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@#Ritodrine hydrochloride (ritodrine) is a β2-adrenoceptor stimulant that has been effectively prescribed for the prevention of premature labor.[1] In clinical practice, one of the biggest drawbacks of β-mimetics is their adverse effects, including arrhythmias, myocardial ischemia, and pulmonary edema, due to their β-sympathomimetic effects.[2] Here, we report a rare pregnant case of spontaneous coronary artery dissection (SCAD) after intravenous infusion of ritodrine.
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Resumen La disección espontánea de la arteria coronaria es una causa no aterosclerótica de infarto de miocardio, la cual es más común en mujeres jóvenes con pocos o ningún factor de riesgo cardiovascular. Es infrecuente, no se asocia a iatrogenia ni trauma, y se presenta por acumulación espontánea de sangre entre las capas de la pared arterial coronaria, por ruptura de la íntima; de ahí que genera una falsa luz que produce compresión externa del verdadero lumen arterial, con lo cual altera el flujo sanguíneo coronario y ocluye la arteria comprometida. Se expone el caso de una mujer de 31 años, sin factores de riesgo cardiovascular, quien ingresó a un servicio de urgencias con dolor torácico típico, de 2 horas de evolución. En el electrocardiograma se apreció elevación del segmento ST en las derivaciones de la cara anteroseptal e inferior, y troponina T de alta sensibilidad positiva, por lo que se realizó terapia trombolítica con tenecteplasa, sin obtener criterios de reperfusión. Se hizo angiografía coronaria, la cual mostró obstrucción total de la arteria coronaria descendente anterior en el tercio medio. El ultrasonido intravascular documentó flap de disección y hematoma en este segmento, los cuales confirmaron la disección coronaria espontánea. Se realizó angioplastia con implante de stent coronario y se restableció la circulación, observando mejoría de los síntomas.
Abstract Spontaneous coronary artery dissection is a non-atherosclerotic cause of myocardial infarction, more frequent in young women with few or no cardiovascular risk factors, it is infrequent, and it is not associated with iatrogenesis or trauma. It occurs due to spontaneous accumulation of blood between the layers of the coronary artery wall, due to rupture of the intima, generating a false lumen that produces external compression of the true arterial lumen, altering coronary blood flow, occluding the compromised artery. It is presented the case of a 31-year-old woman with no cardiovascular risk factors, who was admitted to an emergency department, with typical chest pain of 2 hours of evolution, showing ST-segment elevation in leads of anteroseptal and inferior face on the electrocardiogram and troponin T with high sensitivity positive. Therefore, thrombolytic therapy was performed with tenecteplase, without obtaining reperfusion criteria. Coronary angiography was performed that demonstrates total obstruction of the anterior descending coronary artery in the middle third. Intravascular ultrasound documents the dissection flap and hematoma in this segment that confirm spontaneous coronary dissection, performing angioplasty with implantation of a coronary stent, restoring circulation with improvement of symptoms.
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Um homem de 28 anos com história pregressa de abuso de drogas foi encaminhado para coronariografia de emergência após parada cardíaca. O eletrocardiograma pós-ressuscitação mostrou elevação do segmento ST em V1-V4. A angiografia mostrou dissecção espontânea da artéria coronária, multiarterial e em diversos segmentos. Devido à instabilidade clínica, o paciente foi submetido à intervenção coronária percutânea da artéria descendente anterior. A prevalência da dissecção espontânea da artéria coronária como causa de síndrome coronariana aguda em homens é infrequente. No entanto, nos casos suspeitos, ela deve ser excluída. A parada cardiorrespiratória é um quadro incomum na dissecção espontânea da artéria coronária, e a intervenção coronária percutânea como modalidade terapêutica ainda é uma questão em debate.
A 28-year-old male with a previous history of drug abuse was sent to an emergent coronary angiography, after a cardiac arrest, with a post-resuscitation eletrocardiogram showing ST- segment elevation from V1-V4. Angiography showed multivessel and multisegment spontaneous coronary artery dissection. Due to clinical instability, patient underwent left anterior descending artery percutaneous coronary intervention. Prevalence of spontaneous coronary artery dissection as the cause of acute coronary syndrome is anecdotal in men. Yet, in the right scenarios as in this case, it must be ruled out. Cardiorespiratory arrest is an uncommon presentation of spontaneous coronary artery dissection and percutaneous coronary intervention in spontaneous coronary artery dissection is still a matter of debate.
