180 results on '"Martínez-Quintana E"'
Search Results
2. Cardiopatías congénitas y embarazo
- Author
-
Martínez-Quintana, E., Romero-Requejo, A., and Rodríguez-González, F.
- Published
- 2016
- Full Text
- View/download PDF
3. Association of Taq 1B CETP polymorphism with insulin and HOMA levels in the population of the Canary Islands
- Author
-
López-Ríos, L., Pérez-Jiménez, P., Martínez-Quintana, E., Rodriguez González, G., Díaz-Chico, B.N., Nóvoa, F.J., Serra-Majem, L., and Chirino, R.
- Published
- 2011
- Full Text
- View/download PDF
4. Insuficiencia pulmonar crónica secundaria a tetralogía de Fallot y estenosis pulmonar intervenida. Recambio valvular pulmonar con prótesis metálica
- Author
-
Martínez-Quintana, E., Rodríguez González, F., Ágredo Muñoz, J., García Mendieta, J.S., Brito Pérez, J.M., Llorens León, R., and Nieto Lago, V.
- Published
- 2008
- Full Text
- View/download PDF
5. Ascites after cardiac surgery
- Author
-
Martínez, Quintana E, Monescillo, A, and Rodríguez, González F
- Published
- 2008
6. Painful hypertrophic osteoarthropathy successfully treated with octreotide. The pathogenetic role of vascular endothelial growth factor (VEGF)
- Author
-
Maroto, A. Angel-Moreno, Martínez-Quintana, E., Suárez-Castellano, L., and Pérez-Arellano, J.-L.
- Published
- 2005
7. Papiloflebitis como manifestación de poliarteritis nodosa
- Author
-
Rodríguez-González, F., primary, Reyes-Rodríguez, M., additional, Francisco-Hernández, F., additional, García-García, Ú., additional, and Martínez-Quintana, E., additional
- Published
- 2019
- Full Text
- View/download PDF
8. Congenital rubella syndrome: a matter of concern
- Author
-
Martínez-Quintana E, Castillo-Solórzano C, Nuria Torner, and Rodríguez-González F
- Subjects
Adult ,Male ,lcsh:Arctic medicine. Tropical medicine ,Adolescent ,lcsh:RC955-962 ,Rubella Syndrome, Congenital ,lcsh:Medicine ,Global Health ,Europa (continente) ,Young Adult ,vacunación ,Pregnancy ,islas del pacífico ,Humans ,Rubella Vaccine ,Pregnancy Complications, Infectious ,Child ,Immunization Schedule ,Rubella ,África ,lcsh:Public aspects of medicine ,Vaccination ,prevalencia ,lcsh:R ,Asia Sudoriental ,lcsh:RA1-1270 ,síndrome de rubéola congénita ,rubéola (sarampión alemán) ,Child, Preschool ,Population Surveillance ,Female ,Measles-Mumps-Rubella Vaccine ,Américas ,región mediterránea - Abstract
Congenital rubella syndrome (CRS), an important cause of severe birth defects, remains a public health problem in a significant number of countries. Therefore, global health experts encourage use of rubella vaccination, with the primary aim of preventing CRS. While large-scale rubella vaccination during the last decade has drastically reduced or eliminated both the virus and CRS in Europe and the Americas, many countries in Africa, South-East Asia, the Eastern Mediterranean, and the Western Pacific have not yet incorporated any type of rubella-containing vaccine into their immunization schedule. As a result, through travel and migration, rubella has been imported into countries that had successfully eliminated the virus, leading to outbreaks and the reestablishment of endemic transmission. The objective of this study was to identify the key factors required for CRS elimination (prevalence reduction, vaccination strategies, and surveillance methods) by reviewing publications in PubMed on rubella and CRS (systematic reviews, country experiences, and position papers from the World Health Organization (WHO) and other intergovernmental organizations). Based on the results of the review, to eliminate rubella and CRS in endemic areas and reduce re-emergence in previously disease-free areas, all countries should carry out two types of mass rubella vaccination campaigns: 1) one single mass national immunization campaign targeting all men and women 5-39+ years old (with the upper age limit depending on the year in which the rubella-containing vaccine was introduced and the epidemiology of rubella in the country) and 2) incorporation of an rubella-containing vaccine in routine childhood immunization programs, including regular vaccination campaigns for 12-month-olds and measles follow-up campaigns. In addition to mass rubella immunization campaigns and routine childhood vaccination programs, the following measures should be taken to help fight rubella and CRS: 1) surveillance of the number of susceptible women of childbearing age, and the emergence of imported cases; 2) coverage of susceptible populations with "second-chance" ("catch-up") campaigns (vaccination of older children and adults who may have missed earlier immunization programs); 3) rapid response to outbreaks; 4) strengthening of CRS surveillance; 5) involvement of the private sector in awareness and vaccination campaigns; and 6) reduction of the number of false-positive laboratory test results.
- Published
- 2015
9. Encrucijada entre la cardiopatía isquémica, la miocardiopatía hipertrófica y el corazón de atleta
- Author
-
Martínez-Quintana, E., Jaimes-Vivas, R., and Rodríguez-González, F.
- Published
- 2015
- Full Text
- View/download PDF
10. Trastornos electrocardiográficos tras intoxicación alcohólica aguda
- Author
-
Martínez-Quintana, E., Kloppenburg, S., Ojeda-Sosa, A., and Rodríguez-González, F.
- Published
- 2014
- Full Text
- View/download PDF
11. Clinical features in adult patient with Wolf-Hirschhorn syndrome
- Author
-
Martínez-Quintana, E. and Rodríguez-González, F.
- Published
- 2014
- Full Text
- View/download PDF
12. Síndrome de Holt Oram e hipertensión arterial pulmonar
- Author
-
Martínez-Quintana, E. and Rodríguez-González, F.
- Published
- 2012
- Full Text
- View/download PDF
13. Respuesta hipertensiva severa al ejercicio en paciente con coartación de aorta corregida y presión arterial basal normal
- Author
-
Martínez-Quintana, E., Rodríguez-González, F., and Medina-Gil, J.M.
- Published
- 2011
- Full Text
- View/download PDF
14. Síndrome de Leopard y miocardiopatía hipertrófica
- Author
-
Martínez-Quintana, E. and Rodríguez-González, F.
- Published
- 2011
- Full Text
- View/download PDF
15. Cardiopatías congénitas y deporte
- Author
-
Martínez Quintana, E., Ágredo Muñoz, J., Rodríguez González, F., and Nieto Lago, V.
