16 research outputs found
A myocardialis necrosis mértékének vizsgálata eltérő supraventricularis szívritmuszavarok rádiófrekvenciás katéterablatiós kezelését követően = Assessment of the extent of myocardial necrosis following radiofrequency catheter ablation of different supraventricular arrhythmias
Absztrakt:
Bevezetés: Ismert, hogy katéteres ablatio által okozott
szívizom-károsodás következtében megnő a szívizom-specifikus nekroenzimek
koncentrációja. Célkitűzés: A magas érzékenységű troponin T
(hsTnT) és a szívizom-specifikus kreatin-kináz (CKMB) szintje középtávú
változásának elemzése pitvarfibrilláció (PF), pitvari flutter (PFlu), AV-csomó
reentry tachycardia (AVNRT) rádiófrekvenciás katéteres ablatióját követően,
illetve elektrofiziológiai vizsgálat után. Módszer:
Rádiófrekvenciás ablatión, illetve elektrofiziológiai vizsgálaton átesett
betegeket vontunk be konszekutívan prospektív vizsgálatunkba.
Sorozatvérmintákból meghatároztuk a hsTnT- és a CKMB-szinteket a procedúra előtt
és után közvetlenül, majd 4 és 20 órával és 3 hónappal később.
Eredmények: Negyvenhét, 55 ± 13 év átlagéletkorú beteget
(10 elektrofiziológiai vizsgálat, 12 AVNRT, 13 PFlu és 12 PF) vontunk be
vizsgálatunkba. A hsTnT-szintek minden csoportban szignifikánsan megemelkedtek a
beavatkozást követően, a CKMB csak a PF-csoportban változott. A hsTnT-szint négy
órával a beavatkozást követően az összes ablatión átesett betegnél és az
elektrofiziológiai vizsgálaton átesett betegek 80%-ánál meghaladta a
referenciatartományt. A legmagasabb átlagos hsTnT-koncentrációk EFV, AVNRT, PFlu
esetén 24 ± 11, 260 ± 218 és 541 ± 233 ng/l-nek bizonyultak. A legmagasabb
hsTnT-szint a PF-ablatiós csoportban volt kimutatható 20 órával az ablatio után
(799 ± 433 ng/l). Pozitív korrelációt találtunk a rádiófrekvenciás ablatiót
követő hsTnT-szint és az ablatio ideje között. Következtetések:
A hsTnT alkalmas a rádiófrekvenciás ablatio és az elektrofiziológiai vizsgálat
utáni myocardialis necrosis vizsgálatára, az ablatión átesett betegek
mindegyikénél; elektrofiziológiai vizsgálat után 80%-ban pozitív a hsTnT. A
necrosis mértéke jelentősen függ a beavatkozás típusától, és korrelál az ablatio
kiterjedtségével. A fentiekben leírt megfigyelések iránymutatásként szolgálnak a
rádiófrekvenciás ablatio utáni hsTnT-szint megfelelő értelmezéséhez. Orv Hetil.
2019; 160(14): 540–548.
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Abstract:
Introduction: Levels of cardiac necroenzymes, high-sensitive
troponin (hsTnT) and creatine kinase muscle-brain (CKMB) increase as a result of
a myocardial damage following catheter ablation. Aim: To
analyze the mid-term alteration of hsTnT and CKMB levels following
radiofrequency ablation (RFCA) for atrial fibrillation (AF), atrial flutter
(AFlu), AV-nodal reentry tachycardia (AVNRT) and electrophysiological studies
(EPS) without ablation. Method: Patients undergoing RFCA for
various indications and EPS were consecutively enrolled in our prospective
study. Concentrations of hsTnT and CKMB were measured from serial blood samples
directly before and after the procedure, 4 and 20 hours later and at 3 months
follow-up. Results: Forty-seven patients (10 EPS, 12 AVNRT, 13
AFlu, 12 AF) with mean age of 55 ± 13 were included. hsTnT levels increased
significantly in all groups after the procedures, while CKMB changed only in the
AF group. hsTnT exceeded the reference value in all patients with ablation and
in 80% of patients with EPS 4 hours post-ablation. Peak average hsTnT levels for
EPS, AVNRT, AFlu were 24 ± 11, 260 ± 218 and 541 ± 233 ng/L, respectively. The
highest hsTnT level was measured in the AF group (799 ± 433 ng/L). We found a
positive correlation between hsTnT levels and ablation time after RFCA.
