METHODS AND APPARATUS FOR REDUCING CONTAMINATION IN BLOOD DRAW SAMPLES
20200297261 ยท 2020-09-24
Inventors
Cpc classification
A61B5/150343
HUMAN NECESSITIES
B01L2200/141
PERFORMING OPERATIONS; TRANSPORTING
A61B5/150351
HUMAN NECESSITIES
A61J1/05
HUMAN NECESSITIES
B01L3/502
PERFORMING OPERATIONS; TRANSPORTING
International classification
Abstract
Methods and apparatus are provided for increasing compliance with the discard volume method of blood drawing. The method includes attaching an initial discard container for discarding an initial amount of blood drawn to a standard blood culture bottle. The apparatus, detachable and configurable with a variety of standard blood culture containers, may act as a physical reminder and a convenient handling arrangement for drawing blood according to the preferred discard volume method that reduces sample contamination and false positives. These methods and apparatus may be compatible or retrofit with existing standard blood culture bottles or kits.
Claims
1-20. (canceled)
21. An apparatus for use with a blood culture bottle and for enhancing compliance with the discard volume method for drawing blood from a patient, the apparatus comprising: an initial discard container including: a body with an opening and an inner volume sized to contain an initial amount of blood drawn from the patient, and a cap configured to cover the opening and seal the inner volume; and a connector configured to couple the initial discard container to the blood culture bottle, the connector including a flexible attachment mechanism configured to clip onto the blood culture bottle by a compression fit.
22. The apparatus of claim 21, wherein the inner volume of the initial discard container is between about 5 ml and about 10 ml.
23. The apparatus of claim 21, wherein the connector includes an intermediate portion that separates the flexible attachment mechanism from the initial discard container.
24. The apparatus of claim 21, wherein the connector is integrally connected to the initial discard container.
25. The apparatus of claim 21, wherein the connector includes a second flexible attachment mechanism configured to clip onto the initial discard container.
26. The apparatus of claim 21, wherein the connector includes a second flexible attachment mechanism configured to clip onto a second blood culture bottle by a compression fit.
27. The apparatus of claim 21, wherein the flexible attachment mechanism is configured to releasably attach to one of a neck and a base of the blood culture bottle.
28. The apparatus of claim 21, wherein the connector includes a loop.
29. The apparatus of claim 28, wherein the loop is configured to releasably attach to one of a neck and a base of the blood culture bottle.
30. The apparatus of claim 21, wherein the flexible attachment mechanism is sized to fit around between half of and an entire circumference of the blood culture bottle.
31. A system for reducing blood culture contamination when drawing blood from a patient, the system comprising: an initial discard container sized to contain an initial amount of blood drawn from the patient; a first blood culture bottle larger than the initial discard container and configured to contain subsequent blood drawn from the patient to be tested; a second blood culture bottle larger than the initial discard container and configured to contain subsequent blood drawn from the patient to be tested; and a connector configured to couple the initial discard container to the first blood culture bottle and the second blood culture bottle.
32. The system of claim 31, wherein the connector includes a first flexible attachment mechanism configured to clip onto the first blood culture bottle by a compression fit and a second flexible attachment mechanism configured to clip onto the first blood culture bottle by a compression fit.
33. The system of claim 32, wherein the connector includes a support bar between the first flexible attachment mechanism and the second flexible attachment mechanism.
34. The system of claim 31, wherein each of the first blood culture bottle and the second blood culture bottle includes a neck and a base, wherein the connector is configured to couple the initial discard container to the neck of the first blood culture bottle and the second blood culture bottle.
35. The system of claim 31, wherein the connector is integrally connected to the initial discard container.
36. The system of claim 31, wherein the initial discard container includes an internal volume between about 5 ml and about 10 ml.
37. A method for reducing blood culture contamination when drawing blood from a patient to be tested from a blood culture bottle, the method comprising: providing an initial discard container that is smaller than the blood culture bottle and coupled the blood culture bottle through a connector; drawing an initial amount of blood from the patient to be discarded; disposing the initial amount of blood into the initial discard container; discarding the initial discard container to avoid contamination associated with the initial amount of blood drawn; drawing blood to be tested from the patient; and placing the blood to be tested into the blood culture bottle.
38. The method of claim 37, wherein drawing the initial amount of blood includes drawing between about 5 ml and about 10 ml of blood.
