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2013 Consensus Statement for Early 
Reperfusion and Pharmaco-Invasive approach 
in patients presenting with Chest pain 
Diagnosed as STEMI (ST Elevation 
Myocardial Infarction) in an Indian Setting 
Developed in collaboration with STEMI India 
JJ Dalal,T Alexander,V.Dayasagar et al. 
ORIGINAL ARTICLE 
JAPI.Vol 62.June 2014.
Introduction 
• Coronary Artery Disease (CAD) is currently the most common,non 
communicable disease in India. 
• >65 million people to be affected by 2015. 
• One of the gravest complications of CAD is STEMI. 
• Reperfusion is a time dependent, key strategy in acute STEMI care. 
• Though there are extensive clear guidelines in STEMI 
management,a gap between guidelines and implementation in 
clinical setting still exists.
• In India, the prevalence of STEMI is rising exponentially leading 
to CV morbidity and mortality. Despite advancement in 
reperfusion therapy(pharmacological and interventional),the 
overall utilization, system of care and timely reperfusion remains 
suboptimal.
Challenges for STEMI system of care in India 
• Primary PCI is available to <10% STEMI patients in India. 
• 1.Lack of awareness 
• 2.Lack of transfer facilities. 
Unavailability of hospital with PCI facility. 
• 3.Casualty/ED –to cath lab 
Finance problem 
Obtaining consent 
Cath lab occupied 
Unavailability of cardiologist round the clock.
• Patient awareness and education for early symptom 
identification. 
• Education required for General Practitioners /Physicians to 
implement early time dependent STEMI management. 
• PCI is the GOLD standard, yet remains unaccessible to majority 
of patients.
<90min
Plight of Reperfusion:What happens in real world ? 
• Most complete data about contemporary trends in STEMI 
patients in India comes from CREATE Registry, Kerala ACS 
Registry. 
• CREATE registry, large of its kind on ACS patients from 89 
large hospital centers from 10 regions and 50 cities across 
India. 
• Kerala Registry 25,748 consecutive ACS patients from 2007 
-2009 in 125 hospitals in Kerala.
What is the purpose of this consensus? 
• Alarming treatment delays exist in patients presenting with chest 
pain observed in real world and published evidences. 
• Time to diagnose STEMI and initiation of reperfusion therapy at 
various first medical contacts (FMC) in India is variable. 
• Evidence based explicit recommendations for practicing 
clinicians about time dependent early treatment. 
• Concept of Pharmaco Invasive(PI) approach contextualized to 
the situation in the India.
Process 
• Expert steering committee 
• 150 experts from 16 states in India. 
• Consensus statement
CREATE Registry 
CREATE Developed 
countries 
Number of pts enrolled 20,468 
% of STEMI 60% (12,405) 40% 
Median time for arrival to hospital after 
symptom onset 
300 min 140 -170 min 
For intiation of fibrinolysis 50 min 32-40 min 
Using ambulance 5% 
Fibrinolytic therapy 59% 
Primary PCI 9%
Kerala Registry 
• STEMI was the most common ACS admission. 
• Highest in hospital mortality rates and non fatal events. 
• Less likely to have any formal education. 
• Present more than 6 hrs after symptom onset. 
• 90% received antiplatelets therapy, 
• Thrombolytics were used in 41% of STEMI pts. 
• Inappropriate thrombolysis was relatively high.
What is Pharmaco –Invasive approach 
• It means FIRST administering EARLY fibrinolysis and then 
SYSTEMATICALLY performing an angiography (and then PCI 
if needed) WITHIN 3-24 hrs AFTER the START of 
fibrinolytic therapy,REGARDLESS of whether fibrinolysis 
RESULTS in SUCCESSFUL REPERFUSION or not. 
• In the event of fibrinolytic failure, a Rescue PCI should be 
immediately performed where one need not wait for the initial 3 
hour window.
Why it has to be stressed much 
regarding this approach ? 
• Time is Myocardium. 
• For each 30 min delay in treatment in STEMI patient,1 yr mortality 
increases by 7.5%. 
