Pub Date : 2024-10-18DOI: 10.1016/j.hrtlng.2024.10.004
Runqi Liu , Jinghui Bao , Ying Tang , Danyan Xu , Li Shen , Huali Qin
Background
Patients with coronary artery disease (CAD) combined with type 2 diabetes mellitus (T2DM) develop serious atherosclerotic and diffuse lesions. Inadequate numbers and the dysfunction of CD4+CD25+Foxp3+regulatory T lymphocytes (Treg cells) are common mechanisms underlying the immunopathological damage in CAD and T2DM.
Objectives
We aimed to explore Treg cell changes in patients with CAD complicated with T2DM and to investigate the association between Treg cells and the severity of CAD.
Methods
A total of 257 participants were included in the study, divided into a healthy control group (HC, n = 63), CAD group (n = 106), and CAD complicated with T2DM group (CAD+T2DM, n = 88). Flow cytometry detected Treg cell levels, and serum IL-10, IL-6, and ELISA detected TGF-β.
Results
The sample for this study consisted of 170 males and 87 females, with 88 (34.24 %) participants having diabetes and 169 (65.76 %) without diabetes. The proportion of circulating Treg cells was lower in the CAD and CAD+T2DM groups than in the HC group, and it was lower in the CAD+T2DM group than in the CAD group. The plasma levels of IL-10 and TGF-β were lower in the CAD than in the HC group, and the levels in the CAD+T2DM group were significantly lower than those in the CAD group. However, the plasma IL-6 level changed in the opposite direction. Gensini's score was negatively correlated with Treg cells (R = - 0.57, P < .05). Subgroup analyses and interaction analyses showed that the association of Treg with the Gensini score was robust.
Conclusion
The level of Treg cells was an independent protective factor for patients with CAD and T2DM and was negatively correlated with the Gensini score. Therefore, Treg cells may be used as therapeutic targets for CAD with T2DM patients.
{"title":"Changes in Treg cells and cytokines in the peripheral blood of patients with coronary artery disease combined with type 2 diabetes mellitus","authors":"Runqi Liu , Jinghui Bao , Ying Tang , Danyan Xu , Li Shen , Huali Qin","doi":"10.1016/j.hrtlng.2024.10.004","DOIUrl":"10.1016/j.hrtlng.2024.10.004","url":null,"abstract":"<div><h3>Background</h3><div>Patients with coronary artery disease (CAD) combined with type 2 diabetes mellitus (T2DM) develop serious atherosclerotic and diffuse lesions. Inadequate numbers and the dysfunction of CD4<sup>+</sup>CD25<sup>+</sup>Foxp3<sup>+</sup>regulatory T lymphocytes (Treg cells) are common mechanisms underlying the immunopathological damage in CAD and T2DM.</div></div><div><h3>Objectives</h3><div>We aimed to explore Treg cell changes in patients with CAD complicated with T2DM and to investigate the association between Treg cells and the severity of CAD.</div></div><div><h3>Methods</h3><div>A total of 257 participants were included in the study, divided into a healthy control group (HC, <em>n</em> = 63), CAD group (<em>n</em> = 106), and CAD complicated with T2DM group (CAD+T2DM, <em>n</em> = 88). Flow cytometry detected Treg cell levels, and serum IL-10, IL-6, and ELISA detected TGF-β.</div></div><div><h3>Results</h3><div>The sample for this study consisted of 170 males and 87 females, with 88 (34.24 %) participants having diabetes and 169 (65.76 %) without diabetes. The proportion of circulating Treg cells was lower in the CAD and CAD+T2DM groups than in the HC group, and it was lower in the CAD+T2DM group than in the CAD group. The plasma levels of IL-10 and TGF-β were lower in the CAD than in the HC group, and the levels in the CAD+T2DM group were significantly lower than those in the CAD group. However, the plasma IL-6 level changed in the opposite direction. Gensini's score was negatively correlated with Treg cells (<em>R</em> = - 0.57, <em>P</em> < .05). Subgroup analyses and interaction analyses showed that the association of Treg with the Gensini score was robust.</div></div><div><h3>Conclusion</h3><div>The level of Treg cells was an independent protective factor for patients with CAD and T2DM and was negatively correlated with the Gensini score. Therefore, Treg cells may be used as therapeutic targets for CAD with T2DM patients.</div></div>","PeriodicalId":55064,"journal":{"name":"Heart & Lung","volume":"69 ","pages":"Pages 147-154"},"PeriodicalIF":2.4,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142481334","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-17DOI: 10.1016/j.hrtlng.2024.10.003
Geunyeong Cha PhD (c), MSN, RN , Misook L. Chung PhD, RN , JungHee Kang PhD, RN , Chin-Yen Lin PhD, RN , Martha J. Biddle PhD, RN , Jia-Rong Wu PhD, RN , Terry A. Lennie PhD, RN , Ashmita Thapa BSN, RN , Debra K. Moser PhD, RN
Background
Heart failure (HF) subtype, depressive symptoms, and physical inactivity independently contribute to survival outcomes, but the effect of the interaction of these variables on survival outcomes remains unknown.
Objectives
We aimed to determine whether depressive symptoms and engagement in physical activity differentially interact to predict the combined endpoint of all-cause death or rehospitalization among patients with HF and reduced (HFrEF) or preserved ejection fraction (HFpEF).
Methods
This study was a secondary analysis. The sample was categorized by the presence or absence of depressive symptoms, and engagement or non-engagement in physical activity. Cox proportional hazard modeling was used to predict the combined endpoint of all-cause death or rehospitalization.
Results
A total of 1002 patients with HF were included (mean age 64.3 ± 12.7 years; 637 males [64 %]; 844 White [84 %]). Among them, 35.3 % did not engage in physical activity, while 64.7 % engaged in any level of physical activity, and 29.7 % had depressive symptoms. In both subtypes, depressive symptoms were associated with the highest risk of all-cause death or rehospitalization. Among patients with HFrEF, those with depressive symptoms who did not engage in physical activity were associated with a 136 % higher risk of the combined endpoint, while among those with HFpEF, depressive symptoms and engagement in physical activity were associated with a 78 % higher risk.
