key: cord-1023008-lstj5dkx
authors: Ng, Tien M. H.; Oh, Esther E.; Bae-Shaaw, Yuna H.; Minejima, Emi; Joyce, Geoffrey
title: Acute Bacterial Infections and Longitudinal Risk of Readmissions and Mortality in Patients Hospitalized with Heart Failure
date: 2022-01-29
journal: J Clin Med
DOI: 10.3390/jcm11030740
sha: 8b5f18e0344f0134b9cd9f29a1b1667b9a278ebe
doc_id: 1023008
cord_uid: lstj5dkx

Aims: Infections are associated with worse short-term outcomes in patients with heart failure (HF). However, acute infections may have lasting pathophysiologic effects that adversely influence HF outcomes after discharge. Our objective was to describe the impact of acute bacterial infections on longitudinal outcomes of patients hospitalized with a primary diagnosis of HF. Methods and Results: This paper is based on a retrospective cohort study of patients hospitalized with a primary diagnosis of HF with or without a secondary diagnosis of acute bacterial infection in Optum Clinformatics DataMart from 2010–2015. Primary outcomes were 30 and 180-day hospital readmissions and mortality, intensive care unit admission, length of hospital stay, and total hospital charge, compared between those with or without an acute infection. Cohorts were compared after inverse probability of treatment weighting. Multivariable logistic regression was used to examine relationship to outcomes. Of 121,783 patients hospitalized with a primary diagnosis of HF, 27,947 (23%) had a diagnosis of acute infection. After weighting, 30-day hospital readmissions [17.1% vs. 15.7%, OR 1.11 (1.07–1.15), p < 0.001] and 180-day hospital readmissions [39.6% vs. 38.7%, OR 1.04 (1.01–1.07), p = 0.006] were modestly greater in those with an acute infection versus those without. Thirty-day [5.5% vs. 4.3%, OR 1.29 (1.21–1.38), p < 0.001] and 180-day mortality [10.7% vs. 9.4%, OR 1.16 (1.11–1.22), p < 0.001], length of stay (7.1 ± 7.0 days vs. 5.7 ± 5.8 days, p < 0.001), and total hospital charges (USD 62,200 ± 770 vs. USD 51,100 ± 436, p < 0.001) were higher in patients with an infection. Conclusions: The development of an acute bacterial infection in patients hospitalized for HF was associated with an increase in morbidity and mortality after discharge.

Heart failure (HF) remains a substantial health care challenge, with the majority of costs due to direct medical expenditure, specifically hospitalizations. Despite efforts and legislation aimed at optimizing guideline-directed in-hospital medical therapies and improving transitions of care, 30-day readmission rates remain as high as 50%, with half due to non-cardiovascular conditions [1, 2] . Three-quarters of these early readmissions are considered preventable, including non-adherence to diet and medical regimens, and poor control of comorbidities [3] . Thus, investigation of factors that result in high readmission rates carry paramount clinical and economic significance. The presence of infections in hospitalized patients portends poorer short-term in-hospital outcomes. The association between acute infections, the development of acute coronary syndromes, and increased morbidity and mortality from cardiovascular causes is also recognized [4, 5] . However, little is known about the influence of acute bacterial infections on long-term outcomes of patients with HF, despite there being clear links to pathophysiologic processes that could worsen the progression of HF [6] [7] [8] . This is especially pertinent in the times of the COVID-19 pandemic and research suggesting potential long-lasting effects on cardiac function. A recent longitudinal analysis of patients with new-onset HF identified infections and respiratory conditions as the two most important causes of non-cardiovascular mortality in these individuals [9] . Patients with HF are at increased risk for infection-related admissions and 30-day mortality compared to patients without HF [10] [11] [12] , with infections commonly the direct cause of death [13] . However, after discharge, the impact of acute infections and their management on the clinical and economic outcomes of patients hospitalized primarily for HF has not been systematically assessed. In addition, the characterization of the type of infections that affect patients hospitalized for HF is limited. Describing the epidemiology of infectious complications, especially bacterial infections, and their impact on outcomes is important to understanding how this comorbidity could be targeted to further improve HF outcomes [14] . This study aims to describe the epidemiology of acute infections, specifically bacterial pathogens, as these represent the most common etiology for infected patients hospitalized for HF [15, 16] , and to evaluate their associations to longitudinal HF outcomes.

