# US 12,214,120 B2 · Medical device with improved desufflation > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 12,214,120 B2 - Document ID: US12214120B2 - Status: Granted - Kind: B2 - Application number: 17/236,828 - Filed: 2021-04-21 - Published: 2021-11-25 - Granted: 2025-02-04 - Earliest claimed: 2016-12-16 - Assignees: W.O.M. World of Medicine GmbH - Applicants: W.O.M. World of Medicine GmbH - Inventors: Yves Koth - Web page: https://patentgrep.com/patent/US12214120B2 ## CPC - A61M 13/003: {Blowing gases other than for carrying powders, e.g. for inflating, dilating or rinsing} - A61B 17/3474: {Insufflating needles, e.g. Veress needles} - A61B 2218/008: for smoke evacuation - A61M 2202/02: Gases - A61M 2205/3334: Measuring or controlling the flow rate - A61M 2205/3337: Controlling, regulating pressure or flow by means of a valve by-passing a pump - A61M 2205/3344: Measuring or controlling pressure at the body treatment site - A61M 2205/75: with filters - A61M: DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY (introducing media into or onto the bodies of animals A61D7/00; means for inserting tampons A61F13/26; devices for administering food or medicines orally A61J; containers for collecting, storing or administering blood or medical fluids A61J1/05); DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY (surgery A61B; chemical aspects of surgical articles A61L); DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR {(Electrotherapy, e.g. producing anaesthesia by the use of alternating or intermittent currents A61N1/36021)} - A61B: DIAGNOSIS; SURGERY; IDENTIFICATION (usefulness limited to only animals A61D) ## Abstract The present disclosure is directed to an insufflator which includes a controller, an insufflation line, a desufflation line, and one pressure sensor and one volume flow sensor associated with each of the insufflation line and the desufflation lines. The insufflation line is in fluid communication with a gas source and the desufflation line in fluid communication with a suction pump. Wherein the controller controls ventilation of a gas present in a patient by adjusting an amount of suction in the desufflation line as a function of pressure measurements obtained from the pressure sensors associated with the insufflation line and the desufflation line. Additionally, the controller includes an activation blocking system that prevents suction in the desufflation line when a pressure measured by means of the pressure sensor associated with the insufflation line is lower than a preset threshold value. Still further, the activation blocking system further prevents suction in the desufflation line when the pressure measured by means of the pressure sensor associated with the insufflation line and a pressure measured by means of the pressure sensor associated with the desufflation line are not identical. ## Claims ### Claim 1 A medical device comprising: an insufflator which includes a controller, an insufflation line, a desufflation line, and one pressure sensor and one volume flow sensor associated with each of the insufflation line and the desufflation line; the insufflation line in fluid communication with a gas source and the desufflation line in fluid communication with a suction pump; wherein the controller controls ventilation of a gas present in a patient by adjusting an amount of suction in the desufflation line as a function of a pressure measurements obtained from the pressure sensor associated with the insufflation line and a pressure measurement obtained from the pressure sensor associated with the desufflation line, wherein the controller activates the suction, and estimates an abdominal pressure of the patient using the pressure sensor of the desufflation line by means of a mathematical observer model and compares the estimated abdominal pressure to the pressure measurement of the pressure sensor in the insufflation line, wherein the suction remains activated only with identical values, effectively a difference smaller than 2 mmHg, between the estimated abdominal pressure and the pressure measurement of the pressure sensor in the insufflation line; wherein the controller includes an activation blocking system that prevents the suction in the desufflation line when the pressure measurement by means of the pressure sensor associated with the insufflation line is lower than a preset threshold value, and wherein the activation blocking system further prevents the suction in the desufflation line when the pressure measurement of the pressure sensor associated with the insufflation line and the pressure measurement of the pressure sensor associated with the desufflation line have values which are not identical. ### Claim 2 (depends on 1) The medical device according to claim 1, wherein the suction pump is contained within a housing for the insufflator. ### Claim 3 (depends on 