12 results on '"Amin, Pravin R."'
Search Results
2. 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
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Tirupakuzhi Vijayaraghavan, Bharath Kumar, primary, Granholm, Anders, additional, Myatra, Sheila N., additional, Jha, Vivekanand, additional, Hammond, Naomi, additional, Micallef, Sharon, additional, Munch, Marie Warrer, additional, Kjær, Maj-Brit N., additional, Møller, Morten Hylander, additional, Lange, Theis, additional, Perner, Anders, additional, Venkatesh, Balasubramanian, additional, Munch, Marie W., additional, Tirupakuzhi Vijayaraghavan, Bharath Kumar, additional, Saseedharan, Sanjith, additional, Benfield, Thomas, additional, Wahlin, Rebecka R., additional, Rasmussen, Bodil S., additional, Andreasen, Anne Sofie, additional, Poulsen, Lone M., additional, Cioccari, Luca, additional, Khan, Mohd S., additional, Kapadia, Farhad, additional, Divatia, Jigeeshu V., additional, Brøchner, Anne C., additional, Bestle, Morten H., additional, Helleberg, Marie, additional, Michelsen, Jens, additional, Padmanaban, Ajay, additional, Bose, Neeta, additional, Møller, Anders, additional, Borawake, Kapil, additional, Kristiansen, Klaus T., additional, Shukla, Urvi, additional, Chew, Michelle S., additional, Dixit, Subhal, additional, Ulrik, Charlotte S., additional, Amin, Pravin R., additional, Chawla, Rajesh, additional, Wamberg, Christian A., additional, Shah, Mehul S., additional, Darfelt, Iben S., additional, Jørgensen, Vibeke L., additional, Smitt, Margit, additional, Møller, Morten H., additional, Meyhoff, Tine S., additional, Vesterlund, Gitte K., additional, Hammond, Naomi E., additional, Bassi, Abhinav, additional, John, Oommen, additional, Jha, Anubhuti, additional, Cronhjort, Maria, additional, Jakob, Stephan M., additional, Gluud, Christian, additional, Kadam, Vaijayanti, additional, Marcussen, Klaus V., additional, Hollenberg, Jacob, additional, Hedman, Anders, additional, Nielsen, Henrik, additional, Schjørring, Olav L., additional, Jensen, Marie Q., additional, Leistner, Jens W., additional, Jonassen, Trine B., additional, Kristensen, Camilla M., additional, Clapp, Esben C., additional, Hjortsø, Carl J.S., additional, Jensen, Thomas S., additional, Halstad, Liv S., additional, Bak, Emilie R.B., additional, Zaabalawi, Reem, additional, Metcalf-Clausen, Matias, additional, Abdi, Suhayb, additional, Hatley, Emma V., additional, Aksnes, Tobias S., additional, Gleipner-Andersen, Emil, additional, Alarcón, A.Felix, additional, Yamin, Gabriel, additional, Heymowski, Adam, additional, Berggren, Anton, additional, la Cour, Kirstine, additional, Weihe, Sarah, additional, Pind, Alison H., additional, and Engstrøm, Janus, additional
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- 2023
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3. Encephalitis and myelitis in tropical countries: Report from the Task Force on Tropical Diseases by the World Federation of Societies of Intensive and Critical Care Medicine
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Silva, Gisele Sampaio, Richards, Guy A., Baker, Tim, and Amin, Pravin R.
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- 2017
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4. Pneumonia in the tropics: Report from the Task Force on tropical diseases by the World Federation of Societies of Intensive and Critical Care Medicine
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Nor, Mohd Basri Mat, Richards, Guy A., McGloughlin, Steve, and Amin, Pravin R.
