Method to improve oxygenation in subjects suffering impaired oxygenation

• US 6,694,969 B1
• Filed: 09/22/2000
• Issued: 02/24/2004
• Est. Priority Date: 09/22/1999
• Status: Expired due to Fees

• Current Assignee: Instrumentarium Dental Incorporated (Envista Holdings Corporation)
• Original Assignee: Instrumentarium Dental Incorporated (Envista Holdings Corporation)
• Inventors: Meriläinen, Pekka, Nyman, Görel, Högman, Marieann, Heinonen, Erkki
• Primary Examiner(s): Lewis, Aaron J.
• Application Number:
  US09/668,625
• Time in Patent Office: 1,250 Days
• Field of Search: 128/200.24, 128/203.12, 128/204.23
• US Class Current: 128/200.24
• CPC Class Codes: A61M 16/0081 Bag or bellow in a bottle
• CPC Class Codes: A61M 16/0677 Gas-saving devices therefor
• CPC Class Codes: A61M 16/12 by mixing different gases
• CPC Class Codes: A61M 16/22 Carbon dioxide-absorbing devices ; Other means for removing carbon dioxidecartridges with absorbing substances for respiratory apparatus A62B19/00
• CPC Class Codes: A61M 2016/0024 with an on-off output signal, e.g. from a switch
• CPC Class Codes: A61M 2202/0275 Nitric oxide [NO]

Abstract

A method for improving oxygenation in subjects having essentially healthy lungs, as evidenced by the absence of a diagnosis of lung disease or injury, but having reduced alveolar gas exchange area. This reduction may be caused by such acute circumstances as an unnatural body position, or may be, for example, chronic as caused by obesity. The method employs the administration of nitric oxide (NO) into the breathing gases of such subjects. NO provided to alveoli collapsing during expiration is small compared to those remaining open, thereby to provide net reduction in the shunt and thus an oxygenation improvement. This result may be gained either by precise control of the inspired NO concentration or by pulsed administration of the NO.

Claims

1. A method for improving oxygenation and reducing shunt perfusion in a lung of a subject, the lung having no diagnosis of injury, in which a first portion of alveoli of the lung are collapsed by compression from body organs during an expiratory phase of a respiratory cycle and during the initial portions of an inspiratory phase and are open in the terminal portions of the inspiratory phase, the lungs having a second portion of alveoli that are open during both the inspiratory and expiratory phases of the respiratory cycle, said method comprising the step of:

during inspiration of breathing gases by the subject, (a) delivering NO gas to the second portion of alveoli in an amount to cause vasodilatation of capillaries associated with such alveoli to improve blood oxygenation (b) while minimizing delivery of NO gas to the first portion of alveoli to an amount below that causing vasodilatation of capillaries associated with the first portion of alveoli to avoid increasing shunt perfusion in the lungs.

2. The method according to claim 1 wherein the step of the method is further defined as delivering the NO gas in a pulse dose in the inspired breathing gases of the subject and wherein at least one of the timing and duration of the pulse doses is controlled to achieve the desired delivery of the NO gas.

5. The method according to claim 1 wherein the step of the method is further defined as controlling the concentration of the NO gas in the breathing gases of the subject to a level, which when inhaled, will achieve the desired provision of the NO gas to the second and first alveolar portions of the lung.

6. The method according to claim 5 wherein the step of the method is further defined as continuously delivering NO gas into the breathing gases of the subject.

7. The method according to claim 6 wherein the step of the method is further defined as controlling the delivery rate of NO gas into the breathing gases of the subject.

8. The method according to claim 1 further defined as comprising the step of measuring the subject'"'"'s alveolar-arterial oxygen partial pressure difference and as delivering NO gas when the alveolar-arterial oxygen partial pressure difference is above a predetermined threshold.

9. The method according to claim 8 further defined as delivering NO gas when the partial pressure difference is greater than 20 kPa.

10. The method according to claim 1 further defined as including the step of measuring the subject'"'"'s arterial oxygen partial pressure and as delivering NO gas when the partial pressure is less than a predetermined threshold.

11. The method according to claim 10 further defined as delivering NO gas when the subject'"'"'s arterial oxygen partial pressure is less than 10 kPa.

12. The method according to claim 1 wherein the method is further defined as carried out on an equine subject in a supine position.

13. The method according to claim 1 wherein the method is further defined as carried out on an obese human subject whose obesity reduces the functional residual capacity of the lungs of the subject.

3. The method according to claim 3 wherein the step of the method is further defined as delivering the pulse dose during the first 70% of the time during which the subject is inspiring.

4. The method according to claim 3 wherein the step of the method is further defined as delivering the pulse dose during the first half of the time the subject is inspiring.