Introduction
Partial anomalous pulmonary venous connections (PAPVC) are found in less than 1% of patients with congenital heart disease [1]. The classic description of the anomaly is a right upper lobe vein draining into the right atrium or superior vena cava in a young male patient with an atrial septal defect (ASD). [2,3]. In patients who present with an isolated PAPVC of the left upper lobe or entire left lung to a vertical vein, repair via a closed technique through a left thoracotomy is safe and effective.
Technique
Indications
Operative intervention has been recommended for A) the presence of symptoms or B) in an asymptomatic patient with a pulmonary to systemic flow ratio (Qp:Qs) greater than 1.5:1 or enlargement of right heart chambers, to decrease the likelihood of developing right heart failure or pulmonary vascular obstructive disease [4].
Pre-operative Investigations
A history and physical examination followed by a chest x-ray, electrocardiogram and complete transesophageal echocardiogram TEE is performed. Additional imaging with either computed tomography (CT) [5], magnetic resonance imaging (MRI), a ventilation perfusion scan or angiography [6] is warranted if there is uncertainty regarding the diagnosis, the anatomy or the co-existence of associated cardiac pathology.
Preparation
The patient is intubated with a double lumen endotracheal tube or a bronchial blocker to deflate the left lung, and is positioned on the operating room table with the left side elevated 30 degrees. The TEE probe is inserted to confirm the preoperative investigations and to assess all normal and anomalous pulmonary veins. The patient is prepared and draped in a sterile fashion, incorporating the left groin into the operative field.
Surgical Technique
| Figure 1: Positioning of the patient and exposure of the anomalous venous connection. |
| Figure 2: Repair of the anomalous venous connection. |
Pitfalls
The co-existence of associated cardiac anomalies such as additional anomalous venous connections (particularly right-sided) or an ASD contraindicate use of the left thoracotomy approach.
Discussion
Most series have reported a prevalence of PAPVC of 0.4-0.7%, predominantly in children and young adults. These anomalies are usually right-sided (90%), with large shunts and associated atrial septal defect(s) (80-90%). A review of 45 children and adults from this institution, studied by transesophageal echocardiography, found that 82% of PAPVC originated from the right lung [6]. A recent retrospective study of adult chest computed tomography (CT) scans detected the presence of an asymptomatic PAVC in 0.2% of patients; which was left-sided in 79% and associated with an ASD infrequently (<3%) [5].
The physiologic effect of a PAPVC is the creation of a left to right shunt caused by drainage of one or more pulmonary veins either directly into the right heart, or via a systemic vein. The severity of symptoms correlates with the number of segments involved, the site(s) of connection, the presence of other pulmonary vascular abnormalities or associated cardiac defects [6,7]. Patients more frequently present with symptoms when associated anomalies are present and may require repair using cardiopulmonary bypass [7]. Those with an isolated PAPVC (without an ASD) of the left upper lobe to a vertical vein draining into the left innominate vein, can undergo safe and effective surgical correction via a closed approach utilizing a left thoracotomy.

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