Overview

Definition:
-Fever in a child who has recently returned from an endemic area is a medical emergency and strongly suggestive of malaria until proven otherwise, regardless of chemoprophylaxis use
-Malaria is a life-threatening parasitic disease transmitted by infected Anopheles mosquitoes.
Epidemiology:
-Malaria is endemic in over 90 countries
-Children, especially those under five years, are disproportionately affected and have higher morbidity and mortality
-In India, malaria remains a significant public health problem, particularly in endemic states.
Clinical Significance:
-Delayed diagnosis and treatment of malaria in returning pediatric travelers can lead to severe complications including cerebral malaria, severe anemia, acute respiratory distress syndrome (ARDS), renal failure, and death
-Prompt and accurate testing is paramount for timely intervention.

Clinical Presentation

Symptoms:
-Fever, often high and cyclical
-Chills and rigors
-Profuse sweating
-Headache
-Malaise
-Myalgias
-Nausea and vomiting
-Diarrhea
-Abdominal pain
-Pallor
-Jaundice may develop
-In severe cases: altered mental status, seizures, difficulty breathing, oliguria.
Signs:
-Fever (>37.5°C)
-Tachycardia
-Tachypnea
-Pallor
-Jaundice
-Hepatosplenomegaly
-Signs of dehydration
-Signs of shock
-Neurological deficits (e.g., lethargy, coma) in severe malaria.
Diagnostic Criteria: No specific diagnostic criteria for malaria in returning travelers exist beyond the clinical suspicion combined with a travel history to an endemic region and subsequent laboratory confirmation of Plasmodium parasites.

Diagnostic Approach

History Taking:
-Detailed travel history: destination country/region, duration of stay, dates of travel, activities undertaken (e.g., outdoor exposure, sleeping arrangements), use of malaria chemoprophylaxis (drug, adherence, adverse effects), previous malaria episodes
-Symptom onset and progression
-Febrile pattern
-Any associated symptoms.
Physical Examination:
-General appearance: assess for distress, dehydration, shock
-Vital signs: temperature, pulse, respiratory rate, blood pressure
-Full systemic examination, focusing on: neurological status (GCS), respiratory system (breath sounds), cardiovascular system (heart sounds, perfusion), abdominal examination (hepatosplenomegaly), skin (pallor, jaundice).
Investigations:
-Microscopy: Peripheral blood smear (PBS) for malaria parasites (Giemsa-stained thick and thin films)
-This is the gold standard for diagnosis and species identification
-Sensitivity depends on parasite density and microscopist skill
-Rapid Diagnostic Tests (RDTs): Detect malaria parasite antigens
-Useful for quick diagnosis, especially in resource-limited settings
-However, they cannot quantify parasitemia and may have lower sensitivity for low-grade infections or specific Plasmodium species
-Polymerase Chain Reaction (PCR): Highly sensitive and specific for detecting Plasmodium DNA
-Useful for species identification and detecting low-level parasitemia, but not routinely available for immediate diagnosis
-Complete Blood Count (CBC): Anemia, thrombocytopenia are common
-Liver function tests (LFTs): Elevated bilirubin, transaminases
-Renal function tests (RFTs): Assess for renal impairment
-Blood glucose: Hypoglycemia can occur, especially in severe malaria
-Coagulation profile: May show coagulopathy.
Differential Diagnosis:
-Other febrile illnesses in returning travelers: Dengue fever, Typhoid fever, Viral hepatitis, Rickettsial infections, Bacterial sepsis, Leptospirosis, Viral gastroenteritis
-Non-malarial febrile illnesses acquired locally.

