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- IRMS - Nicolae Testemitanu SUMPh
- 1. COLECȚIA INSTITUȚIONALĂ
- MedEspera: International Medical Congress for Students and Young Doctors
- MedEspera 2020
Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12710/11906
Title: | Takotsubo cardiomyopathy (TTS) – a disease that mimics an acute coronary syndrome |
Authors: | Stepan, Ion Lutica, Nicolae Stepan, Tatiana Secureanu, Marina Tolici, Doina Grib, Andrei |
Keywords: | Stress cardiomyopathy;Takotsubo;acute coronary syndrome;hypokinesia;akinesia |
Issue Date: | 2020 |
Publisher: | MedEspera |
Citation: | STEPAN, Ion, LUTICA, Nicolae, STEPAN, Tatiana, [et al]. Takotsubo cardiomyopathy (TTS) – a disease that mimics an acute coronary syndrome. In: MedEspera: the 8th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2020, p. 222. |
Abstract: | Background. TTS, also known as stress cardiomyopathy and "Broken Heart Syndrome", is a
cardiac syndrome that appears suddenly and implies transient left ventricular systolic
dysfunction leading to heart failure symptoms. It frequently occurs following a significant
stress. Available data report about 1.7-2.2% of patients with suspected ASC to be subsequently
diagnosed with TTS. The aim is to present a TTS clinical case and the differential diagnosis
with an ACS.
Case report. A 62 years old, female, presented with: compressive chest pain, lasting >6 hours
without relieve at rest or on nitrates, shortness of breath at mild exertion and fatigue. Symptoms
onset at 2 days following a major stress (death of the only brother). Other symptoms:
palpitations, dizziness. Objective: mild uncle swelling. Cracking murmurs in the lower lung
fieldson auscultation. Heart rate 86 bpm, BP- 140/80 mmHg, SaO2 – 95%. Laboratory testing:
troponin I – 4.8ng/ml (reference limit 0.3ng/ml), NT-proBNP – 10236pg/ml. ECG: Sinus
rhythm, HR – 86 bpm, normal axis, inverted T-waves in I, II, aVL, V3-V6. Echocardiography:
moderate LV dilatation: diastolic diameter 57mm, systolic diameter 40mm, LV apical akinesia,
middle segments hypokinesia, mild concentric hypertrophy of the LV(septum 12mm, posterior
wall 12mm), moderately abnormal systolic function, EF - 39%. Non-STE ACS was suspected
and the patient was admitted in the CCU for 48h, and a cardiology ward for 4 days afterwards.
Treated with: nitrates, heparins, β-blockers, ACE-inhibitors, aspirin and diuretics.
Coronarography (performed on the 2nd day of admission): no significant lesions identified.
Non-STE ACS ruled out and TTS presumed. At 4 days: troponin I –1,3ng/ml, NT-proBNP–
3455pg/ml. At discharge troponin I –0.14ng/ml, NT-proBNP- 460pg/ml. Echo: mild LV
dilation: diastolic diameter 54mm, systolic diameter 37mm, LV apical hypokinesia, mildly
abnormal systolic function EF – 50%, in rest – the same. At 20 days from symptoms onset:
ECG: HR 74bpm, normalization of the T waves, in –rest the same. Echo: no wall motion
abnormalities, EF 63%, complete recovery of the LV function. TTS confirmed.
Conclusions. TTS is a rare condition which can be suspected when ECG changes and LV wall
motion abnormalities present at echo without respecting a specific coronary pool and no culprit
lesion is identified at coronarography. An ACS is to be, firstly, ruled out. The diagnosis is
confirmed only after the recovery of the LV function. |
URI: | https://medespera.asr.md/wp-content/uploads/ABSTRACT-BOOK.pdf http://repository.usmf.md/handle/20.500.12710/11906 |
Appears in Collections: | MedEspera 2020
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