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- 2017
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5. Intensive Care in India in 2018–2019: The Second Indian Intensive Care Case Mix and Practice Patterns Study
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Kumar, Vivek, primary, Venkataraman, Ramesh, additional, Bajan, Khusrav, additional, Mehta, Yatin, additional, Govil, Deepak, additional, Ramakrishnan, Nagarajan, additional, Zirpe, Kapil, additional, Sircar, Mrinal, additional, Gurav, Sushma, additional, Samavedam, Srinivas, additional, Sahu, Samir, additional, Dixit, Subhal, additional, Myatra, Sheila Nainan, additional, Sathe, Prachee, additional, Bhattacharya, Pradip Kumar, additional, Harne, Rahul, additional, Divatia, Jigeeshu V, additional, D'Silva, Carol, additional, Amin, Pravin R, additional, Kapadia, Farhad N, additional, Pande, Rajesh Kumar, additional, Mehta, Sujata N, additional, Thakur, Leelavati, additional, Rathod, Darshana, additional, Pasha, Shaik Arif, additional, Todi, Subhash Kumar, additional, and the INDICAPS-II investigators, FNU, additional
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- 2022
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6. Effect of 12 mg vs 6 mg of Dexamethasone on the Number of Days Alive Without Life Support in Adults With COVID-19 and Severe Hypoxemia:The COVID STEROID 2 Randomized Trial
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Munch, Marie W, Myatra, Sheila N, Vijayaraghavan, Bharath Kumar Tirupakuzhi, Saseedharan, Sanjith, Benfield, Thomas, Wahlin, Rebecka R, Rasmussen, Bodil S, Andreasen, Anne Sofie, Poulsen, Lone M, Cioccari, Luca, Khan, Mohd S, Kapadia, Farhad, Divatia, Jigeeshu V, Br��chner, Anne C, Bestle, Morten H, Helleberg, Marie, Michelsen, Jens, Padmanaban, Ajay, Bose, Neeta, M��ller, Anders, Borawake, Kapil, Kristiansen, Klaus T, Shukla, Urvi, Chew, Michelle S, Dixit, Subhal, Ulrik, Charlotte S, Amin, Pravin R, Chawla, Rajesh, Wamberg, Christian A, Shah, Mehul S, Darfelt, Iben S, J��rgensen, Vibeke L, Smitt, Margit, Granholm, Anders, Kj��r, Maj-Brit N, M��ller, Morten H, Meyhoff, Tine S, Vesterlund, Gitte K, Hammond, Naomi E, Micallef, Sharon, Bassi, Abhinav, John, Oommen, Jha, Anubhuti, Cronhjort, Maria, Jakob, Stephan M, Gluud, Christian, Lange, Theis, Kadam, Vaijayanti, Marcussen, Klaus V, Hollenberg, Jacob, Hedman, Anders, Nielsen, Henrik, Schj��rring, Olav L, Jensen, Marie Q, Leistner, Jens W, Jonassen, Trine B, Kristensen, Camilla M, Clapp, Esben C, Hjorts��, Carl J S, Jensen, Thomas S, Halstad, Liv S, Bak, Emilie R B, Zaabalawi, Reem, Metcalf-Clausen, Matias, Abdi, Suhayb, Hatley, Emma V, Aksnes, Tobias S, Gleipner-Andersen, Emil, Alarc��n, Arif F, Yamin, Gabriel, Heymowski, Adam, Berggren, Anton, La Cour, Kirstine, Weihe, Sarah, Pind, Alison H, Engstr��m, Janus, Jha, Vivekanand, Venkatesh, Balasubramanian, and Perner, Anders
- Subjects
