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      <title>Wiley: Clinical Cardiology: Table of Contents</title>
      <link>https://onlinelibrary.wiley.com/journal/19328737?af=R</link>
      <description>Table of Contents for Clinical Cardiology. List of articles from both the latest and EarlyView issues.</description>
      <language>en-US</language>
      <copyright>© Wiley Periodicals, Inc.</copyright>
      <managingEditor>wileyonlinelibrary@wiley.com (Wiley Online Library)</managingEditor>
      <pubDate>Thu, 11 Jun 2026 07:47:28 +0000</pubDate>
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      <dc:title>Wiley: Clinical Cardiology: Table of Contents</dc:title>
      <dc:publisher>Wiley</dc:publisher>
      <prism:publicationName>Clinical Cardiology</prism:publicationName>
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         <title>Wiley: Clinical Cardiology: Table of Contents</title>
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         <link>https://onlinelibrary.wiley.com/doi/10.1002/clc.70367?af=R</link>
         <pubDate>Wed, 10 Jun 2026 04:32:14 -0700</pubDate>
         <dc:date>2026-06-10T04:32:14-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/19328737?af=R">Wiley: Clinical Cardiology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
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         <title>IVUS‐Guided Versus Angiography‐Guided PCI for Unprotected Left Main Coronary Artery Disease: A Systematic Review, Meta‐Analysis, and GRADE Assessment of Randomized Trials</title>
         <description>Clinical Cardiology, Volume 49, Issue 6, June 2026. </description>
         <dc:description>graphical abstract for IVUS‐guided versus angiography‐guided pci for unprotected left main coronary artery disease.





ABSTRACT

Background
Intravascular ultrasound (IVUS) has been increasingly used as an adjunctive tool for complex percutaneous interventions (PCIs); however, comparative randomized evidence with conventional angiography in unprotected left main coronary artery (ULMCA) disease remains scarce and fragmented. Therefore, this systematic review and meta‐analysis aimed to assess and synthesize evidence regarding its use in ULMCA disease.


Methods
We performed a systematic literature search across PubMed, Scopus, Web of Science, and Cochrane until April 2026 to identify relevant RCTs comparing IVUS‐guided PCI with conventional angiography‐guided PCI in ULMCA disease. Risk of bias of studies was assessed using the Cochrane RoB‐2 tool. A random‐effects model meta‐analysis was performed in R, with an exploratory univariate meta‐regression of covariates.


Results
Four randomized trials involving 2278 patients with ULMCA disease were included. Compared with angiography‐guided PCI, IVUS guidance was associated with numerically lower risks of all‐cause death, cardiac death, target lesion revascularization, and target vessel revascularization, while myocardial infarction and stent thrombosis were similar between groups.


Conclusion
In patients undergoing PCI for ULMCA disease, IVUS guidance was associated with numerically favorable but statistically nonsignificant reductions in mortality and repeat revascularization, without clear differences in myocardial infarction or stent thrombosis. Although randomized evidence is still lacking to determine clinical superiority, these results justify powered future trials to determine whether the effects of IVUS guidance vary according to prior myocardial infarction status and left ventricular ejection fraction.
</dc:description>
         <content:encoded>&lt;img src="https://onlinelibrary.wiley.com/cms/asset/a2ca00f5-29f1-45bc-a118-418b86b608c7/clc70367-gra-0001-m.png"
     alt="IVUS-Guided Versus Angiography-Guided PCI for Unprotected Left Main Coronary Artery Disease: A Systematic Review, Meta-Analysis, and GRADE Assessment of Randomized Trials"/&gt;&lt;p&gt;graphical abstract for IVUS-guided versus angiography-guided pci for unprotected left main coronary artery disease.
&lt;/p&gt;
&lt;br/&gt;
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Intravascular ultrasound (IVUS) has been increasingly used as an adjunctive tool for complex percutaneous interventions (PCIs); however, comparative randomized evidence with conventional angiography in unprotected left main coronary artery (ULMCA) disease remains scarce and fragmented. Therefore, this systematic review and meta-analysis aimed to assess and synthesize evidence regarding its use in ULMCA disease.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;We performed a systematic literature search across PubMed, Scopus, Web of Science, and Cochrane until April 2026 to identify relevant RCTs comparing IVUS-guided PCI with conventional angiography-guided PCI in ULMCA disease. Risk of bias of studies was assessed using the Cochrane RoB-2 tool. A random-effects model meta-analysis was performed in R, with an exploratory univariate meta-regression of covariates.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Four randomized trials involving 2278 patients with ULMCA disease were included. Compared with angiography-guided PCI, IVUS guidance was associated with numerically lower risks of all-cause death, cardiac death, target lesion revascularization, and target vessel revascularization, while myocardial infarction and stent thrombosis were similar between groups.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;In patients undergoing PCI for ULMCA disease, IVUS guidance was associated with numerically favorable but statistically nonsignificant reductions in mortality and repeat revascularization, without clear differences in myocardial infarction or stent thrombosis. Although randomized evidence is still lacking to determine clinical superiority, these results justify powered future trials to determine whether the effects of IVUS guidance vary according to prior myocardial infarction status and left ventricular ejection fraction.&lt;/p&gt;</content:encoded>
         <dc:creator>
Abdelrahman Elhakim, 
Mostafa Salem, 
Mohammed A. Elbahloul, 
Abdelrahman M. Elettreby, 
Mohamed A. Alsaied, 
Hamza A. Abdul‐Hafez, 
Ghaith Hussein Ahmad Al Bataineh, 
Maab M. Saleh, 
Amer Al Manla, 
Osama Bisht
</dc:creator>
         <category>REVIEW</category>
         <dc:title>IVUS‐Guided Versus Angiography‐Guided PCI for Unprotected Left Main Coronary Artery Disease: A Systematic Review, Meta‐Analysis, and GRADE Assessment of Randomized Trials</dc:title>
         <dc:identifier>10.1002/clc.70367</dc:identifier>
         <prism:publicationName>Clinical Cardiology</prism:publicationName>
         <prism:doi>10.1002/clc.70367</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/clc.70367?af=R</prism:url>
         <prism:section>REVIEW</prism:section>
         <prism:volume>49</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/clc.70383?af=R</link>
         <pubDate>Wed, 10 Jun 2026 04:31:32 -0700</pubDate>
         <dc:date>2026-06-10T04:31:32-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/19328737?af=R">Wiley: Clinical Cardiology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/clc.70383</guid>
         <title>CDK7 as a Potential Exploratory Biomarker for Distinguishing Acute Myocardial Infarction Subtypes via DDR Pathways: Evidence From a Bangladeshi Cohort</title>
         <description>Clinical Cardiology, Volume 49, Issue 6, June 2026. </description>
         <dc:description>Differential expression of DNA damage response genes was evaluated in Bangladeshi AMI patients. CDK7 showed significantly higher expression in NSTEMI compared to STEMI, while ATM, OGG1, and NBN showed no subtype‐specific differences, highlighting potential transcriptional heterogeneity between AMI subtypes.




