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1.
G Ital Cardiol (Rome) ; 24(11): 911-914, 2023 Nov.
Article It | MEDLINE | ID: mdl-37901981

Myocardial contusion is a rare and potentially fatal complication of chest trauma. There is no unique definition for this entity: some authors define myocardial contusion as a mild increase in cardiac biomarkers in the context of chest trauma, while for others the diagnosis requires evidence of pathologic findings at cardiac imaging. Consequently, the real incidence of myocardial contusion remains unknown, varying in reports between 8% and 71%. We describe a case of cardiac contusion secondary to a low-energy blunt chest trauma, manifesting as persistent ST-elevation associated with elevation of myocardial necrosis markers, with consequent myocardial stunning of the right ventricular free wall. As there is no consensus regarding the diagnostic pathway, it is essential to integrate first-level exams (ECG and laboratory findings) with cardiac magnetic resonance imaging, to define the presence of cardiac contusion and its extent, particularly if the echocardiographic data are unconclusive.


Heart Injuries , Myocardial Contusions , Myocardial Infarction , ST Elevation Myocardial Infarction , Thoracic Injuries , Wounds, Nonpenetrating , Humans , Thoracic Injuries/complications , Wounds, Nonpenetrating/complications , Wounds, Nonpenetrating/diagnosis , Heart Injuries/diagnostic imaging , Heart Injuries/etiology , ST Elevation Myocardial Infarction/complications , Myocardial Contusions/complications , Myocardial Infarction/complications , Arrhythmias, Cardiac/diagnosis , Electrocardiography
4.
Arterioscler Thromb Vasc Biol ; 39(5): 915-924, 2019 05.
Article En | MEDLINE | ID: mdl-30894011

Objective- Aim of this study was to evaluate changes in LCAT (lecithin:cholesterol acyltransferase) concentration and activity in patients with an acute coronary syndrome, to investigate if these changes are related to the compromised capacity of HDL (high-density lipoprotein) to promote endothelial nitric oxide (NO) production, and to assess if rhLCAT (recombinant human LCAT) can rescue the defective vasoprotective HDL function. Approach and Results- Thirty ST-segment-elevation myocardial infarction (STEMI) patients were enrolled, and plasma was collected at hospital admission, 48 and 72 hours thereafter, at hospital discharge, and at 30-day follow-up. Plasma LCAT concentration and activity were measured and related to the capacity of HDL to promote NO production in cultured endothelial cells. In vitro studies were performed in which STEMI patients' plasma was added with rhLCAT and HDL vasoprotective activity assessed by measuring NO production in endothelial cells. The plasma concentration of the LCAT enzyme significantly decreases during STEMI with a parallel significant reduction in LCAT activity. HDL isolated from STEMI patients progressively lose the capacity to promote NO production by endothelial cells, and the reduction is related to decreased LCAT concentration. In vitro incubation of STEMI patients' plasma with rhLCAT restores HDL ability to promote endothelial NO production, possibly related to significant modification in HDL phospholipid classes. Conclusions- Impairment of cholesterol esterification may be a major factor in the HDL dysfunction observed during acute coronary syndrome. rhLCAT is able to restore HDL-mediated NO production in vitro, suggesting LCAT as potential therapeutic target for restoring HDL functionality in acute coronary syndrome.


Acute Coronary Syndrome/blood , Acute Coronary Syndrome/physiopathology , Lipoproteins, HDL/blood , Phosphatidylcholine-Sterol O-Acyltransferase/blood , ST Elevation Myocardial Infarction/blood , ST Elevation Myocardial Infarction/enzymology , Biomarkers/blood , Cohort Studies , Female , Humans , Male , Nitric Oxide/metabolism , Prognosis , ST Elevation Myocardial Infarction/diagnostic imaging , Sensitivity and Specificity , Sterol O-Acyltransferase/blood
5.
Am Heart J ; 204: 196-201, 2018 10.
Article En | MEDLINE | ID: mdl-30100052

