Definition
Malaria
is a serious infectious disease spread by certain mosquitoes. It is
most common in tropical climates. It is characterized by recurrent
symptoms of chills, fever,
and an enlarged spleen. The disease can be treated with medication, but
it often recurs. Malaria is endemic (occurs frequently in a particular
locality) in many third world countries. Isolated, small outbreaks
sometimes occur within the boundaries of the United States.
Description
Malaria
is a growing problem in the United States. Although only about 1400 new
cases were reported in the United States and its territories in 2000,
many involved returning travelers. In addition, locally transmitted
malaria has occurred in California, Florida, Texas, Michigan, New
Jersey, and New York City. While malaria can be transmitted in blood,
the American blood supply is not screened for malaria. Widespread
malarial epidemics are far less likely to occur in the United States,
but small localized epidemics could return to the Western world. As of
late 2002, primary care physicians are being advised to screen returning
travelers with fever for malaria, and a team of public health doctors
in Minnesota is recommending screening immigrants, refugees, and
international adoptees for the disease—particularly those from high-risk
areas.
The picture is far more bleak, however,
outside the territorial boundaries of the United States. A recent
government panel warned that disaster looms over Africa from the
disease. Malaria infects between 300 and 500 million people every year
in Africa, India, southeast Asia, the Middle East, Oceania, and Central
and South America. A 2002 report stated that malaria kills 2.7 million
people each year, more than 75 percent of them African children under
the age of five. It is predicted that within five years, malaria will
kill about as many people as does AIDS.
As many as half a billion people worldwide are left with chronic anemia
due to malaria infection. In some parts of Africa, people battle up to
40 or more separate episodes of malaria in their lifetimes. The spread
of malaria is becoming even more serious as the parasites that cause
malaria develop resistance to the drugs used to treat the condition. In
late 2002, a group of public health researchers in Thailand reported
that a combination treatment regimen involving two drugs known as
dihydroartemisinin and azithromycin shows promise in treating
multidrug-resistant malaria in southeast Asia.
Causes and symptoms
Human malaria is caused by four different species of a parasite belonging to genus Plasmodium: Plasmodium falciparum (the most deadly), Plasmodium vivax, Plasmodium malariae, and Plasmodium ovale.
The last two are fairly uncommon. Many animals can get malaria, but
human malaria does not spread to animals. In turn, animal malaria does
not spread to humans.
A person gets malaria
when bitten by a female mosquito who is looking for a blood meal and is
infected with the malaria parasite. The parasites enter the blood stream
and travel to the liver, where they multiply. When they re-emerge into
the blood, symptoms appear. By the time a patient shows symptoms, the
parasites have reproduced very rapidly, clogging blood vessels and
rupturing blood cells.
Malaria cannot be
casually transmitted directly from one person to another. Instead, a
mosquito bites an infected person and then passes the infection on to
the next human it bites. It is also possible to spread malaria via
contaminated needles or in blood transfusions. This is why all blood
donors are carefully screened with questionnaires for possible exposure
to malaria.
It is possible to contract malaria
in non-endemic areas, although such cases are rare. Nevertheless, at
least 89 cases of so-called airport malaria, in which travelers contract
malaria while passing through crowded airport terminals, have been
identified since 1969.
The amount of time
between the mosquito bite and the appearance of symptoms varies,
depending on the strain of parasite involved. The incubation period is
usually between 8 and 12 days for falciparum malaria, but it can be as
long as a month for the other types. Symptoms from some strains of P. vivax may not appear until 8-10 months after the mosquito bite occurred.
The
primary symptom of all types of malaria is the "malaria ague" (chills
and fever). In most cases, the fever has three stages, beginning with
uncontrollable shivering for an hour or two, followed by a rapid spike
in temperature (as high as 106°F), which lasts three to six hours. Then,
just as suddenly, the patient begins to sweat profusely, which will
quickly bring down the fever. Other symptoms may include fatigue, severe headache, or nausea and vomiting.
