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Arrhythmogenic right ventricular cardiomyopathy (ARVC) : Inherited Heart Disease (IHD) Clinic

https://libcat.nshealth.ca/en/permalink/chpams34670
Nova Scotia Health Authority. QEII. Inherited Heart Disease Clinic. Halifax, NS: Nova Scotia Health Authority , 2020.
Pamphlet Number
0630
Available Online
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In arrhythmogenic right ventricular cardiomyopathy (ARVC), the heart muscle is replaced by fat and scar tissue. This can make it harder for the heart to pump blood out to the body. ARVC usually affects the right side of the heart. The fat and scar tissue causes the right side of the heart to stretch. In very bad cases, a weak heart may cause fluid to build up outside of the heart, in the lungs (causing shortness of breath), or the ankles or belly (causing swelling). ARVC also affects the electr…
Available Online
View Pamphlet
Corporate Author
Nova Scotia Health Authority. QEII. Inherited Heart Disease Clinic
Place of Publication
Halifax, NS
Publisher
Nova Scotia Health Authority
Date of Publication
2020
Format
Pamphlet
Language
English
Physical Description
1 electronic document ([6] p.) : digital, PDF file
Subjects (MeSH)
Cardiovascular disorders
Cardiomyopathy
Subjects (LCSH)
Heart--Abnormalities--Patients
Heart--Diseases
Specialty
Cardiovascular system
Abstract
In arrhythmogenic right ventricular cardiomyopathy (ARVC), the heart muscle is replaced by fat and scar tissue. This can make it harder for the heart to pump blood out to the body. ARVC usually affects the right side of the heart. The fat and scar tissue causes the right side of the heart to stretch. In very bad cases, a weak heart may cause fluid to build up outside of the heart, in the lungs (causing shortness of breath), or the ankles or belly (causing swelling). ARVC also affects the electrical activity of the heart and can cause fast, dangerous heart rhythms. The pamphlet gives the most common cause (inherited) of ARVC, symptoms, diagnostic procedures, and treatment (medications, a special pacemaker called an internal cardioverter defibrillator, and rarely a heart transplant). Websites for further information are also noted.
Responsibility
Prepared by: Inherited Heart Disease Clinic, QEII, Halifax
Pamphlet Number
0630
Less detail

