Deshpande, Abhishek https://orcid.org/0000-0001-5522-2995
Walker, Ramara
Schulte, Rebecca
Pallotta, Andrea M.
Tereshchenko, Larisa G.
Hu, Bo
Kadri, Sameer S.
Klompas, Michael
Rothberg, Michael B.
Funding for this research was provided by:
Agency for Healthcare Research and Quality (R01HS028633)
Article History
Received: 18 May 2023
Accepted: 30 August 2023
First Online: 16 September 2023
Declarations
:
: This study was approved by the Cleveland Clinic IRB (#21–863) and the AHRQ. The study is a low-risk quality-improvement initiative performed at the hospital level, making it impractical for patients to opt out of the study. We have study approval from the Cleveland Clinic Institutional Review Board for a waiver of informed consent. The interventions are considered minimal risk because physicians have the ability to override the orders for rapid diagnostic testing and pharmacist recommendations for de-escalation and final decisions will depend on the individual physician’s judgment. All participating providers will receive an information sheet about the study, including a description of measures for protecting confidentiality (Additional file ). Important modifications to the protocol are submitted to the Cleveland Clinic IRB and to ClinicalTrials.gov.
: Not applicable.
: AD has received research support from Seres Therapeutics and was a consultant for Merck, both unrelated to the current study. MK received royalties from UpToDate for chapters on hospital-acquired pneumonia. All other authors declare that they have no competing interests.