Dexamethasone/administration & dosage ,Male ,Mycoses/etiology ,medicine.medical_treatment ,Dexamethasone ,Hypoxemia ,law.invention ,Randomized controlled trial ,law ,medicine ,Shock, Septic/etiology ,Humans ,Single-Blind Method ,Hypoxia ,610 Medicine & health ,Glucocorticoids ,Aged ,Mechanical ventilation ,Dose-Response Relationship, Drug ,Septic shock ,business.industry ,Hypoxia/etiology ,COVID-19 ,Glucocorticoids/administration & dosage ,General Medicine ,Middle Aged ,medicine.disease ,Shock, Septic ,Respiration, Artificial ,COVID-19 Drug Treatment ,Life Support Care ,Dose–response relationship ,Mycoses ,Relative risk ,Anesthesia ,Life support ,COVID-19/complications ,Female ,medicine.symptom ,business ,medicine.drug - Abstract
Importance A daily dose with 6 mg of dexamethasone is recommended for up to 10 days in patients with severe and critical COVID-19, but a higher dose may benefit those with more severe disease. Objective To assess the effects of 12 mg/d vs 6 mg/d of dexamethasone in patients with COVID-19 and severe hypoxemia. Design, Setting, and Participants A multicenter, randomized clinical trial was conducted between August 2020 and May 2021 at 26 hospitals in Europe and India and included 1000 adults with confirmed COVID-19 requiring at least 10 L/min of oxygen or mechanical ventilation. End of 90-day follow-up was on August 19, 2021. Interventions Patients were randomized 1:1 to 12 mg/d of intravenous dexamethasone (n���=���503) or 6 mg/d of intravenous dexamethasone (n���=���497) for up to 10 days. Main Outcomes and Measures The primary outcome was the number of days alive without life support (invasive mechanical ventilation, circulatory support, or kidney replacement therapy) at 28 days and was adjusted for stratification variables. Of the 8 prespecified secondary outcomes, 5 are included in this analysis (the number of days alive without life support at 90 days, the number of days alive out of the hospital at 90 days, mortality at 28 days and at 90 days, and ���1 serious adverse reactions at 28 days). Results Of the 1000 randomized patients, 982 were included (median age, 65 [IQR, 55-73] years; 305 [31%] women) and primary outcome data were available for 971 (491 in the 12 mg of dexamethasone group and 480 in the 6 mg of dexamethasone group). The median number of days alive without life support was 22.0 days (IQR, 6.0-28.0 days) in the 12 mg of dexamethasone group and 20.5 days (IQR, 4.0-28.0 days) in the 6 mg of dexamethasone group (adjusted mean difference, 1.3 days [95% CI, 0-2.6 days]; P���=���.07). Mortality at 28 days was 27.1% in the 12 mg of dexamethasone group vs 32.3% in the 6 mg of dexamethasone group (adjusted relative risk, 0.86 [99% CI, 0.68-1.08]). Mortality at 90 days was 32.0% in the 12 mg of dexamethasone group vs 37.7% in the 6 mg of dexamethasone group (adjusted relative risk, 0.87 [99% CI, 0.70-1.07]). Serious adverse reactions, including septic shock and invasive fungal infections, occurred in 11.3% in the 12 mg of dexamethasone group vs 13.4% in the 6 mg of dexamethasone group (adjusted relative risk, 0.83 [99% CI, 0.54-1.29]). Conclusions and Relevance Among patients with COVID-19 and severe hypoxemia, 12 mg/d of dexamethasone compared with 6 mg/d of dexamethasone did not result in statistically significantly more days alive without life support at 28 days. However, the trial may have been underpowered to identify a significant difference. Trial Registration ClinicalTrials.gov Identifier: NCT04509973 and ctri.nic.in Identifier: CTRI/2020/10/028731.