Brugada syndrome : Inherited Heart Disease (IHD) Clinic

https://libcat.nshealth.ca/en/permalink/chpams35823
Nova Scotia Health Authority. QEII. Inherited Heart Disease Clinic. Halifax, NS: Nova Scotia Health Authority , 2020.
Pamphlet Number
1773
Available Online
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Brugada syndrome is a rare condition where there are changes in the electrical signals that make the heart beat. In Brugada syndrome, the channels in the heart cells do not work properly. The abnormal opening and closing of the channels can lead to dangerous heart rhythms. The heart may beat so fast that it cannot pump blood out to the body. This can cause collapse and, if the rhythm does not stop, sudden death. The pamphlet provides the causes, symptoms, diagnostic tests, treatments and some g…
Available Online
View Pamphlet
Corporate Author
Nova Scotia Health Authority. QEII. Inherited Heart Disease Clinic
Place of Publication
Halifax, NS
Publisher
Nova Scotia Health Authority
Date of Publication
2020
Format
Pamphlet
Language
English
Physical Description
1 electronic document ([6] p.) : digital, PDF file
Subjects (MeSH)
Heart Defects, Congenital
Brugada Syndrome
Subjects (LCSH)
Brugada syndrome
Congenital heart disease
Specialty
Cardiovascular System
Abstract
Brugada syndrome is a rare condition where there are changes in the electrical signals that make the heart beat. In Brugada syndrome, the channels in the heart cells do not work properly. The abnormal opening and closing of the channels can lead to dangerous heart rhythms. The heart may beat so fast that it cannot pump blood out to the body. This can cause collapse and, if the rhythm does not stop, sudden death. The pamphlet provides the causes, symptoms, diagnostic tests, treatments and some general activity guidelines. Websites for further information are also listed.
Responsibility
Prepared by: Inherited Heart Disease Clinic, QEII, Halifax
Pamphlet Number
1773
Less detail
Marc Dewey. (Second edition) --Berlin: Springer , c2014.
Available Online
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Location
Online
Cardiac computed tomography (CT) has become a highly accurate diagnostic modality that continues to attract increasing attention. This extensively illustrated book aims to assist the reader in integrating cardiac CT into daily clinical practice, while also reviewing its current technical status and applications. Clear guidance is provided on the performance and interpretation of imaging using the latest technology, which offers greater coverage, better spatial resolution, and faster imaging whi…
Available Online
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Author
Dewey, Marc
Responsibility
Marc Dewey
Edition
Second edition
Place of Publication
Berlin
Publisher
Springer
Date of Publication
c2014
Physical Description
1 online resource (xiii, 498 pages : illustrations)
ISBN
9783642418839 (electronic bk.)
9783642418822
Subjects (MeSH)
Cardiovascular Diseases - diagnostic imaging
Tomography, Emission-Computed
Subjects (LCSH)
Cardiovascular system - Tomography
Abstract
Cardiac computed tomography (CT) has become a highly accurate diagnostic modality that continues to attract increasing attention. This extensively illustrated book aims to assist the reader in integrating cardiac CT into daily clinical practice, while also reviewing its current technical status and applications. Clear guidance is provided on the performance and interpretation of imaging using the latest technology, which offers greater coverage, better spatial resolution, and faster imaging while also providing functional information about cardiac diseases. The specific features of scanners from all four main vendors, including those that have only recently become available, are presented. Among the wide range of applications and issues discussed are coronary calcium scoring, coronary artery bypass grafts, stents, and anomalies, cardiac valves and function, congenital and acquired heart disease, and radiation exposure. Upcoming clinical uses of cardiac CT, such as hybrid imaging, preparation and follow-up after valve replacement, electrophysiology applications, myocardial perfusion and fractional flow reserve assessment, and plaque imaging, are also explored.
Contents
Introduction -- Technical and Personnel Requirements -- Anatomy -- Cardiac CT in Clinical Practice -- Clinical Indications -- Patient Preparation -- Physics Background and Radiation Exposure -- Examination and Reconstruction -- Examinations on Different CT Scanners -- Reading and Reporting -- Coronary Artery Calcium -- Coronary Artery Bypass Grafts -- Coronary Artery Stents -- Coronary Artery Plaques -- Cardiac Function -- Cardiac Valves -- Transcatheter Aortic Valve Interventions -- Pulmonic Valve Implantation, Mitral Valve Repair, and Left Atrial Appendage Closure -- Myocardial Perfusion and Fractional Flow Reserve -- Hybrid Imaging -- Electrophysiology Interventions -- Coronary Artery Anomalies -- Congenital and Acquired Heart Disease -- Typical Clinical Examples -- Results of Clinical Studies -- Outlook.
Format
e-Book
Location
Online
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Catecholaminergic polymorphic ventricular tachycardia (CPVT) : Inherited Heart Disease (IHD) Clinic

https://libcat.nshealth.ca/en/permalink/chpams36689
Nova Scotia Health Authority. QEII. Inherited Heart Disease Clinic. Halifax, NS: Nova Scotia Health Authority , 2020.
Pamphlet Number
2083
Available Online
View Pamphlet
In CPVT, the channels don’t have a normal response to adrenaline. This causes extra heartbeats to start in the bottom chambers of the heart. This can make the heart beat fast. It might beat so fast that it does not pump blood out to the body. This can cause collapse and, if the rhythm does not stop, sudden death. The pamphlet provides the causes, symptoms, diagnostic tests, treatments, and some general activity guidelines. Websites for further information are also listed.
Available Online
View Pamphlet
Corporate Author
Nova Scotia Health Authority. QEII. Inherited Heart Disease Clinic
Place of Publication
Halifax, NS
Publisher
Nova Scotia Health Authority
Date of Publication
2020
Format
Pamphlet
Language
English
Physical Description
1 electronic document ([6] p.) : digital, PDF file
Subjects (MeSH)
Heart Defects, Congenital
Tachycardia, Ventricular
Subjects (LCSH)
Ventricular tachycardia
Congenital heart disease
Specialty
Cardiovascular System
Abstract
In CPVT, the channels don’t have a normal response to adrenaline. This causes extra heartbeats to start in the bottom chambers of the heart. This can make the heart beat fast. It might beat so fast that it does not pump blood out to the body. This can cause collapse and, if the rhythm does not stop, sudden death. The pamphlet provides the causes, symptoms, diagnostic tests, treatments, and some general activity guidelines. Websites for further information are also listed.
Responsibility
Prepared by: Inherited Heart Disease Clinic, QEII, Halifax
Pamphlet Number
2083
Less detail