Management of acute decompensated heart failure patients presenting with cardiogenic shock (CS) is not straightforward, as few data are available from clinical trials. Stabilization before left ventricle assist device (LVAD) or heart transplantation (HTx) is strongly advocated, as patients undergoing LVAD implant or HTx in critical status have worse outcomes. This was a multicenter phase II study with a Simon 2-stage design, including 24 consecutive patients treated with low-moderate epinephrine doses, whose refractory CS prompted implantation of intra-aortic balloon pump (IABP) which was subsequently upgraded with peripheral venoarterial extracorporeal membrane oxygenation. At admission, patients had severe left ventricular dysfunction and overt CS, 7 patients could be managed only with inotropic therapy, and 16 patients were transitioned to IABP and 1 to IABP and venoarterial extracorporeal membrane oxygenation; the median duration of epinephrine therapy was 7 days (interquartile range 6-15), and the median dose was 0.08 µg/kg/min (interquartile range 0.05-0.1); 21 patients (87.5%) survived at 60 days (primary outcome); among them, 13 (61.9%) underwent LVAD implantation, 2 (9.5%) underwent HTx, and 6 (28.6%) improved on medical treatment, indicating that early and intensive treatment of CS in chronic advanced heart failure patients with low-dose epinephrine and timely short-term mechanical circulatory support leads to satisfactory outcomes.


Adrenergic beta-Agonists/therapeutic use , Epinephrine/therapeutic use , Extracorporeal Membrane Oxygenation , Heart Failure/complications , Intra-Aortic Balloon Pumping , Shock, Cardiogenic/therapy , Vasoconstrictor Agents/therapeutic use , Adrenergic beta-Agonists/adverse effects , Aged , Algorithms , Combined Modality Therapy , Epinephrine/adverse effects , Female , Heart Failure/etiology , Humans , Male , Middle Aged , Prospective Studies , Shock, Cardiogenic/etiology , Treatment Outcome , Vasoconstrictor Agents/adverse effects
6.
Vasc Health Risk Manag ; 14: 109-118, 2018.
Article En | MEDLINE | ID: mdl-29881284

Reference hemoglobin (Hb) values for the definition of anemia are still largely based on the 1968 WHO Scientific Group report, which established a cutoff value of <13 g/dL for adult men and <12 g/dL for adult nonpregnant women. Subsequent studies identified different normal values according to race and age. Estimated prevalence of anemia on admission in the setting of an acute coronary syndrome (ACS) is between 10% and 43% of the patients depending upon the specific population under investigation. Furthermore, up to 57% of ACS patients may develop hospital-acquired anemia (HAA). Both anemia on admission and HAA are associated with worse short- and long-term mortality, even if different mechanisms contribute to their prognostic impact. Baseline anemia can usually be traced back to preexisting disease that should be specifically investigated and corrected whenever possible. HAA is associated with clinical characteristics, medical therapy and interventional procedures, all eliciting cardiovascular adaptive response that can potentially worsen myocardial ischemia. The intrinsic fragility of anemic patients may limit aggressive medical and interventional therapy due to an increased risk of bleeding, and could independently contribute to worse outcome. However, primary angioplasty for ST elevation ACS should not be delayed because of preexisting (and often not diagnosed) anemia; delaying revascularization to allow fast-track anemia diagnosis is usually feasible and justified in non-ST-elevation ACS. Besides identification and treatment of the underlying causes of anemia, the only readily available means to reverse anemia is red blood cell transfusion. The adequate transfusion threshold is still being debated, although solid evidence suggests reserving red blood cell transfusions for patients with Hb level <8 g/dL and considering it in selected cases with Hb levels of between 8 and 10 g/dL. No evidence supports the use of iron supplements and erythropoiesis-stimulating agents in the setting of ACS.