- Subjects
Deporte ,Ejercicio ,Exercise ,Cardiopatías congénitas ,Congenital heart disease ,Sport - Abstract
Las cardiopatías congénitas constituyen cada vez más una causa frecuente de consulta cardiológica. Las nuevas técnicas diagnósticas y terapéuticas han permitido mayor supervivencia y calidad de vida de unos pacientes que desean realizar deporte. Hasta donde pueden llegar no es siempre fácil de determinar. Las guías nos ayudan a la hora de decidir, aunque finalmente es el médico el que debe determinar en cada caso la situación del paciente y el tipo de deporte que podrá realizar dependiendo de la severidad y el tipo de cardiopatía. Congenital heart diseases are a frequent cause of cardiology consultation. New diagnostic and therapeutic techniques have allowed greater survival and quality of life of patients who wish to participate in sports. What they can do is not always easy to determine. Guidelines are helpful at the time of deciding, although finally is the doctor the one that must determine in each case the situation of the patient and the type of exercise they can do depending on the severity and type of cardiopathy.
- Published
- 2008
16. Hipertensión arterial y coartación de aorta intervenida en la infancia
- Author
-
Martínez-Quintana, E., Rodríguez-González, F., and Cuba-Herrera, J.
- Published
- 2010
- Full Text
- View/download PDF
17. Aneurisma idiopático de la arteria pulmonar principal en paciente joven
- Author
-
Martínez-Quintana, E., Rodríguez-González, F., Gómez-Guindal, J.A., and Junquera-Rionda, P.
- Published
- 2010
- Full Text
- View/download PDF
18. A Novel Fibrillin 1 Gene Mutation Leading to Marfan Syndrome with Minimal Cardiac Features
- Author
-
Martínez-Quintana, E., primary, Rodríguez-González, F., additional, Garay-Sánchez, P., additional, and Tugores, A., additional
- Published
- 2014
- Full Text
- View/download PDF
19. Novel Frameshift CHD7 Mutation Related to CHARGE Syndrome
- Author
-
Martínez-Quintana, E., primary, Rodríguez-González, F., additional, Garay-Sánchez, P., additional, and Tugores, A., additional
- Published
- 2013
- Full Text
- View/download PDF
20. Mucopolysaccharidosis Type II and the G374sp Mutation
- Author
-
Martínez-Quintana, E., primary and Rodríguez-González, F., additional
- Published
- 2013
- Full Text
- View/download PDF
21. LEOPARD Syndrome: Clinical Features and Gene Mutations
- Author
-
Martínez-Quintana, E., primary and Rodríguez-González, F., additional
- Published
- 2012
- Full Text
- View/download PDF
22. LEOPARD Syndrome Caused by Tyr279Cys Mutation in the PTPN11 Gene
- Author
-
Martínez-Quintana, E., primary and Rodríguez-González, F., additional
- Published
- 2011
- Full Text
- View/download PDF
23. Aneurisma arterial pulmonar y osteoartropatía hipertrófica en paciente con cardiopatía congénita cianótica
- Author
-
Martínez-Quintana, E., primary and Rodríguez-González, F., additional
- Published
- 2009
- Full Text
- View/download PDF
24. Vasoespasmo coronario inducido por un cuadro vasovagal como forma de presentación de angina variante
- Author
-
Rodríguez-González, F., primary, Martínez-Quintana, E., additional, and Cuba-Herrera, J., additional
- Published
- 2009
- Full Text
- View/download PDF
25. Cardiopatías congénitas y deporte
- Author
-
Martínez Quintana, E., primary, Ágredo Muñoz, J., additional, Rodríguez González, F., additional, and Nieto Lago, V., additional
- Published
- 2008
- Full Text
- View/download PDF
26. Painful hypertrophic osteoarthropathy successfully treated with octreotide. The pathogenetic role of vascular endothelial growth factor (VEGF)
- Author
-
Angel-Moreno Maroto, A., primary, Martínez-Quintana, E., additional, Suárez-Castellano, L., additional, and Pérez-Arellano, J.-L., additional
- Published
- 2005
- Full Text
- View/download PDF
27. Novel Frameshift CHD7 Mutation Related to CHARGE Syndrome.
- Author
-
Martínez-Quintana, E., Rodríguez-González, F., Garay-Sánchez, P., and Tugores, A.
- Published
- 2014
- Full Text
- View/download PDF
28. LEOPARD Syndrome Caused by Tyr279Cys Mutation in the PTPN11 Gene.
- Author
-
Martínez-Quintana, E. and Rodríguez-González, F.
- Published
- 2012
- Full Text
- View/download PDF
29. Cardiogenic shock following blunt chest trauma
- Author
-
Rodríguez-González Fayna and Martínez-Quintana Efrén
- Subjects
Aneurysm ,blunt cardiac injury ,cardiac contusion ,cardiac complications ,echocardiography ,Medical emergencies. Critical care. Intensive care. First aid ,RC86-88.9 - Abstract
Cardiac contusion, usually caused by blunt chest trauma, has been recognized with increased frequency over the past decades. Traffic accidents are the most frequent cause of cardiac contusions resulting from a direct blow to the chest. Other causes of blunt cardiac injury are numerous and include violent fall impacts, interpersonal aggression, explosions, and various types of high-risk sports. Myocardial contusion is difficult to diagnose; clinical presentation varies greatly, ranging from lack of symptoms to cardiogenic shock and arrhythmia. Although death is rare, cardiac contusion can be fatal. We present a case of cardiac contusion due to blunt chest trauma secondary to a fall impact, which manifested as cardiogenic shock.
- Published
- 2010
30. Group Psychological Therapy Program in Adult Patients with Congenital Heart Disease and Anxious-Depressive Symptoms.
- Author
-
Martínez-Quintana E, Codana-Alcántara K, Montesdeoca-Naranjo HM, García-Suárez MI, Fleitas-Álvarez MP, Alcántara-Castellano M, Ruiz-Castellano A, González-Isasi A, Rodríguez-González F, and Bosch-Casañas E
- Subjects
- Humans, Female, Male, Adult, Surveys and Questionnaires, Self Concept, Middle Aged, Treatment Outcome, Psychiatric Status Rating Scales, Depression therapy, Depression psychology, Anxiety therapy, Anxiety psychology, Quality of Life psychology, Heart Defects, Congenital psychology, Heart Defects, Congenital complications, Heart Defects, Congenital therapy, Psychotherapy, Group methods
- Abstract
Introduction : Anxiety and depression are significant mental health concerns for individuals with congenital heart disease (CHD). As group therapy has proven to be a valuable and effective treatment option for managing anxiety and depression, the aim of this study was to determine its effects on patients with CHD and anxious-depressive symptoms. Methods : We used non-pharmacological psychological group intervention, of six weekly sessions of 90 min each, administered by trained personnel, in adult patients with CHD. Measurement tools included quality of life (Euro quality of life-5D questionnaire), self-esteem (Rosenberg Self-Esteem Scale), anxiety (State-Trait Anxiety Inventory), depression (Beck Depression Inventory-II), and satisfaction surveys. Results : A total of 18 out of 21 CHD patients (mean age 35.8 ± 9.0 years old and 13 (72%) females) completed the program. According to CHD complexity, five (28%) patients had mild, six (33%) moderate, and seven (38%) great defects. Patients with CHD scored significantly higher in the Euro quality of life visual analogue scale (7.83 ± 1.4 vs. 7.14 ± 1.6, p = 0.012) and lower in the Beck Depression Inventory-II (12.3 ± 10.9 vs. 18.1 ± 12.1, p = 0.003) post-program than pre-intervention. Meanwhile, the Rosenberg Self-Esteem Scale score was close to reaching statistical significance (27.4 ± 6.0 vs. 25.1 ± 5.4, p = 0.051), while the State-Trait Anxiety Inventory did not. Finally, participants scored high in the satisfaction questionnaire at the end of the sessions, on a scale from 0 to 3, especially in the questions related to feeling comfortable with others (2.5 ± 0.6), recommending the program (2.3 ± 0.6), or being willing to attend future sessions (2.6 ± 0.8). Conclusions : Group psychological therapy proved to be a useful tool to reduce depressive symptomatology after a 6-week program, providing a comfortable environment to patients with CHD.
