ES2354107T3 - Dispositivo de inserción para un equipo de infusión con una primera y segunda unidades de resorte. - Google Patents
Dispositivo de inserción para un equipo de infusión con una primera y segunda unidades de resorte. Download PDFInfo
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/158—Needles for infusions; Accessories therefor, e.g. for inserting infusion needles, or for holding them on the body
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/06—Body-piercing guide needles or the like
- A61M25/0612—Devices for protecting the needle; Devices to help insertion of the needle, e.g. wings or holders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/158—Needles for infusions; Accessories therefor, e.g. for inserting infusion needles, or for holding them on the body
- A61M2005/1581—Right-angle needle-type devices
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/158—Needles for infusions; Accessories therefor, e.g. for inserting infusion needles, or for holding them on the body
- A61M2005/1585—Needle inserters
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/158—Needles for infusions; Accessories therefor, e.g. for inserting infusion needles, or for holding them on the body
- A61M2005/1587—Needles for infusions; Accessories therefor, e.g. for inserting infusion needles, or for holding them on the body suitable for being connected to an infusion line after insertion into a patient
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/02—Access sites
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/31—Details
- A61M5/32—Needles; Details of needles pertaining to their connection with syringe or hub; Accessories for bringing the needle into, or holding the needle on, the body; Devices for protection of needles
- A61M5/3205—Apparatus for removing or disposing of used needles or syringes, e.g. containers; Means for protection against accidental injuries from used needles
- A61M5/321—Means for protection against accidental injuries by used needles
- A61M5/3243—Means for protection against accidental injuries by used needles being axially-extensible, e.g. protective sleeves coaxially slidable on the syringe barrel
- A61M5/326—Fully automatic sleeve extension, i.e. in which triggering of the sleeve does not require a deliberate action by the user
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hematology (AREA)
- Anesthesiology (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Vascular Medicine (AREA)
- Biophysics (AREA)
- Pulmonology (AREA)
- Infusion, Injection, And Reservoir Apparatuses (AREA)
Abstract
Un dispositivo de inserción para un equipo de infusión que comprende un alojamiento (1), un cuerpo (2) portador que porta una pieza (8) de infusión, un anillo central (3) de la aguja provisto de una aguja (6) de inserción, una primera unidad (4) de movimiento para llevar el cuerpo (2) portador y el anillo central (3) de la aguja hasta una posición avanzada, una segunda unidad (5) de movimiento para llevar el anillo central (3) de la aguja hasta una posición de repliegue, y medios para la activación que deberían ser activados al menos una vez a fin de llevar el cuerpo (2) portador y el anillo central (3) de la aguja desde una posición replegada hasta una posición avanzada, y el anillo central (3) de la aguja de nuevo desde la posición avanzada hasta la posición replegada, caracterizado porque la primera unidad (4) de movimiento y la segunda unidad (5) de movimiento están ambas conectadas a una superficie distal del cuerpo (2) portador.
Description
Dispositivo de inserción para un equipo de
infusión con una primera y segunda unidades de resorte.
La presente invención se refiere a un
dispositivo de inserción para un equipo de infusión con el fin de
administrar una sustancia terapéutica de forma intermitente o
continua, tal como, por ejemplo, insulina. El dispositivo de
inserción está constituido por un anillo central de aguja que
comprende una aguja de inserción y dos unidades de resorte que
garantizan la inserción y retirada automáticas de la aguja de
inserción.
