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Neonatal sepsis and mortality in low-income and middle-income countries from a facility-based birth cohort: an international multisite prospective observational study.
Milton, Rebecca; Gillespie, David; Dyer, Calie; Taiyari, Khadijeh; Carvalho, Maria J; Thomson, Kathryn; Sands, Kirsty; Portal, Edward A R; Hood, Kerenza; Ferreira, Ana; Hender, Thomas; Kirby, Nigel; Mathias, Jordan; Nieto, Maria; Watkins, William J; Bekele, Delayehu; Abayneh, Mahlet; Solomon, Semaria; Basu, Sulagna; Nandy, Ranjan K; Saha, Bijan; Iregbu, Kenneth; Modibbo, Fatima Z; Uwaezuoke, Stella; Zahra, Rabaab; Shirazi, Haider; Najeeb, Syed U; Mazarati, Jean-Baptiste; Rucogoza, Aniceth; Gaju, Lucie; Mehtar, Shaheen; Bulabula, Andre N H; Whitelaw, Andrew C; Walsh, Timothy R; Chan, Grace J.
Afiliación
  • Milton R; Institute of Infection and Immunity, Cardiff University, Cardiff, UK; Centre for Trials Research, Cardiff University, Cardiff, UK. Electronic address: miltonrl1@cardiff.ac.uk.
  • Gillespie D; Centre for Trials Research, Cardiff University, Cardiff, UK.
  • Dyer C; Institute of Infection and Immunity, Cardiff University, Cardiff, UK; Centre for Trials Research, Cardiff University, Cardiff, UK.
  • Taiyari K; Centre for Trials Research, Cardiff University, Cardiff, UK.
  • Carvalho MJ; Institute of Infection and Immunity, Cardiff University, Cardiff, UK; Institute of Biomedicine, Department of Medical Sciences, University of Aveiro, Aveiro, Portugal.
  • Thomson K; Institute of Infection and Immunity, Cardiff University, Cardiff, UK; Ineos Institute of Antimicrobial Research, Department of Zoology, University of Oxford, Oxford, UK.
  • Sands K; Institute of Infection and Immunity, Cardiff University, Cardiff, UK; Ineos Institute of Antimicrobial Research, Department of Zoology, University of Oxford, Oxford, UK.
  • Portal EAR; Institute of Infection and Immunity, Cardiff University, Cardiff, UK.
  • Hood K; Centre for Trials Research, Cardiff University, Cardiff, UK.
  • Ferreira A; Institute of Infection and Immunity, Cardiff University, Cardiff, UK.
  • Hender T; Institute of Infection and Immunity, Cardiff University, Cardiff, UK.
  • Kirby N; Centre for Trials Research, Cardiff University, Cardiff, UK.
  • Mathias J; Institute of Infection and Immunity, Cardiff University, Cardiff, UK.
  • Nieto M; Institute of Infection and Immunity, Cardiff University, Cardiff, UK.
  • Watkins WJ; Institute of Infection and Immunity, Cardiff University, Cardiff, UK.
  • Bekele D; St Paul's Hospital Millennium Medical College, Addis Ababa, Ethiopia.
  • Abayneh M; St Paul's Hospital Millennium Medical College, Addis Ababa, Ethiopia.
  • Solomon S; St Paul's Hospital Millennium Medical College, Addis Ababa, Ethiopia.
  • Basu S; Division of Bacteriology, ICMR-National Institute of Cholera and Enteric Diseases Beliaghata, Kolkata, India.
  • Nandy RK; Division of Bacteriology, ICMR-National Institute of Cholera and Enteric Diseases Beliaghata, Kolkata, India.
  • Saha B; Department of Neonatology, Institute of Postgraduate Medical Education and Research, Kolkata, India.
  • Iregbu K; National Hospital, Abuja, Nigeria.
  • Modibbo FZ; Murtala Mohammed Specialist Hospital, Kano, Nigeria.
  • Uwaezuoke S; National Hospital, Abuja, Nigeria.
  • Zahra R; Department of Microbiology, Quaid-i-Azam University, Islamabad, Pakistan.
