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Cardio- and reno-protective effect of remote
ischemic preconditioning in patients undergoing
percutaneous coronary intervention. A prospective,
non-randomized controlled trial

Research Authors
Ayman K.M. Hassan, Hamdy Shams-Eddin, Mona H.M. Abdel-Rahim,
Heba A. Abd El-Hafeez, Sadat Edroos
Research Department
Research Journal
The Egyptian Heart Journal
Research Member
Research Publisher
Elsevier
Research Rank
2
Research Vol
67
Research Website
NULL
Research Year
2015
Research_Pages
315–323
Research Abstract

Abstract Objectives: This study assessed the cardio- and renoprotective effect of remote ischemic
Preconditioning (PreC) in patients undergoing percutaneous coronary intervention (PCI).
Background: Myocyte necrosis and contrast induced nephropathy (CIN) occur frequently in PCI
and are associated with subsequent cardiovascular events. Methods: Two hundred consecutive
patients undergoing elective PCI with normal baseline troponin-I (cTnI) values were recruited.
Subjects were systematically allocated into 2 groups: 100 patients received PreC (created by three
5 min inflations of a blood pressure cuff to 200 mmHg around the upper arm, separated by
5 min intervals of reperfusion) <2 h before the PCI procedure, and control group (n= 100).
Results: The incidence of PCI-related myocardial infarction (MI 4a) at 24 h after PCI was lower in
the PreC group compared with control group (41% vs 64%, P =0.02). Subjects who received PreC
had significant trend toward lower incidence of CIN at 72 h after contrast exposure (4 vs. 11,
P = 0.05) and less chest pain during stent implantation compared to control group. At 3 months,
the major adverse event rate was lower in the PreC group (6 vs. 14 events; P =0.04).
Conclusions: The use of PreC < 2 h before PCI, reduces the incidence of PCI-related MI 4a, tends
to decrease the incidence of CIN and improves ischemic symptoms in patients undergoing elective
PCI. The observed cardio- and renoprotection appears to confer sustained benefit on reduced major adverse events at 3 month follow-up beyond what is seen with judicious pre- and post-hydration
(ClinicalTrials.gov identifier: NCT02313441).