Dilated cardiomyopathy (DCM) : Inherited Heart Disease (IHD) Clinic

https://libcat.nshealth.ca/en/permalink/chpams34671
Nova Scotia Health Authority. QEII. Inherited Heart Disease Clinic. Halifax, NS: Nova Scotia Health Authority , 2020.
Pamphlet Number
0629
Available Online
View Pamphlet
In dilated cardiomyopathy (DCM), the heart muscle becomes weak. This makes it harder for the heart to pump blood out to the body. This causes the bottom chambers to dilate (stretch). A weak heart can also cause fluid to build up in parts of the body like the lungs (causing shortness of breath) and the ankles or belly (causing swelling). DCM may also affect the electrical activity of the heart and can cause fast, dangerous heart rhythms. The pamphlet gives the causes of DCM, symptoms, diagnostic…
Available Online
View Pamphlet
Corporate Author
Nova Scotia Health Authority. QEII. Inherited Heart Disease Clinic
Place of Publication
Halifax, NS
Publisher
Nova Scotia Health Authority
Date of Publication
2020
Format
Pamphlet
Language
English
Physical Description
1 electronic document ([6] p.) : digital, PDF file
Subjects (MeSH)
Cardiovascular disorders
Cardiomyopathy
Subjects (LCSH)
Heart--Hypertrophy
Myocardium--Diseases
Specialty
Cardiovascular system
Abstract
In dilated cardiomyopathy (DCM), the heart muscle becomes weak. This makes it harder for the heart to pump blood out to the body. This causes the bottom chambers to dilate (stretch). A weak heart can also cause fluid to build up in parts of the body like the lungs (causing shortness of breath) and the ankles or belly (causing swelling). DCM may also affect the electrical activity of the heart and can cause fast, dangerous heart rhythms. The pamphlet gives the causes of DCM, symptoms, diagnostic procedures and treatments (medications, a special pacemaker or internal defibrillator and rarely a heart transplant). Websites for further information are also noted.
Notes
Previous title: DCM: Dilated Cardiomyopathy
Responsibility
Prepared by: Inherited Heart Disease Clinic, QEII, Halifax
Pamphlet Number
0629
Less detail

Hypertrophic cardiomyopathy (HCM) : Inherited Heart Disease (IHD) Clinic

https://libcat.nshealth.ca/en/permalink/chpams34669
Nova Scotia Health Authority. QEII. Inherited Heart Disease Clinic. Halifax, NS: Nova Scotia Health Authority , 2020.
Pamphlet Number
0631
Available Online
View Pamphlet
In HCM, there is a thickening of the heart muscle, usually in the wall between the 2 lower chambers (the septum). When the muscle thickens, it gets stiff and makes it hard for the bottom chambers to relax and fill with blood before each heartbeat. Thickening can also make it harder for blood to leave the heart. This can lower the amount of blood the heart can pump out to the rest of the body. Thickening of the heart muscle can create scar tissue. This can make you more at risk of dangerous, fas…
Available Online
View Pamphlet
Corporate Author
Nova Scotia Health Authority. QEII. Inherited Heart Disease Clinic
Place of Publication
Halifax, NS
Publisher
Nova Scotia Health Authority
Date of Publication
2020
Format
Pamphlet
Language
English
Physical Description
1 electronic document ([6] p.) : digital, PDF file
Subjects (MeSH)
Cardiovascular disorders
Cardiomyopathy
Subjects (LCSH)
Heart--Hypertrophy
Myocardium--Diseases
Specialty
Cardiovascular system
Abstract
In HCM, there is a thickening of the heart muscle, usually in the wall between the 2 lower chambers (the septum). When the muscle thickens, it gets stiff and makes it hard for the bottom chambers to relax and fill with blood before each heartbeat. Thickening can also make it harder for blood to leave the heart. This can lower the amount of blood the heart can pump out to the rest of the body. Thickening of the heart muscle can create scar tissue. This can make you more at risk of dangerous, fast heart rhythms. The pamphlet gives the most common cause (inherited) of HCM, symptoms, diagnostic procedures, and treatment (medications, a special pacemaker called an internal cardioverter defibrillator). Websites for further information are also noted.
Responsibility
Prepared by: Inherited Heart Disease Clinic, QEII, Halifax
Pamphlet Number
0631
Less detail

