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Derivation and validation of a novel risk assessment tool to identify children aged 2-59 months at risk of hospitalised pneumonia-related mortality in 20 countries.
Rees, Chris A; Colbourn, Tim; Hooli, Shubhada; King, Carina; Lufesi, Norman; McCollum, Eric D; Mwansambo, Charles; Cutland, Clare; Madhi, Shabir Ahmed; Nunes, Marta; Matthew, Joseph L; Addo-Yobo, Emmanuel; Chisaka, Noel; Hassan, Mumtaz; Hibberd, Patricia L; Jeena, Prakash M; Lozano, Juan M; MacLeod, William B; Patel, Archana; Thea, Donald M; Nguyen, Ngoc Tuong Vy; Kartasasmita, Cissy B; Lucero, Marilla; Awasthi, Shally; Bavdekar, Ashish; Chou, Monidarin; Nymadawa, Pagbajabyn; Pape, Jean-William; Paranhos-Baccala, Glaucia; Picot, Valentina S; Rakoto-Andrianarivelo, Mala; Rouzier, Vanessa; Russomando, Graciela; Sylla, Mariam; Vanhems, Philippe; Wang, Jianwei; Asghar, Rai; Banajeh, Salem; Iqbal, Imran; Maulen-Radovan, Irene; Mino-Leon, Greta; Saha, Samir K; Santosham, Mathuram; Singhi, Sunit; Basnet, Sudha; Strand, Tor A; Bhatnagar, Shinjini; Wadhwa, Nitya; Lodha, Rakesh; Aneja, Satinder.
Afiliação
  • Rees CA; Division of Pediatric Emergency Medicine, Emory University School of Medicine, Children's Healthcare of Atlanta, Atlanta, Georgia, USA.
  • Colbourn T; Institute for Global Health, University College London, London, UK.
  • Hooli S; Section of Pediatric Emergency Medicine, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas, USA.
  • King C; Department of Global Public Health, Karolinska Institutet, Stockholm, Sweden.
  • Lufesi N; Acute Respiratory Illness Unit, Government of Malawi Ministry of Health, Lilongwe, Malawi.
  • McCollum ED; Global Program in Respiratory Sciences, Eudowood Division of Pediatric Respiratory Sciences, Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Mwansambo C; Acute Respiratory Illness Unit, Government of Malawi Ministry of Health, Lilongwe, Malawi.
  • Cutland C; South African Medical Research Council: Vaccines and Infectious Diseases Analytics Research Unit, School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg-Braamfontein, South Africa.
  • Madhi SA; South African Medical Research Council: Vaccines and Infectious Diseases Analytics Research Unit, School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg-Braamfontein, South Africa.
  • Nunes M; South African Medical Research Council: Vaccines and Infectious Diseases Analytics Research Unit, School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg-Braamfontein, South Africa.
  • Matthew JL; Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Addo-Yobo E; Department of Pediatrics, Komfo Anokye Teaching Hospital, Kumasi, Ghana.
  • Chisaka N; World Bank, World Bank, Washington, District of Columbia, USA.
  • Hassan M; Department of Pediatrics, Children's Hospital, Islamabad, Pakistan.
  • Hibberd PL; Department of Global Health, Boston University School of Public Health, Boston, Massachusetts, USA.
  • Jeena PM; Department of Paediatrics and Child Health, University of KwaZulu-Natal Nelson R Mandela School of Medicine, Durban, South Africa.
  • Lozano JM; Division of Medical and Population Health Science Education and Research, Florida International University, Miami, Florida, USA.
  • MacLeod WB; Department of Global Health, Boston University School of Public Health, Boston, Massachusetts, USA.
  • Patel A; Lata Medical Research Foundation, Nagpur and Datta Meghe Institute of Medical Sciences, Sawangi, India.
  • Thea DM; Department of Global Health, Boston University School of Public Health, Boston, Massachusetts, USA.
  • Nguyen NTV; Department of Pediatrics, Children Hospital No 1, Ho Chi Minh City, Viet Nam.
  • Kartasasmita CB; Department of Child Health, Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia.
  • Lucero M; Department of Pediatrics, Research Institute for Tropical Medicine, Muntinlupa City, Philippines.
  • Awasthi S; Department of Pediatrics, King George's Medical University, Lucknow, Uttar Pradesh, India.
  • Bavdekar A; Department of Pediatrics, KEM Hospital Pune, Pune, India.
  • Chou M; Rodolph Mérieux Laboratory, Faculty of Medicine, University of Health Sciences, Phnom Penh, Cambodia.
  • Nymadawa P; Department of Pediatrics, Mongolian Academy of Sciences, Ulaanbaatar, Mongolia.
  • Pape JW; Department of Pediatrics, GHESKIO, Port-au-Prince, Haiti.
  • Paranhos-Baccala G; Pediatrics, Fondation Merieux, Lyon, France.
  • Picot VS; Pediatrics, Fondation Merieux, Lyon, France.
  • Rakoto-Andrianarivelo M; Centre d'Infectiologie, Charles Mérieux, Antanarivo, Madagascar.
  • Rouzier V; Department of Pediatrics, GHESKIO, Port-au-Prince, Haiti.
  • Russomando G; Departamento de Biología Molecular y Genética, Instituto de Investigaciones en Ciencias de la Salud, Asuncion, Paraguay.
  • Sylla M; Department of Pediatrics, Gabriel Touré University Hospital Center, Bamako, Mali.
  • Vanhems P; Unité d'Hygiène, Epidémiologie, Infectiovigilance et Prévention, Hospices Civils de Lyon, Lyon, France.
  • Wang J; MOH Key Laboratory of Systems Biology of Pathogens and Dr Christophe Mérieux Laboratory, Chinese Academy of Medical Sciences & Peking Union, Beijing, China.
  • Asghar R; Department of Paediatrics, Rawalpindi Medical College, Rawalpindi, Pakistan.
  • Banajeh S; Department of Pediatrics, Sana'a University, Sana'a, Yemen.
  • Iqbal I; Department of Pediatrics, Nishtar Medical College, Multan, Pakistan.
  • Maulen-Radovan I; Division de Investigacion Insurgentes, Instituto Nactional de Pediatria, Mexico City, Mexico.
  • Mino-Leon G; Infectious Diseases, Children's Hospital Dr Francisco de Ycaza Bustamante, Guayaquil, Ecuador.
  • Saha SK; Child Health Research Foundation, Dhaka Shishu Hosp, Dhaka, Bangladesh.
  • Santosham M; International Vaccine Access Center (IVAC), Department of International Health, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland, USA.
  • Singhi S; Department of Pediatrics, Medanta, The Medicity, Gurgaon, India.
  • Basnet S; Department of Pediatrics, Tribhuvan University Institute of Medicine, Kathmandu, Nepal.
  • Strand TA; Department of Research, Innlandet Hospital Trust, Lillehammer, Norway.
  • Bhatnagar S; Department of Maternal and Child Health, Translational Health Science and Technology Institute, Faridabad, India.
  • Wadhwa N; Department of Maternal and Child Health, Translational Health Science and Technology Institute, Faridabad, India.
  • Lodha R; Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
  • Aneja S; Department of Pediatrics, Sharda University School of Medical Sciences and Research, Greater Noida, Uttar Pradesh, India.
BMJ Glob Health ; 7(4)2022 04.
Article em En | MEDLINE | ID: mdl-35428680
ABSTRACT