ABSTRACT

Introduction
Acute myocardial infarction (AMI) is a major cause of cardiovascular death, with STEMI and NSTEMI as distinct subtypes. Current diagnostic tools often lack the sensitivity and timeliness to rapidly distinguish these subtypes at early clinical presentation. The DNA damage response (DDR), activated by ischemia and oxidative stress during AMI, represents a promising pathway for identifying novel biomarkers. Despite evidence of its role in myocardial infarction, little is known about DDR gene expression in South Asian populations, particularly in Bangladesh. This study evaluated the expression of four DDR genes; ATM, CDK7, OGG1, and NBN and their potential for distinguishing between STEMI and NSTEMI.


Methods
A total of 70 AMI patients and 60 healthy controls from the Bangladeshi population were recruited. RNA was extracted from blood samples, and gene expression was quantified using qRT‐PCR. Statistical analyses included Mann–Whitney U tests for group differences, linear regression analysis and Spearman's correlation analysis for gene co‐expression.


Results
CDK7 expression was significantly higher in NSTEMI compared to STEMI patients (p &lt; 0.05). However, ATM, OGG1, and NBN did not differ significantly between the subtypes. Co‐expression analysis revealed strong positive correlations among all four genes, with the strongest between ATM and CDK7 (r = 0.76, p &lt; 0.001).


Conclusion
This is the first study in the Bangladeshi population to demonstrate distinct DDR gene expression patterns across AMI subtypes, with CDK7 showing subtype‐specific differential expression between STEMI and NSTEMI. Although the observed discrimination was modest and requires further validation, these findings provide important exploratory insights into ischemia‐associated transcriptional regulation in an underrepresented population.
</dc:description>
         <content:encoded>&lt;img src="https://onlinelibrary.wiley.com/cms/asset/f4a0a24c-234e-4978-9be1-f9fc0987dd25/clc70383-gra-0001-m.png"
     alt="CDK7 as a Potential Exploratory Biomarker for Distinguishing Acute Myocardial Infarction Subtypes via DDR Pathways: Evidence From a Bangladeshi Cohort"/&gt;&lt;p&gt;Differential expression of DNA damage response genes was evaluated in Bangladeshi AMI patients. CDK7 showed significantly higher expression in NSTEMI compared to STEMI, while ATM, OGG1, and NBN showed no subtype-specific differences, highlighting potential transcriptional heterogeneity between AMI subtypes.
&lt;/p&gt;&lt;br/&gt;
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Introduction&lt;/h2&gt;
&lt;p&gt;Acute myocardial infarction (AMI) is a major cause of cardiovascular death, with STEMI and NSTEMI as distinct subtypes. Current diagnostic tools often lack the sensitivity and timeliness to rapidly distinguish these subtypes at early clinical presentation. The DNA damage response (DDR), activated by ischemia and oxidative stress during AMI, represents a promising pathway for identifying novel biomarkers. Despite evidence of its role in myocardial infarction, little is known about DDR gene expression in South Asian populations, particularly in Bangladesh. This study evaluated the expression of four DDR genes; ATM, CDK7, OGG1, and NBN and their potential for distinguishing between STEMI and NSTEMI.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;A total of 70 AMI patients and 60 healthy controls from the Bangladeshi population were recruited. RNA was extracted from blood samples, and gene expression was quantified using qRT-PCR. Statistical analyses included Mann–Whitney U tests for group differences, linear regression analysis and Spearman's correlation analysis for gene co-expression.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;CDK7 expression was significantly higher in NSTEMI compared to STEMI patients (&lt;i&gt;p&lt;/i&gt; &amp;lt; 0.05). However, ATM, OGG1, and NBN did not differ significantly between the subtypes. Co-expression analysis revealed strong positive correlations among all four genes, with the strongest between ATM and CDK7 (r = 0.76, &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001).&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;This is the first study in the Bangladeshi population to demonstrate distinct DDR gene expression patterns across AMI subtypes, with CDK7 showing subtype-specific differential expression between STEMI and NSTEMI. Although the observed discrimination was modest and requires further validation, these findings provide important exploratory insights into ischemia-associated transcriptional regulation in an underrepresented population.&lt;/p&gt;</content:encoded>
         <dc:creator>
Rifat Hossain Ripon, 
Hasnat Zahin, 
Abdullah Al Noman, 
Abdullah Al Saba, 
Mohammad Sayem, 
A.H.M. Nurun Nabi, 
Tahirah Yasmin
</dc:creator>
         <category>CLINICAL ARTICLE</category>
         <dc:title>CDK7 as a Potential Exploratory Biomarker for Distinguishing Acute Myocardial Infarction Subtypes via DDR Pathways: Evidence From a Bangladeshi Cohort</dc:title>
         <dc:identifier>10.1002/clc.70383</dc:identifier>
         <prism:publicationName>Clinical Cardiology</prism:publicationName>
         <prism:doi>10.1002/clc.70383</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/clc.70383?af=R</prism:url>
         <prism:section>CLINICAL ARTICLE</prism:section>
         <prism:volume>49</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/clc.70372?af=R</link>
         <pubDate>Mon, 08 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-08T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/19328737?af=R">Wiley: Clinical Cardiology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/clc.70372</guid>
         <title>Reconsidering the Clinical Utility of a Body Shape Index for Abdominal Aortic Calcification in Hypertension: From Association to Clinical Applicability</title>
         <description>Clinical Cardiology, Volume 49, Issue 6, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Dengfeng Zhang, 
Xiaoling Shang
</dc:creator>
         <category>LETTER TO THE EDITOR</category>
         <dc:title>Reconsidering the Clinical Utility of a Body Shape Index for Abdominal Aortic Calcification in Hypertension: From Association to Clinical Applicability</dc:title>
         <dc:identifier>10.1002/clc.70372</dc:identifier>
         <prism:publicationName>Clinical Cardiology</prism:publicationName>
         <prism:doi>10.1002/clc.70372</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/clc.70372?af=R</prism:url>
         <prism:section>LETTER TO THE EDITOR</prism:section>
         <prism:volume>49</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/clc.70368?af=R</link>
         <pubDate>Sat, 06 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-06T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/19328737?af=R">Wiley: Clinical Cardiology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/clc.70368</guid>
         <title>Admission Shock Index in Acute Aortic Dissection: A Triage Trigger or a Restated Vital Sign?</title>
         <description>Clinical Cardiology, Volume 49, Issue 6, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Shaher Yar, 
Youmna Imtiaz, 
Haniyah Attiq, 
Ishvah Shashwat Nag
</dc:creator>
         <category>LETTER TO THE EDITOR</category>
         <dc:title>Admission Shock Index in Acute Aortic Dissection: A Triage Trigger or a Restated Vital Sign?</dc:title>
         <dc:identifier>10.1002/clc.70368</dc:identifier>
         <prism:publicationName>Clinical Cardiology</prism:publicationName>
         <prism:doi>10.1002/clc.70368</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/clc.70368?af=R</prism:url>
         <prism:section>LETTER TO THE EDITOR</prism:section>
         <prism:volume>49</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/clc.70361?af=R</link>
         <pubDate>Fri, 05 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-05T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/19328737?af=R">Wiley: Clinical Cardiology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/clc.70361</guid>
         <title>Correction to “Prognostic Value of HALP Score in Rheumatic Mitral Stenosis: A Long‐Term Follow‐up Study”</title>
         <description>Clinical Cardiology, Volume 49, Issue 6, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator/>
         <category>CORRECTION</category>
         <dc:title>Correction to “Prognostic Value of HALP Score in Rheumatic Mitral Stenosis: A Long‐Term Follow‐up Study”</dc:title>
         <dc:identifier>10.1002/clc.70361</dc:identifier>
         <prism:publicationName>Clinical Cardiology</prism:publicationName>
         <prism:doi>10.1002/clc.70361</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/clc.70361?af=R</prism:url>
         <prism:section>CORRECTION</prism:section>
         <prism:volume>49</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/clc.70366?af=R</link>
         <pubDate>Fri, 05 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-05T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/19328737?af=R">Wiley: Clinical Cardiology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/clc.70366</guid>
         <title>“Diagnostic Performance of Artificial Intelligence in Evaluating Tricuspid Regurgitation: A Systematic Review and Meta‐Analysis”</title>
         <description>Clinical Cardiology, Volume 49, Issue 6, June 2026. </description>
         <dc:description>Artificial intelligence demonstrates strong diagnostic accuracy for detecting tricuspid regurgitation, particularly with echocardiography‐based models. Despite promising performance, substantial heterogeneity and limited external validation highlight the need for prospective, multicenter studies before routine clinical implementation.





ABSTRACT

Background
Tricuspid regurgitation (TR) is a common valvular heart disease affecting 0.55%–1.6% of adults, rising to 5%–8% in those over 75 years, often secondary to left‐sided pathology or pulmonary hypertension. Moderate‐to‐severe TR independently predicts mortality and heart failure hospitalization, yet underdiagnosis persists due to echocardiography's operator dependence and variability. Artificial intelligence (AI), including machine learning (ML) and deep learning (DL), promises automated detection to enhance sensitivity and reproducibility. This systematic review and meta‐analysis synthesizes evidence on AI's diagnostic performance for TR using echocardiographic or alternative modalities.


