在哪些病理问题和局限性?
IF 1.9 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2019-10-11 eCollection Date: 2019-01-01 DOI: 10.17925/HI.2019.13.1.15
Yu Sato, Salomé H Kuntz, Dipti Surve, Hiroyuki Jinnouchi, Atsushi Sakamoto, Anne Cornelissen, Renu Virmani, Frank Kolodgie, Aloke V Finn

The use of endovascular therapy for peripheral artery disease and coronary artery disease has increased and spread worldwide and is considered as the foremost, guideline-based invasive treatment. Drug-coated balloons (DCBs) utilise anti-proliferative drugs similar to drug-eluting stents; however, the do not leave any permanent metallic scaffold. Excipients and drug formulations play a crucial role in innovative DCB technologies and allow for treatment of lesions where stents are not suitable. Although the significance of downstream embolic effects after DCB use remains uncertain, several preclinical studies suggest such side effects might pose safety concerns. Recently, a meta-analysis of randomised controlled trials of paclitaxel devices suggested an association between increased mortality and paclitaxel device use. Subsequently, unfavourable criticism of paclitaxel devices attracted much attention and gave rise to a discussion about the safety of such devices. In this review, we will focus on the novel DCB technologies from the standpoint of preclinical studies and clinical trials, as well as discuss current controversies regarding the increase in death rates from paclitaxel-coated DCBs versus control devices seen in a recent meta-analysis of randomised controlled clinical trials.

血管内治疗外周动脉疾病和冠状动脉疾病的使用在全球范围内不断增加和普及,被认为是最重要的、以指南为基础的侵入性治疗方法。药物涂层球囊(DCB)使用的抗增生药物与药物洗脱支架类似,但不会留下任何永久性金属支架。辅料和药物配方在创新的 DCB 技术中发挥着至关重要的作用,可用于治疗不适合使用支架的病变。尽管使用 DCB 后下游栓塞效应的意义仍不确定,但一些临床前研究表明,这种副作用可能会带来安全问题。最近,一项关于紫杉醇装置随机对照试验的荟萃分析表明,死亡率的增加与紫杉醇装置的使用有关。随后,对紫杉醇装置的不利批评引起了广泛关注,并引发了对此类装置安全性的讨论。在这篇综述中,我们将从临床前研究和临床试验的角度重点介绍新型 DCB 技术,并讨论近期随机对照临床试验荟萃分析中发现的紫杉醇涂层 DCB 与对照设备相比死亡率增加的争议。
{"title":"What are the Pathological Concerns and Limitations of Current Drug-coated Balloon Technology?","authors":"Yu Sato, Salomé H Kuntz, Dipti Surve, Hiroyuki Jinnouchi, Atsushi Sakamoto, Anne Cornelissen, Renu Virmani, Frank Kolodgie, Aloke V Finn","doi":"10.17925/HI.2019.13.1.15","DOIUrl":"10.17925/HI.2019.13.1.15","url":null,"abstract":"<p><p>The use of endovascular therapy for peripheral artery disease and coronary artery disease has increased and spread worldwide and is considered as the foremost, guideline-based invasive treatment. Drug-coated balloons (DCBs) utilise anti-proliferative drugs similar to drug-eluting stents; however, the do not leave any permanent metallic scaffold. Excipients and drug formulations play a crucial role in innovative DCB technologies and allow for treatment of lesions where stents are not suitable. Although the significance of downstream embolic effects after DCB use remains uncertain, several preclinical studies suggest such side effects might pose safety concerns. Recently, a meta-analysis of randomised controlled trials of paclitaxel devices suggested an association between increased mortality and paclitaxel device use. Subsequently, unfavourable criticism of paclitaxel devices attracted much attention and gave rise to a discussion about the safety of such devices. In this review, we will focus on the novel DCB technologies from the standpoint of preclinical studies and clinical trials, as well as discuss current controversies regarding the increase in death rates from paclitaxel-coated DCBs versus control devices seen in a recent meta-analysis of randomised controlled clinical trials.</p>","PeriodicalId":12836,"journal":{"name":"Heart International","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2019-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524611/pdf/heart-int-13-15.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40664273","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Letter from the Editor-in-Chief. 总编辑的来信。
IF 0.2 Q4 Medicine Pub Date : 2019-10-11 eCollection Date: 2019-01-01 DOI: 10.17925/HI.2019.13.1.12
Magdi El-Omar
{"title":"Letter from the Editor-in-Chief.","authors":"Magdi El-Omar","doi":"10.17925/HI.2019.13.1.12","DOIUrl":"https://doi.org/10.17925/HI.2019.13.1.12","url":null,"abstract":"","PeriodicalId":12836,"journal":{"name":"Heart International","volume":null,"pages":null},"PeriodicalIF":0.2,"publicationDate":"2019-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524609/pdf/heart-int-13-12.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40664276","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
European Bifurcation Club Perspectives on Two-stent Techniques - An Interview. 欧洲分支俱乐部对双支架技术的看法-访谈。
IF 0.2 Q4 Medicine Pub Date : 2019-09-18 eCollection Date: 2019-01-01 DOI: 10.17925/HI.2019.13.1.9
Dr Francesco Burzotta
{"title":"European Bifurcation Club Perspectives on Two-stent Techniques - An Interview.","authors":"Dr Francesco Burzotta","doi":"10.17925/HI.2019.13.1.9","DOIUrl":"https://doi.org/10.17925/HI.2019.13.1.9","url":null,"abstract":"","PeriodicalId":12836,"journal":{"name":"Heart International","volume":null,"pages":null},"PeriodicalIF":0.2,"publicationDate":"2019-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524544/pdf/heart-int-13-09.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40664277","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Role of Optimal Medication Given to Patients with Hypertension and Ischemic Heart Disease Prior to an Acute Coronary Syndrome. 急性冠脉综合征前高血压和缺血性心脏病患者最佳用药的作用
IF 0.2 Q4 Medicine Pub Date : 2017-10-14 eCollection Date: 2017-01-01 DOI: 10.5301/heartint.5000237
Călin Pop, Roberta Florescu, Claudia Matei, Lavinia Pop, Viorel Manea, Coralia Cotoraci, Liana Mos, Antoniu Petris

