Aspirator for pneumostoma management

• US 8,348,906 B2
• Filed: 02/18/2009
• Issued: 01/08/2013
• Est. Priority Date: 02/19/2008
• Status: Expired due to Fees

• Current Assignee: Portaero, Inc
• Original Assignee: Portaero, Inc
• Inventors: Tanaka, Don, Wiesman, Joshua P., Plough, David C.
• Primary Examiner(s): Sirmons, Kevin C
• Assistant Examiner(s): Thomas, Jr., Bradley G
• Application Number:
  US12/388,461
• Publication Number:
  US 20090209917A1
• Time in Patent Office: 1,420 Days
• Field of Search: 604/99.04, 604/104, 604/174, 604/275, 604/246, 604/212, 604/180, 604/167.03, 604/319, 604/35, 604/37, 604/118, 604/276, 128/202.28, 128/278, 12820714-20715, 606/108, 606/167
• US Class Current: 604/212
• CPC Class Codes: A61B 2017/00809 Lung operations
• CPC Class Codes: A61K 9/007 Pulmonary tract; Aromatherapy
• CPC Class Codes: A61M 1/04 Artificial pneumothorax apparatus
• CPC Class Codes: A61M 11/00 Sprayers or atomisers specially adapted for therapeutic purposes in general B05B; aerosol containers B65D83/14
• CPC Class Codes: A61M 11/005 using ultrasonics spraying or atomising liquids using ultrasonic vibrations in general B05B17/06
• CPC Class Codes: A61M 11/042 electrical
• CPC Class Codes: A61M 13/00 Insufflators for therapeutic or disinfectant purposes , i.e. devices for blowing a gas, powder or vapour into the body hand-held units in which gas flow is produced by muscular energy at the moment of use B05B11/062
• CPC Class Codes: A61M 15/0085 using ultrasonics spraying or atomising liquids using ultrasonic vibrations in general B05B17/06
• CPC Class Codes: A61M 15/009 using medicine packages with incorporated spraying means, e.g. aerosol cans pocket atomiser of the injector type A61M11/08
• CPC Class Codes: A61M 15/02 with activated or ionised fluids, e.g. electrohydrodynamic [EHD] or electrostatic devices; Ozone-inhalators with radioactive tagged particles
• CPC Class Codes: A61M 16/0816 Joints or connectors
• CPC Class Codes: A61M 16/0833 T- or Y-type connectors, e.g. Y-piece
• CPC Class Codes: A61M 16/202 electrically actuated
• CPC Class Codes: A61M 2039/0252 for access to the lungs
• CPC Class Codes: A61M 2039/0276 for introducing or removing fluids into or out of the body
• CPC Class Codes: A61M 2202/0208 Oxygen
• CPC Class Codes: A61M 2202/025 Helium
• CPC Class Codes: A61M 2202/064 Powder
• CPC Class Codes: A61M 2205/075 Bulb type
• CPC Class Codes: A61M 2205/7518 bacterial
• CPC Class Codes: A61M 2205/7536 : allowing gas passage, but preventing liquid passage, e.g. liquophobic, hydrophobic, water-repellent membranes
• CPC Class Codes: A61M 25/02 : Holding devices, e.g. on the body
• CPC Class Codes: A61M 25/04 : in the body, e.g. expansible A61M25/10, A61M16/0488 take precedence
• CPC Class Codes: A61M 25/10 : Balloon catheters A61M25/0125 takes precedence; embolectomy A61B17/22032; retractors A61B17/02; inflatable balloons for placing stents or stent-grafts A61F2/958 ; stomach balloons for treatment of obesity A61F5/0003; oesophagal tubes A61J15/00
• CPC Class Codes: A61M 27/00 : Drainage appliance for wounds or the like , i.e. wound drains, implanted drains negative pressure wound therapy devices A61M1/90; implements for holding wound open A61B17/02 ; middle ear drainage A61F11/202
• CPC Class Codes: A61M 39/02 : Access sites
• CPC Class Codes: A61M 39/0247 : Semi-permanent or permanent transcutaneous or percutaneous access sites to the inside of the body peritoneal dialysis catheters A61M1/285; tracheostomy devices A61M16/0465; measuring pressure within the body A61B5/03; colostomy devices A61F5/445; gastrotomy feeding tubes A61J15/0015; means for fixing a feeding tube outside of the body A61J15/0053

Abstract

A pneumostoma management system includes a pneumostoma management device for maintaining the patency of a pneumostoma while controlling the flow of material through the pneumostoma and a pneumostoma aspirator for pneumostoma care. The pneumostoma aspirator includes a bulb or syringe for applying positive or negative pressure, a tube for entering the pneumostoma and a limiting device for limiting the depth of insertion of the tube into a pneumostoma. The pneumostoma aspirator may also be used to introduce irrigation fluid into the pneumostoma and/or remove irrigation fluid and discharge from the pneumostoma.