Methods
Following PRISMA guidelines, we searched PubMed, Embase, Scopus, Web of Science, and EBSCO from inception to August 2025, without language restrictions. Eligibility used PICOS: adults with TR evaluation; AI/ML index tests; clinician‐interpreted echocardiography reference; outcomes, including AUROC, sensitivity, and specificity. Data extraction and quality assessment by two reviewers; random‐effects meta‐analysis for pooled estimates; heterogeneity via I2; certainty per GRADE.


Results
Eight studies were included. Pooled AUROC was 0.89 (95% CI 0.86–0.92) for TR detection. Echocardiography‐based models showed sensitivity 0.87 (95% CI 0.81–0.90), specificity 0.88 (95% CI 0.73–0.95), AUROC 0.92 (95% CI 0.89–0.94); ECG‐based models had AUROC 0.805. Substantial heterogeneity (I2 &gt; 90%) arose from modalities and reference standards; GRADE certainty moderate due to retrospective designs and limited external validation.


Conclusions
AI demonstrates promising diagnostic accuracy for TR, potentially standardizing early detection and triage. However, heterogeneity and methodological gaps necessitate larger prospective, multicenter studies with standardized reporting (e.g., TRIPOD‐AI) to confirm clinical utility.
</dc:description>
         <content:encoded>&lt;img src="https://onlinelibrary.wiley.com/cms/asset/feb1076c-7df4-43a6-a5a6-c65adbedd3e7/clc70366-gra-0001-m.png"
     alt="“Diagnostic Performance of Artificial Intelligence in Evaluating Tricuspid Regurgitation: A Systematic Review and Meta-Analysis”"/&gt;&lt;p&gt;Artificial intelligence demonstrates strong diagnostic accuracy for detecting tricuspid regurgitation, particularly with echocardiography-based models. Despite promising performance, substantial heterogeneity and limited external validation highlight the need for prospective, multicenter studies before routine clinical implementation.
&lt;/p&gt;
&lt;br/&gt;
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Tricuspid regurgitation (TR) is a common valvular heart disease affecting 0.55%–1.6% of adults, rising to 5%–8% in those over 75 years, often secondary to left-sided pathology or pulmonary hypertension. Moderate-to-severe TR independently predicts mortality and heart failure hospitalization, yet underdiagnosis persists due to echocardiography's operator dependence and variability. Artificial intelligence (AI), including machine learning (ML) and deep learning (DL), promises automated detection to enhance sensitivity and reproducibility. This systematic review and meta-analysis synthesizes evidence on AI's diagnostic performance for TR using echocardiographic or alternative modalities.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;Following PRISMA guidelines, we searched PubMed, Embase, Scopus, Web of Science, and EBSCO from inception to August 2025, without language restrictions. Eligibility used PICOS: adults with TR evaluation; AI/ML index tests; clinician-interpreted echocardiography reference; outcomes, including AUROC, sensitivity, and specificity. Data extraction and quality assessment by two reviewers; random-effects meta-analysis for pooled estimates; heterogeneity via I&lt;sup&gt;2&lt;/sup&gt;; certainty per GRADE.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Eight studies were included. Pooled AUROC was 0.89 (95% CI 0.86–0.92) for TR detection. Echocardiography-based models showed sensitivity 0.87 (95% CI 0.81–0.90), specificity 0.88 (95% CI 0.73–0.95), AUROC 0.92 (95% CI 0.89–0.94); ECG-based models had AUROC 0.805. Substantial heterogeneity (I&lt;sup&gt;2&lt;/sup&gt; &amp;gt; 90%) arose from modalities and reference standards; GRADE certainty moderate due to retrospective designs and limited external validation.&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;AI demonstrates promising diagnostic accuracy for TR, potentially standardizing early detection and triage. However, heterogeneity and methodological gaps necessitate larger prospective, multicenter studies with standardized reporting (e.g., TRIPOD-AI) to confirm clinical utility.&lt;/p&gt;</content:encoded>
         <dc:creator>
Pooya Eini, 
Homa Serpoush, 
Mohammad Rezayee, 
Milan Kassulke
</dc:creator>
         <category>REVIEW</category>
         <dc:title>“Diagnostic Performance of Artificial Intelligence in Evaluating Tricuspid Regurgitation: A Systematic Review and Meta‐Analysis”</dc:title>
         <dc:identifier>10.1002/clc.70366</dc:identifier>
         <prism:publicationName>Clinical Cardiology</prism:publicationName>
         <prism:doi>10.1002/clc.70366</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/clc.70366?af=R</prism:url>
         <prism:section>REVIEW</prism:section>
         <prism:volume>49</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/clc.70365?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/19328737?af=R">Wiley: Clinical Cardiology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/clc.70365</guid>
         <title>Generalizability of Low‐Voltage Zone‐Based Risk Scores After Atrial Fibrillation Ablation</title>
         <description>Clinical Cardiology, Volume 49, Issue 6, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Laiba Anwar, 
Aina Gul, 
Javeria Kashaf Zain, 
Muhammad Faizan Khan, 
Syed Huzaifa Khan
</dc:creator>
         <category>LETTER TO THE EDITOR</category>
         <dc:title>Generalizability of Low‐Voltage Zone‐Based Risk Scores After Atrial Fibrillation Ablation</dc:title>
         <dc:identifier>10.1002/clc.70365</dc:identifier>
         <prism:publicationName>Clinical Cardiology</prism:publicationName>
         <prism:doi>10.1002/clc.70365</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/clc.70365?af=R</prism:url>
         <prism:section>LETTER TO THE EDITOR</prism:section>
         <prism:volume>49</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/clc.70363?af=R</link>
         <pubDate>Mon, 01 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-01T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/19328737?af=R">Wiley: Clinical Cardiology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/clc.70363</guid>
         <title>Evaluation of Polygenic Scores and CT Imaging in Risk Factor Modification in Patients With Diabetes: Rationale and Design of the VOLTAIRE Study</title>
         <description>Clinical Cardiology, Volume 49, Issue 6, June 2026. </description>
         <dc:description>Three‐arm randomized trial assessing whether computed tomography coronary angiography or polygenic risk score disclosure, combined with nurse‐led counseling, improves cardiovascular risk factor modification in people with type 2 diabetes.





