Ablation of incessant supraventricular tachycardia in pregnancy (RCD code: VIII-V-3A.O)
Journal Title: Journal of Rare Cardiovascular Diseases - Year 2013, Vol 1, Issue 4
Abstract
We present a case of a 40‑year‑old woman, 4‑months pregnant (in vitro fertilization), admitted to a hospital due to incessant supraventricular tachycardia with a rate of 187 beats/min. Attempts to stop the arrhythmia (3 × cardioversion, verapamil IV) were unsuccessful; after electrical cardioversion, tachycardia recurred after a few sinus beats. In the view of poor arrhythmia tolerance (hypotonia, dyspnea) and the risks associated with incessant tachycardia (placental hypoperfusion, development of tachyarrhythmic cardiomyopathy), it was decided to perform an electrophysiology study and ablation. The procedure was carried out with the use of a computer 3D mapping system (Ensite NavX), aiming to minimize standard fluoroscopy use. The electrophysiology study indicated the presence of focal right‑atrial tachycardia. In this situation, geometry reconstruction and activation mapping of the right atrium was carried out, localizing the arrhythmogenic focus in the inferolateral portion of the tricuspid ring. After several radiofrequency (RF) applications, arrhythmia subsided and sinus rhythm was restored. Total fluoroscopy time in the procedure was only 90 seconds; the total radiation exposure was 12mGy. In addition, the abdomen of the pregnant woman was shielded with lead gowns from both sides, thus nearly completely eliminating the fetal radiation exposure. Unfortunately, after 4 weeks, the arrhythmia returned. A repeated ablation was carried out in an identical fashion as the index procedure, again with only minimal fluoroscopy time (62 s, 10mGy). The rest of pregnancy and labour were uneventful, without recurrence of tachycardia and a healthy baby was delivered. Therapeutic options and literature are reviewed and discussed. JRCD 2013; 1 (4): 24–28
Authors and Affiliations
Marek Jastrzębski, Renata Rajtar-Salwa, Danuta Czarnecka
1st Conference for Adults with Congenital Heart Diseases. “Care for congenital heart disease patients in Poland”
The population of adults with congenital heart disease (ACHD) is heterogeneous with respect to the type and complexity of the defect as well as its clinical manifestations. In many patients congenital heart disease (CHD)...
For one mistake made for not knowing, ten mista kes are made for not looking
And yet again, summer solstice is just behind the cor‑ ner. As the time passes so quickly, do we really have a chance to use it profitability? One way is to study hard and be up‑to‑date. Then we know new and com‑ plex sy...
Spontaneous coronary artery dissection secondary to intimal fibromuscular dysplasia (RCD code: I‑1C.O)
Fibromuscular dysplasia (FMD) is a nonatherosclerotic, noninflammatory arterial disease of unknown etiology. Histologically, FMD is classified on the basis of arterial layer involved into intimal, medial and perimedial...
Nitric oxide signaling in the ischemic postconditioning of human heart muscle (RCD code: III)
Background: Ischemic heart conditioning is well documented to trigger the intrinsic protective mechanisms of resistance against ischemia/reperfusion (I/R) injury. Previous studies on animal model have suggested that the...
Arrhythmias in pregnancy (RCD code: VII‑V)
Cardiovascular diseases in pregnancy are the most common causes of maternal mortality in developed world and an important cause of heart failure, stroke, and arrhythmia. Cardiac disease complicates 0.4–4% of all pregnanc...