Pub Date : 2024-01-01Epub Date: 2024-03-27DOI: 10.1159/000538347
Pingjiang Li, Yuying Cui, Xiaoming Xu, Jianjun Dong, Lin Liao
Background: The mineralocorticoid receptor plays an important pathophysiological role in cardiorenal diseases by causing inflammation and fibrosis. Mineralocorticoid receptor antagonists (MRAs) are well known in treating cardiovascular disease and diverse nephropathies. However, the first-generation MRA (spironolactone) and the second-generation MRA (eplerenone) remain underutilized because of the risk of inducing severe adverse events. As a selective nonsteroidal MRA, finerenone is safer and more effective and improves cardiorenal outcomes in patients with chronic kidney disease (CKD) and type 2 diabetes mellitus (T2DM). However, the effect of finerenone on cardiorenal outcomes in patients of different races and kidney function (estimated glomerular filtration rate) is unclear.
Summary: In this review, we summarized the impact of finerenone on patients with CKD and T2DM from randomized controlled trials. The synthesis of published data aims to address the questions pertaining to the cardiorenal benefits of finerenone among various racial groups and different levels of kidney function.
Key message: Finerenone presents racial differences and effects associated with kidney function in CKD and T2DM patients. Due to the limited data for subgroups, it is prudent to approach the conclusion with caution.
{"title":"Cardiorenal Benefits of Finerenone in Different Races and Kidney Function in Patients with Chronic Kidney Disease.","authors":"Pingjiang Li, Yuying Cui, Xiaoming Xu, Jianjun Dong, Lin Liao","doi":"10.1159/000538347","DOIUrl":"10.1159/000538347","url":null,"abstract":"<p><strong>Background: </strong>The mineralocorticoid receptor plays an important pathophysiological role in cardiorenal diseases by causing inflammation and fibrosis. Mineralocorticoid receptor antagonists (MRAs) are well known in treating cardiovascular disease and diverse nephropathies. However, the first-generation MRA (spironolactone) and the second-generation MRA (eplerenone) remain underutilized because of the risk of inducing severe adverse events. As a selective nonsteroidal MRA, finerenone is safer and more effective and improves cardiorenal outcomes in patients with chronic kidney disease (CKD) and type 2 diabetes mellitus (T2DM). However, the effect of finerenone on cardiorenal outcomes in patients of different races and kidney function (estimated glomerular filtration rate) is unclear.</p><p><strong>Summary: </strong>In this review, we summarized the impact of finerenone on patients with CKD and T2DM from randomized controlled trials. The synthesis of published data aims to address the questions pertaining to the cardiorenal benefits of finerenone among various racial groups and different levels of kidney function.</p><p><strong>Key message: </strong>Finerenone presents racial differences and effects associated with kidney function in CKD and T2DM patients. Due to the limited data for subgroups, it is prudent to approach the conclusion with caution.</p>","PeriodicalId":9584,"journal":{"name":"Cardiorenal Medicine","volume":" ","pages":"227-234"},"PeriodicalIF":3.8,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140304998","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 : 2024-01-01Epub Date: 2024-02-14DOI: 10.1159/000537785
Amir Kazory, Claudio Ronco
{"title":"Advances in Cardiorenal Medicine: The Year 2023 in Review.","authors":"Amir Kazory, Claudio Ronco","doi":"10.1159/000537785","DOIUrl":"10.1159/000537785","url":null,"abstract":"","PeriodicalId":9584,"journal":{"name":"Cardiorenal Medicine","volume":" ","pages":"123-128"},"PeriodicalIF":3.8,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139734575","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 : 2024-01-01Epub Date: 2024-03-12DOI: 10.1159/000538042
Kyung An Kim, Joo Eun Lee, Ik Jun Choi, Kwan Yong Lee, Chan Joon Kim, Mahn-Won Park, Chul Soo Park, Hee-Yeol Kim, Ki-Dong Yoo, Doo Soo Jeon, Myung Ho Jeong, Kiyuk Chang
Introduction: Renin-angiotensin system blockers (RASBs) are known to improve mortality after acute myocardial infarction (AMI). However, there remain uncertainties regarding treatment with RASBs after AMI in patients with renal dysfunction and especially in the setting of acute kidney injury (AKI).
Methods: Patients from a multicenter AMI registry undergoing percutaneous coronary intervention in Korea were stratified and analyzed according to the presence of AKI, defined as an increase in serum creatinine levels of ≥0.3 mg/dL or ≥50% increase from baseline during admission, and RASB prescription at discharge. The primary outcome of interest was 5-year all-cause mortality.
