Sepsis hysteria? Not for children – Authors' reply
Thankfully, paediatric sepsis trials in high-income countries have not used mortality as the primary endpoint for many years, citing “affordability”.2 A point-prevalence study of 6925 children across 128 paediatric intensive care units in 26 countries identified 569 children who fulfilled sepsis cri...
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Veröffentlicht in: | The Lancet (British edition) 2020-10, Vol.396 (10259), p.1333-1334 |
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description | Thankfully, paediatric sepsis trials in high-income countries have not used mortality as the primary endpoint for many years, citing “affordability”.2 A point-prevalence study of 6925 children across 128 paediatric intensive care units in 26 countries identified 569 children who fulfilled sepsis criteria.3 Of these patients, 439 children (77%) had one or more comorbid conditions that could independently limit survival, including solid organ or stem-cell transplants, malignancy, renal disease, and haematological or immunological conditions. The authors estimated that an intervention trial would take 3 years for 2118 patients to be enrolled from 58 paediatric intensive care units for 80% power to detect a 5% absolute risk reduction in mortality. With respect to low-income and middle-income countries, paediatric mortality rates are indeed higher than in high-income countries; however, what is the true incidence, and in what proportion could antibacterial therapy be potentially life-saving? |
doi_str_mv | 10.1016/S0140-6736(20)32144-9 |
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Not for children – Authors' reply</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><source>ProQuest Central UK/Ireland</source><creator>Singer, Mervyn ; Inada-Kim, Matt ; Peters, Mark ; Maitland, Kathryn</creator><creatorcontrib>Singer, Mervyn ; Inada-Kim, Matt ; Peters, Mark ; Maitland, Kathryn</creatorcontrib><description>Thankfully, paediatric sepsis trials in high-income countries have not used mortality as the primary endpoint for many years, citing “affordability”.2 A point-prevalence study of 6925 children across 128 paediatric intensive care units in 26 countries identified 569 children who fulfilled sepsis criteria.3 Of these patients, 439 children (77%) had one or more comorbid conditions that could independently limit survival, including solid organ or stem-cell transplants, malignancy, renal disease, and haematological or immunological conditions. The authors estimated that an intervention trial would take 3 years for 2118 patients to be enrolled from 58 paediatric intensive care units for 80% power to detect a 5% absolute risk reduction in mortality. With respect to low-income and middle-income countries, paediatric mortality rates are indeed higher than in high-income countries; however, what is the true incidence, and in what proportion could antibacterial therapy be potentially life-saving?</description><identifier>ISSN: 0140-6736</identifier><identifier>EISSN: 1474-547X</identifier><identifier>DOI: 10.1016/S0140-6736(20)32144-9</identifier><identifier>PMID: 34338210</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Antibiotics ; Antiinfectives and antibacterials ; Child ; Children ; Clinical trials ; Fatalities ; Hospitals ; Humans ; Hysteria ; Immunology ; Income ; Intensive care ; Intensive care units ; Kidney transplantation ; Malignancy ; Mortality ; Pathogens ; Pediatrics ; Pneumonia ; Risk management ; Sepsis ; Sepsis - diagnosis ; Streptococcus infections ; Transplants</subject><ispartof>The Lancet (British edition), 2020-10, Vol.396 (10259), p.1333-1334</ispartof><rights>2020 Elsevier Ltd</rights><rights>2020. 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Not for children – Authors' reply</title><title>The Lancet (British edition)</title><addtitle>Lancet</addtitle><description>Thankfully, paediatric sepsis trials in high-income countries have not used mortality as the primary endpoint for many years, citing “affordability”.2 A point-prevalence study of 6925 children across 128 paediatric intensive care units in 26 countries identified 569 children who fulfilled sepsis criteria.3 Of these patients, 439 children (77%) had one or more comorbid conditions that could independently limit survival, including solid organ or stem-cell transplants, malignancy, renal disease, and haematological or immunological conditions. The authors estimated that an intervention trial would take 3 years for 2118 patients to be enrolled from 58 paediatric intensive care units for 80% power to detect a 5% absolute risk reduction in mortality. With respect to low-income and middle-income countries, paediatric mortality rates are indeed higher than in high-income countries; however, what is the true incidence, and in what proportion could antibacterial therapy be potentially life-saving?</description><subject>Antibiotics</subject><subject>Antiinfectives and antibacterials</subject><subject>Child</subject><subject>Children</subject><subject>Clinical trials</subject><subject>Fatalities</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Hysteria</subject><subject>Immunology</subject><subject>Income</subject><subject>Intensive care</subject><subject>Intensive care units</subject><subject>Kidney transplantation</subject><subject>Malignancy</subject><subject>Mortality</subject><subject>Pathogens</subject><subject>Pediatrics</subject><subject>Pneumonia</subject><subject>Risk management</subject><subject>Sepsis</subject><subject>Sepsis - diagnosis</subject><subject>Streptococcus infections</subject><subject>Transplants</subject><issn>0140-6736</issn><issn>1474-547X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkLtOwzAUhi0EoqXwCKBIDJQh4GsST1VVcZMqGAoSm-X4orpKk2AnSN14B96QJyG9wMDCdJbv_885HwCnCF4hiJLrGUQUxklKkiGGlwQjSmO-B_qIpjRmNH3dB_1fpAeOQlhACGkC2SHoEUpIhhHsAzozdXAhmq9CY7yTo-ixaiJb-UjNXaG9KaOvj89o3DbzyoeLyJu6WB2DAyuLYE52cwBebm-eJ_fx9OnuYTKexopAwmPElIWc8IzRnHEqCckV18rmCsM0RwRrlFueIS6RxLmWuZVWamRRRyOlEzIAw21v7au31oRGLF1Qpihkaao2CMxY2r1KUtKh53_QRdX6srtOYMpIkkKS8Y5iW0r5KgRvrKi9W0q_EgiKtVax0SrWzgSGYqNVrHNnu_Y2Xxr9m_rx2AGjLWA6He_OeBGUM6Uy2nmjGqEr98-Kbz6yhiE</recordid><startdate>20201024</startdate><enddate>20201024</enddate><creator>Singer, Mervyn</creator><creator>Inada-Kim, Matt</creator><creator>Peters, Mark</creator><creator>Maitland, Kathryn</creator><general>Elsevier Ltd</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>0TT</scope><scope>0TZ</scope><scope>0U~</scope><scope>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7RV</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88C</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8C2</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>ASE</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FPQ</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K6X</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>KB~</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>20201024</creationdate><title>Sepsis hysteria? 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subjects | Antibiotics Antiinfectives and antibacterials Child Children Clinical trials Fatalities Hospitals Humans Hysteria Immunology Income Intensive care Intensive care units Kidney transplantation Malignancy Mortality Pathogens Pediatrics Pneumonia Risk management Sepsis Sepsis - diagnosis Streptococcus infections Transplants |
title | Sepsis hysteria? Not for children – Authors' reply |
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