Evidence map›Paper›PMID 35597905›Full record

ArticleBMC pediatrics2022

Neurocognitive deficits in survivors of childhood acute myeloid leukemia.

Satoko Takahashi, Satomi Sato, Shunji Igarashi, Hitoshi Dairoku, Yuichi Takiguchi, Tetsuya Takimoto

Open access · goldAbstract read
In one paragraph

Article in BMC pediatrics, 2022. 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
2.3field-weighted citation impact, top 12% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  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

6 authors at 5 institutions in 1 country.

Satoko TakahashiDepartment of Pediatrics, Japanese Red Cross Narita Hospital, 90-1 Iida-cho, Narita-shi, Chiba, 286-8523, Japan. satoko_y0115@ga2.so-net.ne.jp.
Satomi SatoGraduate School of Public Health, St. Luke's International University, OMURA Susumu & Mieko Memorial, St. Luke's Center for Clinical Academia, 5th Floor, 3-6-2 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Shunji IgarashiDepartment of Pediatrics, Japanese Red Cross Narita Hospital, 90-1 Iida-cho, Narita-shi, Chiba, 286-8523, Japan.
Hitoshi DairokuSpecified Nonprofit Corporation LD, Dyslexia Center, #315 Applaud Ichikawa, 3-1-1 Ichikawaminami, Ichikawa-shi, Chiba, 272-0033, Japan.
Yuichi TakiguchiDepartment of Medical Oncology, Chiba University Graduate School of Medicine, 1-8-1 Inohana, Chuo-ku, Chiba-shi, Chiba, 260-8677, Japan.
Tetsuya TakimotoChildren's Cancer Center, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.
Japanese Red Cross Narita Hospital · JPChiba University · JPIchikawa Junior and Senior High School · JPNational Center For Child Health and Development · JPSt. Luke's International University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough treatment of acute myeloid leukemia (AML) contains neurotoxic agents, studies investigating neurocognitive outcomes in children with AML are sparse. We evaluated late cognitive effects in children treated with a high-dose cytarabine based regimen, focusing on general intellectual ability and specific neurocognitive domains.

methodsWe evaluated 12 survivors of childhood AML who were treated between 2006 and 2016 and completed the Wechsler Intelligence Scales. One-sample t-tests were used to compare full-scale intelligence quotient (FSIQ) and primary index scores to norms. The overall effect of index scores and subtests was examined with one-way ANOVA. Univariate analyses and multiple regression models examined demographic and clinical characteristics associated with FSIQ.

resultsParticipants who underwent the Wechsler Intelligence Scale for Children demonstrated impairment on working memory index and participants who underwent the Wechsler Adult Intelligence Scale showed low score in the subtests that reflect working memory, whereas they exhibited no statistical differences versus the population means for FSIQ. There were no significant differences in the overall effect of index scores and subtests. On univariate analysis, FSIQ were related to time since diagnosis and age at assessment, and both were significant predictors of FSIQ on multiple linear regression.

conclusionsSurvivors of childhood AML exhibited impairment of working memory, even if their FSIQ was within the normal range. Difficulties in specific cognitive domains are associated with reduced quality of life. It is important to identify survivors who are at risk and provide tailored interventions.

Indexed as

Quality of LifeSurvivorsChildCognitionHumansIntelligence TestsMemory, Short-TermAcute myeloid leukemiaChildhoodNeurocognitive deficitsQuality of lifeWorking memory

Identifiers

PMID35597905
PMCPMC9123816
OpenAlexW4281261054

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.