Primary Pulmonary Hypertension Treated with

Case Report

Acta Cardiol Sin 2006;22:102-6

Primary Pulmonary Hypertension Treated with Endothelin-1 Antagonist, Bosentan: Case Report and Review of the Literature Chun-Chieh Liu,1 Ping-Ying Lee,1,2 Hung-I Yeh1,2, Charles Jia-Yin Hou1 and Cheng-Ho Tsai1,2

Primary pulmonary hypertension (PPH) is a rare and progressive fatal disease. PPH is a diagnosis of exclusion, and median survival from the time of diagnosis is 2.8 years, if without treatment. Current options for treatment include oxygen, anticoagulation, diuretics, digoxin, calcium channel blockers, prostacyclin, and inhaled nitric oxide. However, endothelin-1 receptor antagonist (ERA) is less mentioned. We address a 19-year-old female who presented progressive dyspnea and exercise intolerance for 2 months. After series of studies, severe PPH was diagnosed. She hesitated to receive lung transplantation. Because of worsening of congestive heart failure (CHF), she started treatment with bosentan, an ERA. After 16 weeks of treatment, she experienced a great improvement of CHF and exercise capacity.

Key Words:

Primary pulmonary hypertension · Endothelin receptor antagonist · Bosentan

INTRODUCTION

with intractable severe pulmonary hypertension, who responded well to short-term treatment with bosentan.

Primary pulmonary hypertension (PPH) is characterized by persistent pulmonary artery hypertension (PAH) of unexplained etiology.1 PPH is relatively rare, with an estimated incidence of 1 to 2 per million in the general population.2 The median survival of PPH from the time of diagnosis is 2.8 years, if without treatment.3 Many options for treatment exist, such as oxygen, anticoagulation, diuretics, digoxin, calcium channel blockers (CCBs), prostacyclin, and inhaled nitric oxide (NO). However, bosentan, an endothelin-1 receptor antagonist (ERA) which is approved in the treatment of PPH recently, is less reported. We herein narrate a young female

CASE REPORT A 19-year-old female, suspected of bronchial asthma but unresponsive to bronchodilators, was referred to our Cardiology Clinic owing to exertional dyspnea (New York Heart Association [NYHA] functional class II) for 2 months. Her body height and weight were 148 cm and 47 kg, respectively. She denied hypertension, diabetes mellitus, drug abuse, operation or other major systemic disease history. Her mother died suddenly at 26 years old of unknown cause. Her blood pressure and respiratory rate were 110/70 mmHg and 20/min, respectively. Her physical examinations were unremarkable except bilateral jugular venous engorgement, accentuated P2 and grade III/VI pansystolic murmurs at the left lower sternal border on cardiac auscultation. The arterial blood analysis in room air revealed hypoxemia (pH: 7.469, PaO2: 64.8 mmHg, PaCO2: 20.2 mmHg, HCO3: 14.4 meq/dL, oxygen saturation: 94.4%). The 12-lead electrocardiog-

Received: October 28, 2005 Accepted: December 23, 2005 1 Division of Cardiology, Department of Internal Medicine, Mackay Memorial Hospital, Mackay Medicine, Nursing and Management College; 2Taipei Medical University, Taipei, Taiwan. Address correspondence and reprint requests to: Dr. Ping-Ying Lee, Division of Cardiology, Department of Internal Medicine, Mackay Memorial Hospital, No. 92, Sec. 2, Chung Shan North Road, Taipei 104, Taiwan. Tel: 886-2-2543-3535 ext. 2456; Fax: 886-2-2543-3535 ext. 3238; E-mail: [email protected] Acta Cardiol Sin 2006;22:102-6

