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Eur Respir J 2008; 32:259-264
Copyright ©ERS Journals Ltd 2008

Corticosteroids in severe pneumonia

O. Sibila1,2,4, C. Agustí3,4 and A. Torres3,4

1 Respiratory Dept, Son Dureta University Hospital, Palma de Mallorca, and 2 Caubet-Cimera Foundation, Bunyola, and 3 Respiratory Dept, Institut Clínic del Tòrax, Hospital Clínic, Institut d’Investigacions Biomèdiques August Pi i Sunyer, Barcelona, and 4 Ciber Enfermedades Respiratorias, Spain.

CORRESPONDENCE: A. Torres, Servei de Pneumologia, Institut Clinic del Tórax, Hospital Clinic, Villarroel 170, 08036, Barcelona, Spain. Fax: 34 932275549. E-mail: atorres{at}ub.edu

Keywords: Community-acquired pneumonia, corticosteroids, inflammatory response, nosocomial pneumonia, severe pneumonia

Received: November 16, 2007
Accepted February 18, 2008


   ABSTRACT
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 ABSTRACT
INFLAMMATORY RESPONSE ASSOCIATED...
 GLUCOCORTICOSTEROIDS AND THE...
 ROLE OF GLUCOCORTICOSTEROIDS IN...
 LESSONS TO BE LEARNED...
 SUMMARY
 Statement of interest
 REFERENCES
 
The mortality rate in severe community- or hospital-acquired pneumonia is very high, ranging 20–50%. Despite advances in antimicrobial therapy and supportive measures, this rate has not changed in recent years, suggesting that other factors are also responsible for the poor outcome. An abnormal increase in the local and systemic inflammatory response is associated with poor outcome, and this occurs despite adequate antibiotic therapy.

There is evidence that acute administration of corticosteroids decreases the inflammatory response and might decrease mortality in severe pneumonia. This has been shown in one small randomised controlled study, terminated prematurely due to 0% mortality in the intervention arm. In addition, an experimental study showed that glucocorticosteroids decrease lung inflammatory response and lung bacterial burden, confirming the results obtained through in vitro investigations.

Although these results are promising and suggest a novel role of glucocorticosteroids in pneumonia, the inherent risks and potential side-effects of these drugs require further controlled clinical trials in order to better define the target population before their general use in clinical practice. Specifically, dosage, period of administration, titration, tapering and side-effects are some of the key questions that need to be investigated.

Pneumonia is the most prevalent infectious respiratory disease. It entails high morbidity and mortality and large healthcare system expenses. Community-acquired pneumonia (CAP) is one of the 10 leading causes of death worldwide. Approximately 20% of CAP patients require hospitalisation, 25% of whom are admitted to an intensive care unit (ICU) and have a mortality rate of 30–50% 1.

Despite progress in life-support measures and antimicrobial therapy, the mortality of severe pneumonia has not varied since the mid-1990s 2, 3, suggesting that other factors are of crucial importance in the evolution of this respiratory infection.

One of the key factors determining the progression of pneumonia is the host inflammatory response, which seems to be increased excessively in nonresponding severe pneumonia 4, 5. The purpose of the present article is to review the evidence in the literature supporting a beneficial role of glucocorticosteroids (GCs) as an adjuvant treatment in severe pneumonia.


   INFLAMMATORY RESPONSE ASSOCIATED WITH PNEUMONIA
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It is well known that the arrival of pathogens in the alveolar space creates a complex inflammatory response, with the interaction of several defence mechanisms and the production of a number of inflammatory mediators and acute phase proteins. The aim of this inflammatory response is to control the progression of the infection and to destroy microorganisms, and consists of several pro-inflammatory (tumour necrosis factor (TNF)-{alpha} and interleukin (IL)-1β, -6 and -8) and anti-inflammatory cytokines (IL-10, IL-1 receptor antagonist and the soluble 55-kDa and 75-kDa TNF receptors). Cytokines promote the migration of defence cells, such as neutrophils, lymphocytes and platelets, through the circulatory system to inflammatory sites 6.

