CA2428510C - Blood withdrawal system - Google Patents
Blood withdrawal system Download PDFInfo
- Publication number
- CA2428510C CA2428510C CA002428510A CA2428510A CA2428510C CA 2428510 C CA2428510 C CA 2428510C CA 002428510 A CA002428510 A CA 002428510A CA 2428510 A CA2428510 A CA 2428510A CA 2428510 C CA2428510 C CA 2428510C
- Authority
- CA
- Canada
- Prior art keywords
- lancet
- lancet holder
- housing
- lancing device
- support surface
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000008280 blood Substances 0.000 title abstract description 55
- 210000004369 blood Anatomy 0.000 title abstract description 55
- 230000033001 locomotion Effects 0.000 claims abstract description 68
- 238000000034 method Methods 0.000 claims abstract description 55
- 230000008569 process Effects 0.000 claims abstract description 43
- 230000001012 protector Effects 0.000 claims description 10
- 230000003993 interaction Effects 0.000 claims description 2
- 230000007246 mechanism Effects 0.000 abstract description 23
- 238000010276 construction Methods 0.000 abstract description 10
- 230000006378 damage Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000003825 pressing Methods 0.000 description 4
- 230000001960 triggered effect Effects 0.000 description 4
- 208000027418 Wounds and injury Diseases 0.000 description 3
- 238000013461 design Methods 0.000 description 3
- 208000014674 injury Diseases 0.000 description 3
- 102000004877 Insulin Human genes 0.000 description 2
- 108090001061 Insulin Proteins 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000036512 infertility Effects 0.000 description 2
- 229940125396 insulin Drugs 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
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- 208000012260 Accidental injury Diseases 0.000 description 1
- 238000002266 amputation Methods 0.000 description 1
- 238000000418 atomic force spectrum Methods 0.000 description 1
- 238000009534 blood test Methods 0.000 description 1
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- 230000037406 food intake Effects 0.000 description 1
- 235000012631 food intake Nutrition 0.000 description 1
- 230000036541 health Effects 0.000 description 1
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- 230000037081 physical activity Effects 0.000 description 1
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Classifications
-
- H—ELECTRICITY
- H04—ELECTRIC COMMUNICATION TECHNIQUE
- H04M—TELEPHONIC COMMUNICATION
- H04M1/00—Substation equipment, e.g. for use by subscribers
- H04M1/02—Constructional features of telephone sets
- H04M1/23—Construction or mounting of dials or of equivalent devices; Means for facilitating the use thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/151—Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
- A61B5/15142—Devices intended for single use, i.e. disposable
- A61B5/15144—Devices intended for single use, i.e. disposable comprising driving means, e.g. a spring, for retracting the piercing unit into the housing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/150007—Details
- A61B5/150015—Source of blood
- A61B5/150022—Source of blood for capillary blood or interstitial fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/150007—Details
- A61B5/150175—Adjustment of penetration depth
- A61B5/150183—Depth adjustment mechanism using end caps mounted at the distal end of the sampling device, i.e. the end-caps are adjustably positioned relative to the piercing device housing for example by rotating or screwing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/150007—Details
- A61B5/150374—Details of piercing elements or protective means for preventing accidental injuries by such piercing elements
- A61B5/150381—Design of piercing elements
- A61B5/150412—Pointed piercing elements, e.g. needles, lancets for piercing the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/150007—Details
- A61B5/150374—Details of piercing elements or protective means for preventing accidental injuries by such piercing elements
- A61B5/150381—Design of piercing elements
- A61B5/150503—Single-ended needles
- A61B5/150519—Details of construction of hub, i.e. element used to attach the single-ended needle to a piercing device or sampling device
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/150007—Details
- A61B5/150374—Details of piercing elements or protective means for preventing accidental injuries by such piercing elements
- A61B5/150534—Design of protective means for piercing elements for preventing accidental needle sticks, e.g. shields, caps, protectors, axially extensible sleeves, pivotable protective sleeves
- A61B5/150541—Breakable protectors, e.g. caps, shields or sleeves, i.e. protectors separated destructively, e.g. by breaking a connecting area
- A61B5/150549—Protectors removed by rotational movement, e.g. torsion or screwing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/150007—Details
- A61B5/150374—Details of piercing elements or protective means for preventing accidental injuries by such piercing elements
- A61B5/150534—Design of protective means for piercing elements for preventing accidental needle sticks, e.g. shields, caps, protectors, axially extensible sleeves, pivotable protective sleeves
- A61B5/150694—Procedure for removing protection means at the time of piercing
- A61B5/150717—Procedure for removing protection means at the time of piercing manually removed
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/150007—Details
- A61B5/150885—Preventing re-use
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/151—Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
- A61B5/15101—Details
- A61B5/15103—Piercing procedure
- A61B5/15107—Piercing being assisted by a triggering mechanism
- A61B5/15111—Semi-automatically triggered, e.g. at the end of the cocking procedure, for instance by biasing the main drive spring or when reaching sufficient contact pressure, the piercing device is automatically triggered without any deliberate action by the user
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/151—Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
- A61B5/15101—Details
- A61B5/15115—Driving means for propelling the piercing element to pierce the skin, e.g. comprising mechanisms based on shape memory alloys, magnetism, solenoids, piezoelectric effect, biased elements, resilient elements, vacuum or compressed fluids
- A61B5/15117—Driving means for propelling the piercing element to pierce the skin, e.g. comprising mechanisms based on shape memory alloys, magnetism, solenoids, piezoelectric effect, biased elements, resilient elements, vacuum or compressed fluids comprising biased elements, resilient elements or a spring, e.g. a helical spring, leaf spring, or elastic strap
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/151—Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
- A61B5/15101—Details
- A61B5/15126—Means for controlling the lancing movement, e.g. 2D- or 3D-shaped elements, tooth-shaped elements or sliding guides
- A61B5/1513—Means for controlling the lancing movement, e.g. 2D- or 3D-shaped elements, tooth-shaped elements or sliding guides comprising linear sliding guides
Abstract
The invention discloses a blood withdrawal system for withdrawing blood for diagnostic purposes. The lancing device comprises a drive mechanism which ensures a pain-reduced lancing process for the patient. The drive mechanism is characterized by a robust and simple construction. By means of a trigger mechanism, the lancet is driven by converting a linear movement of a trigger unit into a rotary movement which initiates the lancing process. This allows a simple handling for the patient.
Description
Blood withdrawal system The invention concerns a blood withdrawal system for withdrawing blood for diagnostic purposes.
Lancets are used in the sense of the invention as blood withdrawal systems which are used to puncture an appropriate part of the body in order to remove a small amount of blood from a part of the body for analytical or diagnostic purposes. The blood is frequently drawn from a finger or earlobe. In medical practices lancets are used for this which are inserted into an appropriate part of the body by a doctor or laboratory staff either manually or with the aid of a simple apparatus. The lancet must of course be sharp and sterile. Otherwise there are no especially stringent requirements for medical practices since blood is collected from individual patients at large time intervals and the puncture is carried out by specially trained staff.
Nevertheless the puncture is frequently associated with considerable pain.
If the blood withdrawal system should be suitable for operation by the patients themselves, this makes much higher demands on the system especially with regard to pain-free and reliable blood withdrawal. The independent use of blood withdrawal systems by patients is carried out especially for so-called home monitoring.
In this case the aim is to enable groups of patients that are at special risk to regularly monitor certain analytical values of their blood. This applies among others to diabetics who frequently and regularly check their blood sugar level and adapt it to the requirements by injecting insulin. The insulin requirement depends among other factors on the food intake and physical activity and must be kept as continuously as possible within certain set limits. This is of uttermost importance for the health of the patients and to avoid serious secondary damage such as loss of sight and amputation of parts of the body.
Blood withdrawal systems have been used for a long time which consist of a lancing device and associated lancets that are specially adapted for the respective instrument.
