Prognostic Importance of Cardiomegaly in Patients with Acute Myocardial Infarction

Total Page:16

File Type:pdf, Size:1020Kb

Prognostic Importance of Cardiomegaly in Patients with Acute Myocardial Infarction Emergencias 2015;27:294-300 ORIGINAL ARTICLE Prognostic importance of cardiomegaly in patients with acute myocardial infarction Leticia Jaulent-Huertas 1, Luciano Consuegra-Sánchez 1, Marta Vicente-Gilabert 2, Antonio Melgarejo-Moreno 1, Nuria Alonso-Fernández 1, Angela Díaz-Pastor 1, Germán Escudero-García 1, José Galcerá-Tomás 2 Objectives. To assess the in-hospital and long-term prognostic importance of cardiomegaly demonstrated by a simple Affiliation of authors: admission radiograph in patients hospitalized for acute myocardial infarction. 1Servicio de Cardiología y Medicina Intensiva, Hospital Methods. Prospective study of 7644 patients admitted for acute myocardial infarction; 2 hospitals participated. We Universitario de Santa Lucía, Cartagena, Murcia, Spain. recorded detailed clinical data, especially noting the presence or absence of cardiomegaly in the chest radiograph. 2Servicio de Medicina Intensiva, Adjusted predictive models for all-cause mortality in hospital or after discharge were constructed. The median follow- Hospital Universitario Virgen de la up was 6 years. Arrixaca, Murcia, Spain. Results. Cardiomegaly was detected in 1351 (17.7%) of the patients. Hospital mortality was 11.2% overall; the inci - Corresponding author: dence of long-term mortality was 5.7 per 100 patient-years. Patients with cardiomegaly were older and had more car - Luciano Consuegra Sánchez Unidad de Hemodinámica diovascular risk factors other than current smoking; they also had more concomitant conditions, had undergone few - Cardiaca er revascularization procedures, and received suboptimal care after discharge. Cardiomegaly was associated with Servicio de Cardiología higher in-hospital rates of adverse events, especially heart failure (70.8% in patients with cardiomegaly vs 21.4% in Hospital Universitario de Santa Lucía others, P<.001) and death (27.8% vs 7.7%, P<.001). Cardiomegaly was also an independent predictor of hospital C/ Mezquita, s/n mortality (odds ratio, 1.34; P=.02) as well as mortality after discharge (hazard ratio, 1.16; P<.01). 30202 Cartagena, Murcia, Spain Conclusions. Cardiomegaly was an independent predictor of both hospital mortality and long-term mortality after Email: discharge in this series. [email protected] Keywords: Myocardial infarction. Cardiomegaly. Prognosis. Article information: Received: 5-5-2015 Accepted: 3-6-2015 Online : 9-9-2015 Importancia de la presencia de cardiomegalia en el pronóstico de los pacientes con infarto agudo de miocardio Objetivos. Conocer el significado pronóstico intrahospitalario y a largo plazo de la presencia de cardiomegalia en la radiología simple inicial de los pacientes ingresados por infarto agudo de miocardio. Métodos: Estudio prospectivo de 7.644 pacientes ingresados por un infarto agudo de miocardio en dos hospitales. Se obtuvo información clínica detallada y se prestó especial atención a la presencia/ausencia de cardiomegalia en la ra - diografía de tórax. Realizamos modelos ajustados para predecir mortalidad (por cualquier causa) hospitalaria y tras el alta con una mediana de 6 años. Resultados: 1.351 (17,7%) pacientes presentaron cardiomegalia. La mortalidad hospitalaria global fue 11,2% y la densidad de incidencia de mortalidad a largo plazo fue de 5,7 por cada 100 pacientes-año. Los pacientes con cardio - megalia presentaron mayor edad y más factores de riesgo cardiovascular excepto tabaquismo activo, mayor comorbi - lidad, fueron menos revascularizados y tratados al alta de forma subóptima. Durante la hospitalización, la cardiomega - lia se asoció a mayores tasas de complicaciones, especialmente insuficiencia cardiaca (70,8 vs 21,4%, p < 0,001) y mortalidad (27,8 vs 7,7%, p < 0,001). La cardiomegalia resultó predictor independiente sobre la mortalidad hospitala - ria ( odds ratio = 1,34; p = 0,02) y tras el alta (hazard ratio = 1,16, p < 0,01). Conclusiones: En pacientes con infarto agudo de miocardio la cardiomegalia resultó predictor independiente de mor - talidad hospitalaria y a largo plazo tras el alta. Palabras clave: Infarto de miocardio. Cardiomegalia. Pronóstico. Introduction cal Associations recommend that the assessment of chest pain sufferers should include a detailed medical Chest pain is one of the most common symptoms history and a number of observations, such as: descrip - that drive patients to emergency departments (EDs). tion of the pain, its duration and accompanying The US National Health Statistic Report lists chest pain symptoms, a physical examination to identify high-risk as the second most frequent cause of ED visits 1. Medi - patients and rule out non-cardiac diseases, an electro - 294 Jaulent-Huertas L, et al. Emergencias 2015;27:294-300 cardiogram as an important source of prognostic infor - failure underwent at least one additional posteroante - mation and a determinant of patient selection, cardiac rior (PA) radiograph to confirm the presence of cardio - biomarker tests, especially high-sensitivity cardiac tropo - megaly. nin assay and a plain chest x-ray. All these measures are Brain and retroperitoneal haemorrhages and any necessary for the correct assessment of patients with other haemorrhage causing haemodynamic deteriora - chest pain attending centres with or without chest pain tion and/or need for transfusion of blood or blood pro - units 2. Previous publications suggest that cardiomegaly ducts or major bleeding complications were considered may be an adverse prognostic marker in patients with serious. Long-term follow-up (median: 6 years) was ca - dilated cardiomyopathy 3, valvular heart disease 4, hyper - rried out via telephone calls, medical record reviews, tensive heart disease 5 and ischemic heart disease 6-8 . outpatient follow-up visits and death records. In-hospi - Plain chest x-ray used to be the preferred method tal mortality was not included in these analyses. to assess pulmonary congestion and cardiomegaly (in - The relationship between dichotomous variables creased cardio-thoracic ratio) during the initial assess - was analysed using contingency tables and chi-square ment of acute myocardial infarction (AMI) patients 9-11 . or Fisher's exact tests. Quantitative variables were analy - This method lost its prevalence after the adoption in sed using ANOVA and Kruskal-Wallis tests, as appropria - the late 1960s of the Killip-Kimball classification 12 , a te. Factors associated with in-hospital death were analy - system based on physical examination and with subs - sed using binary multivariate logistic regression. Odds tantial clinical and prognostic value, both in the short ratio (OR) and their 95% confidence intervals (CI) were and long term. Cardiomegaly may not be a reliant mar - determined. Calibration and discrimination of the final ker of ventricular dysfunction 13 , and yet some studies 14,15 model were calculated. Survival after hospital discharge identify it as an adverse prognostic marker during fo - was assessed using Kaplan-Meier survival curves and the llow up. The aim of this study was to analyse the use - resulting groups were compared with Mantel-Haenszel fulness of x-ray measured cardiomegaly for in-hospital tests. To measure associations, we used Cox regression and long-term prognosis of patients visiting the ED for with hazard ratio (HR) and 95% CI. Non-normally dis - chest pain and diagnosed with AMI. tributed variables were base-10 logarithmic transfor - med. Confounding variables for both multivariate mo - dels were: 1) variables that for our study showed Method association with the variable of interest: death from any cause; and 2) variables that showed consistent associa - From January 1998 to March 2014, we conducted tion with the variable of interest in previous studies. an observational and prospective study of all patients Covariates were included using the Enter method. The diagnosed with AMI and consecutively admitted to the log-linear model was tested graphically. The proportio - coronary units of two hospitals in the province of Mur - nal hazards assumption was assessed through a Schoen - cia, Spain: Hospital Universitario Virgen de la Arrixaca, feld residuals test and a graphical method. The percen - municipality of Murcia, and Hospital Universitario de tage of missing values per variable was usually less than Santa Lucia, municipality of Cartagena. Patients with 2% for most (99%) of the variables. The most relevant periprocedural AMI after coronary revascularisation we - first-order interactions were analysed in the adjusted re not included. For the study, AMI was defined as typi - model. Statistical significance was set at the 0.05 level cal chest pain lasting 30 minutes and/or elevated bio - (p <0.05). Statistical analyses were performed with two markers of myocardial necrosis. Subjects included packages: IBM’s PASW version 20 and StataCorp’s STA - patients with ST-segment elevation myocardial infarc - TA version 9.1. tion (STEMI) and non-ST-segment elevation myocardial infarction (NSTEMI). The study was approved by the research ethics Results committees of both medical centers and patients gave their written consent to participate in the study. Table 1 shows the baseline characteristics of the Detailed demographic information of each patient study sample (n = 7,644). The mean age of the pa - was compiled. The initial chest radiograph was assessed tients was 66 ± 13 years, 26.7% women; 37.6% had in terms of four degrees: (1) absence of pulmonary diabetes, 75.2% had suffered STEMI and 24.4% sho - congestion, (2) presence of pulmonary blood flow re - wed signs of heart