Acute Coronary Syndrome/blood , Anemia/blood , Hemoglobins/metabolism , Acute Coronary Syndrome/diagnosis , Acute Coronary Syndrome/mortality , Acute Coronary Syndrome/therapy , Anemia/diagnosis , Anemia/mortality , Anemia/therapy , Biomarkers/blood , Erythrocyte Transfusion , Health Status , Humans , Percutaneous Coronary Intervention , Risk Factors , Treatment Outcome
7.
Eur J Intern Med ; 51: 34-40, 2018 05.
Article En | MEDLINE | ID: mdl-29317139

BACKGROUND: Still there is conflicting evidence about gender-related differences in prognosis among patients with heart failure. This prognostic uncertainty may have implications for risk stratification and planning management strategy. The aim of the present study was to explore the association between gender and one-year mortality in patients admitted with acute decompensated heart failure (ADHF). METHODS: We studied 1513 patients. The Cumulative Incidence Function (CIF) method was used to estimate the absolute rate of mortality, heart transplantation (HT)/ventricular assist device (VAD) implantation, and survival free of HT/VAD implantation at 1year. An interaction analysis was performed to assess the association between covariates, gender, and mortality risk. Propensity score matching and Cox regression were used to compare mortality rates in the gender subgroups. RESULTS: The CIF estimates of 1-year mortality, HT/VAD implantation, and survival free of HT/VAD implantation at 1year were 33.1%, 7.0%, and 59.9% for women and 30.2%, 10.2%, and 59.6% for men, respectively. Except for diabetes, there was no significant interaction between gender, covariates, and mortality risk. In the matched cohort, the hazard ratio of death for women was 1.19 (95% confidence intervals [CIs]: 0.90-1.59; p=.202). After adjusting for age and baseline risk, the hazard ratio of death for women was 1.18 (95% CIs: 0.95-1.43; p=.127). The use of gender-specific predictive models did not allow improving the accuracy of risk prediction. CONCLUSIONS: Our data strongly suggest that women and men have comparable outcome in the year following a hospitalization for ADHF.


Heart Failure/mortality , Heart Failure/surgery , Sex Factors , Acute Disease , Age Distribution , Aged , Aged, 80 and over , Female , Heart Transplantation/statistics & numerical data , Heart-Assist Devices/statistics & numerical data , Hospitalization/statistics & numerical data , Humans , Incidence , Italy/epidemiology , Male , Middle Aged , Prognosis , Propensity Score , Proportional Hazards Models , Sex Distribution
8.
Blood Press ; 27(1): 32-40, 2018 02.
Article En | MEDLINE | ID: mdl-28922954

OBJECTIVE: The role of risk factors on the progression of arterial stiffness has not yet been extensively evaluated. The aim of the current longitudinal study was to evaluate the determinants of the PWV progression over a 4 years follow-up period in hypertensive subjects. MATERIALS AND METHODS: We enrolled 333 consecutive hypertensive outpatients 18-80 aged, followed by the Hypertension Unit of St. Gerardo Hospital (Monza, Italy). At baseline anamnestic, clinical, BP, laboratory data and cfPWV were assessed. We performed a PWV follow-up examination with a median time amounting to 3.75 ± 0.53 years. RESULTS: At baseline the mean age was 54.5 ± 12.6 years, SBP and DBP were 141.3 ± 18.6 and 86.4 ± 10.4 mmHg and PWV was 8.56 ± 1.92 m/s. Despite an improvement in BP control (from 37 to 60%), at follow-up the population showed a PWV increase (ΔPWV 0.87 ± 3.05 m/s). PWV and ΔPWV gradually increased in age decades. In patients with uncontrolled BP values at follow-up ΔPWV showed a greater increase as compared to patients with controlled BP (1.46 ± 3.67 vs 0.62 ± 2.61 m/s, p < .05). The independent predictors of ΔPWV were age, baseline PWV, baseline SBP/MBP and ΔSBP/MBP. CONCLUSIONS: the accelerated arterial aging in treated hypertensive subjects is in large measure explained by age and BP values. PWV changes over time would probably give important information that need further future research studies.


