The present disclosure relates to a connector for a medication dispenser (e.g., an aerosol dispenser), a medication applicator (e.g., an aerosol applicator) including the connector and the medication dispenser, and a breathing system including the medication applicator and a breathing apparatus (e.g., an endotracheal tube, a breathing circuit, or the like).
A quick medication delivery to a patient with accurate dosage during a medical procedure can be lifesaving. For example, anesthesiologist often use an aerosol dispenser to treat intraoperative airway spasms. However, because an entrance of an endotracheal tube (ETT) does not match the aerosol dispenser, these two ends cannot make a firm seal when they are put together, resulting in aerosol leakage and making it difficult to precisely control the dosage delivered to the patient as well as wasting the medication.
Embodiments of the present application relate to a connector for a medication dispenser (e.g., an aerosol dispenser), a medication applicator (e.g., an aerosol applicator) including the connector and the medication dispenser, and a breathing system including the medication applicator and a breathing apparatus (e.g., an endotracheal tube, a breathing circuit, or the like).
In an embodiment, a connector for a medication dispenser includes a first portion coupling the connector to the medication dispenser and a second portion coupling the connector to a breathing apparatus. The first portion has a first opening with a first shape and a first size. The second portion has a second opening with a second shape and a second size that are different from the first shape and the first size of the first opening, respectively.
In an embodiment, a medication applicator includes a medication dispenser and a connector configured to couple the medication dispenser to a breathing apparatus. The connector includes a first portion coupling the connector to the medication dispenser and a second portion coupling the connector to a breathing apparatus. The first portion has a first opening with a first shape and a first size. The second portion has a second opening with a second shape and a second size that are different from the first shape and the first size of the first opening, respectively.
In an embodiment, a breathing system includes a breathing apparatus and a connector configured to couple a medication dispenser to the breathing apparatus. The connector includes a first portion coupling the connector to the medication dispenser and a second portion coupling the connector to the breathing apparatus. The first portion has a first opening with a first shape and a first size. The second portion has a second opening with a second shape and a second size that are different from the first shape and the first size of the first opening, respectively.
Embodiments of the present application relate to a connector for a medication dispenser (e.g., an aerosol dispenser), a medication applicator (e.g., an aerosol applicator) including the connector and the medication dispenser, and a breathing system including the medication applicator and a breathing apparatus (e.g., an endotracheal tube, a breathing circuit, or the like).
In an embodiment, a connector for a medication dispenser includes a first portion coupling the connector to a mouthpiece of an aerosol dispenser and a second portion configured to couple the connector to an adaptor of an ETT. The first portion has a first opening with a substantially rectangular shape matching that of the mouthpiece, and the second portion has a second opening with a circular shape matching that of the adaptor of the ETT. As a result, the connector can make firm seals with the mouthpiece and the adaptor, thereby substantially preventing aerosol leakage, precisely controlling the dosage delivered to a patient, and saving the medication.
In an embodiment, a connector for a medication dispenser includes a first portion coupling the connector to a mouthpiece of an aerosol dispenser and a second portion coupling the connector to a sampling port of a breathing circuit. The first portion has a first opening with a substantially rectangular shape matching that of the mouthpiece, and the second portion has a second opening with a circular shape matching that of an opening of the sampling port. The connector further includes a third portion coupling the connector to the sampling port together with the second portion through Lure lock fitting. As a result, the connector can make firm seals with the mouthpiece and the sampling port, thereby substantially preventing aerosol leakage, precisely controlling the dosage delivered to a patient, and saving the medication. In addition, the connector may be coupled to the sampling port of the breathing circuit without removing the breathing circuit from an ETT, and thus a medical procedure may be performed safely without worrying potential contamination from a patient.
A detailed description of embodiments is provided below along with accompanying figures. The scope of this disclosure is limited only by the claims and encompasses numerous alternatives, modifications and equivalents. Although steps of various processes are presented in a given order, embodiments are not necessarily limited to being performed in the listed order. In some embodiments, certain operations may be performed simultaneously, in an order other than the described order, or not performed at all.
