TY - JOUR
T1 - Heterogeneity of treatment effect of higher dose dexamethasone by geographic region (Europe vs. India) in patients with COVID-19 and severe hypoxemia – a post hoc evaluation of the COVID STEROID 2 trial
AU - Tirupakuzhi Vijayaraghavan, Bharath Kumar
AU - Granholm, Anders
AU - Munch, Marie W.
AU - Kjær, Maj Brit N.
AU - Møller, Morten H.
AU - Perner, Anders
AU - Myatra, Sheila N.
AU - Jha, Vivekanand
AU - Jha, Vivekanand
AU - Jha, Vivekanand
AU - Hammond, Naomi
AU - Micallef, Sharon
AU - Venkatesh, Balasubramanian
AU - Hammond, Naomi
AU - Lange, Theis
AU - Munch, Marie W.
AU - Myatra, Sheila N.
AU - Tirupakuzhi Vijayaraghavan, Bharath Kumar
AU - Saseedharan, Sanjith
AU - Benfield, Thomas
AU - Wahlin, Rebecka R.
AU - Rasmussen, Bodil S.
AU - Andreasen, Anne Sofie
AU - Poulsen, Lone M.
AU - Cioccari, Luca
AU - Khan, Mohd S.
AU - Kapadia, Farhad
AU - Divatia, Jigeeshu V.
AU - Brøchner, Anne C.
AU - Bestle, Morten H.
AU - Helleberg, Marie
AU - Michelsen, Jens
AU - Padmanaban, Ajay
AU - Bose, Neeta
AU - Møller, Anders
AU - Borawake, Kapil
AU - Kristiansen, Klaus T.
AU - Shukla, Urvi
AU - Chew, Michelle S.
AU - Ulrik, Charlotte S.
AU - Kjær, Maj Brit N.
AU - Møller, Morten H.
AU - Meyhoff, Tine S.
AU - Vesterlund, Gitte K.
AU - Gluud, Christian
AU - Lange, Theis
AU - Marcussen, Klaus V.
AU - Nielsen, Henrik
AU - Jensen, Thomas S.
AU - Perner, Anders
AU - the COVID-STEROID 2 collaborators
N1 - Publisher Copyright:
© 2023 The Author(s)
PY - 2024
Y1 - 2024
N2 - Background: In the COVID-STEROID 2 trial there was suggestion of heterogeneity of treatment effects (HTE) between patients enrolled from Europe vs. India on the primary outcome. Whether there was HTE for the remaining patient-centred outcomes is unclear. Methods: In this post hoc analysis of the COVID-STEROID 2 trial, which compared 12 mg vs. 6 mg dexamethasone in adults with COVID-19 and severe hypoxemia, we evaluated HTE by geographical region (Europe vs. India) for secondary outcomes with analyses adjusted for stratification variables. Results are presented as risk differences (RDs) or mean differences (MDs) with 99% confidence intervals (CIs) and P-values from interaction tests. Findings: There were differences in mortality at day 28 (RD for Europe −8.3% (99% CI: −17.7 to 1.0) vs. India 0.1% (99% CI: −10.0 to 10.0)), mortality at day 90 (RD for Europe −7.4% (99% CI: −17.1 to 2.0) vs. India −1.4% (99% CI: −12.8 to 9.8)), mortality at day 180 (RD for Europe −6.7% (99% CI: −16.4 to 2.9) vs. India −1.0% (99% CI: −12.3 to 10.3)), and number of days alive without life support at day 90 (MD for Europe 6.1 days (99% CI: −1.3 to 13.4) vs. India 1.7 days (99% CI: −8.4 to 11.8)). For serious adverse reactions, the direction was reversed (RD for Europe −1.0% (99% CI: −7.1 to 5.2) vs. India −5.3% (99% CI: −16.2 to 5.0). Interpretation: Our analysis suggests higher dose dexamethasone may have less beneficial effects for patients in India as compared with those in Europe; however, the evidence is weak, and this could represent a chance finding. Funding: None for this analysis. The COVID STEROID 2 trial was funded by The Novo Nordisk Foundation and supported by Rigshospitalet's Research Council.
AB - Background: In the COVID-STEROID 2 trial there was suggestion of heterogeneity of treatment effects (HTE) between patients enrolled from Europe vs. India on the primary outcome. Whether there was HTE for the remaining patient-centred outcomes is unclear. Methods: In this post hoc analysis of the COVID-STEROID 2 trial, which compared 12 mg vs. 6 mg dexamethasone in adults with COVID-19 and severe hypoxemia, we evaluated HTE by geographical region (Europe vs. India) for secondary outcomes with analyses adjusted for stratification variables. Results are presented as risk differences (RDs) or mean differences (MDs) with 99% confidence intervals (CIs) and P-values from interaction tests. Findings: There were differences in mortality at day 28 (RD for Europe −8.3% (99% CI: −17.7 to 1.0) vs. India 0.1% (99% CI: −10.0 to 10.0)), mortality at day 90 (RD for Europe −7.4% (99% CI: −17.1 to 2.0) vs. India −1.4% (99% CI: −12.8 to 9.8)), mortality at day 180 (RD for Europe −6.7% (99% CI: −16.4 to 2.9) vs. India −1.0% (99% CI: −12.3 to 10.3)), and number of days alive without life support at day 90 (MD for Europe 6.1 days (99% CI: −1.3 to 13.4) vs. India 1.7 days (99% CI: −8.4 to 11.8)). For serious adverse reactions, the direction was reversed (RD for Europe −1.0% (99% CI: −7.1 to 5.2) vs. India −5.3% (99% CI: −16.2 to 5.0). Interpretation: Our analysis suggests higher dose dexamethasone may have less beneficial effects for patients in India as compared with those in Europe; however, the evidence is weak, and this could represent a chance finding. Funding: None for this analysis. The COVID STEROID 2 trial was funded by The Novo Nordisk Foundation and supported by Rigshospitalet's Research Council.
KW - COVID-19
KW - Developing countries
KW - Randomised controlled trials
KW - Steroids
U2 - 10.1016/j.lansea.2023.100293
DO - 10.1016/j.lansea.2023.100293
M3 - Journal article
C2 - 38234702
AN - SCOPUS:85173170884
VL - 20
JO - The Lancet Regional Health - Southeast Asia
JF - The Lancet Regional Health - Southeast Asia
SN - 2772-3682
M1 - 100293
ER -