Hypertension/physiopathology , Adult , Aged , Disease Progression , Female , Follow-Up Studies , Humans , Male , Middle Aged , Pulse Wave Analysis , Risk Factors
9.
Thromb Res ; 155: 78-85, 2017 Jul.
Article En | MEDLINE | ID: mdl-28521259

BACKGROUND: Deficiency of the von Willebrand factor-cleaving protease ADAMTS13 is central to the pathophysiology of thrombotic thrombocytopenic purpura (TTP), a microangiopathic syndrome that presents as an acute medical emergency. In this review we will explore the evidence of a two-way relationship between TTP and ACS. Moreover, we will review the evidence emerged from epidemiological studies of an inverse relationship between the plasma levels of ADAMTS13 and the risk of ACS. METHODS AND RESULTS: Pubmed, MEDLINE and EMBASE, CINHAL, COCHRANE and Google Scholar databases were searched from inception to January 2017. The search yielded 43 studies representing 23 unique patient cases, 5 case series, 5 cohort studies and 10 case-control studies. Most ACS cases developing in the setting of TTP resolved with standard treatment of the underlying microangiopathy, with only a few requiring coronary invasive management. Antiplatelet therapy was not usually prescribed and all of the currently used P2Y12 were felt to be a potential trigger for a TTP-like syndrome, although our review revealed that the occurrence of TTP in patients treated with new P2Y12 antagonists is rare. Most studies confirmed the inverse association among ADAMTS13 levels and ACS. CONCLUSIONS: The heart is a definite target organ in TTP. The clinical spectrum of its involvement is probably influenced by local factors that add on to the systemic deficiency characteristic of TTP. It follows that patients with TTP should be carefully monitored for ACS events, especially when multiple risk factors for coronary disease exist.


ADAMTS13 Protein/metabolism , Acute Coronary Syndrome/etiology , Acute Coronary Syndrome/metabolism , Purpura, Thrombotic Thrombocytopenic/complications , Purpura, Thrombotic Thrombocytopenic/metabolism , von Willebrand Factor/metabolism , ADAMTS13 Protein/blood , Acute Coronary Syndrome/blood , Acute Coronary Syndrome/therapy , Coronary Vessels/metabolism , Humans , Male , Middle Aged , Platelet Aggregation Inhibitors/therapeutic use , Purinergic P2Y Receptor Antagonists/therapeutic use , Purpura, Thrombotic Thrombocytopenic/blood , Purpura, Thrombotic Thrombocytopenic/therapy
11.
Am J Cardiol ; 118(5): 771-6, 2016 09 01.
Article En | MEDLINE | ID: mdl-27392510

Radiotherapy for breast cancer may expose heart and vessels to late radiation-induced complications. Although recent technical progress in radiation therapy (RT) has been associated with drastic reduction in cardiovascular (CV) mortality, the prolonged life expectancy of patients with cancer requires CV evaluation for many years. The aim of our study was to evaluate local changes in vascular and cardiac function because of previous breast RT. We enrolled 43 patients treated with RT 15 years ago for breast cancer. CV risk factors and atherosclerotic carotid damage were investigated in all women. We divided patients into 2 groups: R (n = 25) treated to right breast and L (n = 18) to left breast. All subjects were submitted to standard echocardiography and functional arteries evaluation by carotid-radial pulse-wave velocity (crPWV; Complior) and AIx (Sphygmocor; Atcor Medical). Global mean age was 69.5 ± 8 years old. CV risk factors were equally allocated in 2 groups. No patients had history of cardiac or artery disease. R had a significantly increased crPWV (9.9 ± 1.4 vs 8.9 ± 1.1, p = 0.001) on right arm compared with left arm, and in L group, crPWV was similarly higher on the left arm than on right arm (9.6 ± 1.5 vs 8.9 ± 1.4, p = 0.011). AIx was significantly increased in the ipsilateral arm only in L (32.1 ± 7.6 vs 28.3 ± 6.8, p = 0.05). Central blood pressure estimation was not different in the right and left arms. No correlations were found with hormone therapy or chemotherapy. Our data show a local arterial stiffening because of radiation that can be involved in increased CV risk in breast cancer-treated patients.


