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"First Case" of Highly Resistant TB Seen in U.S.

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sjf53 View Drop Down
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    Posted: December 27 2009 at 7:43am

 

First Case of Highly Resistant TB Seen in U.S.

Sunday, December 27, 2009

LANTANA, Florida —  It started with a cough, a cool-season hack that refused to go away.

Then came the fevers. They bathed and chilled the skinny frame of Oswaldo Juarez, a 19-year-old Peruvian visiting to study English. His lungs clattered, his chest tightened and he ached with every gasp. During a wheezing fit at 4 a.m., Juarez felt a warm knot rise from his throat. He ran to the bathroom sink and spewed a mouthful of blood.

I'm dying, he told himself, "because when you cough blood, it's something really bad."

It was really bad, and not just for him.

Doctors say Juarez's incessant hack was a sign of what they have both dreaded and expected for years — this country's first case of a contagious, aggressive, especially drug-resistant form of tuberculosis. The Associated Press learned of his case, which until now has not been made public, as part of a six-month look at the soaring global challenge of drug resistance.

Juarez's strain — so-called extremely drug-resistant (XXDR) TB — has never before been seen in the United States, according to Dr. David Ashkin, one of the nation's leading experts on tuberculosis. XXDR tuberculosis is so rare that only a handful of other people in the world are thought to have had it.

"These are the ones we really fear because I'm not sure how we treat them," Ashkin said.

Forty years ago, the world thought it had conquered TB and any number of other diseases through the new wonder drugs: Antibiotics. U.S. Surgeon General William H. Stewart announced it was "time to close the book on infectious diseases and declare the war against pestilence won."

Today, all the leading killer infectious diseases on the planet — TB, malaria and HIV among them — are mutating at an alarming rate, hitchhiking their way in and out of countries. The reason: Overuse and misuse of the very drugs that were supposed to have saved us.

Just as the drugs were a manmade solution to dangerous illness, the problem with them is also manmade. It is fueled worldwide by everything from counterfeit drugmakers to the unintended consequences of giving drugs to the poor without properly monitoring their treatment. Here is what the AP found:

—In Cambodia, scientists have confirmed the emergence of a new drug-resistant form of malaria, threatening the only treatment left to fight a disease that already kills 1 million people a year.

—In Africa, new and harder-to-treat strains of HIV are being detected in about 5 percent of new patients. HIV drug resistance rates have shot up to as high as 30 percent worldwide.

—In the United States, drug-resistant infections killed more than 65,000 people last year, more than prostate and breast cancer combined. More than 19,000 people died from a staph infection alone that has been eliminated in Norway, where antibiotics are stringently limited.

"Drug resistance is starting to be a very big problem. In the past, people stopped worrying about TB, and it came roaring back. We need to make sure that doesn't happen again," said Dr. Thomas Frieden, director of the U.S. Centers for Disease Control and Prevention, who was himself infected with tuberculosis while caring for drug-resistant patients at a New York clinic in the early 1990s. "We are all connected by the air we breathe, and that is why this must be everyone's problem."

This April, the World Health Organization sounded alarms by holding its first drug-resistant TB conference in Beijing. The message was clear — the disease already has spread to all continents and is increasing rapidly. Even worse, WHO estimates only 1 percent of resistant patients received appropriate treatment last year.

"We have seen a huge upburst in resistance," said CDC epidemiologist Dr. Laurie Hicks.

———

Juarez' strain of TB puzzled doctors. He had never had TB before. Where did he pick it up? Had he passed it on? Could they stop it before it killed him?

At first, mainstream doctors tried to treat him. But the disease already had gnawed a golf ball-sized hole into his right lung.

TB germs can float in the air for hours, especially in tight places with little sunlight or fresh air. So every time Juarez coughed, sneezed, laughed or talked, he could spread the deadly germs to others.

"You feel like you're killing somebody, like you could kill a lot of people. That was the worst part," he said.

Tuberculosis is the top single infectious killer of adults worldwide, and it lies dormant in one in three people, according to WHO. Of those, 10 percent will develop active TB, and about 2 million people a year will die from it.

