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1.
J Am Heart Assoc ; 9(4): e014254, 2020 02 18.
Article in English | MEDLINE | ID: mdl-32067585

ABSTRACT

Background Intravenous ferric carboxymaltose (FCM) improves symptoms, functional capacity, and quality of life in heart failure and iron deficiency. The mechanisms underlying these effects are not fully understood. The aim of this study was to examine changes in myocardial iron content after FCM administration in patients with heart failure and iron deficiency using cardiac magnetic resonance. Methods and Results Fifty-three stable heart failure and iron deficiency patients were randomly assigned 1:1 to receive intravenous FCM or placebo in a multicenter, double-blind study. T2* and T1 mapping cardiac magnetic resonance sequences, noninvasive surrogates of intramyocardial iron, were evaluated before and 7 and 30 days after randomization using linear mixed regression analysis. Results are presented as least-square means with 95% CI. The primary end point was the change in T2* and T1 mapping at 7 and 30 days. Median age was 73 (65-78) years, with N-terminal pro-B-type natriuretic peptide, ferritin, and transferrin saturation medians of 1690 pg/mL (1010-2828), 63 ng/mL (22-114), and 15.7% (11.0-19.2), respectively. Baseline T2* and T1 mapping values did not significantly differ across treatment arms. On day 7, both T2* and T1 mapping (ms) were significantly lower in the FCM arm (36.6 [34.6-38.7] versus 40 [38-42.1], P=0.025; 1061 [1051-1072] versus 1085 [1074-1095], P=0.001, respectively). A similar reduction was found at 30 days for T2* (36.3 [34.1-38.5] versus 41.1 [38.9-43.4], P=0.003), but not for T1 mapping (1075 [1065-1085] versus 1079 [1069-1089], P=0.577). Conclusions In patients with heart failure and iron deficiency, FCM administration was associated with changes in the T2* and T1 mapping cardiac magnetic resonance sequences, indicative of myocardial iron repletion. Clinical Trial Registration URL: http://www.clinicaltrials.gov. Unique identifier: NCT03398681.


Subject(s)
Anemia, Iron-Deficiency/drug therapy , Ferric Compounds/administration & dosage , Heart Failure/diagnostic imaging , Iron/metabolism , Magnetic Resonance Imaging , Maltose/analogs & derivatives , Myocardium/metabolism , Administration, Intravenous , Aged , Anemia, Iron-Deficiency/complications , Anemia, Iron-Deficiency/diagnostic imaging , Double-Blind Method , Female , Heart Failure/complications , Heart Failure/metabolism , Hematinics/administration & dosage , Humans , Male , Maltose/administration & dosage , Middle Aged
2.
Rev Port Cardiol (Engl Ed) ; 37(8): 717.e1-717.e5, 2018 Aug.
Article in English, Portuguese | MEDLINE | ID: mdl-29934214

ABSTRACT

Prosthetic valve endocarditis is a major diagnostic challenge in clinical practice, due to the lower sensitivity of the modified Duke criteria and a higher percentage of cases with negative or inconclusive echocardiography results. The delay in establishing medical and surgical treatment increases the morbidity/mortality rate. New imaging techniques and 18F-FDG PET/CT in particular have meant a significant advance in cases of high clinical suspicion and negative or inconclusive echocardiography, increasing the overall sensitivity of the modified Duke criteria. We report the case of a male patient with prosthetic valve endocarditis, where 18F-FDG PET/CT provided the diagnostic key, determining the origin of the endocarditis and avoiding treatment delay.


Subject(s)
Endocarditis, Bacterial/diagnostic imaging , Fluorodeoxyglucose F18 , Heart Valve Prosthesis , Positron Emission Tomography Computed Tomography , Prosthesis-Related Infections/diagnostic imaging , Radiopharmaceuticals , Staphylococcal Infections/diagnostic imaging , Staphylococcus aureus , Endocarditis, Bacterial/etiology , Heart Valve Prosthesis/adverse effects , Humans , Male , Middle Aged , Prosthesis-Related Infections/etiology , Staphylococcal Infections/etiology
3.
Clin Cardiol ; 41(6): 729-735, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29607528