- Published
- 2021
7. Effect of 12 mg vs 6 mg of Dexamethasone on the Number of Days Alive Without Life Support in Adults With COVID-19 and Severe Hypoxemia The COVID STEROID 2 Randomized Trial
- Author
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Munch, Marie W., Myatra, Sheila N., Vijayaraghavan, Bharath Kumar Tirupakuzhi, Saseedharan, Sanjith, Benfield, Thomas, Wahlin, Rebecka R., Rasmussen, Bodil S., Andreasen, Anne Sofie, Poulsen, Lone M., Cioccari, Luca, Khan, Mohd S., Kapadia, Farhad, Divatia, Jigeeshu V., Brochner, Anne C., Bestle, Morten H., Helleberg, Marie, Michelsen, Jens, Padmanaban, Ajay, Bose, Neeta, Møller, Anders, Borawake, Kapil, Kristiansen, Klaus T., Shukla, Urvi, Chew, Michelle S., Dixit, Subhal, Ulrik, Charlotte S., Amin, Pravin R., Chawla, Rajesh, Wamberg, Christian A., Shah, Mehul S., Darfelt, Iben S., Jorgensen, Vibeke L., Smitt, Margit, Granholm, Anders, Kjær, Maj-Brit N., Møller, Morten H., Meyhoff, Tine S., Vesterlund, Gitte K., Hammond, Naomi E., Micallef, Sharon, Bassi, Abhinav, John, Oommen, Jha, Anubhuti, Cronhjort, Maria, Jakob, Stephan M., Gluud, Christian, Lange, Theis, Kadam, Vaijayanti, Marcussen, Klaus V., Hollenberg, Jacob, Hedman, Anders, Nielsen, Henrik, Schjorring, Olav L., Jensen, Marie Q., Leistner, Jens W., Jonassen, Trine B., Kristensen, Camilla M., Clapp, Esben C., Hjortso, Carl J. S., Jensen, Thomas S., Halstad, Liv S., Bak, Emilie R. B., Zaabalawi, Reem, Metcalf-Clausen, Matias, Abdi, Suhayb, Hatley, Emma V., Aksnes, Tobias S., Gleipner-Andersen, Emil, Alarcon, Arif F., Yamin, Gabriel, Heymowski, Adam, Berggren, Anton, La Cour, Kirstine, Weihe, Sarah, Pind, Alison H., Engstrom, Janus, Jha, Vivekanand, Venkatesh, Balasubramanian, Perner, Anders, Munch, Marie W., Myatra, Sheila N., Vijayaraghavan, Bharath Kumar Tirupakuzhi, Saseedharan, Sanjith, Benfield, Thomas, Wahlin, Rebecka R., Rasmussen, Bodil S., Andreasen, Anne Sofie, Poulsen, Lone M., Cioccari, Luca, Khan, Mohd S., Kapadia, Farhad, Divatia, Jigeeshu V., Brochner, Anne C., Bestle, Morten H., Helleberg, Marie, Michelsen, Jens, Padmanaban, Ajay, Bose, Neeta, Møller, Anders, Borawake, Kapil, Kristiansen, Klaus T., Shukla, Urvi, Chew, Michelle S., Dixit, Subhal, Ulrik, Charlotte S., Amin, Pravin R., Chawla, Rajesh, Wamberg, Christian A., Shah, Mehul S., Darfelt, Iben S., Jorgensen, Vibeke L., Smitt, Margit, Granholm, Anders, Kjær, Maj-Brit N., Møller, Morten H., Meyhoff, Tine S., Vesterlund, Gitte K., Hammond, Naomi E., Micallef, Sharon, Bassi, Abhinav, John, Oommen, Jha, Anubhuti, Cronhjort, Maria, Jakob, Stephan M., Gluud, Christian, Lange, Theis, Kadam, Vaijayanti, Marcussen, Klaus V., Hollenberg, Jacob, Hedman, Anders, Nielsen, Henrik, Schjorring, Olav L., Jensen, Marie Q., Leistner, Jens W., Jonassen, Trine B., Kristensen, Camilla M., Clapp, Esben C., Hjortso, Carl J. S., Jensen, Thomas S., Halstad, Liv S., Bak, Emilie R. B., Zaabalawi, Reem, Metcalf-Clausen, Matias, Abdi, Suhayb, Hatley, Emma V., Aksnes, Tobias S., Gleipner-Andersen, Emil, Alarcon, Arif F., Yamin, Gabriel, Heymowski, Adam, Berggren, Anton, La Cour, Kirstine, Weihe, Sarah, Pind, Alison H., Engstrom, Janus, Jha, Vivekanand, Venkatesh, Balasubramanian, and Perner, Anders
- Abstract
Importance A daily dose with 6 mg of dexamethasone is recommended for up to 10 days in patients with severe and critical COVID-19, but a higher dose may benefit those with more severe disease. Objective To assess the effects of 12 mg/d vs 6 mg/d of dexamethasone in patients with COVID-19 and severe hypoxemia. Design, Setting, and Participants A multicenter, randomized clinical trial was conducted between August 2020 and May 2021 at 26 hospitals in Europe and India and included 1000 adults with confirmed COVID-19 requiring at least 10 L/min of oxygen or mechanical ventilation. End of 90-day follow-up was on August 19, 