{"id":6660,"date":"2024-11-19T12:04:22","date_gmt":"2024-11-19T12:04:22","guid":{"rendered":"https:\/\/workhouse.sweetdishy.com\/?p=6660"},"modified":"2024-11-19T12:04:23","modified_gmt":"2024-11-19T12:04:23","slug":"treatment-of-helminthic-infections","status":"publish","type":"post","link":"https:\/\/workhouse.sweetdishy.com\/index.php\/2024\/11\/19\/treatment-of-helminthic-infections\/","title":{"rendered":"TREATMENT OF HELMINTHIC INFECTIONS"},"content":{"rendered":"\n<p>Anthelmintic drugs are used to eradicate or reduce the numbers of helminthic parasites in the<br>intestinal tract or tissues of the body. Most anthelmintics are active against specific parasites;<br>thus, parasites must be identified before treatment is started.<br><strong>Individual Drugs<\/strong><br><strong>Albendazole<\/strong><br>Albendazole, a broad-spectrum oral anthelmintic, is used for pinworm infection, ascariasis,<br>trichuriasis, strongyloidiasis, and infections with both hookworm species. Albendazole is also<br>the drug of choice in hydatid disease and cysticercosis.<br>Anthelmintic Actions: Albendazole blocks glucose uptake by larval and adult stages of<br>susceptible parasites, depleting their glycogen stores and decreasing formation of ATP. As a<br>result the parasite is immobilized and dies. The drug has larvicidal effects in necatoriasis and<br>ovicidal effects in ascariasis, ancylostomiasis, and trichuriasis. The drug is teratogenic and<br><em>embryotoxic in some animal species and contraindicated in the first trimester.<br><strong>Clinical Uses<\/strong><\/em><\/p>\n\n\n\n<ol class=\"wp-block-list\">\n<li>Ascariasis, Trichuriasis, and Hookworm and Pinworm Infections: For pinworm infections,<br>ancylostomiasis, and light ascariasis, necatoriasis, or trichuriasis, a single dose of 400 mg is<br>given orally for adults and in children over two years of age. In pinworm infection, the dose<br>should be repeated in 2 weeks.<\/li>\n\n\n\n<li>Strongyloidiasis: 400 mg twice daily for three days (with meals).<\/li>\n\n\n\n<li>Hydatid Disease: 800 mg\/kg\/d in divided doses for three months<\/li>\n\n\n\n<li>Neurocysticercosis: 15 mg\/kg \/d for 8 days<\/li>\n\n\n\n<li>Other Infections: At a dosage of 200-400 mg twice daily, albendazole is the drug of choice in<br>treatment of cutaneous larval migrans (give daily for 3-5 days) and in intestinal capillariasis<br>(10-day course).<br>Adverse Reactions: Mild and transient epigastric distress, diarrhea, headache, nausea,<br>dizziness. In 3-month treatment courses causes jaundice, nausea, vomiting, abdominal pain,<br>alopecia, rash or pruritus occurs.<br><strong>Diethylcarbamazine Citrate<\/strong><br>Diethylcarbamazine is a drug of choice in the treatment of filariasis, loiasis, and tropical<br>eosinophilia.<br>Anthelmintic Actions: Diethycarbamazine immobilizes microfilariae and alters their surface<br>structure, making them more susceptible to destruction by host defense mechanisms. The<br>mode of action of diethylcarbamazine against adult worms is unknown.<br><strong>Clinical Uses:<\/strong><\/li>\n\n\n\n<li>Wuchereria bancrofti, Loa loa: Diethycarbamazine is the drug of choice for treatment of<br>infections with these parasites, given its high order of therapeutic efficacy and lack of<br>serious toxicity. Microfilariae of all species are rapidly killed; adult parasites are killed more<br>slowly, often requiring several courses of treatment.<\/li>\n\n\n\n<li>Onchocerca volvulus: Diethylcarbamazine temporarily kills microfilariae but are poorly<br>effective against adult worms. If diethylcarbamazine is used in onchocerciasis treatment,<br>suramin (a toxic drug) must be added to the regimen to kill the adult worms.<br><strong>Adverse Reactions<\/strong><br>Reactions to the drug itself are mild and transient includes: headache, malaise, anorexia, and<br>weakness are frequent. Reactions Induced by dying Parasites: As a result of the release of<br>foreign proteins from dying microfilariae or adult worms in sensitized patients. Reactions in<br>onchocerciasis affect the skin and eyes in most patients. The reactions may be severe, if<br>infection is heavy. Vision can be permanently damaged as a result of dying microfilariae in the<br>optic disks and retina. Reactions in W bancrofti, and L loa infections are usually mild in W<br>bancrofti, and occasionally severe in L loa infections. Reactions include fever, malaise, papular<br>rash, headache, gastrointestinal symptoms, cough, chest pains, and muscle or joint pains.