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Resumen: El diagnóstico de disección coronaria espontánea como causa de síndrome coronario agudo ha aumentado desde el surgimiento de las técnicas de imagen intracoronaria. Aún así, continúa siendo una entidad subdiagnosticada. La evidencia en relación con el tratamiento es escasa, pero la conducta conservadora ha demostrado resultados favorables en pacientes seleccionados. Presentamos el caso de una paciente de 55 años en la que se diagnostica infarto de miocardio sin elevación del ST. En la cineangiocoronariografía se sospecha como mecanismo causal la disección coronaria espontánea, lo cual se confirma mediante ultrasonido intravascular. Se optó por un tratamiento conservador con buena evolución.
Summary: The diagnosis of spontaneous coronary artery dissection as a cause of acute coronary syndrome has increased since the arise of intravascular imaging techniques. However, it still remains an underdiagnosed entity. Evidence related to its management is scarce, but conservative strategies have shown favorable outcomes in selected patients. We present the case of a 55-year-old female patient who is diagnosed with a non-ST segment elevation myocardial infarction. Spontaneous coronary artery dissection is suspected in the coronary angiography and then confirmed by intravascular ultrasound. Conservative management was selected, with favorable clinical outcomes.
Resumo: O diagnóstico de dissecção coronariana espontânea como causa da síndrome coronariana aguda aumentou com o surgimento das técnicas de imagem intracoronariana. Apesar disso é uma entidade subdiagnosticada. A evidência sobre o tratamento é escassa, mas o tratamento conservador mostrou resultados favoráveis em pacientes selecionados. Apresentamos o caso de um paciente de 55 anos com diagnóstico de infarto do miocárdio sem supradesnivelamento do segmento ST. Suspeita-se de dissecção coronariana espontânea na angiografia, confirmada por ultrassonografia intravascular. Se optou por tratamento conservador com boa evolução.
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Objective To study the clinical, angiographic and technical characteristics of patients with spontaneous coronary artery dissection (SCAD) undergoing percutaneous coronary intervention (PCI). Methods This was a retrospective single center study where patients with angiographically confirmed SCAD undergoing PCI over a period of 4 years (2013–2017) were analyzed. We also sought to identify the clinical and angiographic predictors of procedural failure during PCI. Results There were a total of 42 patients with angiographically confirmed SCAD during the study period of which 16 patients (38.1%) underwent PCI. 14 out of the 16 patients (87.5%) taken up for PCI had technical success. In all patients the lesion was initially attempted to cross with a floppy wire and if unsuccessful it was escalated to a hydrophilic wire and finally to a stiff wire The SCAD lesion was crossed with a floppy wire in 71.4% of patients, with a hydrophilic wire in 14.2% and a stiff wire in 7.1% of patients. Wire escalation was required in 5 patients (31.3%) and in 60% of cases there was a technical success after wire escalation. Presence of diabetes mellitus, hypertension, dyslipidemia, smoking, coexisting atherosclerosis, diffuse nature of the lesion, and baseline Thrombolysis in Myocardial Infarction (TIMI) ≤ 2 flow did not predict procedural failure during PCI. Conclusion PCI in SCAD is associated with a fair rate of technical success in our population. Choosing an initial floppy wire and then escalating to a hydrophilic wire followed by a stiff wire is an optimal revascularization strategy.
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We report a case of Spontaneous coronary artery dissection associated with fragile X syndrome. The relationship between fragile X syndrome and Spontaneous coronary artery dissection is unclear. However, More research will need about the causes and treatment of Spontaneous coronary artery dissection.
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Female , Humans , Acute Coronary Syndrome , Coronary Vessels , Fragile X SyndromeABSTRACT
Spontaneous coronary artery dissection is a rare condition that usually causes a coronary syndrome, but may also cause sudden death. It is more common in women and is associated with factors such as the peripartum period and oral contraceptive use. We report two cases. A 45-year-old woman with hepatitis C, presenting in the emergency room with angina. An intravascular ultrasound showed a dissecting hematoma involving the left, anterior descending and circumflex coronary arteries. She was initially managed with nitroglycerin, anticoagulation and anti-platelet drugs but due to persistence of symptoms, she required surgical revascularization. A 32-year-old woman presenting in the emergency room with angina. A coronary angiogram revealed a dissection of the anterior descending coronary artery. Eight days later an intravenous ultrasound showed a retrograde progression of the dissection and she was subjected to a surgical revascularization.
