NO supply device with automatic alarm modification when dose changes

Abstract

The invention relates to an apparatus (1) for delivering a gas containing NO comprising NO dose adjustment means (50, 51) for enabling a first dose of NO to be adjusted, and microprocessor (211) control means (210) for determining, from the first dose of NO adjusted, first high and low alarm thresholds corresponding to first maximum and minimum NO contents. NO dose modification means (50, 51) make it possible to modify or adjust the first dose of NO to obtain or set a second dose of NO different from the first dose of NO. The control means (210) are configured to automatically determine, from the second dose of NO, second high and low NO alarm thresholds different from the first high and low NO alarm thresholds. Installation for supplying a gas containing NO (100) comprising such an apparatus for delivering NO (1).

Description

Title of the invention: NO supply apparatus with automatic modification of alarms during dose changes

[0001] The invention relates to a NO delivery apparatus comprising means for automatically modifying alarms during NO dose changes, and an installation for supplying a NO-based gas mixture to a patient, typically an NO / nitrogen (N2) mixture, comprising such a NO delivery apparatus and a medical ventilator delivering an oxygen-based respiratory gas (> 20% approx.).

[0002] Inhaled nitric oxide (NO or NOi) is a gaseous drug commonly used to treat patients suffering from acute pulmonary arterial hypertension, in particular pulmonary vasoconstrictions in adults or children, including newborns (PPHN), as described for example by EP-A-560928 or EP-A-1516639.

[0003] To implement inhaled NO therapy, a gas supply installation, also called an NO administration installation, is used, comprising an NO delivery device and a medical ventilator, i.e. a respiratory assistance device, supplying a patient circuit which generally comprises one or more flexible conduits fluidically connected to a respiratory interface, such as a tracheal intubation probe or the like, used to deliver to the patient to be treated, a final gas mixture containing the NO.

[0004] Such a gas supply installation is described for example by EP3821929. This type of installation is used in a hospital environment to administer NO treatment and thus treat patients who need to inhale NO to treat their pulmonary arterial hypertension. Installations of this type are also described by EP3233171, EP3410927, EP3410927, EP4209243, EP4241817, EP4241812 and EP4295882.

[0005] In such an installation, the NO delivery apparatus makes it possible to inject a gaseous flow based on NO, typically an NO / nitrogen gas mixture, into the patient circuit also supplied with a flow of respiratory gas containing oxygen (at least approximately 20% vol.), such as air or an oxygen / nitrogen mixture (O2 / N2), supplied by the medical ventilator, so as to obtain a combined flow, also called a “final gaseous mixture”, comprising NO at the desired dosage, typically less than 50 ppmv of NO, at least approximately 20% vol. of oxygen and nitrogen (N2), or even unavoidable impurities.

[0006] Flow rate control means of the apparatus make it possible to control or adjust the flow rate of gas containing NO, eg NO / N2 mixture, in order to obtain the desired combined gas mixture, i.e. the final mixture containing NO at the desired dosage.

[0007] In fact, the flow rate of NO-based gas depends in particular on the flow rate of oxygen-based respiratory gas, i.e. air or N2 / O2 mixture, coming from the medical ventilator. It is therefore necessary to continuously measure the flow rate of the oxygen-based respiratory gas using a flow sensor arranged in the patient circuit, upstream of the injection site of the NO-based mixture and to use these measurements to calculate the flow rate of NO-based gas to be supplied.

[0008] However, in practice, more or less significant fluctuations in the NO content of the combined gas mixture are observed, which result from variations in the flow rate of oxygen-based respiratory gas supplied by the medical ventilator.

[0009] It is understood that such variations can be critical for the patient if they are significant and lead to an NO content (very) far from the desired dosage, that is to say if the NO content is excessive or insufficient.

[0010] In order to guarantee increased safety for the patient, the user, such as a healthcare worker, can generally set on the NO delivery device maximum and minimum values ​​(i.e. high and low thresholds) of acceptable NO content in the combined gas mixture.

[0011] By ensuring monitoring, i.e. continuous tracking, of the composition of the combined gas mixture obtained, it can be ensured that the proportion of NO present therein does not deviate too much from the desired dosage. Indeed, in the event that the measured NO content exceeds one of the upper or lower thresholds, an audible alarm and / or a visual alarm can be triggered by the NO delivery device in order to warn the nursing staff and enable them to take corrective measures.

[0012] However, setting the high and low NO alarm thresholds corresponding to the maximum and minimum acceptable NO levels (thresholds) is not easy because these thresholds depend closely on the chosen dose. Therefore, the healthcare staff can make errors in calculating them and / or then entering them into the NO delivery device, and it is easy to understand that any error can endanger the patient.

[0013] Furthermore, when the healthcare personnel, such as a doctor, decides to change the dose of NO in order to adapt the patient's treatment, that is to say to increase or decrease the dose of NO in the combined gas mixture sent to the patient, he must remember to also modify the high and low NO alarm thresholds having been set for the previous dose in order to choose new ones corresponding to the new dose of NO chosen by the doctor.

[0014] Again, besides the fact that the doctor may forget to adapt the alarm thresholds to the new dose of NO, errors may occur when entering the thresholds with the same negative consequences for the patient as mentioned above.

[0015] In all cases, poorly chosen or poorly adjusted alarm thresholds inevitably cause untimely alarm triggering, which leads in particular to noise pollution and increased fatigue for the nursing staff who must constantly intervene to deactivate them, thus diverting them from more critical tasks to be carried out. This then harms the treatment of the patient, in particular their safety.

[0016] A problem is therefore to improve patient safety, in particular to be able to avoid or at least minimize the aforementioned risks and / or untimely alarm triggering, by proposing an improved NO delivery device, i.e. one that is safer with regard to the determination of the NO alarm thresholds, in particular in the event of a change in the NO dose.

[0017] A solution concerns a device for delivering, i.e. supplying, a gas containing NO, such as a NO / N2 gas mixture, comprising NO dose adjustment means configured to allow a user to adjust, i.e. set, select or the like, a first dose of NO (DNOi), and microprocessor control means configured to determine, from said first set dose of NO (DNOi), first high and low alarm thresholds corresponding to a first maximum NO content (Tmaxi) and to a first minimum NO content (Tmini), with: Tmaxl > DNoi > Tminl-

[0018] In addition, the delivery apparatus of the invention further comprises NO dose modification means configured to allow a user to modify or adjust the first NO dose (DNOi) to obtain or set a second NO dose (DN02) different from the first NO dose (DNOi), and the control means are configured to determine, i.e. calculate, modify, adjust or the like, automatically from said second NO dose (DNO2), second high and low NO alarm thresholds different from said first high and low NO alarm thresholds, corresponding to a second maximum NO content (Tmax2) and to a second minimum NO content (Tmin2), with: Tmax2 > DN02 > Tmin2.

[0019] In other words, at the start of treatment of a patient, i.e. just before the start of supplying NO to the patient, the control means of the device automatically determine, i.e. calculate, the values ​​of the first high and low NO alarm thresholds, i.e. said first maximum and minimum NO contents (Tmini, Tmaxi), from the value of the first dose of NO (DNOi) or dosage set by the user, i.e. the doctor or the like, by adding or, conversely, subtracting from 10% to 30% to the NO dose value (DN0) set, preferably of the order of 20% which corresponds to an acceptable tolerance.

[0020] Then, if the user, typically a doctor, decides to change the dosage, i.e. to modify the dose of NO to change it from the first dose of NO (DNOi) to a second dose of NO (DNO2), which is different from the first dose of NO (DNOi), then the device, typically its microprocessor, will automatically calculate, from this second dose of NO (DNO2), second high and low NO alarm thresholds different from said first high and low NO alarm thresholds, corresponding to the second maximum NO (Tmax2) minimum NO (Tmin2) contents, and with: Tmax2 > DN02 > T min2*

[0021] The calculation is done as for the first alarm thresholds, that is to say by applying the same tolerance, for example 20%.

