Study aim
Looking at whether aspirin can help prevent strokes in patients with pneumonia
Inclusion Criteria
- Participants aged ≥ 50 years
- Admitted to hospital with pneumonia, or decision to admit
- Symptoms and signs of acute lower respiratory tract infection
- Radiographic changes in keeping with infection on chest radiograph, CT scan, or lung ultrasound scan
Exclusion Criteria
- Already taking regular prescribed anti-platelet medication, including aspirin, clopidogrel, cangrelor, selexipag, cilostazol, dipyridamole, prasugrel, ticagrelor, abciximab, eptifibatide, tirofiban, epoprostenol, or iloprost
- Known allergy, previous important adverse reaction, or contraindication to aspirin
- At high risk of excessive bleeding (e.g. large trauma or haemorrhage, urgent need for major surgery, or uncorrectable coagulopathy) in the opinion of the treating physician
- Hospital-acquired pneumonia, defined as related to an inpatient hospital stay within the last 10 days, or acquired at least 48 hours after current admission
- Discharged without a 'Decision to Admit' to hospital by urgent care / emergency department
- Unlikely to tolerate or adhere to medication regimen
- Prisoners
- Known to be pregnant
- Life expectancy less than 3 months due to pre-existing condition (e.g. terminal malignancy)
- Presentation more likely due to acute COVID-19 pneumonitis in the opinion of the treating physician — i.e. newly positive PCR or similar antigen test for COVID-19
- Enrolment onto another study where the combined burden on the participant would be too high, or where dual enrolment would compromise one or both studies' objectives
Note: Anti-coagulation medication is not an exclusion criterion; however, the increased bleeding risk should be considered by the clinician.
Step-by-step recruitment guide
Standard working hours (09:00 – 17:00)
1
Contact the ED Research Team when an eligible patient arrives in the ED — send a message via Epic chat to "ED Research Team" or phone 217907.
2
The ED Research Team will see the patient to arrange consent and randomisation.
Out of hours & weekends
1
Send the ED Research Team an Epic message with the patient's details. The team has 7 days from admission to approach the patient to discuss the trial.
Equipment & materials locations