Congenital Heart Disease
Anemia in Adults With Congenital Heart Disease Relates to Adverse Outcome

https://doi.org/10.1016/j.jacc.2009.06.050Get rights and content
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Objectives

To assess the relation of anemia in noncyanotic adults with congenital heart disease (ACHD) to functional capacity and mortality.

Background

Anemia is common in acquired heart failure and affects prognosis. The presence of anemia and its relation to outcome in ACHD remain unknown.

Methods

Data were collected on consecutive noncyanotic ACHD patients attending our tertiary center between 2001 and 2006 in whom hemoglobin concentration was measured. Anemia was defined as hemoglobin concentration <13 g/dl in males and <12 g/dl in females. Cyanotic patients were excluded to avoid confounding from secondary erythrocytosis.

Results

Overall, 830 noncyanotic ACHD patients (age 36.5 ± 15.0 years, 49.6% male) fulfilled the inclusion criteria. The prevalence of anemia was 13.1% and was highest in patients with congenitally corrected transposition of great arteries and Ebstein anomaly of the tricuspid valve. Anemic patients were more likely to be receiving diuretics (p < 0.0001) and have a lower mean corpuscular volume (p = 0.0001), with a trend toward a higher New York Heart Association functional class (p = 0.06). During a median follow-up of 47 months, 55 patients died. Anemic patients had a 3-fold higher mortality risk compared with nonanemic patients, even after propensity score adjustment for clinical variables such as systemic ventricular function, renal impairment, and diuretic therapy (adjusted hazard ratio: 3.00; 95% confidence interval: 1.46 to 6.13).

Conclusions

Anemia is not uncommon in ACHD patients attending tertiary services and is associated with a 3-fold increased risk of death. Screening for anemia should be part of the routine assessment of ACHD patients for risk stratification and treatment when correctable causes are identified.

Key Words

congenital heart defects
anemia
prognosis

Abbreviations and Acronyms

ACHD
adults with congenital heart disease
ccTGA
congenitally corrected transposition of great arteries
MCV
mean corpuscular volume
NYHA
New York Heart Association

Cited by (0)

Dr. Dimopoulos has been supported by the European Society of Cardiology. Dr. Giannakoulas is supported by the Hellenic Heart Foundation, the DG Education & Culture—LLP Programme—Leonardo Da Vinci Mobility, and the Hellenic Cardiological Society. Dr. Karaoli was supported by the European Union (DaVinci programme). Dr. Francis is supported by the British Heart Foundation. The Royal Brompton Adult Congenital Heart Programme and the Department of Clinical Cardiology have received support from the British Heart Foundation and the Clinical Research Committee, Royal Brompton Hospital, London.