Sepsis & infection

Targeted Tissue Perfusion Versus Macrocirculatory-Guided Standard Care in Patients With Septic Shock: A Randomized Clinical Trial—The TARTARE-2S Trial

Crit Care MedPublished Randomised controlled trial

Primary resultResult — go to the resultDifference in medians 0.59 95% CI −3 to 4

Authors' conclusion

In ICU patients with septic shock and lactate greater than 3 mmol/L, targeting tissue perfusion and allowing lower than recommended MAP did not increase the number of days alive with normal lactate and without vasopressor/inotropic drugs at 30 days.

Study context

Population
ICU patients with septic shock and blood lactate greater than 3 mmol/L194 analysed
Participants
219 patients
Comparison
Targeted tissue perfusion vs mean arterial pressure (MAP)-guided standard care
  • TTPn = 111
  • Standard care (SC)n = 108reference
Primary endpoint
Days alive with normal lactate and without vasopressor/inotropic drugs
Follow-up
30 days
Methodological detailsparallel-group, open-label, stratified allocation (trial site, chronic arterial hypertension), multicentre (3 European university hospital ICUs), Enrollment 2016 to 2022
  • Parallel-group
  • Open-label
  • Stratified allocation (trial site, chronic arterial hypertension)
  • Multicentre (3 European university hospital ICUs)
  • Enrollment 2016 to 2022

Primary result

As reported in the abstract

Difference in medians

0.59

95% CI −3 to 4

By group

TTP vs SC
difference in medians 0.59 (95% CI −3 to 4)

Secondary outcomes

Mortality · day 30

Single components of primary outcome, days alive without organ support, mortality · 30 d

Not significantly different between groups

MAP levels

Lower in TTP vs SC

Safety

Serious adverse reactions

Not significantly different between groups

Original publication

Targeted Tissue Perfusion Versus Macrocirculatory-Guided Standard Care in Patients With Septic Shock: A Randomized Clinical Trial—The TARTARE-2S Trial. Crit Care Med. Published 17 October 2025. doi:10.1097/ccm.0000000000006899

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.