2021. Interventions Patients were randomized 1:1 to 12 mg/d of intravenous dexamethasone (n = 503) or 6 mg/d of intravenous dexamethasone (n = 497) for up to 10 days. Main Outcomes and Measures The primary outcome was the number of days alive without life support (invasive mechanical ventilation, circulatory support, or kidney replacement therapy) at 28 days and was adjusted for stratification variables. Of the 8 prespecified secondary outcomes, 5 are included in this analysis (the number of days alive without life support at 90 days, the number of days alive out of the hospital at 90 days, mortality at 28 days and at 90 days, and ≥1 serious adverse reactions at 28 days). Results Of the 1000 randomized patients, 982 were included (median age, 65 [IQR, 55-73] years; 305 [31%] women) and primary outcome data were available for 971 (491 in the 12 mg of dexamethasone group and 480 in the 6 mg of dexamethasone group). The median number of days alive without life support was 22.0 days (IQR, 6.0-28.0 days) in the 12 mg of dexamethasone group and 20.5 days (IQR, 4.0-28.0 days) in the 6 mg of dexamethasone group (adjusted mean difference, 1.3 days [95% CI, 0-2.6 days]; P = .07). Mortality at 28 days was 27.1% in the 12 mg of dexamethasone group vs 32.3% in the 6 mg of dexamethasone group (adjusted relative risk, 0.86
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- 2021
8. Intensive Care in India in 2018-2019: The Second Indian Intensive Care Case Mix and Practice Patterns Study.
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Divatia, Jigeeshu V., Mehta, Yatin, Govil, Deepak, Zirpe, Kapil, Amin, Pravin R., Ramakrishnan, Nagarajan, Kapadia, Farhad N., Sircar, Mrinal, Sahu, Samir, Bhattacharya, Pradip Kumar, Myatra, Sheila Nainan, Samavedam, Srinivas, Dixit, Subhal, Pande, Rajesh Kumar, Mehta, Sujata N., Venkataraman, Ramesh, Bajan, Khusrav, Kumar, Vivek, Harne, Rahul, and Thakur, Leelavati
- Subjects
INTENSIVE care units ,EVALUATION of medical care ,VASOCONSTRICTORS ,RESEARCH ,SCIENTIFIC observation ,CROSS-sectional method ,MEDICAL care costs ,APACHE (Disease classification system) ,MEDICAL care use ,MEDICAL protocols ,ARTIFICIAL respiration ,SEPSIS ,HOSPITAL mortality ,CRITICAL care medicine ,PHYSICIAN practice patterns ,CARDIOTONIC agents ,CAPNOGRAPHY - Abstract
Background: We aimed to study organizational aspects, case mix, and practices in Indian intensive care units (ICUs) from 2018 to 2019, following the Indian Intensive Care Case Mix and Practice Patterns Study (INDICAPS) of 2010--2011. Methods: An observational, 4-day point prevalence study was performed between 2018 and 2019. ICU, patient characteristics, and interventions were recorded for 24 hours, and ICU outcomes till 30 days after the study day. Adherence to selected compliance measures was determined. Data were analyzed for 4,669 adult patients from 132 ICUs. Results: On the study day, mean age, acute physiology and chronic health evaluation (APACHE II), and sequential organ failure assessment (SOFA) scores were 56.9 ± 17.41 years, 16.7 ± 9.8, and 4.4 ± 3.6, respectively. Moreover, 24% and 22.2% of patients received mechanical ventilation (MV) and vasopressors or inotropes (VIs), respectively. On the study days, 1,195 patients (25.6%) were infected and 1,368 patients (29.3%) had sepsis during their ICU stay. ICU mortality was 1,092 out of 4,669 (23.4%), including 737 deaths and 355 terminal discharges (TDs) from ICU. Compliance for process measures related to MV ranged between 62.7 and 85.3%, 11.2 and 47.4% for monitoring delirium, sedation, and analgesia, and 7.7 and 25.3% for inappropriate transfusion of blood products. Only 34.8% of ICUs routinely used capnography. Large hospitals with ≥500 beds, closed ICUs, the APACHE II and SOFA scores, medical admissions, the presence of cancer or cirrhosis of the liver, the presence of infection on the study day, and the need for MV or VIs were independent predictors of mortality. Conclusions: Hospital size and closed ICUs are independently associated with worse outcomes. The proportion of TDs remains high. There is a scope for improvements in processes of care. [ABSTRACT FROM AUTHOR]
