Hydrocortisone treatment in early sepsis-associated acute respiratory distress syndrome: results of a randomized controlled trial

Acute respiratory distress syndrome (ARDS) is a secondary disease that follows—usually within 6–48 h—a primary disease of multifactorial etiology (most frequently pneumonia and extrapulmonary sepsis [1]) associated with severe systemic inflammation. Inflammatory mediators released into the systemic circulation (systemic inflammation) from the site of infection reach the broad pulmonary capillary surface, producing severe and diffuse inflammatory exudate of the pulmonary lobules and resulting in hypoxemic respiratory failure [2]. In addition to the lung, systemic inflammation involves other vital organs, particularly the cardiovascular and renal systems. In ARDS, baseline plasma inflammatory cytokine levels are associated with a significantly increased risk of death after adjustment for tidal volume (6 ml/kg vs. 12 ml/kg) and severity of illness [3], and higher inflammatory cytokine levels are found in the largest subgroup of sepsis-associated ARDS [3]. Sepsis-associated ARDS, in comparison with sepsis without ARDS [4] or non-sepsis-related ARDS [1, 5], is associated with significantly higher morbidity and higher (up to 60 % [4, 6]) mortality.

In sepsis and ARDS, systemic inflammation is activated by the nuclear factor-κB (NF-κB) signaling system and downregulated by activated glucocorticoid receptor α (GRα) [7]. In these patients, inadequate (endogenous glucocorticoid-activated) GRα-mediated downregulation of proinflammatory transcription factor NF-κB in circulating and tissue cells leads to higher initial levels and persistent elevation over time of plasma and bronchoalveolar lavage markers of inflammation, hemostasis, and tissue repair [7]. Inadequate intracellular GRα-mediated anti-inflammatory activity for the severity of the patient’s illness was recently termed critical illness-related corticosteroid insufficiency (CIRCI) [8]. Experimental [9] and clinical research [7] shows that CIRCI can be improved with quantitatively and temporally adequate glucocorticoid administration, and a new meta-analysis provides support for its use in ARDS of multifactorial etiology [10].

Despite the high prevalence and mortality of sepsis-associated ARDS, a prospective randomized controlled trial (RCT) investigating glucocorticoid treatment is lacking. We conducted this RCT to test the hypothesis that the anti-inflammatory action of 7 days of hydrocortisone treatment would result in accelerated disease resolution and lower mortality. The primary outcome was 28-day all-cause mortality; secondary endpoints included 28-day survival without organ support and 60-day mortality.

Figure 1 shows progress through the phases of the trial. The trial was stopped when target recruitment was achieved. Of the 206 randomized patients, 9 (6 hydrocortisone, 3 placebo) withdrew consent after randomization and were excluded from analysis. Two hundred thirteen patients were excluded because they were already receiving hydrocortisone for hemodynamic stabilization of refractory septic shock on high-dose vasopressors. The intention-to-treat analysis included 197 patients (98 hydrocortisone, 99 placebo). For the primary endpoint, none of the patients in the intention-to-treat analysis were lost to follow-up. Unless specified otherwise, comparison between groups is reported as hydrocortisone vs. placebo. The mean time (in hours) from meeting severe sepsis criteria to randomization was similar between groups (11.9 ± 7.9 h vs.14.0 ± 10.2 h; p = 0.21).

The baseline characteristics of each group at study entry were similar (Table 1). Most patients had vasopressor-dependent shock (n = 154; all but 7 with a lactate level >2 mmol/L) [20] and met criteria for moderate to severe ARDS (n = 135). Lactate level (3.9 ± 2.2 mmol/L vs. 4.0 ± 2.5 mmol/L; p = 0.95) and distribution of patients with fluid-responsive shock was similar (6.1 % vs. 4.0 %; p = 0.55). The most common comorbidities were hypertension and diabetes mellitus. The leading cause of sepsis was pneumonia; overall, bacteremia was present in 28 %. During treatment intervention, the treated group had significant improvement in gas exchange and LIS (Fig. 2), as well as a similar rate of extubation (43.3 % vs. 31.6 %; p = 0.11). On study day 7 (mean ± SE), the ratio of partial pressure of oxygen in arterial blood to fraction of inspired oxygen (PaO₂/FiO₂) was 319.1 ± 9.7 vs. 266.3 ± 11.7 (p = 0.001), and the LIS was 1.1 ± 0.1 vs. 1.4 ± 0.1 (p = 0.01). These positive effects persisted at day 14 (last measurement), 7 days after removal of the study drug. In addition, the random coefficients models using the longitudinal data for PaO₂/FiO₂ and LIS revealed that the treatment arm had significantly improved profiles over time (p = 0.002).

