This study evaluated 91 patients who suffered a myocardial infarction but had normal coronary arteries on angiogram. It compared their long-term outcomes to 91 matched patients with coronary artery blockages. The study found that identifiable causes (like coronary spasm or coagulation disorders) were only detected in about 1/3 of normal angiogram patients. Their mortality was similar to those with blockages, but morbidity (e.g. reinfarction) was lower. Poorer prognosis in normal angiogram patients was linked to lower ejection fraction and diabetes.
This study evaluated 91 patients who suffered a myocardial infarction but had normal coronary arteries on angiogram. It compared their long-term outcomes to 91 matched patients with coronary artery blockages. The study found that identifiable causes (like coronary spasm or coagulation disorders) were only detected in about 1/3 of normal angiogram patients. Their mortality was similar to those with blockages, but morbidity (e.g. reinfarction) was lower. Poorer prognosis in normal angiogram patients was linked to lower ejection fraction and diabetes.
This study evaluated 91 patients who suffered a myocardial infarction but had normal coronary arteries on angiogram. It compared their long-term outcomes to 91 matched patients with coronary artery blockages. The study found that identifiable causes (like coronary spasm or coagulation disorders) were only detected in about 1/3 of normal angiogram patients. Their mortality was similar to those with blockages, but morbidity (e.g. reinfarction) was lower. Poorer prognosis in normal angiogram patients was linked to lower ejection fraction and diabetes.
This study evaluated 91 patients who suffered a myocardial infarction but had normal coronary arteries on angiogram. It compared their long-term outcomes to 91 matched patients with coronary artery blockages. The study found that identifiable causes (like coronary spasm or coagulation disorders) were only detected in about 1/3 of normal angiogram patients. Their mortality was similar to those with blockages, but morbidity (e.g. reinfarction) was lower. Poorer prognosis in normal angiogram patients was linked to lower ejection fraction and diabetes.
doi:10.1053/euhj.2000.2553, available online at http://www.idealibrary.com on
Clinical characteristics, aetiological factors and long-term prognosis of myocardial infarction with an absolutely normal coronary angiogram A 3-year follow-up study of 91 patients A. Da Costa, K. Isaaz, E. Faure, S. Mourot, A. Cerisier and M. Lamaud Division of Cardiology, University Jean Monnet of Saint-Etienne, Saint-Etienne, France Objectives The purpose of this study was to evaluate the clinical outcome of a large cohort of patients who suered an acute myocardial infarction with absolutely normal epicardial coronary arteries at the post-myocardial infarc- tion coronary angiogram. The aetiological and prognostic factors in this population were also analysed. Background Few data exist concerning the outcome, and aetiological and prognostic factors, of patients with myo- cardial infarction and angiographically absolutely normal coronary arteries. Methods Ninety-one patients (34 females/57 males; mean age 5013 years, range 2478 years) admitted with an acute myocardial infarction had absolutely normal cor- onary arteries at the angiogram performed 624 days (range 115 days) after the myocardial infarction, dened by smooth contours and no focal reduction (NC). Of the 91 NC patients, 71 were evaluated prospectively, alongside a systematic search of all aetiological factors reported in the literature. The NC patients were matched for age, sex, and the same period of myocardial infarction onset with a group of 91 patients with coronary artery stenosis (>50% diameter stenosis) at the angiogram performed 734 days (range 115 days) after the myocardial infarction (SC). Results The percent of smokers was similar between the two groups; higher prevalence rates of coronary heart disease family history, obesity, hypertension, hyper- cholesterolaemia and diabetes mellitus were found in SC (P=0043 to 00001). In NC, coronary spasm was found in 155%, congenital coagulation disorders in 128%, collagen tissue disorders in 22%, embolization in 22%, and oral contraceptive use in 11%. Left ventricular ejection fraction at hospital discharge was higher in NC (60%13%) than in SC (55%13%, P=004). The mean follow-up was 35 months (range 1100 months). KaplanMeier event-free survival, with the combined end-point dened as