ABSTRACT

Treatment with intravenous ferric carboxymaltose (FCM) has been shown to improve symptoms, functional capacity, and quality of life in patients with heart failure and iron deficiency. However, the underlying mechanisms for these beneficial effects remain undetermined. The aim of this study is to quantify cardiac magnetic resonance changes in myocardial iron content after administration of intravenous FCM in patients with heart failure and iron deficiency and contrast them with parameters of heart failure severity. This is a multicenter, double-blind, randomized study. Fifty patients with stable symptomatic heart failure, left ventricular ejection fraction <50%, and iron deficiency will be randomly assigned 1:1 to receive intravenous FCM or placebo. Intramyocardial iron will be evaluated by T2* and T1 mapping cardiac magnetic resonance sequences before and at 7 and 30 days after FCM. After 30 days, patients assigned to placebo will receive intravenous FCM in case of persistent iron deficiency. The main endpoint will be changes from baseline in myocardial iron content at 7 and 30 days. Secondary endpoints will include the correlation of these changes with left ventricular ejection fraction, functional capacity, quality of life, and cardiac biomarkers. The results of this study will add important knowledge about the effects of intravenous FCM on myocardial tissue and cardiac function. We hypothesize that short-term (7 and 30 days) myocardial iron content changes after intravenous FCM, evaluated by cardiac magnetic resonance, will correlate with simultaneous changes in parameters of heart failure severity. The study is registered at http://www.clinicaltrials.gov (NCT03398681).


Subject(s)
Anemia, Iron-Deficiency/drug therapy , Ferric Compounds/administration & dosage , Heart Failure/drug therapy , Hematinics/administration & dosage , Maltose/analogs & derivatives , Myocardium/metabolism , Aged , Anemia, Iron-Deficiency/blood , Anemia, Iron-Deficiency/diagnosis , Anemia, Iron-Deficiency/physiopathology , Clinical Protocols , Double-Blind Method , Female , Ferric Compounds/adverse effects , Ferric Compounds/metabolism , Heart Failure/blood , Heart Failure/diagnostic imaging , Heart Failure/physiopathology , Hematinics/adverse effects , Hematinics/metabolism , Humans , Infusions, Intravenous , Magnetic Resonance Imaging, Cine , Male , Maltose/administration & dosage , Maltose/adverse effects , Maltose/metabolism , Quality of Life , Recovery of Function , Research Design , Severity of Illness Index , Spain , Stroke Volume , Time Factors , Treatment Outcome , Ventricular Function, Left
4.
Article in English | MEDLINE | ID: mdl-29165095

ABSTRACT

BACKGROUND: People with schizophrenia and other severe mental disorders have an increased mortality mainly attributed to natural causes, specifically cardiovascular disease and cancer. The metabolic syndrome and the Framingham Risk Score are epidemiologic tools related to long-term cardiovascular disease risk and they are increased in people with severe mental disorders. This increase has been attributed both to the disorder itself and to the use of antipsychotic drugs. OBJECTIVE: To quantify the cardiovascular risk in a group of people treated with long-acting injectable antipsychotics. METHODS: This is a cross-sectional study developed in an outpatient mental health clinic in which the prevalence of metabolic syndrome was estimated and the cardiovascular risk was measured using the Framingham Risk Score. All the analyses were separated by gender. RESULTS: 130 people (81 men) were recruited. According to the International Diabetes Federation criteria, 60 participants (46,2%) had metabolic syndrome. The individual criterion most often met in both genders was obesity. The mean Framingham Risk Score for the sample was moderate, 7,7 (SD: 6,3). For women, the risk was lower (mean 5,7, SD: 4,9) than for men (mean=9, SD: 6,7). There were no significant differences in the prevalence of metabolic syndrome and Framingham Risk Scores by longacting injectable antipsychotic or years of treatment. CONCLUSION: The prevalence of metabolic syndrome and the cardiovascular risk are high in people with psychosis treated with long acting injectable antipsychotics. To better address this vulnerability, the recommendations involve both behavioral and pharmacological interventions.