- Published
- 2025
- Full Text
- View/download PDF
31. Risk Factors for Chronic Kidney Disease in Adult Patients with Congenital Heart Disease and Its Relationship with Cardiovascular Mortality.
- Author
-
Martínez-Quintana E and Rodríguez-González F
- Abstract
Background : Patients with congenital heart disease (CHD) show risk factors for chronic kidney disease (CKD) and it is well known that CKD has a large negative impact on survival. Methods : Observational and prospective cohort study. Adult CHD patients and controls were matched for age and sex. Results : A total of 657 CHD adult patients (cases) and 1954 controls were studied. Median age in CHD patients was 30 (17-62) years and 373 (57%) were male. The prevalence of CKD (Glomerular filtration rate (GFR) < 60 mL/min/1.73 m
2 ) was 0.2% and 4.5% in the control and CHD groups, respectively. Binary logistic regression analysis determined as risk factors for CKD in CHD patients: age [1.54 (1.04-1.28), p = 0.009], dyslipidemia [19.8 (1.35-301.1), p = 0.031], low iron concentration [0.96 (0.96-0.93), p = 0.048], cyanosis [25.7 (1.60-411.8), p = 0.022], and Down syndrome [46.8 (8.09-2710), p = 0.003]. During a follow-up time of 6.8 (1.2-10.5) years, cardiovascular mortality occurred in 31 patients with CHD showing, through the Kaplan-Meier test, a worse outcome among patients with CKD ( p < 0.05) as was also seen in the univariate Cox regression survival analysis. However, after adjusting for other variables, this significance was lost, with age remaining as the unique independent prognostic factor. Conclusions : The prevalence of CKD was much higher in patients with CHD than in the control group; age, cyanosis, and Down syndrome were the predictors of a higher risk of CKD among CHD patients. Although CKD was associated with worse survival in CHD patients, only age was identified as an independent prognostic factor for cardiovascular mortality.- Published
- 2024
- Full Text
- View/download PDF
32. C-Reactive Protein and Long-Term Prognosis in Adult Patients with Congenital Heart Disease.
- Author
-
Martínez-Quintana E, Alcántara-Castellano M, García-Suárez MI, and Rodríguez-González F
- Abstract
Background/Objectives : Prognostic biomarkers may provide information about the patient's cardiovascular outcomes. However, there are doubts regarding how high-sensitivity C-reactive protein (hs-CRP) impacts patients with congenital heart disease (CHD). The main objective is to evaluate whether high hs-CRP levels predict a worse prognosis in patients with CHD. Methods : Observational and prospective cohort study. Adult CHD patients and controls were matched for age and sex. Results : In total, 434 CHD patients (cases) and 820 controls were studied. The median age in the CHD patients was 30 (18-62) years and 256 (59%) were male. A total of 51%, 30%, and 19% of patients with CHD had mild, moderate, and great complexity defects, respectively. The body mass index [1.07 (1.01-1.13), p = 0.022)], diabetes mellitus [3.57 (1.07-11.97), p = 0.039], high NT-pro-BNP levels [1.00 (1.00-1.01), p = 0.021], and low serum iron concentrations [0.98 (0.97-0.99), p = 0.001] predicted high hs-CRP levels (≥0.3 mg/dL) in patients with CHD. During a follow-up time of 6.81 (1.17-10.46) years, major cardiovascular events (MACE) occurred in 40 CHD patients, showing the Kaplan-Meier test demonstrated a worse outcome among patients with hs-CRP levels above 0.3 mg/dL ( p = 0.012). Also, hs-CRP showed statistical significance in the univariate Cox regression survival analysis. However, after adjusting for other variables, this significance was lost and the remaining predictors of MACE were age [HR 1.03 (1.01-1.06), p = 0.001], great complexity defects [HR 2.46 (1.07-5.69), p = 0.035], and an NT pro-BNP cutoff value for heart failure > 125 pg/mL [HR 7.73 (2.54-23.5), p < 0.001]. Conclusions : Hs-CRP obtained statistical significance in the univariate survival analysis. However, this significance was lost in the multivariate analysis in favor of age, CHD complexity, and heart failure.
- Published
- 2024
- Full Text
- View/download PDF
33. [Effect of outpatient administration of levosimendan in reducing hospital readmission in patients with heart failure].
- Author
-
Acosta-Armas P, Medina-Gil JM, and Martínez-Quintana E
- Subjects
- Humans, Aged, Male, Female, Middle Aged, Aged, 80 and over, Treatment Outcome, Heart Failure drug therapy, Patient Readmission statistics & numerical data, Simendan therapeutic use, Simendan administration & dosage, Pyridazines therapeutic use, Pyridazines administration & dosage, Cardiotonic Agents therapeutic use, Cardiotonic Agents administration & dosage, Ambulatory Care, Hydrazones therapeutic use, Hydrazones administration & dosage
- Published
- 2023
- Full Text
- View/download PDF
34. Crystalluria in adolescent and adult patients with congenital heart disease.
- Author
-
Martínez-Quintana E and Rodríguez-González F
- Subjects
- Adolescent, Adult, Female, Humans, Male, Young Adult, Calcium Oxalate, Crystalluria, Prospective Studies, Risk Factors, Heart Defects, Congenital complications, Heart Defects, Congenital epidemiology, Kidney Calculi epidemiology, Kidney Calculi complications
- Abstract
Introduction: Crystalluria is a frequent finding in normal individuals and in patients suffering from urolithiasis. As nephrolithiasis has been associated with cardiovascular risk factors and most congenital heart disease (CHD) patients reach adulthood, the objective of this study is to determine the presence of crystalluria and if it influences their cardiovascular outcome., Methods: Case-control and observational prospective study design of patients with CHD older than 14 years with a stable CHD verified with imaging tests and a control population., Results: 214 patients with CHD [median age 21 (17-35) years and 41 (19%) males] and 345 controls were studied and followed up. None of them had symptoms of renal calculi. Nine (4%) patients with CHD and 24 (7%) patients in the control group showed crystalluria (p = 0.180), all of them composed of calcium oxalate. No significant differences were seen in age, sex, body mass index, CHD complexity, cardiovascular risk factors, NYHA functional class, cyanosis, and medical treatment between CHD patients with and without crystalluria. In relation to survival, 18 patients with CHD had a major acute cardiovascular event (MACE) (3 strokes, 2 myocardial infarction, 9 cardiovascular death and 4 non cardiovascular mortality) during the follow up time [7.3 (4.4-8.5) years] without significant differences in the Kaplan-Meier analysis (p = 0.358) between patients with and without crystalluria., Conclusion: No significant differences were found between CHD and control patients in relation to crystalluria and it had no impact on the occurrence of cardiovascular events in the medium term follow up of patients with CHD., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
- Published
- 2023
- Full Text
- View/download PDF
35. Impact of face masks during the treadmill exercise tests.
- Author
-
Wangüemert Pérez F, Wangüemert Guerra M, Caballero Dorta E, Acosta Materan CJ, Tormo Juarez JP, Godoy Camacho C, Cardenes Leon A, Segura Villalobos F, Medina Gil JM, Perez ML, García Salvador JJ, Mateos Cañero GO, Jiménez Rivero C, and Martínez-Quintana E
- Subjects
- Adult, Aged, Female, Humans, Male, Middle Aged, Exercise Test, Masks, Pandemics prevention & control, Retrospective Studies, SARS-CoV-2, COVID-19 epidemiology, COVID-19 prevention & control
- Abstract
Introduction and Objective: There is little literature on the use of face masks in a treadmill test (TMT) during the COVID-19 pandemic. The objective of this study is to analyze the impact of face masks during a TMT performed during the prepandemic (without face mask) and postpandemic (with face mask) era., Methods: Retrospective observational unicentric study of patients undergoing TMT. The inclusion criterion were being over 16years old and having performed at least one TMT in the prepandemic and postpandemic period., Results: One thousand six hundred fifty-five patients were included in the study. Nine hundred thirty-five (56.5%) were men and 720 (43.5%) women. The mean age was 57.3±14.9 and the mean follow-up time was 15.4 months. Fifty-three percent patients had arterial hypertension, 20% dyslipidemia, 12% diabetes mellitus, 8% smoking habit, 19% personal history of ischemic heart disease, 5% COPD, 8% bronchial asthma, and 8% atrial fibrillation. In almost all the variables studied in PE, including the appearance of ventricular arrhythmias, no significant differences were found, neither by age nor sex, except for the existence of a very slight decrease in exercise capacity with mask use in older patients (>65years)., Conclusions: The use of surgical or FFP2 face masks during the TMT did not affect functional capacity, blood pressure, heart rate, or increased ventricular arrhythmias., (Copyright © 2022 Elsevier España, S.L.U. All rights reserved.)
- Published
- 2023
- Full Text
- View/download PDF
36. Clinical and Pharmacological Parameters Determine Relapse During Clopidogrel Treatment of Acute Coronary Syndrome.
- Author
-
Santana-Mateos M, Medina-Gil JM, Saavedra-Santana P, Martínez-Quintana E, Rodríguez-González F, and Tugores A
- Subjects
- Aspirin therapeutic use, Calcium Channel Blockers therapeutic use, Clopidogrel therapeutic use, Cytochrome P-450 CYP2C19 genetics, Humans, Platelet Aggregation Inhibitors, Recurrence, Retrospective Studies, Ticlopidine therapeutic use, Treatment Outcome, Acute Coronary Syndrome drug therapy, Coronary Artery Disease, Diabetes Mellitus, Type 2 drug therapy, Myocardial Infarction drug therapy
- Abstract
The therapeutic efficacy of clopidogrel as an antiplatelet drug varies among individuals, being the mainstream hypothesis that its bioavailability depends on the individual genetic background and/or interactions with other drugs. A total of 477 patients receiving double antiaggregation therapy with aspirin and clopidogrel, after suffering a first event, were followed for 1 year to record relapse, as a surrogate end point to measure their therapeutic response, as defined by presenting with an acute coronary event (unstable angina, ST-segment-elevation myocardial infarction, or non-ST-segment-elevation myocardial infarction), stent thrombosis/restenosis, or cardiac mortality. Anthropometric, clinical, and pharmacological variables along with CYP2C19 genotypes were analyzed for their association with the disease relapse phenotype. Only 75 patients (15%) suffered a relapse, which occurred during the first 6 months of therapy, with a peak at 4.5 months. An initial univariate analysis identified that patients in the relapse group were significantly older (67.4 ± 11.0 vs 61.6 ± 12.3 years old) and presented with diffuse coronary disease, insulin-dependent type 2 diabetes mellitus dyslipidemia, and arterial hypertension. A poor clinical response to the platelet antiaggregation regime also occurred more frequently among patients taking acenocoumarol and calcium channel blockers, along with aspirin and clopidogrel, while no association was found according to CYP2C19 genotypes. A retrospective multivariate analysis indicated that patients belonging to the nonresponder phenotype to treatment with aspirin and clopidogrel were older, presented with diffuse coronary disease, a group largely overlapping with type 2 insulin-dependent diabetes mellitus, and were taking dihidropyrimidinic calcium channel blockers., (© 2021, The American College of Clinical Pharmacology.)
- Published
- 2022
- Full Text
- View/download PDF
37. A Common Variant at the 3'untranslated Region of the CCL7 Gene (rs17735770) Is Associated With Decreased Susceptibility to Coronary Heart Disease.
- Author
-
Medina-Gil JM, Pérez-García A, Saavedra-Santana P, Díaz-Carrasco A, Martínez-Quintana E, Rodríguez-González F, Ramírez CM, Riaño M, Garay-Sánchez P, and Tugores A
- Abstract
Monocytes participate in the development of atherosclerosis through the action of cytokines and other inflammatory mediators. Among them, CCR2 and its ligands, CCL2 and CCL7 play an important role, so the main objective of this work was to determine whether genetic variants affecting their activity were associated with cardiovascular disease. A cohort of 519 patients that have suffered coronary events was analyzed under a propensity score-matching protocol selecting a homogeneous set of cases and controls, according to age, sex, smoking status, dyslipidemia, arterial hypertension and type 2 diabetes as risk factors. While dyslipidemia and arterial hypertension were more prevalent among patients with angina pectoris, current smoking status and elevated inflammatory markers, including total leukocyte and monocyte counts, were more likely associated with acute coronary events. Propensity score matching analysis, performed to eliminate the influence of these risk factors and highlight genetic modifiers, revealed that a single nucleotide variant, rs17735770 at the 3'untranslated region of the CCL7 gene transcript, was associated with decreased cardiovascular risk in a group represented mostly by men, with an average age of 57, and without significant differences in traditional risk factors. Furthermore, the presence of this variant altered the local mRNA structure encompassing a binding site for miR-23ab, resulting in increased translation of a reporter gene in a miR23 independent fashion. The rs17735770 genetic variant led to increased expression of CCL7, a potential antagonist of CCR2 at inflammatory sites, where it could play a meaningful role during the evolution of atherosclerosis., Competing Interests: AD-C was employed by SECUGEN SL, Madrid, Spain and designed all the primers and performed all the sequencing associated with this project at SECUGEN SL, a service paid for by the authors. However, SECUGEN SL was not involved in the study design, collection, analysis, interpretation of data, the writing of this article or the decision to submit it for publication. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2022 Medina-Gil, Pérez-García, Saavedra-Santana, Díaz-Carrasco, Martínez-Quintana, Rodríguez-González, Ramírez, Riaño, Garay-Sánchez and Tugores.)
