Remote pressure sensing system and method thereof

• US 8,702,620 B2
• Filed: 11/03/2009
• Issued: 04/22/2014
• Est. Priority Date: 11/03/2008
• Status: Active Grant

• Current Assignee: GI View Limited Israeli Company of
• Original Assignee: G.I. View Ltd.
• Inventors: Gefen, Ra'anan, Sheps, Tal, Eshel, Reuven, Mendelewicz, Ran, Kinrot, Noam
• Primary Examiner(s): Towa, Rene
• Assistant Examiner(s): ABOUELELA, MAY A
• Application Number:
  US13/126,829
• Publication Number:
  US 20110295146A1
• Time in Patent Office: 1,631 Days
• Field of Search: 600/560, 600/561, 600/481, 600/485, 600/488, 600/587, 600/593, 606/21, 604/21, 604/27
• US Class Current: 600/560
• CPC Class Codes: A61B 1/00082 Balloons
• CPC Class Codes: A61B 1/00156 using self propulsion
• CPC Class Codes: A61B 1/005 Flexible endoscopes
• CPC Class Codes: A61B 1/31 for the rectum, e.g. proctoscopes, sigmoidoscopes , colonoscopes

Abstract

The present invention relates to a monitoring system and method for use with a body of a subject. The system comprises a medical device, having a portion thereof configured to be placed inside the subject'"'"'s body, said portion of the medical device being configured to be propelled by fluid pressure through a body lumen; at least two pressure sensors accommodated remotely from the subject'"'"'s body at two different spaced-apart positions outside the subject'"'"'s body and configured and operable to detect pressure at the two spaced-apart remote positions; said at least two pressure sensors being in fluid communication with at least one site inside the subject'"'"'s body, a relation between the pressure at said at least one site and the pressures at said two spaced-apart remote positions being thereby indicative of the fluid pressure at said at least one site.

Claims

1. A monitoring system for use with a body of a subject, the system comprising:

a medical device, having a portion thereof configured to be placed inside the subjects body, said portion of the medical device being configured to be propelled by fluid pressure through a body lumen;

at least first and second pressure sensors configured to be accommodated remotely from the subjects body at two different spaced-apart positions outside the subjects body and configured and operable to detect pressure at the two spaced-apart remote positions, respectively;

said pressure sensors configured to be in fluid communication with at least one site inside the subject'"'"'s body;

at least one tubular member having a distal end connected to the first pressure sensor and a proximal end connected to the second pressure sensor;

said tubular member being configured and operable as a flow resistor and selected to have a first characteristic resistance to fluid flow;

first and second pressure sensors measuring a pressure gradient across the tubular member;

a distal flow path extending between the tubular member and the medical device and exhibiting a second characteristic resistance to fluid flow; and

a control unit for monitoring and regulating fluid pressure at said at least one site, said control unit utilizing a model based upon a ratio between the first characteristic resistance and the second characteristic resistance to generate an output indicative of the pressure at the at least one site.

2. The system of claim 1, wherein said medical device comprises at least one inflatable balloon;

and said control unit being configured and operable to monitor and regulate fluid pressure within said at least one inflatable balloon.

3. The system of claim 2, wherein said model utilizes a relation between a pressure drop across a resistor defined by a path inside said fluid communication connecting between said at least two pressure sensors.

4. The system of claim 1, wherein said relation is based on mathematical function including a polynomial equation taking into account the resistance of said at least one tubular member.

5. The system of claim 1, wherein said medical device being configured as a two-part device, the two parts being attachable to one another, thereby enabling the part of the device containing said portion which is to be placed inside the subject'"'"'s body, to be disposable.

6. The system of claim 2, wherein said control unit is integrated in an external workstation, said workstation comprising one or more fluid pressure sources in fluid communication with the portion of the device, said one or more source of fluid pressure source is configured and operable to inflate said at least one site at predetermined pressures.

7. The system of claim 1, wherein said medical device includes a guide member at least partially insertable into a body lumen, the guide member including a first passageway connectable to the source of fluid pressure, and at least one inflatable balloon in fluid communication with the guide member.

8. The system of claim 7, wherein said medical device includes a second inflatable balloon spaced apart from said at least one inflatable balloon in fluid communication with the guide member;

said system comprising an additional pair of pressure sensors accommodated at two different spaced-apart auxiliary positions outside the subject'"'"'s body and configured and operable to detect pressure at the two spaced-apart remote auxiliary positions;

an additional relation between the pressure at the second inflatable balloon and the pressures at the two spaced-apart remote auxiliary positions being thereby indicative of the fluid pressure at the second inflatable balloon.

9. The system of claim 8, wherein at least one of said inflatable balloon and said second inflatable balloon comprises at least one piston head configured to be inflated so as to form and maintain a pressure seal with a wall of the body lumen, and be advanced distally through the body lumen in response to fluid pressure from the fluid pressure source applied to an external surface of the piston head.

10. The system of claim 2, wherein one or more fluid pressure source are configured to regulate the pressure in the device in response to the output data.

11. The system of claim 6, wherein the control unit is configured to switch between two different models based on two different directions of fluid between the fluid pressure source and the device.

12. The system of claim 6, wherein the device comprises a distal end of a passageway, the passageway being configured to convey fluid from the fluid pressure source into the body lumen.

13. A monitoring system for use with a body of a subject, the system comprising:

a medical device, comprising at least one inflatable balloon and having a portion thereof configured to be placed inside the subjects body, said portion of the medical device being configured to be propelled by fluid pressure through a body lumen;

at least first and second pressure sensors configured to be accommodated remotely from the subject'"'"'s body at two different spaced-apart positions outside the subjects body and configured and operable to detect pressure at the two spaced-apart remote positions, respectively;

said pressure sensors configured to be in fluid communication with at least one site inside the subjects body;

at least one tubular member having a distal end connected to the first pressure sensor and a proximal end connected to the second pressure sensor;

said tubular member being configured and operable as a flow resistor and selected to have a first characteristic resistance to fluid flow;

first and second pressure sensors measuring a pressure gradient across the tubular member;

a distal flow path extending between the tubular member and the medical device and exhibiting a second characteristic resistance to fluid flow; and

a control unit for monitoring and regulating fluid pressure at said at least one site and within said at least one inflatable balloon;

said control unit being configured and operable to generate an output indicative of a pressure level at the at least one site, utilizing at least one model based upon a ratio between the second characteristic resistance and the first characteristic resistance.

14. The system of claim 13, wherein the pressure level P3 at the at least one site is determined in accordance with the following equation:

15. The system of claim 13, comprising an additional pair of pressure sensor accommodated at two different spaced-apart positions outside the subject'"'"'s body creating an auxiliary channel and configured and operable to detect pressure at the two spaced-apart remote positions;

said control unit being configured and operable to determine an additional relation between the pressure in the auxiliary channel and the pressures at the two spaced-apart remote positions.