All of this process is beneficial as long as it is limited to the control of local infection. If this reaction is overproportioned, several systemic consequences negatively influence the clinical progression of the infection 7.

This excessive inflammatory response is associated with the release of inflammatory mediators that can be detected in serum or bronchoalveolar lavage fluid (BALF) and have been shown to be of diagnostic and prognostic value.

The association between the overproduction of pro-inflammatory cytokines, such as TNF-{alpha} or IL-6, in serum and fatality in septic shock patients has confirmed that cytokines are markers of severity and probably major mediators involved in the pathogenesis of septic shock 8. Studies concerning severe pneumonia have shown that, despite the inflammatory response initially being compartmentalised 9, an increase in inflammatory cytokine levels in serum is also detected and related to poor prognosis 10–13.

In addition, a recent study by Yende et al. 14 has demonstrated that patients with high levels of circulating inflammatory cytokines in clinical stability (prior to infection) have a higher risk of suffering from CAP, suggesting a crucial role of the inflammatory response in all aspects of the pathogenicity of this infection.


   GLUCOCORTICOSTEROIDS AND THE INFLAMMATORY RESPONSE: MOLECULAR MECHANISMS
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GCs inhibit the expression and action of many cytokines involved in the inflammatory response associated with pneumonia. GCs are mainly transported in the blood complexed to transcortin (or corticosteroid-binding globulin) and albumin, although a small proportion is in a free metabolically activate state. The free GC molecules readily cross the plasma membrane into the cytoplasm. Once in the cytoplasm, GCs bind to their specific receptor, the GC receptor (GR){alpha}. GR{alpha} exists as a heterocomplex located in the cytoplasm of nearly all human cells 15. The anti-inflammatory and immunosuppressive effects of GCs are due to three molecular mechanisms 15, 16. First, the ligand-activated GR{alpha} binds as a homodimer to specific DNA sequences, so-called GR-responsive elements, usually located in the promoter regions of target genes, in order to induce transcription, a phenomenon called transactivation. Secondly, indirect negative regulation of gene expression (transrepression) is achieved by GR–protein interaction. The ligand-activated receptor binds as a monomer to key pro-inflammatory transcription factors, such as activator protein-1 and nuclear factor-{kappa}B. The resulting complex inhibits the initiation of transcription of relevant genes. This mechanism has been shown to be involved in the inhibition of different gene products that play a central role in inflammation (table 1Go). The third mechanism is GC signalling through membrane-associated receptors and second messengers (so-called nongenomic pathways). The best-described nongenomic mechanism involves the activation of endothelial nitric oxide synthetase (eNOS). Nontranscriptional activation of eNOS by GR represents a physiologically important signalling pathway by which GCs exert their rapid anti-inflammatory effects. Binding of GCs to the GR stimulates phosphatidylinositol-3’-kinase and Akt kinase, leading to eNOS activation and nitric oxide-dependent vasorelaxation 17.


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  		Table 1— Effect of glucocorticosteroids on gene transcription

 

   ROLE OF GLUCOCORTICOSTEROIDS IN SEVERE PNEUMONIA
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Based on the critical role of the inflammatory response in the progression of infections and the anti-inflammatory potential of GCs, it is not surprising that these drugs have been tested in clinical practice. To date, the results have been controversial, and clear indications for their use are currently sparse. The usefulness of GCs seems to have been demonstrated in infections such as bacterial meningitis and pneumonia caused by Pneumocystis jiroveci 18. In the field of sepsis, the crucial role of the associated inflammatory response to infection has been well demonstrated. In this critical infection, current recommendations support the use of hydrocortisone at a physiological dose (i.e. 200–300 mg hydrocortisone·day–1). These recommendations were based on the encouraging results of four small trials and subsequently one larger trial 19–23. All five trials reported fewer deaths in patients who received GCs. A meta-analysis of these trials suggested that the use of corticosteroids reduced mortality 24. As the balance of evidence regarding GC treatment for septic shock shifted towards the positive, a very important investigation, published in 2008, brought more shadows than light. This study represents the largest multicentric randomised placebo-controlled trial conducted on this topic to date, involving 499 patients with septic shock. The main result of this study was that hydrocortisone at a physiological dose does not decrease mortality in a general population of patients with septic shock, even though the drug hastens reversal of shock 25. All in all, substantial uncertainty regarding the role of GCs in septic shock persists, and some authorities in the field have encouraged the launch of new trials with much higher numbers of patients in order to avoid generating further uncertainty 26.

