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Predicting mortality in sick African children: the FEAST Paediatric Emergency Triage (PET) Score.
George, Elizabeth C; Walker, A Sarah; Kiguli, Sarah; Olupot-Olupot, Peter; Opoka, Robert O; Engoru, Charles; Akech, Samuel O; Nyeko, Richard; Mtove, George; Reyburn, Hugh; Berkley, James A; Mpoya, Ayub; Levin, Michael; Crawley, Jane; Gibb, Diana M; Maitland, Kathryn; Babiker, Abdel G.
Affiliation
  • George EC; Medical Research Council Clinical Trials Unit (MRC CTU) at UCL, London, UK. elizabeth.george@ucl.ac.uk.
  • Walker AS; Medical Research Council Clinical Trials Unit (MRC CTU) at UCL, London, UK. rmjlasw@ucl.ac.uk.
  • Kiguli S; Department of Paediatrics, Mulago Hospital, Makerere University, Kampala, Uganda. skwalube@yahoo.co.uk.
  • Olupot-Olupot P; Department of Paediatrics, Mbale Regional Referral Hospital, Mbale, Uganda. polupotolupot@yahoo.com.
  • Opoka RO; Department of Paediatrics, Mulago Hospital, Makerere University, Kampala, Uganda. opokabob@yahoo.com.
  • Engoru C; Department of Paediatrics, Soroti Regional Referral Hospital, Soroti, Uganda. charlesengoru@yahoo.co.uk.
  • Akech SO; Kilifi Clinical Trials Facility, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. sakech@gmail.com.
  • Nyeko R; Department of Paediatrics, St Mary's Hospital, Lacor, Uganda. richard_nyeko@yahoo.com.
  • Mtove G; Department of Paediatrics, Joint Malaria Programme, Teule Hospital, Muheza, Tanzania. mtoveg2002@yahoo.co.uk.
  • Reyburn H; Department of Paediatrics, Joint Malaria Programme, Teule Hospital, Muheza, Tanzania. hugh.reyburn@lshtm.ac.uk.
  • Berkley JA; Kilifi Clinical Trials Facility, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. jberkley@kemri-wellcome.org.
  • Mpoya A; Kilifi Clinical Trials Facility, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. ampoya@kemri-wellcome.org.
  • Levin M; Wellcome Trust Centre for Clinical Tropical Medicine and Department of Paediatrics, Faculty of Medicine, Imperial College, London, UK. m.levin@imperial.ac.uk.
  • Crawley J; Medical Research Council Clinical Trials Unit (MRC CTU) at UCL, London, UK. jane.crawley@gmail.com.
  • Gibb DM; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK. jane.crawley@gmail.com.
  • Maitland K; Medical Research Council Clinical Trials Unit (MRC CTU) at UCL, London, UK. diana.gibb@ucl.ac.uk.
  • Babiker AG; Kilifi Clinical Trials Facility, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. k.maitland@imperial.ac.uk.
BMC Med ; 13: 174, 2015 Jul 31.
Article in En | MEDLINE | ID: mdl-26228245
BACKGROUND: Mortality in paediatric emergency care units in Africa often occurs within the first 24 h of admission and remains high. Alongside effective triage systems, a practical clinical bedside risk score to identify those at greatest risk could contribute to reducing mortality. METHODS: Data collected during the Fluid As Expansive Supportive Therapy (FEAST) trial, a multi-centre trial involving 3,170 severely ill African children, were analysed to identify clinical and laboratory prognostic factors for mortality. Multivariable Cox regression was used to build a model in this derivation dataset based on clinical parameters that could be quickly and easily assessed at the bedside. A score developed from the model coefficients was externally validated in two admissions datasets from Kilifi District Hospital, Kenya, and compared to published risk scores using Area Under the Receiver Operating Curve (AUROC) and Hosmer-Lemeshow tests. The Net Reclassification Index (NRI) was used to identify additional laboratory prognostic factors. RESULTS: A risk score using 8 clinical variables (temperature, heart rate, capillary refill time, conscious level, severe pallor, respiratory distress, lung crepitations, and weak pulse volume) was developed. The score ranged from 0-10 and had an AUROC of 0.82 (95 % CI, 0.77-0.87) in the FEAST trial derivation set. In the independent validation datasets, the score had an AUROC of 0.77 (95 % CI, 0.72-0.82) amongst admissions to a paediatric high dependency ward and 0.86 (95 % CI, 0.82-0.89) amongst general paediatric admissions. This discriminative ability was similar to, or better than other risk scores in the validation datasets. NRI identified lactate, blood urea nitrogen, and pH to be important prognostic laboratory variables that could add information to the clinical score. CONCLUSIONS: Eight clinical prognostic factors that could be rapidly assessed by healthcare staff for triage were combined to create the FEAST Paediatric Emergency Triage (PET) score and externally validated. The score discriminated those at highest risk of fatal outcome at the point of hospital admission and compared well to other published risk scores. Further laboratory tests were also identified as prognostic factors which could be added if resources were available or as indices of severity for comparison between centres in future research studies.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Infant Mortality / Child Mortality / Emergency Service, Hospital / Hospitals, Pediatric Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Child / Child, preschool / Humans / Infant / Male Country/Region as subject: Africa Language: En Journal: BMC Med Journal subject: MEDICINA Year: 2015 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Infant Mortality / Child Mortality / Emergency Service, Hospital / Hospitals, Pediatric Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Child / Child, preschool / Humans / Infant / Male Country/Region as subject: Africa Language: En Journal: BMC Med Journal subject: MEDICINA Year: 2015 Type: Article