Introduction: Administering optimal cardiovascular medication (OCM) to patients with hypertension (HBP) and ischemic heart disease (IHD) lowers cardiovascular morbidity and mortality.The main objective of this study was to compare in-hospital cardiac mortality among patients with HBP and/or IHD, treated or untreated with OCM, who developed a first episode of acute coronary syndrome (ACS).

Methods: The study was carried out retrospectively and included patients admitted with a first episode of ACS between 2013 and 2016. The patients were divided into three groups: those with HBP, IHD, and a history of HBP + IHD. Patients were then divided into two subgroups: subgroup A consisted of patients undergoing optimal anti-ischemic and/or antihypertensive therapy, while subgroup B consisted of patients without OCM.

Results: This analysis comprised 1096 patients. Mean age was 64.3 ± 18 years. There were 581 patients in subgroup A - 53%, and 515 patients in subgroup B - 47%. Total cardiac mortality was 9.98%, different depending on the groups and subgroups studied: HBP group total - 7%, subgroup A - 5.1%, significantly lower compared to subgroup B - 9.4% (p = 0.05); IHD group total - 12.2%, subgroup A - 9.07%, significantly lower compared to subgroup B - 15.8% (p = 0.05); HBP + IHD group total - 14.35%, subgroup A - 9.9%, significantly lower compared to subgroup B - 18.8% (p = 0.05).

Conclusions: The lack of OCM in patients with HBP and/or IHD is correlated to a significant increase in in-hospital cardiac mortality among patients who develop a first-episode ACS.

