Subcutaneous oxygen tension: A useful adjunct in assessment of perfusion status

OBJECTIVESUsing a new fluorescence-quenching optode which, unlike earlier oximeters, neither consumes oxygen nor generates heat, we sought to determine the effects of hemorrhage and resuscitation on subcutaneous PO2. Additionally, we compared the effects of resuscitation with diaspirin crosslinked h...

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Published in:Critical care medicine Vol. 23; no. 5; pp. 867 - 873
Main Authors: Powell, Craig C, Schultz, Scot C, Burris, David G, Drucker, William R, Malcolm, Diana S
Format: Journal Article
Language:English
Published: Hagerstown, MD Williams & Wilkins 01-05-1995
Lippincott
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Abstract OBJECTIVESUsing a new fluorescence-quenching optode which, unlike earlier oximeters, neither consumes oxygen nor generates heat, we sought to determine the effects of hemorrhage and resuscitation on subcutaneous PO2. Additionally, we compared the effects of resuscitation with diaspirin crosslinked hemoglobin, an oxygen-carrying solution, on subcutaneous PO2 to that of traditional resuscitative fluids. We also compared mean arterial pressure and central venous oxygen saturation, indirect indices of perfusion, to subcutaneous PO2, a direct index of perfusion. DESIGNProspective trial, randomized for selection of treatment regimen. SETTINGShock-trauma laboratory of a medical university. SUBJECTSMale Sprague-Dawley rats, weighing 260 to 380 g. INTERVENTIONSRats were bled 22 mL/kg and resuscitated, 1 min later, with either 66 mL/kg of lactated Ringer's solution, 22 mL/kg of human serum albumin, 22 mL/kg of blood, or 22 mL/kg of diaspirin crosslinked hemoglobin. A fifth group of animals was not resuscitated after hemorrhage. Subcutaneous PO2 and mean arterial pressure were monitored continuously throughout the experiment, while central venous oxygen saturation was measured intermittently. MEASUREMENTS AND MAIN RESULTSSubcutaneous PO2 decreased in response to hemorrhage and, although it did increase after resuscitation with each fluid, no treatment was able to restore subcutaneous PO2 to baseline within 2 hrs postresuscitation. Subcutaneous PO2 continued to decrease after hemorrhage in the unresuscitated animals. In contrast, mean arterial pressure was restored to baseline values in only blood- and diaspirin crosslinked hemoglobin-treated animals, although this effect was lost within 30 mins in the blood-treated group. Only blood restored the central venous oxygen saturation to baseline values in the early postresuscitation period. CONCLUSIONSThe fluorescence-quenching optode consistently followed changes in subcutaneous PO2 during hemorrhage and after resuscitation. Diaspirin crosslinked hemoglobin performed as well as blood in restoring peripheral perfusion, as measured by subcutaneous PO2, while both of these fluids were superior to either lactated Ringer's solution or albumin. Both whole blood and diaspirin crosslinked hemoglobin restored mean arterial pressure to baseline, although the effect of the latter was of a longer duration. The pressor effect of the crosslinked hemoglobin did not affect peripheral perfusion, as reflected by the values for subcutaneous PO2. Subcutaneous PO2 is a useful adjunct in assessment of the adequacy of peripheral perfusion and may help redefine targets for resuscitation.(Crit Care Med 1995; 23:867-873)
AbstractList OBJECTIVESUsing a new fluorescence-quenching optode which, unlike earlier oximeters, neither consumes oxygen nor generates heat, we sought to determine the effects of hemorrhage and resuscitation on subcutaneous PO2. Additionally, we compared the effects of resuscitation with diaspirin crosslinked hemoglobin, an oxygen-carrying solution, on subcutaneous PO2 to that of traditional resuscitative fluids. We also compared mean arterial pressure and central venous oxygen saturation, indirect indices of perfusion, to subcutaneous PO2, a direct index of perfusion.DESIGNProspective trial, randomized for selection of treatment regimen.SETTINGShock-trauma laboratory of a medical university.SUBJECTSMale Sprague-Dawley rats, weighing 260 to 380 g.INTERVENTIONSRats were bled 22 mL/kg and resuscitated, 1 min later, with either 66 mL/kg of lactated Ringer's solution, 22 mL/kg of human serum albumin, 22 mL/kg of blood, or 22 mL/kg of diaspirin crosslinked hemoglobin. A fifth group of animals was not resuscitated after hemorrhage. Subcutaneous PO2 and mean arterial pressure were monitored continuously throughout the experiment, while central venous oxygen saturation was measured intermittently.MEASUREMENTS AND MAIN RESULTSSubcutaneous PO2 decreased in response to hemorrhage and, although it did increase after resuscitation with each fluid, no treatment was able to restore subcutaneous PO2 to baseline within 2 hrs postresuscitation. Subcutaneous PO2 continued to decrease after hemorrhage in the unresuscitated animals. In contrast, mean arterial pressure was restored to baseline values in only blood- and diaspirin crosslinked hemoglobin-treated animals, although this effect was lost within 30 mins in the blood-treated group. Only blood restored the central venous oxygen saturation to baseline values in the early postresuscitation period.CONCLUSIONSThe fluorescence-quenching optode consistently followed changes in subcutaneous PO2 during hemorrhage and after resuscitation. Diaspirin crosslinked hemoglobin performed as well as blood in restoring peripheral perfusion, as measured by subcutaneous PO2, while both of these fluids were superior to either lactated Ringer's solution or albumin. Both whole blood and diaspirin crosslinked hemoglobin restored mean arterial pressure to baseline, although the effect of the latter was of a longer duration. The pressor effect of the crosslinked hemoglobin did not affect peripheral perfusion, as reflected by the values for subcutaneous PO2. Subcutaneous PO2 is a useful adjunct in assessment of the adequacy of peripheral perfusion and may help redefine targets for resuscitation.
