Invasive Cardiology

Increased Vascular Access Complications in Patients with Renal Dysfunction Undergoing Percutaneous Coronary Procedures Using Arteriotomy Closure Devices

Authors: Emad F. Aziz, MB, ChB, DOa, Sandeep Pulimi, MDa, Clinton Coleman, MDb, Calatin Florita, MDc, Dan Musat, MDa, Deborah Tormey, RNa, Ashraf Fawzy, BSa, Steve Lee, BSa, Eyal Herzog, MDa, David L. Coven, MDa, Jacqueline Tamis-Holland, MDa, Mun K. Hong, MDa

ABSTRACT: Background. Arteriotomy closure device (ACD) use has increased following percutaneous transfemoral coronary procedures (PTCP). However, their safety in patients with chronic kidney disease (CKD) is not known. Therefore, we evaluated the complication rates of ACD among patients with CKD. Methods. Six-hundred ten consecutive patients who underwent PTCP and ACD were retrospectively studied. Patients were grouped according to their creatinine clearance (CrCl in ml/min/1.73 m2) calculated by the Cockcroft-Gault formula using the National Kidney Foundation classification system; Stage I (CrCl ≥ 90); Stage II (60–89); Stage III (30–59); Stage IV (15–29); and Stage V (≤ 15). The primary endpoint was the combined incidence of pseudo-aneurysm, retroperitoneal hematoma, femoral artery thrombosis, surgical vascular repair, and groin infection. Results. Among 610 patients 283 (46%) underwent PCI. The primary endpoint was seen in 66 (10.8%) patients. Univariate predictors of primary outcome were lower CrCl (p < 0.001), and presence of peripheral vascular disease (p = 0.03). There was an inverse relationship between CrCl and complication rate. CKD was the strongest independent multivariate predictor for the primary endpoint (OR 1.032; 95% CI 1.019–1.046; p < 0.0001), driven by higher infection (p < 0.0001), thrombosis (p = 0.003) and hematoma (p = 0.007). Conclusions. Renal function appears to be significantly associated with vascular access-site complications. Worsening renal function is associated with higher vascular access site complications, largely driven by an increased infection rate.


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