Stress in adults with congenital heart disease – preliminary results on anxiety, life events, coping and socioeconomic factors (RCD code: IV)
Journal Title: Journal of Rare Cardiovascular Diseases - Year 2014, Vol 1, Issue 6
Abstract
We performed pilot analysis of the anxiety level, frequency of life events and their interactions among adults with congenital heart disease (CHD), and evaluated their coping strategies and socioeconomic functioning. In a cross‑sectional questionnaire study on 30 consecutive ambulatory patients with CHD we addressed these issues by a custom‑designed tool incorporating state‑anxiety scale of the State‑Trait Anxiety Inventory, the brief‑COPE questionnaire (Polish versions) and 10 selected life events. We found that state‑anxiety level adjusted for sex, age and life events differed by CHD defect category (R2 = 0,51; p<0,001). Other factors are characterized and briefly discussed. JRCD 2014; 1 (6): 10–14
Authors and Affiliations
Paweł Iwaszczuk, Lidia Tomkiewicz-Pająk, Klaudia Knap, Piotr Musiałek, Wojciech Szczeklik, Władysław Łosiak, Maria Olszowska
Pulmonary arterial hypertension after systemic‑to‑pulmonary shunt correction (RCD code: II-1A.4d)
Pulmonary arterial hypertension develops in a significant number of patients with congenital heart diseases. Congenital heart diseases predispose to pulmonary vascular remodeling as a result of increased pulmonary blood...
Exercise capacity in adult patients after Fontan procedure. (RCD code: IV-5B.1)
Background: The aim of Fontan procedure is to restore a balance between pulmonary and systemic circulation and improve or nearly normalize arterial saturation in patients with functionally univentricular heart. Neverthel...
Rare diseases and disorders and rare cardiovascular complications
n/a
Cardiac AL Amyloidosis (RCD code: III-3A.2a)
Primary systemic amyloidosis (AL amyloidosis) is the most common subtype of amyloidosis in developed countries. Amyloid fibrils deposition results from an abnormal secondary structure of immunoglobulin light chains produ...
Hypertrophic cardiomyopathy or hereditary hemochromatosis? (RCD code: III‑2B.3.o)
Hemochromatosis is a disease resulting from excessive deposition of iron in parenchymal tissues. The most common form of this disease is associated with the homozygous p.Cys282Tyr mutation of the HFE gene. It leads to mu...