Cargando…

Differential Diagnosis of Hemophagocytic Syndrome by (18)F-FDG PET/CT: A Meta-Analysis

Hemophagocytic syndrome (HPS) is a rare disease in clinical practice, and there are often cases of delayed diagnosis. At present, researchers have applied (18)F-FDG PET/CT in the differential diagnosis of HPS, but no consensus has been formed. Therefore, this study aims to systematically evaluate th...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Jun, He, Bang, Wang, Jian, Ying, Caiyun, Zeng, Lingfeng, Zheng, Shiyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8817876/
https://www.ncbi.nlm.nih.gov/pubmed/35132359
http://dx.doi.org/10.1155/2022/4448993
_version_ 1784645734116622336
author Zhang, Jun
He, Bang
Wang, Jian
Ying, Caiyun
Zeng, Lingfeng
Zheng, Shiyi
author_facet Zhang, Jun
He, Bang
Wang, Jian
Ying, Caiyun
Zeng, Lingfeng
Zheng, Shiyi
author_sort Zhang, Jun
collection PubMed
description Hemophagocytic syndrome (HPS) is a rare disease in clinical practice, and there are often cases of delayed diagnosis. At present, researchers have applied (18)F-FDG PET/CT in the differential diagnosis of HPS, but no consensus has been formed. Therefore, this study aims to systematically evaluate the application value of (18)F-FDG PET/CT in the diagnosis of HPS patients. PubMed, Embase, Cochrane Library, Chinese National Knowledge Infrastructure (CNKI), Wangfang database (Wangfang), and Chinese Biomedical Network (CBM) were searched to collect the relevant studies of (18)F-FDG PET/CT in the diagnosis of HPS. Data from the articles were screened and extracted for meta-analysis using Stata16.0 software. A total of 10 retrospective studies, including 300 patients, were included in this meta-analysis. The meta-analysis results showed that the pooled sensitivity was 0.82 (95% CI: 0.67–0.95), specificity was 0.72 (95% CI: 0.51–0.86), positive likelihood ratio was 2.89 (95% CI: 1.46–5.75), positive likelihood ratio was 0.25 (95% CI: 0.12–0.54), diagnostic odds ratio was 2.89 (95% CI: 1.46–5.75), and AUC was 0.84 (95% CI: 0.81–0.87). The SUVmax in the liver, spleen, lymph nodes, and bone marrow of HPS patients was greater than 2.5, and the SUVmax in the spleen, lymph nodes, and bone marrow of malignant HPS patients was higher than that of benign HPS patients. The difference was statistically significant (P < 0.05). According to the existing literature evidence, (18)F-FDG PET/CT is an effective method for diagnosing HPS.
format Online
Article
Text
id pubmed-8817876
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-88178762022-02-06 Differential Diagnosis of Hemophagocytic Syndrome by (18)F-FDG PET/CT: A Meta-Analysis Zhang, Jun He, Bang Wang, Jian Ying, Caiyun Zeng, Lingfeng Zheng, Shiyi J Healthc Eng Research Article Hemophagocytic syndrome (HPS) is a rare disease in clinical practice, and there are often cases of delayed diagnosis. At present, researchers have applied (18)F-FDG PET/CT in the differential diagnosis of HPS, but no consensus has been formed. Therefore, this study aims to systematically evaluate the application value of (18)F-FDG PET/CT in the diagnosis of HPS patients. PubMed, Embase, Cochrane Library, Chinese National Knowledge Infrastructure (CNKI), Wangfang database (Wangfang), and Chinese Biomedical Network (CBM) were searched to collect the relevant studies of (18)F-FDG PET/CT in the diagnosis of HPS. Data from the articles were screened and extracted for meta-analysis using Stata16.0 software. A total of 10 retrospective studies, including 300 patients, were included in this meta-analysis. The meta-analysis results showed that the pooled sensitivity was 0.82 (95% CI: 0.67–0.95), specificity was 0.72 (95% CI: 0.51–0.86), positive likelihood ratio was 2.89 (95% CI: 1.46–5.75), positive likelihood ratio was 0.25 (95% CI: 0.12–0.54), diagnostic odds ratio was 2.89 (95% CI: 1.46–5.75), and AUC was 0.84 (95% CI: 0.81–0.87). The SUVmax in the liver, spleen, lymph nodes, and bone marrow of HPS patients was greater than 2.5, and the SUVmax in the spleen, lymph nodes, and bone marrow of malignant HPS patients was higher than that of benign HPS patients. The difference was statistically significant (P < 0.05). According to the existing literature evidence, (18)F-FDG PET/CT is an effective method for diagnosing HPS. Hindawi 2022-01-29 /pmc/articles/PMC8817876/ /pubmed/35132359 http://dx.doi.org/10.1155/2022/4448993 Text en Copyright © 2022 Jun Zhang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhang, Jun
He, Bang
Wang, Jian
Ying, Caiyun
Zeng, Lingfeng
Zheng, Shiyi
Differential Diagnosis of Hemophagocytic Syndrome by (18)F-FDG PET/CT: A Meta-Analysis
title Differential Diagnosis of Hemophagocytic Syndrome by (18)F-FDG PET/CT: A Meta-Analysis
title_full Differential Diagnosis of Hemophagocytic Syndrome by (18)F-FDG PET/CT: A Meta-Analysis
title_fullStr Differential Diagnosis of Hemophagocytic Syndrome by (18)F-FDG PET/CT: A Meta-Analysis
title_full_unstemmed Differential Diagnosis of Hemophagocytic Syndrome by (18)F-FDG PET/CT: A Meta-Analysis
title_short Differential Diagnosis of Hemophagocytic Syndrome by (18)F-FDG PET/CT: A Meta-Analysis
title_sort differential diagnosis of hemophagocytic syndrome by (18)f-fdg pet/ct: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8817876/
https://www.ncbi.nlm.nih.gov/pubmed/35132359
http://dx.doi.org/10.1155/2022/4448993
work_keys_str_mv AT zhangjun differentialdiagnosisofhemophagocyticsyndromeby18ffdgpetctametaanalysis
AT hebang differentialdiagnosisofhemophagocyticsyndromeby18ffdgpetctametaanalysis
AT wangjian differentialdiagnosisofhemophagocyticsyndromeby18ffdgpetctametaanalysis
AT yingcaiyun differentialdiagnosisofhemophagocyticsyndromeby18ffdgpetctametaanalysis
AT zenglingfeng differentialdiagnosisofhemophagocyticsyndromeby18ffdgpetctametaanalysis
AT zhengshiyi differentialdiagnosisofhemophagocyticsyndromeby18ffdgpetctametaanalysis