Using a new fluorescence-quenching optode which, unlike earlier oximeters, neither consumes oxygen nor generates heat, we sought to determine the effects of hemorrhage and resuscitation on subcutaneous PO2. Additionally, we compared the effects of resuscitation with diaspirin crosslinked hemoglobin, an oxygen-carrying solution, on subcutaneous PO2 to that of traditional resuscitative fluids. We also compared mean arterial pressure and central venous oxygen saturation, indirect indices of perfusion, to subcutaneous PO2, a direct index of perfusion. Prospective trial, randomized for selection of treatment regimen. Shock-trauma laboratory of a medical university. Male Sprague-Dawley rats, weighing 260 to 380 g. Rats were bled 22 mL/kg and resuscitated, 1 min later, with either 66 mL/kg of lactated Ringer's solution, 22 mL/kg of human serum albumin, 22 mL/kg of blood, or 22 mL/kg of diaspirin crosslinked hemoglobin. A fifth group of animals was not resuscitated after hemorrhage. Subcutaneous PO2 and mean arterial pressure were monitored continuously throughout the experiment, while central venous oxygen saturation was measured intermittently. Subcutaneous PO2 decreased in response to hemorrhage and, although it did increase after resuscitation with each fluid, no treatment was able to restore subcutaneous PO2 to baseline within 2 hrs postresuscitation. Subcutaneous PO2 continued to decrease after hemorrhage in the unresuscitated animals. In contrast, mean arterial pressure was restored to baseline values in only blood- and diaspirin crosslinked hemoglobin-treated animals, although this effect was lost within 30 mins in the blood-treated group. Only blood restored the central venous oxygen saturation to baseline values in the early postresuscitation period. The fluorescence-quenching optode consistently followed changes in subcutaneous PO2 during hemorrhage and after resuscitation. Diaspirin crosslinked hemoglobin performed as well as blood in restoring peripheral perfusion, as measured by subcutaneous PO2, while both of these fluids were superior to either lactated Ringer's solution or albumin. Both whole blood and diaspirin crosslinked hemoglobin restored mean arterial pressure to baseline, although the effect of the latter was of a longer duration. The pressor effect of the crosslinked hemoglobin did not affect peripheral perfusion, as reflected by the values for subcutaneous PO2. Subcutaneous PO2 is a useful adjunct in assessment of the adequacy of peripheral perfusion and may help redefine targets for resuscitation.
OBJECTIVESUsing a new fluorescence-quenching optode which, unlike earlier oximeters, neither consumes oxygen nor generates heat, we sought to determine the effects of hemorrhage and resuscitation on subcutaneous PO2. Additionally, we compared the effects of resuscitation with diaspirin crosslinked hemoglobin, an oxygen-carrying solution, on subcutaneous PO2 to that of traditional resuscitative fluids. We also compared mean arterial pressure and central venous oxygen saturation, indirect indices of perfusion, to subcutaneous PO2, a direct index of perfusion. DESIGNProspective trial, randomized for selection of treatment regimen. SETTINGShock-trauma laboratory of a medical university. SUBJECTSMale Sprague-Dawley rats, weighing 260 to 380 g. INTERVENTIONSRats were bled 22 mL/kg and resuscitated, 1 min later, with either 66 mL/kg of lactated Ringer's solution, 22 mL/kg of human serum albumin, 22 mL/kg of blood, or 22 mL/kg of diaspirin crosslinked hemoglobin. A fifth group of animals was not resuscitated after hemorrhage. Subcutaneous PO2 and mean arterial pressure were monitored continuously throughout the experiment, while central venous oxygen saturation was measured intermittently. MEASUREMENTS AND MAIN RESULTSSubcutaneous PO2 decreased in response to hemorrhage and, although it did increase after resuscitation with each fluid, no treatment was able to restore subcutaneous PO2 to baseline within 2 hrs postresuscitation. Subcutaneous PO2 continued to decrease after hemorrhage in the unresuscitated animals. In contrast, mean arterial pressure was restored to baseline values in only blood- and diaspirin crosslinked hemoglobin-treated animals, although this effect was lost within 30 mins in the blood-treated group. Only blood restored the central venous oxygen saturation to baseline values in the early postresuscitation period. CONCLUSIONSThe fluorescence-quenching optode consistently followed changes in subcutaneous PO2 during hemorrhage and after resuscitation. Diaspirin crosslinked hemoglobin performed as well as blood in restoring peripheral perfusion, as measured by subcutaneous PO2, while both of these fluids were superior to either lactated Ringer's solution or albumin. Both whole blood and diaspirin crosslinked hemoglobin restored mean arterial pressure to baseline, although the effect of the latter was of a longer duration. The pressor effect of the crosslinked hemoglobin did not affect peripheral perfusion, as reflected by the values for subcutaneous PO2. Subcutaneous PO2 is a useful adjunct in assessment of the adequacy of peripheral perfusion and may help redefine targets for resuscitation.(Crit Care Med 1995; 23:867-873)