[0022] The fact that the NO alarm thresholds are automatically and immediately recalculated by the NO delivery device as soon as the user has set the desired second dose of NO (DN02), i.e. the second desired dosage, is an undeniable advantage in terms of safety because errors in calculating or entering values ​​into the device or the possibility that the nursing staff forgets to recalculate these values ​​no longer exist. In addition, this also prevents unexpected alarm triggering, i.e. false alarms. In all cases, patient safety is improved.

[0023] Depending on the embodiment considered, the delivery apparatus of the invention may comprise one or more of the following features: - the control means are configured to automatically calculate (i.e. determine), from the first NO dose (DNOi) set, a first high NO alarm threshold corresponding to a first maximum NO content (Tmaxi), such that: 1.1 . DNOi < Tmaxi < 1.3 . DNOi, i.e. the first maximum NO content (Tmaxi) is 10% to 30% higher than the first NO dose value (DNOi) set. - the control means are configured to automatically calculate (i.e. determine), from the first NO dose (DNOi) set, a first low NO alarm threshold corresponding to a first minimum NO content (Tmini), such that: 0.7 . DNOi < Tmini < 0.9 . DNOi, i.e. the first minimum NO content (Tmini) is 10% to 30% lower than the first NO dose value (DNOi) set. - the control means are configured to calculate (ie determine), from the first dose of NO (DNOi) set, a first high NO alarm threshold corresponding to a first maximum NO content (Tmaxi), such that:

[0024] Tmaxl < 1.25 . DNOi. - the control means are configured to calculate (i.e. determine), from the first dose of NO (DNOi) set, a first high NO alarm threshold corresponding to a first maximum NO content (Tmaxi), such that:

[0025] Tmaxi < 1.20 . DNOi, in particular such that: Tmaxi = 1.20 . DNOi. - the control means are configured to calculate (i.e. determine), from the first dose of NO (DNOi) set, a first low NO alarm threshold corresponding to a first minimum NO content (Tmini), such that:

[0026] 0.75. DNOi < Tminl. - the control means are configured to calculate (ie determine), from the first dose of NO (DNOi) set, a first low NO alarm threshold corresponding to a first minimum NO content (Tmini), such that:

[0027] 0.80 . DNOi < Tmini, in particular such that: 0.80 . DNOi = Tminl. - advantageously, the control means are configured to calculate a first maximum NO content (Tmaxl) such that: Tmaxi - DNOi > 2 ppmv, i.e. the difference between the first dose of NO (DNOi) set and the first maximum NO content (Tmaxl) must be at least 2 ppmv. For example, for a first dose of NO (DNOi) of 10 ppmv, the first maximum NO content (Tmaxi) must be set at least 12 ppmv, i.e. 12 ppmv or more. - the control means are further configured to calculate a first minimum NO content (Tmini) such that: DNOi _Tmini > 2 ppmv, i.e., here too, the difference between the first dose of NO (DNOi) set and the first minimum NO content (Tmini) must be at least 2 ppmv. For example, for a first dose of NO (DNOi) of 10 ppmv, the first minimum NO content (Tmini) must be set at no more than 8 ppmv, i.e. 8 ppm or less. - it includes a graphic display, i.e. a display screen or the like. - the graphic display is configured to display at least said first set NO dose (DNOi) and / or said first maximum and minimum NO contents (Tmini, Tmax[) corresponding to said first high and low alarm thresholds. - the graphic display includes a touch screen (i.e. touch panel) or any other equivalent display device. - the control means are configured to command a display, on the graphic display, of the first maximum NO content (Tmaxi) corresponding to the first high NO alarm threshold. - the control means are configured to command a display on the graphic display of the first minimum NO content (Tmini) corresponding to the first low NO alarm threshold. - the first dose of NO (DNOi) is between 1 and 80 ppmv. - the control means are further configured to determine, eg calculate, automatically, from the second dose of NO (DN02) set, a second high NO alarm threshold corresponding to a second maximum NO content (Tmax2) and a second low NO alarm threshold corresponding to a second minimum NO content (Tmin2), said determination being carried out in the same way as that of the first high NO alarm threshold corresponding to the first maximum NO content (Tmaxi) and the first low NO alarm threshold corresponding to the first minimum NO content (Tminl)- - the control means are further configured to automatically calculate (i.e. determine), from the second dose of NO (DN02) set, a second high NO alarm threshold corresponding to a second maximum NO content (Tmax2), such that: 1.1 . DN02 < Tmax2 < 1.3 . DN02, i.e. the second maximum NO content (Tmax2) is 10% to 30% higher than the second NO dose value (DN02) set. - the control means are configured to automatically calculate, from the second dose of NO (DN02) set, a second low NO alarm threshold corresponding to a second minimum NO content (Tmin2), such that:

[0028] 0.7 . Dn02 < Tmin2 < 0.9 . DN02, i.e. the second minimum NO content (Tmin2) is 10% to 30% lower than the second set NO dose value (DN02). - the control means are configured to calculate, from the second dose of NO (DN02) set, a second high NO alarm threshold corresponding to a second maximum NO content (Tmax2), such that: Tmax2 < 1.25 . DN02. - the control means are configured to calculate, from the second dose of NO (DN02) set, a second high NO alarm threshold corresponding to a second maximum NO content (Tmax2), such that: Tmax2 < 1.20 . DN02, in particular such that: Tmax2 = 1.20 . DN02. - the control means are configured to calculate (i.e. determine), from the second dose of NO (DN02) set, a second low NO alarm threshold corresponding to a second minimum NO content (Tmin2), such that: 0.75. DNo2 < Tmin2. - the control means are configured to calculate, from the second dose of NO (DN02) set, a second low NO alarm threshold corresponding to a second minimum NO content (Tmin2), such that: 0.80 . DN02 < Tmin2, in particular such that: 0.80 . DN02 = Tmin2. - again, advantageously, the control means are configured to calculate a second maximum NO content (Tmax2) such that:

[0029] Tmax2 - Dn02 > 2 ppmv, i.e. the difference between the second dose of NO (DN02) set and the second maximum NO content (Tmax2) must be at least 2 ppmv. - by analogy, the control means are further configured to calculate a second minimum NO content (Tmin2) such that: Dx02 Tmm2 > 2 ppmv, i.e., here too, the difference between the first dose of NO (DN02) set and the second minimum NO content (Tmin2) must be at least 2 ppmv. - the graphic display is further configured to display at least said second dose of NO (DN02) and / or said second maximum and minimum NO contents (Tmin2, Tmax2) corresponding to said second high and low NO alarm thresholds having been determined. - the control means are configured to control a display on the graphic display of the second maximum NO content (Tmax2) corresponding to the second high NO alarm threshold and of the second minimum NO content (Tmin2) corresponding to the second low NO alarm threshold. - the second dose of NO (DNO2) is between 1 and 75 ppmv. - the second dose of NO (DNO2) is lower than the first dose of NO (DNOi) or, alternatively, the second dose of NO (DN02) is greater than the first dose of NO (DNOi). - the difference (in absolute value) between the first dose of NO (DNOi) and the second dose of NO (DN02) is at least 2 ppmv, preferably at least 3 ppmv, preferably at least 4 ppmv, for example at least 5 ppmv. - the graphic display is configured to simultaneously display the second dose of NO (DN02) and the second maximum and minimum levels of NO (Tmin2, Tmax2) corresponding to said second high and low NO alarm thresholds having been determined. - the control means are configured to determine the second minimum and maximum NO contents (Tmin2, Tmax2) such that, when: DN02 < DNOi then . Tmax2 < Tmax|Ct Tmm2 < Tminl* - the control means are configured to determine the second minimum and maximum NO contents (Tmin2, Tmax2) such that, when: DN02> DNOi then: Tmax2 > TTnm2 Tminl* - it further comprises storage means for storing the first dose of NO (DNOi) and / or the second dose of NO (DNO2). - the storage means allow the first maximum NO content (Tmaxi) and / or the first minimum NO content (Tmini) to be stored. the storage means make it possible to store the second maximum NO content (Tmax2) and / or the second minimum NO content (Tmin2). it comprises an internal gas circuit for conveying a gas stream containing NO, i.e. gas passages, gas conduits or the like. the internal gas circuit comprises flow control means configured to control the flow of gas containing NO within said gas circuit. the control means are configured to control (at least) the flow control means to control the supply of gas containing NO as a function of at least said first set dose of NO (DNOi) or, as the case may be, of the second dose of NO (DNO2), i.e. when the dose of NO has been modified with a change from the first dose of NO (DNOi) to the second dose of NO (DNO2). the internal gas circuit of the device carrying the gas containing NO, typically a NO / N2 gas mixture, is fluidically connected to a breathing circuit carrying a breathing gas containing oxygen, such as air or an O2 / N2 gas mixture (>20% O2), to inject the gas containing NO and obtain a combined gas mixture containing NO and oxygen, i.e. the final mixture to be administered to the patient. it comprises NO concentration measuring means for determining the NO content in the combined gas mixture containing NO and oxygen, such as an NO sensor, for example an electrochemical cell. the NO concentration measuring means are arranged to determine the NO content in the combined gas mixture within the internal gas circuit. it includes alarm means, typically an audible and / or visual alarm. the control means are configured to act on alarm means to trigger an alarm, in particular an audible and / or visual alarm. the alarm means may include a buzzer-type device, and / or a loudspeaker, or any other device making it possible to emit an audible sound signal to the human ear, i.e. to the healthcare staff. the alarm means may comprise a light device, for example comprising one or more diodes (LEDs) or the like. the alarm means may include a display of an alert message or the like on the graphic display. the control means are configured to trigger an alarm, i.e. to activate alarm means, when the NO content (i.e. an instantaneous content) in the combined gas mixture is greater than or equal to the first or, as the case may be, the second maximum NO content (Tmaxi, Tmax2) or less than or equal to the first or, as the case may be, the second minimum NO content (Tmini, Tmin2). the control means determine the NO content (i.e. an instantaneous content) in the combined gas mixture from measurements provided by the NO concentration measuring means. the control means are configured to control a display on the graphic display of the NO content in the combined gas mixture having been determined by the NO concentration measuring means. The display is configured to display an alarm message if an alarm is triggered. the dose setting means and / or the NO dose modification means are configured to allow the user to modify, set, adjust or the like the NO dose (DNOi, DNO2) and / or the high and / or low NO alarm thresholds (Tmaxl? Tmax2, Tminl? Tmin2)- the dose adjustment means and / or the NO dose modification means comprise one or more keys or the like, in particular virtual keys displayed by the display screen. it is supplied with a gas containing NO in a given initial proportion, typically a NO / N2 mixture. it is supplied with a gas containing an initial proportion of NO of between 100 and 2000 ppmv, preferably between 100 and 1500 ppmv, typically between 200 and 1000 ppmv. It is supplied with a gaseous mixture of nitrogen and NO. the NO dose adjustment or modification means are configured to allow the user to adjust, adjust or modify a NO dose, i.e. NO content setpoint, corresponding to the desired NO proportion in the combined gas mixture, i.e. after mixing the NO / N2 mixture with the oxygen-based respiratory gas flow, i.e. a NO dosage. the means of adjusting or modifying the NO dose are part of an HMI (human-machine interface) or IGU (graphical user interface). The HMI includes the graphic display. preferably, the means for adjusting the dose or modifying NO comprise one or more touch keys, operable by the user, displayed on a graphic display of the digital screen type with a touch panel, i.e. virtual keys. the dose adjustment means and / or the NO dose modification means comprise a “+” key for incrementing a NO dose value and / or a “-” key for decrementing a NO dose value. Typically, the increment or decrement is + / - 1 ppmv. the dose setting means and / or the NO dose modification means further comprise a validation key for validating / confirming a NO dose value having been set, preferably a virtual validation key displayed by the display screen. alternatively, the means for adjusting or modifying the dose of NO comprise a mechanical selection member, such as one or more digitally actuated buttons or keys, such as a push button or the like, or a rotary button or the like the graphic display is of the color display type. the NO dose adjustment or modification means are configured to allow the user to adjust a NO dose, i.e. a NO content setpoint. the doses or NO content instructions (DNOi, DNO2) are between 1 and 70 ppmv, preferably between 1 and 60 ppmv, advantageously between 1 and 50 ppmv, typically between 5 and 40 ppmv. the storage means include computer memory, such as flash memory, RAM or the like. the flow control means are arranged on the internal gas circuit. the flow control means include valve means, such as solenoid valves or the like. the control means are configured to control the flow control means to allow or prevent the passage of the NO / N2 flow in the internal gas circuit. the flow control means comprise one or more proportional solenoid valves and / or one or more on-off solenoid valves. The main means of flow control include a mass flow controller. - the mass flow controller (MFC) comprises at least one proportional solenoid valve controlled by the control means and a main flow sensor. - the microprocessor control means comprise a (micro)controller or the like. - the microprocessor control means comprise one (or more) (micro)processors arranged on one (or more) electronic card. - the control means comprise one (or more) (micro)processors implementing one or more algorithms, in particular one (or more) algorithms for controlling the flow control means, one (or more) algorithms for processing respiratory gas flow measurements or NO, NO2 and / or O2 concentration measurements.... - the storage means are arranged on the electronic card.

[0030] The invention also relates to an installation for supplying a gas containing NO comprising the NO delivery apparatus according to the invention supplied with a NO / N2 gas mixture by a source of NO / N2 mixture, and a medical ventilator configured to supply a flow of respiratory gas containing O2 to said respiratory circuit.

[0031] According to the embodiment considered, the installation for supplying a gas containing NO of the invention may comprise one or more of the following characteristics: - the medical ventilator is configured to provide a flow of breathing gas containing at least approximately 20% vol. O2, typically a NO / N2 gas mixture or air. - the NO delivery device and the medical ventilator are fluidically connected to the breathing circuit to provide it with gas flows. - a flow sensor is arranged in the respiratory circuit between the medical ventilator and the injection device. - an injection device is arranged in the respiratory circuit, downstream of the flow sensor. - the injection device is configured to allow the NO-containing gas from the NO delivery apparatus to be injected into the O2-containing breathing gas stream from the medical ventilator to obtain the combined gas mixture to be supplied to the patient in need thereof. - the injection device is configured to operate a mixture of the gas containing NO coming from the NO delivery device with the flow of respiratory gas containing O2 conveyed by the respiratory circuit, and obtain a combined gas mixture containing NO and oxygen, or even other compounds such as nitrogen or unavoidable impurities. the injection device comprises a first gas inlet supplied with a flow of respiratory gas containing O2, i.e. coming from the medical ventilator. the injection device further comprises a second gas inlet supplied with gas containing NO from the NO delivery apparatus. the injection device further comprises a gas outlet providing the combined gas mixture containing NO and oxygen, obtained by mixing, within the injection device, the gas containing NO (eg NO / N2 mixture) with the flow of respiratory gas containing O2 (eg air or O2 / N2 mixture). the medical ventilator delivers air or an oxygen / nitrogen mixture, i.e. as a breathing gas containing at least approximately 20% vol. oxygen, preferably at least approximately 21% vol. oxygen. the medical ventilator comprises a motorized blower (i.e. turbine, compressor or the like) delivering the respiratory gas, typically air or an oxygen / nitrogen mixture or, according to another embodiment, an internal gas circuit comprising one or more proportional valves for conveying the gas and controlling its supply, in particular its flow rate. Such a ventilator is generally supplied with respiratory gas by one or more wall outlets supplied with gas by a network of pipes in a hospital establishment or building, typically air or an oxygen / nitrogen mixture. the medical ventilator comprises control means or a device, such as an electronic control card(s). Preferably, the control means of the medical ventilator drive or control the motorized blower or, as the case may be, the proportional valves of the medical ventilator. the medical ventilator is of the HFO type or includes an HFO function, that is, it is capable of producing high-frequency oscillations. the NO source(s) supplying the NO delivery apparatus contains a NO / N2 gas mixture containing between 100 and 2000 ppmv of NO, the remainder being nitrogen (N2), preferably between 100 and 1000 ppmv of NO, conditioned at a pressure of between 10 and 250 bar abs, typically at more than 100 bar abs (before the start of withdrawal). - the source of NO is or includes one (or more) gas cylinders with a capacity of between 0.5 and 50 L (water equivalent). - the gas cylinder(s) comprises a cylindrical body made of steel or aluminium alloy and is equipped with a simple valve (without regulator) or with an integrated regulator or RDI, preferably an RDI, protected by a protective cover, for example made of metal or polymer. - the respiratory circuit (i.e. patient circuit) comprises an inspiratory branch and an expiratory branch, typically flexible pipes forming the inspiratory branch and the expiratory branch, for example polymer pipes. - the inspiratory branch and the expiratory branch, e.g. flexible pipes, are connected to a junction piece, such as a Y piece. - the inspiratory branch and / or the expiratory branch are fluidically connected to a patient respiratory interface, preferably via the junction piece. - the patient respiratory interface includes a tracheal intubation tube or respiratory mask, or other. - the respiratory circuit, in particular the inspiratory branch, may include a gas humidifier. - the gas humidifier is arranged downstream of the injection device, for example an NO injection module, so as to be able to humidify the gas before its administration by inhalation to the patient. - the ventilator and the NO delivery device are electrically powered by one or more electrical current sources, typically the mains (110 / 220V) and / or one or more rechargeable batteries.