Conclusions
Depressive symptoms and lack of physical activity predicted the combined endpoint of all-cause death or rehospitalization among patients with HFrEF, while depressive symptoms alone were the strongest predictor among patients with HFpEF.
{"title":"Association of depressive symptoms and engagement in physical activity with event-free survival in patients with heart failure","authors":"Geunyeong Cha PhD (c), MSN, RN , Misook L. Chung PhD, RN , JungHee Kang PhD, RN , Chin-Yen Lin PhD, RN , Martha J. Biddle PhD, RN , Jia-Rong Wu PhD, RN , Terry A. Lennie PhD, RN , Ashmita Thapa BSN, RN , Debra K. Moser PhD, RN","doi":"10.1016/j.hrtlng.2024.10.003","DOIUrl":"10.1016/j.hrtlng.2024.10.003","url":null,"abstract":"<div><h3>Background</h3><div>Heart failure (HF) subtype, depressive symptoms, and physical inactivity independently contribute to survival outcomes, but the effect of the interaction of these variables on survival outcomes remains unknown.</div></div><div><h3>Objectives</h3><div>We aimed to determine whether depressive symptoms and engagement in physical activity differentially interact to predict the combined endpoint of all-cause death or rehospitalization among patients with HF and reduced (HFrEF) or preserved ejection fraction (HFpEF).</div></div><div><h3>Methods</h3><div>This study was a secondary analysis. The sample was categorized by the presence or absence of depressive symptoms, and engagement or non-engagement in physical activity. Cox proportional hazard modeling was used to predict the combined endpoint of all-cause death or rehospitalization.</div></div><div><h3>Results</h3><div>A total of 1002 patients with HF were included (mean age 64.3 ± 12.7 years; 637 males [64 %]; 844 White [84 %]). Among them, 35.3 % did not engage in physical activity, while 64.7 % engaged in any level of physical activity, and 29.7 % had depressive symptoms. In both subtypes, depressive symptoms were associated with the highest risk of all-cause death or rehospitalization. Among patients with HFrEF, those with depressive symptoms who did not engage in physical activity were associated with a 136 % higher risk of the combined endpoint, while among those with HFpEF, depressive symptoms and engagement in physical activity were associated with a 78 % higher risk.</div></div><div><h3>Conclusions</h3><div>Depressive symptoms and lack of physical activity predicted the combined endpoint of all-cause death or rehospitalization among patients with HFrEF, while depressive symptoms alone were the strongest predictor among patients with HFpEF.</div></div>","PeriodicalId":55064,"journal":{"name":"Heart & Lung","volume":"69 ","pages":"Pages 138-146"},"PeriodicalIF":2.4,"publicationDate":"2024-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142445876","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-15DOI: 10.1016/j.hrtlng.2024.09.012
Amin Khorshid Savar , Hongrui Wang, Nuo Chen, Yunzhang Cheng
Background
The rising heart failure rates globally show the pressing demand for treatment progress, especially in Left Ventricular Assist Devices (LVADs). Axial-flow pump LVADs are gaining notice for their small size, few moving parts, and potential for miniaturization, providing a vital option for heart transplants during donor shortages.
Objectives
Despite several studies on LVADs, there is a notable lack of research specifically comparing axial-flow pumps with similar technology. This gap hinders the identification of the most optimal technology to guide development efforts and meet patient needs. This study aims to comprehensively compare the most commonly used axial-flow pumps and provide a detailed analysis focusing on survival rates and quality of life parameters.
Methods
As a developer of axial-flow pumps (LVADs), our group conducted a systematic review of the current axial-flow pump LVADs. We analyzed studies comparing these devices, focusing on key metrics such as survival rates and quality of life.
Results
The HeartMate 2 and Jarvik 2000 show superior survival rates (up to 86.9 % at 6 months, 96.3 % at 3 years) and (6-month survival 67 %-91 %) respectively, compared to the other axial flow pumps LVAD. The results underscore the importance of choosing the optimal device and informing the direction of future developments.
Conclusion
In this paper, we aim to inform future studies to enhance their effectiveness and advance the overall performance of these devices, ultimately benefiting patients and developers. This review furnishes evidence-based recommendations for the most appropriate axial-flow pumps based on survival rates and quality of life parameters.