39. The method of claim 37, further comprising, prior to drawing the initial amount of blood, decoupling the initial discard container from the blood culture bottle.
40. The method of claim 37, further comprising drawing additional blood to be tested from the patient, and placing the additional blood to be tested into a second blood culture bottle coupled to the connector.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION
[0026] The discard volume method (DVM) can drastically reduce blood sample contamination caused by an initial needle puncture introducing foreign matter from the skin into the blood stream. In particular, the DVM includes taking a small volume of blood collected after the initial needle puncture of the skin and discarding it. The actual blood sample is then drawn and saved for laboratory testing. By making the DVM easier, more accessible, and less costly, more healthcare professionals will implement it, thereby lowering the rate of false positives caused by contamination and saving millions in unnecessary healthcare costs annually.
[0027] The present disclosure provides methods and apparatus for enhancing the convenience and lowering the cost of compliance with the DVM of drawing blood. As discarding the initial volume of blood is key to the DVM, the present disclosure provides an apparatus comprising a container especially for that purpose, thus making the DVM easier to use. The present disclosure seeks to avoid utilizing complex mechanical switching mechanisms to implement the DVM since these systems are not only expensive, but more susceptible to failure because of multiple complications that could break at any time. Further, the present disclosure includes an initial discard container compatible for inclusion with various existing standard blood culture bottles, in some applications with a modular connection. Thus, the initial discard container of the present disclosure provides an improvement over prior systems and may be retrofit to work well with many existing systems used in healthcare facilities.
[0028] In a typical blood culture procedure, a blood sample is collected from one venipuncture and then inoculated into one or more blood culture bottles. An example culture bottle 10 is shown in
[0029] These standard blood culture bottles 10 are sized for particular trays or stacks within computerized detection instrumentation systems and laboratory equipment designed by the same manufacturer. These highly organized systems streamline laboratory processes and incorporate verification steps for reducing errors in results. The FDA classifies blood culture bottles as in vitro diagnostic devices, and they are defined under regulation 21 C.F.R. 866.2860 as part of a microbial growth monitor system. Other equipment and devices used in the blood drawing procedure of a blood culture test are defined under 21 C.F.R. 862.1675 as class II tubes, vials, and other devices for blood-specimen collection. Market regulations and the use of automated laboratory systems have resulted in standardized dimensions for any commercially available blood culture bottles and containers. Table 1 contains details of the most popular manufacturers' standard blood culture bottles.
TABLE-US-00001 TABLE 1 Manufacturer Bottle Volume Cost Becton, Dickinson, & Co. BACTEC 40 mL $10.77 Becton, Dickinson, & Co. SEPTI-CHEK 70 mL $2.00 bioMerieux BacT/Alert 40 mL $6.16 Thermo Scientific VersaTREK REDOX 80 mL $5.50 Thermo Scientific VersaTREK REDOX EZ Draw 40 mL $5.80
[0030] As shown in
[0031] The neck 16 of the blood culture bottle 10 includes an opening at the top which may be sealed by the lid 18. The lid 18 may fit inside the opening of the neck 16 or around the neck 16, such as in a screw-type fitting, for example. The lid 18 may be color coded to represent the anaerobic or aerobic type or to identify the type of culture media within the bottle 10. In an alternate configuration, such as a bioMerieux BacT/Alert bottle, the base 14 of the blood culture bottle 10 may extend to the lid 18 or have a relatively short neck 16 (that is, the blood culture bottle 10 may not include a taper portion 20, or include a very short taper portion 20).
[0032] Current ways of implementing the DVM include using a blood culture bottle 10, such as that shown in
[0033] In one aspect, the present disclosure provides an apparatus for enhancing compliance with the DVM. As shown in
[0034] According to one study of blood culture contamination rates, discarding an initial volume of about 5 ml was effective in lowering false positives by about 30%, versus initial discard volumes of 1-2 ml. In order to meet this metric and in light of ergonomics, a preferred configuration for the initial discard container 22 may be smaller than the standard blood culture bottle 10 and include an inner volume 24 capable of holding about 6.6 ml. Alternatively, the initial discard container 22 may be any other volume within the inner volume 24 above 5 ml, such as between about 5 ml and about 10 ml. Other volumes below 5 ml may also be contemplated.