The use of GCs as an adjunctive therapy in severe pneumonia has not been evaluated so extensively as in septic shock. A pilot study by Montón et al. 27, in patients with severe pneumonia requiring mechanical ventilation, detected a possible immunosuppressive effect of GCs in pneumonia. In this study, a decrease in levels of pro-inflammatory cytokines, such as IL-6 and TNF-{alpha}, was observed in both serum and BALF from patients who had received GCs as a coadjuvant treatment (in most cases, as a bronchodilatory treatment associated with antibiotic treatment). Furthermore, in the group of patients receiving GC treatment, a trend towards lower mortality was also observed, although the population of the study comprised only 20 patients.

The relationship between the intensity of the inflammatory response in severe pneumonia, GC dosage and prognosis was subsequently studied by AgustÍ et al. 28. In this study, the inflammatory response in BALF and serum from patients with severe pneumonia who had received GC treatment for long periods (>30 days) was assessed. Results were compared to those from a group of patients with severe pneumonia without GC treatment and with those from a third group of patients with pneumonia who had received GC treatment for a short period of time (9±7 days, in most cases as a bronchodilatory treatment). These authors observed that the local inflammatory response (in BALF) and systemic inflammatory response (in serum), measured by such relevant cytokines as IL-6 or TNF-{alpha}, was markedly diminished in patients who had received GCs for longer periods of time compared to those who had not received such treatment. Furthermore, short-term administration of GCs had an intermediate effect in the suppression of the inflammatory response.

The mortality of the group of patients with severe pneumonia who had received long-term GC treatment was similar to that of patients who had not received GC treatment. Interestingly, the patients who had received GC treatment for short periods of time and had shown an attenuated inflammatory response exhibited a tendency towards lower mortality 28.

These results suggest that deep attenuation of the inflammatory response by prolonged corticosteroid treatment can be as harmful as an exaggerated inflammatory response, but its moderated attenuation by a short corticosteroid treatment can be beneficial for the modulation of the inflammatory response and for the prognosis of the disease. Studies performed by Keh et al. 29 seem to confirm the beneficial effects of low-dose GC treatment. Those authors demonstrated that low dosages of hydrocortisone achieved rapid haemodynamic stabilisation in patients with septic shock. The study verified that hydrocortisone attenuates the inflammatory and anti-inflammatory response, but does not have a negative effect on the phagocytic function of macrophages and monocytes.

In another work by Ioanas et al. 5, in a series of patients with ICU-acquired pneumonia requiring mechanical ventilation, the authors found that high levels of IL-6 and IL-8 at the time of diagnosis and IL-6 levels on day 3 were the only factors related to the lack of response to empirical antibiotic treatment, suggesting, again, that modulation of the potential inflammatory response could also be beneficial in this subgroup of patients. Furthermore, on multivariate analysis of the several factors that could be related to the lack of response to treatment, the authors found that the concomitant administration of GCs was a protective factor (odds ratio (OR) 0.21).

Meduri et al. 30 investigated prolonged methylprednisolone infusion (1 mg·kg body weight–1·day–1) in a randomised trial in 91 patients with early acute respiratory distress syndrome (ARDS), 43% caused by severe CAP. Methylprednisolone-treated patients with severe CAP showed a higher rate of extubation (61 versus 14%; p = 0.07) and lower C-reactive protein levels (2.5±1.8 versus 12.1±8.1 mg·dL–1; p = 0.06) by day 7. Treatment was associated with a nonsignificant reduction in the median duration of mechanical ventilation (5 versus 10 days; p = 0.13) and hospital mortality (16.5 versus 42.5%; p = 0.3) 30.

