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JOURNAL CLUB
Two-year follow-up data from the STEPP-AMI
study: A prospective, observational, multicenter
study comparing tenecteplase-facilitated PCI versus
primary PCI in Indian patients with STEMI
i n d i a n h e a r t j o u r n a l 6 8 ( 2 0 1 6 ) 1 6 9 – 1 7 3
DR MALLESWARA RAO
INTRODUCTION
• STEMI is a life threatening manifestation of CAD requiring timely
reperfusion
• incidence of STEMI is higher in the Indian population when compared
to developed countries
• Current recommendations maintain PCI as the treatment of choice ,
contingent upon rapid initiation of treatment at centers with a skilled
PCI laboratory within suggested timelines
• unavailability of primary PCI capable hospitals across India and
delays in transport -<10% of patients with STEMI-PCI in India
• patients who do reach the hospital early still have to deal with other issues, such
as arranging for finances, as most Indian patients pay out-of
pocket
• introduction of fibrin-specific lytic agents like tenecteplase (TNK) has improved
the IRA patency rates significantly.
• Rapid fibrinolytic treatment improved the outcomes in patients treated within
an hour of symptom onset, with tapering benefits after 3 hrs
• fibrinolysis -high rates of reocclusion of IRA
• initial bolus lysis followed by early CAG within 3–24 h
of fibrinolysis, with an appropriate PCI ='pharmacoinvasive strategy-good
alternative especially in a developing country such as India.
Comparison of primary angioplasty and pre-
hospital fibrinolysis in acute myocardial
infarction (CAPTIM) trial: a 5-year follow-up
• primary angioplasty (n = 421)VS pre-hospital fibrinolysis (rt-PA) with
immediate transfer to a centre with interventional facilities (n = 419)
all-cause mortality at 5 years
• 9.7% in the pre-hospital fibrinolysis group
• 12.6% in PPCI [ P = 0.18].
patients included within 2 h, 5 year mortality
• 5.8% in the pre-hospital fibrinolysis group
• 11.1% in PPCI [HR 0.50 ( P = 0.04],
Patients included after 2 h, 5 year mortality
• 14.5 vs 14.4% [ P = 0.92].
PRESENT STUDY
• prospective, observational, multicenter pilot study,
• between August 2011 and May 2013
• Study sites, which were capable of performing 24/7 primary
PCI, were selected from Tamilnadu,Karnataka , and Kerala
• 200 patients
• observational study, the treatment options were chosen entirely by
the patient and the attendants
• some patients who presented outside the recommended timelines
for thrombolysis have received lytic therapy .
AIM
• assess the safety, efficacy, and
feasibility of a pharmacoinvasive strategy in comparison to
primary PCI in STEMI
• primary endpoint
• set at 30 days
• composite of death, cardiogenic shock, reinfarction, repeat
revascularization, and congestive heart failure, and extended to 2
years
• Safety end points are bleeding assessed using the
TIMI classification at 30 day
• Baseline characteristics were no different between both groups,
except more patients in arm B were in killip's class I.
• 6.7% (n = 3) patients in arm A had insignificant disease; hence no
intervention was performed for them
• 100% of patients in arm B required angioplasty and stent
implantation.
pharmacoinvasive arm
(arm 'A') -
45 patients
PPCI arm (arm 'B') 155 patients
• Patients in arm A also had better TIMI flow at CAG (TIMI 3 flow in
27.9%), higher radial procedures (76.7%), more IRA patency
(82.2%), and less thrombus burden.
• In arm 'A', 12.1% -failed thrombolysis.
bleeding outcomes
• 2.2% vs. 2.6%, 'p' not significant).
• efficacy end points are studied at 30 days, 3 months, 6 months, 1 year, and 2
years-no difference
• There is trend of benefit for arm B in the initial few months
• Primary endpoint at 30 days -trend toward benefit in the primary PCI group
(11.1% vs.3.9%, p = 0.07, RR = 2.8).
• At the end of 2-year follow-up, the initial benefit from PPCI seems to be
narrowed as more events have occurred in PPCI group (A-17.8% vs. B-13.6%, p =
0.47, RR = 1.31;).
• The additions of events in the primary endpoint of PPCI group are mainly due to
death and repeat revascularization
• This may be partly due to the fact that 6.7%of patients in arm A did
not require a stent placement due to insignificant disease at the
angiogram, which means they are at no risk of stent thrombosis or
restenosis.
• non-urgent basis on which the angioplasty was performed in arm A
may also have influenced the primary endpoint over a period of
time, but this fact needs further large studies to provide
comprehensive evidence.
•
CONCLUSION
• fibrinolysis followed by an early coronary angiogram within 3–24 h
with PCI, if appropriate, resulted in similar outcomes when
compared to primary PCI in patients with STEMI at 2-year
follow-up.
