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Malaria is a disease of the blood that is caused by the Plasmodium parasite. The parasite is transmitted from person to person by a particular type of mosquito. Female Anopheles mosquito is the only mosquito that transmits malaria.
Malaria is a disease of the blood that is caused by the Plasmodium parasite. The parasite is transmitted from person to person by a particular type of mosquito. Female Anopheles mosquito is the only mosquito that transmits malaria.
Malaria is a disease of the blood that is caused by the Plasmodium parasite. The parasite is transmitted from person to person by a particular type of mosquito. Female Anopheles mosquito is the only mosquito that transmits malaria.
#18 Gepulango, Ethel Princess The word malaria comes from 18th century Italian mala meaning "bad" and aria meaning "air".
the term was first used by Dr. Francisco Torti, Italy, when people thought the disease was caused by foul air in marshy areas.
Malaria is a disease of the blood that is caused by the Plasmodium parasite, which is transmitted from person to person by a particular type of mosquito.
THE ANOPHELES MOSQUITO The female Anopheles mosquito is the only mosquito that transmits malaria. Serve as the vector that carries and transfers the infectious agent (Plasmodium) primarily bites between the hours of 9pm and 5am, which is why sleeping under a mosquito net at night is such an important method of prevention.
Plasmodium falciparum - the most serious form of the disease. It is most common in Africa, especially sub- Saharan Africa. Plasmodium vivax - milder form of the disease, generally not fatal. This species is most commonly found in Asia, Latin America, and parts of Africa. Plasmodium malariae - milder form of the disease, generally not fatal. known to stay in the blood of some people for several decades.
Plasmodium ovale. - rarely found outside Africa or the western Pacific islands. Symptoms are similar to those of P. vivax. Plasmodium knowlesi -causes malaria in macaques but can also infect humans.occurs in certain forested areas of South-East Asia.
The morphology of P. knowlesi parasites in human infections: closely resembled those of P. falciparum in the early trophozoite stage and P. malariae in the later stages of the erythrocytic cycle. Malaria commonly occur s in Central America, South America, Caribbean, Africa, and Asia The Malaria Control Program has categorized these 79 provinces based on the 5-year average .This helps the program in prioritizing resources in Categories A & B provinces. Out of the 79 provinces, 57 are malaria endemic provinces. In 2007, 6 provinces have been added in the list of Category D provinces. Involves two hosts, Human and Anopheles mosquitoes
The disease is transmitted to humans when an infected female Anopheles mosquito bites a person and injects the malaria parasites (sporozoites) into the blood.
Sporozoites travel through the bloodstream to the liver, mature, and eventually infect the human red blood cells.
While in red blood cells, the parasites again develop until a mosquito takes a blood meal from an infected human and ingests human red blood cells containing the parasites. Then the parasites reach the Anopheles mosquitos stomach and eventually invade the mosquito salivary glands. When an Anopheles mosquito bites a human, these sporozoites complete and repeat the complex Plasmodium life cycle.
Incubation means the time between becoming infected and the appearance of symptoms. This generally depends on the type of parasite:
P. falciparum - 9 to 14 days P. vivax - 12 to 18 days P. ovale - 12 to 18 days P. malariae - 18 to 40 days
However, incubation periods can vary from as short as 7 days, to several months for P. vivax and P. ovale.
The first symptoms include fever, headache and vomiting. . It is extremely uncommon for malaria to cause skin lesions or rash.
If not treated within 24 hours, P. falciparum malaria can progress to severe illness often leading to death. Children with severe malaria frequently develop one or more of the following symptoms: severe anaemia, respiratory distress in relation to metabolic acidosis, or cerebral malaria.
In adults, multi-organ involvement is also frequent. In malaria endemic areas, persons may develop partial immunity, allowing asymptomatic infections to occur.
Demonstration of the parasites in peripheral blood is important to a diagnosis
Several effective methods of diagnosis have been developed: Fluorescent dye staining DNA probe specific for P. falciparum PCR diagnostics ELISA detection of P. falciparum antigen WHO recommends that all cases of suspected malaria be confirmed using parasite-based diagnostic testing (either microscopy or rapid diagnostic test) before administering treatment. These tests take less than 30 minutes to perform.
Rapid tests can detect proteins called antigens that are present in Plasmodium. However, the reliability of rapid tests varies significantly from product to product. Thus, it is recommended that rapid tests be used in conjunction with microscopy.
the polymerase chain reaction (PCR) ,which detects malaria DNA. Because this test is not widely available, it is important not to delay treatment while waiting for results.
