TY - JOUR
T1 - Effectiveness of neuraminidase inhibitors in reducing mortality in patients admitted to hospital with influenza A H1N1pdm09 virus infection: A meta-analysis of individual participant data: A meta-analysis of individual participant data
AU - PRIDE Consortium Investigators
AU - Muthuri, Stella G.
AU - Venkatesan, Sudhir
AU - Myles, Puja R.
AU - Leonardi-Bee, Jo
AU - Al Khuwaitir, Tarig S.A.
AU - Al Mamun, Adbullah
AU - Anovadiya, Ashish P.
AU - Azziz-Baumgartner, Eduardo
AU - Báez, Clarisa
AU - Bassetti, Matteo
AU - Beovic, Bojana
AU - Bertisch, Barbara
AU - Bonmarin, Isabelle
AU - Booy, Robert
AU - Borja-Aburto, Victor H.
AU - Burgmann, Heinz
AU - Cao, Bin
AU - Carratala, Jordi
AU - Denholm, Justin T.
AU - Dominguez, Samuel R.
AU - Duarte, Pericles A.D.
AU - Dubnov-Raz, Gal
AU - Echavarria, Marcela
AU - Fanella, Sergio
AU - Gao, Zhancheng
AU - Gérardin, Patrick
AU - Giannella, Maddalena
AU - Gubbels, Sophie
AU - Herberg, Jethro
AU - Higuera Iglesias, Anjarath L.
AU - Hoger, Peter H.
AU - Hu, Xiaoyun
AU - Islam, Quazi T.
AU - Jiménez, Mirela F.
AU - Kandeel, Amr
AU - Keijzers, Gerben
AU - Khalili, Hossein
AU - Knight, Marian
AU - Kudo, Koichiro
AU - Kusznierz, Gabriela
AU - Kuzman, Ilija
AU - Kwan, Arthur M.C.
AU - Amine, Idriss Lahlou
AU - Langenegger, Eduard
AU - Lankarani, Kamran B.
AU - Leo, Yee Sin
AU - Linko, Rita
AU - Liu, Pei
AU - Madanat, Faris
AU - Bozkurt, Ilkay
PY - 2014/5/1
Y1 - 2014/5/1
N2 - Background: Neuraminidase inhibitors were widely used during the 2009-10 influenza A H1N1 pandemic, but evidence for their eff ectiveness in reducing mortality is uncertain. We did a meta-analysis of individual participant data to investigate the association between use of neuraminidase inhibitors and mortality in patients admitted to hospital with pandemic influenza A H1N1pdm09 virus infection. Methods: We assembled data for patients (all ages) admitted to hospital worldwide with laboratory confi rmed or clinically diagnosed pandemic influenza A H1N1pdm09 virus infection. We identifi ed potential data contributors from an earlier systematic review of reported studies addressing the same research question. In our systematic review, eligible studies were done between March 1, 2009 (Mexico), or April 1, 2009 (rest of the world), until the WHO declaration of the end of the pandemic (Aug 10, 2010); however, we continued to receive data up to March 14, 2011, from ongoing studies. We did a meta-analysis of individual participant data to assess the association between neuraminidase inhibitor treatment and mortality (primary outcome), adjusting for both treatment propensity and potential confounders, using generalised linear mixed modelling. We assessed the association with time to treatment using time-dependent Cox regression shared frailty modelling. Findings: We included data for 29 234 patients from 78 studies of patients admitted to hospital between Jan 2, 2009, and March 14, 2011. Compared with no treatment, neuraminidase inhibitor treatment (irrespective of timing) was associated with a reduction in mortality risk (adjusted odds ratio [OR] 0.81; 95% CI 0.70-0.93; p=0.0024). Compared with later treatment, early treatment (within 2 days of symptom onset) was associated with a reduction in mortality risk (adjusted OR 0.48; 95% CI 0.41-0.56; p<0.0001). Early treatment versus no treatment was also associated with a reduction in mortality (adjusted OR 0.50; 95% CI 0.37-0.67; p<0.0001). These associations with reduced mortality risk were less pronounced and not signifi cant in children. There was an increase in the mortality hazard rate with each day's delay in initiation of treatment up to day 5 as compared with treatment initiated within 2 days of symptom onset (adjusted hazard ratio [HR 1.23] [95% CI 1.18-1.28]; p<0.0001 for the increasing HR with each day's delay). Interpretation We advocate early instigation of neuraminidase inhibitor treatment in adults admitted to hospital with suspected or proven influenza infection.
AB - Background: Neuraminidase inhibitors were widely used during the 2009-10 influenza A H1N1 pandemic, but evidence for their eff ectiveness in reducing mortality is uncertain. We did a meta-analysis of individual participant data to investigate the association between use of neuraminidase inhibitors and mortality in patients admitted to hospital with pandemic influenza A H1N1pdm09 virus infection. Methods: We assembled data for patients (all ages) admitted to hospital worldwide with laboratory confi rmed or clinically diagnosed pandemic influenza A H1N1pdm09 virus infection. We identifi ed potential data contributors from an earlier systematic review of reported studies addressing the same research question. In our systematic review, eligible studies were done between March 1, 2009 (Mexico), or April 1, 2009 (rest of the world), until the WHO declaration of the end of the pandemic (Aug 10, 2010); however, we continued to receive data up to March 14, 2011, from ongoing studies. We did a meta-analysis of individual participant data to assess the association between neuraminidase inhibitor treatment and mortality (primary outcome), adjusting for both treatment propensity and potential confounders, using generalised linear mixed modelling. We assessed the association with time to treatment using time-dependent Cox regression shared frailty modelling. Findings: We included data for 29 234 patients from 78 studies of patients admitted to hospital between Jan 2, 2009, and March 14, 2011. Compared with no treatment, neuraminidase inhibitor treatment (irrespective of timing) was associated with a reduction in mortality risk (adjusted odds ratio [OR] 0.81; 95% CI 0.70-0.93; p=0.0024). Compared with later treatment, early treatment (within 2 days of symptom onset) was associated with a reduction in mortality risk (adjusted OR 0.48; 95% CI 0.41-0.56; p<0.0001). Early treatment versus no treatment was also associated with a reduction in mortality (adjusted OR 0.50; 95% CI 0.37-0.67; p<0.0001). These associations with reduced mortality risk were less pronounced and not signifi cant in children. There was an increase in the mortality hazard rate with each day's delay in initiation of treatment up to day 5 as compared with treatment initiated within 2 days of symptom onset (adjusted hazard ratio [HR 1.23] [95% CI 1.18-1.28]; p<0.0001 for the increasing HR with each day's delay). Interpretation We advocate early instigation of neuraminidase inhibitor treatment in adults admitted to hospital with suspected or proven influenza infection.
U2 - 10.1016/s2213-2600(14)70041-4
DO - 10.1016/s2213-2600(14)70041-4
M3 - Article
VL - 2
SP - 395
EP - 404
JO - The Lancet. Respiratory medicine
JF - The Lancet. Respiratory medicine
IS - 5
ER -