A housing of the lancing device contains a lancet drive which mechanically punctures the skin with a lancet. A spring is usually used as a drive element for the lancing movement. In the initial phase of development very simple constructions were commonly used in which the lancet was directly attached to one end of a pressure spring arranged in an elongate housing. Such a blood withdrawal device is disclosed for example in the document US 4,469,110. However, the use of the described systems show that in particular the requirement for a less painful blood withdrawal cannot be fulfilled. Recently small, simple-to-operate and relatively low-cost analytical systems have been developed to reduce the pain of puncture which are usually composed of blood test strips and an accompanying evaluation instrument.
Such modern blood withdrawal systems are intended to ensure that blood withdrawal is as painless as possible for the patient and is simple to handle. Therefore in the recent prior art numerous different blood withdrawal systems are known which are suitable for generating the incisions required for blood collection in a simple and relatively painless manner. Such blood withdrawal systems usually comprise a housing with an exit opening for the tip of a lancet and a lancet holder for holding the lancet which can be moved relative to the housing along a predetermined straight puncturing path. The lancet holder is moved during the puncturing and return movement by a lancet drive which has an elastic drive element which is usually a metal spring. In a first position in which the elastic drive element is in a tensioned state, the lancet holder is usually locked by means of a locking device. After such a locking device is released, the elastic drive element relaxes so that the movement of the drive element is converted into a puncturing movement of the lancet drive which moves the lancet held by the lancet holder at high speed along the predetermined lancing path in a puncturing direction until the tip of the lancet emerges from the exit opening of the blood withdrawal system. A wound is generated in a part of the body pressed against the exit opening. Immediately afterwards the lancet is usually retracted by the lancet drive into the housing. The drive units of the modern lancing devices which reduce pain due to a high lancing speed and the retraction of the lancet after the lancing consequently ensure that in the case of the modern lancing devices the blood withdrawal is considerably more pleasant for the patient.
Such blood withdrawal systems of the prior art are described for example in the documents US 4,442,836, US 4,535,769 and US 4,924,897. In the design described in the patent US 4,924,879 a spiral drive spring acts on a wheel whose rotation is converted by means of a lever connected to the wheel into a lancing and retraction movement. It is claimed that the pain is reduced by among others the fact that this movement proceeds very rapidly. However, the construction using precisely manufactured metal parts is complicated and relatively voluminous. Another disadvantage is that the lancet emerges from the exit opening when the lancet drive is tensioned resulting in a risk of injury for the user.
The patent EP 0 582 226 describes another lancing device which is suitable for withdrawing blood samples. A piston driven by a spring means is movably mounted within the lancing device. A lancet which emerges through an opening provided in the housing during a lancing process is located at one end of the piston. The outer periphery of the piston has wings of only limited strength which bear against the housing wall of the lancing device. When the lancing process is carried out the piston is moved in the puncturing direction by means of the spring elements thereby destroying the wings of the plunger so that they no longer rest against the housing.
A disadvantage of this prior art is that the spring elements for driving the piston have to apply sufficient force to firstly destroy the wings of the piston before the piston can be moved in the lancing direction. Furthermore if the wings are not completely destroyed, this can cause frictional effects when the piston moves within the housing in the lancing direction. Hence the conditions of a lancing process are changed depending on the frictional effects so that undefined force curves act during the lancing process. This influences among others the puncturing speed of the lancet into a part of the skin so that the patient has to expect different levels of pain caused by the puncturing.
In addition the lancet has a sterile protector which has to be removed from the needle tip before use. However, the wings may be damaged as a result of a strong pulling motion and this may accidentally trigger a lancing process. Since the described mechanism is only suitable for disposable lancing devices and it is not possible to retension the lancet due to the destroyed wings on the piston, the unused lancet has to be consequently discarded.
Lancets are used in the sense of the invention as blood withdrawal systems which are used to puncture an appropriate part of the body in order to remove a small amount of blood from a part of the body for analytical or diagnostic purposes. The blood is frequently drawn from a finger or earlobe. In medical practices lancets are used for this which are inserted into an appropriate part of the body by a doctor or laboratory staff either manually or with the aid of a simple apparatus. The lancet must of course be sharp and sterile. Otherwise there are no especially stringent requirements for medical practices since blood is collected from individual patients at large time intervals and the puncture is carried out by specially trained staff.
Nevertheless the puncture is frequently associated with considerable pain.
If the blood withdrawal system should be suitable for operation by the patients themselves, this makes much higher demands on the system especially with regard to pain-free and reliable blood withdrawal. The independent use of blood withdrawal systems by patients is carried out especially for so-called home monitoring.
In this case the aim is to enable groups of patients that are at special risk to regularly monitor certain analytical values of their blood. This applies among others to diabetics who frequently and regularly check their blood sugar level and adapt it to the requirements by injecting insulin. The insulin requirement depends among other factors on the food intake and physical activity and must be kept as continuously as possible within certain set limits. This is of uttermost importance for the health of the patients and to avoid serious secondary damage such as loss of sight and amputation of parts of the body.
Blood withdrawal systems have been used for a long time which consist of a lancing device and associated lancets that are specially adapted for the respective instrument.
A housing of the lancing device contains a lancet drive which mechanically punctures the skin with a lancet. A spring is usually used as a drive element for the lancing movement. In the initial phase of development very simple constructions were commonly used in which the lancet was directly attached to one end of a pressure spring arranged in an elongate housing. Such a blood withdrawal device is disclosed for example in the document US 4,469,110. However, the use of the described systems show that in particular the requirement for a less painful blood withdrawal cannot be fulfilled. Recently small, simple-to-operate and relatively low-cost analytical systems have been developed to reduce the pain of puncture which are usually composed of blood test strips and an accompanying evaluation instrument.
Such modern blood withdrawal systems are intended to ensure that blood withdrawal is as painless as possible for the patient and is simple to handle. Therefore in the recent prior art numerous different blood withdrawal systems are known which are suitable for generating the incisions required for blood collection in a simple and relatively painless manner. Such blood withdrawal systems usually comprise a housing with an exit opening for the tip of a lancet and a lancet holder for holding the lancet which can be moved relative to the housing along a predetermined straight puncturing path. The lancet holder is moved during the puncturing and return movement by a lancet drive which has an elastic drive element which is usually a metal spring. In a first position in which the elastic drive element is in a tensioned state, the lancet holder is usually locked by means of a locking device. After such a locking device is released, the elastic drive element relaxes so that the movement of the drive element is converted into a puncturing movement of the lancet drive which moves the lancet held by the lancet holder at high speed along the predetermined lancing path in a puncturing direction until the tip of the lancet emerges from the exit opening of the blood withdrawal system. A wound is generated in a part of the body pressed against the exit opening. Immediately afterwards the lancet is usually retracted by the lancet drive into the housing. The drive units of the modern lancing devices which reduce pain due to a high lancing speed and the retraction of the lancet after the lancing consequently ensure that in the case of the modern lancing devices the blood withdrawal is considerably more pleasant for the patient.
Such blood withdrawal systems of the prior art are described for example in the documents US 4,442,836, US 4,535,769 and US 4,924,897. In the design described in the patent US 4,924,879 a spiral drive spring acts on a wheel whose rotation is converted by means of a lever connected to the wheel into a lancing and retraction movement. It is claimed that the pain is reduced by among others the fact that this movement proceeds very rapidly. However, the construction using precisely manufactured metal parts is complicated and relatively voluminous. Another disadvantage is that the lancet emerges from the exit opening when the lancet drive is tensioned resulting in a risk of injury for the user.
The patent EP 0 582 226 describes another lancing device which is suitable for withdrawing blood samples. A piston driven by a spring means is movably mounted within the lancing device. A lancet which emerges through an opening provided in the housing during a lancing process is located at one end of the piston. The outer periphery of the piston has wings of only limited strength which bear against the housing wall of the lancing device. When the lancing process is carried out the piston is moved in the puncturing direction by means of the spring elements thereby destroying the wings of the plunger so that they no longer rest against the housing.
A disadvantage of this prior art is that the spring elements for driving the piston have to apply sufficient force to firstly destroy the wings of the piston before the piston can be moved in the lancing direction. Furthermore if the wings are not completely destroyed, this can cause frictional effects when the piston moves within the housing in the lancing direction. Hence the conditions of a lancing process are changed depending on the frictional effects so that undefined force curves act during the lancing process. This influences among others the puncturing speed of the lancet into a part of the skin so that the patient has to expect different levels of pain caused by the puncturing.