death, reinfarction, heart failure and stroke was 75% in NC vs 50% in SC (P<00001). Survival rate was 945% in NC compared to 92% in SC (ns). Univariate predictors of events in NC were left ventricular ejection fraction (P=003), age (P=002), diabetes (P=001), and smoking (P=003). Using Cox multivariate analysis, independent predictors of long- term outcome in NC patients were left ventricular ejection fraction (P=0003) and diabetes (P=0004). Conclusion Aetiological factors, predominantly coronary spasm and inherited coagulation disorder, can be detected in only one third of the patients with myocardial infarction and absolutely normal coronary angiograms despite a sys- tematic search in a prospective population. Mortality rates are similar but morbidity is lower in myocardial infarction patients with absolutely normal coronary angiography compared with those with coronary artery stenosis. The only two independent factors predictive of poor outcome in myocardial infarction patients with normal coronary arteries are left ventricular function and diabetes. (Eur Heart J 2001; 22: 14591465, doi:10.1053/ euhj.2000.2553) 2001 The European Society of Cardiology Key Words: Myocardial infarction, prognosis, angio- graphically normal coronaries. See page 1364 for the Editorial comment on this article Revision submitted 27 November 2000, and accepted 29 November 2000. Correspondence: Pr Karl Isaaz, Service de Cardiologie, Ho pital Nord, Centre Hospitalier Universitaire de Saint-Etienne, 42055 Saint-Etienne CEDEX 2, France. 0195-668X/01/221459+07 $35.00/0 2001 The European Society of Cardiology Introduction Although acute myocardial infarction is generally associated with obstructive coronary artery disease, myocardial infarction with normal epicardial coronary arteries have also been documented [122] . The overall prevalence rate of myocardial infarction with a normal coronary angiogram is low, approximately 3%, but appears to vary with age, with higher rates in young patients [57,21] . Various mechanisms have been hypoth- esized [23] including coronary spasm [2430] , acquired or inherited coagulation disorders [3137] , toxic conditions [3841] , embolization [42] . There are limited data in the published literature regarding the long-term follow-up of large series of patients who suered an acute myocardial infarction with an absolutely normal coronary arteriogram. In addition, to our knowledge, a systematic search of the most frequently reported aetio- logical factors has not been done prospectively in a large cohort of patients. The aim of the present study was: (1) to compare the long-term prognosis of a large cohort of myocardial infarction patients with an absolutely normal coronary angiogram with that of myocardial infarction patients with coronary artery obstructive dis- ease; 71 patients (78%) out of our total cohort of patients were studied prospectively and constituted a prospective arm; (2) to systematically seek aetiological factors in the prospective arm of the study and (3) to test whether prognostic factors may be identied within the group of myocardial infarction patients with an absolutely normal coronary angiogram. Methods Patient population Patients who were admitted with acute myocardial infarction to our institution were screened retrospec- tively from January 1990 to September 1994 and then prospectively from October 1994 to December 1998. The diagnosis of myocardial infarction was based on the triad of chest pain, ECG changes, and raised plasma enzyme activity. Ninety-one patients (34 females/ 57 males; mean age 5013 years, range 2478 years) were identied as having angiographically absolutely normal coronary arteries, dened by epicardial vessels, smooth contours and no focal reduction on the coronary angiogram, which was performed 624 days (range 115 days) after myocardial infarction onset (NC). Among these 91 patients, 20 were retrospectively included and 71 (78%) were prospectively studied. Patients in the NC group were matched for age and gender with a group of 91 patients who presented with an acute myocardial infarction during the same period but who had coronary artery stenosis dened by >50% diameter reduction of at least one major epicardial coronary vessel at the angiogram performed 734 days (range 1 to 15 days) after the myocardial infarction (SC). Classication of the patients into the two groups, based on the analysis of the coronary angiogram, was made by three independent experienced angiographers. Age, gender, angiographic left ventricular ejection