Evidence map›Paper›PMID 38982551›Full record

ArticleJournal of intensive care2024

Increasing plasma calprotectin (S100A8/A9) is associated with 12-month mortality and unfavourable functional outcome in critically ill COVID-19 patients.

Ingrid Didriksson, Maria Lengquist, Martin Spångfors, Märta Leffler, Theodor Sievert, Gisela Lilja, Attila Frigyesi, Hans Friberg, Alexandru Schiopu

Registry-linked trialAbstract read
In one paragraph

Article in Journal of intensive care, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04974775 (Swecrit Biobank - Blood Samples From Critically Ill Patients and Healthy Controls), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–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.

NCT04974775 active not recruitingnot on this map

Swecrit Biobank - Blood Samples From Critically Ill Patients and Healthy Controls

TypeobservationalSponsorSkane University HospitalRan2014 to 2026Enrolled8,500ConditionsCritical Illness, Cardiac Arrest, Sepsis, InfluenzaArmsBlood collection, Blood collection, serial sampling
3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Observational
  2. Article
  3. Observational
  4. Article
  5. Article
  6. 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

9 authors.

Ingrid DidrikssonDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, Lund, Sweden. ingrid_kristina_larsdotter.didriksson@med.lu.se.ORCID http://orcid.org/0000-0003-1334-7583
Maria LengquistDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, Lund, Sweden.
Martin SpångforsDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, Lund, Sweden.
Märta LefflerDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, Lund, Sweden.
Theodor SievertDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, Lund, Sweden.
Gisela LiljaDepartment of Neurology, Skåne University Hospital, Lund, Sweden.
Attila FrigyesiDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, Lund, Sweden.
Hans FribergDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, Lund, Sweden.
Alexandru SchiopuDepartment of Translational Medicine, Lund University, Malmö, Sweden.

Funding

Ministerul Educaţiei Naţionale PNRR-C9/18-CF148Riksförbundet HjärtLung 21004021Riksförbundet HjärtLung 21023322Socialstyrelsen 2019:YF0053
6 · The paper itself

Abstract

backgroundCalprotectin (S100A8/A9) is a pro-inflammatory mediator primarily released from neutrophils. Previous studies have revealed associations between plasma calprotectin, disease severity and in-hospital mortality in unselected COVID-19 patients.

objectiveWe aimed to assess whether plasma calprotectin dynamics during the first week of intensive care are associated with mortality and functional outcome in critically ill COVID-19 patients.

methodsThis prospective study included 498 COVID-19 patients admitted to six intensive care units (ICUs) in Sweden between May 2020 and May 2021. Blood samples were collected on ICU admission and on day 7. The primary outcome was 12-month mortality. Secondary outcomes were functional outcome of survivors at 3 and 12 months, and the need for invasive mechanical ventilation (IMV) or continuous renal replacement therapy (CRRT) during the ICU stay. Functional outcome was assessed by the Glasgow Outcome Scale Extended (GOSE, range 1-8, with < 5 representing an unfavourable outcome). Associations between plasma calprotectin and outcomes were examined in binary logistic regression analyses adjusted for age, sex, BMI, hypertension, smoking, and creatinine.

resultsHigh plasma calprotectin on admission and day 7 was independently associated with increased 12-month mortality. Increasing calprotectin from admission to day 7 was independently associated with higher mortality at 12 months [OR 2.10 (95% CI 1.18-3.74), p = 0.012], unfavourable functional outcome at 3 months [OR 2.53 (95% CI 1.07-6.10), p = 0.036], and the use of IMV [OR 2.23 (95% CI 1.10-4.53), p = 0.027)] and CRRT [OR 2.07 (95% CI 1.07-4.00), p = 0.031)]. A receiver operator characteristic (ROC) model including day 7 calprotectin and age was a good predictor of 12-month mortality [AUC 0.79 (95% CI 0.74-0.84), p < 0.001]. Day 7 calprotectin alone predicted an unfavourable functional outcome at 3 months [AUC 0.67 (95% CI 0.58-0.76), p < 0.001].

conclusionIn critically ill COVID-19 patients, increasing calprotectin levels after admission to the ICU are associated with 12-month mortality and unfavourable functional outcome in survivors. Monitoring plasma calprotectin dynamics in the ICU may be considered to evaluate prognosis in critical COVID-19. STUDY REGISTRATION: ClinicalTrials.gov Identifier: NCT04974775, registered April 28, 2020.

Indexed as

CalprotectinCOVID-19ICUInnate immune systemMortality

Identifiers

PMID38982551
PMCPMC11232228

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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.