Beyond Fever, Rash, Joint Pain
Dr Seebat Masrur
FCPS Part 2 Trainee(Cardiology)
Case Scenario
• A 32-year-old woman presents to the emergency
department with
• Sudden onset high-grade fever (103°F), headache, and
severe joint pain in wrists and ankles for 3 days.
• Mild maculopapular rash over trunk and limbs
• Recent travel history Dhaka 10 days prior
Is this dengue fever, or could it be something
else?
Initial Investigations:
• CBC: Mild lymphopenia, mild thrombocytopenia (platelets
~130,000/µL)
• NS1 antigen test for dengue: Negative
• IgM for dengue: Negative but IgG Negative
• Liver function tests: Mildly elevated ALT/AST
What else could present similarly if dengue is
excluded?
Chikungunya Virus
• A single-stranded RNA virus.
• Belongs to the Alphavirus genus within the Togaviridae
family.
• Initially isolated from human serum in Tanzania in 1952,
Chikungunya had, by 2004, spread across Africa, India, and
Southeast Asia, causing significant sporadic epidemics.
• There are three primary lineages: West African, Asian,
and ECSA.
• The name derives from the Kimakonde language, meaning
"to become contorted," a reference to the characteristic
joint pain posture.
Transmission
Transmits Chikungunya, dengue, Zika,
and yellow fever.
Humans serve as the main reservoir of
infection.
Active daytime painless biters with
black-white striped markings.
Lays eggs in tiny water-holding
containers.
Eggs can withstand dryness for 6–8
months.
• Blood-borne transmission is possible
• Rarely, vertical transmission during pregnancy
• No direct human-to-human transmission reported
• Outbreaks fuelled by urbanization, travel, and
vector expansion.
Global
History &
Spread
• First detected: Tanzania, 1952
• Reached Asia via Thailand (1958) → Endemic in
India, Sri Lanka, SE Asia
• Spread to Europe (Italy, 2007) – local transmission
• Landed in the Americas (2013) → Rapid spread
across South America
• Major outbreaks: Réunion (2005–06), India (2006),
Italy (2007, 2017)
• 🔄 From local threat to global concern due to travel
and vector adaptability
Bangladesh –
Epidemiology
• First cases in Rajshahi & Chapainawabganj (2008)
• Outbreaks: Dhaka (2011), Tangail (2012)
• 2017: >13,000 cases across 17 districts
• Likely underreported (limited diagnostics)
• Surges during monsoon and Eid travel
• 2024 resurgence in Dhaka = ⚠️New wave brewing
• ️
🌧️When it rains, it spreads
The Silent Surge
•⚠️Surge in Dhaka: 337 confirmed cases (Jan–
May 2025)
•🚨 Chattogram spike: 984 cases (Jun–Jul); Aedes
larvae found in 50% homes
Clinical
Presentation
• Incubation period: 3-7 days.
(1-12 days).
• Viremia lasts 5-7 days
(diagnostic window)
• Majority of infected
individuals become
symptomatic.
