20 research outputs found
Hybrid minimally invasive epicardial and endocardial 3D-mapping-guided cryoablation for symptomatic pre-excitation syndrome after previous four failed catheter ablations
Minimally invasive hybrid approach for the treatment of Wolff Parkinson-White syndrome is seldom. We report a case of minimally invasive no-x-ray 3D-guided epicardial ablation of accessory pathway in a 23-year-old Caucasian sportsman with pre-excitation and very frequent palpitations with documented symptomatic narrow QRS tachycardia and previous 4 failed percutaneous radiofrequency ablations.Małoinwazyjne, hybrydowe podejście do leczenia zespołu Wolff Parkinsona-White’a jest rzadko stosowane. W pracy przedstawiono przypadek małoinwazyjnej, hybrydowej, 3D-mapowanej nasierdziowej ablacji dodatkowej drogi przewodzenia bez zastosowania skopii u 23-letniego kaukaskiego sportowca z cechami preekscytacji, bardzo częstymi kołataniami oraz z udokumentowanym objawowym częstoskurczem z wąskimi zespołami QRS, leczonym czterokrotną nieskuteczną przezskórną ablacją
Rodzinny napadowy częstoskurcz węzłowy — obserwacja wielopokoleniowej rodziny
We report a three-generation family coming from southeastern region of Poland (Podkarpackie voivodship) with 6 women having normal hearts and presenting with a history of paroxysmal tachycardia with onset of symptoms in the adulthood. Recordings of clinical SVT, dual AVN electrophysiology, induction of typical AVNRT and results of RFCA are available. The history of this family shows the significance of a careful and detailed collection of medical history, and point towards the importance of family screening in AVNRT patients
Feasibility and performance of catheter ablation with zero-fluoroscopy approach for regular supraventricular tachycardia in patients with structural and/or congenital heart disease
Electrocardiographic algorithms to guide a management strategy of idiopathic outflow tract ventricular arrhythmias
The current guidelines of the European Society of Cardiology outlined electrocardiographic
(ECG) differentiation of the site of origin (SoO) in patients with idiopathic ventricular arrhythmias (IVAs). The aim of this study was to compare 3 ECG algorithms for differentiating the SoO and to
determine their diagnostic value for the management of outflow tract IVA. We analyzed 202 patients (mean age [SD]: 45 [16.7] years; 133 women [66%])
with IVAs with the inferior axis (130 premature ventricular contractions or ventricular tachycardias from
the right ventricular outflow tract [RVOT]; 72, from the left ventricular outflow tract [LVOT]), who underwent
successful radiofrequency catheter ablation (RFCA) using the 3‑dimensional
electroanatomical system.
The ECGs before ablation were analyzed using custom‑developed
software. Automated measurements
were performed for the 3 algorithms: 1) novel transitional zone (TZ) index, 2) , and 3) transition
ratio. The results were compared with the SoO of acutely successful RFCA. The algorithm predicted the left‑sided
SoO with a sensitivity and specificity close
to 90%. The TZ index showed higher sensitivity (93%) with lower specificity (85%). In the subgroup
with the transition zone in lead V3 (n = 44, 15 from the LVOT) the sensitivity and specificity of the V2–
transition‑ratio
algorithm were 100% and 45%, respectively. The combined TZ index+ algorithm
(LVOT was considered only when both algorithms suggested the LVOT SoO) can increase the specificity
of the LVOT SoO prediction to 98% with a sensitivity of 88%. The combined TZ‑index
and algorithm allowed an accurate and simple identification
of the SoO of IVA. A prospective study is needed to determine the strategy for skipping the RVOT
mapping in patients with LVOT arrhythmias indicated by the 2 combined algorithms
Long-term follow-up and comparison of techniques in radiofrequency ablation of ventricular arrhythmias originating from the aortic cusps (AVATAR Registry)
Introduction: Radiofrequency ablation (RFA) of outflow tract ventricular arrhythmia (VA) that originates from the aortic cusps can be challenging. Data on long-term efficacy and safety as well as optimal technique after aortic cusp ablation have not previously been reported. Objectives: This aim of the study was to determine the short- and long-term outcomes after RFA of aortic cusp VA, and to evaluate aortic valve injuries according to echocardiographic screening. Patients and methods: This was a prospective multicenter registry (AVATAR, Aortic Cusp Ventricular Arrhythmias: Long Term Safety and Outcome from a Multicenter Prospective Ablation Registry) study. A total of 103 patients at a mean age of 56 years (34–64) from the “Electra” Registry (2005–2017) undergoing RFA of aortic cusps VA were enrolled. The following 3 ablation techniques were used: zero-fluoroscopy (ZF; electroanatomical mapping [EAM] without fluoroscopy), EAM with fluoroscopy, and conventional fluoroscopy-based RFA. Data on clinical history, complications after RFA, echocardiography, and 24-hour Holter monitoring were collected. The follow-up was 12 months or longer. Results: There were no major acute cardiac complications after RFA. In one case, a vascular access complication required surgery. The median (interquartile range [IQR]) procedure time was 75 minutes (IQR, 58–95), median follow-up, 32 months (IQR, 12–70). Acute and long-term procedural success rates were 93% and 86%, respectively. The long-term RFA outcomes were observed in ZF technique (88%), EAM with fluoroscopy (86%), and conventional RFA (82%), without differences. During long-term follow-up, no abnormalities were found within the aortic root. Conclusions: Ablation of VA within the aortic cusps is safe and effective in long-term follow-up. The ZF approach is feasible, although it requires greater expertise and more imaging modalities
Validation of standard and new criteria for the differential diagnosis of narrow QRS tachycardia in children and adolescents
To establish an appropriate treatment strategy and determine if ablation is indicated for patients with narrow QRS complex supraventricular tachycardia (SVT), analysis of a standard 12-lead electrocardiogram (ECG) is required, which can differentiate between the 2 most common mechanisms underlying SVT: atrioventricular nodal reentry tachycardia (AVNRT) and orthodromic atrioventricular reentry tachycardia (OAVRT). Recently, new, highly accurate electrocardiographic criteria for the differential diagnosis of SVT in adults were proposed; however, those criteria have not yet been validated in a pediatric population. All ECGs were recorded during invasive electrophysiology study of pediatric patients (n = 212; age: 13.2 ± 3.5, range: 1–18; girls: 48%). We assessed the diagnostic value of the 2 new and 7 standard criteria for differentiating AVNRT from OAVRT in a pediatric population. Two of the standard criteria were found significantly more often in ECGs from the OAVRT group than from the AVNRT group (retrograde P waves [63% vs 11%, P < 0.001] and ST-segment depression in the II, III, aVF, V1–V6 leads [42% vs 27%; P < 0.05]), whereas 1 standard criterion was found significantly more often in ECGs from the AVNRT group than from the OAVRT group (pseudo r′ wave in V1 lead [39% vs 10%, P < 0.001]). The remaining 6 criteria did not reach statistical significance for differentiating SVT, and the accuracy of prediction did not exceed 70%. Based on these results, a multivariable decision rule to evaluate differential diagnosis of SVT was performed. These results indicate that both the standard and new electrocardiographic criteria for discriminating between AVNRT and OAVRT have lower diagnostic values in children and adolescents than in adults. A decision model based on 5 simple clinical and ECG parameters may predict a final diagnosis with better accuracy
A simplified approach for evaluating sustained slow pathway conduction for diagnosis and treatment of atrioventricular nodal reentry tachycardia in children and adults
Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans
Genome-wide association studies (GWAS) have identified numerous common prostate cancer (PrCa) susceptibility loci. We have
fine-mapped 64 GWAS regions known at the conclusion of the iCOGS study using large-scale genotyping and imputation in
25 723 PrCa cases and 26 274 controls of European ancestry. We detected evidence for multiple independent signals at 16
regions, 12 of which contained additional newly identified significant associations. A single signal comprising a spectrum of
correlated variation was observed at 39 regions; 35 of which are now described by a novel more significantly associated lead SNP,
while the originally reported variant remained as the lead SNP only in 4 regions. We also confirmed two association signals in
Europeans that had been previously reported only in East-Asian GWAS. Based on statistical evidence and linkage disequilibrium
(LD) structure, we have curated and narrowed down the list of the most likely candidate causal variants for each region.
Functional annotation using data from ENCODE filtered for PrCa cell lines and eQTL analysis demonstrated significant
enrichment for overlap with bio-features within this set. By incorporating the novel risk variants identified here alongside the
refined data for existing association signals, we estimate that these loci now explain ∼38.9% of the familial relative risk of PrCa,
an 8.9% improvement over the previously reported GWAS tag SNPs. This suggests that a significant fraction of the heritability of
PrCa may have been hidden during the discovery phase of GWAS, in particular due to the presence of multiple independent
signals within the same regio