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Modelling to inform prophylaxis regimens to prevent human rabies
BACKGROUND: The Strategic Advisory Group of Experts (SAGE) Working Group on rabies vaccines and immunoglobulins was established in 2016 to develop practical and feasible recommendations for prevention of human rabies. To support the SAGE agenda we developed models to compare the relative costs and p...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7612382/ https://www.ncbi.nlm.nih.gov/pubmed/30528846 http://dx.doi.org/10.1016/j.vaccine.2018.11.010 |
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author | Hampson, Katie Abela-Ridder, Bernadette Bharti, Omesh Knopf, Lea Léchenne, Monique Mindekem, Rolande Tarantola, Arnaud Zinsstag, Jakob Trotter, Caroline |
author_facet | Hampson, Katie Abela-Ridder, Bernadette Bharti, Omesh Knopf, Lea Léchenne, Monique Mindekem, Rolande Tarantola, Arnaud Zinsstag, Jakob Trotter, Caroline |
author_sort | Hampson, Katie |
collection | PubMed |
description | BACKGROUND: The Strategic Advisory Group of Experts (SAGE) Working Group on rabies vaccines and immunoglobulins was established in 2016 to develop practical and feasible recommendations for prevention of human rabies. To support the SAGE agenda we developed models to compare the relative costs and potential benefits of rabies prevention strategies. METHODS: We examined Post-Exposure Prophylaxis (PEP) regimens, protocols for administration of Rabies Immunoglobulin (RIG) and inclusion of rabies Pre-Exposure Prophylaxis (PrEP) within the Expanded Programme on Immunization (EPI). For different PEP regimens, clinic throughputs and consumables for vaccine administration, we evaluated the cost per patient treated, costs to patients and potential to treat more patients given limited vaccine availability. RESULTS: We found that intradermal (ID) vaccination reduces the volume of vaccine used in all settings, is less costly and has potential to mitigate vaccine shortages. Specifically, the abridged 1-week 2-site ID regimen was the most cost-effective PEP regimen, even in settings with low numbers of bite patients presenting to clinics. We found advantages of administering RIG to the wound(s) only, using considerably less product than when the remaining dose is injected intramuscularly distant to the wound(s). We found that PrEP as part of the EPI programme would be substantially more expensive than use of PEP and dog vaccination in prevention of human rabies. CONCLUSIONS: These modeling insights inform WHO recommendations for use of human rabies vaccines and biologicals. Specifically, the 1-week 2-site ID regimen is recommended as it is less costly and treats many more patients when vaccine is in short supply. If available, RIG should be administered at the wound only. PrEP is highly unlikely to be an efficient use of resources and should therefore only be considered in extreme circumstances, where the incidence of rabies exposures is extremely high. |
format | Online Article Text |
id | pubmed-7612382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-76123822022-02-16 Modelling to inform prophylaxis regimens to prevent human rabies Hampson, Katie Abela-Ridder, Bernadette Bharti, Omesh Knopf, Lea Léchenne, Monique Mindekem, Rolande Tarantola, Arnaud Zinsstag, Jakob Trotter, Caroline Vaccine Article BACKGROUND: The Strategic Advisory Group of Experts (SAGE) Working Group on rabies vaccines and immunoglobulins was established in 2016 to develop practical and feasible recommendations for prevention of human rabies. To support the SAGE agenda we developed models to compare the relative costs and potential benefits of rabies prevention strategies. METHODS: We examined Post-Exposure Prophylaxis (PEP) regimens, protocols for administration of Rabies Immunoglobulin (RIG) and inclusion of rabies Pre-Exposure Prophylaxis (PrEP) within the Expanded Programme on Immunization (EPI). For different PEP regimens, clinic throughputs and consumables for vaccine administration, we evaluated the cost per patient treated, costs to patients and potential to treat more patients given limited vaccine availability. RESULTS: We found that intradermal (ID) vaccination reduces the volume of vaccine used in all settings, is less costly and has potential to mitigate vaccine shortages. Specifically, the abridged 1-week 2-site ID regimen was the most cost-effective PEP regimen, even in settings with low numbers of bite patients presenting to clinics. We found advantages of administering RIG to the wound(s) only, using considerably less product than when the remaining dose is injected intramuscularly distant to the wound(s). We found that PrEP as part of the EPI programme would be substantially more expensive than use of PEP and dog vaccination in prevention of human rabies. CONCLUSIONS: These modeling insights inform WHO recommendations for use of human rabies vaccines and biologicals. Specifically, the 1-week 2-site ID regimen is recommended as it is less costly and treats many more patients when vaccine is in short supply. If available, RIG should be administered at the wound only. PrEP is highly unlikely to be an efficient use of resources and should therefore only be considered in extreme circumstances, where the incidence of rabies exposures is extremely high. 2019-10-03 2018-12-07 /pmc/articles/PMC7612382/ /pubmed/30528846 http://dx.doi.org/10.1016/j.vaccine.2018.11.010 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hampson, Katie Abela-Ridder, Bernadette Bharti, Omesh Knopf, Lea Léchenne, Monique Mindekem, Rolande Tarantola, Arnaud Zinsstag, Jakob Trotter, Caroline Modelling to inform prophylaxis regimens to prevent human rabies |
title | Modelling to inform prophylaxis regimens to prevent human rabies |
title_full | Modelling to inform prophylaxis regimens to prevent human rabies |
title_fullStr | Modelling to inform prophylaxis regimens to prevent human rabies |
title_full_unstemmed | Modelling to inform prophylaxis regimens to prevent human rabies |
title_short | Modelling to inform prophylaxis regimens to prevent human rabies |
title_sort | modelling to inform prophylaxis regimens to prevent human rabies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7612382/ https://www.ncbi.nlm.nih.gov/pubmed/30528846 http://dx.doi.org/10.1016/j.vaccine.2018.11.010 |
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