Clinical features of Chikungunya fever
Common Infrequent Rare in adults but seen
in
children
Fever
Arthritis/ Arthralgia
Backache
Headache
Rash
Stomatitis
Oral ulcers
Exfoliative dermatitis
Photosensitive
hyperpigmentation
Photophobia
Retro-orbital pain
Vomiting
Diarrhoea
Mental confusion
Signs of meningeal
irritation
Phases
Three primary clinical
presentations of the
disease:
Acute Phase-0–10 days
Subacute-11–90 days
Chronic->90 days (3
months)
Clinical Presentation
Acute Phase
• Sudden high-grade fever (>39°C)
• Symmetric polyarthralgia/arthritis – wrists, hands, ankles, knees
• Maculopapular rash in ~50% (appears a few days after fever)
• Myalgia, headache, conjunctivitis, eye pain, photophobia
• GI symptoms: nausea, vomiting, diarrhea (more in children)
• Rare: Neurological signs – encephalitis, Guillain-Barré syndrome
Subacute
Phase
•Persistent joint pain &
stiffness, esp. in previously
affected joints
•Morning stiffness, reduced
range of motion
•Fatigue, myalgia, emotional
changes (low mood, irritability)
•Inflammatory arthritis (RA-like)
•Skin & hair changes:
Hyperpigmentation, alopecia
Chronic Phase
(Virus-Free but
Still in Pain)
•Occurs in 30–40% of patients
•Joints: Chronic arthritis, synovitis,
osteoarthritis
•Tendons: Tendinitis, tenosynovitis
•Other: Neuropathic pain, stiffness,
postural hypotension
•Psychological: Mood disorders, loss of
physical fitness
•Women Are More Affected
Severe or Atypical presentations
High-risk Populations
• Elderly (>65yrs )
• Infants (Neuro-invasive risks)
• Pregnant Women (vertical transmission)
• People with comorbidities (HTN, DM, CAD, COPD,
CVD)
• Co-Infection: Dengue, HIV, Malaria
Rashes
•Typically appears 2–5 days after fever onset
•Often maculopapular, widespread on trunk,
limbs, face
•May be itchy, non-blanching, and sometimes
accompanied by hyperpigmentation
•More common in children and young adults
•May be transient or persist for several days
CHIKV Arthropathy
•Seen in up to 90% of symptomatic
patients; worse in the morning, improves
with movement
•Pain may follow a saddle-back pattern
(initial relief followed by relapse)
•Often affects previously injured joints
•Stooped posture common due to back
and limb pain
•Large joints (e.g., knees, shoulders)
may show swelling or effusion
•Locally known as "Langra Jor (ল্যাংড়া
জ্বর)", mimicking seronegative RA
RA CHIKV Arthritis
Onset Gradual Acute
Joint Involvement ALL Peripheral >
Central
Spine Cervical LS Spine
Erosions ++ -
Limb Oedema + ++
Diagnostic Approaches
• Goal: Early detection, rule out differentials, confirm ChikV
Clinical features: Fever ≥38.5°C, severe arthralgia/arthritis
• Epidemiological link: Travel to/residence in epidemic zone
within 15 days
• Laboratory confirmation: PCR / Serology
• Key differential exclusion: Dengue, malaria, COVID-19, other
alphaviruses
Investigations
•Select tests based on
timing for accuracy.
•Combine methods in
borderline or late
presentations.
•Always retest 5–7 days
after initial negative if
clinical suspicion remains
high
Time Since
Symptom
Onset
Recommende
d Test
Days 1–7 RT-PCR, Viral
Isolation
Days 5–14 IgM ELISA ±
RT-PCR
>Day 14 IgG serology
(paired
samples)
PCR
• Effective during the acute phase of
infection (within 8 days of symptom
onset)
• Samples can be taken from blood,
cerebrospinal fluid (CSF), or tissue
• After 8 days of symptom onset – viremia
usually resolves, reducing test sensitivity
Serology
•IgM: Becomes detectable around Day
5 and persists for several weeks
•IgG: Emerges approximately by Day
10 and remains for an extended period
Diagnostic criteria include:
•Presence of IgM along with symptoms
•OR a fourfold increase in IgG levels
between paired samples
Basic Laboratory Tests
TEST ABNORMALITY CLINICAL NOTES
CBC (Complete
Blood Count)
- Leukopenia (low
WBC count)
- Lymphopenia
- Thrombocytopenia
(mild or absent)
Mild drop in platelets
but rarely reaches
Dengue-level severity.
ESR/CRP Elevated Suggests systemic
inflammation; helpful in
persistent arthritis.
Liver Function
Test (LFT)
- Elevated ALT/AST Mild hepatic
involvement, more
common in adults.
Creatinine/Urea
Normal or mildy
raised
In rare severe or renal
cases, elevation may
occur.
Urine R/M/E Normal Unless nephritis
 Clinical Criteria
• Acute fever ≥ 38.5°C (101.3°F)
• Severe arthralgia or arthritis
 Epidemiological Criteria
• Travel or residence in
epidemic area
• Within 15 days before
symptom onset
 Laboratory Criteria
• RT-PCR or viral isolation
(BSL3)
• IgM detection + positive
neutralization
• IgG: 4-fold rise in paired sera
(14 days apart)
Case Definitions:
 Possible Case: Clinical +
exposure history, no
alternative diagnosis
 Probable Case: Clinical +
epidemiological match
 Confirmed Case: Positive
lab result regardless of
symptoms
General Principles of Treatment
• Chikungunya is a self-limiting viral illness.
