Malaria: Difference between revisions

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== Diagnostic Tests/Lab Tests/Lab Values  ==
== Diagnostic Tests/Lab Tests/Lab Values  ==


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Malaria should be expected in any traveler who presents with a fever who has returned from a Malarious region within the past year.<sup>6</sup> The standard for diagnoses of malaria is through microscopic analysis of thick and thin blood smear tests.<sup>1</sup>Of the two, a thick blood smear test is more sensitive than a thin blood smear test because a greater volume of blood can be analyzed.<sup>6</sup>However, the thin blood smear can more accurately detect the correct species of malaria that is involved.<sup>1</sup>The test should be repeated 2-3 times if the smear shows a negative result for Malaria because a low parasitic level may not be detected by blood smear in the first test.<sup>1</sup>Diagnosis is determined by examining the parasite density. Parasite density is determined by the percent of infected red blood cells.<sup>6</sup>
 
Rapid Diagnostic Tests (RPTs) are used when blood smears are unavailable or examination is delayed.<sup>2</sup>They are based upon recognition of the antigens Histadine Rich Protein 2 (HRP2) and Parasyte Lactate Dehyrdrogenase (pLDH) by dipstick analysis. The HRP2 antigen detects P. falciparum and pLDH can detect and form of Plasmodium.<sup>2</sup>
 
Lab values can also be a good indication of malarial infection. The following is a list values that can be expected:<br>Hemoglobin- decreased<br>Hematocrit- decreased<br>Leukocytes- high, normal, or low<br>Sodium- slightly low<br>Platelets- normal or slightly low
 
 
 
Diagnosis of severe Malaria can be aided by recognition of specific criteria designated by the World Health Organization.<sup>3 </sup>Any one of the following criteria along with a positive blood smear for the parasite&nbsp;P.falciparum establishes the diagnoses of severe or complicated Malaria:
 
Cerebral Malaria- symptoms include decreased consciousness and seizures<br>Respiratory distress- symptoms include dyspnea and nasal flaring<br>Prostation<br>Hyperparasitemia- described as parasite density greater than or equal to 500,000/mm3<br>Severe anemia- described as hemoglobin less than or equal to 5 g/dL<br>Hypoglycemia- described as blood glucose less than or equal to 5 g/dL<br>Jaundice/icterus- characterized by yellowing of the skin as a result of loss of red blood cells<br>Renal Insufficiency- classified as anuria for at least 24 hours<br>Hemoglobinuria- described as dark colored urine<br>Shock<br>Cessation of eating and drinking<br>Repetitive vomiting<br>Hyperpyrexia- described as axillary temperature greater than or equal to 40 degrees celcius
 
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== Causes  ==
== Causes  ==

Revision as of 23:30, 4 March 2010

Welcome to PT 635 Pathophysiology of Complex Patient Problems This is a wiki created by and for the students in the School of Physical Therapy at Bellarmine University in Louisville KY. Please do not edit unless you are involved in this project, but please come back in the near future to check out new information!!

Original Editors - Students from Bellarmine University's Pathophysiology of Complex Patient Problems project.

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Definition/Description[edit | edit source]

Malaria is a parasitic infection caused by the bite of a female Anopheles mosquito.1 The infection can result from any one of five parasites from the Plasmodium group including Plasmodium flaciparum (P. flaciparum), Plasmodium vivax (P. vivax), Plasmodium ovale (P. ovale), Plasmodium malariae (P. malariae), and Plasmodium knowlesi (P. knowlesi). Malaria causes fever, chills, malaise, headaches, and myalgia and can result in death if not treated appropriately.1 The disease is most prevalent in Sub Suhahran Africa and Southeast Asia.1 It has been eliminated from the United States, but is still one of the most common causes of fever in travelers that have returned from the aforementioned areas.1

Prevalence[edit | edit source]

