June, 1999

Q wave and Non-Q wave Myocardial Infarction: A multivariate analysis of Survival Experience and Clinical Outcome after First Diagnosis at a Tertiary Care Hospital

Pages with reference to book, From 149 To 154
  Rehan M. Karim, Haseeb A. Khawaja, Shabana Naz, Shehzad S. Merchant, lnayat A. Momin, Irfan Lalani, Asif A. Sewani  ( Department of Community, The Aga Khan University Medical College, Karachi. )
Saeed Akhtar  ( Department of Health Sciences, The Aga Khan University Medical College, Karachi. )
Anwar Ahmed  ( Department of Cardiology, The Aga Khan University Medical College, Karachi. )


Introduction: Myocardial infarction (MI) is a well-recognized clinical entity with a worldwide distribution. In the United States alone, 1.5 mfflion cases of MI occur per year. This study compares the in-hospital mortality, 1 year mortality and time to death following a first Q-wave or non Q-wave myocardial infarction (MI).
Methods: One thousand five hundred and ninety-six patients were admitted at the Aga Khan University Hospital with a diagnosis of MI over a period of four years of whom 420 patients met our inclusion criteria. Data was collected from the patients’ medical records and on telephone using a pretested questionnaire. Logistic regression and Cox proportional hazard models were used to analyze the data.
Results: The mean age ±sd of the patients was 59±10 years. Of the total patients, 151(36%) and 269(64%) suffered non-Q wave and Q-wave MI respectively. A higher in hospital mortality was observed in patients with Q-wave MI (n64, 23.8%) than those with non-Q wave MI (n=16 (10.6%); adjusted OR = 2.76, 95% CI:1.5-5.01}. Similarly, patients having Q-wave Ml experienced increased 1 year mortality (n=77, 28.6%) compared to patients suffering non-Q wave MI {n=26 (17.2%); adjusted OR = 2.04,95% CI: 1.21-3.43}.
Conclusion: Patients with Q-wave MI had a worse prognosis compared with patients with non-Q-wave MI and therefore warrant a closer follow up. Further prospective studies are needed to evaluate the efficacy of early aggressive interventions in modifying the natural history of this disease (JPMA 49:149, 1999).


Myocardial infarction (MI) is a well-recognized clinical entity with a worldwide distribution. The World Health Organization defmes MI as a diagnosis when two of the following triad is present: clinical symptoms (i.e.: typical chest pain), cardiac enzyme elevation and ECG changes1. In the United States alone, 1.5 million cases of MI occur per year2. The overall prevalence of coronary heart disease in India was between 32-45/1000 people in different communities, and the prevalence of Ml varied between 10-15/1000 people3,4. Infarction has previously been classified as transmural if ST elevation or Q waves were observed in ECG or sub-endocardial if typical chest pain, creatine phosphokinase (CPK) enzyme elevation, and ST-T wave changes occurred in the absence of flew Q waves. However on pathological examination, most infarctions involve the subendocardium and some transmurai extension is common even in the absence of Q waves on ECG. Thus a more appropriate classification was devised, based on the presence or absence of Q waves5.
The well-established risk factors for MI include old age, male gender, smoking, diabetes, hypertension, hypercholestrolemia and the presence or family history of ischemic heart disease6. Previous studies have shown a higher incidence of non-Q wave MI in the elderly and fema!es7,8,9. Several studies looked at differences between the two types of infarction regarding prevalence of hypertension, smoking, diabetes, hypercholestrolemia and family history of ischemic heart disease10-13. None found any difference in the distribution of these risk factors between the two types of infarctions. Stone et al8, however reported an increased frequency of diabetes in people suffering non-Q wave infarctions. The Framingham14 study reported a higher incidence of hypertension in non-Q wave myocardial infarction group. A history of hypertension remains predictive of adverse outcome, particularly short-term mortality15. For patients less than 65 years of age, hypertension is a moderate risk factor for !ong term mortality16. Diabetic patients had a higher mortality at 28 days post MI17. Cigarette smoking did not show a quantitative relationship with the severity of the acute infarction in terms of short and long term mortality18.
The prognosis after myocardial infarction depends on the infarct size, as demonstrated by the CK levels in blood, left ventricular function, and the use of thrombolytic therapy19,20. Studies have shown that patients with non Q wave MI suffered smaller infarcts, as reflected by lower CPK levels21,22, and higher post MI left ventricular ejection fraction8,22.
People suffering Q wave infarction usually experience higher in hospital mortality. However there is no difference in long term survival when compared to non-Q wave MI8,14,23 This is controversial, and studies showing no difference regarding in hospital mortality21,22, and reduced long term survival for non Q wave infarctions have also been reported24-26.
It has been shown that the total in hospital and 6 month mortality was lower in patients younger than 50 years than those above 50 years27,28. In one study, gender did not affect in-hospital and three-year mortality rates29.
Other studies have demonstrated a higher short-term mortality in women but similar long-term mortality30,31.
Existing literature holds much controversy regarding the prognosis of patient with Q wave and non Q wave infarctions. Therefore, we conducted this study to compare the in hospital mortality, mortality at I year and the time to death in association with the various risk factors proven to have a role in myocardial infarction.

