keyword
https://read.qxmd.com/read/38617758/impact-of-atrial-fibrillation-on-1-year-outcome-in-patients-with-implantable-cardioverter-defibrillator-or-cardiac-resynchronization-therapy-with-defibrillator-results-from-the-german-device-registry
#1
JOURNAL ARTICLE
Sebastian Feickert, Niels Christian Ewertsen, Julia Köbe, Thomas Kleemann, Joachim Jehle, Jochen Senges, Matthias Hochadel, Dietrich Andresen, Christoph Stellbrink, Lars Eckardt, Stefan Spitzer, Johannes Brachmann, Hüseyin Ince, Giuseppe D'Ancona
BACKGROUND: Atrial fibrillation (AF) is a cardiac arrhythmia frequently documented in patients requiring implantable cardioverter defibrillators (ICDs) and/or cardiac resynchronization therapy with defibrillator (CRT-D). Patients with diagnosed AF at the point of ICD or CRT-D implantation may have an impaired follow-up outcome. METHODS: The German DEVICE I-II registry is a nationwide prospective multicentre database of patients implanted with ICD and CRT-D with clinical follow-up data...
March 29, 2024: Journal of Thoracic Disease
https://read.qxmd.com/read/38597211/impact-of-atrial-fibrillation-phenotype-and-left-atrial-volume-on-outcome-after-pulmonary-vein-isolation
#2
JOURNAL ARTICLE
Laurève Chollet, Salik Ur Rehman Iqbal, Severin Wittmer, Gregor Thalmann, Antonio Madaffari, Nikola Kozhuharov, Oskar Galuszka, Thomas Küffer, Christoph Gräni, Nicolas Brugger, Helge Servatius, Fabian Noti, Andreas Haeberlin, Laurent Roten, Hildegard Tanner, Tobias Reichlin
AIMS: Pulmonary vein isolation (PVI) is increasingly performed in patients with atrial fibrillation (AF). Both AF phenotype and left atrial (LA) volume have been shown to influence ablation outcome. The inter-relationship of the two is incompletely understood. We aimed to investigate the impact of AF phenotype vs. LA volume on outcome after PVI. METHODS AND RESULTS: In a retrospective analysis of a prospective registry of patients undergoing a first PVI, the association of AF phenotype and LA volume index (LAVI) was assessed as well as their impact on AF recurrence during follow-up...
March 30, 2024: Europace: European Pacing, Arrhythmias, and Cardiac Electrophysiology
https://read.qxmd.com/read/38596441/systemic-juvenile-idiopathic-arthritis-associated-lung-disease-a-retrospective-cohort-study
#3
JOURNAL ARTICLE
Konstantin E Belozerov, Natalia M Solomatina, Eugenia A Isupova, Alla A Kuznetsova, Mikhail M Kostik
BACKGROUND: Lung damage in systemic juvenile arthritis (sJIA) is one of the contemporary topics in pediatric rheumatology. Several previous studies showed the severe course and fatal outcomes in some patients. The information about interstitial lung disease (ILD) in the sJIA is scarce and limited to a total of 100 cases. AIM: To describe the features of sJIA patients with ILD in detail. METHODS: In the present retrospective cohort study, information about 5 patients less than 18-years-old with sJIA and ILD were included...
March 9, 2024: World Journal of Clinical Pediatrics
https://read.qxmd.com/read/38593150/spatial-characteristics-of-non-communicable-diseases-and-their-associations-to-social-conditions-in-a-large-urban-cohort-in-germany-results-from-the-hamburg-city-health-study
#4
JOURNAL ARTICLE
Valerie Andrees, Ramona Bei der Kellen, Matthias Augustin, Jürgen Gallinat, Volker Harth, Hanno Hoven, Simone Kühn, Anne Lautenbach, Christina Magnussen, Nicole Mohr, Raphael Twerenbold, Ines Schäfer, Benjamin Waschki, Birgit-Christiane Zyriax, Jobst Augustin
BACKGROUND: Non-communicable diseases (NCDs) are responsible for many deaths. They are associated with several modifiable and metabolic risk factors and are therefore prone to significant regional variations on different scales. However, only few intra-urban studies examined spatial variation in NCDs and its association with social circumstances, especially in Germany. Thus, the present study aimed to identify associations of personal risk factors and local social conditions with NCDs in a large German city...
