Evidence map›Paper›PMID 41931323›Full record

ArticleMedicine2026

Feasibility of 80-kVp CTA with reduced iodine contrast in chronic limb-threatening ischemia.

Zequn Li, Yongzhi Zhang, Jian Zhao, Fengkai Wang, Wei Wei, Liqiang Huang

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Article in Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Zequn LiDepartment of Radiology, The Third Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Yongzhi ZhangDepartment of Radiology, The Third Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Jian ZhaoDepartment of Radiology, The Third Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Fengkai WangDepartment of Vascular Interventional Radiology, The Third Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Wei WeiDepartment of Radiology, The Third Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Liqiang HuangDepartment of Radiology, The Third Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.ORCID 0009-0002-5576-4481

Funding

Medical Science Research Project of Hebei NO.20250640
6 · The paper itself

Abstract

backgroundComputed tomography angiography (CTA) is a vital preoperative diagnostic tool for chronic limb-threatening ischemia (CLTI). However, its high radiation dose and reliance on iodine contrast agents pose significant challenges, though studies addressing these challenges in CLTI remain limited. This study evaluates the feasibility of using 80-kVp tube voltage with reduced iodine contrast dosage in CTA for CLTI patients, aiming to minimize radiation exposure and contrast volume while preserving diagnostic image quality.

methodsA total of 74 CLTI patients were prospectively enrolled and divided into 2 groups: the experimental group (n = 37) underwent CTA at 80 kVp with a contrast injection rate of 3.5 mL/s and a total volume of 75 to 85 mL; the control group (n = 37) was scanned at 120 kVp with a contrast injection rate of 4.0 mL/s and a total volume of 95 to 105 mL. Parameters including radiation dose (volume computed tomography (CT) dose index and dose-length product), iodine intake, and image quality (CT attenuation values, noise, signal-to-noise ratio, contrast-to-noise ratio, and subjective scores) were compared.

resultsThe experimental group demonstrated a 19.4% reduction in iodine intake (P < .05) and a 30.1% and 29.3% reduction in volume computed tomography dose index and dose-length product, respectively (P < .05), compared with the control group. The experimental group demonstrated significantly higher CT attenuation values and increased image noise across all measured levels (all P < .05), while maintaining comparable signal-to-noise ratio across all measured levels (all P > .05). Similarly, contrast-to-noise ratio remained equivalent between groups at the lower abdominal aorta, mid-femoral artery, and mid-popliteal artery levels (all P > .05). The subjective image quality scores showed no significant differences between the experimental and control groups, both above (4.70 ± 0.46 vs 4.74 ± 0.44, P = .43) and below (4.08 ± 0.57 vs 4.15 ± 0.60, P = .15) the popliteal artery level.

conclusionLower-limb CTA using 80-kVp tube voltage and reduced iodine contrast dosage is feasible for CLTI patients, providing diagnostic image quality while significantly reducing radiation exposure and contrast volume. This approach offers a safer and more efficient alternative for preoperative evaluation in this population.

Indexed as

Chronic Limb-Threatening IschemiaComputed Tomography AngiographyContrast MediaIodineIschemiaAgedAged, 80 and overFeasibility StudiesFemaleHumansMaleMiddle AgedProspective StudiesRadiation DosageSignal-To-Noise RatioContrast MediaIodinechronic limb-threatening ischemiacomputed tomography angiography (CTA)low iodine contrast doselow tube voltageradiation dose reduction

Identifiers

PMID41931323
PMCPMC13052980

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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.