Abstract:
A safety needle assembly has a collar or ring that is rotatably mounted to a needle hub. The needle assembly may be connected to a syringe by the user grasping the needle hub in first and second embodiments, or turning of the needle sheath in other embodiments. The collar of the needle assembly may be rotated by turning the needle sheath. The needle hub may also interact with the collar by rotating the needle sheath. Mechanisms are provided at both the collar and the housing so that once the contaminated needle is covered, the needle assembly may be removed from the syringe for disposal by rotating the needle housing.
Abstract:
The present invention safety device is a one-piece needle assembly that has a base and a housing pivotally connected to the base. The base has a distal portion to which a needle is fitted. At the base there is formed longitudinally along its distal portion a catch mechanism that may be in the form of an anchor projection. At the back wall of the housing there is extended another catch mechanism that may be configured in the form of two clasping fingers. Also providing in the housing is an integral hook. As the housing and the base are pivoted relative to each other, and as the needle makes contact with the hook, the respective catch mechanisms at the base and the housing also make contact with each other, resulting in the coupling of the catch mechanisms and the coupling of the needle to the hook. As a result, the catch mechanisms are interlocked and the needle is fixedly retained by the hook within the housing. The catch mechanisms may also be configured as a hook and a latch in the form of a rib with an opening whereto the hook is fixedly coupled. The catch mechanisms may further be configured as respective interlockable pairs of loops and bosses. The gauge of the needle may be determined by the color of both the base and the housing, which are molded as a unitary single unit.
Abstract:
A safety needle assembly has a collar or ring that is rotatably mounted to a needle hub, which may be connected to a medical device such as a syringe. The needle assembly may be connected to the syringe by the user grasping the needle hub in first and second embodiments, or turning of the needle sheath in other embodiments. In all of the embodiments, the collar of the needle assembly may be rotated by turning the needle sheath, which is designed to interact with the collar. In some of the embodiments, the needle hub likewise interacts with the collar in such a way that by rotating the needle sheath, the needle hub is likewise rotated for connection to a syringe. When an exposed needle is to be covered, after the needle sheath has been removed, a housing connected to the collar is pivotally moved to cover the needle. Mechanisms are provided at both the collar and the housing so that once the contaminated needle is covered, the needle assembly may be removed from the syringe for disposal by rotating the needle housing. In all of the embodiments disclosed, the needle sheath does not come into contact with the needle hub and the collar is rotatable about the needle hub.
Abstract:
A computer readable storage medium comprises a publication definition module to create and define properties for a publication object. The publication definition module includes executable instructions to associate a set of static documents and a set of report templates with the publication object. Executable instructions define a conditional delivery rule for the publication object. The conditional delivery rule specifies a condition for the inclusion of a report template from the set of report templates to be merged with a static document from the set of static documents.
Abstract:
The present invention relates to methods of treating pulmonary hypertension, facilitating joint fusion, facilitating tendon and ligament repair, reducing the occurrence of secondary fracture, treating avascular necrosis, facilitating cartilage repair, facilitating bone healing after limb transplantation, facilitating liver regeneration, facilitating wound healing, reducing the occurrence of gastric ulceration, treating hypertension, facilitating the growth of tooth enamel or finger or toe nails, treating glaucoma, treating ocular hypertension, and repairing damage caused by metastatic bone disease using an EP2 selective receptor agonist.
Abstract:
A safety needle assembly has a needle hub and a collar. Integrally formed from the proximal portion of the needle hub is a ring that surrounds its luer base. At the distal portion of the needle hub there are coaxially formed circumferential flanges which act to allow the collar to be rotatable about the needle hub. A needle protection housing is connected to the collar and is pivotable to cover the needle that extends from the distal end of the needle hub. Before use, the needle extending from the needle hub is covered by a needle sheath that has a groove formed circumferentially at its proximal end that snap-fits to a circumferential rib formed at the distal end of the collar.
Abstract:
A computer readable storage medium comprises a publication definition module to create and define properties for a publication object. The publication definition module includes executable instructions to associate a set of static documents and a set of report templates with the publication object. Executable instructions define a conditional delivery rule for the publication object. The conditional delivery rule specifies a condition for the inclusion of a report template from the set of report templates to be merged with a static document from the set of static documents.
Abstract:
A system, method and apparatus is provided for pulse width correction in a power driver. In an embodiment, an apparatus includes an operational amplifier having an input and an output. The input of the operational amplifier is coupled to receive an input pulse signal. The apparatus further includes an output stage having an input coupled to the output of the operational amplifier. The output stage also includes a current output configured to couple to a load and to a voltage sense output. The apparatus also includes a comparator having an inverting input coupled to the voltage sense output of the output stage, a non-inverting input configured to couple to an input signal, and an output. Also, the apparatus includes a timing circuit with an input coupled to the output of the comparator and an input coupled to the input signal. The timing circuit also has an output to supply the input pulse signal. The timing circuit measures a delay from a change in the input signal to a change in the output of the comparator. The timing circuit replicates the measured delay as a delay in a change to the input pulse signal.
Abstract:
A method for predicting treatment response of a type II diabetes patient to rosiglitazone is provided. The method involves at least one sample from a patient having type II diabetes and analyzing biomarkers predictive of a patient who will respond to treatment with rosiglitazone. The biomarkers include, at least, interleukin-8, histidine, citrate. These biomarkers are identified in at least one classification analyses selected from the group consisting of a majority-vote based classifier and support-vector machine (SVM) classifier. Also provided is a method for predicting treatment response of a type II diabetes patient to glyburide at 8 weeks post-initiation of therapy. The method involves obtaining a sample from a type II diabetes patient who has been treated with glyburide for about 4 weeks and analyzing biomarkers predictive of a patient who will respond to treatment with glyburide at 8 weeks. The biomarkers useful in this method include, at least, sphingomyelin 23:1 and L-phenylalanine. Also provided are kits useful for the methods of the invention.
Abstract:
A fluid transfer system has a holder that is made of a cylindrical member having a closed end and an open end. The closed end has fitted thereto a luer and a cannula that extends into the interior of the holder. The holder has a distal portion that has a first cross section and a proximal portion that has a second cross section. The cross section of the distal portion is smaller than the cross section of the proximal portion. The distal and proximal portions are joined by a shoulder. The fluid transfer system also includes an adapter that is inserted to the holder from the open end of the holder. The adapter has a base having a central opening and a cylindrical tube that extends from the central opening. The diameter of the cylindrical tube is slightly smaller than the diameter of the distal portion and is configured to accept a first type of fluid collection store such as a vacuum tube. With the adapter removed, the holder can accept a differently dimensioned fluid collection store such as for example a blood culture collection bottle.