• Mortality benefit with primary PCI is lost if PCI related delay 
exceeded 60 min. Nallamothu et al ,Am J Cardiol,2004;94:772-774 
• Practically, early fibrinolytic therapy can compensate for PCI 
related delay. 
• Proportional mortality reduction was significantly higher in patients 
treated within 2 hrs with fibrinolytics.. 
Circulation 2004;109:1223-1225
Indications 
• It is appropriate for patients with STEMI who are eligible for 
treatment with fibrinolytics drugs and in whom 
Transfer time ≥30 min, or 
DTB(door to balloon) time≥90 min, 
[FMC to balloon time > 120 min]. 
• PCI related delay : (door to balloon) – (door to needle) > 60 
minutes. 
Shortening the time to reperfusion of the Infarct related artery. 
Optimal reperfusion strategy for patients with STEMI.
TRIAL EVIDENCE 
• CARESS- in- AMI trial . 
• STREAM trial 
• STEPP AMI 
What do they conclude 
• …..> 80% IRA patency is assosciated with early fibrinolysis 
even when the total ischemic time is about 4 hrs. 
• Significant portion of patients did not require stenting. 
• Lower thrombus burden. 
• No increase in bleeding risk.
Early Reperfusion and 
Pharmaco Invasive approach 
1.FMC at the level of General practitioner or consulting physician in 
private clinic/OPD. 
All patients of chest pain/suspected of AMI on clinical diagnosis should 
receive prophylactic dose of 350 mg soluble/chewable aspirin 
immediately (not enteric coated). 
ECG for diagnosis. 
Clopidogrel (300mg <75 yrs, 75 mg if >75 yrs) and atorvastatin (40-80 
mg) after confirmation by ECG. 
Transfer immediately by ambulance to nearest PCI capable 
hospital/hospitals where fibrinolysis is possible.
• Avoid referring patients to diagnostic centers as they take 3-4 
hrs of precious time for ECG reporting that may add to delay 
in timely interventions. 
• Condition of the patient to be explained to attendants and gain 
their confidence for preparedness for PCI
2.First/Second Medical contact at the level of emergency 
physician at non PCI capable hopsital/nursing home capable of 
fibrinolysis. 
• Transfer to PPCI capable center only if transfer time < 30 min. 
• Call the PPCI capable hospital and send the case. 
• If occupied –thrombolyse and then transfer. 
• If > 30 min - thrombolyse immediately.
3.Medical contact at the level of PPCI capable hospitals 
• Patient counselling 
• ED- cath lab transfer 
• Patient relative unwilling for quick decision. 
• Cath lab occupied. 
• DTB <90 min – PPCI 
• DTB > 90min - fibrinolysis
Choice of agents 
• Tenecteplase 0.53 mg/kg single blous iv over 5 seconds 
(LOE 1 A) 
• Reteplase 10 MU bolus – 30 mins +10 MU bolus 
(LOE grade 1B) 
• Alteplase 15 mg IV bolus,0.75 mg/kg over 30 min ,0.5 mg/kg 
over 60 min (LOE grade 1C) 
• Streptokinase 1.5 MU over 30 -60 min (LOE grade 2B) 
• For streptokinase –perform PCI in the later half of 3-24 hrs. 
• Radial approach is the preferred route.
Choice of fibrinolytics 
FIRST GENERATION SECOND THIRD IN PIPELINE 
Streptokinase Alteplase Increased fibrin 
specificity 
Lanoteplase 
antigenic accelerated dose Resistance to 
plasminogen activators 
Alfimeprase 
IV infusion IV infusion Reteplase 60% 
less fibrin specific 54% Tenecteplase 
TIMI grade 3flow more specific 
32% single bolus 
wt based regimen 
TIMI 3 flow - 63%
PCI 
FMC to PCI capable 
hospital 
Primary 
PCI 
<90 min 
Facilitated 
PCI(use of 
half dose 
of 
fibrinolytic 
s) 
obsolete 
Deferred 
PCI 
Stenting 
later 
Pharmaco Invasive 
approach >90 min 
PCI 3-24 
hrs after 
fibrinolysi 
s 
PCI 14- 
24 hrs 
after STK 
Delayed PCI 
12-72 hrs 
after STEMI 
FMC to Non PCI 
hosptial 
Transport <120 
min (including 
90 min) 
Primary 
PCI 
> 120 
min 
PI approach 
PCI 
Failed 
thrombolysis 
Rescue 
PCI
2013 CONSENSUS STATEMENT ON PHARMACOINVASIVE STRATEGY IN INDIA

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2013 CONSENSUS STATEMENT ON PHARMACOINVASIVE STRATEGY IN INDIA

  • 1. 2013 Consensus Statement for Early Reperfusion and Pharmaco-Invasive approach in patients presenting with Chest pain Diagnosed as STEMI (ST Elevation Myocardial Infarction) in an Indian Setting Developed in collaboration with STEMI India JJ Dalal,T Alexander,V.Dayasagar et al. ORIGINAL ARTICLE JAPI.Vol 62.June 2014.
