A high-risk patient with long-QT syndrome with no response to cardioselective beta-blockers

Heart Vessels. 2015 Sep;30(5):687-91. doi: 10.1007/s00380-014-0530-7. Epub 2014 Jun 11.

Abstract

We present a case of a high-risk 19-year-old female with long-QT syndrome (LQTS) with compound mutations. She had a history of aborted cardiac arrest and syncope and had received treatment with propranolol for 15 years. However, because she developed adult-onset asthma we tried to switch propranolol, a nonselective beta-blocker, to beta-1-cardioselective agents, bisoprolol and metoprolol. These resulted in both a markedly prolonged corrected QT interval and the development of LQTS-associated arrhythmias. Eventually, propranolol was reinitiated at a higher dose with the addition of verapamil, and she has had no further cardiac or asthmatic events for 5 years.

Keywords: Beta-1 selective blocker; Beta-blocker; High-risk patient; Long-QT syndrome; Nonselective beta-blocker.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Antagonists / therapeutic use*
  • Drug Tolerance*
  • Electrocardiography*
  • Female
  • Humans
  • Long QT Syndrome / drug therapy*
  • Long QT Syndrome / physiopathology
  • Young Adult

Substances

  • Adrenergic beta-Antagonists