[0035] The initial discard container 22 may include a cap 26 (or stopper or lid) for sealing the inner volume 24 to prevent blood from leaking. The cap 26 may act as a seal for a vacuum created within the inner volume 24 of the initial discard container 22. The cap 26 may be made of rubber or other material so that a needle may be pushed through the cap 26 to initiate blood flow from the patients' vein into the inner volume 24. The cap 26 may be coated with sterilizing material or a lubricant such as silicone. The cap 26 may be integrally connected to the initial discard container 22 or otherwise attached to keep the two components together. Furthermore, the initial discard container 22 may include additional caps 26. Alternatively, the initial discard container 22 may not include a cap 26 (such as shown in
[0036] In some aspects, the initial discard container 22 may be formed of an inexpensive plastic or other material. The initial discard container 22 may also be sterilized or evacuated during manufacture. In addition or alternatively, the initial discard container 22 may be sterilized prior to use or may include wipes or other components to conveniently sterilize the device or puncture site prior to blood draw. The initial discard container 22 (and/or a comprehensive kit, as further described below) may sustain a long shelf life within healthcare facilities, which may be helpful in managing stock or purchasing in bulk.
[0037] Advantageously, the initial discard container 22 need not include any special substances, such as those in the inner volume 12 of blood culture bottles 10, since the initial blood volume drawn may simply be discarded along with the initial discard container 22. Alternatively, the inner volume 24 of the initial discard container 22 may be coated with a special compound and/or include other broths in order to prevent growth or keep the initial discard container 22 sterile. In this respect, the initial discard container 22 may be kept rather than discarded in order to test the success rate of the DVM in reducing false positives from the initial blood drawn. Also, the initial discard container 22 may include a special formula or other compound that may provide the phlebotomist with an initial visual cue about the contents of the blood. In this way, the initial discard container 22 may act as a diagnostic device.
[0038] In some aspects, the initial discard container 22 may be included in a kit with, for example, two blood culture bottles 10, sterile needles, and/or other equipment. Additionally, the initial discard container 22 may be attachable to and/or detachable from a component of the kit or another commonly used implement in obtaining a blood culture, such as a culture bottle 10, syringe, tubing, or tray. For example, as further described below, the initial discard container 22 may be attachable to and/or detachable from one or both of the blood culture bottles 10 via a snap-off, a tear-off, a lift-off, or another connection.
[0039] In one configuration, an initial discard container 22 may be removably coupled to a blood culture bottle 10. In one non-limiting example, as shown in
[0040] Referring to the example of
[0041] Additionally, in some configurations, as shown in
[0042] Referring now the examples of
[0043] While the above examples describe and illustrate connectors 28, 36 integral with the initial discard container 22, it is contemplated within other configurations to have such connectors 28, 36 be separate from the initial discard container 22. For example, the initial discard container 22 may be held in, received in, or otherwise attached to the connectors 28, 36.
[0044] Referring to the example of
[0045] Referring to the example of
[0046] Referring to the example of
[0047] Referring to the example of
[0048] The connectors of
[0049] Using the connectors described above, or other suitable connectors, the present disclosure provides a method of enhancing compliance with the DVM, thereby reducing blood culture contaminations and false positives in blood tests. Accordingly, an exemplary method may include attaching an initial discard container 22 to a blood culture bottle 10 so that a phlebotomist may easily handle all the implements necessary for obtaining a blood culture from a patient. Alternatively, the method may include forming the initial discard container 22 extending from and/or connected to the blood culture bottle 10. In yet another non-limiting example, the method may include providing a blood culture kit that includes the initial discard container 22 and a connector configured to connect the initial discard container to the blood culture bottle 10.
[0050]
[0051] According to the above-described apparatus and methods, the initial discard container 22 specifically for containing the initial volume of blood drawn from a patient in the DVM may advantageously be included in connection to or packaged with other tools needed for the DVM. Adding the initial discard container 22 for any blood culture preparation enhances usage of the DVM by increasing convenience, decreasing costs, and serving as a physical and visual reminder to follow the steps of the DVM. By enhancing the usage of the DVM, the present disclosure provides ways in which the rate of false positives and blood culture contamination may be reduced.
[0052] The present disclosure has described terms of one or more preferred configurations, and it should be appreciated that many equivalents, alternatives, variations, and modifications, aside from those expressly stated, are possible and within the scope of the present disclosure.