Materials and Methods

A retrospective cohort of patients admitted at the Aga Khan: University Hospital (AKUH), a tertiary care hospital between January 1, 1994 and December 31, 1997 with a diagnosis of Ml was eligible for inclusion in the study. A total of 1596 patients were identified by the indexing and coding department AKUH, of whom 272 died in hospital while 1324 were discharged. Patients were excluded from the study if they had a prior MI, a pre­existing left bundle branch block on ECG, history of prior revascularization(i.e. coronary artery bypass grafting and coronary angioplasty) and if telephone contact was not possible. Patients were telephoned in order to determine their survival status until 1st Jan 1999. The final study sample included 420 patients of whom 80 died in hospital while 340 survived their hospital stay and were interviewed via phone.
Congestive heart failure was taken as documented by the attending physician and/or diffuse bilateral rales on chest auscultation and/or evidence of pulmonary edema on chest X-ray and/or presence of S3 on auscultation. A cardiologist (AA) using the Minnesota code criteria32 determined the type of infarct for Q-wave Ml.
Data management and analysis
The SPSS software package was used for data entry and analysis. Age was categorized into quartiles and used in subsequent analysis. Patients with Q-wave Ml were compared with those suffering non Q-wave Ml with regard to demographic and clinical variables. The student’s t-test or chi-square test was used as appropriate.
In-hospital mortality, mortality at 1 year follow-up and time to death during follow-up were the three outcome variables used in this study. Unadjusted relationship of infarct type (i.e. Q-wave or non Q-wave) with in-hospital mortality and mortality at 1 year was assessed by simple logistic regression. Univariate logistic regression was used to identify potential confounding factors from gender, sex, history of hypertension, diabetes mellitus, smoking and family history of ischemic heart disease. Factors related with the three outcome variables were incorporated multivariable analysis (P 0.2). The final models for ‘in-hospital mortality’ and ‘mortality at 1 year’ were selected through backward stepwise procedure and included factors which were significantly (P <0.05) related to these outcome variables.
Unadjusted survival experience over the study duration was estimated using the Kaplan Meier method to discharge were examined using Cox proportional hazard model. The independent variables considered were the same as for in-hospital mortality and mortality at 1 year.


Table 1 describes the baseline characteristics of patients presenting with Q wave and non Q wave Ml. Patients with Q-wave MI were significantly more likely to have family history of ischemic heart disease (p = 0.026), higher mean CK (p < 0.0001) and receive thrombolytic therapy (p<0.001). The two groups however, did not differ significantly in age, gender. history of smoking, history of diabetes, history of hypertension and congestive heart failure in hospital (Table 1).

In-Hospital Mortality
Eighty patients died during the course of their hospital stay. Amongst 269 patients who suffered Q wave MI, 64(23.8%) died whereas only 16(10.6%) out of 151 patients suffering from non-Q wave MI expired, during their hospital stay.
The final multivariable logistic regression model for in-hospital mortality (Table 2)

demonstrated that age, smoking and infarct type significantly affected outcome. After adjusting for confounders, it was seen that Q-wave Ml patients were more likely to suffer from in-hospital mortality than non-Q wave MI patients (adjusted OR = 2.76, 95%C1 1.5 - 5.01, p 0.001). Smoking had a protective effect on in-hospital mortality (adjusted OR = 0.24, 95%C1 0. 12-0.48, p <0.001). Patients over 67 year of age had increased likelihood of dying during hospital stay compared to patients aged 49 years (adjusted OR = 3.81; 95%Cl: 1.54-9.47. p = 0.004).
Mortality at 1 Year
One year after experiencing their first Ml, 103 patients died. This constituted 77(28.6%) of patients with Q wave Ml and 26 (17.2%) of patients with non-Q wave Ml. The final multivariate logistic regression model (Table 3)

