2014
DOI: 10.1056/nejmoa1403285
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Simvastatin in the Acute Respiratory Distress Syndrome

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Cited by 395 publications
(337 citation statements)
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References 17 publications
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“…infections, [201][202][203] chronic obstructive lung disease, [204][205][206] and acute respiratory distress syndrome 207 ), but those claims have been reliably refuted by randomized trials of adequate size. [208][209][210][211][212] These findings reinforce concerns about basing inference about treatment effects on relatively small numbers of events in randomized trials or on observational studies irrespective of their size. 3,4,213,214 In summary, lowering LDL cholesterol with statin therapy has been shown to prevent both non-fatal and fatal major vascular events in a wide range of circumstances, and the absolute benefits depend chiefly on an individual's absolute risk of such events and on the magnitude of the LDL-reduction that is achieved (as well as the duration of treatment).…”
Section: Other Beneficial Effects That Have Been Attributed To Statinmentioning
confidence: 90%
“…infections, [201][202][203] chronic obstructive lung disease, [204][205][206] and acute respiratory distress syndrome 207 ), but those claims have been reliably refuted by randomized trials of adequate size. [208][209][210][211][212] These findings reinforce concerns about basing inference about treatment effects on relatively small numbers of events in randomized trials or on observational studies irrespective of their size. 3,4,213,214 In summary, lowering LDL cholesterol with statin therapy has been shown to prevent both non-fatal and fatal major vascular events in a wide range of circumstances, and the absolute benefits depend chiefly on an individual's absolute risk of such events and on the magnitude of the LDL-reduction that is achieved (as well as the duration of treatment).…”
Section: Other Beneficial Effects That Have Been Attributed To Statinmentioning
confidence: 90%
“…There was no significant difference between the two groups in OI at day 7 (the primary outcome) or in any other secondary physiological outcomes. The KGF group, compared to placebo, had fewer median ventilatorfree days (1 [0-17] versus 20 [13][14][15][16][17][18][19][20][21][22] days; difference -8 days, 95% CI -17--2; P < 0·001), a longer median duration of ventilation in survivors (16 [13-30] versus 11 [8][9][10][11][12][13][14][15][16] days; difference 6 days, 95% CI 2-14; P = 0·002) and a higher mortality at 28 days (31·0% versus 9·7%; risk ratio 3·2 95% CI 1·0-10·7; P = 0·054).…”
Section: Disseminationmentioning
confidence: 99%
“…The concept of fragility is a construct that may help clarify just how "fragile" the results of a clinical trial may be by describing how many extra (or fewer) outcome events are required to alter a statistically significant result [11]. In both the STATInS and HARP-2 trials [12,13] an alteration of just three events would have yielded statistically significant results in favour of statin use based on mortality outcomes.…”
mentioning
confidence: 99%