Results: In total 9,629 patients were selected for initial analysis, of which 2,405 had an episode of AKI. After adjustment using multivariable Cox regression, treatment with RASBs at discharge was associated with decreased all-cause mortality in the entire cohort (hazard ratio [HR] 0.849, confidence interval [CI] 0.753-0.956), but not for the patients with AKI (HR 0.988, CI 0.808-1.208). In subgroup analysis, RASBs reduced all-cause mortality in patients with stage I AKI (HR 0.760, CI 0.584-0.989) but not for stage II and III AKI (HR 1.200, CI 0.899-1.601, interaction p value 0.002). Similar heterogeneities between RASB use and AKI severity were also observed for other clinical outcomes of interest.
Conclusion: Treatment with RASBs in patients with AMI and concomitant AKI is associated with favorable outcomes in non-severe AKI, but not in severe AKI. Further studies to confirm these results and to develop strategies to minimize the occurrence of adverse effects arising from RASB treatment are needed.
背景:众所周知,肾素-血管紧张素系统阻滞剂(RASBs)可改善急性心肌梗死(AMI)后的死亡率。然而,对于肾功能不全的急性心肌梗死患者,尤其是急性肾损伤(AKI)患者,使用 RASBs 治疗仍存在不确定性:方法:对在韩国接受经皮冠状动脉介入治疗的多中心急性心肌梗死登记患者进行分层,并根据是否存在急性肾损伤(定义为入院时血清肌酐水平比基线增加≥0.3mg/dL或≥50%)以及出院时的RASB处方进行分析。主要研究结果为 5 年全因死亡率:共有 9629 名患者被选中进行初步分析,其中 2405 人发生过 AKI。在使用多变量 Cox 回归进行调整后,出院时接受 RASBs 治疗与整个队列中全因死亡率的降低相关(HR 0.849,CI 0.753-0.956),但与 AKI 患者的相关性不大(HR 0.988,CI 0.808-1.208)。在亚组分析中,RASBs 可降低 I 期 AKI 患者的全因死亡率(HR 0.760,CI 0.584-0.989),但不能降低 II 期和 III 期 AKI 患者的全因死亡率(HR 1.200,CI 0.899-1.601,交互作用 p 值 0.002)。在其他相关临床结果中也观察到了使用RASB和AKI严重程度之间的类似异质性:结论:AMI合并AKI患者接受RASB治疗与非重度AKI患者的良好预后相关,但与重度AKI患者的良好预后无关。需要进一步研究以证实这些结果,并制定策略以尽量减少 RASB 治疗引起的不良反应。
{"title":"Effect of Renin-Angiotensin System Blockers in Acute Myocardial Infarction Patients with Acute Kidney Injury.","authors":"Kyung An Kim, Joo Eun Lee, Ik Jun Choi, Kwan Yong Lee, Chan Joon Kim, Mahn-Won Park, Chul Soo Park, Hee-Yeol Kim, Ki-Dong Yoo, Doo Soo Jeon, Myung Ho Jeong, Kiyuk Chang","doi":"10.1159/000538042","DOIUrl":"10.1159/000538042","url":null,"abstract":"<p><strong>Introduction: </strong>Renin-angiotensin system blockers (RASBs) are known to improve mortality after acute myocardial infarction (AMI). However, there remain uncertainties regarding treatment with RASBs after AMI in patients with renal dysfunction and especially in the setting of acute kidney injury (AKI).</p><p><strong>Methods: </strong>Patients from a multicenter AMI registry undergoing percutaneous coronary intervention in Korea were stratified and analyzed according to the presence of AKI, defined as an increase in serum creatinine levels of ≥0.3 mg/dL or ≥50% increase from baseline during admission, and RASB prescription at discharge. The primary outcome of interest was 5-year all-cause mortality.</p><p><strong>Results: </strong>In total 9,629 patients were selected for initial analysis, of which 2,405 had an episode of AKI. After adjustment using multivariable Cox regression, treatment with RASBs at discharge was associated with decreased all-cause mortality in the entire cohort (hazard ratio [HR] 0.849, confidence interval [CI] 0.753-0.956), but not for the patients with AKI (HR 0.988, CI 0.808-1.208). In subgroup analysis, RASBs reduced all-cause mortality in patients with stage I AKI (HR 0.760, CI 0.584-0.989) but not for stage II and III AKI (HR 1.200, CI 0.899-1.601, interaction p value 0.002). Similar heterogeneities between RASB use and AKI severity were also observed for other clinical outcomes of interest.</p><p><strong>Conclusion: </strong>Treatment with RASBs in patients with AMI and concomitant AKI is associated with favorable outcomes in non-severe AKI, but not in severe AKI. Further studies to confirm these results and to develop strategies to minimize the occurrence of adverse effects arising from RASB treatment are needed.</p>","PeriodicalId":9584,"journal":{"name":"Cardiorenal Medicine","volume":" ","pages":"178-190"},"PeriodicalIF":3.8,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140109290","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}
J.P. Islas Rodríguez, Tomas Miranda-Aquino, Gregorio Romero-González, J. H. Hernández-Del Río, Jahir R. Camacho- Guerrero, Scarlett Covarrubias-Villa, J. B. Ivey-Miranda, Jonathan S. Chávez-Íñiguez