- Published
- 2022
- Full Text
- View/download PDF
38. Gamma-glutamyl transferase and cardiovascular events in patients with congenital heart disease.
- Author
-
Martínez-Quintana E, Pardo-Maiza J, Déniz-Alvarado B, Riaño-Ruiz M, González-Martín JM, and Rodríguez-González F
- Subjects
- Adolescent, Adult, Cohort Studies, Female, Humans, Male, Prospective Studies, Young Adult, Cardiovascular Diseases blood, Cardiovascular Diseases etiology, Heart Defects, Congenital blood, Heart Defects, Congenital complications, gamma-Glutamyltransferase blood
- Abstract
Introduction: Serum gamma-glutamyl transferase activity (GGT) seems to predict cardiovascular events in different populations. However, no data exist on patients with congenital heart disease (CHD)., Methods: Observational, analytic, prospective cohort study design involving CHD patients and a control population to determine the effect of GGT levels on survival., Results: A total of 589 CHD patients (58% males, 29 ± 14 years old) and 2745 matched control patients were followed up. A total of 69 (12%) CHD patients had a major acute cardiovascular event (MACE) during the follow-up time (6.1 [0.7-10.4] years). Patients with CHD and a GGT >60 U/L were significantly older, more hypertensive and dyslipidemic, had a worse NYHA functional class and a greater anatomical complexity than CHD patients with a GGT ≤60 U/L. The binary logistic regression analysis showed that age, a great CHD anatomical complexity, and having atrial fibrillation/flutter were the predictive factors of higher GGT levels (>60 U/L). The Kaplan-Meier analysis showed that patients with CHD and a GGT concentration above 60 UL showed the lowest probability of survival compared to that of CHD with GGT ≤60 U/L and controls irrespective of their GGT concentrations (p < .001). Similarly, the multivariable Cox regression analysis found an independent association between higher GGT levels (>60 U/L) and a worse prognosis (HR 2.44 [1.34-4.44], p = .003) among patients with CHD., Conclusion: Patients with CHD showed significant higher GGT levels than patients in the control group having those with higher GGT concentrations (>60 U/L) the worst survival., (© 2021 Stichting European Society for Clinical Investigation Journal Foundation. Published by John Wiley & Sons Ltd.)
- Published
- 2022
- Full Text
- View/download PDF
39. Blood test assessment of liver ultrasound findings in patients with Fontan surgery.
- Author
-
Martínez-Quintana E and Rodríguez-González F
- Abstract
Hepatic complications are common in patients with Fontan surgery. The objective of this observational study is to compare demographic, clinical and blood test data in patients older than 14 years old with a Fontan procedure (cases) and asymptomatic patients with single non-operated restrictive ventricular septal defect (VSD) (controls) and to determine whether there are differences in blood collection and liver disease scores according to the liver ultrasound findings in the group of Fontan patients. The liver findings were classified as mild (normal or heterogeneous echogenicity) and significant (nodular surface, small hyperechoic nodules or hepatocarcinoma). 74 patients (14 patients with a Fontan procedure and 60 patients with a restrictive VSD) were included in the study. Median age was 18 (14-45) years old and 41 patients were males. Fontan patients had significantly lower platelet count, lower mean platelet volume (MPV) and lower glucose levels than patients with single non-operated restrictive VSD. On the contrary, Fontan patients showed higher liver enzymes [aspartate aminotransferase (AST) and alanine aminotransferase (ALT), gamma-glutamyl transferase (GGT)], N-terminal pro-brain natriuretic peptide (NT-pro-BNP) and thyroid-stimulating hormone (TSH) concentrations than patients with restrictive VSD. 4 out of 14 (29%) patients with Fontan operation and significant liver ultrasound findings showed greater number of cardiac surgeries, lower MPV values and higher GGT and TSH levels than Fontan patients with mild findings. In conclusion, Fontan patients showed higher liver enzymes (AST, ALT and GGT) than controls and Fontan patients with significant liver ultrasound findings had higher GGT and TSH concentrations than Fontan patients with mild findings., Competing Interests: None., (AJCD Copyright © 2021.)
- Published
- 2021
40. Genealogy of patients with congenital heart disease in isolated populations.
- Author
-
Martínez-Quintana E, Sánchez-Matos MM, Rodríguez-González F, and Tugores A
- Abstract
In isolated populations rare genetic diseases are important and relatively frequent. The objective of this study is to determine the geographical aggregates of maternal and paternal ancestors of patients with congenital heart disease (CHD) to determine whether there is an association between the different areas and types of cardiac defects. Descriptive, observational, and cross-sectional study of patients with CHD obtained consecutively in a single adult CHD unit between January 2018 and December 2019 in Gran Canaria (Canary Islands, Spain). To be included in the study, at least one of the grandparents (maternal or paternal) should be born in Gran Canaria. 258 out of 353 CHD patients met the inclusion criteria. 58% of CHD patients were male and the median age was of 28 (21-40) years old. The most frequent types of CHD were cardiac septal defects (76 patients), right side cardiac outflow tract anomalies (74 patients) and left side cardiac outflow tract anomalies (58 patients). 13% of the patients had a family history of CHD, 11% showed consanguinity and 7% had an associated polymalformative syndrome. 20% of the four ancestors were born in the same municipality and a significant association was seen between two areas of Gran Canaria, orographically related, and right-side cardiac outflow tract anomalies (P<0.001). In conclusion in patients with tetralogy of Fallot and/or pulmonary valve stenosis/atresia an ancestry's geographic aggregation was seen., Competing Interests: This work is supported by a competitive, peer reviewed grant from the Distribuidora Industrial, S.A. (DISA) (2018) and the Fundación Canaria Instituto de Investigación Sanitaria de Canarias (FIISC) of the Canary Islands Health Service (PIFUN 40/18)., (AJCD Copyright © 2021.)