  • 2. Introduction • Coronary Artery Disease (CAD) is currently the most common,non communicable disease in India. • >65 million people to be affected by 2015. • One of the gravest complications of CAD is STEMI. • Reperfusion is a time dependent, key strategy in acute STEMI care. • Though there are extensive clear guidelines in STEMI management,a gap between guidelines and implementation in clinical setting still exists.
  • 3. • In India, the prevalence of STEMI is rising exponentially leading to CV morbidity and mortality. Despite advancement in reperfusion therapy(pharmacological and interventional),the overall utilization, system of care and timely reperfusion remains suboptimal.
  • 4. Challenges for STEMI system of care in India • Primary PCI is available to <10% STEMI patients in India. • 1.Lack of awareness • 2.Lack of transfer facilities. Unavailability of hospital with PCI facility. • 3.Casualty/ED –to cath lab Finance problem Obtaining consent Cath lab occupied Unavailability of cardiologist round the clock.
  • 5. • Patient awareness and education for early symptom identification. • Education required for General Practitioners /Physicians to implement early time dependent STEMI management. • PCI is the GOLD standard, yet remains unaccessible to majority of patients.
  • 7. Plight of Reperfusion:What happens in real world ? • Most complete data about contemporary trends in STEMI patients in India comes from CREATE Registry, Kerala ACS Registry. • CREATE registry, large of its kind on ACS patients from 89 large hospital centers from 10 regions and 50 cities across India. • Kerala Registry 25,748 consecutive ACS patients from 2007 -2009 in 125 hospitals in Kerala.
  • 8. What is the purpose of this consensus? • Alarming treatment delays exist in patients presenting with chest pain observed in real world and published evidences. • Time to diagnose STEMI and initiation of reperfusion therapy at various first medical contacts (FMC) in India is variable. • Evidence based explicit recommendations for practicing clinicians about time dependent early treatment. • Concept of Pharmaco Invasive(PI) approach contextualized to the situation in the India.
  • 9. Process • Expert steering committee • 150 experts from 16 states in India. • Consensus statement
  • 10. CREATE Registry CREATE Developed countries Number of pts enrolled 20,468 % of STEMI 60% (12,405) 40% Median time for arrival to hospital after symptom onset 300 min 140 -170 min For intiation of fibrinolysis 50 min 32-40 min Using ambulance 5% Fibrinolytic therapy 59% Primary PCI 9%
  • 11.
  • 12. Kerala Registry • STEMI was the most common ACS admission. • Highest in hospital mortality rates and non fatal events. • Less likely to have any formal education. • Present more than 6 hrs after symptom onset. • 90% received antiplatelets therapy, • Thrombolytics were used in 41% of STEMI pts. • Inappropriate thrombolysis was relatively high.
  • 13. What is Pharmaco –Invasive approach • It means FIRST administering EARLY fibrinolysis and then SYSTEMATICALLY performing an angiography (and then PCI if needed) WITHIN 3-24 hrs AFTER the START of fibrinolytic therapy,REGARDLESS of whether fibrinolysis RESULTS in SUCCESSFUL REPERFUSION or not. • In the event of fibrinolytic failure, a Rescue PCI should be immediately performed where one need not wait for the initial 3 hour window.