As the sweating subsides, the patient typically feels exhausted and
falls asleep. In many cases, this cycle of chills, fever, and sweating
occurs every other day, or every third day, and may last for between a
week and a month. Those with the chronic form of malaria may have a
relapse as long as 50 years after the initial infection.
Falciparum
malaria is far more severe than other types of malaria because the
parasite attacks all red blood cells, not just the young or old cells,
as do other types. It causes the red blood cells to become very
"sticky." A patient with this type of malaria can die within hours of
the first symptoms. The fever is prolonged. So many red blood cells are
destroyed that they block the blood vessels in vital organs (especially
the kidneys), and the spleen becomes enlarged. There may be brain
damage, leading to coma and convulsions. The kidneys and liver may fail.
Malaria in pregnancy can lead to premature delivery, miscarriage, or stillbirth.
Certain
kinds of mosquitoes (called anopheles) can pick up the parasite by
biting an infected human. (The more common kinds of mosquitoes in the
United States do not transmit the infection.) This is true for as long
as that human has parasites in his/her blood. Since strains of malaria
do not protect against each other, it is possible to be reinfected with
the parasites again and again. It is also possible to develop a chronic
infection without developing an effective immune response.
Diagnosis
Malaria
is diagnosed by examining blood under a microscope. The parasite can be
seen in the blood smears on a slide. These blood smears may need to be
repeated over a 72-hour period in order to make a diagnosis. Antibody
tests are not usually helpful because many people developed antibodies
from past infections, and the tests may not be readily available. A new
laser test to detect the presence of malaria parasites in the blood was
developed in 2002, but is still under clinical study.
Two
new techniques to speed the laboratory diagnosis of malaria show
promise as of late 2002. The first is acridine orange (AO), a staining
agent that works much faster (3-10 min) than the traditional Giemsa
stain (45-60 min) in making the malaria parasites visible under a
microscope. The second is a bioassay technique that measures the amount
of a substance called histadine-rich protein II (HRP2) in the patient's
blood. It allows for a very accurate estimation of parasite development.
A dip strip that tests for the presence of HRP2 in blood samples
appears to be more accurate in diagnosing malaria than standard
microscopic analysis.
Anyone who becomes ill
with chills and fever after being in an area where malaria exists must
see a doctor and mention their recent travel to endemic areas. A person
with the above symptoms who has been in a high-risk area should insist
on a blood test for malaria. The doctor may believe the symptoms are
just the common flu virus. Malaria is often misdiagnosed by North
American doctors who are not used to seeing the disease. Delaying
treatment of falciparum malaria can be fatal.
Treatment
Falciparum
malaria is a medical emergency that must be treated in the hospital.
The type of drugs, the method of giving them, and the length of the
treatment depend on where the malaria was contracted and how sick the
patient is.
For all strains except falciparum,
the treatment for malaria is usually chloroquine (Aralen) by mouth for
three days. Those falciparum strains suspected to be resistant to
chloroquine are usually treated with a combination of quinine and
tetracycline. In countries where quinine resistance is developing, other
treatments may include clindamycin (Cleocin), mefloquin (Lariam), or
sulfadoxone/pyrimethamine (Fansidar). Most patients receive an
antibiotic for seven days. Those who are very ill may need intensive
care and intravenous (IV) malaria treatment for the first three days.
Anyone
who acquired falciparum malaria in the Dominican Republic, Haiti,
Central America west of the Panama Canal, the Middle East, or Egypt can
still be cured with chloroquine. Almost all strains of falciparum
malaria in Africa, South Africa, India, and southeast Asia are now
resistant to chloroquine. In Thailand and Cambodia, there are strains of
falciparum malaria that have some resistance to almost all known drugs.
A patient with falciparum malaria needs to be hospitalized and given antimalarial drugs in different
combinations
and doses depending on the resistance of the strain. The patient may
need IV fluids, red blood cell transfusions, kidney dialysis, and
assistance breathing.
A drug called primaquine may prevent relapses after recovery from P. vivax or P. ovale. These relapses are caused by a form of the parasite that remains in the liver and can reactivate months or years later.
