Evidence map›Paper›PMID 40261331›Full record

ReviewOrthopadie (Heidelberg, Germany)2025

Bone marrow lesions related to bone marrow edema syndromes and osteonecrosis.

Gad Shabshin, Nogah Shabshin

Abstract readReview
In one paragraph

Review in Orthopadie (Heidelberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

2 authors.

Gad ShabshinFaculty of Medicine, Tel Aviv University, 35 Klachkin st., Tel Aviv, Israel, 6997801. gadshabshin@mail.tau.ac.il.
Nogah ShabshinDepartment of Radiology, Emek Medical Center, Clalit Health Services, Afula, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone marrow lesions (BML) are abnormalities in the bone marrow identified on magnetic resonance imaging (MRI) and can generally be classified as traumatic or atraumatic. This review focuses on atraumatic bone marrow edema syndromes (BMES) and their imaging evaluation. The MRI remains the modality of choice for assessing BMES, particularly using fluid-sensitive sequences although other sequences such as Dixon and T1-weighted imaging can be of further assistance. Emerging evidence supports dual-energy CT (DECT) as a reliable alternative, with high sensitivity and specificity for detecting bone marrow edema. The term BMES is a collective term for conditions, such as transient osteoporosis (TO) and regional migratory osteoporosis (RMO), predominantly affect weight-bearing bones in middle-aged individuals and pregnant or postpartum females. Subchondral insufficiency fractures of the knee (SIFK) are a key subset of BMES. These fractures most commonly involve the medial femoral condyle (MFC) and are associated with risk factors, such as meniscal root tears and extrusion of the meniscal body. The MRI findings typically include bone marrow edema-like signals and subchondral fracture lines, with additional features, such as secondary osteonecrosis in advanced cases. Prognostic indicators are crucial for stratifying patients and guiding management. Low-grade or reversible lesions often resolve with conservative treatment, whereas high-grade or irreversible lesions may require surgical intervention.Avascular necrosis, another atraumatic BML entity, differs from BMES by its association with systemic factors, such as steroid use or alcohol abuse. Accurate imaging, particularly in the early stages, is vital to distinguish between reversible and irreversible lesions, facilitating timely and appropriate management.

Indexed as

Bone MarrowBone Marrow DiseasesEdemaOsteonecrosisFemaleHumansMagnetic Resonance ImagingSyndromeTomography, X-Ray ComputedAvascular necrosisDual-energy computed tomographyMagnetic resonance imagingSensitivity and specificitySubchondral insufficiency fracture of the knee

Identifiers

PMID40261331
PMCPMC12037679

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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.