- Published
- 2021
41. Mental well-being among patients with congenital heart disease and heart failure during the COVID-19 pandemic.
- Author
-
Martínez-Quintana E, Vega-Acedo LDC, Santana-Herrera D, Pérez-Acosta C, Medina-Gil JM, Muñoz-Díaz E, and Rodríguez-González F
- Abstract
Patients with congenital heart disease (CHD) show increasing survival. We evaluated the influence of COVID-19 confinement on the mental well-being of patients with CHD. Descriptive, cross-sectional, observational epidemiological study in a cohort of 242 patients with CHD over 14 years old recruited consecutively from a single adolescent and adult CHD outpatient unit. Patients were sent an online questionnaire to determine clinical, demographic and the 12-element general health questionnaire (GHQ-12) data during the COVID-19 quarantine. 242 out of 407 (59%) patients with CHD, to whom the questionnaire was sent, responded to the survey. 98 (42%) patients were between 14 and 24 years old and 133 (58%) were over 25 years old. Of the total, 119 (51%) were male. 123 (51%), 88 (36%) and 31 (13%) patients with CHD had mild, moderate, and severe anatomical complexity respectively. 11 (4.5%) out of 242 patients with CC presented heart failure (HF) symptoms, requiring 18% of them admission to the hospital emergency department during the pandemic (P=0.002). In relation to the GHQ-12 questionnaire, patients with CHD and HF enjoyed less their daily activities (81% vs. 51%, P=0.043) and had less self-confidence (46% vs. 18%, P=0.041) than those without HF symptoms. In conclusion, patients with CHD and HF, during the COVID-19 quarantine, presented a lower capacity to enjoy daily activities and self-confidence than CHD without HF symptoms., Competing Interests: None., (AJCD Copyright © 2021.)
- Published
- 2021
42. The effect of physical activity on quality of life and serum glucose and cholesterol levels in patients with congenital heart disease.
- Author
-
Martínez-Quintana E, Estupiñán-León H, Déniz-Déniz L, Rojas-Brito AB, Barreto-Martín A, González-Martín JM, Miranda-Calderín G, Rodríguez-González F, and Tugores A
- Abstract
As physical activity contributes to quality of life and health, we evaluated its association, as measured by the Global physical activity (GPAQ) questionnaire, on the quality of life (QoL) and serum glucose and cholesterol levels of patients with congenital heart disease (CHD). This cross-sectional study was carried out in 200 adult patients with CHD (17 to 58 years old), of whom 45 had simple defects, 122 moderate defects and 33 great anatomical complexity defects. Physiological complexity was defined as stage A in 74 patients, stage B in 29, stage C in 86 and stage D in 11. The energy expenditure was below 600 Metabolic Equivalent of Task (MET)-minutes per week in 56 (28%) patients, while 144 (72%) were above 600 MET-minutes per week. Physically inactive patients with CHD were significantly more dyslipidemic than active ones, but no significant differences in serum glucose and cholesterol levels were observed. Logistic regression analysis showed that physical activity was associated with a better QoL rating [0.28 (0.10-0.17), P=0.014] and health satisfaction [0.24 (0.09-0.62), P=0.003]. Physically active patients with CHD scored 7.7 and 8.9 points higher, on a 100-point scale, in the physical and social relationships domains respectively, than physically inactive ones. No significant differences were seen in the psychological and the environment domains associated with physical activity. Additionally, a worse New York Heart Association (NYHA) functional class (≥ 2) was identified as a risk factor for dissatisfaction with health [OR 7.48, 95% CI (1.55-47.14), P=0.020], having a significantly negative impact of 8.5 and 7.6, on a 100-point scale, in the physical and psychological domains respectively. In conclusion, physically active patients with CHD had a better QoL assessment, were more satisfied with their health and scored higher in the physical and social relationships domains., Competing Interests: None., (AJCD Copyright © 2021.)
- Published
- 2021
43. Evaluation of quality of life in patients with congenital heart disease: an observational case control study.
- Author
-
Martínez-Quintana E, Estupiñán-León H, Rojas-Brito AB, Déniz-Déniz L, Barreto-Martín A, and Rodríguez-González F
- Abstract
Quality of life (QoL) has become an important issue in patients with congenital heart disease (CHD). Accordingly, the focus has shifted from mere survival to a better QoL. The objective of this study is to assess QoL, by examining the World Health Organization QoL-bref (WHOQoL-BREF) questionnaire, in patients with CHD and a control population of a same geographic area matched for age, sex, cardiovascular risk factors and educational level. 154 patients with CHD recruited from a single hospital outpatient clinic and 250 healthy controls were studied between October 2018 and April 2019. Median age in patients with CHD was 27 (20-34) years and 62% were male. 32, 90 and 32 patients with CHD showed mild, moderate, and complex defects, respectively. 131 (53%) controls referred having felt or experienced negative feelings such as bad mood, despair, stress, or depression compared to 53 (34%) patients in the CHD group (P<0.001). Despite needing more medical treatment (P<0.001), patients with CHD enjoyed more their lives (P<0.001), felt their lives made more sense (P<0.001), were happier with themselves (P=0.006) and with their personal relationships (P=0.020), had a greater support from friends (P=0.031) and felt safer in their daily lives (P=0.004) than patients in the control group. Similarly, patient with CHD felt their environment was healthier, had more opportunities for leisure and were happier with their access to healthcare system (P<0.005) than controls. On the contrary, except the need for more medical treatment in patients with great CHD defects (P=0.019), no significant differences were seen in the WHOQoL-BREF survey according to the anatomical complexity. In conclusion, overall patients with CHD scored better in the WHOQoL-BREF questionnaire, especially in the psychological and environment domains, than patients in the control group., Competing Interests: None., (AJCD Copyright © 2021.)
- Published
- 2021
44. COVID-19 quarantine and depression in patients with congenital heart disease.
- Author
-
Martínez-Quintana E, Santana-Herrera D, Vega-Acedo LDC, Pérez-Acosta C, Rodríguez-González F, and Tugores A
- Abstract
COVID-19 outbreak has brought tremendous psychological pressure to the general population, especially to those with associated cardiovascular disease. An online Patient Health Questionnaire (PHQ-9) survey on consecutive congenital heart disease (CHD) patients, was carried out to determine depression during the Spanish coronavirus disease (COVID-19) quarantine. Two-hundred forty-two out of 407 (59%) CHD patients answered the survey, 123 (51%) had mild defects, 88 (36%) moderate and 31 (13%) great defects, most of them between 18 and 24 years old and 51% were male. Patients were dichotomized to no or mild (PHQ-9 < 10) and moderate to severe (≥ 10) depressive symptoms. Thirty-four (14%) patients showed a PHQ-9 ≥ 10 and 10 of them (29%) were under anxiolytic or antidepressant treatment during the quarantine. During the study period, 9 (4%) patients had COVID-19 symptoms. Patients with a NYHA above 2 (P=0.025), living in houses without garden or balcony (P=0.014), needing psychological/psychiatric evaluation/medication in the previous 12 months or being under anxiolytic/antidepressant treatment during the confinement had, significantly, a PHQ-9 score ≥ 10 (P < 0.001). Being under anxiolytic/antidepressant treatment during the coronavirus pandemic [OR 3.92 (95% CI 1.05-14.66), P=0.043] and having previous psychological/psychiatric evaluation in the previous 12 months to the quarantine [OR 3.82 (95% CI 1.16-12.54), P=0.027] were the only variables that reached statistical significance, in the multivariable analysis, as predictors of a pathological PHQ-9 questionnaire (score ≥ 10). In conclusion depression was frequent during the COVID-19 quarantine among CHD patients, with only a third of them being under anxiolytic or antidepressant treatment. Needing psychological/psychiatric evaluation/treatment during the previous 12 months to the lockdown was a predictive factor for an abnormal PHQ-9 score., Competing Interests: None., (AJCD Copyright © 2021.)