Simple TB is simple to treat — as cheap as a $10 course of medication for six to nine months. But if treatment is stopped short, the bacteria fight back and mutate into a tougher strain. It can cost $100,000 a year or more to cure drug-resistant TB, which is described as multi-drug-resistant (MDR), extensively drug-resistant (XDR) and XXDR.

There are now about 500,000 cases of MDR tuberculosis a year worldwide. XDR tuberculosis killed 52 of the first 53 people diagnosed with it in South Africa three years ago.

Drug-resistant TB is a "time bomb," said Dr. Masae Kawamura, who heads the Francis J. Curry National Tuberculosis Center in San Francisco, "a manmade problem that is costly, deadly, debilitating and the biggest threat to our current TB control strategies."

Juarez underwent three months of futile treatment in a Fort Lauderdale hospital. Then, in December 2007, he was sent to A.G. Holley State Hospital, a 60-year-old massive building of brown concrete surrounded by a chain-link fence, just south of West Palm Beach.

"They told me my treatment was going to be two years, and I have only one chance at life," Juarez said. "They told me if I went to Peru, I'm probably going to live one month, and then I'm going to die."

Holley is the nation's last-standing TB sanitarium, a quarantine hospital that is now managing new and virulent forms of the disease.

Tuberculosis has been detected in the spine of a 4,400-year-old Egyptian mummy. In the 1600s, it was known as the great white plague because it turned patients pale. In later centuries, as it ate through bodies, they called it "consumption." By 1850, an estimated 25 percent of Europeans and Americans were dying of tuberculosis, often in isolated sanatoriums like Holley where they were sent for rest and nutrition.

Then in 1944 a critically ill TB patient was given a new miracle antibiotic and immediately recovered. New drugs quickly followed. They worked so well that by the 1970s in the United States, it was assumed the disease was a problem of the past.

Once public health officials decided TB was gone, the disease was increasingly missed or misdiagnosed. Without public funding, it made a comeback among the poor. Then immigration and travel flourished, breaking down invisible walls that had contained TB.

Drug resistance emerged worldwide. Doctors treated TB with the wrong drug combinations. Clinics ran out of drug stocks. And patients cut their treatment short when they felt better, or even shared pills with other family members.

There are two ways to get drug resistant TB. Most cases develop from taking medication inappropriately. But it can also be transmitted like simple TB, a cough or a sneeze.

In the 1980s, HIV and AIDS brought an even bigger resurgence of TB cases. TB remains the biggest killer of HIV patients today.

For decades, drug makers failed to develop new medicines for TB because the profits were not there. With the emergence of resistant TB, several private drug companies have started developing new treatments, but getting an entire regimen on the market could take 24 years. In the meantime, WHO estimates each victim will infect an average of 10 to 15 others annually before they die.

A.G. Holley was back in business.

———

Holley's corridors are long and dark, with fluorescent tubes throwing harsh white light on drab walls. One room is filled with hulking machines once used to collapse lungs, sometimes by inserting ping pong balls. Antique cabinets hold metal tools for spreading and removing ribs — all from a time when TB was rampant and the hospital's 500 beds were filled.

Only 50 beds are funded today, but those are mostly full. More than half the patients are court-ordered into treatment after refusing to take their meds on the outside.

Juarez came voluntarily. In the beginning, he was isolated and forced to wear a mask when he left his room. He could touch his Peruvian family only in pictures taped to the wall. He missed his dad, his siblings, his dog, his parrot, and especially his mother.

"I was very depressed," he said. "I had all this stuff in my mind."

He spent countless hours alone inside the sterile corner room reserved for patients on extended stays — dubbed "the penthouse" because it is bigger and lined by a wall of windows.

His moods ran hot and cold. He punched holes in the walls out of frustration, played loud reggaeton music with a thumping beat and got into fights with other patients. He covered his door's small window with a drawing of an evil clown to keep nurses from peering inside. He made friends with new patients, but was forced to stay long after many of them came, got cured, and left.

