Background Image
Table of Contents Table of Contents
Previous Page  34 / 40 Next Page
Information
Show Menu
Previous Page 34 / 40 Next Page
Page Background

RESEARCH ARTICLE

SA JOURNAL OF DIABETES & VASCULAR DISEASE

76

VOLUME 16 NUMBER 2 • NOVEMBER 2019

Clinical outcome of intracoronary versus intravenous

high-dose bolus administration of tirofiban in diabetic

patients undergoing primary percutaneous coronary

intervention

AHMED A GHONIM, ABDALLA MOSTAFA, AHMED EMARA, ALAA S ALGAZZAR,

MOHAMMED A QUTUB

Correspondence to: Ahmed A Ghonim

Department of Cardiovascular Medicine, Naser Institute for Research and

Therapy, Cairo, Egypt

e-mail:

goodminds@hotmail.com

Abdalla Mostafa, Ahmed Emara

Cardiology Department, Menofia University, Almenofia, Egypt

Alaa S Algazzar

Cardiology Department, Ahmed Maher Teaching Hospital,

Cairo, Egypt

Mohammed A Qutub

Division of Cardiology, Department of Medicine, King Abdulaziz University

Hospital, Jeddah Saudi Arabia

Previously published in

Cardiovasc J Afr

2019;

30

: 285–289

S Afr J Diabetes Vasc Dis

2019;

16

: 76–80

Abstract

Background:

Previous trials remain inconsistent regarding

the advantages and hazards related to intracoronary

(IC) compared with intravenous (IV) administration of

thrombolytics. We aimed to evaluate the safety and

effectiveness of IC versus IV tirofiban administration in

diabetic patients (DM) with acute ST-segment elevation

myocardial infarction (STEMI) during primary percutaneous

coronary intervention (PCI)

Methods:

This trial included95patientswhowere randomised

to high-dose bolus plus a maintenance dose of tirofiban

administered either IV or IC. The groups were compared for

the incidence of composite major adverse cardiac events

(MACE) at 30 days. Levels of cardiac markers were recorded

pre- and post-intervention for myocardial perfusion.

Results:

The MACE were not different between the groups,

but post-procedure myocardial blush grade (MBG) 3 and

thrombolysis in myocardial infarction (TIMI) 3 flow were

significant in the IC group (

p

= 0.45, 0.21, respectively),

favouring the IC strategy. Peak values of both creatine

kinase-muscle/brain (CK-MB) and high-sensitivity troponin T

(hs-TnT) were significantly lower in the IC group (155.68 ±

121, 4291 ± 334 ng/dl) versus the IV group (192.4 ± 86, 5342 ±

286 ng/dl) (

p

= 0.021,

p

= 0.035, respectively). The peak value

was significantly lower in the IC group than the IV group in

terms of ST-segment resolution and 30-day left ventricular

ejection fraction (LVEF) (

p

= 0.016 and 0.023, respectively).

Conclusion:

Thirty days post PCI, IC tirofiban was more

efficient in ameliorating blood flow in the coronary arteries

and myocardial tissue perfusion in DM patients after

STEMI despite bleeding events, and MACE rates showed

no significant difference between the groups. The IC group

showed better improvement in LVEF.

Keywords:

diabetes mellitus, STEMI, intracoronary tirofiban,

primary coronary intervention

Impaired glucose metabolism accelerates the risk of arteriosclerosis

and 80% of patients with diabetes mellitus (DM) die from

cardiovascular diseases.

1

Previous trials have demonstrated a

positive correlation between hyperglycaemia and the occurrence

of heart failure, arrhythmia and other complications. Moreover,

hyperglycaemia significantly increased the mortality rate of patients

with diabetes complicated by myocardial infarction (MI).

2

Acute occlusion of the major epicardial coronary artery usually

leads to acute ST-segment elevation myocardial infarction (STEMI).

Successful recanalisation and patency of the occluded vessels with

percutaneous coronary intervention (PCI) or fibrinolytics diminishes

the infarction size, saves the function of the ventricle and decreases

morbidity and mortality rates.

3,4

Several consequences, such as no reflow and slow flow,

associated with more major adverse cardiac events (MACE),

complications and high mortality rates have been observed in

patients with DM complicated by acute MI (AMI) and undergoing

primary PCI.

5,6

Platelet aggregation into the distal microvasculature

or thrombus embolisation immediately after successful intervention

impairs microvascular flow. Administration of glycoprotein IIb/IIIa

inhibitors (GPI) and many catheter-based strategies have been

attempted to overcome this phenomenon.

7,8

American guidelines recommend tirofiban during PCI in patients

with STEMI for high burden of thrombus or patients who received

inadequate loading of P2Y12 inhibitors, and in patients with non-

ST-elevation acute coronary syndrome (NSTE-ACS) and high risk.

9,10

European guidelines recommend tirofiban use in PCI for bailout

situations if there is angiographic evidence of massive thrombus,

slow or no reflow, or thrombotic complications.

11,12

This trial attempted to assess whether intracoronary (IC)

administration of high-dose bolus plus a maintenance-dose

infusion of tirofiban would lead to better efficacy and safety and

enhance clinical outcomes better than the standard intravenous (IV)

bolus-plus-infusion regimen during PCI for diabetic patients with

acute STEMI.