\vskip1.000000\baselineskip
El documento de la patente de EE.UU. nº
6.387.078 corresponde a un aparato automático de inyección que
inyecta vía intramuscular o transdérmicamente una dosis única,
dosificada previamente, de un medicamento suministrado, y el aparato
de inyección retrae automáticamente la aguja hipodérmica al
dispositivo después que ha concluido la inyección. El usuario
presiona el extremo distal, es decir, el extremo de la aguja, del
dispositivo sobre el lugar de inyección deseado y presiona el
pulsador de accionamiento. Esta acción libera la combinación
émbolo-jeringuilla de su acoplamiento temporal con
el alojamiento. La combinación émbolo-jeringuilla
conjuntamente con el acoplamiento resorte-a-émbolo
se ven entonces forzados a apartarse de su extremo proximal, es
decir, el extremo de accionamiento, del alojamiento mediante un
resorte accionador activado. El resorte accionador impulsa la
combinación émbolo-jeringuilla hacia delante a
través del orificio del alojamiento hasta que la aguja hipodérmica
sale del alojamiento y entra en el tejido del receptor, y el
cilindro de la jeringuilla toca el extremo distal interior del
alojamiento. Durante este movimiento, un resorte de retorno
posicionado entre el conjunto de la jeringuilla y el extremo fijo
distal del alojamiento es comprimido y activado. Cuando el líquido
del aparato de inyección automático es descargado por el émbolo que
está siendo empujado hacia adelante a través del interior del
cilindro de la jeringuilla, el acoplamiento
resorte-a-émbolo entra en contacto con un separador
que desacopla el resorte accionador del émbolo. Sin la influencia
del resorte accionador sobre la combinación
émbolo-jeringuilla, el resorte de retorno activado
fuerza la combinación émbolo-jeringuilla a retraer
hacia atrás el extremo proximal del dispositivo hasta que la aguja
hipodérmica esté replegada totalmente dentro del alojamiento.
Puesto que este aparato automático de inyección
está dirigido a inyecciones de una dosis dosificada previamente de
un medicamento líquido almacenado en las que el émbolo durante la
inyección empuja la dosis líquida del medicamento almacenado fuera
del aparato, la solución no será aplicable para el uso cuando se
inserta un dispositivo de inyección, ya que la manipulación e
inyección de un líquido en condiciones estériles se necesita un
aparato de inyección complicado que requiere interactuar con el
líquido.
El documento WO 2005/046780 (fig.
97-102) describe un dispositivo utilizado para la
inserción automática de una cánula de un dispositivo de infusión
dentro de la piel de un paciente, y después para la retirada
automática de la aguja de inserción. El dispositivo de inserción
tiene la forma de un cilindro oblongo (longitud \approx 4 x el
diámetro) que se abre en un extremo (1984) y está provisto con
medios para la activación en el otro extremo (1952). Cuando el
equipo de infusión se ha cargado en la aguja (1968), el elemento de
cierre (1962) se mueve en dirección del extremo provisto de medios
para la activación por el paciente utilizando salientes (1974),
salientes los cuales son accesibles a través de una ranura (1976)
del alojamiento hasta que las lengüetas (1956) del elemento de
cierre (1962) se acoplan a una superficie externa del alojamiento
(pag. 26, l. 24-27). Entonces, el extremo abierto
(1984) se coloca contra la piel del paciente y se activa el medio de
activación (1952). Cuando se acoplan los rebordes (1954) activados
en el medio de activación, los salientes (1956) son empujados unos
contra otros para desacoplar los salientes del alojamiento. Cuando
los salientes se liberan del alojamiento, el elemento de cierre, el
anillo central de la aguja, el retenedor del cuerpo y el dispositivo
de infusión asociado se mueven por medio de un primer resorte en
dirección al extremo (1984) abierto. El dispositivo de inserción
mueve el dispositivo de infusión hacia la piel del paciente,
insertando de ese modo la aguja y la cánula del dispositivo de
infusión. A medida que la cánula se inserta totalmente, los
salientes (1964) del anillo central (1965) de la aguja acoplan las
superficies (1972) en rampa del manguito (1982), haciendo que los
salientes (1964) sean forzados el uno hacia otro. Cuando los
salientes (1964) han sido forzados suficientemente hacia adentro
para liberar los extremos (1988) del cuerpo (1980) principal, el
segundo resorte (1966) mueve entonces el anillo central (1965) de la
aguja en la dirección del medio (1952) de activación. De este modo,
la aguja es retirada del dispositivo de infusión dejando en su lugar
el dispositivo de infusión sobre la piel al tiempo que el cuerpo
retenedor permanece en una posición contigua al extremo abierto del
manguito de forma que una vez que el dispositivo de inserción se ha
retirado de la piel del paciente, el cuerpo retenedor proteja al
paciente de tener más contacto con
la aguja.
la aguja.