fraction, myocardial infarction location, number of vessels dis- eased in the SC group and risk factors including family history of coronary artery disease, diabetes, cigarette smoking, hypertension, obesity, hypercholesterolaemia were entered into the analysis. Clinical conditions known to be associated with hypercoagulation, such as pregnancy, carcinoma, polycythaemia, collagen tis- sue disorder, oral contraceptive use were sought systematically. Detection of inherited coagulation disorders Inherited coagulation disorders were sought in only two of the 20 patients of the retrospective arm and in all the 71 patients of the prospective arm. Blood samples were taken 4 weeks after myocardial infarction. The absence of an inammatory syndrome was documented by a normal brinogen level. Quantitative measurements of protein C, antithrombin III (ATIII), and plasminogen were performed by colorimetric assay using, respect- ively, coamatic protein C from chromogenix (Mo lndal, Sweden), Stachom ATIII automated, and Stachrom PLG (Diagnostica Stago, Asnie`res, France). Quantita- tive determination of functional protein S, based on the inhibition of factor Va, was established using a clotting assay of protein S (Staclot protein S, Diagnostica Stago). A clotting assay was used for quantitative deter- mination of factor XII. The activated protein C (APC) resistance test was performed as previously described with an ST 888 instrument (Diagnostica Stago) using the coatest activated protein C resistance (APCR, factor V Leiden) test kit from Biogenic. Patients with a ratio <29 were then subjected to factor V genotyping using a polymerase chain reaction technique. Provocative testing for coronary spasm From September 1994 a provocating test using intra- venous ergonovine maleate 04 mg within 2 min, was performed prospectively and systematically in all 71 patients with a normal coronary angiogram to identify coronary artery spasm. The test was considered positive when at least 70% focal reduction of luminal diameter was present. Follow-up Clinical events were dened as follows: (1) heart failure; (2) myocardial infarction recurrence; (3) stroke; and (4) cardiovascular mortality. Clinical evaluation was made with a combined end-point, dened by at least one clinical event. Follow-up (by telephone and interviewing the patients and their family medical doctor) was carried out in December 1998 by three observers blinded to the initial status of the patient. Follow-up was accomplished 1460 A. Da Costa et al. Eur Heart J, Vol. 22, issue 16, August 2001 in 176 of the 182 patients (97%) and three patients were lost to follow-up in each group. Statistical analysis All continuous variables were reported as mean valueSD. Dierences among groups were assessed by one-way ANOVA. Univariate analysis was performed by log rank test, to assess whether clinical variables and left ventricular function were predictors of cardiac events. A P value <005 was considered as signicant. Multivariate Cox analysis incorporating variables with a P value <005 in the univariate model was performed to search for independent predictive factors of cardiac events. Results Baseline characteristics of the two groups Comparison between NC and SC patients regarding baseline clinical data, risk factors, location of myo- cardial infarction and left ventricular dysfunction are presented in Table 1. NC patients did not dier from SC patients regarding age, gender and smoking. Statistically signicant higher prevalence rates of coronary heart disease family history, obesity, hypertension, hypercholesterolaemia and diabetes mellitus were found in SC. Angiographic left ventricular ejection fraction at hospital discharge was higher in NC (60%14%) than in SC (55%13%, P=004). No dierence was found between NC and SC regarding myocardial infarction location. Aetiological factors in patients with myocardial infarction and absolutely normal coronary arteries Aetiological factors of myocardial infarction in NC patients are summarized in Table 2. In the 71 NC patients studied prospectively, a coronary spasm was documented in 155%. Congenital coagulation disorders were found in nine of 73 patients (123%), with eight cases observed in the 71 patients (113%) of the prospec- tive arm. Congenital coagulation disorders were APC resistance in seven patients, factor XII in one patient and protein C deciency in one patient. In the total cohort of the 91 NC patients, we found a collagen tissue disorder in two patients (22%, one patient with systemic lupus