An estimated 500 million cases of Malaria occur each year, with 1-2 million deaths.2  About 90 % of these deaths occur in Sub-Saharan Africa.6 Severe Malaria (caused by P. falciparum) has a mortality rate of about 15-20%.1 About 1,500 cases are diagnosed within United States every year.4 An estimated 50% of the world’s population, about 3.3 billion people, are at risk for Malaria.6 The following areas are most commonly affected by malaria : Africa, India, Pakistan, Southeast Asia, Paupa New Guinea, Haiti, and parts of South America.2 109 countries and territories are affected worldwide and the disease is most prevelant in area of tropical climate, as the Anopheles mosquito is able to live in areas with warm temperatures.6 Transmission of Malaria has been eliminated from the U.S., Puerto Rico, Jamaica, Chile, Israel, Lebanon, North Korea, and Europe. However, Anopheles mosquitos are found throughout the world, except for Antarctica.  As a result, the disease can be re-introduced into any country.

Characteristics/Clinical Presentation[edit | edit source]

The person infected with Malaria will not present with symptoms until about 7 days to 4 weeks after he or she has been bitten.6 However, symptoms may not occur until up to 6 months to 1 year after the bite.2 The bite of a female Anopheles mosquito produces infection and consequent death to erythrocytes, or red blood cells, (see the Plasmodium life cycle in “causes” for more information) which causes hemolysis, anemia, and tissue hypoxia.2 Symptoms could include fever, chills, malaise, headaches, and myalgia. Cough, abdominal pain, and diarrhea may also occur, but are less likely.1 

Infection by the P. Falciparum parasite produces the most severe form of Malaria and is the most life-threatening.4 When diagnosed with Malaria, the patient is classified as either severe (complicated) or uncomplicated. The criteria for diagnosis of severe Malaria is listed in the “diagnosis” section. If infected by P. vivax or P. ovale, the patient may experience relapsing Malaria in which the infection can lie dormant in the body for up to 4 years.4

Associated Co-morbidities[edit | edit source]

Co-morbidities caused by severe Malaria (P. flaciparum) could include cerebral malaria, hypoglycemia, severe anemia, pulmonary edema, respiratory failure, renal failure, and metabolic acidosis.1 Below is a description of each, and an explanation of the pathophisiology as it relates to Malaria.

Cerebral Malaria: This form of Malaria can only be caused by P. Flaciparum.2 It is characterized by “the intense sequestration of parasites in the cerebral microvasculature.3” In other words, the parasite invades the blood vessels of the brain and disallow blood to circulate as it normally would.  Furthermore, oxygen and glucose supply to the brain is compromised because of improper amounts of blood flow.3 Cerebral Malaria causes over 80% of the casualties caused by Malaria.2 Symptoms of cerebral Malaria include seizures, stupor and focal neurological symptoms.2

Hypoglycemia: In children, hypoglycemia is caused by the inability of the liver to make new forms of glucose (hepatic gluconeogenesis) because the hepatocytes (liver cells) have been infected.3 In adults, hypoglycemia is caused by increased amounts of insulin in cells which is a result of stimulation of the islet cells in the pancreas which are responsible for some insulin production.3

Anemia: Loss of red blood cells results not only from phagocytic removal of infected erythrocytes, but also removal of uninfected erythtrocytes.3 The bone marrow, which is responsible for blood cell production,is defected in the Malaria infected individual and the result is a decreased level of erythroprotein production and an increased level of phagocytic activity within red blood cells.3

Pulmonary Edema and Respiratory Failure: Inflammatory cytokines (substances that carry signals between cells) are produced in the lungs in response to erythrocyte sequestration (microvascular obstruction).3 As a result, capillary permeability is increased which can produce pulmonary edema, dyspnea, hypoxia, or acute respiratory distress syndrome.3

Metabolic Acidosis: Lack of oxygen to the tissues produces acidosis (High H+ concentration and low pH). The effects of anemia, microvascular obstruction, and hypovolemia (reduced perfusion of the tissues) can cause this lack of oxygen.3


Medications 
[edit | edit source]