1) The medical device according to claim 1, wherein the insufflator includes a connection port for communicating with the suction pump and the suction pump is external to the insufflator. ### Claim 4 (depends on 3) The medical device according to claim 3, wherein the insufflator includes a control valve for controlling a suction rate of the suction pump. ### Claim 5 (depends on 1) The medical device according to claim 1, wherein the preset threshold value is lower than 5 mm Hg. ### Claim 6 (depends on 1) The medical device according to claim 1, wherein the preset threshold value is lower than 3 mm Hg. ### Claim 7 (depends on 1) The medical device according to claim 1, wherein the controller cyclically pauses the suction, and during the suction pauses compares the pressure measurement of the pressure sensor associated with the insufflation line and the pressure measurement of the pressure sensor associated with the desufflation line, wherein the suction is activated again only with identical values of the pressure measurement of the pressure sensor associated with the insufflation line and the pressure measurement of the pressure sensor associated with the desufflation line. ### Claim 8 (depends on 1) The medical device according to claim 1, wherein the controller compares a sucked-off gas volume obtained using the volume flow sensor associated with the desufflation line to a decrease in the abdominal pressure and wherein the controller suspends the suction, when the comparison of the sucked-off gas volume to the decrease in the abdominal pressure does not correspond to an expected value. ### Claim 9 (depends on 8) The medical device according to claim 8, wherein the controller determines and stores the expected value of the comparison of the sucked off gas volume to the decrease in the abdominal pressure during an insufflation phase by measurement of a rise in the abdominal pressure to an insufflated volume during the insufflation phase. ### Claim 10 (depends on 1) The medical device according to claim 1, wherein the mathematical observer model is configured in a manner of a Luenberger observer. ### Claim 11 (depends on 1) The medical device according to claim 1, wherein the desufflation line is connected to a cylindrical trocar, the cylindrical trocar being configured such that the cylindrical trocar comprises recesses in a cylinder wall. ### Claim 12 (depends on 1) A method for controlled ventilation of a gas present in a patient after a surgery, by means of the medical device according to claim 1, the method comprising activating the suction via the controller only when: a) the pressure measurement of the pressure sensor associated with the insufflation line is higher than the preset threshold value, and b) when the pressure measurement of the pressure sensor associated with the insufflation line and the pressure measurement of the pressure sensor associated with the desufflation line are identical in value; wherein the controller pauses the suction and verifies the pressure the pressure measurement of the pressure sensor associated with the insufflation line and the pressure measurement of the pressure sensor associated with the desufflation line during the suction pauses; and the controller activates the suction pump and determines the abdominal pressure using the pressure sensor of the desufflation line, the pressure being estimated by the mathematical observer model and wherein the controller compares the estimated abdominal pressure to the pressure measurement of the pressure sensor in the insufflation line, wherein the suction remains activated only with identical values effectively a difference smaller than 2 mmHg, between the estimated abdominal pressure and the pressure measurement of the pressure sensor in the insufflation line. ### Claim 13 (depends on 12) The method according to claim 12, wherein the suction is performed at a suction rate of 1 to 5 l/min. ### Claim 14 (depends on 12) The method according to claim 12, wherein the suction is stopped once the abdominal pressure is 5, 4 or 3 mmHg. ### Claim 15 (depends on 12) The method according to claim 12, wherein the preset threshold value is larger than 5 mmHg. ### Claim 16 (depends on 12) The method according to claim 12, wherein the preset threshold value is larger than 3 mmHg. ### Claim 17 (depends on 12) The method according to claim 12, further including a step of providing the insufflator with a connection port for communicating with the suction pump and the suction pump is external to the insufflator. ### Claim 18 (depends on 12) The method according to claim 12, further including a step of providing the insufflator with a control valve for controlling a suction rate of the suction pump. ### Claim 19 (depends on 12) The method according to claim 12, wherein the mathematical observer model is configured in a manner of a Luenberger observer.