demonstrated that age, smoking and infarct type, significantly affected I-year mortality. Patients with Q­wave infarction experienced increased mortality at 1 year follow-up than patients with non- Q wave infarctions (OR = 2.04; 95%Cl 1.21-3.43, p = 0.0076). Smoking had a protective effect on 1 year mortality (OR 0.34, 95%Cl: 0.19-0.6, p = 0.0002). Patients aged 59-66 years were 2.95 times more likely to die with in 1 year compared to patients  49 years (adjusted OR = 2.95, 95% Cl: 1 .23-7.06, p = 0.015). Patients >. 67 years of age had an even higher odds of dying within 1 year after first Ml (adjusted OR = 5.18; 95% Cl: 2.22-12.1, p = 0.0001).
Time to death following hospitalization
The median time to death following the diagnosis of MI was 6 days. Med ian survival time of the patients who died after suffering from non-Q wave Ml and Q-wave Ml was 61 days and 4 days respectively (Figure).

The final multivariate Cox proportional hazard model (Table 4)

demonstrated that age, smoking, revascularization and infarct type, significantly affected time to death following diagnosis of Ml. After adjusting for confounders, the relationship between infarct type and time to death was marginally significant (adjusted RH = 1.45, 95% Cl: 0.98-2.12, p = 0.06). Revascularization (adjusted RH = 0.18; 95%Cl: 0.08-0.42, p = 0.0001) and smoking history (adjusted RH 0.43, 95% CI: 0.28-0.67, p = 0.0002) prolonged survival following first diagnosis of Ml among the study subjects. Patients above 67 years were 2.1 times more likely to die during the total follow-up period than patients below 49 years (adjusted RH = 2.1; 95% Cl: 1.2-3.8, p = 0.01).


This data demonstrates important differences in baseline characteristics and clinical outcome between patients presenting with first Q wave and non-Q wave MI. Majority of the risk factors associated with MI did not show a statistically significant difference in their distribution between Q wave and non-Q wave Ml. This is consistent with data from previous studies10,11 CoIl et al12 showed that patients with non Q wave Ml were significantly younger. On the other hand Nicod et al observed that patients with non-Q wave MI were significantly older7. However he had excluded patients in whom location of infarct could not be determined.
Stone et al observed more diabetics in the group of patients with non-Q wave MI8. In our study sample, family history of IHD was found more frequently in patients with Q wave MI. A higher CK peak value was also found in Q wave vs non-Q wave MI. This is consistent with previous studies23,24. The biological rationale underlying this observation is that patients with non-Q wave Ml’s often exhibit partial coronary occlusion in the infarct territory. On the other hand, patients with Q wave Ml’s often have total coronary artery occlusion in the infarct territory. This leads to increased infarct size and thus higher peak CK levels33,34.
Multivariate analysis indicates that Q wave Ml patients have higher in-hospital mortality than non-Q wave MI patients, with a similar trend being observed for 1 year mortality. This finding corroborates the results of many recent studies19,20,25,26. Regarding long term mortality, patients with Q wave Ml exhibited marginally increased mortality than patients with non-Q wave MI (OR = 1.45, 95% Cl 0.98 - 2). However, much controversy surrounds this issue, since literature is available suggesting that Q wave and non Q wave Ml patients have similar short term20 and long term survival8. However, it should be noted that these studies also included patients with previous MI8,21 used only univariate analysis21 and excluded a subgroup of patients having antero-inferior MI8.
Smoking had a beneficial effect on survival in in-hospital mortality. This finding is supported by previous literature34. The biological rationale for this effect is that smokers develop occlusive coronary thrombi at an earlier stage of atherosclerosis than in non-smokers. Thus, left ventricular function is relatively well preserved following MI in smokers, owing to the less advanced stage of coronary atherosclerosis. Hence, in-hospital mortality is lower in smokers compared to non-smokers. However, smokers tend to suffer a higher frequency of reinfarctions, which reduces their long-term survival34.
The results show a protective effect of smoking on mortality at 1-year follow up as well as for time to death following discharge from hospital. This may be explained by the limited follow-up period of this study.
Patients over 67 years of age had increased risk of dying than patients below 50 years of age for in hospital mortality, I-year mortality and early death following discharge. This is supported by Mocetti et at29 who also showed a higher in hospital and 6 month mortality in patients above 70 years.
In conclusion, patients with first Q-wave MI had a worse prognosis than patients with non Q wave MI. Hence they warrant a closer follow-up and aggressive risk reduction measures. Additional planned prospective studies are needed to evaluate whether early aggressive intervention may beneficially modify the natural history of this disease.
Limitations of the study
Although multivariate analysis was used to adjust for prognostic factors affecting survival after Ml (Q wave v/s. non Q-wave), medications given to patient after hospital discharge could modify the long-term outcome. Such data was not reliably available for many subjects and were therefore, not included in the analysis. Records did not contain adequate data for quantifying time lag between symptom onset and hospital presentation of MI patients. Therefore, the peak CK levels may not be a reliable estimate of the actual infarct size in these patients. Another limitation of the study was that the cause of death could not be ascertained on telephonic interview. For that reason, all cause mortality was used.


