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Volume 24, Issue 1, Pages 30-36 (February 2010)


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Outcome After Implantation of Cardiac Resynchronization/Defibrillation Systems in Patients With Congestive Heart Failure and Left Bundle-Branch Block

Giselher Pfau, MD, Thomas Schilling, MD, DEAACorresponding Author Informationemail address, Alf Kozian, MD, Anke Lux, MSc, A. Götte, MD, Christof Huth, MD§, Thomas Hachenberg, MD, PhD

published online 05 October 2009.

Objective

The implantation of cardiac resynchronization/defibrillation devices (CRT-Ds) increasingly is used in patients with congestive heart failure and left bundle-branch block. There are no data on the effects of anesthesia and surgery on outcome after implantation.

Design

A retrospective, observational study; postoperative survey.

Setting

University hospital.

Participants

Three hundred forty-one patients (258 men/83 women, 63 ± 9 years) with congestive heart failure and left bundle-branch block who underwent CRT-D implantation in 1996 to 2005.

Measurements and Main Results

Perioperative data were retrieved from the patients' records. Cardiologists caring for the patients were contacted to obtain information on current New York Heart Association (NYHA) status and mortality after CRT-D implantation. Preoperatively, 45 patients were classified as NYHA II, 246 as NYHA III, and 50 as NYHA IV. CRT was performed via thoracotomy in 100 and transvenously in 241 cases. General anesthesia (propofol or sevoflurane and remifentanil) was performed in 273 and local anesthesia (lidocaine) in 68 patients. Hypotension occurred mainly during general anesthesia (43% v 4%). The 30-day mortality was 0%. The postoperative survey started in 2006 and was completed by 215 patients. The mean survival time was 77 months; 151 patients survived the study period. Outcome was not influenced by local and general anesthesia. Presence of preoperative NYHA class >II (odds ratio [OR] = 1.6, confidence interval [CI] = 0.5-5.1), mitral regurgitation (OR = 2.5, CI = 1.2-5.5), and serum creatinine >1.1 mg/dL (OR = 3.0, CI = 1.5-6.2) resulted in an inferior prognosis.

Conclusions

In patients with severely impaired cardiac function, general anesthesia for the implantation of a biventricular pacing device can be used with justifiable risk. The method of anesthesia did not influence outcome.

 Department of Anesthesiology and Intensive Care Medicine, Otto-von-Guericke University, Magdeburg, Germany

 Department of Biometrics, Institute for Biometry and Medical Informatics, Otto-von-Guericke University, Magdeburg, Germany

 Department of Cardiology, Angiology and Pneumology, Otto-von-Guericke University, Magdeburg, Germany

§ Department of Cardiovascular and Thoracic Surgery, Otto-von-Guericke University, Magdeburg, Germany

Corresponding Author InformationAddress reprint requests to Thomas Schilling, MD, DEAA, Department of Anesthesiology and Intensive Care Medicine, Otto-von-Guericke University, Leipziger Str 44, D-39120 Magdeburg, Germany

PII: S1053-0770(09)00287-0

doi:10.1053/j.jvca.2009.07.009


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