[0032] According to another aspect, the invention also relates to a method for the therapeutic treatment of a person, i.e. a human patient (i.e. adult, child, adolescent or newborn), suffering from pulmonary hypertension and / or hypoxia, causing pulmonary vasoconstrictions or the like, comprising administration by inhalation to the person in need thereof, of a gas mixture comprising from 1 to 80 ppmv of NO, typically less than 40 ppmv, and at least approximately 20% vol. of oxygen, preferably at least 21% vol.of oxygen approximately, by means of a gas supply installation, such as that described above according to the invention, comprising an NO delivery apparatus according to the invention ensuring delivery of NO, so as to treat (at least partially) said pulmonary hypertension and / or said hypoxia, which may be caused by one (or more) pathology or other pulmonary disorders typically of the PPHN type (persistent pulmonary hypertension of the newborn) or ARDS (acute respiratory distress syndrome), or even generated. by cardiac surgery with the patient being placed on extracorporeal circulation (ECC). Definitions

[0033] Generally speaking, within the framework of the invention: - “ppmv” means parts per million by volume, - “%vol.” means percentage by volume. - “NO” means nitrogen monoxide. - “NO2” means nitrogen dioxide. - “N2” means nitrogen. - “O2” means oxygen. - the terms “concentration”, “quantity”, “proportion”, “dose” and “content” are considered equivalent. - the terms "means of / to / for" are considered to be completely equivalent and substitutable by the terms "device of / to / for", for example the terms "control means" can be replaced by "control device", the terms "valve means" can be replaced by "valve device", the "memorization means" can be replaced by "memorization device" ... - by “flow measurement” we mean a flow value (e.g. a digital value) or a signal representative of such a flow value reflecting or corresponding to a gas flow rate measured by a flow sensor, such as a mass flow sensor. - by “pressure measurement” we mean a pressure value (e.g. a digital value) or a signal representative of such a pressure value reflecting or corresponding to the gas pressure measured by a pressure sensor. - by "concentration measurement" is meant a value of content of a given gaseous compound, such as NO, NO2 or O2, i.e. a numerical value or a signal representative of such a content value reflecting or corresponding to the proportion (i.e. quantity) of the gaseous compound considered in a given gaseous mixture, measured by concentration measuring means, such as electrochemical cell sensors.

[0034] The invention will now be better understood thanks to the following detailed description, given for illustrative but non-limiting purposes, with reference to the appended figures among which:

[0035] [Fig.l] shows schematically an embodiment of a gas administration installation comprising an NO delivery apparatus according to the invention.

[0036] [Fig.2] schematizes an embodiment of the internal architecture of the device of delivery of NO according to the invention, such as that of the installation of [Fig.l].

[0037] [Fig.3] shows schematically an embodiment of the display of different information on the display of an NO delivery device according to the invention, such as that of [Fig.2], in particular of a first dose of NO having been set.

[0038] [Fig.4] schematizes a modification of the dose of NO by the user.

[0039] [Fig.5] is similar to [Fig.3] but schematizes the display obtained after modification of the NO dose by the user.

[0040] [Fig.l] schematizes an embodiment of a gas administration installation 100 according to the invention comprising an NO 1 delivery apparatus according to the invention making it possible to supply a gas mixture based on nitrogen monoxide (NO), typically a NO / N2 gas mixture, and a medical ventilator 50 supplying a gas containing at least 20% vol. of oxygen, typically air, an O2 / N2 gas mixture or other.

[0041] The installation 100 here comprises two pressurized gas cylinders 10 each containing a gas mixture based on NO, namely a NO / N2 gas mixture here containing between 100 and 1000 ppmv of NO (N2 remainder), for example 450 or 800 ppm vol. of NO (N2 remainder), or any other suitable concentration, which supply the NO / N2 mixture to the device or apparatus 1 for delivering or supplying NO, making it possible to monitor and control the supply of the NO / N2 gas mixture.

[0042] The gas cylinders 10 are fluidically connected to the NO supply apparatus 1, via gas supply lines 12, such as flexible pipes or conduits or the like, which may be equipped with devices for regulating and / or monitoring the gas pressure, such as a gas regulator 13, pressure gauges, etc. The gas supply lines 12 are connected to one or more gas inlets 2 of the NO 1 delivery apparatus which supply an internal gas circuit 200, as shown diagrammatically in [Fig. 2], used to convey the gas within the NO 1 supply apparatus, i.e. into the external casing or frame 1.1 of the NO delivery apparatus 1 according to the invention.

[0043] In the embodiment of [Fig.2], the internal gas circuit 200 is connected to two gas inlets 2 arranged in parallel and each supplying a dedicated inlet section 200.3 of the internal gas circuit 200. Control valves 222 or the like control the passage of the NO / N2 flow in these inlet sections 200.3.

[0044] The NO 1 delivery apparatus further comprises an oxygen inlet 3 fluidically connected, via an oxygen supply line 11, such as a flexible hose or the like, to an oxygen source (not shown), for example a pressurized oxygen cylinder or a hospital network, i.e. an oxygen supply pipe oxygen arranged in a hospital building. This allows the internal gas circuit 200 to be supplied with oxygen when necessary.

[0045] The medical ventilator 50, i.e. a respiratory assistance device, provides a flow of oxygen-based respiratory gas, i.e. containing at least approximately 20% by volume of oxygen, preferably at least approximately 21% by volume of oxygen, such as air or an oxygen / nitrogen mixture (N2 / O2).

[0046] The medical ventilator 50 and the NO 1 supply apparatus of the installation 100 are in fluid communication with a respiratory circuit 20, also called a patient circuit, in particular with a gas supply line or inspiratory branch 21 of the respiratory circuit 20, which is used to convey the gas flow to the respiratory interface 40 supplying the therapeutic gas flow to the patient, i.e. a combined gas mixture, i.e. the final mixture, containing the desired NO dosage. This combined gas mixture is obtained by mixing the oxygen-based flow (e.g. air or O2 / N2 mixture) coming from the medical ventilator 50 and the flow containing NO, i.e. the NO / N2 gas mixture, delivered by the NO 1 delivery apparatus.

[0047] To do this, the NO 1 delivery device supplies or injects the NO / N2 mixture into the respiratory circuit 20 carrying the oxygen-based flow, via a conduit or an injection line 23, fluidically connecting the internal gas circuit 200 of the NO 1 delivery device to an injection device 24 arranged on the gas supply line 21.

[0048] The injection device 24 is configured to operate a mixture of the gas containing NO coming from the NO 1 delivery apparatus with the flow of respiratory gas containing O2 coming from the ventilator 50 and conveyed by the inspiratory branch 21 of the respiratory circuit 20, and to obtain a combined gas mixture containing NO and oxygen, that is to say the final gas mixture administered to the patient.