Author Drucker, William R
Powell, Craig C
Schultz, Scot C
Burris, David G
Malcolm, Diana S
AuthorAffiliation From the Department of Surgery (Drs. Powell, Schultz, Drucker, and Malcolm), Uniformed Services University of the Health Sciences; the Department of Surgery (Drs. Powell and Drucker), the National Naval Medical Center Bethesda, MD; and the Department of Trauma/Critical Care (Dr. Burris), Washington Hospital Center, Washington, DC. Supported, in part, by a grant administered by the Henry M. Jackson Foundation for the Advancement of Military Medicine from Baxter Healthcare (Round Lake, IL); Research Work Unit 63706N.M0095.001.9290 and Research Project 63792N.R1889 from InnerSpace (Irvine, CA); and the Naval Medical Research and Development Command, Department of the Navy. The views expressed in this report are those of the authors and do not necessarily represent the official position of the Department of the Navy, the Department of Defense, or any other governmental department or agency. Address requests for reprints to: Dr. Diana S. Malcolm, Department of Surgery, Uniformed Services Un
AuthorAffiliation_xml – name: From the Department of Surgery (Drs. Powell, Schultz, Drucker, and Malcolm), Uniformed Services University of the Health Sciences; the Department of Surgery (Drs. Powell and Drucker), the National Naval Medical Center Bethesda, MD; and the Department of Trauma/Critical Care (Dr. Burris), Washington Hospital Center, Washington, DC. Supported, in part, by a grant administered by the Henry M. Jackson Foundation for the Advancement of Military Medicine from Baxter Healthcare (Round Lake, IL); Research Work Unit 63706N.M0095.001.9290 and Research Project 63792N.R1889 from InnerSpace (Irvine, CA); and the Naval Medical Research and Development Command, Department of the Navy. The views expressed in this report are those of the authors and do not necessarily represent the official position of the Department of the Navy, the Department of Defense, or any other governmental department or agency. Address requests for reprints to: Dr. Diana S. Malcolm, Department of Surgery, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814
Author_xml – sequence: 1
  givenname: Craig C
  surname: Powell
  fullname: Powell, Craig C
  organization: From the Department of Surgery (Drs. Powell, Schultz, Drucker, and Malcolm), Uniformed Services University of the Health Sciences; the Department of Surgery (Drs. Powell and Drucker), the National Naval Medical Center Bethesda, MD; and the Department of Trauma/Critical Care (Dr. Burris), Washington Hospital Center, Washington, DC. Supported, in part, by a grant administered by the Henry M. Jackson Foundation for the Advancement of Military Medicine from Baxter Healthcare (Round Lake, IL); Research Work Unit 63706N.M0095.001.9290 and Research Project 63792N.R1889 from InnerSpace (Irvine, CA); and the Naval Medical Research and Development Command, Department of the Navy. The views expressed in this report are those of the authors and do not necessarily represent the official position of the Department of the Navy, the Department of Defense, or any other governmental department or agency. Address requests for reprints to: Dr. Diana S. Malcolm, Department of Surgery, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814
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  surname: Schultz
  fullname: Schultz, Scot C
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  givenname: Diana S
  surname: Malcolm
  fullname: Malcolm, Diana S
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Keywords Human
Blood gas
Oxymetry
Oxygen
Intensive care
Partial pressure
Surveillance
Perfusion
Hemodynamics
Subcutaneous tissue
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Snippet OBJECTIVESUsing a new fluorescence-quenching optode which, unlike earlier oximeters, neither consumes oxygen nor generates heat, we sought to determine the...
Using a new fluorescence-quenching optode which, unlike earlier oximeters, neither consumes oxygen nor generates heat, we sought to determine the effects of...
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SubjectTerms Analysis of Variance
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Animals
Aspirin - analogs & derivatives
Aspirin - therapeutic use
Biological and medical sciences
Blood Gas Monitoring, Transcutaneous - instrumentation
Blood Gas Monitoring, Transcutaneous - methods
Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care
Evaluation Studies as Topic
Hemoglobins - therapeutic use
Hemorrhage - physiopathology
Hemorrhage - therapy
Intensive care medicine
Male
Medical sciences
Prospective Studies
Random Allocation
Rats
Rats, Sprague-Dawley
Resuscitation - methods
Title Subcutaneous oxygen tension: A useful adjunct in assessment of perfusion status
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https://www.ncbi.nlm.nih.gov/pubmed/7736745
https://search.proquest.com/docview/77255882
Volume 23
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