10 research outputs found
Impact of primary kidney disease on the effects of empagliflozin in patients with chronic kidney disease: secondary analyses of the EMPA-KIDNEY trial
- Author
- Abat S.
- Abd Rahman R.
- Abdul Cader R.
- Abdul Hafidz M. I.
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- Publication venue
- Publication date
- 01/01/2024
- Field of study
Background: The EMPA KIDNEY trial showed that empagliflozin reduced the risk of the primary composite outcome of kidney disease progression or cardiovascular death in patients with chronic kidney disease mainly through slowing progression. We aimed to assess how effects of empagliflozin might differ by primary kidney disease across its broad population. Methods: EMPA-KIDNEY, a randomised, controlled, phase 3 trial, was conducted at 241 centres in eight countries (Canada, China, Germany, Italy, Japan, Malaysia, the UK, and the USA). Patients were eligible if their estimated glomerular filtration rate (eGFR) was 20 to less than 45 mL/min per 1·73 m2, or 45 to less than 90 mL/min per 1·73 m2 with a urinary albumin-to-creatinine ratio (uACR) of 200 mg/g or higher at screening. They were randomly assigned (1:1) to 10 mg oral empagliflozin once daily or matching placebo. Effects on kidney disease progression (defined as a sustained ≥40% eGFR decline from randomisation, end-stage kidney disease, a sustained eGFR below 10 mL/min per 1·73 m2, or death from kidney failure) were assessed using prespecified Cox models, and eGFR slope analyses used shared parameter models. Subgroup comparisons were performed by including relevant interaction terms in models. EMPA-KIDNEY is registered with ClinicalTrials.gov, NCT03594110. Findings: Between May 15, 2019, and April 16, 2021, 6609 participants were randomly assigned and followed up for a median of 2·0 years (IQR 1·5–2·4). Prespecified subgroupings by primary kidney disease included 2057 (31·1%) participants with diabetic kidney disease, 1669 (25·3%) with glomerular disease, 1445 (21·9%) with hypertensive or renovascular disease, and 1438 (21·8%) with other or unknown causes. Kidney disease progression occurred in 384 (11·6%) of 3304 patients in the empagliflozin group and 504 (15·2%) of 3305 patients in the placebo group (hazard ratio 0·71 [95% CI 0·62–0·81]), with no evidence that the relative effect size varied significantly by primary kidney disease (pheterogeneity=0·62). The between-group difference in chronic eGFR slopes (ie, from 2 months to final follow-up) was 1·37 mL/min per 1·73 m2 per year (95% CI 1·16–1·59), representing a 50% (42–58) reduction in the rate of chronic eGFR decline. This relative effect of empagliflozin on chronic eGFR slope was similar in analyses by different primary kidney diseases, including in explorations by type of glomerular disease and diabetes (p values for heterogeneity all >0·1). Interpretation: In a broad range of patients with chronic kidney disease at risk of progression, including a wide range of non-diabetic causes of chronic kidney disease, empagliflozin reduced risk of kidney disease progression. Relative effect sizes were broadly similar irrespective of the cause of primary kidney disease, suggesting that SGLT2 inhibitors should be part of a standard of care to minimise risk of kidney failure in chronic kidney disease. Funding: Boehringer Ingelheim, Eli Lilly, and UK Medical Research Council
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- Publication venue
- 'Elsevier BV'
- Publication date
- 01/07/1994
- Field of study
Controversy exists as to whether neoadjuvant chemotherapy improves survival in patients with invasive bladder cancer, despite randomised controlled trials of more than 3000 patients. We undertook a systematic review and meta-analysis to assess the effect of such treatment on survival in patients with this disease
Augmentation of Heat Transfer and Investigation of Fluid Flow Characteristics of an Impinging Air Jet on to a Flat Plate
- Author
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Leukocyte Adhesion Deficiency-I: Clinical and Molecular Characterization in an Indian Population
- Author
- A Etzioni
- A Majorana
- A Mazzone
- A Mishra
- Ansu Abu Alex
- Anu Korula
- AO Shigeoka
- B Walzog
- Biju George
- DP Cox
- E Vijver van de
- E Vijver van de
- EC Mathew
- ES Harris
- F Lorusso
- FM Pavalko
- J Schymeinsky
- JE Sligh
- JM Schwarz
- KM Shah
- Kotteeswari Kathirvel
- LA Boxer
- M Madkaikar
- M Madkaikar
- M Movahedi
- MR Madkaikar
- N Patkar
- P Kumar
- Prashant Deshpande
- RV Shaji
- S Hanna
- S Matsuura
- S Razvi
- U Khanduri
- Vikram Mathews
- W Qasim
- Y Ohashi
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Indigenous Communication Forms and Their Potential to Convey Food Security Messages in Rural Ethiopia
- Author
- Ahmed J. S.
