Method and device for monitoring loss of body fluid and dislodgment of medical instrument from body
First Claim
1. A hemodialysis site sensor attachable to at least one of a blood line and a fistula needle for alerting medical personnel of the leakage of blood from an access site where the fistula needle enters into a patient'"'"'s body and dislodgment of the fistula needle from the access site, the hemodialysis site sensor comprising:
- a base membrane layer made of a medical-grade, biocompatible material and including an upper side, a lower side adherable to skin of the patient, and one or more holes disposed therein to allow the passage of blood and vapor therethrough;
a second membrane layer including an upper side, a lower side, and one or more holes disposed therein to allow the passage of blood and vapor therethrough;
a third membrane layer including an upper side and a lower side;
an electrical connection adapted to be electrically coupled to an analytical circuit and includinga first sensing array disposed between the upper side of the base membrane layer and the lower side of the second membrane layer,a second sensing array disposed between the upper side of the second membrane layer and the lower side of the third membrane layer, and resistively connected to the first sensing array;
a disconnection mechanism attachable to at least one of the blood line and the fistula needle and severing the electrical connection upon dislodgment of the fistula needle from the access site;
wherein an electrical signal sent through the electrical connection changes when blood contacts at least one of the sensing arrays or the electrical connection is severed by the disconnection mechanism, causing the analytical circuit to actuate an alarm notifying medical personnel of partial or total dislodgment of the fistula needle from the access site.
1 Assignment
0 Petitions
Accused Products
Abstract
A method of alerting medical personnel of a problem during hemodialysis includes providing an active, fail-to-safe site sensor for a fistula needle at an access site during hemodialysis; and automatically alerting medical personnel of a problem during hemodialysis using the active, fail-to-safe site sensor during at least the following: failing of the active, fail-to-safe site sensor; insufficient powering to the active, fail-to-safe site sensor; partial fistula needle dislodging from the access site; and complete needle dislodging from the access site.
-
Citations
11 Claims
-
1. A hemodialysis site sensor attachable to at least one of a blood line and a fistula needle for alerting medical personnel of the leakage of blood from an access site where the fistula needle enters into a patient'"'"'s body and dislodgment of the fistula needle from the access site, the hemodialysis site sensor comprising:
-
a base membrane layer made of a medical-grade, biocompatible material and including an upper side, a lower side adherable to skin of the patient, and one or more holes disposed therein to allow the passage of blood and vapor therethrough; a second membrane layer including an upper side, a lower side, and one or more holes disposed therein to allow the passage of blood and vapor therethrough; a third membrane layer including an upper side and a lower side; an electrical connection adapted to be electrically coupled to an analytical circuit and including a first sensing array disposed between the upper side of the base membrane layer and the lower side of the second membrane layer, a second sensing array disposed between the upper side of the second membrane layer and the lower side of the third membrane layer, and resistively connected to the first sensing array; a disconnection mechanism attachable to at least one of the blood line and the fistula needle and severing the electrical connection upon dislodgment of the fistula needle from the access site; wherein an electrical signal sent through the electrical connection changes when blood contacts at least one of the sensing arrays or the electrical connection is severed by the disconnection mechanism, causing the analytical circuit to actuate an alarm notifying medical personnel of partial or total dislodgment of the fistula needle from the access site. - View Dependent Claims (2, 3)
-
-
4. A method of alerting medical personnel of partial and total dislodgment of a fistula needle from an access site where the fistula needle enters into a patient'"'"'s body during hemodialysis, comprising:
-
providing a site sensor including a base membrane layer made of a medical-grade, biocompatible material and including a lower side adherable to skin of the patient at the access site, and one or more holes disposed therein to allow the passage of blood and vapor therethrough, a top membrane layer, an electrical connection including one or more resistively connected sensing arrays disposed between the base membrane layer and the top membrane layer, and a disconnection mechanism attachable to at least one of the blood line and the fistula needle and severing the electrical connection upon dislodgment of the fistula needle from the access site; providing an analytical circuit in electrical communication with the electrical connection; sending a signal from the analytical circuit to the site sensor and receiving the signal from the site sensor with the analytical circuit, the signal traveling through the one or more resistively connected sensing arrays of the electrical connection; partially dislodging the fistula needle from the access site causing blood to contact the one or more resistively connected sensing arrays and the signal sent from the analytical circuit to change; completely dislodging the fistula needle from the access site causing the disconnection mechanism to sever the electrical connection and the signal sent from the analytical circuit to change; determining with the analytical circuit whether the signal changed outside of a predetermined range; actuating an alarm with the analytical circuit if the signal changed outside of a predetermined range. - View Dependent Claims (5, 6, 7)
-
-
8. A method of alerting medical personnel of a problem during hemodialysis, comprising:
-
providing an active, fail-to-safe site sensor for a fistula needle at an access site during hemodialysis, wherein the active, fail-to-safe sensor includes a base membrane layer made of a medical-grade, biocompatible material and including a lower side adherable to skin of the patient, and one or more holes disposed therein to allow the passage of blood and vapor therethrough, a top membrane layer, an electrical connection including one or more resistively connected sensing arrays disposed between the base membrane layer and the top membrane layer, and an analytical circuit in electrical communication with the one or more resistively connected sensing arrays of the electrical connection and sending an electrical signal therethrough, and automatically alerting medical personnel of a problem during hemodialysis using the active, fail-to-safe site sensor when the difference between the electrical signal sent by the analytical circuit and the electrical signal received by the analytical circuit is beyond a predetermined range, and automatically alerting medical personnel of a problem during hemodialysis using the active, fail-to-safe site sensor during at least the following;
failing of the active, fail-to-safe site sensor, insufficient powering to the active, fail-to-safe site sensor, partial fistula needle dislodging from the access site; and
complete needle dislodging from the access site. - View Dependent Claims (9, 10, 11)
-
Specification