keyword
https://read.qxmd.com/read/38634311/evaluation-of-the-introduction-of-a-single-lead-ecg-device-and-digital-cardiologist-consultation-platform-among-general-practitioners-in-the-netherlands
#1
JOURNAL ARTICLE
Evert P M Karregat, Marlou A de Koning, Jelle C L Himmelreich, David W Koetsier, Jonas S S G de Jong, Eric P Moll van Charante, Ralf E Harskamp, Wim A M Lucassen
AIM: To evaluate the use of a single-lead electrocardiography (1L-ECG) device and digital cardiologist consultation platform in diagnosing arrhythmias among general practitioners (GPs). BACKGROUND: Handheld 1L-ECG offers a user-friendly alternative to conventional 12-lead ECG in primary care. While GPs can safely rule out arrhythmias on 1L-ECG recordings, expert consultation is required to confirm suspected arrhythmias. Little is known about GPs' experiences with both a 1L-ECG device and digital consultation platform for daily practice...
April 18, 2024: Primary Health Care Research & Development
https://read.qxmd.com/read/38633071/observation-of-blood-motion-in-the-internal-jugular-vein-by-contact-and-contactless-photoplethysmography-during-physiological-testing-case-studies
#2
JOURNAL ARTICLE
Gennadi Saiko, Timothy Burton, Yasuyuki Kakihana, Kosaku Hatanaka, Ohtonari Takahito, Alexandre Douplik
Central venous pressure is an estimate of right atrial pressure and is often used to assess hemodynamic status. However, since it is measured invasively, non-invasive alternatives would be of great utility. The aim of this preliminary study was a) to investigate whether photoplethysmography (PPG) can be used to characterize venous system fluid motion and b) to find the model for venous blood volume modulations. For this purpose, we monitored the internal jugular veins using contact (cPPG) and video PPG during clinically validated physiological tests: abdominojugular test (AJT) and breath holding (BH)...
April 1, 2024: Biomedical Optics Express
https://read.qxmd.com/read/38628989/a-rare-case-of-a-patient-being-alert-and-communicative-despite-severe-hypothermia
#3
Emile Jeunesse, Patrick O'Malley, Nick Petrus, Chelsea McCoy
Hypothermia is defined as a significant drop in core body temperature below 35°C (95°F). It is traditionally staged as mild, moderate, severe, and profound at temperatures of 35°C to 32°C (95°F to 89.6°F), 32°C to 28°C (89.6°F to 82.4°F), <28°C (<82.4°F), and <24°C (75.2°F), respectively. It can also be classified into the same stages by clinical presentations. We present a patient that fits into two different stages based on core body temperature and clinical presentation...
March 2024: Curēus
https://read.qxmd.com/read/38627781/cardiac-herniation-post-left-upper-lobectomy-and-thymectomy-a-case-report
#4
JOURNAL ARTICLE
Hiral Jhala, Mathew Thomas
BACKGROUND: Cardiac herniation occurs when there is a residual pericardial defect post thoracic surgery and is recognised as a rare but fatal complication. It confers a high mortality and requires immediate surgical correction upon recognition. We present a case of cardiac herniation occurring post thymectomy and left upper lobectomy. CASE PRESENTATION: Initial presentation: A 48-year-old male, hypertensive smoker presented with progressive breathlessness and was found to have a left upper zone mass confirmed on CT biopsy as carcinoid of unclear origin...
April 16, 2024: Journal of Cardiothoracic Surgery
https://read.qxmd.com/read/38623359/chest-pain-in-a-patient-with-transthyretin-cardiac-amyloidosis-a-case-report
#5
Linfeng Xie, Suxin Luo, Bi Huang
KEY CLINICAL MESSAGE: Patients with transthyretin cardiac amyloidosis (ATTR-CM) commonly present with dyspnea, fatigue, and edema. In our case, the main presentation was exertional angina, which was atypical in patients with ATTR-CM and should be paid more attention to. ABSTRACT: A 54-year-old woman was admitted with a complaint of exertional chest pain, and she had a history of hypertension. The results of the electrocardiogram and echocardiography revealed the clues of cardiac amyloidosis, and the patient was finally diagnosed with transthyretin cardiac amyloidosis, then she received tafamidis, and the symptoms improved significantly...
April 2024: Clinical Case Reports
https://read.qxmd.com/read/38623139/successful-stent-implantation-into-the-patent-ductus-arteriosus-in-complex-cyanotic-congenital-heart-disease
#6
Kunal Bhugaonkar, Kshitij Balwaik, Neha Masne