- Angioni G.
- Ansu-Kyeremeh K.
- Awa N.
- Awa N.
- Barrett C. B.
- Bessette G.
- Carmen R.
- Chapke R.
- Compton J. L.
- CSA (Central Statistical Agency)
- Dagron A. G.
- Dei J. S.
- Devereux S.
- Dissanayake W.
- Dutta J. M.
- FAO (Food and Agriculture Organization)
- FAO (Food and Agriculture Organization)
- FAO (Food and Agriculture Organization)
- Fasil G.
- Fetterman D.
- Flick U.
- Gillespie S.
- Gulilat M.
- Guyomard H.
- Harter L.
- Hoddinott J.
- Holt J.
- Laini V.
- Manyozo L.
- Mda Z.
- Mefalopulos P.
- Mieder W.
- MoFED (Ministry of Finance and Economic Development)
- Myers F.
- National Academy of Sciences
- Nicola P.
- Nigussie E.
- Quarry W.
- Reed T. V.
- Riley M.
- Scott J.
- Servaes J.
- Servaes J.
- Sharkey S.
- Taylor J.
- Tekola Y.
- Tufte T.
- Turay T. M.
- Ugboajah F. O.
- Ushe M. U.
- Wang G.
- Willis K.
- Publication venue
- 'SAGE Publications'
- Publication date
- Field of study
Integrating work-based learning into open distance learning in higher education – examining the prospects in a developing context from a student perspective
- Author
- Abdulai Abukari
- Ajayi J. F.
- Ansu-Kyeremeh K.
- Atkinson G.
- Bawa Kuyini Ahmed
- Boud D.
- Brennan J.
- Brubacher J. S.
- Deb S.
- Evans T.
- Flick U.
- Garnett J.
- Garnett J.
- Garrett R.
- Goksu A.
- Government of Ghana
- Government of Ghana
- Graham G.
- Harry K.
- Hatfield S. B.
- IEDE
- Kapur D.
- Keegan D.
- Kerr C.
- Kolb D. A.
- Koul B. N.
- Lemanski T.
- Macfarlane B.
- Mason J.
- Miles M. B.
- Ministry of Education
- Ministry of Education
- Ministry of Education
- Mnkeni-Saurombe N.
- Nipper S.
- Nixon I.
- Sheridan I.
- Smith P. J.
- The Africa-America Institute
- The Commonwealth of Learning and Asian Development Bank
- Tusting K.
- Uetela P.
- UNESCO
- Ward K.
