Literature DB >> 28606655

Mortality in pulmonary arterial hypertension due to congenital heart disease: Serial changes improve prognostication.

M T U Schuijt1, I M Blok2, A H Zwinderman1, A C M J van Riel2, M J Schuuring2, R J de Winter1, A L Duijnhouwer3, A P J van Dijk3, B J M Mulder2, B J Bouma4.   

Abstract

BACKGROUND: Adult patients with pulmonary arterial hypertension due to congenital heart disease (PAH-CHD) suffer from high mortality. This underlines the importance of adequate risk stratification to guide treatment decisions. Several baseline parameters are associated with mortality, however, their prognostic value may weaken after years of follow-up. Therefore we investigated the prognostic value of serial changes in standard clinical parameters in PAH-CHD.
METHODS: In this prospective observational cohort study we included consecutive PAH-CHD adults, between 2005 and 2016. Control visits to the outpatient clinic were standardized, including functional, biochemical and echocardiographic tests, according to the guidelines. The prognostic value of serial changes was determined with time-dependent Cox regression.
RESULTS: Ninety-two patients with PAH-CHD were included (age 43±15years, 34% male, 38% Down, 73% Eisenmenger). During a median follow-up of 6.0 (IQR 3.7-9.3) years, 35 (38%) patients died. Serial changes in World Health Organization functional classification (WHO-FC, HR 18.34 for onset class IV), six-minute walk distance (6-MWD, HR 0.65 per 50m), oxygen saturation at peak exercise (peak SaO2, HR 0.74 per 5%), NTproBNP (HR 2.25 per 1000ng/l) and echocardiographic right ventricular function (TAPSE, HR 0.80 per 0.5cm) significantly predicted mortality. Moreover, serial changes in these parameters were more potent predictors compared to baseline parameters, based on reduction in -2 log likelihood.
CONCLUSIONS: Serial changes in standard clinical parameters have more prognostic value compared to baseline parameters in PAH-CHD. Our results emphasize the importance of screening for serial changes since periodical assessment could guide treatment decisions to delay disease progression.
Copyright © 2017 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Congenital heart disease; Longitudinal; Predictors; Prognosis; Pulmonary arterial hypertension; Time-dependent

Mesh:

Year:  2017        PMID: 28606655     DOI: 10.1016/j.ijcard.2017.05.101

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN: 0167-5273            Impact factor:   4.164


  5 in total

Review 1.  Adult congenital heart disease with pulmonary arterial hypertension: mechanisms and management.

Authors:  Michail Papamichalis; Andrew Xanthopoulos; Panagiotis Papamichalis; John Skoularigis; Filippos Triposkiadis
Journal:  Heart Fail Rev       Date:  2020-09       Impact factor: 4.214

2.  Contemporary survival of patients with pulmonary arterial hypertension and congenital systemic to pulmonary shunts.

Authors:  Chodchanok Vijarnsorn; Kritvikrom Durongpisitkul; Paweena Chungsomprasong; Densiri Bositthipichet; Salisa Ketsara; Yuttapon Titaram; Prakul Chanthong; Supaluck Kanjanauthai; Jarupim Soongswang
Journal:  PLoS One       Date:  2018-04-17       Impact factor: 3.240

3.  Assessment of right ventricular function in patients with pulmonary arterial hypertension-congenital heart disease and repaired and unrepaired defects: Correlation among speckle tracking, conventional echocardiography, and clinical parameters.

Authors:  Hatice S Kemal; Meral Kayıkçıoğlu; Sanem Nalbantgil; Levent Hürkan Can; Nesrin Moğulkoç; Hakan Kültürsay
Journal:  Anatol J Cardiol       Date:  2020-04       Impact factor: 1.596

4.  Subcutaneous treprostinil in congenital heart disease-related pulmonary arterial hypertension.

Authors:  Nika Skoro-Sajer; Christian Gerges; Olga Hajnalka Balint; Dora Kohalmi; Monika Kaldararova; Iveta Simkova; Johannes Jakowitsch; Harald Gabriel; Helmut Baumgartner; Mario Gerges; Roela Sadushi-Kolici; David S Celermajer; Irene Marthe Lang
Journal:  Heart       Date:  2018-02-07       Impact factor: 5.994

5.  Guideline implementation and early risk assessment in pulmonary arterial hypertension associated with congenital heart disease: A retrospective cohort study.

Authors:  Xiaoxian Deng; Bowen Jin; Shanshan Li; Yaping Li; Hongmei Zhou; Yang Wu; Menghuan Yan; Yuanping Hu; Qiu Qiu; Gangcheng Zhang; Xuan Zheng
Journal:  Clin Respir J       Date:  2019-08-29       Impact factor: 2.570

  5 in total

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