Capnometry system for use with a medical effector system
First Claim
1. A medical-effector-system procedure room unit comprising:
- a) a procedure-room-unit host controller; and
b) a capnometer having a capnometer gas input which receives directly or indirectly respiratory gas obtained from a cannula which is disposable on the face of a patient and having a capnometer signal output operatively connected to the procedure-room-unit host controller, wherein the procedure-room-unit host controller issues a user alert that the capnometer is fluidly connected and/or not fluidly connected to the cannula based at least in part on the capnometer signal output of the capnometer.
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Accused Products
Abstract
Disclosed is a capnometry apparatus for receiving respiratory gas from a respiratory cannula positioned on a patient. An integrated host controller alerts a user if the capnometry apparatus is connected or not connected to the respiratory cannula based in part on a signal output from a capnometer located in the capnometry apparatus. The host controller also includes the functionality to shut off the capnometer pump with or without a time delay when the capnometer signal output indicates the capnometer pump is not connected to the cannula. An ambient-air pressure sensor located in the capnometry apparatus alerts the host controller if the capnometry apparatus has been moved to a new location with a substantially different altitude than the first location, in which case the host controller will issue an alert to a user prompting a calibration of the capnometry apparatus.
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Citations
14 Claims
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1. A medical-effector-system procedure room unit comprising:
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a) a procedure-room-unit host controller; and
b) a capnometer having a capnometer gas input which receives directly or indirectly respiratory gas obtained from a cannula which is disposable on the face of a patient and having a capnometer signal output operatively connected to the procedure-room-unit host controller, wherein the procedure-room-unit host controller issues a user alert that the capnometer is fluidly connected and/or not fluidly connected to the cannula based at least in part on the capnometer signal output of the capnometer. - View Dependent Claims (2)
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- 3. A medical-effector-system procedure room unit comprising a medical-effector-system procedure-room-unit console having a console fan and a capnometer subassembly, wherein the console fan moves air into, through, and out of the procedure-room-unit console, wherein the capnometer subassembly has a capnometer-subassembly gas inlet and a capnometer-subassembly gas outlet, and wherein the capnometer-subassembly gas outlet is disposed to enable gas leaving the capnometer-subassembly gas outlet to be entrained with air moved by the console fan.
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6. A medical-effector-system procedure room unit comprising:
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a) a procedure-room-unit host controller;
b) a capnometer having a capnometer gas input which receives directly or indirectly respiratory gas obtained from a cannula which is disposable on the face of a patient and having a capnometer signal output operatively connected to the procedure-room-unit host controller;
c) an oxygen manifold having an oxygen-delivery flow path including in series a flow-path inlet fluidly-connectable to a source of pressurized oxygen, a flow restrictor, and a flow-path outlet fluidly-connectable to the cannula; and
d) a low side pressure sensor in fluid communication with the flow-path outlet, disposed downstream of any oxygen-manifold flow restrictor, and having a low-side pressure signal output operatively connected to the procedure-room-unit host controller, wherein the procedure-room-unit host controller issues a user alert that the capnometer is fluidly connected and/or not fluidly connected to the cannula based at least in part on the capnometer signal output of the capnometer and the low-side pressure signal output of the low side pressure sensor. - View Dependent Claims (7)
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8. A medical-effector-system procedure room unit comprising:
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a) a procedure-room-unit host controller;
b) a capnometer having a capnometer gas input which receives directly or indirectly respiratory gas obtained from a cannula which is disposable on the face of a patient and having a capnometer signal output operatively connected to the procedure-room-unit host controller; and
c) a capnometer pump operatively connected to the capnometer and controlled by the procedure-room-unit host controller, wherein the procedure-room-unit host controller determines that the capnometer is fluidly connected and/or not fluidly connected to the cannula based at least in part on the capnometer signal output of the capnometer, and wherein the procedure-room-unit host controller shuts off, with or without a time delay, the capnometer pump when the capnometer is not fluidly connected to the cannula. - View Dependent Claims (9)
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10. A medical-effector-system procedure room unit comprising:
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a) a procedure-room-unit host controller;
b) a capnometer having a capnometer gas input which receives directly or indirectly respiratory gas obtained from a cannula which is disposable on the face of a patient and having a capnometer signal output operatively connected to the procedure-room-unit host controller; and
c) an ambient-air pressure sensor having an ambient-air-pressure-sensor signal output operatively connected to the procedure-room-unit host controller;
wherein the procedure-room-unit host controller determines if the medical-effector-system procedure room unit has been moved to a new location having an altitude difference greater than a predetermined altitude difference using at least the ambient-air-pressure-sensor signal output of the ambient-air pressure sensor, and wherein the procedure-room-unit host controller issues a capnometer-calibration user alert when the medical-effector-system procedure room unit has been moved to a new location having an altitude difference greater than the predetermined altitude difference. - View Dependent Claims (11)
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12. A medical-effector-system procedure room unit comprising:
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a) a procedure-room-unit host controller;
b) a cannula disposable on the face of a patient and having a respiratory-gas-sample output operatively connectable to the procedure-room-unit host controller; and
c) an oxygen manifold having a flow-path outlet fluidly-connectable to the cannula and having a variable-size-orifice flow restrictor operatively connected to, and disposed upstream of, the flow-path outlet, wherein the procedure-room-unit host controller determines when the patient is first breathing with a disposed cannula based at least on the respiratory-gas-sample output of the cannula and opens the variable-size-orifice flow restrictor when the patient is first determined to be breathing with a disposed cannula. - View Dependent Claims (13, 14)
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Specification