对高血压(HBP)和缺血性心脏病(IHD)患者给予最佳心血管药物(OCM)可降低心血管发病率和死亡率。本研究的主要目的是比较首次发生急性冠状动脉综合征(ACS)的HBP和/或IHD患者(接受或未接受OCM治疗)的住院心脏死亡率。方法:回顾性研究纳入2013年至2016年间首次发作ACS的患者。患者被分为三组:有HBP、IHD和有HBP + IHD病史的患者。然后将患者分为两个亚组:亚组由接受最佳抗缺血和/或抗高血压治疗的患者组成,而亚组由未接受OCM治疗的患者组成。结果:本分析共纳入1096例患者。平均年龄64.3±18岁。A亚组581例,占53%;B亚组515例,占47%。心脏总死亡率为9.98%,因组和亚组而异:HBP组总死亡率为7%,A亚组为5.1%,显著低于B亚组9.4% (p = 0.05);IHD组总- 12.2%,A亚组- 9.07%,显著低于B亚组- 15.8% (p = 0.05);HBP + IHD组总- 14.35%,A亚组- 9.9%,显著低于B亚组- 18.8% (p = 0.05)。结论:HBP和/或IHD患者缺乏OCM与首发ACS患者院内心脏死亡率显著增加相关。
{"title":"Role of Optimal Medication Given to Patients with Hypertension and Ischemic Heart Disease Prior to an Acute Coronary Syndrome.","authors":"Călin Pop,&nbsp;Roberta Florescu,&nbsp;Claudia Matei,&nbsp;Lavinia Pop,&nbsp;Viorel Manea,&nbsp;Coralia Cotoraci,&nbsp;Liana Mos,&nbsp;Antoniu Petris","doi":"10.5301/heartint.5000237","DOIUrl":"https://doi.org/10.5301/heartint.5000237","url":null,"abstract":"<p><strong>Introduction: </strong>Administering optimal cardiovascular medication (OCM) to patients with hypertension (HBP) and ischemic heart disease (IHD) lowers cardiovascular morbidity and mortality.The main objective of this study was to compare in-hospital cardiac mortality among patients with HBP and/or IHD, treated or untreated with OCM, who developed a first episode of acute coronary syndrome (ACS).</p><p><strong>Methods: </strong>The study was carried out retrospectively and included patients admitted with a first episode of ACS between 2013 and 2016. The patients were divided into three groups: those with HBP, IHD, and a history of HBP + IHD. Patients were then divided into two subgroups: subgroup A consisted of patients undergoing optimal anti-ischemic and/or antihypertensive therapy, while subgroup B consisted of patients without OCM.</p><p><strong>Results: </strong>This analysis comprised 1096 patients. Mean age was 64.3 ± 18 years. There were 581 patients in subgroup A - 53%, and 515 patients in subgroup B - 47%. Total cardiac mortality was 9.98%, different depending on the groups and subgroups studied: HBP group total - 7%, subgroup A - 5.1%, significantly lower compared to subgroup B - 9.4% (p = 0.05); IHD group total - 12.2%, subgroup A - 9.07%, significantly lower compared to subgroup B - 15.8% (p = 0.05); HBP + IHD group total - 14.35%, subgroup A - 9.9%, significantly lower compared to subgroup B - 18.8% (p = 0.05).</p><p><strong>Conclusions: </strong>The lack of OCM in patients with HBP and/or IHD is correlated to a significant increase in in-hospital cardiac mortality among patients who develop a first-episode ACS.</p>","PeriodicalId":12836,"journal":{"name":"Heart International","volume":null,"pages":null},"PeriodicalIF":0.2,"publicationDate":"2017-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.5301/heartint.5000237","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36532120","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Mild troponin I elevation does not predict ischemia on myocardial perfusion imaging 轻度肌钙蛋白I升高不能在心肌灌注显像上预测缺血
IF 0.2 Q4 Medicine Pub Date : 2017-08-02 DOI: 10.5301/HEARTINT.5000236
L. Ha, Farrukh Abbas, M. Rao
Introduction: Data are limited on the degree of mild troponin I elevation and clinical risk factors in predicting myocardial ischemia. Methods: Hospitalized adult patients who underwent myocardial perfusion imaging (MPI) from 2015 to 2016 at Rochester General Hospital and had mild troponin I elevation (>0.1 and <1.5 ng/mL) were included. Predictors of outcomes were determined using logistic regression model. Results: One hundred and sixty-six patients with mild troponin I elevation who underwent MPI were followed. Mean age was 69.6 ± 12.5 years and 53.0% of the patients were female. Fourteen patients (8.4%) presented with typical chest pain (CP), 60 patients (36.1%) had