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Dr Pravin Yerpude
Professor and Head
Dept of Community Medicine
Chhindwara Institute of Medical
Sciences,Chhindwara(M.P.)
 Dengue is caused by
a dengue virus
which are
arboviruses which is
carried by a
mosquito.
 The mosquito is
scientifically called
Aedes aegypti carry
the virus.
 Dengue infection have the potential of rapid
spread leading to an acute public health
problem.
 It is a notifiable disease
 Of all the arthropod –borne viral
diseases,dengue fever is the most common
 Dengue fever is one of the most important
emerging disease of the tropical and sub-
tropical regions affecting urban and
periurban areas
Areas infested with Aedes aegypti
Areas with Aedes aegypti and recent epidemic dengue
 World
 Each year 50 million infections occur
worldwide with 5,00,000 cases of DHF and at
least 12,000 deaths,mainly among children
 Increase of dengue and DHF is due to
uncontrolled population growth and
urbanization without appropriate water
management ,to the global spread of dengue
via travel and trade and to the erosion of
vector control programme
 Currently DFDHF is endemic in-
India, Bangladesh,Indonesia, Madives,
Myanmar, Srilanka, Thailand
 Category A: Indonesia, Myanmar, Thailand
-Major public health problem, Multiple
serotypes
-Increased hospitalization & child hood
mortality, -Rural environment affected
Category B: India, Bangladesh, Madives, Srilanka
-DHF emerging,
- Expanding geographically within the country
- Cyclic epidemic---- more frequent multiple
serotype
Category C: Bhutan, Nepal
-No reported cases with uncertain endemicity
Category D: DPR Korea -Non endemic
7
 India
 Dengue/DHF widely prevalent in India and all
4 serotypes are found
 It is reported from 18 states/UTS with about
450 million population at risk
 2006-12317 cases and 184 deaths
 2007-553 cases and 69 deaths
 2008-1256 cases and 80 deaths
 2009-1553 cases and 96 deaths
 2010-2829 cases and 110 deaths
AGENT
HOST
VECTOR
ENVIRONMENT
 Virus
 Vector
 Flavi RNA virus
 Types- 4 types
Den-1, Den- 2, Den- 3, Den- 4
( All are isolated in India)
 Type 2 is the Commonest
 Each type has different antigenic strain.
 There is no cross immunity
Infection with one serotype-long
lasting immunity to that subtype
Tiger Mosquito
•
Large, multi-striped,
Aerial, slender elongated body covered with scales
 Aedes Aegypti is ( Tiger ).
other types- A. albopictus,
A. polynesiensis,
A. Scutellaris
7- 10
days
Adult- 3 weeks
Egg may survive for many months
 Habitat ie 30°N to 40°S latitude of tropics –
subtropics.
 Hot – humid temp of 16° to 40° C so peri-
monsoon Aug-Nov .
 Flying range- 400 meters
 Usually bites during day time
 Resting habits- Endophily (indoor, dark
places)
Aedes mosquito- Sucking bloodAedes mosquito- Sucking blood
-feeds on many humans,
-Time of biting- daytime
INTRADOMESTIC CONTAINERS
KUNDI (tank)
KOTHIS
DESERT COOLER
22
Cisterns
Fountains Garden tanks
Mosquito Breeding Habitats
Contained Waters
Water-supply related mosquito larval habitats:
 Breeding- lays eggs at the bottom of clean
open domestic, Peridomestic containers
 Larvae stick to the inside walls; but have to
come up to surface to breathe.
 Not a disease of the poorest but of those
who use water tanks, flower pots, coolers,
AC.
 Children most vulnerable to get DHF as low
immunity and interaction with maternal
antibody in infants.
Host
•Children
•Office goers
Environment
•Tropics & subtropics
•Water collection in
artificial container
•16-40 C temp.-
humid climate
Agent- Flavivirus
27
Host
-School going Children
-Office goers
-Urban population
-Over crowding
-Poor sanitation
-All S-E classs
Environment
16- 40 d. C
Humidity
Peri monsoon
Agent
-Dengue virus
- Female Aedes mosquito
 Increased distribution & densities of vector
infestation,
 Unreliable water supply systems
 Increasing non-biodegradable containers and
poor solid waste disposal
 Increased air travel
 Increasing population density in urban areas-
unplanned & uncontrlled urbanization
 Deterioration of public health infrastructure &
surveillance system
1. Virus transmitted
to human in mosquito
saliva
2. Virus replicates
in target organs
3. Virus infects white
blood cells and
lymphatic tissues
4. Virus released and
circulates in blood
3
4
1
2
5. Second mosquito
ingests virus with
blood
6. Virus replicates
in mosquito midgut
and other organs,
infects salivary
glands
7. Virus replicates
in salivary glands
6
7
5
Viremia Viremia
Extrinsic
incubation
Period
(8-10 days)
DAYS
0 5 8 12 16 20 24 28
Human #1 Human #2
Illness
Mosquito feeds /
acquires virus
Mosquito refeeds
transmits virus
Intrinsic
incubation
period
(3-10 days)
Illness
 Incubation period
 5-6 days (3-10 days)
Both Man and Mosquito
Dengue Viral Infection
Asymptomatic Symptomatic
Dengue fever DHF
Undifferentiated No shock
DSS
Classical
Dengue fever
Without
H
,age
With
H’age
Plasma
leakage
 Undifferentiated fever
 Classic dengue fever (DF)
 Dengue hemorrhagic fever (DHF)
 Dengue shock syndrome (DSS)
87% of patients infected were either
asymptomatic or only mildly symptomatic
 High grade fever, Anorexia, Backache, Rash,
bone breaking severe Bodyache, Retrobulbar
pain,Hepatomegaly, Weakness, Depression.
 Dehydration, Abd colic, Constipation, severe
Conjunctivitis, Conjctival H’ge.
 Single phase or 2 peak saddle back (Biphasic
curve) fever- 39-400C, last for 7 days
Pt. is viremic at the time of fever--- Infective
to mosquito
 Rash may be diffuse,flushing,mottling or
fleeting pin-point eruptions on the face,neck
and chest during first half of febrile period
and a maculopapular rash on 3rd or 4th day
 It starts on the chest and trunk and may
spread to the extremities and rarely to the
face
 It may be accompanied by itching
 Inflate blood pressure cuff to a point midway
between systolic and diastolic pressure for 5
minutes
 Positive test:
20 or more petechiae per 1 inch2 (6.25
cm2)
or
20 or more petechiae per 3 cms. diameter
 Skin eruption- 80% of cases Reddish Measly
Face, Gets Redder at 5-6 Days.
 Nose Bleeds occ, Mild Thrombocytopenia &
Leukopenia.
 Tourniquet test may be +ve, BP cuff between
S/D pr. for 5 min.
Suspected C/O of DF
 Acute onset
 High grade fever <7 days duration
 Severe headache, backache
 Joint , post orbital & muscle pain
 With or without rash
Probable C/O of DF
 Suspected case
 High vector velocity
 Presence of confirmed cases in area
 Bd. –ve for Mp, No response to anti-
malarials
 Isolation of virus from the blood in early
phase
 IgM abs. in single serum samples or
 4 fold rise of Abs. in paired serum samples.
 Influenza
 Measles
 Rubella
 Malaria
 Typhoid fever
 Leptospirosis
 Meningococcemia
 Rickettsial infections
 Bacterial sepsis
 Other viral hemorrhagic fevers
56
 Isolation of Dengue virus from serum, plasma,
leucocytes or autopsy samples.
 Demonstration of a fourfold or greater rise in
reciprocal IgG antibody titres to one or more
dengue virus antigen in paired sera samples.
 Demonstaration of dengue virus antigen in
autopsy tissue by immunohistochemistry or
immunofluorescence or in serum samples by EIA
 Detection of viral genomic sequences in autopsy
tissue, serum or CSF sample by PCR (Polymerase
Chain Reaction)
 Most cases of early Classical DF can be
treated at OPD & DHF at small hospitals or
pvt H.
 Only Paracetamol as anti-pyretic.
 No Steroids, aspirin, NSAID, antiplatelet AB eg
cephalosporins, vanco.
 Lots of oral fluids in early illness eg ORS,
chhas, tea etc.
 Observe twice daily if pt. not well.
 DSS in ICU.
58
 Diagnosis of types of D is purely clinical.
 Serrology is no guide to management.
 Mx is the fluid- FLUID & FLUID.
 It is NOT the bleeding or H’ge mx.
If enough fluids are given early; Platelets
are NOT required even for
Thrombocytopenia.
 Blood will increase the viscosity in
Hemoconcentration; may ►thrombosis.