Introduction: In cardiorenal syndrome type 1 (CRS1) vascular congestion is central to the pathophysiology of heart failure and thus a key target for management. The Venous Evaluation by Ultrasound System (VExUS) could guide decongestion effectively and thereby improve outcomes. Methods: In this randomized clinical trial, patients with CRS1 (i.e., increase in creatinine ≥0.3 mg/dL) were randomized to guide decongestion with VExUS compared to usual clinical evaluation. The primary endpoint was to assess kidney function recovery (KFR), and the key secondary endpoint was decongestion evaluated by physical examination and changes in brain natriuretic peptide (BNP) and CA-125. Exploratory endpoints included days of hospitalization and mortality. Results: From March 2022 to February 2023, a total of 140 patients were randomized 1:1 (70 in the VExUS and 70 in the Control group). KFR was not statistically different between groups. However, VExUS improved more than twice the odds to achieve decongestion (OR 2.6, 95% CI 1.9-3.0, p=0.01) and the odds to reach a decrease of BNP >30% (OR 2.4; 95% CI 1.3-4.1, p = 0.01). The survival at 90 days, recongestion and CA-125 were similar between groups. Conclusion: In patients with CRS1, we observed that VExUS-guided decongestion did not improve the probability of KFR but improved the odds to achieve decongestion.
在1型心肾综合征(CRS1)中,血管充血是心衰病理生理学的核心,因此是治疗的关键目标。静脉超声评估系统(VExUS)可以有效地指导去充血,从而改善预后。方法:在本随机临床试验中,随机选择CRS1(即肌酐升高≥0.3 mg/dL)患者,与常规临床评价相比,使用VExUS指导去充血。主要终点是评估肾功能恢复(KFR),关键的次要终点是通过体检和脑钠肽(BNP)和CA-125的变化来评估充血。探索性终点包括住院天数和死亡率。结果:从2022年3月至2023年2月,共140例患者按1:1随机分组(70例为VExUS组,70例为对照组)。KFR组间差异无统计学意义。然而,VExUS实现去充血的几率提高了两倍以上(OR 2.6, 95% CI 1.9-3.0, p=0.01), BNP降低的几率>30% (OR 2.4;95% CI 1.3 ~ 4.1, p = 0.01)。90天存活率、再充血率和CA-125在两组间无明显差异。结论:在CRS1患者中,我们观察到,vexus引导下的去充血并没有提高KFR的概率,但提高了实现去充血的几率。
{"title":"Effect on kidney function recovery guiding decongestion with VExUS in patients with cardiorenal syndrome 1, a randomized control trial","authors":"J.P. Islas Rodríguez, Tomas Miranda-Aquino, Gregorio Romero-González, J. H. Hernández-Del Río, Jahir R. Camacho- Guerrero, Scarlett Covarrubias-Villa, J. B. Ivey-Miranda, Jonathan S. Chávez-Íñiguez","doi":"10.1159/000535641","DOIUrl":"https://doi.org/10.1159/000535641","url":null,"abstract":"Introduction: In cardiorenal syndrome type 1 (CRS1) vascular congestion is central to the pathophysiology of heart failure and thus a key target for management. The Venous Evaluation by Ultrasound System (VExUS) could guide decongestion effectively and thereby improve outcomes. Methods: In this randomized clinical trial, patients with CRS1 (i.e., increase in creatinine ≥0.3 mg/dL) were randomized to guide decongestion with VExUS compared to usual clinical evaluation. The primary endpoint was to assess kidney function recovery (KFR), and the key secondary endpoint was decongestion evaluated by physical examination and changes in brain natriuretic peptide (BNP) and CA-125. Exploratory endpoints included days of hospitalization and mortality. Results: From March 2022 to February 2023, a total of 140 patients were randomized 1:1 (70 in the VExUS and 70 in the Control group). KFR was not statistically different between groups. However, VExUS improved more than twice the odds to achieve decongestion (OR 2.6, 95% CI 1.9-3.0, p=0.01) and the odds to reach a decrease of BNP >30% (OR 2.4; 95% CI 1.3-4.1, p = 0.01). The survival at 90 days, recongestion and CA-125 were similar between groups. Conclusion: In patients with CRS1, we observed that VExUS-guided decongestion did not improve the probability of KFR but improved the odds to achieve decongestion.","PeriodicalId":9584,"journal":{"name":"Cardiorenal Medicine","volume":"27 7","pages":""},"PeriodicalIF":3.8,"publicationDate":"2023-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138593348","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}
{"title":"Acknowledgement to Reviewers","authors":"","doi":"10.1159/000528551","DOIUrl":"https://doi.org/10.1159/000528551","url":null,"abstract":"<br />Cardiorenal Med 2023;13:1–","PeriodicalId":9584,"journal":{"name":"Cardiorenal Medicine","volume":"10 1","pages":""},"PeriodicalIF":3.8,"publicationDate":"2023-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138534442","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 : 2023-01-01Epub Date: 2023-03-23DOI: 10.1159/000528897
Moe Kojima, Naoya Tanabe, Yu Kojima, Koichi Tamura, Hiroo Takahashi, Jun Ito
Introduction: Various methods for vascular access (VA) management have been studied. We investigated the usefulness of a new, simple, and quantitative VA management method using the Pocket LDF® laser blood flowmeter (hereinafter "LDF") that noninvasively measures peripheral circulation flow.
Methods: Peripheral circulation flow was measured in 82 patients (43 men) on maintenance hemodialysis with an arteriovenous fistula (AVF). The shunt symmetry index (SSI) was calculated as peripheral circulation flow in the AVF limb divided by that in the non-AVF limb. SSI was used for microcirculation evaluation and also compared by AVF site. Patients undergoing vascular access interventional therapy (VAIVT) underwent ultrasound evaluation (Doppler ultrasonography) of the AVF and SSI measurement before and after VAIVT. SSI was compared between those who did and did not require VAIVT, and the cutoff value for SSI was determined by receiver operating characteristic curve (ROC) analysis.
Results: As many as 86% of the patients who were measured peripheral circulation flow had SSI <1.0, which indicates that AVF reduced peripheral circulation flow. All patients who underwent VAIVT showed a decrease in SSI to <1.0 after VAIVT, probably due to improvement of stenosis. SSI differed significantly between patients who did and did not require VAIVT (1.20 ± 0.49 vs. 0.65 ± 0.33, p < 0.001), which indicates that SSI is affected by the presence of stenosis in the proximal vein of the VA anastomosis. In patients with SSI ≥1.0, stenosis of the proximal vein of the AVF caused stasis of blood flow, resulting in increased peripheral blood flow. AVF site seems to have no impact on peripheral circulation flow. The SSI cutoff value for the screening of proximal vein stenosis was 1.06 (sensitivity: 0.69, specificity: 0.93, area under the curve: 0.81).
Conclusion: Based on the ROC analysis, we recommend considering AVF ultrasound for SSI >1.06. Our results suggest the usefulness of the described VA management method using the LDF.
导读:血管通路(VA)管理的各种方法已被研究。我们研究了一种新的、简单的、定量的VA管理方法的有效性,该方法使用口袋LDF®激光血流仪(以下简称“LDF”),无创测量外周循环流量。方法:对82例(男性43例)伴有动静脉瘘(AVF)的维持性血液透析患者进行外周循环流量测定。分流对称指数(SSI)计算为AVF肢体周围循环流量除以非AVF肢体的循环流量。采用SSI进行微循环评价,并与AVF位点进行比较。行血管通路介入治疗(VAIVT)的患者在VAIVT前后分别行AVF和SSI的超声评价(多普勒超声)。比较需要和不需要VAIVT的患者的SSI,并通过受试者工作特征曲线(ROC)分析确定SSI的截止值。结果:测量外周循环流量的患者中,高达86%的SSI < 1.0,表明AVF降低了外周循环流量。所有接受VAIVT的患者在VAIVT后SSI下降到< 1.0,可能是由于狭窄的改善。使用和不使用VAIVT的患者SSI差异显著(1.20±0.49 vs 0.65±0.33,p < 0.001),说明SSI受VA吻合口近端静脉狭窄的影响。SSI≥1.0的患者,AVF近端静脉狭窄导致血流淤滞,外周血流量增加。AVF部位似乎对周围循环流量没有影响。筛选近端静脉狭窄的SSI截止值为1.06(敏感性:0.69,特异性:0.93,曲线下面积:0.81)。讨论/结论:基于ROC分析,我们建议对SSI > 1.06的患者考虑AVF超声。我们的研究结果表明,所描述的使用LDF的VA管理方法是有用的。
{"title":"Usefulness of a Novel Vascular Access Management Method Using a Laser Blood Flowmeter.","authors":"Moe Kojima, Naoya Tanabe, Yu Kojima, Koichi Tamura, Hiroo Takahashi, Jun Ito","doi":"10.1159/000528897","DOIUrl":"10.1159/000528897","url":null,"abstract":"<p><strong>Introduction: </strong>Various methods for vascular access (VA) management have been studied. We investigated the usefulness of a new, simple, and quantitative VA management method using the Pocket LDF® laser blood flowmeter (hereinafter \"LDF\") that noninvasively measures peripheral circulation flow.</p><p><strong>Methods: </strong>Peripheral circulation flow was measured in 82 patients (43 men) on maintenance hemodialysis with an arteriovenous fistula (AVF). The shunt symmetry index (SSI) was calculated as peripheral circulation flow in the AVF limb divided by that in the non-AVF limb. SSI was used for microcirculation evaluation and also compared by AVF site. Patients undergoing vascular access interventional therapy (VAIVT) underwent ultrasound evaluation (Doppler ultrasonography) of the AVF and SSI measurement before and after VAIVT. SSI was compared between those who did and did not require VAIVT, and the cutoff value for SSI was determined by receiver operating characteristic curve (ROC) analysis.