Write a short note on chikungunya.
Aetiology
Chikungunya is caused by the chikungunya virus (CHIKV), a single-stranded RNA alphavirus of the Togaviridae family, transmitted by the daytime-biting *Aedes aegypti* and *Aedes albopictus* mosquitoes — the same vectors as dengue, which is why the two frequently co-circulate and co-infect.
The name derives from a Makonde word meaning "that which bends up", describing the stooped posture of patients crippled by joint pain. India has experienced large epidemics since the major resurgence of 2005–06, and the disease is now endemic with recurrent outbreaks, particularly post-monsoon.
Incubation: 2–7 days (range 1–12).
Pathogenesis
The virus replicates in skin fibroblasts and disseminates to muscle, joints, liver and lymphoid tissue, causing a vigorous innate immune and interferon response. Persistent viral antigen and RNA within joint tissue and macrophages, together with an ongoing inflammatory response, is thought to underlie the prolonged arthritis that characterises this infection and distinguishes it from dengue.
Clinical Features
Acute phase (first 1–2 weeks):
- Abrupt high fever — typically sudden in onset, lasting 3–7 days.
- SEVERE, SYMMETRICAL, INCAPACITATING POLYARTHRALGIA — the hallmark. It affects small joints of the hands, wrists, ankles and feet predominantly, is often bilateral, and is frequently so severe that the patient cannot walk, hold objects or stand upright — hence the "bent-up" posture. Frank arthritis with swelling occurs in a substantial proportion.
- Rash — maculopapular, on the trunk and limbs, sometimes with intense pruritus; hyperpigmentation, particularly of the nose ("chik sign") and centrofacial region, is characteristic and may persist.
- Headache, myalgia, backache, fatigue, conjunctivitis, nausea.
- Haemorrhagic manifestations are uncommon and mild — an important contrast with dengue.
Subacute and chronic phase:
- Persistent or relapsing polyarthralgia and arthritis lasting months to YEARS in up to 30–50% — the most important long-term consequence. It is symmetrical, involves small joints, and may closely mimic rheumatoid arthritis, but is seronegative and non-erosive. Morning stiffness, tenosynovitis and Raynaud's phenomenon may occur.
- Fatigue and depression are common.
Severe and atypical disease (in neonates, the elderly and those with comorbidity): encephalitis, myelitis, Guillain–Barré syndrome, myocarditis, hepatitis, acute kidney injury, and bullous skin lesions in infants. Vertical transmission around the time of delivery can cause severe neonatal disease.
CHIKUNGUNYA versus DENGUE — A KEY DIFFERENTIATION
| Feature | Chikungunya | Dengue |
|---|---|---|
| Joint pain | SEVERE, symmetrical, small joints; often persists for months | Aching myalgia and arthralgia; transient |
| Arthritis (swelling) | Common | Rare |
| Fever | High, abrupt, shorter | High, may be biphasic |
| Retro-orbital pain | Less prominent | Prominent |
| Haemorrhage / plasma leak | Rare and mild | Characteristic — the cause of death |
| Shock | Rare | Dengue shock syndrome |
| Platelets | Normal or mildly reduced | Marked thrombocytopenia |
| Leucocytes | Lymphopenia | Leucopenia |
| Rash | Common, may leave pigmentation | Common; "isles of white in a sea of red" in recovery |
| Mortality | Low | Higher, from plasma leakage |
Both may co-infect the same patient, and when in doubt, manage as dengue, since dengue carries the risk of shock and requires the more careful fluid monitoring.
Investigations
- RT-PCR — the test of choice in the first 5–7 days, when viraemia is present.
- IgM ELISA — positive from about day 5, persisting for months.
- IgG — rising titres in paired sera; indicates past infection.
- Test for dengue simultaneously — NS1 antigen and IgM — because co-infection and clinical overlap are common.
- Supporting: lymphopenia (characteristic), mild thrombocytopenia, raised ESR and CRP, mildly raised transaminases. Rheumatoid factor and anti-CCP are negative, which helps distinguish chronic chikungunya arthritis from rheumatoid arthritis.
Management
There is no specific antiviral treatment; management is symptomatic.
Acute phase:
- Rest, adequate oral fluids and hydration.
- Paracetamol for fever and pain.
- AVOID aspirin and NSAIDs until dengue has been reliably excluded — because if the illness is dengue, they increase bleeding risk. Once dengue is excluded, NSAIDs are the mainstay for the joint pain and are considerably more effective than paracetamol alone.
- Cold compresses and gentle mobilisation for joint pain.
Subacute and chronic arthritis:
- NSAIDs as first-line.
- Short courses of corticosteroids for severe persistent inflammatory arthritis unresponsive to NSAIDs.
- Hydroxychloroquine, sulfasalazine or methotrexate for prolonged, disabling, rheumatoid-like disease, managed with rheumatology input.
- Physiotherapy and graded exercise — important and often neglected; maintains joint range and function.
- Patient education about the expected duration, since the persistence of symptoms causes considerable anxiety and repeated investigation.
Prevention
Identical to dengue, and the two programmes are the same: source reduction of *Aedes* breeding sites (domestic water containers, coolers, tyres, discarded receptacles), weekly "dry day" practices, larvicides, personal protection with repellents and full-sleeved clothing (noting the daytime biting habit, so bed nets alone are insufficient), and community participation. Isolate viraemic patients under bed nets during the first week to prevent onward transmission. There is no widely deployed vaccine.
The joint pain is what separates chikungunya from dengue, and it is what persists. In an epidemic setting, a patient with fever and severe symmetrical small-joint pain with swelling has chikungunya; a patient with fever, retro-orbital pain, marked thrombocytopenia and rising haematocrit has dengue. And when a patient presents months later with a seronegative symmetrical polyarthritis after a febrile illness, take an epidemic and travel history — post-chikungunya arthritis is repeatedly misdiagnosed as new-onset rheumatoid arthritis and treated accordingly.
All questions in Infectious Diseases
- Q1Discuss the pathogenesis, clinical features, warning signs, investigations and management of dengue fever. ★
- Q2Discuss the clinical features, complications, investigations and management of severe malaria, including cerebral malaria. ★
- SN1Write a short note on typhoid (enteric) fever.
- SN2Write a short note on COVID-19 and pandemic influenza (H1N1).
- SN3Write a short note on sexually transmitted infections — gonorrhoea and human papillomavirus.
- SN4Write a short note on adult immunisation.
- SN5Write a short note on food poisoning.
- SN6Write a short note on febrile neutropenia.
- SN7Write a short note on varicella (chickenpox) and herpes zoster.
- SN8Write a short note on viral haemorrhagic fevers, including Ebola virus disease.
- SN9Write a short note on leptospirosis.
- SN10Write a short note on scrub typhus and other rickettsial infections.
- SN11Write a short note on visceral leishmaniasis (kala-azar).
- SN12Write a short note on brucellosis.
- SN13Write a short note on rabies, including post-exposure prophylaxis.
- SN14Write a short note on antitubercular therapy, including multidrug-resistant tuberculosis.
- SN15Write a short note on lymphatic filariasis.
- SN16Write a short note on neurocysticercosis.
- SN17Write a short note on chikungunya.