ISRCTN68786381
Active, not recruiting
未知
Evaluation of an integrated care pathway for out-of-hospital treatment of older adults with an acute moderate-to-severe lower respiratory tract infection or pneumonia
Haga Hospital0 sites300 target enrollmentNovember 28, 2022
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Haga Hospital
- Enrollment
- 300
- Status
- Active, not recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
2023 Protocol article in https://doi.org/10.1136/bmjopen-2023-073126 (added 18/08/2023)
Investigators
Eligibility Criteria
Inclusion Criteria
- •Current inclusion criteria as of 18/07/2023:
- •To be eligible to participate in this study, a patient must meet all of the following criteria:
- •1\. Age \=65 years
- •2\. Clinical diagnosis of an acute moderate\-to\-severe (Pneumonia Severity Index (PSI) class \=3 or CURB\-65 \=2\) lower respiratory tract infection or pneumonia
- •3\. Oxygen saturation \=92% and respiratory rate \=24/minute with maximum five litres of oxygen (or adjusted oxygen saturation cut\-offs as clinically indicated (e.g. for patients with chronic obstructive pulmonary disease (COPD)) by the treating physician)
- •4\. Written informed consent (IC) for participation in the study
- •To be eligible to participate in this study, an informal caregiver must meet all of the following criteria:
- •1\. Age \=18 years
- •2\. Being an informal caregiver of a patient included in the study
- •3\. Written IC for participation in the study
Exclusion Criteria
- •Current exclusion criteria as of 18/07/2023:
- •A potential patient who meets any of the following criteria will not be able to participate:
- •1\. Chemotherapy for solid organ malignancy (\<2 months before presentation)
- •2\. Active hematologic malignancy
- •3\. Immunocompromised status (e.g. solid organ transplants)
- •4\. Severe dementia (Clinical Dementia Rating Scale Sum of Boxes (CDR\-SOB) score 16\-18\)
- •Previous exclusion criteria:
- •A potential patient who meets any of the following criteria will not be able to participate:
- •1\. Patients receiving chemotherapy (\<2 months before presentation)
- •2\. Patients with active hematologic malignancy
Outcomes
Primary Outcomes
Not specified
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