Numerous specific details are set forth in the following description. These details are provided to promote a thorough understanding of the scope of this disclosure by way of specific examples, and embodiments may be practiced according to the claims without some of these specific details. Accordingly, the specific embodiments of this disclosure are illustrative, and are not intended to be exclusive or limiting. For the purpose of clarity, technical material that is known in the technical fields related to this disclosure has not been described in detail so that the disclosure is not unnecessarily obscured.
The mediation applicator (e.g., an aerosol applicator) 110 may include a medication dispenser 120 and a connector 160. In an embodiment, the medication dispenser 120 is an aerosol dispenser and may provide one or more aerosol medications stored therein to the breathing apparatus 180 through the connector 160.
The connector 160 may include a first portion coupling the connector 160 to the medication dispenser 120 and a second portion coupling the connector 160 to the breathing apparatus 180. The first portion and the second portion of the connector 160 may form firm seals with the medication dispenser 120 and the breathing apparatus 180, respectively, thereby substantially preventing aerosol leakage, precisely controlling the dosage delivered to a patient, and saving the medication.
The breathing apparatus 180 may couple the connector 160 to the patient. In an embodiment, the breathing apparatus 10 is an ETT, a breathing circuit, or the like.
Referring to
The casing 224 may be fixedly coupled to the container 224 by wrapping a portion of the container 222. The casing 224 may include a mouthpiece (e.g., a mouthpiece 326 in
The connector 260 may couple the mouthpiece of the casing 224 to a portion (e.g., the adaptor 282) of the ETT 280 to form respective seals at both ends of the connector 260. In an embodiment, the connector 260 includes a first portion 262 and a second portion 264, such that the first portion 262 may be coupled to the mouthpiece to form a first seal, and the second portion 264 may be coupled to the adaptor 282 to form a second seal.
The ETT 280 may include the adaptor 282, a tubing 284, a balloon 288, and a cuff 286. For example, the adaptor 282 may couple the ETT 280 to a portion of a breathing circuit (e.g., a breathing circuit 480 in
Referring to
The first portion 362 of the connector 360 may have a first opening OP1 corresponding to an outer perimeter of the mouthpiece 326. In an embodiment, the first opening OP1 of the first portion 362 may have a substantially rectangular shape corresponding to that of an outer surface of the mouthpiece 326, similarly to that of a first opening OP1′ of a connector 660 shown in
The first portion 362 of the connector 360 may have a first length L1 along a first direction (e.g., an axial direction) that is perpendicular to the first opening OP1. In an embodiment, the first length L1 of the first portion 362 of the connector 360 may be in a range from 15 mm to 21 mm.
In an embodiment, the second portion 364 of the connector 360 may have a second opening OP2 corresponding to an outer perimeter of the adaptor 382. For example, the second opening OP2 of the second portion 364 may have a circular shape corresponding to that of an outer surface of a first portion 392 of the adaptor 382.
The second portion 364 of the connector 360 may have a second length L2 along a first direction (e.g., an axial direction) that is perpendicular to the second opening OP2. In an embodiment, the second length L2 of the second portion 364 may be in a range from 15 mm to 21 mm.
The first length L1 and the second length L2 may be sufficiently long (e.g., each being equal to or longer than 15 mm) to ensure securing the inserted mouthpiece 362 and the inserted portion 392 of the adaptor 382, respectively. When a flow of the aerosol medication flows in the first direction (e.g., the axial direction), the flow expands in a second direction (e.g., a radial direction) perpendicular to the first direction. As a result, when the sum of the first length L1 and the second length L2 is excessively long, an outer portion of the medication flow may be significantly interrupted by one or more of an inner surface of the inserted mouthpiece 326, inner surfaces of the first portion 362 and the second portion 364 of the connector 360, and an inner surface of the inserted portion 392 of the adaptor 382. Accordingly, the sum of the first length L1 and the second length L2 may be sufficiently short (e.g., equal to or shorter than 42 mm) to effectively transport the aerosol medication through the connector 360.
