Isoflurane but not mechanical ventilation promotes extravascular fluid accumulation during crystafloid volume loading

被引:67
作者
Connolly, CM
Kramer, GC [1 ]
Hahn, RG
Chaisson, NF
Svensén, CH
Kirschner, RA
Hastings, DA
Chinkes, DL
Prough, DS
机构
[1] Univ Texas, Med Branch, Resuscitat Res Lab, Dept Anesthesiol, Galveston, TX 77555 USA
[2] Univ Texas, Med Branch, Dept Physiol, Resuscitat Res Lab, Galveston, TX 77555 USA
关键词
D O I
10.1097/00000542-200303000-00015
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: The combination of isoflurane anesthesia and mechanical ventilation reduces urinary output and promotes redistribution of a crystalloid bolus into the extravascular space. The authors hypothesized that mechanical ventilation rather than isoflurane causes this alteration. Methods. The fate of a 25-ml/kg, 20-min, 0.9% saline fluid bolus was studied in four different experiments per sheep: while conscious and spontaneously ventilating (CSV), while conscious and mechanically ventilated (CMV), while anesthetized with isoflurane and mechanical ventilated (ISOMV), and while anesthetized with isoflurane and spontaneously ventilating (ISOSV). Results: By calculations based on the indicator dilution and mass balance principles, plasma expansion was similar between protocols. Isoflurane but not mechanical ventilation reduced urinary output and increased interstitial fluid volume (P < 0.001): At 180 min, mean total urinary outputs were 15.6 +/- 2.1 and 15.9 +/- 2.9 ml/kg in the CSV and CMV protocols and 2.7 +/- 0.6 and 3.1 +/- 1.1 ml/kg in the ISOSV and ISOMV protocols, respectively. The net changes in extravascular volume, assumed to be interstitial fluid volume, were 8.6 +/- 3.3 and 8.1 +/- 3.1 ml/kg, and 22.5 +/- 1.5 and 22.1 +/- 1.6 ml/kg in the corresponding protocols. Volume kinetic analysis demonstrated extravascular fluid accumulation associated with isoflurane anesthesia similar to the calculated interstitial accumulation of 20.2 +/- 0.5 and 26.5 +/- 0.3 ml/kg in the ISOSV and ISOMV protocols, respectively. Conclusion: Isoflurane, but not mechanical ventilation, decreased urinary excretion and increased interstitial fluid volume. Volume kinetic analysis indicated "third-space" losses due to isoflurane. Perioperative fluid retention may be associated not only with surgical tissue manipulation, but with anesthesia per se.
引用
收藏
页码:670 / 681
页数:12
相关论文
共 39 条
[1]   Effects of pH on vascular tension: Which are the important mechanisms? [J].
Aalkjaer, C ;
Poston, L .
JOURNAL OF VASCULAR RESEARCH, 1996, 33 (05) :347-359
[2]   PROPOFOL VS ISOFLURANE - ENDOCRINE STRESS-RESPONSE, HEMODYNAMIC REACTION, AND RECOVERY AFTER TOTAL INTRAVENOUS AND INHALATION ANESTHESIA [J].
ADAMS, HA ;
SCHMITZ, CS ;
BALTESGOTZ, B .
ANAESTHESIST, 1994, 43 (11) :730-737
[3]   Isoflurane alters the recirculatory pharmacokinetics of physiologic markers [J].
Avram, MJ ;
Krejcie, TC ;
Niemann, CU ;
Enders-Klein, C ;
Shanks, CA ;
Henthorn, TK .
ANESTHESIOLOGY, 2000, 92 (06) :1757-1768
[4]   Chronic cocaine administration reversibly increases isoflurane minimum alveolar concentration in sheep [J].
Bernards, CM ;
Kern, C ;
Cullen, BF .
ANESTHESIOLOGY, 1996, 85 (01) :91-95
[5]   Volume kinetic analysis of the distribution of 0.9% saline in conscious versus isoflurane-anesthetized sheep [J].
Brauer, KI ;
Svensén, C ;
Hahn, RG ;
Traber, LD ;
Prough, DS .
ANESTHESIOLOGY, 2002, 96 (02) :442-449
[6]   General anesthetic techniques in ruminants [J].
Carroll, GL ;
Hartsfield, SM .
VETERINARY CLINICS OF NORTH AMERICA-FOOD ANIMAL PRACTICE, 1996, 12 (03) :627-+
[7]   RELEASE OF ATRIAL-NATRIURETIC-FACTOR [J].
CHRISTENSEN, G .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1993, 53 (02) :91-100
[8]   ANESTHESIA AND THE KIDNEY [J].
COUSINS, MJ ;
SKOWRONSKI, G ;
PLUMMER, JL .
ANAESTHESIA AND INTENSIVE CARE, 1983, 11 (04) :292-320
[9]   INSENSIBLE WATER-LOSS AND ITS ASSESSMENT IN ADULT PATIENTS - A REVIEW [J].
COX, P .
ACTA ANAESTHESIOLOGICA SCANDINAVICA, 1987, 31 (08) :771-776
[10]   RESPONSE OF SERUM INTERLEUKIN-6 IN PATIENTS UNDERGOING ELECTIVE SURGERY OF VARYING SEVERITY [J].
CRUICKSHANK, AM ;
FRASER, WD ;
BURNS, HJG ;
VANDAMME, J ;
SHENKIN, A .
CLINICAL SCIENCE, 1990, 79 (02) :161-165