</p><p><strong>Results: </strong>As many as 86% of the patients who were measured peripheral circulation flow had SSI <1.0, which indicates that AVF reduced peripheral circulation flow. All patients who underwent VAIVT showed a decrease in SSI to <1.0 after VAIVT, probably due to improvement of stenosis. SSI differed significantly between patients who did and did not require VAIVT (1.20 ± 0.49 vs. 0.65 ± 0.33, p < 0.001), which indicates that SSI is affected by the presence of stenosis in the proximal vein of the VA anastomosis. In patients with SSI ≥1.0, stenosis of the proximal vein of the AVF caused stasis of blood flow, resulting in increased peripheral blood flow. AVF site seems to have no impact on peripheral circulation flow. The SSI cutoff value for the screening of proximal vein stenosis was 1.06 (sensitivity: 0.69, specificity: 0.93, area under the curve: 0.81).</p><p><strong>Conclusion: </strong>Based on the ROC analysis, we recommend considering AVF ultrasound for SSI >1.06. Our results suggest the usefulness of the described VA management method using the LDF.</p>","PeriodicalId":9584,"journal":{"name":"Cardiorenal Medicine","volume":" ","pages":"232-237"},"PeriodicalIF":3.8,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664318/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9165929","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Introduction: Sacubitril/valsartan (S/V) reduces all-cause mortality in patients with heart failure with reduced ejection fraction (HFrEF), but it may decline their estimated glomerular filtration rates (eGFR). In addition to eGFR, this clinical study aimed to develop a blood urea nitrogen (BUN)-based index to evaluate the status of renal perfusion and then identify predictors of all-cause death or heart transplant in patients with HFrEF receiving S/V.
Methods: From the recruited 291 patients with HFrEF who were prescribed S/V from March 2017 to March 2019, we collected demographic, drug history, laboratory, echocardiographic, and clinical data from 1 year before S/V initiation until December 2020. Regression analysis was conducted by fitting Cox's models with time-dependent covariates for the survival time and applying the modern stepwise variable selection procedure. The smoothing spline method was used to detect nonlinearity in effect and yield optimal cut-off values for continuous covariates.
Results: In the Cox's model, decreased hemoglobin level, decreased mean left ventricular ejection fraction, declined daily dose of S/V, decreased eGFR within 3 months, and increased BUN levels within 1 month and 9 months over time were significantly associated with an increased risk of all-cause death or heart transplant in patients with HFrEF.
Conclusions: Adequate maintenance of renal perfusion is crucial for the continuous use of S/V and to avoid worsening renal function in patients with HFrEF. We defined the maximum increase in BUN levels within a specified period as the Worsening Renal Perfusion Index (WRPSV Index) to capture the prognostic effect of renal hypoperfusion in patients with HFrEF.
