Evidence map›Paper›PMID 41816395›Full record

ArticleJournal of thoracic disease2026

Endoscopic stenting as salvage therapy for high-risk Boerhaave's syndrome patients.

Khalid Bhatti, Samuel Wiltshire, Sufia Laulloo, Lydia M Y Chang, Christopher Ball, Vinutha D Shetty

Abstract read
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Article in Journal of thoracic 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.

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0citing papers in PubMed
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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

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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

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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

6 authors.

Khalid BhattiDepartment of Upper GI Surgery, Royal Preston Hospital, Preston, UK.ORCID https://orcid.org/0000-0002-3530-1730
Samuel WiltshireDepartment of Upper GI Surgery, Royal Preston Hospital, Preston, UK.
Sufia LaullooDepartment of Upper GI Surgery, Royal Preston Hospital, Preston, UK.
Lydia M Y ChangDepartment of Upper GI Surgery, Royal Preston Hospital, Preston, UK.
Christopher BallDepartment of General and Upper GI Surgery, Morcombe Hospital, Kendal, UK.
Vinutha D ShettyDepartment of Upper GI Surgery, Royal Preston Hospital, Preston, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Spontaneous oesophageal perforation (Boerhaave's syndrome) is a life-threatening emergency with significant morbidity and mortality. Surgical repair remains a key component of management for selected patients; however, many high-risk patients are unsuitable for operative management. This article discusses how, in these high-risk individuals, minimally invasive strategies such as the use of covered self-expanding metal stents (SEMS) offer a valuable alternative to surgery. Stent therapy aims to achieve rapid control of oesophageal leakage, limit mediastinal contamination, and facilitate early sepsis control. When applied in appropriately selected patients, this approach may reduce procedural morbidity while providing effective source control. Methods: This retrospective cohort study analysed all patients diagnosed with spontaneous oesophageal perforation between 2012 and 2024 at a tertiary referral centre. Patients deemed unfit for surgical intervention following comprehensive clinical assessment and acute multidisciplinary team (MDT) discussion-incorporating physiological status, comorbidities, Charlson Comorbidity Index (CCI), Pittsburgh score, markers of infection, and end-organ function-were managed with covered SEMS. Clinical, biochemical, and outcome data were reviewed. Results: Of 102 patients with oesophageal perforation, 69 were diagnosed with Boerhaave's syndrome. Twenty-two high-risk patients underwent endoscopic stenting with covered SEMS. The in-hospital mortality rate was 45%, predominantly from sepsis and multiorgan failure, while no deaths were directly stent-related. The 1-year survival rate was 50%. Conclusions: Endoscopic stenting offers a feasible and effective salvage option for high-risk Boerhaave's syndrome patients unsuitable for surgery. SEMS likely prevent otherwise inevitable fatalities in this cohort.

Indexed as

Boerhaave’s syndromeendoscopic stentingminimally invasive therapyoesophageal perforationself-expanding metal stents (SEMS)

Identifiers

PMID41816395
PMCPMC12972782

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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.