key: cord-0829699-m4i4oeqs
authors: Mayeux, Jennalyn D.; Pan, Irene Z.; Dechand, John; Jacobs, Joshua A.; Jones, Tara L.; McKellar, Stephen H.; Beck, Emily; Hatton, Nathan D.; Ryan, John J.
title: Management of Pulmonary Arterial Hypertension
date: 2020-11-18
journal: Curr Cardiovasc Risk Rep
DOI: 10.1007/s12170-020-00663-3
sha: f9d15139970b782561a1cf738eb34b8d926006b7
doc_id: 829699
cord_uid: m4i4oeqs

PURPOSE OF REVIEW: This review focuses on the therapeutic management and individualized approach to Group 1 pulmonary arterial hypertension (PAH), utilizing Food and Drug Administration-approved PAH-specific therapies and various interventional and surgical options for PAH. RECENT FINDINGS: The paradigm for the optimal management of PAH has shifted in recent years. Upfront combination therapy with an endothelin receptor antagonist and a phosphodiesterase 5 inhibitor is now widely accepted as standard of care. In addition, there is increasing emphasis on starting prostanoids early in order to delay time to clinical worsening. However, less is known regarding which prostanoid agent to initiate and the optimum time to do so. In order to facilitate shared decision-making, there is an increasing need for decision tools based on guidelines and collective clinical experiences to navigate between pharmacologic and interventional treatments, as well as explore innovative, therapeutic pathways for PAH. SUMMARY: The management of PAH has become increasingly complex. With a growing number of PAH-specific therapies, intimate knowledge of the therapeutics and the potential barriers to adherence are integral to providing optimal care for this high-risk patient population. While current PAH-specific therapies largely mediate their effects through pulmonary vasodilation, ongoing research efforts are focused on ways to disrupt the mechanisms leading to pulmonary vascular remodeling. By targeting aberrations identified in the metabolism and proliferative state of pulmonary vascular cells, novel PAH treatment pathways may be just on the horizon.

Pulmonary hypertension (PH) describes an abnormal elevation in pulmonary arterial blood pressure [1] . The World Health Organization (WHO) classifies PH into five groups based on shared histology and pathophysiology. Group 1 pulmonary arterial hypertension (PAH) is a rare form of PH characterized by plexogenic vascular remodeling. Causes for Group 1 PAH include idiopathic and familial PH, as well as PH associated with conditions such as collagen vascular disease, congenital shunts, cirrhosis and portal hypertension, human immunodeficiency virus (HIV), hemoglobinopathies, and schistosomiasis. Group 1 PAH also includes PH associated with drugs, such as anorexigens or amphetamines. Group 2 PH is the collection of PH syndromes resulting from left ventricular (LV) or left-sided valvular disease, such as heart failure with reduced ejection fraction (HFrEF), heart failure with preserved ejection fraction (HFpEF), or valvular heart disease. Group 3 PH is PH secondary to chronic lung diseases, hypoxia, or both. This group of PH is typically characterized by mild elevations in pulmonary artery pressure (PAP), relative to patients with other types of PH. Group 4 PH is due to pulmonary arterial obstruction and commonly known as chronic thromboembolic pulmonary hypertension (CTEPH). Jennalyn D. Mayeux and Irene Z. Pan contributed equally to this work.

This category of PH is particularly unique as it represents a curable form of PH that does not require lung transplantation. Group 5 PH represents a heterogeneous collection of PH syndromes secondary to systemic diseases (e.g., sarcoidosis, histiocytosis X), hematological disorders (e.g., polycythemia vera, chronic myeloid leukemia), and extrinsic compression of the pulmonary artery. This classification system has practical significance as contemporary PAH treatments have increasingly demonstrated inconsistent benefit and even potential signals of harm across other types of PH [2] .

The focus of this review is the therapeutic management of Group 1 PAH. The review will discuss approved and emerging treatment pathways, Food and Drug Administration (FDA)-approved PAH-specific therapies, and personalization of PAH care, in addition to interventional and surgical options for PAH.

The pathogenesis of PAH is diverse and very complex. As more clinical trial and registry data becomes available, our understanding of the development and progression of this rare disease continues to evolve. Multiple mechanisms occur at the cellular and tissue level that potentiate smooth muscle cell proliferation, endothelial cell dysfunction, inflammation, and remodeling of the pulmonary vasculature. Together, these physiological alterations result in pathologic transformations leading to excessive vasoconstriction, medial hypertrophy, intimal fibrosis, and formation of plexiform lesions [3, 4] . Contemporary PAH therapies target one of three major pathways implicated in disease progression: nitric oxide (NO), endothelin-1 (ET-1), and prostacyclin (PGI 2 ) pathways. In a small minority of patients with PAH, excessive vasoconstriction plays a predominant role in increasing pulmonary vascular resistance (PVR)-mediated in large part by an influx of calcium via long-lasting calcium channels in vascular smooth muscle cells [5] . Targeting one or more of these pathways has become the current standard of practice for the medical management of PAH [6] . Therapies are available orally (Table 1) and in parenteral and inhaled forms ( Table 2) . Clinical trials have shown that these therapies play an important role in improving quality of life, and some have even shown a reduction in mortality rates in PAH (Table 3) . However, PAH remains a high mortality disease with no cure.

In PAH, NO production is chronically impaired. NO is an endothelium-derived vasoactive mediator that increases the production of cyclic guanosine monophosphate (cGMP) through the activation of soluble guanylate cyclase (sGC). In doing so, NO acts to stimulate vasodilation and inhibit proliferation within vascular smooth muscle cells [3, 4] . Currently, there are two drug classes targeting this pathway, phosphodiesterase type-5 inhibitors (PDE5i) and sGC stimulators. Phosphodiesterase type-5 (PDE5) is an enzyme found in high concentrations within the pulmonary vasculature that works to catalyze the conversion of cGMP to guanosine monophosphate (GMP). Inhibitors of the PDE-5 enzyme, such as sildenafil and tadalafil, enhance the NO-dependent, cGMPmediated pathway by preventing the breakdown of cGMP, while riociguat, an sGC stimulator, works directly to increase the production of cGMP, resulting in vasodilation and antiproliferative effects [57] .

Endothelin-1 is a potent vasoconstrictor and key driver of pulmonary vascular remodeling through its actions on endothelin receptor A (ET A ) and endothelin receptor B (ET B ) [3] . Endothelin-1 is upregulated in the vascular endothelial cells of patients with pulmonary hypertension. By binding to ET A and ET B receptors located in smooth muscle cells, ET-1 stimulates cellular proliferation, fibrosis, inflammation, and vasoconstriction [4, 58] . The effects of ET-1 via ET B on endothelial cells result in increased production of prostacyclin and NO and subsequent vasodilation [3, 59] . Both ET A and ET B receptors are found in high concentrations within the pulmonary vasculature, and as such, serve as an important focus for targeted drug therapy [59] . There are currently three FDAapproved endothelin-receptor antagonists (ERA) with varying degrees of affinity for ET A and ET B receptors: ambrisentan, bosentan, and macitentan.

The final pathway involves prostacyclin, a potent vasodilator produced predominantly in the vascular endothelium. The vasodilatory effects of prostacyclin, also referred to as PGI 2 , result from PGI 2 stimulation of the prostaglandin I2 (IP) receptor, leading to increased generation of cyclic adenosine monophosphate (cAMP). Additionally, PGI 2 inhibits platelet aggregation and possesses antiproliferative properties [3, 60] . However, in PAH, PGI 2 synthesis is suppressed, whereas levels of thromboxane A 2 , an endogenous vasoconstrictor and platelet agonist, are increased [61] . Drug therapies targeting this imbalance within the pulmonary arteries include PGI 2 analogs, such as epoprostenol, treprostinil, and iloprost, and PGI 2 receptor agonists, such as selexipag [62] .