  • 14. Why it has to be stressed much regarding this approach ? • Time is Myocardium. • For each 30 min delay in treatment in STEMI patient,1 yr mortality increases by 7.5%. • Mortality benefit with primary PCI is lost if PCI related delay exceeded 60 min. Nallamothu et al ,Am J Cardiol,2004;94:772-774 • Practically, early fibrinolytic therapy can compensate for PCI related delay. • Proportional mortality reduction was significantly higher in patients treated within 2 hrs with fibrinolytics.. Circulation 2004;109:1223-1225
  • 15. Indications • It is appropriate for patients with STEMI who are eligible for treatment with fibrinolytics drugs and in whom Transfer time ≥30 min, or DTB(door to balloon) time≥90 min, [FMC to balloon time > 120 min]. • PCI related delay : (door to balloon) – (door to needle) > 60 minutes. Shortening the time to reperfusion of the Infarct related artery. Optimal reperfusion strategy for patients with STEMI.
  • 16. TRIAL EVIDENCE • CARESS- in- AMI trial . • STREAM trial • STEPP AMI What do they conclude • …..> 80% IRA patency is assosciated with early fibrinolysis even when the total ischemic time is about 4 hrs. • Significant portion of patients did not require stenting. • Lower thrombus burden. • No increase in bleeding risk.
  • 17. Early Reperfusion and Pharmaco Invasive approach 1.FMC at the level of General practitioner or consulting physician in private clinic/OPD. All patients of chest pain/suspected of AMI on clinical diagnosis should receive prophylactic dose of 350 mg soluble/chewable aspirin immediately (not enteric coated). ECG for diagnosis. Clopidogrel (300mg <75 yrs, 75 mg if >75 yrs) and atorvastatin (40-80 mg) after confirmation by ECG. Transfer immediately by ambulance to nearest PCI capable hospital/hospitals where fibrinolysis is possible.
  • 18. • Avoid referring patients to diagnostic centers as they take 3-4 hrs of precious time for ECG reporting that may add to delay in timely interventions. • Condition of the patient to be explained to attendants and gain their confidence for preparedness for PCI
  • 19. 2.First/Second Medical contact at the level of emergency physician at non PCI capable hopsital/nursing home capable of fibrinolysis. • Transfer to PPCI capable center only if transfer time < 30 min. • Call the PPCI capable hospital and send the case. • If occupied –thrombolyse and then transfer. • If > 30 min - thrombolyse immediately.
  • 20. 3.Medical contact at the level of PPCI capable hospitals • Patient counselling • ED- cath lab transfer • Patient relative unwilling for quick decision. • Cath lab occupied. • DTB <90 min – PPCI • DTB > 90min - fibrinolysis
  • 21. Choice of agents • Tenecteplase 0.53 mg/kg single blous iv over 5 seconds (LOE 1 A) • Reteplase 10 MU bolus – 30 mins +10 MU bolus (LOE grade 1B) • Alteplase 15 mg IV bolus,0.75 mg/kg over 30 min ,0.5 mg/kg over 60 min (LOE grade 1C) • Streptokinase 1.5 MU over 30 -60 min (LOE grade 2B) • For streptokinase –perform PCI in the later half of 3-24 hrs. • Radial approach is the preferred route.
  • 22. Choice of fibrinolytics FIRST GENERATION SECOND THIRD IN PIPELINE Streptokinase Alteplase Increased fibrin specificity Lanoteplase antigenic accelerated dose Resistance to plasminogen activators Alfimeprase IV infusion IV infusion Reteplase 60% less fibrin specific 54% Tenecteplase TIMI grade 3flow more specific 32% single bolus wt based regimen TIMI 3 flow - 63%
  • 23.
  • 24. PCI FMC to PCI capable hospital Primary PCI <90 min Facilitated PCI(use of half dose of fibrinolytic s) obsolete Deferred PCI Stenting later Pharmaco Invasive approach >90 min PCI 3-24 hrs after fibrinolysi s PCI 14- 24 hrs after STK Delayed PCI 12-72 hrs after STEMI FMC to Non PCI hosptial Transport <120 min (including 90 min) Primary PCI > 120 min PI approach PCI Failed thrombolysis Rescue PCI