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- 2021
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9. Intensive Care in India: The Indian Intensive Care Case Mix and Practice Patterns Study
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Singh, Virendra, primary, Todi, Subhash, additional, Sahu, Samir, additional, Jani, Charu K., additional, Kulkarni, Atul P., additional, Samaddar, Devi Prasad, additional, Amin, Pravin R., additional, Kapadia, Farhad N., additional, Mehta, Sujata, additional, Bande, BD, additional, Tewari, Reshma, additional, Sathe, Prachee, additional, and LNU, INDICAPS Study Investigators, additional
- Published
- 2016
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10. Intensive Care in India: The Indian Intensive Care Case Mix and Practice Patterns Study.
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Divatia, Jigeeshu V., Amin, Pravin R., Ramakrishnan, Nagarajan, Kapadia, Farhad N., Todi, Subhash, Sahu, Samir, Govil, Deepak, Chawla, Rajesh, Kulkarni, Atul P., Samavedam, Srinivas, Jani, Charu K., Rungta, Narendra, Samaddar, Devi Prasad, Mehta, Sujata, Venkataraman, Ramesh, Hegde, Ashit, Bande, BD, Dhanuka, Sanjay, Singh, Virendra, and Tewari, Reshma
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ARTIFICIAL respiration , *LENGTH of stay in hospitals , *INTENSIVE care units , *MEDICAL care costs , *MORTALITY , *SCIENTIFIC observation , *RESPIRATORY insufficiency , *SEPTIC shock , *SEPSIS , *PHYSICIAN practice patterns , *COST analysis , *CROSS-sectional method - Abstract
Aims: To obtain information on organizational aspects, case mix and practices in Indian Intensive Care Units (ICUs). Patients and Methods: An observational, 4‑day point prevalence study was performed between 2010 and 2011 in 4209 patients from 124 ICUs. ICU and patient characteristics, and interventions were recorded for 24 h of the study day, and outcomes till 30 days after the study day. Data were analyzed for 4038 adult patients from 120 ICUs. Results: On the study day, mean age, Acute Physiology and Chronic Health Evaluation (APACHE II) and sequential organ failure assessment (SOFA) scores were 54.1 ± 17.1 years, 17.4 ± 9.2 and 3.8 ± 3.6, respectively. About 46.4% patients had ≥1 organ failure. Nearly, 37% and 22.2% patients received mechanical ventilation (MV) and vasopressors or inotropes, respectively. Nearly, 12.2% patients developed an infection in the ICU. About 28.3% patients had severe sepsis or septic shock (SvSpSS) during their ICU stay. About 60.7% patients without infection received antibiotics. There were 546 deaths and 183 terminal discharges (TDs) from ICU (including left against medical advice or discharged on request), with ICU mortality 729/4038 (18.1%). In 1627 patients admitted within 24 h of the study day, the standardized mortality ratio was 0.67. The APACHE II and SOFA scores, public hospital ICUs, medical ICUs, inadequately equipped ICUs, medical admission, self‑paying patient, presence of SvSpSS, acute respiratory failure or cancer, need for a fluid bolus, and MV were independent predictors of mortality. Conclusions: The high proportion of TDs and the association of public hospitals, self‑paying patients, and inadequately equipped hospitals with mortality has important implications for critical care in India. [ABSTRACT FROM AUTHOR]
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- 2016
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11. ISCCM Position Statement for Improving Gender Balance in Critical Care Medicine.