Early on, Juarez's treatment was similar to chemotherapy. Drugs were pumped into his bloodstream intravenously three times a day, and he choked down another 30 pills, including some that turned his skin a dark shade of brown. He swallowed them with spoonfuls of applesauce, yogurt, sherbet and chocolate pudding, but once they hit his stomach, waves of nausea sometimes sent him heaving. He would then have to force them all down again.

"When he first came in we really had to throw everything and the kitchen sink at him," said Ashkin, the hospital's medical director, who experimented on Juarez with high doses of drugs, some not typically used for TB. "It was definitely cutting edge and definitely somewhat risky because it's not like I can go to the textbooks or ... journal articles to find out how to do this."

After 17 years of handling complex cases — including TB in the brain and spine — Ashkin had never seen a case so resistant. He believed he would have to remove part of Juarez's lung.

Ashkin dialed Peru to talk to the young man's father.

It is a rare disease, said Ashkin, hard to define. Your son is one of two people in the world known to have had this strain, he said.

"What happened to the other person?" his father asked.

"He died."

———

Juarez's adventure in the United States had turned into a medical nightmare.

About 60 million people visit the U.S. every year, and most are not screened for TB before arrival. Only refugees and those coming as immigrants are checked. The top category of multidrug-resistant patients in the United States — 82 percent of the cases identified in 2007 — was foreign-born patients, according to the CDC.

The results are startling among those tested, said Dr. Angel Contreras, who screens Dominicans seeking to enter the United States on immigrant visas. The high rate of MDR-TB in the Dominican Republic coupled with high HIV rates in neighboring Haiti are a health crisis in the making, he said.

"They're perfect ingredients for a disaster," he said.

Juarez's homeland, Peru, also is a hotspot for multidrug-resistant TB. DNA fingerprinting linked his disease to similar strains found there and in China, but none with the same level of resistance.

"So the question is: Is this a strain that's evolving? That's mutating? That's becoming more and more resistant?" asked Ashkin. "I think the answer is yes."

Doctors grappling with these new strains inadvertently give the wrong medicines, and so the TB mutates to become more aggressive and resistant.

Poor countries also do not have the resources to determine whether a patient's TB is drug-resistant. That requires sputum culturing and drug-susceptibility testing — timely, expensive processes that must be performed in capable labs. WHO is working to make these methods more available in high-risk countries as well as negotiating cheaper prices for second-line drugs.

"There's a lot of MDR and XDR-TB that hasn't been diagnosed in places like South Africa and Peru, Russia, Estonia, Latvia," said Dr. Megan Murray, a tuberculosis expert at Harvard University. "We think it's a big public health threat."

Experts argue if wealthy countries do not help the worst-hit places develop comprehensive TB programs, it puts everyone at risk.

"You're really looking at a global issue,"' said Dr. Lee Reichman, a TB expert at the New Jersey Medical School Global Tuberculosis Institute. "It's not a foreign problem, you can't keep these TB patients out. It's time people realize that."

———

Juarez spent a year and a half living alone in a room plastered with bikini-clad blondes, baseball caps and a poster of Mount Everest for inspiration. There were days when he simply shut down and refused his meds until his family persuaded him to keep fighting.

"I was thinking that maybe if I need to die, then that's what I need to do," he said, perched on his bed in baggy jeans. "I felt like: `I'm never going to get better. I'm never going to get out of here."'

When put side by side, his CAT scans from before and after treatment are hard to believe. The dark hole is gone, and only a small white scar tattoos his lung.

"They told me the TB is gone, but I know that TB, it doesn't have a cure. It only has a treatment like HIV," he said, his English now fluent and his body weight up 32 pounds from when he first arrived. "The TB can come back. I saw people who came back to the hospital twice and some of them died. So, it's very scary."

His treatment cost Florida taxpayers an estimated $500,000, a price tag medical director Ashkin says seems like an astronomical amount to spend on someone who is not an American citizen. But he questions how the world can afford not to treat Juarez and others sick with similar lethal strains.

"This is an airborne spread disease ... so when we treat that individual, we're actually treating and protecting all of us," he said. "This is true homeland security."