Calcium channel blockers (CCB) are indicated in patients with a positive acute vasoreactivity test. Common CCBs used for (Table 1) . Patients should be started on a low dose and gradually titrated up as tolerated [57] . Common adverse drug reactions include peripheral edema, systemic hypotension, nausea, gastrointestinal distress, and bradycardia, in the setting of diltiazem [7, 9, 11] . Monotherapy with a CCB is indicated only in patients who achieve the desired dose, establish improved hemodynamics after 3-4 months of therapy, and maintain WHO Functional Class (FC) I-II status. In patients who cannot tolerate therapy or experience worsening hemodynamics or functionality, alternative PAH-specific therapy is recommended [57] . Calcium channel blockers were initially studied in the acute setting in patients who were given nifedipine 20 mg or diltiazem 60 mg hourly. Of the patients who responded to CCB therapy, the mean reduction in PVR and PAP were 60% and 48%, respectively [63] . A subsequent study demonstrated improved 5-year survival in patients who responded to CCBs compared to those who did not (94% vs. 55%; p = 0.003) [10] . However, less than 10% of PAH patients were found to be long-term responders to CCB therapy [8, 10, 64] .

For over a decade, PDE5is have remained the most widely prescribed class of PAH-specific therapies. These agents are arguably the easiest to initiate due to relative ease of procurement and generic availability. As such, these agents are typically the initial therapy prescribed for patients diagnosed with PAH.

Although initially approved in 1998 for use in erectile dysfunction [65] , the role of sildenafil soon expanded due to its actions on PDE5 receptors within the pulmonary vasculature, and sildenafil was approved by the FDA for the treatment of PAH in 2005 [12] . Early sildenafil trials, the vast majority of which included ≤ 30 patients, tested doses up to 100 mg three times daily [66] . In these studies, sildenafil demonstrated efficacy in a number of clinical outcomes with incremental benefit at higher sildenafil doses. The 2005 SUPER trial, a randomized, placebo-controlled trial, demonstrated improvements in WHO-FC, reduction in mean PAP, and reduction in PVR that incrementally improved with higher doses [13] . No significant difference was found between sildenafil 20 mg, 40 mg, and 80 mg three times daily in WHO-FC II-III, treatment-naïve patients with respect to the primary outcome of 6min walk distance (6MWD) [13] . Moreover, sildenafil has also been shown to improve outcomes even when added to advanced therapies such as intravenous (IV) epoprostenol. [50] TRUST 2010 [51] TRIUMPH I 2010 [52] The 2008 PACES trial randomized patients on IV epoprostenol to sildenafil 80 mg three times daily or placebo [16] . The addition of sildenafil at 80 mg three times daily to an IV prostanoid improved 6MWD in comparison to the placebo arm. This further solidified its place in therapy and added to the data supporting combination therapy. Although there has been some interest over the years regarding use of higher sildenafil doses such as 40 mg or even 80 mg three times daily, the large sample size data available do not support this strategy. Based on data from the SUPER trial, it has been hypothesized that adequate inhibition of PDE5 is achieved with 20 mg dosed three times daily [13] . Thus, 20 mg three times daily became the FDA-approved dose for PAH [12] . Notwithstanding the evidence for higher doses, obtaining insurance approval for doses higher than the FDA-approved dose of 20 mg three times daily is very difficult. The other widely available agent in this class, tadalafil, received FDA-approval in 2009. Tadalafil is more convenient than its predecessor given its longer half-life and once daily dosing [18] . Unlike the mixed data with sildenafil dosing, the PHIRST trial demonstrated tadalafil 40 mg once daily was indisputably the target dose [19] . Tadalafil 40 mg daily demonstrated improvements in 6MWD and time to clinical worsening (TTCW) in a mixture of treatment-naïve patients and patients on background therapy with bosentan. Both PDE5is carry similar adverse effect profiles, the most common being headache, flushing, myalgia, and dyspepsia. These adverse effects rarely result in the need for discontinuation and typically resolve over time.

As a member of the newest class of PAH-specific therapies, riociguat, a sGC stimulator, has established its role among the armamentarium of agents that target the NO pathway. In addition to its role in Group 1 PAH, riociguat is currently the only PAH-specific therapy that also carries FDA approval for Group 4 PH, or inoperable or persistent CTEPH [6, 57] . In the PATENT-1 and CHEST-1 trials, riociguat 2.5 mg three times daily significantly improved the primary outcome of 6MWD by 30 m and 39 m, in PAH and CTEPH, respectively [34, 35] . In PATENT-1, this effect was seen in both treatment-naïve patients, as well as patients on background therapy with an ERA. The secondary endpoints of reduction in PVR and Nterminal probrain natriuretic peptide (NT-proBNP) and improvement in WHO-FC were consistent between both trials. Though only PATENT-1 showed an improvement in TTCW, this endpoint should be interpreted with caution due to the small overall number of events (8 vs. 3) [6] . In addition, the RESPITE trial demonstrated a potential benefit in transitioning from PDE5i therapy to riociguat in WHO-FC III PAH patients on background ERA therapy [67] . The subsequent REPLACE trial showed benefit with switching stable intermediate risk patients from PDE5i therapy to riociguat (https://pharmaceuticalbusiness-review.com/news/ bayer-adempas-phase-4-trial/). Adverse effects were consistent between both trials, most commonly being headache, dyspepsia, dizziness, and hypotension. The latter is an adverse effect that is particularly unique to riociguat as compared to other oral therapies for PAH. The average mean arterial pressure reduction in both trials was 9 mmHg. Thus, riociguat requires slow uptitration to the target dose of 2.5 mg three times daily. It is typically started at 1 mg three times daily and increased by 0.5 mg three times daily at 2 week intervals if systolic blood pressure remains > 95 mmHg. Of note, PDE5is and sGC stimulators should not be used in combination due to the duplication of the NO pathway and pronounced hypotension as evidenced in the PATENT PLUS trial [36] . Riociguat requires females to enroll in the Risk Evaluation and Mitigation Strategy (REMS) program due to the teratogenicity of the drug.

Three ERAs are currently FDA-approved for the treatment of PAH. All three agents are teratogenic and require both prescribers and female patients to be enrolled in the REMS program. The REMS require females of reproductive potential to establish a negative pregnancy test prior to therapy initiation, monthly during therapy, and 1 month following therapy discontinuation. Additionally, bosentan carries an additional REMS program requirement of monthly liver function tests to monitor for hepatotoxicity. Bosentan is the only FDAapproved ERA for the pediatric population and is typically avoided in adults due to hepatotoxic risk. Other common adverse drug reactions for ERAs include edema, headaches, flulike symptoms, nasal congestion, anemia, and urinary tract infection, in the setting of macitentan [21, 23, 30] . Doses for the following agents are as follows: bosentan 62.5-125 mg twice daily, ambrisentan 5-10 mg daily, and macitentan 10 mg daily. Doses for bosentan and ambrisentan are usually started low and titrated up as tolerated. Endothelin receptor antagonists are recommended in WHO-FC II-III patients [57] .

Bosentan has been studied in a wide variety of trials and has been shown to improve cardiac index, PVR, patientreported dyspnea, 6MWD, and TTCW [14, 24, 25, [27] [28] [29] . In the 24-week Study 351 trial, 32 patients with idiopathic or hereditary PAH or PAH associated with scleroderma were randomized to bosentan or placebo. All patients were WHO-FC III and were not on any PAH-specific medications at baseline. Patients on bosentan had a 70-m improvement in 6MWD from baseline as compared to a worsening of 6 m in the placebo group [24] . Bosentan continued to demonstrate improvements in WHO-FC III patients in the SERAPH, BREATHE-1, and BREATHE-5 trials [14, 25, 27] and also showed benefit in WHO-FC II patients in the EARLY trial [28] . The COMPASS2 trial established additional benefits in patients already on stable doses of sildenafil [29] . Within the ARIES-1 and ARIES-2 trials, ambrisentan demonstrated improvements in 6MWD, TTCW, and WHO-FC at 12 weeks and at 48 weeks [22] . Macitentan showed favorable outcomes in TTCW, 6MWD, WHO-FC, and PAH-related death and hospitalization in WHO-FC II-III PAH patients, the majority of which were on concomitant PDE5i in the SERAPHIN trial [31] . In the 2017 MERIT-1 trial, macitentan was also found to reduce PVR and improve cardiac index and 6MWD in WHO-FC II-III CTEPH patients [32] .