Recommended publications
  • Cardiac Involvement in COVID-19 Patients: a Contemporary Review
    Review Cardiac Involvement in COVID-19 Patients: A Contemporary Review Domenico Maria Carretta 1, Aline Maria Silva 2, Donato D’Agostino 2, Skender Topi 3, Roberto Lovero 4, Ioannis Alexandros Charitos 5,*, Angelika Elzbieta Wegierska 6, Monica Montagnani 7,† and Luigi Santacroce 6,*,† 1 AOU Policlinico Consorziale di Bari-Ospedale Giovanni XXIII, Coronary Unit and Electrophysiology/Pacing Unit, Cardio-Thoracic Department, Policlinico University Hospital of Bari, 70124 Bari, Italy; [email protected] 2 AOU Policlinico Consorziale di Bari-Ospedale Giovanni XXIII, Cardiac Surgery, Policlinico University Hospital of Bari, 70124 Bari, Italy; [email protected] (A.M.S.); [email protected] (D.D.) 3 Department of Clinical Disciplines, School of Technical Medical Sciences, University of Elbasan “A. Xhuvani”, 3001 Elbasan, Albania; [email protected] 4 AOU Policlinico Consorziale di Bari-Ospedale Giovanni XXIII, Clinical Pathology Unit, Policlinico University Hospital of Bari, 70124 Bari, Italy; [email protected] 5 Emergency/Urgent Department, National Poisoning Center, Riuniti University Hospital of Foggia, 71122 Foggia, Italy 6 Department of Interdisciplinary Medicine, Microbiology and Virology Unit, University of Bari “Aldo Moro”, Piazza G. Cesare, 11, 70124 Bari, Italy; [email protected] 7 Department of Biomedical Sciences and Human Oncology—Section of Pharmacology, School of Medicine, University of Bari “Aldo Moro”, Policlinico University Hospital of Bari, p.zza G. Cesare 11, 70124 Bari, Italy; [email protected] * Correspondence: [email protected] (I.A.C.); [email protected] (L.S.) † These authors equally contributed as co-last authors. Citation: Carretta, D.M.; Silva, A.M.; D’Agostino, D.; Topi, S.; Lovero, R.; Charitos, I.A.; Wegierska, A.E.; Abstract: Background: The widely variable clinical manifestations of SARS-CoV2 disease (COVID-19) Montagnani, M.; Santacroce, L.
    [Show full text]
  • Mitral Valve Disease in Dogs- Truly Epic Kristin Jacob, DVM, DACVIM CVCA Cardiac Care for Pets Towson, MD
    Mitral Valve Disease in Dogs- Truly Epic Kristin Jacob, DVM, DACVIM CVCA Cardiac Care for Pets Towson, MD Chronic degenerative mitral valvular disease (DMVD) is the most common heart disease in dogs. In dogs with congestive heart failure, 75% have mitral regurgitation/degenerative valvular disease. Almost all have tricuspid regurgitations as well, but clinically the mitral regurgitation is the most significant. Degenerative valvular disease is most common in small breed dogs and more common in males than females. DMVD has been proven to be inherited in the Cavalier King Charles Spaniel and the Dachshund but several other breeds are predisposed, such as Bichons, poodles, Chihuahuas, Miniature Schnauzers, Boston Terriers. The cause of degenerative valvular disease remains unknown. However, the valve changes occur due to a destruction of collagen, deposition of mucopolysaccharide in the spongiosa and fibrosa layer of mitral valve, which also affects chordae tendinea. These changes prevent effective coaptation of the valve leaflets leading to progressive mitral regurgitation. Mitral regurgitation (MR) leads to decreasing forward output and increasing left atrial and left ventricular dilation and remodeling as well as activation of the neurohormonal systems. Typically, patients will have 2-3 years in asymptomatic phase (time between when heart murmur detected) until symptoms develop - congestive heart failure (CHF). We can detect progressive heart enlargement 6-12 months prior to the development of CHF. This means that we have a fairly long time period to intervene with therapy and alter the progression of the disease - we know what’s coming! Eventually left atrial pressure increases sufficiently and pulmonary congestion develops leading to symptoms of CHF and can also lead to pulmonary hypertension.