• No targeted antiviral therapy is currently available.
• Most patients recover within 7–10 days, but joint pain
may persist.
• ✅ Key Focus: Symptomatic relief, prevention of
complications, and follow-up for chronic symptoms.
Acute Phase Management
•Supportive Care: Focus on rest and symptom relief.
•Fever Control: Paracetamol 500–1000 mg every 6 hrs. Avoid
NSAIDs early to rule out dengue.
•Pain Management:Paracetamol for mild cases; add Tramadol or
low-dose NSAID if pain is moderate–severe, only after ruling out
dengue.
•Hydration: Encourage ORS and adequate fluid intake.
•Monitor for Red Flags: Shock, bleeding, neurological
symptoms, hepatitis, or myocarditis.
Subacute Phase Management
• Common Issues: Persistent joint pain, stiffness, arthritis-like
symptoms
• NSAIDs (e.g., naproxen, diclofenac) initiated if dengue
excluded
• Short course of steroids (e.g., prednisolone 10–15 mg/day for
5–10 days) in:
– Severe polyarthritis
– Refractory synovitis
• Supportive Care: Physiotherapy, mental health monitoring, and
psychosocial support (especially in elderly or chronic cases)
Chronic Phase Management
•NSAIDs as needed with safety monitoring
•Low-dose corticosteroids for persistent inflammation
•DMARDs (e.g., methotrexate) in autoimmune arthritis (refer
specialist), Biologics-Etanercept, Infliximab
•Psychological support or antidepressants for mood
symptoms
•Rehabilitation: Graded physiotherapy and occupational
therapy
When to
Start
DMARDs
•Chronic arthritis ≥ 3 months
•Symptoms mimicking rheumatoid arthritis
•Inadequate response to NSAIDs and
corticosteroids
•Presence of synovitis, joint erosion, or
deformity
•Biologics are not first-line in post-viral arthritis
Reserved for
➤ severe, persistent, disabling
arthritis mimicking RA
Initiation requires
➤ rheumatologist’s
evaluation and decision
Prevention is Essential!
• No vaccine available for general population.
• Patients with viremia should avoid mosquito
bites
→ to prevent spread to Aedes mosquitoes.
• ✅ Prevention Measures:
• Use EPA-approved repellents (e.g., DEET,
permethrin-treated clothing)
• Wear long-sleeved clothes & trousers
• Eliminate mosquito breeding sites (stagnant
water)
Chikungunya Vaccine Update
(2024)
 VLA1553 (IXCHIQ™) – Valneva’s live-
attenuated, single-dose vaccine
• ✅ FDA-approved (Nov 2023) for adults ≥18
years
• Efficacy: 98.9% at Day 28, 96.3% at 6
months
• Placebo trial: 98.9% vs. 0% seroconversion
• ➕ Strong safety & durable immunity
 CHIKV-VLP – Emergent’s virus-like particle
vaccine
• In advanced Phase 3; may benefit
elderly/immunocompromised
Prognosis
Mortality is very
low (~0.1%), mainly
in elderly/comorbid
patients
Most recover within
1–2 weeks of acute
illness
30–40% may
develop persistent
joint pain or
arthritis-like
symptoms
Risk of chronic
arthritis ↑ in older
adults, women, and
those with rheumatic
disease
Rare
neurological/cardia
c complications
may occur
With proper care,
long-term outcome
is favorable, but
recovery can take
months to years
Reinfection with CHIKV
•Usually occurs only once due to strong
immune memory
•Infection triggers lifelong immunity via
neutralizing antibodies
•Reinfection is extremely rare, but may
occur with:
•Different viral strain
•Immunocompromised state
•Incomplete immunity
•➤ No large-scale reinfection outbreaks
have been reported
Take-Home Message
•Chikungunya is a mosquito-borne viral illness.
•Presents with sudden fever, rash, headache, and severe
joint pain.
•Chronic joint pain may persist for months or years.
•Always rule out dengue before initiating treatment.
•It is a self-limiting disease; supportive care is essential.
•Prevention through mosquito control is crucial.
