Severe thrombocytopenia in patients with idiopathic pulmonary arterial hypertension provided several strategies for lung transplantation

Case description

A 21-year-old woman was diagnosed with idiopathic pulmonary arterial hypertension (IPAH) at the age of 15 following abnormal electrocardiography findings detected during a routine checkup (Fig. 1a and d). Right heart catheterization revealed the mean pulmonary arterial pressure, right atrial pressure, cardiac index, and pulmonary vascular resistance to be 65 mmHg, 4 mmHg, 2.74 L/min/m², and 13 Wood units, respectively. Her platelet count then was 216,000/µL. She was prescribed tadalafil, followed by ambrisentan and beraprost. Two years later, beraprost was replaced by continuous intravenous epoprostenol therapy. OPEN IN VIEWER

She was listed for bilateral lung transplantation from a brain-dead donor at the age of 19; subsequently, she developed mild thrombocytopenia; within a year, her platelet count decreased to 20,000/µL. We attempted the following additional strategies to ensure maximum support for right heart failure as a therapeutic intervention for thrombocytopenia until lung transplantation (Fig. 1b, e, and k):

Reduction of the epoprostenol dose secondary to a suspicion of epoprostenol-induced thrombocytopenia, following which her platelet count improved to 60,000/µL.

Following lung transplantation, she did not require any further pulmonary vasodilators (Fig. 1c and f). She was maintained on prednisolone and immunosuppressants as required for post-transplantation therapy. Her pulmonary hemodynamics and platelet counts progressively normalized. She is continuing to show good progress at one year following surgery.

Discussion

We presented a case of severe IPAH and thrombocytopenia wherein we attempted to prepare the patient for lung transplantation by several measures including the transition from epoprostenol to treprostinil, intensification of PAH drugs, and administration of TRAs. Post-transplantation, pulmonary hypertension and thrombocytopenia resolved.

PAH is often reported to be complicated by thrombocytopenia, due to several reasons.^1–4 Some conditions responsible for the etiology of PAH may induce platelet aggregation and destruction, resulting in thrombocytopenia. First, congestive splenomegaly may cause thrombocytopenia. Our patient was found to have mild splenomegaly on CT scan and abdominal ultrasound. The spleen size did not show any change following lung transplantation. Platelet counts may decrease with the deterioration of pulmonary hemodynamics as estimated by brain natriuretic peptide (BNP) and transtricuspid pressure gradient (TRPG), although this association is not consistent. It is possible that congestive splenomegaly induced by worsening pulmonary hemodynamics may be one of the critical factors related to thrombocytopenia. Second, one study reported the role of thrombin in the activation and binding of protease-activated receptor-1 on platelets in patients with IPAH. This binding leads to platelet degranulation and adenosine diphosphate release, resulting in platelet aggregation. Moreover, IPAH decreases nitric oxide and soluble guanylyl cyclase production, thus inducing platelet activation and aggregation. ⁵ This may be true in our case as the platelet count increased with a decrease in pulmonary arterial pressure following lung transplantation. Third, microangiopathic thrombocytopenia has been reported to be related to PAH. ⁴ Platelets circulating through the numerous plexiform lesions are often found to be damaged. Fibrin deposition in plexiform lesions on lung pathology and the absence of fibrin deposition on other organs indicate the presence of microangiopathic thrombocytopenia in PAH. ⁴ In our case, lung pathology did not reveal plexiform lesions and fibrin deposition in the pulmonary vessels, suggesting that reasons other than platelet destruction in the microvessels may have been responsible for the condition.

Drug-induced thrombocytopenia, especially with prostacyclin, has been reported in PAH patients.^2,3 Epoprostenol is widely known to be associated with thrombocytopenia. ² Although treprostinil may also induce thrombocytopenia, transitioning from intravenous epoprostenol to treprostinil reportedly improves thrombocytopenia. ³ Epoprostenol has a much higher affinity than treprostinil for the EP3 receptor, which promotes platelet aggregation.^6,7 Thrombocytopenia may be further exacerbated through the platelet EP3 receptor. In our case, thrombocytopenia improved temporarily on switching from epoprostenol to treprostinil and resolved after prostacyclin termination, indicating that drug-induced platelet aggregation may also have contributed to thrombocytopenia.

One study reported ITP-induced thrombocytopenia in some cases with PAH. ¹ Oral prednisolone, intravenous immunoglobulin, or splenectomy were found to yield unsatisfactory results. ¹ In our case, we made a diagnosis of ITP based on elevated PAIgG levels and bone marrow pathology. As described previously, prednisolone administration was not practical. However, TRA increased the platelet count. Our patient is currently on immunomodulators and prednisolone as a part of post-lung transplantation therapy. Hence, it is impossible to rule out ITP as a reason for her thrombocytopenia.

In conclusion, several factors can induce thrombocytopenia in patients with PAH. In our case, PAH etiology, right heart failure, drugs, and ITP may have contributed to severe thrombocytopenia. Considering that the patient’s platelet count returned to normal following lung transplantation and the normalization of pulmonary hemodynamics, it may be inferred that thrombocytopenia may mostly resolve with a new pair of lungs with normal vasculature and reduced RV afterload. Improving thrombocytopenia, even temporarily, is crucial as a bridge to transplantation. A comprehensive approach to cover all possible etiologies for thrombocytopenia may be required in patients with PAH awaiting transplantation.