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No Reflow Phenomenon Incidence and Predictors

2019-07-17 10:04:58 | BioPortfolio

Summary

Background No reflow phenomenon is described in up to 65% of patients undergoing primary percutaneous coronary intervention for ST elevation myocardial infarction (STEMI). It is known to be associated with worse outcomes but predictors of no reflow are not clearly described.

Objectives A single centre case-control observational study of patients presenting with acute myocardial infarction appropriate for PPCI comparing baseline clinical, biochemical and angiographic characteristics between patients with no reflow phenomenon and those without. Aiming to establish incidence for the UK population.

Secondary outcomes will be to gain further insight into those presenting with STEMI for PPCI and develop a risk model to guide management and clinical outcomes of patients to 30days.

Methods This study will prospectively recruit all consecutive patients attending a single centre for primary percutaneous coronary intervention for STEMI. Angiographic assessment of the recanalised epicardial vessel will be used to diagnose no reflow (reduced TIMI flow or blush grade). Baseline demographic, angiographic and biochemical characteristics and outcomes at 30days for reflow and no reflow cohorts will be statistically assessed and compared with logistic regression.

Study Design

Conditions

No Reflow Phenomenon

Intervention

No intervention as observational study

Location

Castle Hill Hospital (Hull and east Yorkshire Hospitals NHS Trust)
Cottingham
East Yorkshire
United Kingdom
HU16 5JQ

Status

Completed

Source

Hull and East Yorkshire Hospitals NHS Trust

Results (where available)

View Results

Links

Published on BioPortfolio: 2019-07-17T10:04:58-0400

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Medical and Biotech [MESH] Definitions

Markedly reduced or absent REPERFUSION in an infarct zone following the removal of an obstruction or constriction of an artery.

A work that reports on the results of a clinical study in which participants may receive diagnostic, therapeutic, or other types of interventions, but the investigator does not assign participants to specific interventions (as in an interventional study).

A study in which observations are made before and after an intervention, both in a group that receives the intervention and in a control group that does not.

A study that uses observations at multiple time points before and after an intervention (the "interruption"), in an attempt to detect whether the intervention has had an effect significantly greater than any underlying trend over time.

A study that compares a group of participants receiving an intervention with a similar group from the past who did not.

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