salient features

Malaria Definition & Organisms

ThisMalaria is a protozoan disease transmitted by the bite of infected Anopheles mosquitoes. It is the most important of the parasitic diseases of humans, with transmission in 107 countries containing 3 billion people and causing 13 million deaths each year. Although there are promising new control and research initiatives, malaria remains today, as it has been for centuries, a heavy burden on tropical communities, a threat to nonendemic countries, and a danger to travelers. !

Plasmodium Falciparam

Plasmodium Vivax

Plasmodium oval

Plasmodium Malariae

Etiology and Pathogenesis

Four species of the genus Plasmodium cause nearly all malarial infections in humans .These are P. falciparum, P. vivax, P. ovale, and P. malariae . Almost all deaths are caused by falciparum malaria.

Human infection begins when a female anopheline mosquito inoculates plasmodial sporozoites from its salivary gland during a blood meal . These microscopic malarial parasites are carried rapidly via the bloodstream to the liver, where they invade hepatic parenchymal cells and begin a period of asexual reproduction.

By this amplification process a single sporozoite eventually may produce from 10,000 to >30,000 daughter merozoites. The swollen infected liver cell eventually bursts, discharging motile merozoites into the bloodstream. These then invade the red blood cells (RBCs) and multiply six- to twentyfold every 4872 h. When the parasites reach densities of ~50/L of blood, the symptomatic stage of the infection begins. immediately but remain dormant for a period ranging from 3 weeks to a year or longer before reproduction begins. These dormant forms, or hypnozoites, are the cause of the relapses that characterize infection with these two species.

In P. vivax and P. ovale infections, a proportion of the intrahepatic forms do not divide

Malignant Malaria
Falciparum Malaria is called as Malignant Malaria due to its potential
To produce more merozoites in

Cerebral

lesser time(5 days) and cause sever complications

To affect all stages f RBCs To block capillaries No exo-erythrocytic cycle

Pulmonary Edema

Hypoglycemia

Why Falciparum Cause Cerebral Malaria?

In P. falciparum infections, membrane protuberances appear on the erythrocyte's surface 1215 h after the cell's invasion. These "knobs" extrude a high-molecular-weight, antigenically variant, strain-specific erythrocyte membrane adhesive protein (PfEMP1) that mediates attachment to receptors on capillary endotheliuman event termed cytoadherence. Several vascular receptors have been identified, of which intercellular adhesion molecule 1 (ICAM-1) is probably the most important in the brain, chondroitin sulfate B in the placenta, and CD36 in most other organs. Thus, the infected erythrocytes stick inside and eventually block capillaries and venules. At the same stage, these P. falciparuminfected RBCs may also adhere to uninfected RBCs to form rosettes

Several days of prodromal symptoms such as malaise, headache, myalgia , anorexia, and mild fever are interrupted by the first paroxysm. Suddenly the patient feels inexplicably cold (in a hot climate) and apprehensive. Mild shivering quickly turns into violent shaking with teethchattering.

Relative Incidence of Severe Complications of Falciparum Malaria

Complication Nonpregnant Adults Pregnant Women Children

Anemia Convulsions Hypoglycemia Jaundice Renal failure Pulmonary edema

+ + + +++ +++ ++

++

+++ + +++ +++ +++ +++ + +++ +++ +

Key: , rare; +, infrequent; ++, frequent; +++, very frequent.

Bad Prognostic Clinical Features

Marked agitation
Hyperventilation (respiratory distress) Hypothermia (<36.5C) Bleeding Deep coma Repeated convulsions
Fits Fever

Cerebral Malaria

Coma

Anuria
Shock

Agitation

Cerebral Malaria

Fundoscopy in Cerebral Malaria

perimacular whitening and palecentered retinal hemorrhages

Blood film for MP

Bad Laboratory Findings

Biochemistry
Hypoglycemia (<2.2 mmol/L) Hyperlactatemia (>5 mmol/L) Acidosis (arterial pH <7.3, serum HCO3 <15 mmol/L) Elevated serum creatinine (>265 mol/L) Elevated total bilirubin (>50 mol/L) Elevated liver enzymes (AST/ALT 3 times Elevated muscle enzymes (CPK , myoglobin ) Elevated urate (>600 mol/L)

Hematology
Leukocytosis (>12,000/L) Severe anemia (PCV <15%) Coagulopathy Decreased platelet count (<50,000/L) Prolonged prothrombin time (>3 s) Prolonged partial thromboplastin time Decreased fibrinogen (<200 mg/dL) Parasitology Hyperparasitemia Increased mortality at >100,000/L High mortality at >500,000/L

Drugs used in Malaria

Primaquin Chlroquine Proguanil

Malaria

Treatmen
Uncomplicated Malaria
Infections due to Plasmodium vivax , Plasmodium malariae , and Plasmodium ovale should be treated with oral chloroquine (total dose,10- 25 mg of base/kg). .

Tropical Splenomegaly is treated by Prguanil 100mg/day+ Folic Acid 5 mg

Chronic Malaria is treated by Primaquine 15mg/day + Chloroquine

Chronic Malaria

Tropical Splenomegaly

Black water Fever

Chloroquine

Primaquine

Prguanil Transfusion + Folic Acid Frusamide Prednisolon

+ Chloroquine

Combination therapy
In much of the tropics, drugresistant P. falciparum has been increasing . It is now accepted that, to prevent resistance, falciparum malaria should be treated with drug combinations and not with single drugs in endemic areas; the same rationale has been applied successfully to the treatment of tuberculosis and HIV/AIDS. Artemisinin combination regimens now constitute first-line recommended treatment for falciparum malaria.

Artemisinin

Falciparum
Quinine

Prevention
Eradication of malaria. Health Education Self Protection Chemoprophylaxis