erythematosus and one patient with sarcoidis), embolization in two patients (22%) and oral contraceptive use in one (11%). Follow-up The mean follow-up was 35 months (range 1100 months). Table 3 shows the events observed during the follow-up in each group. Twenty-two events occurred in the 91 NC patients: heart failure (n=8), myocardial reinfarction (n=5), stroke (n=5) and cardiovascular mortality (n=4). Forty four events occurred in the 91 SC patients (P<00001 vs NC): heart failure (n=19; P=004 vs NC), myocardial reinfarction (n=15; P=002 vs NC), stroke (n=3, P=09) and cardiovascular mortality (n=7, P=038). Although the cardiovascular mortality rate was 76% higher in SC than in NC (8% vs 45%), the dierence did not reach statistical signicance. Kaplan Meier event-free survival, with combined end-point dened by the association of death, reinfarction, heart Table 1 Comparison of clinical characteristics between the two groups NC (n=91) SC (n=91) P value Age (years) 4914 5114 ns Sex (% female) 37% 37% ns Smoking (%) 60% 63% ns Hypertension (%) 154% 35% 0003 Diabetes (%) 10% 24% 0017 Obesity (%) 11% 24% 003 Cholesterol (%) 20% 48% <00001 Family history of CAD (%) 15% 27% 004 LVEF (%) 6013 5513 004 % Anterior MI 5934% 549% ns CAD=coronary artery disease; LVEF=left ventricular ejection fraction; MI=myocardial infarction; NC=patients with absolutely normal coronary arteries; SC=patients with obstructive coronary arteries. Table 2 Aetiological factors in the group of patients with myocardial infarction and normal coronary arteries (in each column, the denominator represents the number of patients in whom the abnormality has been actually sought) Retrospective arm (n=20) Prospective arm (n=71) Overall cohort (n=91) Coronary spasm ND 11/71 (155%) 11/71 (155%) Inherited coagulation disorder 1/2 8/71 (1126%) 9/73 (123%) Embolization 1/20 (5%) 1/71 (14%) 2/91 (22%) Collagen tissue disorder 1/20 (5%) 1/71 (14%) 2/91 (22%) Oral contraceptive use 0/20 1/71 (14%) 1/91 (11%) ND=no data. MI with a normal angiogram 1461 Eur Heart J, Vol. 22, issue 16, August 2001 failure and stroke was 75% in NC vs 61% in SC (P=001). Among 11 variables tested including age, gender, smoking, hypertension, diabetes, obesity, chol- esterol level, family history of ischaemic heart disease, left ventricular ejection fraction, myocardial infarction location, presence of at least one aetiological factor, univariate analysis found that predictors of cardio- vascular events in NC were left ventricular ejection fraction (P=003), age (P=002), diabetes (P=001), and smoking (P=003). Using Cox multivariate analysis, independent predictors of long-term outcome were left ventricular ejection fraction (P=0003) and diabetes (P=0004). In the SC group, among 11 variables tested including age, gender, smoking, hypertension, diabetes, obesity, cholesterol level, family history of ischaemic heart dis- ease, left ventricular ejection fraction, myocardial infarc- tion location, number of vessels diseased, univariate analysis found that predictors of cardiovascular events were left ventricular ejection fraction (P=0009) and hypertension (P=004). Cox multivariate analysis in SC patients showed that only left ventricular ejection fraction (P=002) was an independent predictor of long-term outcome. Discussion Our study suggests that aetiological factors, predomi- nantly coronary spasm and inherited coagulation dis- order, can be detected in only one third of patients with myocardial infarction and an absolutely normal coronary angiogram, despite a systematic search in a prospective population. Although morbidity in these patients is lower than in myocardial infarction patients with coronary artery stenosis, the mortality rate is similar. In myocardial infarction patients with an absolutely normal coronary angiogram, the only two independent prognostic factors are left ventricular function and diabetes. There are limited data in the published literature regarding the long-term follow-up of large series of patients who suered an acute myocardial infarction with an absolutely normal coronary arteriogram. In addition, to our knowledge, a systematic search of the most frequently reported aetiological factors has not been done prospectively in a large cohort of patients. The rst largest cohort, with a long-term follow-up, was reported by Raymond et al. [15] who suggested a 10 year survival rate in 74 patients with myocardial infarction and normal coronary arteries. In the retrospective work by Raymond et al. [15] , only 40 of the 