As the first class of PAH-specific therapies to become available, the prostanoid class came as a breakthrough therapy for this disease. All treatments prior to the FDA approval of epoprostenol were considered adjunctive or supportive therapies [57] . The prostanoid class is indisputably the most diverse class with agents available via oral, inhalation, IV, and subcutaneous (SQ) routes of administration (Fig. 1) . The three parenteral and inhaled prostanoids are epoprostenol, treprostinil, and iloprost.

Parenteral prostanoids (i.e., epoprostenol, treprostinil) have maintained their role as the only class with a class I recommendation for WHO-FC IV patients [57] . Epoprostenol, the sole synthetic prostacyclin, is also the only PAH-specific therapy to have shown improved survival in a randomized, controlled trial [46] . The primary outcome of this 12-week trial, 6MWD, was improved by 31 m compared to placebo. Similarly, the stable prostacyclin analogue, treprostinil, showed 16-m 6MWD improvement as compared to placebo in its respective randomized, controlled trial [50] . Though this improvement in 6MWD may not seem impressive as an overall value when compared to what was shown with PDE5is or ERAs, two key factors must be taken into consideration. First, > 90% of patients were WHO-FC III or IV at baseline between both trials, representing a population with much more advanced disease. Second, the mean dose achieved at 12 weeks was 9.2 and 9.3 ng/kg/min [46, 50] . In our experience, consistent with most practices internationally, maintenance doses of continuous infusion prostanoids are typically targeted to achieve doses of 40 ng/kg/min, or higher, as tolerated. Therefore, as serum concentrations are linearly increased at doses up to 125 ng/kg/min [48] , coupled with further improvement as shown by Simmoneau and colleagues in patients in the highest quartile of treprostinil doses (i.e., > 13.8 ng per kilogram per minute), larger increases in exercise capacity are anticipated at higher doses than mean doses achieved in the trials [50] . Epoprostenol and treprostinil are typically started at 1-2 ng/kg/min and titrated upward at 1-2 ng/kg/min every 12-24 h, as tolerated. The most common and dose-limiting adverse effects of parenteral prostanoids during dose titration are headache, flushing, nausea, vomiting, jaw pain, diarrhea, abdominal pain, leg pain, arthralgias, myalgias, and hypotension. These occur during drug initiation and dose increases and typically resolve over time. Additionally, patients on SC treprostinil experience dose-limiting cutaneous site reactions due to a histamine-mediated response. This also resolves within 5-7 days maintained at a stable dose.

Given the need for continuous infusion of epoprostenol and parenteral treprostinil, the complexity of use of these agents cannot be overstated. First, all patients on chronic IV therapy require placement of an indwelling central venous catheter. Thus, patients must practice adequate line care hygiene to prevent the development of bloodstream infections [48] . Next, with a half-life of 3-5 min [44, 48] , epoprostenol requires fairly capable and health-literate patients to be able to adequately manage a continuous infusion pump. The possibility of interruption in therapy and subsequent rebound PH resulting in death makes epoprostenol a very high-risk therapy [44] . Treprostinil, with a much longer half-life of approximately 4 h [48] , allows more time for patients to reestablish access, making therapy interruption less of a concern and affords the ability to use continuous SC infusion. For patients on continuous SC treprostinil, maintenance of a viable infusion site requires considerable lifestyle modifications as they must continually keep the site dry and intact to maintain site longevity.

The recent introduction of an implantable infusion pump for treprostinil has garnered clinician and patient interest given fewer maintenance requirements by the patient and the ability to shower and swim without concern for getting the pump or the infusion site wet. Long-term studies of the use of the implantable pump have described cases of pump failure and pump pocket infections [68] .

Inhaled therapies offer an alternative route for WHO-FC III-IV patients requiring a prostanoid. Iloprost, a prostacyclin analogue, and inhaled treprostinil, were both shown to improve 6MWD at 12 weeks [52, 54] . Though they obviate the need for central venous access and administration via a continuous infusion, both therapies are limited by frequency of dosing. Iloprost, dosed at 2.5-5 mcg six to nine times daily, requires around-the-clock administration at the target dose [53] . Though it requires less frequent administration, inhaled treprostinil still requires four administrations per day with a goal dose of 9 inhalations (54 mcg) four times daily [49] . Furthermore, the nebulization device required for inhalation of both agents is bulky and must be carried by the patient during any excursions outside of the home if >2 h for iloprost or > 4 h for treprostinil. The dose-limiting side effects of inhaled therapies are similar to parenteral with the addition of cough and throat irritation shortly after drug administration [49, 53] . 

There are numerous challenges to both parenteral and inhaled prostanoid formulations, which require additional resources, time, and education for safe and effective use of these therapies. For these reasons, an oral formulation serves as an attractive alternative. Nearly 20 years after the introduction of IV epoprostenol, the FDA approved oral treprostinil diolamine in an extended release formulation [39] . However, treprostinil diolamine uptake in clinical practice has been limited, in large part due to mixed results in the literature. In the FREEDOM M trial, treprostinil monotherapy in treatment-naïve, WHO-FC II-III PAH patients significantly improved 6MWD [42] . Conversely, in patients already receiving background PAH therapies, oral treprostinil failed to show significant improvement in 6MWD or TTCW in both the FREEDOM C [40] and FREEDOM C2 [41] trials. In the FREEDOM C and FREEDOM C2 trials, approximately 45% and 40% of patients, respectively, were on both an ERA and PDE5i at baseline. More recently, in the 2019 FREEDOM-EV trial, oral treprostinil significantly decreased time to first clinical worsening event by 26% compared to placebo in patients who were recently diagnosed with PAH (median of 6.4 months) and on monotherapy PDE5i or ERA at baseline [43] . The treatment difference was driven by delayed disease progression. On the whole, the evidence for the use of oral treprostinil is conflicting, and its place in clinical practice remains unclear, particularly without any distinctive benefit in the contemporary setting, where upfront combination therapy is now the standard of care.

The recommended starting dose for treprostinil diolamine is 0.25 mg twice daily or 0.125 mg three times daily and is typically increased every 3-4 days as tolerated [39] . Three times daily dosing is preferred in order to avoid large swings in serum drug levels. A large peak:trough ratio may result in increased adverse effects and limit the max daily dose achieved. Furthermore, patients may also experience prolonged periods at low drug levels [69] . Common adverse effects include diarrhea, headache, nausea, flushing, jaw pain, fatigue, and myalgias [39, 70] . Strategies to improve drug tolerability and cut down on the severity of dose-limiting side effects include [1] three times daily dosing; [2] dose titration in increments no greater than 0.125 mg, which can be initiated with one dose first (usually the evening dose); and [3] extending the intervals between dose titrations to allow patients more time to acclimate to the effects of the medication [69] (Fig. 1) . The oral bioavailability of treprostinil diolamine is~17% and should be administered with a 250-cal meal containing 30-50% fat to enhance drug absorption [71] . As with other PAHspecific therapies, abrupt discontinuation of treatment should be avoided. The dose may be reduced in increments of 0.5-1 mg per day, with consideration for tablet strength, as tablets may not be cut or crushed [39] .

The other orally available agent targeting the PGI 2 pathway, selexipag, received FDA approval in 2015. Selexipag is a selective prostacyclin receptor (IP receptor) agonist [37, 72] recommended for use in WHO-FC II-III PAH patients [57] . In the 2015 GRIPHON trial, the primary endpoint of morbidity and mortality occurred in significantly fewer patients on selexipag compared to those in the placebo arm. Study patients were predominantly WHO-FC II-III and on concomitant ERA and/or PDE5i therapy. The treatment effect was driven primarily by disease progression and hospitalization as a result of worsening PAH. 6MWD was also notably improved in the selexipag group. However, selexipag did not significantly reduce all-cause mortality [38] .