Birth-associated structural issues with the heart are known as congenital heart disorders or defects. They might alter the heart's regular blood flow. A 10-month-old female child presented to a tertiary care hospital with symptoms of recurrent cyanotic spells with episodes of desaturation a few months after birth. ECG findings depicted a normal sinus rhythm with a right axis deviation along the right ventricular forces. Two-dimensional echocardiography showed a tetralogy of Fallot with pulmonary atresia with a patent ductus arteriosus from the undersurface of the arch with confluent small pulmonary arteries...
March 2024: Curēus
https://read.qxmd.com/read/38619578/the-role-of-cardiac-magnetic-resonance-in-sports-cardiology-results-from-a-large-cohort-of-athletes
#7
JOURNAL ARTICLE
Viviana Maestrini, Marco Penza, Sara Monosilio, Cristian Borrazzo, Silvia Prosperi, Domenico Filomena, Lucia Ilaria Birtolo, Erika Lemme, Ruggiero Mango, Giuseppe Di Gioia, Gianfranco Gualdi, Maria Rosaria Squeo, Antonio Pelliccia
BACKGROUND: Cardiac magnetic resonance (CMR) provides information on morpho-functional abnormalities and myocardial tissue characterisation. Appropriate indications for CMR in athletes are uncertain. OBJECTIVE: To analyse the CMR performed at our Institute to evaluate variables associated with pathologic findings in a large cohort of athletes presenting with different clinical conditions. METHODS: All the CMR performed at our Institute in athletes aged > 14 years were recruited...
April 15, 2024: Clinical Research in Cardiology: Official Journal of the German Cardiac Society
https://read.qxmd.com/read/38618420/enteric-fever-presenting-with-complete-heart-block-chb-a-rare-case-of-reversible-arrhythmia
#8
Rushikesh H Dhondge, Sourya Acharya, Sunil Kumar, Sachin Agrawal, Shubham V Nimkar
Salmonella enterica serovar Typhi is the causative agent of enteric fever, commonly called "typhoid". This fever can be mistaken for a variety of other febrile disorders. It is an endemic sickness, especially in developing nations. Enteric fever typically manifests with fever, abdominal pain, and constitutional symptoms, making it a diagnostic challenge due to its broad clinical spectrum. Enteric fever also affects various other systems, causing complications, amongst which the cardiovascular system is no exception...
March 2024: Curēus
https://read.qxmd.com/read/38617591/pulmonary-embolism-with-paradoxical-embolization-to-right-coronary-artery-in-the-presence-of-a-large-patent-foramen-ovale-a-case-report
#9
Erik Boberg, Anders Hedman, Jacob Hollenberg
BACKGROUND: Pulmonary embolism (PE) is the leading cause of in-hospital death and the third most frequent cause of cardiovascular death. The clinical presentation of PE is variable, and choosing the appropriate treatment for individual patients can be challenging. CASE SUMMARY: A 64-year-old man presented to hospital with acute chest pain, shortness of breath, and pulmonary oedema. Electrocardiogram revealed ST-elevation myocardial infarction. D-dimer was 18.8 mg/L fibrinogen equivalent units (FEU) (normal <0...
April 2024: European Heart Journal. Case Reports
https://read.qxmd.com/read/38617067/concurrent-myocardial-infarction-in-the-setting-of-thrombotic-thrombocytopenic-purpura-secondary-to-systemic-lupus-erythematosus-a-case-report
#10
Saleh Azadbakht, Bardia Amidi, Narges Naderi, Anwar Sharifaskari, Mahtab Hatami
KEY CLINICAL MESSAGE: In acute thrombotic thrombocytopenic purpura (TTP), apart from urgent treatment, assessing the patient's medical history, especially conditions like systemic lupus erythematosus that could trigger TTP, is crucial. Rarely, TTP patients may experience cardiac conditions as severe as a myocardial infarction. ABSTRACT: A 45-year-old woman manifested severe and acute thrombotic thrombocytopenic purpura (TTP) of unknown origin. The patient's symptoms, the laboratory data, the detection of the reduction in ADAMTS13 activity, and the presence of schistocytes on the peripheral smear confirmed the diagnosis...
April 2024: Clinical Case Reports
https://read.qxmd.com/read/38606204/a-case-report-of-dextrocardia-with-situs-inversus-a-rare-condition-and-its-clinical-importance
#11
Girma Deshimo, Haile Abebe, Getiye Damtew, Enguday Demeke, Seife Feleke
Situs inversus totalis (SIT) is a rare medical condition characterized by a complete mirror-image reversal of the normal positioning of the internal organs. Aristotle initially described situs inversus in animals, while Fabricius first characterized it in humans. Although the specific cause is uncertain, there is evidence of autosomal recessive and X-linked inheritance. Before seeking treatment for an unrelated ailment, many people with SIT are unaware of their distinct anatomy, as in our case. The presented case is a 30-year-old female patient from Central Ethiopia, presented to Hakim Gizaw Teaching Hospital outpatient department of medicine with the complaint of right-sided anterior chest pain for five days...