{"title":"Comparative analysis of survival rate and quality of life in axial-flow pump left ventricular assist devices (LVADs)","authors":"Amin Khorshid Savar , Hongrui Wang, Nuo Chen, Yunzhang Cheng","doi":"10.1016/j.hrtlng.2024.09.012","DOIUrl":"10.1016/j.hrtlng.2024.09.012","url":null,"abstract":"<div><h3>Background</h3><div>The rising heart failure rates globally show the pressing demand for treatment progress, especially in Left Ventricular Assist Devices (LVADs). Axial-flow pump LVADs are gaining notice for their small size, few moving parts, and potential for miniaturization, providing a vital option for heart transplants during donor shortages.</div></div><div><h3>Objectives</h3><div>Despite several studies on LVADs, there is a notable lack of research specifically comparing axial-flow pumps with similar technology. This gap hinders the identification of the most optimal technology to guide development efforts and meet patient needs. This study aims to comprehensively compare the most commonly used axial-flow pumps and provide a detailed analysis focusing on survival rates and quality of life parameters.</div></div><div><h3>Methods</h3><div>As a developer of axial-flow pumps (LVADs), our group conducted a systematic review of the current axial-flow pump LVADs. We analyzed studies comparing these devices, focusing on key metrics such as survival rates and quality of life.</div></div><div><h3>Results</h3><div>The HeartMate 2 and Jarvik 2000 show superior survival rates (up to 86.9 % at 6 months, 96.3 % at 3 years) and (6-month survival 67 %-91 %) respectively, compared to the other axial flow pumps LVAD. The results underscore the importance of choosing the optimal device and informing the direction of future developments.</div></div><div><h3>Conclusion</h3><div>In this paper, we aim to inform future studies to enhance their effectiveness and advance the overall performance of these devices, ultimately benefiting patients and developers. This review furnishes evidence-based recommendations for the most appropriate axial-flow pumps based on survival rates and quality of life parameters.</div></div>","PeriodicalId":55064,"journal":{"name":"Heart & Lung","volume":"69 ","pages":"Pages 127-137"},"PeriodicalIF":2.4,"publicationDate":"2024-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142433397","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-10DOI: 10.1016/j.hrtlng.2024.08.003
Christine R. Hoch PhD, RN, ACNS-BC, Jennifer Klinedinst, Karen Larimer, Stephen S. Gottlieb
<div><h3>Purpose</h3><div>The purpose of this study was to explore the relationship of serum osmolality to HF-related fatigue, controlling for select physiologic covariates.</div></div><div><h3>Background</h3><div>Fatigue is a common symptom of heart failure (HF) associated with deleterious outcomes including increased morbidity and mortality. Underlying physiologic mechanisms of HF-related fatigue are not well understood. Hypervolemia and hypovolemia have been suggested as potential mechanisms of HF-related fatigue. Serum osmolality has been used as a physiologic measure to assess changes in volume status with therapeutic treatments to manage fluid imbalances. Low serum osmolality is associated with increased risk of mortality and hospital readmission in persons with HF. However, the relationship of serum osmolality and HF-related fatigue has not been well described.</div></div><div><h3>Methods</h3><div>We analyzed cross-sectional data from two waves of the National Health and Nutrition Examination Survey (2015-2016 and 2017-2018). Adults who self-reported having HF without co-morbid conditions known to contribute to fatigue were included in the study (unweighted n = 126). Data were weighted to provide US national estimates, and complex sample design used for analyses. Independent t tests and chi-square tests were used to explore differences between fatigued and nonfatigued adults with HF. Logistic regression analyses were used to calculate the odds of having fatigue. Bivariate logistic regression models were performed to assess the individual contributions of select physiologic covariates: age, sex, hemoglobin, body mass index (BMI) and presence of shortness of breath. Covariates with a significance of p≤.10 were included in the final model. Multivariate logistic regression was performed on the presence of fatigue as the outcome with physiologic predictors selected from the bivariate analysis: BMI and serum osmolality.</div></div><div><h3>Results</h3><div>Being female was associated with higher odds of experiencing fatigue when controlling for serum osmolality and body mass index (OR=4.91, p<.001, CI 2.200 – 10.954). Serum osmolality was lower in those that experienced fatigue compared to those without fatigue (t=-2.37, p=.032) Higher serum osmolality was associated with 7.6% lower odds of experiencing fatigue when controlling for sex and BMI (OR=.924, p=.014, CI .870 - .982).</div></div><div><h3>Conclusion</h3><div>Despite the deleterious outcomes associated with HF-related fatigue, physiologic mechanisms remain poorly understood. Serum osmolality may be associated with the experience of fatigue in persons with HF. Serum osmolality reflects the concentration of serum sodium, urea, and glucose. The differences in serum osmolality noted may be explained by dietary sodium, serum blood glucose, fluid restrictions or use of diuretics. Yet, serum osmolality is associated with mortality in persons with HF, suggesting changes in serum osmolality ma
背景疲劳是心力衰竭(HF)的一种常见症状,与发病率和死亡率增加等不良后果相关。HF相关疲劳的基本生理机制尚不十分清楚。高血容量和低血容量被认为是 HF 相关疲劳的潜在机制。血清渗透压已被用作一种生理指标,用于评估治疗过程中容量状态的变化,以控制体液失衡。血清渗透压过低与心房颤动患者的死亡率和再入院风险增加有关。然而,血清渗透压与心房颤动相关疲劳的关系尚未得到很好的描述。方法我们分析了两波全国健康与营养调查(2015-2016 年和 2017-2018 年)的横断面数据。研究纳入了自我报告患有高血压且不合并已知会导致疲劳的疾病的成年人(未加权 n = 126)。数据经过加权处理,以提供美国全国估计值,并采用复杂样本设计进行分析。采用独立 t 检验和卡方检验来探讨患有高血压的疲劳成年人与非疲劳成年人之间的差异。逻辑回归分析用于计算疲劳的几率。双变量逻辑回归模型用于评估特定生理协变量(年龄、性别、血红蛋白、体重指数 (BMI)、呼吸急促)的个体贡献。显著性 p≤.10 的协变量被纳入最终模型。以出现疲劳作为结果,并结合从二元分析中选出的生理预测因素,进行多变量逻辑回归:结果 在控制血清渗透压和体重指数的情况下,女性出现疲劳的几率更高(OR=4.91,p<.001,CI 2.200 - 10.954)。与没有疲劳感的人相比,有疲劳感的人血清渗透压较低(t=-2.37,p=.032)。当控制性别和体重指数时,较高的血清渗透压与较低的7.6%疲劳感几率相关(OR=.924,p=.014,CI.870 - .982)。血清渗透压可能与高血压患者的疲劳体验有关。血清渗透压反映了血清钠、尿素和葡萄糖的浓度。饮食中的钠、血清血糖、液体限制或使用利尿剂都可能导致血清渗透压的差异。然而,血清渗透压与心房颤动患者的死亡率有关,这表明血清渗透压的变化可能告知疾病的严重程度,并可能影响症状的表现。我们的研究结果还表明,与心房颤动相关的疲劳可能具有性别二态性。症状表现的差异可能与生理差异有关。与男性相比,女性的心室质量较小,心肌收缩力增强,细胞周转率较低,血压较低,儿茶酚胺介导的血管收缩较少,全身水分较少。这些生理差异可能会导致疲劳表现和疲劳严重程度。因此,基于性别的干预措施可能有助于控制这一症状。