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Sathe P, Shukla U, Kapadia FN, Ray S, Chanchalani G, Nasa P, Agarwal D, Amin PR, Bandhopadhyay S, Baronia T, Bhagwati AM, Bhattacharya PK, Chaudhry D, Chawla R, Das R, Sinha S, Dixit S, Divatia JV, George N, Govil D, Khanikar RG, Iyer S, Jain PK, Kadapatti K, Krishna B, Kulkarni AP, Mani RK, Mathur R, Mehta Y, Patil LA, Patil VP, Panigrahi B, Prayag S, Rajagopalan RE, Rajesh S, Ramachandran P, Rao M, Reddy C, Samavedam S, Singh SJ, Takkellapati LR, Talekar S, Thakur L, Zirpe KG, and Myatra SN
- Abstract
Gender disparity in Critical Care Medicine (CCM) persists globally, with women being underrepresented. Female Intensivists remain a minority, facing challenges in academic and leadership positions at the workplace and within academic societies. The Indian Society of Critical Care Medicine (ISCCM) recognized the need for addressing issues related to gender parity and constituted its first Diversity Equity and Inclusion (DEI) Committee in 2023. Through a Delphi process involving 38 Panelists including 53% women, consensus and stability were achieved for 18 statements (95%). From these 18 consensus statements, 15 position statements were drafted to address gender balance issues in CCM. These statements advocate for equal opportunities in recruitment, workplace inclusivity, prevention of harassment, and improved female representation in leadership roles, nominated positions, and conferences. While the consensus reflects a significant step toward gender equity, further efforts are required to implement, advocate, and evaluate the impact of these measures. The ISCCM position statements offer valuable guidance for promoting gender balance within society and the CCM community., How to Cite This Article: Sathe P, Shukla U, Kapadia FN, Ray S, Chanchalani G, Nasa P, et al . ISCCM Position Statement for Improving Gender Balance in Critical Care Medicine. Indian J Crit Care Med 2024;28(S2):S288-S296., Competing Interests: Source of support: Nil Conflict of interest: None, (Copyright © 2024; The Author(s).)
- Published
- 2024
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12. Effect of 12 mg vs 6 mg of Dexamethasone on the Number of Days Alive Without Life Support in Adults With COVID-19 and Severe Hypoxemia: The COVID STEROID 2 Randomized Trial.
