Abstract: Embodiments of a computer system, a method, and a computer-program product (e.g., software) for use with the computer system are described. These embodiments may be used to identify and correct errors in financial information that was extracted using character-recognition software, such as optical character recognition software and/or intelligent character recognition software. In particular, potential errors may be identified by comparing the financial information for a current financial transaction of a user with expected financial information from one or more previous financial transactions of the user. Error metrics for these potential errors may be determined and used to correct at least some of the potential errors. For example, values of the Levenshtein edit distance may be determined based on the comparison, and one or more potential errors associated with one or more minimum values of the Levenshtein edit distance may be corrected.

Abstract: An insulating unit that includes at least three transparent and/or semi-transparent sheets and which includes an improved arrangement to secure one or more intermediate sheets to a spacer frame.

Abstract: An insulating unit that includes at least three transparent and/or semi-transparent sheets and which includes an improved arrangement to secure one or more intermediate sheets to a spacer frame.

Abstract: An insulating unit that includes at least three transparent and/or semi-transparent sheets and which includes an improved arrangement to secure one or more intermediate sheets to a spacer frame.

Abstract: The invention is a self-venting blood collection needle assembly for the extraction of at least one fluid sample into an evacuated container for laboratory testing, this blood collection needle assembly providing a clear or translucent flashback chamber for blood to flow into, for visualization by the user to confirm successful vein entry. The self-venting mechanism permits escape of air during use, and which, typically, also prevents an outflow of fluid, such as blood. Thus, air under venous pressure will be allowed to escape from the blood collection needle assembly until blood reaches the venting mechanism.

Abstract: A bowel management system includes a waste collection catheter having at least two distinct sections. The first section is patient proximal when disposed in the patient's rectum and has durometer hardness in the range of about 50 A to about 90 A. The second catheter section is connected to the first section and has durometer hardness in the range of about 5 A to about 49 A. A selectively collapsible, substantially spherical retention balloon is attached coaxially and exterior of the first catheter section such that the proximal-most end of the retention balloon is coincident to the proximal-most end of the first section of the waste collection catheter, the substantially spherical retention balloon having an inflated size so as to be sufficiently large enough to retain the patient proximal end of the catheter in the patient's rectum without being so large as to trigger a defecatory response in the patient.

Abstract: The blood collection set includes an IV needle assembly, a length of flexible plastic tubing extending from the IV needle assembly and a non-patient needle assembly. The set is formed with a venting mechanism that permits an outflow of air, while blocking an outflow of blood or other fluids. Thus, the venting mechanism enables air that had existed in interior portions of the blood collection set to be vented allowing for greater flash visualization on venous entry, and avoids the need to employ a discard tube.

Abstract: The invention provides a method for electronic form filling that enables users to enter data into one source form and have that data transferred into any number of electronic target forms. As the fields are linked through the invention, complete accuracy is provided for any single-entry multiple-target form interactions. The invention works regardless of data standards adoption; does not require target forms to ‘opt-in’; does not store any sensitive, private user information; and is not limited by the state-of-the-art in artificial-intelligence research.

Abstract: The invention is a system (10, 110) for regulating volume in a retention cuff/balloon (20) in an indwelling catheter; i.e., the combination of fixed-volume inflatable retention cuff mountable on a patient proximal end of an indwelling catheter (14) and relief valve (23, 123) connected to the cuff. The relief valve has ends for selective introduction of fluid to the cuff and for connection to an inflation tube. A valve port (24, 124) permits escape of excess fluid when a maximum cuff volume has been exceeded, and inflation tube (22) connects cuff (20) to the relief valve. The inflation tube has ends in fluid-tight connection to an interior of the cuff, and the relief valve to thereby permit the cuff and valve to be in fluid communication with each other for selective filling of the cuff to insert and safely retain an indwelling catheter in a patient for an extended period.

Abstract: A bowel management system includes a waste collection catheter having at least two distinct sections. The first section is patient proximal when disposed in the patient's rectum and has durometer hardness in the range of about 50A to about 90A. The second catheter section is connected to the first section and has durometer hardness in the range of about 5A to about 49A. A selectively collapsible, substantially spherical retention balloon is attached coaxially and exterior of the first catheter section such that the proximal-most end of the retention balloon is coincident to the proximal-most end of the first section of the waste collection catheter, the substantially spherical retention balloon having an inflated size so as to be sufficiently large enough to retain the patient proximal end of the catheter in the patient's rectum without being so large as to trigger a defecatory response in the patient.