atypical CP and 92 patients (55.4%) had no CP on presentation. MPI was positive for ischemia in 45 patients (27.1%). There was no difference in peak troponin I level with ischemia versus no ischemia on MPI (0.34 ng/dL [0.13-0.69] vs. 0.23 ng/dL [0.14-0.50], p value 0.254). Atypical CP did not predict the presence of ischemia on MPI (odds ratio [OR] 1.97, 95% confidence interval [CI] 0.91-4.26). Coronary artery disease (CAD) history (age and sex adjusted p value 0.013), diabetes (adjusted p value 0.036), creatinine ≥2 mg/dL (adjusted p value 0.019) and dialysis (adjusted p value 0.006) were statistically significant predictors of ischemia on MPI. Conclusions: In patients presenting with mild troponin I elevation, peak troponin I level did not predict ischemia on MPI. The presence of CAD history, diabetes, elevated creatinine and dialysis were predictors of ischemia on MPI.
关于轻度肌钙蛋白I升高程度和临床危险因素预测心肌缺血的数据有限。方法:纳入2015 - 2016年在罗切斯特综合医院行心肌灌注显像(MPI)且肌钙蛋白I轻度升高(>.1和<1.5 ng/mL)的住院成年患者。采用logistic回归模型确定预测因素。结果:对166例轻度肌钙蛋白I升高患者行MPI随访。平均年龄69.6±12.5岁,女性占53.0%。14例(8.4%)表现为典型胸痛,60例(36.1%)表现为非典型胸痛,92例(55.4%)表现为无胸痛。45例(27.1%)患者MPI呈缺血阳性。缺血与无缺血时肌钙蛋白I峰值水平在MPI上无差异(0.34 ng/dL [0.13-0.69] vs. 0.23 ng/dL [0.14-0.50], p值0.254)。非典型CP不能预测MPI是否存在缺血(优势比[OR] 1.97, 95%可信区间[CI] 0.91-4.26)。冠状动脉病史(CAD)(年龄和性别校正p值0.013)、糖尿病(校正p值0.036)、肌酐≥2 mg/dL(校正p值0.019)和透析(校正p值0.006)是MPI缺血的有统计学意义的预测因素。结论:在肌钙蛋白I轻度升高的患者中,肌钙蛋白I峰值水平不能预测MPI的缺血。CAD病史、糖尿病、肌酐升高和透析是MPI缺血的预测因素。
{"title":"Mild troponin I elevation does not predict ischemia on myocardial perfusion imaging","authors":"L. Ha, Farrukh Abbas, M. Rao","doi":"10.5301/HEARTINT.5000236","DOIUrl":"https://doi.org/10.5301/HEARTINT.5000236","url":null,"abstract":"Introduction: Data are limited on the degree of mild troponin I elevation and clinical risk factors in predicting myocardial ischemia. Methods: Hospitalized adult patients who underwent myocardial perfusion imaging (MPI) from 2015 to 2016 at Rochester General Hospital and had mild troponin I elevation (>0.1 and <1.5 ng/mL) were included. Predictors of outcomes were determined using logistic regression model. Results: One hundred and sixty-six patients with mild troponin I elevation who underwent MPI were followed. Mean age was 69.6 ± 12.5 years and 53.0% of the patients were female. Fourteen patients (8.4%) presented with typical chest pain (CP), 60 patients (36.1%) had atypical CP and 92 patients (55.4%) had no CP on presentation. MPI was positive for ischemia in 45 patients (27.1%). There was no difference in peak troponin I level with ischemia versus no ischemia on MPI (0.34 ng/dL [0.13-0.69] vs. 0.23 ng/dL [0.14-0.50], p value 0.254). Atypical CP did not predict the presence of ischemia on MPI (odds ratio [OR] 1.97, 95% confidence interval [CI] 0.91-4.26). Coronary artery disease (CAD) history (age and sex adjusted p value 0.013), diabetes (adjusted p value 0.036), creatinine ≥2 mg/dL (adjusted p value 0.019) and dialysis (adjusted p value 0.006) were statistically significant predictors of ischemia on MPI. Conclusions: In patients presenting with mild troponin I elevation, peak troponin I level did not predict ischemia on MPI. The presence of CAD history, diabetes, elevated creatinine and dialysis were predictors of ischemia on MPI.","PeriodicalId":12836,"journal":{"name":"Heart International","volume":null,"pages":null},"PeriodicalIF":0.2,"publicationDate":"2017-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46510802","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
Placement Of Cardiac PacemaKEr Trial (POCKET) - rationale and design: a randomized controlled trial. 心脏起搏器放置试验(POCKET) -基本原理和设计:一项随机对照试验。
IF 0.2 Q4 Medicine Pub Date : 2017-04-14 eCollection Date: 2017-01-01 DOI: 10.5301/heartint.5000235
Peter Magnusson, Leo Wennström, Robert Kastberg, Per Liv

