2022
DOI: 10.1016/j.artd.2022.08.021
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Digital Fluoroscopic Navigation for Limb Length Restoration During Anterior Total Hip Arthroplasty

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Cited by 3 publications
(3 citation statements)
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“…have evaluated the use of DA THA with standard fluoroscopy to guide component placement and reported more accurate postoperative LLD (1.6 mm) compared to non-navigated posterior THA (5.5 mm) ( P < .0001) [ 28 ]. Using fluoroscopic-assisted computer navigation software, O’Leary and colleagues report LLD accuracy within ± 3 mm of the intended target in 66% of THAs, which was a statistical improvement over the LLD accuracy (40% within ± 3 mm of the intended target) using standard fluoroscopy ( P < .01) [ 15 ]. Our data are consistent with the previous authors in that we report a high degree of LLD accuracy using fluoroscopic-assisted AI computer navigation; on final radiographs, 66% of THAs were within 2 mm of the AI-navigated intraoperative LLD, and 98% were within 5 mm.…”
Section: Discussionmentioning
confidence: 99%
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“…have evaluated the use of DA THA with standard fluoroscopy to guide component placement and reported more accurate postoperative LLD (1.6 mm) compared to non-navigated posterior THA (5.5 mm) ( P < .0001) [ 28 ]. Using fluoroscopic-assisted computer navigation software, O’Leary and colleagues report LLD accuracy within ± 3 mm of the intended target in 66% of THAs, which was a statistical improvement over the LLD accuracy (40% within ± 3 mm of the intended target) using standard fluoroscopy ( P < .01) [ 15 ]. Our data are consistent with the previous authors in that we report a high degree of LLD accuracy using fluoroscopic-assisted AI computer navigation; on final radiographs, 66% of THAs were within 2 mm of the AI-navigated intraoperative LLD, and 98% were within 5 mm.…”
Section: Discussionmentioning
confidence: 99%
“…Previous authors have compared the use of fluoroscopic-assisted computer navigation to standard fluoroscopy for assessing LLD, where the primary outcome of interest was the difference between the mean planned and actual LLD. Categorizing this difference into 6 categories (up to 1 mm, 1-2 mm, 2-3 mm, 3-4 mm, 4-5 mm, and >5 mm), the authors performed a sample size calculation and determined that a minimum sample of 100 patients (50 per group) was required to achieve a power of 0.8 [ 15 ]. We further performed a sample size/power calculation (assuming α = 0.05 and power = 0.8) and determined the total sample size required to be 376 subjects (188 in each group) to determine a clinically significant 5% difference between manual and AI groups for ΔLLD within ±5 mm.…”
Section: Methodsmentioning
confidence: 99%
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