Citation: | LI Xueling, WANG Luyao, ZUO Zhengcai, WANG Guihong. Efficacy of sildenafil citrate in treating pulmonary hypertension associated with connective tissue disease[J]. Chinese Journal of General Practice, 2023, 21(11): 1834-1836. doi: 10.16766/j.cnki.issn.1674-4152.003236 |
[1] |
ZHAO J L, WANG Q, WANG Q, et al. 2020 Chinese expert-based consensus on the diagnosis and treatment of connective tissue disease associated pulmonary arterial hypertension[J]. Rheumatol Immunol Res, 2021, 2(2): 63-78. doi: 10.2478/rir-2021-0010
|
[2] |
CHEN H A, HSU T C, YANG S C, et al. Incidence and survival impact of pulmonary arterial hypertension among patients with systemic lupus erythematosus: a nationwide cohort study[J]. Arthritis Res Ther, 2019, 21(1): 82. doi: 10.1186/s13075-019-1868-0
|
[3] |
PAN J, LEI L, ZHAO C, et al. Clinical characteristics and survival of patients with three major connective tissue diseases associated with pulmonary hypertension: a study from China[J]. Exp Ther Med, 2021, 22(3): 925. doi: 10.3892/etm.2021.10357
|
[4] |
LIM Y H, LOW T T, CHAN S P, et al. Pulmonary arterial hypertension in a multi-ethnic Asian population: characteristics, survival and mortality predictors from a 14-year follow-up study[J]. Respirology, 2019, 24(2): 162-170. doi: 10.1111/resp.13392
|
[5] |
POPE J E, DENTON C P, JOHNSON S R, et al. State-of-the-art evidence in the treatment of systemic sclerosis[J]. Nat Rev Rheumatol, 2023, 19(4): 212-226. doi: 10.1038/s41584-023-00909-5
|
[6] |
DEPASCALE R, DEL FRATE G, GASPAROTTO M, et al. Diagnosis and management of lung involvement in systemic lupus erythematosus and Sjögren's syndrome: a literature review[J]. Ther Adv Musculoskelet Dis, 2021, 13: 1759720X211040696. DOI: 10.1177/1759720X211040696.
|
[7] |
LEMMERS J M, FRETHEIM H, KNAAPEN H K, et al. Selexipag treatment in patients with systemic sclerosis-associated pulmonary arterial hypertension in clinical practice, a case series[J]. J Scleroderma Relat Disord, 2020, 5(3): NP7-NP11. DOI: 10.1177/2397198320916082.
|
[8] |
LI M T, WANG Y H, ZHAO J L, et al. Chinese SLE Treatment and Research group (CSTAR) registry 2009—2019: major clinical characteristics of Chinese patients with systemic lupus erythematosus[J]. Rheumatol Immunol Res, 2021, 2(1): 43-47. doi: 10.2478/rir-2021-0001
|
[9] |
GIORDANO N, CORALLO C, CHIRICO C, et al. Pulmonary arterial hypertension in systemic sclerosis: diagnosis and treatment according to the European Society of Cardiology and European Respiratory Society 2015 guidelines[J]. J Scleroderma Relat Disord, 2019, 4(1): 35-42. doi: 10.1177/2397198318808998
|
[10] |
朱玲娴, 赵荫环, 张蕊, 等. 系统性硬化症发生肺动脉高压的独立危险因素分析[J]. 风湿病与关节炎, 2023, 12(1): 14-18.
ZHU L X, ZHAO Y H, ZHANG R, et al. Independent risk factors of pulmonary hypertention in systemic sclerosis[J]. Rheumatism And Arthritis, 2023, 12(1): 14-18.
|
[11] |
谢长好, 李志军. 系统性红斑狼疮的诊断与治疗[J]. 中华全科医学, 2020, 18(4): 527-528. http://www.zhqkyx.net/article/id/240c4592-9f47-4c70-a324-2bf8221505c8
XIE C H, LI Z J. Diagnosis and treatment of systemic lupus erythematosus[J]. Chinese Journal of General Practice, 2020, 18(4): 527-528. http://www.zhqkyx.net/article/id/240c4592-9f47-4c70-a324-2bf8221505c8
|
[12] |
QIAN J Y, DING Y F, YANG X Y, et al. The diagnostic and prognostic value of growth differentiation factor-15 in systemic lupus erythematosus-associated pulmonary arterial hypertension[J]. Pulm Circ, 2023, 13: e12195. DOI: 10.1002/pul2.12195.