The starting dose of selexipag is 200 mcg twice daily. This is typically increased by 200 mcg twice daily at weekly intervals to the highest dose tolerated by the patient up to a maximum dose of 1600 mcg twice daily. Common adverse effects include headache, diarrhea, nausea, flu-like symptoms, and flushing [37] . These side effects typically subside with time and may require increasingly longer periods of adjustment as the doses get higher. A single-dose step-up method may also be implemented for patients experiencing difficulty with dose titrations, where the evening dose is increased first before increasing the morning dose a week later. The expectation for maximally tolerated doses should not be that side effects subside completely, but rather the dose at which the patient experiences side effects that are manageable. Side effect management strategies vary by center (Fig. 1) . Once the side effects become intolerable or unmanageable, the dose is decreased by 200 mcg twice daily and parked. This dosing strategy stems from the GRIPHON trial, which saw all maximally tolerated doses demonstrate similar efficacy for the composite primary endpoint.

Ralinepag is another selective IP receptor agonist currently undergoing phase 3 clinical trials (https://clinicaltrials.gov/ ct2/show/NCT03626688). In the phase 2 clinical trial, ralinepag significantly reduced PVR in PAH patients on background PAH-specific therapies [73] . The extendedrelease formulation being tested in the ongoing phase 3 trial provides the advantage of once daily dosing. Phase 3 study results are expected in 2021-2022 (https://clinicaltrials.gov/ ct2/show/NCT03626688).

As our understanding of PAH further develops, coupled with expanding research, development, and clinical experience with novel PAH-specific therapies, the paradigm for the optimal management of PAH has shifted in recent years. Combination therapy, targeting the NO, ET-1, and PGI 2 pathways, has emerged as the contemporary standard of care in treatment of PAH patients. Historically, combination therapy was implemented in a sequential method based on baseline and subsequent FC, as well as hemodynamic assessments. The AMBITION trial, published in 2015, was a randomized, controlled trial in WHO-FC II-III PAH, treatment naïve patients comparing combination therapy with tadalafil 40 mg daily and ambrisentan 10 mg daily versus tadalafil or ambrisentan monotherapy. The primary endpoint was the first event of clinical failure, time to clinical failure (TTCF), defined as the first occurrence of a composite of death, hospitalization for worsening PAH, disease progression, or unsatisfactory long-term clinical response. Patients started on combination therapy had a significantly longer TTCF (HR 0.50, 95% CI: 0.35-0.72; p < 0.001) [20] . The 2015 European Society of Cardiology/European Respiratory Society (ESC/ ERS) guidelines assigned class I recommendations for combination therapy with the following: macitentan and sildenafil (based on the SERAPHIN trial) [31] , riociguat and bosentan (based on the PATENT-1 trial) [34] , and selexipag and PDE5i or ERA therapy (based on the GRIPHON trial) [38] . Other dual therapy combinations were given a lower level of evidence recommendation [57] .

However, despite a decrease in TTCW, many patients continue to experience worsening symptoms, clinical deterioration, and limited functional status. This has naturally given way to exploring the effects of triple combination therapy on patient outcomes. Three main studies have looked at triple therapy. The first trial, a small pilot study of 19 patients, initiated combination therapy with IV epoprostenol, bosentan, and sildenafil. Overall, the patients had improvements in 6MWD, hemodynamics, FC, and survival [74] . Secondly, the GRIPHON trial demonstrated benefit in adding on selexipag to ERA and PDE5i background therapy [38] . In the GRIPHON trial, 14.7% of patients were on PDE5i monotherapy, 32.4% on ERA monotherapy, and 32.5% on both ERA and PDE5i therapy. Within the pre-specified subgroup analysis, the benefit in the primary outcome was still present within the dual therapy group [38] . Thirdly, the TRITON trial provides more information regarding combination therapy (https://clinicaltrials.gov/ct2/show/NCT02558231). The TRITON study is a multicenter, double-blind, placebocontrolled, phase 3b study with newly diagnosed, treatmentnaïve PAH patients randomized to upfront triple or initial double therapy. Macitentan and tadalafil were initiated at randomization, and selexipag or placebo was added at day 15 (and subsequently uptitrated until week 12). The primary endpoint was change in PVR at week 26. Initial triple and initial double therapy reduced PVR by 54% and 52%, respectively, with no difference between the groups. In addition, both groups saw improvement in 6MWD and NT-proBNP, as well as no worsening in FC, with no difference between groups. Discontinuation rates due to adverse effects were similar between the initial triple and initial dual combination groups (https://www.atsjournals.org/doi/abs/10.1164/ajrccmconference.2020.201.1_MeetingAbstracts.A2928). This raises concern about the role and value of upfront initial triple combination therapy in Group 1 PAH.

As the body of evidence for combination therapy grows, it is important to consider individualized strategies to achieve adequate combination therapies while minimizing adverse side effects that may lead to therapy discontinuation (Fig. 1) . Some of these strategies include staggered therapy initiation and dose titrations, frequent monitoring, and aggressive management of adverse drug reactions [75] . It is essential for clinicians to adapt and tailor recommendations as more data becomes available and to determine the optimal approach to the pharmacologic management of PAH.

When determining the optimal therapeutic approach for PAH patients, there are several best practice guidelines from the ESC/ERS, CHEST, and the World Symposium of Pulmonary Hypertension (WSPH) [6, 57, 76] . Risk is routinely assessed through ECS/ERS and REVEAL 2.0 risk calculators with therapies tailored accordingly [57, 77] . There are currently 14 FDA-approved therapies in the USA, and therapeutic changes may be appropriate months to years after initiation to accommodate clinical status and patient-specific needs.

Once an accurate assessment of all PH risks has been completed, appropriate diagnostic tests have been performed, and WHO Group 1 PAH confirmed, a determination should be made as to whether the patient is high, intermediate, or low risk (Figs. 2 and 3) . The ESC/ERS and REVEAL 2.0 risk categorization guides are frequently used to guide initial therapy class choices [57, 77] . These risk assessments include clinical evaluation for signs of right heart failure, WHO-FC assessment, laboratory values (viz., NT-proBNP levels), imaging findings, and hemodynamics, in addition to the etiology of PAH.

For a new diagnosis of PAH, the 6th WSPH recommends upfront dual combination therapy with an ERA and PDE5i [76] . Although preferable, simultaneous initiation of an ERA and PDE5i can be challenging. Many programs initiate a PDE5i, and within a few days or weeks, rapidly initiate an ERA if upfront dual combination therapy is not feasible (Fig. 3) . Follow-up visits should be scheduled within weeks of therapy initiation to discuss any side effects, as well as provide an opportunity to review the disease state, questions, management of comorbidities, and other supportive measures such as oxygen and diuretics. REMS considerations, if applicable, should also be reviewed. Separating the initiation of a PDE5i and an ERA, even by a few days, often not only helps to facilitate insurance approval of the ERA but also helps to identify adverse effects from a specific therapy. If a PDE5i is not tolerated or is contraindicated, riociguat is preferred and will require additional time for titration. In addition, it may be reasonable to switch from a PDE5i to riociguat in patients who remain at intermediate risk based on the REPLACE trial (Fig.  3) (https://pharmaceutical-business-review.com/news/bayeradempas-phase-4-trial/).

In a low-to-intermediate risk patient on combination therapy, reassessment within 3 months is preferred to evaluate goals, functional response to therapy, and possible need for prostacyclin therapy (Fig. 4) . It is important to continually reassess diagnosis and other risk factors for PH, ensure comorbidities are optimally managed, and review medication (Table 4 ). In a high risk but stable patient, as often indicated by first visit in an ambulatory setting as opposed to the hospital, dual combination therapy is rapidly initiated. Using shared decision-making considers the preferred route of prostanoid therapy early on in the care of the patient. When initiation of a parenteral prostanoid is indicated, prescribing considerations include geographic distance from their PAH care center, social circumstances including availability of support person, patient dexterity, and risk profile for infection.

