Evidence map›Paper›PMID 32518816›Full record

ArticleInternational journal of cardiology. Heart & vasculature2020

Does combination therapy work in chronic thromboembolic pulmonary hypertension?

M C J van Thor, R J Snijder, J C Kelder, J J Mager, M C Post

Erratum issuedAbstract read
In one paragraph

Article in International journal of cardiology. Heart & vasculature, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Trial
  2. Article
  3. Upfront combination therapy with sildenafil and ambrisentan in patients with chronic thromboembolic pulmonary hypertension.Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

M C J van ThorDept of Cardiology, St. Antonius Hospital, Nieuwegein, the Netherlands.
R J SnijderDept of Pulmonology, St. Antonius Hospital, Nieuwegein, the Netherlands.
J C KelderDept of Epidemiology, St. Antonius Hospital, Nieuwegein, the Netherlands.
J J MagerDept of Pulmonology, St. Antonius Hospital, Nieuwegein, the Netherlands.
M C PostDept of Cardiology, St. Antonius Hospital, Nieuwegein, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe current experience with combination therapy in chronic thromboembolic pulmonary hypertension (CTEPH) is limited. We present the first survival results up to 5 years for dual combination therapy versus monotherapy in CTEPH.

methodsAll consecutive, non-operated CTEPH or residual PH after pulmonary endarterectomy patients treated with PH-specific medical therapy between January 2002 and November 2019 were included. We report and compare survival between monotherapy and (upfront or sequential) dual combination therapy until five years after medication initiation.

resultsIn total, 183 patients (mean age 65 ± 14 years, 60% female, 66% WHO FC III/IV, 86% non-operated) were included, of which 83 patients received monotherapy and 100 patients received dual combination therapy. At baseline, patients receiving combination therapy had a higher NT-proBNP (p = 0.02) mean pulmonary artery pressure (p = 0.0001) and pulmonary vascular resistance (p = 0.02), while cardiac index was lower (p = 0.03). Total follow-up duration was 3.3 ± 1.8 years, during which 31 (17%) patients died. Estimated 1-, 3- and 5-year survival for monotherapy were 99%, 92% and 79%, respectively. For combination therapy percentages were 98%, 89% and 70%, respectively. Survival did not significantly differ between both groups (p = 0.22).

conclusionSurvival up to 5 years for patients treated with combination therapy, regardless of the combination strategy, was similar as patients with monotherapy, despite worse clinical and haemodynamic baseline characteristics.

Indexed as

6MWD, 6-minute walking distanceBPA, balloon pulmonary angioplastyChronic thromboembolic pulmonary hypertensionCI, cardiac indexCO, cardiac outputCombination therapyCOPD, chronic obstructive lung diseaseCT, computed tomographyCTEPH, chronic thromboembolic pulmonary hypertensionERA(s), endothelin receptor antagonist(s)FC, functional classHR, hazards regressionIQR, interquartile rangeMonotherapymPAP, mean pulmonary arterial pressureNT-proBNP, N-terminal pro brain natriuretic peptidePAH, pulmonary arterial hypertensionPEA, pulmonary endarterectomyPH, pulmonary hypertensionPVR, pulmonary vascular resistanceRAP, right atrial pressureRHC, right heart catheterisationSD, standard deviationSurvivalWHO, World Health Organization

Identifiers

PMID32518816
PMCPMC7270605

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.