Claims

1. A device for treating a pneumostoma which comprises a surgically-created aperture which passes through a chest wall of a patient and into a lung of a patient without communicating with a pleural cavity of the patient and which enables gases to exit the lung through the chest wall of the patient, the device comprising:

a tube shaped for insertion into the pneumostoma, the tube having sufficient length that upon insertion into the pneumostoma, a proximal end of the tube is positioned exterior to a patient and a distal end of the tube is positioned within the lung of the patient;

an aperture adjacent the distal end of the tube, the aperture sized and positioned to allow ingress of liquid and solid discharge from a lung;

a lumen passing from the aperture to the proximal end of the tube;

a flange projecting from the proximal end of the tube, the flange sized to prevent passage of the flange into the pneumostoma and thereby limit insertion of the tube into the lung; and

a suction device connected to the proximal end of the tube such that, with the tube positioned in a pneumostoma and the flange positioned against the chest wall of the patient, actuation of the suction device applies negative pressure to the lumen at the proximal end of the tube and draws liquid and solid discharge from the lung into the lumen through the aperture adjacent the distal end of the tube.

2. The device of claim 1, wherein the suction device is a manually-actuated suction device.

3. The device of claim 2, wherein the suction device comprises an elastic bulb, such that, with the tube positioned in a pneumostoma and the flange positioned against the chest wall of the patient, the elastic bulb can be manually compressed and released, whereupon the elastic bulb expands and applies negative pressure to the lumen at the proximal end of the tube and draws liquid and solid discharge from the lung into the lumen through the aperture adjacent the distal end of the tube.

4. The device of claim 3, wherein a one-way valve is positioned through a surface of said elastic bulb such that, when the elastic bulb is manually compressed, gases within the elastic bulb are ejected exterior to the patient.

5. The device of claim 4, wherein a one-way valve is positioned between the lumen and the elastic bulb such that, when the elastic bulb is manually compressed, gases within the elastic bulb are prevented from entering the lumen of the tube.

6. The device of claim 5, wherein the tube, the flange and the elastic bulb are permanently connected.

7. The device of claim 6, wherein the tube, the flange, and the bulb are formed in one piece.

8. The device of claim 2, wherein the suction device comprises a syringe having a barrel and a plunger such that, with the tube positioned in a pneumostoma and the flange positioned against the chest wall of the patient, drawing the plunger distally within said barrel applies negative pressure to the lumen at the proximal end of the tube and draws liquid and solid discharge from the lung into the lumen through the aperture adjacent the distal end of the tube.

9. The device of claim 2, further comprising a safety device which limits the negative pressure applied to the lumen by the suction device.

10. The device of claim 2, wherein:

the flange and the tube are permanently connected;

the flange comprises a biocompatible adhesive positioned to releasably secure the flange to the chest wall of the patient;

and wherein the suction device further comprises a releasable coupling which releasably connects the suction device to the proximal end of the tube.

11. The device of claim 1 wherein the suction device comprises a battery-operated device including a motor coupled to one of a fan and a pump such that, with the tube positioned in a pneumostoma and the flange positioned against the chest wall of the patient, operation of the motor applies negative pressure to the proximal end of the tube and draws liquid and solid discharge from the lung into the lumen through the aperture adjacent the distal end of the tube.

