prolonged weaning, prolonged invasive ventilation, weaning failure J44 J84 F05 F10.4 F19.4 G62.80 G72.80 N17 N18 E66.01 E66.02 E10 E11 E12 E13 E14
Conditions
Interventions
Group 1: Patients - written survey:
at discharge: EQ-5D
after three months: EQ-5D, PEACS
after six months: EQ-5D, PAM, PHQ9, PEF
after 12 months: EQ-5D
patient interviews: after discharge
Group 2: re
Sponsors
Universitätsklinikum Heidelberg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Inclusion criteria for the health economic evaluation: - Age = 30 - Invasively ventilated for = 96 h - Alive 11 days after the day of intubation - Insured with the statutory health insurance AOK Baden-Württemberg - No evidence for a degenerative disease that would justify the need for an invasive ventilation Inclusion criteria for the process evaluation: INTERVIEWS - Patients: All patients who take part in the PRiVENT-study with oral German language skills and who sign the interview consent form - Relatives: All relatives of patients who take part in the PRiVENT-study with oral German language skills, aged 18 years or older who give their consent to be interviewed - Healthcare professionals: Healthcare professionals working in one of the participating weaning centres or intensive care units of the PRiVENT-study with oral German language skills are considered eligible if they are 18 years or older and agree to the interview - Stakeholders: Representatives of health insurance companies, self-help groups and politicians committed to health policy, who have oral German language skills, are 18 years or older and consent to take part in an interview QUANTITATIVE SURVEYS - Patients: All patients who have written or oral German language skills and have themselves given consent to participate in the PRiVENT-study - Healthcare staff: All those involved in the care of patients who take part in the PRiVENT-study, i.e. doctors, nurses, respiratory therapists, physiotherapists, etc. working in one of the participating weaning centres or intensive care units, aged 18 years or older, who have written or oral German language skills, and agree to take part in the survey
Exclusion criteria
Exclusion criteria: All those who do not meet the above inclusion criteria will be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Health economic evaluation: cost savings resulting from the successful PRiVENT-intervention; process evaluation: implementation of the PRiVENT-intervention as a whole and its individual components | — |
Secondary
| Measure | Time frame |
|---|---|
| Health economic evaluation: The costs associated with the PRiVENT-intervention, direct health care costs of patients with long-term invasive ventilation, patients’ quality of life associated with invasive long-term ventilation as well as with a successful PRiVENT-intervention. Process evaluation: impact on healthcare professionals' job satisfaction and interprofessional collaboration, and PRiVENT patients' decision-making behavior, quality of life, activity levels, and hospital discharge experiences. | — |
Countries
Germany
Contacts
Public ContactJohanna Forstner
Universitätsklinikum Heidelberg
Outcome results
None listed