  • Shirazi H; Pakistan Institute of Medical Sciences, Islamabad, Pakistan.
  • Najeeb SU; Department of Microbiology, Quaid-i-Azam University, Islamabad, Pakistan.
  • Mazarati JB; University Teaching Hospital, Kigali, Rwanda.
  • Rucogoza A; University Teaching Hospital, Kigali, Rwanda.
  • Gaju L; University Teaching Hospital, Kigali, Rwanda.
  • Mehtar S; Department of Global Health, Stellenbosch University, Cape Town, South Africa.
  • Bulabula ANH; Infection Control Africa Network, Cape Town, South Africa.
  • Whitelaw AC; Division of Medical Microbiology at the National Health Laboratory Services Tygerberg and Stellenbosch University, Cape Town, South Africa.
  • Walsh TR; Institute of Infection and Immunity, Cardiff University, Cardiff, UK; Ineos Institute of Antimicrobial Research, Department of Zoology, University of Oxford, Oxford, UK.
  • Chan GJ; St Paul's Hospital Millennium Medical College, Addis Ababa, Ethiopia; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA; Department of Epidemiology, Harvard T H Chan School of Public Health, Boston, MA, USA.
Lancet Glob Health ; 10(5): e661-e672, 2022 05.
Article en En | MEDLINE | ID: mdl-35427523
BACKGROUND: Neonatal sepsis is a primary cause of neonatal mortality and is an urgent global health concern, especially within low-income and middle-income countries (LMICs), where 99% of global neonatal mortality occurs. The aims of this study were to determine the incidence and associations with neonatal sepsis and all-cause mortality in facility-born neonates in LMICs. METHODS: The Burden of Antibiotic Resistance in Neonates from Developing Societies (BARNARDS) study recruited mothers and their neonates into a prospective observational cohort study across 12 clinical sites from Bangladesh, Ethiopia, India, Pakistan, Nigeria, Rwanda, and South Africa. Data for sepsis-associated factors in the four domains of health care, maternal, birth and neonatal, and living environment were collected for all mothers and neonates enrolled. Primary outcomes were clinically suspected sepsis, laboratory-confirmed sepsis, and all-cause mortality in neonates during the first 60 days of life. Incidence proportion of livebirths for clinically suspected sepsis and laboratory-confirmed sepsis and incidence rate per 1000 neonate-days for all-cause mortality were calculated. Modified Poisson regression was used to investigate factors associated with neonatal sepsis and parametric survival models for factors associated with all-cause mortality. FINDINGS: Between Nov 12, 2015 and Feb 1, 2018, 29 483 mothers and 30 557 neonates were enrolled. The incidence of clinically suspected sepsis was 166·0 (95% CI 97·69-234·24) per 1000 livebirths, laboratory-confirmed sepsis was 46·9 (19·04-74·79) per 1000 livebirths, and all-cause mortality was 0·83 (0·37-2·00) per 1000 neonate-days. Maternal hypertension, previous maternal hospitalisation within 12 months, average or higher monthly household income, ward size (>11 beds), ward type (neonatal), living in a rural environment, preterm birth, perinatal asphyxia, and multiple births were associated with an increased risk of clinically suspected sepsis, laboratory-confirmed sepsis, and all-cause mortality. The majority (881 [72·5%] of 1215) of laboratory-confirmed sepsis cases occurred within the first 3 days of life. INTERPRETATION: Findings from this study highlight the substantial proportion of neonates who develop neonatal sepsis, and the high mortality rates among neonates with sepsis in LMICs. More efficient and effective identification of neonatal sepsis is needed to target interventions to reduce its incidence and subsequent mortality in LMICs. FUNDING: Bill & Melinda Gates Foundation.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sepsis / Nacimiento Prematuro / Sepsis Neonatal Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Newborn / Pregnancy Idioma: En Revista: Lancet Glob Health Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sepsis / Nacimiento Prematuro / Sepsis Neonatal Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Newborn / Pregnancy Idioma: En Revista: Lancet Glob Health Año: 2022 Tipo del documento: Article