Hamzaoui Olfa, Goury Antoine, Teboul Jean-Louis
Service de Médecine intensive réanimation polyvalente, Hôpital Robert Debré, CHU de Reims Université de Reims, 51092 Reims, France.
"Hémostase et Remodelage Vasculaire Post-Ischémie"-EA 3801, Unité HERVI, 51100 Reims, France.
J Clin Med. 2023 Jul 10;12(14):4589. doi: 10.3390/jcm12144589.
Septic shock is mainly characterized-in addition to hypovolemia-by vasoplegia as a consequence of a release of inflammatory mediators. Systemic vasodilatation due to depressed vascular tone results in arterial hypotension, which induces or worsens organ hypoperfusion. Accordingly, vasopressor therapy is mandatory to correct hypotension and to reverse organ perfusion due to hypotension. Currently, two vasopressors are recommended to be used, norepinephrine and vasopressin. Norepinephrine, an α-agonist agent, is the first-line vasopressor. Vasopressin is suggested to be added to norepinephrine in cases of inadequate mean arterial pressure instead of escalating the doses of norepinephrine. However, some questions about the bedside use of these vasopressors remain. Some of these questions have been well answered, some of them not clearly addressed, and some others not yet answered. Regarding norepinephrine, we firstly reviewed the arguments in favor of the choice of norepinephrine as a first-line vasopressor. Secondly, we detailed the arguments found in the recent literature in favor of an early introduction of norepinephrine. Thirdly, we reviewed the literature referring to the issue of titrating the doses of norepinephrine using an individualized resuscitation target, and finally, we addressed the issue of escalation of doses in case of refractory shock, a remaining unanswered question. For vasopressin, we reviewed the rationale for adding vasopressin to norepinephrine. Then, we discussed the optimal time for vasopressin administration. Subsequently, we addressed the issue of the optimal vasopressin dose, and finally we discussed the best strategy to wean these two vasopressors when combined.
脓毒性休克的主要特征除血容量不足外,还包括因炎症介质释放导致的血管麻痹。血管张力降低引起的全身血管扩张导致动脉低血压,进而诱发或加重器官灌注不足。因此,必须使用血管升压药来纠正低血压并逆转因低血压导致的器官灌注不足。目前,推荐使用两种血管升压药,去甲肾上腺素和血管加压素。去甲肾上腺素是一种α受体激动剂,是一线血管升压药。在平均动脉压不足的情况下,建议在去甲肾上腺素基础上加用血管加压素,而不是增加去甲肾上腺素的剂量。然而,关于这些血管升压药在床边使用的一些问题仍然存在。其中一些问题已经得到很好的解答,一些问题没有得到明确解决,还有一些问题尚未得到解答。关于去甲肾上腺素,我们首先回顾了支持选择去甲肾上腺素作为一线血管升压药的论据。其次,我们详细阐述了近期文献中支持早期使用去甲肾上腺素的论据。第三,我们回顾了关于使用个体化复苏目标滴定去甲肾上腺素剂量问题的文献,最后,我们讨论了难治性休克时剂量增加的问题,这是一个尚未得到解答的问题。对于血管加压素,我们回顾了在去甲肾上腺素基础上加用血管加压素的基本原理。然后,我们讨论了血管加压素给药的最佳时机。随后,我们讨论了血管加压素的最佳剂量问题,最后我们讨论了联合使用这两种血管升压药时撤药的最佳策略。