2024: PloS One
https://read.qxmd.com/read/38592243/cardiac-mechanics-and-valvular-and-vascular-abnormalities-in-hypereosinophilic-syndrome
#5
REVIEW
Attila Nemes
Hypereosinophilic syndrome (HES) is considered to be a rare myeloproliferative disease that is characterized by persistent eosinophilia with associated multiple-organ damage. The heart is often involved in HES, representing a major cause of morbidity and mortality. HES is a heterogeneous group of disorders; the majority of the cases are idiopathic. Summarizing the findings regarding myocardial, valvular, and vascular abnormalities in a series of patients with HES, most studies found normal left ventricular (LV) volumes with reduced LV global longitudinal strain and LV apical rotation and twist in HES cases, accompanied by increased left atrial (LA) volumes and stroke volumes, reduced peak LA circumferential strain (representing systolic abnormalities), and mitral annular dilation and functional deterioration...
February 28, 2024: Journal of Clinical Medicine
https://read.qxmd.com/read/38586757/methylphenidate-induced-non-ischemic-heart-failure-with-reduced-ejection-fraction-and-mild-pulmonary-hypertension
#6
Derek Ugwendum, Yolande Mbome, Divine Besong Arrey Agbor, Umida Burkhanova, Rita Offor, Ikpechukwu J Okorie, Asher Gorantla, Frances A Amokaye, Muhammed Atere, Jay Nfonoyim
Attention-deficit hyperactivity disorder (ADHD) is a neurodevelopmental disorder that is commonly diagnosed during childhood. Patients present with hyperactive-impulsive behavior and/or inappropriate inattention which may persist through adulthood. Central nervous system stimulants have been used to manage patients with ADHD. Methylphenidate which is used as a first-line therapy has been shown to have adverse cardiovascular effects in these patients. This is a case of a young male with a history of ADHD since childhood on methylphenidate who was diagnosed with acute non-ischemic heart failure with an ejection fraction of 15-20%...
March 2024: Curēus
https://read.qxmd.com/read/38584678/nf-%C3%AE%C2%BAb-affected-the-serum-levels-of-tnf-%C3%AE-and-il-1%C3%AE-via-activation-of-the-mapk-nf-%C3%AE%C2%BAb-signaling-pathway-in-rat-model-of-acute-pulmonary-microthromboembolism
#7
JOURNAL ARTICLE
Yanfen Zhong, Binbin Liang, Xiaofeng Zhang, Jingtao Li, Decai Zeng, Tongtong Huang, Ji Wu
Pulmonary thromboembolism caused by thrombi blocking major pulmonary artery and its branches, is a frequently encountered phenomenon and an important cause of high morbidity and mortality in lung diseases and may develop into persistent pulmonary hypertension (PH). Nuclear factor-κB (NF-κB) signaling pathway had been reported participated in the formation and development of PH by promoting inflammatory response. The aim of this study was to investigate the effects of NF-κB activation on the serum levels of tumor necrosis factor α (TNF-α) and interleukin-1β (IL-1β) in acute pulmonary microthromboembolism (APMTE) rats...
April 2024: Pulmonary Circulation
https://read.qxmd.com/read/38583684/adapting-nitric-oxide-a-review-of-its-foundation-uses-in-austere-medical-conditions-and-emerging-applications
#8
JOURNAL ARTICLE
Brian Strickland, N Stuart Harris
Nitric oxide was first identified as a novel and effective treatment for persistent pulmonary hypertension of the newborn (PPHN), and has since been found to be efficacious in treating acute respiratory distress syndrome (ARDS) and pulmonary hypertension. Physicians and researchers have also found it shows promise in resource-constrained settings, both within and outside of the hospital, such as in high altitude pulmonary edema (HAPE) and COVID-19. The treatment has been well tolerated in these settings, and is both efficacious and versatile when studied across a variety of clinical environments...