74 studied patients had absolutely normal coronary arteries and, aetiologi- cal factors were not systematically sought. In terms of factors predictive of clinical outcome, Raymond et al. [15] did not analyse statistics comparing survivors and non- survivors in the group of patients with a normal cor- onary angiogram. More recently, out of a total of 8839 patients who had had a history of myocardial infarction, Zimmerman et al. [21] reported a better survival rate at 7 years in the 720 patients with either angiographically normal coronary arteries or minimal to moderate dis- ease, including stenosis with a diameter reduction up to 69%, than in the remaining patients with obstructive coronary artery disease. Zimmerman et al. did not, however, perform an analysis of either prognostic fac- tors or aetiological mechanisms within the subgroup of patients with absolutely normal coronary arteries [21] . Pathophysiology of myocardial infarction with normal epicardial coronary arteries Various mechanisms have been suggested to explain the occurrence of myocardial infarction despite normal epi- cardial coronary arteries including coronary spasm, acquired or inherited coagulation disorders, toxic agents, embolization, connective tissue disease. Coronary artery spasm has been proposed as a classic aetiological factor of myocardial infarction with normal coronary arteries [2430] , but the actual prevalence rate has remained ill-dened due to the lack of ergonovine tests in large series of patients. In their study, Raymond et al. found that coronary artery spasm was present in ve of the 16 patients (31%) in whom an ergonovine maleate test was performed [15] . The same prevalence was found by Legrand et al. [7] and Lindsay and Pichard [9] who evaluated, respectively, 18 and nine patients. According to our results with a systematically performed ergonovine maleate test in a larger population of myocardial infarction patients with normal coronary arteries, the prevalence rate of coronary artery spasm appears to be lower than that previously reported in small sample size populations, since we documented a spasm in only 11 of the tested 71 patients (155%). Congenital coagulation abnormalities have also been hypothesized as possible mechanisms of myocardial infarction with angiographically normal coronary arteries [31,3337] . Owing to the small size of the popu- lation sample in previous studies, there was no con- clusive answer [3336] . Recently, a multicentre study has found a higher prevalence rate of factor V Leiden, a newly described congenital coagulation disorder, in patients with myocardial infarction and normal Table 3 Comparison of outcome at long-term follow-up between patients with absolutely normal coronary arteries and those with obstructive coronary arteries NC SC P value Follow-up (months) 3317 3518 ns Events Heart failure 8/88 (91%) 19/88 (22%) 004 Stroke 5/88 (57%) 3/88 (34%) ns Reinfarction 5/88 (57%) 15/88 (17%) 002 Cardiovascular mortality 4/88 (45%) 7/88 (8%) ns Combined end-point 22/88 (25%) 44/88 (50%) <00001 1462 A. Da Costa et al. Eur Heart J, Vol. 22, issue 16, August 2001 coronary arteries, compared with myocardial infarction patients and coronary artery stenosis or healthy subjects [37] . In our study, congenital disorders of coagulation, including activated protein C resistance, Factor XII and deciency in protein C, were found in only eight of the 71 patients (113%) in whom such abnormalities were systematically and prospec- tively sought. This prevalence rate of congenital co- agulation abnormalities is lower than that of 182% we reported previously in a much smaller cohort of younger patients [36] . Our data show that aetiological factors of myocardial infarction, with angiographically absolutely normal cor- onary arteries, are detected in only one third of patients, even when a systematic search of all causal factors reported in the published literature is performed. These results may be partially explained by limitations of the angiography technique per se, a normal coronary angio- gram being not necessarily synonymous with structur- ally normal vessel. This calls for further prospec- tive studies on the pathophysiological mechanisms of myocardial infarction. Long-term prognosis of myocardial infarction patients with normal coronary angiogram: is it so good as believed? Only two large trials have previously been published on the long-term survival rate of patients with myocardial infarction and a normal coronary angiogram. The rst large cohort