Pulmonary Disorders I
Corticosteroids
Proposed rationale for corticosteroid use in ARDS was to prevent fibroproliferation with subsequent
alveolar fibrosis from a proinflammatory response.
Steroids may improve oxygenation, but randomized trials found no definitive mortality benefit.
Although the optimal timing of use remains unknown, consideration may be given in patients
with early (less than 7 days) and late (7 days or more), whereas initiation beyond 14 days after
onset was associated with higher death rates in the LaSRS trial. (N Engl J Med 2006;354:1671-84;
patients initiated on steroids after 14 days of ARDS onset may be misleading. It should be noted this
specific cohort had significant baseline characteristic variation or difference as well as atypically
low death rates in the control group for 60-day (8%) and 180-day (12%) mortality (N Engl J Med
2006;354:1671-84). Furthermore, no significant differences in mortality were found between
steroid and control groups in the greater than 14 days cohort after adjusting for important baseline
Update: Guidelines on Use of Corticosteroids updated their recommendations from 2017, removing
the specification of βearly moderate to severe ARDS.β Both the SCCM and the 2024 ATS ARDS
guidelines suggest the use of corticosteroids and provide no specific recommendation to choose
between steroid molecules.
The DEXA-ARDS clinical trial was the first randomized, placebo-controlled clinical trial
2020;8:267-76). The corticosteroid group consisted of dexamethasone 20 mg intravenously daily
over the first 5 days, followed by 10 mg intravenously daily for up to 10 days or upon extubation
(if occurring prior to day 10). Dexamethasone was associated with increased mean ventilator-
free days over placebo at 1 month (12.3 Β± 9.9 and 7.5 Β± 9.9 days, respectively; p<0.0001). Other
secondary outcomes, including mortality (all-cause, ICU, in-hospital) and MV duration (among all
ICU survivors at day 60), significantly favored the dexamethasone group. Of note, hyperglycemia,
secondary infections, and barotrauma were similar between study groups. The novelty of this trial
compared with previously published corticosteroid studies was the concurrent use of contemporary
lung-protective MV strategies.
| d. | Published guidelines provide minimal direction for clinical practice decision-making regarding |
|---|
the best approach for corticosteroid use in ARDS (BMJ Open Respir Res. 2019;6:e000420; Ann
selected patients with ARDS, whereas neither of the 2019 guidelines provides any recommendations
because of the paucity of quality data (Table 4).
Source
Summary
GRADE Recommendation
Annane 2017
Suggest use in early moderate to severe ARDS
(Pao2/Fio2 < 200 mm Hg AND within 14 d of onset)
Conditional recommendation;
moderate quality of evidence
Griffiths 2019
Limited quality data, resulting in inability to
make a recommendation; rather, states that further
research is warranted
Research recommendation
Papazian 2019
Not reported
Not reported
2024;52(5):e219-e233 2024
Suggest use in adult critically ill patients with
ARDS
Conditional recommendation;
moderate quality of evidence
Qadir 2024
Suggest use in patients with ARDS
Conditional recommendation;
moderate quality of evidence
Abbreviations: ARDS, acute respiratory distress syndrome; Fio2, fraction of inspired oxygen.