In addition the lancet has a sterile protector which has to be removed from the needle tip before use. However, the wings may be damaged as a result of a strong pulling motion and this may accidentally trigger a lancing process. Since the described mechanism is only suitable for disposable lancing devices and it is not possible to retension the lancet due to the destroyed wings on the piston, the unused lancet has to be consequently discarded.
Furthermore U.S. Pat. No. 4,416,279 discloses a blood withdrawal system in which the lancet holder is moved along an inclined ramp located in the housing in an opposite direction to the lancing direction by rotating an external part of the housing. This movement tensions a spring member which serves as the drive element for the lancet holder. The sloping surface protruding into the housing has a plateau on which the lancet holder can be temporarily held after a first rotary movement of the external housing member. In this position the lancet holder is pulled back in the opposite direction to lancing to such an extent that the lancet can be removed from the lancet holder and exchanged. By continuing the rotation the lancet holder is moved further along the sloping surface in the opposite direction to lancing, further tensioning the spring element until the lancet holder is moved beyond the sloping surface and is driven by the force of the spring in the puncturing direction. The lancet tip emerges from the housing.
A disadvantage of the prior art is that the rotational movement of the outer housing member makes it more difficult for the user to handle the blood withdrawal system. In order to tension the blood withdrawal system and simultaneously position the finger pad at the exit opening of the blood withdrawal system, the patient has to position his finger in a holder provided. The holder also serves to fix the position of the blood withdrawal system on the finger tip while the user rotates the outer housing member with the other hand. The said blood withdrawal system proves to be extremely unwieldy and is very difficult to operate particularly by elderly persons.
SUMMARY OF THE INVENTION
The object of the present invention provides a blood withdrawal system and a method for blood withdrawal in which the described disadvantages of the prior art are avoided. The system and the method are simple. The pain caused by the puncture is reduced by a rapid drive movement of the lancet holder. The construction of the blood withdrawal system is robust and cost-effective.
In accordance with one aspect of the present invention there is provided a lancing device comprising - a housing defining an opening in which a lancet holder containing a lancet is movably mounted, - wherein the lancet holder is connected to a spring member and the lancet holder comprises at least one bearing member, and - at least one support surface is - 4a -arranged in the housing in such a manner that the bearing member rests on the support surface in a first position of the lancet holder, and - a trigger unit which transfers the lancet holder into a second position wherein a release button of the trigger unit carries out a linear movement and the linear movement is converted into a rotary movement of the bearing member and the support surface relative to one another such that the bearing member in the second position of the lancet holder falls from the support surface which at least partially relaxes a spring element that was tensioned before the falling movement and the lancet holder moves relative to the housing such that the tip of the lancet emerges from the opening of the housing, wherein the rotary movement is carried out by the lancet holder.
In accordance with another aspect of the present invention there is provided a method for triggering a lancing process with a lancing device comprising - supporting a lancet holder on a support surface in the inside of a housing of a lancing device, -actuating a trigger unit of the lancing device such that at least a part of the trigger unit carries out a linear movement, - converting the linear movement of the trigger unit into a rotation of the lancet holder and the support surface relative to one another until the lancet holder falls from the support surface and the lancet holder carries out a falling movement during which, - a tip of a lancet of the lancet holder emerges through an opening of the housing to carry out a lancing process.
The invention encompasses a blood withdrawal system having a housing in which an opening is located, and a lancet holder containing a lancet is movably mounted in the housing. The lancet holder has at least one bearing member. A support surface is also located in the housing which is positioned such that the bearing member rests on the support surface in a first position of the lancet holder. The blood withdrawal system also comprises a triggering unit with a release button. The triggering unit converts a linear movement of the release button into a rotation of the bearing member and the support surface relative to one another by which means the lancet holder is transferred into a second position and falls from the support surface. A
spring element of the blood withdrawal system is connected to the lancet holder and is transformed by the falling movement of the bearing member from a pretensioned state into an at least partially relaxed state. As a result of the movement of the lancet holder relative to the housing, the tip of the lancet emerges from the opening of the housing so that it can puncture a part of the body that is positioned there.
The blood withdrawal system according to the invention is characterized by a simple robust construction. There are no special requirements with regard to form or material for the bearing member or the support surface. Within the scope of the invention a wide variety of designs are possible which enable the lancet holder to be supported by the support surface. This enables the lancing device to be manufactured with large tolerances without effecting the function of the blood withdrawal device.
This simplifies the manufacturing process and hence reduces the production costs for the lancing device. This is a decisive advantage especially for disposable lancing devices that are manufactured in large numbers.
As a result of the described mechanism the puncturing movement of the lancet holder or the lancet is carried out so rapidly that the puncture pain is minimized. As soon as the lancet holder falls from the support surface in the lancing direction, the lancing process is initiated. The potential energy stored in the system is at a maximum. In contrast to the prior art in which the lancing process is for example triggered by breaking off small hooks, the active force of moment of the system is constant in each lancing process since for example additional frictional effects caused by irregular detachment of the small hooks do not occur. This ensures a lancing process under constant, reproducible conditions.
The conversion of a linear movement of the release button into a rotary movement makes the operation of the blood withdrawal system particularly user-friendly since the patient can for example actuate the lancing device by pressing the release button and thus does not have to carry out complicated handling steps.
In principle a wide variety of embodiments of the triggering unit are conceivable for triggering a lancing process which convert a linear movement of the release button into a relative rotation of the bearing member and the support surface. For example a linear movement of the release button can be converted into a rotation of the lancet holder, or embodiments are encompassed in which the support surfaces rotate relative to a part of the housing or relative to the lancet holder. In such a construction actuation of the release button causes a rotary movement of the support surface whereby for example a part of the housing to which the support surface is attached can also be rotated.
In a preferred embodiment the linear movement of the release button occurs perpendicularly to the plane of rotation so that for example the blood withdrawal system is operated by pressing the release button along the puncturing direction.
In an advantageous embodiment it has also proven to be expedient for the lancet holder to comprise two bearing members which each rest on a support surface of the housing. This ensures that the lancet holder is supported symmetrically by a simple housing construction. Of course an embodiment is also conceivable which contains more than two bearing members and several support surfaces. In principle the number of bearing members and of the corresponding support surfaces is unlimited so that usually a construction is selected in which the lancet holder is supported optimally and can be manufactured at low costs.
In order to convert the linear movement into a rotary movement of the bearing member and the support surface relative to one another, several designs of the triggering unit are also conceivable. In a preferred embodiment of the triggering unit it contains a rotary drive element which is pressed by the linear movement of the release button against the bearing member such that the bearing member falls from the support surface. The rotary drive element for example has an elastic ram and the support surface can contain a depression in which the bearing member of the lancet holder is supported. A linear movement of the release button presses the elastic ram from above against the bearing member of the lancet holder and deforms it in this process. If the bearing member is in a depression of the support surface, the ram can also reach underneath the bearing member due to the deformation and lever it out of the depression in the support surface. As a result the lancet holder falls from the support surface and a lancing process is triggered. However, a ramp extending into the inside of the housing is also conceivable as a rotary drive element. In this case the ramp is pressed against the bearing member by the linear movement of the release button which pushes it from the support surface and the lancet holder makes a falling movement.
Due to the falling movement of the bearing member and thus of the lancet holder, the spring element is relaxed, In the sense of this invention this is also understood as a process in which the spring element only passes through a relaxed state and is subsequently again converted into a tensioned state.
For example the falling movement of the lancet holder can be stopped by a stop provided for this purpose so that only a defined part of the lancet extends from the housing. The limit stop which consequently determines the puncture depth of the blood withdrawal system can in this connection advantageously be a component of a cap provided for this purpose which is mounted movably on the housing of the system or is a component of the housing itself. It is possible for the cap to be attached movably on the housing in or against the lancing direction such that in the case of a limit stop on the housing the distance between the stop and the exit opening of the cap is varied. If the stop is a component of the cap the position of the stop and thus the puncture depth can be changed by moving the cap in the direction of or opposite to the direction of lancing, or it can be changed by a rotation of the cap in which the axial position of the cap remains constant. In such an embodiment the cap contains several stops at different levels which come into use depending on the rotary movement of the cap and which define the puncture depth. Such a system for regulating the puncture depth is described for example in the document EP 1 534.