Background: A pacemaker system consists of one or two leads connected to a device that is implanted into a pocket formed just below the collarbone. This pocket is typically subcutaneous, that is, located just above the pectoral fascia. Even though the size of pacemakers has decreased markedly, complications due to superficial implants do occur. An alternative technique would be intramuscular placement of the pacemaker device, but there are no randomized controlled trials (RCTs) to support this approach, which is the rationale for the Placement Of Cardiac PacemaKEr Trial (POCKET). The aim is to study if intramuscular is superior to subcutaneous placement of a pacemaker pocket.

Methods: In October 2016, we started to enroll 200 consecutive patients with an indication for bradycardia pacemaker implantation. Patients are randomized to random block sizes, stratified by age group (cut-off: 65 years) and sex, and then randomized to either subcutaneous or intramuscular implant. A concealed allocation procedure is employed, using sequentially numbered, sealed envelopes. Pocket site is blinded to the patient and in all subsequent care. The primary endpoint is patient overall satisfaction with the pocket location at 24 months as measured using a visual analog scale (VAS) 0-10. Secondary endpoints are: complications, patient-reported satisfaction at 1, 12, and 24 months (overall satisfaction, pain, discomfort, degree of unsightly appearance, movement problems, and sleep problems due to device).

Conclusions: POCKET is a prospective interventional RCT designed to evaluate if intramuscular is superior to subcutaneous placement of a bradycardia pacemaker during a two-year follow-up.

背景:起搏器系统由一根或两根连接到一个装置的导线组成,该装置被植入锁骨下方形成的口袋中。这个口袋通常位于皮下,即位于胸筋膜上方。尽管起搏器的尺寸已经明显减小,但由于浅表植入引起的并发症仍然存在。另一种技术是肌肉内放置起搏器装置,但没有随机对照试验(rct)支持这种方法,这是心脏起搏器放置试验(POCKET)的基本原理。目的是研究肌肉内放置心脏起搏器是否优于皮下放置。方法:2016年10月,我们开始招募200例有心动过缓起搏器植入指征的连续患者。患者被随机分配到随机块大小,按年龄组(截止年龄:65岁)和性别分层,然后随机分配到皮下或肌肉内植入。采用了一种隐蔽的分配程序,使用顺序编号的密封信封。口袋部位对患者和所有后续护理都是不可见的。主要终点是患者在24个月时对口袋位置的总体满意度,使用视觉模拟评分(VAS) 0-10进行测量。次要终点是:并发症、患者在1、12和24个月时报告的满意度(总体满意度、疼痛、不适、外观不美观程度、运动问题和由器械引起的睡眠问题)。结论:POCKET是一项前瞻性介入随机对照试验,旨在评估在两年随访期间,肌内植入心动过缓起搏器是否优于皮下植入。
{"title":"Placement Of Cardiac PacemaKEr Trial (POCKET) - rationale and design: a randomized controlled trial.","authors":"Peter Magnusson,&nbsp;Leo Wennström,&nbsp;Robert Kastberg,&nbsp;Per Liv","doi":"10.5301/heartint.5000235","DOIUrl":"https://doi.org/10.5301/heartint.5000235","url":null,"abstract":"<p><strong>Background: </strong>A pacemaker system consists of one or two leads connected to a device that is implanted into a pocket formed just below the collarbone. This pocket is typically subcutaneous, that is, located just above the pectoral fascia. Even though the size of pacemakers has decreased markedly, complications due to superficial implants do occur. An alternative technique would be intramuscular placement of the pacemaker device, but there are no randomized controlled trials (RCTs) to support this approach, which is the rationale for the Placement Of Cardiac PacemaKEr Trial (POCKET). The aim is to study if intramuscular is superior to subcutaneous placement of a pacemaker pocket.</p><p><strong>Methods: </strong>In October 2016, we started to enroll 200 consecutive patients with an indication for bradycardia pacemaker implantation. Patients are randomized to random block sizes, stratified by age group (cut-off: 65 years) and sex, and then randomized to either subcutaneous or intramuscular implant. A concealed allocation procedure is employed, using sequentially numbered, sealed envelopes. Pocket site is blinded to the patient and in all subsequent care. The primary endpoint is patient overall satisfaction with the pocket location at 24 months as measured using a visual analog scale (VAS) 0-10. Secondary endpoints are: complications, patient-reported satisfaction at 1, 12, and 24 months (overall satisfaction, pain, discomfort, degree of unsightly appearance, movement problems, and sleep problems due to device).</p><p><strong>Conclusions: </strong>POCKET is a prospective interventional RCT designed to evaluate if intramuscular is superior to subcutaneous placement of a bradycardia pacemaker during a two-year follow-up.</p>","PeriodicalId":12836,"journal":{"name":"Heart International","volume":null,"pages":null},"PeriodicalIF":0.2,"publicationDate":"2017-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.5301/heartint.5000235","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35585980","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 9
The inhibitory effects of polysaccharide peptides (PsP) of Ganoderma lucidum against atherosclerosis in rats with dyslipidemia. 灵芝多糖肽(PsP)对血脂异常大鼠动脉粥样硬化的抑制作用。
IF 0.2 Q4 Medicine Pub Date : 2017-04-12 eCollection Date: 2017-01-01 DOI: 10.5301/heartint.5000234
Titin Andri Wihastuti, Teuku Heriansyah

