Evidence mapPaperPMID 42298739Full record

ArticleActa anaesthesiologica Scandinavica2026

Effects of Sedation, TEmperature and Pressure After Cardiac Arrest and REsuscitation on Major Adverse Kidney Events (STEPCARE-MAKE): A Protocol for a Pre-Planned Sub-Study of a Randomized Clinical Trial.

Keski-Keturi M, Niemelä V H, Young P, Nielsen N, Wise M P, Reinikainen M, Bass F, Lilja G, Dankiewicz J, Hammond N and 67 more

Abstract readClinical Trial Protocol
In one paragraph

Article in Acta anaesthesiologica Scandinavica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing 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.

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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

77 authors.

Keski-Keturi MEmergency Medicine and Services, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.ORCID https://orcid.org/0009-0007-3759-8164
Niemelä V HDepartment of Anaesthesia and Intensive Care, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Young PIntensive Care Unit, Wellington Hospital, Wellington, New Zealand.
Nielsen NDepartment of Clinical Sciences Lund, Anesthesia and Intensive Care, Lund University, Lund, Sweden.
Wise M PAdult Critical Care, University Hospital of Wales, Cardiff, UK.
Reinikainen MInstitute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland.ORCID https://orcid.org/0000-0001-6878-3740
Bass FCritical Care Program, the George Institute for Global Health, UNSW, Sydney, Australia.
Lilja GNeurology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.ORCID https://orcid.org/0000-0003-1860-1456
Dankiewicz JDepartment of Clinical Sciences Lund, Section of Cardiology, Skåne University Hospital, Lund, Sweden.
Hammond NCritical Care Program, the George Institute for Global Health, UNSW, Sydney, Australia.
Hästbacka JTampere University Hospital, Wellbeing Services County of Pirkanmaa and Tampere University, Faculty of Medicine and Health Technology, Tampere, Finland.
Levin HDepartment of Clinical Sciences Lund, Lund University, Lund, Sweden.
Moseby-Knappe MDepartment of Clinical Sciences Lund, Lund University, Lund, Sweden.ORCID https://orcid.org/0000-0001-8160-5957
Saxena MCritical Care Division and Department of Intensive Care Medicine, The George Institute for Global Health, Sydney, Australia.
Tiainen MDepartment of Neurology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.ORCID https://orcid.org/0000-0001-5107-1990
Ceric AAnesthesia & Intensive Care, Department of Clinical Sciences, Lund University, Skane University Hospital, Malmö, Sweden.
Kamp C BCopenhagen Trial Unit, Centre for Clinical Intervention Research, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-7756-4694
Sillassen C D BCopenhagen Trial Unit, Centre for Clinical Intervention Research, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.ORCID https://orcid.org/0009-0004-9247-5245
Alexandersson DDepartment of Clinical Sciences Lund, Anesthesia and Intensive Care, Lund University, Lund, Sweden.
Schmidbauer SDepartment of Clinical Sciences Lund, Anesthesia and Intensive Care, Lund University, Lund, Sweden.
Tirkkonen JIntensive Care Unit, Tampere University Hospital, Tampere, Finland.
Oksanen TDepartment of Anaesthesia and Intensive Care, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Säkkinen HResearch Unit of Translational Medicine, Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.
Bendel SInstitute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland.ORCID https://orcid.org/0000-0002-1209-8397
Düring JDepartment of Clinical Sciences, Anesthesia and Intensive Care, Lund University, Skåne University Hospital, Malmö, Sweden.
Lybeck ADepartment of Intensive and Perioperative Care, Skåne University Hospital, Lund University, Lund, Sweden.ORCID https://orcid.org/0000-0001-7574-3958
Johnsson JDepartment of Anesthesia and Intensive Care, Helsingborg Hospital, Helsingborg, Sweden.ORCID https://orcid.org/0000-0003-0651-3811
Unden JDepartment of Intensive and Perioperative Care, Skåne University Hospital, Lund University, Lund, Sweden.
Lundin ADepartment of Anaesthesiology and Intensive Care Medicine, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID https://orcid.org/0000-0002-6623-6847
Kåhlin JPerioperative Medicine and Intensive Care (PMI), Karolinska University Hospital, Stockholm, Sweden.ORCID https://orcid.org/0000-0001-5266-5272
Grip JPerioperative Medicine and Intensive Care (PMI), Karolinska University Hospital, Stockholm, Sweden.
Lotman ENorth Estonia Medical Centre, Tallinn, Estonia.
Romundstad LDepartment of Anesthesia and Intensive Care Medicine, Division of Emergencies and Critical Care, Oslo University Hospital, Oslo, Norway.
Seidel PDepartment of Intensive Care Medicine, Stavanger University Hospital, Stavanger, Norway.
Stammet PDepartment of Anaesthesia and Intensive Care Medicine Centre, Hospitalier de Luxembourg, Luxembourg, Luxembourg.ORCID https://orcid.org/0000-0002-0298-1012
Graf TUniversity Heart Center Lübeck, University Hospital Schleswig-Holstein, Lübeck, Germany.
Mengel AHertie Institute of Clinical Brain Research, Tuebingen, Germany.
Leithner CDepartment of Neurology, Freie Universität and Humboldt-Universität Zu Berlin, Charité-Universitätsmedizin Berlin, Berlin, Germany.ORCID https://orcid.org/0000-0002-8277-846X
Nee JDepartment of Nephrology and Medical Intensive Care, Charité - Universitaetsmedizin Berlin, Berlin, Germany.
Druwé PDepartment of Intensive Care Medicine, Ghent University Hospital, Ghent, Belgium.
Ameloot KDepartment of Cardiology, Ziekenhuis Oost-Limburg, Genk, Belgium.
McGuigan P JWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
White JCEDAR (Centre for Healthcare Evaluation, Device Assessment and Research), Cardiff and Vale University Health Board Cardiff, Cardiff, UK.
Govier MBristol Royal Infirmary, University Hospitals Bristol and Weston, Bristol, UK.
Ostermann MGuy's & St Thomas' Hospital, London, UK.
Hopkins PIntensive Care Medicine Centre for Human & Applied Physiological Sciences, School of Basic & Medical Biosciences, Faculty of Life Sciences and Medicine King's College, London, UK.
Proudfoot ADepartment of Perioperative Medicine, Barts Heart Centre, St Bartholomew's Hospital, London, UK.
Handslip RSt George's University Hospital NHS Foundation Trust, London, UK.
Pogson DDepartment of Critical Care, Portsmouth University Hospitals Trust Cosham, Portsmouth, UK.
Jackson PLeeds Teaching Hospitals NHS Trust, Leeds, UK.
Nichol AAustralian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, Victoria, Australia.
Haenggi MInstitute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.ORCID https://orcid.org/0000-0001-5845-031X
Hilty M PInstitute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
Iten MDepartment of Intensive Care Medicine, Inselspital University Hospital Bern, Bern, Switzerland.
Schrag CKlinik für Intensivmedizin, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Nafi MIstituto Cardiocentro Ticino, Lugano, Switzerland.
Joannidis MDivision of Intensive Care and Emergency Medicine, Department of Internal Medicine, Medical University Innsbruck, Innsbruck, Austria.
Robba CAOM, IRCCS Policlinico San Martino, Genoa, Italy.
Belohlavek J2nd Dept. of Internal Medicine, Cardiovascular Medicine, General University Hospital and 1st Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.
Rob D2nd Department of Medicine, Department of Cardiovascular Medicine, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic.
Arabi YKing Saud Bin Abdulaziz University for Health Sciences and King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.ORCID https://orcid.org/0000-0001-5735-6241
Al-Fares ADepartment of Anesthesia, Critical Care Medicine, and Pain Medicine, Al-Amiri Hospital, Ministry of Health, Kuwait City, Kuwait.
Yew Woon CTan Tock Seng Hospital, Singapore, Singapore.
Aneman AIntensive Care Unit, Liverpool Hospital, South Western Sydney Local Health District, Sydney, New South Wales, Australia.ORCID https://orcid.org/0000-0003-2096-5304
Stewart ALiverpool Hospital, Sydney, New South Wales, Australia.
Arnott CCritical Care Program, the George Institute for Global Health, UNSW, Sydney, Australia.
Ramanan MDepartment of Cardiology, Royal Prince Alfred Hospital, Sydney, Australia.
Panwar RCritical Care Division, the George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia.
Delaney ATampere University Hospital, Wellbeing Services County of Pirkanmaa and Tampere University, Faculty of Medicine and Health Technology, Tampere, Finland.
Reade MNorthern Clinical School, Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.ORCID https://orcid.org/0000-0003-1570-0707
Venkatesh BCritical Care Program, the George Institute for Global Health, UNSW, Sydney, Australia.
Taccone FDepartment of Intensive Care, Hospital Universitaire de Bruxelles (HUB), Universite Libre de Bruxelles (ULB), Brussels, Belgium.ORCID https://orcid.org/0000-0003-0830-1628
Pekkarinen P TDepartment of Anaesthesia and Intensive Care, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.ORCID https://orcid.org/0000-0002-8203-3409
Friberg HIntensive and Perioperative Care, Skåne University Hospital, Malmö, Sweden.
Cronberg TNeurology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Jakobsen J CIntensive Care Unit, Tampere University Hospital, Tampere, Finland.
Skrifvars M BDepartment of Anaesthesia and Intensive Care, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.ORCID https://orcid.org/0000-0002-0341-0262