ABSTRACT

Background
The contemporary management of type 2 diabetes (T2D) involves a multifaceted model of care integrating intensive management of lipids, blood pressure, and glucose, along with lifestyle modifications. Despite these efforts, cardiovascular disease (CVD) remains a leading cause of morbidity and mortality among patients with T2D, largely due to suboptimal adherence to preventive strategies. The VOLTAIRE trial aims to assess the impact of providing personalized cardiovascular risk information derived from computed tomography coronary angiography (CTCA) and a polygenic risk score (PRS) on cardiovascular risk factor modification.


Objectives
VOLTAIRE evaluates whether integrating CTCA and PRS into risk counseling enhances adherence to lifestyle and pharmacological interventions, ultimately improving cardiovascular outcomes among patients with T2D.


Methods
VOLTAIRE is a prospective three‐arm, parallel‐group, randomized controlled trial enrolling participants aged 40 years or older with T2D and no established atherosclerotic CVD. Participants are randomized 1:1:1 to receive: (1) risk factor counseling plus CTCA result, (2) risk factor counseling plus PRS result, or (3) standard risk factor counseling (control). Nurse‐led motivational interviewing is used for risk counseling. The primary outcome is change in non‐calcified plaque volume measured by serial CTCA at 12 months. Secondary outcomes include low‐density lipoprotein cholesterol levels, adherence to medication, patient engagement, CVD knowledge improvements, and psychological outcomes over 12 months. Enrollment began in August 2023.


Discussion
VOLTAIRE seeks to determine if coupling nurse‐led risk factor counseling with personalized CTCA or PRS information improves cardiovascular outcomes, adherence, and participant engagement in T2D management.
</dc:description>
         <content:encoded>&lt;img src="https://onlinelibrary.wiley.com/cms/asset/421283fa-b799-4b06-bd75-949da0ab6cd2/clc70363-gra-0001-m.png"
     alt="Evaluation of Polygenic Scores and CT Imaging in Risk Factor Modification in Patients With Diabetes: Rationale and Design of the VOLTAIRE Study"/&gt;&lt;p&gt;Three-arm randomized trial assessing whether computed tomography coronary angiography or polygenic risk score disclosure, combined with nurse-led counseling, improves cardiovascular risk factor modification in people with type 2 diabetes.
&lt;/p&gt;
&lt;br/&gt;
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;The contemporary management of type 2 diabetes (T2D) involves a multifaceted model of care integrating intensive management of lipids, blood pressure, and glucose, along with lifestyle modifications. Despite these efforts, cardiovascular disease (CVD) remains a leading cause of morbidity and mortality among patients with T2D, largely due to suboptimal adherence to preventive strategies. The VOLTAIRE trial aims to assess the impact of providing personalized cardiovascular risk information derived from computed tomography coronary angiography (CTCA) and a polygenic risk score (PRS) on cardiovascular risk factor modification.&lt;/p&gt;
&lt;h2&gt;Objectives&lt;/h2&gt;
&lt;p&gt;VOLTAIRE evaluates whether integrating CTCA and PRS into risk counseling enhances adherence to lifestyle and pharmacological interventions, ultimately improving cardiovascular outcomes among patients with T2D.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;VOLTAIRE is a prospective three-arm, parallel-group, randomized controlled trial enrolling participants aged 40 years or older with T2D and no established atherosclerotic CVD. Participants are randomized 1:1:1 to receive: (1) risk factor counseling plus CTCA result, (2) risk factor counseling plus PRS result, or (3) standard risk factor counseling (control). Nurse-led motivational interviewing is used for risk counseling. The primary outcome is change in non-calcified plaque volume measured by serial CTCA at 12 months. Secondary outcomes include low-density lipoprotein cholesterol levels, adherence to medication, patient engagement, CVD knowledge improvements, and psychological outcomes over 12 months. Enrollment began in August 2023.&lt;/p&gt;
&lt;h2&gt;Discussion&lt;/h2&gt;
&lt;p&gt;VOLTAIRE seeks to determine if coupling nurse-led risk factor counseling with personalized CTCA or PRS information improves cardiovascular outcomes, adherence, and participant engagement in T2D management.&lt;/p&gt;</content:encoded>
         <dc:creator>
Ruofei Chen, 
Adam J. Nelson, 
Sophia Zoungas, 
Robyn A. Clark, 
Sean Tan, 
Esther F. Davis, 
Melissa C. Southey, 
Domenic Sacca, 
Andrew Lin, 
Giuseppe Di Giovanni, 
Masashi Fujino, 
Tayla Micheli, 
Stephen J. Nicholls
</dc:creator>
         <category>CLINICAL STUDY DESIGN</category>
         <dc:title>Evaluation of Polygenic Scores and CT Imaging in Risk Factor Modification in Patients With Diabetes: Rationale and Design of the VOLTAIRE Study</dc:title>
         <dc:identifier>10.1002/clc.70363</dc:identifier>
         <prism:publicationName>Clinical Cardiology</prism:publicationName>
         <prism:doi>10.1002/clc.70363</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/clc.70363?af=R</prism:url>
         <prism:section>CLINICAL STUDY DESIGN</prism:section>
         <prism:volume>49</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/clc.70343?af=R</link>
         <pubDate>Sat, 30 May 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-05-30T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/19328737?af=R">Wiley: Clinical Cardiology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/clc.70343</guid>
         <title>Symptom Denial and Cultural Constraints: A Qualitative Exploration of Pre‐Hospital Delay Determinants in Myocardial Infarction Patients in China</title>
         <description>Clinical Cardiology, Volume 49, Issue 6, June 2026. </description>
         <dc:description>This study reveals that heart attack patients often dangerously delay emergency care due to unrecognized symptoms, passive endurance, and traditional cultural constraints, like fearing to burden families. Crucially, family involvement acts as a double‐edged sword, either accelerating or further delaying life‐saving treatment.