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Humans , Female , Adult , Middle Aged , Vascular Diseases/congenital , Coronary Vessel Anomalies/diagnostic imaging , Vascular Diseases/surgery , Vascular Diseases/diagnostic imaging , Coronary Angiography , Coronary Vessel Anomalies/surgeryABSTRACT
Spontaneous coronary artery dissection is an extremely rare cause of acute coronary syndrome. Although it predominantly affects young women in the peripartum period, it can also occur in men. The left coronary artery is most frequently involved. The usual presentation is ST segment elevation myocardial infarction. Although several treatment modalities have been proposed, the optimal treatment options still remain to be established. This current case report focuses on a 40- year-old male presented with acute coronary syndrome and subsequently was found to have coronary artery dissection.
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Spontaneous coronary artery dissection (SCAD) is a very rare cause of peripheral artery thromboembolism. It is especially rare to show symptoms of acute limb ischemia without chest symptoms during a hospital visit. In this case, a rare case of SCAD led to left heart failure and caused left ventricle thrombi, which in turn caused peripheral thromboembolism.
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Arteries , Coronary Vessels , Extremities , Heart Failure , Heart Ventricles , Ischemia , Thorax , ThromboembolismABSTRACT
Background: A 43 year old woman presented with chest pain followed by cardiac arrest recovered after defibrillation. Coronary angiography revealed a narrowed anterior descending coronary artery but no intraluminal thrombi. Optic coherence tomography showed intramural hematoma and the patient was treated medically with aspirin, clopidogrel and atorvastatin. Two weeks later the pain recurred and coronary angiography revealed similar findings. After medical treatment with heparin followed by aspirin and clopidogrel she has remained stable.
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Humans , Female , Adult , Coronary Disease/complications , Coronary Disease/diagnostic imaging , Heart Arrest/etiology , Aortic Dissection/complications , Aortic Dissection/diagnostic imaging , Coronary Vessels/pathology , Tomography, Optical Coherence , Electrocardiography , Hematoma/etiology , Hematoma/diagnostic imagingSubject(s)
Humans , Adult , Acute Coronary Syndrome/etiology , Acute Coronary Syndrome/therapy , IschemiaABSTRACT
Acute coronary syndrome (ACS) due to spontaneous coronary artery dissection (SCAD) is rare. Further, concurrent ACS with a cerebrovascular accident is improbable, but possible. We report a case of a young man, with a history of Hodgkin’s lymphoma treated with a combination of chemotherapy and radiotherapy ten years ago, presented with acute coronary syndrome caused by an extensive dissection of the right coronary artery, together with acute ischemic stroke. Survivors of Hodgkin’s lymphoma are at increased risk for cardiovascular complications due to radiation, which can expedite atherosclerosis and can, eventually, give rise to dissection and cerebrovascular disease, as exemplified in our case. This case report and review outlines the incidence, epidemiology, causes, pathophysiology, diagnosis and treatment of spontaneous coronary artery dissection. Our case report is a remainder to clinicians to be mindful of concomitant occurrence of these two conditions and highlights the significant impact the treatment of each has on the other, especially when the literature does not have clear recommendations about simultaneous management. Spontaneous coronary artery dissection with concomitant ischemic cerebrovascular stroke poses a therapeutic dilemma and requires a multi-disciplinary team to appropriately manage the patient.
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Spontaneous coronary artery dissection is a rare but often fatal cause of acute myocardial ischemia that occurs in young or middle-aged and otherwise healthy patients. We report a case of spontaneous left main coronary artery dissection in a young woman who was treated with emergency coronary artery bypass grafting. She improved after surgery but required a long recuperative period because of her cardiac failure and multiple organ failure, developed expiring on the 78th postoperative day. Spontaneous coronary artery dissection is unpredictable, and sudden death is the usual mode of clinical presentation. Prompt diagnosis and coronary artery revascularization are essential in order to achieve a favorable outcome in such cases.
