Loa loa

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Background

  • “African Eye Worm”
  • Generally thought to be a harmless infection[1]
  • Neglected tropical disease - very few studies have been done; most information is from case reports
  • Transmitted by Tabanid flies (genus Chrysops)
    • Mainly active during the day and prefer humans to other hosts[2]
  • Unlick Onchocerciasis Loa Loa does not damage visual acuity even while migrating through the eyeCite error: Invalid <ref> tag; invalid names, e.g. too many
  • Majority of cases in western and central Africa
    • Countries with the highest disease burden: Angola, Benin, Cameroon, Central African Republic, Chad, Democratic Republic of the Congo, Equatorial Guinea, Gabon, Nigeria, Republic of Congo, Sudan

Risk Factors

  • Living or traveling to western and central Africa
  • Cases have been reported in urban and rural settings in these countries; however, majority occur in densely forested areas
  • Working outside during the day, working in wet or muddy areas
  • Prevalence higher in males, probably due to different occupational exposures
  • Prevalence increases with age, probably due to chronicity of infection and lack of symptoms

Clinical Features

  • Usually asymptomatic
    • Symptoms can begin within 2 months of exposure
    • Case reports suggests symptoms may not show up for >20 years post-exposure
  • Infection is generally noticed when the patient sees a white worm migrating through the subconjuctiva or sclera of their eye
  • Calabar swellings – pruritic transient swellings in the subcutaneous tissues as the worm migrates through, usually on the limbs, especially forearms, and near joints
  • Pruritus, joint or muscle pain, headache
  • Can cause severe disease rarely
    • Encephalopathy, endomyocardial fibrosis, pulmonary infiltrates, renal failure

Differential Diagnosis

Travel-related skin conditions

See also domestic U.S. ectoparasites

Diagnosis

  • Clinical diagnosis if you can see the worm in the subconjuctiva
  • Marked eosinophilia and elevated IgE
  • Presence of Loa Loa larvae in the blood, CSF, urine, or sputum – through microscopy or DNA PCR
    • Blood levels peak between 10 am – 3 pm
    • Difficult since adult worms must be depositing larvae to be detected, which they may not do for years and density of larvae may be too low to be detected
  • Loa Loa antibodies in the serum

Management

  • Eye worm removal
    • Use local anesthesia to make small incision in conjunctiva to extract worm with forceps
  • Diethylcarbamazine (DEC)
    • Only treatment that is definitively curative killing both larvae and adult worms
    • May need 2-3 courses of treatment
    • First course should last 3-4 weeks
      • Starting doses should be divided into BID or TID doses starting at 3-6 mg/day and doubling daily until up to 400 mg/day is reached
      • Side effects occur in >50% of people – pruritus, rashes, edema, headaches, fever, pleural effusion, laryngeal edema
      • Give antihistamines or corticosteroids at the same time to reduce side effects
    • Associated with severe encephalopathy if Loa Loa burden is high
  • 2nd line – Ivermectin or Albendazole
    • Ivermectin kills only larvae so is not curative, may be more effective if given monthly
      • Given as a single dose 150 ug/kg, then repeated every 1-3 months
    • Albendazole kills only adult worms so is not curative, treatment is very slow, and may not be effective if high worm burden
      • Given as 200 mg BID for 21 days
    • Both treatments may be more effective as a therapy to decrease disease burden so that follow-up treatment with DEC is less likely to cause encephalopathy

Complications

  • Infection-associated encephalopathy
  • Treatment-associated encephalopathy
    • Characteristically accompanied by retinal hemorrhages
    • Aphasia, incontinence, extrapyramidal signs
    • Generally fatal or resulting in severe morbidity

Prevention

  • Personal protective measures against flies – long sleeves, light-colored clothes, nets/screens, insecticide
  • Mass treatment in endemic communities is being currently evaluated to determine if it would be safe and effective

See Also

Sources

  1. Metzer, WG, Mordmuller, B. “Loa Loa – does it deserve to be neglected?” Lancet Infect Dis. 2014 Apr; 14 (4):353-7. Epub 2013 Dec 12.
  2. Boussinesq, M. "Loiasis." Annals of Tropical Medicine and Parasitology 100.8 (2006): 715-31