studied with a long-term follow-up was reported by Raymond et al. [15] , who described ndings in 74 patients with myocardial infarction and normal coronary arteries over a mean follow-up period of 105 years. In the retrospective work by Raymond et al. [15] , only 40 of the 74 studied patients had absolutely normal coronary arteries. In their study, Raymond et al. [15] found a 85% survival rate at follow-up in patients with a normal coronary arterio- gram vs 73% in 74 patients with coronary occlusive disease. More recently, in a total of 8839 patients who had had a history of myocardial infarction, Zimmerman et al. [21] reported an excellent survival rate of 91% at 7 years in the 720 patients with zero-vessel disease compared with that of 75% (P<00001) in the remaining patients with obstructive coronary artery disease. Zero- vessel disease was dened in the study by Zimmerman et al. [21] as either angiographically normal coronary arteries or minimal to moderate disease, including stenosis with a diameter reduction of up to 69%. When patients with zero-vessel disease were further stratied, there was no signicant dierence in survival rates among patients with normal arteries, and minimal or moderate disease, but the re-infarction rate was higher in those with minimal and moderate disease (11% and 16% respectively) than in patients with angiographically normal arteries (5%, P=00002). In agreement with these two previous studies [15,21] , we have found a high survival rate of 955% at 3 years in our 91 patients with myocardial infarction and abso- lutely normal coronary arteries. However, despite this excellent survival rate, the morbidity of these patients seems to be signicant since the combined end-points, including the other major cardiac events (heart failure, stroke, re-infarction), were observed in 20%. Our results regarding overall complications are in agreement with the ndings of Maggi et al. [20] who showed, in a smaller group of 41 patients with myocardial infarction and completely normal coronary arteries, that the incidence of complications including angina, re-infarction and death was 19% after 12 years of follow-up. Prognostic factors in myocardial infarction with normal coronary angiogram By univariate analysis we identied four factors associ- ated with a poor prognosis in our patients with myo- cardial infarction and normal coronary arteries: left ventricular ejection fraction, age, smoking and diabetes. Multivariate analysis showed that the only two indepen- dent predictive factors were left ventricular ejection fraction and diabetes. These two variables have been demonstrated as major long-term prognostic factors in patients with myocardial infarction and coronary artery stenosis [43,44] . To our knowledge, our study is the rst to demonstrate the independent prognostic role of left ventricular ejection fraction and diabetes in myocardial infarction patients with absolutely angiographically normal coronary arteries. Diabetes may play a role in the prognosis of these patients through its related micro- vascular dysfunction which may enhance left ventricular remodelling [45] . Study limitations Twenty of our 91 studied patients have been evaluated retrospectively and our study has therefore the inherent limitations of this design. In particular, several aetiologi- cal factors, such as coronary artery spasm and coagula- tion disorders, have been evaluated prospectively in only 71 patients. However, our study provides the largest prospective series of patients with myocardial infarction and absolutely normal coronary arteries in whom aetio- logical factors reported in the literature have been systematically sought. A larger prospective and multi- centre study would have been better suited to the objectives. The other signicant limitation is probably due to the absence of endovascular analysis with recent technologies such as coronary angioscopy and intra- vascular ultrasound, which would allow a better analysis of the vessel structure and have enabled the limitations of the angiographic technique to be circumvented. Conclusions Patients with myocardial infarction and an absolutely normal coronary angiogram have a better long-term MI with a normal angiogram 1463 Eur Heart J, Vol. 22, issue 16, August 2001 prognosis than those with coronary artery stenosis, but the combined morbidity and mortality are not negligible in this subset of patients. The only two independent predictive factors of poor outcome in patients with myocardial infarction and absolutely