    [Show full text]
  • Clinical Manifestation and Survival of Patients with I Diopathic Bilateral
    ORIGINAL ARTICLE Clinical Manifestation and Survival of Patients with Mizuhiro Arima, TatsujiI diopathicKanoh, Shinya BilateralOkazaki, YoshitakaAtrialIwama,DilatationAkira Yamasaki and Sigeru Matsuda Westudied the histories of eight patients who lacked clear evidence of cardiac abnormalities other than marked bilateral atrial dilatation and atrial fibrillation, which have rarely been dis- cussed in the literature. From the time of their first visit to our hospital, the patients' chest radio- graphs and electrocardiograms showed markedly enlarged cardiac silhouettes and atrial fibrilla- tion, respectively. Each patient's echocardiogram showed a marked bilateral atrial dilatation with almost normal wall motion of both ventricles. In one patient, inflammatory change was demonstrated by cardiac catheterization and endomyocardial biopsy from the right ventricle. Seven of our eight cases were elderly women.Over a long period after the diagnosis of cardiome- galy or arrhythmia, diuretics or digitalis offered good results in the treatment of edema and congestion in these patients. In view of the clinical courses included in the present study, we conclude that this disorder has a good prognosis. (Internal Medicine 38: 112-118, 1999) Key words: cardiomegaly, atrial fibrillation, elder women,good prognosis Introduction echocardiography. The severity of mitral and tricuspid regur- gitation was globally assessed by dividing into three equal parts Idiopathic enlargement of the right atrium was discussed by the distance from the valve orifice. The regurgitant jet was de- Bailey in 1955(1). This disorder may be an unusual congenital tected on color Doppler recording in the four-chamber view malformation. A review of the international literature disclosed and classified into one of the three regions (-: none, +: mild, that although several cases have been discussed since Bailey's ++:moderate, +++: severe).
    [Show full text]
  • Case Report Chagas Cardiomyopathy Presenting As Symptomatic Bradycardia: an Underappreciated Emerging Public Health Problem in the United States
    Hindawi Case Reports in Cardiology Volume 2017, Article ID 5728742, 5 pages https://doi.org/10.1155/2017/5728742 Case Report Chagas Cardiomyopathy Presenting as Symptomatic Bradycardia: An Underappreciated Emerging Public Health Problem in the United States Richard Jesse Durrance,1 Tofura Ullah,1 Zulekha Atif,1 William Frumkin,2 and Kaushik Doshi1 1 Department of Internal Medicine, Jamaica Hospital Medical Center, 8900 Van Wyck Expressway, Jamaica, NY 11418, USA 2Department of Cardiology, Jamaica Hospital Medical Center, 8900 Van Wyck Expressway, Jamaica, NY 11418, USA Correspondence should be addressed to Richard Jesse Durrance; [email protected] Received 13 February 2017; Accepted 18 July 2017; Published 16 August 2017 Academic Editor: Aiden Abidov Copyright © 2017 Richard Jesse Durrance et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Chagas cardiomyopathy (CCM) is traditionally considered a disease restricted to areas of endemicity. However, an estimated 300,000 people living in the United States today have CCM, of which its majority is undiagnosed. Wepresent a case of CCM acquired in an endemic area and detected in its early stage. A 42-year-old El Salvadoran woman presented with recurrent chest pain and syncopal episodes. Significant family history includes a sister inEl Salvador who also began suffering similar episodes. Physical exam and ancillary studies were only remarkable for sinus bradycardia. The patient was diagnosed with symptomatic sinus bradycardia and a pacemaker was placed. During her hospital course, Chagas serology was ordered given the epidemiological context from which she came.