This retrospective cohort study utilized pre-existing de-identified data on adult patients ≥ 18 years enrolled in the Optum Clinformatics DataMart, which covers 14 million privately insured and Medicare Advantage beneficiaries, from 1 January 2010 to 30 June 2015. The de-identified Clinformatics ® Data Mart (OptumInsight, Eden Prairie, MN, USA) is a large-scale dataset of patients with both medical and pharmacy coverage from a large commercial insurer in the United States. All adult patients hospitalized with a primary diagnosis of HF with or without a secondary diagnosis of an acute bacterial infection during the study period were included in the analysis. All diagnoses were identified by ICD-9 codes (see Appendices A and B). Patients were excluded if they were <18 years of age, pregnant, incarcerated, had <6 months of follow-up data after index hospital admission, or had infection listed as the primary diagnosis. Patients were categorized into two separate cohorts for comparison: (1) hospitalized patients with HF with a secondary diagnosis of acute infection, and (2) hospitalized patients with HF without an acute infection diagnosis. Patient data were analyzed from index hospitalization to 6 months after discharge. The study was approved by the institutional review board of the University of Southern California (HS-18-00104).

The main outcomes of interest were 30-and 180-day hospital readmissions and mortality (after discharge), length of hospital stay, admission to the intensive care unit (ICU), and total hospital charges. In addition, the types of acute infections and etiology of hospital readmissions (primary diagnosis listed for hospital re-admission) were ascertained.

Enrollment data on patient demographics (age, gender, marital status) were linked to longitudinal claims capturing admission and discharge dates, discharge to long-term care (LTC), diagnosis of HF (Appendix A), type of acute infection (Appendix B), prescription medications 90 days before and after index hospitalization according to generic drug name, Elixhauser Comorbidity Index, and chronic comorbid diagnoses. The primary diagnoses during hospital readmissions were also obtained.

As a reflection of the large sample size, at baseline, almost all patient characteristics were statistically significantly different between the cohorts of patients with HF with or without infection. To minimize the effect of these competing differences on the influence of the presence of infection, inverse probability of treatment weighting (IPTW) was applied. The sample with IPTW was weighed to adjust for the propensity score, removing the bias associated with differences in the observed covariates in two groups [17] . The propensity score for infection was estimated using logistic regression with relevant covariates (age, gender, discharge to LTC, Elixhauser Comorbidity Index, and comorbidity). The propensity score (p) was then used to weigh the observations in each comparison group so that the patients with infection were given weight of 1/p and the patients without infection were given weight of 1/(1 − p). Elixhauser Comorbidity Index is a well-validated scoring system to characterize the risk of in-hospital mortality using 31 comorbid conditions and a scoring system of −7 to +12, with higher score indicating greater risk of mortality [18] . The primary and secondary outcomes were measured as both categorical variables (frequencies with percentages) and continuous variables [means with standard deviations (SD)]. Continuous and categorical variables were compared between the two cohorts using the Student's t-test and the chi-squared test, respectively. Multivariable logistic regression was used after the weighting adjustment. A p-value of <0.05 was considered statistically significant and 95% confidence intervals were reported for all odds ratios. Statistical analyses were performed using SAS, version 9.4 (SAS Institute, Cary, NC, USA).

A secondary exploratory analysis was also conducted to determine whether any patient characteristics could independently predict increased risk for acute infections. All subjects in the original non-matched cohort were included. Independent variables evaluated using univariable logistic regression with significance level p-value of 0.1 were age, gender, Elixhauser Comorbidity Index, and comorbid conditions (including diabetes mellitus, hypertension, ischemic heart disease, acute or chronic renal failure, obesity, and anemia), cigarette smoking, and statin therapy within 120 days prior to hospitalization. These variables were selected based on available evidence suggesting association with HF outcomes and the hypothetical obtainability of information from the database. Based on the univariable regression results, age, gender, acute renal failure, ischemic heart disease, Elixhauser Comorbidity Index, anemia, obesity, statin therapy prior to hospitalization, and cigarette smoking were further evaluated using a multivariable logistic regression model. The variables were entered in a stepwise manner. Odds ratio and 95% confidence interval (CI) were estimated for the 8 predictive variables in the final model with respect to the event of acute infection during hospitalization.

A total of 121,882 patients had an index hospitalization with a primary diagnosis of HF. After excluding 99 patients, due to exclusion criteria or missing data, and weighing (IPTW), 27,912 patients (23%) with HF as a primary diagnosis also had an acute infection secondary diagnosis, while 93,855 patients (77%) did not. A CONSORT diagram illustrates who was included and excluded in Supplemental Figure S1 . Baseline characteristics before and after IPTW are reported in Table 1 . The mean age of weighted cohorts was 74.5 years, 50% female, 22% discharged to LTC, and mean Elixhauser Comorbidity Index was 4.2. For cardiac comorbidities, 80% had hypertension, 56% had dyslipidemia, 24% had coronary artery disease, and 45% had arrhythmias (any arrhythmia history), whereas for non-cardiac comorbid conditions, 45% had diabetes, 38% had respiratory disorder, and 37% had anemia. ACE inhibitor = angiotensin converting enzyme inhibitor, ARB = angiotensin receptor blocker, HF = heart failure, LTC = long-term care facility, MRA = mineralocorticoid receptor antagonist, SD = standard deviation.

The major acute infections as secondary diagnoses in patients with HF were commonly identified as pneumonia (60.7%), urinary tract infection (29.9%), or cellulitis (8.7%), while the incidence of sepsis (1.0%) and septic shock (0.7%) was uncommon. Acute infections by type are outlined in Table 2 . Table 3 . The inclusion of variables for state-level education and median household income did not substantially change the ORs related to re-hospitalizations and mortality from the original model. Since pneumonia and urinary tract infections comprised the majority of the infections, we repeated the outcomes analyses based on these subgroups. When infection was limited to pneumonia, all clinical outcomes remained significantly greater in patients with HF and pneumonia compared to those without infection, except for 180-day readmissions. When infection was limited to urinary tract infection, all clinical outcomes remained greater as well, although the need for ICU admission was not different. Subgroup results are provided in Supplemental Table S1 .

Patients with HF and an acute infection were more likely to be admitted to an ICU compared to those without an acute infection [37.1% vs. 33.8%, OR 1.16 (1.13-1.19), p < 0.001]. The length of hospital stay was longer in those with an acute infection, with an absolute difference of 1.4 hospital days. Total hospital charge was also greater in those with an acute infection (USD 62,200 ± 770 vs. 51,100 ± 436, p < 0.001), an absolute cost difference of about USD 11,000. For patients readmitted within 30 days, the most frequent primary diagnoses were HF, infection, and acute kidney failure for both cohorts, although numeric differences in the absolute frequency of each diagnosis existed. The ten most frequent primary diagnoses for 30-day readmissions are outlined in Table 4 . For the exploratory predictors of infection analysis using the unweighted data, patients with HF who developed acute infections were more likely to be older in age (mean 76.7 y vs. 73.8 y), female (57% vs. 47%), have acute renal failure (34.9% vs. 29.5%), and have anemia (40.1% vs. 35.6%) (p < 0.0001). Upon multivariable analysis, the significant predictors for increased risk of infection were female gender and acute renal failure, while a history of ischemic heart disease, obesity, and statin therapy was associated with a lower risk of infection. Predictors for acute infection are presented in Supplemental Table S2 .

Modifiable comorbid conditions are recognized as significant predictors of outcomes in patients with HF; however, there are limited data related to longitudinal influence of acute infections. This study examined the morbidity and mortality after discharge in patients hospitalized with a primary diagnosis of HF who were also diagnosed with an acute bacterial infection using data from a large national claims database. In the current study, 23% of patients hospitalized primarily for HF developed an acute bacterial infection. The development of an acute infection was associated with an elevated risk for poor clinical and economic outcomes. After propensity matching with IPTW to balance the groups, the odds of 30-day re-hospitalization and 30-day mortality were 10% and 30% higher, respectively, compared to patients who did not develop an acute infection. The increased risk was sustained to 180 days, although slightly attenuated. The development of an acute infection was also associated with a higher proportion of ICU utilization, an increase in mean hospital length of stay by 1.4 days, and higher total hospital charges.