The first portion 392 of the adaptor 382 functioning as an entrance of an ETT (e.g., the ETT 280 in
The connector 360 according to an embodiment of the present disclosure may have the first opening OP1 and the second opening OP2 that differ in shape. For example, the connector 360 may have the first opening OP1 matching the substantially rectangular cross-section of the mouthpiece 326 and the second opening OP2 matching the circular cross-section of the first portion 392 of the adaptor 382. As a result, the connector 360 can make firm seals with the mouthpiece 326 and the adaptor 382, thereby substantially preventing aerosol leakage, precisely controlling the dosage delivered to the patient, and saving the medication. The first opening OP1 and the second opening OP2 also may differ in size. For example, a first area of the first opening OP1 may be in a range from 250 mm2 to 425 mm2, and a second area of the second opening OP2 may be in a range from 160 mm2 to 240 mm2. For example, a ratio of the first area of the first opening OP1 over the second area of the second opening OP1 may be in a range from 1.1 to 2.7.
The breathing circuit 480 includes a first adaptor 430, a sampling port 432, a hose 486, and a second adaptor 436. The first adaptor 430 may be coupled to an adaptor 482 of an ETT. Although not shown in
The connector 460 may couple a mouthpiece of a casing 424 of the medication dispenser 420 to a sampling port 432 of the breathing circuit 480. In an embodiment, the connector 460 may be coupled to the sampling port 460 through Lure lock fitting. Although the breathing circuit 480 shown in the embodiment of
The connector 660 may include a first portion 662, a second portion 668, and a third portion 666. An aerosol dispenser (e.g., the aerosol dispenser 420 in
The first portion 662 of the connector 660 may have a first opening OP1′ corresponding to an outer perimeter of the mouthpiece. In an embodiment, the first opening OP1′ of the first portion 662 may have a substantially rectangular shape corresponding to that of an outer surface of the mouthpiece. For example, with respect to the orientation shown in
The first portion 662 of the connector 660 may have a first length L1 along a first direction (e.g., an axial direction) that is perpendicular to the first opening OP1′. In an embodiment, the first length L1 of the first portion 662 of the connector 660 may be in a range from 15 mm to 21 mm.
The second portion 668 and the third portion 666 of the connector 660 may be coupled to the sampling port. In an embodiment, the second portion 668 and the third portion 666 of the connector 660 may be coupled to the sampling port through Lure lock fitting. For example, an outer surface of the second portion 668 of the connector 660 may be inserted into an opening of the sampling port, and an inner surface of the third portion 666 of the connector 660 may be threadedly coupled to an outer surface of the sampling port, thereby forming a firm seal to substantially prevent aerosol leakage. Referring back to
The third portion 666 of the connector 660 may have a second length L2 along a first direction (e.g., an axial direction) that is perpendicular to the second opening OP2′. In an embodiment, the second length L2 of the third portion 666 may be in a range from 4 mm to 12 mm.
The second portion 668 of the connector 660 may protrude from the third portion 666 in the axial direction by a third length L3. In an embodiment, the third length L3 may be in a range from 1.5 mm to 3.5 mm.
The connector 660 according to an embodiment of the present disclosure may have the first opening OP1′ and the second opening OP2′ that differ in shape. For example, the connector 660 may have the first opening OP1′ matching the substantially rectangular cross-section of the mouthpiece of the aerosol dispenser and the second opening OP2′ matching a portion of the circular cross-section of the opening of the sampling port. Thus, the connector 660 can make firm seals with the mouthpiece and the sampling port, thereby substantially preventing aerosol leakage, precisely controlling the dosage delivered to the patient, and saving the medication. The first opening OP1 and the second opening OP2 also may differ in size. For example, a first area of the first opening OP1′ may be in a range from 250 mm2 to 425 mm2, and a second area of the second opening OP2′ may be in a range from 2 mm2 to 5 mm2. For example, a ratio of the first area of the first opening OP1′ over the second area of the second opening OP1′ may be in a range from 50 to 200.
Aspects of the present disclosure have been described in conjunction with the specific embodiments thereof that are proposed as examples. Numerous alternatives, modifications, and variations to the embodiments as set forth herein may be made without departing from the scope of the claims set forth below. Accordingly, embodiments as set forth herein are intended to be illustrative and not limiting.
The present disclosure claims priority to U.S. provisional Application No. 63/036,334 filed on Jun. 8, 2020, which is incorporated by reference herein for all purposes.
Number | Date | Country | |
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63036334 | Jun 2020 | US |