1. A Systematic Review on the Role of Βeta-Blockers in Reducing Cardiac Arrhythmias in Long QT Syndrome Subtypes 1-3
- Author
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Hajra Khurshid, Waleed Sultan, Israa A Qureshi, Michael Alfonso, Anjli Tara, Alisha Sapkota, Sheila W Ruo, Myat Win, Terry R Went, Dwayne A Wiltshire, Nasrin Jahan, and Amudhan Kannan
- Subjects
medicine.medical_specialty ,congenital, hereditary, and neonatal diseases and abnormalities ,medicine.drug_class ,Long QT syndrome ,Population ,Cardiology ,arrhythmia ,QT interval ,sudden cardiac death ,Sudden cardiac death ,Nadolol ,Internal medicine ,medicine ,Internal Medicine ,nadolol ,cardiovascular diseases ,long qt syndrome ,education ,Beta blocker ,education.field_of_study ,business.industry ,General Engineering ,propanolol ,medicine.disease ,atenolol ,beta blocker ,Systematic review ,business ,Cohort study ,medicine.drug - Abstract
Long QT syndrome (LQTS) is one of the most common inherited cardiac channelopathies with a prevalence of 1:2000. The condition can be congenital or acquired with 15 recognized genotypes; the most common subtypes are LQTS 1, 2, and 3 making up to 85%-90% of the cases. LQTS is characterized by delayed ventricular cardiomyocyte repolarization manifesting on the surface electrocardiogram (EKG) by a prolonged corrected QT (QTc) interval. The mainstay of treatment for this condition involves in part or combination medical therapy via β-blockers as first-line (or other anti-arrhythmic), left cardiac sympathectomy, or implantable cardiac defibrillator placement. Given the high rate of adverse cardiac events (ACE) or sudden cardiac death (SCD) in this population of patients with this disease, this review seeks to highlight the genotype-specific treatment consensus in β-blocker therapy of the most common subtypes. A database search of PubMed, PMC, and Medline was conducted to ascertain the most recent data in the last five years on the management of LQTS types 1-3 and the role of β-blockers in reducing ACE in these types. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines were adhered to in the study selection, and selected studies focused on humans, written in the English Language, and within the last five years of LQTS subtypes 1, 2, and 3. Eleven relevant studies were selected after considering inclusion criteria, exclusion criteria, and quality appraisal within the last five years, focusing on β-blocker selection directed based on the subtypes of LQTS. Two meta-analyses, one cohort study, and eight reviews provided significant data that non-selective β-blockers unequivocally are of benefit in these LQTS types. Summary of findings suggested nadolol followed by propranolol yields the best results in LQTS 1, while nadolol would yield the best effect in LQTS 2 and 3.
- Published
- 2021