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 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
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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) |
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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 – sequence: 2 givenname: Scot C surname: Schultz fullname: Schultz, Scot C – sequence: 3 givenname: David G surname: Burris fullname: Burris, David G – sequence: 4 givenname: William R surname: Drucker fullname: Drucker, William R – sequence: 5 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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References | Hunt (R11-15-20160304) 1987; 11 Schultz (R15-15-20160304) 1993; 35 Hunt (R12-15-20160304) 1967; 18 Schultz (R14-15-20160304) 1993; 122 Chang (R25-15-20160304) 1983; 197 Kandel (R29-15-20160304) 1983; 143 Sheldon (R22-15-20160304) 1983; 94 Benesch (R19-15-20160304) 1973; 55 Hunt (R10-15-20160304) 1972; 135 Kivisaari (R23-15-20160304) 1973; 125 Hamilton (R18-15-20160304) 1992; 20 Gottrup (R5-15-20160304) 1987; 15 Przybelski (R17-15-20160304) 1991; 117 Amberson (R28-15-20160304) 1949; 1 Gosain (R13-15-20160304) 1991; 109 Scalea (R27-15-20160304) 1988; 28 Chang (R7-15-20160304) 1983; 197 Heppenstall (R26-15-20160304) 1974; 75 Nikki (R24-15-20160304) 1972; 4 VanEsbroeck (R4-15-20160304) 1992; 79 Gottrup (R6-15-20160304) 1989; 17 Stephens (R9-15-20160304) 1971; 173 Gys (R3-15-20160304) 1988; 16 Jonsson (R8-15-20160304) 1987; 74 Heymann (R2-15-20160304) 1977; 20 Brantigan (R21-15-20160304) 1974; 37 |
References_xml | – volume: 16 start-page: 1222 year: 1988 ident: R3-15-20160304 publication-title: Crit Care Med doi: 10.1097/00003246-198812000-00009 contributor: fullname: Gys – volume: 11 start-page: 126 year: 1987 ident: R11-15-20160304 publication-title: World J Surg doi: 10.1007/BF01656394 contributor: fullname: Hunt – volume: 20 start-page: 55 year: 1977 ident: R2-15-20160304 publication-title: Prog Cardiovasc Dis doi: 10.1016/S0033-0620(77)80005-4 contributor: fullname: Heymann – volume: 135 start-page: 561 year: 1972 ident: R10-15-20160304 publication-title: Surg Gynecol Obstet contributor: fullname: Hunt – volume: 122 start-page: 301 year: 1993 ident: R14-15-20160304 publication-title: J Lab Clin Med contributor: fullname: Schultz – volume: 17 start-page: 904 year: 1989 ident: R6-15-20160304 publication-title: Crit Care Med doi: 10.1097/00003246-198909000-00013 contributor: fullname: Gottrup – volume: 125 start-page: 623 year: 1973 ident: R23-15-20160304 publication-title: Am J Surg doi: 10.1016/0002-9610(73)90149-9 contributor: fullname: Kivisaari – volume: 197 start-page: 470 year: 1983 ident: R25-15-20160304 publication-title: Ann Surg doi: 10.1097/00000658-198304000-00017 contributor: fullname: Chang – volume: 197 start-page: 470 year: 1983 ident: R7-15-20160304 publication-title: Ann Surg doi: 10.1097/00000658-198304000-00017 contributor: fullname: Chang – volume: 117 start-page: 143 year: 1991 ident: R17-15-20160304 publication-title: J Lab Clin Med contributor: fullname: Przybelski – volume: 55 start-page: 245 year: 1973 ident: R19-15-20160304 publication-title: Anal Biochem doi: 10.1016/0003-2697(73)90309-6 contributor: fullname: Benesch – volume: 74 start-page: 263 year: 1987 ident: R8-15-20160304 publication-title: Br J Surg doi: 10.1002/bjs.1800740413 contributor: fullname: Jonsson – volume: 173 start-page: 515 year: 1971 ident: R9-15-20160304 publication-title: Ann Surg doi: 10.1097/00000658-197104000-00006 contributor: fullname: Stephens – volume: 37 start-page: 117 year: 1974 ident: R21-15-20160304 publication-title: J Appl Physiol doi: 10.1152/jappl.1974.37.1.117 contributor: fullname: Brantigan – volume: 4 start-page: 146 year: 1972 ident: R24-15-20160304 publication-title: Ann Clin Res contributor: fullname: Nikki – volume: 18 start-page: 3 year: 1967 ident: R12-15-20160304 publication-title: Surg Forum contributor: fullname: Hunt – volume: 28 start-page: 725 year: 1988 ident: R27-15-20160304 publication-title: J Trauma doi: 10.1097/00005373-198806000-00001 contributor: fullname: Scalea – volume: 75 start-page: 874 year: 1974 ident: R26-15-20160304 publication-title: Surgery contributor: fullname: Heppenstall – volume: 143 start-page: 1400 year: 1983 ident: R29-15-20160304 publication-title: Arch Intern Med doi: 10.1001/archinte.1983.00350070120019 contributor: fullname: Kandel – volume: 35 start-page: 619 year: 1993 ident: R15-15-20160304 publication-title: J Trauma doi: 10.1097/00005373-199310000-00019 contributor: fullname: Schultz – volume: 79 start-page: 584 year: 1992 ident: R4-15-20160304 publication-title: Br J Surg doi: 10.1002/bjs.1800790640 contributor: fullname: VanEsbroeck – volume: 109 start-page: 523 year: 1991 ident: R13-15-20160304 publication-title: Surgery contributor: fullname: Gosain – volume: 15 start-page: 1030 year: 1987 ident: R5-15-20160304 publication-title: Crit Care Med doi: 10.1097/00003246-198711000-00008 contributor: fullname: Gottrup – volume: 94 start-page: 399 year: 1983 ident: R22-15-20160304 publication-title: Surgery contributor: fullname: Sheldon – volume: 1 start-page: 469 year: 1949 ident: R28-15-20160304 publication-title: J Appl Physiol doi: 10.1152/jappl.1949.1.7.469 contributor: fullname: Amberson – volume: 20 start-page: S106 year: 1992 ident: R18-15-20160304 publication-title: Crit Care Med contributor: fullname: Hamilton |
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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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