This study represents the largest examination of the prevalence and impact of acute infections in a large U.S. population with a primary admission diagnosis of HF. A previous study in Israel including over 9000 older adults with HF reported 38% of all hospital admissions during a 9-year study period were due to infections [10] . Patients with infectionrelated hospital admissions had an increase in 6-month and annual readmission rates as well as 30-day and 1-year mortality compared to non-infected patients [10] . A singlecenter study of 260 patients at a tertiary university hospital in Brazil found that 45.8% of patients developed an acute infection during HF hospitalization, which was associated with increased in-hospital mortality (26.9% vs. 17%, p = 0.05), but a decrease in mortality after discharge (11.5% vs. 22%, p = 0.046) [19] . However, confounding risk factors for increased in-hospital mortality, such as renal failure, were not accounted for, and it was unknown when mortality after discharge occurred. A recent prospective cohort study of 711 patients with HF in the United Kingdom (UK) identified infection as the cause for readmission in 25% of cases, along with worse survival post discharge [11] . Importantly, cardiovascular causes still accounted for a larger percentage of readmissions (39% overall with 14% due to acute decompensated heart failure) which is in agreement with our results. Infectionrelated re-hospitalizations were also found in another prospective cohort to independently predict poorer survival [12] .

In the current study, an overall 30-day hospital readmission rate of approximately 17% was observed, which is slightly less than the estimated 20-25% risk of hospital readmission reported in patients with generalized HF [20] [21] [22] . The observed 30-day mortality rate was 5.5% in our cohort with HF and acute infection and 4.3% in those without infection, which is consistent with prior studies that report a 30-day mortality range of 2-20% [10] . There appeared to be an attenuation of re-hospitalization risk with infection based on the 180-day hospitalization odds ratios. This likely reflects other factors which contribute to the outcomes of patients at 180 days, possibly diluting the observed effect or association of the acute infection to 30-day outcomes. In a recent post hoc analysis utilizing clinical trial data of patients with HF, the cumulative incidence of clinical outcomes after hospitalization for pneumonia also attenuated over time [23] .

The results have potentially important clinical and policy implications. It has been suggested that 75% of early readmissions are largely preventable and, thus, an area of focus by the U.S. Center for Medicare and Medicaid Services in reducing the national burden of HF costs [1] . Thirty-day performance measures are closely monitored in the U.S., as outcomes during this timeframe are thought to reflect in-hospital HF treatment and adequate transitions of care [1] . Our results indicate that hospitalized patients with HF who experience a complication of acute infection had increased risk of 30-day readmissions and mortality, suggesting that procedures and pathways to optimize infection outcomes should be applied specifically to HF. A recent longitudinal analysis of 86,000 individuals with incident HF also specifically identified infections as an important opportunity to positively impact HF prognosis [9] . The prevention of hospital-acquired infections, early detection of infection using procalcitonin, early initiation of optimal antibiotics, and adequate duration of therapy may prevent and reduce risk of hospital readmissions in patients with HF [14, 16, 24, 25] . The data for procalcitonin for guiding antibiotic decision making remains mixed, but has been more consistently shown to aid in antibiotic de-escalation or discontinuation [26, 27] . In the HF population, a procalcitonin-guided approach to early antibiotic initiation failed to improve outcomes in a multicenter study [28] ; however, it may be useful in conjunction with other signs and symptoms of inflammation from infection. In a large multi-center U.S. registry study of adults 65 years and older, in-hospital worsening of HF was directly associated with increased mortality, hospital readmissions, and Medicare payments at 30 days [22] . Improving the quality of care during hospitalizations remains an important aspect of HF management and may reduce costs arising from future readmissions.

The association between acute infections and poorer outcomes is plausible, both clinically and pathophysiologically. In our analysis of predictors of acute infections, older age, female gender, acute renal failure, and anemia were all associated with increased risk. Renal failure and anemia are well recognized for their association to poorer prognosis in HF [22, 29, 30] , and thus it could be hypothesized that the link between infections and worse outcomes is an epiphenomenon. However, the lack of predictive value of the Elixhauser comorbidity score for infection and the IPTW analysis that eliminated baseline differences in these covariates support the independent risks associated with acute infection. Pathophysiologically, infections and HF share at least two common pathways-inflammation and neurohormonal activation [31, 32] . Severe infections that require hospitalization have been identified as a potential trigger of the inflammatory process and a risk factor for coronary artery disease. In addition, the risk of subsequent and delayed cardiovascular disease is reported to be six-fold during the first year after infection [33, 34] . Recently, a 13-year study looking at 1.2 million patients admitted to UK hospitals reported that patients with a prior infection had higher incidence of ischemic heart disease and stroke, which was associated with significantly higher mortality than the general population [35] . This suggests that infections cause local and systemic inflammation and have procoagulant properties that can contribute to the cardiovascular disease process. Infection-induced inflammation may also impair inotropy and contribute to adverse cardiac remodeling, negatively influencing patients with HF [36] [37] [38] . Inflammation and immune system function are also closely tied to activation of the sympathetic nervous system, and the counter-regulation of these systems may be an important mechanism of worse prognosis in patients with HF who develop infections [31, 39] . Our findings of an inverse association between history of ischemic heart disease, obesity, and statin use to risk of infection was not expected. However, one potential explanation is that our analysis first captured re-hospitalization and, since the more common reason for hospitalization in these patients was cardiovascular and not infectious, it may appear as an observed "protective" association. Two recent analyses examining reasons for hospitalizations post-myocardial infarction also found that the majority were cardiac [40, 41] . Statins, which exert anti-inflammatory and possible immunomodulatory effects, may lower the risk of infections although it remains an area of controversy [42] [43] [44] .

