Pulmonary arterial hypertension is a serious disease with significant morbidity and mortality. Although it can occur idiopathically, it is more commonly associated with other cardiac or lung diseases. While most of the available therapies have been tested in adult populations and most therapies in children remain off-label, new reports and randomized trials are emerging that inform the treatment of pediatric populations. This review discusses currently available therapies for pediatric pulmonary hypertension, their biological rationales, and evidence for their clinical effectiveness.
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Pediatric pulmonary hypertension remains a devastating illness that requires more study to appropriately adapt therapies for the unique features of the pediatric lung and its vasculature.
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Much progress has been made over the last decade, and therapies are now available that better target specific abnormalities in vascular signaling.
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Future study will likely focus on a better understanding of the signaling pathways and how they interact. For example, the combination of strategies that increase cyclic guanosine monophosphate and cyclic adenosine monophosphate together may be more effective than either treatment alone.
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It is hoped that earlier identification, combined with the development of novel and more specific therapies, will improve the life span and quality of life of these children.
Normal pulmonary vascular transition
During fetal life the placenta serves as the organ of gas exchange, and the fetal circulation uses a series of adaptive mechanisms to maximize delivery of oxygen to metabolically active organs such as the brain, gut, and kidney. The most highly oxygenated blood enters the fetus via the umbilical vein. To efficiently direct oxygenated blood to the systemic circulation and minimize oxygen loss, almost 90% of fetal blood flow is diverted past the lungs via anatomic shunts through the foramen ovale and the ductus arteriosus. While the lung rapidly grows its network of small pulmonary arteries during the second half of gestation, blood flow in the pulmonary circulation remains highly restricted by hypoxic pulmonary vasoconstriction of small pulmonary arteries, which is reversed at birth by the sudden increase in lung oxygenation when the newborn takes his or her first breath. After birth, a rapid decrease in pulmonary vascular resistance and increase in pulmonary vascular flow occurs in response to lung expansion, increased oxygen tension, and increased pH. Pulmonary artery pressure and vascular resistance decrease more slowly, with pulmonary arterial pressure reaching its nadir approximately 2 to 3 weeks after birth. However, the responsiveness to hypoxia is retained into adulthood, and pulmonary hypertension can be easily triggered in the newborn period by hypoxic lung disease, apnea, or other causes.
Definition and classification of pediatric pulmonary hypertension
Pulmonary hypertension is necessary to support gas exchange in the fetus, but if pulmonary arterial pressure is elevated after birth or during infancy or childhood, pulmonary hypertension becomes a serious medical problem with substantial mortality and morbidity. Pulmonary hypertension is classically defined as a mean pulmonary artery pressure of at least 25 mm Hg at rest, with a pulmonary capillary wedge pressure of 15 mm Hg or less. Numerous disease processes can produce pulmonary hypertension in both adults and children, but these 2 populations are quite different when considering classification, genetic causes and, in some cases, treatment. This difference exists largely because the exposure of the developing lung to pathologic and/or environmental insults affects lung adaptation, development, and growth, leading to far greater complexity of phenotypes. The classifications of pulmonary hypertension introduced at the World Health Organization Symposium in 1998 and subsequently modified at the Venice and Dana Point Symposia were primarily designed for use in adult diseases, and have been difficult to apply to pediatric populations. A new pediatric classification scheme was developed by an expert panel in Panama City in 2011 to better address the developmental underpinnings of pulmonary vascular disease in children. For instance, while idiopathic pulmonary arterial hypertension occurs in children, pulmonary hypertension very commonly occurs in association with congenital heart disease, or other lung diseases such as lung hypoplasia or bronchopulmonary dysplasia (BPD). The latter group appears to be growing, and represents a significant proportion of patients followed by pediatric pulmonary hypertension programs. Pulmonary hypertension affects roughly one-third of infants with moderate to severe BPD, and results in greater morbidity and mortality, poor growth and neurodevelopmental outcome, long-term mechanical ventilation support, and death due to right heart dysfunction and multiorgan failure. Pulmonary vascular disease also contributes to the morbidity and mortality of other pediatric diseases such as sickle cell disease, interstitial lung diseases, and cystic fibrosis. Relatively little is known about the epidemiology of pediatric pulmonary hypertension, and comprehensive registries to support phenotyping and clinical research are needed.