normal coronary arteries are left ventricular function and diabetes. Despite a systematic search, aetiological factors are found in only one third of patients and further prospec- tive studies are needed to improve our understanding of the pathophysiology of myocardial infarction with normal coronary arteries. References [1] Bruschke AVG, Bryneel KKJ, Bloch A, Van Harpe G. Acute myocardial infarction without obstructive coronary artery disease demonstrated by selective cine arteriography. Br Heart J 1971; 33: 58594. [2] Arnett EN, Roberts WC. Acute myocardial infarction and angiographically normal coronary arteries. Circulation 1976; 53: 395400. [3] Rosenblatt A, Selzer A. The nature and clinical features of myocardial infarction with normal coronary arteriogram. Circulation 1977; 55: 57880. [4] Erlebacher JA. Transmural myocardial infarction with normal coronary arteries. Am Heart J 1979; 98: 42130. [5] Betriu A, Pare JC, Sanz GI et al. Myocardial infarction with normal coronary arteries: a prospective clinical-angiographic study. Am J Cardiol 1981; 48: 2832. [6] Proudt WL, Welch C, Siqueira C, Morcef FP, Sheldon WC. Prognosis of 1000 young women studied by coronary angio- graphy. Circulation 1981; 64: 118590. [7] Legrand V, Deliege M, Henrard L, Boland J, Kulbertus H. Patients with myocardial infarction and normal coronary arteriogram. Chest 1982; 6: 67885. [8] Ciraulo DA, Bresnahan GF, Frankel PS, Isely PE, Zimmerman WR, Chesne RB. Transmural myocardial infarc- tion with normal coronary angiograms and with single vessel coronary obstruction. Chest 1983; 2: 196202. [9] Lindsay J, Pichard AD. Acute mycocardial infarction with normal coronary arteries. Am J Cardiol 1984; 54: 9024. [10] Morris DC, Hurst JW, Logue RB. Myocardial infarction in young women. Am J Cardiol 1976; 38: 299304. [11] Khan AH, Haywood LJ. Myocardial infarction in nine patients with radiologically patent coronary arteries. N Engl J Med 1974; 291: 42731. [12] Proudt WL, Bruschke AVG, Sones FM. Clinical course of patients with normal and slightly or moderately abnormal coronary arteriograms: 10-years follow-up of 521 patients. Circulation 1980; 62: 7127. [13] McKenna WJ, Schew CYC, Oakley CM. Myocardial infarc- tion with normal coronary angiogram: possible mechanisms of smoking risk in coronary artery disease. Br Heart J 1980; 43: 4938. [14] Thompson SI, Vieweg WVR, Alpert JS, Hagan AD. Incidence and age distribution of patients with myocardial infarction and normal coronary arteriograms. Cathet Cardiovasc Diagn 1977; 3: 3: 19. [15] Raymond R, Lynch J, Underwood D, Leatherman J, Razavi M. Myocardial infarction and normal coronary arteriogra- phy: ten year clinical and risk analysis of 74 patients. J Am Coll Cardiol 1988; 11: 4717. [16] Alpert JS. Myocardial infarction with angiographically normal coronary arteries. Arch Intern Med 1994; 154: 2659. [17] Alpert JS. Myocardial infarction with angiographically normal coronary arteries. Arch Intern Med 1994; 154: 245. [18] Shari M, Frohlich TG, Silverman IM. Myocardial infarction with angiographically normal coronary arteries. Chest 1995; 107: 3640. [19] Fournier JA, Sanchez-Gonzales A, Quero J et al. Normal angiogram after myocardial infarction in young patients: a prospective clinical angiographic and long term follow-up study. Int J Cardiol 1997; 60: 2817. [20] Maggi A, Metra M, Niccoli L et al. Prognosis in patients with myocardial infarction and angiographically normal coronary arteries. Cardiologia 1994; 39: 23541. [21] Zimmerman FH, Cameron A, Fisher LD, Grace NG. Myo- cardial infarction in young adults: angiographic characteriz- ation, risk factors and prognosis (coronary artery surgery registry). J Am Coll Cardiol 1995; 26: 65461. [22] Fournier JA, Sanchez A, Quero J, Fernandez-Cortacero JAP, Gonzales-Barbero A. Myocardial infarction in men aged 40 years or less: a prospective clinical angiographic study. Clin Cardiol 1996; 19: 6316. [23] Cheitlin MD, McAllister HA, De Castro CM. Myocardial infarction without atherosclerosis. JAMA 1975; 231: 951 8. [24] Heupler FA. Syndrome of symptomatic coronary arterial spasm with nearly normal coronary angiograms. Am J Cardiol 1979; 45: 87381. [25] Gersh BJ, Bassendine MF, Forman R, Walls RS, Beck W. Coronary artery spasm and myocardial infarction in the absence of angiographically demonstrable obstructive coronary disease. Mayo Clin Proc 1981; 56: 7008. Table 4 Prognosis factors in the group of patients with myocardial infarction and normal coronary arteries Patients with events (n=22) Patients without events (n=66) P value Age (years) 5313 4913 0025 Sex (% female) 41% 20% ns Smoking (%) 64% 56% 0026 Hypertension (%) 23% 15% ns Diabetes (%) 15% 5% 001 Obesity (%) 23% 9% ns Cholesterol (%) 18% 21% ns Family history of CAD (%) 5% 20% ns % anterior MI 59% 59% ns Aetiological factor 363% 182% ns LVEF (%) 5314 6113 003 CAD=coronary artery disease; MI=myocardial infarction; LVEF=left ventricular ejection fraction. 