Management

Initial Management:
-Immediate commencement of empirical antimalarial treatment if malaria is strongly suspected and diagnosis cannot be rapidly confirmed
-Supportive care: hydration (oral or intravenous fluids), antipyretics (paracetamol)
-Obtain blood for diagnostic tests before starting treatment if possible.
Medical Management:
-Antimalarial treatment depends on the suspected or confirmed Plasmodium species, severity of illness, age, weight, and local drug resistance patterns
-For *Plasmodium falciparum* malaria: Artemisinin-based combination therapy (ACT) is the first-line treatment in most regions
-In India, specific ACT regimens (e.g., Artemether-Lumefantrine) are recommended
-For *Plasmodium vivax* and *P
-ovale*: Treatment involves an asexual blood stage treatment followed by a radical cure with an 8-aminoquinoline (e.g., primaquine) to eradicate dormant liver hypnozoites
-Glucose-6-phosphate dehydrogenase (G6PD) deficiency testing is crucial before primaquine administration to prevent hemolytic anemia
-Uncomplicated malaria: Oral ACT
-Severe malaria: Intravenous artesunate is the drug of choice, followed by oral ACT
-Specific dosages vary by age and weight and should be guided by national/WHO guidelines.
Surgical Management: Not applicable for malaria itself, but surgical intervention may be required for complications such as splenic rupture or bowel obstruction if present.
Supportive Care:
-Close monitoring of vital signs, fluid balance, neurological status
-Management of complications: seizures (benzodiazepines), ARDS (mechanical ventilation), renal failure (dialysis), anemia (blood transfusion), hypoglycemia (intravenous glucose)
-Nutritional support
-Isolation is not necessary for malaria treatment.

Complications

Early Complications:
-Cerebral malaria (coma, seizures, neurological deficits)
-Severe anemia
-Acute respiratory distress syndrome (ARDS)
-Acute kidney injury (AKI)
-Hypoglycemia
-Metabolic acidosis
-Shock
-Jaundice
-Hemolysis
-Splenic rupture (rare).
Late Complications:
-Post-malarial neurological sequelae (rare)
-Anemia requiring prolonged management
-Relapses of vivax/ovale malaria if radical cure is inadequate.
Prevention Strategies:
-Travellers should be educated about malaria risks and preventive measures: chemoprophylaxis (appropriate drug selection and adherence), use of insect repellent, protective clothing, mosquito nets, and staying in screened or air-conditioned accommodations
-Prompt medical attention for any febrile illness during or after travel.

Prognosis

Factors Affecting Prognosis:
-Prompt diagnosis and treatment are critical
-The Plasmodium species involved (*P
-falciparum* being the most dangerous)
-The parasite density
-The patient's age and immune status
-Presence and severity of complications
-Adherence to treatment
-Access to appropriate medical care.
Outcomes:
-With prompt diagnosis and appropriate treatment, the prognosis for uncomplicated malaria is generally excellent
-Severe malaria can be life-threatening and carries a significant risk of mortality and long-term sequelae, particularly in young children.
Follow Up:
-Children treated for uncomplicated malaria usually require a short follow-up to ensure resolution of symptoms and absence of anemia
-Those treated for severe malaria require close monitoring for any residual neurological deficits or organ dysfunction
-Children treated for P
-vivax or P
-ovale malaria require follow-up to ensure completion of radical cure, particularly the primaquine course, and monitoring for G6PD deficiency related complications.

Key Points

Exam Focus:
-Always consider malaria in a febrile traveler from an endemic area
-Microscopic examination of blood smear is gold standard
-RDTs are useful but have limitations
-ACTs are first-line for P
-falciparum
-Primaquine requires G6PD testing for radical cure of P
-vivax/ovale
-Severe malaria is a medical emergency.
Clinical Pearls:
-Do not rely solely on chemoprophylaxis
-it is not 100% effective
-Test ALL febrile travelers returning from endemic areas, even if they have taken prophylaxis
-A negative RDT does not rule out malaria if suspicion is high
-send PBS
-Be vigilant for complications of severe malaria, especially in young children.
Common Mistakes:
-Delayed diagnosis due to considering other common febrile illnesses without adequate travel history
-Inadequate investigations or misinterpretation of results
-Inappropriate antimalarial treatment selection (e.g., using non-effective drugs for the region or Plasmodium species)
-Failure to administer radical cure for P
-vivax/ovale
-Forgetting to test for G6PD deficiency before primaquine use
-Underestimating the severity of malaria in children.