Filtered bag-valve mask resuscitators are disclosed. Proper ventilation can be delivered to patients with significantly reduced risk of exposing healthcare providers to severe airborne diseases, while not compromising the quality of care and allowing the option of using aerosolized medications. A filtered bag-valve mask resuscitator can also include an angled segment having a lumen configured to deliver gases to and/or from a filter.

A system includes a guidance device that provides feedback to a user to compress a patient's chest at a rate of between about 90 and 110 compressions per minute and at a depth of between about 4.5 centimeters to about 6 centimeters. The system includes a pressure regulation system having a pressure-responsive valve that is configured to be coupled to a patient's airway. The pressure-responsive valve is configured to remain closed during successive chest compressions in order to permit removal at least about 200 ml from the lungs in order to lower intracranial pressure to improve survival with favorable neurological function. The pressure-responsive valve is configured to remain closed until the negative pressure within the patient's airway reaches about −7 cm H.sub.2O, at which time the pressure-responsive valve is configured to open to provide respiratory gases to flow to the lungs through the pressure-responsive valve.

An example device comprises: a cradle to support a resuscitator bag; a paddle arm comprising: a paddle surface disposed opposite the cradle; and a pair of arms extending from the paddle surface; a housing comprising: top, bottom, front and rear sides, and an opening at the front side, towards the top side; the paddle surface extending through the opening; the pair of arms, of the paddle arm, rotatably attached to the housing at an end opposite the paddle surface towards the rear side; a nut assembly rotatably attached to the pair of arms therebetween; a screw threaded through the nut assembly; and a motor rotatably attached to the housing towards the bottom side of the housing; the motor configured to: drive the screw relative to the nut assembly to move the paddle arm towards and away from the cradle, to compress and release the resuscitator bag when located therebetween.

In alternative embodiments, provided are mechanical ventilators and methods for making and using them.

A ventilator includes at-least one air vessel, at-least one inflation bag, at-least one connecting member, a bag holder and at-least one controller member. The at-least one connecting member connects to the at-least one air vessel. The bag holder may hold the inflation bag. The at-least one controller member operates the at-least one inflation bag thereby changing size of the inflation bag to vary a tidal volume and an inspiration-expiration ratio of the ventilator. In another aspect, at-least one controller member is mounted on the bag holder. Further, the at-least one controller member slides within the bag holder to change the shape of the inflation bag to vary a tidal volume and an inspiration-expiration ratio of the ventilator.

A nasal ventilation mask supplies breathing gas to an airway of a patient. The mask has a housing defining an internal cavity and having a peripheral end defining an end opening. The end opening is in fluid communication with the internal cavity. The end opening is configured to be positioned over an airway on a face of the patient. A sealing member is connected to the housing proximate the end opening. The sealing member extends towards the internal cavity and is configured to abut the face of the patient and deflect towards the internal cavity. The housing further defines a connector assembly having an opening in fluid communication with the internal cavity. The connector assembly is configured to be operably connected to a supply of breathing gas.

A manual resuscitator regulating system for regulating the rate and volume of ventilation during manual resuscitation. The manual resuscitator regulating system may include an intake assembly configured to permit a selected volume of gas to flow into a chamber over a predetermined amount of time and/or an outtake assembly configured to permit a selected volume of gas flow out of the chamber over a predetermined amount of time. The intake assembly and/or the outtake assembly may include one or more adjustment mechanisms configured to allow a user to selectively adjust volume. The intake assembly and the outtake assembly may be configured to coordinate with one another to deliver a selected tidal volume and/or volume of gas. The manual resuscitator regulating system may include a placement indicator configured to indicate or guide a user where to squeeze or compress the chamber.

A resuscitation bag system (1) useable for resuscitating a person in cardiac arrest, and having a gas control unit (90) with a first valve (92) fluidly connected to a first (922) and to a second conduit (923), the first (922) and second conduits (923) being arranged in parallel and further fluidly connected to the first conduit element (56), the first conduit (922) having a first flow restriction (924) configured for limiting the gas flow to a first flowrate, and the second conduit (923) comprising second flow restriction (925) configured for limiting the gas flow to a second flowrate, with the second flowrate being less than the first flowrate.

An emergency respirator ventilator that comprising an air cylinder and piston/piston rod for compressing an air bag to transmit air to a patient, e.g., during situations where fully equipped ventilators are not immediately available.

A device includes a body defining a respiration passage in fluidic communication with a filter fitting disposed on a first end of the body and a mask fitting disposed on a second end of the body, and a treatment passage in fluidic communication with the mask fitting. A treatment fitting is disposed on the body and is coupleable to a treatment source such that a seal in the treatment fitting transitions from a closed state to an open state to allow fluidic communication between the treatment source and the treatment passage. The device configured to permit (i) inhalation air and/or exhaled breath to be drawn and/or expelled through the filter fitting, the respiration passage, and the mask fitting and (ii) a respiratory therapeutic to be drawn from the treatment source coupled to the treatment fitting, through the treatment passage, and through the mask fitting.