• These findings lend further support to the adoption
of a pharmacoinvasive strategy where patient and system related
delays are inherent
THANKYOU

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Pci vs tlt 2

  • 1. JOURNAL CLUB Two-year follow-up data from the STEPP-AMI study: A prospective, observational, multicenter study comparing tenecteplase-facilitated PCI versus primary PCI in Indian patients with STEMI i n d i a n h e a r t j o u r n a l 6 8 ( 2 0 1 6 ) 1 6 9 – 1 7 3 DR MALLESWARA RAO
  • 2.
  • 4. • STEMI is a life threatening manifestation of CAD requiring timely reperfusion • incidence of STEMI is higher in the Indian population when compared to developed countries • Current recommendations maintain PCI as the treatment of choice , contingent upon rapid initiation of treatment at centers with a skilled PCI laboratory within suggested timelines • unavailability of primary PCI capable hospitals across India and delays in transport -<10% of patients with STEMI-PCI in India
  • 5. • patients who do reach the hospital early still have to deal with other issues, such as arranging for finances, as most Indian patients pay out-of pocket • introduction of fibrin-specific lytic agents like tenecteplase (TNK) has improved the IRA patency rates significantly. • Rapid fibrinolytic treatment improved the outcomes in patients treated within an hour of symptom onset, with tapering benefits after 3 hrs • fibrinolysis -high rates of reocclusion of IRA • initial bolus lysis followed by early CAG within 3–24 h of fibrinolysis, with an appropriate PCI ='pharmacoinvasive strategy-good alternative especially in a developing country such as India.
  • 6.
  • 7.
  • 8.
  • 9.
  • 10.
  • 11.
  • 12.
  • 13.
  • 14.
  • 15.
  • 16.
  • 17. Comparison of primary angioplasty and pre- hospital fibrinolysis in acute myocardial infarction (CAPTIM) trial: a 5-year follow-up • primary angioplasty (n = 421)VS pre-hospital fibrinolysis (rt-PA) with immediate transfer to a centre with interventional facilities (n = 419) all-cause mortality at 5 years • 9.7% in the pre-hospital fibrinolysis group • 12.6% in PPCI [ P = 0.18]. patients included within 2 h, 5 year mortality • 5.8% in the pre-hospital fibrinolysis group • 11.1% in PPCI [HR 0.50 ( P = 0.04], Patients included after 2 h, 5 year mortality • 14.5 vs 14.4% [ P = 0.92].
  • 18. PRESENT STUDY • prospective, observational, multicenter pilot study, • between August 2011 and May 2013 • Study sites, which were capable of performing 24/7 primary PCI, were selected from Tamilnadu,Karnataka , and Kerala • 200 patients • observational study, the treatment options were chosen entirely by the patient and the attendants • some patients who presented outside the recommended timelines for thrombolysis have received lytic therapy .
  • 19. AIM • assess the safety, efficacy, and feasibility of a pharmacoinvasive strategy in comparison to primary PCI in STEMI
  • 20. • primary endpoint • set at 30 days • composite of death, cardiogenic shock, reinfarction, repeat revascularization, and congestive heart failure, and extended to 2 years • Safety end points are bleeding assessed using the TIMI classification at 30 day
  • 21. • Baseline characteristics were no different between both groups, except more patients in arm B were in killip's class I. • 6.7% (n = 3) patients in arm A had insignificant disease; hence no intervention was performed for them • 100% of patients in arm B required angioplasty and stent implantation. pharmacoinvasive arm (arm 'A') - 45 patients PPCI arm (arm 'B') 155 patients
  • 22.
  • 23.
  • 24.
  • 25. • Patients in arm A also had better TIMI flow at CAG (TIMI 3 flow in 27.9%), higher radial procedures (76.7%), more IRA patency (82.2%), and less thrombus burden. • In arm 'A', 12.1% -failed thrombolysis.
  • 26. bleeding outcomes • 2.2% vs. 2.6%, 'p' not significant). • efficacy end points are studied at 30 days, 3 months, 6 months, 1 year, and 2 years-no difference • There is trend of benefit for arm B in the initial few months • Primary endpoint at 30 days -trend toward benefit in the primary PCI group (11.1% vs.3.9%, p = 0.07, RR = 2.8). • At the end of 2-year follow-up, the initial benefit from PPCI seems to be narrowed as more events have occurred in PPCI group (A-17.8% vs. B-13.6%, p = 0.47, RR = 1.31;). • The additions of events in the primary endpoint of PPCI group are mainly due to death and repeat revascularization
  • 27. • This may be partly due to the fact that 6.7%of patients in arm A did not require a stent placement due to insignificant disease at the angiogram, which means they are at no risk of stent thrombosis or restenosis. • non-urgent basis on which the angioplasty was performed in arm A may also have influenced the primary endpoint over a period of time, but this fact needs further large studies to provide comprehensive evidence. •
  • 28. CONCLUSION • fibrinolysis followed by an early coronary angiogram within 3–24 h with PCI, if appropriate, resulted in similar outcomes when compared to primary PCI in patients with STEMI at 2-year follow-up. • These findings lend further support to the adoption of a pharmacoinvasive strategy where patient and system related delays are inherent