The disclosed technology relates generally to medical devices, and more particularly, some embodiments relate to systems and methods for such devices.
In general, one aspect disclosed features a cap for disinfecting a medical device, the cap comprising: a cylindrical receiving portion having an opening configured to receive a medical device, the cylindrical receiving portion comprising internal threads configured to mate with external threads of the medical device; disinfectant disposed within the cylindrical receiving portion; a cylindrical stem disposed longitudinally within the cylindrical receiving portion; and an annular sponge disposed about the cylindrical stem and contacting the disinfectant.
Embodiments of the cap may include one or more of the following features. In some embodiments, the annular sponge is made of polyurethane. In some embodiments, the annular sponge is approximately ¼ inch thick. Some embodiments comprise one or more longitudinal grooves formed in the cylindrical stem. Some embodiments comprise a removable seal configured to retain the disinfectant within the cylindrical receiving portion. In some embodiments, the medical device comprises one of: a female luer lock; or a needleless valve.
In general, one aspect disclosed features a cap for disinfecting a medical device, the cap comprising: a cylindrical receiving portion having an opening configured to receive a medical device; a cylindrical stem disposed longitudinally within the cylindrical receiving portion; and disinfectant disposed within the cylindrical receiving portion.
Embodiments of the cap may include one or more of the following features. In some embodiments, the cylindrical receiving portion comprises: internal threads configured to mate with external threads of the medical device. Some embodiments comprise an annular sponge disposed about the cylindrical stem and contacting the disinfectant. In some embodiments, the annular sponge is made of polyurethane. In some embodiments, the annular sponge is approximately ¼ inch thick. Some embodiments comprise one or more longitudinal grooves formed in the cylindrical stem. Some embodiments comprise a removable seal configured to retain the disinfectant within the cylindrical receiving portion. In some embodiments, the disinfectant is 70/30 isopropyl alcohol. In some embodiments, the medical device comprises one of: a female luer lock; or a needleless valve.
In general, one aspect disclosed features a method of disinfecting a medical device, the method comprising: providing a medical device; providing a cap, the cap comprising: a cylindrical receiving portion having an opening configured to receive a medical device, a cylindrical stem disposed longitudinally within the cylindrical receiving portion, and disinfectant disposed within the cylindrical receiving portion; and inserting the medical device into the cylindrical receiving portion of the cap such that the disinfectant contacts the medical device. Embodiments of the method may include one or more of the following features. In some embodiments, the cylindrical receiving portion comprises internal threads configured to mate with external threads of the medical device, the method further comprising: turning the cap with respect to the medical device such that the internal threads of the cap engage external threads of the medical device. In some embodiments, the cap comprises an annular sponge disposed about the cylindrical stem and contacting the disinfectant, the method further comprising: turning the cap with respect to the medical device such that the internal threads of the cap engage external threads of the medical device and the annular sponge is compressed to release the disinfectant. Some embodiments comprise removing the medical device from the cylindrical receiving portion of the cap; and allowing the disinfectant to dissipate from the medical device. In some embodiments, the medical device comprises one of: a female luer lock; or a needleless valve.
The present disclosure, in accordance with one or more various embodiments, is described in detail with reference to the following figures. The figures are provided for purposes of illustration only and merely depict typical or example embodiments.
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The figures are not exhaustive and do not limit the present disclosure to the precise form disclosed.
It is often desirable to administer fluids to patients intravenously. Intravenous fluid delivery systems often include connectors that allows the patient to leave the fluid delivery system temporarily, for example when the patient would like to visit the bathroom. But while disconnected, the connectors are exposed to the environment, and may become contaminated. To reduce the risk of contamination, the connectors are usually disinfected before reconnection. For example, the connectors may be disinfected using a swab containing a disinfectant fluid.
Embodiments of the disclosed technology provide medical disinfectant caps for disinfecting medical devices, and methods for using the medical disinfectant caps to disinfect medical devices. The disclosed medical disinfectant caps may include internal threads for mating with the external threads of a medical device. The caps may include disinfectant. A medical device may be disinfected by simply threading the cap onto the medical device, thereby allowing the disinfectant to contact and disinfect the medical device. The disinfectant may be 70/30 isopropyl alcohol. In the disclosed embodiments, the kill levels achieved may match or exceed competition kill levels.
In some embodiments, the caps include a sponge soaked with the disinfectant. In these embodiments, threading the cap onto the medical devices compresses the sponge, thereby releasing the disinfectant to contact and disinfect the medical device.
The caps may include a cylindrical stem disposed longitudinally within the cap. The stem may be configured to prevent the disinfectant from entering an interior space of the medical device, while allowing the disinfectant to bathe exterior surfaces of the medical device. These embodiments are especially useful for disinfecting female luer locks, and similar medical devices.
In some embodiments having a stem, one or more longitudinal grooves may be formed in the stem to allow the disinfectant to flow past the stem. These embodiments are especially useful for disinfecting needleless valves, and similar medical devices.
In embodiments having a stem, the sponge soaked with disinfectant may be annular and disposed about the cylindrical stem. In some embodiments, the caps may be sealed with a removable seal to retain the disinfectant until use.
The cap 100 may include a cylindrical stem 108 disposed longitudinally within the cylindrical receiving portion 102. The cylindrical stem 108 may prevent the disinfectant from entering the interior of a medical device such as a female luer lock.
In some embodiments, the cap 100 may include an annular sponge.
In some embodiments, the stem of the cap may include one or more longitudinal grooves.
The cylindrical stem 308 may include one or more longitudinal grooves 310. The grooves 310 may allow the disinfectant to flow past the stem 308 to bathe an interior surface of a medical device such as a needless valve, and similar medical devices.
In some embodiments, the cap 100 may be sealed with a removable seal prior to use.
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The elements of the process 1600 are presented in one arrangement. However, it should be understood that one or more elements of the process may be performed in a different order, in parallel, omitted entirely, and the like. Furthermore, the process 1600 may include other elements in addition to those presented.
Referring to
The process 1600 may include providing a medical disinfectant cap, the cap comprising a cylindrical receiving portion having an opening configured to receive a medical device, a cylindrical stem disposed longitudinally within the cylindrical receiving portion, and disinfectant disposed within the cylindrical receiving portion, at 1604.
With continued reference to
The process 1600 may include removing the medical device from the cylindrical receiving portion of the cap, at 1608, and allowing the disinfectant to dissipate from the medical device, at 1610. For example, the disinfectant may dissipate in approximately one minute. At this point, the medical device is disinfected, and may be connected to the IV system again.
As used herein, the term “or” may be construed in either an inclusive or exclusive sense. Moreover, the description of resources, operations, or structures in the singular shall not be read to exclude the plural. Conditional language, such as, among others, “can,” “could,” “might,” or “may,” unless specifically stated otherwise, or otherwise understood within the context as used, is generally intended to convey that certain embodiments include, while other embodiments do not include, certain features, elements and/or steps.
Terms and phrases used in this document, and variations thereof, unless otherwise expressly stated, should be construed as open ended as opposed to limiting. Adjectives such as “conventional,” “traditional,” “normal,” “standard,” “known,” and terms of similar meaning should not be construed as limiting the item described to a given time period or to an item available as of a given time, but instead should be read to encompass conventional, traditional, normal, or standard technologies that may be available or known now or at any time in the future. The presence of broadening words and phrases such as “one or more,” “at least,” “but not limited to” or other like phrases in some instances shall not be read to mean that the narrower case is intended or required in instances where such broadening phrases may be absent.
A person of ordinary skill in the art will recognize that they may make many changes to the details of the above-described memory device without departing from the underlying principles. Only the following claims, however, define the scope of the memory device.