{"title":"Heart Failure Related Fatigue and Serum Osmolality: An Exploratory Analysis of the National Health and Nutrition Examination Survey","authors":"Christine R. Hoch PhD, RN, ACNS-BC, Jennifer Klinedinst, Karen Larimer, Stephen S. Gottlieb","doi":"10.1016/j.hrtlng.2024.08.003","DOIUrl":"10.1016/j.hrtlng.2024.08.003","url":null,"abstract":"<div><h3>Purpose</h3><div>The purpose of this study was to explore the relationship of serum osmolality to HF-related fatigue, controlling for select physiologic covariates.</div></div><div><h3>Background</h3><div>Fatigue is a common symptom of heart failure (HF) associated with deleterious outcomes including increased morbidity and mortality. Underlying physiologic mechanisms of HF-related fatigue are not well understood. Hypervolemia and hypovolemia have been suggested as potential mechanisms of HF-related fatigue. Serum osmolality has been used as a physiologic measure to assess changes in volume status with therapeutic treatments to manage fluid imbalances. Low serum osmolality is associated with increased risk of mortality and hospital readmission in persons with HF. However, the relationship of serum osmolality and HF-related fatigue has not been well described.</div></div><div><h3>Methods</h3><div>We analyzed cross-sectional data from two waves of the National Health and Nutrition Examination Survey (2015-2016 and 2017-2018). Adults who self-reported having HF without co-morbid conditions known to contribute to fatigue were included in the study (unweighted n = 126). Data were weighted to provide US national estimates, and complex sample design used for analyses. Independent t tests and chi-square tests were used to explore differences between fatigued and nonfatigued adults with HF. Logistic regression analyses were used to calculate the odds of having fatigue. Bivariate logistic regression models were performed to assess the individual contributions of select physiologic covariates: age, sex, hemoglobin, body mass index (BMI) and presence of shortness of breath. Covariates with a significance of p≤.10 were included in the final model. Multivariate logistic regression was performed on the presence of fatigue as the outcome with physiologic predictors selected from the bivariate analysis: BMI and serum osmolality.</div></div><div><h3>Results</h3><div>Being female was associated with higher odds of experiencing fatigue when controlling for serum osmolality and body mass index (OR=4.91, p<.001, CI 2.200 – 10.954). Serum osmolality was lower in those that experienced fatigue compared to those without fatigue (t=-2.37, p=.032) Higher serum osmolality was associated with 7.6% lower odds of experiencing fatigue when controlling for sex and BMI (OR=.924, p=.014, CI .870 - .982).</div></div><div><h3>Conclusion</h3><div>Despite the deleterious outcomes associated with HF-related fatigue, physiologic mechanisms remain poorly understood. Serum osmolality may be associated with the experience of fatigue in persons with HF. Serum osmolality reflects the concentration of serum sodium, urea, and glucose. The differences in serum osmolality noted may be explained by dietary sodium, serum blood glucose, fluid restrictions or use of diuretics. Yet, serum osmolality is associated with mortality in persons with HF, suggesting changes in serum osmolality ma","PeriodicalId":55064,"journal":{"name":"Heart & Lung","volume":"68 ","pages":"Pages 381-382"},"PeriodicalIF":2.4,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142418510","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-10DOI: 10.1016/j.hrtlng.2024.08.004
Jessica Bocchino MSN, RN-BC, Zoya Shir, Valerie Mc Donough
Purpose
The purpose of this Quality Improvement Project was to identify heart failure patients who met criteria for an Implanted Cardiac Defibrillator.
Background
Patients with heart failure are at risk of ventricular arrhythmias. Implantable cardiac defibrillators (ICDs) can significantly reduce sudden cardiac death. Unfortunately, ICD implantation is often underutilized. Based on studies, the American College of Cardiology and American Heart Association recommend ICDs in patients with depressed Ejection Fractions (EF) and heart failure. The Centers for Medicare & Medicaid Services have approved reimbursement for ICD placement in patients meeting criteria.
Methods
The Heart Failure Coordinators at Hackensack University Medical Center screened heart failure patients admitted to the hospital. Through real time screening and participation in Multidisciplinary Rounds (MDRs) we reviewed patients echocardiograms for ejection fractions (EF) of < _35%, New York Heart Association (NYHA) class I-III and ensured the patient had received optimal medical therapy for at least 3 months. Those with a terminal illness, life expectancy, cognitive or severe psychiatric illness were not included. If patients met criteria a recommendation was sent to the provider for a possible consultation to Electrophysiology (EP). Additionally, the Heart Failure Algorithm was modified to suggest EP consults for patients with EF< 35%.
Results
Improvements in our compliance to the Get With The Guidelines- Heart Failure (GWTG-HF) Quality Measure AHAHF12: ICD Counseling or ICD Placed or Prescribed at Discharge increased by 20% from Quarter 1 203 to Quarter 2 2023 and additionally increased by 7% in Quarter 3. Through daily screening and the use of the Heart Failure Algorithm, cases were identified and presented at our monthly Heart Failure Adjudication meetings. These presentations not only assisted in referrals to EP, but also captured our audience. The presentations increased the awareness of our medical centers providers.
Conclusion
The use of daily screening increased referrals to Electrophysiology and identification of patients that met criteria for for device therapy. Consideration of ICD implantation must be a shared decision making process. As the population for heart failure continues to grow, device therapy can improve overall survival. It is vital to remain aware of technologies and devices that can refine management of complexed heart failure care.