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Spontaneous coronary artery dissection (SCAD) is a rare disease that occurs most commonly in young people, especially in peripartum or postpartum women without traditional risk factors for coronary artery disease. We describe the case of a 30-year-old woman who suddenly died approximately 2 weeks postpartum period. She was otherwise healthy with no cardiac risk factors. On autopsy, the coronary artery showed 4cm long segment of dissection, starting from the left main artery to anterior descending branch. Microscopic finding of the dissection revealed a tear between tunica media and adventitia, creating an intramural hematoma. The left ventricle showed multifocal areas of acute myocardial infarction with reperfusion injury. SCAD should be considered in the differential diagnosis of any young person sustaining an acute myocardial infarction, especially women in the postpartum state.
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Adult , Female , Humans , Adventitia , Arteries , Autopsy , Coronary Artery Disease , Coronary Vessels , Death, Sudden , Diagnosis, Differential , Heart Ventricles , Hematoma , Myocardial Infarction , Peripartum Period , Postpartum Period , Rare Diseases , Reperfusion Injury , Risk Factors , Tunica MediaABSTRACT
Spontaneous coronary artery dissection (SCAD) is an uncommon cause of acute myocardial ischemia, which frequently presents as sudden death. The pathophysiology and treatment of SCAD have not been fully determined. Herein, a case of SCAD, manifesting as variant angina, which rapidly progressed during an ergonovine test, in which 3 drug-eluting stents were deployed using intravascular an ultrasound guidance, with an excellent immediate result, is reported.
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Coronary Vessels , Death, Sudden , Drug-Eluting Stents , Ergonovine , Myocardial Ischemia , Stents , Ultrasonography , Ultrasonography, InterventionalABSTRACT
Spontaneous coronary artery dissection (SCAD) is a rare disease that occurs most commonly in young people, especially in peripartum or postpartum women. It is usually catastrophic and fatal. The etiology of dissection is still under discussion. Possible factors are inflammation, changes of flow dynamics, and preexisting intima lesions. The treatment of choice for spontaneous coronary artery dissection is still not settled. The authors report a twenty-nine year-old woman with coronary lesions diagnosed as spontaneous coronary artery dissection which developed during exercise and was treated with intracoronary stenting.
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Female , Humans , Coronary Vessels , Inflammation , Peripartum Period , Postpartum Period , Rare Diseases , StentsABSTRACT
Spontaneous coronary artery dissection is a rere incident occurring usually in young patients, predominautly in females. It is usually fatal and found postmortem. It is also a rare cause of acute myocardial infarction. We present the case of a twenty nine-year-old-man with spontaneous right coronary artery dissection found angiographically which caused an inferior wall myocardial infarction. He was treated with medical therapy only amd after uneventful hospital course, he was discharged with medication. Three months later, coronary angiography was done to follow up the lesion and found that the site was completely healed.
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Female , Humans , Coronary Angiography , Coronary Vessels , Follow-Up Studies , Inferior Wall Myocardial Infarction , Myocardial InfarctionABSTRACT
Spontaneous coronary artery dissection(SCD) is a rare entity that is infrequently diasnosed antemortem. The majority of patients have presented with acute myocardial infaction or sudden death. the etiology, prognosis and treatment of this entity remain ill-defined. We report two cases of SCD which were diagnosed by coronary agniogram and intracoronary ultrasound.
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Humans , Coronary Vessels , Death, Sudden , Prognosis , UltrasonographyABSTRACT
Objective To study the incidence and the effect of intracoronary stenting for spontaneous coronary artery dissection (SCAD). Methods Data from coronary angiography performed in 2?216 patients were analyzed to discover SCAD. Intracoronary stents were implanted in the patients with SCAD suited for percutaneous coronary intervention (PCI). Aspirin, clopidogrel, heparin or low molecular weight heparin were used on demand during the operation-around period. Results Twenty-six cases of SCAD [19 males, 7 females, mean age (60.9?11.6) years] were discovered. The incidence was 1.17%. Among the 26 patients, 15 suffered from acute myocardial infarction and 11 unstable angina. SCAD occurred in 28 blood vessels of the 26 cases, of which, 1 was in LM, 9 in LAD, 4 in LCX and 14 in RCA. Twenty-three stents were implanted in 19 coronary arteries of 18 patients (15 stentings after PTCA and 4 direct stentings). After PCI, remaining stenosis of one SCAD lesion was