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1. Lower vs Higher Oxygenation Target and Days Alive Without Life Support in COVID-19:The HOT-COVID Randomized Clinical Trial

2. Lower vs Higher Oxygenation Target and Days Alive Without Life Support in COVID-19: The HOT-COVID Randomized Clinical Trial.

3. Induced hypothermia in patients with septic shock and respiratory failure (CASS): a randomised, controlled, open-label trial

5. Mild induced hypothermia and coagulation and platelet function in patients with septic shock: Secondary outcome of a randomized trial

6. The Nordic perioperative and intensive care registries—Collaboration and research possibilities

7. The Nordic perioperative and intensive care registries-Collaboration and research possibilities

8. Mild induced hypothermia and coagulation and platelet function in patients with septic shock:Secondary outcome of a randomized trial

11. Prediction of non-recovery from ventilator-demanding acute respiratory failure, ARDS and death using lung damage biomarkers: data from a 1200-patient critical care randomized trial

12. Goal directed fluid removal with furosemide versus placebo in intensive care patients with fluid overload: A trial protocol for a randomised, blinded trial (GODIF trial)

13. A policy for diversity, equity, inclusion and anti-racism in the Scandinavian Society of Anaesthesiology and Intensive Care Medicine (SSAI)

14. Goal directed fluid removal with furosemide versus placebo in intensive care patients with fluid overload:A trial protocol for a randomised, blinded trial (GODIF trial)

16. A policy for diversity, equity, inclusion and anti‐racism in the Scandinavian Society of Anaesthesiology and Intensive Care Medicine (SSAI)

17. Preferences for the measurement and supplementation of magnesium, phosphate and zinc in ICUs:The international WhyTrace survey

18. Lower or Higher Oxygenation Targets for Acute Hypoxemic Respiratory Failure

19. Lower or Higher Oxygenation Targets for Acute Hypoxemic Respiratory Failure

20. Hydroxyethyl Starch 130/0.4 versus Ringerʼs Acetate in Severe Sepsis

21. Preferences for the measurement and supplementation of magnesium, phosphate and zinc in ICUs: The international WhyTrace survey

23. The handling oxygenation targets in the intensive care unit (HOT‐ICU) trial: Detailed statistical analysis plan

24. Handling Oxygenation Targets in the Intensive Care Unit (HOT-ICU)-Protocol for a randomised clinical trial comparing a lower vs a higher oxygenation target in adults with acute hypoxaemic respiratory failure

25. Biomarker-assisted identification of sepsis-related acute liver impairment:A frequent and deadly condition in critically ill patients

26. Low Incidence of Biphasic Allergic Reactions in Patients Admitted to Intensive Care after Anaphylaxis

27. Handling Oxygenation Targets in the Intensive Care Unit (HOT-ICU) - Protocol for a randomised clinical trial comparing a lower vs a higher oxygenation target in adults with acute hypoxaemic respiratory failure

28. Predicting recovery from acute kidney injury in critically ill patients:Development and validation of a prediction model

31. The Procalcitonin And Survival Study (PASS) – A Randomised multi-center investigator-initiated trial to investigate whether daily measurements biomarker Procalcitonin and pro-active diagnostic and therapeutic responses to abnormal Procalcitonin levels, can improve survival in intensive care unit patients. Calculated sample size (target population): 1000 patients

32. Induced hypothermia in patients with septic shock and respiratory failure (CASS):a randomised, controlled, open-label trial

33. Preferences for the measurement and supplementation of magnesium, phosphate and zinc in ICUs: The international WhyTrace survey.

34. Induced hypothermia in patients with septic shock and respiratory failure (CASS): a randomised, controlled, open-label trial

35. Endothelial Damage Signals Refractory Acute Kidney Injury in Critically Ill Patients

37. Induced Hypothermia in Patients with Septic Shock and Ventilator-demanding Respiratory Failure

38. Prediction of non-recovery from ventilator-demanding acute respiratory failure, ARDS and death using lung damage biomarkers:data from a 1200-patient critical care randomized trial

39. Begrænset evidens for monitorering og behandling af fosfatmangel hos kritisk syge patienter

40. Profound Endothelial Damage Predicts Impending Organ Failure and Death in Sepsis

41. Invasive Candida Infections and the Harm From Antibacterial Drugs in Critically Ill Patients:Data From a Randomized, Controlled Trial to Determine the Role of Ciprofloxacin, Piperacillin-Tazobactam, Meropenem, and Cefuroxime

42. Invasive Candida Infections and the Harm From Antibacterial Drugs in Critically Ill Patients

43. Non-recognized Liver Impairment in Infected Critically Ill Patients Is Frequent and Hazardous

44. The potential of antimicrobials to induce thrombocytopenia in critically ill patients:data from a randomized controlled trial

45. Transfusion requirements in septic shock (TRISS) trial - comparing the effects and safety of liberal versus restrictive red blood cell transfusion in septic shock patients in the ICU:protocol for a randomised controlled trial

46. Kidney failure related to broad-spectrum antibiotics in critically ill patients:secondary end point results from a 1200 patient randomised trial

47. Procalcitonin-guided interventions against infections to increase early appropriate antibiotics and improve survival in the intensive care unit: a randomized trial

48. The Procalcitonin And Survival Study (PASS) - a randomised multi-center investigator-initiated trial to investigate whether daily measurements biomarker Procalcitonin and pro-active diagnostic and therapeutic responses to abnormal Procalcitonin levels, can improve survival in intensive care unit patients. Calculated sample size (target population): 1000 patients

49. The Potential of Antimicrobials to Induce Thrombocytopenia in Critically Ill Patients: Data from a Randomized Controlled Trial

50. Transfusion requirements in septic shock (TRISS) trial - comparing the effects and safety of liberal versus restrictive red blood cell transfusion in septic shock patients in the ICU: protocol for a randomised controlled trial

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