Background: Atherosclerosis occurs as a result of low-density lipoprotein (LDL) deposits oxidation. Endothelial dysfunction is an early process of atherosclerosis. Restoring endothelial lining back to normal by endothelial progenitor cells (EPCs) is critical for slowing or reversing vascular disease progression. Oxidative stress from hydrogen peroxide (H2O2) is increased in dyslipidemia so that antioxidant agent is required to prevent destruction of blood vessels.

Objectives: This study aims to report Ganoderma lucidum polysaccharide peptide (PsP) effects in atherogenic process by measuring H2O2 level, IL-10 level, and EPC number in blood serum, and also intima-media thickness of aorta in dyslipidemia Wistar rat model by giving them a hypercholesterol diet (HCD).

Materials and methods: The study was an experimental in vivo post-test with control group design. Thirty-five Wistar rats (Rattus norwegicus) were divided into five groups (normal diet group, HCD group, and hypercholesterol groups that received 50 mg/kg, 150 mg/kg, and 300 mg/kg bodyweight PsP).

Results: Each treatment group showed significant results for the administration of PsP using the one-way analysis of variance test (p<0.050) for the reduction of H2O2 (p = 0.003), levels of IL-10 (p = 0.027), number of EPC in the blood serum (p = 0.011), and the intima-media thickness of the aorta (p = 0.000). PsP from G. lucidum is a potent antioxidant and may prevent atherogenesis process in patients with dyslipidemia.

Conclusions: The optimum doses of PsP in this study is 300 mg/kg bodyweight. Further studies are required to determine the antioxidant effects of PsP G. lucidum and its benefits in the management of dyslipidemia.

背景:动脉粥样硬化是低密度脂蛋白(LDL)沉积氧化的结果。内皮功能障碍是动脉粥样硬化的早期过程。内皮祖细胞(EPCs)恢复内皮内膜正常是减缓或逆转血管疾病进展的关键。过氧化氢(H2O2)的氧化应激在血脂异常时增加,因此需要抗氧化剂来防止血管的破坏。目的:本研究通过高胆固醇饮食(HCD)对血脂异常Wistar模型大鼠血清中H2O2水平、IL-10水平、EPC数及主动脉内膜-中膜厚度的测定,研究灵芝多糖肽(PsP)在动脉粥样硬化过程中的作用。材料与方法:采用对照组设计的实验性体内后验法。将35只Wistar大鼠分为5组(正常饮食组、HCD组和高胆固醇组,分别给予50 mg/kg、150 mg/kg和300 mg/kg体重的PsP)。结果:各治疗组PsP给药的单因素方差分析(p2O2 (p = 0.003))、血清IL-10水平(p = 0.027)、血清EPC数量(p = 0.011)、主动脉内膜-中膜厚度(p = 0.000)均有显著性结果。灵芝中的PsP是一种有效的抗氧化剂,可以防止血脂异常患者的动脉粥样硬化过程。结论:本研究中PsP的最佳剂量为300 mg/kg体重。需要进一步的研究来确定PsP G. lucidum的抗氧化作用及其在血脂异常治疗中的益处。
{"title":"The inhibitory effects of polysaccharide peptides (PsP) of <i>Ganoderma lucidum</i> against atherosclerosis in rats with dyslipidemia.","authors":"Titin Andri Wihastuti,&nbsp;Teuku Heriansyah","doi":"10.5301/heartint.5000234","DOIUrl":"https://doi.org/10.5301/heartint.5000234","url":null,"abstract":"<p><strong>Background: </strong>Atherosclerosis occurs as a result of low-density lipoprotein (LDL) deposits oxidation. Endothelial dysfunction is an early process of atherosclerosis. Restoring endothelial lining back to normal by endothelial progenitor cells (EPCs) is critical for slowing or reversing vascular disease progression. Oxidative stress from hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) is increased in dyslipidemia so that antioxidant agent is required to prevent destruction of blood vessels.</p><p><strong>Objectives: </strong>This study aims to report <i>Ganoderma lucidum</i> polysaccharide peptide (PsP) effects in atherogenic process by measuring H<sub>2</sub>O<sub>2</sub> level, IL-10 level, and EPC number in blood serum, and also intima-media thickness of aorta in dyslipidemia Wistar rat model by giving them a hypercholesterol diet (HCD).</p><p><strong>Materials and methods: </strong>The study was an experimental in vivo post-test with control group design. Thirty-five Wistar rats (Rattus norwegicus) were divided into five groups (normal diet group, HCD group, and hypercholesterol groups that received 50 mg/kg, 150 mg/kg, and 300 mg/kg bodyweight PsP).</p><p><strong>Results: </strong>Each treatment group showed significant results for the administration of PsP using the one-way analysis of variance test (p<0.050) for the reduction of H<sub>2</sub>O<sub>2</sub> (p = 0.003), levels of IL-10 (p = 0.027), number of EPC in the blood serum (p = 0.011), and the intima-media thickness of the aorta (p = 0.000). PsP from <i>G. lucidum</i> is a potent antioxidant and may prevent atherogenesis process in patients with dyslipidemia.</p><p><strong>Conclusions: </strong>The optimum doses of PsP in this study is 300 mg/kg bodyweight. Further studies are required to determine the antioxidant effects of PsP <i>G. lucidum</i> and its benefits in the management of dyslipidemia.</p>","PeriodicalId":12836,"journal":{"name":"Heart International","volume":null,"pages":null},"PeriodicalIF":0.2,"publicationDate":"2017-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.5301/heartint.5000234","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35585978","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
Calculating the 30-day Survival Rate in Acute Myocardial Infarction: Should we Use the Treatment Chain or the Hospital Catchment Model? 计算急性心肌梗死的30天生存率:我们应该使用治疗链还是医院集水区模型?
IF 0.2 Q4 Medicine Pub Date : 2017-02-12 eCollection Date: 2017-01-01 DOI: 10.5301/heartint.5000238
Jan Norum, Tonya M Hansen, Anders Hovland, Lise Balteskard, Bjørn Haug, Frank Olsen, Thor Trovik

Introduction: Acute myocardial infarction (AMI) is a potentially deadly disease and significant efforts have been concentrated on improving hospital performance. A 30-day survival rate has become a key quality of care indicator. In Northern Norway, some patients undergoing AMI are directly transferred to the Regional Cardiac Intervention Center at the University Hospital of North Norway in Tromsø. Here, coronary angiography and percutaneous coronary intervention is performed. Consequently, local hospitals may be bypassed in the treatment chain, generating differences in case mix, and making the treatment chain model difficult to interpret. We aimed to compare the treatment chain model with an alternative based on patients' place of living.