ABSTRACT

Objective
To explore the pre‐hospital delay experiences of myocardial infarction patients in China from a patient‐centered perspective.


Background
Pre‐hospital delay remains a globally prevalent issue, influenced by subjective and context‐dependent factors that are not easily captured through quantitative methods. Traditional metrics may oversimplify the psychological processes involved and fail to account for individual variability and contextual influences.


Design
A descriptive qualitative study.


Methods
Semi‐structured interviews were conducted with MI patients at a tertiary hospital in Qingdao between November 18 and 30, 2024. Participants were selected through purposeful sampling. Thematic analysis was performed using MAXQDA software to code and analyze the qualitative data. The study followed the COREQ checklist.


Findings
We interviewed 16 patients and conducted four core themes: (1) limited disease awareness, (2) inappropriate symptom response strategies, (3) constraints of traditional cultural beliefs and (4) family influence on decision‐making, along with 12 subthemes.


Conclusion
Patients' pre‐hospital delays frequently stem from cognitive limitations in symptom recognition coupled with maladaptive coping strategies contributes to treatment postponement. Notably, familial decision‐making intervention demonstrates potential in mitigating such delays. And traditional Chinese culture exerts a profound influence on pre‐hospital delays among elderly MI patients.


Implications for Patients
Patients' experiences of pre‐hospital delay in myocardial infarction reveal its key determinants. Healthcare providers should develop targeted interventions tailored to patients' cognition, culture, and family situations to enhance intervention effectiveness.


