Evidence map›Paper›PMID 42783040›Full record

ReviewJournal of cardiovascular development and disease2026

Multimodal Management of Chronic Thromboembolic Pulmonary Hypertension: A Narrative Review of Treatment Selection and Sequencing.

Houda Gharsalli, Mohammed Alshahrani, Olfa Harbi, Nawal Alwadai, Abdalla M Al-Asiri, Fatmah Alahmari, Amal Alqahtani, Najla Al-Jahash, Lobna Abbag, Saud Alqahtani and 1 more

Abstract readReview
In one paragraph

Review in Journal of cardiovascular development and disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Houda GharsalliPulmonology Department, Aseer Central Hospital, Abha 62523, Saudi Arabia.
Mohammed AlshahraniPulmonology Department, Aseer Central Hospital, Abha 62523, Saudi Arabia.
Olfa HarbiPulmonology Section, Medical Department, Imam Abdulrahman Al-Faisal Hospital, Riyadh 11461, Saudi Arabia.
Nawal AlwadaiPulmonology Department, Aseer Central Hospital, Abha 62523, Saudi Arabia.
Abdalla M Al-AsiriPulmonology Department, Aseer Central Hospital, Abha 62523, Saudi Arabia.
Fatmah AlahmariDepartment of Internal Medicine, Aseer Central Hospital, Abha 62523, Saudi Arabia.
Amal AlqahtaniDepartment of Internal Medicine, Aseer Central Hospital, Abha 62523, Saudi Arabia.
Najla Al-JahashDepartment of Internal Medicine, Aseer Central Hospital, Abha 62523, Saudi Arabia.ORCID 0009-0007-3164-2785
Lobna AbbagDepartment of Internal Medicine, Aseer Central Hospital, Abha 62523, Saudi Arabia.
Saud AlqahtaniDepartment of Internal Medicine, Aseer Central Hospital, Abha 62523, Saudi Arabia.ORCID 0009-0005-2091-2642
Khaled Abdulwahab AmerDepartment of Internal Medicine, Aseer Central Hospital, Abha 62523, Saudi Arabia.ORCID 0000-0003-2931-7039

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic thromboembolic pulmonary hypertension (CTEPH) is a treatable yet frequently underdiagnosed late complication of acute pulmonary embolism, in which incompletely resolved thromboemboli organise into fibrotic obstructions of the pulmonary arteries and, together with a secondary small-vessel arteriopathy affecting both obstructed and non-obstructed territories, raise pulmonary vascular resistance, impose right ventricular pressure overload, and-if left untreated-progress to right heart failure and death. Three established therapies address the disease at distinct anatomical levels: pulmonary endarterectomy, the potentially curative treatment of choice for surgically accessible disease; balloon pulmonary angioplasty, for distal inoperable lesions or residual disease; and pulmonary hypertension-targeted medical therapy, for the accompanying microvasculopathy. Their evaluation in randomised controlled trials and large registries has produced a multimodal paradigm in which these treatments are combined and sequenced according to operability and lesion distribution. This narrative review synthesises evidence published through January 2026 to accomplish the following: (i) summarise and critically appraise the contemporary evidence for each modality, distinguishing guideline-supported recommendations from observational, proof-of-concept, and expert-opinion-based practice; (ii) describe how treatments are selected, sequenced, and bridged in relation to operability and to residual or recurrent pulmonary hypertension after endarterectomy; and (iii) situate treatment within the broader chronic thromboembolic pulmonary disease spectrum and the case-finding pathway after pulmonary embolism. Rather than proposing a validated algorithm, it emphasises that, because each modality carries distinct indications and risks, decisions should be individualised through multidisciplinary assessment at expert centres, with early referral central to optimising outcomes.

Indexed as

anticoagulationballoon pulmonary angioplastychronic thromboembolic pulmonary hypertensionmultimodal managementnarrative reviewpulmonary endarterectomypulmonary hypertension-targeted therapy

Identifiers

PMID42783040
PMCPMC13607472

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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.