Chikungunya primary prevention: Difference between revisions
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| style="padding: 5px 5px; background: #F5F5F5;" | 1−2 | | style="padding: 5px 5px; background: #F5F5F5;" | 1−2 | ||
| style="padding: 5px 5px; background: #F5F5F5;" |1−2 | | style="padding: 5px 5px; background: #F5F5F5;" | 1−2 | ||
| style="padding: 5px 5px; background: #F5F5F5;" | II | | style="padding: 5px 5px; background: #F5F5F5;" | II | ||
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|+'''WHO recommended insecticides for use as indoor residual sprays''' | |||
! style="background: #4479BA; width: 300px;" | {{fontcolor|#FFF|Insecticide compounds and formulations}} | |||
! style="background: #4479BA; width: 150px;" | {{fontcolor|#FFF|Class group}} | |||
! style="background: #4479BA; width: 150px;" | {{fontcolor|#FFF|Dosage (g a.i./m<sup>2</sup>)}} | |||
! style="background: #4479BA; width: 150px;" | {{fontcolor|#FFF|Mode of action}} | |||
! style="background: #4479BA; width: 150px;" | {{fontcolor|#FFF|Duration of effective action (months)}} | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" | DDT WP | |||
| style="padding: 5px 5px; background: #F5F5F5;" | OC | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 1−2 | |||
| style="padding: 5px 5px; background: #F5F5F5;" | contact | |||
| style="padding: 5px 5px; background: #F5F5F5;" | >6 | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" | Malathion WP | |||
| style="padding: 5px 5px; background: #F5F5F5;" | OP | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 2 | |||
| style="padding: 5px 5px; background: #F5F5F5;" | contact | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 2-3 | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" | Fenitrothion WP | |||
| style="padding: 5px 5px; background: #F5F5F5;" | OP | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 2 | |||
| style="padding: 5px 5px; background: #F5F5F5;" | contact & airborne | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 3-6 | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" | Pirimiphos-methyl WP & EC | |||
| style="padding: 5px 5px; background: #F5F5F5;" | OP | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 1−2 | |||
| style="padding: 5px 5px; background: #F5F5F5;" | contact & airborne | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 2-3 | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" | Bendiocarb WP | |||
| style="padding: 5px 5px; background: #F5F5F5;" | C | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 0.1−0.4 | |||
| style="padding: 5px 5px; background: #F5F5F5;" | contact & airborne | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 2-6 | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" | Propoxur WP | |||
| style="padding: 5px 5px; background: #F5F5F5;" | C | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 1−2 | |||
| style="padding: 5px 5px; background: #F5F5F5;" | contact & airborne | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 3-6 | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" | Alpha-cupermethrin WP & SC | |||
| style="padding: 5px 5px; background: #F5F5F5;" | PY | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 0.02−0.03 | |||
| style="padding: 5px 5px; background: #F5F5F5;" | contact | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 4-6 | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" | Bifenthrin WP | |||
| style="padding: 5px 5px; background: #F5F5F5;" | PY | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 0.025−0.05 | |||
| style="padding: 5px 5px; background: #F5F5F5;" | contact | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 3-6 | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" | Cyfluthrin WP | |||
| style="padding: 5px 5px; background: #F5F5F5;" | PY | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 0.02−0.05 | |||
| style="padding: 5px 5px; background: #F5F5F5;" | contact | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 3-6 | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" | Deltamethrin WP, WG | |||
| style="padding: 5px 5px; background: #F5F5F5;" | PY | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 0.02−0.025 | |||
| style="padding: 5px 5px; background: #F5F5F5;" | contact | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 3-6 | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" | Etofenprox WP | |||
| style="padding: 5px 5px; background: #F5F5F5;" | PY | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 0.1−0.3 | |||
| style="padding: 5px 5px; background: #F5F5F5;" | contact | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 3-6 | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;" | Lambda-cyhalothrin WP, CS | |||
| style="padding: 5px 5px; background: #F5F5F5;" | PY | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 0.02−0.03 | |||
| style="padding: 5px 5px; background: #F5F5F5;" | contact | |||