Este dispositivo de inserción es más bien
complejo y la longitud del dispositivo se define por las unidades
individuales que forman las piezas funcionales del dispositivo, ya
que estas unidades tienen que ser colocadas más o menos extremo con
extremo. Una característica que ilustra la complejidad de la unidad
es el hecho de que los dos resortes respectivamente desvían el
alojamiento del elemento de cierre y el cuerpo retenedor del anillo
central de la aguja, al tiempo que un cuerpo principal se coloca
entre los dos sistemas de resorte para transferir la fuerza del
primer resorte al segundo resorte.
\newpage
El documento de US 2003/0199823 describe un
dispositivo de inserción del mismo tipo que en el documento WO
2005/046780, es decir, un dispositivo que tiene dos resortes que
funcionan en cada una de las direcciones y que están colocados para
prolongarse mutuamente.
El documento DE 203 20 207 describe un
dispositivo utilizado para una inserción automática de una cánula de
un dispositivo de infusión que tiene un repliegue automático de la
aguja de inserción. Este dispositivo puede tener dos resortes
colocados uno junto al otro, aunque los dos resortes funcionan
simultáneamente en la misma dirección.
Según la presente invención, las dos unidades de
resorte funcionan directamente de forma conjunta, ya que la primera
unidad de resorte afecta directamente el movimiento del cuerpo
portador mientras que el segundo sistema de resorte está afectado de
forma directa por el movimiento del cuerpo portador. Que las
unidades de resorte afecten directamente o estén afectadas
directamente por el cuerpo portador significa que las unidades de
resorte están conectadas al cuerpo portador de forma directa o a
través de una pieza que transfiere la potencia ya sea inalterada o
bajo modificaciones controladas.
\vskip1.000000\baselineskip
El objeto de la invención es proporcionar un
dispositivo de inserción sencillo, poco costoso, para un dispositivo
de infusión, dispositivo de inserción el cual sería fácil y seguro
de manipular durante su uso por el usuario, y seguro de eliminar
después de su utilización.
La invención se refiere a un dispositivo de
inserción para un equipo de infusión que comprende un alojamiento,
un cuerpo portador para porta una pieza de infusión, un anillo
central de la aguja, una primera unidad de movimiento para llevar el
cuerpo portador a una posición avanzada, y una segunda unidad de
movimiento para llevar el cuerpo portador a una posición de
repliegue, en el que el dispositivo de inserción tiene medios para
la activación, que se deberían activar al menos una vez a fin de
llevar el cuerpo portador desde una posición de repliegue hasta una
posición avanzada, y de nuevo desde una posición avanzada hasta una
posición de repliegue.
En una realización preferida, el dispositivo de
inserción tiene medios de activación que deben ser activados sólo
una vez a fin de tanto llevar el cuerpo portador desde una posición
de repliegue hasta una posición avanzada como nuevamente desde una
posición avanzada hasta una posición replegada.
Preferiblemente, la primera unidad de movimiento
y la segunda unidad de movimiento se colocan al menos parcialmente
en paralelo una de la otra, donde "paralelo" se entiende que no
está en "serie". "En serie" significa que una unidad de
movimiento se coloca prolongando a la otra, según se describió, por
ejemplo, en el documento WO 2005/046780.
En una realización preferida, la primera unidad
de movimiento y la segunda unidad de movimiento están colocadas el
menos parcialmente en paralelo una con respecto a la otra dentro del
alojamiento.
