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Cardiology Research

Case Report

Volume 9, Number 5, October 2018, pages 330-333

Patent Ductus Venosus and Congenital Heart Disease: A Case Report and Review

Patent ductus venosus (PDV) is an uncommon vascular malformation, classified as a type of intrahepatic shunt [1]. In utero, the ductus venosus connects the left portal vein to the inferior vena cava, allowing a portion of the venous blood to bypass the liver and return to the heart. After birth, the ductus venosus generally closes between days of life 2 to 18 in term infants [2-5]. The natural decrease in portal venous pressure after birth contributes to the closure process [6-8]. Prostaglandins play a role in maintaining the patency of the ductus venosus while a product of the cytochrome P-450 system is postulated to contribute to its constriction [2, 9-12]. If the ductus venosus fails to close, clinical signs may include galactosemia, hypoxemia, encephalopathy with hyperammonia, and hepatic dysfunction with disturbances of coagulation function and hyperbilirubinemia [1]. We report an infant with complex congenital heart disease (CHD) who developed coagulopathy and hyperammonemia during the preoperative period secondary to PDV. Once the diagnosis was made, hybrid stage 1 palliation was performed to allow for discontinuation of the prostaglandin infusion and facilitate PDV closure. Previous reports of PDV in CHD are presented, its etiology and clinical consequences reviewed, and options for therapeutic treatment discussed.

Institutional Review Board approval is not required for single case reports at Nationwide Children’s Hospital (Columbus, Ohio). A full term, 3 kg male infant presented in cardiogenic shock with poor perfusion on the second day of life. Workup including echocardiography revealed a type B interrupted aortic arch with a large malpositioned ventricular septal defect (VSD) and a patent ductus arteriosus (PDA). On admission to the cardiac intensive care unit, the capillary blood gas showed a pH of 6.92, PaCO2 22 mm Hg, and a base deficit of 27 mmol/L. Initial laboratory values were notable for coagulopathy and hyperammonemia (107 µmol/L) with signs of shock liver (elevated AST and ALT to 1,124 U/L and 526 U/L respectively). The patient’s trachea was intubated, a prostaglandin E (PGE) infusion was started, and resuscitation provided by the administration of isotonic fluid and sodium bicarbonate. After initial resuscitation and initiation of the PGE infusion, his clinical status and laboratory parameters steadily improved. A left lower extremity catheter-associated deep vein thrombosis was noted and therapeutic unfractionated heparin therapy was started. On day of life (DOL) 12, worsening coagulation function was noted with a prothrombin time of 18.9 s, INR of 1.63, and hyperammonemia (133 µmol/L). The AST/ALT and total bilirubin did not significantly increase at this time; however, intermittent hypoglycemia was noted despite a glucose infusion rate of 10 mg/kg/min. On DOL 13, the serum lactate increased and the patient’s trachea was reintubated. Planned surgical intervention was delayed due to the hepatic dysfunction and clinical decompensation. Since an ultrasound showed that the femoral vein thrombosis was non-occlusive and had not increased in size, the heparin infusion was discontinued on DOL 14. The workup for hepatic dysfunction and coagulopathy included a normal ferritin to rule out neonatal hemochromatosis, negative herpes simplex virus polymerase chain reaction, and a normal single nucleotide polymorphism microarray. A normal factor VIII level ruled out a consumptive process while low factor V and factor VII levels were consistent with decreased hepatic production. An abdominal ultrasound demonstrated a large patent ductus venosus with steal of blood flow from the portal vein and portosystemic shunting (Fig. 1). This was determined to be the cause of his hepatic dysfunction, coagulation disturbance, and hyperammonemia. As there was concern that the PGE infusion and high central venous pressures related to the CHD were contributing to the patency of the ductus venosus, the decision was made to proceed with surgical intervention. The coagulation disturbance was treated with fresh frozen plasma and he was taken to the operating room for a hybrid stage 1 palliation procedure on DOL 17. The PGE infusion was discontinued at the time of the procedure. Postoperatively, the coagulation disturbance, hypoglycemia, and hyperammonemia resolved. Follow-up ultrasound on DOL 21 showed a decrease in the size of the ductus venosus and by 6 weeks of age, the PDV had closed.

Click for large image

Figure 1. Hepatic and abdominal ultrasound showing hepatic vein confluence with the inferior vena cava (1); patent ductus venosus (2); and hepatic vein (3).

Various factors may be responsible for hepatic dysfunction and its resultant laboratory alterations (hyperammonemia, hyperbilirubinemia, and coagulation disturbances) in the critically ill term neonate with CHD. Our patient presented in shock with end-organ dysfunction which could explain the associated hepatic dysfunction early in his clinical course. However, the hyperammonemia, hypoglycemia, and worsening coagulation function on DOL 12 were not accompanied by other signs of shock or hemodynamic decompensation. They occurred at a time when his clinical status was improving. An extensive workup was negative except for an abdominal ultrasound which showed a PDV and portosystemic shunting of the venous blood. Shunting of blood across a PDV has been shown to impair ammonia detoxification, blood coagulation and regulation of serum bile acids, with the clinical impact dictated by the percentage of blood that is shunted [13, 14]. Although PDV is a rare cause of hepatic dysfunction in the neonate, it may occur in patients receiving PGE infusions or those with elevated right-sided filling pressures due to CHD. Clinical signs and symptoms include hepatic dysfunction with coagulation disturbances, hyperbilirubinemia, and hyperammonemia as noted in our patient.

Of the 106 reported cases of PDV that we found in our literature review, 26 were in patients who also had CHD [1, 6, 7, 15-28]. Of the PDV cases reported in CHD patients, all patients presented in childhood, with either clinical symptoms or incidental findings noted on imaging. Nineteen of the 26 patients presented at less than 2 years of age. The most common presenting symptoms in this population were hyperammonemia with encephalopathy, hyperbilirubinemia, and galactosemia. Only two previous cases of PDV in CHD patients presented with coagulation disturbances (prolonged PT and PTT) [1, 20]. Other presenting symptoms included liver tumors, pulmonary hypertension (not secondary to CHD), elevated AST/ALT, developmental delay and membranoproliferative glomerulonephritis. The most common types of CHD associated with PDV included ventricular septal defect, atrial septal defect, and patent ductus arteriosus, although several previous case reports do not specify the type of CHD. Management strategies varied between conservative management (dietary restrictions and lactulose to treat hyperammonemia), endovascular closure, surgical ligation, and liver transplantation. Seven of the patients were reported to have died, most often due to cardiac complications from their CHD.

There is a recognized association between extrahepatic shunts and CHD [29]. Many authors have also speculated regarding the association of PDV, an intrahepatic shunt, and CHD [15, 17, 18]. Fugelseth et al demonstrated that high right-sided pressures due to CHD or pulmonary hypertension may lead to shunting through a PDV, potentially maintaining ductus venosus patency or contributing to its clinical significance [3]. Additionally, prostaglandins have been shown to play a role in maintaining the patency of the ductus venosus [2, 9-12]. Thus, in our patient, both the prostaglandin infusion and increased right-sided pressures may have contributed to ductus venosus patency, illustrating two factors which could place CHD patients at a higher risk for clinically significant PDV.

A PDV rarely closes spontaneously and is the most likely of the intrahepatic shunts to require surgical closure or a catheter-based intervention [30]. Alternatively, patients with CHD may require a palliative procedure or full correction of their CHD to lower right sided pressures and permit discontinuation of the PGE infusion to encourage closure of the PDV. Given the reported low likelihood of spontaneous closure of PDV, the spontaneous closure of our patient’s PDV off PGE supports our assumption that the PGE infusion was contributing to patency of the ductus venosus. We would speculate that patients with a PDV on a PGE infusion, especially those with elevated right sided pressures, may experience a higher rate of spontaneous resolution than other PDV patients once the PGE infusion is discontinued. However, if a palliative procedure or full correction of the CHD is not feasible, surgical or catheter-based intervention may be necessary for closure of a PDV in select CHD patients, including those with persistent clinical manifestations. As noted by other authors, the adequacy of the portal venous system must be assessed before closure is attempted, both through imaging of the portal venous system and measurement of the rise in portal venous pressure with temporary occlusion of the PDV [1, 14]. If a PDV is closed without an adequate portal venous system the patient can develop acute portal venous congestion and bowel ischemia [31].

Given the likely effect of PGE infusion and elevated right-sided pressures on the ductus venosus, a PDV is an important consideration in the differential diagnosis of hepatic dysfunction in neonates with CHD presenting with hyperbilirubinemia, coagulation disturbances or hyperammonemia. We would suggest a management strategy that minimizes factors contributing to PDV patency, such as a PGE infusion or high right-sided pressures, to encourage spontaneous closure of the PDV. This may require modification of the surgical plan for repair or palliation of CHD. When this is not possible, interventional or surgical closure of the PDV may be necessary if the portal venous system is found to be adequate.

Conflict of Interest

The authors have no conflict of interest to report.

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