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Atorvastatin for reduction of 28-day mortality in severe and critical COVID-19 patients: a randomized controlled trial
被引:2
|作者:
Eltahan, Naglaa Hamdi
[1
]
Elsawy, Neamat Hamdy
[2
,3
]
Abdelaaty, Kholoud M.
[4
]
Elhamaky, Amal Salah
[5
]
Hassan, Ahmed H.
[6
]
Emara, Moataz Maher
[7
]
机构:
[1] Minist Hlth & Populat, Sherbin Cent Hosp, Sherbin, Egypt
[2] Minist Hlth & Populat, Epidemiol & Surveillance Dept, Prevent Sect, Fowa Hlth Dist, Fowa, Egypt
[3] Minist Hlth & Populat, Fowa Cent Hosp, Dept Clin Res, Fowa, Egypt
[4] Mansoura Univ, Specialized Med Hosp, Mansoura, Egypt
[5] Minist Hlth & Populat, Mansoura Specialized Hosp, Mansoura, Egypt
[6] Mansoura Univ, Mansoura Univ Hosp, Mansoura, Egypt
[7] Mansoura Univ, Dept Anesthesiol & Intens Care & Pain Med, Fac Med, 60 Elgomhoria St, Mansoura 35516, Egypt
关键词:
COVID-19;
SARS-CoV-2;
Coronavirus;
Statins;
hmg coa;
Atorvastatin;
Mortality;
D O I:
10.1186/s12931-024-02732-2
中图分类号:
R56 [呼吸系及胸部疾病];
学科分类号:
摘要:
BackgroundCOVID-19 is an abnormal host response to the SARS-CoV-2 infection, which is associated with endothelial dysfunction and multi-organ failure. Atorvastatin has been proposed to reduce COVID-19 severity and mortality in chronic and de-novo users.MethodsThis randomized double-blind trial included 220 COVID-19 patients admitted to Mansoura University's isolation hospital in Egypt. One hundred and ten cases were given 40 mg of atorvastatin once daily for 28 days (group A), while 110 received a placebo (group B). All patients received treatment as per hospital protocol. The primary outcome is all-cause mortality at 28 days. We also tracked 6-month mortality, time to clinical improvement, the risk of invasive mechanical ventilation, acute kidney injury, potential adverse events, and hospital and intensive care length of stay.ResultsThe 28-day all-cause mortality was 52/104 (50%) in group A vs. 54/103 (52.4%) in group B, odds ratio (OR) = 0.907 (0.526, 1.565), P = 0.727; adjusted OR = 0.773 (0.407, 1.47), P = 0.433. Six-month mortality occurred in 53/102 (52%) and 59/79 (60.8%) in group A vs. B, respectively, P = 0.208. Among hospital survivors in group A vs. group B, the median time to clinical improvement was 10 days (7-14) vs. 10 (7-15), P = 0.715; the duration of hospital stay was 10 days (7-14) vs. 10 (8-17), P = 0.378. Discontinuation was higher in group B (four vs. one), but statistically insignificant, P = 0.369.ConclusionsIn adults with severe or critical COVID-19, atorvastatin did not reduce the risk of 28-day or 6-month mortality and did not shorten the length of hospital stay or time to clinical improvement.Trial registration Clinical Trial Registry (NCT04952350) on July 1st, 2021. https://clinicaltrials.gov/ct2/show/NCT04952350ConclusionsIn adults with severe or critical COVID-19, atorvastatin did not reduce the risk of 28-day or 6-month mortality and did not shorten the length of hospital stay or time to clinical improvement.Trial registration Clinical Trial Registry (NCT04952350) on July 1st, 2021. https://clinicaltrials.gov/ct2/show/NCT04952350
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