Caminos Eguillor Juan Francisco, Ferrara Gonzalo, Kanoore Edul Vanina Siham, Buscetti María Guillermina, Canales Héctor Saúl, Lattanzio Bernardo, Gatti Luis, Gutierrez Facundo Javier, Dubin Arnaldo
Facultad de Ciencias Médicas, Universidad Nacional de La Plata, Cátedras de Farmacología Aplicada y Terapia Intensiva, 60 y 120, 1900 La Plata, Argentina.
Facultad de Ciencias Médicas, Universidad Nacional de La Plata, Cátedras de Farmacología Aplicada y Terapia Intensiva, 60 y 120, 1900 La Plata, Argentina.
Microvasc Res. 2023 May;147:104490. doi: 10.1016/j.mvr.2023.104490. Epub 2023 Jan 31.
Rewarming is a recommended therapy during the resuscitation of hypothermic patients with hemorrhagic shock. In experimental models, however, it increases inflammatory response and mortality. Although microcirculation is potential target of inflammation, the microvascular effects of rewarming during the resuscitation of hemorrhagic shock have not been studied. Our goal was to assess the systemic and microcirculatory effects of an increase in core temperature (T°) during the retransfusion of hemorrhagic shock in sheep. Our hypothesis was that rewarming could hamper microcirculation.
In anesthetized and mechanically ventilated sheep, we measured systemic, intestinal, and renal hemodynamics and oxygen transport. O consumption (VO) and respiratory quotient were measured by indirect calorimetry. Cortical renal, intestinal villi and sublingual microcirculation were assessed by IDF-videomicroscopy. After basal measurements, hemorrhagic shock was induced and T° was reduced to ~33 °C. After 1 h of shock and hypothermia, blood was retransfused and Ringer lactate solution was administered to prevent arterial hypotension. In the control group (n = 12), T° was not modified, while in the intervention (rewarming) group, it was elevated ~3 °C. Measurements were repeated after 1 h.
During shock, both groups showed similar systemic and microvascular derangements. After retransfusion, VO remained decreased compared to baseline in both groups, but was lower in the control compared to the rewarming group. Perfused vascular density has a similar behavior in both groups. Compared to baseline, it remained reduced in peritubular (control vs. rewarming group, 13.8 [8.7-17.5] vs. 15.7 [10.1-17.9] mm/mm, PNS) and villi capillaries (14.7 [13.6-16.8] vs. 16.3 [14.2-16.9] mm/mm, PNS), and normalized in sublingual mucosa (19.1 [16.0-20.3] vs. 16.6 [14.7-17.2] mm/mm, PNS).
This is the first experimental study assessing the effect of rewarming on systemic, regional, and microcirculatory perfusion in hypothermic hemorrhagic shock. We found that a 3 °C increase in T° neither improved nor impaired the microvascular alterations that persisted after retransfusion. In addition, sublingual mucosa was less susceptible to reperfusion injury than villi and renal microcirculation.
复温是失血性休克低温患者复苏过程中的推荐治疗方法。然而,在实验模型中,复温会增加炎症反应和死亡率。尽管微循环是炎症的潜在靶点,但失血性休克复苏过程中复温对微血管的影响尚未得到研究。我们的目标是评估绵羊失血性休克再输血过程中核心温度(T°)升高对全身和微循环的影响。我们的假设是复温可能会阻碍微循环。
在麻醉并机械通气的绵羊中,我们测量了全身、肠道和肾脏的血流动力学以及氧输送。通过间接测热法测量氧耗(VO)和呼吸商。通过IDF视频显微镜评估肾皮质、肠绒毛和舌下微循环。在进行基础测量后,诱导失血性休克并将T°降至约33°C。休克和低温1小时后,进行输血并给予乳酸林格液以防止动脉低血压。在对照组(n = 12)中,T°未改变,而在干预(复温)组中,T°升高约3°C。1小时后重复测量。
在休克期间,两组均表现出相似的全身和微血管紊乱。输血后,两组的VO均较基线水平降低,但对照组低于复温组。两组的灌注血管密度表现相似。与基线相比,肾小管周围(对照组与复温组,13.8 [8.7 - 17.5] vs. 15.7 [10.1 - 17.9] mm/mm,PNS)和绒毛毛细血管(14.7 [13.6 - 16.8] vs. 16.3 [14.2 - 16.9] mm/mm,PNS)的灌注血管密度仍降低,而舌下黏膜的灌注血管密度恢复正常(19.1 [16.0 - 20.3] vs. 16.6 [14.7 - 17.2] mm/mm,PNS)。
这是第一项评估复温对低温失血性休克全身、局部和微循环灌注影响的实验研究。我们发现T°升高3°C既未改善也未损害输血后持续存在的微血管改变。此外,舌下黏膜比绒毛和肾脏微循环对再灌注损伤的敏感性更低。