59
 Fluids
 Rest
 Antipyretics (avoid aspirin and non-
steroidal anti-inflammatory drugs)
 Monitor blood pressure, hematocrit,
platelet count, level of consciousness
60
 Continue monitoring after defervescence
 If any doubt, provide intravenous fluids,
guided by serial hematocrits, blood pressure,
and urine output
 The volume of fluid needed is similar to the
treatment of diarrhea with mild to moderate
isotonic dehydration (5%-8% deficit)
61
It is not a complication of dengue
fever but has separate etio-
pathognesis
Bitten dengue virus
Bitten dengue virus
Specific Antibodies to
Same type virus
Neutralizing antibody to Dengue 1 virus
Dengue 1 virus
Homologous Antibodies Form
Non-infectious Complexes
Non-neutralizing antibody
Complex formed by neutralizing antibody and virus
Bitten dengue virus
Specific Antibodies to
dengue virus
Bitten dengue virus
Other sub-type
Non-neutralizing antibody to Dengue 1
virus
Dengue 2 virus
Heterologous Antibodies Form
Infectious Complexes
Complex formed by non-neutralizing
antibody and virus
Bitten dengue virus
Specific Antibodies to
dengue virus
Bitten dengue virus
Other sub-type
Immune reaction
Ag-Ab complex
Bitten dengue virus
Specific. Antibodies to
dengue virus
Bitten dengue virus
Other sub-type
Immune reaction
Ag-Ab complex
Capillary leakage
DHF
 Antibody-Ag complex-can enter a greater
proportion of cells of the mononuclear
lineage, thus increasing virus production
 Infected monocytes release vasoactive
mediators, resulting in increased vascular
permeability and hemorrhagic manifestations
that characterize DHF and DSS
Hyperendemicity
circulation
of diff. types of viruses
probability
of secondary infection
probability of
immune enhancement
Increased probability of DHF
Dengue- Hemorrhagic formDengue- Hemorrhagic form
• Hemorrhagic arm
DENGUE FEVER
 Skin hemorrhages: petechiae,
purpura, ecchymoses
 Gingival bleeding
 Nasal bleeding
 Gastro-intestinal bleeding:
hematemesis, melena, hematochezia
 Hematuria
 Increased menstrual flow
 Plasma Leakage as Cap Damage - at 5-7
days. Internal Dehydration ► Giddiness, Low
Pulse Volume, Narrow Pulse pr, ↓ Urine o/p.
This lasts for few hrs in Majority.
 Acute Hepatomegaly.
 Hemoconcentration
 Fine Morbiliform, Annular Rash over Limbs,
Decrease Platelets found ONLY in DHF.
Done 48 h apart.
 H/o acute fever
 Hemorrhagic manifestations
 Low platelet count (100,000/mm3 or less)
 Objective evidence of “leaky capillaries:”
◦ elevated hematocrit (>20% over baseline)
◦ low albumin
◦ pleural or other effusions
4 Necessary Criteria:
 Grade 1
◦ Fever and nonspecific constitutional symptoms
◦ Positive tourniquet test is only hemorrhagic
manifestation
 Grade 2
◦ Grade 1 manifestations + spontaneous bleeding
 Grade 3
◦ Signs of circulatory failure (rapid/weak pulse, narrow
pulse pressure, hypotension, cold/clammy skin)
 Grade 4
◦ Profound shock (undetectable pulse and BP)
Presence of thrombocytopenia with haemoconcentration
differentiate DF from other Ds.
 Oliguria, dark urine.
 Children most vulnerable to get DHF as low
immunity and interaction with maternal Ab in
infants.
 Cool limbs.
 Rt hypochondrial pain.
 Severe DHF leaks persist for 72 hrs.
fluid leaks into serous cavities
eg Peritoneum, Pleura, Pericardium.
Abdominal distension, colic, low Pulse Pr.
 Congestive phase after the leaks stop.
 Untreated DHF► DSS ►DIC. So recognize
early.
 4 criteria for DHF
 Evidence of circulatory failure :
◦ Rapid and weak pulse
◦ Narrow pulse pressure ( 20 mm Hg) OR
hypotension for age
◦ Cold, clammy skin and altered mental status
 Frank shock is direct evidence of circulatory
failure
Pt dies of Shock, not bleeding
Warning Signs for DSS
When Patients Develop
DSS:
• 3 to 6 days after onset of
symptoms
Initial Warning Signals:
• Disappearance of fever
• Drop in platelets
• Increase in hematocrit
Alarm Signals:
• Severe abdominal pain
• Prolonged vomiting
• Abrupt change from fever
to hypothermia
• Change in level of
consciousness (irritability
or somnolence)
Four Criteria for DHF:
• Fever
• Hemorrhagic manifestations
• Excessive capillary
permeability
•  100,000/mm3 platelets
 Decreased level of consciousness:
lethargy, confusion, coma
 Seizures
 Nuchal rigidity
 Paresis
 Blood pressure
 Evidence of bleeding in skin or other sites
 Hydration status
 Evidence of increased vascular
permeability-- pleural effusions, ascites
 Tourniquet test
 Virus strain (genotype)
◦ Epidemic potential: viremia level,
infectivity
 Virus serotype
◦ DHF risk is greatest for DEN-2,
followed by DEN-3, DEN-4 and
DEN-1
 Virus strain– with two or more serotypes
circulating simultaneously at high levels
(hyperendemic transmission)
 Pre-existing anti-dengue antibody
◦ previous infection
◦ maternal antibodies in infants
 Host genetics
 Age- Children
 Higher risk in secondary infections
 Fever surveillance
 Diagnosis based on standared case definitions.