[0049] More specifically, the injection device 24 comprises a first gas inlet supplied with a flow of respiratory gas containing O2 coming from the medical ventilator 50, a second gas inlet supplied with gas containing NO, i.e. coming from the NO 1 delivery apparatus, and a gas outlet providing the combined gas mixture containing NO and oxygen, obtained by mixing, within the injection device 24, the gas containing NO with the flow of respiratory gas containing O2.

[0050] In other words, the flow of NO / N2 supplied by the injection line 23 then mixes (thanks to the injection device 24) with the flow of oxygen-based gas (> 20% O2), e.g. air or an oxygen / nitrogen mixture, delivered by the medical ventilator 50 and conveyed by the inspiratory branch 21 of the patient circuit 20 so as to obtain a final mixture, i.e. the combined mixture, to be administered to the patient containing essentially NO at the desired dosage, nitrogen (N2) and oxygen (O2), and possibly unavoidable impurities (eg argon, CO2, NO2, ....), i.e. a final gas mixture NO / N2 / O2.

[0051] The inspiratory branch 21 of the circuit 20 further comprises a gas humidifier 30 arranged downstream of the injection device 24. It makes it possible to humidify the final gas flow, e.g. the combined gas mixture NO / N2 / O2, before it is administered by inhalation to the patient to be treated, by means of a respiratory interface 40, such as a tracheal intubation probe, a respiratory mask or the like.

[0052] A line for recovering gases exhaled by the patient forms an expiratory branch 22 of the patient circuit 20. It is fluidically connected to the inspiratory branch 21 via a connecting piece 25, such as a Y-shaped piece.

[0053] The inspiratory branch 21 is, at its upstream end, fluidically connected to an outlet port 51 of the medical ventilator 50, such as a connector, fitting or the like, so as to recover and convey the oxygen-based gas, typically air or N2 / O2 mixture supplied by the medical ventilator 50, while the expiratory branch 22 conveying the exhaled gases is fluidically connected to an inlet port 52 of the medical ventilator 50, such as a connector, fitting or the like, so as to return to the medical ventilator 50 all or part of the flow of gases exhaled by the patient. The expiratory branch 22 may comprise one or more optional components, for example a CO2 removal device 35, i.e. a CO2 trap, such as a hot tank or the like, making it possible to remove the CO2 present in the gases exhaled by the patient, a filter or the like.

[0054] Furthermore, a flow sensor 25, for example of the hot wire or pressure differential type, is arranged on the respiratory circuit 20, in particular on the inspiratory branch 21, between the ventilator 50 and the injection device 24. The flow sensor 25 is connected to a sensor connection port 27, of the NO 1 delivery device, via one or more flow measurement lines 26 connecting to said sensor connection port 27. It is used to measure the flow rate of gas delivered by the ventilator 50, such as air or N2 / O2, circulating in the inspiratory branch 21, upstream of the injection device.

[0055] These flow rate measurements made by the flow sensor 25 make it possible to more effectively control or regulate the delivery of the NO (i.e. N2 / O2) flow by the NO 1 delivery apparatus, in particular the NO flow rate, since the flow rate measurements made by the flow sensor 25 are returned, via the flow rate measurement line 26 (i.e. electrical cables or the like) and the sensor connection port 27, to (micro)processor control means 210 of the NO 1 delivery apparatus, typically a controller, which process these flow rate measurements as explained below and illustrated in [Fig.2]. The sensor connection port 27 is electrically connected to the control means 210. control 210 via one or more electrical connections, for example electric cables or the like.

[0056] The NO 1 supply apparatus comprises a rigid casing 1.1, for example made of polymer, comprising the internal gas circuit 200 on [Fig.2], typically gas lines, passages or conduits or the like, which fluidically connects the gas inlet (or inlets) 21 of the NO 1 supply apparatus to the injection line 23 so as to convey the flow of NO-based gas between them.

[0057] In the embodiment shown schematically in [Fig. 2], a portion of the internal gas circuit 200 comprises two gas sections arranged in parallel, namely a main section 200.1 and a secondary section 200.2, called the emergency section. The main section 200.1 and the secondary section 200.2 are fluidically connected to each other and to the rest of the gas circuit 200 at upstream 260 and downstream 261 connection sites located, respectively, upstream and downstream of the main and secondary flow control means 220, 221.

[0058] In normal operation of the device 1, the flow of NO / N2 passes through the main section 200.1, whereas in the event of a malfunction rendering the main flow control means 220 non-operational, the flow of NO / N2 is diverted and then passes through the emergency section 200.2.

[0059] Of course, according to another embodiment (not shown), the internal gas circuit 200 could be configured differently, for example comprising a single gas line instead of the two sections 200.1, 200.2. However, in this embodiment, a malfunction of the main flow control means 220 could not be taken into account and the apparatus 1 would then become non-functional.

[0060] Generally speaking, the main and secondary flow control means 220, 221, such as main and secondary valve means 2200, 2210, shown diagrammatically in [Fig. 2], i.e. one or more valve devices, for example one or more proportional solenoid valves controlled by the control means 210, are arranged on the internal gas circuit 200, in particular on the main 200.1 and secondary 200.2 sections, and serve to control or adjust the gas flow which circulates therein towards the injection line 23, i.e. towards the injection device 24, whether in normal operating mode or in emergency mode.

[0061] Preferably, the main section 200.1 comprises a proportional solenoid valve 220 and an additional flow sensor 230, typically a mass flow controller or MFC, while the secondary section 200.2 comprises one (or more) all-or-nothing (TOR) type solenoid valves 221, preferably controlled in pulsed mode.

[0062] Preferably, the main and secondary flow control means 220, 221 of the NO 1 supply apparatus are controlled, i.e. monitored, by the means control 210, i.e. one (or more) control devices or (micro)controllers, arranged in the housing 1.1 of the NO 1 supply device.

[0063] Typically, the control means 210 comprise one or more electronic cards comprising one or more microprocessors 211 implementing one or more algorithms. The control means 210 make it possible in particular to adjust or control the flow rate of NO-based gas by controlling all or part of the valve means 2200, 2210, typically to open or close one or more (electro)valves, to obtain a flow rate of NO-based gas, typically to authorize or stop the gas flow rate.

[0064] Of course, the control means 210 also make it possible to carry out calculations and / or to control or command all the electromechanical elements of the device 1, such as the sensors, the displays, etc.

[0065] As explained below, the control means 210 can determine the flow rate of NO to be supplied to obtain the desired NO content in the combined mixture, i.e. the desired NO dosage, in particular from a set NO content setpoint adjusted and / or set by the user, i.e. a dose of NO (DN0) adjusted by the user, namely a first dose of NO (DNOi) or subsequently a second dose of NO (DN02) as explained below, from the composition of the NO / N2 gas mixture, in particular from the NO content in this NO / N2 gas mixture which can be stored by the device 1, and from one or more flow rate measurements carried out by the flow sensor 25 arranged on the inspiratory branch 21 and connected by a flow rate measurement line 26 to the NO 1 supply device, in particular to the control means 210, via the connection port to sensor 27.

[0066] The internal gas circuit 200 of the NO 1 supply apparatus may also comprise other elements or components, in particular one (or more) pressure sensor 250, one (or more) additional flow sensor or flow meter and / or calibrated orifice devices 240 or others. These other elements may be arranged upstream and / or downstream of the flow control means 220, 221, i.e. the valve means, for example an additional flow sensor may be used to determine the flow rate of NO-based gas circulating in all or part of the internal gas circuit 200, in particular to ensure that it complies with the desired flow rate.

[0067] In [Fig.2], it can be seen that the main section 200.1 comprises an additional flow sensor 230 arranged upstream of the flow control means 220, such as valve means 2200, for example one or more solenoid valves, preferably a proportional solenoid valve, controlling the passage of gas in the main section 200.1. This assembly forms a mass flow controller (MFC).