Literature characterizing infections in patients with HF is emerging. The current study reflects a large national diverse population, and the most common acute infections in patients hospitalized with HF were pneumonia and urinary tract infections. Both of these infection subgroups had an increase in 30-day mortality and hospital readmissions. These findings are consistent with results from a large UK database study where respiratory and urinary tract infections were independently associated with an increase in myocardial infarction and stroke during the 3-day post-infectious period [45] . Respiratory infections in particular have also been independently associated with higher in-hospital mortality in patients with HF and mentioned in large registries and observational cohort studies as the most common type of infection in hospitalized HF patients [12, 36, 46, 47] . Another study found that 52.6% of patients hospitalized with HF developed a lower respiratory tract infection and 15.7% developed a urinary tract infection, further supporting these infections as an important area for future research [10] .

Data describing specific prevention methods of hospital-acquired infections in the HF population is lacking. However, general recommendations to minimize infection risk for the most common hospital-acquired infections are likely applicable to the patient hospitalized for HF. This includes optimal management of comorbidities, eliminating catheters or lines as soon as possible, appropriate ventilator care for intubated patients, discontinuing unnecessary stress-ulcer prophylaxis and antibiotics to prevent Clostridium difficile infection, appropriate hand hygiene and patient isolation precautions, and ensuring that vaccinations are up to date.

There are several limitations to our study that deserve mention. First, inherent limitations of utilizing coded data for diagnoses are well described and apply to our analyses. However, the database has been used for similar type of epidemiologic studies that have been well validated. In retrospect, some ICD-9 subcodes that could indicate bacterial infections were omitted from the original analysis. When outcomes were re-analyzed using a revised ICD-9 code set which expanded potential capture of intestinal infections (008.x), pneumonia (482.x), more specific codes for septicemia from only bacterial organisms (038.x), unspecified site bacterial infections (041.x), meningitis (320.x), bacterial endocarditis (421.x), peritonitis (567.x), liver abscess (572.x), and some others, the odds ratios were similar, confirming the association of increased risk. Importantly, all these broad infection sources were included in the original set of ICD-9 codes. Due to the lack of availability of in-hospital data, medication use at the time of admission and discharge was estimated by evaluating prescription charges 90 days before and after the index hospitalization. Lastly, the Optum Clinformatics database has limited patient-level clinical data, so we were unable to identify specific HF characteristics and biomarkers (e.g., left ventricular ejection fraction, blood pressure, laboratory values, etc.) with prognostic importance to further risk-stratify and control these differences in our analyses.

Further study is needed to continue to advance our understanding of how infections intersect with HF outcomes. Since we did not evaluate non-bacterial acute infections (i.e., fungal or viral infections), it would be valuable to determine specific pathogens that are more commonly seen in patients hospitalized with HF. This could potentially further validate studies that support regular use of influenza and pneumococcal vaccinations in patients with HF, since this is a seemingly cost-effective intervention that could improve quality of life and clinical outcomes [36, 48] . Lastly, the establishment of acute infections as a modifiable risk factor for HF outcomes would support the added value of adequate antimicrobial management and provide a basis for future studies to evaluate the impact of these interventions on HF outcomes.

In conclusion, acute bacterial infections are a common occurrence in patients hospitalized with HF and are associated with an increase in longitudinal hospital readmissions and mortality after discharge. Patients hospitalized with HF who develop an infection also have increased hospital length of stay and total hospital charge.

Supplementary Materials: The following supporting information can be downloaded at: https: //www.mdpi.com/article/10.3390/jcm11030740/s1, Figure S1 . Assessment for Study Eligibility: Diagram of eligibility criteria for inclusion into (A) heart failure with infection or (B) heart failure without infection cohorts. 

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