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Published on: July 18, 2014
Cardiac interventions in patients with achondroplasia: a systematic review
Amrita Sukhavasi1, Thomas J O'Malley1, Elizabeth J Maynes1
1Division of Cardiothoracic Surgery, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Insights
Cardiac interventions in patients with dwarfism, including achondroplasia, show promising safety outcomes. This systematic review highlights that common cardiac procedures can be performed effectively, with necessary equipment adjustments for this unique population.
Area of Science:
- Cardiology
- Genetics
- Surgical Innovation
Background:
- Patients with achondroplasia and other forms of dwarfism exhibit higher cardiovascular disease rates.
- Limited research exists on cardiac surgical or percutaneous intervention outcomes in this population.
Purpose of the Study:
- To systematically review and analyze outcomes of cardiac interventions in patients with dwarfism.
- To identify challenges and necessary adaptations for cardiac procedures in this unique patient group.
Main Methods:
- Systematic electronic literature search for achondroplasia, dwarfism, and cardiac intervention.
- Inclusion of 14 articles detailing 14 patient cases.
- Extraction and analysis of patient-level data, including demographics, comorbidities, and procedural details.
Main Results:
- Median age 55.5 years, height 102.0 cm; 57.1% male.
- Common comorbidities included coronary artery disease (53.8%) and prior myocardial infarction (30.8%).
- Cardiac surgeries included coronary artery bypass grafting, aortic valve replacement, and aortic dissection repair; no mortality reported.
Conclusions:
- Common cardiac procedures appear to be safe for patients with dwarfism.
- Procedural success may require specific equipment modifications to accommodate patient anatomy.
Abstract:
Patients with achondroplasia and other causes of dwarfism suffer from increased rates of cardiovascular disease relative to the remainder of the population. Few studies have examined these patients when undergoing cardiac surgery or percutaneous intervention. This systematic review examines the literature to determine outcomes following cardiac intervention in this unique population. An electronic search was performed in the English literature to identify all reports of achondroplasia, dwarfism, and cardiac intervention. Of the 5,274 articles identified, 14 articles with 14 cases met inclusion criteria. Patient-level data was extracted and analyzed. Median patient age was 55.5 [interquartile ranges (IQR), 43.8, 59.8] years, median height 102.0 [98.8, 112.5] cm, median BMI 32.1 [27.0, 45.9], and 57.1% (8/14) were male. Of these 14 patients, nine had the following documented skeletal abnormalities: 66.7% (6/9) had scoliosis, 66.7% (6/9) had kyphosis, 11.1% (1/9) had lordosis, 11.1% (1/9) pectus carinatum and 11.1% (1/9) spinal stenosis. Coronary artery disease was present in 53.8% (7/13), and 30.8% (4/13) patients previously suffered a myocardial infarction. Of the eight patients who underwent cardiac surgery, 37.5% (3/8) underwent multivessel coronary artery bypass grafting, 37.5% (3/8) underwent aortic valve replacement, 25.0% (2/8) underwent type A aortic dissection repair, and the remaining 12.5% (1/8) underwent pulmonary thromboendarterectomy. Six patients underwent percutaneous intervention. Median cardiopulmonary bypass time was 136.5 [110.0, 178.8] minutes. Median arterial cannula size was 20.0 [20.0, 24.0] Fr. Bicaval cannulation was performed in all cases describing cannulation strategy (5/5). Median superior vena cava cannula size was 28.0 [28.0, 28.0] Fr, and inferior vena cava cannula size was 28.0 [28.0, 28.0] Fr. No mortality was reported with a median follow up time of 6.0 [6.0, 10.5] months. In conclusion, Common cardiac procedures can be performed with reasonable safety in this patient population. Operative adjustments may need to be made with respect to equipment to accommodate patient-specific needs.
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