- Published
- 2021
45. Proteinuria versus albuminuria in 24-hour urine collection: prevalence and clinical outcome in non-hypoxemic adult patients with congenital heart disease.
- Author
-
Martínez-Quintana E, Barreto-Martín A, Estupiñán-León H, Rojas-Brito AB, Déniz-Déniz L, and Rodríguez-González F
- Abstract
Congenital heart disease (CHD) patients, especially cyanotic ones, usually have renal function impairment. However, little information exists in non-cyanotic CHD patients. The objective of this study is to determine renal failure in non-hypoxemic CHD patients by measuring the amount of protein and albumin released in urine over a 24-hour period and determining the glomerular filtration rate (GFR). Prospective study of consecutive outpatient non-hypoxemic CHD patients followed up in a single tertiary referral hospital. Demographic, clinical, blood test and 24-hour urine collection were recorded. 264 CHD patients, 22 (18-343) years old and 160 (61%) males, were followed up during 9.2 (5.9-11.1) years. 137 (52%), 96 (36%) and 31 (18%) CHD patients had mild, moderate, and great anatomical CHD defects. 44 (17%) and 32 (12%) CHD patients showed proteinuria (≥ 150 mg/24 hours) and albuminuria (> 30 mg/24 hours) respectively. 35 out of 44 (79%) CHD patients with proteinuria (≥ 150 mg/24 hours) showed normal to mild albuminuria levels (< 30 mg/24 hours). Variables associated with proteinuria were male sex, body mass index, auricular fibrillation/flutter, arterial hypertension, diabetes mellitus and being under angiotensin-converting enzyme (ACE) inhibitor and an angiotensin receptor blocker (ARB), loop diuretics or anti-aldosterone treatment. Major adverse cardiovascular events (MACE), defined as cardiovascular and non-cardiovascular deaths, stroke, myocardial infarction and heart failure requiring hospitalization, occurred in 16 (6%) patients during the follow up time. Multivariate Cox regression analysis showed that older patients, patients with a great CHD complexity and patients with proteinuria [6.99 (1.90-24.74), P=0.003] had a significant higher risk of MACE. Proteinuria is frequent among non-hypoxemic CHD patients and occurs mostly in those with a GFR above 60 ml/min/1.73 m
2 and normal to mild albuminuria levels. Having proteinuria, but not albuminuria, was independently associated with a worse outcome., Competing Interests: None., (AJCD Copyright © 2021.)- Published
- 2021
46. Malnutrition is independently associated with an increased risk of major cardiovascular events in adult patients with congenital heart disease.
- Author
-
Martínez-Quintana E, Sánchez-Matos MM, Estupiñán-León H, Rojas-Brito AB, González-Martín JM, Rodríguez-González F, and Tugores A
- Subjects
- Adolescent, Adult, Body Mass Index, Female, Heart Defects, Congenital diagnosis, Heart Defects, Congenital mortality, Heart Defects, Congenital physiopathology, Heart Disease Risk Factors, Humans, Hypoalbuminemia epidemiology, Male, Malnutrition diagnosis, Malnutrition mortality, Malnutrition physiopathology, Nutrition Assessment, Prevalence, Prognosis, Prospective Studies, Risk Assessment, Spain epidemiology, Time Factors, Young Adult, Heart Defects, Congenital epidemiology, Malnutrition epidemiology, Nutritional Status, Survivors
- Abstract
Background and Aims: Malnutrition is found frequently during chronic diseases, and its prevalence and relation to disease outcome in adult patients with congenital heart disease (CHD) remains unknown., Methods and Results: A cohort of 393 consecutive stable congenital heart disease (CHD) patients was followed up in a single dedicated clinical unit. Demographic, clinical and laboratory parameters, along with a nutritional risk index (NRI), were studied, as well as major acute cardiovascular events (MACE), defined as arterial thrombotic events, heart failure requiring hospitalization or cardiovascular and non-cardiovascular mortality. The median age of the patients was 23 years (17-35) and 225 (57%) were males. Median plasma albumin concentration was 4.5 (4.2-4.7) g/dL, the body mass index was 23 (21-27) kg/m
2 , the NRI was 112 (106-118), and 33 (8%) patients showed malnutrition (NIR<100). A worse NYHA functional class (II and III), total cholesterol and serum glucose levels were significant risk factors associated with malnutrition (NRI<100) in CHD patients. During a median follow-up of 8 (5-10) years, 39 (10%) CHD patients suffered a MACE. Multivariable Cox regression analysis showed that older patients (years) [HR 1.06 (1.04-1.09), p < 0.001], CHD patients with great anatomical complexity [HR 4.24 (2.17-8.27), p < 0.001] and those with a lower NRI [HR 0.95 (0.93-0.98), p = 0.001] had a significant worse MACE-free survival, being the NRI a better predictor of MACE than albumin concentration., Conclusions: A low NRI is independently associated with a significant increased risk of MACE in CHD patients., Competing Interests: Declaration of competing interest No conflicts of interest., (Copyright © 2020 The Italian Diabetes Society, the Italian Society for the Study of Atherosclerosis, the Italian Society of Human Nutrition and the Department of Clinical Medicine and Surgery, Federico II University. Published by Elsevier B.V. All rights reserved.)- Published
- 2021
- Full Text
- View/download PDF
47. Predicting sudden cardiac death in adults with congenital heart disease.
- Author
-
Oliver JM, Gallego P, Gonzalez AE, Avila P, Alonso A, Garcia-Hamilton D, Peinado R, Dos-Subirà L, Pijuan-Domenech A, Rueda J, Rodriguez-Puras MJ, Garcia-Orta R, Martínez-Quintana E, Datino T, Fernandez-Aviles F, and Bermejo J
- Subjects
- Adult, Case-Control Studies, Female, Humans, Incidence, Logistic Models, Male, Middle Aged, Prognosis, Prospective Studies, Risk Assessment, Death, Sudden, Cardiac epidemiology, Death, Sudden, Cardiac etiology, Heart Defects, Congenital complications
- Abstract
Objectives: To develop, calibrate, test and validate a logistic regression model for accurate risk prediction of sudden cardiac death (SCD) and non-fatal sudden cardiac arrest (SCA) in adults with congenital heart disease (ACHD), based on baseline lesion-specific risk stratification and individual's characteristics, to guide primary prevention strategies., Methods: We combined data from a single-centre cohort of 3311 consecutive ACHD patients (50% male) at 25-year follow-up with 71 events (53 SCD and 18 non-fatal SCA) and a multicentre case-control group with 207 cases (110 SCD and 97 non-fatal SCA) and 2287 consecutive controls (50% males). Cumulative incidences of events up to 20 years for specific lesions were determined in the prospective cohort. Risk model and its 5-year risk predictions were derived by logistic regression modelling, using separate development (18 centres: 144 cases and 1501 controls) and validation (two centres: 63 cases and 786 controls) datasets., Results: According to the combined SCD/SCA cumulative 20 years incidence, a lesion-specific stratification into four clusters-very-low (<1%), low (1%-4%), moderate (4%-12%) and high (>12%)-was built. Multivariable predictors were lesion-specific cluster, young age, male sex, unexplained syncope, ischaemic heart disease, non-life threatening ventricular arrhythmias, QRS duration and ventricular systolic dysfunction or hypertrophy. The model very accurately discriminated (C-index 0.91; 95% CI 0.88 to 0.94) and calibrated (p=0.3 for observed vs expected proportions) in the validation dataset. Compared with current guidelines approach, sensitivity increases 29% with less than 1% change in specificity., Conclusions: Predicting the risk of SCD/SCA in ACHD can be significantly improved using a baseline lesion-specific stratification and simple clinical variables., Competing Interests: Competing interests: None declared., (© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.)