Reference
•World Health Organization (WHO). Guidelines on Clinical Management
of Chikungunya Virus Infection, 2023–2024. Available at:
https://www.who.int
•Directorate General of Health Services (DGHS), Bangladesh. National
Guideline for Clinical Management of Chikungunya Fever. Dhaka: Ministry
of Health and Family Welfare, Bangladesh; 2024.
•Sharif AR, Dey SK, Rahman MS, et al. Molecular characterization of
Chikungunya virus during the 2017 outbreak in Dhaka, Bangladesh. Int J
Infect Dis. 2019;87:36–37. doi:10.1016/j.ijid.2019.08.100
•Harrison’s Principles of Internal Medicine (21st ed.)
Chapter: Arboviruses
•Oxford Handbook of Tropical Medicine (5th ed.)
•Centers for Disease Control and Prevention (CDC). Chikungunya Virus:
Clinical & Laboratory Evaluation. Yellow Book 2024. Available at:
https://www.cdc.gov/chikungunya
THANK YOU
Feature Chikungunya Zika
Fever (>38.5°C) +++ +
Arthralgia +++ (severe, disabling) + (mild to moderate)
Arthritis + -
Rash ++ (maculopapular) +++ (maculopapular)
Headache ++ +
Myalgia + +
Conjunctivitis - ++ (non-purulent)
Neurological symptoms Rare Possible (e.g., GBS)
Hemorrhage +/- -
Thrombocytopenia + Rare
Lymphopenia +++ +
Vertical transmission Rare Reported
Microcephaly risk No Yes (congenital)
Sub-Acute Arthritic Phase (2 Weeks–3 Months)
• Focus: Control inflammation, prevent chronicity
• PCM ± weak opioids for pain control
• Prednisolone 10–15 mg/day, taper over 8–12 weeks
• Gabapentin for persistent neuropathic symptoms
• Use VAS scale for pain monitoring
• Avoid NSAIDs while on steroids; no DMARDs yet
Chronic Phase (>3 Months)
• Focus: Prevent joint damage, long-term care
• Refer to Rheumatology for evaluation
• Use DMARDs: MTX, HCQ, Leflunomide
• ± low-dose steroids if symptoms persist
• Add physiotherapy, occupational therapy, joint
support
• Combination DMARDs preferred if severe arthritis
Viral Lineage
•There are three primary lineages: West African, Asian, and
ECSA.
•The Indian Ocean Lineage (IOL) is a highly virulent sub-
lineage within ECSA.
•It first appeared during the Réunion outbreak (2005–06).
•The Bangladesh outbreaks (2017, 2024) have been
associated with ECSA-IOL.
•It is effectively transmitted by Aedes albopictus
mosquitoes.
•Infection leads to severe joint pain and extended
arthralgia.
Newborns & Infants
• Clinical Presentation (3–7 days after birth):
• Fever, rash, poor feeding, lethargy, irritability.
• Limb edema, cyanosis, hyperalgesia.
• Neurological signs: seizures, encephalopathy, hypotonia.
• Rare: Myocarditis, hepatitis, coagulopathy.
• Prognosis:
• Most recover, but long-term neurodevelopmental delay
reported in severe neonatal cases.
• Close pediatric follow-up essential.
Chikungunya in Pregnancy
•Maternal Risk:
•Chikungunya is usually not more severe in pregnant women.
•Most cases are self-limiting, similar to non-pregnant adults.
•Vertical Transmission:
•Risk is highest when maternal infection occurs near delivery.
•Transmission is mainly intrapartum; rarely transplacental.
• No evidence of teratogenicity or fetal malformations.
Neonatal Outcomes:
• Infected neonates may develop encephalopathy, seizures, or
multi-organ involvement.
• Symptoms typically start 3–7 days after birth.
Feature Dengue Chikungunya
Onset
Usually 3–6 days after fever
onset
Appears 2–5 days after fever
onset
Type
Maculopapular or
petechial; may include
purpura
Maculopapular, morbilliform
(measles-like), or
scarlatiniform
Distribution Trunk, face, and
extremities
Mainly trunk and limbs, may
involve palms/soles
Itching Often absent or mild Frequently intensely itchy
Associated Signs "White islands in a sea of
red" (classic sign)
Rash may desquamate (peel
off) during recovery
Duration 2–3 days, self-limiting 3–7 days, sometimes
recurring

Chikungunya gudeilines 2023 based on recent avances

  • 1.