    [Show full text]
  • Pathology of Idiopathic Cardiomegaly in Amaica
    Br Heart J: first published as 10.1136/hrt.33.2.193 on 1 March 1971. Downloaded from British Heart_Journal, I97I, 33, I93-202. Pathology of idiopathic cardiomegaly in amaica Marie Campbell, J. M. Summerell, G. Bras, J. A. Hayes, and K. L. Stuart From Department of Pathology and Department of Medicine, University of the West Indies, Kingston 7, Jamaica Twenty-one cases of idiopathic cardiomegaly which came to necropsy have been reviewed. A Investigations included injection and x-ray studies, careful microscopical examination and skip serial sectioning of the conduction systems. The obvious feature was gross cardiomegaly in the absence of atheroma of the large coronary vessels and an associatedfibrosis of the right and left bundle-branches. Three hearts showed thickening of the intramural vessels of 8o0 to 4OOt di- ameter. We suggest that such changes may be one of the causes of the ischaemic electrocardio- graphic findings reported in previous epidemiological surveys. In I963 Stuart and Hayes described patients in similar surveys in the U.S.A. or Britain. with cardiomegaly of unexplained aetiology The cardiothoracic ratio calculated from the seen clinically and at necropsy at the Univer- antero-posterior chest x-ray was also higher sity Hospital of the West Indies (U.H.W.I.) than in a similar study from Wales (Stuart et _. in Jamaica. This paper suggested that a form al., I962; Ashcroft and Miall, I969). These ofidiopathic cardiomegaly occurred with some findings are difficult to explain in a commun- -_ frequency in the Jamaican community. Their ity in which coronary atheroma and myocar- http://heart.bmj.com/ patients were mainly from the lower income dial infarction are not frequent (Robertson, group, the average length of illness being i8 I959).
    [Show full text]
  • Profile for Estimating Risk of Heart Failure
    ORIGINAL INVESTIGATION Profile for Estimating Risk of Heart Failure William B. Kannel, MD, MPH; Ralph B. D’Agostino, PhD; Halit Silbershatz, PhD; Albert J. Belanger, MS; Peter W. F. Wilson, MD; Daniel Levy, MD Context: We devised a risk appraisal function to assess pacity or chest x-ray film because these may not be readily the hazard of heart failure in persons who are predis- available in some clinical settings. posed by coronary disease, hypertension, or valvular heart disease. Results: Using the risk factors that make up the multi- variate risk formulation—derived from ordinary office Objective: To provide general practitioners and intern- procedures—the probability of developing heart failure ists with a cost-effective method to select people at high can be estimated and compared with the average risk for risk who are likely to have impaired left ventricular sys- persons of the same age and sex. Using this risk profile, tolic function and may therefore require further evalu- 60% of events in men and 73% in women occurred in ation and aggressive preventive measures. subjects in the top quintile of multivariate risk. Methods: The routinely measured risk factors used in Conclusions: Using this multivariate risk formula- constructing the heart failure profile include age, elec- tion, it is possible to identify high-risk candidates for trocardiographic left ventricular hypertrophy, cardio- heart failure who are likely to have a substantial yield megaly on chest x-ray film, heart rate, systolic blood pres- of positive findings when tested for objective evidence sure, vital capacity, diabetes mellitus, evidence of of presymptomatic left ventricular dysfunction.
    [Show full text]
  • Cardiothoracic Ratio and Left Heart Valves Regurgitation Kardiyotorasik Oran Ve Sol Kalp Kapak Yetersizli¤I
    150 Editorial Comment Editöryel Yorum Cardiothoracic ratio and left heart valves regurgitation Kardiyotorasik oran ve sol kalp kapak yetersizli¤i Valvular heart disease is one of the most important heart It has been demonstrated that the traditional linear disorders that causes heart failure in children and it can be cardiothoracic ratio shows an inverse correlation with the left congenital or acquired. Almost all acquired valvular heart ventricular ejection fraction (5). Recent studies have shown the diseases are rheumatic in origin. Mitral valve involvement chest radiography to have a relatively high specificity in occurs in about three quarters of all cases of rheumatic heart predicting cardiac enlargement on echocardiography (6). disease and aortic valve involvement in about one quarter (1). Davidson et al. (7) demonstrated that, although there was Mitral regurgitation (MR) is the most common valvular involve- good correlation between the radiographic total cardiac volume ment in children with rheumatic heart disease and aortic and echocardiographic ventricular volumes, especially for regurgitation (AR) is less common. Apart from rheumatic heart left-sided lesions in children, cardiothoracic ratio and cardiac disease, the major causes of MR and AR are infective endocarditis, frontal area did not correlate with echocardiographic measure- collagen-vascular disease, cardiomyopathy, congenital heart ments. However, Satou et al. (6) found that chest radiography disease and annular abnormalities (1). The left ventricle initially has a limited ability to accurately detect cardiac enlargement in compensates in acute MR, in part by emptying more completely children referred to a pediatric cardiac clinic. and in part by increasing preload, i.e., by use of the Frank-Starling In the study published in the current issue of the Anatolian principle.