[0068] Furthermore, the secondary section 200.2 comprises a calibrated orifice device 240 arranged downstream of secondary flow control means 221, such as means with secondary valve 2210, preferably one or more solenoid valves, controlling the flow rate of gas in the secondary section 200.2.

[0069] Advantageously, the solenoid valve of the secondary flow control means 221 is of the all-or-nothing (TOR) type, i.e. capable of adopting 2 “stable” positions, namely an open position allowing the gas flow to pass and a closed position preventing any circulation of gas flow.

[0070] Furthermore, the additional flow meter or flow sensor 230 of the MFC may be of the pressure differential type, mass or other, and cooperates with the control means 210 to provide them with flow rate measurements of the N0 / N2 flow.

[0071] Usually, the NO 1 supply apparatus also comprises a graphical user interface or GUI comprising a graphical display 4, preferably a touch screen, i.e. a touch panel, used to display various information or data, icons, curves, alarms, etc., as well as virtual selection keys and / or blocks or windows, used in particular to make choices, selections or to enter information, such as desired values ​​(e.g. flow rate, NO dosage, etc.), or any other information or data useful to the healthcare personnel. Preferably, the display is in color but it can also be in black and white.

[0072] However, according to another embodiment, the device 1 may also comprise one or more mechanical selection members, i.e. non-virtual, such as one or more selection buttons or keys actuated by digital pressure from the user, one or more rotary selection buttons or other. The selections or choices made via this or these mechanical selection members may be displayed on the graphic display 4 of the IGU.

[0073] In particular, the first dose of NO (DNOi) and second dose of NO (DN02) can be set or selected via one or more virtual selection keys and / or blocks or windows displayed by the graphic display 4, in particular when it has a touch screen.

[0074] The electrical power supply of the NO 1 supply apparatus, in particular of the components requiring electrical current to operate, such as the control means 210, the graphic display 4, etc., is conventionally provided by a source of electrical current and / or electrical power supply means (not shown), for example a connection to the mains current (110 / 220V) of the electrical cord and connection plug type, and / or one (or more) electrical power supply batteries, preferably rechargeable, and / or a current transformer. The electrical power supply of the medical ventilator 50 is provided in a similar manner, in particular by a connection to the mains current or an internal battery.

[0075] Furthermore, the installation 100 also comprises a gas sampling line 60 which fluidically connects the inspiratory branch 21 to the NO 1 supply device.

[0076] The gas sampling line 60 makes it possible to monitor, i.e. to follow up, the composition of the combined gas mixture containing NO, O2, etc., in order to ensure that the contents of NO, O2 and also of toxic NO2 species that may be formed are compliant, in particular that the proportion of NO is indeed between fixed high and low NO alarm thresholds, i.e. between acceptable maximum and minimum NO contents. Otherwise, the control means of the device 1 trigger an audible alarm and / or a visual alarm in order to alert the healthcare personnel, by activating (i.e. controlling / commanding) the alarm means.

[0077] The gas sampling line 60, also called the monitoring line, is fluidically connected, at a connection site 61 in [Fig.l], to the gas supply line 21, between the humidifier 30 and the junction piece 25, i.e. the Y-shaped piece, typically in the immediate vicinity of the junction piece 25, and also to an inlet port 62 of the NO 1 supply device, for example a port 62 carried by a connector, fitting or the like, allowing the connection of the gas sampling line 60, such as a flexible pipe or the like.

[0078] The gas sampling line 60 makes it possible to take gas samples and convey them to the NO 1 supply device where they are analyzed in an internal gas analyzer (not shown), that is to say within a calibration line comprising at least one sensor, in particular one or more electrochemical cells, electrically connected to the control means, in order to verify their conformity.

[0079] As already stated, it is appropriate to check that the composition of the final gas, i.e. the combined gas mixture, is consistent with that of the desired NO / N2 / O2 gas mixture to be administered to the patient, in particular to ensure that it does not contain an excessive quantity of toxic NO2 species, that its oxygen content is not hypoxic, and that its NO content corresponds to the desired dosage (neither too high nor too low), i.e. the dose of NO to be administered by inhalation which is chosen by the healthcare personnel, i.e. a doctor or similar, namely the first dose of NO (DNOi) or the second dose of NO (Dn02) in the event of modification of the first dose of NO (DNOi).

[0080] This conformity verification is conventionally carried out by means of dedicated NO, NO2 and O2 concentration measuring means, typically NO2, NO and O2 sensors, for example electrochemical cells or the like, which must be calibrated periodically, for example every week.

[0081] The control means 210 of the device 1 are further configured to recover and process, i.e. analyze, the signals coming from the various means for measuring the concentration of NO, NO2 and O2, such as sensors, of the gas analyzer, which is arranged in the device 1, and to act in response to these signals, in particular to carry out a calibration of the sensors, trigger audible and / or visual alarms, etc.

[0082] Generally speaking, the control means 210 with (micro)processor 211, such as a controller, determine the set flow rate of gas containing NO to be supplied to the injection device 24 and control the flow control means 220, 221, such as proportional solenoid valves 220 and / or TOR 221, to supply the gas containing NO at the set flow rate. The determination of the set flow rate of NO is carried out from a measurement of the respiratory gas flow rate, i.e. flow rate value or signal, carried out and supplied by the flow sensor 25 to the control means 210, of a set NO content corresponding to the final proportion of NO desired in the combined gas mixture, typically set by the user, i.e.nursing staff, and the initial proportion of NO in the gas containing NO supplying the NO 1 delivery device, i.e. the quantity of NO present in the NO / N2 mixture coming from the gas cylinders 10, typically between 200 and 1000 ppmv, for example 450 or 800 ppmv.

[0083] Preferably, the NO content in the NO / N2 gas mixture supplying the device 1 can be stored by the storage means 212 of the device 1.

[0084] Furthermore, the NO content in the NO / N2 gas mixture supplying the device 1 may be adjustable or not, i.e. memorized once and for all or adjustable by the user, within a dedicated or similar menu of the device 1, for example by using, here again, adjustment means, such as one or more keys, rotary knobs, cursors or others.

[0085] The first desired dose of NO (DNOi), which is typically between 1 and 80 ppmv, i.e. the NO setpoint value at the start of a treatment, must be entered by the user, for example via the HMI, using dose adjustment means or the like, such as one or more keys, rotary knobs, sliders or the like, preferably via one or more virtual keys displayed on the display screen 4.

[0086] As already explained, in order to be able to detect and warn the user, i.e. the healthcare staff, in the event of excessive or, conversely, insufficient NO concentration in the combined gas mixture supplied to the patient, it is essential to set the high and low NO alarm thresholds, i.e. (at least) a high threshold and a low threshold, corresponding to the maximum and minimum acceptable NO levels taking into account the fluctuations in NO concentration that may exist due to possible variations in particular in the flow rate of oxygen-based respiratory gas coming from the medical ventilator 50.

[0087] Thus, just before starting a treatment, for example when putting the device 1 into service, it is appropriate to define first high and low alarm thresholds corresponding to a first maximum NO content (Tmaxi) and to a first minimum NO content (Tmini), with: Tmax[ > DNOi > Tmini.

[0088] The setting of these high and low NO alarm thresholds (i.e. Tmaxi, Tmini) is done automatically, via the control means 210, as soon as the first dose of NO (DNOi) desired by the user, i.e. a doctor for example, is set, which avoids calculation errors and also errors linked to the entry of these NO alarm thresholds in the NO delivery device. Patient safety is improved.

[0089] More precisely, to do this, the control means 210 automatically calculate or determine, from the first dose of NO set (DNOi) having been chosen by the doctor or the like, the first high and low alarm thresholds corresponding to a first maximum NO content (Tmaxi) and to a first minimum NO content (Tmini), with: Tmax1 > Dn01 > Tmini.

[0090] Once the first desired dose of NO (DNOi), i.e. the desired dosage, typically between 1 and 80 ppmv, preferably less than or equal to 60 ppmv, more preferably less than or equal to 40 ppmv, for example of the order of 20 ppmv, has been set by the user using the NO dose setting means, such as one or more virtual keys displayed by the graphic display 4, the chosen value corresponding to the first dose of NO (DNOi) set, is used by the control means 210 to automatically calculate or determine first high and low NO alarm thresholds as follows: - the first high NO alarm threshold corresponds to a first maximum NO content (Tmaxi), such that: 1.1 . DNOi < Tmaxi < 1.3 . DNOi, preferably

[0091] Tmaxi < 1.25. DNOi, more preferably Tmaxi < 1.2.DNOi, for example

[0092] Tmaxl = 1.2.DNOi, and - the first low NO alarm threshold corresponding to a first minimum NO content (Tmini), such that: 0.7 . DNOi < Tmini < 0.9 . DNOi, preferably

[0093] 0.75 . DNOi < Tmini, more preferably 0.80 . DNOi < Tmini, for example

[0094] Tminl = 0.8.DNOi.

[0095] In other words, before or when starting a treatment, the control means 210 of the device 1 automatically determine the first values ​​of the high and low NO alarm thresholds (Tmaxi, TminJ by adding or, conversely, subtracting from 10% to 30% (i.e. a tolerance), preferably approximately 20%, to the value of the first dose of NO (DNOi) set, depending on the tolerance value (%) that can be accepted, i.e. the fluctuations in NO contents in the combined gas mixture that can be tolerated within the framework of the patient's treatment.

[0096] The tolerance value (%) may be non-modifiable, for example set in the factory and stored in the device, or, according to another embodiment, may be modifiable by the user, for example within a configuration menu of the device 1. The percentage (%) of tolerance may depend on different factors, for example for a particular treatment protocol.

[0097] The tolerance value (%) and / or the calculation formulas including this tolerance value (%) are stored within the device 1, for example within the storage means 212. For example a tolerance of 20% which is applied to the calculation of all the NO alarm thresholds.

[0098] Once determined, the first maximum NO content (Tmaxi) corresponding to the first high NO alarm threshold and the first minimum NO content (Tmini) corresponding to the first low NO alarm threshold are preferentially stored, i.e. recorded, by the storage means 212.

[0099] For example, for a first dose of NO (DNOi) set at 20 ppmv by the doctor or the like, the delivery device 1 of the invention, typically its control means 210, automatically calculates first high and low NO alarm thresholds between 14 and 18 ppmv for the first minimum NO content (Tmini) and between 22 and 26 ppmv for the first maximum NO content (Tmaxi).

[0100] If the percentage (%) of tolerance has been set at 20% due to adjustments made for example in the factory, the calculation formulas above then boil down to: - Tmaxi = 1.20.DNOi, for the first high NO alarm threshold, i.e. 20% more than the first dose of NO (DNOi) set, and - Tmini = 80. DNOi for the first low NO alarm threshold, i.e. 20% less than the first NO dose (DNOi) set.

[0101] Therefore, for the first dose of NO (DNOi) set at 20 ppmv, the device 1 can then automatically calculate first high and low NO alarm thresholds equal to 16 ppmv for the first minimum NO content (Tmini) and 24 ppmv for the first maximum NO content (Tmaxi), i.e. first high and low thresholds equal to 20 ppmv + / - 20% (i.e. + / - 4 ppmv).

[0102] In all cases, in particular for the set NO doses (DN0) which are less than 10 ppmv, the control means 210 are configured to calculate and / or set first maximum and minimum NO contents (Tmaxi, Tmini) preferably deviating by at least 2 ppmv from the first set NO dose (DNOi), i.e.: Tmaxl - DNOi > 2 ppmv and DNOi _Tminl > 2 ppmv.

[0103] For example, for a first dose of NO (DN0) set at 5 ppmv and a tolerance of 20%, the control means 210 are configured to calculate and / or set first maximum and minimum NO contents (Tmaxi, Tmini) of 3 ppmv for the first minimum NO content (Tmini) and 7 ppmv for the first maximum NO content (Tmaxi), whereas in theory they should be 4 ppmv and 6 ppmv, respectively.

[0104] Such a deviation of at least 2 ppmv from the set NO dose (DN0) makes it possible to avoid too frequent alarm triggering while guaranteeing good safety for the patient.

[0105] Once the first high and low NO alarm thresholds have been determined, they are preferably displayed by the graphic display 4, as illustrated in [Fig.3], which schematizes a display in a first dedicated window 41, of the first maximum NO content (Tmaxi) corresponding to the first high NO alarm threshold, namely here 24 ppmv, and of the first minimum NO content (Tmini) corresponding to the first low NO alarm threshold, namely here 16 ppmv.

[0106] It can be seen that the instantaneous value of NO content (NOinst) is also displayed in the first window 41, namely here 0.8 ppmv, which is measured by the NO concentration measuring means, such as an NO sensor. In this case, since the treatment has not yet started (displayed information: WAITING - Patient Not Treated), the NO value in the flow sent to the patient is almost zero (0.8 ppmv) because the flow of respiratory gas coming from the medical ventilator 50 has not yet been mixed with the flow of NO / N2 mixture coming from the device 1. Therefore, the NO concentration measuring means only determine a negligible quantity in the air flow, i.e. in the form of traces or unavoidable impurities.

[0107] [Fig.3] therefore illustrates the display 4 after setting the first dose of NO (DN0) by the user and calculating the first alarm thresholds (Tmaxi, Tmini) but just before the start of the patient's treatment, which can then begin after the user presses the virtual start button 45 displayed on the graphic display 4. Moreover, we also see that the first dose of NO (DNOi) set, that is to say the dosage, is also displayed within a second window 42, namely here 20 ppmv.

[0108] The NO concentration measuring means provide the NO measurements (i.e. value or signal) to the control means 210 which process them to possibly trigger alarms and / or control their display on the display 4, in order to ensure effective monitoring of the operation of the device 1 and / or the installation 100.

[0109] In addition, the display 4 also displays the NO2 and O2 concentrations measured by the NO2 and O2 concentration measuring means, typically NO2 and O2 sensors, for example electrochemical cells or the like, and processed by the control means 210, which also control their display on the display 4, namely here in third and fourth windows 43, 44.

[0110] We see that the NO2 content measured and displayed in the third window 43 is equal here to 0 ppmv, which is normal since the treatment has not yet started, therefore no oxidation of the NO molecules to form the toxic NO2 species could have taken place.

[0111] On the other hand, it is noted that the supply of the flow of respiratory gas containing oxygen, such as air or a gas mixture formed of 21% O2 and remainder N2 for example, coming from the ventilator 50 has started since the O2 concentration measuring means have detected an oxygen content of approximately 21% vol. in the gas flow present in the respiratory circuit 20. This oxygen content is displayed in the fourth window 44.

[0112] Once the first dose of NO has been set (DNOi) by the user and the first high and low alarm thresholds corresponding to the first maximum NO (Tmaxi) and minimum NO (Tmini) levels calculated by the device 1, for example 16 and 24 ppmv in [Fig.3], the treatment of a patient can be launched by the user, i.e. the nursing staff.

[0113] The NO is then distributed by the apparatus 1 at a given flow rate making it possible to obtain the desired NO dosage in the combined gas mixture, namely a dosage corresponding to the first dose of NO set (DNOi) by the user. This is done by controlling all or part of the flow control means 220, 221, as already explained.

[0114] However, if the doctor or the like realizes that the dose of NO provided is not suitable for the patient, i.e. that it is too high or too low, then he can modify this first dose of NO (DNOi), via NO dose modification means, namely as previously one or more virtual keys for example, to adopt a second dose of NO (DN02) different from the first dose of NO (DNOi).

[0115] For example, if the first dose of NO (DNOi) having been set, i.e. the starting dosage, was 20 ppmv, as illustrated in [Fig.3], and the doctor thinks that it is too strong for the patient in question, he can decide to reduce it for example to 16 ppmv (or conversely, to increase it if too weak).

[0116] In this case, as shown diagrammatically in [Fig.4], it actuates means for modifying the NO dose, such as one or more virtual keys displayed by the graphic display 4 with touch screen, for example “+” or “-” keys, used to increment or decrement the value displayed by the graphic display 4 so as to modify the first dose of NO (DNOi), namely here 20 ppmv, to obtain or fix the desired second dose of NO (DN02), namely here 16 ppmv.

