Long-term effects of sildenaril in a patient with scleroderma-associated pulmonary hypertension and Raynaud's syndrome

被引:8
|
作者
Rosenkranz, S
Caglayan, E
Diet, F
Karasch, T
Weihrauch, J
Wassermann, K
Erdmann, E
机构
[1] Univ Cologne, Innere Med Klin 3, D-50924 Cologne, Germany
[2] Univ Cologne, Dermatol Klin & Poliklin, D-50924 Cologne, Germany
关键词
D O I
10.1055/s-2004-829025
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
History: A 65-year-old woman was admitted because of dyspnea at rest and peripheral edema due to scleroderma-associated pulmonary fibrosis and hypertension, as well as Raynaud's phenomenon. Diagnostic features, treatment and course: She had a marked restrictive ventilatory disorder with severe impairment of diffusion capacity. Right heart catheterization demonstrated a mean pulmonary artery pressure of 50 mmHg. She was able to walk only 220 m. All usual methods of treatment failed to give satisfactory results so that sildenafil (phospherodiesterase type-5 \PDE-5\ inhibitor; Viagra(R) was given, even though it is not licensed for this indications (,,off-label", as a therapeutic attempt. This achieved definite reduction in pulmonary arterial pressure and significantly improved the clinical symptoms. In particular, it drastically reduced the level of atrial natriuretic peptide, an important prognostic marker in right heart failure. Sildenafil also significantly raised peripheral perfusion and the signs of Raynaud's syndrome. Conclusion: PDE-5 inhibitors are efficacious in scleroderma-associated pulmonary hypertension and may also provide a new option in the treatment of Raynaud's disease.
引用
收藏
页码:1736 / 1740
页数:5
相关论文
共 50 条
  • [1] Long-term outcomes of epoprostenol in scleroderma-associated pulmonary hypertension.
    Schachna, L
    Tarver, J
    Krishnan, J
    Houston-Harris, T
    Wigley, FM
    White, B
    Gaine, SP
    Rosas, I
    ARTHRITIS AND RHEUMATISM, 2000, 43 (09): : S316 - S316
  • [2] Sildenafil improved pulmonary hypertension and peripheral blood flow in a patient with scleroderma-associated lung fibrosis and the Raynaud phenomenon
    Rosenkranz, S
    Diet, F
    Karasch, T
    Weihrauch, J
    Wassermann, K
    Erdmann, E
    ANNALS OF INTERNAL MEDICINE, 2003, 139 (10) : 871 - 873
  • [3] Mortality prediction in scleroderma-associated pulmonary hypertension
    House, CV
    Coleiro, B
    Mukerjee, D
    Black, CM
    Coghlan, JG
    CIRCULATION, 1999, 100 (18) : 588 - 588
  • [4] Recent advances in scleroderma-associated pulmonary hypertension
    Highland, Kristin B.
    CURRENT OPINION IN RHEUMATOLOGY, 2014, 26 (06) : 637 - 645
  • [5] Risk assessment in Scleroderma-associated pulmonary arterial hypertension
    Mercurio, Valentina
    Diab, Nermin
    Peloquin, Grace
    Housten-Harris, Traci
    Damico, Rachel
    Kolb, Todd M.
    Mathai, Stephen C.
    Hassoun, Paul M.
    VASCULAR PHARMACOLOGY, 2020, 132
  • [6] Antibodies to fibroblasts in idiopathic and scleroderma-associated pulmonary hypertension
    Tamby, M. C.
    Humbert, M.
    Guilpain, P.
    Servettaz, A.
    Dupin, N.
    Christner, J. J.
    Simonneau, G.
    Fermanian, J.
    Weill, B.
    Guillevin, L.
    Mouthon, L.
    EUROPEAN RESPIRATORY JOURNAL, 2006, 28 (04) : 799 - 807
  • [7] A PUZZLING CASE: CHRONIC THROMBOEMBOLIC PULMONARY HYPERTENSION VS SCLERODERMA-ASSOCIATED PULMONARY HYPERTENSION
    Bhatti, Waqas
    Noor, Ahmed
    Masood, Jamil
    CHEST, 2019, 156 (04) : 772A - 772A
  • [8] Esophageal Dysmotility in Patients With Scleroderma-Associated Pulmonary Arterial Hypertension
    Selvachandran, Adarsha
    Yap, Vanessa
    Foley, Raymond
    Datta, Debapriya
    CHEST, 2017, 152 (04) : 987A - 987A
  • [9] Increased oxidative stress is scleroderma-associated pulmonary hypertension.
    Stein, M
    Robbins, IM
    Christman, BW
    Loyd, JE
    Morrow, JD
    ARTHRITIS AND RHEUMATISM, 1999, 42 (09): : S189 - S189
  • [10] Practical approach to screening for scleroderma-associated pulmonary arterial hypertension
    Fischer, Aryeh
    Bull, Todd M.
    Steen, Virginia D.
    ARTHRITIS CARE & RESEARCH, 2012, 64 (03) : 303 - 310