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Hypertension is the leading modifiable risk factor for global cardiovascular disease, responsible for an estimated 10.8 million deaths and more than 200 million disability-adjusted life years annually.1 Despite the availability of effective pharmacological and lifestyle interventions, prevalence continues to rise, particularly in low- and middle-income countries (LMICs), where over three-quarters of all cases now occur.2 The condition’s […]

Pressure ulcer: an unreported complication of the Safeguard® hemostasis device. No need to crack under pressure

Claudio Moretti, Giorgio Quadri, Fiorenzo Gaita, Imad Sheiban
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Published Online: Aug 3rd 2018 Heart International 2011;6(1):e3 DOI: https://doi.org/10.4081/hi.2011.e3
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1

Abstract

Overview

Diagnostic cardiac catheterizations are predominantly
performed using the femoral
artery access. Several devices have been
developed to aid in the closure of femoral arteriotomy.
Safeguard® is a new pneumatic compression
device that has been developed for compression
of the femoral artery after brief manual
compression. We hereby report the case of
an elderly patient who underwent a percutaneous
coronary intervention via the femoral
artery in whom a Safeguard™ device, left
overnight because of persistent oozing, provoked
an extensive pressure ulcer. Knowledge
of this potential complication is important to
minimize its occurance and provide appropriate
treatment.

Keywords

Cardiac catheterization, closure vascular access, femoral closure device, vascular access complication.

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Article Information

Correspondence

Claudio Moretti, Division of Cardiology, University of Turin, San Giovanni Battista “Molinette” Hospital, Corso Bramante 88–90, 10126 Turin, Italy. Tel. +39.011.6334195 – Fax: +39.011.6967053. E-mail: drclamore@yahoo.it

Received

2011-05-07

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