In July, at age 21 — 19 months after checking in — Juarez swallowed his last pills, packed a few small suitcases and wheeled them down the hospital's long corridor.

The last time doctors saw him, he was walking out of the sanitarium into south Florida's soupy heat.

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Post Options Post Options   Thanks (0) Thanks(0)   Quote Mary008 Quote  Post ReplyReply Direct Link To This Post Posted: December 27 2009 at 11:20am

.

 National Media needs to beef up research.
 
 
 
Not True....
 
 
 
.
.
First Case of Highly Resistant TB Seen in U.S.
......................................................................................
 
Associated Press
 
 
............................................
 
 
Extensively Drug-Resistant Tuberculosis
 
(XDR) TB
 
 
A total of 83 cases of XDR-TB were reported in the United States from
 
1993 to 2007.
 
 
 
 
source-
 

JAMA. 2008 Nov 12;300(18):2153-60.

Extensively drug-resistant tuberculosis in the United States, 1993-2007.

 
 
 
 
................................
 
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Mary008 Quote  Post ReplyReply Direct Link To This Post Posted: December 27 2009 at 11:51am
.
 
 
Because we Can Not Control immigration...
 
of people into the US (and Canada)
 
 
It may have been a wise decision to implement The Goal of National Health Care For
 
the USA.
 
...................................................................................................................................
 
 
 
 
 
 
 
Can J Infect Dis Med Microbiol. 2007 September; 18(5): 289–291.  PMCID: PMC2533560
Copyright © 2007, Pulsus Group Inc. All rights reserved
 
 
The emergence of extensively drug-resistant tuberculosis (TB): TB/HIV coinfection,
 
multidrug-resistant TB and the resulting public health threat from extensively drug-
 
resistant TB, globally
 
and in Canada
 
 
Paul E Alexander, MHSc1 and Prithwish De, MHSc PhD candidate2

source-
 
...................................................................................................................

 
 
 
Curr Opin Infect Dis.
...................................
.............................................
..........................................................
 
 
2009 Apr; 22
(2):167-73.
.........................................................................
 
Extensively drug-resistant tuberculosis.

...........................................................................
 
LoBue P.
 
Division of Tuberculosis Elimination,
 
Centers for Disease Control and Prevention,
 
1600 Clifton Road, Atlanta, GA 30333, USA. plobue@cdc.gov
 
 
 
 
PURPOSE OF REVIEW:
 
 
To describe the origin, epidemiology, diagnosis, treatment, prevention, and control of

extensively drug-resistant tuberculosis (XDR TB).

RECENT FINDINGS:

 XDR TB is defined as the occurrence of TB in persons whose
 
Mycobacterium tuberculosis isolates
 
are resistant to isoniazid and rifampin
 
and to any fluoroquinolone and at least
 
one of three injectable second-line drugs
 
(i.e., amikacin, kanamycin, or capreomycin).

 
 
 
As of June 2008, XDR TB has been found in
 
49 countries
 
 
including the United States.

 
 
It generally takes several weeks to detect XDR TB using conventional
 
culture-based methods, although some progress is being made in

developing rapid molecular tests. Treatment for XDR TB is difficult,

usually requiring at least 18-24 months of four to six second-line anti-

TB drugs.

Treatment success rates are generally 30-50%,

with very poor outcomes in HIV-infected patients.

 
 
Management of contacts to infectious XDR TB patients is complicated
 
by the lack of a proven effective treatment
f
or XDR latent tuberculosis infection.

 
 
SUMMARY:
 
XDR TB is an emerging global health threat.

The disease is difficult and expensive to diagnose and treat, and outcomes are f
 
requently poor.

New rapid diagnostic tests and new classes of anti-TB drugs are needed to successfully
 
combat this global problem.
 
 
PMID: 19283912 [PubMed - indexed for MEDLINE]
 
nkpos=4
 
 
 
.........................
 
 
 
 
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Post Options Post Options   Thanks (0) Thanks(0)   Quote sjf53 Quote  Post ReplyReply Direct Link To This Post Posted: December 27 2009 at 3:07pm

Thanks Mary.  I thought the same thing.