Subject(s)
Antipsychotic Agents/adverse effects , Cardiovascular Diseases/epidemiology , Mental Disorders/drug therapy , Metabolic Syndrome/epidemiology , Adult , Aged , Antipsychotic Agents/administration & dosage , Cardiovascular Diseases/chemically induced , Cardiovascular Diseases/mortality , Cost of Illness , Cross-Sectional Studies , Delayed-Action Preparations , Female , Habits , Health Behavior , Health Status , Humans , Injections , Life Style , Male , Mental Disorders/epidemiology , Mental Disorders/psychology , Metabolic Syndrome/chemically induced , Metabolic Syndrome/mortality , Middle Aged , Prevalence , Risk Assessment , Risk Factors , Severity of Illness Index , Spain/epidemiology , Young Adult
5.
JACC Heart Fail ; 4(11): 833-843, 2016 11.
Article in English | MEDLINE | ID: mdl-27522630

ABSTRACT

OBJECTIVES: This study sought to evaluate the prognostic effect of carbohydrate antigen-125 (CA125)-guided therapy (CA125 strategy) versus standard of care (SOC) after a hospitalization for acute heart failure (AHF). BACKGROUND: CA125 has emerged as a surrogate of fluid overload and inflammatory status in AHF. After an episode of AHF admission, elevated values of this marker at baseline as well as its longitudinal profile relate to adverse outcomes, making it a potential tool for treatment guiding. METHODS: In a prospective multicenter randomized trial, 380 patients discharged for AHF and high CA125 were randomly assigned to the CA125 strategy (n = 187) or SOC (n = 193). The aim in the CA125 strategy was to reduce CA125 to ≤35 U/ml by up or down diuretic dose, enforcing the use of statins, and tightening patient monitoring. The primary endpoint was 1-year composite of death or AHF readmission. Treatment strategies were compared as a time to first event and longitudinally. RESULTS: Patients allocated to the CA125 strategy were more frequently visited, and treated with ambulatory intravenous loop diuretics and statins. Likewise, doses of oral loop diuretics and aldosterone receptor blockers were more frequently modified. The CA125 strategy resulted in a significant reduction of the primary endpoint, whether evaluated as time to first event (66 events vs. 84 events; p = 0.017) or as recurrent events (85 events vs. 165 events; incidence rate ratio: 0.49; 95% confidence interval: 0.28 to 0.82; p = 0.008). The effect was driven by significantly reducing rehospitalizations but not mortality. CONCLUSIONS: The CA125 strategy was superior to the SOC in terms of reducing the risk of the composite of 1-year death or AHF readmission. This effect was mainly driven by significantly reducing the rate of rehospitalizations. (Carbohydrate Antigen-125-guided Therapy in Heart Failure [CHANCE-HF]; NCT02008110).


Subject(s)
CA-125 Antigen/blood , Heart Failure/therapy , Acute Disease , Adrenergic beta-Antagonists/therapeutic use , Aged , Aged, 80 and over , Angiotensin Receptor Antagonists/therapeutic use , Angiotensin-Converting Enzyme Inhibitors/therapeutic use , Benzazepines/therapeutic use , Cardiac Pacing, Artificial , Cardiovascular Agents/therapeutic use , Cause of Death , Defibrillators, Implantable , Female , Heart Failure/blood , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Ivabradine , Male , Middle Aged , Mineralocorticoid Receptor Antagonists/therapeutic use , Monitoring, Physiologic , Mortality , Myocardial Revascularization , Natriuretic Peptide, Brain/blood , Patient Care Planning , Patient Readmission , Peptide Fragments/blood , Sodium Potassium Chloride Symporter Inhibitors/therapeutic use , Spain , Treatment Outcome
8.
Rev. esp. cardiol. (Ed. impr.) ; 68(2): 121-128, feb. 2015. tab
Article in Spanish | IBECS | ID: ibc-132555