<br><strong>Ivermectin<\/strong><br>Ivermectin is the drug of choice in individual and mass treatment of onchocerciasis and for<br>strongyloidiasis. The drug is rapidly absorbed. The drug has a wide tissue distribution. It<br>apparently enters the eye slowly and to a limited extent. Excretion of the drug and its<br>metabolites is almost exclusively in the feces.<br>Anthelmintic Actions: Ivermectin paralyze nematodes and arthropods by intensifying GABAmediated transmission of signals in peripheral nerves. In onchocerciasis, ivermectin is<br>microfilaricidal and affects embryogenesis. The mode of action of ivermectin on microfilariae is<br>uncertain.<br>Clinical Uses: Onchocerciasis, Bancroftian Filariasis, Strongyloidiasis, scabies and cutaneous<br><strong>larva migrans<\/strong><br>Adverse Reactions: The adverse effects of ivermectin are the Mazotti reaction, which starts on<br>the first day after a single oral dose and peaks on the second day. The reaction is due to killing<br>of microfilariae and its intensity correlates with skin microfilaria loads. The Mazotti reaction<br>includes fever, headache, dizziness, somnolence, weakness, rash, increased pruritus, diarrhea,<br>joint and muscle pains, hypotension, tachycardia, lymphadenitis, lymphangitis, and peripheral<br>edema. The Mazotti reaction diminishes with repeated dosing. Steroids may be necessary for<br>several days.<br><strong>Levamisole<\/strong><br>Levamisole hydrochloride is highly effective in eradicating Ascaris and moderately effective<br>against both species of hookworm.<br><strong>Mebendazole<\/strong><br>Mebendazole has a broad spectrum of anthelmintic activity and a low incidence of adverse<br>effects. Poorly absorbed after oral adminstration. It rapidly metabolized and excreted mostly in<br>the urine, either unchanged or as decarboxylated derivatives.<br>Mebendazole inhibits microtubule synthesis in nematodes, thus irreversibly impairing glucose<br>uptake. As a result, intestinal parasites are immobilized or die slowly.<br><strong>Clinical Uses:<\/strong> The drug can be taken before or after meals; the tablets should be chewed<br>before swallowing.<\/li>\n\n\n\n<li>Pinworm Infection: Give 100 mg once and repeat the dose at 2 and 4 weeks<\/li>\n\n\n\n<li>Ascaris lumbricoides, Trichuris trichiura, and Hookworm<\/li>\n\n\n\n<li>Hydatid Disease: Mebendazole is the alternative.<\/li>\n\n\n\n<li>Taeniasis: In Taenia solium infection, mebendazole has a theoretic advantage over<br>niclosamide in that proglottids are expelled intact.<\/li>\n\n\n\n<li>Strongyloidiasis.<br>Adverse Reactions: Mild nausea, vomiting, diarrhea, and abdominal pain have been reported<br>infrequently, more often in children heavily parasitized by Ascaris.<br><strong>Metrifonate<\/strong><br>Metrifonate is a safe, alternative drug for the treatment of Schistosoma haematobium infections.<br>Metrifonate, an organophosphate compound, is rapidly absorbed after oral administration.<br>Clearance appears to be through nonenzymatic transformation to its active metabolite<br>(dichlorvos). Metrifonate and the active metabolite are well distributed to the tissues and are<br>completely eliminated in 24-48 hours.<br>Adverse Reactions: mild and transient cholinergic symptoms, including nausea and vomiting,<br>diarrhea, abdominal pain, bronchospasm, headache, sweating, fatigue, weakness, dizziness,<br>and vertigo.<br><strong>Niclosamide<\/strong><br>Niclosamide is a drug of choice for the treatment of most tapeworm infections. It appears to be<br>minimally absorbed from the gastrointestinal tract: neither the drug nor its metabolites have<br>been recovered from the blood or urine.<br>Clinical Uses: Niclosamide should be given in the morning on an empty stomach. The tablets<br>must be chewed thoroughly and are then swallowed with water.<\/li>\n\n\n\n<li>T saginata, T solium, and Diphyllobothrium latum: A single 2 g dose of niclosamide results in<br>cure rates of over 85% for D latum and about 95% for T saginata.<\/li>\n\n\n\n<li>Hymenolepis nana and H: Niclosamide is effective against the adult parasites in the lumen of<br>the intestine. The minimum course of treatment must be 7 days<\/li>\n\n\n\n<li>Intestinal Fluke Infections: Niclosamide can be used as an alternative drug for the treatment<br>of intestinal flukes.