April 5, 2024: Nitric Oxide: Biology and Chemistry
https://read.qxmd.com/read/38576766/new-therapeutic-strategy-with-extracorporeal-membrane-oxygenation-for-refractory-hepatopulmonary-syndrome-after-liver-transplant-a-case-report
#9
Belinda Sánchez Pérez, María Pérez Reyes, Jose Aranda Narvaez, Julio Santoyo Villalba, Jose Antonio Perez Daga, Claudia Sanchez-Gonzalez, Julio Santoyo-Santoyo
BACKGROUND: Due to the lack of published literature about treatment of refractory hepatopulmonary syndrome (HPS) after liver transplant (LT), this case adds information and experience on this issue along with a treatment with positive outcomes. HPS is a complication of end-stage liver disease, with a 10%-30% incidence in cirrhotic patients. LT can reverse the physiopathology of this process and restore normal oxygenation. However, in some cases, refractory hypoxemia persists, and extracorporeal membrane oxygenation (ECMO) can be used as a rescue therapy with good results...
March 18, 2024: World Journal of Transplantation
https://read.qxmd.com/read/38574463/isolated-partial-anomalous-pulmonary-veins-a%C3%A2-10-year-experience-at-a-single-center
#10
JOURNAL ARTICLE
Can Jin, Yongtao Wu, Zhiyi Wang, Xiaoran Liu, Qiang Wang
INTRODUCTION: Isolated partial anomalous pulmonary venous connection (PAPVC) is difficult to diagnose, and surgical indications remain controversial. We reviewed 10 y of isolated PAPVC cases. METHODS: The data of patients with isolated PAPVC admitted to the Anzhen Congenital Heart Disease Department from 2010 to 2019 were reviewed retrospectively. RESULTS: Thirty patients, aged between 4 mo and 32 y, were included in this study...
April 3, 2024: Journal of Surgical Research
https://read.qxmd.com/read/38572485/dedifferentiated-early-postnatal-lung-myofibroblasts-redifferentiate-in-adult-disease
#11
JOURNAL ARTICLE
Rachana R Chandran, Taylor S Adams, Inamul Kabir, Eunate Gallardo-Vara, Naftali Kaminski, Brigitte N Gomperts, Daniel M Greif
Alveolarization ensures sufficient lung surface area for gas exchange, and during bulk alveolarization in mice (postnatal day [P] 4.5-14.5), alpha-smooth muscle actin (SMA)+ myofibroblasts accumulate, secrete elastin, and lay down alveolar septum. Herein, we delineate the dynamics of the lineage of early postnatal SMA+ myofibroblasts during and after bulk alveolarization and in response to lung injury. SMA+ lung myofibroblasts first appear at ∼ P2.5 and proliferate robustly. Lineage tracing shows that, at P14...
2024: Frontiers in Cell and Developmental Biology
https://read.qxmd.com/read/38567662/association-of-cardiopulmonary-hemodynamics-and-mortality-in-veterans-with-liver-cirrhosis-a-retrospective-cohort-study
#12
JOURNAL ARTICLE
Arun Jose, Natalia Rahman, Alexander R Opotowsky, Thomas J Glorioso, Stephen W Waldo, Katarina Zeder, Arnold Seto, Jean M Elwing, Francis X McCormack, Bradley A Maron
BACKGROUND: Portopulmonary hypertension (PoPH), associated with increased mortality, can limit treatment options for liver diseases. Data on the continuum of clinical risk related to cardiopulmonary hemodynamics in PoPH are lacking. METHODS AND RESULTS: As part of the United States national Veterans Affairs Clinical Assessment, Reporting, and Tracking database, we performed a retrospective cohort study of adults with cirrhosis undergoing right heart catheterization between October 1, 2017, and September 30, 2022...
