Background: Congenital heart disease (CHD) is a major contributor to morbidity and infant mortality and imposes the highest burden on global healthcare costs. Early diagnosis and prompt treatment of CHD contribute to enhanced neonatal outcomes and survival rates; however, there is a shortage of proficient examiners in remote regions. Artificial intelligence (AI)-powered ultrasound provides a potential solution to improve the diagnostic accuracy of fetal CHD screening.
Methods: A literature search was conducted across seven databases for systematic review. Articles were retrieved based on PRISMA Flow 2020 and inclusion and exclusion criteria. Eligible diagnostic data were further meta-analyzed, and the risk of bias was tested using Quality Assessment of Diagnostic Accuracy Studies-Artificial Intelligence.
Findings: A total of 374 studies were screened for eligibility, but only 9 studies were included. Most studies utilized deep learning models using either ultrasound or echocardiographic images. Overall, the AI models performed exceptionally well in accurately identifying normal and abnormal ultrasound images. A meta-analysis of these nine studies on CHD diagnosis resulted in a pooled sensitivity of 0.89 (0.81-0.94), a specificity of 0.91 (0.87-0.94), and an area under the curve of 0.952 using a random-effects model.
Conclusion: Although several limitations must be addressed before AI models can be implemented in clinical practice, AI has shown promising results in CHD diagnosis. Nevertheless, prospective studies with bigger datasets and more inclusive populations are needed to compare AI algorithms to conventional methods.
Systematic Review Registration: https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42023461738, PROSPERO (CRD42023461738).
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http://dx.doi.org/10.3389/fcvm.2025.1473544 | DOI Listing |
Anal Chem
March 2025
College of Chemistry, Jilin Province Research Center for Engineering and Technology of Spectral Analytical Instruments, Jilin University, Qianjin Street 2699, Changchun 130012, China.
The lack of precise, real-time analytical tools for monitoring tumor microenvironment changes during treatment hinders advancements in integrated diagnostic and therapeutic platforms. Traditional caspase-3 monitoring strategies are limited by their inability to address drug resistance and newly discovered apoptotic pathways, leading to reduced accuracy and practicality. To overcome these limitations, we developed a fluorescence-based "Trojan horse" nanosystem, PFpR@CM, featuring high-sensitivity Caspase-1 detection, tumor-targeted delivery, and photothermal therapy.
View Article and Find Full Text PDFTrans R Soc Trop Med Hyg
March 2025
Molecular Epidemiology department, ICMR-National Institute of Malaria Research, Sector 8, Dwarka, 110077 New Delhi, India.
Background: Rapid diagnostic tests (RDTs) are vital for malaria diagnosis, especially in resource-limited areas. RDTs targeting histidine-rich protein 2 (PfHRP2) and its structural homologue PfHRP3 are commonly used for detecting Plasmodium falciparum. However, genetic deletions in these proteins can affect test accuracy.
View Article and Find Full Text PDFChatGPT and other artificial intelligence (AI) tools can modify nutritional management in clinical settings. These technologies, based on machine learning and deep learning, enable the identification of risks, the proposal of personalized interventions, and the monitoring of patient progress using data extracted from clinical records. ChatGPT excels in areas such as nutritional assessment by calculating caloric needs and suggesting nutrient-rich foods, and in diagnosis, by identifying nutritional issues with technical terminology.
View Article and Find Full Text PDFBackground: The Sysmex DI-60 system (Sysmex, Kobe, Japan) is an automated cell image analyzer that captures and analyzes cell images. The aim of this study was to evaluate the performance of DI-60 for leukocyte differential count in comparison with manual differential count and XN-20.
Methods: A total of 205 samples were analyzed and the agreement between DI-60 pre-classification and post-verification by medical technicians was determined.
Background: Tuberculosis is still a significant global health challenge, with latent tuberculosis infection (LTBI) posing a risk for the development of active disease. This study aimed to compare the performance of the STAN-DARD F TB-Feron FIA test with the QuantiFERON-TB Gold Plus, a test endorsed by the World Health Organization (WHO), in detecting LTBI.
Methods: We included 137 participants, out of which 58.
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