(What Clinicians Need to Know about Dengue in the United States

CDC
258 followers
Oct 29, 2026
(What Clinicians Need to Know about Dengue in the United States
AI Generated·May contain errors
Video Summary
AI GeneratedThis CDC presentation provides clinicians with comprehensive guidance on dengue fever, covering its transmission, clinical progression, and diagnosis. It highlights a significant surge in U.S. cases, particularly a major local outbreak in Florida, and emphasizes the critical importance of identifying warning signs and managing fluid intake to prevent mortality from severe plasma leakage.
Good afternoon, everyone.
I'm Captain Ibad Khan, and I'm representing
the Clinician Outreach and Communication
Activity, COCA, with the Office
of Emergency Risk Communication at the Centers for Disease
Control and Prevention.
I'd like to welcome you to today's COCA Call,
What Clinicians Need to Know About Dengue
in the United States.
All participants joining us today are in listen-only mode.
To view live captions, from your menu bar,
click More, select Language and Speech, then
click Show Live Captions.
If you prefer to view only the contents
on the slide without the distraction
of seeing the thumbnail view of the gallery of the attendees,
you can switch your settings to focus mode.
To enable focus mode, once again go to your menu bar,
click view, then click focus on content.
Free continuing education is offered for this webinar
and instructions on how to earn continuing education will
be provided at the end of the
The end of the COCA Call.
In compliance with continuing education requirements,
all planners, presenters, and moderators must
disclose all financial relationships
in any amount with ineligible companies over the
previous 24 months, as well as any use of unlabeled product
or products under investigational
use.
CDC, our planners, presenters,
and moderator wish to disclose they have no financial relationships
With ineligible companies.
whose primary business is producing, marketing, selling, reselling,
or distributing healthcare products used by or on patients.
In addition, content will not include any discussion of the unlabeled
use of a product or a product under investigational use.
CDC did not accept financial or in-kind support
from ineligible companies for this continuing education activity.
CDC complies with applicable federal civil rights laws.
and does not discriminate based on race,
color, national origin, age, disability,
religion, or sex. To learn more about this,
visit www.hhs.gov forward slash civil rights.
At the conclusion of today's session,
participants will be able to accomplish the following.
Summarize dengue epidemiology and transmission in the United States.
List the clinical features of dengue.
Explain dengue diagnostic testing for patients with suspected dengue,
and describe appropriate treatments
for dengue patients according to severity classification.
After today's presentations, there will be a Q&A session.
You may submit questions
at any time during today's presentation via the
Microsoft Teams platform.
Please note that the ability to ask a question during the live
This webinar is limited by Microsoft to the first 1,000 attendees
who join the webinar.
If you are unable to ask a question during the webinar,
you may submit your question
after the live session by emailing coca at cdc.gov.
Kindly note that we receive many more questions
than we can answer during our webinars.
If you're a patient, please refer
your questions to your healthcare provider.
If you're a member of the media and have a question,
please contact CDC Media Relations
at www.cdc.gov forward slash media.
Click Contact Media Relations at the bottom of the page
and complete the request for comment form.
I would now like to welcome our presenters for today's COCA Call.
We are very pleased to have with us Dr. Laura Adams, an epidemiologist,
and Dr. Liliana Sanchez-Gonzalez,
who is a medical epidemiologist, both from the dengue
branch in the Division of Vector-Borne Diseases
at the National Center for Emerging and Zoonotic
Infectious Diseases at the Centers for Disease Control and Prevention.
It is my pleasure now to turn it over to Dr. Adams.
Dr. Adams, please proceed.
Thank you very much.
Today, we're going to be talking about what
clinicians need to know about dengue in the
United States.
Next slide.
We'll be starting with some background on dengue
and then get into a bit about the current
situation currently in the U.S.
Next slide.
We'll start with a quick overview of dengue basics.
Next slide.
Dengue is caused by infection with any one
of four distinct dengue viruses.
Infection with one dengue virus provides lifelong immunity
to that specific virus,
but only short-term cross-protective
immunity against other dengue viruses.
This means individuals can potentially be infected multiple times.
Next slide.
Dengue virus transmission most commonly occurs through
the bite of an infected mosquito.
Aedes aegypti is the most common vector, shown on the top right.
However, Aedes albopictus, shown on the bottom,
can also sustain transmission.
Other modes of transmission for dengue virus are much less common
but include perinatal transmission
from a mother to a baby, through breast milk,
blood transfusion or organ transplantation,
needle stick or other hospital or laboratory accident,
and rarely sexual transmission.
Next slide. Aedes mosquitoes lay their eggs
on the inner walls of water holding containers
like tires, pots, and buckets shown in the images below
and are common in urban areas. Next slide.
Dengue virus transmission occurs when a person
who is acutely infected with dengue virus
gets bitten by a mosquito.
During the extrinsic incubation period, the virus replicates in the
mosquito for 8 to 12 days before
the mosquito can transmit dengue virus to another person.
After the infected mosquito bites another person,
there's an intrinsic incubation period of around
3 to 14 days before symptoms develop. Next slide.