| style="padding: 5px 5px; background: #F5F5F5;" | 3-6 | |||
|- | |||
| style="padding: 5px 5px; background: #FFF;" colspan="4"|CS = capsule suspension; EC = emulsifiable concentrate; SC = suspension concentrate; WG = water dispersible granule; WP = wettable; OC = Organochlorines; OP = Organophosphates; C = Carbamates; PY = Pyrethroids | |||
|- | |||
| style="padding: 5px 5px; background: #FFF;" colspan="4"| <SMALL>Table adapted from ''Preparedness and Response for Chikungunya Virus: Introduction in the Americas. PAHO © 2011.''<ref name=PAHO2011>{{cite book | last = | first = | title = Preparedness and response for Chikungunya virus introduction in the Americas | publisher = Pan American Health Organization CDC, Center for Disease Control and Prevention | location = Washington, DC | year = 2011 | isbn = 978-92-75-11632-6 }}</ref></SMALL> | |||
|- | |||
|} | |||
==Response to Chikungunya Virus Infection Introduction <SMALL><SMALL><SMALL><SMALL><SMALL>Adapted from ''Preparedness and Response for Chikungunya Virus: Introduction in the Americas. PAHO © 2011.''<ref name=PAHO2011>{{cite book | last = | first = | title = Preparedness and response for Chikungunya virus introduction in the Americas | publisher = Pan American Health Organization CDC, Center for Disease Control and Prevention | location = Washington, DC | year = 2011 | isbn = 978-92-75-11632-6 }}</ref></SMALL></SMALL></SMALL></SMALL></SMALL>== | ==Response to Chikungunya Virus Infection Introduction <SMALL><SMALL><SMALL><SMALL><SMALL>Adapted from ''Preparedness and Response for Chikungunya Virus: Introduction in the Americas. PAHO © 2011.''<ref name=PAHO2011>{{cite book | last = | first = | title = Preparedness and response for Chikungunya virus introduction in the Americas | publisher = Pan American Health Organization CDC, Center for Disease Control and Prevention | location = Washington, DC | year = 2011 | isbn = 978-92-75-11632-6 }}</ref></SMALL></SMALL></SMALL></SMALL></SMALL>== |
Revision as of 21:48, 16 June 2014
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Alejandro Lemor, M.D. [2]; Alonso Alvarado, M.D. [3]; Vendhan Ramanujam M.B.B.S [4]
Overview
In the absence of an effective vaccine to prevent chikungunya virus infection, the only available tool to prevent the infection is by reducing the human-vector contact.
Integrated Vector Management Program Adapted from Preparedness and Response for Chikungunya Virus: Introduction in the Americas. PAHO © 2011.[1]
The primary vectors of chikungunya virus infection are Aedes aegypti or Aedes albopictus. Therefore, vector control planning efforts should focus on suppression of both the mosquito populations in order to prevent the likelihood of chikungunya virus infection establishment and to lay the foundation for emergency interventions in the event of an outbreak. Since the biology and control procedures for Aedes aegypti are similar to those for Aedes albopictus, surveillance and control recommendations developed for dengue management as a component of the Integrated Management Strategy for Dengue Prevention and Control (IMS-Dengue) may be utilized and intensified in order to respond to a chikungunya virus infection introduction. Successful Integrated Vector Management (IVM) for chikungunya virus infection requires trained experts in medical entomology and vector control, sufficient resources, and a sustained commitment.
Vector Surveillance and Identification of High Risk Areas
- Given the similarity in transmission cycles of both Dengue and Chikungunya viruses, in areas where dengue is endemic, a retrospective analysis of Dengue virus transmission during previous years should be conducted during the chikungunya virus infection planning phase to indicate the areas where chikungunya virus infection is expected to circulate.
- Depending on the risk of transmission, stratification is done and it is used to assign resources and priorities.
- Surveillance methods for Aedes aegypti and Aedes albopictus are varied and include methods to monitor egg production, larval sites, pupal abundance, and adult abundance.
- It must also be able to detect and identify hidden and difficult to control larval sites (e.g., cryptic locations such as septic tanks, storm drains, sump pumps, and vacant lots) and other productive sites, as well as the readily identified and commonly found larval habitats.
Personal Protection
- The likelihood of the infection can be reduced by the use of personal repellents on skin or clothing. DEET (N,N-diethyl-m-toluamide) and picaridin (also known as KBR3023 or Bayrepel™) are effective repellents widely available in the America.
- Infants and others sleeping or resting during the day should use bednets to avoid infection. It is of particular importance that individuals who are potentially infected with Chikungunya virus during an outbreak rest beneath an IT bednet to avoid mosquito bites and further spread of infection.
