Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 7 de 7
Filter
1.
Eur J Cardiothorac Surg ; 20(3): 573-6, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11509281

ABSTRACT

Primary spontaneous coronary artery dissection is one of the rare causes of acute myocardial infarction. Previous studies reports that it is mostly seen in middle aged women in the last trimester of pregnancy and early postpartum period. Clinical presentation of the disease is variable in pattern and severity related to extent and development rate of dissection. In the last 2 years, nine non-pregnant primary spontaneous coronary artery dissection cases were found in coronary angiography among 3750 patients prediagnosed as coronary artery disease. The cases were presented and discussed with review of the pertinent literature.


Subject(s)
Aortic Dissection/complications , Coronary Aneurysm/complications , Coronary Artery Disease/complications , Aged , Aortic Dissection/diagnostic imaging , Coronary Aneurysm/diagnostic imaging , Coronary Angiography , Coronary Artery Disease/diagnostic imaging , Female , Humans , Male , Middle Aged , Pregnancy , Pregnancy Complications, Cardiovascular , Risk Factors
2.
Cardiology ; 89(2): 130-3, 1998.
Article in English | MEDLINE | ID: mdl-9524014

ABSTRACT

OBJECTIVES: Although the pathophysiology of syndrome X (angina pectoris, positive ECG test findings and normal coronary arteriogram) is unclear, it is generally accepted that intracellular metabolic changes resulting from abnormal constriction of prearteriolar vessels due to endothelium-dependent vasodilation abnormalities may play a role in the pathogenesis. We established the effect of long-term treatment with cilazapril, an angiotensin-converting enzyme inhibitor, which prevents the effect of angiotensin II in the tonic control of vascular resistance. METHODS: 18 patients (15 women and 3 men, mean age 43.2 +/- 4.6 years) with syndrome X were included in this study. A randomized double-blind crossover placebo-controlled trial was done. After a 1-week washout period, patients received either cilazapril 2 x 2.5 mg or placebo for 3 weeks, followed by 3 weeks of the other therapy. At the end of two periods, an exercise ECG test (modified Bruce protocol) was employed. RESULTS: The magnitude of ST segment depression was significantly decreased during treatment with cilazapril compared with placebo. On the other hand, total exercise time and time to 1 mm ST segment depression were significantly prolonged by cilazapril. However, rate pressure products were not significantly different at peak exercise at or at 1 mm of ST segment depression during both therapies. CONCLUSION: Cilazapril exerted a beneficial therapeutic effect in cases with syndrome X. The possible mechanism of this effect may be a modulation of coronary tone at the microcirculation level.


Subject(s)
Angiotensin-Converting Enzyme Inhibitors/therapeutic use , Cilazapril/therapeutic use , Microvascular Angina/drug therapy , Adult , Cross-Over Studies , Double-Blind Method , Electrocardiography , Exercise Test , Female , Heart Rate , Humans , Male , Microvascular Angina/physiopathology
4.
J Invasive Cardiol ; 9(8): 529-533, 1997 Oct.
Article in English | MEDLINE | ID: mdl-10762954
5.
J Card Surg ; 11(5): 371-5, 1996.
Article in English | MEDLINE | ID: mdl-8969385

ABSTRACT

Primary spontaneous coronary artery dissection is an unusual occurrence. There have been less than 150 cases reported in world literature. This process frequently occurs in relatively young women, particularly in the peripartum or early postpartum period. This article reports the clinical course of one patient with primary spontaneous left main coronary artery dissection who was treated with coronary artery bypass grafting. To our knowledge, it is the second case to be treated with the use of left internal mammary artery.


Subject(s)
Aortic Dissection/surgery , Coronary Aneurysm/surgery , Adult , Aortic Dissection/complications , Cineangiography , Coronary Aneurysm/complications , Coronary Artery Bypass , Female , Humans , Myocardial Infarction/etiology , Myocardial Revascularization , Saphenous Vein/transplantation , Surgical Flaps/methods
6.
Heart Vessels ; 11(3): 165-8, 1996.
Article in English | MEDLINE | ID: mdl-8897066

ABSTRACT

A 34-year-old man presenting with angina both at rest and on exertion was investigated. He developed severe ST segment elevation and a brief period of ventricular tachycardia during an exercise tolerance test. On coronary angiography, 60% fixed luminal narrowing was observed in the proximal left anterior descending coronary artery and a severe spasm developed at this site, leading to temporary total occlusion of the vessel. Successful coronary angioplasty (PTCA) was performed on this lesion, with a residual 15% narrowing. However, the patient had a recurrence of angina 3 weeks later, despite being administered high doses of nitrate and calcium antagonist. During control angiography, the lesion severity was unchanged, but spasm developed again following contrast injection. At this time, a Palmaz-Schatz stent was implanted. Calcium antagonist, nitrate, Ticlopidine and low molecular weight heparin therapy was started. There was no recurrence of symptoms during a 3-month follow-up. The exercise tolerance test, and myocardial perfusion scintigraphy findings were normal and the stent was patent without restenosis at the end of the 3-month follow-up. Intracoronary stent implantation for persistent coronary spasm refractory to conventional medical therapy can be considered a feasible and attractive treatment modality for the control of symptoms.


Subject(s)
Angioplasty, Balloon, Coronary , Coronary Vasospasm/therapy , Stents , Adult , Angina Pectoris, Variant/diagnosis , Angina Pectoris, Variant/physiopathology , Angina Pectoris, Variant/therapy , Angioplasty, Balloon, Coronary/instrumentation , Coronary Angiography , Coronary Vasospasm/diagnosis , Coronary Vasospasm/etiology , Exercise Test , Follow-Up Studies , Hemodynamics/physiology , Humans , Male , Ventricular Function, Left/physiology
7.
Int J Cardiol ; 54 Suppl: S135-6, 1996 Aug.
Article in English | MEDLINE | ID: mdl-9119514

ABSTRACT

Takayasu arteritis is a non-specific inflammatory process of unknown etiology affecting the aorta and its branches. A retrospective study was done in 14 patients diagnosed as Takayasu arteritis. Eleven patients were female and three were male. Ages ranged from 12 to 30 years. Seven patients had type I arteritis, three patients type II arteritis, and four patients type III Takayasu arteritis. Successful angioplasty was performed in five cases.


Subject(s)
Cross-Cultural Comparison , Takayasu Arteritis/diagnosis , Adolescent , Adult , Angioplasty, Balloon , Child , Female , Humans , Magnetic Resonance Imaging , Male , Retrospective Studies , Takayasu Arteritis/classification , Takayasu Arteritis/therapy , Treatment Outcome , Turkey
SELECTION OF CITATIONS
SEARCH DETAIL
...