Another randomised study by Annane et al. 21 in patients with septic shock showed that 28-day mortality among patients with severe CAP was 45 and 65% for patients randomised to low-dose hydrocortisone (n = 47) and placebo (n = 54), respectively (OR 0.44; 95% confidence interval (CI) 0.20–0.98; p = 0.044).

Finally, a recent retrospective study in 308 patients with severe CAP (defined as classes IV and V of the prognostic severity index score) showed that mortality was decreased in those patients who had received simultaneous administration of systemic corticosteroids along with antibiotic treatment (OR 0.28; 95% CI 0.113–0.732) 31.

The only randomised controlled study in humans regarding the role of GCs in severe pneumonia was published in 2005 by Confalonieri et al. 32. These authors assessed the efficiency and safety of the administration of a continuous infusion of hydrocortisone in a double-blind randomised placebo-controlled trial including 46 patients with severe CAP requiring ICU admission. Of these patients, 23 received an intravenous bolus of hydrocortisone at a dose of 200 mg followed by a perfusion of 10 mg·h–1 for 7 days. These authors demonstrated a mortality reduction in the group treated with hydrocortisone (0 versus 30%; p = 0.009), a better modulation of the systemic inflammatory response (determined by serum C-reactive protein level) and a significant improvement in the main clinical end-points, such as chest radiographic results, multiple organ dysfunction score (severity scale), arterial oxygen tension (Pa,O2)/inspiratory oxygen fraction (FI,O2) ratio, and duration of ICU and hospital stay.

Although the intimal mechanisms by which the inflammatory response modulated by GCs can interfere with pulmonary infection are not well elucidated, in vitro studies and experimental work in animals have provided some clues regarding this issue. The present authors’ group has developed an experimental model of Pseudomonas aeruginosa pneumonia in ventilated pigs 10, in which the effect of GCs has been studied by comparing three groups of animals with severe pneumonia (those without treatment, those with antibiotic treatment and those with antibiotic treatment plus GCs). In this model, pigs treated with antibiotics plus GCs experienced, after 96 h of pneumonia onset, a decrease in the local inflammatory response compared to the other groups. Furthermore, animals treated with antibiotics plus GCs presented lower bacterial counts in both BALF and pulmonary tissue obtained at the end of the study, a finding that was related to a tendency to suffer from less-severe lesions, as revealed by a histopathological study 33. In this sense, Meduri et al. 34 have demonstrated, in an in vitro study, that certain bacterial strains possess receptors for the cytokines IL-1β and TNF-{alpha}, and that the exposure of bacteria to these cytokines enhances their growth and virulence. It has been proposed that GCs might restore the impaired capacity of phagocytic cells produced by excessive inflammation. Exposing human monocytic (U937) cells to progressively higher concentrations of lipopolysaccharide (LPS) enhanced the intracellular survival and replication of various species of bacteria. More importantly, when exposed to graded concentrations of methylprednisolone, U937 cells previously stimulated with LPS were able to suppress bacterial replication efficiently in a concentration-dependent manner. Finally, TNF-{alpha}, IL-1β and IL-6 mRNA levels in LPS-activated cells were reduced by treatment of such cells with methylprednisolone 34.


   LESSONS TO BE LEARNED FROM SEPSIS AND ACUTE RESPIRATORY DISTRESS SYNDROME
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Although the previously mentioned findings seem to point towards a beneficial effect of GC treatment in severe pneumonia, definitive confirmation of these potential benefits is required. In this sense, many lessons can be learned from studies performed in patients with septic shock and ARDS.

