Cargando…

Systematic review of the clinical manifestations of glucose-6-phosphate dehydrogenase deficiency in the Greater Mekong Subregion: implications for malaria elimination and beyond

INTRODUCTION: To achieve malaria elimination in the Greater Mekong Subregion (GMS) by 2030, proper case management is necessary. 8-aminoquinolines, such as primaquine, are the only available medicines effective in preventing relapse of the hypnozoite stage of Plasmodium vivax, as well as the onward...

Descripción completa

Detalles Bibliográficos
Autores principales: Ong, Ken Ing Cherng, Kosugi, Hodaka, Thoeun, Sophea, Araki, Hitomi, Thandar, Moe Moe, Iwagami, Moritoshi, Hongvanthong, Bouasy, Brey, Paul T, Kano, Shigeyuki, Jimba, Masamine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5656182/
https://www.ncbi.nlm.nih.gov/pubmed/29082022
http://dx.doi.org/10.1136/bmjgh-2017-000415
_version_ 1783273667523772416
author Ong, Ken Ing Cherng
Kosugi, Hodaka
Thoeun, Sophea
Araki, Hitomi
Thandar, Moe Moe
Iwagami, Moritoshi
Hongvanthong, Bouasy
Brey, Paul T
Kano, Shigeyuki
Jimba, Masamine
author_facet Ong, Ken Ing Cherng
Kosugi, Hodaka
Thoeun, Sophea
Araki, Hitomi
Thandar, Moe Moe
Iwagami, Moritoshi
Hongvanthong, Bouasy
Brey, Paul T
Kano, Shigeyuki
Jimba, Masamine
author_sort Ong, Ken Ing Cherng
collection PubMed
description INTRODUCTION: To achieve malaria elimination in the Greater Mekong Subregion (GMS) by 2030, proper case management is necessary. 8-aminoquinolines, such as primaquine, are the only available medicines effective in preventing relapse of the hypnozoite stage of Plasmodium vivax, as well as the onward transmission of Plasmodium falciparum. However, primaquine can cause haemolysis in individuals who have glucose-6-phosphate dehydrogenase deficiency (G6PDd). We conducted a systematic review on the reported clinical manifestations of G6PDd to provide a comprehensive overview of the situation in the GMS. METHODS: The protocol for this systematic review was registered on PROSPERO: International prospective register of systematic reviews (CRD42016043146). We searched the PubMed/MEDLINE, CINAHL, and Web of Science databases for published articles describing the clinical manifestations of G6PDd in the GMS. We included articles of all study designs from inception until 31 July 2016, reporting the clinical manifestations of G6PDd. We then performed a narrative synthesis of these articles. RESULTS: We included 56 articles in this review, 45 of which were from Thailand. Haemolysis in G6PD-deficient individuals was caused not only by primaquine but also by other medicines and infections. Other clinical manifestations of G6PDd that were found were favism, neonatal jaundice and chronic non-spherocytic haemolytic anaemia. G6PDd also influenced the clinical presentations of genetic disorders and infections, such as thalassemia and typhoid fever. CONCLUSION: As G6PDd also affects the clinical presentations of other infections, the benefits of G6PD testing and proper record keeping transcend those of malaria case management. Therefore, healthcare workers at the community level should be made familiar with complications resulting from G6PDd as these complications extend beyond the scope of malaria.
format Online
Article
Text
id pubmed-5656182
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BMJ Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-56561822017-10-27 Systematic review of the clinical manifestations of glucose-6-phosphate dehydrogenase deficiency in the Greater Mekong Subregion: implications for malaria elimination and beyond Ong, Ken Ing Cherng Kosugi, Hodaka Thoeun, Sophea Araki, Hitomi Thandar, Moe Moe Iwagami, Moritoshi Hongvanthong, Bouasy Brey, Paul T Kano, Shigeyuki Jimba, Masamine BMJ Glob Health Research INTRODUCTION: To achieve malaria elimination in the Greater Mekong Subregion (GMS) by 2030, proper case management is necessary. 8-aminoquinolines, such as primaquine, are the only available medicines effective in preventing relapse of the hypnozoite stage of Plasmodium vivax, as well as the onward transmission of Plasmodium falciparum. However, primaquine can cause haemolysis in individuals who have glucose-6-phosphate dehydrogenase deficiency (G6PDd). We conducted a systematic review on the reported clinical manifestations of G6PDd to provide a comprehensive overview of the situation in the GMS. METHODS: The protocol for this systematic review was registered on PROSPERO: International prospective register of systematic reviews (CRD42016043146). We searched the PubMed/MEDLINE, CINAHL, and Web of Science databases for published articles