Inherited Heart Disease (IHD) Clinic

https://libcat.nshealth.ca/en/permalink/chpams36693
Nova Scotia Health Authority. QEII. Inherited Heart Disease Clinic. Halifax, NS: Nova Scotia Health Authority , 2020.
Pamphlet Number
2088
Available Online
View Pamphlet
The Inherited Heart Disease (IHD) Clinic is for people with a suspected or diagnosed heart problem that may be inherited (be passed from parents to their children). The Clinic does genetic testing (blood tests) and helps people manage their condition. Inherited heart disease can be diagnosed at any age. You may have a wide range of symptoms, from no symptoms at all to sudden cardiac death (heart stops working). The pamphlet explains the roles of the Clinic team members, how to get referred, how…
Available Online
View Pamphlet
Corporate Author
Nova Scotia Health Authority. QEII. Inherited Heart Disease Clinic
Place of Publication
Halifax, NS
Publisher
Nova Scotia Health Authority
Date of Publication
2020
Format
Pamphlet
Language
English
Physical Description
1 electronic document ([6] p.) : digital, PDF file
Subjects (MeSH)
Cardiovascular disorders
Heart Diseases - congenital
Subjects (LCSH)
Congenital heart disease
Specialty
Cardiovascular System
Abstract
The Inherited Heart Disease (IHD) Clinic is for people with a suspected or diagnosed heart problem that may be inherited (be passed from parents to their children). The Clinic does genetic testing (blood tests) and helps people manage their condition. Inherited heart disease can be diagnosed at any age. You may have a wide range of symptoms, from no symptoms at all to sudden cardiac death (heart stops working). The pamphlet explains the roles of the Clinic team members, how to get referred, how to get ready for your appointment, tests you may have, how to register for your appointment, what will happen during and after your appointment (followup), and research. An FAQ section is also listed.
Responsibility
Prepared by: Inherited Heart Disease Clinic, QEII, Halifax
Pamphlet Number
2088
Less detail

Long QT Syndrome (LQTS) : Inherited Heart Disease (IHD) Clinic

https://libcat.nshealth.ca/en/permalink/chpams34686
Nova Scotia Health Authority. QEII. Inherited Heart Disease Clinic. Halifax, NS: Nova Scotia Health Authority , 2020.
Pamphlet Number
1021
Available Online
View Pamphlet
LQTS is a rare disease where there are changes in the electrical signals that make the heart beat. In LQTS, channels in the heart cells do not work properly. The abnormal opening and closing of the channels can lead to dangerous heart rhythms. The heart may beat so fast that it cannot pump blood out to the body. This can cause collapse and, if the rhythm does not stop, sudden death. The pamphlet provides the causes, symptoms, diagnostic tests, treatment, and some general activity guidelines. We…
Available Online
View Pamphlet
Corporate Author
Nova Scotia Health Authority. QEII. Inherited Heart Disease Clinic
Place of Publication
Halifax, NS
Publisher
Nova Scotia Health Authority
Date of Publication
2020
Format
Pamphlet
Language
English
Physical Description
1 electronic document ([6] p.) : digital, PDF file
Subjects (MeSH)
Heart Defects, Congenital
Long QT syndrome - congresses
Subjects (LCSH)
Long QT syndrome
Congenital heart disease
Specialty
Cardiovascular system
Abstract
LQTS is a rare disease where there are changes in the electrical signals that make the heart beat. In LQTS, channels in the heart cells do not work properly. The abnormal opening and closing of the channels can lead to dangerous heart rhythms. The heart may beat so fast that it cannot pump blood out to the body. This can cause collapse and, if the rhythm does not stop, sudden death. The pamphlet provides the causes, symptoms, diagnostic tests, treatment, and some general activity guidelines. Websites for further information are also noted.
Notes
Previous title: LQTS : long QT syndrome
Responsibility
Prepared by: Inherited Heart Disease Clinic, QEII, Halifax
Pamphlet Number
1021
Less detail

8 records – page 1 of 1.