- Publication venue
- 'Informa UK Limited'
- Publication date
- Field of study
Abstracts of National Conference on Research and Developments in Material Processing, Modelling and Characterization 2020
- Author
- A Chakraborty
- A K Bandhyopadhyay
- A K Halder
- A L S Brahma Reddy
- A. A. KRISHNA VAMSI
- A. K. Sahu
- A. M. Vora
- A. R. Tanna
- A. R. Vhanmane
- A. Sirisha Bhadrakali
- A.K. Chandan
- A.R. Vhanmane
- Abdhesh Kumar
- Abdhesh Prasad
- Abhishek Barua
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- Ashis K. Panda
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- Ashok Kumar
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- Atosh Kumar Sinha
- Atosh Kumar Sinha
- Atosh Kumar Sinha
- Avanish Chandan
- Avanish K Chandana
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- Avik Mondal
- Avinash K. Parkhe
- Avinash Parkhe
- Awadhesh Kumar
- Awadhesh Kumar Yadav
- Ayan Banik
- B K Jha
- B. Om Prakash
- Bandi Ramanjulu
- Baruah Mayuri
- Basavraj M. Angadi
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- Bishnu Kumar Das
- Biswajit Das
- Boopathiraja Kunnathur Periyasamy
- Braj Bihari Prasad
- Budhram Boipai
- C P Paul
- C. P. Paul
- C. S. Mandloi
- C. Tarasasanka
- C. V. Papade
- C.K. Dhanapal
- C.V. Papade
- Ch. SundarSingh
- Chandrakant S. Ulhe
- Chetan C. Jadhav
- Chetan Jadhav
- Chhabi Ram Matawale
- Chidambaram TN
- Chiradeep Ghosh
- D S Padan
- D. B. Naga Muruga
- D. Patel
- D.Dhanunjaya
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- Elango Murugappan
- Faisal Rahmani
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- G K Dey
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- G. Madhusudan Reddy
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- G.K. Bansal
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- Gaurav K Bansala
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- Girijesh Kumar
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- Goutam Mukhopadhyay
- H. H. Joshi
- Harpreet Singh
- Himanshu Shekhar Mishra
- Hrishikesh Jugade
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- J K Goswamy
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- Jay Chakraborty
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- N Chikkanna
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- Nitu Rani
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- O.Y. Venkata Subba Reddy
- O.Y. Venkata Subba Reddy
- Obulesu Mopuri
- P Chandramohan
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- P V S Lakshminarayana
- P. Chand
- P. K. Swain
- P. Mastanaiah
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- Prabhash Gokarn
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- Pradeep R
- Pradnya Patil
- Pradyumn K Arya
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- Prakash Kumar
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- Priya Choudhary
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- Promod Kumar
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- Purnanand Pathak
- Puspanjali Mohanta
- R Gaurav Kumar
- R Gupta
- R Kumar
- R N Singh
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- R. Ganapathi
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- Rathnakumar K
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- Ratnesh Gupta
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- Roshan Sharma
- Ruban Whenish
- Rupesh Kumar Khutey
- S B Singh
- S BHATTACHARYA
- S G Chowdhury
- S K Tripathi
- S MAMMEN
- S Sadhu
- S SENGUPTA
- S. Anand
- S. Deepak Kumar
- S. DHEERAJ KUMAR
- S. Ghosh Chowdhury
- S. Gopikumar
- S. K. Nath
- S. K. Parida
- S. K. Sahoo
- S. K. Tripathy
- S. N. Joshi
- S. Rajpal
- S. Santhi
- S. Sowmya
- S. Uma
- S.R. kumar
- S.R. Kumar
- S.R. Kumar
- Sabir Ali
- Sachin Kore
- Sachin Pawar
- Sachin Sonawane
- Sadanand A. Namjoshi
- Sahebagouda Sanganagoudar
- Sajan Kapil
- Samadhan J. Shinde
- Sambasiva Rao Mukkollu
- Sameer Ranjan
- Samit Kumar Singh
- Sampad Kumar Panda
- Sandeep S. Wangikar
- Sandeep Wangikar
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- Sangita K. Swain
- Sanjay Kumar
- Sanjay Kumar Jha
- Sanjay Kushwaha
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- Sanjeev Kumar
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- Satyendra Kumar Patel
- Saurabhkumar jha
- Saurav Suman
- Sayed Abbas Ali