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nography and laboratory studies showed no evidence of pulmonary embolism, obstructive or restrictive pulmonary disease, portal hypertension, connective tissue disease or HIV infection. A right cardiac catheterization study demonstrated as follows: pulmonary capillary wedge pressure (PCWP) 13 mm Hg, main pulmonary artery pressure (PAP) 83/42 mmHg (mean 58 mmHg), RV 86/9 mmHg, mean right atrium (RA) pressure 14 mmHg, cardiac output (CO) 4.3 L/min, cardiac index (CI) 3.1 L/min, and main pulmonary artery oxygen saturation 75%. The patient’s PAP did not reduce after administration of nifedipine (10 mg) or nitroglycerin (0.6 mg). Also, pulmonary angiography showed neither pulmonary arterial/venous occlusive disease nor congenital cardiac anomalies. On the basis of above findings, she was confirmed to have PPH. Lung transplantation was suggested, but she declined. High dosage of CCBs, such as nifedipine (30 mg/day) and diltiazem (90 mg/day) had been used but discontinued owing to hypotension. Therefore, she was treated with oral anticoagulant, warfarin (10 mg/day) and adjusted to keep the international normalized ratio between 2 and 3. Nocturnal oxygen (3 L/min) was also supplied. Unfortunately, severe dyspnea (NYHA functional class IV; WHO classification of PAH, functional class IV) happened after 2-year follow-up. Repeat UCG showed conspicuous RV and small LV (40 mm and 16 mm in end-diastole, respectively) and very high PASP (136 mmHg) [Figure 2A]. The patient still hesitated to undergo lung transplantation. After discussion, she agreed to take oral ERA, bosentan at a dose of 62.5 mg twice daily for the first month, then 125 mg twice daily for the next 3 months, starting June 4, 2005. After the first-month treatment, she got a significant improvement of dyspnea on exertion (NYHA functional class IV to class II) and completed the following course without adverse effects. Liver function tests and hematocrit were checked monthly and were within the normal ranges. After treatment for 4 months, the UCG also showed increased LV size in concordance with reduced RV size (36 mm and 32 mm in end-diastole, respectively), reduced PASP (from 136 to 120 mmHg) and severity of TR (from grade 4 to 1), and RA size (from 30 to 24 mm) (LV ejection fraction 70%) [Figure 2B]. Follow-up right cardiac catheterization revealed a significant lowering of mean RA pressure to 6 mmHg (from 14 to 6 mmHg), but no significant change

raphy (ECG) revealed sinus rhythm, right axis deviation, and right ventricular hypertrophy [Figure 1A]. The chest x-ray showed enlarged right ventricle (RV) with prominent pulmonary vascular trunk [Figure 1B]. The echocardiography (UCG) demonstrated dilated RV with interventricular septal paradox as well as severe tricuspid regurgitation (TR) with an estimated pulmonary artery systolic pressure (PASP) of approximately 88 mmHg. The left ventricle (LV) function was normal (LV ejection fraction 67%). There were no increased thickness of pericardium, no pericardial effusion and no intra- or extra-cardiac shunting demonstrated by 2-dimensional and color doppler UCG. A series of examinations such as ventilation/perfusion lung scan, pulmonary function test, abdominal so-

Figure 1. A. The 12-lead ECG reveals sinus rhythm, right axis deviation, and right ventricular hypertrophy. B. The chest x-ray shows enlarged RV with prominent pulmonary vascular trunk.

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Figure 2. A. UCG in apical four-chamber view demonstrates profound dilatation of RA and RV but small LV (30, 40 mm and 16 mm in end-diastole, respectively), and B. Follow-up UCG after administration of bosentan for 16 weeks shows RA and RV diameter decreased to 24 and 32 mm, respectively and LV diameter increased to 36 mm.

