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    Performance of Biopsy Needle With Therapeutic Injection System to Prevent Bleeding Complications

    Source: Journal of Medical Devices:;2013:;volume( 007 ):;issue: 001::page 11002
    Author:
    Wong, Philip
    ,
    Johnson, Kent J.
    ,
    Warner, Roscoe L.
    ,
    Merz, Scott I.
    ,
    Kruger, Grant H.
    ,
    Weitzel, William F.
    DOI: 10.1115/1.4023274
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Renal disease is epidemic in the United States with approximately 8 أ— 106 people having chronic kidney disease. Renal biopsies are widely used to provide essential diagnostic information to physicians. However, the risk of bleeding complications possibly leading to lifethreatening situations results in the contraindication of biopsy in certain patient populations. Safer renal biopsies will allow more accurate diagnosis and better management of this epidemic health problem. We report the preclinical testing of a novel biopsy device called the therapeutic injection system (TIS). The device introduces a third stage to the standard twostage sidecut percutaneous biopsy process. The third stage is designed to reduce bleeding complications by injecting a hemostatic plug at the time of biopsy. Laboratory evaluation and preliminary in vivo animal testing using an anticoagulated porcine model of the TIS and Bard Monoptyآ® (Bard Medical, Covington, GA) control device were performed. The hemostatic material Gelfoamآ® (Pfizer, Brussels, Belgium) was selected as the active material comprising the hemostatic plugs. The performance of two composite plugs, one composed of polyvinyl alcohol (PVA) combined in 2:1 and 12:1 ratios with the hemostatic material, and one plug composed of 100% hemostatic material were tested. Stroke sequence and hemostatic plug deployment were verified by sequential firing of the TIS biopsy needle into clear gelatin and ex vivo bovine kidney specimens. In vivo trials with porcine specimens revealed a significant reduction in blood loss (8.1 آ± 3.9 ml, control versus 1.9 آ± 1.6 ml, 12:1 PVA/hemostatic, TIS, خ±â€‰= 0.01, n = 6). The 100% hemostatic plug showed a substantial and immediate reduction in blood loss (9.2 ml, control versus 0.0 ml, TIS, n = 1). The prototype device was shown to work repeatedly and reliably in laboratory trials. Initial results show promise in this approach to control post biopsy bleeding. This solution maintains the simplicity and directness of the percutaneous approach, while not significantly changing the standard percutaneous biopsy procedure.
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      Performance of Biopsy Needle With Therapeutic Injection System to Prevent Bleeding Complications

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    contributor authorWong, Philip
    contributor authorJohnson, Kent J.
    contributor authorWarner, Roscoe L.
    contributor authorMerz, Scott I.
    contributor authorKruger, Grant H.
    contributor authorWeitzel, William F.
    date accessioned2017-05-09T01:01:21Z
    date available2017-05-09T01:01:21Z
    date issued2013
    identifier issn1932-6181
    identifier othermed_7_1_011002.pdf
    identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/152661
    description abstractRenal disease is epidemic in the United States with approximately 8 أ— 106 people having chronic kidney disease. Renal biopsies are widely used to provide essential diagnostic information to physicians. However, the risk of bleeding complications possibly leading to lifethreatening situations results in the contraindication of biopsy in certain patient populations. Safer renal biopsies will allow more accurate diagnosis and better management of this epidemic health problem. We report the preclinical testing of a novel biopsy device called the therapeutic injection system (TIS). The device introduces a third stage to the standard twostage sidecut percutaneous biopsy process. The third stage is designed to reduce bleeding complications by injecting a hemostatic plug at the time of biopsy. Laboratory evaluation and preliminary in vivo animal testing using an anticoagulated porcine model of the TIS and Bard Monoptyآ® (Bard Medical, Covington, GA) control device were performed. The hemostatic material Gelfoamآ® (Pfizer, Brussels, Belgium) was selected as the active material comprising the hemostatic plugs. The performance of two composite plugs, one composed of polyvinyl alcohol (PVA) combined in 2:1 and 12:1 ratios with the hemostatic material, and one plug composed of 100% hemostatic material were tested. Stroke sequence and hemostatic plug deployment were verified by sequential firing of the TIS biopsy needle into clear gelatin and ex vivo bovine kidney specimens. In vivo trials with porcine specimens revealed a significant reduction in blood loss (8.1 آ± 3.9 ml, control versus 1.9 آ± 1.6 ml, 12:1 PVA/hemostatic, TIS, خ±â€‰= 0.01, n = 6). The 100% hemostatic plug showed a substantial and immediate reduction in blood loss (9.2 ml, control versus 0.0 ml, TIS, n = 1). The prototype device was shown to work repeatedly and reliably in laboratory trials. Initial results show promise in this approach to control post biopsy bleeding. This solution maintains the simplicity and directness of the percutaneous approach, while not significantly changing the standard percutaneous biopsy procedure.
    publisherThe American Society of Mechanical Engineers (ASME)
    titlePerformance of Biopsy Needle With Therapeutic Injection System to Prevent Bleeding Complications
    typeJournal Paper
    journal volume7
    journal issue1
    journal titleJournal of Medical Devices
    identifier doi10.1115/1.4023274
    journal fristpage11002
    journal lastpage11002
    identifier eissn1932-619X
    treeJournal of Medical Devices:;2013:;volume( 007 ):;issue: 001
    contenttypeFulltext
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    DSpace software copyright © 2002-2015  DuraSpace
    نرم افزار کتابخانه دیجیتال "دی اسپیس" فارسی شده توسط یابش برای کتابخانه های ایرانی | تماس با یابش
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