    Beyond Fever, Rash,Joint Pain Dr Seebat Masrur FCPS Part 2 Trainee(Cardiology)
  • 2.
    Case Scenario • A32-year-old woman presents to the emergency department with • Sudden onset high-grade fever (103°F), headache, and severe joint pain in wrists and ankles for 3 days. • Mild maculopapular rash over trunk and limbs • Recent travel history Dhaka 10 days prior
  • 3.
    Is this denguefever, or could it be something else? Initial Investigations: • CBC: Mild lymphopenia, mild thrombocytopenia (platelets ~130,000/µL) • NS1 antigen test for dengue: Negative • IgM for dengue: Negative but IgG Negative • Liver function tests: Mildly elevated ALT/AST What else could present similarly if dengue is excluded?
  • 4.
    Chikungunya Virus • Asingle-stranded RNA virus. • Belongs to the Alphavirus genus within the Togaviridae family. • Initially isolated from human serum in Tanzania in 1952, Chikungunya had, by 2004, spread across Africa, India, and Southeast Asia, causing significant sporadic epidemics. • There are three primary lineages: West African, Asian, and ECSA. • The name derives from the Kimakonde language, meaning "to become contorted," a reference to the characteristic joint pain posture.
  • 5.
    Transmission Transmits Chikungunya, dengue,Zika, and yellow fever. Humans serve as the main reservoir of infection. Active daytime painless biters with black-white striped markings. Lays eggs in tiny water-holding containers. Eggs can withstand dryness for 6–8 months.
  • 6.
    • Blood-borne transmissionis possible • Rarely, vertical transmission during pregnancy • No direct human-to-human transmission reported • Outbreaks fuelled by urbanization, travel, and vector expansion.
  • 7.
    Global History & Spread • Firstdetected: Tanzania, 1952 • Reached Asia via Thailand (1958) → Endemic in India, Sri Lanka, SE Asia • Spread to Europe (Italy, 2007) – local transmission • Landed in the Americas (2013) → Rapid spread across South America • Major outbreaks: Réunion (2005–06), India (2006), Italy (2007, 2017) • 🔄 From local threat to global concern due to travel and vector adaptability
  • 8.
    Bangladesh – Epidemiology • Firstcases in Rajshahi & Chapainawabganj (2008) • Outbreaks: Dhaka (2011), Tangail (2012) • 2017: >13,000 cases across 17 districts • Likely underreported (limited diagnostics) • Surges during monsoon and Eid travel • 2024 resurgence in Dhaka = ⚠️New wave brewing • ️ 🌧️When it rains, it spreads
  • 9.
    The Silent Surge •⚠️Surgein Dhaka: 337 confirmed cases (Jan– May 2025) •🚨 Chattogram spike: 984 cases (Jun–Jul); Aedes larvae found in 50% homes
  • 10.
    Clinical Presentation • Incubation period:3-7 days. (1-12 days). • Viremia lasts 5-7 days (diagnostic window) • Majority of infected individuals become symptomatic.
  • 11.
    Clinical features ofChikungunya fever Common Infrequent Rare in adults but seen in children Fever Arthritis/ Arthralgia Backache Headache Rash Stomatitis Oral ulcers Exfoliative dermatitis Photosensitive hyperpigmentation Photophobia Retro-orbital pain Vomiting Diarrhoea Mental confusion Signs of meningeal irritation
  • 12.
    Phases Three primary clinical presentationsof the disease: Acute Phase-0–10 days Subacute-11–90 days Chronic->90 days (3 months)
  • 13.
    Clinical Presentation Acute Phase •Sudden high-grade fever (>39°C) • Symmetric polyarthralgia/arthritis – wrists, hands, ankles, knees • Maculopapular rash in ~50% (appears a few days after fever) • Myalgia, headache, conjunctivitis, eye pain, photophobia • GI symptoms: nausea, vomiting, diarrhea (more in children) • Rare: Neurological signs – encephalitis, Guillain-Barré syndrome
  • 14.
    Subacute Phase •Persistent joint pain& stiffness, esp. in previously affected joints •Morning stiffness, reduced range of motion •Fatigue, myalgia, emotional changes (low mood, irritability) •Inflammatory arthritis (RA-like) •Skin & hair changes: Hyperpigmentation, alopecia
  • 15.
    Chronic Phase (Virus-Free but Stillin Pain) •Occurs in 30–40% of patients •Joints: Chronic arthritis, synovitis, osteoarthritis •Tendons: Tendinitis, tenosynovitis •Other: Neuropathic pain, stiffness, postural hypotension •Psychological: Mood disorders, loss of physical fitness •Women Are More Affected
  • 16.
    Severe or Atypicalpresentations
  • 17.
    High-risk Populations • Elderly(>65yrs ) • Infants (Neuro-invasive risks) • Pregnant Women (vertical transmission) • People with comorbidities (HTN, DM, CAD, COPD, CVD) • Co-Infection: Dengue, HIV, Malaria
  • 18.
    Rashes •Typically appears 2–5days after fever onset •Often maculopapular, widespread on trunk, limbs, face •May be itchy, non-blanching, and sometimes accompanied by hyperpigmentation •More common in children and young adults •May be transient or persist for several days
  • 19.
    CHIKV Arthropathy •Seen inup to 90% of symptomatic patients; worse in the morning, improves with movement •Pain may follow a saddle-back pattern (initial relief followed by relapse) •Often affects previously injured joints •Stooped posture common due to back and limb pain •Large joints (e.g., knees, shoulders) may show swelling or effusion •Locally known as "Langra Jor (ল্যাংড়া জ্বর)", mimicking seronegative RA
  • 20.
    RA CHIKV Arthritis OnsetGradual Acute Joint Involvement ALL Peripheral > Central Spine Cervical LS Spine Erosions ++ - Limb Oedema + ++
  • 21.
    Diagnostic Approaches • Goal:Early detection, rule out differentials, confirm ChikV Clinical features: Fever ≥38.5°C, severe arthralgia/arthritis • Epidemiological link: Travel to/residence in epidemic zone within 15 days • Laboratory confirmation: PCR / Serology • Key differential exclusion: Dengue, malaria, COVID-19, other alphaviruses
  • 22.
    Investigations •Select tests basedon timing for accuracy. •Combine methods in borderline or late presentations. •Always retest 5–7 days after initial negative if clinical suspicion remains high Time Since Symptom Onset Recommende d Test Days 1–7 RT-PCR, Viral Isolation Days 5–14 IgM ELISA ± RT-PCR >Day 14 IgG serology (paired samples)
  • 23.
    PCR • Effective duringthe acute phase of infection (within 8 days of symptom onset) • Samples can be taken from blood, cerebrospinal fluid (CSF), or tissue • After 8 days of symptom onset – viremia usually resolves, reducing test sensitivity
  • 24.
    Serology •IgM: Becomes detectablearound Day 5 and persists for several weeks •IgG: Emerges approximately by Day 10 and remains for an extended period Diagnostic criteria include: •Presence of IgM along with symptoms •OR a fourfold increase in IgG levels between paired samples
  • 25.
    Basic Laboratory Tests TESTABNORMALITY CLINICAL NOTES CBC (Complete Blood Count) - Leukopenia (low WBC count) - Lymphopenia - Thrombocytopenia (mild or absent) Mild drop in platelets but rarely reaches Dengue-level severity. ESR/CRP Elevated Suggests systemic inflammation; helpful in persistent arthritis. Liver Function Test (LFT) - Elevated ALT/AST Mild hepatic involvement, more common in adults. Creatinine/Urea Normal or mildy raised In rare severe or renal cases, elevation may occur. Urine R/M/E Normal Unless nephritis
  • 27.
     Clinical Criteria •Acute fever ≥ 38.5°C (101.3°F) • Severe arthralgia or arthritis  Epidemiological Criteria • Travel or residence in epidemic area • Within 15 days before symptom onset  Laboratory Criteria • RT-PCR or viral isolation (BSL3) • IgM detection + positive neutralization • IgG: 4-fold rise in paired sera (14 days apart) Case Definitions:  Possible Case: Clinical + exposure history, no alternative diagnosis  Probable Case: Clinical + epidemiological match  Confirmed Case: Positive lab result regardless of symptoms
  • 28.
    General Principles ofTreatment • Chikungunya is a self-limiting viral illness. • No targeted antiviral therapy is currently available. • Most patients recover within 7–10 days, but joint pain may persist. • ✅ Key Focus: Symptomatic relief, prevention of complications, and follow-up for chronic symptoms.
  • 29.
    Acute Phase Management •SupportiveCare: Focus on rest and symptom relief. •Fever Control: Paracetamol 500–1000 mg every 6 hrs. Avoid NSAIDs early to rule out dengue. •Pain Management:Paracetamol for mild cases; add Tramadol or low-dose NSAID if pain is moderate–severe, only after ruling out dengue. •Hydration: Encourage ORS and adequate fluid intake. •Monitor for Red Flags: Shock, bleeding, neurological symptoms, hepatitis, or myocarditis.
  • 30.
    Subacute Phase Management •Common Issues: Persistent joint pain, stiffness, arthritis-like symptoms • NSAIDs (e.g., naproxen, diclofenac) initiated if dengue excluded • Short course of steroids (e.g., prednisolone 10–15 mg/day for 5–10 days) in: – Severe polyarthritis – Refractory synovitis • Supportive Care: Physiotherapy, mental health monitoring, and psychosocial support (especially in elderly or chronic cases)
  • 31.
    Chronic Phase Management •NSAIDsas needed with safety monitoring •Low-dose corticosteroids for persistent inflammation •DMARDs (e.g., methotrexate) in autoimmune arthritis (refer specialist), Biologics-Etanercept, Infliximab •Psychological support or antidepressants for mood symptoms •Rehabilitation: Graded physiotherapy and occupational therapy
  • 32.
    When to Start DMARDs •Chronic arthritis≥ 3 months •Symptoms mimicking rheumatoid arthritis •Inadequate response to NSAIDs and corticosteroids •Presence of synovitis, joint erosion, or deformity •Biologics are not first-line in post-viral arthritis Reserved for ➤ severe, persistent, disabling arthritis mimicking RA Initiation requires ➤ rheumatologist’s evaluation and decision
  • 33.
    Prevention is Essential! •No vaccine available for general population. • Patients with viremia should avoid mosquito bites → to prevent spread to Aedes mosquitoes. • ✅ Prevention Measures: • Use EPA-approved repellents (e.g., DEET, permethrin-treated clothing) • Wear long-sleeved clothes & trousers • Eliminate mosquito breeding sites (stagnant water)
  • 34.
    Chikungunya Vaccine Update (2024) VLA1553 (IXCHIQ™) – Valneva’s live- attenuated, single-dose vaccine • ✅ FDA-approved (Nov 2023) for adults ≥18 years • Efficacy: 98.9% at Day 28, 96.3% at 6 months • Placebo trial: 98.9% vs. 0% seroconversion • ➕ Strong safety & durable immunity  CHIKV-VLP – Emergent’s virus-like particle vaccine • In advanced Phase 3; may benefit elderly/immunocompromised
  • 35.
    Prognosis Mortality is very low(~0.1%), mainly in elderly/comorbid patients Most recover within 1–2 weeks of acute illness 30–40% may develop persistent joint pain or arthritis-like symptoms Risk of chronic arthritis ↑ in older adults, women, and those with rheumatic disease Rare neurological/cardia c complications may occur With proper care, long-term outcome is favorable, but recovery can take months to years
  • 36.
    Reinfection with CHIKV •Usuallyoccurs only once due to strong immune memory •Infection triggers lifelong immunity via neutralizing antibodies •Reinfection is extremely rare, but may occur with: •Different viral strain •Immunocompromised state •Incomplete immunity •➤ No large-scale reinfection outbreaks have been reported
  • 37.
    Take-Home Message •Chikungunya isa mosquito-borne viral illness. •Presents with sudden fever, rash, headache, and severe joint pain. •Chronic joint pain may persist for months or years. •Always rule out dengue before initiating treatment. •It is a self-limiting disease; supportive care is essential. •Prevention through mosquito control is crucial.
  • 38.
    Reference •World Health Organization(WHO). Guidelines on Clinical Management of Chikungunya Virus Infection, 2023–2024. Available at: https://www.who.int •Directorate General of Health Services (DGHS), Bangladesh. National Guideline for Clinical Management of Chikungunya Fever. Dhaka: Ministry of Health and Family Welfare, Bangladesh; 2024. •Sharif AR, Dey SK, Rahman MS, et al. Molecular characterization of Chikungunya virus during the 2017 outbreak in Dhaka, Bangladesh. Int J Infect Dis. 2019;87:36–37. doi:10.1016/j.ijid.2019.08.100 •Harrison’s Principles of Internal Medicine (21st ed.) Chapter: Arboviruses •Oxford Handbook of Tropical Medicine (5th ed.) •Centers for Disease Control and Prevention (CDC). Chikungunya Virus: Clinical & Laboratory Evaluation. Yellow Book 2024. Available at: https://www.cdc.gov/chikungunya
  • 39.
  • 41.
    Feature Chikungunya Zika Fever(>38.5°C) +++ + Arthralgia +++ (severe, disabling) + (mild to moderate) Arthritis + - Rash ++ (maculopapular) +++ (maculopapular) Headache ++ + Myalgia + + Conjunctivitis - ++ (non-purulent) Neurological symptoms Rare Possible (e.g., GBS) Hemorrhage +/- - Thrombocytopenia + Rare Lymphopenia +++ + Vertical transmission Rare Reported Microcephaly risk No Yes (congenital)
  • 42.
    Sub-Acute Arthritic Phase(2 Weeks–3 Months) • Focus: Control inflammation, prevent chronicity • PCM ± weak opioids for pain control • Prednisolone 10–15 mg/day, taper over 8–12 weeks • Gabapentin for persistent neuropathic symptoms • Use VAS scale for pain monitoring • Avoid NSAIDs while on steroids; no DMARDs yet
  • 43.
    Chronic Phase (>3Months) • Focus: Prevent joint damage, long-term care • Refer to Rheumatology for evaluation • Use DMARDs: MTX, HCQ, Leflunomide • ± low-dose steroids if symptoms persist • Add physiotherapy, occupational therapy, joint support • Combination DMARDs preferred if severe arthritis
  • 44.
    Viral Lineage •There arethree primary lineages: West African, Asian, and ECSA. •The Indian Ocean Lineage (IOL) is a highly virulent sub- lineage within ECSA. •It first appeared during the Réunion outbreak (2005–06). •The Bangladesh outbreaks (2017, 2024) have been associated with ECSA-IOL. •It is effectively transmitted by Aedes albopictus mosquitoes. •Infection leads to severe joint pain and extended arthralgia.
  • 45.
    Newborns & Infants •Clinical Presentation (3–7 days after birth): • Fever, rash, poor feeding, lethargy, irritability. • Limb edema, cyanosis, hyperalgesia. • Neurological signs: seizures, encephalopathy, hypotonia. • Rare: Myocarditis, hepatitis, coagulopathy. • Prognosis: • Most recover, but long-term neurodevelopmental delay reported in severe neonatal cases. • Close pediatric follow-up essential.
  • 46.
    Chikungunya in Pregnancy •MaternalRisk: •Chikungunya is usually not more severe in pregnant women. •Most cases are self-limiting, similar to non-pregnant adults. •Vertical Transmission: •Risk is highest when maternal infection occurs near delivery. •Transmission is mainly intrapartum; rarely transplacental. • No evidence of teratogenicity or fetal malformations. Neonatal Outcomes: • Infected neonates may develop encephalopathy, seizures, or multi-organ involvement. • Symptoms typically start 3–7 days after birth.
  • 47.
    Feature Dengue Chikungunya Onset Usually3–6 days after fever onset Appears 2–5 days after fever onset Type Maculopapular or petechial; may include purpura Maculopapular, morbilliform (measles-like), or scarlatiniform Distribution Trunk, face, and extremities Mainly trunk and limbs, may involve palms/soles Itching Often absent or mild Frequently intensely itchy Associated Signs "White islands in a sea of red" (classic sign) Rash may desquamate (peel off) during recovery Duration 2–3 days, self-limiting 3–7 days, sometimes recurring

Editor's Notes

  • #12 The disease is self-limiting. The disease is a complex spectrum varied from typical, atypical and severe disease. The co-morbidities or co-infections may modify the clinical spectrum and even death. The genetic background may change the clinical picture.