Objectives: This study aimed to evaluate the feasibility of reduced full-of-view synthetic high-b value diffusion-weighted images (rFOV-syDWIs) in the clinical application of cervical cancer based on image quality and diagnostic efficacy.

Methods: We retrospectively evaluated the data of 35 patients with cervical cancer and 35 healthy volunteers from May to November 2021. All patients and volunteers underwent rFOV-DWI scans, including a 13b-protocol: b = 0, 25, 50, 75, 100, 150, 200, 400, 600, 800, 1000, 1200, and 1500 s/mm and a 5b-protocol: b = 0, 100, 400, 800,1500 s/mm. rFOV-syDWIs with b values of 1200 (rFOV-syDWI) and 1500 (rFOV-syDWI) were generated from two different multiple-b-value image datasets using a mono-exponential fitting algorithm. According to homoscedasticity and normality assessed by the Levene's test and Shapiro-Wilk test, the inter-modality differences of quantitative measurements were, respectively, examined by Wilcoxon signed-rank test or paired t test and the inter-group differences of ADC values were examined by independent t test or Mann-Whitney U test.

Results: A higher inter-reader agreement between SNRs and CNRs was found in 13b-protocol and 5b-protocol rFOV-syDWI compared to 13b-protocol rFOV-sDWI (p < 0.05). AUC of 5b-protocol syADC and syADC was equal or higher than that of 13b-protocol sADC and sADC.

Conclusions: rFOV-syDWIs provide better lesion clarity and higher image quality than rFOV-sDWIs. 5b-protocol rFOV-syDWIs shorten scan time, and synthetic ADCs offer reliable diagnosis value as scanned 13b-protocol DWIs.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842823PMC
http://dx.doi.org/10.1186/s13244-022-01350-0DOI Listing

Publication Analysis

Top Keywords

reduced full-of-view
8
full-of-view synthetic
8
cervical cancer
8
b = 0 100
8
test
5
feasibility study
4
study reduced
4
synthetic high-b-value
4
high-b-value diffusion-weighted
4
diffusion-weighted imaging
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!