<br>Adverse Reactions: Adverse effects, mild, and transitory. It causes nausea, vomiting, diarrhea,<br>and abdominal discomfort.<br><strong>Oxamniquine<\/strong><br>Oxamniquine is used for the treatment of S mansoni infections. It is active against both mature<br>and immature stages of S mansoni. It has also been used extensively for mass treatment.<br>Oxamniquine is readily absorbed orally.<br>Clinical Uses: Oxamniquine is safe and effective in all stages of S mansoni disease, including<br>advanced hepatosplenomegaly. It is better tolerated if given with food, although food delays<br>absorption. In mixed infections with S mansoni and S haematobium, oxamniquine has been<br>successfully used in combination with metrifonate.<br>Adverse Reactions: Central nervous system symptoms are most common; nausea and<br>vomiting, diarrhea, colic, pruritus, and urticaria also occur.<br><strong>Piperazine<br><\/strong>The piperazine salts are alternative drugs in the treatment of ascariasis. Piperazine is readily<br>absorbed from the gastrointestinal tract, and maximum plasma levels are reached in 2-4 hours.<br>Most of the drug is excreted unchanged in the urine in 2-6 hours.<br>Anthelmintic Actions: Piperazine causes paralysis of Ascaris by blocking acetylcholine at the<br>myoneural junction. The paralyzed roundworms are unable to maintain their position in the host<br>and are expelled live by normal peristalsis.<br>Clinical Uses: Ascariasis<br>Adverse Reactions: Piperazine cause nausea, vomiting, diarrhea, abdominal pain, dizziness,<br>and headache.<br><strong>Praziquantel<br><\/strong>Praziquantel is effective in the treatment of schistosome infections of all species and most other<br>trematode and cestode infections, including cysticercosis. The drug&#8217;s safety and effectiveness<br>as a single oral dose have also made it useful in mass treatment of several of the infections. It<br>is rapidly absorbed after oral administration. Most of the drug is rapidly metabolized to inactive<br>products after a first pass in the liver. Excretion is mainly via the kidneys and bile.<br>Anthelmintic Actions: Praziquantel drug increases cell membrane permeability to calcium,<br>resulting in marked contraction, followed by paralysis of worm musculature. Vacuolization and<br>disintegration of the tegumen occur, and parasite death follows.<br><strong>Clinical Uses:<\/strong><\/li>\n\n\n\n<li>Schistosomiasis: Praziquantel is the drug of choice for all forms of schistosomiasis.<\/li>\n\n\n\n<li>Taeniasis and Diphyllobothriasis: A single dose of praziquantel, 10 mg\/kg.<\/li>\n\n\n\n<li>Neurocysticercosis: The praziquantel dosage is 50 mg\/kg\/d in three divided doses for 14<br>days.<br>193<\/li>\n\n\n\n<li>H nana: Praziquantel is the drug of choice for H nana infections and the first drug to be<br>highly effective. A single dose of 25 mg\/kg is used.<br>Adverse Reactions: Most frequent are headache, dizziness, drowsiness, and lassitude; others<br>include nausea, vomiting, abdominal pain, loose stools, pruritus, urticaria, arthralgia, myalgia,<br>and low-grade fever. Praziquantel appears to be better tolerated in children than in adults.<br>Adverse effects may be more frequent in heavily infected patients, especially in S mansoni<br>infections.<br><strong>Pyrantel Pamoate<\/strong><br>Pyrantel pamoate is a broad-spectrum anthelmintic highly effective for the treatment of pinworm<br>and Ascaris. Pyrantel pamoate because it is poorly absorbed from the gastrointestinal tract, it is<br>active mainly against luminal organisms.<br>Anthelmintic Actions: Pyrantel is effective against mature and immature forms of susceptible<br>helminths within the intestinal tract but not against migratory stages in the tissues or against<br>ova. The drug is a depolarizing neuromuscular blocking agent that causes release of<br>acetylcholine and inhibition of cholinesterase; this results in stimulation of ganglionic receptors<br>and worm paralysis, which is followed by expulsion from the host&#8217;s intestinal tract.<br>Clinical Uses: The standard dose is 11 mg (base)\/kg (maximum, 1 g), given with or without<br>food. Pyrantel is given as a single dose and repeated in 2 and 4 weeks is effective in<br>Enterobius vermicularis, A lumbricoides, and hookworm infections.