2021
DOI: 10.11622/smedj.2019137
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Novel method of intraoperative liver tumour localisation with indocyanine green and near-infrared imaging

Abstract: Online first papers have undergone full scientific review and copyediting, but have not been typeset or proofread. To cite this article, use the DOIs number provided. Mandatory typesetting and proofreading will commence with regular print and online publication of the online first papers of the SMJ.

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Cited by 13 publications
(14 citation statements)
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References 35 publications
(55 reference statements)
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“…However, the flexibility of medical resource allocation might be poorer and the waiting time before surgery would be prolonged in this setting. A small retrospective study indicated that a shorter injection time can also result in a satisfactory imaging effect [ 16 ]. However, as the ICG administration timing remains inconclusive, another cohort study was begun last year [ 21 ].…”
Section: Discussionmentioning
confidence: 99%
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“…However, the flexibility of medical resource allocation might be poorer and the waiting time before surgery would be prolonged in this setting. A small retrospective study indicated that a shorter injection time can also result in a satisfactory imaging effect [ 16 ]. However, as the ICG administration timing remains inconclusive, another cohort study was begun last year [ 21 ].…”
Section: Discussionmentioning
confidence: 99%
“…Despite all these advantages, ICG fluorescence navigation has some inherent drawbacks. First, ICG is usually injected intravenously a few days prior to the operation and bile metabolism malfunctions in diseased (especially cirrhotic) liver, and residual ICG will affect the observation [ 13 , 16 ]. Second, regenerated nodules might show as false-positive if the bile duct is compressed [ 9 ].…”
Section: Introductionmentioning
confidence: 99%
“…Based on sequence information, mouse OATP1B2 is orthologous to human OATP1B1 and OATP1B3 (approximately 70% shared identity), whereas mouse OATP1A1 is orthologous to human OATP1A2, which is expressed in the brain [20]. A subsequent study indicated that the uptake deficit of liver-specific MRI contrast agents in Slco1a/1b knockout mice could be rescued by knock-in of human OATP1B1/1B3 [17]. The different enhancement levels between Gd-EOB-DTPA and Gd-BOPTA in OATP1B1/1B3 knock-in mice may be due to the expression ratio of OATP1B1 and OATP1B3, as evidenced in our observation that OATP1B1 is a better transporter for Gd-BOPTA than OATP1B3 is.…”
Section: Discussionmentioning
confidence: 99%
“…Previous inhibition studies and activity modification via the protein kinase C pathway showed that Gd-BOPTA is transported through OATPs and that its efflux from hepatocytes is via multiple resistanceassociated protein 3 [15,16]. However, other results identified human OATP1B1 and OATP1B3 expression in Slco1a/1b knockout mice and that OATP1B1/1B3 could not fully rescue the transportation of Gd-BOPTA in knockout mice [17]. According to these studies, the OATP family transportability toward Gd-BOPTA is not determined and we intend to use a cell line transduction model to investigate the Gd-BOPTA transport capabilities of human OATP1B1 and OATP1B3 separately.…”
Section: Introductionmentioning
confidence: 95%
“…and the lack of standardised and validated quantitative models. In this issue of the Singapore Medical Journal, Lim et al (15) described their experience with NIR imaging using ICG for intraoperative liver tumour localisation in 32 patients. A total of 46 lesions were resected, including 23 hepatocellular carcinomas, 12 colorectal liver metastases and 11 benign lesions.…”
mentioning
confidence: 99%