1. Beaglehole-R, Stewart-AW, Butler-M. Comparability of old and new World Health Organization criteria for definite myocardial infarction. lnt-J­Epidemiol. 1987; 16: 373-6.
2. Antman EM, Braunwald E. Acute myocardial infarction. In: Fauci AS, Braunwald E, Isselbacher Ki., eds. Harrison’s Principals of Internal Medicine. 14th ed. McGraw Hill, New York, 1998; Vol.1, pp. 1352.65.
3. Chadha-SL, Radhakrishnan-S, Ramachandran-K et al. Epidemiological study of coronary heart disease in urban population of Delhi. lndian-J-Med-Res. 1990; 92: 424-30.
4. Gopinath-N, Chadha-SL, Jain-P et al. An epiderniological study of coronary heart disease in different ethnic groups in Delhi urban population. J-Assoc­Physicians-India. 1995; 43: 30-3.
5. Massie BM, Amidon TM. Acute myocardial infarction. In: Tiemey LM, McPhee Si, Papadakis MA, eds. Current Medical Diagnosis and Treatment. 38th ed. CAppleton and Lange, Connecticut, 1999, pp. 372-84..
6. Assmann-G, Schulte-H, Cullen-P. New and classical risk factors- the Munster heart study. Eur-J-Med-Res. 1997 16; 2: 237-42.
7. Nicod-P, Gilpin-E, Dittrich-H et al. Short and long tenn clinical outcome after o wave and non-Q wave myocardial infarction in a large patient population. Circulation. 1989; 79: 528-36.
8. Stone-PH, Raabe-DS, Jaffe-AS et al. Prognostic significance of location and type of myocardial infarction: independant adverse outcome associated with anterior location. J-Am-Coll-Cardiol. 1988; 11: 453-63.
9. Hendel-RC. Myocardial infarction in women, Cardiology. 1990: 77 suppl 2:41-57.
10. Thanavaro S, Krone Ri, Kleigei RE et at. In-hospital prognosis of patients with first non-transmural and transmural infarctions. Circulation 1980; 61: 29-33.
11. Krone RJ, Friedman E, Thanavaro S et at. Long term prognosis after first Q wave or non-Q wave myocardial infarction: analysis of 593 patients. Am-J­Cardiol. 1983; 52: 234-39.
12. CoIl S, Castaner A, Sanz G et al. Prevalence and prognosis after a first non­transmural Ml. Am-J-Cardiol. 1983; 51: 1584-88.
13. Connoly DC, Elveback CR. Coronary heart disease in residents of Rochester, Minnesota, VI: hospital and post hospital course of patients with transmural and sub-endocardial myocardial infarction. Mayo Clin Proc 1985; 60:375-81.
14. Berger CJ, Murabito JM, Evans JC et al. Prognosis after first myocardial infarction. JAMA 1992; 268: 1545-51 .
15. Haider-AW, Chen-L, Larson-MG et al. Antecedent hypertension confers increased risk for adverse outcomes after initial myocardial infarction. Hypertension. 1997; 30: 1020-4.
16. Gustaffson-F, Kober-L, Ottesen-MM et al. Long term prognosisafter acute Ml in patients with a history of arterial hypertension. TRACE Study group. Eur-Heart-J. 1998; 19: 588-94.
17. Davis-TM, Parsons-RW, Hobbs-MS et at. Arrythmias and mortality after myocardial infarction in diabetic patients. Diabetes-Care. 1998; 21: 637-40.
18. Gottlieb-S, Fallavollita-J, Brown-M et al. Cigarette smoking and the age at onset of a first non fatal myocardial infarction. Coron-Artery-Dis. 1994; 5:687-94.
19. Peel AF, Semple T, Wang I et al. A coronary prognostic index for grading severity of infarction. Br Heart J 1962; 24: 745-60.
20. Henning H, Gilpin F, Corell JW. Prognosis after acute myocardial infarction. A multivariate analysis of mortality and survival. Circulation. 1979; 59: 1124-36.