{"title":"The Worsening Renal Perfusion Index Predicts the Prognoses of Heart Failure Patients Treated with Sacubitril/Valsartan.","authors":"Wan-Tseng Hsu, Yu-Yang Cheng, Tsun-Yu Yang, Chao-Kai Chang, Yi-Hsuan Lin, Chii-Ming Lee, Tao-Min Huang","doi":"10.1159/000534095","DOIUrl":"10.1159/000534095","url":null,"abstract":"<p><strong>Introduction: </strong>Sacubitril/valsartan (S/V) reduces all-cause mortality in patients with heart failure with reduced ejection fraction (HFrEF), but it may decline their estimated glomerular filtration rates (eGFR). In addition to eGFR, this clinical study aimed to develop a blood urea nitrogen (BUN)-based index to evaluate the status of renal perfusion and then identify predictors of all-cause death or heart transplant in patients with HFrEF receiving S/V.</p><p><strong>Methods: </strong>From the recruited 291 patients with HFrEF who were prescribed S/V from March 2017 to March 2019, we collected demographic, drug history, laboratory, echocardiographic, and clinical data from 1 year before S/V initiation until December 2020. Regression analysis was conducted by fitting Cox's models with time-dependent covariates for the survival time and applying the modern stepwise variable selection procedure. The smoothing spline method was used to detect nonlinearity in effect and yield optimal cut-off values for continuous covariates.</p><p><strong>Results: </strong>In the Cox's model, decreased hemoglobin level, decreased mean left ventricular ejection fraction, declined daily dose of S/V, decreased eGFR within 3 months, and increased BUN levels within 1 month and 9 months over time were significantly associated with an increased risk of all-cause death or heart transplant in patients with HFrEF.</p><p><strong>Conclusions: </strong>Adequate maintenance of renal perfusion is crucial for the continuous use of S/V and to avoid worsening renal function in patients with HFrEF. We defined the maximum increase in BUN levels within a specified period as the Worsening Renal Perfusion Index (WRPSV Index) to capture the prognostic effect of renal hypoperfusion in patients with HFrEF.</p>","PeriodicalId":9584,"journal":{"name":"Cardiorenal Medicine","volume":" ","pages":"310-323"},"PeriodicalIF":3.8,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664343/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10242170","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-01-01Epub Date: 2023-08-16DOI: 10.1159/000531631
Gema Miñana, Miguel González-Rico, Rafael de la Espriella, Daniel González-Sánchez, Marco Montomoli, Eduardo Núñez, Agustín Fernández-Cisnal, Sandra Villar, Jose Luis Górriz, Julio Núñez
Introduction: Spot urinary sodium emerged as a useful parameter for assessing decongestion in patients with congestive heart failure (CHF). Growing evidence endorses the therapeutic role of continuous ambulatory peritoneal dialysis (CAPD) in patients with refractory CHF and kidney disease. We aimed to examine the long-term trajectory of urinary, peritoneal, and total (urinary plus peritoneal) sodium removal in a cohort of patients with refractory CHF enrolled in a CAPD program. Additionally, we explored whether sodium removal was associated with the risk of long-term mortality and episodes of worsening heart failure (WHF).
Methods: We included 66 ambulatory patients with refractory CHF enrolled in a CAPD program in a single teaching center. 24-h peritoneal, urinary, and total sodium elimination were analyzed at baseline and after CAPD initiation. Its trajectories over time were calculated using joint modeling of longitudinal and survival data. Within the framework of joint frailty models for recurrent and terminal events, we estimated its prognostic effect on recurrent episodes of WHF.
Results: At the time of enrollment, the mean age and estimated glomerular filtration rate were 72.8 ± 8.4 years and 28.5 ± 14.3 mL/min/1.73 m2, respectively. The median urinary sodium at baseline was 2.34 g/day (1.40-3.55). At a median (p25%-p75%) follow-up of 2.93 (1.93-3.72) years, we registered 0.28 deaths and 0.24 episodes of WHF per 1 person-year. Compared to baseline (urinary), CAPD led to increased sodium excretion (urinary plus dialyzed) since the first follow-up visit (p < 0.001). Over the follow-up, repeated measurements of total sodium removal were associated with a lower risk of death and episodes of WHF.
Conclusions: CAPD increased sodium removal in patients with refractory CHF. Elevated sodium removal identified those patients with a lower risk of death and episodes of WHF.
