Evidence map›Paper›PMID 28214496›Full record

ReviewJournal of vascular surgery. Venous and lymphatic disorders2017

New diagnostic modalities in the evaluation of lymphedema.

Thomas F O'Donnell, John C Rasmussen, Eva M Sevick-Muraca

Abstract readReview
In one paragraph

Review in Journal of vascular surgery. Venous and lymphatic disorders, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 2% of its field
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

54 citing papers in PubMed, 1 synthesis or guideline pooled it, 163 citations in OpenAlex.

  1. Biomaterials in the clinical treatment of lymphedema-a systematic review.Journal of vascular surgery. Venous and lymphatic disorders · 2024
    Pooled it
  2. Review
  3. Article
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  6. Review
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  12. Review
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  15. Supermicrosurgical lymphovenous anastomosis.Journal of the Chinese Medical Association : JCMA · 2024
    Review
  16. Lymphoscintigraphy is frequently recommended but seldom used in a "real world setting".Journal of vascular surgery. Venous and lymphatic disorders · 2024
    Article
  17. Evaluation of Primary Lymphedema with Intranodal Lymphangiography.Cardiovascular and interventional radiology · 2024
    Observational
  18. Review
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  20. Review
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

3 authors at 2 institutions in 1 country.

Thomas F O'DonnellCardiovascular Center at Tufts Medical Center, Tufts University School of Medicine, Boston, Mass. Electronic address: todonnell@tuftsmedicalcenter.org.
John C RasmussenThe Center for Molecular Imaging, The Brown Foundation Institute of Molecular Medicine for the Prevention of Human Diseases at the University of Texas Health Science Center at Houston, Houston, Tex.
Eva M Sevick-MuracaThe Center for Molecular Imaging, The Brown Foundation Institute of Molecular Medicine for the Prevention of Human Diseases at the University of Texas Health Science Center at Houston, Houston, Tex.
Brown Foundation · USTufts University · US

Funding

Task Specific Project 4U54CA136404 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI SEVICK, EVA M. · 2008 to 2012
$5.1M
Functional lymph angiography with NIR imagingR01HL092923 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI SEVICK, EVA M. · 2008 to 2011
$1.5M
Lymphatic contribution to progressive peripheral vascular disease and ulcerationR21HL132598 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI RASMUSSEN, JOHN CHARLES, SEVICK, EVA M. · 2016 to 2017
$424k
NCI NIH HHS U54 CA136404NHLBI NIH HHS R01 HL092923NHLBI NIH HHS R21 HL132598
6 · The paper itself

Abstract

objectiveCurrently, lymphedema (LED) is typically diagnosed clinically on the basis of a patient's history and characteristic physical findings. Whereas the diagnosis of LED is sometimes confirmed by lymphoscintigraphy (LSG), the technique is limited in both its ability to identify disease and to guide therapy. Recent advancements provide opportunities for new imaging techniques not only to assist in the diagnosis of LED, based on anatomic changes, but also to assess contractile function and to guide therapeutic intervention. The purpose of this contribution was to review these imaging techniques.

methodsLiterature for each technique is reviewed and discussed, and the evidence for each of these new diagnostic techniques was assessed on several criteria to determine if each could (1) establish whether disease is present, (2) determine the severity of the disease process, (3) define the pathophysiologic mechanism of the disease process, (4) demonstrate whether intervention is possible as well as what type, and (5) objectively grade the response to therapy.

resultsLSG is currently the standard test to confirm LED. Duplex ultrasound (DUS) is a simple, readily available noninvasive test that can identify LED by specific tissue characteristics as well as the response to therapy. Magnetic resonance imaging and computed tomography scans similarly demonstrate the alterations in epidermal and subcutaneous tissue, but the latter can also detect obstructing neoplasms as a cause of secondary LED. Moreover, magnetic resonance lymphangiography details lymphatic vessels and nodes and their function. Newer fluorescence imaging techniques provide opportunities to image lymphatic anatomy and function. Visible microlymphangiography by fluorescein sodium is limited by tissue light absorption to imaging depths of 200 μm. Near-infrared fluorescence lymphatic imaging, a newer test using intradermal injection of indocyanine green, can penetrate several centimeters of tissue and can visualize the initial and conducting lymphatics, the lymph node basins, and the active function of lymphangions (the key module) in exquisite detail.

conclusionsThe availability and the noninvasive nature of DUS should make this modality the first choice for establishing the diagnosis of LED based on tissue changes. Further studies comparing DUS with LSG, however, are needed. The costs of magnetic resonance imaging and computed tomography limit their adoption as a means to regularly assess the lymphatics. Whereas lymphatic truncal anatomy and transit times can be delineated by the older technique of LSG, near-infrared fluorescence lymphatic imaging is rapid, highly sensitive, and repeatable and provides exquisite detail for lymphatic vessel anatomy and function of the lymphangions as well as the response to therapy.

Indexed as

Contrast MediaFluorescenceHumansLymphatic SystemLymphedemaLymphographyMagnetic Resonance AngiographySensitivity and SpecificityTomography, X-Ray ComputedUltrasonography, DopplerContrast Media

Identifiers

PMID28214496
PMCPMC5325714
OpenAlexW2572796183

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.