{"title":"Does Your Patient Need An Implanted Cardiac Defibrillator?","authors":"Jessica Bocchino MSN, RN-BC, Zoya Shir, Valerie Mc Donough","doi":"10.1016/j.hrtlng.2024.08.004","DOIUrl":"10.1016/j.hrtlng.2024.08.004","url":null,"abstract":"<div><h3>Purpose</h3><div>The purpose of this Quality Improvement Project was to identify heart failure patients who met criteria for an Implanted Cardiac Defibrillator.</div></div><div><h3>Background</h3><div>Patients with heart failure are at risk of ventricular arrhythmias. Implantable cardiac defibrillators (ICDs) can significantly reduce sudden cardiac death. Unfortunately, ICD implantation is often underutilized. Based on studies, the American College of Cardiology and American Heart Association recommend ICDs in patients with depressed Ejection Fractions (EF) and heart failure. The Centers for Medicare & Medicaid Services have approved reimbursement for ICD placement in patients meeting criteria.</div></div><div><h3>Methods</h3><div>The Heart Failure Coordinators at Hackensack University Medical Center screened heart failure patients admitted to the hospital. Through real time screening and participation in Multidisciplinary Rounds (MDRs) we reviewed patients echocardiograms for ejection fractions (EF) of < _35%, New York Heart Association (NYHA) class I-III and ensured the patient had received optimal medical therapy for at least 3 months. Those with a terminal illness, life expectancy, cognitive or severe psychiatric illness were not included. If patients met criteria a recommendation was sent to the provider for a possible consultation to Electrophysiology (EP). Additionally, the Heart Failure Algorithm was modified to suggest EP consults for patients with EF< 35%.</div></div><div><h3>Results</h3><div>Improvements in our compliance to the Get With The Guidelines- Heart Failure (GWTG-HF) Quality Measure AHAHF12: ICD Counseling or ICD Placed or Prescribed at Discharge increased by 20% from Quarter 1 203 to Quarter 2 2023 and additionally increased by 7% in Quarter 3. Through daily screening and the use of the Heart Failure Algorithm, cases were identified and presented at our monthly Heart Failure Adjudication meetings. These presentations not only assisted in referrals to EP, but also captured our audience. The presentations increased the awareness of our medical centers providers.</div></div><div><h3>Conclusion</h3><div>The use of daily screening increased referrals to Electrophysiology and identification of patients that met criteria for for device therapy. Consideration of ICD implantation must be a shared decision making process. As the population for heart failure continues to grow, device therapy can improve overall survival. It is vital to remain aware of technologies and devices that can refine management of complexed heart failure care.</div></div>","PeriodicalId":55064,"journal":{"name":"Heart & Lung","volume":"68 ","pages":"Page 383"},"PeriodicalIF":2.4,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142418511","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-10DOI: 10.1016/j.hrtlng.2024.08.006
Oriane Chausiaux PhD, MsC, BsC, MPhil, Gareth Williams, Melanie Keyser, Michał Nieznański, Philip Downer, Anna Zieba, Lewis Bond, Jakub Zieba, Shamus Husheer
Purpose
This study evaluates the implications of deploying a telemonitoring device in the homes of patients with heart failure through family doctors.
Background
In recent years, a decline in in-person primary healthcare consultations has posed significant challenges, especially for elderly patients with heart failure, who often contend with multiple comorbidities. A notable concern is their lack of awareness regarding symptom changes, such as weight gain, breathlessness, or swelling of the feet.
Methods
A cohort of 122 patients from 11 primary care practices across the UK were equipped with connected weighing scales and an AI monitoring device, including an internet dongle when necessary. These patients primarily resided in socioeconomically deprived areas. The study focused on device acceptability, utilization rates, and the impact of generated alerts on clinical teams. Initially planned for a six-month duration, a majority of participants opted to extend their use of the AI-device.
Results
The deployment targeted high-risk patients with heart failure, characterized by complex health conditions and histories of non-adherence with self-checks.
Data availability was high, with usage statistics indicating:
Weighing scale usage (at least once = 60.7%; at least 16days/mth = 5.7%)
AI-device usage (at least once = 100%; at least 16days/mth = 71.3%)
This indicates the AI device's passive, automated nature may enhance data collection from traditionally disengaged patient groups. Acceptability was high, with few rejections and of the 40% of participants responding to usability surveys, 92% would likely recommend the device to a friend. Alert management did not significantly burden GP teams, with most alerts being relevant to heart failure or other critical conditions needing attention (COPD exacerbation, COVID-19 infection, lymphoedema etc.). GP feedback was notably positive, especially from practices with a dozen or more participating patients.
Conclusion
Despite the challenging chosen patient group (representative of the high-risk heart failure population in the area), data acquisition was excellent, allowing clinicians to get an overview of the patient's health status remotely. While the investigation was not a randomized controlled trial (RCT), anecdotal evidence suggests early problem identification without significantly increasing GP workload. Further research is essential before broader implementation. The pivotal trial for the AI-device is expected to take place in the US in 2025.
