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LEISHMANIASIS
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TYPES A) Cutaneous B) Mucocutaneous C) Visceral
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Life Cycle
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The parasite in blood stream * Is transmitted from animals to humans by the bite of infected sand fly. * Diagnosed by the presence of parasite in biopsy from skin. * Treatment is limited due to toxicities & failure of drugs.
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Sodium Stibogluconate Pentavalent antimonial drug
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Pharmacokinetics Not absorbed orally Given IV/ IM for 20 days for cutaneous leishmaniasis & 28 days for visceral and mucocutaneous disease. Distributed in extravascular compartement.
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Partially metabolized Excreted in urine
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Mechanism Of Action Unknown Production of oxygen free radicals
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Adverse Effects GIT upset Fever, headache, arthralgia, rash. IMI----( local pain & sterile abscess). QT prolongation. Hemolytic anaemia
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Pentamidine Alternative to Na stibogluconate for the treatment of visceral leishmaniasis. For cutaneous lesion
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Pharmacokinetics Not absorbed orally Given IV/ IM. Accumulative drug & eliminated slowly in urine ( elimination half-life 12 days). Not effectively cross blood brain barrier Can be inhaled as a nebulized powder.
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Mechanism of Action Unknown
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Clinical uses Pneumocystosis Prophylaxis against pneumocystosis in immunocompromised individuals. African trypanosomiasis ( sleeping sickness). Alternative to sodium stibogluconate for visceral leishmaniasis.
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Adverse Effects Rapid IVI can lead to severe hypotension, tachycardia, dizziness, dyspnea ( should be given slowly over 2 hours). IMI – pain & sterile abscess
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Pancreatic toxicity( acute pancreatitis) Hypoglycemia Hyperglycemia Reversible renal insufficiency Rash Metallic taste
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Fever Thrombocytopenia Cardiac arrhythmias GIT upset Cough, dyspnea, bronchospasm ( with the inhaled drug ) Headache, Arthralgia
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Miltefosine An alkylphosphocholine analog Used for the treatment of visceral leishmaniasis Given orally
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Adverse Effects Vomiting & diarrhea Elevation in liver enzymes Teratogenic
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Amphotericin B Antifungal drug Used as alternative therapy for visceral leishmaniasis.
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