Percutaneous Ultrasound Gastrostomy (PUG): Engineering and Feasibility Assessment of a Pediatric Device

Information

  • Research Project
  • 9909329
  • ApplicationId
    9909329
  • Core Project Number
    R43DK123910
  • Full Project Number
    1R43DK123910-01
  • Serial Number
    123910
  • FOA Number
    PA-18-574
  • Sub Project Id
  • Project Start Date
    9/20/2019 - 5 years ago
  • Project End Date
    2/28/2020 - 4 years ago
  • Program Officer Name
    DENSMORE, CHRISTINE L
  • Budget Start Date
    9/20/2019 - 5 years ago
  • Budget End Date
    2/28/2020 - 4 years ago
  • Fiscal Year
    2019
  • Support Year
    01
  • Suffix
  • Award Notice Date
    9/19/2019 - 5 years ago
Organizations

Percutaneous Ultrasound Gastrostomy (PUG): Engineering and Feasibility Assessment of a Pediatric Device

The goal of this project is to test a potentially safer, more accessible method for placement of gastrostomy feeding tubes in pediatric patients. Millions of patients worldwide require enteral nutrition, and hundreds of thousands of gastrostomy (feeding tube placement) procedures are performed annually in the United States alone, over 10,000 of which are in children. The current standard of practice for placement of nearly all feeding tubes worldwide is called the Percutaneous Endoscopic Gastrostomy (PEG) method. PEG is costly, complex, and potentially risky to perform, as it is performed in a surgical suite about 85% of the time, requiring specialty providers and sophisticated imaging instruments. Open surgical gastrostomy is another alternative, but is more invasive. We have invented a new device and method, using magnets and low-cost, non-invasive ultrasound, called the Point-of-Care Ultrasound Magnet Aligned Gastrostomy (PUMA-G) device, which will improve and simplify the gastrostomy procedure on many dimensions. The PUMA-G device is applied using the Percutaneous Ultrasound Gastrostomy (PUG) procedure. The most important difference between our method and PEG, is that the PUMA-G device will eliminate several safety risks of PEG while also allowing up to 80% of all gastrostomy procedures to be performed at the patient?s bedside - without specialist consultants, expensive imaging, and surgical suite time (for the remaining 20% of cases, the PUMA-G device will be contraindicated, and a conventional PEG or open surgical gastrostomy may be performed). Migration of methods from the surgical theatre to the patient bedside has successfully occurred for many different specialty procedures over the previous two decades, and in each instance has led to substantially reduced cost and improved patient satisfaction, with comparable or better safety outcomes. PUMA-G has been designed, built, and tested successfully in adults, with over 15 successful live canine experiments and 6 live human patient cases to date. Recently, many world-class pediatricians who have seen the PUMA-G device have recognized it as a superior method for use in children, and have requested a PUMA-G device be built which is sized and designed for use in smaller patients. This project will design, test, and validate in a live rabbit model a smaller PUMA-G device for safer and less costly ultrasound gastrostomy in children.

IC Name
NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
  • Activity
    R43
  • Administering IC
    DK
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    224614
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    847
  • Ed Inst. Type
  • Funding ICs
    NIDDK:224614\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    COAPTECH, LLC
  • Organization Department
  • Organization DUNS
    080322442
  • Organization City
    BALTIMORE
  • Organization State
    MD
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    212024268
  • Organization District
    UNITED STATES