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RESEARCH ARTICLE

SA JOURNAL OF DIABETES & VASCULAR DISEASE

44

VOLUME 17 NUMBER 2 • NOVEMBER 2020

Table 1.

Patient characteristics according to glycaemia status at

admission

AH

NAH

Characteristics

n

= 474

n

= 694

p

-value

Age (years), m ± SD

57.9 ± 11.0

54.7 ± 11.8 < 0.001

Age > 60 years

193 (40.7)

220 (31.7)

0.001

Female gender

42 (19.8)

94 (15.1)

0.10

Hypertension

312 (65.8)

377 (54.3)

< 0.001

Diabete mellitus

262 (55.3)

70 (10.1)

< 0.001

Active smoking

113 (23.8)

222 (32.0)

0.002

Dyslipidaemia

149 (31.4)

216 (31.1)

0.91

Familial history of CAD

27 (5.7)

44 (6.3)

0.65

History of MI

42 (8.9)

58 (8.4)

0.76

History of stroke

24 (5.1)

23 (3.3)

0.13

Admission delay (hours),

m (IQR)

15 (5–52)

20 (5–48)

0.37

Systolic BP (mmHg),

m ± SD

148.8 ± 34.3

143.5 ± 29.1

0.01

Diastolic BP (mmHg),

m ± SD

92.1 ± 21.2

88.1 ± 19.0 < 0.001

Heart rate (bpm),

m ± SD

89.4 ± 20.9

81.8 ± 18.8 < 0.001

Congestive heart failure

168 (35.4)

144 (20.7)

< 0.001

LVEF < 40%

210 (44.3)

198 (28.5)

< 0.001

ECG findings 0.005

Anterior ACS

274 (57.8)

321 (63.6)

Inferior ACS

169 (35.7)

315 (45.4)

Lateral ACS

31 (6.5)

58 (8.4)

Troponine Ic peak (μg/l),

m (IQR)

13.1 (5.2–30.0) 4.9 (1.4–15.0)

0.004

CPK peak (UI/l), m (IQR)

1083 (436–2680) 714 (245–1900) < 0.001

CKMB peak (UI/l), m (IQR)

91 (40–242)

65 (26–171) < 0.001

STEMI

369 (77.8)

431 (62.1)

< 0.001

Atrial fibrillation

16 (3.4)

22 (3.2)

0.84

SVT/VF

18 (3.8)

25 (3.6)

0.86

Cardiogenic shock

31 (6.5)

20 (2.9)

0.002

PCI

81 (17.1)

139 (20.1)

0.21

DAPT

455 (65.6)

327 (69.0)

0.22

Death

72 (15.2)

34 (4.9)

< 0.001

Length of stay (days),

m ± SD

9.0 ± 5.9

8.4 ± 5.3

0.03

Severity of CAD

n

= 144

n

= 420

0.51

Non significant CAD

23 (16.0)

59 (14.0)

1-vessel CAD

48 (34.0)

162 (38.6)

2-vessel CAD

44 (30.6)

135 (32.1)

3-vessel CAD

28 (19.4)

64 (15.2)

Data are in

n

(%), means ± standard deviation or median (interquartile range).

AH: admission hyperglycaemia. NAH: absence of admission hyperglycaemia.

CAD: coronary artery disease. BP: blood pressure. MI: myocardial infarction.

LVEF: left ventricular ejection fraction. STEMI: ST-segment elevation myocardial

infarction. SVT/VF: sustained ventricular tachycardia/ventricular fibrillation.

DAPT: dual antiplatelet therapy. PCI: percutaneous coronary intervention.

curve = 0.636; sensitivity 61%, specificity 67%;

p

< 0.001) (Fig. 1).

Considering the value of 140 mg/dl (7.8 mmol/l), we found similar

sensitivity and specificity (sensitivity 62%, specificity 60%).