Persistent pulmonary hypertension of the newborn (PPHN) is a unique and specific type of pulmonary hypertension that occurs in the neonatal period as a failure to achieve the normal drop in pulmonary vascular resistance in the early neonatal period. PPHN is a syndrome that complicates a wide range of neonatal cardiopulmonary diseases, and affects up to 10% of all preterm and term neonates that require neonatal intensive care unit (NICU) support for respiratory failure. Moderate or severe PPHN affects up to 2 to 6 per 1000 live births, and complicates the course of 10% of all infants admitted to the NICU. These circulatory abnormalities are also responsible for an 8% to 10% risk of death and a 25% risk of long-term neurodevelopmental morbidity. The long-term impact of PPHN on pediatric and adult pulmonary vascular function is another important area for future research.
Definition and classification of pediatric pulmonary hypertension
Pulmonary hypertension is necessary to support gas exchange in the fetus, but if pulmonary arterial pressure is elevated after birth or during infancy or childhood, pulmonary hypertension becomes a serious medical problem with substantial mortality and morbidity. Pulmonary hypertension is classically defined as a mean pulmonary artery pressure of at least 25 mm Hg at rest, with a pulmonary capillary wedge pressure of 15 mm Hg or less. Numerous disease processes can produce pulmonary hypertension in both adults and children, but these 2 populations are quite different when considering classification, genetic causes and, in some cases, treatment. This difference exists largely because the exposure of the developing lung to pathologic and/or environmental insults affects lung adaptation, development, and growth, leading to far greater complexity of phenotypes. The classifications of pulmonary hypertension introduced at the World Health Organization Symposium in 1998 and subsequently modified at the Venice and Dana Point Symposia were primarily designed for use in adult diseases, and have been difficult to apply to pediatric populations. A new pediatric classification scheme was developed by an expert panel in Panama City in 2011 to better address the developmental underpinnings of pulmonary vascular disease in children. For instance, while idiopathic pulmonary arterial hypertension occurs in children, pulmonary hypertension very commonly occurs in association with congenital heart disease, or other lung diseases such as lung hypoplasia or bronchopulmonary dysplasia (BPD). The latter group appears to be growing, and represents a significant proportion of patients followed by pediatric pulmonary hypertension programs. Pulmonary hypertension affects roughly one-third of infants with moderate to severe BPD, and results in greater morbidity and mortality, poor growth and neurodevelopmental outcome, long-term mechanical ventilation support, and death due to right heart dysfunction and multiorgan failure. Pulmonary vascular disease also contributes to the morbidity and mortality of other pediatric diseases such as sickle cell disease, interstitial lung diseases, and cystic fibrosis. Relatively little is known about the epidemiology of pediatric pulmonary hypertension, and comprehensive registries to support phenotyping and clinical research are needed.
Persistent pulmonary hypertension of the newborn (PPHN) is a unique and specific type of pulmonary hypertension that occurs in the neonatal period as a failure to achieve the normal drop in pulmonary vascular resistance in the early neonatal period. PPHN is a syndrome that complicates a wide range of neonatal cardiopulmonary diseases, and affects up to 10% of all preterm and term neonates that require neonatal intensive care unit (NICU) support for respiratory failure. Moderate or severe PPHN affects up to 2 to 6 per 1000 live births, and complicates the course of 10% of all infants admitted to the NICU. These circulatory abnormalities are also responsible for an 8% to 10% risk of death and a 25% risk of long-term neurodevelopmental morbidity. The long-term impact of PPHN on pediatric and adult pulmonary vascular function is another important area for future research.
