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1.
Front Cardiovasc Med ; 10: 1121083, 2023.
Article in English | MEDLINE | ID: mdl-37588035

ABSTRACT

Introduction: The role of myocardial strain in risk prediction for acute myocarditis (AMC) patients, measured by cardiac magnetic resonance (CMR), deserves further investigation. Our objective was to evaluate the association between myocardial strain measured by CMR and clinical events in AMC patients. Material and methods: This was a prospective single-center study of patients with AMC. We included 100 patients with AMC with CMR confirmation. The primary outcome was the composite of all-cause mortality, heart failure and AMC recurrence in 24 months. A subgroup analysis was performed on a sample of 36 patients who underwent a second CMR between 6 and 18 months. The association between strain measures and clinical events or an increase in left ventricular ejection fraction (LVEF) was explored using Cox regression analysis. Global peak radial, circumferential and longitudinal strain in the left and right ventricles was assessed. ROC curve analysis was performed to identify cutoff points for clinical event prediction. Results: The mean follow-up was 18.7 ± 2.3 months, and the composite primary outcome occurred in 26 patients. The median LVEF at CMR at baseline was 57.5% (14.6%). LV radial strain (HR = 0.918, 95% CI: 0.858-0.982, p = 0.012), LV circumferential strain (HR = 1.177, 95% CI: 1.046-1.325, p = 0.007) and LV longitudinal strain (HR = 1.173, 95% CI: 1.031-1.334, p = 0.015) were independently associated with clinical event occurrence. The areas under the ROC curve for clinical event prediction were 0.80, 0.79 and 0.80 for LV radial, circumferential, and longitudinal strain, respectively. LV longitudinal strain was independently correlated with prognosis (HR = 1.282, CI 95%: 1.022-1.524, p = 0.007), even when analyzed together with ejection fraction and delayed enhancement. LV and right ventricle (RV) strain were not associated with an increase in LVEF. Finally, when the initial CMR findings were compared with the follow-up CMR findings, improvements in the measures of LV and RV myocardial strain were observed. Conclusion: Measurement of myocardial strain by CMR can provide prognostic information on AMC patients. LV radial, circumferential and longitudinal strain were associated with long-term clinical events in these patients.

2.
J Card Fail ; 29(4): 463-472, 2023 04.
Article in English | MEDLINE | ID: mdl-36243338

ABSTRACT

BACKGROUND: Congestion is central to the pathophysiology of heart failure (HF); thus, tracking congestion is crucial for the management of patients with HF. In this study we aimed to compare changes in inferior vena cava diameter (IVCD) with venous pressure following manipulation of volume status during ultrafiltration in patients with cardiac dysfunction. METHODS AND RESULTS: Patients with stable hemodialysis and with systolic or diastolic dysfunction were studied. Central venous pressure (CVP) and peripheral venous pressure (PVP) were measured before and after hemodialysis. IVCD and PVP were measured simultaneously just before dialysis, 3 times during dialysis and immediately after dialysis. Changes in IVCD and PVP were compared at each timepoint with ultrafiltration volumes. We analyzed 30 hemodialysis sessions from 20 patients. PVP was validated as a surrogate for CVP. Mean ultrafiltration volume was 2102 ± 667 mL. IVCD discriminated better ultrafiltration volumes ≤ 500 mL or ≤ 750 mL than PVP (AUC 0.80 vs 0.62, and 0.80 vs 0.56, respectively; both P< 0.01). IVCD appeared to track better ultrafiltration volume (P< 0.01) and hemoconcentration (P< 0.05) than PVP. Changes in IVCD were of greater magnitude than those of PVP (average change from predialysis: -58 ± 30% vs -28 ± 21%; P< 0.001). CONCLUSIONS: In patients undergoing ultrafiltration, changes in IVCD tracked changes in volume status better than venous pressure.


Subject(s)
Heart Diseases , Heart Failure , Humans , Heart Failure/therapy , Vena Cava, Inferior/diagnostic imaging , Central Venous Pressure/physiology , Renal Dialysis , Venous Pressure
3.
Clin Res Cardiol ; 107(1): 76-86, 2018 Jan.
Article in English | MEDLINE | ID: mdl-28921054