La invención comprende también un dispositivo de
inserción para un equipo de infusión que comprende un alojamiento,
un cuerpo portador para porta una pieza de infusión, un anillo
central de la aguja, una primera unidad de resorte y una segunda
unidad de resorte, en el que
- el alojamiento está provisto de un medio guía
sobre la superficie interna para guiar el movimiento del cuerpo
portador,
- el anillo central de la aguja comprende una
aguja de inserción para penetrar la piel,
- el cuerpo portador tiene una posición
replegada y una posición avanzada, y en la posición de repliegue
antes de la inserción el cuerpo portador y el anillo central de la
aguja se bloquean entre sí.
- el cuerpo portador está provisto de medios
para guiar que corresponden a los medios para guiar que se
encuentran sobre el alojamiento,
- la primera unidad de resorte desvía el
alojamiento y el cuerpo portador, y la segunda unidad de resorte
desvía el cuerpo portador y el anillo central de la aguja.
\vskip1.000000\baselineskip
En una realización preferida, la primera y
segunda unidades de resorte están ambas conectadas a una superficie
distal del cuerpo portador.
En otra realización preferida, el cuerpo
portador permanece en una posición avanzada después de la inserción
de la aguja.
En otra realización preferida, la pieza de
infusión está provista de una superficie proximal adhesiva.
En otra realización preferida, la pieza de
infusión está provista de una superficie distal adhesiva.
En otra realización preferida, se sujeta de
forma liberable una almohadilla adhesiva a una pieza proximal del
alojamiento, y la almohadilla adhesiva puede cubrir una abertura
proximal del alojamiento a través de la cual se transportará la
pieza de infusión.
En otra realización preferida, la primera unidad
de resorte y la segunda unidad de resorte comprenden respectivamente
un resorte de compresión.
En otra realización preferida, el cuerpo
portador está provisto de al menos una superficie inclinada cuya
superficie está en contacto con una pieza giratoria del anillo
central de la aguja, pieza giratoria la cual puede girar en relación
con la pieza principal del anillo central de la aguja al que está
fijada la aguja de inserción, y el alojamiento está provisto de un
elemento que evita que la pieza giratoria del anillo central de la
aguja gire cuando el cuerpo portador se encuentre en una posición
replegada.
La invención también comprende un método para
insertar una pieza de infusión, en el que la pieza de infusión se
encuentra fijada de forma liberable a un anillo central de la aguja,
y el anillo central de la aguja se encuentra fijado de forma
liberable a un cuerpo portador que porta la pieza de infusión desde
una posición de replegada hasta una posición avanzada, en el que
- una unidad de resorte desviada activado por el
usuario mueve el cuerpo portador, el anillo central de la aguja y la
pieza de infusión hacia delante desde una posición replegada, hasta
que una superficie proximal de la pieza de infusión entra en
contacto con la piel de los pacientes o contacta con una pieza
conectada a la piel del paciente;
- en esta posición avanzada, el anillo central
de la aguja se libera del cuerpo portador y una unidad de resorte
desviada mueve el anillo central de la aguja apartándolo del cuerpo
portador, dando como resultado el repliegue del anillo central de la
aguja; entonces, la pieza de infusión es liberada del cuerpo
portador, y el alojamiento -que incluye el cuerpo portador y el
anillo central de la aguja- se retira del paciente.
\vskip1.000000\baselineskip
La invención se explica con mayor detalle a
continuación con referencia a los dibujos que se acompañan, en los
que se muestra una realización preferida de la invención.