1464 A. Da Costa et al. Eur Heart J, Vol. 22, issue 16, August 2001 [26] Bott-Silverman C, Heupler FA. Natural history of pure coronary artery spasm in patients treated medically. J Am Coll Cardiol 1983; 2: 2005. [27] Vincent GM, Anderson JL, Marshall HW. Coronary spasm producing coronary thrombosis and myocardial infarction. N Engl J Med 1983; 309: 2203. [28] Conti CR. Myocardial infarction: thoughts about pathogen- esis and the role of coronary spasm. Am Heart J 1985; 110: 18793. [29] Madias JE. The long term outcome of patients who suered an acute myocardial infarction in the midst of recurrent attacks of variant angina. Clin Cardiol 1986; 9: 22784. [30] Di Clemente D, Borghi A, Morgagni CL, Costa GM, Rusticalli G, Bugiardini R. Acute myocardial infarction with normal coronary arteries: role of microvascular dysfunction. Cardiologia 1994; 39: 82734. [31] Brecker SJD, Stevenson RN, Roberts R, Uthayakumar S, Timmis AD, Balcon R. Acute myocardial infarction in patients with normal coronary arteries. BMJ 1993; 307: 12556. [32] Da Costa A, Guy JM, Rousset H et al. Antiphospholipids and the heart. Arch Mal Coeur 1993; 307: 12567. [33] Holm J, Zo ller B, Svensson PJ et al. Myocardial infarction associated with homozygous resistance to activated protein C. Lancet 1994; 344: 9523. [34] Kyriakidis M, Androulakis A, Triposkiadis F et al. Lack of a thrombotic tendency in patients with acute myocardial infarction and angiographically normal coronary arteries. Circulation 1995; 86: 224. [35] Ardissino D, Peyvandi F, Merlini PA et al. Factor V (Arg 506-Gln) mutation in young survivors of myocardial infarction. Thromb Haemost 1996; 75: 7012. [36] Da Costa A, Tardy BR, Isaaz K et al. Prevalence of factor V leiden and other inherited thrombophilias in young patients with myocardial infarction and normal coronary arteries. Heart 1998; 80: 33840. [37] Mansourati J, Da Costa A, Munier S et al. Prevalence of factor V Leiden in patients with myocardial infarction and normal coronary angiography. Thromb Haemost 2000; 83: 8225. [38] Isner JM, Estes NAM, Thompson PD et al. Acute cardiac events temporally related to cocaine abuse. N Engl J Med 1986; 315: 143843. [39] Minor RL, Scott BD, Brown DD, Winniford MD. Cocaine induced myocardial infarction in patients with normal coronary arteries. Ann Intern Med 1991; 115: 797806. [40] Regan TJ, Wu CF, Weisse AB, Moschos CB, Ahme SS, Lyons MM. Acute myocardial infarction in toxic cardiomyopathy without coronary obstruction. Circulation 1975; 51: 453 61. [41] Zainea M, Duvernoy WFC, Chauhan A, David S, Soto E, Small D. Acute myocardial infarction in angiographically normal coronary arteries following induction of general anesthesia. Arch Intern Med 1994; 154: 24958. [42] Gonzales M, Herandez E, Aranda JM, Linares E, Cortes F, Contron G. Acute myocardial infarction due to intracoronary occlusion after elective cardioversion for atrial brillation in a patient with angiographically nearly normal coronary arteries. Am Heart J 1981; 102: 9324. [43] Lee KL, Woodlief LH, Topol EJ et al. Predictors of 30 days mortality in the era of reperfusion for acute myocardial infarction. Results from an international trial of 41 021 patients. Circulation 1995; 91: 165968. [44] Butler R, MacDonald TM, Struthers AD, Morris AD. The clinical implications of diabetic heart disease. Eur Heart J 1998; 19: 161727. [45] Iwasaka T, Takhashi N, Nakamura S et al. Residual left ventricular pump function after acute myocardial infarction in NIDDM patients. Diabetes Care 1992; 15: 15226. MI with a normal angiogram 1465 Eur Heart J, Vol. 22, issue 16, August 2001
(Autism and Child Psychopathology Series) Johnny L. Matson (Eds.) - Clinical Guide To Toilet Training Children - Springer International Publishing (2017)
Age +estimated+glomerular+filtration+rate+and+ejection+fraction+score+predicts+contrast-Induced+acute+kidney+injury+in+patients+with+diabetes+and+chronic+kidney+disease +insight+from+the+TRACK-D+study
Application of Strain and Other Echocardiographic Parameters in The Evaluation of Early and Long-Term Clinical Outcomes After Cardiac Surgery Revascularization