Categories
Ailmemts & Remedies

Arrhythmia

Definition:
The heart is a pump that functions by pushing the blood through its four chambers. The blood is “pushed” through in a controlled sequence of muscular contractions. The sequence is controlled by bundles of cells which control the electrical activity of the heart. When the sequence is disturbed, heart arrhythmias occur.

Arrhythmias are abnormal rhythms of the heart.  Arrhythmias cause the heart to pump blood less effectively.  Most cardiac arrhythmias are temporary and benign.  Most temporary and benign arrhythmias are those where your heart skips a beat or has an extra beat. The occasional skip or extra beat is often caused by strong emotions or exercise. Nonetheless, some arrhythmias may be life-threatening and require treatment.

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Types of Arrhythmias:
Arrhythmias can be divided into two main categories ventricular and supraventricular.  Supraventricular arrhythmias occur in the heart’s two upper chambers called the atrium.  Ventricular arrhythmias occur in the heart’s two lower chambers called the ventricles.


Electrical conduction in the heart originates in the SA node and travels through the AV node to the ventricles, resulting in a heart beat.
Supraventricular and Ventricular arrhythmias are further defined by the speed of the heartbeats: very slow, very fast and fast uncoordinated.  A very slow heart rate is called bradycardia.  In bradycardia, the heart rate is less than 60 beats per minute. A very fast heart rate is called Tachycardia meaning the heart beats faster than 100 beats per minute. A fast uncoordinated heart rate is called Fibrillation.  Fibrillation is the most serious form of arrhythmia are contractions of individual heart muscle fibers.  Arrhythmias cause nearly 250,000 deaths each year.

Supraventricular Arrhythmia

A very common long term arrhythmia is atrial fibrillation. Atrial fibrillation is very abnormal.  A normal heart beats between 60 and 100 times a minute. However, in atrial fibrillation, the atria (upper lobes of the heart) beat 400 to 600 times per minute. In response to this, the ventricles usually beat irregularly at a rate of 170 to 200 times per minute. So in Atrial Fibrillation, the upper part of the heart may beat up to 8 times as much as a normal heart.  Unfortunately, atrial fibrillation is seen in many types of heart disease; once established, it usually lasts a lifetime.

Ventricular Arrhythmia
One of the most serious arrhythmias is sustained ventricular tachycardia. In sustained ventricular tachycardia, there are consecutive impulses that arise from the ventricles at a heart rate of 100 beats or more per minute until stopped by drug treatment or electrical conversion. This condition is very dangerous.  It is dangerous because it may degenerate further into a totally disorganized electrical activity known as ventricular fibrillation. In ventricular fibrillation, heart’s action is so disorganized that it quivers and does not contract, thus failing to pump blood.

SADS:
SADS, or sudden arrhythmic death syndrome, is a term used to describe sudden death due to cardiac arrest brought on by an arrhythmia in the absence of any structural heart disease on autopsy. The most common cause of sudden death in the US is coronary artery disease.[citation needed] Approximately 300,000 people die suddenly of this cause every year in the US.[citation needed] SADS occurs from other causes. There are many inherited conditions and heart diseases that can affect young people and subsequently cause sudden death. Many of these victims have no symptoms before dying suddenly.

Causes of SADS in young people include viral myocarditis, long QT syndrome, Brugada syndrome, Catecholaminergic polymorphic ventricular tachycardia, hypertrophic cardiomyopathy and arrhythmogenic right ventricular dysplasia

Signs and symptoms:
The term cardiac arrhythmia covers a very large number of very different conditions.

The most common symptom of arrhythmia is an abnormal awareness of heartbeat, called palpitations. These may be infrequent, frequent, or continuous. Some of these arrhythmias are harmless (though distracting for patients) but many of them predispose to adverse outcomes.

Some arrhythmias do not cause symptoms, and are not associated with increased mortality. However, some asymptomatic arrhythmias are associated with adverse events. Examples include a higher risk of blood clotting within the heart and a higher risk of insufficient blood being transported to the heart because of weak heartbeat. Other increased risks are of embolisation and stroke, heart failure and sudden cardiac death.

If an arrhythmia results in a heartbeat that is too fast, too slow or too weak to supply the body’s needs, this manifests as a lower blood pressure and may cause lightheadedness or dizziness, or fainting.

Some types of arrhythmia result in cardiac arrest, or sudden death.

Medical assessment of the abnormality using an electrocardiogram is one way to diagnose and assess the risk of any given arrhythmia.

Causes:
Many types of heart disease cause arrhythmia.  Coronary disease is often a trigger.  It triggers arrhythmia because coronary heart disease produces scar tissue in the heart.  This scar tissue disrupts the transmission of signals which control the heart rhythm.  Some people are born with arrhythmias, meaning the condition is congenital. Atherosclerosis is also a factor in causing arrhythmia. Other medical conditions such as diabetes and high blood pressure also are factors. Furthermore,  stress, caffeine, smoking, alcohol, and some over-the-counter cough and cold medicines can affect your heart’s natural beating pattern.

Diagnosis:
Many different techniques are used to diagnose arrhythmia.  The techniques include:

•A standard electrocardiogram (ECG or EKG).
An EKG is the best test for diagnosing arrhythmia. This test helps doctors analyze the electrical currents of your heart and determines the type of arrhythmia you have.

•Holter monitoring.
Holter monitoring gets a continuous reading of your heart rate and rhythm over a 24-hour period (or more). You wear a recording device (the Holter monitor), which is connected to small metal disks on your chest. With certain types of monitors, you can push a “record” button to capture a rhythm when you feel symptoms. Doctors can then look at a printout of the recording to find out what causes your arrhythmia.

•Trans telephonic monitoring. Transtelephonic monitoring documents problems that may not be detected within a 24-hour period. The devices used for this type of test are smaller than a Holter monitor. One of the devises is about the size of a beeper, the other device is worn like a wristwatch. Like with Holter monitoring, you wear the recording device. When you feel the symptoms of an arrhythmia, you can telephone a monitoring station, where a record can be made. If you cannot get to a telephone during your symptoms, you can turn on the device’s memory function. Later, you can send the recorded information to a monitoring station by using a telephone. These devices also work during episodes of fainting.

•Electrophysiology studies (EPS). Electrophysiology studies are usually performed in a cardiac catheterization laboratory. In this procedure, a long, thin tube (called a catheter) is inserted through an artery in your leg and guided to your heart. A map of electrical impulses from your heart is sent through the wire to find out what kind of arrhythmia you have and where it starts. During the study, doctors can give you controlled electrical impulses to show how your heart reacts. Medicines may also be tested at this time to see which medicines will stop the arrhythmia. Once the electrical pathways causing the arrhythmia are found, radio waves can be sent through the catheter to destroy them.

•A tilt-table exam. A tilt-table exam is a way to evaluate your heart’s rhythm in cases of fainting. The test is noninvasive, which means that doctors will not use needles or catheters. Your heart rate and blood pressure are monitored as you lie flat on a table. The table is then tilted to 65 degrees. The changing angle puts stress on the area of the nervous system that maintains your heart rate and blood pressure. Doctors can see how your heart responds under carefully supervised conditions of stress.

Treatment:

Treatment of arrhythmia depend on the type of arrhythmia, the patients age, physical condition and age.  Methods are available for prevention of arrhythmia.  These methods include relaxation techniques to reduce stress, limit intake of caffeine, nicotine, alcohol and stimulant drugs. Many arrhythmias require no treatment, they are naturally controlled by the body’s immune system. However if it is  necessary that arrhythmias must be controlled, they can be controlled by drugs, Cardioversion, Automatic implantable defibrillators or an Artificial pacemaker. Arrhythmias are very serious.

Arrhythmias that start in the lower chambers of the heart (the ventricles) are more serious than those that start in the upper chambers (the atria).

Management:
The method of cardiac rhythm management depends firstly on whether or not the affected person is stable or unstable. Treatments may include physical maneuvers, medications, electricity conversion, or electro or cryo cautery.

Physical maneuvers
A number of physical acts can increase parasympathetic nervous supply to the heart, resulting in blocking of electrical conduction through the AV node. This can slow down or stop a number of arrhythmias that originate above or at the AV node (you may click to see: supraventricular tachycardias). Parasympathetic nervous supply to the heart is via the vagus nerve, and these maneuvers are collectively known as vagal maneuvers.

Antiarrhy
thmic drugsMain article: Antiarrhythmic agents
There are many classes of antiarrhythmic medications, with different mechanisms of action and many different individual drugs within these classes. Although the goal of drug therapy is to prevent arrhythmia, nearly every antiarrhythmic drug has the potential to act as a pro-arrhythmic, and so must be carefully selected and used under medical supervision.

Other drugs

A number of other drugs can be useful in cardiac arrhythmias.

Several groups of drugs slow conduction through the heart, without actually preventing an arrhythmia. These drugs can be used to “rate control” a fast rhythm and make it physically tolerable for the patient.

Some arrhythmias promote blood clotting within the heart, and increase risk of embolus and stroke. Anticoagulant medications such as warfarin and heparins, and anti-platelet drugs such as aspirin can reduce the risk of clotting.

Electricity
Dysrhythmias may also be treated electrically, by applying a shock across the heart — either externally to the chest wall, or internally to the heart via implanted electrodes.

Cardioversion is either achieved pharmacologically or via the application of a shock synchronised to the underlying heartbeat. It is used for treatment of supraventricular tachycardias. In elective cardioversion, the recipient is usually sedated or lightly anesthetized for the procedure.

Defibrillation differs in that the shock is not synchronised. It is needed for the chaotic rhythm of ventricular fibrillation and is also used for pulseless ventricular tachycardia. Often, more electricity is required for defibrillation than for cardioversion. In most defibrillation, the recipient has lost consciousness so there is no need for sedation.

Defibrillation or cardioversion may be accomplished by an implantable cardioverter-defibrillator (ICD).

Electrical treatment of dysrhythmia also includes cardiac pacing. Temporary pacing may be necessary for reversible causes of very slow heartbeats, or bradycardia, (for example, from drug overdose or myocardial infarction). A permanent pacemaker may be placed in situations where the bradycardia is not expected to recover.

Electrical cautery
Some cardiologists further sub-specialise into electrophysiology. In specialised catheter laboratories, they use fine probes inserted through the blood vessels to map electrical activity from within the heart. This allows abnormal areas of conduction to be located very accurately, and subsequently destroyed with heat, cold, electrical or laser probes.

This may be completely curative for some forms of arrhythmia, but for others, the success rate remains disappointing. AV nodal reentrant tachycardia is often curable. Atrial fibrillation can also be treated with this technique (e.g. pulmonary vein isolation), but the results are less reliable.

Click  to learn more about  arrhythmia

Disclaimer: This information is not meant to be a substitute for professional medical advise or help. It is always best to consult with a Physician about serious health concerns. This information is in no way intended to diagnose or prescribe remedies.This is purely for educational purpose.

Resources:
http://www.mamashealth.com/ardiag.asp
http://www.mamashealth.com/arrhythmia.asp
http://hrssc.com/hrssc-patient-resource-how-to-diagnose-arrhythmias.html
http://www.nsmc.partners.org/web/service/heart_arrhythmia
http://www1.ecardio.com/PS/Cardiac.aspx
http://www.medicompinc.com/holter_service.html

http://www.nhlbi.nih.gov/health/dci/Diseases/ekg/ekg_during.html

http://commons.wikimedia.org/wiki/File:Heart_conduct_atrialfib.gif

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Categories
Herbs & Plants

Elephant Tree

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Botanical Name: Bursera microphylla
Family: Burseraceae
Genus: Bursera
Species: B. microphylla
Kingdom: Plantae
Order: Sapindales

Common Name : Elephant Tree

Habitat: This tree is native to Northern Mexico, in the states of Baja California, Baja California Sur, Sinaloa, Sonora and Zacatecas; and the Southwestern United States, in Southern California and Arizona); especially desert ecoregions.

Description:
Bursera microphylla is a shrub or small tree, to 16 feet, widespreading, with a very short, thick, trunk. and its bark is light gray to white, with younger branches having a reddish color. The light foliage is made up of long, straight, flat, legume-like leaves which are composed of paired leaflets. It flowers in rounded yellow buds which open into small, star-shaped white or cream flowers. The fruit is a drupe containing a yellow stone.

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Leaf: Alternate, pinnate, drought deciduous, 11-21 ovate to lanceolate, entire, 1/4 inch long leaflets per leaf, 1 to 1 1/2 inches overall, with a camphor-like odor.
Flower: Small, creamy white, borne on long stalks, usually clustered in 3’s, midsummer.
Fruit: Reddish brown, maturing late fall, 1/3 inch long, splitting into 3 pieces at maturity.
Twig: Resinous and stout, reddish brown.
Bark: Tight and smooth, very attractive, outer layer pale creamy white to gray-brown, peeling to reveal gray-green (photosynthetic), innermost bark reddish, spouting resin when cut.

This mysterious tree of the desert can readily attain a height of six meters in the southwestern USA, with its thick tortuous smooth trunks arrayed in a multifurcate branching habit; moreover, a mature specimen may reach six to seven meters in lateral spread with a characteristic open crown. In some parts of Mexico the height may reach as much as 15 meters with correspondingly greater spread. Young trees have a light reddish trunk, but mature trees have a characteristic white peeling bark. Glabrous leaves manifest an aroma of camphor, and are pinnately compound in a planar geometry with length of two to eight centimeters; the paired leaflets may number anywhere from seven to 33, with the odd terminal leaflet being lone

The drupe type leathery fruits are oval in shaped and tri-valved, with the stone being yellow. Stamens number from six to ten (Jepson) Flower buds are yellow, while the opened cream to white star shaped flower is five petalled with minute green five millimeter sepals and petals measuring four millimeters; blooming time is typically in June and July. Diagnostic features differentiating this plant from its genus member B. fagaroides include the notably longer (up to four cm) and more acute leaflets of the latter.

Medicinal Uses:
The Cahuilla Indian people of the Colorado Desert region of California, according to legend, used the red sap of the Elephant Tree as a panacea medicine.

The bark is flaky and papery like a birch tree and can carry a red hue with age. The leaves give off a camphor smell when crushed. Native Americans considered it a valuable tree with healing powers, probably due to the camphor oils it contains.

The Cahuilla Indians extracted the sap to be used as a generalized cure for a gamut of illnesses. (Bean) In present day the resin is dried and prepared as a substance similar to myrrh, mirroring the use of its Asian family member tree. In Sonora tannin has been historically extracted from the bark for export; (Kearney) in the same Mexican state the gum has been used to treat venereal disease. The copal form resin of intermediate polymerization has been harvested from several Mexican regions historically for manufacture of cement and varnish, and has also been used in medicinal treatment for scorpion stings; there is data to suggest B. fagaroides may have been more common for the latter uses, as well as incense burned in Aztec and Mayan temples in prehistorical times.

The resin was an Aztec remedy.  In the 16th century, Fray Bernardino de Sahagun wrote that a little ground copal, the size of a small fingernail, added to water and drunk only7 once a day on an empty stomach would cure diarrhea.  The resin, bark and leaves are steeped in tequila or grain alcohol to make a tincture that is applied to gum sores, cold sores, and abscessed teeth.  The dried stems and leaves are drunk in a tea to relieve painful urination, and as a stimulating expectorant for slowly healing bronchitis and chest colds.  A tea of the leaves or the leaves and bark is used as a tonic to fortify the immune system.

Disclaimer:
The information presented herein is intended for educational purposes only. Individual results may vary, and before using any supplements, it is always advisable to consult with your own health care provider.

Resources:
http://cnre.vt.edu/dendro/dendrology/syllabus/factsheet.cfm?ID=765
http://en.wikipedia.org/wiki/Bursera_microphylla
http://www.ubcbotanicalgarden.org/potd/2008/09/bursera_microphylla.php
http://www.globaltwitcher.com/artspec_information.asp?thingid=90792

http://tchester.org/bd/species/burseraceae/bursera_microphylla.html

http://swbiodiversity.org/images/vasc_herbarium_images/Burseraceae/photos/Bursera_buds.jpg

http://www.herbnet.com/Herb%20Uses_DE.htm

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Categories
Healthy Tips

Few Tips to Improve Your Slumber Tonight

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Sleep is important for your physical and emotional health. Sleep may help you stay healthy by keeping your immune system strong. Getting enough sleep can help your mood and make you feel less stressed.

But we all have trouble sleeping sometimes. This can be for many reasons. You may have trouble sleeping because of depression, insomnia, fatigue, or Sjögren’s syndrome. If you are depressed, feel anxious, or have post-traumatic stress disorder (PTSD), you may have trouble falling or staying asleep.

Whatever the cause, there are things you can do:

Your sleeping area :
•Use your bedroom only for sleeping
•Move the TV out of your bedroom
•Keep your bedroom quiet and dark
Your evening and bedtime routine

•Get regular exercise — but not within 3 to 4 hours before bedtime
•Create a relaxing bedtime routine
•Go to bed at the same time every night
•Consider using a sleep mask and earplugs
If you can’t sleep
•Imagine yourself in a peaceful, pleasant place
•Don’t drink any liquids after 6 PM if waking up during the night to go to the bathroom is a problem


Your activities during the day
Your habits and activities can affect how well you sleep. Here are some tips.
•Exercise during the day. Don’t exercise after 5 p.m. because it may be harder to fall asleep.
•Get outside during daylight hours. Spending time in sunlight helps to reset your body’s sleep and wake cycles.
•Don’t drink or eat anything that has caffeine in it, such as coffee, tea, cola, and chocolate.
•Don’t drink alcohol before bedtime. Alcohol can cause you to wake up more often during the night.
•Don’t smoke or use tobacco, especially in the evening. Nicotine can keep you awake.
•Don’t take naps during the day, especially close to bedtime.
•Don’t take medicine that may keep you awake, or make you feel hyper or energized, right before bed. Your doctor can tell you if your medicine may do this and if you can take it earlier in the day.

If you can’t sleep because you are in great pain or have an injury, you often feel anxious at night, or you often have bad dreams or nightmares, talk to your doctor.

Source: Health.com April 24, 2008

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Categories
Ailmemts & Remedies

Anthrax

Alternative Names: Woolsorter’s disease; Ragpicker’s disease; Cutaneous anthrax; Gastrointestinal anthrax.

Definition:
Anthrax is a life-threatening infectious disease that normally affects animals, especially ruminants (such as goats, cattle, sheep, and horses). Anthrax can be transmitted to humans by contact with infected animals or their products.
CLICK & SEE
Anthrax is an acute disease caused by the bacterium Bacillus anthracis. Most forms of the disease are lethal. There are effective vaccines against anthrax, and some forms of the disease respond well to antibiotic treatment.

Like many other members of the genus Bacillus, Bacillus anthracis can form dormant endospores (often referred to as “spores” for short, but not to be cnfused with fungal spores) that are able to survive in harsh conditions for decades or even centuries. Such spores can be found on all continents, even Antarctica.  When spores are inhaled, ingested, or come into contact with a skin lesion on a host they may reactivate and multiply rapidly.

Anthrax spores can be produced in vitro and used as a biological weapon. Anthrax does not spread directly from one infected animal or person to another; it is spread by spores. These spores can be transported by clothing or shoes. The dead body of an animal that died of anthrax can also be a source of anthrax spores.

In recent years, anthrax has received a great deal of attention as it has become clear that the infection can also be spread by a bioterrorist attack or by biological warfare.

Symptoms:

There are three different types of anthrax.
1.Cutaneous anthrax ,2.Inhalational anthrax  and 3.Intestinal anthrax

1.Cutaneous anthrax – this type accounts for about 95 per cent of cases. People handling dead animals – such as abattoir workers and tanners – are at most risk. Infection occurs when the bacterium comes into direct contact with a cut or abrasion in the skin.

At first the skin itches. This is soon followed by the appearance of a small, raised itchy bump that looks like an insect bite. This skin lesion is commonly located on the head, forearms or hands.

Within one to two days the skin lesion develops into a vesicle and becomes a painless ulcer, usually about 1cm to 3cm in diameter. After two to six days the black dying central area of the ulcer that’s characteristic of cutaneous anthrax is apparent.

If left untreated, cutaneous anthrax infection can spread and cause blood poisoning, which is fatal in up to 20 per cent of cases, but with effective antibiotic treatment few deaths occur.

2.Inhalational anthrax – when inhaled, the larger spores lodge in the windpipe or throat, while smaller ones lodge further down the respiratory tract in the lungs. The anthrax bacteria produce toxins that enter the bloodstream and cause haemorrhaging and tissue decay.

Initial symptoms of inhalational anthrax, which is rare, are mild and non-specific, similar to the symptoms of a flu-like infection. These include tiredness, weakness, fever, mild non-productive cough and chest pain.

If left untreated, over the next two to six days this mild phase becomes severe, causing breathing problems, sepsis and bleeding. By the time the infection has reached this stage it’s usually fatal.

3.Intestinal anthrax
– a very rare form of food poisoning that may follow the ingestion of contaminated meat.

Initial symptoms are nausea, vomiting, loss of appetite and fever. As the infection becomes more severe, abdominal pain, vomiting of blood and severe diarrhoea occur.

Intestinal anthrax is often fatal.

Cause:-
Bacteria :-

Bacillus anthracis is a rod-shaped, Gram-positive, aerobic bacterium about 1 by 9 micrometers in length. It was shown to cause disease by Robert Koch in 1876. The bacterium normally rests in endospore form in the soil, and can survive for decades in this state. Herbivores are often infected whilst grazing or browsing, especially when eating rough, irritant or spiky vegetation: the vegetation has been hypothesized to cause wounds within the gastrointestinal tract permitting entry of the bacterial endo-spores into the tissues, though this has not been proven. Once ingested or placed in an open cut, the bacterium begins multiplying inside the animal or human and typically kills the host within a few days or weeks. The endo-spores germinate at the site of entry into the tissues and then spread via the circulation to the lymphatics, where the bacteria multiply.

Exposure:-

Occupational exposure to infected animals or their products (such as skin, wool, and meat) is the usual pathway of exposure for humans. Workers who are exposed to dead animals and animal products are at the highest risk, especially in countries where anthrax is more common. Anthrax in livestock grazing on open range where they mix with wild animals still occasionally occurs in the United States and elsewhere. Many workers who deal with wool and animal hides are routinely exposed to low levels of anthrax spores but most exposures are not sufficient to develop anthrax infections. It is presumed that the body’s natural defenses can destroy low levels of exposure. These people usually contract cutaneous anthrax if they catch anything. Throughout history, the most dangerous form of inhalational anthrax was called Woolsorters’ disease because it was an occupational hazard for people who sorted wool. Today this form of infection is extremely rare, as almost no infected animals remain. The last fatal case of natural inhalational anthrax in the United States occurred in California in 1976, when a home weaver died after working with infected wool imported from Pakistan. The autopsy was done at UCLA hospital. To minimize the chance of spreading the disease, the deceased was transported to UCLA in a sealed plastic body bag within a sealed metal container.

Pulmonary:

Respiratory infection in humans initially presents with cold or flu-like symptoms for several days, followed by severe (and often fatal) respiratory collapse. Historical mortality was 92%, but, when treated early (seen in the 2001 anthrax attacks), observed mortality was 45%. Distinguishing pulmonary anthrax from more common causes of respiratory illness is essential to avoiding delays in diagnosis and thereby improving outcomes. An algorithm for this purpose has been developed. Illness progressing to the fulminant phase has a 97% mortality regardless of treatment.

Gastrointestinal:-

Gastrointestinal infection in humans is most often caused by eating anthrax-infected meat and is characterized by serious gastrointestinal difficulty, vomiting of blood, severe diarrhea, acute inflammation of the intestinal tract, and loss of appetite. Some lesions have been found in the intestines and in the mouth and throat. After the bacterium invades the bowel system, it spreads through the bloodstream throughout the body, making even more toxins on the way. Gastrointestinal infections can be treated but usually result in fatality rates of 25% to 60%, depending upon how soon treatment commences.  This form of anthrax is the rarest form. In the United States, there is only one official case reported in 1942 by the CDC.

Cutaneous :

Anthrax skin lesionCutaneous (on the skin) anthrax infection in humans shows up as a boil-like skin lesion that eventually forms an ulcer with a black center (eschar). The black eschar often shows up as a large, painless necrotic ulcer (beginning as an irritating and itchy skin lesion or blister that is dark and usually concentrated as a black dot, somewhat resembling bread mold) at the site of infection. In general, cutaneous infections form within the site of spore penetration between 2 and 5 days after exposure. Unlike bruises or most other lesions, cutaneous anthrax infections normally do not cause pain.

Mode of infection :-
Inhalational anthrax, mediastinal wideningAnthrax can enter the human body through the intestines (ingestion), lungs (inhalation), or skin (cutaneous) and causes distinct clinical symptoms based on its site of entry. In general, an infected human will be quarantined. However, anthrax does not usually spread from an infected human to a noninfected human. But, if the disease is fatal to the person’s body, its mass of anthrax bacilli becomes a potential source of infection to others and special precautions should be used to prevent further contamination. Inhalational anthrax, if left untreated until obvious symptoms occur, may be fatal.

Anthrax can be contracted in laboratory accidents or by handling infected animals or their wool or hides. It has also been used in biological warfare agents and by terrorists to intentionally infect as exemplified by the 2001 anthrax attacks.

Diagnosis:
Other than Gram Stain of specimens, there are no specific direct identification techniques for identification of Bacillus species in clinical material. These organisms are Gram-positive but with age can be Gram-variable to Gram-negative. A specific feature of Bacillus species that makes it unique from other aerobic microorganisms is its ability to produce spores. Although spores are not always evident on a Gram stain of this organism, the presence of spores confirms that the organism is of the genus Bacillus.

All Bacillus species grow well on 5% Sheep blood agar and other routine culture media. PLET (polymyxin-lysozyme-EDTA-thallous acetate) can be used to isolate B.anthracis from contaminated specimens, and bicarbonate agar is used as an identification method to induce capsule formation.

Bacillus sp. will usually grow within 24 hours of incubation at 35 degrees C, in ambient air (room temperature) or in 5% CO2. If bicarbonate agar is used for identification then the media must be incubated in 5% CO2.

B.anthracis appears as medium-large, gray, flat, irregular with swirling projections, often referred to as “medusa head” appearance, and is non-hemolytic on 5% sheep blood agar. It is non-motile, is susceptible to penicillin and produces a wide zone of lecithinase on egg yolk agar. Confirmatory testing to identify B.anthracis includes gamma bacteriophage testing, indirect hemagglutination and enzyme linked immunosorbent assay to detect antibodies.

Treatment:
Anthrax cannot be spread directly from person to person, but a patient’s clothing and body may be contaminated with anthrax spores. Effective decontamination of people can be accomplished by a thorough wash-down with antimicrobial effective soap and water. Waste water should be treated with bleach or other anti-microbial agent. Effective decontamination of articles can be accomplished by boiling contaminated articles in water for 30 minutes or longer. Chlorine bleach is ineffective in destroying spores and vegetative cells on surfaces, though formaldehyde is effective. Burning clothing is very effective in destroying spores. After decontamination, there is no need to immunize, treat or isolate contacts of persons ill with anthrax unless they were also exposed to the same source of infection. Early antibiotic treatment of anthrax is essential—delay significantly lessens chances for survival. Treatment for anthrax infection and other bacterial infections includes large doses of intravenous and oral antibiotics, such as fluoroquinolones, like ciprofloxacin (cipro), doxycycline, erythromycin, vancomycin or penicillin. In possible cases of inhalation anthrax, early antibiotic prophylaxis treatment is crucial to prevent possible death. In May 2009, Human Genome Sciences submitted a Biologic License Application (BLA, permission to market) for its new drug, raxibacumab (brand name ABthrax) intended for emergency treatment of inhaled anthrax.[28] If death occurs from anthrax the body should be isolated to prevent possible spread of anthrax germs. Burial does not kill anthrax spores.

If a person is suspected as having died from anthrax, every precaution should be taken to avoid skin contact with the potentially contaminated body and fluids exuded through natural body openings. The body should be put in strict quarantine. A blood sample taken in a sealed container and analyzed in an approved laboratory should be used to ascertain if anthrax is the cause of death. Microscopic visualization of the encapsulated bacilli, usually in very large numbers, in a blood smear stained with polychrome methylene blue (McFadyean stain) is fully diagnostic, though culture of the organism is still the gold standard for diagnosis. Full isolation of the body is important to prevent possible contamination of others. Protective, impermeable clothing and equipment such as rubber gloves, rubber apron, and rubber boots with no perforations should be used when handling the body. No skin, especially if it has any wounds or scratches, should be exposed. Disposable personal protective equipment is preferable, but if not available, decontamination can be achieved by autoclaving. Disposable personal protective equipment and filters should be autoclaved, and/or burned and buried. Bacillus anthracis bacillii range from 0.5–5.0 ?m in size. Anyone working with anthrax in a suspected or confirmed victim should wear respiratory equipment capable of filtering this size of particle or smaller. The US National Institute for Occupational Safety and Health (NIOSH) and Mine Safety and Health Administration (MSHA) approved high efficiency-respirator, such as a half-face disposable respirator with a high-efficiency particulate air (HEPA) filter, is recommended.[29] All possibly contaminated bedding or clothing should be isolated in double plastic bags and treated as possible bio-hazard waste. The victim should be sealed in an airtight body bag. Dead victims that are opened and not burned provide an ideal source of anthrax spores. Cremating victims is the preferred way of handling body disposal. No embalming or autopsy should be attempted without a fully equipped biohazard laboratory and trained and knowledgeable personnel.

Delays of only a few days may make the disease untreatable and treatment should be started even without symptoms if possible contamination or exposure is suspected. Animals with anthrax often just die without any apparent symptoms. Initial symptoms may resemble a common cold—sore throat, mild fever, muscle aches and malaise. After a few days, the symptoms may progress to severe breathing problems and shock and ultimately death. Death can occur from about two days to a month after exposure with deaths apparently peaking at about 8 days after exposure.[30] Antibiotic-resistant strains of anthrax are known.

In recent years there have been many attempts to develop new drugs against anthrax, but existing drugs are effective if treatment is started soon enough.

Early detection of sources of anthrax infection can allow preventive measures to be taken. In response to the anthrax attacks of October 2001 the United States Postal Service (USPS) installed BioDetection Systems (BDS) in their large scale mail cancellation facilities. BDS response plans were formulated by the USPS in conjunction with local responders including fire, police, hospitals and public health. Employees of these facilities have been educated about anthrax, response actions and prophylactic medication. Because of the time delay inherent in getting final verification that anthrax has been used, prophylactic antibiotic treatment of possibly exposed personnel must be started as soon as possible.

Prognosis:
When treated with antibiotics, cutaneous anthrax is likely to get better. However, up to 20% of people who do not get treatment may die due to anthrax-related blood infections.

People with second-stage inhalation anthrax have a poor outlook, even with antibiotic therapy. Up to 90% of cases in the second stage are fatal.

Gastrointestinal anthrax infection can spread to the bloodstream, and may result in death.

Possible Complications:

Cutaneous anthrax:
•Spread of infection into the bloodstream

Inhalational anthrax:

•Hemorrhagic meningitis
•Swelling of lymph nodes in the chest (mediastinal adenopathy)
•Fluid buildup in the chest (pleural effusion)
•Shock
•Death

Gastrointestinal anthrax
•Severe bleeding (hemorrhage)
•Shock
•Death

Prevention:
There are two main ways to prevent anthrax.

For people who have been exposed to anthrax (but have no symptoms of the disease), doctors may prescribe preventive antibiotics, such as ciprofloxacin, penicillin, or doxycycline, depending on the strain of anthrax.

An anthrax vaccine is available to certain military personnel, but not to the general public. It is given in a series of six doses over 18 months. There is no known way to spread cutaneous anthrax from person to person. People who live with someone who has cutaneous anthrax do not need antibiotics unless they have also been exposed to the same source of anthrax.

An anthrax vaccine licensed by the U.S. Food and Drug Administration (FDA) and produced from one non-virulent strain of the anthrax bacterium, is manufactured by BioPort Corporation, subsidiary of Emergent BioSolutions. The trade name is BioThrax, although it is commonly called Anthrax Vaccine Adsorbed (AVA). It was formerly administered in a six-dose primary series at 0, 2, 4 weeks and 6, 12, 18 months, with annual boosters to maintain immunity. On December 11, 2008, the FDA approved the removal of the 2-week dose, resulting in the currently recommended five-dose series.

Unlike NATO countries, the Soviets developed and used a live spore anthrax vaccine, known as the STI vaccine, produced in Tbilisi, Georgia. Its serious side-effects restrict use to healthy adults.

Disclaimer: This information is not meant to be a substitute for professional medical advise or help. It is always best to consult with a Physician about serious health concerns. This information is in no way intended to diagnose or prescribe remedies.This is purely for educational purpose.

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Herbs & Plants

Brugmansia

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Botanical Name :Brugmansia spp
Family: Solanaceae
Subfamily: Solanoideae
Tribe: Datureae
Genus: Brugmansia
Kingdom: Plantae

Order: Solanales

Species:Sanguinea

Synonyms:Datura candida (Pers.) Safford,Datura brugmansia

Common Name :Belladonna Tree, Bloodred Angel’s Trumpet, Borrachero Rojo, Chamico, El Guantug,  Floripondio, Guantug, Huacacachu, Huanto, Humoco, Misha Colorada, Perecillo, Poroporo, Red Brugmansia, Tonga, Yerba de Huaca

Habitat :Brugmansia trees are native to subtropical regions of South America, along the Andes from Colombia to northern Chile, and also in southeastern Brazil,
where it grows on sloping terrain under damp conditions.

Description:

Brugmansia Sanguinea is a perennial shrub-like tree, indigenous to the midlands of South America. It can grow 15 feet (5 meters ) tall, with long thin oval shaped leaves that grow up to 16 inches (40 cm) long and 6 inches (15 cm) wide. The flowers are up to 9 inches (23 cm) long, narrow and trumpet shaped, and range in color from a light pink to a deep blood-red, but it can also produce flowers that are pure yellow, yellow–red, green¬–red and pure red. Unlike the closely related Golden Angel’s Trumpet, the Sanguinea’s flowers do not produce an aromatic fragrance and tend to be slightly smaller.

CLICK TO SEE THE PICTURES…..(01)...(1)....  (2)..(3)..….(4).…………..
Click to see more pictures:
Brugmansia are long-lived, woody trees or bushes, with pendulous, not erect, flowers, that have no spines on their fruit.It is a genus of seven species of flowering plants  Datura species are herbaceous bushes with erect (not pendulous) flowers, and most have spines on their fruit.

Cultivation:
Brugmansia are easily grown in a moist, fertile, well-drained soil, in full sun to part shade, in frost-free climates. They begin to flower in mid to late spring in warm climates and continue into the fall, often continuing as late as early winter in warm conditions. In cool winters, outdoor plants need protection, but the roots are hardy and will resprout in April or May. The species from the higher elevations, in B. section Sphaerocarpium, prefer moderate temperatures and cool nights, and may not flower if temperatures are very hot. Most Brugmansias may be propagated easily by rooting 10–20 cm cuttings taken from the end of a branch during the summer.

Chemical Constituents:The plant’s stems, flowers, leaves and seed are known to contain large quantities of tropane alkaloids. Recent research has shown that the main active compound in this plant is Scopolamine, it also contains aposcopolamine, atropine, hyoscyamine, meteloidine, and norscopolamine. All of these compounds may be illegal in most parts of the world when extracted from their naturally occurring sources.

Medicinal Uses:
Although the plant is poisonous, natives in Brazil smoke the leaves for a strong narcotic effect that it is said to relieve asthma.
(Schultes, R. E. 1976. Ethnobotany.)

It seems that almost every tribe in region had a different medicinal use for this magical plant, most prominently it was used to treat rheumatism and arthritis. It has also been used to treat sore throats, stomach pains caused by parasitic worms, to cleanse wounds of infected pus, and to help sooth irritated bowels and reduce flatulence. Due to many undesirable side effects and after effects there are no currently accepted medicinal uses for this plant. Although, today in Ecuador, the pharmaceutical industry grows Brugmansia to produce pure Scopolamine for medicinal purposes.

Traditional preparations : There are several traditional ways in which the seeds, flowers, and leaves were prepared to produce various intoxicating drinks, teas and powders. The native Canelo Indians would scrape the pith from the stem and flowers and squeeze out the juices, which were then consumed straight away. Other preparations include steeping the leaves and flowers in hot water to make delirium inducing teas; in some areas the seeds would be dried and powered and then added to Chica, a fermented maize beer; there are also reports of Indians mixing the dried leaves with tobacco and smoking the resulting blend. One of the most powerful decoctions was exclusively made and consumed by shaman, they boiled the fruits and seeds of the plant to produce a potent drink called tonga.

Other Uses:
Traditional uses: Mestizo Shamans have used the Bloodred Angel’s Trumpet as a sacrament in their burial ceremonies and grieving rituals. It was believed that widows would be gently lulled into the afterworld by consuming a hallucinogenic maize beer, Chicha, while they were being buried alive with their deceased husband. Chicha was made from corn, tobacco and the Sanguinea flowers and allowed to ferment. Modern day shaman’s use this traveling plant to communicate with their ancestors as well as the animal spirit world, diagnose disease, find lost objects, prophesize and to predict the future. The native tribes still use the seeds, mixing them in with coffee, to induce sexual arousal or to harm someone and put them into a coma or even kill them, depending on the dosage.

As with Datura, all parts of Brugmansia are highly toxic. The plants are sometimes ingested for recreational or shamanic intoxication as the plant contains the tropane alkaloids scopolamine and atropine; however because the potency of the toxic compounds in the plant is variable, the degree of intoxication is unpredictable and can be fatal.

Ritualized Brugmansia consumption is an important aspect of the shamanic complexes noted among many indigenous peoples of western Amazonia, such as the Jivaroan speaking peoples. Likewise, it is a central component in the cosmology and shamanic practices of the Urarina peoples of Loreto, Peru.

Planted in ganden for beautification.

Scientific Research:
Brugmansia ×candida is a hybrid between Brugmansia aurea with Brugmansia versicolor. This hybrid can be found growing wild in nature therefore it is a “natural hybrid”.

Native Legends and Names:
Brugmansia is named after Sebald Justin Brugmans (1763-1819).
Even though Brugmansia has been in the USA for many many years, it has always been portrayed as a “Plant of Evil” and something undesirable to have growing in your yard.

Known Hazards:All parts of plant are poisonous if ingested or absorbed through the mucous membranes. Be careful to not rub your eyes after touching Brugmansia.

Disclaimer:
The information presented herein is intended for educational purposes only. Individual results may vary, and before using any supplements, it is always advisable to consult with your own health care provider.

Resources:
http://treesandshrubs.about.com/od/commonshrubs/p/angelstrumpet.htm
http://en.wikipedia.org/wiki/Brugmansia
http://www.ntbg.org/plants/plant_details.php?plantid=11850
http://www.entheology.org/edoto/anmviewer.asp?a=31&z=5

http://en.wikipedia.org/wiki/File:Brugmansia_arborea_with_fruit.jpg

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