April 3, 2024: Journal of the American Heart Association
https://read.qxmd.com/read/38564376/single-cell-rna-sequencing-reveals-repair-features-of-human-umbilical-cord-mesenchymal-stromal-cells
#13
JOURNAL ARTICLE
Chanèle Cyr-Depauw, David P Cook, Ivana Mižik, Flore Lesage, Arul Vadivel, Laurent Renesme, Yupu Deng, Shumei Zhong, Pauline Bardin, Liqun Xu, Marius A Möbius, Jenny Marzahn, Daniel Freund, Duncan J Stewart, Barbara C Vanderhyden, Mario Rüdiger, Bernard Thébaud
RATIONALE: The chronic lung disease bronchopulmonary dysplasia (BPD) is the most severe complication of extreme prematurity. BPD results in impaired lung alveolar and vascular development and long-term respiratory morbidity, for which only supportive therapies exist. Umbilical cord-derived mesenchymal stromal cells (UC-MSCs) improve lung structure and function in experimental BPD. Results of clinical trials with MSCs for many disorders do not yet match the promising preclinical studies...
April 2, 2024: American Journal of Respiratory and Critical Care Medicine
https://read.qxmd.com/read/38552044/abca3-mutation-induced-congenital-pulmonary-surfactant-deficiency-a-case-report
#14
JOURNAL ARTICLE
Chunxia Lei, Chunhui Wan, Caixia Liu
INTRODUCTION: Congenital surfactant deficiency, often caused by mutations in genes involved in surfactant biosynthesis such as ABCA3, presents a significant challenge in neonatal care due to its severe respiratory manifestations. This study aims to analyze the clinical data of a newborn male diagnosed with pulmonary surfactant metabolism dysfunction type 3 resulting from ABCA3 gene mutations to provide insights into the management of this condition. PATIENT CONCERNS: A newly born male child aged 1 day and 3 hours was referred to our department due to poor crying and shortness of breath...
March 29, 2024: Medicine (Baltimore)
https://read.qxmd.com/read/38551880/-copd-diagnostic-and-severity-assessment
#15
JOURNAL ARTICLE
Lucile Regard, Nicolas Roche
COPD: DIAGNOSTIC AND SEVERITY ASSESSMENT. Chronic obstructive pulmonary disease (COPD) is a frequent and underdiagnosed respiratory disease and a leading cause of morbidity and mortality. It should be suspected in patients aged 40 and over presenting with persistent respiratory symptoms (cough, sputum, shortness of breath, recurrent respiratory tract infections) and a history of exposure to risk factors for the disease (smoking, occupational or domestic exposure to noxious particles). Spirometry is required to confirm the diagnosis of COPD, showing persistent airflow limitation with a post-bronchodilator FEV1/FCV inférieur 0...
March 2024: La Revue du Praticien
https://read.qxmd.com/read/38551716/role-of-albumin-infusion-in-cirrhosis-associated-complications
#16
REVIEW
Mohamed A Heybe, Kosha J Mehta
Cirrhosis is an advanced-stage liver disease that occurs due to persistent physiological insults such as excessive alcohol consumption, infections, or toxicity. It is characterised by scar tissue formation, portal hypertension, and ascites (accumulation of fluid in the abdominal cavity) in decompensated cirrhosis. This review evaluates how albumin infusion ameliorates cirrhosis-associated complications. Since albumin is an oncotic plasma protein, albumin infusion allows movement of water into the intravascular space, aids with fluid resuscitation, and thereby contributes to resolving cirrhosis-induced hypovolemia (loss of extracellular fluid) seen in ascites...