Patient tolerability, both physically and financially, should be considered. In the USA, we remain subject to insurance formularies, hospital availability, and patient cost sharing. Clinicians play an important role in advocating on behalf of patients for insurance approval of PAH-specific therapies (Table 5 ). However, this requires dedication of additional time and resources and more importantly, can delay time to initiation of therapy for up to a month or more. Each patient case should be individualized according to the risk assessment, medication preference (taking into consideration comorbidities), and potential cost hurdles based on experience with insurance formularies.

While pharmacotherapy remains the cornerstone of treatment, PAH remains a progressive, fatal disease with a fair amount of heterogeneity in response to pharmacotherapy [78] . Several non-pharmacologic options have been explored as adjunct therapies and have shown improvement in hemodynamics and quality of life in high risk PAH populations in small clinical experiences [79] [80] [81] [82] . However, given the lack of data surrounding these techniques, non-pharmacologic therapies discussed in this section are largely considered palliative or a bridge to transplantation at this point.

Balloon atrial septostomy involves the creation of a rightto-left shunt using percutaneous balloon dilations across the interatrial septum, reducing right ventricular pressure and volume. This consequentially increases cardiac output which augments systemic oxygen transport despite decreasing systemic oxygen saturation [80, 83] . The idea behind creation of an interatrial shunt dates back to the 1980s when patients with patent foramen ovale and PAH with resultant right-to-left shunting were noted to have improved survival compared to those without shunting [84] . Decades following this discovery, the precise role for atrial septostomy remains uncertain, and data regarding its use largely comes from small case series and case reports. The most recent data available suggests a hemodynamic and symptomatic benefit in patients with WHO-FC IV symptoms due to right sided heart failure despite optimal pharmacologic therapy [80, 82, 85] . In this patient population, patients were noted to have increased cardiac index, decreased right atrial pressure, and improvement in 6MWD following atrial septostomy. However, the impact of atrial septostomy on long-term survival has not been established, and current guidelines recommend considering atrial septostomy only as a palliative or bridging measure in experienced centers [86] . Furthermore, baseline right atrial pressures of > 20 mmHg or resting arterial oxygen saturations < 85% are contraindications to atrial septostomy due to the hemodynamic alterations that occur following the procedure. and management remains important to patient-centered care (especially in those with overlapping cardiac and/or lung disease). Monotherapy may be appropriate for some. Patients should be counseled that PAH-specific therapies oftentimes do no immediately improve symptoms or functional status and may take weeks or months to notice improvement. Oxygen, diuretics, and other supportive therapies remain important in reaching low risk status. Vasoreactivity should always be assessed when appropriate (i.e., idiopathic, familial, or drug/toxin-induced PH), and CCB therapy initiated as indicated. A more convenient therapy does not always equate to improved tolerability.

Side effects of one medication within a drug class may not be as frequent or severe with another medication within the same therapeutic class. Connective tissue disease patients often have overlapping interstitial lung disease. Use extra caution and monitor closely for side effects and deterioration with vasodilators. Toxin-induced patients, particularly those currently using methamphetamines, may struggle with medication compliance and adherence to REMS requirements. Initiation of medications with REMS requirements need to be carefully considered, particularly in women of child-bearing potential and the ability to reliably perform monthly pregnancy testing. 

Initially described decades ago for the management of certain congenital heart diseases, a Potts anastomosis/shunt involves a surgical anastomosis of the left pulmonary artery to the descending aorta via a left thoracotomy. More recently, a technique for transcatheter Potts shunt creation was also described, though data regarding this approach is sparse [87] . A Potts shunt creates a right-to-left shunt that theoretically avoids arterial oxygen desaturation above the level of the anastomosis, sparing cerebral and coronary circulation. Thus far, the most robust evidence for Potts shunting as an adjunctive treatment in PAH is in children. A small case series of 24 children undergoing surgical Potts anastomosis (ages 1.5-17 years) 

Similar to renal denervation for systemic hypertension, modification of sympathetic pulmonary innervation has been proposed as a potential target for pulmonary arterial hypertension therapy. While results from animal models demonstrating the role of sympathetic tone in pathogenesis and as a potential target for intervention have been promising, relevance to human disease remains unproven [89, 90] . A first-in-man, single center study of 13 patients undergoing pulmonary arterial denervation demonstrated significant reduction in mean PAP, NT-proBNP, and improvement in 6MWD, pulmonary arterial compliance, and functional capacity compared to a control group at 3 months [91] . Additionally, no major complications of the procedure were reported. In the multicenter, open-label TROPHY trial, intravascular ultrasound pulmonary artery denervation decreased PVR and was associated with an improved 6MWD [92] . While these results are encouraging, further investigation and confirmation of these findings are required before this strategy can be adopted into clinical practice.

Atrial septal defects (ASDs) are among the most common of congenital heart diseases, and PAH has been associated with ASDs in 4-34% of patients [93, 94] . Based on the most 2018 AHA/ACC guideline for the management of adults with congenital heart disease, closure of an ASD is currently indicated to reduce right atrial and right ventricular pressure/volume if there is evidence of right-sided enlargement and net left-to-right shunting with pulmonary-systemic blood flow ratio (Qp:Qs) > 1.5, provided the PAP is less than 50% of systemic blood pressure and PVR is less than one-third of the systemic vascular resistance (Class I, Level of Evidence B) [95] . Closure of an ASD in adults with PAP greater than two-thirds systemic pressure, PVR greater than two-thirds systemic, or net right-toleft shunting is not recommended (Class III, level of evidence C) [95] . However, there are no set guidelines regarding atrial septal defect closure in the presence of net left-to-right shunting with PAP or PVR between one-half and two-thirds systemic pressure or resistance [95] . Despite the lack of conclusive data, pulmonary vasodilator testing is generally recommended in this scenario for patients with a baseline pulmonary vascular resistance index (PVRI) of 6-9 WU*m2. A 20% decrease in PVR, a 20% decrease in pulmonary vascular resistance:systemic vascular resistance (PVR:SVR) ratio, a final PVRI < 6 WU*m2, and final PVR:SVR ratio < 33% with vasodilator challenge likely indicate a favorable response after atrial septal defect closure, though this is largely based on small case series and expert consensus [96] .

While medical therapies for PAH have made great strides in recent years, lung transplantation remains an important therapy for patients with severe disease refractory to medical therapy. Although transplantation for PAH is a relatively rare indication (~5% of all lung transplants) compared to COPD PH exist -Therapies often may only be filled at a specific specialty pharmacy or may be less expensive at payer-preferred pharmacies which can be less convenient Medication cost -Medication price is often not readily available to prescribers and may first require prior authorization and then coordination with pharmacy and/or insurance to assess affordability -Generics may cost more out-of-pocket if a copay card is available through the branded drug manufacturer -Copay cards offered by drug manufacturers are restricted to commercial patients only (cannot be used with Medicare, Medicaid, Tricare, etc.) -Encourage patient to consider total yearly out-of-pocket costs as monthly expenses may fluctuate throughout the year and satisfy various insurance structures including: • Annual deductibles • Maximum out-of-pocket for commercial insurance • Coverage gap (i.e., donut hole) and catastrophic coverage for Medicare Patient assistance (primarily based on financial need) -Additional financial support may be available and requires patient effort and initiative. Often entails formal income and residency verification. Examples include: • Non-profit grants primarily for Medicare patients • Manufacturer assistance for branded therapies if grants are not available • Specialty pharmacy assistance in select cases (patient must ask pharmacy) -Uninsured patients or those who have received an insurance denial and subsequent appeal denial for a branded therapy for an FDA-approved indication may qualify for patient assistance through the manufacturer at zero cost or interstitial lung disease, referral is appropriate when the patient's predicted 2-3-year survival is estimated to be < 50% [57] . Perioperative risk is minimized with early referral before severe cardiac dysfunction and hepatic congestion develop. Widely accepted criteria for the referral for transplant evaluation consist of the following:

& WHO-FC III of IV symptoms despite maximal medical therapy & A markedly low (< 350 m) or declining 6MWD & Cardiac index of < 2 L/min/m 2 & Central venous pressure ≥ 15 mmHg Listing for lung transplantation is appropriate with deterioration of functional status and hemodynamics. Not all patients with PAH, however, are candidates for transplantation, and the usual contraindications (active/recent malignancy, substance abuse, poor social support, non-adherence) still apply. Since 2005, organs in the USA have been allocated under a new system called the Lung Allocation Score, or LAS. It serves as a severity of illness score ranging from 0 (well) to 100 (ill). The LAS weighs the probability of death in 1 year without transplant against the probability of death 1 year posttransplant. The purpose of implementing the LAS was to decrease deaths on the wait list, and it lowered wait-list mortality for all etiologies of lung failure except PAH. These changes relatively disadvantaged patients with PAH from getting an organ with some evidence of increased wait-list mortality [97, 98] . This led to LAS exceptions relating to evidence of worse prognosis, specifically cardiac dysfunction (elevated central venous pressure and/or low cardiac index) [98] .

