阅读说明：本技术 食管压力测量导管 (Esophageal pressure measuring catheter ) 是由 罗格·克里斯蒂安·弗林克 劳伦斯·巴斯蒂安·约瑟夫·霍根伯克 特尼斯·亨德里克·沙尔特 于 2020-02-25 设计创作，主要内容包括：一种食管压力测量导管,包括具有近端和远端的管,其中管的远端被设置成插入患者的食管内,其中管设有至少一个压力传感器,用于测量患者的食管区域内的压力,其中管设有邻近所述至少一个压力传感器的至少一个可充气气囊,并且其中气囊的边缘与压力传感器的中心之间的距离小于20mm。(An esophageal pressure measurement catheter comprising a tube having a proximal end and a distal end, wherein the distal end of the tube is configured to be inserted into an esophageal tube of a patient, wherein the tube is provided with at least one pressure sensor for measuring pressure within the esophageal region of the patient, wherein the tube is provided with at least one inflatable balloon adjacent to the at least one pressure sensor, and wherein the distance between the edge of the balloon and the center of the pressure sensor is less than 20 mm.)

1. An esophageal pressure measurement catheter comprising a tube having a proximal end and a distal end, wherein said distal end of said tube is configured to be inserted into the esophagus of a patient, wherein said tube is provided with at least one pressure sensor for measuring the pressure within the esophageal region of a patient, characterized in that said tube is provided with at least one inflatable balloon adjacent to said at least one pressure sensor, wherein the distance between the edge of said balloon and the center of said pressure sensor is less than 20 mm.

2. The esophageal pressure measurement catheter of claim 1, wherein the tube comprises a feeding lumen for delivering liquid food, medication and/or gastric acid to and/or from the stomach of the patient.

3. The esophageal pressure-measuring catheter of claim 1 or 2, wherein the tube comprises a pressure sensor lumen for receiving a connector of the at least one pressure sensor.

4. The esophageal pressure-measuring catheter of claim 1, 2, or 3, wherein the tube comprises a balloon inflation lumen for delivering a fluid, such as air, to the at least one inflatable balloon.

5. The esophageal pressure measurement catheter of any of the preceding claims, wherein the balloon is inflatable to a diameter of between 7mm and 18mm, preferably between 10mm and 15 mm.

6. Esophageal pressure measurement catheter according to any of the previous claims, wherein the distance between the edge of the balloon and the center of the pressure sensor is less than 10mm, preferably less than 7mm, more preferably less than 5mm, most preferably less than 3 mm.

7. The esophageal pressure measurement catheter of any of the preceding claims, wherein the balloon has a spherical shape or the balloon has a cylindrical shape with a substantially rectangular longitudinal cross-section.

8. The esophageal pressure measurement catheter of any of the preceding claims, wherein the tube has a length of at least 80cm, preferably at least 95 cm.

9. The esophageal pressure-measuring catheter of any of the preceding claims, wherein the tube has a diameter of between 2mm and 6 mm.

10. The esophageal pressure measurement catheter of any of the preceding claims, wherein the at least one pressure sensor is a solid-state pressure sensor.

11. The esophageal pressure measurement catheter of any of the preceding claims, wherein the balloon is made of urethane, PET, and/or nylon.

12. The esophageal pressure-measuring catheter of any of the preceding claims, wherein the balloon has a wall thickness of between 0.01mm and 0.06 mm.

13. The esophageal pressure measurement catheter of any of the preceding claims, wherein the balloon has feet on either side for securing the balloon on the tube, wherein the length of the feet in the axial direction is less than 7mm, preferably less than 5mm, more preferably less than 3 mm.

14. Esophageal pressure measurement catheter according to any of the preceding claims, wherein on each side of the at least one pressure sensor the tube is provided with two inflatable balloons adjacent to the at least one pressure sensor, wherein the distance between the edge of each balloon and the center of the pressure sensor is less than 20mm, preferably less than 10mm, more preferably less than 7mm, more preferably less than 5mm, most preferably less than 3 mm.

15. Esophageal pressure measurement catheter according to any of the preceding claims, wherein the tube is provided with a plurality of the pressure sensors distributed along the length of the tube, each sensor being provided with at least one inflatable balloon adjacent to the at least one pressure sensor, wherein the distance between the edge of the balloon and the center of the pressure sensor is less than 20mm, preferably less than 10mm, more preferably less than 7mm, more preferably less than 5mm, most preferably less than 3 mm.

Technical Field

The present invention relates to an esophageal pressure-measuring catheter comprising a tube having a proximal end and a distal end, wherein the distal end of the tube is arranged to be inserted into the esophageal duct of a patient, wherein the tube is provided with at least one pressure sensor for measuring the pressure in the esophageal region of the patient.

Disclosure of Invention

When measuring the pressure in the esophagus of a patient, one problem is that any interaction between the esophageal wall and the pressure sensor (e.g., the wall contacting the pressure sensor) can negatively affect the measurement. The present invention is directed to a more reliable esophageal pressure-measuring catheter.

To this end, the tube is provided with at least one inflatable bladder adjacent to the at least one pressure sensor, wherein the distance between the edge of the bladder and the center of the pressure sensor is less than 20 mm. The balloon, when inflated, acts as a spacer keeping the esophageal wall away from the pressure sensor, making the measurement more accurate.

The at least one pressure sensor is preferably a solid state pressure sensor. The tube preferably comprises a pressure sensor cavity for accommodating a connection of the at least one pressure sensor. The tube preferably includes a balloon inflation lumen for delivering a fluid (e.g., air) to the at least one inflatable balloon. The tube also preferably comprises a feeding lumen for delivering liquid food, medication and/or gastric acid to and/or from the stomach of the patient.