That is why I put quotations around "First Case" in the topic thread.
I forgot to add the question mark.
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Mary008 Quote  Post ReplyReply Direct Link To This Post Posted: December 27 2009 at 8:11pm
hi, good find.    trying to remember if there are  4 or 5 Pandemics now....
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Medclinician Quote  Post ReplyReply Direct Link To This Post Posted: December 28 2009 at 6:26am
Mary we have been monitoring this guy who has been in forced isolation for more than a year. One case which was highly publicized of a returning person crossing the Canadian border and then waved through say 'you don't look that sick'.

This strain is found in up to 7 locations globally but probably is more widespread. It is extremely dangerous in that if it does spread- it is a nasty lifetime disease for which we have no cure.

There have been questions of the humanity of keep people with this type of infection in enforced confinement. I would agree with that as opposed the other option.

Med
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Mary008 Quote  Post ReplyReply Direct Link To This Post Posted: December 28 2009 at 9:10pm
.
 
 
 
 
BMJ 1994;308:807-808 (26 March)

News

New York makes progress in fight against tuberculosis

Fred B. Charatan 

New York City is gaining ground in its battle against tuberculosis,

 
with a 15% fall in the number of new cases reported last year.
 
The city still has three times as many new cases of tuberculosis as
 
any other city in the US, but these latest figures--which show a
 
drop from 3811 cases in 1992 to 3235 last year--represent the first decrease in a decade.

The rate of tuberculosis in New York City is 44 cases per 100 000

population--more than four times the national average.
 
 
...............
 
She was born to Johannes Dircksen Hoes (1753-1789), and Maria Quakenbush (1754-
 
1852) who were of Dutch ancestry. She was taught in a local Kinderhook school by master
 
Vrouw Lange. Like Martin, she was raised in a Dutch home and never did lose her distinct
 
Dutch accent. Van Buren was devoted to his shy, blue-eyed bride, whom he always called
 
"Jannetje", a Dutch petform of Johanna.
 
 
Wife of Pres. Martin Van Buren
 
Hannah  Van Buren
March 8, 1783 – February 5, 1819
 
After 10 years of marriage, Mrs. Van Buren contracted tuberculosis
and died on February 5, 1819, at age 35.
 
wikipedia
...............................................................
 
 
Some earlier history of this disease....   
 
 
 
Some knew it as "Consumption"
 
 
 
 
Tuberculosis Sanatorium
...............................................
Glen Lake Children's Camp
.................................................

is a former children's camp for victims of tuberculosis.

The camp was part of the Glen Lake Sanatorium on the border of Minnetonka and Eden Prairie, Minnesota. Although the main sanatorium buildings were demolished in 1993, the children's camp portion remained intact.
 
The camp is Minnesota's only known surviving camp for children who had tuberculosis, and it reflects the philanthropic efforts of its founders, George H. and Leonora Christian. It was listed on the National Register of Historic Places on August 5, 1999.[2]

Tuberculosis was becoming a major health problem in Minnesota around the turn of the 20th century, with more than

20,000 Minnesotans dying of the disease between 1887 and 1899.

The Minnesota Legislature created the
Minnesota State Sanatorium for Consumptives
on Leech Lake near Walker, Minnesota in 1907. The sanatorium at Leech Lake wasn't able to handle the increasing demand for tuberculosis patients, so the Legislature passed a bill allowing counties to build their own sanatoria. Hennepin County began construction of the Glen Lake Sanatorium in 1914, and it opened in 1916.[2]
The children's camp was established by George H. and Leonora Christian.
 
 
George H. Christian was a flour buyer who partnered with Governor Cadwallader C. Washburn. Leonora dedicated herself to the fight against tuberculosis, and in 1906, she established a summer camp in Minneapolis for children with tuberculosis.

