Boldt J, Mueller M, Menges T, Papsdorf M, Hempelmann G
Department of Anaesthesiology and Intensive Care Medicine, Justus-Liebig-University Giessen, Germany.
Br J Anaesth. 1996 Oct;77(4):480-7. doi: 10.1093/bja/77.4.480.
Various vasoactive substances are involved in the regulation of the macro- and microcirculation. We have investigated if these regulators change during long-term volume therapy with human albumin (HA) or hydroxyethylstarch solution (HES) in trauma and sepsis patients. To maintain pulmonary capillary wedge pressure (PCWP) at 10-15 mm Hg, either 20% HA (HA-trauma, n = 14; HA-sepsis, n = 14) or 10% low-molecular weight HES solution (HES-trauma, n = 14; HES-sepsis, n = 14) were infused for 5 days, otherwise patient management did not differ between the two groups (trauma/sepsis). Mean arterial pressure (MAP), heart rate (HR), PCWP and cardiac index (CI) were monitored in all patients. Liver function was assessed using the monoethylglycinexylidide (MEGX) test, and gastric intramucosal pH (pHi) was monitored by tonometry to assess splanchnic perfusion. Plasma concentrations of vasopressin, endothelin-1, adrenaline, noradrenaline, atrial natriuretic peptide and 6-keto-prostaglandin F1 alpha were measured from arterial blood samples. All measurements were carried out on the day of admission to the intensive care unit (trauma patients) or on diagnosis of sepsis, and daily over the next 5 days at 12:00. MAP, HR and PCWP did not differ between the corresponding subgroups (trauma/sepsis). Cl increased significantly more in the HES than in the HA groups. pHi and MEGX plasma concentrations did not differ in the trauma patients throughout the study. Both were lower than normal in the sepsis groups and increased more markedly in the HES than in the albumin-treated patients (P < 0.05). In the trauma patients, concentrations of all vasoactive regulators were very similar in both groups. In both sepsis groups, vasopressors (vasopressin, endothelin-1, noradrenaline and adrenaline) were significantly increased above normal at baseline and decreased more markedly in HES than in HA patients. Concentrations of atrial natriuretic peptide increased only in the HA patients (from 159 (SD 31) to 215 (38) pg ml-1 on day 2). Plasma concentrations of 6-keto-prostaglandin F1 alpha decreased significantly only in the HES sepsis patients (from 112 (25) to 47 (15) pg ml-1).
多种血管活性物质参与体循环和微循环的调节。我们研究了在创伤和脓毒症患者中,使用人白蛋白(HA)或羟乙基淀粉溶液(HES)进行长期容量治疗期间,这些调节因子是否会发生变化。为了将肺毛细血管楔压(PCWP)维持在10 - 15 mmHg,分别输注20% HA(创伤组HA - trauma,n = 14;脓毒症组HA - sepsis,n = 14)或10%低分子量HES溶液(创伤组HES - trauma,n = 14;脓毒症组HES - sepsis,n = 14),持续5天,除此之外两组(创伤/脓毒症)的患者管理并无差异。监测所有患者的平均动脉压(MAP)、心率(HR)、PCWP和心脏指数(CI)。使用单乙基甘氨酰二甲苯胺(MEGX)试验评估肝功能,并通过张力测定法监测胃黏膜内pH值(pHi)以评估内脏灌注。从动脉血样本中测量血管加压素、内皮素 - 1、肾上腺素、去甲肾上腺素、心房利钠肽和6 - 酮 - 前列腺素F1α的血浆浓度。所有测量均在重症监护病房入院当天(创伤患者)或脓毒症诊断时进行,并在接下来的5天每天12:00进行。相应亚组(创伤/脓毒症)之间的MAP、HR和PCWP无差异。HES组的CI升高幅度明显大于HA组。在整个研究过程中,创伤患者的pHi和MEGX血浆浓度无差异。脓毒症组两者均低于正常水平,且HES组的升高幅度明显大于白蛋白治疗组患者(P < 0.05)。在创伤患者中,两组所有血管活性调节因子的浓度非常相似。在两个脓毒症组中,血管加压药(血管加压素、内皮素 - 1、去甲肾上腺素和肾上腺素)在基线时显著高于正常水平,且HES组的下降幅度明显大于HA组患者。心房利钠肽浓度仅在HA组患者中升高(第2天从159(标准差31)升高至215(38)pg/ml)。仅在HES脓毒症患者中,6 - 酮 - 前列腺素F1α的血浆浓度显著降低(从112(25)降至47(15)pg/ml)。