Patient or Public Contribution
Patients and family members contributed to the data collected.
</dc:description>
         <content:encoded>&lt;img src="https://onlinelibrary.wiley.com/cms/asset/d8ebd485-b3fe-444d-b1b9-26af882b22f8/clc70343-gra-0001-m.png"
     alt="Symptom Denial and Cultural Constraints: A Qualitative Exploration of Pre-Hospital Delay Determinants in Myocardial Infarction Patients in China"/&gt;&lt;p&gt;This study reveals that heart attack patients often dangerously delay emergency care due to unrecognized symptoms, passive endurance, and traditional cultural constraints, like fearing to burden families. Crucially, family involvement acts as a double-edged sword, either accelerating or further delaying life-saving treatment.
&lt;/p&gt;
&lt;br/&gt;
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Objective&lt;/h2&gt;
&lt;p&gt;To explore the pre-hospital delay experiences of myocardial infarction patients in China from a patient-centered perspective.&lt;/p&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Pre-hospital delay remains a globally prevalent issue, influenced by subjective and context-dependent factors that are not easily captured through quantitative methods. Traditional metrics may oversimplify the psychological processes involved and fail to account for individual variability and contextual influences.&lt;/p&gt;
&lt;h2&gt;Design&lt;/h2&gt;
&lt;p&gt;A descriptive qualitative study.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;Semi-structured interviews were conducted with MI patients at a tertiary hospital in Qingdao between November 18 and 30, 2024. Participants were selected through purposeful sampling. Thematic analysis was performed using MAXQDA software to code and analyze the qualitative data. The study followed the COREQ checklist.&lt;/p&gt;
&lt;h2&gt;Findings&lt;/h2&gt;
&lt;p&gt;We interviewed 16 patients and conducted four core themes: (1) limited disease awareness, (2) inappropriate symptom response strategies, (3) constraints of traditional cultural beliefs and (4) family influence on decision-making, along with 12 subthemes.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;Patients' pre-hospital delays frequently stem from cognitive limitations in symptom recognition coupled with maladaptive coping strategies contributes to treatment postponement. Notably, familial decision-making intervention demonstrates potential in mitigating such delays. And traditional Chinese culture exerts a profound influence on pre-hospital delays among elderly MI patients.&lt;/p&gt;
&lt;h2&gt;Implications for Patients&lt;/h2&gt;
&lt;p&gt;Patients' experiences of pre-hospital delay in myocardial infarction reveal its key determinants. Healthcare providers should develop targeted interventions tailored to patients' cognition, culture, and family situations to enhance intervention effectiveness.&lt;/p&gt;
&lt;h2&gt;Patient or Public Contribution&lt;/h2&gt;
&lt;p&gt;Patients and family members contributed to the data collected.&lt;/p&gt;</content:encoded>
         <dc:creator>
Yunjie Tang, 
Danqing Hu, 
Jing Han
</dc:creator>
         <category>CLINICAL ARTICLE</category>
         <dc:title>Symptom Denial and Cultural Constraints: A Qualitative Exploration of Pre‐Hospital Delay Determinants in Myocardial Infarction Patients in China</dc:title>
         <dc:identifier>10.1002/clc.70343</dc:identifier>
         <prism:publicationName>Clinical Cardiology</prism:publicationName>
         <prism:doi>10.1002/clc.70343</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/clc.70343?af=R</prism:url>
         <prism:section>CLINICAL ARTICLE</prism:section>
         <prism:volume>49</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/clc.70362?af=R</link>
         <pubDate>Thu, 28 May 2026 03:35:24 -0700</pubDate>
         <dc:date>2026-05-28T03:35:24-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/19328737?af=R">Wiley: Clinical Cardiology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/clc.70362</guid>
         <title>Issue Information</title>
         <description>Clinical Cardiology, Volume 49, Issue 6, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator/>
         <category>ISSUE INFORMATION</category>
         <dc:title>Issue Information</dc:title>
         <dc:identifier>10.1002/clc.70362</dc:identifier>
         <prism:publicationName>Clinical Cardiology</prism:publicationName>
         <prism:doi>10.1002/clc.70362</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/clc.70362?af=R</prism:url>
         <prism:section>ISSUE INFORMATION</prism:section>
         <prism:volume>49</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/clc.70349?af=R</link>
         <pubDate>Thu, 28 May 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-05-28T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/19328737?af=R">Wiley: Clinical Cardiology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/clc.70349</guid>
         <title>The Linear Association Between A Body Shape Index and Abdominal Aortic Calcification in Individuals With Hypertension</title>
         <description>Clinical Cardiology, Volume 49, Issue 6, June 2026. </description>
         <dc:description>Higher A Body Shape Index (ABSI) was independently associated with increased abdominal aortic calcification (AAC) risk in hypertensive individuals and showed a linear positive relationship with AAC risk. ABSI may serve as a supplementary risk indicator, although its discriminative ability was limited.





ABSTRACT

Objective
This study aimed to evaluate the association between A Body Shape Index (ABSI) and abdominal aortic calcification (AAC) in individuals with hypertension.


Methods
This cross‐sectional analysis utilized data from 1486 participants in the National Health and Nutrition Examination Survey (NHANES). The relationship between ABSI and AAC was evaluated through logistic regression, subgroup analyses, receiver operating characteristic (ROC) curve assessment, and restricted cubic spline (RCS) modeling.


Results
Multivariable logistic regression revealed that each standard deviation increase in ABSI corresponded to a 16.2% elevated AAC risk (OR = 1.162, 95% CI: 1.025–1.318, p = 0.019). Compared with the lowest quartile (Q1), individuals in Q3 and Q4 had significantly higher risks of AAC, with ORs of 1.554 (95% CI: 1.096–2.204, p = 0.013) and 1.503 (95% CI: 1.047–2.157, p = 0.027), respectively. Subgroup analyses revealed a robust association between ABSI and AAC that was consistently observed across strata. ROC curve analysis revealed that ABSI provided moderate discriminative ability for AAC detection in the overall cohort (AUC = 0.625, 95% CI: 0.596–0.654, p &lt; 0.001), males (AUC = 0.632, 95% CI: 0.589–0.675, p &lt; 0.001), and females (AUC = 0.627, 95% CI: 0.588–0.666, p &lt; 0.001). RCS analysis, in both unadjusted and multivariable‐adjusted models, RCS analysis confirmed a dose‐dependent positive relationship between ABSI and AAC risk (P for nonlinearity &gt; 0.05).