21. Ogawa-U, Haze-K, Saito-M etal. Comparison of clinical features of Q-wave and non-Q-wave MI. Am-Heart-J. 1986; 111: 513-8.
22. Kishi-K, Uiasa-Y, Kinoshita-M et al. Clinical features and long tern outcome of non—Q—wave inyocardial infarction in the elderly: comparison with Q—wave Ml. J-Cardiol.1994; 24: 433-7.
23. Lavie-CJ,Gersh-BJ. Acute Myocardial Infarction. Mayo Clin Proc., 1990,65: 53 1-48.
24. Goodman-SG,Langer-A,Ross-AM et al. Non-Q-wave versus Q-wave Ml after thrombolylie therapy. Circulation. 1998; 97: 444-50.
25. Mahoney C, Hindman MC, Avonin N et al. Prognostic differences in subgroups of patients with electrocardiographic evidence of subendocardial or transmural Ml. Am J Med., 1980; 69: 183-86.
26. Cannom DS, Levy W, Colten LS. The short and long term prognosis of patients with transmural and non transmural myocardial infarction. Am J Med 1976: 61: 452-58.
27. Moccetti-T Malacrida-K, Pasoui-E et al. Epiderniologic variables and outcome of 1972 young patients with acute Ml (GISSI—2). Arch—Intent—Med., 1997; 157: 865-9.
28. Chaikhouni—A, Chouhan—L, Banua—A et al. Mvocardial infarction in Qatar. Clin-Cardiol. 1993; 16: 227-30.
29. Fiebach—N H. Visroli-CM. l-Iorwitz—Rl. Difference between women and men in survival after myocaridal infarction. JAMA .1990; 263: 1092-6.
30. Kober-L. Ottesen-M, Rasmussen-S et al. Influence of gender on short-and long-tenn mortality alter acute Ml. Ti’ace Study. Amn-J-Cardiol. 1996; 77: 1052-6.
31. Maynard-C, Everv-NR, Martin-iS et al. Association of gender and survival in patients with acute mvocardial infarction. Arch—lnteni—Med. 1997; 1 57: 1379-84.
32. Aguirre—FV, Younis—LT, Chaitman—l3R et al. Early and I—year clinical outcome of patients evolving non Q—w ave versus Q—wave mvocardial infarction after thrombolysis. Circulation. 1995:91: 25.41-48.
33. DeWood-MA, Spores-J, Notske-R et al. Prevalence of coronary occlusion during the early hours of transmural myocardial infarction. N EngI J Med 1980; 303: 897,
34. Molstad-P. First mvocardial infarction in smokers. Eur-Heart-J. 1991: 12: 753-9.

Pages with reference to book, From 149 To 154

News & Events

The DIABETES AND RAMADAN International Alliance 3rd Forum will be held in Dubai on 17th April, 2015. Important topics as Education, acute emergencies, CREED Study, Insulin in Ramadan, Incretins in Ramadan,and many more will be discussed. The Forum will provide intense learning opportunity to all participants. The International Faculty will include President, IDF and many others.

The Sixth Regional Conference on Medical Journals in the Eastern Mediterranean Region(EMMJ6) will take place from February 18-20,2015 in Shiraz,Islamic Republic of Iran.
Important dates:
Abstract Submission Deadline: January 15,2015
Abstract Acceptance Notification: January 22,2015
Registration (Conference and Workshops) Deadline: January 30,2015


Sindh Institute of Urology and Transplantation (SIUT), Karachi will celebrate 40 years of its services by holding an International Symposium on Recent Advances in Urology, Nephrology, GI Hepatology, Paediatrics, Transplantation & Bioethics from 8th to 12th December, 2015.Social and economic aspects of health care especially in a developing country will also be included.
Important Dates: Last date for Abstract submission:31st July 2015
Last Date for early registration: 30. September, 2015