Evidence map›Paper›PMID 19441867›Full record

ReviewDrugs2009

Novel approaches for pharmacological management of atrial fibrillation.

Joachim R Ehrlich, Stanley Nattel

Abstract readReview
PubMed Publisher
In one paragraph

Review in Drugs, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
6.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 74 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 3 countries.

Joachim R EhrlichDivision of Cardiology, Goethe-University, Frankfurt, Germany. j.ehrlich@em.uni-frankfurt.de
Stanley Nattel
Goethe Institute · GBMcGill University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the light of the progressively increasing prevalence of atrial fibrillation (AF), medical awareness of the need to develop improved therapeutic approaches for the arrhythmia has also risen over the last decade. AF reduces quality of life and is associated with increased morbidity and mortality. Despite several setbacks as a result of negative results from rhythm control trials, the potential advantages of sinus-rhythm (SR) maintenance have motivated continued efforts to design novel pharmacological options aiming to terminate AF and prevent its recurrence, with a hope that optimized medical therapy will improve outcomes in AF patients. Pathophysiologically, AF is associated with electrical and structural changes in the atria, which increase the propensity to arrhythmia perpetuation but may eventually allow for new modalities for therapeutic intervention. Antiarrhythmic drug therapy has traditionally targeted ionic currents that modulate excitability and/or repolarization of cardiac myocytes. Despite efficacious suppression of ventricular and supraventricular arrhythmias, traditional antiarrhythmic drugs present problematic risks of pro-arrhythmia, potentially leading to excess mortality in the case of Na+-channel blockers or IKr (IKr=the rapid component of the delayed rectifier potassium current) blockers. New anti-AF agents in development do not fit well into the classical Singh and Vaughan-Williams formulation, and are broadly divided into 'atrial-selective compounds' and 'multiple-channel blockers'. The prototypic multiple-channel blocker amiodarone is the most efficient presently available compound for SR maintenance, but the drug has extra-cardiac adverse effects and complex pharmacokinetics that limit widespread application. The other available drugs are not nearly as efficient for SR maintenance and have a greater risk of proarrhythmia than amiodarone. Two new antiarrhythmic drugs are on the cusp of introduction into clinical practice. Vernakalant affects several atrially expressed ion channels and has rapid unbinding Na+-channel blocking action along with promising efficacy for AF conversion to SR. Dronedarone is an amiodarone derivative with an electrophysiological profile similar to its predecessor but lacking most amiodarone-associated adverse effects. Furthermore, dronedarone has shown benefits for important clinical endpoints, including cardiovascular mortality in specific AF populations, the first AF-suppressing drug to do so in prospective randomized clinical trials. Agents that modulate non-ionic current targets (termed 'upstream' therapies) may help to modify the substrate for AF maintenance. Among these, drugs such as angiotensin II type 1 (AT1) receptor antagonists, immunosuppressive agents or HMG-CoA reductase inhibitors (statins) deserve mention. Finally, drugs that block atrial-selective ion-channel targets such as the ultra-rapid delayed rectifier current (IKur) and the acetylcholine-regulated K+-current (IKACh) are presently in development. The introduction of novel antiarrhythmic agents for the management of AF may eventually improve patient outcomes. The potential value of a variety of other novel therapeutic options is currently under active investigation.

Indexed as

Drug Delivery SystemsAnimalsAnti-Arrhythmia AgentsAtrial FibrillationClinical Trials as TopicHumansTreatment OutcomeAnti-Arrhythmia Agents

Identifiers

PMID19441867
OpenAlexW2034943103

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.