Methods: Between 2013 and 2015, a total of 3,155 patients were registered in the Norwegian Patient Registry database. All patients were categorized according to their local hospital's catchment area. The method of Guo-Romano, with an indifference interval of 0.02, was used to test whether a hospital was an outlier or not. We adjusted for age, sex, comorbidity, and number of prior hospitalizations.

Conclusions: We revealed the 30-day AMI survival figure ranging between 88.0% and 93.5% (absolute difference 5.5%) using the hospital catchment method. The treatment chain rate ranged between 86.0% and 94.0% (absolute difference 8.0%). The latter figure is the one published as the National Quality of Care Measure in Norway. Local hospitals may get negative attention even though their catchment area is well served. We recommend the hospital catchment method as the first choice when measuring equality of care.

简介:急性心肌梗死(AMI)是一种潜在的致命疾病,人们一直在努力提高医院的表现。30天存活率已成为一项关键的护理质量指标。在挪威北部,一些接受急性心肌梗死的患者被直接转移到位于特罗姆瑟的北挪威大学医院的区域心脏干预中心。在这里,进行冠状动脉造影和经皮冠状动脉介入治疗。因此,当地医院可能在治疗链中被绕过,产生病例组合的差异,使治疗链模型难以解释。我们的目的是将治疗链模型与基于患者居住地的替代方案进行比较。方法:2013年至2015年间,共有3155名患者在挪威患者注册数据库中登记。所有患者根据当地医院的集水区进行分类。采用Guo-Romano法检验医院是否属于异常值,无差异区间为0.02。我们调整了年龄、性别、合并症和既往住院次数。结论:采用医院集水法,AMI患者30天生存率在88.0% ~ 93.5%之间(绝对差5.5%)。治疗链率为86.0% ~ 94.0%,绝对差8.0%。后一个数字是挪威作为国家护理质量衡量标准公布的数字。当地医院可能会受到负面关注,即使他们的服务范围很好。我们推荐医院集水法作为衡量护理公平性的首选方法。
{"title":"Calculating the 30-day Survival Rate in Acute Myocardial Infarction: Should we Use the Treatment Chain or the Hospital Catchment Model?","authors":"Jan Norum,&nbsp;Tonya M Hansen,&nbsp;Anders Hovland,&nbsp;Lise Balteskard,&nbsp;Bjørn Haug,&nbsp;Frank Olsen,&nbsp;Thor Trovik","doi":"10.5301/heartint.5000238","DOIUrl":"https://doi.org/10.5301/heartint.5000238","url":null,"abstract":"<p><strong>Introduction: </strong>Acute myocardial infarction (AMI) is a potentially deadly disease and significant efforts have been concentrated on improving hospital performance. A 30-day survival rate has become a key quality of care indicator. In Northern Norway, some patients undergoing AMI are directly transferred to the Regional Cardiac Intervention Center at the University Hospital of North Norway in Tromsø. Here, coronary angiography and percutaneous coronary intervention is performed. Consequently, local hospitals may be bypassed in the treatment chain, generating differences in case mix, and making the treatment chain model difficult to interpret. We aimed to compare the treatment chain model with an alternative based on patients' place of living.</p><p><strong>Methods: </strong>Between 2013 and 2015, a total of 3,155 patients were registered in the Norwegian Patient Registry database. All patients were categorized according to their local hospital's catchment area. The method of Guo-Romano, with an indifference interval of 0.02, was used to test whether a hospital was an outlier or not. We adjusted for age, sex, comorbidity, and number of prior hospitalizations.</p><p><strong>Conclusions: </strong>We revealed the 30-day AMI survival figure ranging between 88.0% and 93.5% (absolute difference 5.5%) using the hospital catchment method. The treatment chain rate ranged between 86.0% and 94.0% (absolute difference 8.0%). The latter figure is the one published as the National Quality of Care Measure in Norway. Local hospitals may get negative attention even though their catchment area is well served. We recommend the hospital catchment method as the first choice when measuring equality of care.</p>","PeriodicalId":12836,"journal":{"name":"Heart International","volume":null,"pages":null},"PeriodicalIF":0.2,"publicationDate":"2017-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.5301/heartint.5000238","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36532121","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
期刊
Heart International
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
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
×
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
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
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