Literature DB >> 15631529

Perioperative pharmacotherapy in patients with left ventricular assist devices.

Nicholas C Dang1, Yoshifumi Naka.   

Abstract

Heart failure remains the leading cause of death in Western countries, affecting 4.9 million individuals and causing >300 000 deaths annually in the US alone. The disease is highly prevalent in the elderly population and often follows a course of progressive disability and deterioration. An estimated 15 000 patients with end-stage heart failure could benefit from heart transplant each year. Yet, as a result of a significant shortage of donor organs, only 2500 hearts are donated annually, and approximately one-third of patients awaiting heart transplant die each year. Mechanical circulatory support, primarily in the form of left ventricular assist devices (LVADs), has come to the forefront of treatment for severe congestive heart failure by providing a feasible alternative to patients who might otherwise die awaiting heart transplant. The arrival of LVADs has resulted in a dramatic shift in the management of heart failure, one that will undoubtedly affect and include a vast proportion of elderly patients. While LVADs represent a surgical approach to a disease that has traditionally been managed medically, the pharmacological application throughout the perioperative period remains of critical importance. Five primary classes of drugs bear specific application to the LVAD population: (i) drugs that provide haemodynamic support; (ii) antimicrobials; (iii) anticoagulants and antiplatelets; (iv) agents that promote myocardial recovery; and (v) miscellaneous other medications. Drugs that provide haemodynamic support are subdivided into inotropes, vasopressors and pulmonary vasodilators. Some combination of these medications is usually administered within the perioperative period in order to maintain stable patient haemodynamics and assure proper LVAD function. Antimicrobials are of paramount importance in the pre-, intra- and postoperative periods to minimise the risk of infection, an unfortunately common complication of LVAD therapy that can have potentially morbid consequences. Anticoagulants and antiplatelet medications are necessary for certain types of LVADs and serve to curb the incidence of device thrombus formation and associated embolic phenomena. Pharmacotherapeutic agents that facilitate myocardial recovery are being investigated as adjuncts to LVAD support so that bridge to recovery can become a realistic outcome for a growing number of LVAD patients. The miscellaneous class of medications used with LVADs includes those that minimise the risk of bleeding in select patients and those that enhance proper vitamin and nutrient status in the postoperative period, the attainment of which may serve vital to a successful recovery.

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Year:  2004        PMID: 15631529     DOI: 10.2165/00002512-200421150-00003

Source DB:  PubMed          Journal:  Drugs Aging        ISSN: 1170-229X            Impact factor:   4.271


  128 in total

Review 1.  Use of inhaled nitric oxide perioperatively and in intensive care patients.

Authors:  E Haddad; S M Lowson; R A Johns; G F Rich
Journal:  Anesthesiology       Date:  2000-06       Impact factor: 7.892

2.  Long-term use of a left ventricular assist device for end-stage heart failure.

Authors:  E A Rose; A C Gelijns; A J Moskowitz; D F Heitjan; L W Stevenson; W Dembitsky; J W Long; D D Ascheim; A R Tierney; R G Levitan; J T Watson; P Meier; N S Ronan; P A Shapiro; R M Lazar; L W Miller; L Gupta; O H Frazier; P Desvigne-Nickens; M C Oz; V L Poirier
Journal:  N Engl J Med       Date:  2001-11-15       Impact factor: 91.245

Review 3.  Use of vasopressor agents in critically ill patients.

Authors:  John A Kellum; Michael R Pinsky
Journal:  Curr Opin Crit Care       Date:  2002-06       Impact factor: 3.687

4.  Effect of prostaglandin E1 infusion in severe chronic heart failure.

Authors:  R Pacher; B Stanek; M Hülsmann; H Sinzinger
Journal:  Prostaglandins       Date:  1997-04

Review 5.  Vasopressin: new uses in critical care.

Authors:  Peter Chen
Journal:  Am J Med Sci       Date:  2002-09       Impact factor: 2.378

6.  Management of vasodilatory shock after cardiac surgery: identification of predisposing factors and use of a novel pressor agent.

Authors:  M Argenziano; J M Chen; A F Choudhri; S Cullinane; E Garfein; A D Weinberg; C R Smith; E A Rose; D W Landry; M C Oz
Journal:  J Thorac Cardiovasc Surg       Date:  1998-12       Impact factor: 5.209

Review 7.  Pathogenesis and management of acute heart failure and cardiogenic shock: role of inotropic therapy.

Authors:  A I McGhie; R A Golstein
Journal:  Chest       Date:  1992-11       Impact factor: 9.410

Review 8.  Bridge to recovery with the use of left ventricular assist device and clenbuterol.

Authors:  Jimmy K F Hon; Magdi H Yacoub
Journal:  Ann Thorac Surg       Date:  2003-06       Impact factor: 4.330

Review 9.  Interactions between the recipient immune system and the left ventricular assist device surface: immunological and clinical implications.

Authors:  Silviu Itescu; Ranjit John
Journal:  Ann Thorac Surg       Date:  2003-06       Impact factor: 4.330

10.  Artificial circulatory support with textured interior surfaces. A counterintuitive approach to minimizing thromboembolism.

Authors:  E A Rose; H R Levin; M C Oz; O H Frazier; Q Macmanus; N A Burton; E A Lefrak
Journal:  Circulation       Date:  1994-11       Impact factor: 29.690

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  2 in total

Review 1.  Clinical pharmacology considerations for children supported with ventricular assist devices.

Authors:  Jennifer Sherwin; Elizabeth Thompson; Kevin D Hill; Kevin Watt; Andrew J Lodge; Daniel Gonzalez; Christoph P Hornik
Journal:  Cardiol Young       Date:  2018-07-11       Impact factor: 1.093

2.  Left ventricular assist device implantation in high risk destination therapy patients: an alternative surgical approach.

Authors:  Louis E Samuels; Elena Casanova-Ghosh; Roberto Rodriguez; Christopher Droogan
Journal:  J Cardiothorac Surg       Date:  2012-03-12       Impact factor: 1.637

  2 in total

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