<br><strong>Suramin<\/strong><br>Suramin is an alternative drug for the eradication of adult parasites of Onchocerca volvulus and<br>a drug of choice in the treatment of the hemolymphatic stage of African trypanosomiasis due to<br>Trypanosoma brucei gambiense and Trypanosoma brucei rhodesiense. Suramin is a<br>nonspecific inhibitor of many enzymes. Toxic reactions are frequent and sometimes severe,<br>including nausea, vomiting, urticaria, fever, nephrotoxicity, peripheral neuritis, anemia, jaundice,<br>and exfoliative dermatitis. The drug should be given only under expert guidance.<br>Thiabendazole<br>Thiabendazole is the drug of choice for the treatment of strongyloidiasis and an alternative drug<br>for cutaneous larva migrans. It may also be tried in trichinosis and visceral larva migrans, given<br>in the absence of other effective drugs. It is no longer recommended for the treatment of<br>pinworm, ascarid, trichurid, or hookworm infection unless the safer drugs of choice are not<br>available. Thiabendazole is rapidly absorbed after ingestion. The drug is almost completely<br>metabolized in the liver. Ninety percent of the drug is excreted in the urine.<br>Anthelmintic Actions: Thiabendazole has anti-inflammatory properties, which may be an<br>important factor in its ability to relieve symptoms in some parasitic diseases. It also has<br>immunomodulating effects on T cell function appears to be an immunorestorative agent.<br>Thiabendazole also has antipyretic and mild antifungal and scabicidal actions. Thiabendazole&#8217;s<br>vermicidal action may be a result of interference with microtubule aggregation acting through<br>inhibition of the enzyme fumarate reductase. The drug has ovicidal effects for some parasites.<br>Clinical Uses: The standard dose is 25 mg\/kg (maximum, 1.5 g). The drug should be given after<br>meals. Effective in Strongyloides stercoralis (The standard dose is given twice daily for 2 days).<br>In patients with hyperinfection syndrome, the standard dose is continued twice daily for 5-7<br>days. Thiabendazole is highly effective in the treatment of cutaneous larva migrans. Cutaneous<br>Larva Migrans (Creeping Eruption) The standard dose is given twice daily for 2 days.<br>Adverse Reactions: Adverse effects are generally mild and transient but can be severe; the<br>most common are dizziness, anorexia, nausea, and vomiting.<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"<p>Anthelmintic drugs are used to eradicate or reduce the numbers of helminthic parasites in theintestinal tract or tissues of the body. Most anthelmintics are active against specific parasites;thus, parasites must be identified before treatment is started.Individual DrugsAlbendazoleAlbendazole, a broad-spectrum oral anthelmintic, is used for pinworm infection, ascariasis,trichuriasis, strongyloidiasis, and infections with both hookworm species. Albendazole [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":6511,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[684],"tags":[],"class_list":["post-6660","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-chemotherapeutic-agents"],"jetpack_featured_media_url":"https:\/\/workhouse.sweetdishy.com\/wp-content\/uploads\/2024\/11\/3755529.png","_links":{"self":[{"href":"https:\/\/workhouse.sweetdishy.com\/index.php\/wp-json\/wp\/v2\/posts\/6660","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/workhouse.sweetdishy.com\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/workhouse.sweetdishy.com\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/workhouse.sweetdishy.com\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/workhouse.sweetdishy.com\/index.php\/wp-json\/wp\/v2\/comments?post=6660"}],"version-history":[{"count":1,"href":"https:\/\/workhouse.sweetdishy.com\/index.php\/wp-json\/wp\/v2\/posts\/6660\/revisions"}],"predecessor-version":[{"id":6661,"href":"https:\/\/workhouse.sweetdishy.com\/index.php\/wp-json\/wp\/v2\/posts\/6660\/revisions\/6661"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/workhouse.sweetdishy.com\/index.php\/wp-json\/wp\/v2\/media\/6511"}],"wp:attachment":[{"href":"https:\/\/workhouse.sweetdishy.com\/index.php\/wp-json\/wp\/v2\/media?parent=6660"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/workhouse.sweetdishy.com\/index.php\/wp-json\/wp\/v2\/categories?post=6660"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/workhouse.sweetdishy.com\/index.php\/wp-json\/wp\/v2\/tags?post=6660"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}