Abstract: Apparatus for adding a beneficial agent to a liquid for drinking during oral administration includes a support structure extending transversely across an imperforate walled zone such as the upper end or neck of a bottle or vessel, or of a funnel-like adapter attached to the top of the vessel, with a retention pocket with liquid penetrable walls held by the support structure and comprising at least one beneficial agent secured therein whereby the beneficial agent is taken up in the liquid for drinking during or just prior to oral administration. The beneficial agent may be in either or both of controlled release dosage form or non-controlled release dosage form and may be one or more of nutrients, medicaments, probiotics, electrolytes, rehydration solutions and diagnostic agents, to which a flavoring agent may be added.

Abstract: An apparatus for supplying an enteral or parenteral fluid to a patient is a cooperative assembly of a rotary peristaltic pump and a fluid delivery set. The peristaltic pump has (a) a housing and (b) a peristaltic rotor projecting from the housing on a rotatable drive shaft. The housing has first and second receptacles for retaining and supporting the fluid delivery set. The fluid delivery set has (a) a drip chamber, or sight chamber, (b) a plurality of lengths or segments of flexible tubing, and (c) fluid connection elements therefor. The fluid delivery set defines a fluid pathway from a supply container of the enteral or parenteral fluid to a connector element adapted to be connected to a device for introducing the fluid into the patient. Preferably the fluid delivery set has a tension responsive pinch valve to prevent bolus feeding in the event that the fluid delivery set becomes displaced from the pump housing.

Abstract: A tubing connector has first and second tubular legs joined together to provide a continuous fluid pathway therethrough with the fluid pathway having a bend of about 78 to 102 degrees therein. A foreshortened retention tab extends laterally from the tubing connector at about the bend in a direction opposed to the second leg of the tubing connector. A handle extends from the tubing connector at about a right angle to both the first and second legs and the retention tab. The tubing connector may be employed as a component of a fluid delivery set used with a pump for enteral or parenteral feeding of a patient.

Abstract: An apparatus is useful for dye marking a liquid enteral nutritional product during delivery thereof from a supply container to a feeding tube delivering the nutritional product to the gastrointestinal tract of a patient. A formulation chamber, such as a drip chamber, is connectable to the supply container. At least one sustained release reservoir containing a physiologically acceptable marker dye is positioned within the formulation chamber, or if not, is included as part of a kit. The sustained release reservoir may be in the form of a coated tablet, osmotically driven device, coated capsule, microencapsulated microspheres, agglomerated molecular sieving material, or chopped hollow fibers having permeable walls. A liquid communication means connects the formulation chamber to the feeding tube of a patient. The marker dye may be a colorant dye or a fluorescing dye or a mixture thereof.

Abstract: An apparatus and method are disclosed for modifying a liquid enteral nutritional product during delivery thereof from a supply to a feeding tube delivering the modified liquid enteral nutritional product to the gastrointestinal tract of a patient. At least one beneficial agent not in controlled release dosage form in a useful, dose unit, amount, is disposed within a formulation chamber so as to be taken up in a liquid enteral nutritional product traversing the formulation chamber while feeding the modified nutritional product into the gastrointestinal tract of a patient. The beneficial additive(s) are selected from nutrients, medicaments, probiotics, or diagnostic agents, or mixtures thereof, each in a dosage form that is dispersible in the medium of the liquid enteral nutritional product in less than two hours.

Abstract: A method for dye marking a liquid enteral nutritional product during delivery thereof from a supply container to a feeding tube delivering the nutritional product to the gastrointestinal tract of a patient includes the steps of: (1) providing apparatus such as a formulation chamber, e.g., a drip chamber, connectable to the supply container, with at least one sustained release reservoir containing a physiologically acceptable and dispersible marker dye positioned within the formulation chamber, and, liquid communication means connecting the formulation chamber to the feeding tube of a patient; (2) providing a supply container containing the nutritional product; (3) connecting the formulation chamber to the supply container and the liquid commmunication means to the feeding tube; and (4) flowing the dye-marked nutritional product through the apparatus and into the feeding tube.

Abstract: A method is disclosed for modifying a liquid enteral nutritional product during delivery thereof from a supply container to a feeding tube delivering the nutritional product to the gastrointestinal tract of a patient. During enteral tube feeding the nutritional product passes through a formulation chamber, e.g., a drip chamber, having located therein at least one controlled release dosage form unit containing at least one beneficial agent. The beneficial agent may be selected from nutrients, medicaments, probiotics, or diagnostic agents or mixtures thereof, and any such together with a physiologically acceptable marker dye in controlled release dosage form and/or the same or different additional beneficial agent not in controlled release dosage form. Controlled release dosage forms may be of a conventional sustained release type or an osmotically driven delivery device.

Abstract: An apparatus is disclosed for modifying a liquid enteral nutritional product during delivery thereof from a supply thereof, such as a hangable container, to a feeding tube delivering the liquid enteral nutritional product to the gastrointestinal tract of a patient. The apparatus has at least one formulation chamber, such as a drip chamber, with at least one controlled release dosage form unit in the form of a coated tablet, osmotically driven device, coated capsule, microencapsulated microspheres, agglomerated molecular sieving type material, or a quantity of fine hollow permeable fibers located therein. The controlled release dosage form unit or units contain at least one beneficial agent selected from nutrients, medicaments, probiotics, or diagnostic agents or mixtures thereof, to any of which a physiologically acceptable marker dye in controlled release dosage form and/or the same or different beneficial agent not in controlled release dosage form may be added.

Abstract: Apparatus for adding a beneficial agent to a liquid for drinking during oral administration includes a support structure extending transversely across an imperforate walled zone such as the upper end or neck of a bottle or vessel, or of a funnel-like adapter attached to the top of the vessel, with a retention pocket with liquid penetrable walls held by the support structure and comprising at least one beneficial agent secured therein whereby the beneficial agent is taken up in the liquid for drinking during or just prior to oral administration. The beneficial agent may be in either or both of controlled release dosage form or non-controlled release dosage form and may be one or more of nutrients, medicaments, probiotics, electrolytes, rehydration solutions and diagnostic agents, to which a flavoring agent may be added.

Abstract: A fluid delivery set has three lengths of flexible tubing. The first length of flexible tubing at one end is connectable to or integral with a supply container for enteral or parenteral fluid, and at the other end is connected to the inlet of a drip chamber. The second length of flexible tubing is connected at one end to the outlet of the drip chamber, and at the other end to the inlet of a retention/connector device that has about a 90.degree. bend therein. The third length of flexible tubing is connected at one end to outlet of the retention/connector device, and at the other end is connectable to or integral with a means for introducing an enteral or parenteral fluid into the body of a patient. Preferably, a tension responsive pinch valve is operatively associated with the second length of flexible tubing.

Abstract: The present invention is an improved stylet for a enteric or nasoenteric feeding tubes. In broadest terms, the present invention comprises: a stylet for a feeding tube, the stylet having: (a) a stylet hub having a bore therethrough and adapted to be attached to one end of the feeding tube, the bore having an inner surface; (b) a longitudinally extending reinforcement member adapted to extend through the feeding tube, the reinforcement member having a proximal end; and (c) a hollow member having an outer surface and having an aperture, the hollow member disposed in the bore so as to hold the inlet end of the reinforcement member between the outer surface and the inner surface through an interference fit.