- Use of IT bednets has an additional benefit of killing mosquitoes that come into contact with the net, which may reduce vector-human contact for other household members.
- A number of pesticide products may be used to safely treat bednets, or long-lasting pretreated nets can be obtained commercially.
Insecticide | Formulation | Dosage (milligrams of active ingredient per square meter of netting) |
---|---|---|
Alpha-cypermethrin | SC 10% | 20−40 |
Cyfluthrin | EW 5% | 50 |
Deltamethrin | SC 1%; WT 25%; and WT 25% + Binderd (K-O TAB 1-2-3) | 15−25 |
Etofenprox | EW 10% | 200 |
Lambda-cyhalothrin | CS 2.5% | 10−15 |
Permethrin | EC 10% | 200−500 |
EC = emulsifiable concentrate; EW = emulsion, oil in water; CS = capsule suspension; SC = suspension concentrate; WT = water dispersible tablet | ||
Table adapted from Preparedness and Response for Chikungunya Virus: Introduction in the Americas. PAHO © 2011.[1] |
Product name | Product type |
---|---|
ICON® MAXX | Lambda-cyhalothrin 10% CS + Binder (Target dose of 50 mg/m2) |
CS = capsule suspension | |
Table adapted from Preparedness and Response for Chikungunya Virus: Introduction in the Americas. PAHO © 2011.[1] |
Household Prevention
- The use of intact screens on windows and doors will reduce entry of vectors into the home.
- Mosquito proofing water storage vessels will reduce oviposition sites and local production.
- Within a household, use of IT bednets72 and IT curtains73 also reduce vector-human contact.
- The number of adult mosquitoes in a home may be reduced by using commercially available pyrethroid-based aerosol sprays and other products designed for the home, such as mosquito coils and electronic mat vaporizers. Aerosol sprays may be applied throughout the home, but areas where adult mosquitoes rest (dark, cooler areas) must be targeted, including bedrooms, closets, clothing hampers, etc. Care should be taken to emphasize proper use of these products when advocating their application to the public, in order to reduce unnecessary exposure to pesticides.
Neighborhood and Community Prevention
- Neighborhood and community prevention for a Chikungunya virus introduction in the Americas should be based on methods developed for dengue control that will reduce the probability that a viremic human arriving in the Americas will be fed upon by Aedes aegypti or Aedes albopictus mosquitoes, thereby leading to secondary transmission and potential establishment of the virus.
- Dengue programs for controlling Aedes aegypti have traditionally focused on control of immature mosquitoes, often through the community’s involvement in environmental management and source reduction thereby stressing on the importance of incorporating community involvement into an IVM program.
Vector Control Procedures
There are a number of vector control procedures that should be consulted when establishing or improving existing programs, which are considered to mitigate the risk of virus expansion.
Environmental Management
- Reduce larval habitats
- Manage (wash/cover) containers
- Discard/recycle containers
- Reduce human-vector contact
- Install window screens
Larval Control
- Source reduction
- Biological control
- Chemical control
Insecticide | Formulation | Dosage (mg/L of active ingredient for control of container-breeding mosquitoes) | WHO hazard classification of active ingredient |
---|---|---|---|
Organophosphates | |||
Pirimiphos-methyl | EC | 1 | III |
Temephos | EC, GR | 1 | U |
Insect growth regulators | |||
Diflubenzuron | DT, GR, WP | 1 | U |
rs-methoprenee | EC | 1 | U |
Novaluron | EC | 0.01-0.05 | NA |
Pyriproxyfene | GR | 0.01 | U |
Biopesticides | |||
Bacillus thuringiensise israelenses | WG | 1-5 mg/L | U |
Spinosad | DT, GR, SC | 0.1-0.5 | U |
DT = tablet for direct application; GR = granule; EC = emulsifiable concentrate; WG = water-dispersible granule; WP = wettable power; SC = suspension concentrate | |||
Class II = moderately hazardous; Class III = slightly hazardous; Class U = Unlikely to pose an acute hazard in normal use; NA = not available | |||
