Patent ductus arteriosus: Difference between revisions
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==Background== | ==Background== | ||
* | *Ductus arteriosus is a blood vessel connecting main pulmonary artery to proximal descending aorta | ||
* | **Shunts blood from right ventricle to bypass fetus's non-functioning lungs in utero | ||
*In PDA, ductus fails to close after birth | |||
*Second most common congenital heart disease | |||
*Approximately 1 in 1600 to 5000 live births in the US.<ref>Mitchell, S. C., Korones, S. B., Berendes, H. W. Congenital heart disease in 56,109 births: incidence and natural history. Circulation 43: 323-332, 1971.</ref> | |||
===Pathophysiology=== | ===Pathophysiology=== | ||
[[File:PDA.png|thumb]] | [[File:PDA.png|thumb]] | ||
*Ductus arteriosus shunts blood from the pulmonary artery to the aorta bypassing the lungs while in utero | *Ductus arteriosus shunts blood from the pulmonary artery to the aorta bypassing the lungs while in utero | ||
*Normally closes soon after birth via complex process | *Normally closes soon after birth via complex process | ||
*In | **Regulated by oxygen tension and decreases in prostaglandin E2 | ||
* | **Becomes ligamentum arteriosum | ||
* | *In PDA, ductus fails to close | ||
*Some congenital heart defects, such as [[transposition of the great arteries]], are incompatible with life ''''without''' a PDA; may be necessary to allow oxygenated and deoxygenated blood to mix | **Results in shunting of blood between aorta and pulmonary artery | ||
**Some oxygenated blood from high-pressure aorta shunts to lower pressure pulmonary artery | |||
**A large shunt can cause increased fluid return to lungs and increased lung pressure, leading to [[pulmonary hypertension]] | |||
*Some congenital heart defects, such as [[transposition of the great arteries]], are incompatible with life ''''without''' a PDA; may be necessary to allow oxygenated and deoxygenated blood to mix | |||
**In these cases [[prostaglandin E1|prostaglandins]] are used to keep the ductus arteriosus '''open'''. | **In these cases [[prostaglandin E1|prostaglandins]] are used to keep the ductus arteriosus '''open'''. | ||
Revision as of 14:39, 9 March 2019
Background
- Ductus arteriosus is a blood vessel connecting main pulmonary artery to proximal descending aorta
- Shunts blood from right ventricle to bypass fetus's non-functioning lungs in utero
- In PDA, ductus fails to close after birth
- Second most common congenital heart disease
- Approximately 1 in 1600 to 5000 live births in the US.[1]
Pathophysiology
- Ductus arteriosus shunts blood from the pulmonary artery to the aorta bypassing the lungs while in utero
- Normally closes soon after birth via complex process
- Regulated by oxygen tension and decreases in prostaglandin E2
- Becomes ligamentum arteriosum
- In PDA, ductus fails to close
- Results in shunting of blood between aorta and pulmonary artery
- Some oxygenated blood from high-pressure aorta shunts to lower pressure pulmonary artery
- A large shunt can cause increased fluid return to lungs and increased lung pressure, leading to pulmonary hypertension
- Some congenital heart defects, such as transposition of the great arteries, are incompatible with life 'without a PDA; may be necessary to allow oxygenated and deoxygenated blood to mix
- In these cases prostaglandins are used to keep the ductus arteriosus open.
Clinical Features
- Continuous machine like heart murmur
- Differential cyanosis (cyanosis of lower extremities and not the upper extremities)
- Dyspnea
- Tachycardia
- Widened pulse pressure
Differential Diagnosis
- Acute pericarditis
- Aortopulmonary Septal Defect
- Coarctation of the Aorta
- Coronary Artery Fistula
- Pediatric Acute Respiratory Distress Syndrome
- Pediatric Sinus of Valsalva Aneurysm
- Pediatric Tachycardia
- Pulmonic Valvular Stenosis
- Sickle cell anemia
- Tetralogy of Fallot With Absent Pulmonary Valve
Congenital Heart Disease Types
- Cyanotic
- Acyanotic
- AV canal defect
- Atrial septal defect (ASD)
- Ventricular septal defect (VSD)
- Cor triatriatum
- Patent ductus arteriosus (PDA)
- Pulmonary/aortic stenosis
- Coarctation of the aorta
- Differentiation by pulmonary vascularity on CXR[2]
- Increased pulmonary vascularity
- Decreased pulmonary vascularity
- Tetralogy of fallot
- Rare heart diseases with pulmonic stenosis
Evaluation
Echocardiography demonstrating PDA[3]
- Careful physical examination demonstrating characteristic machine like murmur
- Echocardiography
- Laboratory tests are usually not helpful. MRA and Cardiac CT can also be used as diagnostic tools
Management
- Spontaneous closure is usually common but if significant respiratory distress or impaired oxygen delivery is present, therapy is usually required.
Medical Therapy
- IV indomethacin: usually effective when administered in the first 10-14 days of life.
Surgical Therapy:
Cardiac catheterization and catheter closure in addition to surgical ligation are also options if medical therapy fails.
Disposition
See Also
External Links
References
- ↑ Mitchell, S. C., Korones, S. B., Berendes, H. W. Congenital heart disease in 56,109 births: incidence and natural history. Circulation 43: 323-332, 1971.
- ↑ Knipe K et al. Cyanotic congenital heart diseases. Radiopaedia. http://radiopaedia.org/articles/cyanotic-congenital-heart-disease
- ↑ http://www.thepocusatlas.com/pediatrics/