2024: Case Reports in Medicine
https://read.qxmd.com/read/38601046/the-added-value-of-three-dimensional-transthoracic-echocardiography-in-mitral-annular-disjunction-a-case-report
#12
Konstantinos Papadopoulos, Ignatios Ikonomidis, Mani A Vannan
BACKGROUND: Mitral annular disjunction (MAD) refers to the arrhythmic mitral valve prolapse (MVP) syndrome associated with ventricular arrhythmias and sudden cardiac death. Although the pathophysiology of this disease is still under investigation, specific imaging criteria that establish the diagnosis have been recognized. In this article, we demonstrate most of these criteria using three-dimensional transthoracic echocardiography (3D-TTE) and provide added value in the management of MAD syndrome...
2024: Frontiers in Cardiovascular Medicine
https://read.qxmd.com/read/38599558/brugada-phenocopy-vs-brugada-syndrome-delineating-the-differences-for-optimal-diagnosis-and-management
#13
REVIEW
Galih Januar Adytia, Henry Sutanto
Brugada syndrome (BrS) is a genetic disorder known for its characteristic electrocardiogram (ECG) patterns and increased risk of sudden cardiac death. Brugada phenocopy (BrP) presents similar ECG patterns but is distinguished by its reversible nature when the underlying conditions are resolved. This article delineates the intricacies of BrP, emphasizing its etiology, clinical presentation, diagnosis, treatment, and prognosis. The article categorizes BrP based on various underlying causes, including metabolic disturbances, myocardial infarction, and mechanical compression, among others...
April 8, 2024: Current Problems in Cardiology
https://read.qxmd.com/read/38597764/-stress-echocardiography-in-low-risk-acute-coronary-syndrome-without-persistent-st-segment-elevation-diagnostic-algorithm
#14
JOURNAL ARTICLE
E E Abramenko, T R Ryabova, V V Ryabov, A A Boshchenko, R S Karpov
This review addresses the capabilities of stress EchoCG as a simple, non-invasive, non-radiation method for diagnosing occult disorders of coronary blood flow in patients with non-ST-elevation acute coronary syndrome on a low-risk electrocardiogram. The capabilities of the enhanced stress EchoCG protocol are based on supplementing the standard detection of transient disturbances of local contractility, generally associated with coronary artery obstruction, with an assessment of the heart rate reserve, coronary reserve and other parameters...
March 31, 2024: Kardiologiia
https://read.qxmd.com/read/38597534/electrocardiographic-and-autonomic-nervous-system-changes-after-changes-in-the-posture-of-children-and-adolescents-with-duchenne-muscular-dystrophy
#15
JOURNAL ARTICLE
Rose Mary Ferreira Lisboa da Silva, Nathalia Mussi Monteze, Juliana Gurgel Giannetti, Zilda Maria Alves Meira
BACKGROUND: Duchenne Muscular Dystrophy (DMD) is a rare inherited neuromuscular disease. At first, cardiac involvement may be asymptomatic. Therefore, assessing patients using non-invasive methods can help detect any changes. OBJECTIVES: Analyze the electrocardiogram (ECG) test and heart rate variability (HRV) of the DMD group and compare the information with that of the age-matched control group. METHODS: A prospective study with 27 male patients with DMD (11...
2024: Arquivos Brasileiros de Cardiologia
https://read.qxmd.com/read/38590089/pause-dependent-paroxysmal-episode-of%C3%A2-third-degree-atrioventricular-block-triggered-by%C3%A2-premature-atrial-contraction
#16
JOURNAL ARTICLE
Chengye Di, Wenhua Lin
BACKGROUND Paroxysmal third-degree atrioventricular block (AVB) can exhibit a vast array of symptoms, but commonly, paroxysmal AVB leads to presyncope, syncope, or possibly sudden cardiac death. We present a rare case of pause-dependent paroxysmal AVB that was triggered by a premature atrial contraction. CASE REPORT A 65-year-old man with frequent episodes of presyncope and syncope for 3 weeks was admitted to our hospital for further diagnosis. A resting 12-lead electrocardiogram showed an incomplete right bundle branch block, and a 24-h Holter recording showed multiple episodes of third-degree AVB...
April 9, 2024: American Journal of Case Reports