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- Serfraj Alam
- Shailesh Dewangan
- Shailesh kumar Prasad
- Shalini Jaiswal
- Shamanth V
- Shamas U Din Hajam
- Shanjul Shrivastava
- Sharath P C
- Shashi B. Prasad
- Shashi Bhushan Prasad
- Shashikant Rajpal
- Shashikant Rajpal
- Shazee Rahmani
- Shitanshu Shekhar Chakraborty
- Shiv B Singh
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- Sufian Raja
- Sujith Bobba
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- Suman Mukhopadhyay
- Suman Sadhu
- Sumanta Mukherjee
- Surajit Sinha
- Surendra Kumar Lader
- Suresh Babu G
- Suresh Kumar
- Suresh Kumar
- Surjya K Pal
- Surya Narayan Panda
- Susanta Kumar Sahoo
- Sushant Kumar Pradhan
- Sushant Patil
- Swagataa Dutta
- Swarup Bag
- Swarup Bag
- Swedha N
- Swetha N
- T Venugopal
- T. Anand
- T. Muthumanickam
- T. Raghavendra
- T. Ram Prabhu
- T. Sheela
- Tapas Kumar Bandyopadhyay
- Tavneet Kaur
- Tej Pratap
- Trilok Chauhan
- Tushar Banerjee
- U K Mondal
- UC Jha
- Uday Shanker Dixit
- Udit Kumar
- V C Srivastava
- V Ranjith Kumar
- V. Rajinikanth
- V. Tejaswini
- V.C. Srivastava
- V.Venkatesh
- Vaibhav Gaur
- Vaishnavi Lakheri
- Vandana B. Parmar
- Vandana Kumari Jha
- Vikas Kumar Choubey
- Vikash Kumar
- VikashKumar
- Vikram Kumar S. Jain
- Vinod Kumar
- Vinod Kumar
- Viranshu Kumar
- Vishaldatt Kohir
- Vivek Kumar
- Vrushali P. Hingane
- VSM Ramakrishna R
- Y. Harold Robinson
- Y.N.V. Sai Ram
- Yash Khandelwal
- Yash Khaturia
- Yelamarthy Sai Nishanth
- YNV Sai Ram
- Publication venue
- AIJR Books
- Publication date
- 06/02/2021
- Field of study
This book presents the abstracts of the papers presented to the Online National Conference on Research and Developments in Material Processing, Modelling and Characterization 2020 (RDMPMC-2020) held on 26th and 27th August 2020 organized by the Department of Metallurgical and Materials Science in Association with the Department of Production and Industrial Engineering, National Institute of Technology Jamshedpur, Jharkhand, India.
Conference Title: National Conference on Research and Developments in Material Processing, Modelling and Characterization 2020Conference Acronym: RDMPMC-2020Conference Date: 26–27 August 2020Conference Location: Online (Virtual Mode)Conference Organizer: Department of Metallurgical and Materials Engineering, National Institute of Technology JamshedpurCo-organizer: Department of Production and Industrial Engineering, National Institute of Technology Jamshedpur, Jharkhand, IndiaConference Sponsor: TEQIP-
Effects of empagliflozin on progression of chronic kidney disease: a prespecified secondary analysis from the empa-kidney trial
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- Abat S
- Abd Rahman R
- Abdul Cader R
- Abdul Hafidz MI
- Abdul Wahab MZ
- Abdul-Samad T
- Abdullah NK
- Abe M
- Abraham N
- Acheampong S
- Achiri P
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- Zulkipli FH
- Publication venue
- Publication date
- 01/01/2023
- Field of study
Background: Sodium-glucose co-transporter-2 (SGLT2) inhibitors reduce progression of chronic kidney disease and the risk of cardiovascular morbidity and mortality in a wide range of patients. However, their effects on kidney disease progression in some patients with chronic kidney disease are unclear because few clinical kidney outcomes occurred among such patients in the completed trials. In particular, some guidelines stratify their level of recommendation about who should be treated with SGLT2 inhibitors based on diabetes status and albuminuria. We aimed to assess the effects of empagliflozin on progression of chronic kidney disease both overall and among specific types of participants in the EMPA-KIDNEY trial. Methods: EMPA-KIDNEY, a randomised, controlled, phase 3 trial, was conducted at 241 centres in eight countries (Canada, China, Germany, Italy, Japan, Malaysia, the UK, and the USA), and included individuals aged 18 years or older with an estimated glomerular filtration rate (eGFR) of 20 to less than 45 mL/min per 1·73 m2, or with an eGFR of 45 to less than 90 mL/min per 1·73 m2 with a urinary albumin-to-creatinine ratio (uACR) of 200 mg/g or higher. We explored the effects of 10 mg oral empagliflozin once daily versus placebo on the annualised rate of change in estimated glomerular