- Author
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Munch MW, Myatra SN, Vijayaraghavan BKT, Saseedharan S, Benfield T, Wahlin RR, Rasmussen BS, Andreasen AS, Poulsen LM, Cioccari L, Khan MS, Kapadia F, Divatia JV, Brøchner AC, Bestle MH, Helleberg M, Michelsen J, Padmanaban A, Bose N, Møller A, Borawake K, Kristiansen KT, Shukla U, Chew MS, Dixit S, Ulrik CS, Amin PR, Chawla R, Wamberg CA, Shah MS, Darfelt IS, Jørgensen VL, Smitt M, Granholm A, Kjær MN, Møller MH, Meyhoff TS, Vesterlund GK, Hammond NE, Micallef S, Bassi A, John O, Jha A, Cronhjort M, Jakob SM, Gluud C, Lange T, Kadam V, Marcussen KV, Hollenberg J, Hedman A, Nielsen H, Schjørring OL, Jensen MQ, Leistner JW, Jonassen TB, Kristensen CM, Clapp EC, Hjortsø CJS, Jensen TS, Halstad LS, Bak ERB, Zaabalawi R, Metcalf-Clausen M, Abdi S, Hatley EV, Aksnes TS, Gleipner-Andersen E, Alarcón AF, Yamin G, Heymowski A, Berggren A, La Cour K, Weihe S, Pind AH, Engstrøm J, Jha V, Venkatesh B, and Perner A
- Subjects
- Aged, COVID-19 complications, COVID-19 mortality, Dexamethasone adverse effects, Dose-Response Relationship, Drug, Female, Glucocorticoids adverse effects, Humans, Hypoxia etiology, Hypoxia therapy, Male, Middle Aged, Mycoses etiology, Respiration, Artificial, Shock, Septic etiology, Single-Blind Method, Dexamethasone administration & dosage, Glucocorticoids administration & dosage, Life Support Care, COVID-19 Drug Treatment
- Abstract
Importance: A daily dose with 6 mg of dexamethasone is recommended for up to 10 days in patients with severe and critical COVID-19, but a higher dose may benefit those with more severe disease., Objective: To assess the effects of 12 mg/d vs 6 mg/d of dexamethasone in patients with COVID-19 and severe hypoxemia., Design, Setting, and Participants: A multicenter, randomized clinical trial was conducted between August 2020 and May 2021 at 26 hospitals in Europe and India and included 1000 adults with confirmed COVID-19 requiring at least 10 L/min of oxygen or mechanical ventilation. End of 90-day follow-up was on August 19, 2021., Interventions: Patients were randomized 1:1 to 12 mg/d of intravenous dexamethasone (n = 503) or 6 mg/d of intravenous dexamethasone (n = 497) for up to 10 days., Main Outcomes and Measures: The primary outcome was the number of days alive without life support (invasive mechanical ventilation, circulatory support, or kidney replacement therapy) at 28 days and was adjusted for stratification variables. Of the 8 prespecified secondary outcomes, 5 are included in this analysis (the number of days alive without life support at 90 days, the number of days alive out of the hospital at 90 days, mortality at 28 days and at 90 days, and ≥1 serious adverse reactions at 28 days)., Results: Of the 1000 randomized patients, 982 were included (median age, 65 [IQR, 55-73] years; 305 [31%] women) and primary outcome data were available for 971 (491 in the 12 mg of dexamethasone group and 480 in the 6 mg of dexamethasone group). The median number of days alive without life support was 22.0 days (IQR, 6.0-28.0 days) in the 12 mg of dexamethasone group and 20.5 days (IQR, 4.0-28.0 days) in the 6 mg of dexamethasone group (adjusted mean difference, 1.3 days [95% CI, 0-2.6 days]; P = .07). Mortality at 28 days was 27.1% in the 12 mg of dexamethasone group vs 32.3% in the 6 mg of dexamethasone group (adjusted relative risk, 0.86 [99% CI, 0.68-1.08]). Mortality at 90 days was 32.0% in the 12 mg of dexamethasone group vs 37.7% in the 6 mg of dexamethasone group (adjusted relative risk, 0.87 [99% CI, 0.70-1.07]). Serious adverse reactions, including septic shock and invasive fungal infections, occurred in 11.3% in the 12 mg of dexamethasone group vs 13.4% in the 6 mg of dexamethasone group (adjusted relative risk, 0.83 [99% CI, 0.54-1.29])., Conclusions and Relevance: Among patients with COVID-19 and severe hypoxemia, 12 mg/d of dexamethasone compared with 6 mg/d of dexamethasone did not result in statistically significantly more days alive without life support at 28 days. However, the trial may have been underpowered to identify a significant difference., Trial Registration: ClinicalTrials.gov Identifier: NCT04509973 and ctri.nic.in Identifier: CTRI/2020/10/028731.
- Published
- 2021
- Full Text
- View/download PDF
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