Vascular complications associated with arteriotomy closure devices in patients undergoing percutaneous coronary procedures
A meta-analysis
Eugenia Nikolsky, MD, PhD*,
Roxana Mehran, MD, FACC*,
Amir Halkin, MD*,
Eve D. Aymong, MD, FACC*,
Gary S. Mintz, MD, FACC*,
Zoran Lasic, MD, FACC*,
Manuela Negoita, MD*,
Martin Fahy, MSc*,
Shoshana Krieger, BA*,
Issam Moussa, MD, FACC*,
Jeffrey W. Moses, MD, FACC*,
Gregg W. Stone, MD, FACC*,
Martin B. Leon, MD, FACC*,
Stuart J. Pocock, PhD and
George Dangas, MD, PhD, FACC*,*
* Cardiovascular Research Foundation and the Lenox Hill Heart and Vascular Institute, New York, New York, USA
London School of Hygiene and Tropical Medicine, London, United Kingdom

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Figure 1 Odds ratio (OR) and 95% confidence interval (CI) of vascular access-related complication rate in patients with Angio-Seal and mechanical compression (control) in diagnostic (Dx), percutaneous coronary intervention (PCI), mixed (Dx+PCI), or any setting. RCT = randomized controlled trials. *Fixed effects model; random effects model.
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Figure 2 Odds ratio (OR) and 95% confidence interval (CI) of vascular access-related complication rate in patients with VasoSeal and mechanical compression (control) in diagnostic (Dx), percutaneous coronary intervention (PCI), mixed, or any setting. *Fixed effects model. RCT = randomized controlled trials.
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Figure 3 Odds ratio (OR) and 95% confidence interval (CI) of vascular access-related complication rate in patients with Perclose and mechanical compression (control) in diagnostic (Dx), percutaneous coronary intervention (PCI), mixed, or any setting. *Fixed effects model; random effects model. RCT = randomized controlled trials.
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Figure 4 Odds ratio (OR) and 95% confidence interval (CI) of vascular access-related complication rate in patients with any arteriotomy closure device (ACD) and mechanical compression (control) in diagnostic (Dx), percutaneous coronary intervention (PCI), mixed, or any setting. Diamonds = all studies; squares = randomized studies.
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