Comments on “Efficacy and safety of adjunctive corticosteroids in the treatment of severe community-acquired pneumonia: a systematic review and meta-analysis of randomized controlled trials”

Heterogeneity among different studies The authors pooled results from seven studies from 1993 to 2023 and used the I2 statistic to assess the heterogeneity. The authors reached the conclusion that “low heterogeneity in most outcomes” was observed based on low I2 estimates. However, tests for heterogeneity using the I2 statistic is often underpowered, especially with a small number of included study; it is thus insufficient to conclude that the studies have low heterogeneity based on the I2 statistic alone. In addition, a close examination of the seven included studies would reveal several potentially important sources of heterogeneity. First, the definition of comparison for each randomized controlled trial (RCT) is different as the standard of care has changed significantly over the past 30 years. The increasing prevalence of antimicrobial resistance leading to varying choices of antibiotics, adoption of high flow nasal cannulation, and changing ventilation strategies are some examples [2–4]. Second, different regimens of corticosteroids were administered in each RCT, which should result in significant variability among the studies included. Third, different patient populations were included in each RCT. For example, Torres et al.’s study focused only on patients with C-reactive protein (CRP) > 150 mg/L at admission while other studies did not exclude patients based on their CRP levels [5]. The pooled estimates should thus be interpreted with caution and consideration for the qualitative differences among the studies. To account for the low power of the I2 statistic, it may be of interest to still conduct an exploratory analysis of the potential sources of heterogeneity using meta-regression.


COMMENT
Comments on "Efficacy and safety of adjunctive corticosteroids in the treatment of severe community-acquired pneumonia: a systematic review and meta-analysis of randomized controlled trials" Ming-hao Luo 1,2 , Zengyi Wan 3 , Guo-wei Tu 1 and Zhe Luo 1* Dear editor, We read with great interest the article by Wu et al., in which they studied the efficacy and safety of adjunctive corticosteroids in severe community-acquired pneumonia [1].The authors ought to be congratulated for such an updated review.However, we have concerns regarding the conclusion of analysis.

Heterogeneity among different studies
The authors pooled results from seven studies from 1993 to 2023 and used the I 2 statistic to assess the heterogeneity.The authors reached the conclusion that "low heterogeneity in most outcomes" was observed based on low I 2 estimates.However, tests for heterogeneity using the I 2 statistic is often underpowered, especially with a small number of included study; it is thus insufficient to conclude that the studies have low heterogeneity based on the I 2 statistic alone.
In addition, a close examination of the seven included studies would reveal several potentially important sources of heterogeneity.First, the definition of comparison for each randomized controlled trial (RCT) is different as the standard of care has changed significantly over the past 30 years.The increasing prevalence of antimicrobial resistance leading to varying choices of antibiotics, adoption of high flow nasal cannulation, and changing ventilation strategies are some examples [2][3][4].Second, different regimens of corticosteroids were administered in each RCT, which should result in significant variability among the studies included.Third, different patient populations were included in each RCT.For example, Torres et al. 's study focused only on patients with C-reactive protein (CRP) > 150 mg/L at admission while other studies did not exclude patients based on their CRP levels [5].The pooled estimates should thus be interpreted with caution and consideration for the qualitative differences among the studies.To account for the low power of the I 2 statistic, it may be of interest to still conduct an exploratory analysis of the potential sources of heterogeneity using meta-regression.
administered "200 mg daily for either 4 or 7 days as determined by clinical improvement, followed by tapering for a total of 8 or 14 days, " not "200 mg daily for either 4 or 8 days" [6].It should thus be included in the tapering subgroup and the > 8 days of treatment subgroup in the subgroup analysis.Further, the mortality outcomes from the included studies were not consistent and did not always match the primary outcome of this meta-analysis (i.e., 30-day all-cause mortality) (Table 1).

Subgroup analysis
The authors conducted subgroup analysis based on predefined criteria and found that mortality benefits were consistently observed in most of the subgroup analyses, particularly for patients aged 60 years or older, without initial septic shock, with ICU admission, use of hydrocortisone and receiving corticosteroid for a duration of ≤ 8 days and not undergoing corticosteroid tapering.However, it should be noted that some subgroups were derived from only one study, in addition to the point mentioned above that a few studies were misclassified.More importantly, the level of CRP was not considered in the subgroup analysis even if previous trials revealed its clinical significance.In a study conducted by Dequin et al., although overall mortality benefits were observed, subgroup analysis revealed no significant difference in the number of deaths among patients with a CRP of under 15 mg/dL (− 2.4 percentage points; 95% CI − 10.7 to 6.0) [6].The use of CRP, whether as an inclusion criterion in future clinical trials or as part of subgroup analysis, needs to be emphasized (Table 1).
Overall, the published meta-analysis has offered important information regarding the rationale of corticosteroids in patients with severe community-acquired pneumonia.But the improvement in mortality, and the population in which corticosteroids would reveal the most benefits should be interpreted critically and reviewed with caution.Further studies are urged to offer more definitive answers.

Table 1
Mortality type and CRP reported in the included study CRP C-reactive protein, ICU intensive care unit Reported in baseline and was compared on day 2, 4, 6 and 8 El-Ghamrawy et al. [9] 2006 Reported mortality rate without specifying the type Not indicated Confalonier et al. [10] 2005 Mortality by day 8, ICU mortality, hospital mortality and 60-day mortality Reported in baseline and was compared on day 1, 2, 3, 6 and 8 Marik et al. [11] 1993 Reported mortality rate without specifying the type Not indicated