The balloon, when inflated under normal, design nominal operating conditions, preferably has a diameter of between 7mm and 18mm, more preferably between 10mm and 15 mm. The distance between the edge of the balloon and the center of the pressure sensor is preferably less than 10mm, more preferably less than 7mm, more preferably less than 5mm, most preferably less than 3 mm. Preferably, the balloon has a spherical shape or the balloon has a cylindrical shape with a substantially rectangular longitudinal cross-section. Preferably, the balloon is located on a side of the pressure sensor that is closer to the proximal end of the tube than to the distal end of the tube. The balloon is preferably made of urethane, PET and/or nylon. The wall thickness of the balloon is preferably between 0.01mm and 0.06 mm. The balloon has feet on either side for securing the balloon to the tube, and the feet are preferably less than 7mm, more preferably less than 5mm, most preferably less than 3 mm.

The length of the tube is preferably at least 80cm, preferably at least 95 cm. The diameter of the tube is preferably between 2mm and 6 mm. Preferably, adjacent to and on each side of the at least one pressure sensor, the tube is provided with two inflatable balloons, wherein the distance between the edge of each balloon and the centre of the pressure sensor is less than 20mm, preferably less than 10mm, more preferably less than 7mm, more preferably less than 5mm, most preferably less than 3 mm. Preferably the tube is provided with a plurality of said pressure sensors distributed along the length of the tube, each sensor being provided with at least one inflatable bladder adjacent to said at least one pressure sensor, wherein the distance between the edge of the bladder and the centre of the pressure sensor is less than 20mm, preferably less than 10mm, more preferably less than 7mm, more preferably less than 5mm, most preferably less than 3 mm. At least one of the pressure sensors is preferably disposed near the distal end of the tube, for example at the last 25%, 10% or 5% of the length of the tube.

Drawings

The invention will now be illustrated by way of preferred embodiments with reference to the accompanying drawings, in which:

FIG. 1 is a side view of an esophageal pressure-measuring catheter in accordance with the present invention;

FIG. 2 is a top view of the esophageal pressure measuring catheter of FIG. 1;

FIG. 3 is a cross-sectional view of the esophageal pressure measuring catheter of FIG. 1;

FIG. 4 is a side view of a balloon for use with an esophageal pressure-measuring catheter in accordance with the present invention; and

figure 5 is a side view of another embodiment of a balloon for use with an esophageal pressure measuring catheter in accordance with the present invention.

Detailed Description

According to fig. 1 to 3, the esophageal pressure measuring catheter 1 comprises a flexible tube 2. The tube may be generally 95-125cm long and about 4mm in diameter. The tube is provided with an intestine feeding cavity 3, a sensor cavity 4 and an air bag inflation cavity 5, the intestine feeding cavity 3, the sensor cavity 4 and the air bag inflation cavity 5 leaving the tube 2 through a three-bifurcation piece 6.

During pressure measurements, which may last more than several days, the enteral feeding chamber 3 is used to feed liquid food, administer medication and/or suction to the patient.

The pressure is measured by a plurality of solid state pressure sensors 7, the plurality of solid state pressure sensors 7 being distributed along the length of the tube 2 and being in open communication with the oesophagus of the patient through corresponding apertures in the wall of the tube 2. The sensor 7 is connected by a connecting member 71 within the sensor chamber 4 to a sensor connector 72, such as an RJ45 connector, located at the proximal outer end of the sensor chamber 4.

Adjacent each pressure sensor 7, an inflatable medical balloon 8 is disposed on the tube 2. The balloon 8 may be made of urethane, for example. The distance between the edge of the inflated balloon 8 and the center of the pressure sensor is, for example, about 4mm, and the diameter of the inflated balloon is, for example, about 12mm to 15 mm. In this way, the balloon acts as a spacer, which prevents the esophageal wall from contacting or coming close to the pressure sensor 7.

In another preferred embodiment, the balloons 8 are arranged at a distance of about 3mm on each side of each pressure sensor 7, thereby improving the spacer function against the esophageal wall touching or approaching the pressure sensors 7 compared to an embodiment where one balloon 8 is arranged per pressure sensor 7.

Fig. 4 shows an example of the airbag 8, the airbag 8 including a spherical inflatable portion 81 and two leg portions 82 at each end for mounting the airbag 8 on the tube 2. The leg portion is about 3mm long in the axial direction.

Fig. 5 shows another example of the balloon 8, the balloon 8 comprising a cylindrical inflatable portion 81 and two leg portions 82 at each end for mounting the balloon 8 on the tube 2. The leg portion is about 3mm long in the axial direction. The inflatable portion 81 has a substantially rectangular longitudinal cross-section, thereby improving the spacer function of preventing the wall of the esophagus from contacting or approaching the pressure sensor 7, compared to the embodiment of fig. 4.

Thus, the invention has been described with reference to the preferred embodiments. However, it should be understood that this disclosure is only illustrative. Various details of structure and function are set forth, however, variations of these details within the full scope extended by the general meaning of the terms in which the appended claims are expressed should be considered within the principles of the invention. The specification and drawings should be used to interpret the claims. The claims should not be construed to limit the scope of protection sought to the strict literal language of the words used in the claims, and the description and drawings are used solely for the purpose of resolving ambiguities in the claims. For the purpose of determining the scope of protection sought in the claims, any element that is equivalent to the element indicated in the claims should be considered in full. An element should be considered equivalent to an element specified in the claims, at least if it performs substantially the same function in substantially the same way to produce substantially the same result as the element specified in the claims.