Pharmacotherapy for pulmonary hypertension
The aims of therapy for pulmonary arterial hypertension are selective pulmonary vasodilation, restoration of normal endothelial function, and reversal of remodeling of the pulmonary vasculature. All of these serve to reduce right ventricular afterload and prevent right ventricular failure. The choice of agents will often depend on the severity and acuity of illness; for instance, acute pulmonary vasodilation is needed for PPHN and acute pulmonary hypertensive crises after cardiopulmonary bypass, but long-term therapy may focus more on vascular remodeling. The main therapeutic avenues involve the nitric oxide (NO), prostacyclin, and endothelin pathways, which are summarized in excellent recent comprehensive reviews. It is also of importance that the scientific understanding and therapeutic management of pulmonary hypertension are changing rapidly.
Nitric Oxide
NO is synthesized from the terminal nitrogen of l- arginine by the enzyme nitric oxide synthase (NOS). Three isoforms of NOS are present in the lung, although endothelial NOS (eNOS) is regarded as the most important regulator of NO production in the lung vasculature. NO is a gas molecule that diffuses freely from the endothelium to the vascular smooth muscle cell. The biological effects of NO in vascular smooth muscle are mediated primarily through activation of soluble guanylate cyclase, which converts guanosine triphosphate to cyclic guanosine monophosphate (cGMP) ( Fig. 1 ). cGMP serves as a second messenger that relaxes vascular smooth muscle through activation of cGMP-gated ion channels and activation of cGMP-dependent protein kinase. However, recent studies indicate that alternative NO signaling pathways may also exist through reaction of NO with protein thiols to form S -nitrosothiols, which may induce vasodilation or protein modification.
Lung eNOS mRNA and protein are present in the early fetus, but both increase toward the end of gestation, readying the lung to adapt to the postnatal need for pulmonary vasodilation. This increase in lung eNOS content explains the emergence of responsiveness to endothelium-dependent vasodilators, such as oxygen and acetylcholine, in late gestation. Many factors associated with pulmonary hypertension have the capacity to perturb eNOS function, even if protein levels are sufficient. Presumably this is because the normal catalytic function of eNOS depends on numerous posttranslational modifications, including association with the chaperone protein Hsp90 and availability of essential substrates and cofactors including l- arginine, tetrahydrobiopterin (BH 4 ), nicotinamide adenine dinucleotide phosphate (reduced), and calcium/calmodulin. Depletion of Hsp90 or biopterin will reduce production or bioavailability of NO, and will also uncouple eNOS, resulting in incomplete reduction of molecular oxygen with subsequent formation of superoxide, essentially turning the enzyme into a source of oxidant stress.
NO is currently approved by the Food and Drug Administration (FDA) only for treatment of PPHN in the neonatal period. Because eNOS is decreased or dysfunctional in PPHN, inhaled NO (iNO) is thought to provide specific replacement therapy that is inhaled directly to airspaces approximating the pulmonary vascular bed. While most commonly administered with mechanical ventilation, iNO can also be provided via continuous positive airway pressure or nasal cannula devices, although the concentration may need to be increased to account for the entrainment of room air.
The safety and efficacy of iNO for PPHN have been particularly well studied through large placebo-controlled trials. iNO significantly decreases the need for extracorporeal membrane oxygenation (ECMO) support in newborns with PPHN, although mortality or length of hospitalization was not affected in any study. Data from the large registry maintained by the Extracorporeal Life Support Organization also indicate a 40% reduction in the number of neonates cannulated for ECMO, coincident with the FDA approval of iNO. By encompassing a range of disease severity, these studies also highlight that starting iNO for respiratory failure that is in earlier stages of evolution (for an oxygenation index of 15–25) does not decrease the incidence of ECMO and/or death, or improve other patient outcomes. On the other hand, delaying iNO initiation until respiratory failure is advanced (oxygenation index of >40) may increase length of time on oxygen. In longer-term follow-up, iNO did not significantly alter the incidence of chronic lung disease or neurodevelopmental impairment relative to placebo.
