Pregnancy and congenital complete atrioventricular block: management during pregnancy and the periparturient period

Journal Title: Journal of Rare Cardiovascular Diseases - Year 2018, Vol 3, Issue 6

Abstract

Complete atrioventricular block (AVB) is rare during pregnancy. Congenital atrioventricular block is the most common type of heart block in this group of patients. About one‐third of female patients with complete AVB remain asymptomatic until adulthood and may be first diagnosed during pregnancy. We present a case of a 31‐year‐old pregnant woman with complete AVB who was in her final stage of pregnancy. After reviewing the various advantages and disadvantages of feasible approaches with the patient, we decided to use fluoroscopy‐guided temporary backup pacemaker implantation. Estimated radiation skin dose was small and safe. The patient agreed to this treatment plan. Four days prior to scheduled cesarean delivery (39 weeks of gestation), during a one‐day stay in the hospital, the pa‐ tient underwent single‐chamber temporary pacemaker implantation (using transvenous active fixation lead and external re‐sterilized pacemaker). The abdominal and pelvic regions were covered with a lead shield. The caesarean delivery was uneventful and the baby was healthy with an Apgar score of 10. JRCD 2018; 3 (6): 204–208.

Authors and Affiliations

Andrzej Ząbek, Barbara Małecka, Paweł Tomasz Matusik, Maciej Dębski, Krzysztof Boczar, Jacek Lelakowski

Keywords

Related Articles

Eosinophilic myocarditis: Gardia lamblia infestation and Garcinia cambogia. Coincidence or causality? (RCD code: III‑1B.1.o)

Eosinophilic myocarditis is a rare form of myocardial inflammation that may lead to heart failure and death, if left untreated. A previously healthy 26-year-old man was admitted to the department with chest pain and dysp...

Hereditary haemorrhagic telangiectasia in Benghazi, Libya; a population‑based study of incidence and prevalence (RCD code: I‑O)

Background: Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant genetic disorder characterised by the formation of aberrant arteriovenous malformations (AVMs). Few studies have described the epidemiolog...

Right ventricular free wall motion abnormalities as a simple method of assessment in patients with pulmonary hypertension (RCD code: II‐1A.O)

Background: Pulmonary hypertension (PH) is a cardiovascular pathology leading to right-sided heart failure. A qualitative assessment of right ventricular (RV) function in echocardiography provides valuable information on...

Pulmonary artery pressure matters – how to efficiently improve survival in pulmonary arterial hypertension (RCD code: II‐1A.1)

Pulmonary arterial hypertension is a disease characterized by poor prognosis despite treatment. Even in a modern era of pharmaco- therapy there is a strong need to further improve survival of patients. The current therap...

Heart in Fabry Disease

Fabry disease is one of the lysosomal storage disorders, that results from progressive multiorgan accumulation of glycoproteins. It is caused by mutations of the GLA gene, which encodes alpha-galactosidase A. The  incide...

Download PDF file
  • EP ID EP286459
  • DOI 10.20418/jrcd.v3i6.313.g224
  • Views 95
  • Downloads 0

How To Cite

Andrzej Ząbek, Barbara Małecka, Paweł Tomasz Matusik, Maciej Dębski, Krzysztof Boczar, Jacek Lelakowski (2018). Pregnancy and congenital complete atrioventricular block: management during pregnancy and the periparturient period. Journal of Rare Cardiovascular Diseases, 3(6), 204-208. https://europub.co.uk/articles/-A-286459