Malaria is treated with various drugs based upon three characteristics about the nature of the infection that affect the selection of the drug including the species of Plasmodium, whether the case in complicated or uncomplicated (see explanation in the “characteristics” section), and the resistance of a certain species of Plasmodium to the drug.The infection has developed resisitane to certain drugs in various regions of the world. Therefore, some drugs have been rendered ineffective in the treatment of certain species of the Plasmodium parasite which has been contracted from certain areas of the world .4 Furthermore, if a woman who has been infected with Malaria is pregnant, many of the below drugs are contraindicated. The main medications used include the following:

1.) Cholorquine Phosphate2
a.) species of plasmodium: P. vivax, P. malariae, P. ovale, and sensitive strains of P. Flaciparum
b.) type of medication: oral or parenteral
c.) side effects: parenteral dose can be associated with hypotension, cardiac arrest, and seizures
If it used for acute malarial attacks it can produce gastrointestinal upset, pruritis, headache, and visual disturbance.

2.) Mefloquine2
a.) species of plasmodium: used for Chloroquine resistant P. flaciparum
b.) type of medication: oral
c.) side effects: nausea, vomiting, abdominal pain, and dizziness

3.) Quinine2
a.) species of plasmodium: all forms of Plasmodium but more commonly used for Chloroquine resistant P. flaciparum
b.) type of medication: oral, intravenous, rectal, or intramuscular
c.) side effects: The intravenous dose can cause cardiac arrhythmias and hypotension. The oral dose can cause nausea, vomiting, diarrhea, and hypoglycemia.

4.) Proguanil/Atovaquone2
a.) species of plasmodium: all forms of Plasmodium but more commonly used for Chloroquine resistant P. flaciparum
b.) type of medication: oral
c.) side effects:  

5.) Primaquine2
a.) species of plasmodium: most commonly used for the liver phase of P. vivax and P. ovale
b.) type of medication: oral
c.) side effects: gastrointestinal distress, should not be used during pregnancy

6.) Doxcycline, Tetracycline, Clindamycin2
a.) species of plasmodium: should be used in coordination with Quinine and is most commonly used for chloroquine resistant flaciparum
b.) type of medication: oral
c.) side effects: can be associated with sun sensitization and should not be used during pregnancy

Species and Drug of Choice:[edit | edit source]

1.) Uncomplicated Malaria P. Falciparum with Chloroquine Resistance (Countries with resistance include all those that are classified as malarious regions except Central America west of the Panama Canal, Haiti, Dominican Republic and most of the Middle East.5
Treatment Options:
a.) Atovaquone-proguanil
b.) Artemether-lumefantrine
c.) Quinine Sulphate plus one of the following: Doxcycline, Tetracycline, Clindamycin
d.) Mefloquine


2.) Uncomplicated Malaria P. Falciparum Cholorquine Sensitive (Countries that are Cholorquine sensitive include all those that are classified as malarious regions except Central America west of the Panama Canal, Haiti, Dominican Republic and most of the Middle East.5
Treatment Options:
a.) Cholorquine Phosphate
b.) Hydrooxychloroquine


3.) Uncomplicated Malaria P. Malariae or P Knowlesi 5
Treatment Options:
a.) Cholorquine Phosphate
b.) Hydrooxychloroquine


4.) Uncomplicated Malaria P. Vivax or P. Ovale Cholorquine Sensitive 5
Treatment Options:
a.) Quinine Sulphate plus either Doxycycline or Tetracycline plus Primaquine Phosphate
b.) Atovaquone-proguanil plus Primaquine Phosphate
c.) Mefloquine plus Primaquine Phosphate


5.) Uncomplicated Malaria P. Vivax with Cholorquine Resistance 5
Treatment Options:
a.) Quinine Sulphate plus one of the following: Doxcycline, Tetracycline, Clindamycin
b.) Atovaquone-proguanil plus Primaquine Phosphate
c.) Mefloquine plus Primaquine Phosphate


6.) Uncomplicated Malaria, Treatment for women who are pregnant 5
Chloroquine-Sensitive (any species):
a.) Cholorquine Phosphate
b.) Hydrooxychloroquine