describing the clinical manifestations of G6PDd in the GMS. We included articles of all study designs from inception until 31 July 2016, reporting the clinical manifestations of G6PDd. We then performed a narrative synthesis of these articles. RESULTS: We included 56 articles in this review, 45 of which were from Thailand. Haemolysis in G6PD-deficient individuals was caused not only by primaquine but also by other medicines and infections. Other clinical manifestations of G6PDd that were found were favism, neonatal jaundice and chronic non-spherocytic haemolytic anaemia. G6PDd also influenced the clinical presentations of genetic disorders and infections, such as thalassemia and typhoid fever. CONCLUSION: As G6PDd also affects the clinical presentations of other infections, the benefits of G6PD testing and proper record keeping transcend those of malaria case management. Therefore, healthcare workers at the community level should be made familiar with complications resulting from G6PDd as these complications extend beyond the scope of malaria. BMJ Publishing Group 2017-08-19 /pmc/articles/PMC5656182/ /pubmed/29082022 http://dx.doi.org/10.1136/bmjgh-2017-000415 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/
spellingShingle Research
Ong, Ken Ing Cherng
Kosugi, Hodaka
Thoeun, Sophea
Araki, Hitomi
Thandar, Moe Moe
Iwagami, Moritoshi
Hongvanthong, Bouasy
Brey, Paul T
Kano, Shigeyuki
Jimba, Masamine
Systematic review of the clinical manifestations of glucose-6-phosphate dehydrogenase deficiency in the Greater Mekong Subregion: implications for malaria elimination and beyond
title Systematic review of the clinical manifestations of glucose-6-phosphate dehydrogenase deficiency in the Greater Mekong Subregion: implications for malaria elimination and beyond
title_full Systematic review of the clinical manifestations of glucose-6-phosphate dehydrogenase deficiency in the Greater Mekong Subregion: implications for malaria elimination and beyond
title_fullStr Systematic review of the clinical manifestations of glucose-6-phosphate dehydrogenase deficiency in the Greater Mekong Subregion: implications for malaria elimination and beyond
title_full_unstemmed Systematic review of the clinical manifestations of glucose-6-phosphate dehydrogenase deficiency in the Greater Mekong Subregion: implications for malaria elimination and beyond
title_short Systematic review of the clinical manifestations of glucose-6-phosphate dehydrogenase deficiency in the Greater Mekong Subregion: implications for malaria elimination and beyond
title_sort systematic review of the clinical manifestations of glucose-6-phosphate dehydrogenase deficiency in the greater mekong subregion: implications for malaria elimination and beyond
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5656182/
https://www.ncbi.nlm.nih.gov/pubmed/29082022
http://dx.doi.org/10.1136/bmjgh-2017-000415
work_keys_str_mv AT ongkeningcherng systematicreviewoftheclinicalmanifestationsofglucose6phosphatedehydrogenasedeficiencyinthegreatermekongsubregionimplicationsformalariaeliminationandbeyond
AT kosugihodaka systematicreviewoftheclinicalmanifestationsofglucose6phosphatedehydrogenasedeficiencyinthegreatermekongsubregionimplicationsformalariaeliminationandbeyond
AT thoeunsophea systematicreviewoftheclinicalmanifestationsofglucose6phosphatedehydrogenasedeficiencyinthegreatermekongsubregionimplicationsformalariaeliminationandbeyond
AT arakihitomi systematicreviewoftheclinicalmanifestationsofglucose6phosphatedehydrogenasedeficiencyinthegreatermekongsubregionimplicationsformalariaeliminationandbeyond
AT thandarmoemoe systematicreviewoftheclinicalmanifestationsofglucose6phosphatedehydrogenasedeficiencyinthegreatermekongsubregionimplicationsformalariaeliminationandbeyond
AT iwagamimoritoshi systematicreviewoftheclinicalmanifestationsofglucose6phosphatedehydrogenasedeficiencyinthegreatermekongsubregionimplicationsformalariaeliminationandbeyond
AT hongvanthongbouasy systematicreviewoftheclinicalmanifestationsofglucose6phosphatedehydrogenasedeficiencyinthegreatermekongsubregionimplicationsformalariaeliminationandbeyond
AT breypault systematicreviewoftheclinicalmanifestationsofglucose6phosphatedehydrogenasedeficiencyinthegreatermekongsubregionimplicationsformalariaeliminationandbeyond
AT kanoshigeyuki systematicreviewoftheclinicalmanifestationsofglucose6phosphatedehydrogenasedeficiencyinthegreatermekongsubregionimplicationsformalariaeliminationandbeyond
AT jimbamasamine systematicreviewoftheclinicalmanifestationsofglucose6phosphatedehydrogenasedeficiencyinthegreatermekongsubregionimplicationsformalariaeliminationandbeyond