Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Circulation. 2002;106:373-378
Published online before print June 24, 2002, doi: 10.1161/01.CIR.0000021428.94652.04
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
106/3/373    most recent
01.CIR.0000021428.94652.04v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kleinsasser, A.
Right arrow Articles by Loeckinger, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kleinsasser, A.
Right arrow Articles by Loeckinger, A.
Right arrowPubmed/NCBI databases
Medline Plus Health Information
*CPR
Related Collections
Right arrow Animal models of human disease
Right arrow Pulmonary biology and circulation

(Circulation. 2002;106:373.)
© 2002 American Heart Association, Inc.


Basic Science Reports

Decompression-Triggered Positive-Pressure Ventilation During Cardiopulmonary Resuscitation Improves Pulmonary Gas Exchange and Oxygen Uptake

Axel Kleinsasser, MD; Karl H. Lindner, MD; Andreas Schaefer, MD; Alexander Loeckinger, MD

From the Department of Medicine, Division of Physiology, University of California, San Diego (A.K.), and the Department of Anesthesiology and Critical Care Medicine, Leopold-Franzens University, Innsbruck, Austria (K.H.L., A.S., A.L.).

Correspondence to Axel Kleinsasser, MD, Department of Medicine, Division of Physiology, University of California, San Diego, 9500 Gilman Dr, CA 92093-0623A. E-mail akleinsasser{at}ucsd.edu

Background Intermittent positive-pressure ventilation (IPPV) is the "gold standard" of ventilation during cardiopulmonary resuscitation (CPR), but continuous positive airway pressure (CPAP) is increasingly discussed as an alternative. This study investigated hemodynamics and pulmonary gas exchange applying CPAP enhanced with pressure support ventilation (CPAPPSV) during CPR.

Methods and Results Twenty-four pigs were subjected to ventricular fibrillation and CPR with CPAPPSV, CPAP, or IPPV. Measurements were taken before (hemodynamics, blood gases, inert gas measurements) and 10 (hemodynamics, blood gases) and 20 (hemodynamics, blood gases, inert gas measurements) minutes after induction of ventricular fibrillation. Although no significant intergroup differences in hemodynamics were found, arterial partial pressure of oxygen (PaO2) was significantly higher during CPAPPSV compared with CPAP or IPPV (98±10, 61±27, and 71±30 mm Hg, respectively, P<0.05). CPAPPSV resulted in an alveolar-arterial partial pressure of oxygen difference of 56±17 mm Hg, whereas during CPAP, 83±21 mm Hg was detected, and during IPPV, 98±29 mm Hg was detected (P<0.05). Pulmonary blood flow to lung units with a normal {image}A/{image} ratio in percent of cardiac output was 76±17% during CPAPPSV, 61±21% during CPAP (P<0.01), and 54±13% during IPPV (P<0.01). Oxygen uptake ({image}O2) was significantly higher during CPAPPSV than with the other ventilation modes (P<0.05) and comparable to the baseline value in intragroup comparison. Return of spontaneous circulation was recorded in 8 of 8 animals in the CPAPPSV group, in 6 of 8 in the CPAP group, and in 3 of 8 in the IPPV group.

Conclusions CPAPPSV provides a straightforward and effective alternative to IPPV or CPAP during CPR that provides significantly higher PaO2 and {image}O2.


Key Words: heart arrest • cardiopulmonary resuscitation • lung • oxygen