https://read.qxmd.com/read/38586535/unusual-presentation-of-benzodiazepine-withdrawal-with-takotsubo-syndrome-a-case-report
#17
Isabel Durães Campos, Helena Moreira, Francisco Portal, José Artur Paiva
BACKGROUND: Thousands of people suffer from anxiety, depression, and insomnia every day, with benzodiazepines being one of the strategies used to treat these conditions. Withdrawal from its long-term use can lead to potentially life-threatening complications, including Takotsubo syndrome. The authors highlight an atypical case of Takotsubo syndrome secondary to benzodiazepine withdrawal, a rare life-threatening complication of acute substance withdrawal. CASE SUMMARY: A 58-year-old female presented to the emergency department with altered mental status and acute pulmonary oedema after discontinuing her prescribed benzodiazepines 3 days prior to presentation...
April 2024: European Heart Journal. Case Reports
https://read.qxmd.com/read/38585551/a-novel-variant-in-akap9-gene-a-controversial-gene-in-long-qt-syndrome
#18
JOURNAL ARTICLE
Murat Erdogan, Suleyman Sunkak, Oguzhan Bahadır, Muhammet Ensar Doğan, Yasin Ada, Burhan Balta
INTRODUCTION: Long QT syndrome (LQTS) is a common congenital cause of fatal cardiac arrhythmia. Characteristic clinical findings are prolonged QT interval and ventricular arrhythmia on electrocardiogram (ECG), syncope, seizure, and sudden death. It is a genetically heterogeneous disease. To date, disease-causing variant have been reported in seventeen genes. The AKAP9 is still considered controversial among those genes. CASE REPORT: We report the case of a 10-year-old female who was born from a non-consanguineous Turkish couple...
March 2024: Molecular Syndromology
https://read.qxmd.com/read/38585407/ventricular-predominance-in-biventricular-arrhythmogenic-cardiomyopathy-should-new-subtype-criteria-be-recognized
#19
Santiago Luna-Alcala, Mauricio Garcia-Cardenas, Enrique C Guerra, Pavel Martinez-Dominguez, Aldo Cabello-Ganem, Leonardo Proaño-Bernal, Cristian A Chava-Ponte, Arturo Hernandez-Pacherres, Nilda Espinola-Zavaleta
Arrhythmogenic cardiomyopathy is a biventricular disease in which the effect on the left ventricle can be either equivalent to or more severe than that on the right ventricle. It is a rare disease due to its low reported prevalence and typically becomes clinically evident during the second to fourth decade of life. It represents 4% of sudden cardiac death cases referred for autopsy and 10% of cases of unexplained cardiac arrest. We present a challenging case report of a 68-year-old man who arrived at the emergency room with chest discomfort, palpitations, and light-headedness before a syncopal episode with urinary incontinence...
June 2024: Radiology Case Reports
https://read.qxmd.com/read/38584762/diagnosis-of-behcet-s-disease-in-a-young-male-patient-with-acute-bilateral-pulmonary-embolism-a-case-report-and-literature-review
#20
Mohammad Hadi Tajik Jalayeri, Mahdi Mazandarani, Narges Lashkarbolouk
Behcet's disease (BD) is a chronic and inflammatory vasculitis characterized by recurrent oral and genital aphthous ulcers, uveitis, and skin lesions. Although there is a high rate of deep vein thrombosis in BD, pulmonary arterial thromboembolism (PTE) is a rare complication. We present a 30-year-old patient who was admitted with pleuritic chest pain, non-massive hemoptysis since 4 days ago and medical history of intermittent genial aphthous lesions, and skin lesions. During our evaluation, he had an S1Q3T3 pattern in the electrocardiogram, a high level of D-dimer, a low level of FDP and fibrinogen along with pulmonary emboli in lobar and segmental branches of the right pulmonary artery and segmental branches of left lower lobe pulmonary artery were detected in his pulmonary CT Angiography...
2024: Respiratory Medicine Case Reports
keyword
keyword
166508
1
2
Fetch more papers »
Fetching more papers... Fetching...
Remove bar
Read by QxMD icon Read
×

Save your favorite articles in one place with a free QxMD account.

×

Search Tips

Use Boolean operators: AND/OR

diabetic AND foot
diabetes OR diabetic

Exclude a word using the 'minus' sign

Virchow -triad

Use Parentheses

water AND (cup OR glass)

Add an asterisk (*) at end of a word to include word stems

Neuro* will search for Neurology, Neuroscientist, Neurological, and so on

Use quotes to search for an exact phrase

"primary prevention of cancer"
(heart or cardiac or cardio*) AND arrest -"American Heart Association"

We want to hear from doctors like you!

Take a second to answer a survey question.