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Published on: July 18, 2014
Adult Congenital Heart Disease: Report from a Public Reference Hospital in Northeastern Brazil
Maria Suely Bezerra Diogenes1, Acrísio Sales Valente1, Hermano Alexandre Lima Rocha1,2
1Hospital de Messejana Dr. Carlos Alberto Studart Gomes, Fortaleza, Ceará, Brazil.
Insights
Adults with congenital heart disease (CHD) require increased health professional attention. Late diagnosis of atrial septal defects (ASD) leads to complications, highlighting a significant concern in managing adult CHD.
Area of Science:
- Cardiology
- Public Health
- Clinical Medicine
Background:
- The global population of adults with congenital heart disease (CHD) is rising, necessitating enhanced focus from healthcare providers.
- Understanding the clinical and demographic characteristics of this population is crucial for effective management.
Purpose of the Study:
- To delineate the clinical demographic profile of adults with CHD.
- To determine the frequency of different CHD types and their invasive treatment status.
- To analyze the data from a public reference hospital in northeastern Brazil.
Main Methods:
- A retrospective cross-sectional study was conducted.
- Data were collected from 704 patients between August 2016 and August 2020.
- A virtual database was utilized for data extraction.
Main Results:
- The study included patients aged 17–81 years, with a mean age of 32±14 years. Atrial septal defect (ASD) was the most common diagnosis (30.7%).
- Moderate complexity defects were prevalent (71.5%). Arrhythmias (24%) and severe pulmonary hypertension (9.8%) were common complications.
- Over half of the patients (51.6%) underwent corrective surgery, while 14.5% required no treatment.
Conclusions:
- Atrial septal defect (ASD) was the leading diagnosis among adults with CHD in this cohort.
- A significant frequency of unrepaired ASD cases was observed, often due to late diagnosis.
- Late diagnosis contributes to complications and underscores a critical area for clinical concern and intervention.
Introduction:
The increasing worldwide number of adults with congenital heart disease (CHD) demands greater attention from health professionals. The purpose of this report is to describe the clinical demographic profile, frequency, and invasive treatment status of adults with CHD in a public reference hospital in northeastern Brazil.
Methods:
This is a retrospective cross-sectional study including 704 patients attended between August 2016 and August 2020. Data were collected from virtual database.
Results:
Patients' age varied from 17 to 81 years (mean 32±14; median 27 years); 294 (41.8%) patients were male, and 410 (58,2%) were female; 230 (32,7%) had diagnosis from age 18 and up. Cardiac complexity categories were "simple defects" (134 [19%] patients), "moderate complexity" (503 [71.5%]), and "great complexity" (67 [9.5%]). Atrial septal defect (ASD) was diagnosed in 216 (30.7%) patients, ventricular septal defect (VSD) in 101 (14.3%), tetralogy of Fallot in 93 (13.2%), and other CHD in 294 (41.8%). New York Heart Association (NYHA) functional classes were I (401 [57%]), II (203 [28.8%]), III (76 [10.8%]), and IV (24 [3.4%]). Complications were arrhythmias (173 [24%]) and severe pulmonary hypertension (69 [9.8%]). Invasive treatments were corrective surgery (364 (51.6%]), reoperation (28 [4.0%]), palliation (11 [1.6%]), interventional catheterization (12 [1.7%]), surgery plus interventional catheterization (5 [0.7%]), and preoperation (91 [12.9%]). Treatment was not required in 102 (14,5%) patients, and 91 (12.9%) were inoperable.
Conclusion:
The leading diagnosis was ASD. Frequency of unrepaired patients was high, mainly ASD, due to late diagnosis, which favored complications and denotes a matter of great concern.
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