Can we eradicate trachoma? A survey of stakeholders.


Journal

The British journal of ophthalmology
ISSN: 1468-2079
Titre abrégé: Br J Ophthalmol
Pays: England
ID NLM: 0421041

Informations de publication

Date de publication:
08 2021
Historique:
received: 03 01 2020
accepted: 27 07 2020
revised: 25 07 2020
pubmed: 29 8 2020
medline: 25 9 2021
entrez: 29 8 2020
Statut: ppublish

Résumé

Although tremendous progress towards the 2020 goal of global elimination of trachoma as a public health problem has been made, it will not be achieved. Future targets are now being considered. One option is changing the goal to We conducted a survey at the beginning of a trachoma eradication session at the 2019 Coalition for Operational Research on Neglected Tropical Diseases meeting in National Harbor, Maryland, USA. We asked respondents what the most important goal of azithromycin mass drug administration was for trachoma (control, elimination of infection or eradication) and if and when they believed trachoma eradication would occur. We then asked what the biggest obstacles were to global eradication. Fifty-six surveys were returned (95%). Most (91%) participants reported that the most important goal of azithromycin mass drug administration was control or elimination of infection, and 24% of participants reported that global eradication was not possible. Of the 76% who reported a year by which they believed trachoma could be eradicated, most fell between 2040 and 2050. Commonly cited barriers to global eradication included lack of surveillance tools to confirm eradication or monitor for infection recrudescence (32%) and lack of resources (23%). Development of alternative indicators for trachoma surveillance and continued investment in trachoma programmes, particularly focused support in the most heavily affected populations, might increase enthusiasm for the feasibility of eradication.

Sections du résumé

BACKGROUND/AIMS
Although tremendous progress towards the 2020 goal of global elimination of trachoma as a public health problem has been made, it will not be achieved. Future targets are now being considered. One option is changing the goal to
METHODS
We conducted a survey at the beginning of a trachoma eradication session at the 2019 Coalition for Operational Research on Neglected Tropical Diseases meeting in National Harbor, Maryland, USA. We asked respondents what the most important goal of azithromycin mass drug administration was for trachoma (control, elimination of infection or eradication) and if and when they believed trachoma eradication would occur. We then asked what the biggest obstacles were to global eradication.
RESULTS
Fifty-six surveys were returned (95%). Most (91%) participants reported that the most important goal of azithromycin mass drug administration was control or elimination of infection, and 24% of participants reported that global eradication was not possible. Of the 76% who reported a year by which they believed trachoma could be eradicated, most fell between 2040 and 2050. Commonly cited barriers to global eradication included lack of surveillance tools to confirm eradication or monitor for infection recrudescence (32%) and lack of resources (23%).
CONCLUSIONS
Development of alternative indicators for trachoma surveillance and continued investment in trachoma programmes, particularly focused support in the most heavily affected populations, might increase enthusiasm for the feasibility of eradication.

Identifiants

pubmed: 32855161
pii: bjophthalmol-2020-315815
doi: 10.1136/bjophthalmol-2020-315815
pmc: PMC8311100
mid: EMS106913
doi:

Substances chimiques

Anti-Bacterial Agents 0
Azithromycin 83905-01-5

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1059-1062

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Informations de copyright

© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Catherine E Oldenburg (CE)

Department of Ophthalmology, University of California, San Francisco, California, USA catherine.oldenburg@ucsf.edu.
Department of Epidemiology and Biostatistics, University of California, San Francisco, California, USA.

Solomon Aragie (S)

The Carter Center, Addis Ababa, Ethiopia.

Abdou Amza (A)

Faculté Des Sciences De La Santé, Université Abdou Moumouni De Niamey, Niamey, Niger.
Programme National De Santé Oculaire, Niamey, Niger.

Anthony W Solomon (AW)

Department of Control of Neglected Tropical Diseases, World Health Organization, Geneva, Switzerland.

Jessica Brogdon (J)

F.I. Proctor Foundation, University of California, San Francisco, California, USA.

Benjamin F Arnold (BF)

Department of Ophthalmology, University of California, San Francisco, California, USA.
F.I. Proctor Foundation, University of California, San Francisco, California, USA.

Jeremy D Keenan (JD)

Department of Ophthalmology, University of California, San Francisco, California, USA.
Department of Epidemiology and Biostatistics, University of California, San Francisco, California, USA.
F.I. Proctor Foundation, University of California, San Francisco, California, USA.

Thomas M Lietman (TM)

Department of Ophthalmology, University of California, San Francisco, California, USA.
Department of Epidemiology and Biostatistics, University of California, San Francisco, California, USA.
F.I. Proctor Foundation, University of California, San Francisco, California, USA.

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Classifications MeSH