Iliocaval and Iliofemoral Venous Stenting for Obstruction Secondary to Tumor Compression: Single Center Experience. (Record no. 14259)

MARC details
000 -LEADER
fixed length control field 03191nam a22003617a 4500
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fixed length control field 240723s20232023 xxu||||| |||| 00| 0 eng d
024 ## - OTHER STANDARD IDENTIFIER
Standard number or code PMC10705686 [pmc]
040 ## - CATALOGING SOURCE
Original cataloging agency Ovid MEDLINE(R)
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
PMID 38076963
245 ## - TITLE STATEMENT
Title Iliocaval and Iliofemoral Venous Stenting for Obstruction Secondary to Tumor Compression: Single Center Experience.
251 ## - Source
Source Research Square. 2023 Nov 28
252 ## - Abbreviated Source
Abbreviated source Res Sq. 2023 Nov 28
253 ## - Journal Name
Journal name Research square
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Year 2023
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Publication date 2023 Nov 28
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Manufacturer FY2024
265 ## - SOURCE FOR ACQUISITION/SUBSCRIPTION ADDRESS [OBSOLETE]
Publication status epublish
265 ## - SOURCE FOR ACQUISITION/SUBSCRIPTION ADDRESS [OBSOLETE]
Medline status PubMed-not-MEDLINE
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Abstract Background: Cancer patients with pelviabdominal masses can suffer from lower extremity symptoms due to venous compression. The effectiveness of venous stenting has been established in extrinsic venous compression in benign conditions like May-Thurner syndrome. In this retrospective study we evaluate the efficacy and safety of caval, iliocaval and iliofemoral venous stenting for cases of extrinsic venous compression caused by malignant masses in cancer patients.
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Abstract Conclusion: Venous stenting is a safe procedure and should be considered as part of the palliative care for patients with debilitating lower extremity symptoms related to iliocaval and iliofemoral venous compression.
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Abstract Methods: IRB-approved retrospective review of patients who underwent iliofemoral venography with venoplasty and stenting between January 2018 and February 2022 was performed. Patients with extrinsic venous compression caused by malignant masses were included. Data on patient demographics, pre-procedure symptoms, procedural technique, stent characteristics, outcomes and follow-up were collected. Descriptive statistics were used to assess technical success, clinical success, primary stent patency and adverse events of the procedure.
520 ## - SUMMARY, ETC.
Abstract Results: Thirty-seven patients (19 males, 18 females) who underwent 45 procedures were included. Deep venous thrombosis (DVT) was present in 21 (57%) patients. Twenty-nine patients (78%, 95% CI 62-90%) reported clinical improvement of the presenting symptoms. The median overall survival after the procedure was 4.7 months (95% CI 3.58-5.99). Eight (22%) patients were alive at last follow up with median follow up of 10.33 months (Range 2-25 months). Twenty-six patients had patent stents on their last follow up imaging (70%, 95% CI 61%-91%). Two patients had a small access site hematoma which resolved spontaneously. Two patients developed moderate, and 1 patient developed severe adverse events related to post procedure therapeutic anticoagulation.
546 ## - LANGUAGE NOTE
Language note English
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Indexing Automated
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Institution MedStar Washington Hospital Center
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Department Radiology
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Medline publication type Preprint
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Local Authors Aly, Ahmed K
Institution Code MWHC
790 ## - Authors
All authors Aly AK, Moussa A, Chevallier O, Kishore S, Petre E, Friedman A, Bryce Y, Gonzalez-Aguirre A, Camacho J, Santos E, Ridouani F
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DOI <a href="https://dx.doi.org/10.21203/rs.3.rs-3588250/v1">https://dx.doi.org/10.21203/rs.3.rs-3588250/v1</a>
Public note https://dx.doi.org/10.21203/rs.3.rs-3588250/v1
858 ## - ORCID
ORCID text Aly, Ahmed K
Orcid <a href="https://orcid.org/0000-0002-1050-3205">https://orcid.org/0000-0002-1050-3205</a>
Name https://orcid.org/0000-0002-1050-3205
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Journal Article
Item type description Article
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Withdrawn status Lost status Damaged status Not for loan Collection Home library Current library Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
              07/23/2024   38076963 38076963 07/23/2024 07/23/2024 Journal Article

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