Breast Neoplasms/radiotherapy , Carotid Arteries/diagnostic imaging , Echocardiography , Radial Artery/diagnostic imaging , Radiotherapy, Adjuvant/adverse effects , Vascular Stiffness/radiation effects , Aged , Body Mass Index , Echocardiography/methods , Female , Follow-Up Studies , Humans , Middle Aged , Risk Assessment , Risk Factors , Time Factors
12.
Am J Hypertens ; 29(2): 158-62, 2016 Feb.
Article En | MEDLINE | ID: mdl-26031304

BACKGROUND: In the last 2 decades, new drugs that oppose the effects of vascular endothelial growth factor receptor (VEGFR), and thus angiogenesis, have considerably improved treatment of solid tumors. These anti-VEGFR drugs, however, are burdened by several side effects, particularly relevant on heart and vessels. The aim of this study was to analyze the changes in cardiovascular structure and function associated with use of anti-VEGFR drugs. METHODS: Twenty-nine patients (27 affected by renal and 2 by thyroid cancer), received treatment with anti-VEGFR drugs. Brachial blood pressure (BP), central BP, carotid-femoral pulse wave velocity (cfPWV), augmentation index (Aix), and several echocardiographic markers of systolic and diastolic left ventricular functions including global longitudinal strain were measured before starting treatment (T0), after 2 (T1), and 6 weeks (T2) of treatment. RESULTS: Anti-VEGFR treatment was accompanied by a significant increase of both peripheral (systolic BP +13±15.5mm Hg, diastolic BP +7.1±9.3mm Hg, P < 0.001) and central BP (systolic BP +14±14.2mm Hg, diastolic BP +7.3±10.4mm Hg, P < 0.001) and a significant raise of cfPWV (+1.3±1.8 m/sec, P = 0.003). There was also a significant alteration of markers of diastolic and subclinical left ventricular systolic function, including global longitudinal strain (-19.9±3.8% at T0, -17.8±2.6% at T2, P < 0.05). All the changes were already evident at T1, worsened at T2 in patients who maintained oncological treatment, but disappeared at T2 in patients in whom treatment was stopped. CONCLUSIONS: All the changes regarding BP and cfPWV appear early after treatment initiation and seem to be reversible if treatment is stopped, instead diastolic and systolic left ventricular function are persistently altered by anti-VEGFR drugs.


Antineoplastic Agents/adverse effects , Arteries/drug effects , Blood Pressure/drug effects , Heart/drug effects , Receptors, Vascular Endothelial Growth Factor/antagonists & inhibitors , Aged , Carcinoma, Renal Cell/drug therapy , Female , Humans , Indazoles , Indoles/adverse effects , Kidney Neoplasms/drug therapy , Male , Middle Aged , Niacinamide/adverse effects , Niacinamide/analogs & derivatives , Phenylurea Compounds/adverse effects , Pulse Wave Analysis , Pyrimidines/adverse effects , Pyrroles/adverse effects , Sorafenib , Sulfonamides/adverse effects , Sunitinib , Thyroid Neoplasms/drug therapy , Vascular Stiffness/drug effects
14.
High Blood Press Cardiovasc Prev ; 22(4): 373-9, 2015 Dec.
Article En | MEDLINE | ID: mdl-25986075

Early vascular aging is a process characterized by a reduction in arterial elastin with an increase in collagen that has been related to cardiovascular risk factor and can determine an increased arterial stiffness and central blood pressure. It can be measured by several non invasive methods and in different arterial segment. The present paper will focus on functional (local stiffness parameter) and structural (intima media thickness) carotid arteries alterations typically evaluated by ultrasound methods. Methodological, research and clinical issue has been reviewed.


Carotid Arteries/pathology , Carotid Artery Diseases/pathology , Vascular Remodeling , Adult , Age Factors , Arterial Pressure , Carotid Arteries/diagnostic imaging , Carotid Arteries/metabolism , Carotid Arteries/physiopathology , Carotid Artery Diseases/diagnostic imaging , Carotid Artery Diseases/metabolism , Carotid Artery Diseases/physiopathology , Carotid Intima-Media Thickness , Collagen/metabolism , Elastin/metabolism , Humans , Middle Aged , Predictive Value of Tests , Vascular Stiffness , Young Adult
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