P. Falciparum with Chloroquine Resistance:
a.) Quinine Sulphate plus Clindamycin


P. Vivax with Cholorquine Resistance
a.) Quinine Sulphate


6.) Complicated (Severe) Malaria 5
Treatment Options:
a.) Quinidine gluconate plus one of the following: Doxcycline, Tetracycline, Clindamycin


For a complete list of dosages for each drug please visit the Center for Disease Control Website at www.cdc.gov/malaria/pdf/treatmenttable.pdf


Prevention:
[edit | edit source]

The primary mode of prophylaxis (prevention) for years has been the use of Chloroquine. However, with chloroquine resistance present in most malarious countries, the choice of drug is now based upon whether or not the country is chloroquine resistant.1 The choice of drug may also rely upon the patient. As mentioned before, some drugs are contraindicated for pregnancy as well as small children.

1.) Country with Chlorquine Resistance Treatment Options:
a.) Doxycycline Prophylaxis
b.) Atovaquone-proguanil

2.) Country without Chloroquine Resistance
a.) Chloroquine Prophylaxis

3.) Country with Chlorquine Resistance Treatment Options for Child < 5 kg or 1st Trimester of pregnancy
a.) Mefloquine Prophylaxis


For more information regarding the best choice of prophylactic drug, visit the center for disease control website at: www.cdc.gov/malaria/traverler/drugs.html

Diagnostic Tests/Lab Tests/Lab Values[edit | edit source]

Malaria should be expected in any traveler who presents with a fever who has returned from a Malarious region within the past year.6 The standard for diagnoses of malaria is through microscopic analysis of thick and thin blood smear tests.1Of the two, a thick blood smear test is more sensitive than a thin blood smear test because a greater volume of blood can be analyzed.6However, the thin blood smear can more accurately detect the correct species of malaria that is involved.1The test should be repeated 2-3 times if the smear shows a negative result for Malaria because a low parasitic level may not be detected by blood smear in the first test.1Diagnosis is determined by examining the parasite density. Parasite density is determined by the percent of infected red blood cells.6

Rapid Diagnostic Tests (RPTs) are used when blood smears are unavailable or examination is delayed.2They are based upon recognition of the antigens Histadine Rich Protein 2 (HRP2) and Parasyte Lactate Dehyrdrogenase (pLDH) by dipstick analysis. The HRP2 antigen detects P. falciparum and pLDH can detect and form of Plasmodium.2

Lab values can also be a good indication of malarial infection. The following is a list values that can be expected:
Hemoglobin- decreased
Hematocrit- decreased
Leukocytes- high, normal, or low
Sodium- slightly low
Platelets- normal or slightly low


Diagnosis of severe Malaria can be aided by recognition of specific criteria designated by the World Health Organization.3 Any one of the following criteria along with a positive blood smear for the parasite P.falciparum establishes the diagnoses of severe or complicated Malaria:

Cerebral Malaria- symptoms include decreased consciousness and seizures
Respiratory distress- symptoms include dyspnea and nasal flaring
Prostation
Hyperparasitemia- described as parasite density greater than or equal to 500,000/mm3
Severe anemia- described as hemoglobin less than or equal to 5 g/dL
Hypoglycemia- described as blood glucose less than or equal to 5 g/dL
Jaundice/icterus- characterized by yellowing of the skin as a result of loss of red blood cells
Renal Insufficiency- classified as anuria for at least 24 hours
Hemoglobinuria- described as dark colored urine
Shock
Cessation of eating and drinking
Repetitive vomiting
Hyperpyrexia- described as axillary temperature greater than or equal to 40 degrees celcius


Causes[edit | edit source]

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Systemic Involvement[edit | edit source]

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Medical Management (current best evidence)[edit | edit source]

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Physical Therapy Management (current best evidence)[edit | edit source]

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Alternative/Holistic Management (current best evidence)[edit | edit source]

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Differential Diagnosis[edit | edit source]

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Case Reports[edit | edit source]

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Resources
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Recent Related Research (from Pubmed)[edit | edit source]

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References[edit | edit source]

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