Evidence map›Paper›PMID 36062611›Full record

ArticleJournal of intensive care medicine2023

Vasopressin Response and Clinical Trajectory in Septic Shock Patients.

Seth R Bauer, Gretchen L Sacha, Matthew T Siuba, Lu Wang, Xiaofeng Wang, Rachel G Scheraga, Vidula Vachharajani

Open access · greenAbstract read
In one paragraph

Article in Journal of intensive care medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. [Vasoactive agents in septic shock-individualized strategies].Medizinische Klinik, Intensivmedizin und Notfallmedizin · 2025
    Review
  4. Article
  5. Review
  6. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Seth R BauerDepartment of Pharmacy, 2569Cleveland Clinic, Cleveland, OH, USA.ORCID 0000-0002-0420-0320
Gretchen L SachaDepartment of Pharmacy, 2569Cleveland Clinic, Cleveland, OH, USA.ORCID 0000-0002-0070-8100
Matthew T SiubaCleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, OH, USA.
Lu WangDepartment of Pharmacy, 2569Cleveland Clinic, Cleveland, OH, USA.
Xiaofeng WangCleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, OH, USA.
Rachel G ScheragaCleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, OH, USA.
Vidula VachharajaniCleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, OH, USA.
Cleveland Clinic · USCleveland Clinic Lerner College of Medicine · US

Funding

Bioenergetic and Epigenetic Reprogramming by Obesity in SepsisR01GM099807 · NIGMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI VACHHARAJANI, VIDULA · 2012 to 2020
$3.1M
TRPV4 Regulates Mechanosensitive Macrophage Functions in Lung InjuryR01HL155064 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI SCHERAGA, RACHEL GREENBERG · 2021 to 2025
$2.1M
Personalized vasopressor therapy in patients with septic shockK08GM147806 · NIGMS · CLEVELAND CLINIC LERNER COM-CWRU · PI SETH BAUER · 2022 to 2026
$886k
NHLBI NIH HHS R01 HL155064NIGMS NIH HHS K08 GM147806NIGMS NIH HHS R01 GM099807
6 · The paper itself

Abstract

backgroundIn septic shock, vasopressors aim to improve tissue perfusion and prevent persistent organ dysfunction, a characteristic of chronic critical illness (CCI). Adjunctive vasopressin is often used to decrease catecholamine dosage, but the association of vasopressin response with subsequent patient outcomes is unclear. We hypothesized vasopressin response is associated with favorable clinical trajectory.

methodsWe included patients with septic shock receiving vasopressin as a catecholamine adjunct in this retrospective cohort study. We defined vasopressin response as a lowering of the catecholamine dose required to maintain mean arterial pressure ≥65 mm Hg, 6 h after vasopressin initiation. Clinical trajectories were adjudicated as early death (ED; death before day 14), CCI (ICU stay ≥14 days with persistent organ dysfunction), or rapid recovery (RR; not meeting ED or CCI criteria). Trajectories were placed on an ordinal scale with ED the worst outcome, CCI next, and RR the best outcome. The association of vasopressin response with clinical trajectory was assessed with multivariable ordinal logistic regression.

resultsIn total 938 patients were included; 426 (45.4%) were vasopressin responders. The most frequent trajectory was ED (49.8%), 29.7% developed CCI, and 20.5% had rapid recovery. In survivors to ICU day 14 (those without ED), 59.2% had CCI and 40.8% experienced RR. Compared with vasopressin non-responders, vasopressin responders less frequently experienced ED (42.5% vs. 55.9%) and more frequently experienced RR (24.6% vs. 17.0%;

conclusionsVasopressin responsive status was associated with improved clinical trajectory in septic shock patients. Early vasopressin response is a potential novel prognostic marker for short-term clinical trajectory.

Indexed as

Shock, SepticCatecholaminesCritical IllnessHumansMultiple Organ FailureRetrospective StudiesVasoconstrictor AgentsVasopressinsCatecholaminesVasoconstrictor AgentsVasopressinschronic critical illnessclinical trajectorysepsisseptic shockvasoconstrictor agentsvasopressin

Identifiers

PMID36062611
PMCPMC10236982
OpenAlexW4294586338

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.