liver function test, HIV testing, and cardiac catheterization.5 Currently, treatment options for PPH include diuretics, digoxin, CCBs, prostacyclin and its analogues, inhaled NO, ERAs, and adjunctive therapies, such as anticoagulants and oxygen. Poor response has been documented with diuretics, digoxin, and CCBs.6-8 Additionally, intravenous prostacyclin and inhaled NO must given via continuous infusion and inhalation device, respectively.9-10 Patients with pulmonary hypertension were reported to have high concentrations of endothelin-1 (ET-1) in the plasma and lungs.11 ET-1 is a potent vasoconstrictor as well as smooth-muscle mitogen. Two separate receptors of ET-1 exist. ET-A receptors, mainly found in vascular smooth muscle cells, can induce vasoconstriction by increasing intracellular calcium. On the other hand, ET-B receptors, mainly expressed by endothelial cells, can stimulate the release of vasodilating agents, such as nitric oxide and prostacyclin. Either selective blocking of ET-A receptors alone or non-selective blocking of both receptors can dilate the local vessels. 11-15 Bosentan (TracleerTM, Actelion, Switzerland), a non-selective antagonist administrated orally, has been approved for the

of the PAP (117/43, mean 67 mmHg), RV pressure (127/12 mmHg), PCWP (14 mmHg), CO (3.6 L/min), CI (2.7 L/min). Therefore, bosentan has been continuously given.

DISCUSSION PPH is defined clinically as the presence of PAH (mean PAP > 25 mmHg at rest, or > 30 mmHg with exercise), associated with a normal PCWP and the absence of secondary etiology.1-3 The first complaint of most patients is dyspnea. Other symptoms include fatigue (1947%; along the course of the disease), palpitations (533%), syncope (8-36%), leg edema (3-37%), and chest pain (5-47%).4 Conditions such as thromboembolic disease, collagen disease, congenital heart disease, valvular heart disease, underlying lung disease, and liver disease must be excluded. Drug history, such as usage of appetite-suppressant drug (fenfluramine), should also be obtained. The workup studies should include chest x-ray, ECG, UCG, pulmonary function tests, ventilation perfusion lung scan, the tests for collagen vascular disease (antinuclear antibodies, anti-double strain DNA, etc.), Acta Cardiol Sin 2006;22:102-6

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treatment of PPH in humans.11 The cost of each dose (either 62.5 mg or 125 mg) is NT$1,892, and the total cost for our patient is about NT$1,380,000 each year. The recommended dose of bosentan is initially 62.5 mg twice daily for 4 weeks, followed by a maintenance dose of 125 mg twice daily. The adverse effects of bosentan include serious hepatotoxicity and fetal damage. It is contraindicated in patients with moderate to severe liver impairment and pregnancy. Other side effects are headache, nasopharyngitis, flushing, edema, hypotension, palpitation, fatigue, and pruritis. Decreased hemoglobin level was also reported. Furthermore, up to 7% of patients in clinical trials developed a drug-related hepatitis that required dose reduction or cessation of therapy. Therefore, liver function tests and hemoglobin/hematocrit must be monitored monthly. The effect of bosentan on cardiopulmonary hemodynamics includes a decrease in pulmonary vascular resistance, which may account for the improved 6-minute walking distance and symptoms of CHF.11 Bosentan also reduces the rate of clinical worsening.12 Regarding our patient, after 4-month treatment with bosentan, CHF symptoms and exercise capacity improved in association with significant decrease in RV size (40 to 32 mm), RA pressure (14 to 6 mmHg), the severity of TR (grade 4 to 1), and increase in LV size (16 to 36 mm). Survival of PPH is directly related to NYHA functional class. It tends to have a worse prognosis if RA pressure is greater than 20 mmHg, mean PAP greater than 85 mmHg, and CI less than 2 L/min/M2.4 However, in recent studies of PPH, the duration of bosentan used was only 12 to 16 weeks, which was not sufficient to test for survival.11-14 Larger and longer-term studies are required.