{"title":"Peritoneal and Urinary Sodium Removal in Refractory Congestive Heart Failure Patients Included in an Ambulatory Peritoneal Dialysis Program: Valuable for Monitoring the Course of the Disease.","authors":"Gema Miñana, Miguel González-Rico, Rafael de la Espriella, Daniel González-Sánchez, Marco Montomoli, Eduardo Núñez, Agustín Fernández-Cisnal, Sandra Villar, Jose Luis Górriz, Julio Núñez","doi":"10.1159/000531631","DOIUrl":"10.1159/000531631","url":null,"abstract":"<p><strong>Introduction: </strong>Spot urinary sodium emerged as a useful parameter for assessing decongestion in patients with congestive heart failure (CHF). Growing evidence endorses the therapeutic role of continuous ambulatory peritoneal dialysis (CAPD) in patients with refractory CHF and kidney disease. We aimed to examine the long-term trajectory of urinary, peritoneal, and total (urinary plus peritoneal) sodium removal in a cohort of patients with refractory CHF enrolled in a CAPD program. Additionally, we explored whether sodium removal was associated with the risk of long-term mortality and episodes of worsening heart failure (WHF).</p><p><strong>Methods: </strong>We included 66 ambulatory patients with refractory CHF enrolled in a CAPD program in a single teaching center. 24-h peritoneal, urinary, and total sodium elimination were analyzed at baseline and after CAPD initiation. Its trajectories over time were calculated using joint modeling of longitudinal and survival data. Within the framework of joint frailty models for recurrent and terminal events, we estimated its prognostic effect on recurrent episodes of WHF.</p><p><strong>Results: </strong>At the time of enrollment, the mean age and estimated glomerular filtration rate were 72.8 ± 8.4 years and 28.5 ± 14.3 mL/min/1.73 m2, respectively. The median urinary sodium at baseline was 2.34 g/day (1.40-3.55). At a median (p25%-p75%) follow-up of 2.93 (1.93-3.72) years, we registered 0.28 deaths and 0.24 episodes of WHF per 1 person-year. Compared to baseline (urinary), CAPD led to increased sodium excretion (urinary plus dialyzed) since the first follow-up visit (p < 0.001). Over the follow-up, repeated measurements of total sodium removal were associated with a lower risk of death and episodes of WHF.</p><p><strong>Conclusions: </strong>CAPD increased sodium removal in patients with refractory CHF. Elevated sodium removal identified those patients with a lower risk of death and episodes of WHF.</p>","PeriodicalId":9584,"journal":{"name":"Cardiorenal Medicine","volume":"13 1","pages":"211-220"},"PeriodicalIF":3.8,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664341/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10367791","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-01-01Epub Date: 2023-10-12DOI: 10.1159/000534252
Guyu Zeng, Deshan Yuan, Peizhi Wang, Tianyu Li, Lin Jiang, Lianjun Xu, Jian Tian, Xueyan Zhao, Xinxing Feng, Dong Wang, Yin Zhang, Kai Sun, Jingjing Xu, Ru Liu, Bo Xu, Wei Zhao, Rutai Hui, Runlin Gao, Lei Song, Jinqing Yuan
Introduction: Limited data are available on the long-term impact of mild renal dysfunction (estimated glomerular filtration rate [eGFR] 60-89 mL/min/1.73 m2) in patients with three-vessel coronary disease (3VD).
Methods: A total of 5,272 patients with 3VD undergoing revascularization were included and were categorized into 3 groups: normal renal function (eGFR ≥90 mL/min/1.73 m2, n = 2,352), mild renal dysfunction (eGFR 60-89, n = 2,501), and moderate renal dysfunction (eGFR 30-59, n = 419). Primary endpoint was all-cause death. Secondary endpoints included cardiac death and major adverse cardiac and cerebrovascular events (MACCE), a composite of death, myocardial infarction, and stroke.
Results: During the median 7.6-year follow-up period, 555 (10.5%) deaths occurred. After multivariable adjustment, patients with mild and moderate renal dysfunction had significantly higher risks of all-cause death (adjusted hazard ratio [HR]: 1.36, 95% confidence interval [CI]: 1.07-1.70; adjusted HR: 2.06, 95% CI: 1.53-2.78, respectively) compared with patients with normal renal function. Patients after coronary artery bypass grafting (CABG) had a lower rate of all-cause death and MACCE than those undergoing percutaneous coronary intervention (PCI) in the normal and mild renal dysfunction group but not in the moderate renal dysfunction group. Results were similar after propensity score matching.
Conclusions: In patients with 3VD, even mild renal impairment was significantly associated with a higher risk of all-cause death. The superiority of CABG over PCI diminished in those with moderate renal dysfunction. Our study alerts clinicians to the early screening of mild renal impairment in patients with 3VD and provides real-world evidence on the optimal revascularization strategy in patients with renal impairment.
