Combining different diagnostic studies of lymphatic filariasis for risk mapping in Papua New Guinea: a predictive model from microfilaraemia and antigenaemia prevalence surveys

Abstract Background The Global Programme to Eliminate Lymphatic Filariasis has encouraged countries to follow a set of guidelines to help them assess the need for mass drug administration and evaluate its progress. Papua New Guinea (PNG) is one of the highest priority countries in the Western Pacifi...

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Main Authors: Alvaro Berg Soto, Zhijing Xu, Peter Wood, Nelly Sanuku, Leanne J. Robinson, Christopher L. King, Daniel Tisch, Melinda Susapu, Patricia M. Graves
Format: Article
Language:English
Published: BMC 2018-12-01
Series:Tropical Medicine and Health
Subjects:
Online Access:http://link.springer.com/article/10.1186/s41182-018-0123-8
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author Alvaro Berg Soto
Zhijing Xu
Peter Wood
Nelly Sanuku
Leanne J. Robinson
Christopher L. King
Daniel Tisch
Melinda Susapu
Patricia M. Graves
author_facet Alvaro Berg Soto
Zhijing Xu
Peter Wood
Nelly Sanuku
Leanne J. Robinson
Christopher L. King
Daniel Tisch
Melinda Susapu
Patricia M. Graves
author_sort Alvaro Berg Soto
collection DOAJ
description Abstract Background The Global Programme to Eliminate Lymphatic Filariasis has encouraged countries to follow a set of guidelines to help them assess the need for mass drug administration and evaluate its progress. Papua New Guinea (PNG) is one of the highest priority countries in the Western Pacific for lymphatic filariasis and the site of extensive research on lymphatic filariasis and surveys of its prevalence. However, different diagnostic tests have been used and thresholds for each test are unclear. Methods We reviewed the prevalence of lymphatic filariasis reported in 295 surveys conducted in PNG between 1990 and 2014, of which 65 used more than one test. Results from different diagnostics were standardised using a set of criteria that included a model to predict antigen prevalence from microfilariae prevalence. We mapped the point location of each of these surveys and categorised their standardised prevalence estimates. Results Several predictive models were produced and investigated, including the effect of any mass drug administration and number of rounds prior to the surveys. One model was chosen based on goodness of fit parameters and used to predict antigen prevalence for surveys that tested only for microfilariae. Standardised prevalence values show that 72% of all surveys reported a prevalence above 0.05. High prevalence was situated on the coastal north, south and island regions, while the central highland area of Papua New Guinea shows low levels of prevalence. Conclusions Our study is the first to provide an explicit predictive relationship between the prevalence values based on empirical results from antigen and microfilaria tests, taking into account the occurrence of mass drug administration. This is a crucial step to combine studies to develop risk maps of lymphatic filariasis for programme planning and evaluation, as shown in the case of Papua New Guinea.
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spelling doaj.art-5c140a2152804d748d6933b6abe4b7042022-12-22T02:45:57ZengBMCTropical Medicine and Health1349-41472018-12-0146111110.1186/s41182-018-0123-8Combining different diagnostic studies of lymphatic filariasis for risk mapping in Papua New Guinea: a predictive model from microfilaraemia and antigenaemia prevalence surveysAlvaro Berg Soto0Zhijing Xu1Peter Wood2Nelly Sanuku3Leanne J. Robinson4Christopher L. King5Daniel Tisch6Melinda Susapu7Patricia M. Graves8Information Resources, James Cook UniversityResearch School of Population Health, Australian National UniversityCollege of Public Health, Medical and Veterinary Sciences, James Cook UniversityVector Borne Diseases Unit, PNG Institute of Medical ResearchVector Borne Diseases Unit, PNG Institute of Medical ResearchSchool of Medicine and Veterans Affairs Administration, Case Western Reserve UniversityDepartment of Population and Quantitative Health Science, Case Western Reserve UniversityMalaria and Vector Borne Diseases, Public Health, Department of HealthCollege of Public Health, Medical and Veterinary Sciences, James Cook UniversityAbstract Background The Global Programme to Eliminate Lymphatic Filariasis has encouraged countries to follow a set of guidelines to help them assess the need for mass drug administration and evaluate its progress. Papua New Guinea (PNG) is one of the highest priority countries in the Western Pacific for lymphatic filariasis and the site of extensive research on lymphatic filariasis and surveys of its prevalence. However, different diagnostic tests have been used and thresholds for each test are unclear. Methods We reviewed the prevalence of lymphatic filariasis reported in 295 surveys conducted in PNG between 1990 and 2014, of which 65 used more than one test. Results from different diagnostics were standardised using a set of criteria that included a model to predict antigen prevalence from microfilariae prevalence. We mapped the point location of each of these surveys and categorised their standardised prevalence estimates. Results Several predictive models were produced and investigated, including the effect of any mass drug administration and number of rounds prior to the surveys. One model was chosen based on goodness of fit parameters and used to predict antigen prevalence for surveys that tested only for microfilariae. Standardised prevalence values show that 72% of all surveys reported a prevalence above 0.05. High prevalence was situated on the coastal north, south and island regions, while the central highland area of Papua New Guinea shows low levels of prevalence. Conclusions Our study is the first to provide an explicit predictive relationship between the prevalence values based on empirical results from antigen and microfilaria tests, taking into account the occurrence of mass drug administration. This is a crucial step to combine studies to develop risk maps of lymphatic filariasis for programme planning and evaluation, as shown in the case of Papua New Guinea.http://link.springer.com/article/10.1186/s41182-018-0123-8Lymphatic filariasisPapua New GuineaPrevalencePredictive modelDiagnostic testsRisk map
spellingShingle Alvaro Berg Soto
Zhijing Xu
Peter Wood
Nelly Sanuku
Leanne J. Robinson
Christopher L. King
Daniel Tisch
Melinda Susapu
Patricia M. Graves
Combining different diagnostic studies of lymphatic filariasis for risk mapping in Papua New Guinea: a predictive model from microfilaraemia and antigenaemia prevalence surveys
Tropical Medicine and Health
Lymphatic filariasis
Papua New Guinea
Prevalence
Predictive model
Diagnostic tests
Risk map
title Combining different diagnostic studies of lymphatic filariasis for risk mapping in Papua New Guinea: a predictive model from microfilaraemia and antigenaemia prevalence surveys
title_full Combining different diagnostic studies of lymphatic filariasis for risk mapping in Papua New Guinea: a predictive model from microfilaraemia and antigenaemia prevalence surveys
title_fullStr Combining different diagnostic studies of lymphatic filariasis for risk mapping in Papua New Guinea: a predictive model from microfilaraemia and antigenaemia prevalence surveys
title_full_unstemmed Combining different diagnostic studies of lymphatic filariasis for risk mapping in Papua New Guinea: a predictive model from microfilaraemia and antigenaemia prevalence surveys
title_short Combining different diagnostic studies of lymphatic filariasis for risk mapping in Papua New Guinea: a predictive model from microfilaraemia and antigenaemia prevalence surveys
title_sort combining different diagnostic studies of lymphatic filariasis for risk mapping in papua new guinea a predictive model from microfilaraemia and antigenaemia prevalence surveys
topic Lymphatic filariasis
Papua New Guinea
Prevalence
Predictive model
Diagnostic tests
Risk map
url http://link.springer.com/article/10.1186/s41182-018-0123-8
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