[1]Maron BA, Abman SH, Elliott CG, et al. Pulmonary arterial hypertension: diagnosis, treatment, and novel advances[J]. Am J Respir Crit Care Med, 2021, 203(12):1472-1487. DOI: 10.1164/rccm.202012-4317SO.
[2]Ruopp NF, Cockrill BA. Diagnosis and treatment of pulmonary arterial hypertension: a review[J]. JAMA, 2022, 327(14):1379-1391. DOI: 10.1001/jama.2022.4402.
[3]Beshay S, Sahay S, Humbert M. Evaluation and management of pulmonary arterial hypertension[J]. Respir Med, 2020, 171:106099. DOI: 10.1016/j.rmed.2020.106099.
[4]Coons JC, Pogue K, Kolodziej AR, et al. Pulmonary arterial hypertension: a pharmacotherapeutic update[J]. Curr Cardiol Rep, 2019, 21(11):141. DOI: 10.1007/s11886-019-1235-4.
[5]Li D, Shao NY, Moonen JR, et al. ALDH1A3 coordinates metabolism with gene regulation in pulmonary arterial hypertension[J]. Circulation, 2021, 143(21):2074-2090. DOI: 10.1161/CIRCULATIONAHA.120.048845.
[6]Ramirez RL, Pienkos SM, de Jesus Perez V, et al. Pulmonary arterial hypertension secondary to drugs and toxins[J]. Clin Chest Med, 2021, 42(1):19-38. DOI: 10.1016/j.ccm.2020.11.008.
[7]白波,陈波,李广洪,等.D-二聚体水平升高与继发性新生儿持续性肺动脉高压的关系探讨[J].国际医药卫生导报,2024,30(8):1348-1352.DOI:10.3760/cma.j.issn.1007-1245.2024.08.025.
[8]Chen CY, Hung CC, Chiang CH, et al. Pulmonary arterial hypertension in the elderly population[J]. J Chin Med Assoc, 2022, 85(1):18-23. DOI: 10.1097/JCMA.0000000000000658.
[9]张靖宇,曾利,王翠,等.血清BNP、VEGF、TGF-β1水平变化在新生儿持续性肺动脉高压病情评估中的临床意义[J].中华全科医学,2020,18(1):7-9,44.DOI:10.16766/j.cnki.issn.1674-4152.001154.
[10]曾贞,陶沙.CT肺动脉成像联合心脏超声对肺动脉高压患者心功能损害的诊断价值[J].中国现代医学杂志,2022,32(3):87-92.DOI:10.3969/j.issn.1005-8982.2022.03.016.
[11]江芳强,莫佳妮.二维斑点追踪技术与心脏超声评估肺动脉高压患者右心室功能的临床价值比较[J].影像研究与医学应用,2023,7(10):107-109.DOI:10.3969/j.issn.2096-3807.2023.10.034.
[12]杨媛华.«中国肺动脉高压诊断与治疗指南(2021版)»解读——肺动脉高压的诊断[J].中国实用内科杂志,2021,41(8):696-699.DOI:10.19538/j.nk2021080107.
[13]Alzghoul BN, Abualsuod A, Alqam B, et al. Cocaine use and pulmonary hypertension[J]. Am J Cardiol, 2020, 125(2):282-288. DOI: 10.1016/j.amjcard.2019.10.008.
[14]Constantine A, Dimopoulos K. Pulmonary artery denervation for pulmonary arterial hypertension[J]. Trends Cardiovasc Med, 2021, 31(4):252-260. DOI: 10.1016/j.tcm.2020.04.005.
[15]Ojopi EPB, Tonon CR, Okoshi K, et al. Pulmonary arterial hypertension and cardioprotective interventions[J]. Arq Bras Cardiol, 2024, 121(7):e20240445. DOI: 10.36660/abc.20240445.
[16]Vonk MC, Vandecasteele E, van Dijk AP. Pulmonary hypertension in connective tissue diseases, new evidence and challenges[J]. Eur J Clin Invest, 2021, 51(4):e13453. DOI: 10.1111/eci.13453.
[17]Pizarro C, Nickenig G, Skowasch D. Diagnosis and therapy of pulmonary arterial hypertension[J]. Dtsch Med Wochenschr, 2023, 148(23):1491-1497. DOI: 10.1055/a-2012-0430.
[18]Kubota K, Miyanaga S, Akao M, et al. Association of delayed diagnosis of pulmonary arterial hypertension with its prognosis[J]. J Cardiol, 2024, 83(6):365-370. DOI: 10.1016/j.jjcc.2023.08.004.
[19]Gerhardt F, Fiessler E, Olsson KM, et al. Positive vasoreactivity testing in pulmonary arterial hypertension: therapeutic consequences, treatment patterns, and outcomes in the modern management era[J]. Circulation, 2024, 149(20):1549-1564. DOI: 10.1161/CIRCULATIONAHA.122.063821.
[20]Boucly A, Beurnier A, Turquier S, et al. Risk stratification refinements with inclusion of haemodynamic variables at follow-up in patients with pulmonary arterial hypertension[J]. Eur Respir J, 2024, 64(3):2400197. DOI: 10.1183/13993003.00197-2024.
|