Cargando…

Building Perinatal Pathology Research Capacity in Sub-Saharan Africa

INTRODUCTION: Over two million stillbirths and neonatal deaths occur in sub-Saharan Africa (sSA) annually. Despite multilateral efforts, reducing perinatal mortality has been slow. Although targeted pathologic investigation can often determine the cause of perinatal death, in resource-limited settin...

Descripción completa

Detalles Bibliográficos
Autores principales: Bebell, Lisa M., Ngonzi, Joseph, Meier, Frederick A., Carreon, Chrystalle Katte, Birungi, Abraham, Kerry, Vanessa B., Atwine, Raymond, Roberts, Drucilla J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304650/
https://www.ncbi.nlm.nih.gov/pubmed/35872791
http://dx.doi.org/10.3389/fmed.2022.958840
_version_ 1784752136830058496
author Bebell, Lisa M.
Ngonzi, Joseph
Meier, Frederick A.
Carreon, Chrystalle Katte
Birungi, Abraham
Kerry, Vanessa B.
Atwine, Raymond
Roberts, Drucilla J.
author_facet Bebell, Lisa M.
Ngonzi, Joseph
Meier, Frederick A.
Carreon, Chrystalle Katte
Birungi, Abraham
Kerry, Vanessa B.
Atwine, Raymond
Roberts, Drucilla J.
author_sort Bebell, Lisa M.
collection PubMed
description INTRODUCTION: Over two million stillbirths and neonatal deaths occur in sub-Saharan Africa (sSA) annually. Despite multilateral efforts, reducing perinatal mortality has been slow. Although targeted pathologic investigation can often determine the cause of perinatal death, in resource-limited settings, stillbirths, early neonatal deaths, and placentas are rarely examined pathologically. However, the placenta is a key source of diagnostic information and is the main determinant of fetal growth and development in utero, influencing child health outcomes. METHODS: In 2016, our collaborative intercontinental group began investigating infectious perinatal death and adverse child health outcomes in Uganda. We developed and initiated a 4-day combined didactic/practical curriculum to train health workers in placental collection, gross placental examination, and tissue sampling for histology. We also trained a local technician to perform immunohistochemistry staining. RESULTS: Overall, we trained 12 health workers who performed gross placental assessment for > 1,000 placentas, obtaining > 5,000 formalin-fixed tissue samples for research diagnostic use. Median placental weights ranged from 425 to 456 g, and 33.3% of placentas were < 10th percentile in weight, corrected for gestational age. Acute chorioamnionitis (32.3%) and maternal vascular malperfusion (25.4%) were common diagnoses. DISCUSSION: Through a targeted training program, we built capacity at a university-affiliated hospital in sSA to independently perform placental collection, gross pathologic examination, and placental tissue processing for histology and special stains. Our training model can be applied to other collaborative research endeavors in diverse resource-limited settings to improve research and clinical capacity and competency for diagnostics and management of stillbirth, neonatal death, and child health outcomes.
format Online
Article
Text
id pubmed-9304650
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-93046502022-07-23 Building Perinatal Pathology Research Capacity in Sub-Saharan Africa Bebell, Lisa M. Ngonzi, Joseph Meier, Frederick A. Carreon, Chrystalle Katte Birungi, Abraham Kerry, Vanessa B. Atwine, Raymond Roberts, Drucilla J. Front Med (Lausanne) Medicine INTRODUCTION: Over two million stillbirths and neonatal deaths occur in sub-Saharan Africa (sSA) annually. Despite multilateral efforts, reducing perinatal mortality has been slow. Although targeted pathologic investigation can often determine the cause of perinatal death, in resource-limited settings, stillbirths, early neonatal deaths, and placentas are rarely examined pathologically. However, the placenta is a key source of diagnostic information and is the main determinant of fetal growth and development in utero, influencing child health outcomes. METHODS: In 2016, our collaborative intercontinental group began investigating infectious perinatal death and adverse child health outcomes in Uganda. We developed and initiated a 4-day combined didactic/practical curriculum to train health workers in placental collection, gross placental examination, and tissue sampling for histology. We also trained a local technician to perform immunohistochemistry staining. RESULTS: Overall, we trained 12 health workers who performed gross placental assessment for > 1,000 placentas, obtaining > 5,000 formalin-fixed tissue samples for research diagnostic use. Median placental weights ranged from 425 to 456 g, and 33.3% of placentas were < 10th percentile in weight, corrected for gestational age. Acute chorioamnionitis (32.3%) and maternal vascular malperfusion (25.4%) were common diagnoses. DISCUSSION: Through a targeted training program, we built capacity at a university-affiliated hospital in sSA to independently perform placental collection, gross pathologic examination, and placental tissue processing for histology and special stains. Our training model can be applied to other collaborative research endeavors in diverse resource-limited settings to improve research and clinical capacity and competency for diagnostics and management of stillbirth, neonatal death, and child health outcomes. Frontiers Media S.A. 2022-07-08 /pmc/articles/PMC9304650/ /pubmed/35872791 http://dx.doi.org/10.3389/fmed.2022.958840 Text en Copyright © 2022 Bebell, Ngonzi, Meier, Carreon, Birungi, Kerry, Atwine and Roberts. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Bebell, Lisa M.
Ngonzi, Joseph
Meier, Frederick A.
Carreon, Chrystalle Katte
Birungi, Abraham
Kerry, Vanessa B.
Atwine, Raymond
Roberts, Drucilla J.
Building Perinatal Pathology Research Capacity in Sub-Saharan Africa
title Building Perinatal Pathology Research Capacity in Sub-Saharan Africa
title_full Building Perinatal Pathology Research Capacity in Sub-Saharan Africa
title_fullStr Building Perinatal Pathology Research Capacity in Sub-Saharan Africa
title_full_unstemmed Building Perinatal Pathology Research Capacity in Sub-Saharan Africa
title_short Building Perinatal Pathology Research Capacity in Sub-Saharan Africa
title_sort building perinatal pathology research capacity in sub-saharan africa
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304650/
https://www.ncbi.nlm.nih.gov/pubmed/35872791
http://dx.doi.org/10.3389/fmed.2022.958840
work_keys_str_mv AT bebelllisam buildingperinatalpathologyresearchcapacityinsubsaharanafrica
AT ngonzijoseph buildingperinatalpathologyresearchcapacityinsubsaharanafrica
AT meierfredericka buildingperinatalpathologyresearchcapacityinsubsaharanafrica
AT carreonchrystallekatte buildingperinatalpathologyresearchcapacityinsubsaharanafrica
AT birungiabraham buildingperinatalpathologyresearchcapacityinsubsaharanafrica
AT kerryvanessab buildingperinatalpathologyresearchcapacityinsubsaharanafrica
AT atwineraymond buildingperinatalpathologyresearchcapacityinsubsaharanafrica
AT robertsdrucillaj buildingperinatalpathologyresearchcapacityinsubsaharanafrica