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Neutrophil/Lymphocyte (N/L) Ratio and Long Term Follow-up in ST-elevation Myocardial Infarction

T

TC Erciyes University

Status

Completed

Conditions

ST Elevated Myocardial Infarction

Treatments

Procedure: primary percutaneous coronary intervention, each groups

Study type

Observational

Funder types

Other

Identifiers

NCT01663194
mgkaya-makpek

Details and patient eligibility

About

Although the pre-procedural neutrophil to lymphocyte ratio (N/L) has been associated with adverse outcomes among patients with coronary artery disease, its role during the acute phase of ST-segment elevation myocardial infarction (STEMI) has not been fully investigated. This study sought to investigate the association of the pre-procedural N/L ratio within-hospital and long-term outcomes among STEMI patients undergoing primary percutaneous coronary intervention (PCI).

Full description

Inflammation plays a role in the initiation and progression of the atherosclerotic process. Due to a growing recognition of its role, recent studies have focused on inflammatory markers and their association with outcomes in patients with ST-segment elevation myocardial infarction (STEMI). Recently, our single center study demonstrated that preprocedural neutrophil/lymphocyte (N/L) ratio is an independent predictor of impaired coronary flow after primary percutaneous coronary intervention (PCI) and of in-hospital major advanced cardiac events (MACE) in patients with STEMI.Several previous studies also evaluated the role of N/L ratio in long-term outcomes among patients with STEMI; however, they evaluated the association between long-term mortality and in-hospital N/L ratio, they were single-center studies and they evaluated a relatively small study population.

In the present multicenter experience, the investigators aimed to investigate the association of the preprocedural N/L ratio with the in-hospital and long-term outcomes in patients with STEMI undergoing primary PCI.

Enrollment

1,034 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

ST elevated myocardial infarction

Exclusion criteria

Treatment with fibrinolytic drugs in the previous 24 hours Active infection Previously documented history of a systemic inflammatory process Known malignancy End-stage liver disease Renal failure

Trial design

1,034 participants in 3 patient groups

N/L ratio tertile 2
Description:
patients were divided in to the tertiles
Treatment:
Procedure: primary percutaneous coronary intervention, each groups
N/L ratio tertile 3
Description:
patients were divided in to the tertiles
Treatment:
Procedure: primary percutaneous coronary intervention, each groups
N/L ratio tertile 1
Description:
patients were divided in to the tertiles
Treatment:
Procedure: primary percutaneous coronary intervention, each groups

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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