Table adapted from Preparedness and Response for Chikungunya Virus: Introduction in the Americas. PAHO © 2011.[1] |
Adult Mosquito Control
- Use of IT bednets
- Use of IT curtains
- Lethal ovitraps
- Space sprays
- Indoor residual treatments
Insecticide | Chemical | Cold aerosols [Dosage of active ingredient (g/ha)] | Thermal fogs [Dosage of active ingredient (g/ha)] | WHO hazard classification of active ingredient |
---|---|---|---|---|
Fenitrothion | Organophosphate | 250−300 | 250−300 | II |
Malathion | Organophosphate | 112−600 | 500−600 | III |
Pirimiphos-methyl | Organophosphate | 230−330 | 180−200 | III |
Bioresmethrin | Pyrethroid | 5 | 10 | U |
Cyfluthrin | Pyrethroid | 1−2 | 1−2 | II |
Cypermethrin | Pyrethroid | 1−3 | − | II |
Cyphenothrin | Pyrethroid | 2−5 | 5−10 | II |
d,d-trans-Cyphenothrin | Pyrethroid | 1−2 | 2.5−5 | NA |
Deltamethrin | Pyrethroid | 0.5−1.0 | 0.5−1.0 | II |
D-Phenothrin | Pyrethroid | 5−20 | - | U |
Etofenprox | Pyrethroid | 10−20 | 10−20 | U |
λ Cyhalothrin | Pyrethroid | 1.0 | 1 | II |
Permethrin | Pyrethroid | 5 | 10 | II |
Resmethrin | Pyrethroid | 2-4 | 4 | III |
Class II = moderately hazardous; class III = slightly hazardous; class U = unlikely to pose an acute hazard in normal use; NA = not available | ||||
Table adapted from Preparedness and Response for Chikungunya Virus: Introduction in the Americas. PAHO © 2011.[1] |
Insecticide compounds and formulations | Class group | Dosage (g a.i./m2) | Mode of action | Duration of effective action (months) |
---|---|---|---|---|
DDT WP | OC | 1−2 | contact | >6 |
Malathion WP | OP | 2 | contact | 2-3 |
Fenitrothion WP | OP | 2 | contact & airborne | 3-6 |
Pirimiphos-methyl WP & EC | OP | 1−2 | contact & airborne | 2-3 |
Bendiocarb WP | C | 0.1−0.4 | contact & airborne | 2-6 |
Propoxur WP | C | 1−2 | contact & airborne | 3-6 |
Alpha-cupermethrin WP & SC | PY | 0.02−0.03 | contact | 4-6 |
Bifenthrin WP | PY | 0.025−0.05 | contact | 3-6 |
Cyfluthrin WP | PY | 0.02−0.05 | contact | 3-6 |
Deltamethrin WP, WG | PY | 0.02−0.025 | contact | 3-6 |
Etofenprox WP | PY | 0.1−0.3 | contact | 3-6 |
Lambda-cyhalothrin WP, CS | PY | 0.02−0.03 | contact | 3-6 |
CS = capsule suspension; EC = emulsifiable concentrate; SC = suspension concentrate; WG = water dispersible granule; WP = wettable; OC = Organochlorines; OP = Organophosphates; C = Carbamates; PY = Pyrethroids | ||||
Table adapted from Preparedness and Response for Chikungunya Virus: Introduction in the Americas. PAHO © 2011.[1] |
Response to Chikungunya Virus Infection Introduction Adapted from Preparedness and Response for Chikungunya Virus: Introduction in the Americas. PAHO © 2011.[1]
- Immediately upon confirmation of the first autochthonous Chikungunya virus case, the health department should inform the IVM program regarding the onset date and location of the case. Vector control procedures must be intensified to effectively reduce the abundance of infected vectors in order to halt transmission in the areas of the case(s).
- Simultaneously, emergency response committees at local and national levels should be informed of the situation and activated. Initial efforts should focus on containing virus transmission and preventing expansion. If virus containment fails, or if cases are not detected until the outbreak has spread over a large geographic area, intensive vector control efforts will need to be expanded to a larger scale program.
Risk and Outbreak Communication Adapted from Preparedness and Response for Chikungunya Virus: Introduction in the Americas. PAHO © 2011.[1]
- Communications are an integrated, coordinated effort involving all disciplines and components for preparation and response.
- Timely communication with stakeholders is crucial for enlisting the community’s participation and to avoid confusion and misinformation.
- As Chikungunya virus is novel in the Americas, the media, the public and many officials will need to be educated about the disease, the mode of transmission, the lack of specific therapeutic treatment, means of symptomatic and supportive treatment, and effective control measures.