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The burden, prevention and care of infants and children with congenital anomalies in sub-Saharan Africa: A scoping review.
Leke, Aminkeng Zawuo; Malherbe, Helen; Kalk, Emma; Mehta, Ushma; Kisa, Phylis; Botto, Lorenzo D; Ayede, Idowu; Fairlie, Lee; Maboh, Nkwati Michel; Orioli, Ieda; Zash, Rebecca; Kusolo, Ronald; Mumpe-Mwanja, Daniel; Serujogi, Robert; Bongomin, Bodo; Osoro, Caroline; Dah, Clarisse; Sentumbwe-Mugisha, Olive; Shabani, Hamisi Kimaro; Musoke, Philippa; Dolk, Helen; Barlow-Mosha, Linda.
Afiliación
  • Leke AZ; Institute for Nursing and Health Research, Centre for Maternal, Fetal and Infant Research, Ulster University, Newtownabbey, United Kingdom.
  • Malherbe H; Centre for Infant and Maternal Health Research, Health Research Foundation, Buea, Cameroon.
  • Kalk E; Research & Epidemiology, Rare Diseases South Africa NPC, Bryanston, Sandton, South Africa.
  • Mehta U; Centre for Infectious Disease Epidemiology & Research, School of Public Health, University of Cape Town, Cape Town, South Africa.
  • Kisa P; Centre for Infectious Disease Epidemiology & Research, School of Public Health, University of Cape Town, Cape Town, South Africa.
  • Botto LD; Makerere University College of Health Sciences, Kampala, Uganda.
  • Ayede I; Division of Medical Genetics, University of Utah, Salt Lake City, Utah, United States of America.
  • Fairlie L; International Center on Birth Defects, University of Utah, Salt Lake City, Utah, United States of America.
  • Maboh NM; Department of Paediatrics, College of Medicine, University of Ibadan and University College Hospital, Ibadan, Nigeria.
  • Orioli I; Faculty of Health Sciences, Wits Reproductive Health and HIV Institute, University of the Witwatersrand, Johannesburg, South Africa.
  • Zash R; Centre for Infant and Maternal Health Research, Health Research Foundation, Buea, Cameroon.
  • Kusolo R; Genetics Department, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Mumpe-Mwanja D; ReLAMC: Latin American Network for Congenital Malformation Surveillance, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Serujogi R; The Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana and Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States of America.
  • Bongomin B; Makerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.
  • Osoro C; Makerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.
  • Dah C; Makerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.
  • Sentumbwe-Mugisha O; Gulu University Faculty of Medicine: Gulu, Gulu, UG/ World Health Organization, Kampala, Uganda.
  • Shabani HK; Kenya Medical Research Institute, Centre for Global Health Research, Nairobi, Kenya.
  • Musoke P; Centre de Recherche en Santé de Nouna, Nouna, Burkina Faso.
  • Dolk H; World Health Organization, Kampala, Uganda.
  • Barlow-Mosha L; Neurosurgery Department, Muhimbili Orthopaedic Institute, Dar es salaam, Tanzania.
PLOS Glob Public Health ; 3(6): e0001850, 2023.
Article en En | MEDLINE | ID: mdl-37379291
ABSTRACT
The aim of this scoping review was to determine the scope, objectives and methodology of contemporary published research on congenital anomalies (CAs) in sub-Saharan Africa (SSA), to inform activities of the newly established sub-Saharan African Congenital Anomaly Network (sSCAN). MEDLINE was searched for CA-related articles published between January 2016 and June 2021. Articles were classified into four main areas (public health burden, surveillance, prevention, care) and their objectives and methodologies summarized. Of the 532 articles identified, 255 were included. The articles originated from 22 of the 49 SSA countries, with four countries contributing 60% of the articles Nigeria (22.0%), Ethiopia (14.1%), Uganda (11.7%) and South Africa (11.7%). Only 5.5% of studies involved multiple countries within the region. Most articles included CA as their primary focus (85%), investigated a single CA (88%), focused on CA burden (56.9%) and care (54.1%), with less coverage of surveillance (3.5%) and prevention (13.3%). The most common study designs were case studies/case series (26.6%), followed by cross-sectional surveys (17.6%), retrospective record reviews (17.3%), and cohort studies (17.2%). Studies were mainly derived from single hospitals (60.4%), with only 9% being population-based studies. Most data were obtained from retrospective review of clinical records (56.1%) or via caregiver interviews (34.9%). Few papers included stillbirths (7.5%), prenatally diagnosed CAs (3.5%) or terminations of pregnancy for CA (2.4%).This first-of-a-kind-scoping review on CA in SSA demonstrated an increasing level of awareness and recognition among researchers in SSA of the contribution of CAs to under-5 mortality and morbidity in the region. The review also highlighted the need to address diagnosis, prevention, surveillance and care to meet Sustainable Development Goals 3.2 and 3.8. The SSA sub-region faces unique challenges, including fragmentation of efforts that we hope to surmount through sSCAN via a multidisciplinary and multi-stakeholder approach.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies / Systematic_reviews Idioma: En Revista: PLOS Glob Public Health Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies / Systematic_reviews Idioma: En Revista: PLOS Glob Public Health Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido