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In-Hospital Mortality clinical trials

View clinical trials related to In-Hospital Mortality.

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NCT ID: NCT06248346 Completed - Clinical trials for In-hospital Mortality

Association Between Administration of Dexmedetomidine and Postoperative Mortality in Hospitals

Start date: September 1, 2014
Phase:
Study type: Observational

The present multicentre retrospective cohort study aimed to investigate the association between intraoperative administration of dexmedetomidine and postoperative mortality in hospitals. The investigators set out to test the hypothesis that perioperative dexmedetomidine use, as an adjunct to general anesthesia, diminishes postoperative mortality in hospitals across all categories of surgical patients.

NCT ID: NCT05821491 Completed - Geriatric Clinical Trials

Prognosis of Geriatric Patients With Non-bedded Night in the Emergency Department: a Multicenter Cohort Study

NoBedNight
Start date: December 12, 2022
Phase:
Study type: Observational

Retrospective, multicenter, French cohort study. Data from patients over 75 years of age who visited the emergency department on 12 and 13 December 2022 could be collected until their discharge from hospital and for a maximum of 30 days. Data from patients who spent the night on a stretcher (stretcher group) as well as from a group of patients who spent the night in a bed (hospital bed group) after a visit to the emergency department will be collected. The characteristics of the patients and their stay in the emergency room will be collected, and their hospital stay (truncated at 30 days) will be analyzed in terms of morbidity and mortality. Main objective: To study the truncated 30-day in-hospital mortality of patients who spent a night on a stretcher in the emergency department. Secondary objectives: To describe the characteristics and hospital stay of patients who spent a night on a stretcher To compare the morbidity and mortality of patients who spent the night on a stretcher with patients who spent the night in an inpatient bed after an emergency visit;

NCT ID: NCT02599636 Active, not recruiting - Clinical trials for In-Hospital Mortality

To Survive After ICU Discharge

Start date: October 2015
Phase: N/A
Study type: Observational

Many factors before and after ICU stay determine the outcome of patients at ICU discharge, the type of illness, physical dependence and other sequelae can be a trigger for complications in hospital ward which can induce ICU readmission and worse outcome. The quality of medical assistance during all the hospitalisation should be guaranteed and many complications or fatal events could be avoidable. The objective of the present study is to demonstrate that collaboration between the intensivist and other medical teams in ward can reduce ICU readmission and hospital mortality after ICU discharge.

NCT ID: NCT01998191 Active, not recruiting - Clinical trials for In Hospital Mortality

Avoidable Mortality Case Note Review Trial

Start date: February 2014
Phase: N/A
Study type: Interventional

TITLE A randomized controlled trial to assess the best method for evaluating avoidable mortality in hospitals using medical record review. DESIGN Randomised controlled trial This trial will be conducted in concordance with the CONSORT guidelines for randomised controlled trials. AIMS Compare explicit versus implicit case review methods for detecting avoidable mortality in patients who have died in hospital Assess the accuracy and efficiency of physicians versus nurses in detecting avoidable mortality in patients who have died in hospital OUTCOME MEASURES Rate of adverse event detection between explicit and implicit review methods Type of adverse event detection between explicit and implicit review methods Kappa score of agreement for inter-rater reliability for the above outcomes: - Between individual reviewers within using the same review method - Between different reviewer types. PARTICIPANTS Physician reviewers and nurses No patient participation. Case records of patients who had inpatient hospital mortality will be reviewed. ELIGIBILITY Over 18, Able to consent, English Language Speaking, Able to participate in case note review training, appropriate level of clinical experience. DURATION 2 years with extension if required and reviewed.