The overwhelming majority of patients receiving lung transplantation for PAH receive bilateral lung transplants (BLT) rather than single lung transplants (SLT), although the evidence to support this practice is fairly weak. Proponents of SLT cite the benefits of lower perioperative morbidity, improved graft function, and more equitable organ allocation, while proponents for BLT argue for possible improved longterm survival, and patients are easier to manage in both the early and late term due to less V/Q mismatching. Despite the controversy, the overwhelming majority of patients (91%) with PAH receive BLT with good results [99] . Heart-lung transplantation is an option for patients with end-stage PAH and severe cardiac dysfunction. It is usually reserved for patients with PAH related to congenital heart disease and represents < 2% of lung transplants [99] . In general, patients with PAH have higher perioperative risks, and conditional survival (at 1 year) is superior to COPD and interstitial lung disease.

As previously stated, currently available therapies for treating PAH target endothelial cell dysregulation and smooth muscle cell tone and proliferation through three mechanistic pathways: the ET-1 pathway, the NO pathway, and the PGI 2 pathway [1, 100] . However, pathologic mechanisms leading to the characteristic histologic findings and dysfunctional pulmonary vascular endothelium in PAH are complex and include dysregulated inflammation with immune activation, oxidative stress, an imbalance of proliferative and anti-proliferative signaling, growth factor activation, dysfunctional metabolism, and altered hormonal signaling [101, 102] . Recent efforts have focused on exploiting the multiple mechanisms leading to pulmonary vascular remodeling seen in PAH to develop novel therapeutics. Various pathways for target include suppressing inflammation and modulating the immune response, altering oxidant stress mechanisms, restoring the balance between pro-proliferative and antiproliferative signaling, and targeting growth factor signaling pathways pertinent to BMPR2 regulation [101, 103, 104] .

Sustained inflammation and immune activation lead to increased cytokine and chemokine production with subsequent perivascular infiltration of macrophages, granulocytes, mast cells, dendritic cells, B and T lymphocytes, and natural killer T cells [101] . There is evidence that the presence of soluble factors and cell surface molecules (i.e., IL-1, IL-6, TNF-α, CRP, and MCP-1) and activation of signaling pathways play critical roles in promoting vascular remodeling, portend a worse prognosis, and may serve as biomarkers of disease progression or, importantly, future therapeutic options [105] [106] [107] [108] [109] [110] . Recent studies have examined anakinra and tocilizumab, IL-1 and IL-6 receptor antagonists, respectively, for their use in PAH. The safety and feasibility of anakinra was investigated in a small, single-arm open label study [111] . Although the study was not designed to show improvement in clinical or functional outcomes, the authors were able to demonstrate nonsignificant improvements in clinical heart failure symptoms, lower IL-6 levels, and an inverse relationship between high sensitivity C-reactive protein levels and peak oxygen consumption. Tocilizumab was also shown to be a safe and feasible treatment option in PAH patients and demonstrated reduced C-reactive protein levels but failed to show a treatment effect in any of the measured clinical endpoints in a small exploratory open-label study [112] . These authors were able to provide clear proof of principle, safety, and feasibility data that support conducting future studies with a focus on clinically meaningful endpoints. Plasmablasts in idiopathic PAH have shown clonality similar to that observed in autoimmune diseases, and the CD-20 antibody, rituximab, has been studied for safety and efficacy of B cell depletion in systemic sclerosis associated-PAH; the safety profile was promising, and there were trends toward clinical improvements [113, 114] .

Mitochondrial generation of reactive oxygen species have been implicated in the development of PAH; inhibition of oxidative stress mechanisms has been proposed to attenuate pulmonary vascular remodeling seen in PAH [115, 116] . Bardoxalone methyl activates Nrf2, a transcription factor that regulates the expression of antioxidant proteins and suppresses the activation of the pro-inflammatory NFκB pathway, and has shown promising results. In the multicenter, phase 2 LARIAT trial, patients with PAH on stable background therapy and WHO-FC II or III were assigned to bardoxalone methyl or placebo (https://clinicaltrials.gov/ct2/ show/NCT02036970). After 16 weeks of therapy, there was a significant improvement 6MWD in the treatment group as compared to the placebo group. The follow-up CATALYST and RANGER were discontinued during the COVID19 pandemic, and it was noted that bardoxalone was unlikely to meet its primary endpoint in the study (6MWD) (https:// clinicaltrials.gov/ct2/show/NCT02657356, https:// clinicaltrials.gov/ct2/show/NCT03068130, https:// pulmonaryhypertensionnews.com/2020/04/01/reata-stopspah-bardoxolone-trials-amid-covid-19-concerns/). Impaired BMPR2 signaling is the most common genetic mechanism implicated in PAH and contributes to the development of pulmonary vascular disease through exaggerated TGF-β signaling [117] . Because the BMPR2 receptor is a TGF-β receptor subtype, targeting TGF-β signaling with sotatercept, an activin receptor type 2A fusion protein that acts as a ligand trap to competitively bind and neutralize TGF-β ligands, is an exciting therapeutic prospect that attenuates PAH through reversing pulmonary artery remodeling, improving RV geometry, and restoring RV function in one preclinical model [118] [119] [120] . In the recently completed PULSAR trial, 106 patients with PAH on baseline therapies were treated with sotatercept or placebo (https://clinicaltrials.gov/ct2/ show/NCT03496207). Preliminary results indicate that after 6 weeks, there were improvements in right heart strain, exercise capacity, and a statistically significant reduction in PVR compared to placebo. The SPECTRA study is underway to examine the effects of sotatercept in adults with PAH and WHO-FC III symptoms (https://clinicaltrials.gov/ ct2/show/NCT03738150).

Modification of abnormal growth factor signaling in PAH is an area of active interest; tyrosine kinase inhibitors have shown mixed results in the treatment of PAH [103] . Imatinib demonstrated an improvement in exercise capacity and hemodynamics in the IMPRES trial but disappointingly had serious adverse events (subdural hemorrhage in patients receiving vitamin K antagonists) that prevented further use in the treatment of PAH [121, 122] . GB002 is an inhaled nonselective inhibitor of platelet-derived growth factor receptor-α and -β that showed a reduced right ventricular systolic pressure and mean PAP, as well as reduced pulmonary arteriolar muscularization, restoration of BMPR2 signaling, and reduced NT-proBNP and cytokine levels in GB002-treated animals [123] . A phase 1 trial to investigate safety, pharmacokinetics, and pharmacodynamics of GB002 in patients with PAH is currently underway (https://clinicaltrials.gov/ct2/ show/NCT03926793). Given the wide range of possibilities for developing novel therapies that modulate underlying pathobiological mechanisms underpinning this disease, future researchers must collaborate to prioritize pre-clinical and clinical studies of new therapeutics.

More than 75% of all cases of PH are attributed to left heart disease or chronic lung diseases [124, 125] . Despite the fact that PAH only accounts for 3% of all cases of PH, significant efforts to understand the pathologic mechanisms underpinning PAH have been undertaken, which have led to the development of investigational novel therapies targeting implicated pathogenic pathways [103] . There is much need for a similar approach to PH in left heart disease and chronic lung disease-associated PH.

