Evidence map›Paper›PMID 40061558›Full record

ArticleJTCVS open2025

Surgical resection of diffuse pulmonary arteriovenous malformations (PAVMs).

Aden R Falk, Lindsay J Nitsche, Colleen E Bontrager, Sarah Bond, Lauren A Beslow, Alexandra J Borst, Jennifer Pogoriler, Paul J Devlin, Elizabeth Goldmuntz, Sunil Singhal and 2 more

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In one paragraph

Article in JTCVS open, 2025. 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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Thoracoscopic Right SSurgical case reports · 2026
    Article
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Aden R FalkDivision of Cardiothoracic Surgery, Children's Hospital of Philadelphia, Philadelphia, Pa.
Lindsay J NitscheDivision of Cardiothoracic Surgery, Children's Hospital of Philadelphia, Philadelphia, Pa.
Colleen E BontragerDivision of Cardiothoracic Surgery, Children's Hospital of Philadelphia, Philadelphia, Pa.
Sarah BondDivision of Cardiothoracic Surgery, Children's Hospital of Philadelphia, Philadelphia, Pa.
Lauren A BeslowDivision of Neurology, Children's Hospital of Philadelphia, Philadelphia, Pa.
Alexandra J BorstDivision of Hematology/Oncology, Department of Pediatrics, University of North Carolina, Chapel Hill, NC.
Jennifer PogorilerDivision of Anatomic Pathology, Children's Hospital of Philadelphia, Philadelphia, Pa.
Paul J DevlinDivision of Cardiothoracic Surgery, Children's Hospital of Philadelphia, Philadelphia, Pa.
Elizabeth GoldmuntzDivision of Cardiology, Children's Hospital of Philadelphia, Philadelphia, Pa.
Sunil SinghalDivision of Cardiac Surgery, Hospital of the University of Pennsylvania, Philadelphia, Pa.
Scott O TrerotolaDivision of Interventional Radiology, Hospital of the University of Pennsylvania, Philadelphia, Pa.
Stephanie M FullerDivision of Cardiothoracic Surgery, Children's Hospital of Philadelphia, Philadelphia, Pa.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Patients with pulmonary arteriovenous malformations (PAVM) can have significant morbidity and mortality. Surgical resection in isolation or with embolization is reported to treat diffuse-type PAVMs. Herein, we describe outcomes for children and adults for whom PAVMs were managed with elective surgical resection. Methods: This retrospective analysis includes all patients treated with surgical resection for PAVM from August 1, 2009, to July 20, 2023. Demographic, diagnostic, treatment, and follow-up information were abstracted from medical records. Descriptive statistics were used. Results: Among 18 patients who underwent surgical resection of PAVMs, 12 had hereditary hemorrhagic telangiectasia. Primary indications for surgery included hemoptysis (n = 4), dyspnea (n = 8), persistence of PAVM following embolotherapy (n = 5), and stroke (n = 1). Selected PAVMs were diffuse-type (n = 14) or highly complex (n = 4). Eight patients underwent embolotherapy before surgery. Most resections were performed via thoracotomy (16/18), with 2 video-assisted thoracoscopic surgeries. Resection consisted of lobectomy (n = 14), segmentectomy (n = 3), or pneumectomy (n = 1). Median oxygen saturation improved from 90% preoperatively to 97% postoperatively. The majority (17/18) of patients were extubated in the operating room, with no major complications. The median hospital length of stay was 4.5 days (range, 2-9 days), with a median of 1 intensive care unit day (range, 1-5 days). At median follow-up of 16 months (range, 6 months-12.1 years), median oxygen saturation was 98%, no bleeding recurred, and 100% survived. Conclusions: Although embolization has been the main therapy for most PAVMs, surgical resection of diffuse-type PAVMs is safe and effective. Outcomes were excellent with improvement of oxygen saturation and functional status.

Indexed as

anatomic lung resectionembolotherapyhereditary hemorrhagic telangiectasiapulmonary arteriovenous malformation

Identifiers

PMID40061558
PMCPMC11883706

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Registered trials

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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.