INTRODUCTION:

Existing risk assessment tools to identify children at risk of hospitalised pneumonia-related mortality have shown suboptimal discriminatory value during external validation. Our objective was to derive and validate a novel risk assessment tool to identify children aged 2-59 months at risk of hospitalised pneumonia-related mortality across various settings.

METHODS:

We used primary, baseline, patient-level data from 11 studies, including children evaluated for pneumonia in 20 low-income and middle-income countries. Patients with complete data were included in a logistic regression model to assess the association of candidate variables with the outcome hospitalised pneumonia-related mortality. Adjusted log coefficients were calculated for each candidate variable and assigned weighted points to derive the Pneumonia Research Partnership to Assess WHO Recommendations (PREPARE) risk assessment tool. We used bootstrapped selection with 200 repetitions to internally validate the PREPARE risk assessment tool.

RESULTS:

A total of 27 388 children were included in the analysis (mean age 14.0 months, pneumonia-related case fatality ratio 3.1%). The PREPARE risk assessment tool included patient age, sex, weight-for-age z-score, body temperature, respiratory rate, unconsciousness or decreased level of consciousness, convulsions, cyanosis and hypoxaemia at baseline. The PREPARE risk assessment tool had good discriminatory value when internally validated (area under the curve 0.83, 95% CI 0.81 to 0.84).

CONCLUSIONS:

The PREPARE risk assessment tool had good discriminatory ability for identifying children at risk of hospitalised pneumonia-related mortality in a large, geographically diverse dataset. After external validation, this tool may be implemented in various settings to identify children at risk of hospitalised pneumonia-related mortality.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pneumonia Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans / Infant Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pneumonia Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans / Infant Idioma: En Ano de publicação: 2022 Tipo de documento: Article