Study/year | Country | Study design | No. total (statins/non-statins) | Patient characteristics | Jadad score | Statins group | Control group |
---|---|---|---|---|---|---|---|
Novak V et al.[17]/2009 | Israel | Double-blind placebo controlled randomized clinical trial. | 83 (42/41) | Not receiving statin therapy during the three months preceding the index admission, within 12Â h of admission to a general medical ward with a suspected or documented bacterial infection, and prescribed intravenous antibiotics therapy by their physicians. | 5 points | 40Â mg of simvastatin orally immediately following enrollment, and daily 20Â mg of simvastatin after that, until hospital discharge or the development of severe sepsis. | Placebo |
Kruger PS et al.[18]/2011 | Australia | Prospective randomized double-blind placebo-controlled trial | 150 (75/75) | Patients with any of 97 potential infection-related diagnoses; admitted to both the general wards or the intensive care unit; preexisting statin therapy and the treating physician prepared to either continue or discontinue this therapy | 5 points | 20Â mg of atorvastatin orally or via nasogastric tube at the earliest opportunity and was continued daily for the duration of hospital admission up to a maximum of 28Â days. | Placebo |
Patel JM et al.[19]/2012 | UK | phase II randomized double-blind placebo-controlled trial | 100 (49/51) | Documented new proven or suspected infection and the presence of any two of the signs and symptoms of infection (white blood cell >11 or <4 × 109/L, temperature >38°C or <36°C, heart rate >90 bpm, or respiratory rate >20/minute) for less than 24 hours. | 4 points | Atorvastatin 40 mg daily was administered orally within 24 hours of randomization. Treatment continued for the duration of their hospital stay or 28 days if earlier | Placebo |
Kruger P et al.[20]/2013 | Australia | Phase II, prospective, randomized, double-blind, placebo controlled trial | 250 (123/127) | Critically ill, had strongly suspected or proven infection, fulfilled three or more of the features of systemic inflammatory response syndrome within the 48Â hours and had an organ dysfunction of less than 24Â hours duration | 4 points | Take statins more than two weeks prior to hospital admission; Atorvastatin 20Â mg was orally or via nasogastric tube given following randomisation then continued daily until Day 14 or until death or discharge from the intensive care unit | Placebo |
Papazian L et al.[21]/2013 | France | Randomized, placebo-controlled, double-blind parallel-group trial | 284 (146/138) | Received mechanical ventilation in the intensive care unit for at least two days and had suspected ventilator-associated pneumonia, statins therapy started on the same day as antibiotic therapy | 5 points | Simvastatin 60Â mg given via a nasogastric tube or orally from study inclusion to ICU discharge, death or Day 28 | Placebo |