Funding

Academy of FinlandFinska LäkarsällskapetMedicinska Understödsföreningen Liv och HälsaSigrid Juséliuksen SäätiöSouth Swedish health RegionStiftelsen Dorothea Olivia, Karl Walter och Jarl Walter Perkléns MinneSvenska KulturfondenSwedish health care, ALF projectThe Swedish Research Council
6 · The paper itself

Abstract

backgroundAcute kidney injury (AKI) is a common and serious complication after cardiac arrest, affecting more than 30% of initially successfully resuscitated patients, with around 10% receiving Kidney Replacement Therapy (KRT). Currently, treatment options to prevent renal complications are limited. In this predefined sub-study of the Sedation, TEmperature and Pressure after Cardiac Arrest and REsuscitation (STEPCARE) trial, we evaluate the effects of sedation depth, fever management strategies, and mean arterial pressure (MAP) targets on the risk of major adverse kidney events (MAKE) in post-cardiac arrest patients.

methodsSTEPCARE-MAKE is a predefined prospective sub-study of the international, randomized clinical STEPCARE trial. The main trial will enroll 3500 patients and employs a 2 × 2 × 2 factorial design, randomizing participants across three interventions: (1) deep sedation for 36 h or minimal sedation, (2) fever management with or without a feedback-controlled device, and (3) MAP target ≥ 65 mmHg or ≥ 85 mmHg. The primary outcome is the composite outcome MAKE, which includes death from any cause by day 30, initiation of KRT, or persistent renal dysfunction, defined as the final creatinine value ≥ 200% of the baseline at the time of discharge from the primary hospital or at day 30, whichever occurs first. Differences between baseline and the highest in-hospital creatinine, baseline and the last measured in-hospital creatinine, baseline and 72-h creatinine, and baseline and the highest creatinine within 72 h will be reported as secondary outcomes.

conclusionThe findings of this sub-study will provide new evidence on the renal effects of the STEPCARE trial interventions and may inform the future of individualized kidney-protective treatment approaches.

Indexed as

Acute Kidney InjuryBody TemperatureDeep SedationHeart ArrestFeverHumansProspective StudiesRandomized Controlled Trials as Topic

Identifiers

PMID42298739
PMCPMC13269662

What Socratic holds

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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 Socratic graph.