La fig. 1 es una vista lateral de una
realización del dispositivo de inserción de la invención, en el que
el cuerpo portador y el dispositivo de infusión se encuentran en una
posición replegada;
la fig. 2 es una vista lateral del dispositivo
de inserción con el cuerpo portador y el dispositivo de infusión en
una posición avanzada, en el que el anillo central del cuerpo de la
aguja se encuentra fijado al cuerpo portador;
la fig. 3 es una vista lateral del dispositivo
de inserción con el cuerpo portador y el dispositivo de infusión en
una posición avanzada, en el que el anillo central de la aguja ha
sido liberado del cuerpo portador;
la fig. 4 es una vista lateral del dispositivo
de inserción con el cuerpo portador y el dispositivo de infusión en
una posición avanzada, en el que el anillo central de la aguja se
encuentra en una posición replegada;
la fig. 5 es una vista lateral del dispositivo
de inserción después que este ha sido retirado del paciente, dejando
la pieza de infusión sobre la piel del paciente.
En este documento, "distal" describe una
superficie o una pieza alejada o colocada lejos del paciente cuando
el dispositivo de inserción está posicionado con el extremo de la
aguja dirigido hacia el paciente. "Proximal" describe una
superficie o una pieza girada en dirección a o colocada cerca del
paciente.
La realización del dispositivo de inserción de
la fig. 1 tiene un alojamiento 1 con una longitud un poco más
pequeña que el diámetro (longitud \approx 1 x el diámetro). El
diseño de este dispositivo de inserción se define fundamentalmente
por el uso y no por las unidades que lo constituyen dentro del
dispositivo de inserción. Las unidades que constituyen el
dispositivo son pocas y pequeñas, y el diseño del dispositivo de
inserción, tal como el tamaño y la forma, resulta de un deseo de
hacer que el dispositivo sea fácil de almacenar y fácil de manipular
por el usuario, incluso si el usuario tiene reducida la habilidad de
sus manos.
El dispositivo de inserción comprende un cuerpo
2 portador con al menos dos elementos 2a de cierre que sobresalen de
una superficie distal del cuerpo portador. Un anillo central 3 de la
aguja está colocado entre los dos elementos 2a de cierre, y el
anillo central de la aguja está provisto de elementos 3a que
sobresalen de una superficie distal del anillo central de la aguja y
que corresponden al medio 2a de cierre del cuerpo 2 portador. Estos
elementos 3a que sobresalen pueden girar hacia el centro del
dispositivo a lo largo de un eje a través del cual ellos se fijan
también a la pieza principal del anillo central 3 de la aguja.
Además, el anillo central de la aguja está provisto de una aguja 6
de inserción que sobresale de una superficie proximal del anillo
central de la aguja. Antes de la inserción, se fija una pieza 8 de
infusión al cuerpo 2 portador, la pieza de infusión está provista de
una cánula que está unida a la aguja de inserción de tal manera que
la inserción de la aguja 6 dará como resultado la inserción de la
cánula. Una almohadilla 7 adhesiva con una superficie proximal
adhesiva cubre la abertura proximal del alojamiento 1. La superficie
adhesiva de la almoha-
dilla 7 normalmente se cubrirá con un revestimiento que se puede soltar, a fin de proteger la superficie adhesiva.
dilla 7 normalmente se cubrirá con un revestimiento que se puede soltar, a fin de proteger la superficie adhesiva.
Durante la inserción, el anillo central 3 de la
aguja se mueve desde la posición de repliegue hasta una posición
avanzada, y de nuevo a una posición de repliegue mediante un sistema
de resortes. El sistema de las figuras 1-5 comprende
dos resortes, un primer resorte 4 y un segundo resorte 5. De acuerdo
con la ley de Hooke, la fuerza ejercida por un resorte depende del
desplazamiento del resorte x y de la constante k del resorte:
F_{resorte} = -k x. Cada uno de los resortes 4 y 5 se pueden
sustituir por más de un resorte, entonces la unidad de resorte que
sustituye, por ejemplo, el primer resorte 4 mostrado en las figuras
1-5, debería ejercer la fuerza:
en la que k_{1}, k_{2} .......,
k_{n} son las constantes del resorte para los resortes
individuales, y F_{resorte} = -k \cdot x, en la que
k = k_{1} + k_{2} + ... + k_{n}.
k = k_{1} + k_{2} + ... + k_{n}.
