Vasoactive drugs for the treatment of pulmonary hypertension associated with interstitial lung diseases: a systematic review

被引:0
作者
Bongiovanni, Gabriele [1 ]
Tonutti, Antonio [1 ]
Stainer, Anna [1 ,2 ]
Nigro, Mattia [1 ]
Kellogg III, Dean L. [3 ,4 ]
Nambiar, Anoop [3 ,4 ]
Gramegna, Andrea [5 ,6 ,7 ]
Mantero, Marco [5 ,6 ,7 ]
Voza, Antonio [8 ]
Blasi, Francesco [5 ,6 ,7 ]
Aliberti, Stefano [1 ,2 ]
Amati, Francesco [1 ,2 ]
机构
[1] Humanitas Univ, Dept Biomed Sci, Via Rita Levi Montalcini 4, I-20072 Pieve Emanuele, Milan, Italy
[2] IRCCS Humanitas Res Hosp, Resp Unit, Via Manzoni 56, I-20089 Rozzano, Milan, Italy
[3] Univ Texas Hlth San Antonio, Dept Med, Div Pulm & Crit Care, San Antonio, TX USA
[4] South Texas Vet Hlth Care Syst, San Antonio, TX USA
[5] Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Milan, Italy
[6] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Resp Unit, Milan, Italy
[7] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Cyst Fibrosis Adult Ctr, Milan, Italy
[8] IRCCS Humanitas Res Hosp, Emergency Med Unit, Via Manzoni 56, I-20089 Milan, Italy
关键词
Interstitial Fibrosis; Primary Pulmonary Hypertension; DOUBLE-BLIND; ARTERIAL-HYPERTENSION; INHALED TREPROSTINIL; FIBROSIS; SCLEROSIS; SAFETY; MULTICENTER; SILDENAFIL; DIAGNOSIS; RIOCIGUAT;
D O I
10.1136/bmjresp-2023-002161
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Objectives Vasoactive drugs have exhibited clinical efficacy in addressing pulmonary arterial hypertension, manifesting a significant reduction in morbidity and mortality. Pulmonary hypertension may complicate advanced interstitial lung disease (PH-ILD) and is associated with high rates of disability, hospitalisation due to cardiac and respiratory illnesses, and mortality. Prior management hinged on treating the underlying lung disease and comorbidities. However, the INCREASE trial of inhaled treprostinil in PH-ILD has demonstrated that PH-ILD can be effectively treated with vasoactive drugs.Methods This comprehensive systematic review examines the evidence for vasoactive drugs in the management of PH-ILD.Results A total of 1442 pubblications were screened, 11 RCTs were considered for quantitative synthesis. Unfortunately, the salient studies are limited by population heterogeneity, short-term follow-up and the selection of outcomes with uncertain clinical significance.Conclusions This systematic review underscores the necessity of establishing a precision medicine-oriented strategy, directed at uncovering and addressing the intricate cellular and molecular mechanisms that underlie the pathophysiology of PH-ILD.PROSPERO registration number CRD42023457482.
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页数:14
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  • [1] Treatable Traits in Systemic Sclerosis
    Amati, Francesco
    Bongiovanni, Gabriele
    Tonutti, Antonio
    Motta, Francesca
    Stainer, Anna
    Mangiameli, Giuseppe
    Aliberti, Stefano
    Selmi, Carlo
    De Santis, Maria
    [J]. CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY, 2023, 65 (02) : 251 - 276
  • [2] Treatable traits in interstitial lung diseases: a call to action
    Amati, Francesco
    Spagnolo, Paolo
    Oldham, Justin M.
    Ryerson, Christopher J.
    Stainer, Anna
    Gramegna, Andrea
    Mantero, Marco
    Lacedonia, Donato
    Sverzellati, Nicola
    Richeldi, Luca
    Blasi, Francesco
    Aliberti, Stefano
    [J]. LANCET RESPIRATORY MEDICINE, 2023, 11 (02) : 125 - 128
  • [3] Atkins D, 2004, BMJ-BRIT MED J, V328, P1490
  • [4] Bosentan for Sarcoidosis-Associated Pulmonary Hypertension A Double-Blind Placebo Controlled Randomized Trial
    Baughman, Robert P.
    Culver, Daniel A.
    Cordova, Francis C.
    Padilla, Maria
    Gibson, Kevin F.
    Lower, Elyse E.
    Engel, Peter J.
    [J]. CHEST, 2014, 145 (04) : 810 - 817
  • [5] Efficacy and safety of sildenafil added to pirfenidone in patients with advanced idiopathic pulmonary fibrosis and risk of pulmonary hypertension: a double-blind, randomised, placebo-controlled, phase 2b trial
    Behr, Juergen
    Nathan, Steven D.
    Wuyts, Wim A.
    Bishop, Nesrin Mogulkoc
    Bouros, Demosthenes E.
    Antoniou, Katerina
    Guiot, Julien
    Kramer, Mordechai R.
    Kirchgaessler, Klaus-Uwe
    Bengus, Monica
    Gilberg, Frank
    Perjesi, Andras
    Harari, Sergio
    Wells, Athol U.
    [J]. LANCET RESPIRATORY MEDICINE, 2021, 9 (01) : 85 - 95
  • [6] The safety of iloprost in systemic sclerosis in a real-life experience
    Bellando-Randone, S.
    Bruni, C.
    Lepri, G.
    Fiori, G.
    Bartoli, F.
    Conforti, M. L.
    Moggi-Pignone, A.
    Guiducci, S.
    Giuggioli, D.
    Colaci, M.
    Spinella, A.
    Ferri, C.
    Matucci-Cerinic, M.
    [J]. CLINICAL RHEUMATOLOGY, 2018, 37 (05) : 1249 - 1255
  • [7] Systemic Sclerosis-Associated Pulmonary Arterial Hypertension
    Chaisson, Neal F.
    Hassoun, Paul M.
    [J]. CHEST, 2013, 144 (04) : 1346 - 1356
  • [8] Inhaled treprostinil: a therapeutic review
    Channick, Richard N.
    Voswinckel, Robert
    Rubin, Lewis J.
    [J]. DRUG DESIGN DEVELOPMENT AND THERAPY, 2012, 6 : 19 - 28
  • [9] An overview of the biology of a long-acting inhaled treprostinil prodrug
    Chapman, Richard W.
    Corboz, Michel R.
    Malinin, Vladimir S.
    Plaunt, Adam J.
    Konicek, Donna M.
    Li, Zhili
    Perkins, Walter R.
    [J]. PULMONARY PHARMACOLOGY & THERAPEUTICS, 2020, 65
  • [10] Role of endothelin in fibrosis and anti-fibrotic potential of bosentan
    Clozel, M
    Salloukh, H
    [J]. ANNALS OF MEDICINE, 2005, 37 (01) : 2 - 12