Discussion

Whereas estimation of the prevalence of DM in ACS patients is

known in sub-Saharan Africa, ranging from 25 to 41%,

11,16

to

our knowledge this is the first study reporting the prevalence of

blood glucose levels at admission and their prognostic value on

in-hospital mortality in our practice. The prevalence of admission

hyperglycaemia (40.6%) was higher than the prevalence of DM

(28.4%). This high rate of acute hyperglycaemia is consistent

with available data in the literature in wealthy countries, where

the prevalence of hyperglycaemia > 140 mg/dl (7.8 mmol/l) ranges

from 39 to 58%.

1,2,5

However, the blood glucose cut-off point

differs across studies, and it has been reported that up to 71% of

ACS patients had acute hyperglycaemia.

3

The prognostic impact of hyperglycaemia on admission in

patients hospitalised for ACS has been established in numerous

studies.

7-10

The Cooperative Cardiovascular Project

7

is the most

important registry (

n

= 141 680) that evaluated the relationship

between mortality rate and admission blood glucose after ACS.

Mortality at 30 days and one year evolved linearly with blood

glucose levels at admission (≤ 110, 110–140, 140–170, 170–240

and ≥ 240 mg/dl) (6.11, 6.11–7.8, 7.8–9.44, 9.44–13.32 and ≥

13.32 mmol/l). As in our study, the risk of mortality was higher in

patients without a history of DM.

7

In a recent meta-analysis including 214 219 patients, admission

hyperglycaemia significantly increased hospital mortality rate (HR

= 3.62;

p

< 0.0001), and this impact persisted at 30 days (HR =

4.81,

p

< 0.0001) and long term up to 108 months (HR = 2.02,

p

< 0.0001).

3

In STEMI patients who underwent primary PCI,

hyperglycaemia was associated with a higher rate of complications

and mortality, including the risk of recurrence of myocardial

infarction and heart failure.

17

Table 2.

Predictors of in-hospital death. Univariate analysis

Death during

Alive at

hospita-

discharge

lization

Predictors

(

n

= 1062) (

n

= 106)

HR

95% CI

p

-value

Age > 60 years 361 (34.0)

52 (49.1)

1.87 1.25–2.79 0.002

Female gender

195 (18.4)

30 (28.3)

1.75 1.12–2.75 0.01

Hypertension

619 (58.3)

70 (66.0)

1.39 0.91–2.12 0.12

Diabete mellitus 288 (27.1)

44 (41.5)

1.91 1.27–2.87 0.002

Active smoking 313 (29.5)

22 (20.8)

0.63 0.38–1.02 0.06

Dyslipidaemia

342 (32.2)

23 (21.7)

0.58 0.36–0.94 0.03

History of MI

92 (8.7)

8 (7.5)

0.86 0.40–1.82 0.69

Admission delay

(hours), m (IQR) 18 (5–48)

25 (6–72)

0.02

Congestive heart

failure

249 (23.4)

63 (59.4)

4.78 3.17–7.23 < 0.001

LVEF < 40%

322 (30.3)

86 (81.1)

9.88 5.97–16.36 < 0.001

Anterior ACS

527 (49.6)

68 (64.2)

1.82 1.20–2.75 0.004

Admission

hyperglycaemia 402 (37.9)

72 (67.9)

3.48 2.27–5.32 < 0.001

STEMI

707 (66.6)

93 (87.7)

3.59 1.98–6.51 0.01

Atrial fibrillation

35 (3.3)

3 (2.8)

0.85 0.26–2.83 0.54

SVT/VF

33 (3.1)

10 (9.4)

3.24 1.55–6.79 < 0.001

Cardiogenic

shock

23 (2.2)

28 (26.4) 16.22 8.92–29.48 < 0.001

DAPT

716 (67.4)

66 (62.3)

0.80 0.53–1.21 0.28

PCI

212 (20.0)

8 (7.5)

0.32 0.16–0.68 0.002

Data are in

n

(%) or median (interquartile range). HR: hazard ratio. 95%

CI: 95% confidence interval. MI: myocardial infarction. LVEF: left ventricular

ejection fraction. ACS: acute coronary syndrome. STEMI: ST-segment

elevation myocardial infarction. SVT/VF: sustained ventricular tachycardia/

ventricular fibrillation.

DAPT: dual antiplatelet therapy. PCI: percutaneous coronary intervention