 Reporting of DF|DHF to state health authority
 5% samples of clinically diagnosed cases during
an epidemic should be tested for confirmatory
lab. Diagnosis.
 Instruct peripheral health staff to report
increasing no. of cases clustering of acute
febrile illness compatible with case definition.
 Primary
 Secondary- Early diagnosis & treatment
 Tertiary- Mx of shock
 Surveillance
AIM:-
Early detection of an outbreak
To initiate timely preventive & control
measures
Should be carried out regularly
1) House Index- Percentage of houses
positive for larvae of aedes.
2) Breteau Index- No of containers positive
`for aedes aegypti per 100
houses
3) Container Index- Percentage of
containers positive for aedes breeding
Index
High risk of
transmission
Low risk of
transmission
BRETEAU >50 <5
HOUSE >10% < 1%
Intermediate risk of transmission- Between These
value
Pre existing heterotypic dengue
antibody is a risk factor for DHF
Tetravalent dengue vaccine –
Phase 2 trial completed successfully in
Thailand
Other approaches-
Infectious cDNA cloned derived vaccine,
inactivated whole virion vaccine
Prevention
Primary
Breeding
Community
awareness
Mosquito
bite
Laws,
Monitoring &
Surveillance
Personal
protection
Mosquito control
measures
Vaccine
Integrated
Vector
Control
Measures
98
Extensive use of fish Scraps/tyre removal
Deweeding of ponds/rivers
Health education
99
Integrated vector control measures
Biological
(larvicidal fish)
Health
awareness
Chemical
(Fogging)
Environmental
(Waste management)
1. Environmental Management
2. Biological Control
3. Chemical Control
4. Improving health standard
Larval control methods are more effective
than adult control measures to achieve
long term sustainable control
10
0
2
 AIM-
To prevent or minimize vector breeding
Reduce human vector contact
10
1
10
2
•Mosquito proofing of
tanks
•Covering of storage
containers
 Mosquito proofing of tanks
 Covering of storage containers
 Cleaning the water storage container of air
cooler every week.
 Solid wastes (tins, buckets, automobile
tyres,coconut shells should be buried or
properly disposed to prevent water
collection.)
 Personal protective measures e.g. proper
clothing(long sleeves & trousers), use of
mosquito repellants-mats, coils, aerosols &
mosquito nets.
10
3
A. Larvivorus Fish: Gambusia affinis,
B. Bacteria: Bacillus thuringiensis, Bacillus
sphaericus- available as powder or slow
release formulation (Tablets, pellets,
briquettes)
C. Cyclopoids (Mesocyclops) are useful for
large containers e.g.-wells, tanks, tyres
D. Larval traps
10
4
 Adult form of mosquito-
Fenthion,
malathion &
fenitrothion
 Larvicide-
Temophos
 Methods of application-
Space spray,
larvicide application
10
5
10
6
use of mosquito repellants-mats,
coils, aerosols & mosquito nets.
Mosquito barriers are needed until fever
subsides, to prevent Aedes mosquitoes
from biting patients and acquiring virus
Keep patient in screened sickroom or
under a mosquito net
 First must educate the
public in the basics of
dengue, such as:
◦ Where the mosquito lays her
eggs
◦ The link between larvae and
adult mosquitoes
◦ General information about
dengue transmission,
symptoms and treatment
10
7
 Remove water from coolers(weekly), small
containers
 Insecticide spray in the house
 Wear mosquito bite protecting clothes
 Use mosquito Netrepellentsmats
 Use coils  mats even during day
10
8
 Diagnosis is purely clinical.
 Serology is no guide to management.
 Only Paracetamol as anti-pyretic
 Mx is the fluid- FLUID & FLUID.
 Blood transfusion will increase the viscosity
in Hemoconcentration; may ►thrombosis.
 Fluids
 Rest
 Antipyretics (avoid aspirin and non-
steroidal anti-inflammatory drugs)
 Monitor blood pressure, hematocrit,
platelet count, level of consciousness
 Blood transfusion is contra-indicated
Host
-School going Children
-Office goers
-Urban population
-Over crowding
-Poor sanitation
-All S-E classs
Environment
16- 40 d. C
Humidity
Peri monsoon
Agent
-Dengue virus
- Female Aedes mosquito
Prevention
Primary
IVCM*
Behavioural change
Vector control
Environment Biological Chemical
Vaccine
Secondary Tertiary
Early
diagnosis
& Mx
Mx of
Cx
Surveillance
*IVCM- Integrated vector control measures

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Dengue fever pravin yerpude

  • 1. Dr Pravin Yerpude Professor and Head Dept of Community Medicine Chhindwara Institute of Medical Sciences,Chhindwara(M.P.)
  • 2.  Dengue is caused by a dengue virus which are arboviruses which is carried by a mosquito.  The mosquito is scientifically called Aedes aegypti carry the virus.
  • 3.  Dengue infection have the potential of rapid spread leading to an acute public health problem.  It is a notifiable disease
  • 4.  Of all the arthropod –borne viral diseases,dengue fever is the most common  Dengue fever is one of the most important emerging disease of the tropical and sub- tropical regions affecting urban and periurban areas
  • 5. Areas infested with Aedes aegypti Areas with Aedes aegypti and recent epidemic dengue
  • 6.  World  Each year 50 million infections occur worldwide with 5,00,000 cases of DHF and at least 12,000 deaths,mainly among children  Increase of dengue and DHF is due to uncontrolled population growth and urbanization without appropriate water management ,to the global spread of dengue via travel and trade and to the erosion of vector control programme
  • 7.  Currently DFDHF is endemic in- India, Bangladesh,Indonesia, Madives, Myanmar, Srilanka, Thailand  Category A: Indonesia, Myanmar, Thailand -Major public health problem, Multiple serotypes -Increased hospitalization & child hood mortality, -Rural environment affected Category B: India, Bangladesh, Madives, Srilanka -DHF emerging, - Expanding geographically within the country - Cyclic epidemic---- more frequent multiple serotype Category C: Bhutan, Nepal -No reported cases with uncertain endemicity Category D: DPR Korea -Non endemic 7
  • 8.  India  Dengue/DHF widely prevalent in India and all 4 serotypes are found  It is reported from 18 states/UTS with about 450 million population at risk  2006-12317 cases and 184 deaths  2007-553 cases and 69 deaths  2008-1256 cases and 80 deaths  2009-1553 cases and 96 deaths  2010-2829 cases and 110 deaths
  • 11.  Flavi RNA virus  Types- 4 types Den-1, Den- 2, Den- 3, Den- 4 ( All are isolated in India)  Type 2 is the Commonest  Each type has different antigenic strain.  There is no cross immunity
  • 12. Infection with one serotype-long lasting immunity to that subtype
  • 14. • Large, multi-striped, Aerial, slender elongated body covered with scales
  • 15.  Aedes Aegypti is ( Tiger ). other types- A. albopictus, A. polynesiensis, A. Scutellaris
  • 17. Egg may survive for many months
  • 18.  Habitat ie 30°N to 40°S latitude of tropics – subtropics.  Hot – humid temp of 16° to 40° C so peri- monsoon Aug-Nov .
  • 19.  Flying range- 400 meters  Usually bites during day time  Resting habits- Endophily (indoor, dark places)
  • 20. Aedes mosquito- Sucking bloodAedes mosquito- Sucking blood -feeds on many humans, -Time of biting- daytime
  • 22. 22 Cisterns Fountains Garden tanks Mosquito Breeding Habitats Contained Waters
  • 23. Water-supply related mosquito larval habitats:
  • 24.
  • 25.  Breeding- lays eggs at the bottom of clean open domestic, Peridomestic containers  Larvae stick to the inside walls; but have to come up to surface to breathe.
  • 26.  Not a disease of the poorest but of those who use water tanks, flower pots, coolers, AC.  Children most vulnerable to get DHF as low immunity and interaction with maternal antibody in infants.
  • 27. Host •Children •Office goers Environment •Tropics & subtropics •Water collection in artificial container •16-40 C temp.- humid climate Agent- Flavivirus 27
  • 28. Host -School going Children -Office goers -Urban population -Over crowding -Poor sanitation -All S-E classs Environment 16- 40 d. C Humidity Peri monsoon Agent -Dengue virus - Female Aedes mosquito
  • 29.  Increased distribution & densities of vector infestation,  Unreliable water supply systems  Increasing non-biodegradable containers and poor solid waste disposal
  • 30.  Increased air travel  Increasing population density in urban areas- unplanned & uncontrlled urbanization  Deterioration of public health infrastructure & surveillance system
  • 31. 1. Virus transmitted to human in mosquito saliva 2. Virus replicates in target organs 3. Virus infects white blood cells and lymphatic tissues 4. Virus released and circulates in blood 3 4 1 2
  • 32. 5. Second mosquito ingests virus with blood 6. Virus replicates in mosquito midgut and other organs, infects salivary glands 7. Virus replicates in salivary glands 6 7 5
  • 33. Viremia Viremia Extrinsic incubation Period (8-10 days) DAYS 0 5 8 12 16 20 24 28 Human #1 Human #2 Illness Mosquito feeds / acquires virus Mosquito refeeds transmits virus Intrinsic incubation period (3-10 days) Illness
  • 34.  Incubation period  5-6 days (3-10 days)
  • 35.
  • 36. Both Man and Mosquito
  • 37.
  • 38. Dengue Viral Infection Asymptomatic Symptomatic Dengue fever DHF Undifferentiated No shock DSS Classical Dengue fever Without H ,age With H’age Plasma leakage
  • 39.  Undifferentiated fever  Classic dengue fever (DF)  Dengue hemorrhagic fever (DHF)  Dengue shock syndrome (DSS)
  • 40.
  • 41. 87% of patients infected were either asymptomatic or only mildly symptomatic
  • 42.  High grade fever, Anorexia, Backache, Rash, bone breaking severe Bodyache, Retrobulbar pain,Hepatomegaly, Weakness, Depression.  Dehydration, Abd colic, Constipation, severe Conjunctivitis, Conjctival H’ge.  Single phase or 2 peak saddle back (Biphasic curve) fever- 39-400C, last for 7 days
  • 43. Pt. is viremic at the time of fever--- Infective to mosquito
  • 44.  Rash may be diffuse,flushing,mottling or fleeting pin-point eruptions on the face,neck and chest during first half of febrile period and a maculopapular rash on 3rd or 4th day  It starts on the chest and trunk and may spread to the extremities and rarely to the face  It may be accompanied by itching
  • 45.
  • 46.
  • 47.
  • 48.
  • 49.
  • 50.  Inflate blood pressure cuff to a point midway between systolic and diastolic pressure for 5 minutes  Positive test: 20 or more petechiae per 1 inch2 (6.25 cm2) or 20 or more petechiae per 3 cms. diameter
  • 51.  Skin eruption- 80% of cases Reddish Measly Face, Gets Redder at 5-6 Days.  Nose Bleeds occ, Mild Thrombocytopenia & Leukopenia.  Tourniquet test may be +ve, BP cuff between S/D pr. for 5 min.
  • 52. Suspected C/O of DF  Acute onset  High grade fever <7 days duration  Severe headache, backache  Joint , post orbital & muscle pain  With or without rash
  • 53.
  • 54. Probable C/O of DF  Suspected case  High vector velocity  Presence of confirmed cases in area  Bd. –ve for Mp, No response to anti- malarials
  • 55.  Isolation of virus from the blood in early phase  IgM abs. in single serum samples or  4 fold rise of Abs. in paired serum samples.
  • 56.  Influenza  Measles  Rubella  Malaria  Typhoid fever  Leptospirosis  Meningococcemia  Rickettsial infections  Bacterial sepsis  Other viral hemorrhagic fevers 56
  • 57.  Isolation of Dengue virus from serum, plasma, leucocytes or autopsy samples.  Demonstration of a fourfold or greater rise in reciprocal IgG antibody titres to one or more dengue virus antigen in paired sera samples.  Demonstaration of dengue virus antigen in autopsy tissue by immunohistochemistry or immunofluorescence or in serum samples by EIA  Detection of viral genomic sequences in autopsy tissue, serum or CSF sample by PCR (Polymerase Chain Reaction)
  • 58.  Most cases of early Classical DF can be treated at OPD & DHF at small hospitals or pvt H.  Only Paracetamol as anti-pyretic.  No Steroids, aspirin, NSAID, antiplatelet AB eg cephalosporins, vanco.  Lots of oral fluids in early illness eg ORS, chhas, tea etc.  Observe twice daily if pt. not well.  DSS in ICU. 58
  • 59.  Diagnosis of types of D is purely clinical.  Serrology is no guide to management.  Mx is the fluid- FLUID & FLUID.  It is NOT the bleeding or H’ge mx. If enough fluids are given early; Platelets are NOT required even for Thrombocytopenia.  Blood will increase the viscosity in Hemoconcentration; may ►thrombosis. 59
  • 60.  Fluids  Rest  Antipyretics (avoid aspirin and non- steroidal anti-inflammatory drugs)  Monitor blood pressure, hematocrit, platelet count, level of consciousness 60
  • 61.  Continue monitoring after defervescence  If any doubt, provide intravenous fluids, guided by serial hematocrits, blood pressure, and urine output  The volume of fluid needed is similar to the treatment of diarrhea with mild to moderate isotonic dehydration (5%-8% deficit) 61
  • 62.
  • 63. It is not a complication of dengue fever but has separate etio- pathognesis
  • 65. Bitten dengue virus Specific Antibodies to Same type virus
  • 66. Neutralizing antibody to Dengue 1 virus Dengue 1 virus Homologous Antibodies Form Non-infectious Complexes Non-neutralizing antibody Complex formed by neutralizing antibody and virus
  • 67. Bitten dengue virus Specific Antibodies to dengue virus Bitten dengue virus Other sub-type
  • 68. Non-neutralizing antibody to Dengue 1 virus Dengue 2 virus Heterologous Antibodies Form Infectious Complexes Complex formed by non-neutralizing antibody and virus
  • 69. Bitten dengue virus Specific Antibodies to dengue virus Bitten dengue virus Other sub-type Immune reaction Ag-Ab complex
  • 70. Bitten dengue virus Specific. Antibodies to dengue virus Bitten dengue virus Other sub-type Immune reaction Ag-Ab complex Capillary leakage DHF
  • 71.  Antibody-Ag complex-can enter a greater proportion of cells of the mononuclear lineage, thus increasing virus production  Infected monocytes release vasoactive mediators, resulting in increased vascular permeability and hemorrhagic manifestations that characterize DHF and DSS
  • 72. Hyperendemicity circulation of diff. types of viruses probability of secondary infection probability of immune enhancement Increased probability of DHF
  • 73. Dengue- Hemorrhagic formDengue- Hemorrhagic form • Hemorrhagic arm
  • 75.  Skin hemorrhages: petechiae, purpura, ecchymoses  Gingival bleeding  Nasal bleeding  Gastro-intestinal bleeding: hematemesis, melena, hematochezia  Hematuria  Increased menstrual flow
  • 76.  Plasma Leakage as Cap Damage - at 5-7 days. Internal Dehydration ► Giddiness, Low Pulse Volume, Narrow Pulse pr, ↓ Urine o/p. This lasts for few hrs in Majority.  Acute Hepatomegaly.  Hemoconcentration  Fine Morbiliform, Annular Rash over Limbs,
  • 77. Decrease Platelets found ONLY in DHF. Done 48 h apart.
  • 78.  H/o acute fever  Hemorrhagic manifestations  Low platelet count (100,000/mm3 or less)  Objective evidence of “leaky capillaries:” ◦ elevated hematocrit (>20% over baseline) ◦ low albumin ◦ pleural or other effusions 4 Necessary Criteria:
  • 79.  Grade 1 ◦ Fever and nonspecific constitutional symptoms ◦ Positive tourniquet test is only hemorrhagic manifestation  Grade 2 ◦ Grade 1 manifestations + spontaneous bleeding  Grade 3 ◦ Signs of circulatory failure (rapid/weak pulse, narrow pulse pressure, hypotension, cold/clammy skin)  Grade 4 ◦ Profound shock (undetectable pulse and BP) Presence of thrombocytopenia with haemoconcentration differentiate DF from other Ds.
  • 80.  Oliguria, dark urine.  Children most vulnerable to get DHF as low immunity and interaction with maternal Ab in infants.  Cool limbs.  Rt hypochondrial pain.
  • 81.  Severe DHF leaks persist for 72 hrs. fluid leaks into serous cavities eg Peritoneum, Pleura, Pericardium. Abdominal distension, colic, low Pulse Pr.  Congestive phase after the leaks stop.  Untreated DHF► DSS ►DIC. So recognize early.
  • 82.  4 criteria for DHF  Evidence of circulatory failure : ◦ Rapid and weak pulse ◦ Narrow pulse pressure ( 20 mm Hg) OR hypotension for age ◦ Cold, clammy skin and altered mental status  Frank shock is direct evidence of circulatory failure
  • 83. Pt dies of Shock, not bleeding
  • 84. Warning Signs for DSS When Patients Develop DSS: • 3 to 6 days after onset of symptoms Initial Warning Signals: • Disappearance of fever • Drop in platelets • Increase in hematocrit Alarm Signals: • Severe abdominal pain • Prolonged vomiting • Abrupt change from fever to hypothermia • Change in level of consciousness (irritability or somnolence) Four Criteria for DHF: • Fever • Hemorrhagic manifestations • Excessive capillary permeability •  100,000/mm3 platelets
  • 85.  Decreased level of consciousness: lethargy, confusion, coma  Seizures  Nuchal rigidity  Paresis
  • 86.  Blood pressure  Evidence of bleeding in skin or other sites  Hydration status  Evidence of increased vascular permeability-- pleural effusions, ascites  Tourniquet test
  • 87.  Virus strain (genotype) ◦ Epidemic potential: viremia level, infectivity  Virus serotype ◦ DHF risk is greatest for DEN-2, followed by DEN-3, DEN-4 and DEN-1
  • 88.  Virus strain– with two or more serotypes circulating simultaneously at high levels (hyperendemic transmission)  Pre-existing anti-dengue antibody ◦ previous infection ◦ maternal antibodies in infants  Host genetics  Age- Children  Higher risk in secondary infections
  • 89.  Fever surveillance  Diagnosis based on standared case definitions.  Reporting of DF|DHF to state health authority  5% samples of clinically diagnosed cases during an epidemic should be tested for confirmatory lab. Diagnosis.  Instruct peripheral health staff to report increasing no. of cases clustering of acute febrile illness compatible with case definition.
  • 90.  Primary  Secondary- Early diagnosis & treatment  Tertiary- Mx of shock  Surveillance
  • 91. AIM:- Early detection of an outbreak To initiate timely preventive & control measures Should be carried out regularly
  • 92. 1) House Index- Percentage of houses positive for larvae of aedes. 2) Breteau Index- No of containers positive `for aedes aegypti per 100 houses 3) Container Index- Percentage of containers positive for aedes breeding
  • 93. Index High risk of transmission Low risk of transmission BRETEAU >50 <5 HOUSE >10% < 1% Intermediate risk of transmission- Between These value
  • 94.
  • 95.
  • 96. Pre existing heterotypic dengue antibody is a risk factor for DHF Tetravalent dengue vaccine – Phase 2 trial completed successfully in Thailand Other approaches- Infectious cDNA cloned derived vaccine, inactivated whole virion vaccine
  • 98. 98 Extensive use of fish Scraps/tyre removal Deweeding of ponds/rivers Health education
  • 99. 99 Integrated vector control measures Biological (larvicidal fish) Health awareness Chemical (Fogging) Environmental (Waste management)
  • 100. 1. Environmental Management 2. Biological Control 3. Chemical Control 4. Improving health standard Larval control methods are more effective than adult control measures to achieve long term sustainable control 10 0 2
  • 101.  AIM- To prevent or minimize vector breeding Reduce human vector contact 10 1
  • 103.  Mosquito proofing of tanks  Covering of storage containers  Cleaning the water storage container of air cooler every week.  Solid wastes (tins, buckets, automobile tyres,coconut shells should be buried or properly disposed to prevent water collection.)  Personal protective measures e.g. proper clothing(long sleeves & trousers), use of mosquito repellants-mats, coils, aerosols & mosquito nets. 10 3
  • 104. A. Larvivorus Fish: Gambusia affinis, B. Bacteria: Bacillus thuringiensis, Bacillus sphaericus- available as powder or slow release formulation (Tablets, pellets, briquettes) C. Cyclopoids (Mesocyclops) are useful for large containers e.g.-wells, tanks, tyres D. Larval traps 10 4
  • 105.  Adult form of mosquito- Fenthion, malathion & fenitrothion  Larvicide- Temophos  Methods of application- Space spray, larvicide application 10 5
  • 106. 10 6 use of mosquito repellants-mats, coils, aerosols & mosquito nets. Mosquito barriers are needed until fever subsides, to prevent Aedes mosquitoes from biting patients and acquiring virus Keep patient in screened sickroom or under a mosquito net
  • 107.  First must educate the public in the basics of dengue, such as: ◦ Where the mosquito lays her eggs ◦ The link between larvae and adult mosquitoes ◦ General information about dengue transmission, symptoms and treatment 10 7
  • 108.  Remove water from coolers(weekly), small containers  Insecticide spray in the house  Wear mosquito bite protecting clothes  Use mosquito Netrepellentsmats  Use coils mats even during day 10 8
  • 109.
  • 110.  Diagnosis is purely clinical.  Serology is no guide to management.  Only Paracetamol as anti-pyretic  Mx is the fluid- FLUID & FLUID.  Blood transfusion will increase the viscosity in Hemoconcentration; may ►thrombosis.
  • 111.  Fluids  Rest  Antipyretics (avoid aspirin and non- steroidal anti-inflammatory drugs)  Monitor blood pressure, hematocrit, platelet count, level of consciousness  Blood transfusion is contra-indicated
  • 112. Host -School going Children -Office goers -Urban population -Over crowding -Poor sanitation -All S-E classs Environment 16- 40 d. C Humidity Peri monsoon Agent -Dengue virus - Female Aedes mosquito
  • 113. Prevention Primary IVCM* Behavioural change Vector control Environment Biological Chemical Vaccine Secondary Tertiary Early diagnosis & Mx Mx of Cx Surveillance *IVCM- Integrated vector control measures