Data for the primary and secondary outcomes are shown in Table 2. By day 28, the treated group had a nonsignificant reduction in duration (days) of MV (10.4 ± 9.4 days vs. 12.4 ± 11.0 days; p = 0.16) and vasopressor support (4.8 ± 3.0 days vs. 6.8 ± 5.7 days; p = 0.16), as well as a nonsignificant increase in patients alive on day 28 without organ support. To evaluate time to survival without organ support at 28 days, a Kaplan-Meier curve was plotted (Fig. 3a). After adjustment by Cox regression analysis for two covariates found to be significant in the multivariate survival model (Table 3), the hydrocortisone cohort showed an HR of 0.74 (95 % CI 0.51–1.07; p = 0.107).

Unadjusted mortality at day 28 and day 60 was similar (Table 2). Subgroup analysis for the relative risk of death at days 28 and 60 is shown in Table 4. After adjustment by Cox regression analysis for covariates we found significant in the multivariate survival model (Table 3), the HRs for death at days 28 and 60 were 0.80 (95 % CI 0.46–1.41; p = 0.44) and 0.81 (95 % 0.51–1.28; p = 0.37), respectively. The APACHE II score was the most significant (p = 0.001) variable detected in the survival models (Table 3). A Kaplan-Meier curve adjusted for vasopressor-dependent shock and LIS at study entry was generated for the subgroups of patients with APACHE II score <25 vs. ≥25 by treatment (Fig. 3b). After adjustment for the presence of vasopressor-dependent shock and LIS, in the largest subgroup with APACHE II score <25 (n = 126), the HR for probability of survival at 28 days was 0.57 (95 % CI 0.24–1.36, p = 0.20), and at 60 days it was 0.69 (95 % CI 0.36–1.31; p = 0.25). In the subgroup with APACHE II score ≥25 (n = 71), the HR for probability of survival at 28 days was 1.05 (95 % CI 0.49–2.23; p = 0.60), and at 60 days it was 0.97 (95 % CI 0.50–1.88; p = 0.92).

With the exception of hyperglycemia (80.6 % vs. 67.7 %; p = 0.04), the rate of adverse events was similar (Table 5). The incidence of hyperglycemia in patients with (80 % vs. 70 %; p = 0.45) and without (81 % vs. 66 %; p = 0.09) underlying diabetes was similar. Neither diabetes nor hyperglycemia (at study entry or after randomization) had an impact on survival (data not shown).

This is the first prospective trial investigating a 7-day course of low-dose hydrocortisone treatment in patients with sepsis-associated early ARDS. Hydrocortisone treatment was associated with rapid and sustained improvement in pulmonary physiology and a nonsignificant increase (65.3 % vs. 55.6 %; p = 0.19) in patients alive on day 28 without organ support. The significant physiological improvements did not translate into an overall survival benefit for the whole group (HR 0.80, 95 % CI 0.46–1.41; p = 0.44), however, and for the largest subgroup of patients with APACHE II score <25 (HR 0.57, 95 % CI 0.24–1.36; p = 0.20). Importantly, in agreement with the literature on sepsis [21] and ARDS [10], we did not find an increased risk of complications, with the exception of hyperglycemia, and hyperglycemia did not affect outcome. Our findings are placed in the context of the limitations of the trial and the updated literature.

Our study has several limitations. First, and most important, our study was significantly underpowered by the recruitment of patients with less severe illness and lower mortality. While the original sample size calculation was based on a control mortality of 60 %, originating from the findings of the largest prior trial [6], our control 28-day mortality was almost half that and similar to the most recent report [5]. This is partly attributable to two main factors: (1) exclusion of a large number of patients who, during the screening process, were already receiving hydrocortisone treatment for refractory septic shock [14]; and (2) improved outcome as a result of implementing the international guidelines of the Surviving Sepsis Campaign [14]. In comparison with prior RCTs, our trial differs by not including longitudinal measurements of systemic inflammatory response syndrome parameters or markers of systemic inflammation [6, 22‐27] and an assessment of adrenal function [6, 26].

Seven RCTs published in the English language investigated prolonged glucocorticoid treatment in ARDS [6, 22‐27]. In each trial, glucocorticoid treatment was associated with a significant reduction in markers of systemic inflammation (inflammatory cytokines and/or C-reactive protein levels) and improvement in lung function. Three trials investigated hydrocortisone treatment in sepsis [22, 23] or septic shock-associated ARDS [6]. The largest study [6] is a post hoc analysis of 177 patients with ARDS from a trial of vasopressor-dependent septic shock investigating hydrocortisone (dosage similar to our trial) and fludrocortisone (50 μg daily) treatment [28]. In the largest trial [6], among those randomized to receive the active drug, the larger subgroup (n = 129) of nonresponders to a short corticotropin test, contrary to responders (n = 48), had more days alive and off a mechanical ventilator (5.6 ± 8.8 days vs. 2.6 ± 6.6 days; p = 0.006) and improved survival (47 % vs. 25 %; p = 0.021). Two other trials [22, 23] of patients with severe community-acquired pneumonia included 94 patients on MV with early ARDS (16 % with shock). In both trials [22, 23], a hydrocortisone bolus (200 mg) followed by an infusion (240–300 mg/24 h) was associated with a significant reduction in duration of MV; one research group reported improved survival [22].

