Contemporary Trends in the All-Cause Mortality of Heart Failure in Diabetic Patients Compared with Non-Diabetic Patients on Medical Management

2019 ◽  
Author(s):  
Bin Zhong ◽  
Yazhu Wang ◽  
Zhe Wang ◽  
Yingquan Chen
BMJ Open ◽  
2017 ◽  
Vol 7 (8) ◽  
pp. e016179 ◽  
Author(s):  
Chin-Sung Kuo ◽  
Yung-Tai Chen ◽  
Chien-Yi Hsu ◽  
Chun-Chin Chang ◽  
Ruey-Hsing Chou ◽  
...  

ObjectivesThe association between hepatitis B virus (HBV) infection and cardiovascular disease remains uncertain. This study explored long-term hard endpoints (ie, myocardial infarction and ischaemic stroke) and all-cause mortality in diabetic patients with chronic HBV infection in Taiwan from 2000 to 2013.DesignThis study was retrospective, longitudinal and propensity score-matched.Setting Nationwide claims data for the period 2000–2013 were retrieved from Taiwan’s National Health Insurance Research Database.ParticipantsThe study included 40 162 diabetic patients with chronic HBV infection (HBV cohort) and 40 162 propensity score-matched diabetic patients without HBV infection (control cohort). Chronic HBV infection was identified based on three or more outpatient clinic visits or one hospital admission with a diagnosis of HBV infection.Main outcome measuresPrimary outcomes were major adverse cardiovascular events (MACE, including myocardial infarction and ischaemic stroke), heart failure and all-cause mortality.ResultsDuring the median follow-up period of 5.3±3.4 years, the HBV cohort had significantly lower risks of myocardial infarction (adjusted HR (aHR)=0.49; 95% CI 0.42 to 0.56), ischaemic stroke (aHR=0.61; 95% CI 0.56 to 0.67), heart failure (aHR=0.50; 95% CI 0.43 to 0.59) and all-cause mortality (aHR=0.72; 95% CI 0.70 to 0.75) compared with the control cohort. The impact of HBV infection on the sequential risk of MACE was greater in patients with fewer diabetic complications.ConclusionsChronic HBV infection was associated with decreased risk of MACE, heart failure and all-cause mortality in patients with diabetes. Further research is needed to investigate the mechanism underlying these findings.


2019 ◽  
Vol 10 (1) ◽  
pp. 1-10 ◽  
Author(s):  
Kevin Bryan Lo ◽  
Fahad Gul ◽  
Pradhum Ram ◽  
Aaron Y. Kluger ◽  
Kristen M. Tecson ◽  
...  

Background: Previous meta-analyses demonstrated the benefits of sodium-glucose cotransporter 2 inhibitors (SGLT2i) primarily on patients with established atherosclerotic cardiovascular disease (ASCVD), but with questionable efficacy on patients at risk of ASCVD. Additionally, evidence of beneficial cardiorenal outcomes in patients with estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m2 with the CV outcomes trials remains unclear. Canagliflozin, one of the SGLT2i, has recently been studied in a large randomized controlled trial in diabetic patients with chronic kidney disease. Thus, there is a need to understand the combined outcomes on the population targeted for treatment with SGLT2i as a whole, regardless of ASCVD status. This meta-analysis will therefore assess the efficacy of SGLT2i in cardiovascular and renal outcomes in general, and in patients with eGFR under 60 mL/min/1.73 m2 in particular. Methods: We searched PubMed and Cochrane databases for randomized, placebo-controlled studies involving SGLT2i. We examined composite cardiovascular outcomes of death from cardiovascular causes, nonfatal myocardial infarctions, nonfatal stroke, and heart failure hospitalizations. Renal composite outcomes and progression of albuminuria were also analyzed. Pooled relative risks (RR) and their 95% confidence intervals (CI) were calculated using a fixed-effects model. Results: The search yielded a total of 252 articles. Four studies were ultimately included in the meta-analysis after exclusion of other irrelevant studies. The pooled RR (95% CI) for the composite cardiovascular outcome was 0.93 (0.87–0.99) with a number needed to treat (NNT) of 167 in the general study population and 0.89 (0.77–1.02) in patients with eGFR <60 mL/min/1.73 m2. The pooled RR for all-cause mortality was 0.9 (0.84–0.97) with NNT = 143. The pooled RR for death from cardiovascular causes alone was 0.89 (0.81–0.99) in the general population and 0.82 (0.62–1.07) in patients with eGFR <60 mL/min/1.73 m2. The pooled RR for heart failure hospitalizations was 0.71 (0.63–0.79) with NNT = 91. With respect to renal outcomes, the pooled RR for the composite renal outcome was 0.63 (0.56–0.71) with NNT = 67; this was true even in patients with eGFR <60 mL/min/1.73 m2 0.67 (0.59–0.76). Lastly, the pooled RR for progression of albuminuria was 0.80 (0.76–0.84). Conclusion: SGLT2i are associated with significantly lower major adverse cardiovascular events, heart failure hospitalizations, and all-cause mortality. The evidence is strongest in reducing heart failure hospitalizations. However, the evidence is weaker when it comes to the population subset with eGFR <60 mL/min/1.73 m2. SGLT2i are also associated with significantly lower adverse renal events, with these effects apparent even in the population with eGFR <60 mL/min/1.73 m2.