March 29, 2024: Clinical and Experimental Medicine
https://read.qxmd.com/read/38550721/whole-exome-sequencing-identifies-dync2h1-mutations-as-a-cause-of-jeune-asphyxiating-thoracic-dystrophy-without-extra-skeletal-organ-involvement
#17
Ali Alsuheel Asseri, Ahmad A Alzoani, Mohammed Almahdi, Hussein Almahdi, Nouf Almushayt, Noha Saad Alyazidi, Basmah Mohammed Al Mufarrih
Jeune syndrome, or asphyxiating thoracic dystrophy (JATD), is a rare autosomal recessive skeletal dysplasia with heterogeneous genetic and clinical phenotypes, which primarily affects cartilage and bone development. Herein, we report a patient with a lethal form of SRTD3 without polydactyly (JATD), which led to severe restrictive lung disease and fatal respiratory failure. A full-term boy was born to a 30-year-old mother who was known to have hypothyroidism and was on thyroxine. The parents were first-degree cousins and had one healthy older son...
2024: International Medical Case Reports Journal
https://read.qxmd.com/read/38547510/sulforaphane-improves-redox-homeostasis-and-right-ventricular-contractility-in-a-model-of-pulmonary-hypertension
#18
JOURNAL ARTICLE
Adriana Conzatti, Rafael Colombo, Rafaela Siqueira, Cristina Campos-Carraro, Patrick Turck, Alexandre Luz de Castro, Adriane Belló-Klein, Alex Sander da Rosa Araujo
Pulmonary arterial hypertension (PAH) is characterized by increased pulmonary vascular resistance, imposing overload on the right ventricle (RV) and imbalance of redox state. Our study investigated the influence of treatment with sulforaphane (SFN), found in cruciferous vegetables, on right ventricle (RV) remodeling and redox homeostasis in monocrotaline-induced pulmonary arterial hypertension (PAH). Male Wistar rats were separated into four groups: control (CTR); control + sulforaphane (CTR + SFN); monocrotaline (MCT); monocrotaline + sulforaphane (MCT + SFN)...
March 14, 2024: Journal of Cardiovascular Pharmacology
https://read.qxmd.com/read/38541781/analysis-of-patients-with-severe-ards-on-vv-ecmo-treated-with-inhaled-no-a-retrospective-observational-study
#19
JOURNAL ARTICLE
Stefan Muenster, Jennifer Nadal, Jens-Christian Schewe, Heidi Ehrentraut, Stefan Kreyer, Christian Putensen, Stefan Felix Ehrentraut
(1) Background : This retrospective study focused on severe acute respiratory distress syndrome (ARDS) patients treated with veno-venous (VV) extracorporeal membrane oxygenation (ECMO) and who inhaled nitric oxide (NO) for pulmonary arterial hypertension (PAH) and/or right ventricular failure (RV failure). (2) Methods : Out of 662 ECMO-supported patients, 366 received VV ECMO, including 48 who inhaled NO. We examined the NO's indications, dosing, duration, and the ability to lower PAH. We compared patients with and without inhaled NO in terms of mechanical ventilation duration, ECMO weaning, organ dysfunction, in-hospital mortality, and survival...
March 8, 2024: Journal of Clinical Medicine
https://read.qxmd.com/read/38536822/immediate-postnatal-prediction-of-death-or-bronchopulmonary-dysplasia-among-very-preterm-and-very-low-birth-weight-infants-based-on-gradient-boosting-decision-trees-algorithm-a-nationwide-database-study-in-japan
#20
JOURNAL ARTICLE
Kota Yoneda, Tomohisa Seki, Yoshimasa Kawazoe, Kazuhiko Ohe, Naoto Takahashi
INTRODUCTION: Bronchopulmonary dysplasia (BPD) poses a substantial global health burden. Individualized treatment strategies based on early prediction of the development of BPD can mitigate preterm birth complications; however, previously suggested predictive models lack early postnatal applicability. We aimed to develop predictive models for BPD and mortality based on immediate postnatal clinical data. METHODS: Clinical information on very preterm and very low birth weight infants born between 2008 and 2018 was extracted from a nationwide Japanese database...
2024: PloS One
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