Pulmonary hypertension in left heart disease and chronic lung disease-associated pulmonary hypertension encompass heterogeneous groups of multiple diseases that portend a poor prognosis [126, 127] . Pulmonary hypertension in left heart disease includes HFrEF, HFpEF, valvular heart disease, and heart disease resulting from chronic arrhythmias [128] . The traditional thinking is that PH in left heart disease results from passive pulmonary vascular congestion related to increased left-sided filling pressures (defined hemodynamically as isolated post-capillary PH with mean PAP > 20 mmHg, pulmonary arterial wedge pressure (PAWP) > 15 mmHg, and a PVR < 3 WU). However, in some instances, the elevated left-sided pressures do not completely account for remodeling that may develop over time and thus lead to combined pre-and postcapillary PH (defined hemodynamically as mean PAP > 20 mmHg, PAWP > 15 mmHg, and a PVR > 3 WU that resembles the "pulmonary vascular phenotype" of PAH (with mean PAP > 20 mmHg, PAWP < 15 mmHg, and a PVR > 3 WU) [128] . Chronic lung disease-associated PH occurs most commonly in COPD and interstitial lung diseases and although is defined by the same hemodynamic properties as PAH (pre-capillary PH or a "pulmonary vascular phenotype"), it represents independent complex and multifactorial pathologic processes [129] . It is not surprising then that defining these groups solely based on strict hemodynamic definitions is problematic. To date, most studies using currently available advanced therapies (i.e., pulmonary vasodilators) in PH in left heart disease have focused on patients with HFrEF and isolated post-capillary PH; all such studies have been negative, or proved to be harmful [126, 128] . Studies of pulmonary vasodilators in chronic lung disease-associated PH have been limited to patients with COPD or idiopathic pulmonary fibrosis, only one of the many subtypes of fibrosing lung diseases. While mostly disappointing, recent studies using inhaled NO [130] and inhaled treprostinil showed promising results in patients with idiopathic pulmonary fibrosis and any form of interstitial lung disease, respectively (https:// clinicaltrials.gov/ct2/show/NCT02630316).

If we are to advance our understanding of the pathophysiology of and treatment options for PH in left heart disease and chronic lung disease-associated PH, we need to focus attention on defining clinical and hemodynamic sub-phenotypes, discovering disease-specific biomarkers, establishing scoring and risk stratification systems, and developing carefully controlled trials that do not exclude disease subtypes (such as HFpEF, left heart disease with combined pre-and postcapillary PH, undefined subtypes of idiopathic interstitial pneumonias, or other chronic lung diseases) [126, 129] . Improved understanding and effective treatments of WHO Groups 2 and 3 PH must include a multimodality approach that combines currently available disease-specific standard of care therapies with novel therapies targeting the underlying pathology that leads to PH.

The management of PAH is increasingly complex. Specialized centers are best suited to provide the comprehensive care management required. With the growing number of therapeutics clinically available, intimate knowledge of pharmacology and side effects is integral to providing optimal care for this vulnerable and high-risk patient population. In addition, patients with PAH often present with multiple comorbidities further complicating management or even call to question the type of PH. Interventional strategies remain largely palliative in nature or serve as a bridge to transplantation.

Funding Dr. Ryan and his research is supported by funding from The Reagan Corporation, The Gordon Family, and The Cushman Family.

Conflict of Interest Irene Pan, John Dechand, Josh Jacobs, Tara Jones, Stephen McKellar, Emily Beck and Nathan Hatton declare that they have no conflict of interest.

John Ryan has received speaker honorarium from Janssen and Bayer and has provided consulting services for Janssen and Bayer.

Jennalyn Mayeux has received speaker honorarium from Janssen and has participated in an advisory board for Bayer.

Human and Animal Rights and Informed Consent This article does not contain any studies with human or animal subjects performed by any of the authors.

Pulmonary arterial hypertension: pathogenesis and clinical management

A concerning trend for patients with pulmonary hypertension in the era of evidence-based medicine

Cellular and molecular pathobiology of pulmonary arterial hypertension

Pathways in pulmonary arterial hypertension: the future is here

The role of calcium channel blockers for the treatment of pulmonary arterial hypertension: how much do we actually know and how could they be positioned today

Therapy for pulmonary arterial hypertension in adults: update of the CHEST guideline and expert panel report

Amlodpine (Norvasc). package insert

Long-term response to calcium channel blockers in idiopathic pulmonary arterial hypertension

Nifedipine (Procardia XL). package insert

The effect of high doses of calcium-channel blockers on survival in primary pulmonary hypertension

Diltiazem (Cardizem). package insert. Bridgewater: Bausch Health

Sildenafil (Revatio). package insert

Sildenafil citrate therapy for pulmonary arterial hypertension

Sildenafil versus endothelin receptor antagonist for pulmonary hypertension (SERAPH) study

A randomized, placebo-controlled, double-blind, crossover study to evaluate the efficacy of oral sildenafil therapy in severe pulmonary artery hypertension

Addition of sildenafil to long-term intravenous epoprostenol therapy in patients with pulmonary arterial hypertension: a randomized trial

Sildenafil dosed concomitantly with bosentan for adult pulmonary arterial hypertension in a randomized controlled trial

Adcirca). package insert. Indianapolis: Eli Lilly

Tadalafil therapy for pulmonary arterial hypertension

Initial use of ambrisentan plus tadalafil in pulmonary arterial hypertension

Ambrisentan for the treatment of pulmonary arterial hypertension: results of the ambrisentan in pulmonary arterial hypertension, randomized, double-blind, placebo-controlled, multicenter, efficacy (ARIES) study 1 and 2

Bosentan (Tracleer). package insert

Effects of the dual endothelin-receptor antagonist bosentan in patients with pulmonary hypertension: a randomised placebo-controlled study

Bosentan therapy for pulmonary arterial hypertension

Combination of bosentan with epoprostenol in pulmonary arterial hypertension: BREATHE-2

Bosentan therapy in patients with Eisenmenger syndrome: a multicenter, double-blind, randomized, placebo-controlled study

Treatment of patients with mildly symptomatic pulmonary arterial hypertension with bosentan (EARLY study): a double-blind, randomised controlled trial

Bosentan added to sildenafil therapy in patients with pulmonary arterial hypertension

South San Francisco: Actelion

Macitentan and morbidity and mortality in pulmonary arterial hypertension

Macitentan for the treatment of inoperable chronic thromboembolic pulmonary hypertension (MERIT-1): results from the multicentre, phase 2, randomised, double-blind, placebo-controlled study

Riociguat (Adempas). package insert. Whippany: Bayer

Riociguat for the treatment of pulmonary arterial hypertension

Riociguat for the treatment of chronic thromboembolic pulmonary hypertension

PATENT PLUS: a blinded, randomised and extension study of riociguat plus sildenafil in pulmonary arterial hypertension

Selexipag (Uptravi). package insert

Selexipag for the treatment of pulmonary arterial hypertension

Oral treprostinil for the treatment of pulmonary arterial hypertension in patients on background endothelin receptor antagonist and/or phosphodiesterase type 5 inhibitor therapy (the FREEDOM-C study): a randomized controlled trial

Oral treprostinil for the treatment of pulmonary arterial hypertension in patients receiving background endothelin receptor antagonist and phosphodiesterase type 5 inhibitor therapy (the FREEDOM-C2 study): a randomized controlled trial

Efficacy and safety of oral treprostinil monotherapy for the treatment of pulmonary arterial hypertension: a randomized, controlled trial

Combination therapy with oral treprostinil for pulmonary arterial hypertension. A double-blind placebo-controlled clinical trial

Epoprostenol (Veletri). package insert

Treatment of primary pulmonary hypertension with continuous intravenous prostacyclin (epoprostenol). Results of a randomized trial

A comparison of continuous intravenous epoprostenol (prostacyclin) with conventional therapy for primary pulmonary hypertension

Continuous intravenous epoprostenol for pulmonary hypertension due to the scleroderma spectrum of disease. A randomized, controlled trial

Continuous subcutaneous infusion of treprostinil, a prostacyclin analogue, in patients with pulmonary arterial hypertension: a double-blind, randomized, placebo-controlled trial

