Subarachnoid Hemorrhage Clinical Trial
Official title:
Incidence, Influencing Factors and Outcome of Takotsubo Cardiomyopathy in Patients Suffering From Acute Non-traumatic Subarachnoid Hemorrhage
Verified date | June 2022 |
Source | University of Debrecen |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Pupose: Takotsubo cardiomyopathy is a rare and not well-known complication of the subarachnoid hemorrhage. This form of heart failure, called as "broke heart" or "apical ballooning syndrome", was first described by Japanese authors at the beginning of 1990's. 1.5-2.2% of acute coronary syndrome is Takotsubo cardiomyopathy. Its predisposing factors, hypothetical parthenogenesis, diagnostic criteria and therapeutic methods are already known from the literature. The study intends to include all patients over 18 years of age who were admitted to our clinic within 48 hours after the bleeding regardless of gender, neurological status or age. Data to be registered within 24 hours after admittance: Instruments: - Intracranial blood flow characteristics:TCCD - using Transcranial Color Doppler; systolic, diastolic and mean blood flow velocity, Systolic / Diastolic ratio, pulsatility index - ECG abnormalities: Corrected QT Interval (QTc), T wave, ST segment, arrhythmia - Echocardiography (Ejection fraction%, exact location and degree of cardiac wall motion abnormalities) - documented with video recording Hypothesis: The risk of Takotsubo cardiomyopathy (TS) is increased if SAH is associated with more severe state, a greater degree of bleeding, intraventricular and/ or intracerebral hemorrhage. The definitive care of patients is postponed due to the appearance of TS, which could affect the final outcome.
Status | Completed |
Enrollment | 137 |
Est. completion date | December 31, 2018 |
Est. primary completion date | June 30, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Acute subarachnoid hemorrhage - Admittance to the neurosurgery intensive care unit within 48 hours after the bleeding has occurred - Over 18 years of age - No prior cardiological diseases in medical history Exclusion Criteria: - Known myocardial diseases (previous myocardial infarction) - Preexisting heart failure - Previously known structural heart disease (severe, clinically significantvalve insufficiency, and / or significant stenosis) - Preexisting myocarditis - Preexisting phaecromocytoma - Preexisting hypertrophic cardiomyopathy (Left ventricle > 15 mm) - Preexisting coronary artery stenosis that requires dilation (patients should be excluded if coronary artery stenosis with dilation need is confirmed during the follow-up period) |
Country | Name | City | State |
---|---|---|---|
Hungary | UNIVERSITY OF DEBRECEN FACULTY OF MEDICINE Department of Anesthesiology and Intensive Care | Debrecen | Hajdú-Bihar |
Lead Sponsor | Collaborator |
---|---|
University of Debrecen |
Hungary,
Castillo Rivera AM, Ruiz-Bailén M, Rucabado Aguilar L. Takotsubo cardiomyopathy--a clinical review. Med Sci Monit. 2011 Jun;17(6):RA135-47. Review. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | ECG abnormalities:Corrected QT Interval (QTc), T wave, ST segment, arrhythmia | 12-lead ECD | Data to be registered within 24 hours after admittance | |
Primary | ECG abnormalities:Corrected QT Interval (QTc), T wave, ST segment, arrhythmia | 12-lead ECD | The following diagnostic steps should be repeated after 1 month | |
Primary | urine metanephrine, normetanephrine levels | The amount of urine collected in 24 hours and determination of urine metanephrine, normetanephrine levels | The amount of urine collected in 24 hours | |
Primary | urine metanephrine, normetanephrine levels | The level of metanephrine and normetanephrine from 24-hour collected urine should be measured again after 1 and 6 months in case of patients where TS was diagnosed. | The following diagnostic steps should be repeated after 1 month | |
Primary | Enzyme level associated with myocardial tissue necrosis | Cardiac troponin I (cTnI), creatine kinase (CK), CK-MB, Brain natriuretic peptide (BNP), N-terminal prohormone of brain natriuretic peptide (NT-proBNP) | Data to be registered within 24 hours after admittance | |
Primary | Enzyme level associated with myocardial tissue necrosis | Cardiac troponin I (cTnI), creatine kinase (CK), CK-MB, Brain natriuretic peptide (BNP), N-terminal prohormone of brain natriuretic peptide (NT-proBNP) | The following diagnostic steps should be repeated after 1 month | |
Primary | Ejection fraction%, exact location and degree of cardiac wall motion abnormalities | Echocardiography documented with video recording | Data to be registered within 24 hours after admittance | |
Primary | Ejection fraction%, exact location and degree of cardiac wall motion abnormalities | Echocardiography documented with video recording | The following diagnostic steps should be repeated after 1 month | |
Secondary | New York Heart Association scores (NYHA scores) Glasgow outcome scale (GOS) - survival index Neurological status | Clinical outcome (GOS), quality of life (Bartel Index) and Karnofsky scores | The following examinations should be carried out after 6 months: |
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