Abstract: An inflation system (10, 110, 120, 130) for a balloon catheter assembly (12) includes an inflation tube (22), the first end of which is connectable to an inflation fluid reservoir (24, 30) and the second end of which is connectable to and opens into an inflatable cuff (20) on a main catheter (14) of the balloon catheter assembly, to permit the fluid reservoir to be in fluid communication with the cuff. A fluid reservoir is connectable to the inflation tube and is fillable with cuff inflation fluid only to a predetermined, fixed volume, to thereby permit no more than such volume of fluid to be transferred from the reservoir to the cuff during use of the system, to prevent over-inflation of the cuff and thereby avoid potential trauma to the patient.

Abstract: A bowel management system includes a waste collection catheter having at least two distinct sections. The first section is patient proximal when disposed in the patient's rectum and has durometer hardness in the range of about 50 A to about 90 A. The second catheter section is connected to the first section and has durometer hardness in the range of about 5 A to about 49 A. A selectively collapsible, substantially spherical retention balloon is attached coaxially and exterior of the first catheter section such that the proximal-most end of the retention balloon is coincident to the proximal-most end of the first section of the waste collection catheter, the substantially spherical retention balloon having an inflated size so as to be sufficiently large enough to retain the patient proximal end of the catheter in the patient's rectum without being so large as to trigger a defecatory response in the patient.

Abstract: A bowel management system includes a rectal catheter; and at least one physiologic sensor. The rectal catheter has a portion in contact with a patient's body internally thereof during use of the system, to thereby determine a preselected physiologic parameter of a patient having the rectal catheter inserted into the patient's bowel. The position of the sensor relative to the rectal catheter portion is such that the sensor is disposed in close proximity to the internal tissue of the patient, or within the fecal flow, when the bowel management system is place for use within the patient.

Abstract: The invention is a self-venting blood collection needle assembly for the extraction of at least one fluid sample into an evacuated container for laboratory testing, this blood collection needle assembly providing a clear or translucent flashback chamber for blood to flow into, for visualization by the user to confirm successful vein entry. The self-venting mechanism permits escape of air during use, and which, typically, also prevents an outflow of fluid, such as blood. Thus, air under venous pressure will be allowed to escape from the blood collection needle assembly until blood reaches the venting mechanism.

Abstract: The blood collection set includes an IV needle assembly, a length of flexible plastic tubing extending from the IV needle assembly and a non-patient needle assembly. The set is formed with a venting mechanism that permits an outflow of air, while blocking an outflow of blood or other fluids. Thus, the venting mechanism enables air that had existed in interior portions of the blood collection set to be vented allowing for greater flash visualization on venous entry, and avoids the need to employ a discard tube.

Abstract: The present invention is a holder assembly having a holder housing, collar and safety shield. The safety shield is pivotably attached to the collar. The collar is receiving within a recess defined by the annular skirt and needle receiving port of the holder housing. The collar and attached safety shield may thus be rotated about the holder housing and an attached needle assembly, thereby allowing a user to freely position the safety shield during needle insertion and preventing the dislocation of safety shield from the holder housing.

Abstract: Disclosed are different titanium aluminide (Ti—Al) honeycomb panel structures formed from a gamma-based Ti—Al (&ggr;-Ti—Al) or orthorhombic Ti—Al (O—Ti—Al) honeycomb core brazed to a &ggr;-Ti—Al or O—Ti—Al facing sheet(s), where a metal braze filler foil containing copper and one or more other metals is used to join the faying surface of the honeycomb core and the faying surface of the facing sheet(s). The structures and method of the invention are useful where high strength, lightweigth materials are required, such as in aircraft and other aerospace-related applications.

Abstract: An interpretive language comprises instructions making up part of the first sequence of instructions (a test "script"). The first language comprises a first set of instructions, the first set of instructions causes a first computer system (a "host" in a preferred embodiment) to issue a series of commands to a second computer system (a "target") in order to cause the second computer system to emulate user activity on the second computer system. User activity includes emulating typing text and/or moving a mouse cursor position. The language further comprises a second set of instructions which cause the first computer system to issue a series of commands to the second computer system in order to cause the second computer system to respond to the first computer system with its state. This state includes user interface objects, and applications running in the target, etc.

Abstract: An endotracheal respiration system which includes a respirator manifold with a port for attachment and detachment of an accessory device thereto without interruption of continuous respiratory support of the patient. A particular embodiment includes a suctioning system for removal of fluids from a patient's lungs during respiratory support. The manifold of the respiration system includes an accessory access port which has a normally closed valve therein which remains closed regardless of the pressure changes within the manifold. However, the normally closed valve is positioned in the port such that placement of a specially designed male adaptor located on the suctioning device forces the normally closed valve to an open position, thus allowing passage of a suction catheter through the manifold into the patient.