{"title":"Insights from Implementing an AI-Enabled Peripheral Edema Monitor in UK-based Community Settings for Therapeutic Decision-Making","authors":"Oriane Chausiaux PhD, MsC, BsC, MPhil, Gareth Williams, Melanie Keyser, Michał Nieznański, Philip Downer, Anna Zieba, Lewis Bond, Jakub Zieba, Shamus Husheer","doi":"10.1016/j.hrtlng.2024.08.006","DOIUrl":"10.1016/j.hrtlng.2024.08.006","url":null,"abstract":"<div><h3>Purpose</h3><div>This study evaluates the implications of deploying a telemonitoring device in the homes of patients with heart failure through family doctors.</div></div><div><h3>Background</h3><div>In recent years, a decline in in-person primary healthcare consultations has posed significant challenges, especially for elderly patients with heart failure, who often contend with multiple comorbidities. A notable concern is their lack of awareness regarding symptom changes, such as weight gain, breathlessness, or swelling of the feet.</div></div><div><h3>Methods</h3><div>A cohort of 122 patients from 11 primary care practices across the UK were equipped with connected weighing scales and an AI monitoring device, including an internet dongle when necessary. These patients primarily resided in socioeconomically deprived areas. The study focused on device acceptability, utilization rates, and the impact of generated alerts on clinical teams. Initially planned for a six-month duration, a majority of participants opted to extend their use of the AI-device.</div></div><div><h3>Results</h3><div>The deployment targeted high-risk patients with heart failure, characterized by complex health conditions and histories of non-adherence with self-checks.</div><div>Data availability was high, with usage statistics indicating:</div><div>Weighing scale usage (at least once = 60.7%; at least 16days/mth = 5.7%)</div><div>AI-device usage (at least once = 100%; at least 16days/mth = 71.3%)</div><div>This indicates the AI device's passive, automated nature may enhance data collection from traditionally disengaged patient groups. Acceptability was high, with few rejections and of the 40% of participants responding to usability surveys, 92% would likely recommend the device to a friend. Alert management did not significantly burden GP teams, with most alerts being relevant to heart failure or other critical conditions needing attention (COPD exacerbation, COVID-19 infection, lymphoedema etc.). GP feedback was notably positive, especially from practices with a dozen or more participating patients.</div></div><div><h3>Conclusion</h3><div>Despite the challenging chosen patient group (representative of the high-risk heart failure population in the area), data acquisition was excellent, allowing clinicians to get an overview of the patient's health status remotely. While the investigation was not a randomized controlled trial (RCT), anecdotal evidence suggests early problem identification without significantly increasing GP workload. Further research is essential before broader implementation. The pivotal trial for the AI-device is expected to take place in the US in 2025.</div></div>","PeriodicalId":55064,"journal":{"name":"Heart & Lung","volume":"68 ","pages":"Page 385"},"PeriodicalIF":2.4,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142418513","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-10DOI: 10.1016/j.hrtlng.2024.08.005
Matthew Dewhurst MBBS, MRCP, MD NHS, Karen Hann, Iain Matthew, Lisa Gallagher, Gemma McCafferty, Hayley McKie, Sara Pick, Debbie Hughes, Louise Clayton, Will Nicolson, Susan Gent, Ganesan Kumar, Phil Keeling
<div><h3>Purpose</h3><div>This study (NCT04072744) investigates the Heartfelt device's ability to predict heart failure events by monitoring peripheral edema, comparing its accuracy and data reliability against traditional daily weight monitoring. It aims to determine the device's effectiveness in providing early warnings to healthcare providers, patients, and caregivers about impending heart failure decompensations and assesses whether adjustments in alert sensitivity could improve patient outcomes, identifying the most efficient approach for ongoing heart failure management.</div></div><div><h3>Background</h3><div>The Heartfelt device, a CE-marked device covered by FDA exemption, allows heart failure monitoring at home by using 3D imaging and AI to detect peripheral edema changes autonomously, requiring no patient input to collect data. In Europe it is regulated to send alerts on potential heart failure risks to patients, families, or providers based on its findings.</div></div><div><h3>Methods</h3><div>The FOOT study enrolled 26 patients from five UK NHS hospitals between February 2020 and June 2022. They used the Heartfelt HF3 device at home, which operated normally but logged data and alerts without informing patients or healthcare teams to prevent bias, as well as Bluetooth scales for daily weight tracking as part of standard care. After six months, clinical records were reviewed for heart failure incidents.</div></div><div><h3>Results</h3><div>In the cohort using the Heartfelt device, 9 heart failure events were recorded in 8 patients, including 2 outpatient visits, 6 hospital admissions, and one fatality, with the device providing an average lead time of 13 days (6.5-20) for deterioration. For standard care (daily weighing), there was an average of 1.1 days [0.3-4.1] of data each week versus 5.9 days [4.9-6.6] of foot volume data weekly recorded by the Heartfelt device. Before 5 of the hospitalizations and one death, the Heartfelt device issued alerts within the preceding two weeks. Alerts also preceded both outpatient incidents; however, the devices had been persistently alerting approximately weekly for several weeks prior, potentially due to excessively sensitive thresholds, so the outpatient events were counted as missed. In total, 6 out of the 9 heart failure events were deemed to be successfully predicted in advance.</div><div>Most patients lacked consistent weighing scale data due to adherence issues despite patients being told to follow the advice of regular weighing during the study. Yet, the weight data available indicated that at least 2 events (1 hospitalization and 1 death) could have been predicted.</div></div><div><h3>Conclusion</h3><div>The Heartfelt device demonstrates superior capability in detecting peripheral edema indicative of heart failure worsening, offering more reliable data collection than traditional weight monitoring. Its predictive alerts potentially afford clinicians and caregivers an early warning system, a
{"title":"Assessing the Heartfelt Device's Predictive Value in Heart Failure Management: Findings from the Multicenter FOOT Trial (UK)","authors":"Matthew Dewhurst MBBS, MRCP, MD NHS, Karen Hann, Iain Matthew, Lisa Gallagher, Gemma McCafferty, Hayley McKie, Sara Pick, Debbie Hughes, Louise Clayton, Will Nicolson, Susan Gent, Ganesan Kumar, Phil Keeling","doi":"10.1016/j.hrtlng.2024.08.005","DOIUrl":"10.1016/j.hrtlng.2024.08.005","url":null,"abstract":"<div><h3>Purpose</h3><div>This study (NCT04072744) investigates the Heartfelt device's ability to predict heart failure events by monitoring peripheral edema, comparing its accuracy and data reliability against traditional daily weight monitoring. It aims to determine the device's effectiveness in providing early warnings to healthcare providers, patients, and caregivers about impending heart failure decompensations and assesses whether adjustments in alert sensitivity could improve patient outcomes, identifying the most efficient approach for ongoing heart failure management.</div></div><div><h3>Background</h3><div>The Heartfelt device, a CE-marked device covered by FDA exemption, allows heart failure monitoring at home by using 3D imaging and AI to detect peripheral edema changes autonomously, requiring no patient input to collect data. In Europe it is regulated to send alerts on potential heart failure risks to patients, families, or providers based on its findings.</div></div><div><h3>Methods</h3><div>The FOOT study enrolled 26 patients from five UK NHS hospitals between February 2020 and June 2022. They used the Heartfelt HF3 device at home, which operated normally but logged data and alerts without informing patients or healthcare teams to prevent bias, as well as Bluetooth scales for daily weight tracking as part of standard care. After six months, clinical records were reviewed for heart failure incidents.</div></div><div><h3>Results</h3><div>In the cohort using the Heartfelt device, 9 heart failure events were recorded in 8 patients, including 2 outpatient visits, 6 hospital admissions, and one fatality, with the device providing an average lead time of 13 days (6.5-20) for deterioration. For standard care (daily weighing), there was an average of 1.1 days [0.3-4.1] of data each week versus 5.9 days [4.9-6.6] of foot volume data weekly recorded by the Heartfelt device. Before 5 of the hospitalizations and one death, the Heartfelt device issued alerts within the preceding two weeks. Alerts also preceded both outpatient incidents; however, the devices had been persistently alerting approximately weekly for several weeks prior, potentially due to excessively sensitive thresholds, so the outpatient events were counted as missed. In total, 6 out of the 9 heart failure events were deemed to be successfully predicted in advance.</div><div>Most patients lacked consistent weighing scale data due to adherence issues despite patients being told to follow the advice of regular weighing during the study. Yet, the weight data available indicated that at least 2 events (1 hospitalization and 1 death) could have been predicted.</div></div><div><h3>Conclusion</h3><div>The Heartfelt device demonstrates superior capability in detecting peripheral edema indicative of heart failure worsening, offering more reliable data collection than traditional weight monitoring. Its predictive alerts potentially afford clinicians and caregivers an early warning system, a","PeriodicalId":55064,"journal":{"name":"Heart & Lung","volume":"68 ","pages":"Pages 383-385"},"PeriodicalIF":2.4,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142418512","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-10DOI: 10.1016/j.hrtlng.2024.08.002
MaryBeth Vieira PhD, RN, CNE, Kristen A. Sethares
Purpose
There is a need to examine genderized societal roles in women for reasons for gaps in physical activity levels to create community engaged action models to address these factors with the primary goal of decreasing all cause cardiovascular disease. The purpose of this study was to examine sociodemographic, contextual, system-related, and personal factors contributing to physical activity levels in women at risk through a community engaged approach
Background
Cardiovascular disease remains the leading cause of death across the population. Black and Hispanic women have persistently high CVD risk factors with all cause CVD highest in Black women. Heart failure which is an end result of many cardiovascular diseases is 19% higher in the Black population than the white population. One way to decrease the risk of cardiovascular disease is through physical activity. 24.3% of adults meet physical activity guidelines. Women, particularly those with economic, educational, and access disparities report the lowest levels of physical activity.
Methods
Focus groups were utilized to interview nine adult female community members in an area of high diversity and potential for sociodemographic disparities. Community stakeholders were recruited, hired, and trained by the PI to lead focus groups and analyze data. Semi-structured interviews were used to discuss facilitators, barriers, preferences, and perspectives related to physical activity in the context of participants’ lifestyle. The research team analyzed and coded the transcripts and identified themes contributing to physical activity. Lincoln and Guba's criteria were applied for rigor.
Results
Themes identified barriers to physical activity including access (cost, location, programming, community events, and safety), family factors (childcare), and discomfort with exercising in mixed gender environments. Genderized roles in family management were apparent with strong themes of prioritization of family needs over self, planning self-care around and after family needs, and lack of time related to these priorities. Difficulty with self-regulation, goal setting, and planning related to physical activity. There was lack of knowledge regarding purposes of physical activity in that participants felt more influenced by societal pressures of “ideal image” for women vs a goal of personal health promotion. Social support was a strong facilitator.
Conclusion
Themes indicated barriers particular to gender and socioeconomics that are consistent with high rates of cardiovascular risk in this population. Programming must be initiated to specifically address the needs identified by the participants in the study in order to increase physical activity, decrease risk factors and disease incidence, thus decreasing incidence of heart failure in the population.