12. A medical device for treating a pneumostoma which comprises a surgically-created aperture which passes through a chest wall of a chest of a patient and into a lung of a patient without communicating with a pleural cavity of the patient and which enables gases to exit the lung through the chest wall of the patient, the medical device comprising:

a flange sized and configured such that the flange cannot be inserted into the pneumostoma, the flange positioned to engage the chest of the patient;

a tube projecting from the flange, the tube configured such that, with the flange engaging the chest of the patient, the tube is positioned in the pneumostoma such that a proximal end of the tube is external to the patient and a distal end of the tube is positioned within the lung of the patient;

a lumen extending along the tube from the proximal end of the tube;

at least one aperture communicating with the lumen, the at least one aperture positioned such that, with the flange engaging the chest of the patient, the at least one aperture is positioned within the lung of the patient; and

a suction device connected to the proximal end of the tube such that, with the at least one aperture positioned within the lung of the patient, actuation of the suction device applies negative pressure to the lumen at the proximal end of the tube and draws liquid and solid discharge from the lung into the lumen through the at least one aperture.

13. The medical device of claim 12, wherein the suction device is a manually-actuated suction device.

14. The device of claim 12, wherein the suction device comprises an elastic bulb such that, with the at least one aperture positioned within the lung of the patient, the elastic bulb can be manually compressed and released whereupon the elastic bulb expands and applies negative pressure to the lumen at the proximal end of the tube and draws liquid and solid discharge from the lung into the lumen through the aperture adjacent the distal end of the tube.

15. The medical device of claim 12, wherein the suction device comprises a one-way valve and an elastic bulb such that, with the at least one aperture positioned within the lung of the patient, the elastic bulb can be manually compressed and released whereupon the elastic bulb expands and applies negative pressure to the lumen at the proximal end of the tube and draws liquid and solid discharge from the lung into the lumen through the aperture adjacent the distal end of the tube.

16. The medical device of claim 12, wherein the tube, the flange and the suction device are permanently connected.

17. The medical device of claim 12, wherein the suction device comprises a syringe having a barrel and a plunger such that, with the at least one aperture positioned within the lung of the patient, drawing the plunger distally within said barrel applies negative pressure to the lumen at the proximal end of the tube and draws liquid and solid discharge from the lung into the lumen through the aperture adjacent the distal end of the tube.

18. The device of claim 12, further comprising a safety device which limits the negative pressure applied to the lumen by the suction device.

19. The device of claim 12, wherein:

the flange and the tube are permanently connected;

the flange comprises a biocompatible adhesive positioned to releasably secure the flange to the chest wall of the patient;

and wherein the suction device further comprises a releasable coupling which releasably connects the suction device to the proximal end of the tube.

20. The device of claim 12, wherein the suction device comprises a battery-operated device including a motor coupled to one of a fan and a pump such that, with the at least one aperture positioned within the lung of the patient, operation of the motor applies negative pressure to the proximal end of the tube and draws liquid and solid discharge from the lung into the lumen through the aperture adjacent the distal end of the tube.

21. A system for treating a pneumostoma which comprises a surgically-created aperture which passes through a chest wall of a chest of a patient and into a lung of a patient without communicating with a pleural cavity of the patient and which enables gases to exit the lung through the chest wall of the patient, the system comprising:

a pneumostoma management device which includes,

a flange sized and configured such that the flange cannot be inserted in the pneumostoma, the flange positioned to engage the chest of the patient,

a tube projecting from the flange, the tube configured such that, with the flange engaging the chest of the patient, the tube is positioned in the pneumostoma such that a proximal end of the tube is external to the patient and a distal end of the tube is positioned within the lung of the patient,

a lumen extending along the tube from the proximal end of the tube, and

an aperture communicating with the lumen, the aperture positioned such that, with the flange engaging the chest of the patient, the aperture is positioned within the lung of the patient; and

a pneumostoma aspirator which includes,

a coupling configured to releasably secure the pneumostoma aspirator to the pneumostoma management device; and

a suction device connected to coupling such that, with the aperture positioned within the lung of the patient and the coupling releasably secured to the pneumostoma management device, actuation of the suction device applies negative pressure to the lumen at the proximal end of the tube and draws liquid and solid discharge from the lung into the lumen through the aperture.

22. The pneumostoma management system of claim 21, wherein the coupling is configured to releasably secure the pneumostoma aspirator directly to the flange of the pneumostoma management device.

23. The pneumostoma management system of claim 21, wherein the coupling is configured to releasably secure the pneumostoma aspirator directly to the tube of the pneumostoma management device.

24. The pneumostoma management system of claim 21, wherein the coupling has a self-seating and centering section which can mate with at least one of the of the tube and the flange of the pneumostoma management device.

25. The pneumostoma management system of claim 21, wherein the pneumostoma aspirator can self-seat against at least one of the tube and the flange of the pneumostoma management device.