2020 ◽  
Vol 41 (Supplement_2) ◽  
Author(s):  
J Perea Armijo ◽  
J Lopez Aguilera ◽  
C Duran Torralba ◽  
J.C Castillo Dominguez ◽  
M Anguita Sanchez

Abstract Introduction Diabetes Mellitus (DM) is a very prevalent metabolic disease in our environment which represents a very frequent comorbidity in patients with heart failure (HF) and is associated with a poorer prognosis. Our aim is to characterize the population with HF that has DM, and to analyze its treatment and impact on the long-term prognosis in terms of mortality and hospital readmissions due to heart failure. Material and methods We selected HF cases assisted at the heart failure unit of the HURS, and classified the patients into two groups: Group 1 (without DM) and Group 2 (with DM). Clinical, echocardiographic, and treatment variables were collected, and the impact of DM and its treatment was evaluated in the long term as far as all-cause mortality and hospital readmissions due to heart failure. Results A total of 396 patients were selected, out of which 151 had DM (38.1%). The mean age of the cohort was 66±14 years, with a male predominance (66.2%). In relation to non-diabetics, Group 2 had a higher percentage of hypertension (83% vs 56%; p=0.000), hypercholesterolemia (74% vs 40%; p=0.000), ischemic etiology (48% vs 22%; p=0.000), chronic renal disease (40% vs 25%; p=0.001), anemia (35% vs 25%; p=0.037), peripheral vascular disease (38% vs 12%; p=0,000), and there was also greater use of ACEi (73% vs 62%; p=0,022) and thiazides (24% vs 9%; p=0,000). Regarding the treatment used in Group 2 for the metabolic control of hyperglycemia, a predominance of metformin (54.3%), I-SGLT2 (39.7%) and insulin (39.1%) was observed while there was a lower percentage of sulphonylureas (6%). With a mean 70±6 months of follow-up, Group 2 had a similar rate of hospital readmission for HF as non-diabetic patients (49.2% vs 52%; p=0.778). Likewise, with a mean of 58.5±7 months of follow-up, diabetic patients had a similar rate of all-cause mortality as non-diabetic patients (24% vs 22.8%; p=0.460). In relation to the use of I-SGLT2, with a mean of 116.5±7 months of follow-up, HF patients taking I-SGLT2 had a lower all-cause mortality rate than those not taking I-SGLT2 (3.8% vs 30.6%; p=0.019). In diabetic patients taking I-SGLT2, with a mean of 116.5±5 months of follow-up, they had a lower all-cause mortality rate than those not taking I-SGLT2 (3.8% vs 35.8%; p=0.002). In diabetic patients taking sulphonylureas, with a mean of 33±5 months of follow-up, they had a higher all-cause mortality rate than those not taking sulphonylureas (44.4% vs 14.8%; p=0.006). Conclusion Diabetic patients with HF have a greater number of comorbidities, although, in our series, it has not been associated with a poorer prognosis in terms of mortality or readmissions due to heart failure. Regarding the treatment used for the metabolic control of hyperglycemia, patients with HF and DM who are treated with I-SGLT2 have a lower all-cause mortality rate. However, diabetic patients with HF who were taking sulfonylureas had a poorer prognosis in terms of mortality. Kaplan-Meier Analysis Funding Acknowledgement Type of funding source: None


Author(s):  
Chintan V. Dave ◽  
Seoyoung C. Kim ◽  
Allison B. Goldfine ◽  
Robert J. Glynn ◽  
Angela Tong ◽  
...  

