Q-stars in scalar-tensor gravitational theories

We study q-stars in Brans-Dicke gravitational theory. We find that when the Brans-Dicke constant, $\omega_{\textrm{BD}}$, tends to infinity, the results of General Relativity are reproduced. For other values of $\omega_{\textrm{BD}}$, the particle number, mass and radius of the star and the absolute value of the matter field are a few percent larger than in the case of General Relativity. We also investigate the general scalar-tensor gravitational theory and find that the star parameters are a few percent larger than in the case of General Relativity.Comment: 14 pages, to appear in Phys. Lett.

Q-stars in 2+1 dimensions

We study q-stars with one or two scalar fields, non-abelian, and fermion-scalar q-stars in 2+1 dimensions in an anti de Sitter or flat spacetime. We fully investigate their properties, such as mass, particle number, radius, numerically, and focus on the matter of their stability against decay to free particles and gravitational collapse. We also provide analytical solutions in the case of flat spacetime and other special cases.Comment: 37 pg, to appear in Nucl. Phys.

Q-stars in extra dimensions

We study q-stars with global and local U(1) symmetry in extra dimensions in asymptotically anti de Sitter or flat spacetime. The behavior of the mass, radius and particle number of the star is quite different in 3 dimensions, but in 5, 6, 8 and 11 dimensions is similar to the behavior in 4.Comment: 18 pages, to appear in Phys. Rev.

Efficacy and Safety of Appropriate Shocks and Antitachycardia Pacing in Transvenous and Subcutaneous Implantable Defibrillators: Analysis of All Appropriate Therapy in the PRAETORIAN Trial.

BACKGROUND: The PRAETORIAN trial (A Prospective, Randomized Comparison of Subcutaneous and Transvenous Implantable Cardioverter Defibrillator Therapy) showed noninferiority of subcutaneous implantable cardioverter defibrillator (S-ICD) compared with transvenous implantable cardioverter defibrillator (TV-ICD) with regard to inappropriate shocks and complications. In contrast to TV-ICD, S-ICD cannot provide antitachycardia pacing for monomorphic ventricular tachycardia. This prespecified secondary analysis evaluates appropriate therapy and whether antitachycardia pacing reduces the number of appropriate shocks. METHODS: The PRAETORIAN trial was an international, investigator-initiated randomized trial that included patients with an indication for implantable cardioverter defibrillator (ICD) therapy. Patients with previous ventricular tachycardia <170 bpm or refractory recurrent monomorphic ventricular tachycardia were excluded. In 39 centers, 849 patients were randomized to receive an S-ICD (n=426) or TV-ICD (n=423) and were followed for a median of 49.1 months. ICD programming was mandated by protocol. Appropriate ICD therapy was defined as therapy for ventricular arrhythmias. Arrhythmias were classified as discrete episodes and storm episodes (≥3 episodes within 24 hours). Analyses were performed in the modified intention-to-treat population. RESULTS: In the S-ICD group, 86 of 426 patients received appropriate therapy, versus 78 of 423 patients in the TV-ICD group, during a median follow-up of 52 months (48-month Kaplan-Meier estimates 19.4% and 17.5%; P=0.45). In the S-ICD group, 83 patients received at least 1 shock, versus 57 patients in the TV-ICD group (48-month Kaplan-Meier estimates 19.2% and 11.5%; P=0.02). Patients in the S-ICD group had a total of 254 shocks, compared with 228 shocks in the TV-ICD group (P=0.68). First shock efficacy was 93.8% in the S-ICD group and 91.6% in the TV-ICD group (P=0.40). The first antitachycardia pacing attempt successfully terminated 46% of all monomorphic ventricular tachycardias, but accelerated the arrhythmia in 9.4%. Ten patients with S-ICD experienced 13 electrical storms, versus 18 patients with TV-ICD with 19 electrical storms. Patients with appropriate therapy had an almost 2-fold increased relative risk of electrical storms in the TV-ICD group compared with the S-ICD group (P=0.05). CONCLUSIONS: In this trial, no difference was observed in shock efficacy of S-ICD compared with TV-ICD. Although patients in the S-ICD group were more likely to receive an ICD shock, the total number of appropriate shocks was not different between the 2 groups. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01296022