Evidence map›Paper›PMID 30700943›Full record

ArticleWorld journal of gastroenterology2019

Treatment for gastric 'indefinite for neoplasm/dysplasia' lesions based on predictive factors.

Mi Jung Kwon, Ho Suk Kang, Hyeon Tae Kim, Jin Woo Choo, Bo Hyun Lee, Sung Eun Hong, Kun Ha Park, Dong Min Jung, Hyun Lim, Jae Seung Soh and 6 more

Abstract read
In one paragraph

Article in World journal of gastroenterology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. [Approach for the Management of Indefinite-for-neoplasia Lesions Detected on Gastric Mucosal Biopsy].The Korean journal of helicobacter and upper gastrointestinal research · 2023
    Review
  3. Review
  4. Article
  5. 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

16 authors.

Mi Jung KwonDepartment of Pathology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang 14068, South Korea.
Ho Suk KangDepartment of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang-si 431-796, South Korea. hskang76@hallym.or.kr.
Hyeon Tae KimDepartment of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang-si 431-796, South Korea.
Jin Woo ChooDepartment of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang-si 431-796, South Korea.
Bo Hyun LeeDepartment of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang-si 431-796, South Korea.
Sung Eun HongDepartment of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang-si 431-796, South Korea.
Kun Ha ParkDepartment of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang-si 431-796, South Korea.
Dong Min JungDepartment of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang-si 431-796, South Korea.
Hyun LimDepartment of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang-si 431-796, South Korea.
Jae Seung SohDepartment of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang-si 431-796, South Korea.
Sung Hoon MoonDepartment of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang-si 431-796, South Korea.
Jong Hyeok KimDepartment of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang-si 431-796, South Korea.
Hye-Rim ParkDepartment of Pathology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang 14068, South Korea.
Soo Kee MinDepartment of Pathology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang 14068, South Korea.
Jin Won SeoDepartment of Pathology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang 14068, South Korea.
Ji-Young ChoeDepartment of Pathology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang 14068, South Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastric 'indefinite for neoplasm/dysplasia' (IFND) is a borderline lesion that is difficult to diagnose as either regenerative or neoplastic. There is a need for guidance in the identification of a subset of patients, who have an IFND lesion with a higher risk of malignant potential, to enable risk stratification and optimal management.

aimTo determine the clinical and pathologic factors for the accurate diagnosis of gastric IFND lesions.

methodsIn total, 461 gastric lesions diagnosed

resultsFour clinical factors [age ≥ 60 years (2.445, 95%CI: 1.305-4.580,

conclusionMore than two clinical and pathologic factors each had significant cut-off values for gastric carcinoma diagnosis; in such cases, endoscopic resection should be considered.

Indexed as

AdenocarcinomaAdolescentAdultAgedAged, 80 and overBiopsyDelayed DiagnosisDiagnosis, DifferentialFemaleGastric MucosaGastritisGastroscopyHumansMaleMiddle AgedPatient SelectionBiopsyDiagnostic delayEndoscopic surgical procedureGastric cancerPrognosis

Identifiers

PMID30700943
PMCPMC6350171

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.