A disadvantage of the prior art is that the rotational movement of the outer housing member makes it more difficult for the user to handle the blood withdrawal system. In order to tension the blood withdrawal system and simultaneously position the finger pad at the exit opening of the blood withdrawal system, the patient has to position his finger in a holder provided. The holder also serves to fix the position of the blood withdrawal system on the finger tip while the user rotates the outer housing member with the other hand. The said blood withdrawal system proves to be extremely unwieldy and is very difficult to operate particularly by elderly persons.
SUMMARY OF THE INVENTION
The object of the present invention provides a blood withdrawal system and a method for blood withdrawal in which the described disadvantages of the prior art are avoided. The system and the method are simple. The pain caused by the puncture is reduced by a rapid drive movement of the lancet holder. The construction of the blood withdrawal system is robust and cost-effective.
In accordance with one aspect of the present invention there is provided a lancing device comprising - a housing defining an opening in which a lancet holder containing a lancet is movably mounted, - wherein the lancet holder is connected to a spring member and the lancet holder comprises at least one bearing member, and - at least one support surface is - 4a -arranged in the housing in such a manner that the bearing member rests on the support surface in a first position of the lancet holder, and - a trigger unit which transfers the lancet holder into a second position wherein a release button of the trigger unit carries out a linear movement and the linear movement is converted into a rotary movement of the bearing member and the support surface relative to one another such that the bearing member in the second position of the lancet holder falls from the support surface which at least partially relaxes a spring element that was tensioned before the falling movement and the lancet holder moves relative to the housing such that the tip of the lancet emerges from the opening of the housing, wherein the rotary movement is carried out by the lancet holder.
In accordance with another aspect of the present invention there is provided a method for triggering a lancing process with a lancing device comprising - supporting a lancet holder on a support surface in the inside of a housing of a lancing device, -actuating a trigger unit of the lancing device such that at least a part of the trigger unit carries out a linear movement, - converting the linear movement of the trigger unit into a rotation of the lancet holder and the support surface relative to one another until the lancet holder falls from the support surface and the lancet holder carries out a falling movement during which, - a tip of a lancet of the lancet holder emerges through an opening of the housing to carry out a lancing process.
The invention encompasses a blood withdrawal system having a housing in which an opening is located, and a lancet holder containing a lancet is movably mounted in the housing. The lancet holder has at least one bearing member. A support surface is also located in the housing which is positioned such that the bearing member rests on the support surface in a first position of the lancet holder. The blood withdrawal system also comprises a triggering unit with a release button. The triggering unit converts a linear movement of the release button into a rotation of the bearing member and the support surface relative to one another by which means the lancet holder is transferred into a second position and falls from the support surface. A
spring element of the blood withdrawal system is connected to the lancet holder and is transformed by the falling movement of the bearing member from a pretensioned state into an at least partially relaxed state. As a result of the movement of the lancet holder relative to the housing, the tip of the lancet emerges from the opening of the housing so that it can puncture a part of the body that is positioned there.
The blood withdrawal system according to the invention is characterized by a simple robust construction. There are no special requirements with regard to form or material for the bearing member or the support surface. Within the scope of the invention a wide variety of designs are possible which enable the lancet holder to be supported by the support surface. This enables the lancing device to be manufactured with large tolerances without effecting the function of the blood withdrawal device.
This simplifies the manufacturing process and hence reduces the production costs for the lancing device. This is a decisive advantage especially for disposable lancing devices that are manufactured in large numbers.
As a result of the described mechanism the puncturing movement of the lancet holder or the lancet is carried out so rapidly that the puncture pain is minimized. As soon as the lancet holder falls from the support surface in the lancing direction, the lancing process is initiated. The potential energy stored in the system is at a maximum. In contrast to the prior art in which the lancing process is for example triggered by breaking off small hooks, the active force of moment of the system is constant in each lancing process since for example additional frictional effects caused by irregular detachment of the small hooks do not occur. This ensures a lancing process under constant, reproducible conditions.
The conversion of a linear movement of the release button into a rotary movement makes the operation of the blood withdrawal system particularly user-friendly since the patient can for example actuate the lancing device by pressing the release button and thus does not have to carry out complicated handling steps.
In principle a wide variety of embodiments of the triggering unit are conceivable for triggering a lancing process which convert a linear movement of the release button into a relative rotation of the bearing member and the support surface. For example a linear movement of the release button can be converted into a rotation of the lancet holder, or embodiments are encompassed in which the support surfaces rotate relative to a part of the housing or relative to the lancet holder. In such a construction actuation of the release button causes a rotary movement of the support surface whereby for example a part of the housing to which the support surface is attached can also be rotated.
In a preferred embodiment the linear movement of the release button occurs perpendicularly to the plane of rotation so that for example the blood withdrawal system is operated by pressing the release button along the puncturing direction.
In an advantageous embodiment it has also proven to be expedient for the lancet holder to comprise two bearing members which each rest on a support surface of the housing. This ensures that the lancet holder is supported symmetrically by a simple housing construction. Of course an embodiment is also conceivable which contains more than two bearing members and several support surfaces. In principle the number of bearing members and of the corresponding support surfaces is unlimited so that usually a construction is selected in which the lancet holder is supported optimally and can be manufactured at low costs.
In order to convert the linear movement into a rotary movement of the bearing member and the support surface relative to one another, several designs of the triggering unit are also conceivable. In a preferred embodiment of the triggering unit it contains a rotary drive element which is pressed by the linear movement of the release button against the bearing member such that the bearing member falls from the support surface. The rotary drive element for example has an elastic ram and the support surface can contain a depression in which the bearing member of the lancet holder is supported. A linear movement of the release button presses the elastic ram from above against the bearing member of the lancet holder and deforms it in this process. If the bearing member is in a depression of the support surface, the ram can also reach underneath the bearing member due to the deformation and lever it out of the depression in the support surface. As a result the lancet holder falls from the support surface and a lancing process is triggered. However, a ramp extending into the inside of the housing is also conceivable as a rotary drive element. In this case the ramp is pressed against the bearing member by the linear movement of the release button which pushes it from the support surface and the lancet holder makes a falling movement.
Due to the falling movement of the bearing member and thus of the lancet holder, the spring element is relaxed, In the sense of this invention this is also understood as a process in which the spring element only passes through a relaxed state and is subsequently again converted into a tensioned state.
For example the falling movement of the lancet holder can be stopped by a stop provided for this purpose so that only a defined part of the lancet extends from the housing. The limit stop which consequently determines the puncture depth of the blood withdrawal system can in this connection advantageously be a component of a cap provided for this purpose which is mounted movably on the housing of the system or is a component of the housing itself. It is possible for the cap to be attached movably on the housing in or against the lancing direction such that in the case of a limit stop on the housing the distance between the stop and the exit opening of the cap is varied. If the stop is a component of the cap the position of the stop and thus the puncture depth can be changed by moving the cap in the direction of or opposite to the direction of lancing, or it can be changed by a rotation of the cap in which the axial position of the cap remains constant. In such an embodiment the cap contains several stops at different levels which come into use depending on the rotary movement of the cap and which define the puncture depth. Such a system for regulating the puncture depth is described for example in the document EP 1 534.
After the lancet holder has hit the stop it is usually retracted in the opposite direction as described by means of a return mechanism such that the lancet tip no longer protrudes from the opening of the housing.
In principle the described system is suitable for disposable lancing devices as well as for lancing devices for multiple use. The system is preferably in a tensioned state as soon as the bearing member rests on the support surface. This state has proven to be particularly suitable for disposable lancing devices since a device for tensioning the spring element is often not provided. Disposable lancing devices are then already delivered in a tensioned state to the customer. In this case the customer only has to operate the release button to initiate the lancing process.