    [Show full text]
  • Familial Cardiomegaly by R
    Br Heart J: first published as 10.1136/hrt.18.2.251 on 1 April 1956. Downloaded from FAMILIAL CARDIOMEGALY BY R. T. GAUNT AND M. A. LECUTIER From the Departments of Pathology and Medicine, Royal Hospital, Chesterfield Received July 9, 1955 William Evans (1949) described a series of cases of cardiac enlargement in which none of the usual causes of cardiomegaly was present, and among this series of nine cases there were three who were related (a mother and two sons). Moreover, the mode of death in several relatives suggested that a similar condition may have been present in other members of the family. A similar family history had been reported previously in patients with unexplained cardiomegaly on two occasions (Case Records, Massachusetts General Hospital, 1942) and Addarii and Mahaim (1946). A necropsy carried out on one member of the family described by Evans showed an unusual finding in that there were extensive glycogen deposits in the heart muscle; in addition there were areas of dense fibrosis with hypertrophy of remaining fibres. Similar deposits of gly- cogen were also found in the vastus externus muscle. Glycogen is found in the heart muscle in some cases of Von-Gierke's disease but Evans did not consider his case to be an example of this condition as there was no evidence of a failure of glycogenolysis. Moreover, death has always occurred at an early age in the recorded cases of Von-Gierke's disease that have shown cardiac involvement. Evans concluded that this was a definite syndrome possibly related to Friedreich's ataxia and suggested that it be called familial cardiomegaly.
    [Show full text]
  • Mitral Stenosis
    Valvular heart diseases METHODIC MATERIALS FOR INTERNATIONAL STUDENTS (IV-VI year) Author: N.A.Filippova, assistant professor Published: 2004 Valvular heart disease with mitral valve affection Normal mitral valve Anatomy The normal mitral valve is a complex structure, consisting of leaflets, annulus, chordae tendineae, and papillary muscles. Its anatomy as studied at autopsy shows an unusual degree of variation between normal subjects. Of the two leaflets, the anterior one is the larger, both from base to margin, and also in its perimeter. It is attached to the root of the aorta and the membranous septum at the base of the heart, and is continuous with the chordae peripherally. It thus passes across the centre of the left ventricular cavity, dividing the inlet from the outlet portion. The posterior cusp is attached to the mitral ring and to the anterior cusp at both commissures. It is continuous with the posterior wall of the left atrium, and is divided into three portions by two scallops. The chordae arise from the ventricular margins of both cusps, and are inserted into the heads of the papillary muscles. There are multiple subdivisions in the chordae as they pass from papillary muscles to the cusps, which form an effective secondary pathway, additional to the main one between the cusps, for blood to enter the ventricle. There are two papillary muscles, one anteromedial and the other posterolateral. In general, the former is larger, and has a more uniform structure than the latter which may be double. Both may have up to six heads, giving rise to chordae.
