Hello friends. In this PPT I am talking about antiprotozoal drugs. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology ...
Hello friends. In this PPT I am talking about antiprotozoal drugs. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Size: 3.04 MB
Language: en
Added: Apr 02, 2023
Slides: 40 pages
Slide Content
Antiprotozoal drugs Dr. Karun Kumar Senior Lecturer Dept. of Pharmacology
Antimalarial Drugs Aims of using drugs To prevent clinical attack of malaria ( prophylactic ) To treat clinical attack of malaria ( clinical curative) To completely eradicate the parasite from the patient’s body (radical curative ) To cut down human-to-mosquito transmission ( gametocidal )
Classification
When a person is bitten by an infected mosquito, Plasmodium sporozoites enter the liver, form tissue schizonts , and undergo exoerythrocytic schizogony to produce merozoites The merozoites released from the liver invade erythrocytes and form trophozoites that undergo erythrocytic schizogony
Some trophozoites develop into male and female gametocytes, which must subsequently pass back into a mosquito before they can develop into sporozoites and repeat the infection cycle
Erythrocytic schizontocides A ct on erythrocytic schizogony Tissue schizontocides Act on preerythrocytic as well as exoerythrocytic (P. vivax ) stages in liver Gametocides K ill gametocytes in blood Primaquine blocks exoerythrocytic schizogony (tissue schizontocide ) Causal prophylaxis Symptoms of malaria (fever, chills & rigors) correspond to erythrocytic stage
Causal prophylaxis Pre erythrocytic phase (in liver), which is the cause of malarial infection and clinical attacks, is the target for this purpose Primaquine ; not used in mass programmes , because of its toxic potential Proguanil for P.f ., but not used in India, because of weak activity against liver stages of P.v ., and rapid development of resistance when used alone
Suppressive prophylaxis The schizontocides which suppress the erythrocytic phase and thus attacks of malarial fever can be used as prophylactics Though the exoerythrocytic phase in case of vivax and other relapsing malarias continues , clinical disease does not appear Mefloquine & Doxy. are used for malaria prophylaxis by travellers
Clinical cure The erythrocytic schizontocides are used to terminate an episode of malarial fever High-efficacy drugs Artemisinin , CQ , Amodiaquine , quinine, mefloquine , halofantrine , Lumefantrine and Atovaquone Low-efficacy drugs Proguanil , pyrimethamine , sulfonamides , tetracyclines and clindamycin
The faster acting drugs are preferred , particularly in falciparum malaria where delay in treatment may result in death even if the parasites are cleared from blood by the drug The exoerythrocytic phase (hypnozoites) of vivax and ovale persists which can cause relapses subsequently without reinfection
Erythrocytic schizontocides are radical curatives for falciparum, but not for vivax or ovale malaria However, recrudescences occur in falciparum infection if the blood is not totally cleared of the parasites by the drug
Erythrocytic schizontocides ( cl.cure ) Kill schizonts in the blood (T/t of acute attacks & suppressive prophylaxis) MACHAR Pe attack Mefloquine Atovaquone Chloroquine Halofantrine (and Lumefantrine ) Artemisinins ResQ (Quinine) Proguanil , Pyrimethamine
T/t of uncomplicated malaria A. Vivax (also ovale , malariae ) malaria Chloroquine 600 mg (10 mg/kg) followed by 300 mg (5 mg/kg) after 8 hours and then for next 2 days ( total 25 mg/kg over 3 days) + Primaquine 15 mg (0.25 mg/kg) daily × 14 days In CQ resist., Quinine 600 mg (10 mg/kg) 8 hourly × 7 days + Doxycycline 100 mg daily × 7 days or + Clindamycin 600 mg 12 hourly × 7 days + Primaquine (as above) or ACT + Primaquine (as above)
B. Chloroquine -sensitive falciparum malaria Chloroquine (as above) + Primaquine 45 mg (0.75 mg/kg) single dose (as gametocidal ) C. Chloroquine -resistant falciparum malaria Artesunate 100 mg BD (4 mg/kg/day) × 3 days + Sulfadoxine 1500 mg (25 mg/kg) + Pyrimethamine 75 mg (1.25 mg/kg) single dose In India (including under NVBDCP) all P.f . cases, irrespective of CQ-resistance status, are treated with artemisinin based combination therapy (ACT )
Radical cure In case of vivax and ovale malaria , drugs which attack the exoerythrocytic stage (hypnozoites) given together with a clinical curative achieve total eradication of the parasite from the patient’s body A radical curative is needed in relapsing malaria, while in falciparum malaria — adequate treatment of clinical attack leaves no parasite in the body DOC for radical cure of vivax and ovale malaria is Primaquine 15 mg daily for 14 days
Gametocidal Elimination of the male and female gametes of Plasmodia formed in the patient’s blood Gametocidal action is of no benefit to the patient being treated, but will reduce the transmission to mosquito Primaquine is gametocidal to all species of Plasmodia , while artemisinins have weak lethal action on early-stage but not mature gametes