- Published
- 2021
- Full Text
- View/download PDF
48. Mediterranean diet adherence in patients with congenital heart disease.
- Author
-
Martínez-Quintana E, Rojas-Brito AB, Estupiñán-León H, and Rodríguez-González F
- Abstract
The Mediterranean diet, based on a rural life where people ate what they grew, has shown cardiovascular benefits. Cross-sectional study of congenital heart disease (CHD) patients recruited consecutively from a single hospital outpatient clinic with the aim of determining their adherence to the Mediterranean diet according to the PREDIMED questionnaire. CHD complexity was categorized as simple, moderate, or great and demographic, clinical and blood test data were recorded. 200 CHD patients, median age 28 (16-54) years old and 120 (60%) males were studied. 45 (22.5%), 122 (61%) and 33 (16.5%) CHD patients had simple, moderate, and great complexity defects respectively. PREDIMED score was classified as low (score 0-5), intermediate (6-9) or high (> 9). 146 (83%) CHD patients showed a suboptimal Mediterranean diet adherence (PREDIMED score < 9) with less than half of patients eating enough vegetables, fruits, legumes, fish or nuts but with a high intake of butter/margarine, commercial sweets and carbonated beverages. No significant differences were seen between sex, body mass index, cardiovascular risk factors, CHD complexity or the educational level and the PREDIMED scores. Only being married was associated with a significant lower Mediterranean diet adherence (P=0.019). Meanwhile, no statistical significance was observed between serum glucose, creatinine, uric acid, albumin, LDL cholesterol, HDL cholesterol or triglycerides levels according to the PREDIMED classification (low, intermediate or high adherence). Conclusions: CHD patients have a low adherence to the Mediterranean diet with a low intake of vegetables, fruits, legumes, and fish., Competing Interests: None., (AJCD Copyright © 2020.)
- Published
- 2020
49. Red blood cell distribution width in addition to N-terminal prohormone of B-type natriuretic peptide concentration improves assessment of risk of cardiovascular events in adult patients with congenital heart disease.
- Author
-
Martínez-Quintana E, Estupiñán-León H, Riaño-Ruiz M, Rodríguez-González F, and Tugores A
- Subjects
- Adolescent, Adult, Biomarkers blood, Case-Control Studies, Female, Heart Defects, Congenital blood, Heart Defects, Congenital complications, Humans, Male, Middle Aged, Predictive Value of Tests, Prognosis, Prospective Studies, Risk Assessment, Risk Factors, Young Adult, Erythrocyte Indices, Heart Defects, Congenital diagnosis, Natriuretic Peptide, Brain blood, Peptide Fragments blood
- Abstract
Background: Red blood cell distribution width (RDW) is a predictor of adverse outcomes in patients with heart disease., Aim: To establish predictors of high RDW values in patients with congenital heart disease (CHD), and their relationship with cardiovascular events., Methods: Overall, 561 patients with stable CHD who attended a single outpatient clinic and a matched control population of 2128 patients were studied. Exclusion criteria were renal failure, anaemia, receiving iron therapy and cyanosis. Blood tests included glucose, creatinine, iron, apoferritin, liver enzymes and a complete blood count. C-reactive protein and N-terminal prohormone of B-type natriuretic peptide (NT-pro-BNP) concentrations were also measured in patients with CHD. Major adverse cardiac events (MACE) were defined as cardiovascular/total mortality, arterial thrombotic events, arrhythmias, major bleedings, pulmonary embolism or heart failure needing hospital admission., Results: The median age in patients with CHD was 23 (17-36) years and the median follow-up time was 5.8 (3.2-8.7) years; 103 (4.8%) controls and 40 (7.1%) patients with CHD had an RDW>15% (P=0.032). During follow-up, MACE were reported in 48 patients. CHD of great complexity, cardiovascular risk factors, low haemoglobin concentration and high NT-pro-BNP concentration were risk factors for an RDW>15%. Kaplan-Meier analysis showed a significantly worse cardiovascular outcome in patients with CHD with an RDW>15% (P<0.001). The multivariable survival analysis determined that age, CHD of great complexity, high NT-pro-BNP concentration and an RDW>15% were independent predictive factors for MACE., Conclusion: RDW and NT-pro-BNP concentration are independent analytical predictors of MACE in patients with CHD., (Copyright © 2020 Elsevier Masson SAS. All rights reserved.)
- Published
- 2020
- Full Text
- View/download PDF
50. Prevalence and predictors of psychological distress in congenital heart disease patients.
- Author
-
Martínez-Quintana E, Girolimetti A, Jiménez-Rodríguez S, Fraguela-Medina C, Rodríguez-González F, and Tugores A
- Subjects
- Adult, Cross-Sectional Studies, Female, Heart Defects, Congenital therapy, Humans, Male, Prevalence, Risk Factors, Young Adult, Heart Defects, Congenital psychology, Psychological Distress
- Abstract
Objective: To determine psychological distress in congenital heart disease (CHD) patients., Methods: Cross-sectional study among consecutive CHD patients recruited from a single hospital outpatient clinic to determine anxiety and depression according to the Hospital Anxiety and Depression Scale (HADS) questionnaire., Results: One hundred and sixty-nine CHD patients [29 (19-39) years old, 100 (59%) males] were studied. A total of 25% and 9% of CHD patients showed anxiety and depression symptoms, respectively. Patients with an HADS score ≥ 8 had a significantly worse New York Heart Association (NYHA) functional class, needed more psychological support, had more mental health history, and took more anxiolytic/antidepressant medication than the CHD patients with an HADS score below 8. A worse NYHA functional class [OR, 1.88 (1.01-3.52)] proved to be a predictor of a borderline/abnormal HADS score., Conclusion: Psychological distress has a high prevalence among CHD patients and having an NYHA Class II and III is a significant predictor of an HADS score ≥ 8., (© 2020 Wiley Periodicals, Inc.)
- Published
- 2020
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.