Implantation of bone marrow stromal cells into ischemic myocardium prevents late myocardial remodeling

Implantation of bone marrow stromal cells into ischemic myocardium prevents late myocardial remodeling

332A small ABSTRACTS myocardial din,(lmg/kg infarcts - Myocardial were and 5 q/kg, observed in the n=lZ)significantly heart. reduced Treat...

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332A small

ABSTRACTS myocardial

din,(lmg/kg

infarcts

- Myocardial

were

and 5 q/kg,

observed

in the

n=lZ)significantly

heart.

reduced

Treatment

by microthrombi.

This model

with

the area and number

cardial infarction(pc0.01 conpared with control). CONCLUSIONS: model of minor myocardial infarction in rats in which the small occluded

JACC

Ischemia and Infarction

is useful to investigate

r-RGD-Hiruof minor myo-

We present a new coronary arteries are

the pathophysiology

and

treatment of minor myocardial infarction which is ccmmcn in interventional treatment. RRGD-Hirudin may be beneficial in the treatment of minor myocardial infarction induced

Moderate/Severe

by PTCA.

(%)

Bleeding

ICH (%)

of Bone Marrow Stromal Cells Into lschamic Myocardium Prevents Late Myocardial Remodeling

YaoLlana

Tanq

Medicine,

Gainesville,

M Ian Phillips,

Republic

myocardial

Qiang Zhao, Junbo

FL, Shanghai

Ge, University

Institute of Cardiovascular

30.Day

of Florida, College

Diseases,

infarction

of

Shanghai,

process

IS a major cause of heart failure and deaths

(Ml). Marrow stromal cell (MSCs) was shown to enhance

Mortality

(%)

Odds Ratio

(n = 1038)

(n = 2304)

17.1

11.6

1.71

1.24. 2.36

0.001

0.48

0.89

0.75

0.262.13

0.586

3.7

4.9

0.78

0.54-

0.214

Methods

Autologous

MSCs were induced

into a zone made ischemic

1 week after Ml via intramyocardial(n=lO) or intracoronary rats received medium (intramyocardial, n=lO; intracoronaiy,

~70 % 1 week after Ml were included.

Histology

after

12:12

by coronary

artery

Scar area index and the scar thickness

Results Eight weeks after implantations, serial section of transplanted area showing regenerated muscle tissue surrounded by host infarction scar in PTAH-stained heart seclefl

ventricular

end-diastolic

diameter

reduced

increased

in MSCs

group

control group. P-zO.01). Moreover, the myccytes were significantly larger than that of control 0.021+0.009

significantly

in

MSCs

group

mm vs. 0.968+0.094 mm in control group, p
and the scar thickness

(1.45iO.32

mm vs. 0.88i0.29mm

in

at the peri-infarct zcne of MSCs group group (diameter:0.033+0.011 mm vs.

mm, P
Conclusion Our data indicate that MSCs implantation and improved scar healing by regeneration of muscular

reversed myocardial tissue after Ml.

remodeling

Holaer Thiele,

Lothar Engelmann,

Hartmann,

University

Background:

Kathleen

Dietrich Pfeiffer,

of Leipzig

in acute

and restoration

Leipzig,

benefit mainly

myocardial of a normal

due to encountered

Sunday, March 30, 2003, Noon-2:00 McCormick Place, Hall A

+ abciximab)

81 min. in COMBO

Duke Clinical

Research

PCI group

bleeding

Vie Hasselblad,

Durham,

Sabina

with in-hospital

conservative

and as delayed

only in comparison

endpoint

GP Ilb/llla

rescue/early

PCI after full-dose

a meta-analysis

of data from

repedusion

regimens

for STEMI

(ASSENT

bleeding

Christopher

fibrinolytic

11 clinical

1,2, and 3, GUSTO

Results:

Patients

treated

with GP Ilb/llla

stratified inhibitors

Boston,

or a prehospital

initi-

MRI. The secondary

therapy

have not

trials evaluating

new

Ill and V, TIMI 108 and

scale,

intracranial

by the adjunctive were younger

hemorrhage

use of GP llbillla

(mean

age 57.3 vs.

Valenti,

Leonardo

Florence,

Maurizio

Hospital,

PCl+stent

was

was 107+ PCI-group

by CK-release

with abciximab

results in a an improved

which

about

the benefit

of abciximab

ever, these studies stents. Methods:

enrolled

To determine

Trapani,

Buenos

Background: Previous randomized alone in pts with acute myocardial

was

com-

is feasible

tissue perfu-

leads to a trend of smaller

infarcts

p.m.

Randomized Alone With in Acute of the (ACE) Trial

the impact

Hospital,

studies comparing stent plus abclximab with stent infarction (AMI) have produced conflicting results

as adjunctive

mainly

Cesar F. Vigo, Careggi

Aires, Argentina

low-risk

treatment patients,

of abciximab

to infarct artery stenting.

How-

or were done with first generation therapy

as adjunct

to infarct

artery

stenting in AMI, 400 pts. without any restriction based on age or clinical status on presentation, were randomized at 4 sites to primary stenting alone (n =200) or stenting plus abciximab

had diabetes

arction.

are listed in the table.

physlcian

to 105+ 127 min. in the facilitated

was similar in both groups without an excess in bleeding

Bolognese.