    [Show full text]
  • Cough As a Cause and Consequence of Heart Dysfunction - Current State of Art
    Physiol. Res. 69 (Suppl. 1): S105-S121, 2020 https://doi.org/10.33549/physiolres.934408 REVIEW Cough as a Cause and Consequence of Heart Dysfunction - Current State of Art Elzbieta M. GRABCZAK1, Sebastian STEC2, Marta DABROWSKA1, Jana PLEVKOVA3, Rafal KRENKE1 1Department of Internal Medicine, Pulmonary Diseases and Allergy, University Clinical Centre, Medical University of Warsaw, Poland, 2MediNice Research and Development Centre, Krosno, Poland, 3Department of Pathophysiology, Jessenius Faculty of Medicine in Martin, Comenius University Bratislava, Martin, Slovak Republic Received October 5, 2019 Accepted November 25, 2019 Summary diseases. Even though cough is triggered exclusively by The cough reflex is an airway defensive process that can be vagal reflex and is aimed at the airway defence, it can be modulated by afferent inputs from organs located also out of the elicited and modulated by afferent inputs from respiratory system. A bidirectional relationship between cough extrapulmonary organs, e.g. esophagus or external and heart dysfunctions are presented in the article, with the auditory canal (Canning et al. 2014, Widdicombe 1995), special insights into an arrhythmia-triggered cough. Albeit rare, because the cough is related to stimulation of vagal cough induced by cardiac pathologies (mainly arrhythmias) afferents, irrespective of the organ localization seems to be an interesting and underestimated phenomenon. (Widdicombe 1995). Although the vagal nerve plays This condition is usually associated with the presence of a fundamental role in cough, the significance of abnormal heart rhythms and ceases with successful treatment of convergence of other than vagal afferent inputs to the arrhythmia either by pharmacotherapy or by radiofrequency neuronal clusters in the brainstem - known as the cough ablation of arrhythmogenic substrate.
    [Show full text]
  • Firefighter Suffers Heart Attack After Participating in a Parade – New York
    2016 08 August 29, 2016 Firefighter Suffers Heart Attack After Participating in a Parade – New York Executive Summary On August 22, 2015, a 40-year-old male volunteer fire fighter (FF) responded with an assistant chief to aide in command of a fire at an assisted living facility. On arrival, he found the fire had been extinguished. He departed to a neighboring town and marched approximately 1 mile in a parade. Approximately 90 minutes after completing the parade, the FF became unresponsive when being driven back to the fire station by another Fire Department (FD) member. The driver proceeded directly to a nearby ambulance station. Cardiopulmonary resuscitation (CPR) was initiated. Following placement of an automated external defibrillator, three shocks were provided. The FF was transported to the hospital emergency department (ED) where his EKG indicated a heart attack. Despite advance care he was pronounced dead at 2305 hours. The death certificate and autopsy listed atherosclerotic coronary heart disease as the immediate cause of death. Cardiomegaly and obesity were identified as significant conditions contributing to death. The autopsy revealed severe stenosis in the left anterior descending coronary artery, cardiomegaly, and left ventricular hypertrophy. NIOSH investigators concluded that the physical stress of participating in a parade on a warm summer day may have triggered his heart attack. Key Recommendation • Phase in a mandatory comprehensive wellness and fitness program for fire fighters. The National Institute for Occupational Safety and Health (NIOSH), an institute within the Centers for Disease Control and Prevention (CDC), is the federal agency responsible for conducting research and making recommendations for the prevention of work-related injury and illness.
    [Show full text]
  • Familial Cardiomegaly
    Br Heart J: first published as 10.1136/hrt.11.1.68 on 1 January 1949. Downloaded from FAMILIAL CARDIOMEGALY BY WILLIAM EVANS From the Cardiac Department of the London Hospital Received November 8, 1948 When valvular, hypertensive, and congenital heart While under observation for two mqnths, the disease have been excluded as causes of cardiac extrasystoles became more frequent and when attacks enlargement, some rarer condition should be sought, of paroxysmal tachycardia increased in number and but only after excluding bradycardia, pericardial severity, the patient was handicapped in his work at disease, sternal depression, or an elevated diaphragm, times by giddiness. At last, when tachycardia which by themselves without real enlargement pro- (Fig. 2) persisted for two days, pulmonary aedema duce an exaggerated cardiac silhouette on cardio- (Fig. 4) developed and he died on the third day. scopy. Such being eliminated, there remains a Summary of Necropsy (P.M. 121/1947). By group where the cause of cardiac enlargement is Professor Dorothy Russell of the Bernhard Baron obscure, and it is the purpose of this paper to Institute of Pathology. describe cases with common subjective and objective Acute pulmonary a?dema. Heart failure. Familial symptoms, and to propose a syndrome that serves Cardiomegaly. Clear yellow pericardial effusion to explain a hitherto ambiguous form of cardiac (4 oz.). Slight whitish opacity of most of visceral enlargement and facilitates clinical diagnosis of the pericardium over both ventricles. Milk-spot (2X5 condition. by 1X2 cm.) on anterior surface of right ventricle. Foramen ovale patent (about 1 cm. diameter), the NoTEs OF THREE CASES IN ONE FAMILY orifice being valvular.
    [Show full text]