US2005004478A1PendingUtilityA1

Implantable device for monitoring aneurysm sac parameters

Priority: May 31, 2001Filed: Mar 2, 2004Published: Jan 6, 2005
Est. expiryMay 31, 2021(expired)· nominal 20-yr term from priority
Inventors:Matthew J. Fitz
A61B 5/0031A61B 5/02158A61B 5/02014A61B 2560/0257A61B 5/076
45
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Claims

Abstract

A device for measuring physiological parameters within an aneurysm sac that has been excluded from blood flow by an endoprosthesis. The device is comprised of at least two sensors, one placed in the aneurysm sac and another in a systemic artery. A differential between the readings of the two sensors can then be calculated, making the device easily calibrated in vivo and insensitive to changes in atmospheric pressure.

Claims

exact text as granted — not AI-modified
1 . A device for measuring at least one physiological parameter in a body, said device comprising: 
 a. an endoprosthesis located within said body, said endoprosthesis defining an inner surface and an outer surface,    b. a first sensing means adapted for chronic implantation within said body, said first sensing means disposed closer to said outer surface of said endoprosthesis than to said inner surface of said endoprosthesis,    c. a second sensing means adapted for chronic implantation within said body, said second sensing means disposed closer to said inner surface of said endoprosthesis than to said outer surface of said endoprosthesis,    d. a means for wireless data transmission,    e. a power source.    
     
     
         2 . The device according to  claim 1 , wherein said endoprosthesis is bifurcated.  
     
     
         3 . The device according to  claim 1 , wherein said physiological parameter is a pressure whereby said second sensing means can be used to compensate for changes in atmospheric pressure.  
     
     
         4 . The device according to  claim 1 , wherein said first sensing means is attached to said endoprosthesis.  
     
     
         5 . The device according to  claim 1 , wherein said second sensing means is attached to said endoprosthesis.  
     
     
         6 . The device according to  claim 1 , wherein said first sensing means is selected from the group consisting of piezoelectric, semiconductor, catheter, acoustic, and ultrasonic sensors.  
     
     
         7 . The device according to  claim 1 , wherein said second sensing means is selected from the group consisting of piezoelectric, semiconductor, catheter, acoustic, and ultrasonic sensors.  
     
     
         8 . The device according to  claim 1 , wherein said data processing means is adapted for chronic implantation within said body.  
     
     
         9 . The device according to  claim 1 , wherein said data processing means is external to said body.  
     
     
         10 . A method for measuring a physiological parameter in a body, comprising the steps of: 
 a. chronically implanting an endoprosthesis within said body, said endoprosthesis defining an inner surface and an outer surface,    b. chronically implanting a first sensing means closer to said outer surface than to said inner surface,    c. chronically implanting a second sensing means closer to said inner surface than to said outer surface,    d. transmitting data,    e. providing a power source.    
     
     
         11 . The method of  claim 10 , wherein said physiological parameter is a pressure.  
     
     
         12 . The method of  claim 10 , wherein said physiological parameter is a flow velocity.  
     
     
         13 . The method of  claim 10 , wherein said physiological parameter is a pressure waveform.  
     
     
         14 . The method of  claim 10 , wherein said first sensing means is selected from the group consisting of piezoelectric, semiconductor, catheter, acoustic, and ultrasonic sensors.  
     
     
         15 . The method of  claim 10 , wherein said second sensing means is selected from the group consisting of piezoelectric, semiconductor, catheter, acoustic, and ultrasonic sensors.  
     
     
         16 . A method for measuring a physiological parameter in a body, comprising the steps of: 
 a. chronically implanting a first sensing means within said body,    b. chronically implanting a second sensing means within said body,    c. chronically implanting a means for wireless data transmission,    d. providing a power source,    whereby a signal can be provided if said physiological parameter reaches a predetermined value.    
     
     
         17 . The device according to  claim 16 , wherein said first sensing means is selected from the group consisting of piezoelectric, semiconductor, catheter, acoustic, and ultrasonic sensors.  
     
     
         18 . The method of  claim 16 , wherein said second sensing means is selected from the group consisting of piezoelectric, semiconductor, catheter, acoustic, and ultrasonic sensors.  
     
     
         19 . The method of  claim 16 , wherein said physiological parameter is a pressure.  
     
     
         20 . The method of  claim 16 , wherein said physiological parameter is a flow velocity.  
     
     
         21 . The method of  claim 16 , wherein said physiological parameter is a pressure waveform.

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