ABSTRACT

Mineralocorticoid receptor antagonists (MRAs) constitute a beneficial therapy in chronic heart failure, but their use in the acute heart failure (AHF) setting remains rather unexplored. To assess the effect of MRAs administered during hospitalization on in-hospital outcomes of patients with AHF, we performed a post-hoc analysis of the Acute Heart Failure Global Registry of Standard Treatment (ALARM-HF). Patients of the original study cohort (n = 4953) were categorized according to in-hospital MRA treatment status as MRA-treated (n = 1439) and untreated (n = 3514) subjects. Nearest-neighbor propensity score with 1:1 matching yielded a subsample of pairs of MRA-treated and MRA-untreated patients (n = 1003 in each treatment group) that were balanced in an extensive list of baseline characteristics. In-hospital mortality between MRA-treated and untreated patients were assessed by Cox regression analysis before and after adjustment for known prognostic factors and other concomitantly administered intravenous and oral HF specific therapies. In the matched cohort, in-hospital mortality was 4.2 vs 10.8% in MRA-treated vs untreated patients. Treatment with MRAs was associated with a reduction of in-hospital mortality [HR 0.372 (95% CI, 0.261-0.532), p < 0.001]. This association remained significant after adjustment for known prognostic factors and co-administered intravenous and oral HF therapies [HR: 0.618 (95% CI, 0.383-0.995), p = 0.048]. In conclusion, MRA therapy administered during hospitalization for AHF was associated with reduced in-hospital mortality. The role of MRAs in AHF deserves further examination in adequately powered randomized controlled studies.


Subject(s)
Heart Failure/drug therapy , Mineralocorticoid Receptor Antagonists/therapeutic use , Aged , Aged, 80 and over , Australia , Chi-Square Distribution , Europe , Female , Heart Failure/diagnosis , Heart Failure/mortality , Heart Failure/physiopathology , Hospital Mortality , Humans , Male , Mexico , Middle Aged , Mineralocorticoid Receptor Antagonists/adverse effects , Multivariate Analysis , Propensity Score , Proportional Hazards Models , Recovery of Function , Registries , Retrospective Studies , Risk Factors , Stroke Volume/drug effects , Time Factors , Treatment Outcome , Ventricular Function, Left/drug effects
4.
Arq Bras Cardiol ; 90(3): 211-5, 2008 Mar.
Article in English, Portuguese | MEDLINE | ID: mdl-18392402

ABSTRACT

In countries where it is available, early levosimendan infusion can be considered for patients who remain symptomatic with dyspnea at rest despite initial therapy, particularly those with a history of chronic heart failure or chronically treated with beta-blockers. Hypotensive patients or patients with active ischemia are not the best candidates for levosimendan administration and should have these problems addressed first.


Subject(s)
Cardiotonic Agents/therapeutic use , Heart Failure/drug therapy , Hydrazones/therapeutic use , Pyridazines/therapeutic use , Vasodilator Agents/therapeutic use , Acute Disease , Adrenergic beta-Antagonists/adverse effects , Cardiotonic Agents/administration & dosage , Contraindications , Hemodynamics/drug effects , Humans , Hydrazones/administration & dosage , Hypotension/complications , Ischemia/complications , Phosphodiesterase Inhibitors/adverse effects , Pyridazines/administration & dosage , Simendan , Syndrome , Vasodilator Agents/administration & dosage
5.
Arq. bras. cardiol ; Arq. bras. cardiol;90(3): 231-235, mar. 2008. tab
Article in English, Portuguese | LILACS | ID: lil-479625

ABSTRACT

Nos países em que é comercializada, a administração precoce de levosimendana deve ser considerada em pacientes que permanecem sintomáticos e com dispnéia em repouso apesar da terapia inicial, principalmente aqueles com história de insuficiência cardíaca crônica ou em tratamento prolongado com betabloqueadores. Pacientes hipotensos ou com isquemia ativa não são os melhores candidatos para receber infusão de levosimendana e precisam, primeiro, ter esses problemas tratados.


In countries where it is available, early levosimendan infusion can be considered for patients who remain symptomatic with dyspnea at rest despite initial therapy, particularly those with a history of chronic heart failure or chronically treated with beta-blockers. Hypotensive patients or patients with active ischemia are not the best candidates for levosimendan administration and should have these problems addressed first.


Subject(s)
Humans , Cardiotonic Agents/therapeutic use , Heart Failure/drug therapy , Hydrazones/therapeutic use , Pyridazines/therapeutic use , Vasodilator Agents/therapeutic use , Acute Disease , Adrenergic beta-Antagonists/adverse effects , Cardiotonic Agents/administration & dosage , Cardiotonic Agents , Hemodynamics/drug effects , Hydrazones/administration & dosage , Hydrazones , Hypotension/complications , Ischemia/complications , Phosphodiesterase Inhibitors/adverse effects , Pyridazines/administration & dosage , Pyridazines , Syndrome , Vasodilator Agents/administration & dosage , Vasodilator Agents
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