In order to avoid contamination the reuse of the disposable lancing device is undesirable and is often actively prevented. This can for example be accomplished by the absence of a tensioning device in the disposable lancing device which simplifies the construction of the lancing device. On the other hand a mechanism is conceivable in which the lancet is actively blocked after use. In this case improper retensioning can be prevented by for example the spring element pressing the bearing member against the support surface from below after the lancing process. Hence this embodiment prevents the bearing member from being positioned on the support surface. In general a wide variety of embodiments are possible that prevent a disposable lancing device from being retensioned.
If the blood withdrawal system is to be suitable for repeated use, the system comprises a device for tensioning the drive element so that the lancing device does not have to be delivered in a tensioned state. In order to avoid unnecessary material stress of the bearing member and the support surface, the drive element in another advantageous embodiment is present in a relaxed or at least partially relaxed state with the bearing member resting on the support surface. Then the drive element is firstly tensioned in an advantageous manner before or during actuation of the trigger unit before a relative rotation of the lancet holder and the support surface is initiated.
Material fatigue of the disposable lancing devices can of course also be avoided by using such a mechanism. However, it may prove to be advantageous to select particularly robust material properties of the bearing members so that the bearing members can withstand the load in a stressed state without difficulty. The tension acting on the bearing members can then be selected such that it does not lead to damage of the bearing members. The puncture speed of the lancing device can be increased according to the tension present in the system to minimize the pain caused by the incision.
Another important aspect in constructing a lancing aid is to prevent unintentional triggering of a lancing process particularly when a sterile protector is removed.
Various mechanisms are possible for this which ensure the lancet remains in the housing. This protects the user from injury by accidental triggering of the lancing device. Moreover such locking mechanisms ensure the sterility of the lancet before the lancing process. Preferred embodiments of a locking mechanism can comprise locking members as a component of the triggering unit which prevent a rotation of the bearing member and the support surface relative to one another as long as the release button is not actuated. Such locking members can, however, also be components of the housing of the lancing device or be located on a detachable sterile protector which is suitable for the sterile storage of the lancet. A
combination of the described features is of course also possible such that an interaction of one or more locking members e.g. on the lancet holder and housing prevent an accidental triggering of the system. In this connection one of the described embodiments may prove to be advantageous depending on other functions of the lancing device such as a puncture depth adjustment. If the locking mechanism is a component of the sterile protector, a relative rotation of the bearing member and the support surface is prevented as long as the sterile protector has not been detached from the lancet. For example the sterile protector in this case comprises barbs which prevent the lancet holder from moving parallel to the lancing direction. If the support surface advantageously has a depression, this can prevent the bearing members from being lifted out of the depression in the support surface. Such an embodiment proves to be particularly advantageous for example in a puncture depth adjustment in which the axial position of the cap is fixed and cannot be changed.
Another subject matter of the invention is a method for triggering a lancing process with a lancing device. In this case a lancet holder firstly rests on a support surface inside a housing of a lancing device. The operator actuates a trigger unit of the lancing device by means of a linear movement. In this process the linear movement of at least a part of the trigger unit is converted into a rotation of the lancet holder and the support surface relative to one another until the lancet holder falls from the support surface and makes a falling movement. As a result of the falling movement a tip of a lancet of the lancet holder emerges through an opening of a housing so that a lancing process can be carried out.
Preferred embodiments of the method are derived as already described.
The invention is illustrated in the following on the basis of examples in the figures.
Figure 1: side-view of a blood withdrawal system Figure 2: top-view of the lancet holder within the housing Figure 3: triggering a lancing process Figure 4: mechanism for adjusting the puncture depth Figure 5: locking mechanism for preventing an unintentional lancing process Figure 1 illustrates the components of a blood withdrawal system before it is assembled. The blood withdrawal system is provided with a housing 9 in which the lancet holder is inserted. The lancet holder is movably mounted in the housing such that it can carry out a lancing process along the puncturing direction. For this purpose the system also comprises drive elements which are connected to and act on the lancet holder. In the example shown the drive elements are in each case a spring (4 and 8). In this connection as shown in figure 1, the lancet holder can either rest loosely on a spring element or abut a spring element within the scope of the invention without a permanent connection between the spring element and lancet holder. In the sense of the invention the connection between the lancet holder and a drive element is characterized in that a force is transferred from the drive element onto the lancet holder. However, embodiments are also possible in which the lancet holder is permanently connected to a drive element. Moreover the lancet holder is positioned in the housing in such a manner that it can rotate perpendicular to the lancing direction during the lancing process as illustrated by the following figures.
In principle the described system is suitable for disposable lancing devices as well as for lancing devices for multiple use. The system is preferably in a tensioned state as soon as the bearing member rests on the support surface. This state has proven to be particularly suitable for disposable lancing devices since a device for tensioning the spring element is often not provided. Disposable lancing devices are then already delivered in a tensioned state to the customer. In this case the customer only has to operate the release button to initiate the lancing process.
In order to avoid contamination the reuse of the disposable lancing device is undesirable and is often actively prevented. This can for example be accomplished by the absence of a tensioning device in the disposable lancing device which simplifies the construction of the lancing device. On the other hand a mechanism is conceivable in which the lancet is actively blocked after use. In this case improper retensioning can be prevented by for example the spring element pressing the bearing member against the support surface from below after the lancing process. Hence this embodiment prevents the bearing member from being positioned on the support surface. In general a wide variety of embodiments are possible that prevent a disposable lancing device from being retensioned.
If the blood withdrawal system is to be suitable for repeated use, the system comprises a device for tensioning the drive element so that the lancing device does not have to be delivered in a tensioned state. In order to avoid unnecessary material stress of the bearing member and the support surface, the drive element in another advantageous embodiment is present in a relaxed or at least partially relaxed state with the bearing member resting on the support surface. Then the drive element is firstly tensioned in an advantageous manner before or during actuation of the trigger unit before a relative rotation of the lancet holder and the support surface is initiated.
Material fatigue of the disposable lancing devices can of course also be avoided by using such a mechanism. However, it may prove to be advantageous to select particularly robust material properties of the bearing members so that the bearing members can withstand the load in a stressed state without difficulty. The tension acting on the bearing members can then be selected such that it does not lead to damage of the bearing members. The puncture speed of the lancing device can be increased according to the tension present in the system to minimize the pain caused by the incision.
Another important aspect in constructing a lancing aid is to prevent unintentional triggering of a lancing process particularly when a sterile protector is removed.
Various mechanisms are possible for this which ensure the lancet remains in the housing. This protects the user from injury by accidental triggering of the lancing device. Moreover such locking mechanisms ensure the sterility of the lancet before the lancing process. Preferred embodiments of a locking mechanism can comprise locking members as a component of the triggering unit which prevent a rotation of the bearing member and the support surface relative to one another as long as the release button is not actuated. Such locking members can, however, also be components of the housing of the lancing device or be located on a detachable sterile protector which is suitable for the sterile storage of the lancet. A
combination of the described features is of course also possible such that an interaction of one or more locking members e.g. on the lancet holder and housing prevent an accidental triggering of the system. In this connection one of the described embodiments may prove to be advantageous depending on other functions of the lancing device such as a puncture depth adjustment. If the locking mechanism is a component of the sterile protector, a relative rotation of the bearing member and the support surface is prevented as long as the sterile protector has not been detached from the lancet. For example the sterile protector in this case comprises barbs which prevent the lancet holder from moving parallel to the lancing direction. If the support surface advantageously has a depression, this can prevent the bearing members from being lifted out of the depression in the support surface. Such an embodiment proves to be particularly advantageous for example in a puncture depth adjustment in which the axial position of the cap is fixed and cannot be changed.
Another subject matter of the invention is a method for triggering a lancing process with a lancing device. In this case a lancet holder firstly rests on a support surface inside a housing of a lancing device. The operator actuates a trigger unit of the lancing device by means of a linear movement. In this process the linear movement of at least a part of the trigger unit is converted into a rotation of the lancet holder and the support surface relative to one another until the lancet holder falls from the support surface and makes a falling movement. As a result of the falling movement a tip of a lancet of the lancet holder emerges through an opening of a housing so that a lancing process can be carried out.
Preferred embodiments of the method are derived as already described.
The invention is illustrated in the following on the basis of examples in the figures.