|
[13] |
WEATHERALD J, HUMBERT M. PDE5 to keep them alive: the use of phosphodiesterase type-5 inhibitors in severe pulmonary hypertension associated with interstitial lung disease[J]. Respirology, 2023, 28(3): 212-214. doi: 10.1111/resp.14399
|
[14] |
王建军, 吕群, 龚玲, 等. 原发性干燥综合征合并间质性肺病患者临床与影像特点分析[J]. 中华全科医学, 2019, 17(8): 1275-1278. doi: 10.16766/j.cnki.issn.1674-4152.000920
WANG J J, LYU Q, GONG L, et al. Analysis of clinical and imaging features of primary Sjogren ' s syndrome complicated with interstitial lung disease[J]. Chinese Journal of General Practice, 2019, 17(8): 1275-1278. doi: 10.16766/j.cnki.issn.1674-4152.000920
|
[15] |
SANGANI R A, LUI J K, GILLMEYER K R, et al. Clinical characteristics and outcomes in pulmonary manifestations of systemic sclerosis: contribution from pulmonary hypertension and interstitial lung disease severity[J]. Pulm Circ, 2022, 12(4): e12117. DOI: 10.1002/pul2.12117.
|
[16] |
VILELA V S, DIAS M M, SALGADO Â A, et al. Pulmonary hypertension in systemic sclerosis: diagnosis by systematic screening and prognosis after three years follow-up[J]. BMC Pulm Med, 2021, 21(1): 251. doi: 10.1186/s12890-021-01618-z
|
[17] |
朱轩池, 刘秀梅. 系统性硬化症相关肺动脉高压的治疗进展[J]. 临床与病理杂志, 2021, 41(7): 1696-1702.
ZHU X C, LIU X M. Progress in the treatment of systemic sclerosis-associated pulmonary arterial hypertention[J]. J Clin Pathol Res, 2021, 41(7): 1696-1702.
|
[18] |
VONK M C, VANDECASTEELE E, VAN DIJK A P. Pulmonary hypertension in connective tissue diseases, new evidence and challenges[J]. Eur J Clin Invest, 2020, 51(4): e13453. DOI: 10.1111/eci.13453.
|
[19] |
TRAN-DUY A, MORRISROE K, CLARKE P, et al. Cost-effectiveness of combination therapy for patients with systemic sclerosis-related pulmonary arterial hypertention[J]. J Am Heart Assoc, 2021, 10(7): e015816. DOI: 10.1161/JAHA.119.015816.
|
[20] |
AHMED W S, GEETHAKUMARI A M, BISWAS K H. Phosphodiesterase 5(PDE5): structure-function regulation and therapeutic application of inhibitors[J]. Biomed Pharmacother, 2021, 134: 111128. DOI: 10.1016/j.biopha.2020.111128.
|
[21] |
RUARO B, CONFALONIERI M, SALTON F, et al. The relationship between pulmonary damage and peripheral vascular manifestations in systemic sclerosis patients[J]. Pharmaceuticals(Basel), 2021, 14(5): 403. doi: 10.3390/ph14050403
|
[22] |
刘玉芳, 石磊. 波生坦治疗结缔组织病相关肺动脉高压临床疗效观察及安全性分析[J]. 中国药物与临床, 2019, 19(6): 867-869.
LIU Y F, SHI L. Clinical efficacy and safety of bosentan in treatment of connective tissue disease associated pulmonary arterial hypertention[J]. Chinese Remedies &Clinics, 2019, 19(6): 867-869.
|
[23] |
WANG Q, QIAN J Y, LI M T, et al. Risk assessment in systemic lupus erythematosus-associated pulmonary arterial hypertension: CSTAR-PAH cohort study[J]. Ther Adv Chronic dis, 2022, 13: 20406223221112528. DOI: 10.1177/20406223221112528.
|