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Dengue Seroepidemiology in India.

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Title: Dengue Seroepidemiology in India.


1
Dengue Seroepidemiology in India.
Rohit Arora, Sanofi Pasteur
2
Dengue in the Past Quarter
  • This map may be used as a guide for the
    assessment of dengue risk throughout the world.
    The blue regions represent areas of ongoing
    transmission risk as defined by the Centers for
    Disease Control and Prevention (CDC) based on
    data from Ministries of Health, international
    health organizations, journals, and knowledgeable
    experts (last updated in 2010 for the 2012 CDC
    Yellow Book). Recent reports (e.g., official,
    newspaper, other media) of local and regional
    dengue or imported cases of dengue collected by
    HealthMap are shown as red markers linked to the
    respective reports.

http//www.healthmap.org/dengue/index.php .
Accessed on 22/1/2012
3
Dengue Seroepidemiology in India
Decade wise circulation of various serotypes of
Dengue in published literature
All 4 serotypes of Dengue have been known to
circulate in the country since many decades.
Chakravarti A,, Arora R, Luxemberger S. Fifty
years of dengue in India. Transactions of the
Royal Society of Tropical Medicine (Under Review)
4
Active surveillance estimates of under reporting
in SEA countries
5
Under-reporting Large Scale, Multi-year School
based Active surveillance for Dengue in Southern
Vietnam

6
Surveillance estimates of under reporting of
Dengue in India
  • Although Dengue is a notifiable disease, but
    there is still a significant factor of
    under-reporting.
  • It is often difficult to estimate the true factor
    of under-reporting which may hugely vary due to
    differential access to healthcare infrastructure.
  • This is compounded further by the non-regulated
    private healthcare setup where a substantial
    number of cases go unreported.

Transactions of the Royal Society of Tropical
Medicine and Hygiene (2008) 102, 570577
7
Community-based dengue surveillance in India
(DNG09)
  • Principal Objectives
  • To estimate the population-based incidence of
    symptomatic laboratory-confirmed dengue
    infections in the catchment population of
    selected cohorts across India (associated with
    community centers)
  • Study design
  • Prospective epidemiological study.
  • Sample size
  • During the determined period of data collection,
    all patients presenting to the study sites and
    fulfilling the inclusion criteria described below
    will be enrolled.
  • Dengue Confirmation
  • Detection of dengue viral RNA by
    reverse-transcriptase polymerase chain reaction
    (RT-PCR) will be performed in acute blood sample.
  • Serology by (ELISA) for IgG and IgM dengue
    antibody.

8
The Challenges.
  • Significant lack of population-based estimates of
    incidence of laboratory confirmed dengue
    infection.
  • Even areas with confirmed dengue reports and high
    risk levels based on socio-demographic factors
    have no documented data.
  • A retrospective investigation of morbidity data
    in GIS mapped outbreak area revealed that dengue
    was never diagnosed in any of the health centres.
  • Given this lack of previous accurate
    documentation of dengue, a seroprevalence study
    was planned
  • to assess the prevalence of dengue-specific
    antibodies which will allow assessing if there
    has been dengue transmission in the community in
    recent years.

2007
9
Prospective dengue seroprevalence study in 5 to
10 year-old children in India.
  • Most frequent diagnosis in these centres has been
    of
  • Acute Respiratory Infection (ARI), and except the
    respiratory signs, the other ARI symptoms (e.g.
    fever, muscle aches, headache) are compatible
    with a possible diagnosis of dengue.
  • A seroprevalence study was proposed, in a sample
    of children registered in the health centres
  • to assess the prevalence of dengue-specific
    antibodies which will allow assessing if there
    has been dengue transmission in the community in
    recent years (5 years).
  • Seroprevalence in children age between the age of
    5 to10 shall be able to provide insight into
    approximate average annual incidence of new
    dengue infection over the last 5-10 years.
  • It was thought to additionally analyze
    JE-specific antibodies in this population
  • To determine exposure of the Japanese
    Encephalitis Virus (Flavivirus) in this
    non-endemic area with close migratory connections
    with endemic zones (eastern UP)

10
Prospective dengue seroprevalence study in 5 to
10 year-old children in India.
  • Primary Objective
  • To determine the prevalence of specific
    antibodies (IgG) against dengue in healthy 5 to
    10 year old children in India through IgG testing
    using the commercially available kit "EL1500G"
    from Focus Diagnostics (California, US)
  • Secondary Objective(s)
  • To determine the dengue virus serotype
    (DENV-1,2,3 and/or 4) specific to the antibodies
    in positive (IgG) samples through PRNT50
  • To estimate the prevalence of specific antibodies
    (IgG) against Japanese encephalitis in healthy 5
    to 10 year-old children in India through JE IgG
    antibodies testing though Indirect ELISA using
    commercial available kits (InBios, USA)

11
Prospective dengue seroprevalence study in 5 to
10 year-old children in India.
  • Source and study population
  • Children, 5 to 10 years of age, in India.
  • Initially 2 study sites in Delhi. Is being
    progressively be expanded to 10 sites across
    India
  • For the two study site in Delhi, the population
    is being drawn from children registered in health
    centres invited to participate during household
    visits performed by social workers of the health
    centres.
  • Delhi Gate (Centre 001)
  • Balmiki Basti (Centre 002)
  • Dengue and JE antibodies testing is being
    conducted in Department of Microbiology at
    Maulana Azad Medical College, Delhi (Dr. Anita
    Chakravarti)

12
Prospective dengue seroprevalence study in 5 to
10 year-old children in India.
  • Sample size and power calculation
  • This study is descriptive and therefore no
    hypothesis is being tested. The sample has been
    arbitrarily set at 323 subjects in each site.
  • Assuming a prevalence rate of 30, a sample of
    323 subjects will ensure a precision of 5 for
    the 2-sided 95 confidence interval around the
    seroprevalence point estimate.

13
THANKS
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