背景:关于轻度肾功能不全(eGFR 60-89 ml/min/1.73m2)对三血管冠状动脉疾病(3VD)患者的长期影响的数据有限,轻度肾功能障碍(eGFR 60-89,n=2501)和中度肾功能障碍(e GFR 30-59,n=419)。主要终点为全因死亡。次要终点包括心脏性死亡和主要不良心脑血管事件(MACCE),这是死亡、心肌梗死和中风的综合因素。结果在平均7.6年的随访期内,555例(10.5%)死亡。经过多变量调整后,与肾功能正常的患者相比,轻度和中度肾功能障碍患者的全因死亡风险显著较高(调整后的HR:1.36,95%CI 1.07-1.70;调整后的HR分别为2.06,95%CI 1.53-2.78)。在正常和轻度肾功能不全组中,冠状动脉旁路移植术(CABG)后的患者的全因死亡率和MACCE低于经皮冠状动脉介入治疗(PCI)的患者,但在中度肾功能不全组中没有。倾向评分匹配后的结果相似。结论在3VD患者中,即使是轻微的肾损伤也与更高的全因死亡风险显著相关。在中度肾功能不全患者中,冠状动脉旁路移植术优于经皮冠状动脉介入治疗。我们的研究提醒临床医生对3VD患者的轻度肾损伤进行早期筛查,并为肾损伤患者的最佳血运重建策略提供了现实世界的证据。
{"title":"Mild Renal Function Impairment and Long-Term Outcomes in Patients with Three-Vessel Coronary Artery Disease: A Cohort Study.","authors":"Guyu Zeng, Deshan Yuan, Peizhi Wang, Tianyu Li, Lin Jiang, Lianjun Xu, Jian Tian, Xueyan Zhao, Xinxing Feng, Dong Wang, Yin Zhang, Kai Sun, Jingjing Xu, Ru Liu, Bo Xu, Wei Zhao, Rutai Hui, Runlin Gao, Lei Song, Jinqing Yuan","doi":"10.1159/000534252","DOIUrl":"10.1159/000534252","url":null,"abstract":"<p><strong>Introduction: </strong>Limited data are available on the long-term impact of mild renal dysfunction (estimated glomerular filtration rate [eGFR] 60-89 mL/min/1.73 m2) in patients with three-vessel coronary disease (3VD).</p><p><strong>Methods: </strong>A total of 5,272 patients with 3VD undergoing revascularization were included and were categorized into 3 groups: normal renal function (eGFR ≥90 mL/min/1.73 m2, n = 2,352), mild renal dysfunction (eGFR 60-89, n = 2,501), and moderate renal dysfunction (eGFR 30-59, n = 419). Primary endpoint was all-cause death. Secondary endpoints included cardiac death and major adverse cardiac and cerebrovascular events (MACCE), a composite of death, myocardial infarction, and stroke.</p><p><strong>Results: </strong>During the median 7.6-year follow-up period, 555 (10.5%) deaths occurred. After multivariable adjustment, patients with mild and moderate renal dysfunction had significantly higher risks of all-cause death (adjusted hazard ratio [HR]: 1.36, 95% confidence interval [CI]: 1.07-1.70; adjusted HR: 2.06, 95% CI: 1.53-2.78, respectively) compared with patients with normal renal function. Patients after coronary artery bypass grafting (CABG) had a lower rate of all-cause death and MACCE than those undergoing percutaneous coronary intervention (PCI) in the normal and mild renal dysfunction group but not in the moderate renal dysfunction group. Results were similar after propensity score matching.</p><p><strong>Conclusions: </strong>In patients with 3VD, even mild renal impairment was significantly associated with a higher risk of all-cause death. The superiority of CABG over PCI diminished in those with moderate renal dysfunction. Our study alerts clinicians to the early screening of mild renal impairment in patients with 3VD and provides real-world evidence on the optimal revascularization strategy in patients with renal impairment.</p>","PeriodicalId":9584,"journal":{"name":"Cardiorenal Medicine","volume":" ","pages":"354-362"},"PeriodicalIF":3.8,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664319/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41192139","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Fluid overload in different acute or chronic clinical settings results in unfavorable outcomes. The use of restrictive strategies for fluid control or the use of diuretics is frequently ineffective and requires extracorporeal ultrafiltration for the removal of excess volume. These extracorporeal treatments are performed with bulky machinery and require highly specialized personnel. The creation of a miniaturized device for extracorporeal ultrafiltration (artificial diuresis) would fill the technological gap in this sector by responding to the needs of cost containment and rehabilitation of the patient. In this article, we explain the rationale that led to the design of this device.
{"title":"Rationale and Need for Simpler and Effective Miniaturized Bedside Ultrafiltration Devices.","authors":"Claudio Ronco, Alessandra Brendolan, Luca Sgarabotto","doi":"10.1159/000528684","DOIUrl":"10.1159/000528684","url":null,"abstract":"<p><p>Fluid overload in different acute or chronic clinical settings results in unfavorable outcomes. The use of restrictive strategies for fluid control or the use of diuretics is frequently ineffective and requires extracorporeal ultrafiltration for the removal of excess volume. These extracorporeal treatments are performed with bulky machinery and require highly specialized personnel. The creation of a miniaturized device for extracorporeal ultrafiltration (artificial diuresis) would fill the technological gap in this sector by responding to the needs of cost containment and rehabilitation of the patient. In this article, we explain the rationale that led to the design of this device.</p>","PeriodicalId":9584,"journal":{"name":"Cardiorenal Medicine","volume":" ","pages":"34-37"},"PeriodicalIF":3.8,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10356512","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}