Chloroquine Rapidly acting erythrocytic schizontocide against all species of plasmodia; controls most clinical attacks in 1–2 days with disappearance of parasites from peripheral blood in 1–3 days Actively concentrated by sensitive intraerythrocytic plasmodia; higher concentration is found in infected RBCs than in noninfected ones DOC for T/t & prophyl . o f non-falciparum malaria & CQ sensitive P. falciparum malaria
Mechanism of action By accumulating in the acidic vacuoles of the parasite and because of its weakly basic nature, it ↑ vacuolar pH and thereby interferes with degradation of haemoglobin by parasitic lysosomes Polymerization of toxic haeme generated from digestion of haemoglobin to nontoxic parasite pigment haemozoin is inhibited by the formation of CQ- haeme complex
Haeme itself or its complex with CQ then damages the plasmodial membranes Clumping of pigment and changes in parasite membranes follow Other related antimalarials like quinine, mefloquine , lumefantrine , pyronaridine appear to act in an analogous manner
Adverse effects Nausea , vomiting, anorexia, uncontrollable itching, epigastric pain, uneasiness, difficulty in accommodation and headache are frequent and quite unpleasant Prolonged use of high doses can result in blindness due to retinal damage
Mefloquine Fast acting erythrocytic schizontocide , but slower than CQ or quinine due to prolonged absorption after oral ingestion. Effective against CQ-sensitive as well as resistant plasmodia A single dose controls fever and eliminates circulating parasites in infections caused by P. falciparum or P. vivax
However, relapses occur frequently subsequently in vivax malaria Also an efficacious suppressive prophylactic for multiresistant P. falciparum and other types of malaria Bitter in taste S/E D izziness , nausea, vomiting, diarrhoea , abdominal pain, sinus bradycardia and Q-T prolongation
Use MDR P. falciparum Due to potential toxicity , cost and long t½, use is restricted In combination with artesunate as ACT for uncomplicated falciparum malaria, including CQ-resistant and CQ + sulfa- pyrimethamine (S/P) resistant cases For prophylaxis of malaria among travellers to areas with multidrug resistance
Sulfonamide-Pyrimethamine (S/P) Pyrimethamine has high affinity for the plasmodial DHFRase enzyme Sulfadoxine and sulfamethopyrazine are ultralong acting sulfonamides — attain low blood concentrations , but are able to synergise with pyrimethamine which also has long t½
Combination has the potential to cause serious adverse effects ( exfoliative dermatitis, Stevens Johnson syndrome, etc.) due to the sulfonamide Use is restricted to single dose t/t of uncomplicated CQ-resistant falciparum malaria 1 st line ACT regimen used under NVBDCP in India
Primaquine Has a marked effect on primary as well as secondary hepatic phases of the malarial parasite Highly active against gametocytes and hypnozoites A/E Abd . pain , g.i . upset , weakness or uneasiness in chest (S/E); can be minimized by taking the drug with meals. CNS and CV symptoms are infrequent. Leucopenia occurs rarely with larger doses. Most imp. toxic potential is dose related haemolysis , methaemoglobinaemia , tachypnoea and cyanosis
Use Vivax malaria R adical cure of relapsing ( vivax ) malaria. G-6-PD status of the patient should be tested before giving 14 day primaquine course. It is to be taken with food to reduce g.i . side effects. Falciparum malaria S ingle 45 mg dose is given with the curative dose of CQ or ACT to kill the gametes and cut down transmission to mosquito
Artemisinin derivatives Fastest acting drugs against malaria Used for t/t of MDR malaria & cerebral malaria Short acting drugs , monotherapy needs to be extended beyond the disappearance of the parasites to prevent recrudescence Recrudescence can be totally prevented by combining 3 day artemisinin with a long acting drug
A/E N , V, abd . pain , itching and drug fever . Headache , tinnitus, dizziness, bleeding, dark urine , S-T segment changes, Q-T prolongation subside when the patient improves or drug is stopped Use Uncomplicated falciparum malaria ( CQ-resistant as well as sensitive ). DCGI has prohibited use of oral artemisinins as single drugs. FDCs are encouraged Severe and complicated falciparum malaria Artesunate ( i.v. or i.m .) OR Artemether ( i.m .) OR Arteether ( i.m .) given till the patient is fit to take oral medication, followed by 3 day oral ACT
ACT regimens for uncomplicated falciparum malaria Artesunate-mefloquine (AS/MQ ) Artesunate 100 mg BD (4 mg/kg/day) × 3 days + mefloquine 750 mg (15 mg/kg) on 2nd day and 500 mg (10 mg/kg) on 3rd day (total 25 mg/kg ) Artesunate-sulfadoxine + pyrimethamine (AS/S/P ) Artesunate 100 mg BD (4 mg/kg/day) × 3 days + sulfadoxine 1500 mg (25 mg/kg) and Pyrimethamine 75 mg (1.25 mg/kg) single dose
Summary
Antiamoebic drugs Drugs useful in infection caused by the anaerobic protozoa Entamoeba histolytica Diloxanide furoate DOC for asympt . Intest . Amebiasis & carriers Metronidazole DOC for amoebic liver abscess & intestinal wall disease