\vskip1.000000\baselineskip
El primer resorte 4 y el segundo resorte 5
pueden comprender ambos resortes de compresión y de tensión.
En la realización de las figuras
1-5, el alojamiento 1 está provisto de medios guía
1a y 1b. Los medios guía 1a y 1b comprenden paredes paralelas, una
pared 1a interior y una pared 1b exterior, que sobresalen de la
superficie interior distal del alojamiento 1. Los elementos 2a de
cierre del cuerpo 2 portador y los elementos 3a que sobresalen del
anillo central 3 de la aguja se encuentran colocados entre las
paredes 1a y 1b paralelas. Los elementos 2a de cierre tienen una o
más superficies inclinadas que entran en contacto con una pieza de
los elementos 3a que sobresalen. Cuando el cuerpo 2 portador se
extrae o se empuja hacia la piel del paciente, los elementos 2a de
cierre ejercerán una fuerza sobre o en perpendicular a cada una de
las superficies inclinadas. Esta fuerza tiene un componente paralelo
a las paredes 1a y 1b que apuntan en la misma dirección que el
movimiento, y otro componente perpendicular al primer componente que
apunta hacia la pared 1a interior. Mientras que la pared 1a interior
esté presente, una fuerza del mismo tamaño aunque en dirección
opuesta que el segundo componente empujará de nuevo desde la pared
1a interna manteniendo el elemento 3a que sobresale en una posición
estable entre las paredes 1a y 1b. Cuando la pared 1a interior no
está presente, el segundo componente de la fuerza ejercida por el
elemento de cierre empujará los elementos 3a que sobresalen hacia el
centro del dispositivo.
Cuando los elementos 3 que sobresalen han sido
liberados de la interconexión con los elementos 2a de cierre, el
anillo central de la aguja no se ve influenciado por una fuerza en
dirección de la pieza de infusión, y la fuerza ejercida por el
segundo resorte 5 superará la fricción entre la aguja de inserción y
la cánula que se extiende desde la pieza 8 de infusión y mueve el
anillo central 3 de la aguja lejos de la pieza 8 de infusión.
En la fig. 1, el cuerpo 2 portador se encuentra
colocado y bloqueado en una posición replegada. La aguja 6 de
inserción la cual se encuentra unida a la cánula se observa por
debajo de la pieza 8 de infusión. Ambas unidades 4 y 5 de resorte se
encuentran desviadas, y los elementos 2a de cierre están
interconectados con los elementos 3a que sobresalen del anillo
central 3 de la aguja debido al soporte de las paredes 1a
interiores.
Cuando el usuario desea insertar el dispositivo
de infusión, el dispositivo se coloca primero en el lugar de
inserción en el paciente. Entonces, el dispositivo de inserción es
activado por el usuario desbloqueando el cuerpo 2 portador del
alojamiento 1.
No se muestra en esta realización cómo se
realiza el desbloqueo del cuerpo 2 portador, aunque una forma es
proporcionar al cuerpo 2 portador dos miembros que sobresalgan por
las aberturas del alojamiento 1 opuestos entre sí. El desbloqueo del
cuerpo portador se realiza entonces por el usuario presionando sobre
el alojamiento 1 en dos puntos opuestos colocados sobre una línea
perpendicular a la línea formada por los dos elementos que
sobresalen del cuerpo 2 portador. Presionando sobre los dos puntos
sobre la línea perpendicular se originará una deformación del
alojamiento 1 e incrementará la distancia entre las dos aberturas
correspondientes en el alojamiento 1, los elementos que sobresalen
del cuerpo portador se liberarán entonces del alojamiento 1.
Cuando el dispositivo de inserción se activa, el
primer resorte 4 intenta regresar a la posición no desviada y al
hacer esto arrastra al cuerpo 2 portador y a la pieza 8 de infusión
a una posición avanzada que se muestra en la fig, 2.