Exercise improvement and plasma biomarker changes with intravenous treprostinil therapy for pulmonary arterial hypertension: a placebo-controlled trial

Addition of inhaled treprostinil to oral therapy for pulmonary arterial hypertension: a randomized controlled clinical trial

Iloprost (Ventavis). package insert

Inhaled iloprost for severe pulmonary hypertension

Randomized study of adding inhaled iloprost to existing bosentan in pulmonary arterial hypertension

Combining inhaled iloprost with bosentan in patients with idiopathic pulmonary arterial hypertension

ESC/ERS guidelines for the diagnosis and treatment of pulmonary hypertension: the joint task force for the diagnosis and treatment of pulmonary hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS): endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC), International Society for Heart and Lung Transplantation (ISHLT)

Expression of endothelin-1 in the lungs of patients with pulmonary hypertension

Medical treatment of pulmonary arterial hypertension. Semin Respir Crit Care Med

Prostanoids for pulmonary arterial hypertension

An imbalance between the excretion of thromboxane and prostacyclin metabolites in pulmonary hypertension

Transitioning Between Prostanoid Therapies in Pulmonary Arterial Hypertension

High-dose calcium channel-blocking therapy for primary pulmonary hypertension: evidence for long-term reduction in pulmonary arterial pressure and regression of right ventricular hypertrophy

Long-term response to calcium-channel blockers in nonidiopathic pulmonary arterial hypertension

Sildenafil (Viagra). package insert

Fe ld m a n J P. Phosphodiesterase-5 inhibitors in management of pulmonary hypertension: safety, tolerability, and efficacy. Drug Healthc Patient Saf

RESPITE: switching to riociguat in pulmonary arterial hypertension patients with inadequate response to phosphodiesterase-5 inhibitors

Long-term results of the DelIVery for pulmonary arterial hypertension trial

Recommendations for the use of oral treprostinil in clinical practice: a Delphi consensus project pulmonary circulation

Oral treprostinil in the treatment of pulmonary arterial hypertension

The effect of different meal compositions on the oral bioavailability of treprostinil diolamine in healthy volunteers

Pharmacokinetics and tolerability of the novel oral prostacyclin IP receptor agonist selexipag

Efficacy and safety of ralinepag, a novel oral IP agonist, in PAH patients on mono or dual background therapy: results from a phase 2 randomised, parallel group, placebo-controlled trial

Upfront triple combination therapy in pulmonary arterial hypertension: a pilot study

Pulmonary arterial hypertension: combination therapy in practice

An overview of the 6th World Symposium on Pulmonary Hypertension

Predicting survival in patients with pulmonary arterial hypertension: the REVEAL risk score calculator 2.0 and comparison with ESC/ERS-based risk assessment strategies

Survival in patients with idiopathic, familial, and anorexigen-associated pulmonary arterial hypertension in the modern management era

Interventional and surgical therapeutic strategies for pulmonary arterial hypertension: beyond palliative treatments

Graded balloon dilation atrial septostomy in severe primary pulmonary hypertension. A therapeutic alternative for patients nonresponsive to vasodilator treatment

Atrial septostomy improves survival in select patients with pulmonary hypertension

Atrial septostomy in treatment of end-stage right heart failure in patients with pulmonary hypertension

Interventional and surgical modalities of treatment for pulmonary arterial hypertension

Factors that influence the outcome of primary pulmonary hypertension

Balloon atrial septostomy in pulmonary arterial hypertension: effect on survival and associated outcomes

Updated treatment algorithm of pulmonary arterial hypertension

Transcatheter Potts shunt creation in patients with severe pulmonary arterial hypertension: initial clinical experience

Palliative Potts shunt for the treatment of children with drug-refractory pulmonary arterial hypertension: updated data from the first 24 patients

Pulmonary artery denervation attenuates pulmonary arterial remodeling in dogs with pulmonary arterial hypertension induced by dehydrogenized monocrotaline

Transthoracic pulmonary artery denervation for pulmonary arterial hypertension

Pulmonary artery denervation to treat pulmonary arterial hypertension: the single-center, prospective, first-in-man PADN-1 study (first-in-man pulmonary artery denervation for treatment of pulmonary artery hypertension)

Intravascular ultrasound pulmonary artery denervation to treat pulmonary arterial hypertension (TROPHY1): multicenter, Early Feasibility Study

Pulmonary arterial hypertension in adults born with a heart septal defect: the euro heart survey on adult congenital heart disease

Incidence of secondary pulmonary hypertension in adults with atrial septal or sinus venosus defects

AHA/ACC guideline for the Management of Adults with Congenital Heart Disease: executive summary: a report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines

Atrial septal defect with pulmonary hypertension: when/how can we consider closure?

International guidelines for the selection of lung transplant candidates: 2006 update-a consensus report from the Pulmonary Scientific Council of the International Society for Heart and Lung Transplantation

Impact of the lung allocation score on lung transplantation for pulmonary arterial hypertension

The registry of the International Society for Heart and Lung Transplantation: thirtythird adult lung and heart-lung transplant report-2016; focus theme: primary diagnostic indications for transplant

Treatment of pulmonary arterial hypertension

New molecular targets of pulmonary vascular remodeling in pulmonary arterial hypertension: importance of endothelial communication

Pathology and pathobiology of pulmonary hypertension: state of the art and research perspectives

Clinical trial design and new therapies for pulmonary arterial hypertension

Current and future treatments of pulmonary arterial hypertension

Ectopic upregulation of membrane-bound IL6R drives vascular remodeling in pulmonary arterial hypertension

Interleukin-6 overexpression induces pulmonary hypertension

Inflammation in pulmonary arterial hypertension

Proinflammatory signature of the dysfunctional endothelium in pulmonary hypertension. Role of the macrophage migration inhibitory factor/CD74 complex

Blocking macrophage leukotriene b4 prevents endothelial injury and reverses pulmonary hypertension

Leukotriene B4 activates pulmonary artery adventitial fibroblasts in pulmonary hypertension

IL-1 blockade reduces inflammation in pulmonary arterial hypertension and right ventricular failure: a single-arm, open-label, phase IB/II pilot study

Clinical trial protocol for TRANSFORM-UK: a therapeutic open-label study of tocilizumab in the treatment of pulmonary arterial hypertension

Circulating plasmablasts are elevated and produce pathogenic anti-endothelial cell autoantibodies in idiopathic pulmonary arterial hypertension

Safety and efficacy of B-cell depletion with rituximab for the treatment of systemic sclerosis-associated pulmonary arterial hypertension in a multi-center NIH clinical trial

Oxidative stress in severe pulmonary hypertension

Oxidative stress in patients with primary pulmonary hypertension

TGFbeta and BMPR2 signaling in PAH: two black sheep in one family

A selective transforming growth factor-beta ligand trap attenuates pulmonary hypertension

ACTRIIA (sotatercept) reverses pulmonary vascular remodeling to attenuate pulmonary arterial hypertension (PAH) by rebalancing TGF-b/ BMP singaling in a preclinical model

ACTRIIA-fc rebalances BMP and activin/TGF-b signaling to attenuate experimental pulmonary hypertension

Imatinib mesylate as add-on therapy for pulmonary arterial hypertension: results of the randomized IMPRES study

Long-term safety and efficacy of imatinib in pulmonary arterial hypertension

Gb002, a novel inhaled pdgfr kinase inhibitor, demonstrates efficacy in the su5416 hypoxia rad model of pulmonary arterial hypertension (PAH)

Haemodynamic definitions and updated clinical classification of pulmonary hypertension

Pulmonary hypertension: prevalence and mortality in the Armadale echocardiography cohort

Left ventricular heart failure and pulmonary hypertension

Pulmonary hypertension due to interstitial lung disease

Pulmonary hypertension due to left heart disease

Pulmonary hypertension in chronic lung disease and hypoxia

A randomized, double-blind, placebo-controlled study to assess the safety and efficacy of pulsed, inhaled nitric oxide at a dose of 30 mug/kg ideal body weight/hr in subjects at risk of pulmonary hypertension associated with pulmonary fibrosis receiving oxygen therapy

Publisher's Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations