A ventilation system includes an electrochemical filter for depleting alkyl phenols, especially 2,6-diisopropyl phenol, in breathing gas. A method uses the filter for removing alkyl phenols, especially 2,6-diisopropyl phenol, from breathing gas.

The present invention relates to the art of automatic regulation of pulmonary devices for imitating, assisting and/or enforcing the breathing process by converting Bag-Valve-Mask (BVM) or a similar device to enhance both phases of breathing: inhalation and exhalation while applying a variable pressure during the breathing process. It also replaces a mechanical chest compression to the sternum area for automatic pneumatic compression, and it could be complimented with the use of a Tens unit, can be used for extended period of time with a high level of reliability, simplicity, efficacy and low cost. The unique filtration system's goal in this invention is safety of the treating patient as well as assisting personnel. This portable and light device is recommended to be used as a resuscitator for the patients with mild to extremely suppressed or without respiratory drive. The source of power can be electrical, battery operated, manual or a combination thereof.

An anesthetic gas delivery system includes a gas machine for supplying anesthetic gas to a patient; a scavenging control system that controls a level of vacuum suction to evacuate waste anesthetic gas; and a user interface electronically coupled to the scavenging control system. The scavenging control system includes an air flow sensor external from the gas machine that measures the flow rate of the waste anesthetic gas through the scavenging control system; a control valve, such as a proportional solenoid valve, that is controllable to adjust the level of vacuum suction to adjust the flow rate of the waste anesthetic gas; and electronic control circuitry that is configured to receive a measured flow rate from the sensor and to control the control valve to adjust the level of vacuum suction based on the flow rate measured by the sensor. The electronic control circuitry further is configured to transmit flow rate information corresponding to the flow rate measured by the sensor to the user interface.

A patient treatment system includes a ventilation bag, and a monitoring device which is configured so as to be connectable to the ventilation bag. The monitoring device measures the pulse rate derived from the heart rate of a neonate, from signals of ECG electrodes which are connected to the monitoring device. In a case where an abnormality of measurement information of the pulse rate is detected, the monitoring device notifies of first information prompting ventilation by the ventilation bag.

Embodiments of the present invention provide systems and methods for delivering respiratory treatment to a patient. For example, a treatment system may include a mechanism for delivering a positive pressure breath to a patient, and one or more limb flow control assemblies which modulate gas flow to and from the patient. Exemplary treatment techniques are embodied in anesthesia machines, mechanical ventilators, and manual ventilators.

A process for operating a ventilator (12) and a ventilator (12) operating according to the process are provided. A pressure target value (p.sub.z) is determined during a phase of exhalation (48) as a function of a compliance (C) determined in relation to the lungs (14) of a patient being ventilated by means of the ventilator (12).

An arrangement and process supply a patient-side coupling unit with a gas mixture including a first gas component and a second gas component. A first duct (K.1) directs the first gas component from a first source (E) to a mixing point (8). The second gas component flows from a second source (25) to a buffer reservoir (5) and from the buffer reservoir (5) through a second duct (K.2) to the mixing point (8). The gas mixture flows from the mixing point (8) through an inspiration duct (K.30) to the patient-side coupling unit. A pneumatic control line (28) provides a control fluid connection between the first duct (K.1) and the buffer reservoir (5). A pressure balancing is effected between the pressure inside (In.O2, In.k1) the buffer reservoir (5), the pressure in the first duct (K.1), and the pressure in the second duct (K.2).

The present invention provides a portable, light-weight, breathing device and methods of use for delivering pristine, fresh air or varying high concentrations of oxygen with or without aroma, i.e., essential oils for stimulating appetite, boosting mood or decreasing stress and anxiety. The breathing device comprises an air container having a breathing air bag therein which contains the fresh air or the varying concentrations of oxygen optionally with the one or more essential oils, tubing for delivering the fresh air or oxygen to a breathing mask, and a plurality of movable valves included in the mask which directs air or oxygen into or out of the mask depending on whether the user is inhaling or exhaling. The breathing device also comprises the use of a can of compressed fresh air or oxygen with or without aroma to be used with an air reservoir or with an expandable air bag.

A breathing circuit for use in conjunction with a ventilator serving a mechanically-ventilated patient includes an expiratory gas airflow pathway; an inspiratory gas airflow pathway; and a gas mixing mechanism operable to mix inspiratory gas and expiratory gas in an amount sufficient to equilibrate the patient's PETCO.sub.2 and arterial PCO.sub.2 such that the patient's PETCO.sub.2 is a clinically reliable approximation of the patient's PaCO.sub.2.

The present invention is a mechanical ventilation device which delivers intermittent positive pressure ventilation by compressing AMBU. As the device uses existing AMBU for the ventilation, it is intended to automate the process of hand ventilation and will hence keep the costs and skill requirement low. Due to usage of the AMBU and simple mechanics, it is easy to manufacture and maintain the device.