Four trials investigated prolonged methylprednisolone treatment in early [26, 27] and late [24, 25] ARDS and were the subject of a recent individual patient data (IPD) meta-analysis (n = 322) [10]. By study day 28, the methylprednisolone group had fewer patients dying while on MV (12 % vs. 29 %; p < 0.001) and more patients successfully extubated (80 % vs. 50 %; p < 0.001); hospital mortality was decreased (20 % vs. 33 %; p = 0.006). Importantly, each trial [24‐27] consistently reported a 9- to 10-day reduction in duration of MV during methylprednisolone administration (Table S3 supplementary material in [10]). All but one trial [25] incorporated slow tapering of the study drug after extubation; lack of slow tapering contributed to increased return to MV [25].

Our trial is a single-center RCT, which may raise concerns regarding the generalization of the results based on participants’ characteristics and the intervention tested. In comparison with our study, severity of illness scores and LISs were higher in five RCTs [6, 24‐27] and similar in two RCTs [22, 23]. Fundamental variables of the treatment protocol that may significantly affect overall response to glucocorticoid treatment in ARDS include study drug, dosage, and duration of administration, including tapering [7]. Our treatment intervention was comparable to the one investigated in the two RCTs with lower severity of illness [22, 23] and differed from the other five RCTs by study drug (hydrocortisone vs. hydrocortisone plus fludrocortisone [6] or methylprednisolone [24‐27]), duration of treatment (7 days vs. 14–28 days [24‐27]), and tapering (lack of tapering vs. slow tapering [24, 26, 27]).

In the past exogenous glucocorticoids were thought to be qualitatively indistinguishable because they act via the same receptor, but qualitative differences have been discovered, and one glucocorticoid cannot be simply replaced by another [29]. In reference to the RCTs described above [6, 24‐27], hydrocortisone has (1) less anti-inflammatory potency when it is not combined with fludrocortisone (a drug with both mineralocorticoid and glucocorticoid activities) and (2) lesser direct inhibitory NF-κB activity than methylprednisolone (half-maximal inhibitory concentration for NF-κB inhibition 16 and 2.8, respectively) [30]. Methylprednisolone, because of its greater penetration in lung tissue and longer residence time [31], is the most frequently used intravenous glucocorticoid for the treatment of severe acute inflammatory lung diseases [32].

New understanding of the central role played by glucocorticoids in resolution of inflammation and restoration of tissue homeostasis [33] provides support for longer duration of treatment incorporating slow tapering (up to 4 weeks). A recent IPD meta-analysis demonstrates that lack of glucocorticoid tapering after extubation of patients with ARDS is frequently associated with clinical deterioration and return to MV [10]. Similarly, researchers in a comparison study of two concurrent RCTs—hydrocortisone 7-day infusion vs. prolonged methylprednisolone—reported that removing hydrocortisone without tapering led to a rebound of systemic inflammation with worsening organ dysfunction requiring reintubation [34]. In our study, we did not measure markers of inflammation and cannot comment on the presence of rebound inflammation. After completion of study treatment, however, the hydrocortisone group continued to demonstrate improved gas exchange and LIS, and the two groups had a similar rate of reintubation by day 28. While these findings may suggest that a clinically significant rebound effect is less likely, most patients (n = 55) had hydrocortisone treatment discontinued prior to extubation, masking a possible rebound.

Our trial does not confirm the benefits reported on the basis of prior RCTs for reduction in duration of MV and intensive care unit stay [22‐27] or survival [22‐24, 26, 27]. Our study is underpowered for the exploratory analysis to demonstrate a survival benefit in patients with APACHE II scores <25. It is likely that this cohort had a lesser degree of systemic inflammation than patients with APACHE II scores ≥25. Lacking measurement of markers of systemic inflammation over time, we cannot comment on whether our treatment protocol was less effective in achieving a significant anti-inflammatory effect in those with APACHE II scores ≥25.

In sepsis-associated ARDS, early administration of hydrocortisone 50 mg intravenously every 6 h for 7 days was safe and associated with improved lung function without a significant survival benefit. Our study is underpowered for the exploratory analysis to demonstrate a survival benefit in patients with APACHE II scores <25.