Conclusion
Higher ABSI levels show a significant, independent association with increased AAC risk in hypertensive patients, suggesting potential clinical value as a indicator for early vascular calcification detection in this population.
</dc:description>
         <content:encoded>&lt;img src="https://onlinelibrary.wiley.com/cms/asset/ca8a02aa-a0cd-407b-99d7-bb55ddd09ba5/clc70349-gra-0001-m.png"
     alt="The Linear Association Between A Body Shape Index and Abdominal Aortic Calcification in Individuals With Hypertension"/&gt;&lt;p&gt;Higher A Body Shape Index (ABSI) was independently associated with increased abdominal aortic calcification (AAC) risk in hypertensive individuals and showed a linear positive relationship with AAC risk. ABSI may serve as a supplementary risk indicator, although its discriminative ability was limited.
&lt;/p&gt;
&lt;br/&gt;
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Objective&lt;/h2&gt;
&lt;p&gt;This study aimed to evaluate the association between A Body Shape Index (ABSI) and abdominal aortic calcification (AAC) in individuals with hypertension.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;This cross-sectional analysis utilized data from 1486 participants in the National Health and Nutrition Examination Survey (NHANES). The relationship between ABSI and AAC was evaluated through logistic regression, subgroup analyses, receiver operating characteristic (ROC) curve assessment, and restricted cubic spline (RCS) modeling.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Multivariable logistic regression revealed that each standard deviation increase in ABSI corresponded to a 16.2% elevated AAC risk (OR = 1.162, 95% CI: 1.025–1.318, &lt;i&gt;p&lt;/i&gt; = 0.019). Compared with the lowest quartile (Q1), individuals in Q3 and Q4 had significantly higher risks of AAC, with ORs of 1.554 (95% CI: 1.096–2.204, &lt;i&gt;p&lt;/i&gt; = 0.013) and 1.503 (95% CI: 1.047–2.157, &lt;i&gt;p&lt;/i&gt; = 0.027), respectively. Subgroup analyses revealed a robust association between ABSI and AAC that was consistently observed across strata. ROC curve analysis revealed that ABSI provided moderate discriminative ability for AAC detection in the overall cohort (AUC = 0.625, 95% CI: 0.596–0.654, &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001), males (AUC = 0.632, 95% CI: 0.589–0.675, &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001), and females (AUC = 0.627, 95% CI: 0.588–0.666, &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001). RCS analysis, in both unadjusted and multivariable-adjusted models, RCS analysis confirmed a dose-dependent positive relationship between ABSI and AAC risk (P for nonlinearity &amp;gt; 0.05).&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;Higher ABSI levels show a significant, independent association with increased AAC risk in hypertensive patients, suggesting potential clinical value as a indicator for early vascular calcification detection in this population.&lt;/p&gt;</content:encoded>
         <dc:creator>
Xinyi Qiu, 
Zhenwei Wang
</dc:creator>
         <category>CLINICAL ARTICLE</category>
         <dc:title>The Linear Association Between A Body Shape Index and Abdominal Aortic Calcification in Individuals With Hypertension</dc:title>
         <dc:identifier>10.1002/clc.70349</dc:identifier>
         <prism:publicationName>Clinical Cardiology</prism:publicationName>
         <prism:doi>10.1002/clc.70349</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/clc.70349?af=R</prism:url>
         <prism:section>CLINICAL ARTICLE</prism:section>
         <prism:volume>49</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/clc.70360?af=R</link>
         <pubDate>Thu, 28 May 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-05-28T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/19328737?af=R">Wiley: Clinical Cardiology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/clc.70360</guid>
         <title>Concerns Regarding the Design, Methodology, and Potential Biases in the Türkiye Heart Failure (TURK‐HF) Registry</title>
         <description>Clinical Cardiology, Volume 49, Issue 6, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Çağrı Zorlu
</dc:creator>
         <category>LETTER TO THE EDITOR</category>
         <dc:title>Concerns Regarding the Design, Methodology, and Potential Biases in the Türkiye Heart Failure (TURK‐HF) Registry</dc:title>
         <dc:identifier>10.1002/clc.70360</dc:identifier>
         <prism:publicationName>Clinical Cardiology</prism:publicationName>
         <prism:doi>10.1002/clc.70360</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/clc.70360?af=R</prism:url>
         <prism:section>LETTER TO THE EDITOR</prism:section>
         <prism:volume>49</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/clc.70358?af=R</link>
         <pubDate>Thu, 28 May 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-05-28T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/19328737?af=R">Wiley: Clinical Cardiology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/clc.70358</guid>
         <title>Clarifying the Scope of Native EHRA Type 2 Valvular Disease and Event Reporting in Anticoagulated Patients With Atrial Fibrillation</title>
         <description>Clinical Cardiology, Volume 49, Issue 6, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Jiaqi Chen, 
Mangmang Xu
</dc:creator>
         <category>LETTER TO THE EDITOR</category>
         <dc:title>Clarifying the Scope of Native EHRA Type 2 Valvular Disease and Event Reporting in Anticoagulated Patients With Atrial Fibrillation</dc:title>
         <dc:identifier>10.1002/clc.70358</dc:identifier>
         <prism:publicationName>Clinical Cardiology</prism:publicationName>
         <prism:doi>10.1002/clc.70358</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/clc.70358?af=R</prism:url>
         <prism:section>LETTER TO THE EDITOR</prism:section>
         <prism:volume>49</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/clc.70359?af=R</link>
         <pubDate>Thu, 28 May 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-05-28T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/19328737?af=R">Wiley: Clinical Cardiology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/clc.70359</guid>
         <title>Hand Dysfunction After Intervention via Distal Versus Conventional Transradial Access: A Meta‐Analysis of Randomized Trials</title>
         <description>Clinical Cardiology, Volume 49, Issue 6, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Fareena Ishtiaq
</dc:creator>
         <category>LETTER TO THE EDITOR</category>
         <dc:title>Hand Dysfunction After Intervention via Distal Versus Conventional Transradial Access: A Meta‐Analysis of Randomized Trials</dc:title>
         <dc:identifier>10.1002/clc.70359</dc:identifier>
         <prism:publicationName>Clinical Cardiology</prism:publicationName>
         <prism:doi>10.1002/clc.70359</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/clc.70359?af=R</prism:url>
         <prism:section>LETTER TO THE EDITOR</prism:section>
         <prism:volume>49</prism:volume>
         <prism:number>6</prism:number>
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