Evidence map›Paper›PMID 34222154›Full record

ArticleFrontiers in pediatrics2021

Diagnostic Time Lag of Pediatric Haemophagocytic Lymphohistiocytosis and Patient Characteristics: A Retrospective Cohort Study.

Xun Li, Haipeng Yan, Zhenghui Xiao, Xinping Zhang, Jiaotian Huang, Shi-Ting Xiang, Mincui Zheng, Zhenya Yao, Ping Zang, Desheng Zhu and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pediatrics, 2021. 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
1.3field-weighted citation impact, top 19% 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, 11 citations in OpenAlex.

  1. Article
  2. Diagnostic delay in monogenic disease: A scoping review.Genetics in medicine : official journal of the American College of Medical Genetics · 2024
    Article
  3. Article
  4. Article
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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

12 authors at 1 institution in 1 country.

Xun LiPediatrics Research Institute of Hunan Province, Hunan Children's Hospital, Changsha, China.
Haipeng YanDepartment of Pediatric Intensive Care Unit, Hunan Children's Hospital, Changsha, China.
Zhenghui XiaoDepartment of Pediatric Intensive Care Unit, Hunan Children's Hospital, Changsha, China.
Xinping ZhangDepartment of Pediatric Intensive Care Unit, Hunan Children's Hospital, Changsha, China.
Jiaotian HuangDepartment of Pediatric Intensive Care Unit, Hunan Children's Hospital, Changsha, China.
Shi-Ting XiangPediatrics Research Institute of Hunan Province, Hunan Children's Hospital, Changsha, China.
Mincui ZhengDepartment of Pediatric Hematology, Hunan Children's Hospital, Changsha, China.
Zhenya YaoDepartment of Pediatric Intensive Care Unit, Hunan Children's Hospital, Changsha, China.
Ping ZangDepartment of Pediatric Intensive Care Unit, Hunan Children's Hospital, Changsha, China.
Desheng ZhuDepartment of Pediatric Intensive Care Unit, Hunan Children's Hospital, Changsha, China.
Liping LiPediatrics Research Institute of Hunan Province, Hunan Children's Hospital, Changsha, China.
Xiulan LuDepartment of Pediatric Intensive Care Unit, Hunan Children's Hospital, Changsha, China.
Hunan Children's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The difficulties and challenges of applying the HLH-2004 diagnostic criteria to early identification and diagnosis of haemophagocytic lymphohistiocytosis have been fully addressed in previous studies. However, the distribution of the diagnostic time lag of haemophagocytic lymphohistiocytosis and related patient characteristics remain unclear. This study investigated the time lags between symptom onset and diagnosis and between hospital admission and diagnosis among pediatric patients with haemophagocytic lymphohistiocytosis, and identified factors that associated with a shorter or longer diagnostic time lag. The cohort of patients with haemophagocytic lymphohistiocytosis was drawn from a tertiary children's hospital and consisted of 122 pediatric patients. The distributions of symptom-to-diagnosis and admission-to-diagnosis time lags were assessed. Clinical characteristics within 48 h of admission and the fulfillment of HLH-2004 diagnostic criteria were compared among admission-to-diagnosis time lag categories. Logistic regression analyses were conducted to identify factors associated with an admission-to-diagnosis time lag >3 days. The median interval from first symptom onset to HLH diagnosis was 12 days (range 4-71 days) and the median interval from hospital admission to HLH diagnosis was 2 days (range 0-23 days). The following factors were negatively associated with admission-to-diagnosis > 3 days: Epstein-Barr virus infection; admission through pediatric intensive care unit; diagnosis established without NK-cell activity and soluble CD25 tests; the performance of all readily available diagnostic tests for HLH (within 48 and 72 h); concurrent fever, splenomegaly, and cytopenias within 48 h; hemophagocytosis, hypertriglyceridemia and/or hypofibrinogenemia within 48 h; and elevated ferritin, total bilirubin, alanine aminotransferase, and prothrombin time within 48 h. Our findings suggest that performance of adequate diagnostic tests for HLH is essential for early diagnosis of HLH. Once suspected, immediate and adequate diagnostic tests for HLH should be arranged for PICU patients. Improvements in diagnostic procedures and monitoring plans are needed to promote early diagnosis of HLH.

Indexed as

diagnostic criteriahaemophagocytic lymphohistiocytosishaemophagocytosisrisk factortime lag

Identifiers

PMID34222154
PMCPMC8247774
OpenAlexW3175949006

What OpenQuestion holds

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LicenceCC BY
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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.