Another
new drug, halofantrine, is available abroad. While it is licensed in
the United States, it is not marketed in this country and it is not
recommended by the Centers for Disease Control and Prevention in
Atlanta.
Alternative treatments
The
Chinese herb qiinghaosu (the Western name is artemisinin) has been used
in China and southeast Asia to fight severe malaria, and became
available in Europe in 1994. Because this treatment often fails, it is
usually combined with another antimalarial drug (mefloquine) to boost
its effectiveness. It is not available in the United States and other
parts of the developed world due to fears of its toxicity, in addition
to licensing and other issues.
A Western herb called wormwood (Artemesia annua) that is taken as a daily dose can be effective against malaria. Protecting the liver with herbs like goldenseal (Hydrastis canadensis), Chinese goldenthread (Coptis chinensis), and milk thistle (Silybum marianum)
can be used as preventive treatment. Preventing mosquitoes from biting
you while in the tropics is another possible way to avoid malaria.
As of late 2002, researchers are studying a traditional African herbal remedy against malaria. Extracts from Microglossa pyrifolia, a trailing shrub belonging to the daisy family (Asteraceae), show promise in treating drug-resistent strains of P. falciparum.
Prognosis
If
treated in the early stages, malaria can be cured. Those who live in
areas where malaria is epidemic, however, can contract the disease
repeatedly, never fully recovering between bouts of acute infection.
Prevention
Several
researchers are currently working on a malarial vaccine, but the
complex life cycle of the malaria parasite makes it difficult. A
parasite has much more genetic material than a virus or bacterium. For
this reason, a successful vaccine has not yet been developed.
Malaria is an especially difficult disease to prevent by vaccination
because the parasite goes through several separate stages. One recent
promising vaccine appears to have protected up to 60% of people exposed
to malaria. This was evident during field trials for the drug that were
conducted in South America and Africa. It is not yet commercially
available.
The World Health Association (WHO)
has been trying to eliminate malaria for the past 30 years by
controlling mosquitoes. Their efforts were successful as long as the
pesticide DDT killed mosquitoes and antimalarial drugs cured those who
were infected. Today, however, the problem has returned a hundred-fold,
especially in Africa. Because both the mosquito and parasite are now
extremely resistant to the insecticides designed to kill them,
governments are now trying to teach people to take antimalarial drugs as
a preventive medicine and avoid getting bitten by mosquitoes.
A
newer strategy as of late 2002 involves the development of genetically
modified non-biting mosquitoes. A research team in Italy is studying the
feasibility of this means of controlling malaria.
Travelers
to high-risk areas should use insect repellant containing DEET for
exposed skin. Because DEET is toxic in large amounts, children should
not use a concentration higher than 35%. DEET should not be inhaled. It
should not be rubbed onto the eye area, on any broken or irritated skin,
or on children's hands. It should be thoroughly washed off after coming
indoors.
Those who use the following preventive measures get fewer infections than those who do not:
- Between dusk and dawn, remain indoors in well-screened areas.
- Sleep inside pyrethrin or permethrin repellent-soaked mosquito nets.
- Wear clothes over the entire body.
Anyone visiting endemic areas should take
antimalarial drugs starting a day or two before they leave the United
States. The drugs used are usually chloroquine or mefloquine. This
treatment is continued through at least four weeks after leaving the
endemic area. However, even those who take antimalarial drugs and are
careful to avoid mosquito bites can still contract malaria.
International
travelers are at risk for becoming infected. Most Americans who have
acquired falciparum malaria were visiting sub-Saharan Africa; travelers
in Asia and South America are less at risk. Travelers who stay in air
conditioned hotels on tourist itineraries in urban or resort areas are
at lower risk than backpackers, missionaries, and Peace Corps
volunteers. Some people in western cities where malaria does not usually
exist may acquire the infection from a mosquito carried onto a jet.
This is called airport or runway malaria.
Source.Medical Dictionary
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