Among people who are infected with dengue virus,
about 60 to 80% will have asymptomatic or subclinical infections.
Of the 20 to 40% who are symptomatic,
around 1 to 5% will progress to severe dengue.
And among those with severe dengue,
most will survive, but up to 5% can be fatal.
Next slide.
Multiple factors can affect an individual's risk for severe dengue.
There's a known risk by age with higher risk among infants born
to seropositive mothers as well as elderly populations.
Underlying comorbidities can also be associated with worse outcomes,
including asthma, diabetes, obesity, hypertension,
and the other factors listed on the slide.
Pregnancy has also been associated
with a higher risk for progression to severe dengue.
Finally, the number of dengue infections
and the time between those infections can also play a role.
Although severe dengue can occur during any dengue infection,
there's a higher risk on the
second dengue infection compared to the first,
third, or fourth infection. Next slide.
For dengue prevention,
recommendations include using EPA-registered insect repellents
and wearing protective clothing like
loose-fitting long-sleeve shirts and pants.
People can also take action to control mosquitoes indoors and outdoors.
This includes cleaning
or eliminating water holding containers where mosquitoes can lay eggs
and using screens or air conditioning if possible.
Next slide. Dengue vaccines are
becoming available globally and three
of them have completed phase three trials which are shown here.
However, none are currently available
in the U.S. Dengvaxia was licensed in the U.S.
But the manufacturer stopped production
and all remaining doses expired earlier this year.
The TAC-003 vaccine and the TV-003 vaccine have been licensed
in other countries but are not licensed in the U.S.
The number of doses required and ages eligible vary by vaccine.
Pre-vaccination screening was required for Dengvaxia
but has not been required for the other vaccines
in the countries where they're licensed.
And efficacy against biologically confirmed dengue
for all three vaccines has varied
based on serostatus, or if the person has had dengue before or not,
as well as by dengue
virus serotype.
Next slide.
Next, let's talk briefly about the current dengue situation.
Next slide.
This figure shows dengue cases reported
to the Pan American Health Organization from
countries across the Americas.
And you can see that dengue cases have
increased steadily over the past 25 years.
This is not a linear increase
because this is mainly driven by outbreaks, which occur
around every three to five years in endemic areas.
This increase has also been driven by larger outbreaks
in endemic areas, as well as increasing
frequency of locally acquired cases in new areas.
Next slide.
Dengue occurs in tropical and subtropical areas globally,
as shown by this map of dengue
cases reported to the World Health Organization so far this year.
Next slide.
In U.S. states, dengue cases usually occur among travelers
to endemic areas.
This figure shows the number
of travel-associated dengue cases reported to CDC from 2010 to 2025,
with a peak in 2024 of more than 3,700 cases,
driven by large outbreaks globally.
Next slide. This figure shows dengue cases among travelers
this year, shown in the green bars,
compared to the most recent five years,
which are shown in the background lines.
First, you can see that there are clear seasonal trends
with higher case numbers among travelers
usually occurring in the second half of the year.
For 2026 specifically, we've seen an increase in
recent weeks, although these numbers are similar
to the past few years, which as you saw in the
previous slide have been the highest years on record.
Next slide. Although dengue is not
considered endemic in the continental U.S.,
competent dengue mosquito vectors are present
in many U.S. states.
The figure on the left shows the estimated range of Aedes aegypti,
and the right shows the range of Aedes albopictus.
Next slide.
We have seen sporadic locally acquired cases and small
outbreaks occur in multiple U.S. states over the past 15 years.
The highest number has been reported from Florida.
We've also seen cases in recent years in Texas, California,
and Arizona, as well as the first locally acquired case identified
in Virginia earlier this year.
Dengue is considered endemic in six U.S. territories
and Freely Associated States.
Next slide. In late September of this year,
an emergency was declared in three Florida counties
due to local dengue transmission.
These local cases included one death due to dengue. Next slide.
Locally acquired dengue cases in Florida have increased rapidly
in 2026, shown here in the red
line, with other high transmission years shown for context,
and cases continue to be reported.
This is the largest locally-acquired dengue outbreak
in Florida since the 1930s.
Next slide.
In total, 288 travel-associated dengue cases have
been identified in Florida this year
as of October 15th.
368 locally-acquired cases have been reported from eight counties.
The majority of these are in the Tampa Bay area,
primarily from Hillsborough County.
Twenty mosquito pools have also tested positive for dengue virus.
Next slide.
Among the locally acquired dengue cases in Florida,
the majority have been infected with
dengue virus two.
Approximately half were male and the median age is 43 years.
Although cases
have been reported among all age groups,
about 45 percent occurred among adults 30 to 49 years old.
Nearly half of the cases, or 47 percent, required hospitalization.
Next slide. The summary points from this section
are that dengue is a growing health threat globally.
Dengue cases among travelers to the U.S. are increasing in recent weeks
and we've seen ongoing
local transmission of dengue virus in multiple Florida counties.
Public health partners can
continue to encourage dengue prevention among people traveling
to and living in areas with
active dengue virus transmission. Next slide.
Thank you and I'll turn it over to Dr. Sanchez-Gonzalez
for the next section.
Now I will talk about dengue clinical features,
the diagnostic testing approach, and management
recommendations based on the patient's clinical presentation.
Next slide. Let's start with the
clinical presentation. Next.
The most common initial presentation of dengue is characterized
by a high fever, usually with abrupt onset.
Fever is present in almost all patients with dengue,
and it is commonly accompanied by aches and pains,
including headache, retro-orbital pain,
Myalgia and arthralgia.
Dengue is sometimes called breakbone fever
because these aches and pains can be intense
and debilitating.
Nausea and vomiting are also common, as is anorexia.
Skin manifestations, including rash and petechia,
are frequently reported, and about a third
of patients may also have mucosal bleeding,
such as epistaxis, gum bleeding, or hematuria.
Other symptoms can include diarrhea, dysgeusia,
lymphadenopathy, and conjunctival injection.
Respiratory symptoms, including cough,
runny nose, and sore throat can occur, but they
are much less common.
Next slide.
We should suspect dengue in any patient
who lives or has traveled to an area with dengue
transmission within the last two weeks,
who is febrile, and who presents with two of the
criteria listed here, nausea or vomiting,
rash, aches and pains, a positive tourniquet
test or petechiae, and leukopenia.
Any warning sign also counts as a clinical criterion,
but we review them in the next slides.
Once we suspect dengue,
we need to determine the patient's clinical severity classification.
Next slide. Patients
who meet the clinical criteria listed here again and do not have
warning signs are classified as having dengue
or dengue without warning signs. Next slide.
We should assess warning signs in all patients with suspected
or confirmed dengue as they
indicate a higher risk of progression to severe disease
and require close monitoring.
Warning signs include abdominal pain or pain to palpation,
persistent vomiting, including
here is a suggested definition,
fluid accumulation such as ascites or pleural effusions, any
mucosal bleeding such as epistaxis,
hematuria, or abnormal vaginal bleeding.
Altered mental status, commonly reported as lethargy,
restlessness, or drowsiness,
liver enlargement, or hemoconcentration,
a progressive increase in hematocrit.
Patients with one or more warning signs
are classified as having dengue with warning signs.
Next slide.
Patients are classified as having severe dengue
if they have any severe manifestation.
If they have severe plasma leakage,
which is the hallmark of severe dengue,
that is leading to shock or respiratory distress.
Next
slide.
Let's now talk about the dengue clinical course.
The incubation period after a mosquito bite can range
from 3 to 14 days, as mentioned
before, although it is usually short, about 3 to 5 days.
After the incubation period,
symptomatic dengue generally follows three clinical phases.
Next slide.
The first phase is the febrile phase.
This is when patients have the symptoms that we just reviewed,
including fever, that gives
this phase its name.
Fever and other symptoms usually last two to seven days,
and this is when most symptomatic
patients will seek medical care.
Patients are viremic during this phase, and as you see here,
they might also be viremic for a couple of days before symptoms begin.
This means that a mosquito
that bites them at this time can become infected
and continue with the transmission cycle.
Clinical problems during this phase include dehydration,
electrolyte disturbances,
And we've got febrile seizures, especially in younger children.
Defervescence, which is the abatement of fever,
usually occurs between days 3 and 8 of the
illness.
Most patients improve as the fever resolves,
however, some patients enter the critical
phase that usually lasts 1 to 2 days
and is when capillary permeability increases.
This can lead to plasma leakage,
which is the movement of fluid out of the blood vessels
into the interstitial space.
Most warning signs are associated with plasma leakage
and are commonly seen toward the end of
the febrile phase or during the critical phase.
Severe manifestations also can develop during
this phase. Severe plasma leakage can result in shock
which is the most common severe manifestation
and recognizing the critical phase is key to monitoring
and managing patients appropriately.
Next slide. The final phase is a recovery
or convalescent phase
that usually lasts about three to five days.
During this phase the fluid that moved
into the tissues early is gradually reabsorbed.
Potential clinical problems here
include hypervolemia or pulmonary edema
and this can occur when patients receive excessive intravenous fluids,
IV fluids, during earlier phases of illness
and this highlights why judicious IV fluid
administration is very important especially
in patients with relevant coexisting conditions.
So these, febrile, critical, and recovery,
are the three typical clinical phases of the
Next slide.
Rashes are very common in patients with dengue
With the abrupt onset of fever, patients may have marked flushing,
redness of the face, neck, and chest,
as shown in the first picture here.
During the febrile phase, patients might develop a macular
or maculopapular rash that often starts
on the trunk and spreads to the face and limbs.
It is usually blanchable, as shown in the last
image here, and it might later become scaly.
The first and the second images here show the
same patient, because patients
with dengue can have different rashes during different phases
of the illness. Next slide. During the recovery phase,
patients can develop a characteristic confluent rash
with areas of spared skin
It is commonly described as islands of white in a sea of red,
or Herman's rash, and this
rash often desquamates and can be extremely itchy
In some patients, itching is the reason they seek medical care.
The appearance of the rash can vary depending
on the patient's skin complexion, and here
you can see four different patients
with the characteristic rash of the recovery phase
Next slide.
Let's pause here for a knowledge check.
We have a 27-year-old woman
who returned four days ago from a one-week trip to Puerto Rico.
She has had four days of fever, headache, myalgia, and macular rash.
Since yesterday, her fever has subsided
with a maximum temperature of 37.4.
Today, she comes with abdominal pain
and unexpected new onset heavy menstrual bleeding.
Her vital signs are normal,
and she has no respiratory distress or signs of shock.
What is the most appropriate clinical
severity classification for this patient?
Dengue without warning signs, dengue with warning signs,
severe dengue, or this patient
does not meet clinical criteria.
I'll give you a few seconds to consider the options.
Next slide.
The correct answer is B, dengue with warning signs
This patient has abdominal pain, which is a warning sign,
and she's also reported abnormal
menstrual bleeding.
Remember that any mucosal bleeding is a warning sign in dengue,
and it is important to ask
about bleeding that might not be obvious during
the physical examination, including changes
in the color of the urine or stools and changes in menstrual flow
Next slide.
Severe plasma leakage is the main pathophysiological process
that can lead to severe dengue
So how do we recognize plasma leakage?
The key sign is hemoconcentration.
We identify this when the hematocrit
is at least 20% above the patient's baseline,
if you have a baseline available,
or 20% above the normal expected value for the patient's sex and age.
Hemoconcentration can be also recognized
when the hematocrit drops by 20% or more
after IV fluid administration,
without evidence of bleeding that would explain this change.
In this situation, the IV fluids may be diluting
the hemoconcentration caused by plasma leakage,
so it is very important that you obtain
a complete blood count during the first assessment of a
patient with suspected dengue that you can use
as your baseline for monitoring.
Another important sign is clinical fluid accumulation such
as ascites or pleural effusion.
Clinical assessment might identify fluid accumulation
Your patients may have respiratory distress,
abdominal discomfort, or flank pain.
And imaging, including chest x-rays or abdominal ultrasounds,
can help identify or confirm smaller amounts of fluid accumulation.
Next slide.
Shock is the most common manifestation of severe dengue.
And unrecognized shock continues to be a common cause
of death among patients with dengue.
It's therefore very important to look for early signs of shock,
not only hypotension.
One early sign of shock is a narrowing pulse pressure.
This means that the difference between the systolic
and diastolic blood pressure values is 20 or less.
In patients with substantial plasma leakage,
compensatory mechanisms can maintain adequate circulation for a while,
increasing the diastolic pressure,
and this narrows the difference between the two pressure values.
If plasma leakage continues without adequate fluid replacement,
then hypotension and shock can develop.
Other signs of early shock include delayed capillary refill
or other evidence of poor peripheral perfusion.
Tachycardia in the absence of fever
is another important sign, particularly in children.
Next slide.
The most common laboratory findings in dengue are leukopenia,
hemoconcentration, and thrombocytopenia.
During the febrile phase, in yellow.
Laboratory results may still be normal.
Toward the end of the febrile phase
and at the beginning of the critical phase,
patients may develop leukopenia with neutropenia, the brown line here,
and lymphocytosis, the black line.
Hemoconcentration, here in blue,
also develops around the beginning of the critical phase
because plasma is leaving the intravascular space
and is increasing the concentration of red blood cells.
And the hematocrit usually begins
to recover as the critical phase ends.
Platelets, here in purple, may take longer to decrease,
so a normal platelet count during
the febrile phase does not rule out dengue.
The lowest platelet count usually coincides
with the highest hematocrit during the critical
phase, and platelets might take longer to recover.
Thrombocytopenia can persist well into the recovery phase.
Next slide.
Other laboratory findings might include mild elevation
in liver enzymes, AST and ALT,
especially AST, even in non-severe cases.
Hyponatremia, prolonged coagulation times,
and low serum albumin related to plasma leakage
can also be present.
Depending on the patient's clinical severity,
you can find other lab abnormalities, including
metabolic acidosis, increased creatinine,
elevated troponins, or elevated B-type natriuretic
peptides.
Several biomarkers have been associated
with progression to severe dengue, but there are
not currently universally recommended biomarkers
that are reliable to predict progression to severe
disease. Next slide.
Dengue has a broad differential diagnosis that includes viral
bacterial and parasitic infections, among other conditions.
You can see here the most common.
And as with other diseases,
to determine the most relevant differential diagnosis,
we should consider the patient's clinical presentation,
exposure and travel history, and epidemiological trends.
In areas with other arboviruses, such as chikungunya,
zika, and yellow fever circulate,
they should be considered. Febrile illnesses with rash,
including measles and rubella, can also resemble dengue.
During the first days of illness,
respiratory viruses such as influenza or COVID-19 can
present with symptoms that are very similar to those of dengue,
and clinical differentiation
can be really challenging.
As the respiratory virus season begins in the US,
it is important to consider the epidemiology
and the seasonality of these pathogens
to guide clinical suspicion and testing.
Next slide.
The key messages from this section, dengue is a dynamic disease.
The clinical presentation can change quickly.
Every time we evaluate a patient with dengue,
we should look for warning signs and manifestations
of severe dengue.
These findings will guide clinical classification and management.
Plasma leakage and progression
to severe dengue usually occur during the critical phase, and
shock rather than bleeding is the most common severe manifestation.
So early recognition and close monitoring
of the critical phase, warning signs, and
signs of shock is essential for patients with dengue.
Next slide.
Now let's talk about diagnostic tests.
Next slide.
First, if you suspect dengue,
clinical management should not be delayed
while waiting for laboratory confirmation.
Monitor and manage your patient as a patient with dengue.
Next slide.
In the U.S., dengue is a nationally notifiable disease,
so suspected or confirmed cases should be reported
to your state or local health department.
If needed, the arboviral surveillance teams
can help you arrange diagnostic testing.
Rapid tests are not widely available in the US
and none are FDA approved, and there are some
private laboratories that can offer different options
for dengue testing. Recommended testing
approach depends on how many days have passed since symptom onset.
Next slide. Let's look at the
figure on the left. Days of symptoms are on the x-axis
and sensitivity of the test is on the y-axis.
The yellow shade shows the typical longest duration of fever,
seven days, and this is
the main window we have to detect viruses and confirm the diagnosis.
Dengue NS1, or the non-structural protein 1,
is here in blue, is most detectable during
the first seven to nine days of illness.
Dengue viral RNA, here in purple,
is detected mainly during the seven first days of illness.
IgM antibody, shown in black,
generally becomes detectable around day four and can remain
detectable for up to 90 days.
So, during the first seven days of illness,
as shown on the right, we recommend ordering
an RT-PCR test plus IgM test or an NS1 antigen test and an IgM test,
these to increase the
likelihood of confirming a dengue diagnosis.
Next slide.
After seven days of illness,
an IgM ELISA test is the primary recommended test.
You can still consider RT-PCR or NS1 antigen testing,
especially if you have symptomatic
patients, although sensitivity is lower than it
is during the first seven days of illness.
It is important to remember that if you order only
an IgM test during the first few days
of illness, the result might be negative,
even when the patient has dengue, as you can
see on the graph.
And then there is cross-reactivity with other flaviviruses,
such as West Nile virus.
Positive IgM results that we get among local
acquired cases might need additional testing
for confirmation, such as plaque reduction neutralization.
Next slide.
So let's apply this to the same patient.
Remember, she has had four days of fever and other general symptoms.
Her fever began to subside yesterday,
and today she's presenting with runny eyes.
What would be the most appropriate
diagnostic approach for this patient?
We should not test because her fever has begun to subside.
We should order an NS1 antigen testing
because she's within the first seven days of illness.
We order a dengue RT-PCR or NS1 test and a dengue IgM antibody test.
And we only order IgM antibody testing
because she's on day four already.
I'll give you a few seconds to consider the options here.
Next slide.
The correct answer is C, order a dengue RT-PCR or NS1 test,
plus a dengue IgM antibody test.
She's within the first seven days of illness,
so testing should include a method that detects
the virus or part of the virus, along with IgM antibody.
IgM alone could be negative early in the illness,
as here in day four, and testing should be
ordered for all patients with suspected dengue,
even if the fever has started to resolve.
Next slide.
Let's now discuss clinical management.
Next slide.
There are some antivirals, monoclonal antibodies,
and other medications that have shown promising
results in early clinical trials for the management of dengue.
However, treatment of dengue remains largely supportive.
Appropriate monitoring and IV fluid management
can greatly reduce mortality among patients
with dengue, and we assign patients to management groups A,
B, or C based on clinical presentation
for coexisting conditions and laboratory findings.
The majority of patients can be managed at home.
And for those who require hospitalization,
judicious IV fluid administration is the main tool we have
to prevent poor clinical outcomes.
Next slide.
Oh, sorry, can you...
Previous slide, please.
I forgot to mention the CDC pocket guide
that is shown here on the right
was included in the resources for this call,
and it provides a practical approach
to classifying patients with dengue
and following the management algorithms.
Next slide, please.
Patients can be classified as group
A and managed as outpatients when they have no
warning signs, they can tolerate oral fluids,
and they have a normal urine output.
Most patients will meet criteria for this group,
so most patients with dengue can be
managed at home.
Ideally, these patients should be assessed every day
with a complete blood count until
they are out of the critical phase.
In practical terms, this means that we monitor
these patients until 48 hours after the fever
goes away or after the fever subsides.
At each assessment we look for signs of dehydration,
defervescence and warning signs.
It is key that we provide clear instructions to the patients
so that they know which warning signs require
immediate medical attention and they can return.
In children, adequate oral fluid intake has
been associated with lower rates of hospitalization.
Abundant oral fluids should be encouraged in all patients with dengue
Recent WHO guidelines published in 2025 reviewed
a substantial body of evidence available and they
suggest the use of protocolized oral fluid treatment
for patients with dengue. This means
giving the patient a specific oral hydration plan to follow at home.
They also suggest paracetamol
for pain or fever and they recommend against aspirin
and NSAIDs because we are not certain
is safe for patients with dengue
and they could increase the risk of bleeding.
Fevered patients should rest and sleep under a mosquito net.
This helps prevent mosquitoes from biting the patient,
becoming infected, and they continue transmission.
Next slide.
Patients are assigned to group B when they have warning signs.
Any coexisting conditions that increase the risk
of severe disease, including pregnancy,
we recommend hospitalization of all pregnant women with dengue,
or social circumstances that would prevent them
from returning quickly to the hospital if need.
These patients should be placed under medical observation
or hospitalized, we order baseline
laboratory testing, placement of an IV line,
not all patients in this group will require IV fluids,
careful monitoring of intake and output,
and if the oral fluid intake is inadequate
or the patient presents with warning signs,
IV fluids should be administered
According to the appropriate algorithm,
we'll see more in the next slides.
Hematocrit should generally be monitored every four
to six hours for these patients,
but this will depend on the patient's condition clinical presentation.
Next slide.
There are several important principles
for fluid management in patients with dengue.
We limit IV fluids during the febrile phase.
IV fluids are usually only needed for 24
to 48 hours during the critical phase.
We use isotonic solutions,
and the goal is to give the minimum amount needed to restore
intravascular volume, maintain good perfusion,
and maintain good urine output.
Most importantly, we reassess
the patient after fluid administration changes and look
for clinical response.
We monitor perfusion, urine output, and hematocrit,
and we base the IV fluid rates on ideal body
weight.
The 2025 WHO guidelines suggest the use
of crystalloid fluids over colloids for all
patients with dengue and recommend using capillary refill time
and serum lactate in addition
to standard clinical assessment to guide the IV fluid management.
Next slide.
Patients with severe dengue manifestations
are assigned to group C and require emergency
treatment.
This includes patients with shock,
respiratory distress caused by severe plasma leakage,
severe bleeding, or severe organ involvement.
These patients require hospitalization, often in an intensive care unit.
We order baseline lab testing,
blood type and screen, oxygen support, and we manage
them with fluid boluses 10 to 20 ml per kilogram.
Hemodynamic status should be monitored continuously when possible,
and hematocrit may be needed
to be checked every one to four hours in this patient,
depending on clinical presentation
and response.
Intake and output should be monitored closely,
and because these patients receive large quantities
of IV fluids, we must also monitor for signs of fluid overload,
including tachypnea, increased
liver size, and peripheral edema.
Next slide, please.
In 2025, the Pan American Health Organization conducted
a detailed review of evidence available
and published a guideline with additional recommendations
for the management of severe
dengue, especially for patients in the intensive care unit.
Key from this guideline is the recommendation
of considering the early use of vasopressive agents
in patients with dengue and persistent hypotension,
norepinephrine for adults and epinephrine for
children, and the use of serum lactate,
capillary refill time, and point-of-care ultrasound to help
guide fluid management. Next slide, please.
And here I wanted to show you what would be the
management for our patient with dengue with warning signs
that we discussed previously in the knowledge checks
This is the algorithm in the CDC pocket guide for patients in group B.
And inside the blue lines, you can see that for this patient,
we would obtain an initial
complete blood count.
In the second box, we would administer crystalloid IV fluids
at a rate of 10 ml per kilogram
in one hour.
The third box, we would reassess the patient for clinical response.
Then on the right, if the patient does not respond,
we can administer additional IV fluids
at the same rate of 10 ml per kilogram.
If the patient responds, on the left you can see the box,
we follow a stepwise decrease
of the amount of IV fluids.
We move to 5 to 7 ml per kilogram per hour for a couple of hours,
then to 3 to 5 ml per
kilogram per hour for another couple of hours, and so on.
We always reassess the clinical status
of the patient with every change in the IV fluid
rate.
And as you can see, the IV fluid rate can go up
and down several times during the management
of a patient with dengue.
And requires frequent monitoring of clinical response.
Managing IV fluids in a patient
with dengue might require intensive human resources to
continuously track clinical response and adjust the IV fluid rates.
This is one of the reasons why dengue
outbreaks can overwhelm health systems.
We know that this careful approach works
and most patients respond to this dynamic IV fluid
management.
Next slide.
What we do not do with patients with dengue.
We do not use corticosteroids routinely
because there is no evidence that they provide any
benefit in patients with dengue.
We do not use NSAIDs because we don't have evidence
that they are safe in patients with
dengue and they can increase the risk of bleeding.
We do not give intramuscular injections
because of the risk of bleeding.
We do not give prophylactic platelet transfusions
as they are not beneficial in patients with
dengue and they can increase the risk of adverse events.
Next slide.
Before discharge, patients should meet several criteria.
They should have been without fever for at least 48 hours,
indicating that they are out of the critical phase.
They should have a stable hematocrit without IV fluids,
indicating that there is no plasma leakage.
They should show an increasing trend in platelet count.
And here, please note that there is no specific
recommended number, but rather an increasing trend
in the serial measurements of platelets meets this criteria.
And they should also have an overall improvement in clinical status.
Next slide.
So let's summarize the main messages
in the second part of this call.
First, we should suspect dengue in any feverish patient with an
appropriate exposure within the previous 14 days.
Second, we should determine the patient's clinical severity,
the phase of disease, and the risk factors for severe dengue.
Third, we should identify warning signs and early signs of shock.
And remember that shock, rather than bleeding,
is the most common severe manifestation.
Fourth, we order diagnostic testing based
on the time since symptom onset.
Within the first seven days, we use RT-PCR or NS1 together with IgM.
Fifth, we classify patients into groups, group A, B, or C,
based on their clinical findings,
coexisting conditions, and laboratory findings.
And finally, we use a stepwise approach to IV fluid management.
We give enough fluids to restore intravascular volume
and to maintain good perfusion and urine output,
and then we reassess frequently to adjust rates as necessary.
Next slide.
For additional training,
CDC offers a series of three interactive web-based modules on dengue.
They are designed for clinicians,
public health professionals, and health educators.
They include clinical cases
and each activity offers free continuing education.
We encourage you to complete these trainings.
Next slide.
Thank you for your attention.
We welcome your questions.
You can also contact the CDC Dengue team
for questions at dengue at cdc.gov.
And I will now turn it over to Captain Ken.
Thank you.
Presenters, thank you so much for providing
this timely information to our audience.
We will now go into our Q&A session.
For our audience, you may submit questions via
the Microsoft Teams platform.
Again, please note the ability to ask a question during
the live webinar is limited by Microsoft
to the first 1,000 attendees who join the webinar.
Please keep your questions related to the clinical nature,
since our audience is supposed
to be clinicians and healthcare providers.
Those are the questions we'll be addressing.
And if you are unable to ask a question during the webinar,
or we're not able to get to your
question, you may submit your question after
the live session by emailing coca at cdc.gov.
So our first question for our presenters asks,
would you consider acute kidney injury or end
stage renal disease patients on dialysis to be in group B?
And would you recommend hospitalization
during their illness? Well, can you hear me now?
Yes, we can hear you. Okay.
Yes, that's a good question.
Yes, acute kidney injury, it is one of the criteria that we consider
as a factor for increased risk to progression to severe disease,
along with pregnancy, coagulopathies.
We recommend hospitalization of these patients if they have suspected
or confirmed dengue.
Yes, they're both there.
For other coexisting conditions, high blood pressure,
obesity, the others that Dr. Adams
mentioned, we work with those patients on a case-by-case basis,
and we determine if
the patient needs to be hospitalized.
But for pregnant women, patients with acute kidney injury,
and patients with coagulopathies
or taking anticoagulant therapy, we recommend them to be hospitalized.
Thank you very much. Can you also differentiate,
while we're speaking about
We're talking about...
patient care like this, can you differentiate between indications
for oral versus IV rehydration
for patients with dengue?
Not sure if I understood the question.
In general or for a specific group?
Group B.
I think let's speak generally,
but if it's more relevant to group B, then we can, if
that's one of the criteria is to determine between oral
and IV, I think that's what this
question is trying to get at, if I was to just read between the lines.
Okay, yes.
So intolerance to oral fluids is one of the criteria that we take.
Thank
To determine if a patient needs to be hospitalized,
if there is no tolerance to
oral fluids that we would recommend the patient
to be kept under observation because of the
importance of hydration in patients with dengue.
In many cases we start IV fluid management and we
you.
continue to monitor tolerance to oral fluids
and we start oral fluids as soon as possible
Because we know that it is...
Because these.
We recommend continued
trying oral hydration in
all patients with dengue
as soon as possible
because this has a lot of benefits in these patients.
So it is one of the criteria we use to determine
if they should be kept in a hospital.
But it's also one of the main interventions we have
to improve patients with dengue.
Great. Thank you so much.
And along the same lines of assessment, we have a question that asks,
what bedside findings can help clinicians
recognize early shock before hypotension develops?
So I mentioned some of them.
Narrowing pulse pressure is very important.
We should not wait until the patient has hypotension
to consider this patient to be in shock.
And narrowing pulse pressure, the difference between the systolic
and diastolic blood pressures being 20 or less,
indicates that the patient might be entering into shock.
So that's a very important one.
And we, in patients with dengue,
always record the blood pressure and always record the pulse pressure.
Yeah, sure. We also look for signs of peripheral
low perfusion, so capillary refill time
is very important to assess in patients with dengue,
as well as, you know, if the extremities are warm,
if we have thready pulses, any additional
manifestations of low peripheral perfusion.
And in children, it's very important in all patients
really to remember that sometimes we start seeing them
to be tachycardic, high heart rate,
without fever, and that can indicate that they
are also starting to have some hemodynamic
compromise. Thank you for that.
And you talked about children and elderly patients. We have a
I have a question about another specific patient population.
For pregnant patients that have either confirmed or suspected dengue,
what immediate inpatient
management steps should be prioritized,
and when is transfer to a tertiary center appropriate?
Yes, so very important for pregnant patients.
The current recommendations is to always
hospitalize pregnant patients.
There is currently some efforts to review the available evidence
for specific questions with pregnant women,
but as of now, the recommendation is that
Every pregnant woman with Dengue should be hospitalized.
Important to remember
that not all pregnant women will require IV fluids.
And as with other patients,
we administer IV fluids in them when they are necessary
because they don't tolerate oral fluids
or because there are warning signs.
We also have a more restrictive fluid strategy with pregnant women.
We use usually lower.
IV fluids rates for them, 5 to 10, for example,
ml per kilogram when we manage shock with them.
And if the patient is in labor or is close to labor,
medical care should be provided in a
tertiary hospital. There is increase of hemorrhage
and other complications for mother and baby. And
And so if the...
Dengue diagnosis is done close to labor or in patients with labor,
that'll be the recommendation.
The route of delivery in patients with dengue,
pregnant patients with dengue,
is based on individual circumstances.
And as I mentioned, there are some reviews
um
underway to review the evidence
and provide additional specific recommendations for
pregnant women. But as of now, those would be the recommendations.
Great. Thank you. Next question asks,
is there a hematocrit level at which you would consider
you.
a transfusion? And if so, what is it?
Oh, that's a very interesting question. So for
patients with dengue,
it's important to remember that there are no
Recommendations for prophylactic transfusions of any kind.
Platelets go down and there could be very important thrombocytopenia,
but if the patient is not bleeding,
there is no recommendation to any transfusion for platelets.
If there is bleeding, of course, we follow the normal,
the regular guidelines for transfusion
in patients with bleeding,
but there are no special considerations for patients with dengue,
no prophylactic transfusions.
We don't do, we don't treat the number of platelets,
we treat the patient.
For hematocrit levels, which we follow the...
The general recommendations for transfusion among other patients,
what we mostly see with patients
with dengue is hemoconcentration,
so an increase in the hematocrit during the critical phase,
and
and we follow general guidelines for transfusion
as we would do with any other patients.
Thank
We really don't do anything different
if the patient doesn't have active bleeding.
you
Great. Thank you. And we have time for just one last question.
for
you.
And the question asks,
your
how can clinicians distinguish dengue
from other conditions on a differential diagnosis, such as
patience.
chikungunya, Zika, malaria, leptospirosis, or even bacterial sepsis?
That is a question that I don't know
if I have enough time to answer, but
Yes, dengue can look a lot like other things, and so we recommend,
as with any other disease, to have great information about the exposure
of the patient, travel history, and also consider the epidemiology
and the seasonality of the different diseases.
Pathogens that might be causing day illness.
For clinical manifestations,
during the first two or three days of disease,
it's really hard to differentiate between dengue and other diseases.
It can be really hard,
but there are some clinical cues that can help with dengue.
Flushing is very characteristic of patients with dengue,
and we've seen in some analysis that we've done
that that helps differentiate a little bit.
Again,
Thrombocytopenia and leukopenia are more common
in patients with dengue than they are in patients
with chikungunya or Zika, for example.
There are a few clinical symptoms and clinical lab findings
that can help guide suspicion
while you have access to testing results for diagnosis.
Thank you so much.
However, the main recommendation,
because it might be many times very difficult to differentiate if you
don't have testing available right away, is that if you suspect dengue,
you monitor that patient as a patient with dengue.
You teach the patient about warning signs.
You are aware of warning signs and evaluate warning signs
in all of these patients so that you don't miss.
If this patient has dengue, you don't miss the critical phase
and you don't miss warning signs and progression to severe disease.
Wonderful. Thank you so much for that comprehensive response.
I think it's a perfect question to end our call on today.
This concludes our Q&A session,
and I want to thank everyone for joining us today
with a special thanks to our presenters
for sharing their time and expertise with us on this timely topic.
CDC has fully transitioned from the training
and continuing education online TCEO system
that provides access to CDC educational activities
for continuing education to CDC Train.
If you do not already have a Train account,
please create one at www.train.org forward slash CDC Train.
All continuing education for COCA calls
is issued online through CDC Train.
Those who participate in today's live COCA call
and wish to receive continuing education,
please complete the online evaluation
and post-test by November 23, 2026
with the course code WC5003-102226.
The registration code is COCA102226.
Those who participate in the on-demand activity
and wish to receive continuing education,
Should complete the online evaluation between November 24,
2026 and November 24, 2028
and use course code WD5003-102226.
The fully closed captioned video and transcript of today's COCA call
will be available on demand next week
at www.cdc.gov forward slash COCA.
For more details about this COCA call,
and upcoming COCA calls,
and to subscribe to receive announcements for future COCA calls,
please visit www.cdc.gov forward slash COCA
forward slash hcp forward slash trainings
forward slash index dot html.
You will also receive other COCA products to help keep you
informed about emerging and existing public health topics.
Again, thank you for joining
us for today's COCA call and have a great day.
