Boys Before Flower: Korean serial full download torrent

Boys Before Flower: Korean serial full download torrent

Boys Before Flowers : Korean Serial songs and Movie download

Story

Boys Before Flower

Boys Before Flower

Jan Di is an average girl whose family owns a dry cleaning store located near the luxurious and well known Shin Hwa College. Jan Di meets the four richest and most spoiled boys known as the F4. After saving a boyfrom jumping off the roof of Shinhwa High School, she is admitted into the school on a swimming scholarship. Jan Di tries to avoid confrontation with the F4 at all cost because she knows what happens to those that stand against them. However, when Jan Di’s friend, Oh Min Ji, accidentally gets ice cream on the leader of the F4’s shoes, she’s forced to declare war on the leader of the F4, Goo Joon Pyo.

Broadcasted – 2009-Jan-05 to 2009-Mar-31
Genre – Romance, Comedy
Country – South Korea
Audio – Korean
Subtitles – English
Episode Run Time – 1hr
Total Episodes – 25
Status – Completed [25/25]

Torrent Download
Boys Before Flowers (1) | English Subtitles
Boys Before Flowers (2)
Boys Before Flowers (3-4)
Boys Before Flowers (5-6)
Boys Before Flowers (7-8)
Boys Before Flowers (9-10)
Boys Before Flowers (11-12)
Boys Before Flowers (13-14)
Boys Before Flowers (15-16)
Boys Before Flowers (17)
Boys Before Flowers (18-19)
Boys Before Flowers (20-21)
Boys Before Flowers (22-23)
Boys Before Flowers (24-25)

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CT Scan : A diagnostic Breakthrough in Medicine




Computed tomography (CT), originally known as computed axial tomography (CAT or CT scan) and body section roentgenography, is a medical imaging method employing tomography where digital geometry processing is used to generate a three-dimensional image of the internals of an object from a large series of two-dimensional X-ray images taken around a single axis of rotation. The word "tomography" is derived from the Greek tomos (slice) and graphein (to write). CT produces a volume of data which can be manipulated, through a process known as windowing, in order to demonstrate various structures based on their ability to block the X-ray beam. Although historically (see below) the images generated were in the axial or transverse plane (orthogonal to the long axis of the body), modern scanners allow this volume of data to be reformatted in various planes or even as volumetric (3D) representations of structures.


History
The first commercially viable CT scanner was invented by Godfrey Newbold Hounsfield in Hayes, England at Thorn EMI Central Research Laboratories using X-rays. Hounsfield conceived his idea in 1967, and it was publicly announced in 1972. It is claimed that the CT scanner was "the greatest legacy" of the Beatles; the massive profits from their record sales enabled EMI to fund scientific research.[1] Allan McLeod Cormack of Tufts University, Massachusetts, USA independently invented a similar process and they shared a Nobel Prize in medicine in 1979.

The prototype CT scanner
The original 1971 prototype took 160 parallel readings through 180 angles, each 1° apart, with each scan taking a little over five minutes. The images from these scans took 2.5 hours to be processed by algebraic reconstruction techniques on a large computer.
The first production X-ray CT machine (called the EMI-Scanner) was limited to making tomographic sections of the brain, but acquired the image data in about 4 minutes (scanning two adjacent slices) and the computation time (using a Data General Nova minicomputer) was about 7 minutes per picture. This scanner required the use of a water-filled Perspex tank with a pre-shaped rubber "head-cap" at the front, which enclosed the patient's head. The water-tank was used to reduce the dynamic range of the radiation reaching the detectors (between scanning outside the head compared with scanning through the bone of the skull). The images were relatively low resolution, being composed of a matrix of only 80 x 80 pixels. The first EMI-Scanner was installed in Atkinson Morley's Hospital in Wimbledon, England, and the first patient brain-scan was made with it in 1972.

a historic EMI-Scanner
In the U.S., the first installation was at the Mayo Clinic. As a tribute to the impact of this system on medical imaging the Mayo Clinic has an EMI scanner on display in the Radiology Department.
The first CT system that could make images of any part of the body, and did not require the "water tank" was the ACTA scanner designed by Robert S. Ledley, DDS at Georgetown University.

Life Saving Techniques





1. Place the child on a hard, flat surface.
2 .Look into the mouth and throat to ensure that the airway is clear. If an object is present, try to sweep it out with your fingers. If unsuccessful and the object is blocking the airway, apply the Heimlich maneuver (see p. 1205). If vomiting occurs, turn the child onto his or her side and sweep out the mouth with two fingers.
3. Tilt the head back slightly to open the airway.

4. Place your mouth tightly over the nose and mouth. Blow two quick, shallow breaths (smaller breaths than you would give to an adult). Watch for the chest to rise.
5. Remove your mouth. Look for the chest to fall as the child exhales.
6. Listen for the sounds of breathing. Feel for the child’s breath on your cheek. If breathing does not start on its own, repeat the procedure.


Mouth-to-Mouth Resuscitation on a Child Age 8 or Older or on an Adult
1. Make sure the person is lying on a hard, flat surface. Look into the mouth and throat to ensure that the airway is clear. If an object is present, try to sweep it out with your fingers (wear disposable surgical gloves if they are available). Apply the Heimlich maneuver (see p. 1205) if unsuccessful and the object is blocking the airway. If vomiting occurs, turn the person on his or her side and sweep out the mouth with two fingers. Do not place your finger in the mouth if the person is rigid or is having a seizure.
2. Tilt the head back slightly to open the airway. Put upward pressure on the jaw to pull it forward.
3. Pinch the nostrils closed with thumb and index finger. Place your mouth tightly over the person’s mouth. Use a mouthpiece if one is available. Blow two quick breaths and watch for the person’s chest to rise.
4. Release the nostrils. Look for the person’s chest to fall as he or she exhales. Listen for the sounds of breathing. Feel for the person’s breath on your cheek. If the person does not start breathing on his or her own, repeat the procedure.

Skin Care for A Better You

SKIN CARE:


For Healthy Skin
F
or Healthy Skin
Skin has three layers-epidermis ,dermis and hypodermis. Epidermis the top most layer. It has melanocytes which gives brown tint to the skin. Below it is dermis .It has fibrous tissue , collagen and elastin. Hypodermis the deepest layer containing connective tissue and fat cells keeps the skin warm and protects it.
TYPE OF SKIN:
NORMAL: Fine textured , soft and smooth.
DRY: Tight , flaky and predisposing to facial lines.
OILY: Greasy skin due sebum production.Looks shiny with enlarged pores leading to blemishes and blackhead.
SENSITIVE :Fine ,translucent,suffer from redness and irritation.
COMBINATION:T –Zone is oily and the rest of the skin is dry (cheeks ,eyes ,cheeks )
DAILY REGIME FOR A HEALTHY SKIN:
HealthySkin
HealthySkin
CLEANSING: Helps to remove dirt ,sweat and make up .Must do atleast twice a day or more for oily skin. Use a cream cleanser for a dry skin. Apply cleansing for 1min in outward and upward in circulation motion.Soaps also can be used by everyone.Must see that they are not harsh.
Toning: Cleansing must be followed by toning . It helps to remove any leftover grease or make up .Closes the pores and refines the skin. Alcohol must be used for dry skin.
MOISTURING :Only time our body retains moisture is just after bath.pat the skin and apply moisturizer to the skin according to the skin type .It must even in oily skin.
SUN PROTECTION: Sun protecting factor(SPF) must be used according to the skin tyope and the intensity of the sun, Time you can stay out in the sun- multiply the SPF with 10 (e.g. 20 SPF means 200 mins i.e. 3 hrs and 20 mins ) recommended is 15-30 .
Tips for sun protection:
Avoid sun for long between 11:00am to 4:00pm in summer.
Drink plenty of water.
Cool yourself with warm shower (extreme temperature is bad for skin ) ,use uv blocking sun glasses ,use a umbrella or a hat.
WEEKLY REGIMEN:
EXFOLIATION: Removing dead skin as it the skin looks dull .must be frequent in older age. Fine grains are good.apricot,strawberries with milk,oat meal,rice bran with glycerine.
FACEMASK: They are stimulating for skin.
Fuller earth with egg white for oily skin.
Egg yolk with honey is for dry skin.
Article By- Dr. Akriti Sharma

Source : www.medchrome.com

Swine Flu vs Bird flu

Swine Flu or Bird Flu
Which do you fear?
Or Zombie Flu ?
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Stye : External Hordeolum



An External hordeolum
Sty



is an acute small staphylococcal abscess of a lash follicle and its associated gland of Zeis or moll.

Signs:
Tender Inflamed swelling in the lid Margin, which points anteriorly thought the skin.
More than one lesion may be present and occasionally minute abscess may involve the entire lid margin.
In severe case a mild preseptal cellulitis may be present.

Treatment:
No treatment is required in most cases because styes frequently resove spontaneously or discharge anteriorly
Hot compresses
Epilation
Systemic Antibiotics may be necessary.

Schizophrenia: A short summary

Historical Background: in 1896, Emil Kraepelin differentiated psychiatric illness into 2 major groups.
  • Dementia Precox
  • Mani depressive illness( psychosis)
Eugen Bleuer's Fundamental Symptoms of Schizophremi: Ambivalence Autism Affective Flattening Association disorder

First Rank symptoms
I. Hallucinations

1. Audible thoughts/thought echo 2. Voices heard arguing 3. Voices giving running commentary II. Thought Alienation Phenomenon a) Thought withdrawal b) Thought insertion c) Thought broadcasting
III. Passivity Phenomenon A. Made feelings B. Made volition C. Made impulses IV. Delusional Perception

Epidemiology; Point prevalence of Schizophrenia is 0.5 to 1 %. The Incidence is about 0.5 in 1000 persons

Clinical features
Thought and speech Disorders Autistic thinking, loosening of association, thought blocking, neologism, paraphasias, mutism, perseveration, verbigeration Delusions: primary and secondary Disorders Of Perception Hallucinations Disorders of Affect Disorders of Motor Behaviour Negative Symptoms Suicidal Tendency

Clinical types: Simple Schizophrenia Hebephrenic Schizophrenia Catatonic Schizophrenia Residual Schicophrenia Undifferentiated Schizophrenia Post-schizophrenic depression Others

Bad Prognostic Factors
Male Negative Symptoms Early Onset Insidious progression Chronic Course

Diagnostic Criteria:
According to DSM IV TR 2 or more of the following is required with 6 months of duration of disease with at least 1 month of Active symptoms 1. Delusion Hallucinations Bizzare Behaviour Bizzare thoughts

MANAGEMENT:
1. Pharmacological Treatment: Generally the treatment is continued for 6 months to 1 year for the first episode, for 1-2 year for subsequent episodes. Fluphenazine 25-30 mg IM every 2-3 weeks Penfluridol Flupenthixol Haloperidol ECT ( Electroconvulsive Therapy) Miscellaneous Treatments Limbic Leucotomy Psychosocial Treatment.

Organic Metal Disorders and Delirium


Organic Mental Disorders are behavioral or psychological disorders associated with permanent or transient brain dysfunction and include only those mental and behavioral disorders that are due to demonstrable cerebral disease or disorders, either primary or secondary. Sub Categories of Organic Mental Disorders: OMD are
  • Delirium
  • Dementia
  • Organic Amnestic Syndrome
  • Other organic mental disorders
Delirium:
commonest type
synonyms: Acute Confusional state, acute brain syndrome, acute organic reaction, toxic psychosis, metabolic encephalopathy.

Clinical Features:
1. A relative Acute Onset
2. Clouding of Consciousness
3.Disorientation to time place and person.
other: Disturbed sleep-wake sleep cycle
sun downing( aggravated in the evening and night)
Motor disturbances- asterixis,Carphologia. etc
Psychomotor disturbances

Diagnosis:
According to ICD10
Symptoms should be present in each one area:
1. Impairment of attention and consciousness
2.Global disturbance of cognition
3. Psychomotor disturances
4.Disturbed slepp wake sleep cycle
5. Emotional disturbances.

Important causes of Delirium are:
  1. Metabolic causes: hypoxia, narcosis,hypoglycemia, CCF, Metabolic acidosis or alkalosis, fever , anemia, shock.
  2. Endocrine : Hypo/hyper thyroid,adrenal,pituitary and parathyroid.
  3. Drug: Digitalis, quinidine, alcohol, anti hypertensives, sedatives,barbiturates,TCA, Antipsychotics.
  4. Nutritional deficiency: Thiamin, Niacin, Pyridoxine, folic acid, B12
  5. Systemic Infections.
  6. Intracranial causes: Epilepsy, tumors, migraine, head injury, infections
  7. post operative
Management of Delirium:
Ix: CBC, BGA, Sugar level, po2 and co2, TFT, serum b1 and foalte, toxic screen, csf, etc
Identificaton of the cause and its immediate correction.
Symptomatic measures
Supportive medical and nursing ccare.

Conjunctivitis




Conjunctivitis is an inflammation or infection of the conjunctiva, the thin transparent layer of tissue that lines the inner surface of the eyelid and covers the white part of the eye. Conjunctivitis, often called “pink eye,” is a common eye disease, especially in children. It may affect one or both eyes. Some forms of conjunctivitis can be highly contagious and easily spread in schools and at home. While conjunctivitis is usually a minor eye infection, sometimes it can develop into a more serious problem.

Conjunctivitis may be caused by a viral or bacterial infection. It can also occur due to an allergic reaction to irritants in the air like pollen and smoke, chlorine in swimming pools, and ingredients in cosmetics or other products that come in contact with the eyes. Sexually transmitted diseases like Chlamydia and gonorrhea are less common causes of conjunctivitis.

symptoms:

* A gritty feeling in one or both eyes
* Itching or burning sensation in one or both eyes
* Excessive tearing
* Discharge coming from one or both eyes
* Swollen eyelids
* Pink discoloration to the whites of one or both eyes
* Increased sensitivity to light

What causes conjunctivitis?
Allergic Conjunctivitis occurs more commonly among people who already have seasonal allergies.

Allergic Conjunctivitis occurs more commonly among people who already have seasonal allergies.

The cause of conjunctivitis varies depending on the offending agent. There are three main categories of conjunctivitis: allergic, infectious and chemical:
Allergic Conjunctivitis

* Allergic Conjunctivitis occurs more commonly among people who already have seasonal allergies. At some point they come into contact with a substance that triggers an allergic reaction in their eyes.

* Giant Papillary Conjunctivitis is a type of allergic conjunctivitis caused by the chronic presence of a foreign body in the eye. This condition occurs predominantly with people who wear hard or rigid contact lenses, wear soft contact lenses that are not replaced frequently, have an exposed suture on the surface or the eye, or have a glass eye.

Infectious Conjunctivitis

* Bacterial Conjunctivitis is an infection most often caused by staphylococcal or streptococcal bacteria from your own skin or respiratory system. Infection can also occur by transmittal from insects, physical contact with other people, poor hygiene (touching the eye with unclean hands), or by use of contaminated eye makeup and facial lotions.

* Viral Conjunctivitis is most commonly caused by contagious viruses associated with the common cold. The primary means of contracting this is through exposure to coughing or sneezing by persons with upper respiratory tract infections. It can also occur as the virus spreads along the body’s own mucous membranes connecting lungs, throat, nose, tear ducts, and conjunctiva.

* Ophthalmia Neonatorum is a severe form of bacterial conjunctivitis that occurs in newborn babies. This is a serious condition that could lead to permanent eye damage unless it is treated immediately. Ophthalmia neonatorum occurs when an infant is exposed to Chlamydia or gonorrhea while passing through the birth canal.

Chemical Conjunctivitis

Chemical Conjunctivitis can be caused by irritants like air pollution, chlorine in swimming pools, and exposure to noxious chemicals.

[back to top]
How is conjunctivitis diagnosed?
Comprehensive Eye Exam

Conjunctivitis can be diagnosed through a comprehensive eye examination.

Conjunctivitis can be diagnosed through a comprehensive eye examination. Testing, with special emphasis on evaluation of the conjunctiva and surrounding tissues, may include:

* Patient history to determine the symptoms the patient is experiencing, when the symptoms began, and the presence of any general health or environmental conditions that may be contributing to the problem.

* Visual acuity measurements to determine the extent to which vision may be affected.

* Evaluation of the conjunctiva and external eye tissue using bright light and magnification.

* Evaluation of the inner structures of the eye to ensure that no other tissues are affected by the condition.

* Supplemental testing may include taking cultures or smears of conjunctival tissue, particularly in cases of chronic conjunctivitis or when the condition is not responding to treatment.

Using the information obtained from these tests, your optometrist can determine if you have conjunctivitis and advise you on treatment options.

[back to top]
How is conjunctivitis treated?

Treatment of conjunctivitis is directed at three main goals:

1. To increase patient comfort.
2. To reduce or lessen the course of the infection or inflammation.
3. To prevent the spread of the infection in contagious forms of conjunctivitis.

The appropriate treatment for conjunctivitis depends on its cause:

* Allergic conjunctivitis – The first step should be to remove or avoid the irritant, if possible. Cool compresses and artificial tears sometimes relieve discomfort in mild cases. In more severe cases, non-steroidal anti-inflammatory medications and antihistamines may be prescribed. Cases of persistent allergic conjunctivitis may also require topical steroid eye drops.

* Bacterial conjunctivitis – This type of conjunctivitis is usually treated with antibiotic eye drops or ointments. Improvement can occur after three or four days of treatment, but the entire course of antibiotics needs to be used to prevent recurrence.

* Viral Conjunctivitis – There are no available drops or ointments to eradicate the virus for this type of conjunctivitis. Antibiotics will not cure a viral infection. Like a common cold, the virus just has to run its course, which may take up to two or three weeks in some cases. The symptoms can often be relieved with cool compresses and artificial tear solutions. For the worst cases, topical steroid drops may be prescribed to reduce the discomfort from inflammation, but do not shorten the course of the infection. Some doctors may perform an ophthalmic iodine eye wash in the office in hopes of shortening the course of the infection. This newer treatment has not been well studied yet, therefore no conclusive evidence of the success exists.

* Chemical Conjunctivitis – Treatment for chemical conjunctivitis requires careful flushing of the eyes with saline and may require topical steroids. The more acute chemical injuries are medical emergencies, particularly alkali burns, which can lead to severe scarring, intraocular damage or even loss of the eye.

Contact Lens Wearers
Contact lens wearers may need to discontinue wearing their lenses while the conjunctivitis is active.

Contact lens wearers may need to discontinue wearing their lenses while the conjunctivitis is active.

Contact lens wearers may need to discontinue wearing their lenses while the condition is active. Your doctor can advise you on the need for temporary restrictions on contact lens wear.

If the conjunctivitis developed due to wearing contact lenses, your eye doctor may recommend that you switch to a different type of contact lens or disinfection solution. Your optometrist might need to alter your contact lense prescription to a type of lens that you replace more frequently to prevent the conjunctivitis from recurring.
Self-care

Practicing good hygiene is the best way to control the spread of conjunctivitis. Once an infection has been diagnosed, follow these steps:

* Don't touch your eyes with your hands.
* Wash your hands thoroughly and frequently.
* Change your towel and washcloth daily, and don't share them with others.
* Discard eye cosmetics, particularly mascara.
* Don't use anyone else's eye cosmetics or personal eye-care items.
* Follow your eye doctor's instructions on proper contact lens care.

You can soothe the discomfort of viral or bacterial conjunctivitis by applying warm compresses to your affected eye or eyes. To make a compress, soak a clean cloth in warm water and wring it out before applying it gently to your closed eyelids.

For allergic conjunctivitis, avoid rubbing your eyes. Instead of warm compresses, use cool compresses to soothe your eyes. Over the counter eye drops are available. Antihistamine eye drops should help to alleviate the symptoms, and lubricating eye drops help to rinse the allergen off of the surface of the eye.

See your doctor of optometry when you experience conjunctivitis to help diagnose the cause and the proper course of action.

Removal of Guinea worm Methos Video

Guinea Worm : Dracunculiais CDC article




Source: CDC

What is dracunculiasis?

Dracunculiasis, more commonly known as Guinea worm disease (GWD), is a preventable infection caused by the parasite Dracunculus medinensis. Infection affects poor communities in remote parts of Africa that do not have safe water to drink.

Currently, many organizations, including The Global 2000 program of The Carter Center of Emory University, UNICEF, Centers for Disease Control and Prevention (CDC), and the World Health Organization (WHO) are helping the last 5 countries in the world (Sudan, Ghana, Mali, Niger, and Nigeria) to eradicate the disease. Since 1986, when an estimated 3.5 million people were infected annually, the campaign has eliminated much of the disease.

In 2007, only 9,585 cases of GWD were reported. Most of those cases were from Sudan (61%) and Ghana (35%). All affected countries are aiming to eliminate Guinea worm disease as soon as possible.

How does Guinea worm disease spread?

Approximately 1 year after a person drinks contaminated water, the adult female Guinea worm emerges from the skin of the infected person. Persons with worms protruding through the skin may enter sources of drinking water and unwittingly allow the worm to release larvae into the water. These larvae are ingested by microscopic copepods (tiny "water fleas") that live in these water sources. Persons become infected by drinking water containing the water fleas harboring the Guinea worm larvae.

Once ingested, the stomach acid digests the water fleas, but not the Guinea worm larvae. These larvae find their way to the small intestine, where they penetrate the wall of the intestine and pass into the body cavity. During the next 10-14 months, the female Guinea worm larvae grow into full size adults, 60-100 centimeters (2-3 feet) long and as wide as a cooked spaghetti noodle. These adult femal worms then migrate and emerge from the skin anywhere on the body, but usually on the lower limbs.

A blister develops on the skin at the site where the worm will emerge. This blister causes a very painful burning sensation and it ruptures within 24-72 hours. Immersion of the affected limb into water helps relieve the pain but it also triggers the Guinea worm to release a milky white liquid containing millions of immature larvae into the water, thus contaminating the water supply and starting the cycle over again. For several days after it has emerged from the ulcer, the female Guinea worm is capable of releasing more larvae whenever it comes in contact with water.



What are the signs and symptoms of Guinea worm disease?

Infected persons do not usually have symptoms until about one year after they become infected. A few days to hours before the worm emerges, the person may develop a fever, swelling, and pain in the area. More than 90% of the worms appear on the legs and feet, but may occur anywhere on the body.

People, in remote, rural communities who are most commonly affected by Guinea worm disease (GWD) frequently do not have access to medical care. Emergence of the adult female worm can be very painful, slow, and disabling. Frequently, the skin lesions caused by the worm develop secondary bacterial infections, which exacerbate the pain, and extend the period of incapacitation to weeks or months. Sometimes permanent disability results if joints are infected and become locked.



What is the treatment for Guinea worm disease?

There is no drug to treat Guinea worm disease (GWD) and no vaccine to prevent infection. Once the worm emerges from the wound, it can only be pulled out a few centimeters each day and wrapped around a piece of gauze or small stick. Sometimes the worm can be pulled out completely within a few days, but this process usually takes weeks or months. Analgesics, such as aspirin or ibuprofen, can help reduce swelling; antibiotic ointment can help prevent bacterial infections. The worm can also be surgically removed by a trained doctor in a medical facility before an ulcer forms.



Where is Guinea worm disease found?

Dracunculiasis now occurs only in 5 countries in sub-Saharan Africa. Transmission of the disease is most common in very remote rural villages and in areas visited by nomadic groups. In 2007, the two most endemic countries, Sudan and Ghana, reported 9,173; 5,815 and 3,358 cases of Guinea worm disease (GWD), respectively. Other endemic countries reporting cases of GWD in 2007 were: Mali (313 cases), Nigeria (73 cases), and Niger (14 cases).

Asia is now free of the disease. Transmission of GWD no longer occurs in several African countries, including Benin, Burkina Faso, Cameroon, Central African Republic, Chad, Cote d'Ivoire, Ethiopia, Kenya, Mauritania, Senegal, Togo, and Uganda. No locally acquired cases of disease have been reported in these countries in the last year or more. The treat of case importations from the remaining endemic countries requires that surveillance be maintained in formerly endemic areas until offical certification. The World Health Organization has certified 180 countries free of transmission of dracunculiasis, including six formerly endemic countries: Pakistan (in 1996), India (in 2000), Senegal and Yemen (in 2004), Central African Republic and Cameroon (in 2007).



Who is at risk for infection?

Anyone who drinks standing pond water contaminated by persons with GWD is at risk for infection. People who live in villages where the infection is common are at greatest risk.



Is Guinea worm disease a serious illness?

Yes. The disease causes preventable suffering for infected persons and is a heavy economic and social burden for affected communities. Emgerence of the adult female worms can be very painful, slow, and disabling. Parents who have active Guinea worm disease may not be able to care for their children. They are also prevented from working in their fields and tending their animals. Because worm emergence usually occurs during planting and harvesting season, heavy crop losses may result leading to financial problems for the entire family. Children may be required to work the fields or tend animals in place of their disabled parents, preventing them from attending school. Therefore, GWD is both a disease of poverty and also a cause of poverty because of the disability it causes.



Is a person immune to Guinea worm disease once he or she has it?

No. Infection does not produce immunity, and many people in affected villages suffer disease year after year.



How can Guinea worm disease be prevented?

Because GWD can only be transmitted via drinking contaminated water, educating people to follow these simple control measures can completely prevent illness and eliminate transmission of the disease:

Drink only water from underground sources (such as from borehole or hand-dug wells) free from contamination.
Prevent persons with an open Guinea worm ulcer from entering ponds and wells used for drinking water.
Always filter drinking water, using a cloth filter, to remove the water fleas.
Additionally, unsafe sources of drinking water can be treated with an approved larvicide, such as ABATE®*, that kills copepods, and communities can be provided with new safe sources of drinking water, or have existing dysfunctional ones repaired.

*Use of trade names is for identification only and does not imply endorsement by the Public Health Service or by the U.S. Department of Health and Human Services.

Headache : Most common causes

# Infection

* Common cold
* Flu
* Fever - headaches are common with fever from any type of infection
* Ear infection
* Tooth infection (type of Dental conditions)
* Sinus infection
* Pneumonia
* Measles
* Mumps
* Tonsillitis
* Sinus blockage
* Coughing - too much coughing can cause a form of traction headache.

# Various possible types of headache:

* Migraine
* Cluster headache
* Tension headache
* See also types of headache

# Lifestyle causes

* Hangover
* Excessive alcohol
* Stress
* Fatigue
* Tension
* Tiredness
* Excessive smoking

# Dyspepsia
# Eye conditions

* Glaucoma
* Eyestrain

# Medical procedures

* Spinal tap treatment
* Epidural - this anaesthetic procedure (common for childbirth) can occasionally cause damage to the spinal area and cause headache.

# Systemic or metabolic conditions

* Hypertension
* Thyroid disease
* Anemia
* Kidney failure (type of Kidney disease)
* Uremia
* Lead poisoning - African Folk Remedies - Kohl - headache
* Various toxins - see toxin causes of headache

# Brain or head conditions

* Meningitis
* Encephalitis
* Head injury
* Brain injury
* Mild traumatic brain injury
* Concussion
* Temporal arteritis
* Heatstroke
* Sunstroke
* Blood clots - in the brain, these can cause a stroke.
* Brain aneurysm
* Subdural hematoma
* Stroke
* Transient ischemic attacks
* Subarachnoid hemorrhage
* Brain tumor
* Benign intracranial hypertension
* Trigeminal neuralgia

Management Of a Comatose Child : Emergency


Manage .... Read more



Malaria : Epidemiology, signs and symptoms

FActs about Malaria
  1. Malaria is a life-threatening disease caused by parasites that are transmitted to people through the bites of infected mosquitoes.
  2. A child dies of malaria every 30 seconds.
  3. There were 247 million cases of malaria in 2006, causing nearly one million deaths, mostly among African children.
  4. Malaria is preventable and curable.
  5. Approximately half of the world's population is at risk of malaria, particularly those living in lower-income countries.
  6. Travellers from malaria-free areas to disease "hot spots" are especially vulnerable to the disease.Malaria takes an economic toll - cutting economic growth rates by as much as 1.3% in countries with high disease rates.

Malaria is caused by parasites of the species Plasmodium. The parasites are spread to people through the bites of infected mosquitoes.


There are four types of human malaria:

Plasmodium falciparum
Plasmodium vivax
Plasmodium malariae
Plasmodium ovale.
Plasmodium falciparum and Plasmodium vivax are the most common. Plasmodium falciparum is the most deadly.




Common symptoms of malaria
In the early stages, malaria symptoms are sometimes similar to those of many other infections caused by bacteria, viruses, or parasites. Symptoms may include:
Fever.
Chills.
Headache.
Sweats.
Fatigue.
Nausea and vomiting.
Other common symptoms of malaria include:
Dry (nonproductive) cough.
Muscle and/or back pain.
Enlarged Spleen

Complications of Malaria( Falciparum):
Cerebral malaria
Algid Malaria
ARDS
Convulsion
Coma
Acute Renal Failure
Hypoglycemia
hyperthermia
hyperparasitemia
severe anemia


Symptomatic diagnosis
Using Giemsa-stained blood smears from children in Malawi, one study showed that when clinical predictors (rectal temperature, nailbed pallor, and splenomegaly) were used as treatment indications, rather than using only a history of subjective fevers, a correct diagnosis increased from 21% to 41% of cases and unnecessary treatment for malaria was significantly decreased.

Microscopic examination of blood films
Field tests
In areas where microscopy is not available, or where laboratory staff are not experienced at malaria diagnosis, there are antigen detection tests that require only a drop of blood. Immunochromatographic tests (also called: Malaria Rapid Diagnostic Tests, Antigen-Capture Assay or "Dipsticks") have been developed, distributed and fieldtested. These tests use finger-stick or venous blood, the completed test takes a total of 15–20 minutes, and a laboratory is not needed. The threshold of detection by these rapid diagnostic tests is in the range of 100 parasites/µl of blood compared to 5 by thick film microscopy. The first rapid diagnostic tests were using P. falciparum glutamate dehydrogenase as antigen.[42] PGluDH was soon replaced by P.falciparum lactate dehydrogenase, a 33 kDa oxidoreductase [EC 1.1.1.27]. It is the last enzyme of the glycolytic pathway, essential for ATP generation and one of the most abundant enzymes expressed by P.falciparum. PLDH does not persist in the blood but clears about the same time as the parasites following successful treatment. The lack of antigen persistence after treatment makes the pLDH test useful in predicting treatment failure. In this respect, pLDH is similar to pGluDH. The OptiMAL-IT assay can distinguish between P. falciparum and P. vivax because of antigenic differences between their pLDH isoenzymes. OptiMAL-IT will reliably detect falciparum down to 0.01% parasitemia and non-falciparum down to 0.1%. Paracheck-Pf will detect parasitemias down to 0.002% but will not distinguish between falciparum and non-falciparum malaria. Parasite nucleic acids are detected using polymerase chain reaction. This technique is more accurate than microscopy. However, it is expensive, and requires a specialized laboratory. Moreover, levels of parasitemia are not necessarily correlative with the progression of disease, particularly when the parasite is able to adhere to blood vessel walls. Therefore more sensitive, low-tech diagnosis tools need to be developed in order to detect low levels of parasitaemia in the field. Areas that cannot afford even simple laboratory diagnostic tests often use only a history of subjective fever as the indication to treat for malaria. Using Giemsa-stained blood smears from children in Malawi, one study showed that unnecessary treatment for malaria was significantly decreased when clinical predictors (rectal temperature, nailbed pallor, and splenomegaly) were used as treatment indications, rather than the current national policy of using only a history of subjective fevers (sensitivity increased from 21% to 41%).


Molecular methods
Molecular methods are available in some clinical laboratories and rapid real-time assays (for example, QT-NASBA based on the polymerase chain reaction) are being developed with the hope of being able to deploy them in endemic areas.

Rapid antigen tests
OptiMAL-IT will reliably detect falciparum down to 0.01% parasitemia and non-falciparum down to 0.1%. Paracheck-Pf will detect parasitemias down to 0.002% but will not distinguish between falciparum and non-falciparum malaria. Parasite nucleic acids are detected using polymerase chain reaction. This technique is more accurate than microscopy. However, it is expensive, and requires a specialized laboratory. Moreover, levels of parasitemia are not necessarily correlative with the progression of disease, particularly when the parasite is able to adhere to blood vessel walls. Therefore more sensitive, low-tech diagnosis tools need to be developed in order to detect low levels of parasitaemia in the field.

Tropical diseases in Asia

Malaria
Cholera
Dysentery
Intestinal Worms
Dengue Fever
Yellow Fever
Schistosomiasis
Leprosy
Filariasis
Trypanosomiasis
Hepatitis
Chlamydia Trachomatis

Pneumonia : xRay Consolidation

Picture a:??? Anyone can explain-post comment
Picture b: Right lower zone Consolidation

Classification: Pneumonia

Early classification schemes



Initial descriptions of pneumonia focused on the anatomic or pathologic appearance of the lung, either by direct inspection at autopsy or by its appearance under a microscope.

A lobar pneumonia is an infection that only involves a single lobe, or section, of a lung. Lobar pneumonia is often due to Streptococcus pneumoniae (though Klebsiella pneumoniae is also possible.)
Multilobar pneumonia involves more than one lobe, and it often causes a more severe illness.
Bronchial pneumonia affects the lungs in patches around the tubes (bronchi or bronchioles).
Interstitial pneumonia involves the areas in between the alveoli, and it may be called "interstitial pneumonitis." It is more likely to be caused by viruses or by atypical bacteria.

The discovery of x-rays made it possible to determine the anatomic type of pneumonia without direct examination of the lungs at autopsy and led to the development of a radiological classification. Early investigators distinguished between typical lobar pneumonia and atypical (e.g. Chlamydophila) or viral pneumonia using the location, distribution, and appearance of the opacities they saw on chest x-rays. Certain x-ray findings can be used to help predict the course of illness, although it is not possible to clearly determine the microbiologic cause of a pneumonia with x-rays alone.

With the advent of modern microbiology, classification based upon the causative microorganism became possible. Determining which microorganism is causing an individual's pneumonia is an important step in deciding treatment type and length. Sputum cultures, blood cultures, tests on respiratory secretions, and specific blood tests are used to determine the microbiologic classification. Because such laboratory testing typically takes several days, microbiologic classification is usually not possible at the time of initial diagnosis.

Combined clinical classification
Traditionally, clinicians have classified pneumonia by clinical characteristics, dividing them into "acute" (less than three weeks duration) and "chronic" pneumonias. This is useful because chronic pneumonias tend to be either non-infectious, or mycobacterial, fungal, or mixed bacterial infections caused by airway obstruction. Acute pneumonias are further divided into the classic bacterial bronchopneumonias (such asStreptococcus pneumoniae), the atypical pneumonias (such as the interstitial pneumonitis of Mycoplasma pneumoniae or Chlamydia pneumoniae), and the aspiration pneumonia syndromes.

Chronic pneumonias, on the other hand, mainly include those of Nocardia, Actinomyces and Blastomyces dermatitidis, as well as the granulomatous pneumonias (Mycobacterium tuberculosis and atypical mycobacteria, Histoplasma capsulatum and Coccidioides immitis).

The combined clinical classification, now the most commonly used classification scheme, attempts to identify a person's risk factors when he or she first comes to medical attention. The advantage of this classification scheme over previous systems is that it can help guide the selection of appropriate initial treatments even before the microbiologic cause of the pneumonia is known. There are two broad categories of pneumonia in this scheme: community-acquired pneumonia and hospital-acquired pneumonia. A recently introduced type of healthcare-associated pneumonia (in patients living outside the hospital who have recently been in close contact with the health care system) lies between these two categories.

Community-acquired pneumonia
Community-acquired pneumonia (CAP) is infectious pneumonia in a person who has not recently been hospitalized. CAP is the most common type of pneumonia. The most common causes of CAP vary depending on a person's age, but they include Streptococcus pneumoniae, viruses, the atypical bacteria, and Haemophilus influenzae. Overall, Streptococcus pneumoniae is the most common cause of community-acquired pneumonia worldwide. Gram-negative bacteria cause CAP in certain at-risk populations. CAP is the fourth most common cause of death in the United Kingdom and the sixth in the United States. The term "walking pneumonia" has been used to describe a type of community-acquired pneumonia of less severity (because of the fact that the sufferer can continue to "walk" rather than require hospitalization). Walking pneumonia is usually caused by the atypical bacteria mycoplasma pneumonia.

Hospital-acquired pneumonia
Hospital-acquired pneumonia, also called nosocomial pneumonia, is pneumonia acquired during or after hospitalization for another illness or procedure with onset at least 72 hrs after admission. The causes, microbiology, treatment and prognosis are different from those of community-acquired pneumonia. Up to 5% of patients admitted to a hospital for other causes subsequently develop pneumonia. Hospitalized patients may have many risk factors for pneumonia, including mechanical ventilation, prolonged malnutrition, underlying heart and lung diseases, decreased amounts of stomach acid, and immune disturbances. Additionally, the microorganisms a person is exposed to in a hospital are often different from those at home . Hospital-acquired microorganisms may include resistant bacteria such as MRSA, Pseudomonas, Enterobacter, andSerratia. Because individuals with hospital-acquired pneumonia usually have underlying illnesses and are exposed to more dangerous bacteria, it tends to be more deadly than community-acquired pneumonia.Ventilator-associated pneumonia (VAP) is a subset of hospital-acquired pneumonia. VAP is pneumonia which occurs after at least 48 hours of intubation and mechanical ventilation.

Other types of pneumonia
Severe acute respiratory syndrome (SARS)
SARS is a highly contagious and deadly type of pneumonia which first occurred in 2002 after initial outbreaks in China. SARS is caused by the SARS coronavirus, a previously unknown pathogen.
Bronchiolitis obliterans organizing pneumonia (BOOP)
BOOP is caused by inflammation of the small airways of the lungs. It is also known as cryptogenic organizing pneumonitis (COP).
Eosinophilic pneumonia
Eosinophilic pneumonia is invasion of the lung by eosinophils, a particular kind of white blood cell. Eosinophilic pneumonia often occurs in response to infection with a parasite or after exposure to certain types of environmental factors.
Chemical pneumonia
Chemical pneumonia (usually called chemical pneumonitis) is caused by chemical toxicants such as pesticides, which may enter the body by inhalation or by skin contact. When the toxic substance is an oil, the pneumonia may be called lipoid pneumonia.
Aspiration pneumonia
Aspiration pneumonia (or aspiration pneumonitis) is caused by aspirating foreign objects which are usually oral or gastric contents, either while eating, or after reflux or vomiting which results inbronchopneumonia. The resulting lung inflammation is not an infection but can contribute to one, since the material aspirated may contain anaerobic bacteria or other unusual causes of pneumonia. Aspiration is a leading cause of death among hospital and nursing home patients, since they often cannot adequately protect their airways and may have otherwise impaired defenses.

Dust pneumonia
Dust pneumonia describes disorders caused by excessive exposure to dust storms, particularly during the Dust Bowl in the United States. With dust pneumonia, dust settles all the way into the alveoli of the lungs, stopping the cilia from moving and preventing the lungs from ever clearing themselves.

Necrotizing pneumonia, although overlapping with many other classifications, includes pneumonias that cause substantial necrosis of lung cells, and sometimes even lung abscess. Implicated bacteria are extremely commonly anaerobic bacteria, with or without additional facultatively anaerobic ones like Staphylococcus aureus, Klebsiella pneumoniae and Streptococcus pyogenes. Type 3 pneumococcus is uncommonly implicated.

Opportunistic pneumonia includes those that frequently strike immunocompromised victims. Main pathogens are cytomegalovirus, Pneumocystis jiroveci, Mycobacterium avium-intracellulare, invasiveaspergillosis, invasive candidiasis, as well as the "usual bacteria" that strike immunocompetent people as well.

USMLE case: surgery or medicine

A 13-year-old boy has a 3-day history of low-grade fever, upper respiratory symptoms, and a sore throat. A few hours before his presentation to the emergency room, he has an abrupt onset of high fever, difficulty swallowing, and poor handling of his secretions. He indicates that he has a marked worsening in the severity of his sore throat. His pharynx has a fluctuant bulge in the posterior wall. Which of the following is the most appropriate initial therapy for this patient?

A.Narcotic analgesics
B.Trial of oral penicillin V
C.Surgical consultation for incision and drainage under general anesthesia
D.Rapid streptococcal screen
E.Monospot test

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Seasonal hyperacute panuveitis (SHAPU) In Nepal


Seasonal hyperacute panuveitis (SHAPU), characterized by an unusual form of unilateral severe hyper acute diffused intraocular inflammation, is one of the mysterious eye diseases of which the definite cause and treatment remains yet to be tound out. In this study, a total of six cases were included. Aqueous and vitreous samples were subjected to direct microscopy and culture (bacterial or fungal). Of the six cases included, two yielded Streptococcus pneumoniae and one Acinetobactor sp. on culture. All three culture positive samples showed pus cells in direct microscopic examination (gram stain). All cases were subjected to vitrectomy and intravitreal antibiotic and steroid injection, along with oral antibiotics and steroid. Five cases were also treated with antiviral agent. After treatment four cases showed reversal of hypotony and three cases recovered some vision.

Moths have been reported to increase the prevalence of this disease. Complications can be as devastating as blindness.

Read NMJ journal Article...Read

Swine Flu 4 vaccines Declared

The US Food and Drug Administration (FDA) announced today that it has approved 4 vaccines against the 2009 influenza A (H1N1) virus, formerly known as "swine flu." The vaccine lots are expected to be available and distributed within the next 4 weeks.

FDA Commissioner of Food and Drugs Margaret A. Hamburg, MD, said she thought Tuesday's approval was good news for the nation's response to the H1N1 influenza virus. "This vaccine will help protect individuals from serious illness and death from influenza," she said.

The approval comes at a time when the Centers for Disease Control and Prevention (CDC) is reporting that visits to physicians around the country for influenza-like illness are increasing and are higher than expected at this time of year. The vaccines that are currently available against 3 seasonal influenza virus strains will not protect against the 2009 H1N1 virus.

The FDA said that the vaccines, based on early data, effectively elicit an immune response in most healthy adults about 8 to10 days after vaccination. Clinical studies are still underway to produce an optimal dose for children, with results expected in the near future.

Meanwhile, the CDC stresses that influenza is primarily spread through person-to-person contact, by the coughing or sneezing of infected people, and recommends that infected people stay home and limit their contact with others to keep from infecting them.

The newly approved vaccines are being made by CSL Limited, MedImmune LLC, Novartis Vaccines and Diagnostics Limited, and Sanofi Pasteur Inc. All 4 firms reportedly use the same processes to manufacture the H1N1 vaccines. As with the seasonal influenza vaccine, some lots of the H1N1 vaccine will contain the preservative thimerosal and others will not. The FDA has been continuing its efforts toward reducing thimerosal used in vaccines.

The FDA warns that persons with known allergies to chicken eggs or any other substance in the vaccine should probably not be vaccinated, although in the ongoing clinical trials, the vaccines have been well tolerated. The most common adverse effect is soreness at the injection site; other adverse effects can include a mild fever, body aches, and fatigue for a couple of days after vaccination. For the nasal spray delivery system, the most common adverse effects were runny nose, nasal congestion in all ages, sore throats in adults, and fever in children aged 2 to 6 years.

The FDA is working with different organizations regarding adverse event monitoring, information sharing, and an overall analysis during and after the 2009 H1N1 vaccination program, according to the news release. "As with any medical product, unexpected or rare serious adverse events may occur," the FDA notes.

Tonsillectomy surgery Best Video

The Best Tonsillectomy video on youtube

3 minutes video, Details video

Tetralogy of Fallot



Tetralogy of Fallot

is the most common Cyanotic heart disease in children. The condition causes mixing of deoxygenated blood with the oxygenated blood being pumped out of the heart and into the circulatory system of blood vessels, Causing-

  • hypoxemia.

  • cyanosis, a bluish color of the skin, lips, and membranes inside the mouth and nose.
The 4 abnormalities (tetralogy) of the heart described by Fallot include the following:
  • Right ventricular hypertrophy: Narrowing or blockage of the pulmonary valve and/or muscle under the pulmonary valve coming out of the right ventricle. This restriction to blood outflow causes an increase in right ventricular work and pressure, leading to right ventricular thickening or hypertrophy.

  • Ventricular septal defect (VSD): This is a hole in the heart wall (septum) that separates the 2 ventricles. The hole is usually large and allows oxygen-poor blood in the right ventricle to pass through, mixing with oxygen-rich blood in the left ventricle. This poorly oxygenated blood is then pumped out of the left ventricle to the rest of the body. The body gets some oxygen, but not all that it needs. This lack of oxygen in the blood causes cyanosis.

  • Abnormal position of the aorta: The aorta, the main artery carrying blood out of the heart and into the circulatory system, exits the heart from a position overriding the right and left ventricles. (In the normal heart, the aorta exits from the left ventricle.) This is not of major importance in infants.

  • Pulmonary valve stenosis (PS): The major issue with tetralogy of Fallot is the degree of pulmonary valve stenosis, since VSD is always present. If the stenosis is mild, minimal cyanosis occurs, since blood still mostly travels to the lungs. However, if the PS is moderate to severe, a smaller amount of blood reaches the lungs, since most is shunted right-to-left through the VSD
Investigations:

CXR - baseline
ECG - yearly to assess rhythm and QRS duration
TTE - regularly (yearly or more frequent if severe PR and RV dysfunction, can be 2 or 3 yearly if very good surgical result and no new symptoms) (NB. It is easy to under estimate the degree of PR by colour follow alone) To assess pulmonary valve function, proximal PA anatomy, RV size and function, LV function, aortic root size and degree of aortic regurgitation.
Catheterisation - for dilatation / stenting of pulmonary arteries
MRI - becoming investigation of choice for proximal pulmonary artery anatomy, RV size and function and assessment of pulmonary regurgitation
Holter - for symptoms and screening for VT or high grade ectopy in those with marked RV dilatation or QRS > 180ms
Exercise test / CPEX - exercise capacity serial assessment, pre-pregnancy counselling

Additional investigations - EP studies for those with symptomatic atrial or ventricular arrhythmias or unexplained syncope or pre-syncope


Indications for intervention

Unrepaired tetralogy of Fallot (at any age)
Significant RVOT or branch PA stenosis (RV pressure > half systemic)
Severe pulmonary regurgitation with dilatation and dysfunction of the RV
Aortic regurgitation
Arrhythmias in presence of repairable haemodynamic sequela

TREATMENT OPTIONS
Surgery (+/- anti-arrhythmia procedures)

Percutaneous pulmonary valve implantation (for those with an RV to PA conduit of suitable size only)

Percutaneous pulmonary artery angioplasty and stenting

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