filtration rate (eGFR slope), a tertiary outcome. We studied the acute slope (from randomisation to 2 months) and chronic slope (from 2 months onwards) separately, using shared parameter models to estimate the latter. Analyses were done in all randomly assigned participants by intention to treat. EMPA-KIDNEY is registered at ClinicalTrials.gov, NCT03594110. Findings: Between May 15, 2019, and April 16, 2021, 6609 participants were randomly assigned and then followed up for a median of 2·0 years (IQR 1·5-2·4). Prespecified subgroups of eGFR included 2282 (34·5%) participants with an eGFR of less than 30 mL/min per 1·73 m2, 2928 (44·3%) with an eGFR of 30 to less than 45 mL/min per 1·73 m2, and 1399 (21·2%) with an eGFR 45 mL/min per 1·73 m2 or higher. Prespecified subgroups of uACR included 1328 (20·1%) with a uACR of less than 30 mg/g, 1864 (28·2%) with a uACR of 30 to 300 mg/g, and 3417 (51·7%) with a uACR of more than 300 mg/g. Overall, allocation to empagliflozin caused an acute 2·12 mL/min per 1·73 m2 (95% CI 1·83-2·41) reduction in eGFR, equivalent to a 6% (5-6) dip in the first 2 months. After this, it halved the chronic slope from -2·75 to -1·37 mL/min per 1·73 m2 per year (relative difference 50%, 95% CI 42-58). The absolute and relative benefits of empagliflozin on the magnitude of the chronic slope varied significantly depending on diabetes status and baseline levels of eGFR and uACR. In particular, the absolute difference in chronic slopes was lower in patients with lower baseline uACR, but because this group progressed more slowly than those with higher uACR, this translated to a larger relative difference in chronic slopes in this group (86% [36-136] reduction in the chronic slope among those with baseline uACR <30 mg/g compared with a 29% [19-38] reduction for those with baseline uACR ≥2000 mg/g; ptrend<0·0001). Interpretation: Empagliflozin slowed the rate of progression of chronic kidney disease among all types of participant in the EMPA-KIDNEY trial, including those with little albuminuria. Albuminuria alone should not be used to determine whether to treat with an SGLT2 inhibitor. Funding: Boehringer Ingelheim and Eli Lilly
Impact of primary kidney disease on the effects of empagliflozin in patients with chronic kidney disease: secondary analyses of the EMPA-KIDNEY trial
- Author
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- Abd Rahman R
- Abdul Cader R
- Abdul Hafidz MI
- Abdul Wahab MZ
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- Publication venue
- Publication date
- 01/01/2023
- Field of study
Background: The EMPA-KIDNEY trial showed that empagliflozin reduced the risk of the primary composite outcome of kidney disease progression or cardiovascular death in patients with chronic kidney disease mainly through slowing progression. We aimed to assess how effects of empagliflozin might differ by primary kidney disease across its broad population. Methods: EMPA-KIDNEY, a randomised, controlled, phase 3 trial, was conducted at 241 centres in eight countries (Canada, China, Germany, Italy, Japan, Malaysia, the UK, and the USA). Patients were eligible if their estimated glomerular filtration rate (eGFR) was 20 to less than 45 mL/min per 1·73 m2, or 45 to less than 90 mL/min per 1·73 m2 with a urinary albumin-to-creatinine ratio (uACR) of 200 mg/g or higher at screening. They were randomly assigned (1:1) to 10 mg oral empagliflozin once daily or matching placebo. Effects on kidney disease progression (defined as a sustained ≥40% eGFR decline from randomisation, end-stage kidney disease, a sustained eGFR below 10 mL/min per 1·73 m2, or death from kidney failure) were assessed using prespecified Cox models, and eGFR slope analyses used shared parameter models. Subgroup comparisons were performed by including relevant interaction terms in models. EMPA-KIDNEY is registered with ClinicalTrials.gov, NCT03594110. Findings: Between May 15, 2019, and April 16, 2021, 6609 participants were randomly assigned and followed up for a median of 2·0 years (IQR 1·5-2·4). Prespecified subgroupings by primary kidney disease included 2057 (31·1%) participants with diabetic kidney disease, 1669 (25·3%) with glomerular disease, 1445 (21·9%) with hypertensive or renovascular disease, and 1438 (21·8%) with other or unknown causes. Kidney