The EJHF last Editor's legacy: how can a high impact factor be built?

Marco Metra1

  • 1Cardiology, Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.

ESC Heart Failure
|August 24, 2017
PubMed

Insights

The European Journal of Heart Failure (EJHF) achieved a high impact factor due to impactful publications, including European Society of Cardiology guidelines. Key topics driving citations include heart failure with preserved ejection fraction and advanced heart failure.

Area of Science:

  • Cardiology
  • Bibliometrics
  • Scientific Publishing

Background:

  • The European Journal of Heart Failure (EJHF) has achieved a significant impact factor, positioning it as a leading cardiology publication.
  • This analysis explores the factors contributing to EJHF's high journal ranking and citation rates.

Discussion:

  • The publication of European Society of Cardiology guidelines for acute and chronic heart failure significantly boosted EJHF's citations.
  • Other influential content includes position statements, reviews, and research on landmark topics in heart failure.
  • Articles focusing on heart failure with preserved ejection fraction and advanced heart failure have garnered substantial attention and citations.

Key Insights:

  • Epidemiology, biomarkers, medical treatments, and devices are prominent areas of interest within EJHF.
  • The journal's success is linked to its ability to publish influential, highly cited content, particularly clinical guidelines.
  • High citation rates correlate with publications addressing specific clinical presentations like heart failure with preserved ejection fraction and advanced heart failure.

Outlook:

  • Sustaining a high impact factor requires anticipating and publishing emerging important research.
  • EJHF's success provides a model for other journals aiming to enhance their influence and impact.
  • Future challenges involve continued innovation in content strategy to maintain leadership in cardiology publishing.

Related Concept Videos

Hydrogen Bonds00:26

Hydrogen Bonds

Hydrogen BondsHydrogen bonds are weak attractions between atoms that have formed other chemical bonds. One of these atoms is electronegative, like oxygen, and has a partial negative charge. The other is a hydrogen atom that has bonded with another electronegative atom and has a partial positive charge.Hydrogen Bonds Control the World!Because hydrogen has very weak electronegativity when it binds with a strongly electronegative atom, such as oxygen or nitrogen, electrons in the bond are...
Electrophilic 1,2- and 1,4-Addition of HX to 1,3-Butadiene01:17

Electrophilic 1,2- and 1,4-Addition of HX to 1,3-Butadiene

The electrophilic addition of hydrogen halides such as HBr to alkenes and nonconjugated dienes gives a single product as per Markovnikov’s rule.
Electrophilic Addition of HX to 1,3-Butadiene: Thermodynamic vs Kinetic Control01:23

Electrophilic Addition of HX to 1,3-Butadiene: Thermodynamic vs Kinetic Control

The addition of a hydrogen halide to 1,3-butadiene gives a mixture of 1,2- and 1,4-adducts. Since more substituted alkenes are more stable, the 1,4-adduct is expected to be the major product. However, the product distribution is strongly influenced by temperature; low temperature favors the 1,2-adduct, whereas the 1,4-adduct is predominant at high temperature.
Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism01:18

Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism

Birch reduction uses solvated electrons as reducing agents. The reaction converts benzene to 1,4-cyclohexadiene. The reaction proceeds by the transfer of a single electron to the ring to form a benzene radical anion. This anion is highly basic—it abstracts a proton from the alcohol to form a cyclohexadienyl radical. Another single electron transfer gives the cyclohexadienyl anion. A proton transfer from the alcohol forms 1,4-cyclohexadiene. Since this reduction occurs via radical anion...
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene01:13

Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene

Bromination and chlorination of aromatic rings by electrophilic aromatic substitution reactions are easily achieved, but fluorination and iodination are difficult to achieve. Fluorine is so reactive that its reaction with benzene is difficult to control, resulting in poor yields of monofluoroaromatic products. To address this, Selectfluor reagent is used as a fluorine source in which a fluorine atom is bonded to a positively charged nitrogen.
Hydrogen Bonds01:04

Hydrogen Bonds

A hydrogen bond is formed when a weakly positive hydrogen atom already bonded to one electronegative atom (for example, the oxygen in the water molecule) is attracted to another electronegative atom from another polar molecule, such as water (H2O), hydrogen fluoride (HF), or ammonia (NH3). The huge electronegativity difference between the H atom (2.1) and the atom to which it is bonded (4.0 for an F atom, 3.5 for an O atom, or 3.0 for an N atom), combined with the very small size of an H atom...