Figure 1: side-view of a blood withdrawal system Figure 2: top-view of the lancet holder within the housing Figure 3: triggering a lancing process Figure 4: mechanism for adjusting the puncture depth Figure 5: locking mechanism for preventing an unintentional lancing process Figure 1 illustrates the components of a blood withdrawal system before it is assembled. The blood withdrawal system is provided with a housing 9 in which the lancet holder is inserted. The lancet holder is movably mounted in the housing such that it can carry out a lancing process along the puncturing direction. For this purpose the system also comprises drive elements which are connected to and act on the lancet holder. In the example shown the drive elements are in each case a spring (4 and 8). In this connection as shown in figure 1, the lancet holder can either rest loosely on a spring element or abut a spring element within the scope of the invention without a permanent connection between the spring element and lancet holder. In the sense of the invention the connection between the lancet holder and a drive element is characterized in that a force is transferred from the drive element onto the lancet holder. However, embodiments are also possible in which the lancet holder is permanently connected to a drive element. Moreover the lancet holder is positioned in the housing in such a manner that it can rotate perpendicular to the lancing direction during the lancing process as illustrated by the following figures.
The lancet holder itself has a sterile protector (7) which is placed over a lancet to ensure the sterility of a lancet before use and to prevent accidental injury by the lancet tip. The spring (8) is firstly inserted into the housing (9). This prevents the lancet from being retracted into the housing after the lancing process when the lancing device is used subsequently. The spring (8) is also referred to as a return spring. The lancet holder is inserted inside the spring (8) and the housing (9). The lancet holder is also provided with bearing members (5) which rest within the housing on support surfaces (not shown) provided for this purpose. The spring (4) as well as the spring (8) interact with the lancet holder in such a manner that when the bearing members (5) rest on the support surfaces within the housing (9), the spring (4) (drive spring) is tensioned whereas the spring (8) (return spring) is relaxed.
During the lancing process the drive spring (4) relaxes while accelerating the lancet holder. This executes a falling movement and strikes the return spring (8) which is thereby tensioned. The lancet holder falls within the housing down to a stop.
The lancet holder is pulled back again by the return spring (8) which is then fully tensioned. At this time the drive spring (4) is relaxed. After the puncture and before the lancing device may be retensioned, both springs (4 and 8) are completely relaxed and rest against the lancet holder. A cap (10) is movably mounted on the housing at the lower end of the housing (9) such that the extent to which the lancet tip emerges from the housing can be changed by rotating the cap. Different puncture depths can be set for the lancet on the basis of this adjustable distance. The regulation of the puncture depth is also described in the following on the basis of figure 4. At the upper end of the housing the trigger unit (1) closes the upper opening of the housing. In the example shown the trigger unit comprises a release button (2) and two small elastic hooks (3) as rotary drive elements. When the release button (2) is moved along the lancing direction of the lancet, the small hooks (3) cause the lancet holder to rotate.
Figure 2 shows a top-view of a lancing device in which the lancet holder (6) is located in a first position in the lancet housing (9). In the example shown the lancet holder (6) has two bearing members (5) which are in the form of holding arms. In the first position the holding arms (5) rest on the support surfaces (20) of the housing (9). A
rotation of the lancet holder (6) moves the bearing members into a second position (shown with dashed lines) in which they no longer rest on the support surfaces. The lancet holder connected to the bearing members can now move in the lancing direction. A puncture process is carried out by movement of the lancet holder in the lancing direction.
Figure 3 illustrates the triggering of a lancing process based on a lancing device which, as already shown, has an elastic hook as the rotary drive element.
Figure 3a shows the housing (9) of the lancing device in which the housing interior can be viewed through a break in the housing wall shown schematically. The housing (9) is closed by a release button (2) and a cap (10). A hook (3) is connected as a rotary drive element to the release button (2). The lancet holder (6) which is driven by a spring (4) is located in the interior of the housing. The lancet holder (6) has a bearing member in the form of a kinked rod (5) by means of which the lancet holder (6) is mounted on a support surface (20) of the housing (9). The support surface (20) of the housing has a depression which facilitates the positioning of the bearing member on the support surface. When the bearing members (5) rest on the support surface (20), the spring (4) is compressed. At this time the rotary drive element (3) is positioned next to the bearing member. The lancing process is triggered by pressing the release button (2) along the lancing direction as indicated by the arrow in figure 3a. In this process the small elastic hook (3) is deformed when the release button is pressed down and engages in the depression of the support surface (20) such that the lancet holder rotates and the bearing member (5) falls from the support surface as shown in figure 3b. The falling movement causes the lancet holder (6) to move in the lancing direction which relaxes the spring (4). The falling movement of the lancet holder continues until a stop (30) is reached within the housing (9) which is struck by the bearing member (5) and stops the falling movement of the lancet holder. As a result the tip of the lancet (21) emerges from an opening (not shown) of the housing. The extent by which the lancet tip (21) emerges from the housing, can be varied by means of the cap (10) which thus enables an adjustment of the puncture depth of the blood withdrawal system as already described. The lancet tip is retracted into the housing by means of the return spring (8) so that the lancet does not remain in the body member after perforating a site on the skin.
During the lancing process the drive spring (4) relaxes while accelerating the lancet holder. This executes a falling movement and strikes the return spring (8) which is thereby tensioned. The lancet holder falls within the housing down to a stop.
The lancet holder is pulled back again by the return spring (8) which is then fully tensioned. At this time the drive spring (4) is relaxed. After the puncture and before the lancing device may be retensioned, both springs (4 and 8) are completely relaxed and rest against the lancet holder. A cap (10) is movably mounted on the housing at the lower end of the housing (9) such that the extent to which the lancet tip emerges from the housing can be changed by rotating the cap. Different puncture depths can be set for the lancet on the basis of this adjustable distance. The regulation of the puncture depth is also described in the following on the basis of figure 4. At the upper end of the housing the trigger unit (1) closes the upper opening of the housing. In the example shown the trigger unit comprises a release button (2) and two small elastic hooks (3) as rotary drive elements. When the release button (2) is moved along the lancing direction of the lancet, the small hooks (3) cause the lancet holder to rotate.
Figure 2 shows a top-view of a lancing device in which the lancet holder (6) is located in a first position in the lancet housing (9). In the example shown the lancet holder (6) has two bearing members (5) which are in the form of holding arms. In the first position the holding arms (5) rest on the support surfaces (20) of the housing (9). A
rotation of the lancet holder (6) moves the bearing members into a second position (shown with dashed lines) in which they no longer rest on the support surfaces. The lancet holder connected to the bearing members can now move in the lancing direction. A puncture process is carried out by movement of the lancet holder in the lancing direction.
Figure 3 illustrates the triggering of a lancing process based on a lancing device which, as already shown, has an elastic hook as the rotary drive element.
Figure 3a shows the housing (9) of the lancing device in which the housing interior can be viewed through a break in the housing wall shown schematically. The housing (9) is closed by a release button (2) and a cap (10). A hook (3) is connected as a rotary drive element to the release button (2). The lancet holder (6) which is driven by a spring (4) is located in the interior of the housing. The lancet holder (6) has a bearing member in the form of a kinked rod (5) by means of which the lancet holder (6) is mounted on a support surface (20) of the housing (9). The support surface (20) of the housing has a depression which facilitates the positioning of the bearing member on the support surface. When the bearing members (5) rest on the support surface (20), the spring (4) is compressed. At this time the rotary drive element (3) is positioned next to the bearing member. The lancing process is triggered by pressing the release button (2) along the lancing direction as indicated by the arrow in figure 3a. In this process the small elastic hook (3) is deformed when the release button is pressed down and engages in the depression of the support surface (20) such that the lancet holder rotates and the bearing member (5) falls from the support surface as shown in figure 3b. The falling movement causes the lancet holder (6) to move in the lancing direction which relaxes the spring (4). The falling movement of the lancet holder continues until a stop (30) is reached within the housing (9) which is struck by the bearing member (5) and stops the falling movement of the lancet holder. As a result the tip of the lancet (21) emerges from an opening (not shown) of the housing. The extent by which the lancet tip (21) emerges from the housing, can be varied by means of the cap (10) which thus enables an adjustment of the puncture depth of the blood withdrawal system as already described. The lancet tip is retracted into the housing by means of the return spring (8) so that the lancet does not remain in the body member after perforating a site on the skin.