ABSTRACT

Introducción y objetivos La morbilidad y la mortalidad después de un ingreso por insuficiencia cardiaca aguda siguen siendo extremadamente elevadas. En este contexto, se ha demostrado que las concentraciones plasmáticas del antígeno carbohidrato 125 muestran correlación con la gravedad de la sobrecarga hídrica y el riesgo de muerte y reingreso. Los datos preliminares indican un posible papel del antígeno carbohidrato 125 como guía para el tratamiento. El objetivo de este estudio es evaluar el efecto pronóstico de una estrategia de tratamiento guiada por el antígeno carbohidrato 125 comparada con el tratamiento estándar en pacientes dados de alta recientemente tras un ingreso por insuficiencia cardiaca aguda. Métodos Ensayo clínico multicéntrico, aleatorizado y a ciego simple, de evaluación de la eficacia en pacientes recientemente dados de alta tras una insuficiencia cardiaca aguda (< 180 días), en clase funcional II-IV de la New York Heart Association y con antígeno carbohidrato 125 > 35 U/ml. Se utilizó un esquema de aleatorización para asignar a los participantes (en relación 1:1) a tratamiento guiado por el antígeno carbohidrato 125 (destinado a mantener valores normales) o tratamiento estándar. El tratamiento guiado se centra principalmente en la frecuencia de monitorización y ajuste de dosis de los tratamientos descongestivos y las estatinas. Hasta el 10 de diciembre de 2013, se había incluido en el estudio a 383 pacientes. El objetivo principal era la combinación de mortalidad por cualquier causa o rehospitalización por insuficiencia cardiaca aguda a 1 año. Se planificó el análisis según el criterio de intención de tratar. Conclusiones: El descubrimiento de estrategias terapéuticas novedosas o mejores formas de optimizar los tratamientos establecidos ha pasado a ser una prioridad de la asistencia sanitaria en la insuficiencia cardiaca. Este estudio aporta nuevos conocimientos importantes acerca del potencial del antígeno carbohidrato 125 como instrumento útil para la monitorización y ajuste de la posología de los tratamientos en los casos en que la utilización óptima no está bien definida, como ocurre con los diuréticos y las estatinas


Introduction and objectives Morbidity and mortality after admission for acute heart failure remain prohibitively high. In that setting, plasma levels of antigen carbohydrate 125 have shown to correlate with the severity of fluid overload and the risk of mortality and readmission. Preliminary data suggests a potential role of antigen carbohydrate 125 to guide therapy. The objective of this study is to evaluate the prognostic effect of an antigen carbohydrate 125-guided management strategy vs standard therapy in patients recently discharged for acute heart failure. Methods This is a multicenter, randomized, single-blind, efficacy trial study of patients recently discharged from acute heart failure (< 180 days), New York Heart Association functional class II-IV and antigen carbohydrate 125 > 35 U/ml. A randomization scheme was used to allocate participants (in a 1:1 ratio) to receive therapy guided by antigen carbohydrate 125 (aiming to keep normal values) or standard treatment. Mainly, antigen carbohydrate 125-guided therapy is focused on the frequency of monitoring and titration of decongestive therapies and statins. As of December 10, 2013, there were 383 patients enrolled. The primary outcome was the composite of 1-year all-cause mortality or rehospitalization for acute heart failure. Analysis was planned to be intention-to-treat. Conclusions Discovering novel therapeutic strategies or finding better ways of optimizing established treatments have become a health care priority in heart failure. This study will add important knowledge about the potential of antigen carbohydrate 125 as a management tool for monitoring and titration of therapies where optimal utilization has not been well defined, such as diuretics and statins (AU)


Subject(s)
Humans , CA-125 Antigen/analysis , Heart Failure/physiopathology , Natriuretic Peptide, Brain/analysis , Prognosis , Biomarkers/analysis , Angiotensin Receptor Antagonists/therapeutic use , Diuretics/therapeutic use , Hydroxymethylglutaryl-CoA Reductase Inhibitors , Length of Stay/statistics & numerical data
9.
Rev Esp Cardiol (Engl Ed) ; 68(2): 121-8, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25623430

ABSTRACT

INTRODUCTION AND OBJECTIVES: Morbidity and mortality after admission for acute heart failure remain prohibitively high. In that setting, plasma levels of antigen carbohydrate 125 have shown to correlate with the severity of fluid overload and the risk of mortality and readmission. Preliminary data suggests a potential role of antigen carbohydrate 125 to guide therapy. The objective of this study is to evaluate the prognostic effect of an antigen carbohydrate 125-guided management strategy vs standard therapy in patients recently discharged for acute heart failure. METHODS: This is a multicenter, randomized, single-blind, efficacy trial study of patients recently discharged from acute heart failure (< 180 days), New York Heart Association functional class II-IV and antigen carbohydrate 125 > 35 U/ml. A randomization scheme was used to allocate participants (in a 1:1 ratio) to receive therapy guided by antigen carbohydrate 125 (aiming to keep normal values) or standard treatment. Mainly, antigen carbohydrate 125-guided therapy is focused on the frequency of monitoring and titration of decongestive therapies and statins. As of December 10, 2013, there were 383 patients enrolled. The primary outcome was the composite of 1-year all-cause mortality or rehospitalization for acute heart failure. Analysis was planned to be intention-to-treat. CONCLUSIONS: Discovering novel therapeutic strategies or finding better ways of optimizing established treatments have become a health care priority in heart failure. This study will add important knowledge about the potential of antigen carbohydrate 125 as a management tool for monitoring and titration of therapies where optimal utilization has not been well defined, such as diuretics and statins. TRIAL REGISTRATION: ClinicalTrials.gov number: NCT02008110.