{"title":"Prevention of Heart Failure in Women with Disparities.","authors":"MaryBeth Vieira PhD, RN, CNE, Kristen A. Sethares","doi":"10.1016/j.hrtlng.2024.08.002","DOIUrl":"10.1016/j.hrtlng.2024.08.002","url":null,"abstract":"<div><h3>Purpose</h3><div>There is a need to examine genderized societal roles in women for reasons for gaps in physical activity levels to create community engaged action models to address these factors with the primary goal of decreasing all cause cardiovascular disease. The purpose of this study was to examine sociodemographic, contextual, system-related, and personal factors contributing to physical activity levels in women at risk through a community engaged approach</div></div><div><h3>Background</h3><div>Cardiovascular disease remains the leading cause of death across the population. Black and Hispanic women have persistently high CVD risk factors with all cause CVD highest in Black women. Heart failure which is an end result of many cardiovascular diseases is 19% higher in the Black population than the white population. One way to decrease the risk of cardiovascular disease is through physical activity. 24.3% of adults meet physical activity guidelines. Women, particularly those with economic, educational, and access disparities report the lowest levels of physical activity.</div></div><div><h3>Methods</h3><div>Focus groups were utilized to interview nine adult female community members in an area of high diversity and potential for sociodemographic disparities. Community stakeholders were recruited, hired, and trained by the PI to lead focus groups and analyze data. Semi-structured interviews were used to discuss facilitators, barriers, preferences, and perspectives related to physical activity in the context of participants’ lifestyle. The research team analyzed and coded the transcripts and identified themes contributing to physical activity. Lincoln and Guba's criteria were applied for rigor.</div></div><div><h3>Results</h3><div>Themes identified barriers to physical activity including access (cost, location, programming, community events, and safety), family factors (childcare), and discomfort with exercising in mixed gender environments. Genderized roles in family management were apparent with strong themes of prioritization of family needs over self, planning self-care around and after family needs, and lack of time related to these priorities. Difficulty with self-regulation, goal setting, and planning related to physical activity. There was lack of knowledge regarding purposes of physical activity in that participants felt more influenced by societal pressures of “ideal image” for women vs a goal of personal health promotion. Social support was a strong facilitator.</div></div><div><h3>Conclusion</h3><div>Themes indicated barriers particular to gender and socioeconomics that are consistent with high rates of cardiovascular risk in this population. Programming must be initiated to specifically address the needs identified by the participants in the study in order to increase physical activity, decrease risk factors and disease incidence, thus decreasing incidence of heart failure in the population.</div></div>","PeriodicalId":55064,"journal":{"name":"Heart & Lung","volume":"68 ","pages":"Page 381"},"PeriodicalIF":2.4,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142418509","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-08DOI: 10.1016/j.hrtlng.2024.09.017
Tianwei Meng , Weidong Wu , Boyu Wang , Chengjia Li , Jiarui Li , Jiawen Liu , Jianying Wang , Rui Qie
Background
Chronic Pulmonary Heart Disease (CPHD) significantly impacts global health, especially among middle-aged and older adults. In China, the Traditional Chinese Medicine (TCM) technique of Resolving Phlegm and Activating Blood (RPAB) is widely used to treat CPHD, although high-quality evidence supporting its efficacy remains limited.
Objectives
The purpose of this study was to rigorously assess the clinical efficacy of RPAB for CPHD and elucidate the mechanisms underlying its primary herbal components.
Methods
Through a detailed search of literature in both Chinese and English and strict inclusion and exclusion criteria, 18 randomized controlled trials (RCTs) were selected for meta-analysis. We identified RPAB's core herbal combinations using association rule analysis. This method statistically analyzes the frequency and correlation of herbal medicine usage. We then analyzed the chemical components of these combinations and investigated their potential intervention mechanisms on CPHD through network pharmacology.
Results
The combination of RPAB with Western medicine was superior to Western medicine alone in improving blood gas analysis and pulmonary function and reducing plasma viscosity in CPHD patients. The core herbal combination identified was Astragalus membranaceus (Fisch.) Bunge, Ligusticum chuanxiong Hort. ex S. H. Qiu & al., and Stellaria alsine Grimm (ALS). This combination targeted 588 therapeutic and 27 core targets. It influenced ten core compounds across 34 pathways, primarily through the chemokine signaling pathway and the JAK-STAT signaling pathway.
Conclusion
RPAB with Western medicine significantly improves CPHD treatment outcomes. The study highlights the therapeutic potential of the ALS combination, which operates through multiple pathways to remodel pulmonary arteries, decrease inflammation, and lessen oxidative stress. These insights support the clinical application of RPAB in CPHD treatment and open new avenues for research and therapeutic development.
{"title":"Treating chronic pulmonary heart disease with traditional Chinese medicine: Systematic evaluation and mechanistic insights into the resolving phlegm and activating blood approach","authors":"Tianwei Meng , Weidong Wu , Boyu Wang , Chengjia Li , Jiarui Li , Jiawen Liu , Jianying Wang , Rui Qie","doi":"10.1016/j.hrtlng.2024.09.017","DOIUrl":"10.1016/j.hrtlng.2024.09.017","url":null,"abstract":"<div><h3>Background</h3><div>Chronic Pulmonary Heart Disease (CPHD) significantly impacts global health, especially among middle-aged and older adults. In China, the Traditional Chinese Medicine (TCM) technique of Resolving Phlegm and Activating Blood (RPAB) is widely used to treat CPHD, although high-quality evidence supporting its efficacy remains limited.</div></div><div><h3>Objectives</h3><div>The purpose of this study was to rigorously assess the clinical efficacy of RPAB for CPHD and elucidate the mechanisms underlying its primary herbal components.</div></div><div><h3>Methods</h3><div>Through a detailed search of literature in both Chinese and English and strict inclusion and exclusion criteria, 18 randomized controlled trials (RCTs) were selected for meta-analysis. We identified RPAB's core herbal combinations using association rule analysis. This method statistically analyzes the frequency and correlation of herbal medicine usage. We then analyzed the chemical components of these combinations and investigated their potential intervention mechanisms on CPHD through network pharmacology.</div></div><div><h3>Results</h3><div>The combination of RPAB with Western medicine was superior to Western medicine alone in improving blood gas analysis and pulmonary function and reducing plasma viscosity in CPHD patients. The core herbal combination identified was <em>Astragalus membranaceus</em> (Fisch.) Bunge, <em>Ligusticum chuanxiong</em> Hort. ex S. H. Qiu & al., and <em>Stellaria alsine</em> Grimm (ALS). This combination targeted 588 therapeutic and 27 core targets. It influenced ten core compounds across 34 pathways, primarily through the chemokine signaling pathway and the JAK-STAT signaling pathway.</div></div><div><h3>Conclusion</h3><div>RPAB with Western medicine significantly improves CPHD treatment outcomes. The study highlights the therapeutic potential of the ALS combination, which operates through multiple pathways to remodel pulmonary arteries, decrease inflammation, and lessen oxidative stress. These insights support the clinical application of RPAB in CPHD treatment and open new avenues for research and therapeutic development.</div></div>","PeriodicalId":55064,"journal":{"name":"Heart & Lung","volume":"69 ","pages":"Pages 111-126"},"PeriodicalIF":2.4,"publicationDate":"2024-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142395371","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}