Conclusions: The hsTnT levels significantly change after
EPS and RFCA, in all patients who underwent ablation, and in 80% of those with
EPS had hsTnT positivity in the early post-procedural phase. hsTnT levels
depended significantly on the type of the subgroups and correlated with the
ablation time. Awareness of those observations is essential to correctly
interpret elevated hsTnT levels following RFCA. Orv Hetil. 2019; 160(14):
540–548
Left atrial appendage size is a marker of atrial fibrillation recurrence after radiofrequency catheter ablation in patients with persistent atrial fibrillation
Introduction There are no consistently confirmed predictors of atrial fibrillation (AF) recurrence after catheter ablation. Therefore, we aimed to study whether left atrial appendage volume (LAAV) and function influence the long-term recurrence of AF after catheter ablation, depending on AF type.Methods AF patients who underwent point-by-point radiofrequency catheter ablation after cardiac computed tomography (CT) were included in this analysis. LAAV and LAA orifice area were measured by CT. Uni- and multivariable Cox proportional hazard regression models were performed to determine the predictors of AF recurrence.Results In total, 561 AF patients (61.9 +/- 10.2 years, 34.9% females) were included in the study. Recurrence of AF was detected in 40.8% of the cases (34.6% in patients with paroxysmal and 53.5% in those with persistent AF) with a median recurrence-free time of 22.7 (9.3-43.1) months. Patients with persistent AF had significantly higher body surface area-indexed LAV, LAAV, and LAA orifice area and lower LAA flow velocity, than those with paroxysmal AF. After adjustment left ventricular ejection fraction (LVEF) Conclusion The current study demonstrates that beyond left ventricular systolic dysfunction, LAA enlargement is associated with higher rate of AF recurrence after catheter ablation in persistent AF, but not in patients with paroxysmal AF.</p
The Value of Voltage Histogram Analysis Derived Right Atrial Scar Burden in the Prediction of Left Atrial Scar Burden
Introduction. Growing evidence suggests that fibrotic changes can be observed in atrial fibrillation (AF) in both atria. Quantification of the scar burden during electroanatomical mapping might have important therapeutic and prognostic consequences. However, as the current invasive treatment of AF is focused on the left atrium (LA), the role of the right atrium (RA) is less well understood. We aimed to characterize the clinical determinates of the RA low-voltage burden and its relation to the LA scaring. Methods. We have included 36 patients who underwent catheter ablation for AF in a prospective observational study. In addition to LA mapping and ablation, high-density RA bipolar voltage maps (HD-EAM) were also reconstructed. The extent of the diseased RA tissue (≤0.5 mV) was quantified using the voltage histogram analysis tool (CARTO®3, Biosense Webster). Results. The percentage of RA diseased tissue burden was significantly higher in patients with a CHA2DS2-VASc score ≥ 2 p=0.0305, higher indexed LA volume on the CTA scan and on the HD‐EAM (p=0.0223 and p=0.0064, respectively), or higher indexed RA volume on the HD‐EAM p=0.0026. High RA diseased tissue burden predicted the presence of high LA diseased tissue burden (OR = 7.1, CI (95%): 1.3–38.9, p=0.0145), and there was a significant correlation of the same (r = 0.6461, p<0.0001). Conclusions. Determining the extent of the right atrial low-voltage burden might give useful clinical information. According to our results, the diseased tissue burden correlates well between the two atria: the right atrium mirrors the left atrium
Synthesis and cell growth inhibitory activity of six non-glycosaminoglycan‐type heparin‐analogue trisaccharides
The design and synthesis of heparin mimetics with high anticancer activity but no anticoagulant activity is an important task in medicinal chemistry. Here, we present the efficient synthesis of five Glc‐GlcA‐Glc sequenced and one Glc‐IdoA‐Glc sequenced non‐glycosaminoglycan, heparin‐related trisaccharides with various sulfation/sulfonylation and methylation patterns. The cell growth inhibitory effects of the compounds were tested against four cancerous human cell lines and two non‐cancerous cell lines. Two D‐glucuronate-containing tetra‐ O ‐sulfated, partially methylated trisaccharides displayed remarkable and selective cell growth inhibitory effects on ovary carcinoma (A2780) and melanoma (WM35) cells. Methyl substituents on the glucuronide unit proved to be detrimental while acetyl substituents were beneficial to the cytostatic activity of the sulfated derivatives