Published: 26 January 2022
Authors: Deirdre B. Fitzgerald , Grant W. Waterer , Charley Budgeon , Ranjan Shrestha , Edward T. Fysh , Sanjeevan Muruganandan , Christopher Stanley , Tajalli Saghaie , Arash Badiei , Calvin Sidhu , Hilman Harryanto , Victor Duong, Maree Azzopardi, David Manners, Norris S. H. Lan, Natalia D. Popowicz , Carolyn J. Peddle-McIntyre, Najib M.Rahman , Catherine A. Read , Ai Ling Tan , Seng Khee Gan, Kevin Murray, and Y. C. Gary Lee
Source: This abstract has been sourced from NZ Respiratory Research Review Issue 208
Rationale: Pleural effusion commonly complicates community-acquired pneumonia and is associated with intense pleural inflammation. Whether antiinflammatory treatment with corticosteroids improves outcomes is unknown.
Objectives: To assess the effects of corticosteroids in an adult population with pneumonia-related pleural effusion.
Methods: The STOPPE (Steroid Therapy and Outcome of Parapneumonic Pleural Effusions) trial was a pilot, multicenter, double-blinded, placebo-controlled, randomized trial involving six Australian centers. Patients with community-acquired pneumonia and pleural effusion were randomized (2:1) to intravenous dexamethasone (4 mg twice daily for 48 h) or placebo and followed for 30 days. Given the diverse effects of corticosteroids, a comprehensive range of clinical, serological, and imaging outcomes were assessed in this pilot trial (ACTRN12618000947202).
Measurements and Main Results: Eighty patients were randomized (one withdrawn before treatment) and received dexamethasone (n = 51) or placebo (n = 28). This pilot trial found no preliminary evidence of benefits of dexamethasone in improving time to sustained (>12 h) normalization of vital signs (temperature, oxygen saturations, blood pressure, heart, and respiratory rates): median, 41.0 (95% confidence interval, 32.3–54.5) versus 27.8 (15.4–49.5) hours in the placebo arm (hazard ratio, 0.729 [95% confidence interval, 0.453–1.173]; P = 0.193). Similarly, no differences in C-reactive protein or leukocyte counts were observed, except for a higher leukocyte count in the dexamethasone group at Day 3. Pleural drainage procedures were performed in 49.0% of dexamethasone-treated and 42.9% of placebo-treated patients (P = 0.60). Radiographic pleural opacification decreased over time with no consistent intergroup differences. Mean duration of antibiotic therapy (22.4 [SD, 15.4] vs. 20.4 [SD, 13.8] d) and median hospitalization (6.0 [interquartile range, 5.0–10.0] vs. 5.5 [interquartile range, 5.0–8.0] d) were similar between the dexamethasone and placebo groups. Serious adverse events occurred in 25.5% of dexamethasone-treated and 21.4% of placebo-treated patients. Transient hyperglycemia more commonly affected the dexamethasone group (15.6% vs. 7.1%).
Conclusions: Systemic corticosteroids showed no preliminary benefits in adults with parapneumonic effusions.
Clinical trial registered with www.anzctr.org.au (ACTRN12618000947202).
Link to abstract
NZ Respiratory Research Review Issue 208