Subject(s)
CA-125 Antigen/blood , Cardiovascular Agents/therapeutic use , Disease Management , Heart Failure/drug therapy , Patient Discharge/trends , Risk Assessment , Acute Disease , Adult , Aged , Biomarkers/blood , Cause of Death/trends , Female , Follow-Up Studies , Heart Failure/blood , Heart Failure/mortality , Humans , Male , Middle Aged , Prognosis , Prospective Studies , Single-Blind Method , Spain/epidemiology , Survival Rate/trends , Time Factors
12.
Blood Press ; 19(2): 104-9, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20070252

ABSTRACT

BACKGROUND: The relationship between basal heart rate (HR) and the occurrence of myocardial ischemia, sudden death, cardiovascular mortality have been described. Therefore, further studies are warranted to evaluate the behaviour of heart rate in different scenarios. We sought to determine whether ambulatory heart rate is associated with the presence of target organ damage (TOD) in hypertensive patients. PATIENTS AND METHODS: Crossectional study of essential hypertensive patients in whom a twenty-four hour ambulatory blood pressure monitoring (ABPM) was performed. The relationship between TOD and 24 hour ambulatory heart rate (HR) was analyzed. RESULTS: Five hundred and sixty-six patients with arterial hypertension were included (55.8% male, mean age 59.9 +/- 14.2 years). 15% were smokers, 62.2% had dyslipidemia, 18.4% diabetes mellitus. Heart rate values were higher during activity as compared to the resting period (72.8 vs 63.3 bpm, p < 0.001). Heart rate, in both periods, was not associated with the presence of TOD. Nevertheless, the patients with nocturnal HR > or = 65 bpm have high risk and a high prevalence of TOD. This relationship was also present in multivariate analysis (HR 2.41; CI 95% 1.41-4.11; p=0.001). CONCLUSION: An elevated nocturnal HR, > or = 65 bpm, obtained with ABPM registry, is associated with the presence of TOD in hypertensive patients. ABPM is a powerful tool for hypertensive patients not only to monitor BP control but also to obtain information on HR which may provide additional information about current and future cardiovascular risk.


Subject(s)
Heart Rate/physiology , Hypertension/complications , Antihypertensive Agents/therapeutic use , Blood Pressure , Blood Pressure Monitoring, Ambulatory , Brain Ischemia/complications , Brain Ischemia/drug therapy , Cardiovascular Diseases/complications , Cardiovascular Diseases/drug therapy , Cross-Sectional Studies , Female , Humans , Hypertension/drug therapy , Hypertension/physiopathology , Male , Middle Aged , Myocardial Ischemia/complications , Myocardial Ischemia/drug therapy , Risk Factors , Surveys and Questionnaires
13.
Comput Methods Programs Biomed ; 98(2): 161-71, 2010 May.
Article in English | MEDLINE | ID: mdl-20004039

ABSTRACT

In Intensive Care Units doctors have to manage several alarm situations in patients. When a doctor analyzes the state of the patient, (s)he has to decide if there is an alarm situation and make decisions about what actions to perform. It is desirable to detect these situations before they occur, because the solution could be easier and the doctor has more time to react. An intelligent system could analyze the information, extract conclusions, format and order the causes leading to the severe condition. This would be helpful for a doctor, and would make the decision-making process easier. A system capable of performing such operations is presented here. This is not a diagnosis application but a tool to detect alarm situations for patient safety. A prototype capable of making retrospective evaluation of the condition of the patients has been developed. This system is based on the MCRDR technology, which has been extended to deal with the requirements of this domain. The evaluation of the system is also reported in this paper.


Subject(s)
Artificial Intelligence , Decision Support Systems, Clinical/statistics & numerical data , Decision Support Techniques , Clinical Alarms/statistics & numerical data , Decision Making , Expert Systems , Fuzzy Logic , Humans , Intensive Care Units/statistics & numerical data , Knowledge Bases , Monitoring, Physiologic/statistics & numerical data
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