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去甲肾上腺素极早期应用于感染性休克患者的效果:一项基于倾向评分的分析。

Effects of very early start of norepinephrine in patients with septic shock: a propensity score-based analysis.

作者信息

Ospina-Tascón Gustavo A, Hernandez Glenn, Alvarez Ingrid, Calderón-Tapia Luis E, Manzano-Nunez Ramiro, Sánchez-Ortiz Alvaro I, Quiñones Egardo, Ruiz-Yucuma Juan E, Aldana José L, Teboul Jean-Louis, Cavalcanti Alexandre Biasi, De Backer Daniel, Bakker Jan

机构信息

Department of Intensive Care Medicine, Fundación Valle del Lili, Universidad Icesi, Cali, Colombia.

Translational Medicine Laboratory in Critical Care and Advanced Trauma Surgery, Fundación Valle del Lili, Universidad Icesi, Cali, Colombia.

出版信息

Crit Care. 2020 Feb 14;24(1):52. doi: 10.1186/s13054-020-2756-3.

Abstract

BACKGROUND

Optimal timing for the start of vasopressors (VP) in septic shock has not been widely studied since it is assumed that fluids must be administered in advance. We sought to evaluate whether a very early start of VP, even without completing the initial fluid loading, might impact clinical outcomes in septic shock.

METHODS

A total of 337 patients with sepsis requiring VP support for at least 6 h were initially selected from a prospectively collected database in a 90-bed mixed-ICU during a 24-month period. They were classified into very-early (VE-VPs) or delayed vasopressor start (D-VPs) categories according to whether norepinephrine was initiated or not within/before the next hour of the first resuscitative fluid load. Then, VE-VPs (n = 93) patients were 1:1 propensity matched to D-VPs (n = 93) based on age; source of admission (emergency room, general wards, intensive care unit); chronic and acute comorbidities; and lactate, heart rate, systolic, and diastolic pressure at vasopressor start. A risk-adjusted Cox proportional hazard model was fitted to assess the association between VE-VPs and day 28 mortality. Finally, a sensitivity analysis was performed also including those patients requiring VP support for less than 6 h.

RESULTS

Patients subjected to VE-VPs received significantly less resuscitation fluids at vasopressor starting (0[0-510] vs. 1500[650-2300] mL, p < 0.001) and during the first 8 h of resuscitation (1100[500-1900] vs. 2600[1600-3800] mL, p < 0.001), with no significant increase in acute renal failure and/or renal replacement therapy requirements. VE-VPs was related with significant lower net fluid balances 8 and 24 h after VPs. VE-VPs was also associated with a significant reduction in the risk of death compared to D-VPs (HR 0.31, CI95% 0.17-0.57, p < 0.001) at day 28. Such association was maintained after including patients receiving vasopressors for < 6 h.

CONCLUSION

A very early start of vasopressor support seems to be safe, might limit the amount of fluids to resuscitate septic shock, and could lead to better clinical outcomes.

摘要

背景

由于假定必须先给予液体治疗,因此脓毒性休克中血管升压药(VP)开始使用的最佳时机尚未得到广泛研究。我们试图评估即使在未完成初始液体负荷的情况下非常早期开始使用VP是否会影响脓毒性休克的临床结局。

方法

在24个月期间,从一家拥有90张床位的混合重症监护病房(ICU)前瞻性收集的数据库中,最初筛选出总共337例需要VP支持至少6小时的脓毒症患者。根据在首次复苏性补液负荷的下一小时内或之前是否开始使用去甲肾上腺素,将他们分为极早期(VE-VP组)或延迟使用血管升压药组(D-VP组)。然后,根据年龄、入院来源(急诊室、普通病房、重症监护病房)、慢性和急性合并症以及开始使用血管升压药时的乳酸、心率、收缩压和舒张压,将VE-VP组(n = 93)患者与D-VP组(n = 93)进行1:1倾向匹配。采用风险调整的Cox比例风险模型评估VE-VP组与28天死亡率之间的关联。最后,进行敏感性分析,纳入那些需要VP支持少于6小时的患者。

结果

VE-VP组患者在开始使用血管升压药时接受的复苏液体显著较少(0[0 - 510] vs. 1500[650 - 2300] mL,p < 0.001),且在复苏的前8小时内接受的液体也显著较少(1100[500 - 1900] vs. 2600[1600 - 3800] mL,p < 0.001),急性肾衰竭和/或肾脏替代治疗需求没有显著增加。VE-VP组在使用血管升压药后8小时和24小时的净液体平衡显著更低。与D-VP组相比,VE-VP组在第28天的死亡风险也显著降低(HR 0.31,CI95% 0.17 - 0.57,p < 0.001)。纳入接受血管升压药治疗<6小时的患者后,这种关联仍然存在。

结论

非常早期开始血管升压药支持似乎是安全的,可能会限制用于复苏脓毒性休克的液体量,并可能带来更好的临床结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e10d/7023737/66bfc2675579/13054_2020_2756_Fig1_HTML.jpg

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