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Initial United States experience with the Paracor HeartNet myocardial constraint device for heart failure.

Publication ,  Journal Article
Klodell, CT; McGiffin, DC; Rayburn, BK; Sun, B; Abraham, WT; Conte, JV; Russell, SD; Pae, WE; Boehmer, JP; Aranda, JM
Published in: J Thorac Cardiovasc Surg
January 2007

OBJECTIVE: This study was undertaken to review the initial results and surgical safety data for the US Food and Drug Administration safety and feasibility trial of the Paracor HeartNet (Paracor Medical, Inc, Sunnyvale, Calif.) myocardial constraint device. METHODS: Patients with New York Heart Association functional class II or III heart failure underwent device implantation (n = 21) through a left minithoracotomy. RESULTS: The average age was 53 years (31-72 years). There were 18 men and 3 women, and 17 patients had nonischemic etiology of heart failure. Mean heart failure duration was 8.3 years (1.4-18.8 years). Average ejection fraction was 22% (11%-33%), with an average left ventricular end-diastolic dimension of 74 mm (55-94 mm). Previous medical therapy included angiotensin-converting enzyme inhibitors, beta-blockers, diuretics, digoxin, and aldosterone receptor blockers. At implantation, 17 patients had implantable electronic devices: 1 biventricular pacemaker, 11 biventricular pacemakers with cardioverter-defibrillators, and 5 implantable cardioverter-defibrillators. Patient comorbidities included hypertension in 10 cases, diabetes mellitus in 8, myocardial infarction in 1, and ventricular tachycardia in 8. Mean operative time was 68 minutes (42-102 minutes), and implantation time averaged 15 minutes (5-51 minutes). The average time to ambulation was 1.6 days (1-4 days). The intensive care unit stay averaged 3.3 days (1-16 days), and hospital stay averaged 6.3 days (4-16 days). Atrial fibrillation occurred in 2 patients, and there were 2 in-hospital deaths. CONCLUSIONS: The Paracor device can be implanted in patients with heart failure and reduced left ventricular function with a high degree of success. Significant surgical complications were infrequent. The initial US experience supports the conduct of a randomized, controlled, pivotal trial.

Duke Scholars

Published In

J Thorac Cardiovasc Surg

DOI

EISSN

1097-685X

Publication Date

January 2007

Volume

133

Issue

1

Start / End Page

204 / 209

Location

United States

Related Subject Headings

  • Ultrasonography
  • Respiratory System
  • Postoperative Complications
  • Pacemaker, Artificial
  • Middle Aged
  • Male
  • Humans
  • Heart Failure
  • Female
  • Defibrillators, Implantable
 

Citation

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ICMJE
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Klodell, C. T., McGiffin, D. C., Rayburn, B. K., Sun, B., Abraham, W. T., Conte, J. V., … Aranda, J. M. (2007). Initial United States experience with the Paracor HeartNet myocardial constraint device for heart failure. J Thorac Cardiovasc Surg, 133(1), 204–209. https://doi.org/10.1016/j.jtcvs.2006.08.070
Klodell, Charles T., David C. McGiffin, Barry K. Rayburn, Benjamin Sun, William T. Abraham, John V. Conte, Stuart D. Russell, Walter E. Pae, John P. Boehmer, and Juan M. Aranda. “Initial United States experience with the Paracor HeartNet myocardial constraint device for heart failure.J Thorac Cardiovasc Surg 133, no. 1 (January 2007): 204–9. https://doi.org/10.1016/j.jtcvs.2006.08.070.
Klodell CT, McGiffin DC, Rayburn BK, Sun B, Abraham WT, Conte JV, et al. Initial United States experience with the Paracor HeartNet myocardial constraint device for heart failure. J Thorac Cardiovasc Surg. 2007 Jan;133(1):204–9.
Klodell, Charles T., et al. “Initial United States experience with the Paracor HeartNet myocardial constraint device for heart failure.J Thorac Cardiovasc Surg, vol. 133, no. 1, Jan. 2007, pp. 204–09. Pubmed, doi:10.1016/j.jtcvs.2006.08.070.
Klodell CT, McGiffin DC, Rayburn BK, Sun B, Abraham WT, Conte JV, Russell SD, Pae WE, Boehmer JP, Aranda JM. Initial United States experience with the Paracor HeartNet myocardial constraint device for heart failure. J Thorac Cardiovasc Surg. 2007 Jan;133(1):204–209.
Journal cover image

Published In

J Thorac Cardiovasc Surg

DOI

EISSN

1097-685X

Publication Date

January 2007

Volume

133

Issue

1

Start / End Page

204 / 209

Location

United States

Related Subject Headings

  • Ultrasonography
  • Respiratory System
  • Postoperative Complications
  • Pacemaker, Artificial
  • Middle Aged
  • Male
  • Humans
  • Heart Failure
  • Female
  • Defibrillators, Implantable