Italy, Otamendi

angiographic The primary

outcomes

endpoint

David Antoniucci. Alfred0 Rodriguez, Albrecht Hempel, Angela Migliorini, Guide Parodi, Antonio L. Bartorelli, Antonio Colombo, Giovanni M. Santoro, Guia Moschi. Renato

58.3 yrs), heavier (mean weight 84.8 vs. 81.6 kg), less commonly female (18.5% vs. 20.8%), less commonly had an anterior infarct (40.9% vs. 42.4%), and rncre commonly (17.0% vs. 14.7%). Unadjusted

(r&8)

A Prospective Multicenter International Trial Comparing Infarct Artery Stenting Infarct Artery Stenting Plus Abcixlmab Myocardial Infarction: Principal Report Abciximab andsarbostent Evaluation

8. Granger,

improve cutccmes when used during (STEMI), but the risks and benefits of

by the GUSTO

(ICH). and 30-day mortality were evaluated inhibitors within the first 24 hours.

fibrinolytic

12:24

14. In-TIME-2. SPEED, FASTER, and INTEGRITI). Patients (n = 3,342) treated with fulldose fibrinolytic therapy who then underwent early PCI within 24 hours were included. The risks of moderate/severe

Since the reduced

therapy

enhancement

sion as shown by the ST-segment resolution, without excess in encountered complications.

Murphy,

NC, TIMI Study Group,

inhibitors infarctton

been well-characterized. Methods: We performed

complications.

plicatlons in the facilitated group. (14% vs. 13%, p=n.s.). Conclusion: The prehospital combined thrombolytic therapy

Background: Glycoprotein (GP) llbillla primary PCI for ST-elevation myocardial dunng

has been shown to achieve a 50% TIMI-3and PTCA have failed to show a mortality

(772 56% vs. 58+ 47%. p=O.O4). Infarct size measured

ondary combined

MA

inhibitors

by

900* 817 in the COMBO only versus 847t 482 pmol/l/h in the facilitated PCI-group (~~0.07) and 1 I+ 8% versus 7+ 8% in the delayed enhancement MRI (p=O.16). The sec-

p.m.

Robert A. Harrington,

Institute,

determined

(p=n.s.). In the facilitated PC&group TIMI-3-flow before intervention was 65% and after 98%, respectively. 90-min ST-segment resolution was mere complete in the facilitated

Kenneth W. Mahaffey, Christopher P. Cannon, A. Michael Lincoff. C. Michael Gibson, Paul W. Armstrong, Frans J. van de Wed, Robert M. Califf, Eric J. Topol, Eugene Braunwald,

is mainly

uation.

1025MP-165 Ohman.

(AMI)

a composite of mortality, reAMI, major bleeding and stroke. Results: Mean time from symptom onset to arrival of the emergency

Safety of Adjunctive Glycoprotein llblllla Blockade During Rescue/Early Percutaneous Coronary Intervention Following Full-Dose Fibrinolytic Therapy for Acute Myocardial Infarction E. Magnus

infarction

flow in the infarct related artery. However,

therapy in combination with a platelet glycoprotein llblllla inhibitor (COMBO) has recently shown to reduce the rate of AMI related complications, ‘“facilitated” PCI needs new eval-

and these results show that “facilitated”

Elliott M. Antman,

Schuler,

ated COMBO therapy with immediate in-hospital “facilitated’ PCl+stent (n=62). Primary endpoints were ST-segment resolution at 90 min., infarct size expressed as area under

SESSION

Robed Tuttle,

Starch, Kazem Rahimi,

Kappl, Gerhard

Methods: Since 12/2000 120 patients with an AMI were randomized in Leipzig, Germany within 6 hours after symptom onset to either a prehospital COMBO (half dose

1025MP Moderated Poster Session...Controversies in Adjunctive Therapy for Acute ST Elevation Myocardial Infarction

T. Roe, Robert P. Giugliano,

Mathias

Germany

reperfusion therapy for AMI with thrombolysis flow only. Early trials combining thrombolysis

the curve of CK-release

1025MP-163

Elsner, Wulf-Hinrich

Enno Boudriot,

- Heart Center,

Prognosis

early repelfusion

Reteplase POSTER

Prehospital

is mea-

Michael

p.m.

in ThrombolyticlAbciximab Therapy Comparison to Facilitated Percutaneous Coronary Intervention After Combined Prehospital Thrombolysis in Acute Myocardial Infarction

1025MP-164

(n=lO) implantation. n=lO). Rats with EF

study were done by HE and PTAH stain.

(0.706*0.150 also reduced

PValue

angiogen-

sured by computer-assistant planimetry as indices of myccardial remodeling 0 weeks after implatation. The diameter of myocytes in the p&infarct zcne were also measured.

Matthew

95% Cl

Conclusions: In this post-hoc, non-randomized analysis, the use of GP Ilb/llla inhibitors during rescue/early PCI following full-dose fibrinolytic therapy was associated with a higher rate of non-ICH bleeding complications. Prospective, randomized clinical trials are therefore needed to delineate the risks and benefits of this treatment strategy.

esis and regenerate cardiomyocytes in rat ischemic heart model. This study is designed to test the effectiveness of MSCs implantation to reverse myocardial remodeling.

tion.

No GP Ilb/ llla

1.15

of China

Background The remodeling

ligation Control

GP Ilbl llla

Implantation

1024-116

People’s

March 19,2003

(n=200).

The stent used was the Carbostant

(Sorin.

Italy). There

were no

exclusion criteria except for a reference Infarct artery diameter < 2.5 mm. endpoint of the study was the 1 -month composite incidence of death, reinf-

repeat target vessel revascularization

(TVR), and stroke (MACCE).

Results: Mean age 63.7 f 12.7; ) 70 yrs 36%; female 23%; diabetes 17%; anterior AMI 43%; cardiogenic shock 9%; not-low-risk patients (TIMI criteria) 66%; median time from