Background: Several glucagon-like peptide agonists (GLP-1RA) and sodium-glucose co-transporter 2 inhibitors (SGLT2i) have demonstrated cardiovascular benefit in type 2 diabetes in large randomized controlled trials in patients with established cardiovascular disease or multiple risk factors. However, few trial participants were on both agents and it remains unknown whether the addition of SGLT2i to GLP-1RA therapy has further cardiovascular benefits. Methods: Patients adding either SGLT2i or sulfonylureas to baseline GLP-1RA were identified within 3 US claims datasets (2013-2018) and were 1:1 propensity score matched (PSM) adjusting for >95 baseline covariates. The primary outcomes were 1) composite cardiovascular endpoint (CCE; comprised of myocardial infarction, stroke, and all-cause mortality) and 2) heart failure hospitalization. Adjusted hazard ratios (HR) and 95% confidence intervals (CI) were estimated in each dataset and pooled via fixed-effects meta-analysis. Results: Among 12,584 propensity-score matched pairs (mean [SD] age 58.3 [10.9] year; male (48.2%)) across the 3 datasets, there were 107 CCE events [incidence rate per 1,000 person-years (IR) = 9.9; 95% CI: 8.1, 11.9] among SGLT2i initiators compared to 129 events [IR = 13.0; 95% CI: 10.9, 15.3] among sulfonylurea initiators corresponding to an adjusted pooled HR of 0.76 (95% CI: 0.59, 0.98); this decrease in CCE was driven by numerical decreases in the risk of MI (HR 0.71, 95% CI: 0.51, 1.003) and all-cause mortality (HR 0.68, 95% CI: 0.40, 1.14) but not stroke (HR 1.05, 95% CI: 0.62, 1.79). For the outcome of heart failure hospitalization, there were 141 events [IR = 13.0; 95% CI: 11.0, 15.2] among SGLT2i initiators versus 206 [IR = 20.8; 95% CI: 18.1, 23.8] events among sulfonylurea initiators corresponding to an adjusted pooled HR of 0.65 (95% CI: 0.50, 0.82). Conclusions: Risk of residual confounding cannot be fully excluded. Individual therapeutic agents within each class may have different magnitudes of effect. In this large real-world cohort of diabetic patients already on GLP-1RA, addition of SGLT2i - compared to addition of sulfonylurea - conferred greater cardiovascular benefit. The magnitude of the cardiovascular risk reduction was comparable to the benefit seen in cardiovascular outcome trials of SGLT2i versus placebo where baseline GLP-1RA use was minimal.


2020 ◽  
Vol 41 (Supplement_2) ◽  
Author(s):  
D.N Afaga ◽  
J.C.A Esguerra ◽  
M.L.R Europa ◽  
I.T.G Cabaluna

Abstract Background Glucagon-like peptide 1 receptor agonists' (GLP-1 RA) effect on secondary prevention of MACE has yet to be investigated in diabetic patients with chronic heart failure. Purpose We aimed to determine the effectiveness of GLP-1 RA as adjunct to standard treatment among diabetic patients with chronic heart failure (LVEF &lt;50%), in preventing major adverse cardiovascular events (MACE): cardiovascular death, nonfatal myocardial infarction, and nonfatal stroke. Methods We searched for eligible trials reporting MACE, all-cause mortality, hospitalization for heart failure, improvement of LVEF and functional capacity (6-minute walk test). Fixed-effects model was used to estimate overall risk ratio for MACE, all-cause mortality and hospitalization for heart failure, while mean difference was used for estimation of improvement of LVEF and functional capacity. Review Manager 5.3 was used for analysis. Results Ten studies (56,597 patients) were included: LIVE, FIGHT, ZHANG, LEADER, ELIXA, SUSTAIN-6, PIONEER-6, EXSCEL, HARMONY, and REWIND. Addition of GLP-1 RA and Liraglutide did not significantly reduce MACE (RR 0.90, CI 95% [0.78–1.03]), (RR 0.91, CI 95% [0.69–1.20]). Moreover, Liraglutide did not significantly reduce cardiovascular death (RR 0.99, CI 95% [0.14–7.15]). No significant effect on LVEF and functional capacity was demonstrated in this study. Conclusion GLP-1 RA use in diabetic patients with chronic heart failure may have modest effect on functional capacity but did not significantly affect MACE, all-cause mortality, and LVEF. Funding Acknowledgement Type of funding source: Private hospital(s). Main funding source(s): Department of Internal Medicine, Manila Doctors Hospital


2008 ◽  
Vol 7 ◽  
pp. 19-19
Author(s):  
B PONIKOWSKA ◽  
E JANKOWSKA ◽  
K WEGRZYNOWSKATEODORCZYK ◽  
S POWIERZA ◽  
L BORODULINNADZIEJA ◽  
...  

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