Reconsidering the limited role of right heart catheterization on severe pulmonary hypertension-due to progressive interstitial lung disease in young male patient : a case report

https://doi.org/10.19106/JMedSci005502202307

Megawati Abubakar(1), Anggoro Budi Hartopo(2*), Ika Trisnawati(3), Eko Budiono(4), Dyah Wulan Anggrahini(5), Lucia Kris Dinarti(6)

(1) Department of Cardiology and Vascular Medicine, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada/Dr. Sardjito Hospital, Yogyakarta,
(2) Department of Cardiology and Vascular Medicine, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada/Dr. Sardjito Hospital, Yogyakarta,
(3) Division of Pulmonology, Department of Internal Medicine, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada/Dr. Sardjito Hospital, Yogyakarta, Indonesia
(4) Division of Pulmonology, Department of Internal Medicine, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada/Dr. Sardjito Hospital, Yogyakarta, Indonesia
(5) Department of Cardiology and Vascular Medicine, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada/Dr. Sardjito Hospital, Yogyakarta,
(6) Department of Cardiology and Vascular Medicine, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada/Dr. Sardjito Hospital, Yogyakarta,
(*) Corresponding Author

Abstract


Pulmonary hypertension (PH)-associated with interstitial lung disease (ILD) develops as a consequence of progressive underlying lung disease or disproportionately to the underlying disease. The PH investigation by right heart catheterization (RHC) for defining PH severity is recommended in patients with ILD who show more severe symptoms than expected from lung disease, appearance of right heart failure, and clinical deterioration not matched by the declining lung function. In patient with progressive ILD, RHC is only considered if it affects the future treatment such as lung transplantation or enrollment in clinical trial/registry. The decision to undertake the RHC in progressive ILD was still fraught with doubts. Here we reported a young adult male patient with ILD whom developed progressive signs and symptoms.  By RHC, he had severe precapillary PH with hemodynamic parameters indicated the presence of pulmonary vascular disease. A PH-specific treatment, sildenafil citrate, was administered, and patient responded well and was clinically stable during the addition of sildenafil citrate. This case highlights the clinical implication of performing RHC in progressive ILD, which can change the treatment decision by PH-specific drugs. Therefore, the RHC decision making in patient with progressive ILD need reconsideration.


Keywords


interstitial lung disease; pulmonary hypertension; heart catheterization; pulmonary arterial remodeling; sildenafil citrate

Full Text:

PDF


References


1.Simonneau G, Montani D, Celermajer DS, Denton CP, Michael A Gatzoulis MA, Krowka M, et al. Haemodynamic definitions and updated clinical classification of pulmonary hypertension. Eur Respir J 2019; 53(1):1801913.
https://doi.org/10.1183/13993003.01913-2018
2.Galiè N, Humbert M, Vachiery JL, Gibbs S, Lang I, Torbicki A, et al. 2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: The Joint Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS): Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC), International Society for Heart and Lung Transplantation (ISHLT). Eur Respir J 2015; 46(4):903-75.
https://doi.org/10.1183/13993003.01032-2015
3.Caminati A, Cassandro R, Harari S. Pulmonary hypertension in chronic interstitial lung diseases. Eur Respir Rev 2013; 22(129):292-301.
https://doi.org/10.1183/09059180.00002713
4.Corte TJ, Wort SJ, Wells AU. Pulmonary hypertension in idiopathic pulmonary fibrosis: a review. Sarcoidosis Vasc Diffuse Lung Dis 2009; 26(1):7-19.
5.Seeger W, Adir Y, Barberà JA, Champion H, Coghlan JG, Cottin V, et al. Pulmonary hypertension in chronic lung diseases. J Am Coll Cardiol 2013; 62(25 Suppl):D109-16.
https://doi.org/10.1016/j.jacc.2013.10.036
6.Nathan SD, Barbera JA, Gaine SP, Harari S, Martinez FJ, Olschewski H, et al. Pulmonary hypertension in chronic lung disease and hypoxia. Eur Respir J 2019; 53(1):1801914.
https://doi.org/10.1183/13993003.01914-2018
7.Dinarti LK, Hartopo AB, Kusuma AD, Satwiko MG, Hadwiono MR, Pradana AD, et al. The COngenital HeARt Disease in adult and Pulmonary Hypertension (COHARD-PH) registry: a descriptive study from single-center hospital registry of adult congenital heart disease and pulmonary hypertension in Indonesia. BMC Cardiovasc Disord 2020; 20(1):163.
https://doi.org/10.1186/s12872-020-01434-z
8.Hartopo AB, Arfian N, Nakayama K, Suzuki Y, Yagi K, Emoto N. Endothelial-derived endothelin-1 promotes pulmonary vascular remodeling in bleomycin-induced pulmonary fibrosis. Physiol Res 2018; 67(Suppl 1):S185-97.
https://doi.org/10.33549/physiolres.933812
9.Spiekerkoetter E, Goncharova EA, Guignabert C, Stenmark K, Kwapiszewska G, Rabinovitch M, et al. Hot topics in the mechanisms of pulmonary arterial hypertension disease: cancer-like pathobiology, the role of the adventitia, systemic involvement, and right ventricular failure. Pulm Circ 2019; 9(4):2045894019889775.
https://doi.org/10.1177/2045894019889775
10.Copeland CR, Lancaster LH. Management of Progressive Fibrosing Interstitial Lung Diseases (PF-ILD). Front Med (Lausanne) 2021; 8:743977.
https://doi.org/10.3389/fmed.2021.743977
11.Farmakis IT, Vazakidis P, Doundoulakis I, Arvanitaki A, Zafeiropoulos S, Boutou A, et al. Haemodynamic effects of PAH-targeted therapies in pulmonary hypertension due to lung disease: A systematic review and meta-analysis. Pulm Pharmacol Ther 2021; 68:102036.
https://doi.org/10.1016/j.pupt.2021.102036
12.Barnes H, Brown Z, Burns A, Williams T. Phosphodiesterase 5 inhibitors for pulmonary hypertension. Cochrane Database Syst Rev 2019; 1(1):CD012621.
https://doi.org/10.1002/14651858.CD012621.pub2
13.Hurdman J, Condliffe R, Elliot CA, Swift A, Rajaram S, Davies C, et al. Pulmonary hypertension in COPD: results from the ASPIRE registry. Eur Respir J 2013; 41(6):1292-301.
https://doi.org/10.1183/09031936.00079512
14.Fossati L, Müller-Mottet S, Hasler E, Speich R, Bloch KE, Huber LC, et al. Long-term effect of vasodilator therapy in pulmonary hypertension due to COPD: a retrospective analysis. Lung 2014; 192(6):987-95.
https://doi.org/10.1007/s00408-014-9650-1
15.Tea I, Hussain I. Under pressure: right heart catheterization and provocative testing for diagnosing pulmonary hypertension. Methodist Debakey Cardiovasc J 2021; 17(2):92-100.
https://doi.org/10.14797/AFUI4711



DOI: https://doi.org/10.19106/JMedSci005502202307

Article Metrics

Abstract views : 979 | views : 1309




Copyright (c) 2023 Megawati Abubakar, Anggoro Budi Hartopo, Ika Trisnawati, Eko Budiono, Dyah Wulan Anggrahini, Lucia Kris Dinarti

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.