[0117] Once the second dose of NO (DNO2) is set, it can be validated via a validation key 51 for example, which is activated by a digital press from the user.

[0118] Therefore, according to the invention, the control means 210 are configured to automatically calculate, from said second dose of NO (DNO2), i.e. here 16 ppmv, second high and low NO alarm thresholds (Tmax2, Tmin2) different from the first high and low NO alarm thresholds (Tmaxi, Tmini), corresponding to second maximum NO (Tmax2) and minimum NO (Tmin2) contents, with:

[0119] Tmax2 > Dn02 > Tmin2

[0120] The calculation of these second high and low NO alarm thresholds (Tmax2, Tmin2) is done like that of the first high and low NO alarm thresholds (Tmaxi, Tmini), as explained above, and this, with the same tolerance value.

[0121] Thus, if for a second dose of NO (DN02) set at 16 ppmv (for a first dose of NO (DNOi) previously set at 20 ppmv) and a tolerance set at + / - 20%, the device 1 can automatically calculate second high and low NO alarm thresholds equal to 13 ppmv for the second minimum NO content (Tmin2) and to 19 ppmv for the second maximum NO content (Tmax2), i.e. first high and low thresholds equal to 16 ppmv + / - 20% (i.e. + / - 3 ppmv).

[0122] As previously, in particular for NO doses less than 10 ppmv, the control means 210 are configured to calculate and / or set second maximum and minimum NO contents (Tmax2, Tmin2) preferably deviating by at least 2 ppmv from the second NO dose (DN02) set.

[0123] Then, as illustrated in [Fig.5], the displays operated on the graphic display 4 change, that is to say are updated, to display not only the “new” or second dose of NO (DN02) but also the “new” or second maximum and minimum levels of NO (Tmin2, Tmax2) corresponding to the second high and low NO alarm thresholds having been determined automatically from the second dose of NO (DN02) chosen by the user.

[0124] Of course, if the user were to change the NO dosage again, i.e. to apply a third dose of NO (or even other doses of NO, for example a fourth, a fifth, etc.), then the device 1 would operate in the same way to calculate “new” or third (or more) maximum and minimum NO contents (Tmi„3, Tmax3).

[0125] In all cases, programming the device 1 so that it automatically updates the alarm levels in the event of a change in the NO dose, i.e. the dosage, is advantageous because it avoids the triggering of untimely alarms which could occur if the user forgets to carry out such an adaptation of the alarm levels or in the event that he makes a mistake in calculating the levels of the new alarms and then enters erroneous threshold values.

[0126] Then, during operation of the apparatus 1, when the control means 210 detect a concentration of NO in the combined NO / O2 / N2 mixture greater than the first maximum NO content (Tmaxi) or, in the event of a change in NO content, a second maximum NO content (Tmax2), i.e. exceeding the high threshold (Tmaxi, Tmax2), or, conversely, less than the first minimum NO content (T mini), or, in the event of a change in NO content, a second minimum NO content (Tmin2), i.e. exceeding the low threshold (Tmini, Tmin2), they act on alarm means of the apparatus 1 to trigger an alarm, which may be audible, for example a sound from a buzzer or the like, and / or visual, for example an alert message displayed on the graphic display 4, in order to warn the nursing staff that the NO content of the combined gas mixture is too high or, conversely, too low.

[0127] Of course, other alarms can be triggered by the control means 210 in the event of detection of an excessively high NO2 content, for example exceeding approximately 1 to 3 ppmv or an excessively low oxygen content, for example less than approximately 19 to 20% vol. These alarms can be set in the factory and / or optionally, can be modified by the user.

[0128] A gas administration installation 100 including an NO 1 delivery apparatus according to the invention comprising means for automatically modifying the alarm thresholds, during dose changes, can be used to administer nitric oxide (NO) by inhalation, i.e. the final mixture obtained NO / O2 / N2, to people, i.e. patients, suffering from acute pulmonary arterial hypertension, in particular to operate a dilation of their pulmonary vessels and an increase in their oxygenation by improving pulmonary gas exchange, in particular to treat Pulmonary Arterial Hypertension of the Newborn or PPHN, Acute Respiratory Distress Syndrome or ARDS observed mainly in adults, or pulmonary hypertension (PH) in cardiac surgery in adults or children.

Claims

Claims

1. Apparatus (1) for delivering a gas containing NO comprising: - NO dose adjustment means (50, 51) configured to allow a user to adjust a first dose of NO (DNOi), and - microprocessor (211) control means (210) configured to determine from said first set dose of NO (DNOi), first high and low alarm thresholds corresponding to a first maximum NO content (Tmaxi) and to a first minimum NO content (Tmini), with: Tmaxl > DNoi > Tminb characterized in that: - it further comprises NO dose modification means (50, 51) configured to allow a user to modify or adjust the first dose of NO (DNOi) to obtain or set a second dose of NO (DN02) different from the first dose of NO (DNOi), and - the control means (210) are configured to automatically determine from said second dose of NO (DNO2),second high and low NO alarm thresholds different from said first high and low NO alarm thresholds, corresponding to a second maximum NO content (Tmax2) and to a second minimum NO content (Tmin2), with: Tmax2 > DNO2 > Tmin2-,

2. Apparatus according to claim 1, characterized in that the first dose of NO (DNOi) is between 1 and 80 ppmv.

3. Apparatus according to one of the preceding claims, characterized in that it further comprises a graphic display (4) configured to display at least: - the first dose of NO set (DNOi) and the first maximum and minimum levels of NO (Tmini, Tmaxi) corresponding to the first high and low alarm thresholds, or - the second dose of NO (DN02) and the second maximum and minimum levels of NO (Tmin2, Tmax2) corresponding to the second high and low NO alarm thresholds having been determined.

4. Apparatus according to one of the preceding claims, characterized in that the control means (210) are configured to determine the second minimum and maximum NO contents (Tmin2, Tmax2) such that: — when: DNo2 < DNoi then: Tmax2 < Tmaxiet Tm;n2 < Tm;ni or when . Dno2 > D^oi then . Tmax2 > Tmaxiet Tmm2 > Tmmi.

5. Apparatus according to claim 1, characterized in that it further comprises an internal gas circuit (200) for conveying a flow of gas containing NO, comprising flow control means (220, 221) configured to control the flow of gas containing NO within said gas circuit (200).

6. Apparatus according to claim 5, characterized in that the microprocessor (211) control means (210) are configured to control at least the flow control means (220, 221) to control the supply of gas containing NO as a function of at least said first set NO dose (DNOi) or the second set NO dose (DN02).

7. Apparatus according to claim 5, characterized in that: - the internal gas circuit (200) of the apparatus (1) conveying the gas containing NO is fluidically connected to a respiratory circuit (20; 21) conveying a respiratory gas containing oxygen to inject the gas containing NO therein and obtain a combined gas mixture containing NO and oxygen, - and the control means (210) are configured to trigger an alarm by activating alarm means, when the NO content in the combined gas mixture is greater than or equal to the first or, as the case may be, the second maximum NO content (T max, T max 2) or less than or equal to the first or, as the case may be, the second minimum NO content (T min, T min 2).

8. Apparatus according to claim 7, characterized in that NO concentration measuring means are arranged to determine the NO content in the combined gas mixture within the internal gas circuit (200) and the control means (210) are configured to control a display (41) on the display graph (4) of the NO content (NOinst) in the combined gas mixture having been determined by NO concentration measuring means.

9. Apparatus according to claim 1, characterized in that the NO dose adjustment or NO dose modification means (50, 51) comprise one or more virtual keys displayed on the graphic display (4).

10. Installation for supplying a gas containing NO (100) comprising the NO delivery apparatus (1) according to one of the preceding claims supplied with a NO / N2 gas mixture by a source of NO / N2 mixture, and a medical ventilator (50) configured to supply a flow of respiratory gas containing O2 to said respiratory circuit (20; 21).

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