En esta posición avanzada, la aguja 6 de
inserción y la cánula adjunta han penetrado la almohadilla 7
adhesiva colocada en el extremo proximal del alojamiento 1. Los
elementos 3a que sobresalen del anillo central 3 de la aguja en la
fig. 2 se han liberado del soporte de las paredes 1a interiores, y,
tan pronto como ha tenido lugar la liberación de las paredes 1a
internas, los elementos 3a que sobresalen del anillo central de la
aguja serán forzados hacia el centro del dispositivo de inserción
hasta la posición que se muestra en la fig. 3.
Inmediatamente después, los elementos 3a que
sobresalen del anillo central de la aguja se liberan de las paredes
1a interiores, la fuerza hacia arriba desde la unidad 5 de resorte
arrastrará el anillo central 3 de la aguja hasta la posición que se
muestra en la fig. 4, donde el anillo central 6 de la aguja y la
aguja 6 de inserción están totalmente cubiertas por el alojamiento
1.
En la fig. 5 se muestra cómo se ha asegurado la
pieza 8 de infusión a la almohadilla 7 adhesiva, la almohadilla 7 se
asegura al paciente, y entonces el dispositivo de inserción se
retira y puede ser eliminado de una forma segura conjuntamente, ya
que la aguja 6 de inserción contaminada se coloca detrás de las
paredes protectoras del alojamiento 1 del dispositivo de
inserción.
Claims (10)
1. Un dispositivo de inserción para un equipo de
infusión que comprende un alojamiento (1), un cuerpo (2) portador
que porta una pieza (8) de infusión, un anillo central (3) de la
aguja provisto de una aguja (6) de inserción, una primera unidad (4)
de movimiento para llevar el cuerpo (2) portador y el anillo central
(3) de la aguja hasta una posición avanzada, una segunda unidad (5)
de movimiento para llevar el anillo central (3) de la aguja hasta
una posición de repliegue, y medios para la activación que deberían
ser activados al menos una vez a fin de llevar el cuerpo (2)
portador y el anillo central (3) de la aguja desde una posición
replegada hasta una posición avanzada, y el anillo central (3) de la
aguja de nuevo desde la posición avanzada hasta la posición
replegada, caracterizado porque la primera unidad (4) de
movimiento y la segunda unidad (5) de movimiento están ambas
conectadas a una superficie distal del cuerpo (2) portador.
2. Un dispositivo de inserción según la
reivindicación (1), caracterizado porque la primera unidad
(4) de movimiento y la segunda unidad (5) de movimiento se
encuentran colocadas dentro del alojamiento (1).
3. Un dispositivo de inserción según cualquiera
de las reivindicaciones 1-2, en el que:
- -
- el alojamiento (1) está provisto de medios guía (1a, 1b) en la superficie interna, para guiar el movimiento del cuerpo (2) portador,
- -
- el anillo central (3) de la aguja comprende una aguja (6) de inserción para perforar la piel,
- -
- el cuerpo (2) portador tiene al menos una posición de repliegue y una posición avanzada, y en la posición de repliegue antes de la inserción, el cuerpo (2) portador y el anillo central (3) de la aguja se encuentran bloqueados entre sí,
- -
- el cuerpo (2) portador está provisto de medios guía (2a) que corresponden a los medios (1a, 1b) guía del alojamiento (1),
- -
- la primera unidad (4) de movimiento se encuentra desviada del alojamiento (1) y el cuerpo (2) portador, y la segunda unidad (5) de movimiento desvía el cuerpo (2) portador y el anillo central (3) de la aguja.
\vskip1.000000\baselineskip
4. Un dispositivo de inserción según las
reivindicaciones 1-3, caracterizado porque el
cuerpo (2) portador permanece en una posición avanzada después de la
inserción de la aguja (6).
5. Un dispositivo de inserción según las
reivindicaciones 1-3, caracterizado porque la
pieza (8) de infusión está provista de una superficie proximal
adhesiva.
