Protozoal Parasites

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Leishmaniasis

A chronic systemic infectious disease transmitted by the bite of a sand fly.

Cause

  • Flagellated protozoa Leishmania species

Clinical features

Visceral Leishmaniasis (Kala-azar)

  • Chronic disease characterized by fever, hepatosplenomegaly, lymphadenopathy, anaemia, leucopenia, progressive emaciation and weakness
  • Fever of gradual onset, irregular, with 2 daily peaks and alternating periods of apyrexia
  • The disease progresses over several months and is fatal if not treated
  • After recovery from Kala-azar, skin (cutaneous) leishmaniasis may develop

Cutaneous and Mucosal Leishmaniasis (Oriental sore)

  • Starts as papule, enlarges to become an indolent ulcer
  • Secondary bacterial infection is common

Differential diagnosis

  • Other causes of chronic fever, e.g. brucellosis
  • (For dermal leishmaniasis) Other causes of cutaneous lesions, e.g. leprosy

Investigations

  • Stained smears from bone marrow, spleen, liver, lymph nodes, or blood to demonstrate Leishman Donovan bodies
  • Culture of the above materials to isolate the parasites
  • Serological tests, e.g. indirect fluorescent antibodies
  • Leishmanin skin test (negative in Kala-azar)

Management

Refer all cases to regional referral hospital

Treatment LOC

Cutaneous Leishmaniasis (all patients)

  • Frequently heals spontaneously but if severe or persistent, treat as for Visceral Leishmaniasis below

Visceral Leishmaniasis (Kala-azar): All patients

  • Combination: Sodium stibogluconate 20 mg /kg per day IM or IV for 17 days
  • Plus paromomycin 15 mg/kg [11 mg base] per day IM for 17 days

Alternative first line treatment is:

  • Sodium Stibogluconate 20 mg/kg per day for 30 days (in case paromomycin is contraindicated)

In relapse or pregnancy

  • Liposomal amphotericin B (e.g. AmBisome) 3 mg/kg per day for 10 days

In HIV+ patients

  • Liposomal amphotericin B 5 mg/kg per day for 8 days
RR

Post Kala-Azar Dermal Leishmaniasis (PKDL)

  • Rare in Uganda
  • Sodium Stibogluconate injection 20 mg/kg/day until clinical cure. Several weeks or even months of treatment are necessary
 

 

Note:

  • Continue treatment until no parasites detected in 2 consecutive splenic aspirates taken 14 days apart
  • Patients who relapse after a 1st course of treatment with Sodium stibogluconate should immediately be re- treated with Ambisome 3 mg/kg/day for 10 days

Prevention

  • Case detection and prompt treatment
  • Residual insecticide spraying
  • Elimination of breeding places

Human African Trypanosomiasis (Sleeping Sickness)

A disease caused by trypanosomes (a protozoa) and transmitted to humans by several species of tsetse fly

Cause

  • Trypanosoma rhodesiense (mostly in the Central and Eastern regions of Uganda)
  • Trypanosoma gambiense (mostly in West Nile region)

Clinical features

  • May be history of tsetse fly bite and swelling at site of bite after 7-14 days (more often in rhodesiense, rarely in T. Gambiense)

T.Rhodesiense

  • Incubation is 2-3 weeks
  • Early stage (haemolymphatic stage): headache not responding to common analgesics, fever, generalised lymphadenopathy, joint pains
  • Late stage (meningoencephalitis stage): after some weeks, neurological and psychiatric symptoms like apathy, day sleepiness, paralysis, seizures
  • If not treated: cachexia, lethargy, coma and death within 3-6 months

T.gambiense

  • Similar to the rhodesiense but less acute and with slower progression
  • Incubation can last several years

Differential diagnosis

  • Malaria, meningitis
  • TB, HIV/AIDS

Investigations

  • Blood: Slides for trypanosomes
  • CSF: For trypanosomes, lymphocyte count
  • Aspirate from chancre/lymph node: for trypanosomes

Management

This is based on the findings of the CSF analysis, determining the stage of disease. To determine the medicine of choice, the disease is divided into two stages: early and late stage

STAGE

FEATURES

Early (first) stage

  • CSF is normal
  • Lymphocytes <5 cells/mm3
  • Total protein <37 mg/dl (by dye-binding protein assay) or < 25 mg/dl (by Double Standard & Centrifuge Method)
  • Absence of trypanosomes (by Double Standard and Centrifuge Method)

Late (second) stage

  • Lymphocytes > 5 cell/ mm3 And/or
  • Presence of trypanosomes

Patient with suspected or diagnosed sleeping sickness should be managed at referral facilities.

Treatment

Treatment LOC

Early (first) stage

T. rhodesiense sleeping sickness

For both children and adults

Suramin IV

A test dose of 5 mg/kg of body weight should first be administered to test for anaphylactic reaction

Followed by five injections of 20 mg/kg every 5 days interval

Day 0: 5 mg/kg body weight

Day 3: 20 mg/kg body weight

Day 8: 20 mg/kg body weight

Day 13: 20 mg/kg body weight

Day 18: 20 mg/kg body weight

Day 23: 20 mg/kg body weight If anaphylaxis: do not administer

T. gambiense sleeping sickness

For both children and adults

Pentamidine IM 4 mg/kg daily for 7 days

Give food 1 hour before to prevent hypoglycaemia

The patient should be in a supine position during administration and 1 hour after to prevent hypertension

RR

Late (second) stage

T. rhodesiense sleeping sickness

For both children and adults

  • IV Melarsoprol 2.2 mg/kg body weight daily for 10 days

T.gambiense sleeping sickness Children ≤ 12 years and <35 kg

  • Eflornithine IV 150 mg/kg 6 hourly for 14 days (total dose of 600 mg/kg/day.) Dilute 150 mg/kg dose of eflornithine into the 100 ml of distilled water. Administer the infusion over at least 2 hours

Children >12 years up to 15 years

  • Eflornithine IV 100 mg/kg 6 hourly for 14 days (total dose of 400 mg/kg per day). Dilute the eflornithine dose of 100 mg/kg into the 100 ml of distilled water. Administer the infusion over at least 2 hours (rate 20 drops/minute)
 RR

Adults >15 years

  • Nifurtimox/Elfornithine combination therapy (NECT)
  • Nifurtimox: 5 mg/kg every 8 hours orally for 10 days (15 mg/kg/day)
  • Plus Eflornithine 200 mg/kg 12 hourly for 7 days (400 mg/kg/day). Dilute Eflornithine dose of 200 mg/kg into 250 ml of distilled water and administer the infusion over at least 2 hours (50 drops/minute)
  • Infusions are given slowly to prevent convulsions

Relapses

  • IV melarsoprol 2.2 mg/kg once daily for 10 days
Note: 

Corticosteroids: Should be given to patients with late trypanosomiasis on melarsoprol who may have hypoadrenalism - the steroids may also reduce any drug reactions

Do not give hydrocortisone after day 24, even though the melarsoprol treatment is not yet complete

If prednisolone is used instead of hydrocortisone, the anti-inflammatory action is similar but the correction of the hypoadrenalism will be much less marked

Suramin: Do not use this medicine for early or late stage T. gambiense treatment in onchocerciasis-endemic areas as it may cause blindness in any onchocerciasis-infected patients by killing the filariae in the eye

 

Prevention

  • Trapping of tsetse flies
  • Clearing of bushes around homes and paths
  • Early detection and treatment of cases