The first studies conducted in patients with sepsis and pneumonia suggested a rapid improvement of symptoms in patients receiving GCs, although effects on mortality were not evidenced, and some cases were associated with a higher number of side-effects and with poorer prognosis once the steroid treatment was suspended 20. Indeed, the potential for harmful side-effects due to GC treatment in these patients and the rebound effects that their tapering can cause in the evolution of the inflammatory process are the subject of intense debate 35. The prolonged use of GCs can alter the phagocytic action of macrophages and alveolar granulocytes, which can facilitate the acquisition of severe bacterial and opportunistic infections 36. Several studies involving patients with sepsis and ARDS have suggested that high-dose GCs increase the risk of secondary infections 37–39; however, a meta-analysis of moderate-dose GCs for sepsis did not substantiate this observation 40. The randomised controlled trial promoted by the National Heart, Lung, and Blood Institute (Bethesda, MD, USA), which included 188 patients with ARDS, did not detect an increased rate of nosocomial infection in the methylprednisolone group 41. Indeed, in this study, there were more cases of nosocomial pneumonia, septic shock and positive blood culture in the placebo group. The ARDS Network protocol did not incorporate infection surveillance, making it impossible to estimate the impact of undiagnosed infections on outcome. Failed or delayed recognition of nosocomial infections in the presence of a blunted febrile response represents a serious threat and may be more common than initially suspected. In the two randomised trials that incorporated infection surveillance 30, 42, nosocomial infections were frequently (56%) identified in the absence of fever.

Another important aspect to bear in mind is the duration of suppression of the GC treatment. There is ample evidence that rapid tapering of GC treatment can induce a haemodynamic and immunological rebound effect if pro-inflammatory cytokine levels increase again and their receptors continue being suppressed 43. Studies conducted in patients with septic shock have demonstrated that hydrocortisone infusion produces a significant decrease in the circulating levels of proteins dependent upon the transcription factor nuclear factor-{kappa}B, such as phospholipase A2, IL-6 and -8, and soluble E-selectin 29. The suppression of the treatment provokes a rebound effect in most of these mediators, which highlights the short-acting anti-inflammatory action of hydrocortisone and the need to provide prolonged treatment in order to achieve a durable anti-inflammatory effect 29, 44. As acknowledged by the authors of the ARDS Network trial, rapid tapering and removal of methylprednisolone probably contributed to the deterioration in Pa,O2/FI,O2 ratio and higher rate of intubation in the treatment arm 41.

Another concerning issue is the influence of GCs on muscle function. Certainly, the effects of moderate-dose GCs in crtically ill patients are now well understood. Recent studies of patients receiving assisted ventilation have found a strong association between corticosteroid treatment and muscle weakness 45, 46. In the ARDS Network trial, the overall rate of clinically suspected neuromyopathy was similar in the two groups evaluated; however, all nine reports of serious adverse events related to neuropathy or myopathy were in patients treated with methylprednisolone 41.


   SUMMARY
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 LESSONS TO BE LEARNED...
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In summary, there is evidence of efficacy of GCs in severe infections including severe pneumonia. Prolonged GC treatment in sepsis and ARDS is uniformly associated with significant improvement in various physiological and clinical parameters, such as improvement in Pa,O2/FI,O2 ratio, hastened reversal of shock and significant reduction in levels of markers of systemic inflammation and duration of mechanical ventilation and ICU stay 47.

In severe pneumonia, scientific evidence is still scarce. Current information suggests that treatment with low dosages of GC is able to modulate (or diminish) the inflammatory response associated with pneumonia and improve prognosis in this disease, mainly in cases in which an increased host inflammatory response has been demonstrated.

Although the only randomised controlled trial of glucocorticosteroids in severe pneumonia showed an improvement in mortality, lessons learned from sepsis and acute respiratory distress syndrome impose the exercise of considerable caution. Reliable treatment recommendations will be possible only if a much larger trial is conducted and many different key points are considered. It is of the utmost importance that studies are designed not only to give a better understanding of the effect of glucocorticosteroids in severe pneumonia but also to determine the type of glucocorticosteroid (hydrocortisone or methylprednisolone), the dosage to be administered and the duration and tapering of the treatment. A series of preventative measures must be implemented in the design of new trials in order to avoid severe harmful secondary effects, including: 1) intensive infection surveillance, 2) avoidance of paralytic agents, 3) avoidance of rebound inflammation with premature discontinuation of treatment, and 4) strict control of hyperglycaemia.


   Statement of interest
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None declared.


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