Figure 4 shows a blood withdrawal system having a similar construction as already shown in figures 1 to 3. The system is shown with one side open in order to show an example of a mechanism for regulating the puncture depth. The lancing device shown in figure 4 illustrates a state in which the lancet protrudes from the lower end of the housing (9). After the lancing process has been initiated by the release button (2), the lancet holder (6) falls along the lancing direction. A falling movement takes place until the lancet holder (6) impacts a stop (30) of the housing (9) so that the falling movement is stopped. In the example shown the bearing member (5) which is used to support the lancet holder on the support surfaces (20) is also used as a counter flange with respect to the stop (30). Hence no additionally constructional measures are necessary to define the falling movement of the lancet holder. In the lancing device shown the stop (30) is a component of the housing (9) cannot be changed. Under these conditions the path along which the lancet holder falls is independent of the selected puncture depth. This ensures a constant moment of force in each puncture process. In order to change the puncture depth, the cap (10) which is movably mounted on the housing (9) is moved along the lancing direction or in the opposite direction as shown by the arrow (31) in figure 4. The distance between the stop (30) of the housing (9) and the opening of the cap (10) from which the lancet emerges can thus be altered by rotating the cap (10). The distance between the stop (30) and the opening is shown in figure 4 by the arrow (32). Consequently the extent by which the lancet protrudes from the housing is defined by this distance.
When changing the puncture depth there are several methods that can be used to position the cap along the path (31). For example this can be accomplished by rotating the cap relative to the housing. It is, however, also possible for the cap (10) to be moved towards or away from the stop (30) by pulling or pushing in direction (31).
In general the cap (10) can be positioned in an infinitely variable manner or in defined steps. Furthermore it has proven to be advantageous for the lancing device to have locking members (not shown) which hold the cap in a predetermined position so that it is not displaced when the cap (10) is placed on a body part. In an advantageous embodiment the resulting puncture depth of the lancet is indicated to the user by a scale. A wide variety of mechanisms are in principle possible for adjusting the puncture depth.
When changing the puncture depth there are several methods that can be used to position the cap along the path (31). For example this can be accomplished by rotating the cap relative to the housing. It is, however, also possible for the cap (10) to be moved towards or away from the stop (30) by pulling or pushing in direction (31).
In general the cap (10) can be positioned in an infinitely variable manner or in defined steps. Furthermore it has proven to be advantageous for the lancing device to have locking members (not shown) which hold the cap in a predetermined position so that it is not displaced when the cap (10) is placed on a body part. In an advantageous embodiment the resulting puncture depth of the lancet is indicated to the user by a scale. A wide variety of mechanisms are in principle possible for adjusting the puncture depth.
For example a mechanism for adjusting the puncture depth is described in the Patent US 4,895,147. In this case the puncture depth of the blood withdrawal system is adjusted by moving a stop of the lancet housing along the lancing direction of the lancing device or in the opposite direction. In this case the lancet holder is connected to a control member which falls against the stop when the lancing process is triggered so that the falling movement of the lancet holder is stopped. The length of the path along which the lancet holder falls is determined in such a mechanism depending on the position of the movable stop. Consequently this results in different moments of acting force depending on the puncture depth.
The document US 6,056,765 discloses another mechanism for changing the puncture depth of a blood withdrawal system. In this case the lancet is movably mounted in the lancet holder. The puncture depth is changed by inserting the needle by different distances into the lancet holder whereas the stop for the lancet holder is permanently positioned in the housing.
In principle there are a wide variety of methods for adjusting the puncture depth since the blood withdrawal system does not impose any further conditions on the lancing device due to its triggering mechanism that would represent a limitation to such mechanisms.
Figure 5 illustrates an example of a locking mechanism which prevents unintentional triggering of a lancing process. Figure 5 shows the upper region of the housing (9) which effects the triggering of a lancing process. In order to prevent an unintentional triggering, the trigger unit (1) has a locking member (40) in addition to the release button (2) and the rotary drive elements (3). The locking member (40) is in the form of a rod extending into the inside of the housing (9). If the release button is not actuated the rod (40) is positioned between the housing (9) and the lancet holder (6).
The lancet holder (6) has a notch (42) into which the locking member (40) engages.
The described positioning prevents a rotation of the lancet holder. The locking member (40) is only pressed against a slanted surface (41) of the housing (9) when the release button is pressed in the lancing direction. Further pressure on the release button guides the locking member along the slope (41) and spreads it outwards.
The lateral stretching of the locking member occurs to such an extent that the rod no longer engages in the notch (42) of the lancet holder. At the same time the holding arms (3) are pressed against the bearing members (5) and rotate the lancet holder which at this time is no longer blocked by the locking member (40). The rotation occurs until the bearing member (5) falls down from the support surface of the housing and triggers a lancing process. In this case the support surface (20) can, as already shown, have a depression in which the bearing member is positioned.
However, it is also conceivable that such a depression in the support surface is omitted since the locking member ensures a secure mounting of the bearing members on the support surface. If such a depression in the support surface is omitted, this for example has the advantage that larger tolerances can be allowed in the manufacture of the blood withdrawal system since it is no longer necessary to exactly adapt the lancet holder to the housing. The manufacturing costs of such a blood withdrawal system are thus reduced.
The locking mechanism shown illustrates an advantageous embodiment in addition to the locking systems that have already been described. However, in principle any embodiments are conceivable which prevent an unintentional triggering of a lancing process. This is advantageously accomplished in that a rotation of the lancet holder relative to the support surfaces is blocked.
The document US 6,056,765 discloses another mechanism for changing the puncture depth of a blood withdrawal system. In this case the lancet is movably mounted in the lancet holder. The puncture depth is changed by inserting the needle by different distances into the lancet holder whereas the stop for the lancet holder is permanently positioned in the housing.
In principle there are a wide variety of methods for adjusting the puncture depth since the blood withdrawal system does not impose any further conditions on the lancing device due to its triggering mechanism that would represent a limitation to such mechanisms.
Figure 5 illustrates an example of a locking mechanism which prevents unintentional triggering of a lancing process. Figure 5 shows the upper region of the housing (9) which effects the triggering of a lancing process. In order to prevent an unintentional triggering, the trigger unit (1) has a locking member (40) in addition to the release button (2) and the rotary drive elements (3). The locking member (40) is in the form of a rod extending into the inside of the housing (9). If the release button is not actuated the rod (40) is positioned between the housing (9) and the lancet holder (6).
The lancet holder (6) has a notch (42) into which the locking member (40) engages.
The described positioning prevents a rotation of the lancet holder. The locking member (40) is only pressed against a slanted surface (41) of the housing (9) when the release button is pressed in the lancing direction. Further pressure on the release button guides the locking member along the slope (41) and spreads it outwards.
The lateral stretching of the locking member occurs to such an extent that the rod no longer engages in the notch (42) of the lancet holder. At the same time the holding arms (3) are pressed against the bearing members (5) and rotate the lancet holder which at this time is no longer blocked by the locking member (40). The rotation occurs until the bearing member (5) falls down from the support surface of the housing and triggers a lancing process. In this case the support surface (20) can, as already shown, have a depression in which the bearing member is positioned.
However, it is also conceivable that such a depression in the support surface is omitted since the locking member ensures a secure mounting of the bearing members on the support surface. If such a depression in the support surface is omitted, this for example has the advantage that larger tolerances can be allowed in the manufacture of the blood withdrawal system since it is no longer necessary to exactly adapt the lancet holder to the housing. The manufacturing costs of such a blood withdrawal system are thus reduced.
The locking mechanism shown illustrates an advantageous embodiment in addition to the locking systems that have already been described. However, in principle any embodiments are conceivable which prevent an unintentional triggering of a lancing process. This is advantageously accomplished in that a rotation of the lancet holder relative to the support surfaces is blocked.
