Evidence map›Paper›PMID 39806688›Full record

Observational studyBMJ open2024

Treating shock with norepinephrine administered in midline catheters in an intermediary care unit: a retrospective cohort study.

Hanna Karlsson, Ajnaz Afrasiabi, Marcus Ohlsson, Viktor Månsson, Hannes Hartman, Gustav Torisson

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in BMJ open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06121115 (Norepinephrine Administration Through a Midline Catheter in an Intermediate Care Unit - a Retrospective Study of Complications and Patient Outcomes), which is not on this map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT06121115 completednot on this map

Norepinephrine Administration Through a Midline Catheter in an Intermediate Care Unit - a Retrospective Study of Complications and Patient Outcomes

TypeobservationalSponsorRegion SkaneRan2023 to 2024Enrolled473ConditionsSeptic Shock, Norepinephrine Adverse Reaction, Hypotension and ShockArmsNorepinephrine
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
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

6 authors.

Hanna KarlssonDepartment of Infectious Diseases, Skånes universitetssjukhus Malmö, Malmö, Skåne, Sweden.
Ajnaz AfrasiabiDepartment of Internal Medicine, Skånes universitetssjukhus Malmö, Malmö, Skåne, Sweden.
Marcus OhlssonDepartment of Internal Medicine, Skånes universitetssjukhus Malmö, Malmö, Skåne, Sweden.ORCID 0000-0003-0043-1727
Viktor MånssonDepartment of Infectious Diseases, Skånes universitetssjukhus Malmö, Malmö, Skåne, Sweden.
Hannes HartmanDepartment of Internal Medicine, Skånes universitetssjukhus Malmö, Malmö, Skåne, Sweden.
Gustav TorissonDepartment of Infectious Diseases, Skånes universitetssjukhus Malmö, Malmö, Skåne, Sweden gustav.torisson@med.lu.se.ORCID 0000-0001-9012-2068

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesA rising incidence of septic shock as well as recommendations for early vasopressor initiation has increased the number of patients eligible for norepinephrine (NE). Traditionally, NE has been administered through central lines, in intensive care units, due to the risk of extravasation in peripheral lines. The aim of the current study is to determine the rate of complications and patient outcomes when NE is administered through midline catheters (MCs) in intermediary care units (IMCUs).

designRetrospective cohort study.

settingThree IMCUs in southern Sweden

participantsPatients with septic shock who received NE through a MC from September 2020 through March 2023. PRIMARY AND SECONDARY OUTCOME MEASURES: The primary outcome was a major complication to treatment, defined as extravasation of NE, catheter-associated venous thromboembolism and catheter-associated bloodstream infection (BSI). Secondary outcomes included patient outcomes after intermediary care (either deceased, discharged to regular ward care or intensive care) and the need for additional central lines.

resultsOf 474 eligible patients, 472 were included, with a median (IQR) age of 73.5 (65-80) years, with 281 (60%) men. The median (IQR) duration of NE infusion was 21 (9-38) hours, with a median (IQR) dosage of 0.12 (0.08-0.20) µg/kg/min. Major complications occurred in 12 cases (2.5%), with one suspected extravasation, seven thromboembolic events and four catheter-related BSIs. After intermediary care, 334 patients (71%) were discharged to regular ward care, 66 patients (14%) were escalated to intensive care and 72 (15%) died in intermediary care, of whom 69 had a documented ceiling of care decision. 100 patients (21%) received a central line.

conclusionNE administration in MCs was associated with a low rate of short-term complications and could decrease the need for central lines. MCs can enable the initial management of circulatory failure outside intensive care, but more studies are needed to determine the long-term value of IMCUs. TRIAL REGISTRATION NUMBER: NCT06121115.

Indexed as

NorepinephrineShock, SepticVasoconstrictor AgentsAgedAged, 80 and overCatheter-Related InfectionsFemaleHumansIntensive Care UnitsMaleRetrospective StudiesSwedenVenous ThromboembolismNorepinephrineVasoconstrictor AgentsAdult intensive & critical careINFECTIOUS DISEASESInpatients

Identifiers

PMID39806688
PMCPMC11683991

What OpenQuestion holds

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Registered trials

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.