6. Un dispositivo de inserción según las
reivindicaciones 1-5, caracterizado porque la
pieza (8) de infusión está provista de una superficie distal
adhesiva.
7. Un dispositivo de inserción según las
reivindicaciones 3, 5 o 6, caracterizado porque una
almohadilla (7) adhesiva se encuentra fijada de forma liberable a
una pieza proximal del alojamiento (1).
8. Un dispositivo de inserción según la
reivindicación 7, caracterizado porque la almohadilla (7)
adhesiva cubre una abertura proximal del alojamiento (1) a través
del cual se transportará la pieza (8) de infusión.
9. Un dispositivo de inserción según la
reivindicación 7, caracterizado porque tanto la primera
unidad (4) como la segunda unidad (5), respectivamente, comprenden
un resorte de compresión.
10. Un dispositivo de inserción según las
reivindicaciones 1-9, caracterizado porque el
cuerpo (2) portador está provisto de al menos una superficie
inclinada, superficie la cual está en contacto con una pieza (3a)
giratoria del anillo central (3) de la aguja, pieza (3a) giratoria
la cual puede girar con relación a la pieza principal del anillo
central (3) de la aguja a la que está fijada la aguja de inserción,
y el alojamiento (1) está provisto de un elemento (1a) para evitar
que la pieza (3a) giratoria del anillo central (3) de la aguja gire
cuando el cuerpo (2) portador se encuentre en una posición
replegada.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05019774.8A EP1762259B2 (en) | 2005-09-12 | 2005-09-12 | Inserter for an infusion set with a first and second spring units |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2354107T3 true ES2354107T3 (es) | 2011-03-10 |
Family
ID=35645677
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES05019774T Expired - Lifetime ES2354107T3 (es) | 2005-09-12 | 2005-09-12 | Dispositivo de inserción para un equipo de infusión con una primera y segunda unidades de resorte. |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US10369277B2 (es) |
| EP (1) | EP1762259B2 (es) |
| AT (1) | ATE480278T1 (es) |
| DE (1) | DE602005023458D1 (es) |
| DK (1) | DK1762259T3 (es) |
| ES (1) | ES2354107T3 (es) |
| NO (1) | NO20064096L (es) |
| PL (1) | PL1762259T3 (es) |
| PT (1) | PT1762259E (es) |
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-
2005
- 2005-09-12 PT PT05019774T patent/PT1762259E/pt unknown
- 2005-09-12 DE DE602005023458T patent/DE602005023458D1/de not_active Expired - Lifetime
- 2005-09-12 EP EP05019774.8A patent/EP1762259B2/en not_active Expired - Lifetime
- 2005-09-12 PL PL05019774T patent/PL1762259T3/pl unknown
- 2005-09-12 ES ES05019774T patent/ES2354107T3/es not_active Expired - Lifetime
- 2005-09-12 AT AT05019774T patent/ATE480278T1/de active
- 2005-09-12 DK DK05019774.8T patent/DK1762259T3/da active
-
2006
- 2006-09-11 US US11/519,137 patent/US10369277B2/en active Active
- 2006-09-12 NO NO20064096A patent/NO20064096L/no not_active Application Discontinuation
-
2019
- 2019-08-02 US US16/530,926 patent/US11617827B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| EP1762259B1 (en) | 2010-09-08 |
| ATE480278T1 (de) | 2010-09-15 |
| PL1762259T3 (pl) | 2011-03-31 |
| NO20064096L (no) | 2007-03-13 |
| US11617827B2 (en) | 2023-04-04 |
| US20190351137A1 (en) | 2019-11-21 |
| DE602005023458D1 (de) | 2010-10-21 |
| EP1762259B2 (en) | 2025-01-01 |
| EP1762259A1 (en) | 2007-03-14 |
| DK1762259T3 (da) | 2011-01-03 |
| US10369277B2 (en) | 2019-08-06 |
| PT1762259E (pt) | 2010-12-10 |
| US20070093754A1 (en) | 2007-04-26 |
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