Claims (22)
1. Lancing device comprising - a housing defining an opening in which a lancet holder containing a lancet is movably mounted, - wherein the lancet holder is connected to a spring member and the lancet holder comprises at least one bearing member, and - at least one support surface is arranged in the housing in such a manner that the bearing member rests on the support surface in a first position of the lancet holder, and - a trigger unit which transfers the lancet holder into a second position wherein a release button of the trigger unit carries out a linear movement and the linear movement is converted into a rotary movement of the bearing member and the support surface relative to one another such that the bearing member in the second position of the lancet holder falls from the support surface which at least partially relaxes a spring element that was tensioned before the falling movement and the lancet holder moves relative to the housing such that the tip of the lancet emerges from the opening of the housing, wherein the rotary movement is carried out by the lancet holder.
2. Lancing device as claimed in claim 1, in which the spring element is connected to the lancet holder in such a manner that the spring element is in a tensioned state when the bearing member rests on the support surface.
3. Lancing device as claimed in claim 1 or 2, in which the linear movement of the release button occurs along a longitudinal axis of the housing.
4. Lancing device as claimed in any one of claims 1 to 3, in which the trigger unit comprises a rotary drive element which is pressed against the bearing member by the linear movement of the release button such that the bearing member falls from the support surface.
5. Lancing device as claimed in claim 4, in which the rotary drive element comprises at least one elastic ram which is deformed by the movement of the release button.
6. Lancing device as claimed in claim 4, in which the rotary drive element has at least one slanted ramp that extends into the interior of the housing.
7. Lancing device as claimed in any one of claims 1 to 6, in which the bearing member is pressed by the spring member or another spring member against an underside of the support surface after the lancet emerges through the opening of the housing.
8. Lancing device as claimed in any one of claims 1 to 7, in which the lancet holder comprises two bearing members.
9. Lancing device as claimed in any one of claims 1 to 8, in which the support surface has a depression in which the bearing member of the lancet holder is mounted.
10. Lancing device as claimed in any one of claims 1 to 9, in which the trigger unit has a locking member which prevents a relative rotation of the bearing member and the support surface provided the release button is not actuated.
11. Lancing device as claimed in claim 10, in which the locking member engages in a recess of the lancet holder.
12. Lancing device as claimed in any one of claims 1 to 11, in which the housing has a locking member which prevents an unintentional relative rotation of the bearing member and the support surface.
13. Lancing device as claimed in any one of claims 1 to 12, in which the lancing device has a detachable sterile protector for the lancet which comprises a locking member which prevents a relative rotation of the bearing member and the support surface provided the sterile protector is not detached from the lancet.
14. Lancing device as claimed in claim 13, in which the sterile protector comprises a barb which prevents the lancet holder from moving parallel to the lancing direction of the lancet.
15. Lancing device as claimed in any one of claims 1 to 14, in which the housing has a stop which stops the falling movement of the lancet holder.
16. Lancing device as claimed in claim 15, in which the falling movement of the lancet holder is stopped by an interaction of the stop and at least one bearing member.
17. Lancing device as claimed in any one of claims 1 to 16, in which the opening of the housing is located in a cap which is movably mounted on the housing.
18. Method for triggering a lancing process with a lancing device comprising - supporting a lancet holder on a support surface in the inside of a housing of a lancing device, - actuating a trigger unit of the lancing device such that at least a part of the trigger unit carries out a linear movement, - converting the linear movement of the trigger unit into a rotation of the lancet holder and the support surface relative to one another until the lancet holder falls from the support surface and the lancet holder carries out a falling movement during which a tip of a lancet of the lancet holder emerges through an opening of the housing to carry out a lancing process.
19. Method as claimed in claim 18, in which a retensioning of the lancet is prevented.
20. Method as claimed in claim 18 or 19, in which the linear movement of the trigger unit is perpendicular to the plane of the rotary movement.
21. Method as claimed in claim 18, in which a lancing device as claimed in any one of claims 1 to 17 is used.
22. Lancing device as claimed in claim 1, which is suitable for a method as claimed in one of the claims 19 or 20.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10222235.5 | 2002-05-16 | ||
| DE10222235A DE10222235A1 (en) | 2002-05-16 | 2002-05-16 | Blood Collection system |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2428510A1 CA2428510A1 (en) | 2003-11-16 |
| CA2428510C true CA2428510C (en) | 2007-07-24 |
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ID=29285584
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002428510A Expired - Lifetime CA2428510C (en) | 2002-05-16 | 2003-05-13 | Blood withdrawal system |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US7238192B2 (en) |
| EP (1) | EP1371329B1 (en) |
| JP (2) | JP3993529B2 (en) |
| KR (2) | KR100819399B1 (en) |
| CN (1) | CN100401982C (en) |
| AT (1) | ATE540614T1 (en) |
| AU (1) | AU2003204154B2 (en) |
| BR (1) | BR0301333A (en) |
| CA (1) | CA2428510C (en) |
| DE (1) | DE10222235A1 (en) |
| ES (1) | ES2379064T3 (en) |
| HK (1) | HK1060967A1 (en) |
| MX (1) | MXPA03004254A (en) |
| PL (1) | PL209556B1 (en) |
| SG (1) | SG120929A1 (en) |
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-
2002
- 2002-05-16 DE DE10222235A patent/DE10222235A1/en not_active Ceased
-
2003
- 2003-05-13 ES ES03010642T patent/ES2379064T3/en not_active Expired - Lifetime
- 2003-05-13 EP EP03010642A patent/EP1371329B1/en not_active Expired - Lifetime
- 2003-05-13 AT AT03010642T patent/ATE540614T1/en active
- 2003-05-13 KR KR1020030030140A patent/KR100819399B1/en active IP Right Grant
- 2003-05-13 SG SG200302790A patent/SG120929A1/en unknown
- 2003-05-13 AU AU2003204154A patent/AU2003204154B2/en not_active Ceased
- 2003-05-13 CA CA002428510A patent/CA2428510C/en not_active Expired - Lifetime
- 2003-05-13 BR BR0301333-2A patent/BR0301333A/en not_active Application Discontinuation
- 2003-05-14 MX MXPA03004254A patent/MXPA03004254A/en active IP Right Grant
- 2003-05-14 US US10/437,717 patent/US7238192B2/en active Active
- 2003-05-15 JP JP2003137847A patent/JP3993529B2/en not_active Expired - Lifetime
- 2003-05-16 CN CNB03123819XA patent/CN100401982C/en not_active Expired - Lifetime
- 2003-05-16 PL PL360198A patent/PL209556B1/en unknown
-
2004
- 2004-06-09 HK HK04104129.2A patent/HK1060967A1/en not_active IP Right Cessation
-
2005
- 2005-05-12 JP JP2005140156A patent/JP4086859B2/en not_active Expired - Lifetime
-
2006
- 2006-02-13 KR KR1020060013653A patent/KR20060023591A/en not_active Application Discontinuation
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| US7238192B2 (en) | 2007-07-03 |
| US20030216767A1 (en) | 2003-11-20 |
| ATE540614T1 (en) | 2012-01-15 |
| SG120929A1 (en) | 2006-04-26 |
| HK1060967A1 (en) | 2004-09-03 |
| JP4086859B2 (en) | 2008-05-14 |
| CA2428510A1 (en) | 2003-11-16 |
| AU2003204154A1 (en) | 2003-12-04 |
| EP1371329A1 (en) | 2003-12-17 |
| JP3993529B2 (en) | 2007-10-17 |
| BR0301333A (en) | 2004-08-24 |
| KR100819399B1 (en) | 2008-04-04 |
| KR20060023591A (en) | 2006-03-14 |
| MXPA03004254A (en) | 2005-11-23 |
| JP2003325484A (en) | 2003-11-18 |
| PL209556B1 (en) | 2011-09-30 |
| CN100401982C (en) | 2008-07-16 |
| EP1371329B1 (en) | 2012-01-11 |
| JP2005261967A (en) | 2005-09-29 |
| CN1462608A (en) | 2003-12-24 |
| ES2379064T3 (en) | 2012-04-20 |
| DE10222235A1 (en) | 2003-11-27 |
| AU2003204154B2 (en) | 2008-02-07 |
| PL360198A1 (en) | 2003-11-17 |
| KR20030089448A (en) | 2003-11-21 |
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