disease progression occurred in 384 (11·6%) of 3304 patients in the empagliflozin group and 504 (15·2%) of 3305 patients in the placebo group (hazard ratio 0·71 [95% CI 0·62-0·81]), with no evidence that the relative effect size varied significantly by primary kidney disease (pheterogeneity=0·62). The between-group difference in chronic eGFR slopes (ie, from 2 months to final follow-up) was 1·37 mL/min per 1·73 m2 per year (95% CI 1·16-1·59), representing a 50% (42-58) reduction in the rate of chronic eGFR decline. This relative effect of empagliflozin on chronic eGFR slope was similar in analyses by different primary kidney diseases, including in explorations by type of glomerular disease and diabetes (p values for heterogeneity all >0·1). Interpretation: In a broad range of patients with chronic kidney disease at risk of progression, including a wide range of non-diabetic causes of chronic kidney disease, empagliflozin reduced risk of kidney disease progression. Relative effect sizes were broadly similar irrespective of the cause of primary kidney disease, suggesting that SGLT2 inhibitors should be part of a standard of care to minimise risk of kidney failure in chronic kidney disease. Funding: Boehringer Ingelheim, Eli Lilly, and UK Medical Research Council
Azithromycin in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial
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- Publication venue
- 'Elsevier BV'
- Publication date
- 01/02/2021
- Field of study
Background Azithromycin has been proposed as a treatment for COVID-19 on the basis of its immunomodulatory actions. We aimed to evaluate the safety and efficacy of azithromycin in patients admitted to hospital with COVID-19. Methods In this randomised, controlled, open-label, adaptive platform trial (Randomised Evaluation of COVID-19 Therapy [RECOVERY]), several possible treatments were compared with usual care in patients admitted to hospital with COVID-19 in the UK. The trial is underway at 176 hospitals in the UK. Eligible and consenting patients were randomly allocated to either usual standard of care alone or usual standard of care plus azithromycin 500 mg once per day by mouth or intravenously for 10 days or until discharge (or allocation to one of the other RECOVERY treatment groups). Patients were assigned via web-based simple (unstratified) randomisation with allocation concealment and were twice as likely to be randomly assigned to usual care than to any of the active treatment groups. Participants and local study staff were not masked to the allocated treatment, but all others involved in the trial were masked to the outcome data during the trial. The primary outcome was 28-day all-cause mortality, assessed in the intention-to-treat population. The trial is registered with ISRCTN, 50189673, and ClinicalTrials.gov, NCT04381936. Findings Between April 7 and Nov 27, 2020, of 16 442 patients enrolled in the RECOVERY trial, 9433 (57%) were eligible and 7763 were included in the assessment of azithromycin. The mean age of these study participants was 65·3 years (SD 15·7) and approximately a third were women (2944 [38%] of 7763). 2582 patients were randomly allocated to receive azithromycin and 5181 patients were randomly allocated to usual care alone. Overall, 561 (22%) patients allocated to azithromycin and 1162 (22%) patients allocated to usual care died within 28 days (rate ratio 0·97, 95% CI 0·87–1·07; p=0·50). No significant difference was seen in duration of hospital stay (median 10 days [IQR 5 to >28] vs 11 days [5 to >28]) or the proportion of patients discharged from hospital alive within 28 days (rate ratio 1·04, 95% CI 0·98–1·10; p=0·19). Among those not on invasive mechanical ventilation at baseline, no significant difference was seen in the proportion meeting the composite endpoint of invasive mechanical ventilation or death (risk ratio 0·95, 95% CI 0·87–1·03; p=0·24). Interpretation In patients admitted to hospital with COVID-19, azithromycin did not improve survival or other prespecified clinical outcomes. Azithromycin use in patients admitted to hospital with COVID-19 should be restricted to patients in whom there is a clear antimicrobial indication. Funding UK Research and Innovation (Medical Research Council) and National Institute of Health Research