According to the CDC, the following drugs are commonly used for treating malaria: artemether-lumefantrine (Coartem) atovaquone-proguanil (Malarone) chloroquine clindamycin (used in combination with quinine) doxycycline (used in combination with quinine) mefloquine (Lariam) quinidine quinine artesunate
Most medications are available only as tablets or pills. Intravenous treatment with quinidine may be needed in severe malaria or when the patient cannot take oral medications.
Patients with P. vivax or P. ovale may not be completely cured by the above medications, even though the symptoms resolve. This is because the parasites can hide in the liver. A medication called primaquinine is used to eradicate the liver form, but this drug cannot be given to people who are deficient in an enzyme called G6PD.
The best available treatment, particularly for P. falciparum malaria, is artemisinin-based combination therapy (ACT).
Artemether-lumefantrine: Coartem as the 1st line treatment of uncomplicated P. falciparum cases, followed by Primaquine on the 4th day of treatment.
Treatment of severe P.falciparum is a combination therapy of quinine ampule/tablet plus any of the following antibiotics: Tetracycline, Doxycycline or Clindamycin.
P. vivax cases are treated with Chloroquine for 3 days and Primaquine for 14 days
PfSPZ, an unusual experimental malaria vaccine, developed by Sanaria Inc. of Rockville, Maryland, USA, has shown great promise in an early-stage clinical trial. Trial researchers said the vaccine may provide 100% protection against malaria infection in healthy adults.It is said that PfSPZ has the best result for a malaria vaccine so far. . It uses weakened forms of the whole, immature "sporozoite" phase of the parasite, and not an assortment of parasite proteins to induce an immune response.
On October 10th, 2013, that a large-scale Phase III African trial using the experimental malaria vaccine RTS,S continued protecting young children up to 18 months after vaccination. The trial showed that RTS,S reduced cases of clinical malaria in young children by 46% after the first vaccine, compared to children of the same aged (5-17 months) who received a control vaccine. Babies aged six to twelve weeks had a 27% lower clinical malaria incidence.
Vector control is the main way to reduce malaria transmission at the community level
Two forms of vector control are effective in a wide range of circumstances.
Insecticide-treated mosquito nets (ITNs) Long-lasting insecticidal nets (LLINs) are the preferred form of ITNs for public health distribution programmes. The most cost effective way to achieve this is through provision of free LLINs, so that everyone sleeps under a LLIN every night.
Indoor spraying with residual insecticides Indoor residual spraying (IRS) with insecticides is a powerful way to rapidly reduce malaria transmission. Its full potential is realized when at least 80% of houses in targeted areas are sprayed. Indoor spraying is effective for 36 months, depending on the insecticide used and the type of surface on which it is sprayed. Longer-lasting forms of existing IRS insecticides, as well as new classes of insecticides for use in IRS programmes, are under development.
Antimalarial medicines can also be used to prevent malaria: For travellers, malaria can be prevented through chemoprophylaxis, which suppresses the blood stage of malaria infections, thereby preventing malaria disease. WHO recommends intermittent preventive treatment with sulfadoxine-pyrimethamine for pregnant women living in high transmission areas, at each scheduled antenatal visit after the first trimester. In 2012, WHO recommended Seasonal Malaria Chemoprevention as an additional malaria prevention strategy for areas of the Sahel sub-Region of Africa.
administration of monthly courses of amodiaquine plus sulfadoxine-pyrimethamine to all children under 5 years of age during the high transmission season.
The vision of the Malaria Control Program is a malaria-free Philippines by 2020. Strategies of the MCP include the following: 1) Early diagnosis and prompt treatment 2) Vector control insecticide-treated mosquito net as main vector control strategy, complemented by indoor residual spraying 3) early management and disease surveillance 4) monitoring and evaluation drug and insecticide resistance monitoring; drug quality monitoring (pilot study to determine the baseline profile); Quality Assurance for microscopy (GF sites) and Philippine Malaria Information System at the provincial level. Health services, including malaria control program has been devolved to the local government units (Local GovernmentCode of 1991). The Department of Health has further undergone reorganization to address its new role and mandate under a decentralized set-up. The functions of the DOH are policy formulation, advocacy, program development, standard setting, technical assistance, regulation and monitoring.
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