Provided is an orogastric tube guide that can be used to accurately and quickly place an orogastric tube into the esophagus of a subject. In some embodiments, the orogastric tube guide is placed into the mouth of the subject after the subject has been intubated with an endotracheal tube. When placed in the midline of the subject's mouth, the disclosed orogastric tube guide aims placement of an orogastric tube towards the subject's esophagus. The orogastric tube guide also optionally contains a bite block to prevent a patient's teeth from clamping down on an endotracheal tube. The orogastric tube guide also optionally contains ports that can be attached to air tubing for providing supplemental oxygen after endotracheal extubation, thereby avoiding the need for nasal cannula.

An intubating device is provided for use with an endotracheal tube. In some embodiments, the intubating device includes a sheath having a distal end and a proximal end, and the sheath is configured to be introduced into a body cavity. The sheath has a rigid section, and the sheath has a flexible section at the distal end. The flexible section is selectively bendable. A control housing is located at the proximal end. The control housing includes a deflector for selectively bending the flexible section of the sheath. In some embodiments, an intubating device includes a sheath having a malleable first section and a second section that is selectively bendable located at a distal end of the sheath.

A medicament delivery device (“MDD”) having a delivery tube and a laryngeal mask having an anterior patient-contacting surface. In some embodiments of the invention, the laryngeal mask has an epiglottis-holding ridge. In some embodiments of the invention, the laryngeal mask has a cuff-portion providing at least a portion of an anterior patient-contacting surface, the cuff-portion being shaped and positioned to create a side-groove facing away from the anterior patient-contacting surface. In some embodiments of the invention, the laryngeal mask has a plurality of ridges on a posterior-side of the laryngeal mask opposite the anterior patient-contacting surface (the “posterior-side ridges”), the posterior-side ridges being shaped and positioned relative to the anterior patient-contacting surface so as to push against the patient and thereby push the anterior patient-contacting surface against the patient.

An add-on device and method for an Endo-Tracheal Tube (ETT), the add-on device including a lengthy body having a major arc-shaped cross section sized and shaped to tightly fit over an ETT, at least one longitudinal cavity passing along the lengthy body, including a distal suction cavity ending with a suction inlet at a distal end of the lengthy body; and a distal suction outlet channel extending from a proximal end of the lengthy body, the channel is a continuous extension of the distal suction cavity and configured to provide suction to the distal suction cavity. The add-on device senses moisture at a distal end of the add-on device, and in case of detection of excessive wetness, provides suction to the distal end of the device through a cavity passing along the device, the suction is provided via a suction outlet channel extending from a proximal end of the device.

Endotracheal devices and methods of using endotracheal devices are provided. The devices include a first elongated conduit having an internal dimension, a second elongated conduit having an external dimension less than the internal dimension of the first conduit, and a manipulation rod operatively mounted to the second conduit, where the manipulation rod allows an operator to move the second conduit within the first conduit. The manipulation rod may be used translate and/or rotate the second conduit within the first conduit. The first and second elongated conduits may be provided with inflatable cuffs to minimize the passage of fluids. Though aspects of the invention may be uniquely adapted for insertion through the trachea and into a bronchus, aspects of the invention may be used for other bodily passages.

Embodiments of the present invention disclose a suction stylet assembly for endotracheal intubation. The assembly includes an elongated tubular member, the elongated tubular member having one or more apertures proximate to a first end, and a handle in communication with a second end of the elongated tubular member. The handle member includes a first passageway connecting the elongated tubular member to a hose fitting on the handle member, the hose fitting configured to receive a hose that provides suction in removing bodily fluids. The handle member further includes an aperture located on a side of the handle member, the aperture forming a second passageway through the handle member running between the side and the first passageway, the aperture configured to permit a user to selectively block the aperture, thereby selectively controlling suction provided between the hose fitting and the elongated tubular member.

A device for delivering a substance to an airway of a patient may include a laryngeal mask airway device, at least one substance delivery reservoir coupled with the laryngeal mask airway device for delivering the substance to the airway of the patient, and at least one conduit coupled with the laryngeal mask airway. The at least one conduit may have a proximal end configured to couple with a source of the substance residing outside the patient and a distal end in fluid communication with the at least one substance delivery reservoir.

The mucus-removing device is adapted for use with a patient. The patient is further defined with a tracheostomy tube. The mucus-removing device is configured for use with the tracheostomy tube. The mucus-removing device generates a vacuum at the tracheostomy tube such that mucus is withdrawn from the pulmonary system through the tracheostomy tube and into the mucus-removing device. The mucus-removing device generates the vacuum at the tracheostomy for a fixed period of time. The periodic nature of the generation of the vacuum allows the patient to breath comfortably during the removal process. The mucus-removing device comprises a pump, a hose, a tracheostomy tube connector, and a control system. The hose attaches the pump to the tracheostomy tube connector. The tracheostomy tube connector attaches the mucus-removing device to the tracheostomy tube of the patient. The control system regulates the operation of the pump.

A system selectively delivers either breath-synchronized, flow-targeted ventilation (BSFTV) or closed-system positive pressure ventilation (CSPPV) to augment respiration of a patient with a standard tracheal tube. A removable adaptor has a cap that can be removably attached to the proximal connector of the tracheal tube in BSFTV mode, and an inner cannula that extends within the tracheal tube to effectively divide it into two lumens. The adaptor includes a ventilator connector for removably engaging a ventilator hose to deliver air/oxygen through the adaptor and one lumen of the tracheal tube with a flow rate varying over each respiratory cycle in a predetermined waveform synchronized with the patient's respiratory cycle to augment the patient's spontaneous respiration. The adaptor also includes a port allowing the spontaneously-breathing patient to freely inhale and exhale in open exchange with the atmosphere through the other lumen.

Methods of delivering medicament and a medicament delivery device (MDD) are described. Such an MDD may have a laryngeal mask configured to fit against a patient at an area surrounding the patient's laryngeal inlet, and thereby cover a laryngeal inlet of the patient, and a delivery tube having interior wall surfaces defining a medicament channel. Medicament may be conveyed via the medicament channel toward the laryngeal mask. The MDD may have at least two gas channels. The gas channels may be in gas-communication with the laryngeal mask.