pertension. Chest 1993;104:236-50. 2. Abenhaim L, Moride Y, Brenot F, et al. Appetite-suppressant drugs and the risk of primary pulmonary hypertension. N Engl J Med 1996;335:609. 3. McLaughlin V, Shillington A, Rich S. Survival of primary pulmonary hypertension; the impact of epoprostenol therapy. Circulation 2002;106:1477-1482. 4. Stuart L, Patricia R, William F. Primary pulmonary hypertension and cor pulmonale. Cardiol Rev 2002;10:265-278. 5. Fein SA, Frishman WH. The pathophysiology and management of primary pulmonary hypertension. Cardiol Clin 1987;5:563576. 6. Reeves JT, Groves BM, Turkevich D. The case for treatment of selected patients with primary pulmonary hypertension. Am Rev Respir Dis 1986;134:342-46. 7. Nauser T, Stiles S. Diagnosis and treatment of pulmonary hypertension. Am Fam Physician 2001:63:1789-1798. 8. Rich S, Kaufman E, Levy P. The effect of high doses of calcium channel blockers on survival in primary pulmonary hypertension. N Engl J Med 1992;327:76-81. 9. Barst RJ, Rubin LJ, McGoon MD, Caldwell EJ, Long WA, Levy PS. Survival in primary pulmonary hypertension with long-term continuous intravenous prostacyclin. Ann Intern Med. 1994; 121:409-15. 10. Hasuda T, Satoh T, Shimouchi A, Sakamaki F, Kyotani S, Matsumoto T. Improvement in exercise capacity with nitric oxide inhalation in patients with precapillary pulmonary hypertension. Circulation 2000;101:2066-70. 11. Channick RN, Simonneau G, Sitbon O, et al. Effects of the dual endothelin-receptor antagonist bosentan in patients with pulmonary hypertension: a randomized placebo-controlled study. Lancet 2001;358:1119-1123. 12. Williamson DJ, Wallman LL, Jones R, et al. Hemodynamic effects of bosentan, an endothelin receptor antagonist, in patients with pulmonary hypertension. Circulation 2000;102:411-418. 13. Rubin LJ, Badesch DB, Barst RJ, et al. Bosentan therapy for pulmonary arterial hypertension. N Engl J Med 2002;346:896903. 14. Barst RJ, Langleben D, Frost E, Horn EM, Oudiz R, Shapiro S, et al. Sitaxsentan therapy for pulmonary arterial hypertension. Am J Respir Crit Care Med 2004;169:441-7. 15. MacLean MR. Endothelin-1: A mediator of pulmonary hypertension? Pulm Pharmacol Ther 1998;11:125-32.

REFERENCES 1. Rubin LJ. ACCP consensus statement: primary pulmonary hy-

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Case Report

Acta Cardiol Sin 2006;22:102−6

原發性肺動脈高壓以內皮素-1 拮抗劑, Bosentan 治療：病例報告和文獻回顧劉俊傑 1 李秉穎 1,2 葉宏一 1,2 侯嘉殷 1 蔡正河 1,2 台北市馬偕醫護管理專科學校暨馬偕紀念醫院心臟內科1 台北市臺北醫學大學2

原發性肺動脈高壓是一種罕見和持續性惡化與致命的疾病。在臨床上呈現持續性的高肺動脈壓而無其它的致病因素。它的診斷是利用排除法。如果沒有治療的話，從診斷確定開始，平均存活約 2.8 年。目前治療的方法包括氧氣輔助、使用抗凝血劑、利尿劑、毛地黃、鈣離子阻斷劑、前列腺素和吸入性一氧化氮；然而，內皮素-1 受體拮抗劑較少被報告。我們提出一位 19 歲的女性表現二個月持續性呼吸困難和運動不能，經過一系列的檢查之後，診斷為重度原發性肺動脈高壓。建議接受肺移植手術，但病人猶豫不決。因為心臟衰竭愈來愈惡化，開始接受內皮素-1 受體拮抗劑 Bosentan 治療。經過 16 週的治療後，病人的心臟衰竭症狀和運動功能有明顯改善。

關鍵詞：原發性肺動脈高壓、內皮素拮抗劑、Bosentan。

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