Based on the available data, iNO should be initiated at a dose of 20 ppm, after confirming PPHN and ruling out congenital heart disease and left ventricular dysfunction. A failure to respond to 20 ppm is only rarely followed by improvement at higher doses. The greatest improvement in oxygenation occurs in infants with extrapulmonary right-to-left shunting but without significant pulmonary parenchymal disease. Even if the total pulmonary vascular resistance (PVR) does not decrease, iNO can improve oxygenation through a microselective effect that reduces intrapulmonary shunting. When iNO is stopped abruptly, rebound pulmonary hypertension can develop. This potentially life-threatening phenomenon can occur even if no improvement in oxygenation has been observed, and has raised questions about whether vascular cells respond to NO by upregulating vasoconstrictor pathways. However, from a practical standpoint, the clinical problem can usually be overcome by weaning iNO to 1 ppm before discontinuation.
iNO is used to treat many other forms of pediatric and neonatal pulmonary hypertension, although its role in those settings is less well defined. For instance, randomized studies have not demonstrated a consistent improvement in oxygenation in infants with congenital diaphragmatic hernia, although there appear to be benefits of stabilizing infants and preventing cardiac arrest before ECMO. Up to one-third of premature infants with BPD will develop some degree of pulmonary hypertension or cor pulmonale, and alterations in NO signaling appear to play a role in the vascular and lung injury. A recent case series indicates that iNO may reduce established BPD-associated pulmonary hypertension to a greater degree than oxygen alone. On the other hand, large clinical trials have shown inconsistent benefit when iNO is used to prevent BPD.
Outside of the NICU setting, the most common clinical use of iNO is for the infant or child with congenital heart disease with associated pulmonary hypertension. Postoperatively, iNO is frequently used to prevent or treat pulmonary hypertensive crises, improve oxygenation, and increase cardiac output. Pulmonary hypertension commonly develops in infants with congenital heart lesions associated with pulmonary overcirculation, such as truncus arteriosus or atrioventricular canal. If the heart lesion is not corrected, medial and intimal thickening occur in the pulmonary vasculature over time, which eventually leads to luminal obliteration. Acute life-threatening exacerbation of pulmonary hypertension following cardiopulmonary bypass is a serious clinical problem even in very young infants. In addition, children undergoing cavopulmonary connections for single ventricle lesions require low PVR for surgical success. Several small single-center studies indicate that iNO can attenuate pulmonary hypertension in at-risk postoperative patients, reduce the number of pulmonary hypertension crises, and shorten time on mechanical ventilation. In one larger randomized trial of pediatric patients, iNO (20 ppm) significantly decreased PVR and pulmonary hypertensive crises, and shortened the time to extubation readiness. Responsivity to iNO has also been proposed as predictive of successful operability in patients with pulmonary hypertension associated with congenital heart disease.
In clinical studies of pediatric patients with severe acute respiratory distress syndrome (ARDS), iNO produced selective pulmonary vasodilation and improved systemic oxygenation. However, subsequent randomized controlled trials did not demonstrate a beneficial effect on mortality or duration of mechanical ventilation in pediatric or adult patients. Although a transient improvement in oxygenation was observed in most of these studies, it has been speculated that because most patients dying from acute respiratory distress syndrome suffer from multiple organ systems failure, lung-selective therapy such as iNO may not improve the overall survival rate. These results likely indicate that the problem of pediatric respiratory failure involves much more than vascular dysfunction, and that there is still much to be learned about the role of NO in primary lung injury.
As our understanding of NO signaling evolves, strategies will emerge that enhance function of the native NOS enzyme. For instance, sufficient synthesis of l- arginine is necessary for optimal NOS function, and exogenous l- arginine supplementation enhances NOS activity in vitro. Although arginine supplementation has been less successful when attempted in vivo, l- arginine can be endogenously synthesized from l- citrulline by a recycling pathway consisting of 2 enzymes, argininosuccinate synthase and argininosuccinate lyase. Recent studies indicate that providing exogenous l- citrulline may reverse NOS dysfunction in animal models of neonatal pulmonary hypertension. In clinical studies, oral l- citrulline increased levels of both plasma citrulline and arginine in high-risk children undergoing cardiopulmonary bypass. Intravenous l- citrulline has been shown to be safe and well tolerated in children undergoing cardiopulmonary bypass, and clinical trials are under way.
Sildenafil
cGMP is the second messenger that regulates contractility of smooth muscle through activation of cGMP-dependent kinases, phosphodiesterases, and ion channels. In vascular smooth muscle cells, NO-mediated activation of soluble guanylate cyclase is a major source of cGMP production. Because cGMP is such a central mediator of vascular contractility, it is not surprising that its concentrations are regulated within a relatively narrow range to allow fine-tuning of vascular responses to oxygen, NO, and other stimuli.
Phosphodiesterases are a large family of enzymes that hydrolyze and inactivate cGMP and cyclic adenosine monophosphate (cAMP), thus regulating their concentrations and effects as well as facilitating cross-talk between the 2 cyclic nucleotides. Type 5 phosphodiesterase (PDE5) is especially highly expressed in the lung, and not only uses cGMP as a substrate but also contains a specific cGMP-binding domain that serves to activate its catabolic activity. As the primary enzyme responsible for regulating cGMP, PDE5 may well represent the most important regulator of NO-mediated vascular relaxation in the normal pulmonary vascular transition after birth.
Fetal and neonatal lung development, along with commonly used therapies, appears to regulate PDE expression and activity. In developing lambs and rats, PDE5 is expressed according to specific developmental trajectories that result in a peak of expression during late fetal life, followed by an acute decrease around the time of birth. This drop in PDE5 activity would be expected to amplify the effects of NO produced by birth-related stimuli such as oxygen and shear stress . By contrast, when pulmonary vessels of fetal lambs undergo remodeling by chronic intrauterine pulmonary hypertension, PDE5 activity increases relative to controls. Even more striking is that after birth, PDE5 activity does not decrease in this lamb model of PPHN, but rather increases dramatically to levels well above those observed in spontaneously breathing or ventilated control lambs. This abnormal increase in activity would be expected to diminish responses to both endogenous and exogenous NO, and could explain the incomplete clinical efficacy of iNO in some patients. It is also interesting that recent reports indicate that PDE5 is highly expressed in the remodeled human right ventricle, raising the possibility that sildenafil therapy may improve right ventricular function.
Although sildenafil is presently only approved by the FDA for the treatment of pulmonary hypertension in adult patients, it is frequently used in children. The first clinical report of sildenafil use in children was to facilitate weaning from iNO following corrective surgery for congenital heart disease. In this initial case series, enteral sildenafil increased circulating cGMP and allowed 2 of 3 infants to wean from iNO without rebound pulmonary hypertension. Subsequent case series expanded these initial observations to show that enteral sildenafil may facilitate iNO discontinuation in infants with critical illness, and may also reduce duration of mechanical ventilation and length of stay in the intensive care unit.
A recent large trial randomized children (approximately two-thirds of whom had pulmonary hypertension associated with cardiac disease) to low-, medium-, or high-dose sildenafil versus placebo for 16 weeks. The investigators concluded that sildenafil monotherapy for 16 weeks is well tolerated for pediatric pulmonary hypertension. The primary end point of improvement in peak oxygen consumption during exercise testing was only marginally different between sildenafil and placebo ( P = .056), but greater effects were noted in the medium-dose and high-dose groups. Adverse events included pyrexia, upper respiratory infections, increased erections, and nausea. Patients who completed the 16-week trial were eligible to receive sildenafil for extended treatment (STARTS-2). Although there was not a placebo arm, the investigators noted that survival rates compared favorably with historical rates. The data also suggest that the overall profile favors the medium dose (roughly 0.5–1 mg/kg given 3 times daily), and there should be consideration for adjusting sildenafil to a medium dose for long-term use. The clinical use of enteral sildenafil has also been reported in infants with PPHN, including one small, randomized controlled trial with oral sildenafil that showed a dramatic improvement in oxygenation and survival.
Enteral administration of sildenafil could raise concerns about gastrointestinal absorption, particularly in critically ill patients who may have compromised intestinal perfusion. An intravenous preparation of sildenafil was approved for clinical use in 2010. Two studies have reported the use of intravenous sildenafil in critically ill children. One enrolled pediatric patients with postoperative pulmonary hypertension after cardiac surgery to 1 of 3 intravenous doses of sildenafil or placebo for a minimum of 24 hours. Median time to extubation and length of time in intensive care was reduced in the sildenafil arm, although the study was underpowered. An open-label pilot trial in infants with PPHN demonstrated that intravenous sildenafil, delivered as a continuous infusion, improved oxygenation. Furthermore, 7 infants received sildenafil without prior use of iNO, and all experienced a significant improvement in oxygenation within 4 hours after sildenafil administration. Only 1 of these 7 infants required iNO, and the other 6 infants improved and survived to hospital discharge without requiring either iNO or ECMO. A randomized controlled trial is currently under way to evaluate the efficacy of intravenous sildenafil in infants with moderate PPHN ( NCT01409031 ).
Sildenafil is also an attractive therapeutic option for infants with chronic pulmonary hypertension caused by congenital diaphragmatic hernia or bronchopulmonary dysplasia, because it can be given orally and over longer periods of time with apparent low toxicity. In a rat model of hyperoxia-induced BPD, chronic use of sildenafil decreased medial wall thickness and right ventricular hypertrophy, and improved lung alveolarization. A clinical case series examined the effect of oral sildenafil in 25 infants and children (<2 years old) with pulmonary hypertension caused by chronic lung disease (mostly BPD). Most patients showed some improvement after a median treatment interval of 40 days, and the majority of infants were able to wean off iNO. Five patients died after initiation of sildenafil treatment, but none died of refractory pulmonary hypertension or right heart failure. A similar approach might benefit some infants with chronic pulmonary hypertension associated with lung hypoplasia. These important pilot studies suggest that sildenafil is well tolerated in infants with pulmonary hypertension caused by chronic lung disease, and paves the way to further studies in this especially challenging population.
An interesting recent study showed that in a rat model of congenital diaphragmatic hernia, antenatal administration of sildenafil to the dam reduced PDE5 activity and increased cGMP, and produced striking reductions in the vascular findings of persistent pulmonary hypertension. This finding is the first indication that pulmonary hypertension can be treated before birth, and will likely open up a productive line of investigation in antenatal diagnosis and treatment.
Tadalafil is a longer-acting selective PDE5 inhibitor recently approved by the FDA for the treatment of adult pulmonary hypertension. A recent retrospective report examined pediatric patients with pulmonary hypertension who were converted from sildenafil to tadalafil to achieve once-daily dosing at 1 mg/kg/d. In addition to the ease of administration, about half of the patients exhibited significant improvements in mean pulmonary arterial pressure and PVR index measured at heart catheterization. Side-effect profiles were similar for the 2 agents. These results indicate that tadalafil may be safe for pediatric patients with pulmonary arterial hypertension, and has the advantages of only once-daily dosing.
Prostanoids
A complementary vasodilatory pathway in the fetal lung is mediated by prostacyclin (PGI 2 ) and cAMP (see Fig. 1 ). Prostacyclin is a metabolite of arachidonic acid that is endogenously produced by the vascular endothelium. The vascular effects of PGI 2 are mediated through its binding to a membrane IP receptor that activates adenylate cyclase and increases cAMP, which triggers relaxation of smooth muscle cells through reducing intracellular calcium concentrations. Prostacyclin production appears to increase in late gestation and early postnatal life, indicating its importance in promoting the neonatal pulmonary vascular transition. Pulmonary hypertension in both neonates and older children is characterized by a decrease in the biosynthesis of prostacyclin accompanied by increased synthesis of the vasoconstrictor thromboxane A 2 . Furthermore, the PGI 2 receptor (IP) is decreased in adult and pediatric patients with pulmonary hypertension, and animal studies point to its contribution to altered vasodilation in PPHN. Prostacyclin is a potent vasodilator in both the systemic and pulmonary circulations and also has antiplatelet effects. Prostacyclin was one of the earliest pulmonary vasodilators used for clinical treatment of pulmonary hypertension, and was approved by the FDA in 1995 for the treatment of severe chronic pulmonary arterial hypertension.
At present, several prostanoid drug preparations are available for clinical use. Epoprostenol, delivered as a continuous intravenous infusion, remains a mainstay of therapy, and has been shown to improve pulmonary hemodynamics, quality of life, exercise capacity, and survival in adults and children with idiopathic and secondary pulmonary hypertension. These significant long-term effects may occur even if short-term vasodilation is not observed, suggesting beneficial effects on platelet aggregation, inhibition of smooth muscle cell growth, and/or protection of right ventricular function. The optimal dose of intravenous epoprostenol is not well defined, although children usually need higher doses than adults. In some children, rapid dosage escalation of infusions of PGI 2 may be necessary to promote acute pulmonary vasodilation, and tolerance can develop that requires periodic dose escalation. Adverse effects include inhibition of platelet aggregation, systemic vasodilation, and alterations in hepatic enzymes, and common side effects include diarrhea and jaw pain. Epoprostenol requires dedicated venous access, typically through a central venous line. The drug is chemically unstable at neutral pH and room temperature, and its short half-life requires continuous intravenous infusion with cold packs to maintain drug stability. Sudden interruption of the medication can lead to severe rebound pulmonary hypertension.
While used commonly for chronic management, intravenous epoprostenol is less frequently used for acute pulmonary hypertension, because of the risks of ventilation-perfusion mismatch and systemic hypotension. For this reason, inhaled, oral, and subcutaneous routes of delivery have been pursued. When given as an inhaled aerosol, the vasodilator effects of PGI 2 tend to be limited to the pulmonary circulation, making this strategy appealing when acute pulmonary vasodilation is needed. Reports in children have been generally positive, although to date there are few studies reporting the use of inhaled PGI 2 in neonates with PPHN. The author’s experience suggests that inhaled PGI 2 is well tolerated and may assist in recovery without ECMO in infants with severe pulmonary hypertension and inadequate response to iNO. Although the optimal dosing of inhaled PGI 2 in critically ill mechanically ventilated infants is not known, short-term studies in newborn lambs with pulmonary hypertension suggest that doses up to 500 ng/kg/min produce progressive improvements in pulmonary artery pressure, PVR, and pulmonary blood flow. In the author’s clinical experience, doses of 50 to 100 ng/kg/min produce rapid improvement in oxygenation in infants who are refractory to iNO. Concerns regarding the use of inhaled PGI 2 include airway irritation from the alkaline solution needed to maintain drug stability, rebound pulmonary hypertension if the drug is abruptly discontinued, loss of medication into the circuit owing to condensation, and alteration of characteristics of mechanical ventilation from the added gas flow needed for the nebulization. Prolonged use of continuous inhaled PGI 2 could also lead to damage of mechanical ventilator valves. Further investigations will likely focus on preparations specifically designed for inhalation, such as iloprost or treprostinil, as discussed below. An oral agent, beraprost, is a prostacyclin analogue that is less potent than epoprostenol, but chemically stable with a longer half-life of approximately 1 hour. Beraprost is currently only approved for the treatment of pulmonary hypertension in Japan and South Korea, although new oral prostanoids are currently under investigation in adult populations.
Iloprost is a chemically stable prostacyclin analogue with a half-life to 20 to 30 minutes that has been studied as an inhaled compound. The advantages of an inhaled agent include improved selectivity for the pulmonary vascular bed, which is superior for patients with acute pulmonary hypertensive crisis with hemodynamic compromise and low cardiac output. This approach may improve ventilation-perfusion mismatch and oxygenation, and successful use has been reported in pediatric populations, including those with PPHN and postcardiopulmonary bypass, and those refractory to iNO or sildenafil. Acute bronchoconstriction is a potential adverse event, and compliance can be poor because of the need for frequent aerosol administrations, up to 8 to 12 times daily.
Treprostinil is a prostacyclin analogue that is stable at room temperature and neutral pH, and with a longer half-life of about 3 hours. Treprostinil is approved by the FDA for the treatment of chronic pulmonary hypertension in adults, and can be delivered via continuous subcutaneous or intravenous infusion as well as by inhalation. Subcutaneous treprostinil produces short-term improvements in exercise tolerance and hemodynamics in some adults with pulmonary arterial hypertension, but severe local site discomfort and induration can limit its tolerance. Subcutaneous treprostinil has been used to transition some children who were chronically stable on intravenous epoprostenol, and may improve the clinical course in children as an add-on therapy. Placebo-controlled trials have demonstrated improved exercise tolerance, clinical symptoms, and hemodynamics in patients with pulmonary hypertension, including children.
PDE3 Inhibition: Milrinone
Similar to the NO-cGMP pathway, prostacyclin-cAMP signaling is regulated by cAMP-hydrolyzing PDE isoforms such as PDE3 and PDE4. The author’s group recently reported that PDE3A expression and activity in the resistance pulmonary arteries increases dramatically by 24 hours after birth. These results were unexpected, as one would have predicted that PDE3 activity would decrease after birth to facilitate cAMP accumulation, similar to the patterns reported for PDE5. It was also observed that addition of iNO dramatically increased PDE3 levels, which suggests that inhibition of PDE3 activity might enhance the vasodilatory effects of iNO/cGMP signaling in addition to its expected effects on the cAMP pathways.
Milrinone is an inhibitor of PDE3 activity that is frequently used in pediatric patients to improve myocardial contractility after cardiac surgery. Milrinone may also bypass abnormalities in endogenous PGI 2 production and/or enhance availability of cAMP, which could be useful for acute treatment of pulmonary hypertension. Recent studies have shown a potential effect on the pulmonary vascular bed as well as synergistic effects with inhaled prostanoids. In animal studies, milrinone decreases pulmonary artery pressure and resistance, and acts additively with iNO. Clinical reports indicate that milrinone may decrease rebound pulmonary hypertension after iNO is stopped, and may enhance pulmonary vasodilation of infants with PPHN refractory to iNO. A study to better define the pharmacokinetic profile of milrinone in infants with PPHN is ongoing ( NCT01088997 ), and should lead to clinical trials designed to test its efficacy.
Endothelin Receptor Antagonists: Bosentan
Endothelin-1 (ET-1) is a 21-amino-acid protein formed by serial enzymatic cleavage of a larger prepropeptide to the vasoactive form, and is one of the most potent vasoconstrictors described in the pulmonary vasculature ( Fig. 2 ). ET-1 is principally produced in endothelial cells in response to hypoxia, and is known to promote endothelial cell dysfunction, proliferation and remodeling of smooth muscle cells, inflammation, and fibrosis. ET-1 binds to 2 receptor subtypes, ET receptors A and B, and the binding of ET-1 to the ETA receptor on smooth muscle cells produces vasoconstriction. Increased ET-1 production and altered ET-receptor activity have been consistently reported in neonatal and adult animal models of pulmonary hypertension, and lung ET-1 expression and plasma ET levels were elevated in severe pulmonary arterial hypertension in adults. In several animal and human studies, plasma ET-1 concentrations are consistently increased during and following cardiopulmonary bypass, suggesting a role for ET-1 in the pathophysiology of pulmonary hypertension induced by cardiopulmonary bypass. ET-1 is believed to play a role in the pathogenesis of neonatal pulmonary hypertension, and endothelin blockade augments pulmonary vasodilation. A recent prospective examination of 40 newborns with congenital diaphragmatic hernia and poor outcome also indicated that plasma ET-1 levels were highly correlated with the severity of pulmonary hypertension.
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