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1.
G Ital Cardiol (Rome) ; 23(3): 214-216, 2022 Mar.
Article in Italian | MEDLINE | ID: mdl-35343503

ABSTRACT

We describe the case of a patient presenting with acute myocardial infarction complicated by cardiogenic shock in the setting of an unknown bioprosthetic aortic valve endocarditis and in absence of obstructive coronary artery disease. Given the angiographic finding, the most likely etiology was external compression by a perivalvular abscess, which was confirmed during autopsy. Although rare, coronary artery compression should be considered in the differential diagnosis of acute coronary syndromes complicating infective endocarditis.


Subject(s)
Endocarditis, Bacterial , Endocarditis , Heart Valve Prosthesis , Myocardial Infarction , Coronary Angiography/adverse effects , Coronary Vessels , Endocarditis/complications , Endocarditis, Bacterial/complications , Endocarditis, Bacterial/diagnosis , Heart Valve Prosthesis/adverse effects , Humans , Myocardial Infarction/complications , Myocardial Infarction/diagnosis
2.
ESC Heart Fail ; 8(6): 4955-4967, 2021 12.
Article in English | MEDLINE | ID: mdl-34533287

ABSTRACT

AIMS: We assessed the outcome of hospitalized coronavirus disease 2019 (COVID-19) patients with heart failure (HF) compared with patients with other cardiovascular disease and/or risk factors (arterial hypertension, diabetes, or dyslipidaemia). We further wanted to determine the incidence of HF events and its consequences in these patient populations. METHODS AND RESULTS: International retrospective Postgraduate Course in Heart Failure registry for patients hospitalized with COVID-19 and CArdioVascular disease and/or risk factors (arterial hypertension, diabetes, or dyslipidaemia) was performed in 28 centres from 15 countries (PCHF-COVICAV). The primary endpoint was in-hospital mortality. Of 1974 patients hospitalized with COVID-19, 1282 had cardiovascular disease and/or risk factors (median age: 72 [interquartile range: 62-81] years, 58% male), with HF being present in 256 [20%] patients. Overall in-hospital mortality was 25% (n = 323/1282 deaths). In-hospital mortality was higher in patients with a history of HF (36%, n = 92) compared with non-HF patients (23%, n = 231, odds ratio [OR] 1.93 [95% confidence interval: 1.44-2.59], P < 0.001). After adjusting, HF remained associated with in-hospital mortality (OR 1.45 [95% confidence interval: 1.01-2.06], P = 0.041). Importantly, 186 of 1282 [15%] patients had an acute HF event during hospitalization (76 [40%] with de novo HF), which was associated with higher in-hospital mortality (89 [48%] vs. 220 [23%]) than in patients without HF event (OR 3.10 [2.24-4.29], P < 0.001). CONCLUSIONS: Hospitalized COVID-19 patients with HF are at increased risk for in-hospital death. In-hospital worsening of HF or acute HF de novo are common and associated with a further increase in in-hospital mortality.


Subject(s)
COVID-19 , Heart Failure , Aged , Female , Heart Failure/epidemiology , Hospital Mortality , Humans , Male , Registries , Retrospective Studies , SARS-CoV-2
3.
Int J Cardiol ; 272: 255-259, 2018 Dec 01.
Article in English | MEDLINE | ID: mdl-30131229

ABSTRACT

BACKGROUND: Ambulatory Advanced Heart Failure (AAHF) is characterized by recurrent HF hospitalizations, escalating diuretic requirements, intolerance to neurohormonal antagonists, end-organ dysfunction, short-term reduced life expectancy despite optimal medical management (OMM). The role of intermittent inotropes in AAHF is unclear. The RELEVANT-HF registry was designed to obtain insight on the effectiveness and safety of compassionate scheduled repetitive 24-hour levosimendan infusions (LEVO) in AAHF patients. METHODS: 185 AAHF NYHA class III-IV patients, with ≥2 HF hospitalizations/emergency visits in the previous 6 months and systolic dysfunction, were treated with LEVO at tailored doses (0.05-0.2 µg/kg/min) without prior bolus every 3-4 weeks. We compared data on HF hospitalizations (percent days spent in hospital, DIH) in the 6 months before and after treatment start. RESULTS: Infusion-related adverse events occurred in 23 (12.4%) patients the commonest being ventricular arrhythmias (16, 8.6%). During follow-up, 37 patients (20%) required for clinical instability treatment adjustments (decreases in infusion dose, rate of infusion or interval). From the 6 months before to the 6 months after treatment start we found lower DIH (9.4 (8.2) % vs 2.8 (6.6) %, p < 0.0001), cumulative number (1.3 (0.6) vs 1.8 (0.8), p = 0.0001) and length of HF admissions (17.4 (15.6) vs 21.6 (13.4) days, p = 0.0001). One-year survival was 86% overall and 78% free from death/LVAD/urgent transplant. CONCLUSIONS: In AAHF patients, who remain symptomatic despite OMM, LEVO is well tolerated and associated with lower overall length of hospital stay during six months. This multicentre clinical experience underscores the need for a randomized controlled trial of LEVO impact on outcomes in AAHF patients.


Subject(s)
Ambulatory Care/trends , Cardiotonic Agents/administration & dosage , Heart Failure/diagnosis , Heart Failure/drug therapy , Aged , Cohort Studies , Drug Administration Schedule , Female , Heart Failure/physiopathology , Humans , Length of Stay/trends , Male , Middle Aged , Registries , Treatment Outcome
4.
J Interv Card Electrophysiol ; 51(3): 245-252, 2018 Apr.
Article in English | MEDLINE | ID: mdl-29502194

ABSTRACT

PURPOSE: Latency during left ventricle (LV) pacing has been suggested as a potential cause of ineffectual biventricular pacing. We assessed the incidence, predictors, and impact on outcome of increased LV latency in 274 patients undergoing cardiac resynchronization therapy (CRT). METHODS: On implantation, the latency interval was defined as the shortest stimulus-to-QRS onset interval in any lead of the 12-lead ECG. A stimulus-to-QRS onset interval ≥ 40 ms was used to define the presence of increased LV latency. RESULTS: Increased LV latency was observed in 55 patients (20%). On multivariate analysis, only ischemic etiology proved to be a predictor of increased LV latency. On 12-month echocardiographic evaluation, 68% patients showed a ≥ 15% decrease in LV end systolic volume (74% patients with increased LV latency, 67% patients without increased LV latency (p = 0.58). The presence of increased LV latency was not associated with a different clinical response to CRT. CONCLUSIONS: Increased LV latency occurred in almost 20% of patients undergoing CRT and was more frequent in patients with ischemic heart disease. The presence of increased LV latency does not seem to have an impact on echocardiographic or clinical response to CRT.


Subject(s)
Cardiac Pacing, Artificial/methods , Electrocardiography , Heart Failure/therapy , Myocardial Ischemia/therapy , Aged , Analysis of Variance , Cardiac Pacing, Artificial/mortality , Cardiac Resynchronization Therapy/methods , Cardiac Resynchronization Therapy/mortality , Cohort Studies , Echocardiography , Female , Heart Failure/diagnostic imaging , Heart Failure/mortality , Humans , Male , Middle Aged , Multivariate Analysis , Myocardial Ischemia/diagnosis , Myocardial Ischemia/mortality , Prognosis , Prospective Studies , Registries , Risk Assessment , Severity of Illness Index , Survival Rate , Treatment Outcome , Ventricular Dysfunction, Left/diagnostic imaging , Ventricular Dysfunction, Left/therapy
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