The camp moved to Glenwood Park (now Theodore Wirth Park) in 1909, staffed by the Visiting Nurses Association. In 1925, the Visiting Nurses Association determined that they could no longer operate the camp. The Children's Aid Society, a foundation established by George H. Christian in 1916, offered to build a permanent children's camp. Glen Lake Sanatorium was willing to provide land and management. Glen Lake Children's Camp opened on June 12, 1925.[2]
 
 
When antibiotic treatments became available for tuberculosis in the 1940s, the era of tuberculosis treatment began to draw to a close.
The children's camp ceased operation in 1950, and the Leech Lake Sanatorium closed in 1962 and transferred its patients to Glen Lake.
The last tuberculosis patient was discharged in 1976.
The sanatorium complex, with the exception of the children's camp, was demolished in 1993.

In 1997, most of the land became the Glen Lake Golf and Practice Center operated by Three Rivers Park District.

The children's camp is still in operation, leased to Friendship Ventures and operated by Eden Wood Center.[2]
 
........................................................................
 
 
 
Transmission
.......................

Further information: Transmission (medicine)
When people suffering from active pulmonary TB cough, sneeze, speak, or spit, they expel infectious aerosol droplets 0.5 to 5 µm in diameter. A single sneeze can release up to 40,000 droplets.[29] Each one of these droplets may transmit the disease, since the infectious dose of tuberculosis is very low and inhaling less than ten bacteria may cause an infection.[30][31]
 
 
 
People with prolonged, frequent, or intense contact are at particularly high risk of becoming infected, with an estimated 22% infection rate.
 
 
A person with active but untreated tuberculosis can infect 10–15 other people per year.[3] Others at risk include people in areas where TB is common, people who inject drugs using unsanitary needles, residents and employees of high-risk congregate settings, medically under-served and low-income populations, high-risk racial or ethnic minority populations, children exposed to adults in high-risk categories, patients immunocompromised by conditions such as HIV/AIDS, people who take immunosuppressant drugs, and health care workers serving these high-risk clients.[32]
 
 
Transmission can only occur from people with active - not latent -TB [1].
 
 
The probability of transmission from one person to another depends upon the number of infectious droplets expelled by a carrier,
 
 
 the effectiveness of ventilation,
 
 the duration of exposure,
 
and the virulence of the M. tuberculosis strain.[8]
 
 
The chain of transmission can, therefore, be broken by isolating patients with active disease and starting effective anti-tuberculous therapy.
 
 
(This is why people were sent away to a Sanatorium to   isolate and "cure")
 
 
After two weeks of such treatment, people with non-resistant active TB generally cease to be contagious.  
 
(then why did they keep the Peruvian Man in Hospital for 2 years?  Perhaps because the drug therapy needs to be closley monitored )
 
If someone does become infected, then it will take at least 21 days, or three to four weeks, before the newly infected person can transmit the disease to others.[33]
 
 
TB can also be transmitted by eating meat infected with TB. Mycobacterium bovis causes TB in cattle. (See details below.)
 
( Folks... don't do Steak TarTare. )
 
Tatar-1.jpg
 
 
 
 
 
 
 
Pathogenesis
......................
 
About 90% of those infected with Mycobacterium tuberculosis have asymptomatic, latent TB infection (sometimes called LTBI), with only a 10% lifetime chance that a latent infection will progress to TB disease.[1] However, if untreated, the death rate for these active TB cases is more than 50%.[34]
 
 
TB infection begins when the mycobacteria reach the pulmonary alveoli, where they invade and replicate within the endosomes of alveolar macrophages.[1][35] The primary site of infection in the lungs is called the Ghon focus, and is generally located in either the upper part of the lower lobe, or the lower part of the upper lobe[1]. Bacteria are picked up by dendritic cells, which do not allow replication, although these cells can transport the bacilli to local (mediastinal) lymph nodes. Further spread is through the bloodstream to other tissues and organs where secondary TB lesions can develop in other parts of the lung (particularly the apex of the upper lobes), peripheral lymph nodes, kidneys, brain, and bone.[1][36] All parts of the body can be affected by the disease, though it rarely affects the heart, skeletal muscles, pancreas and thyroid.[37]
Tuberculosis is classified as one of the granulomatous inflammatory conditions. Macrophages, T lymphocytes, B lymphocytes and fibroblasts are among the cells that aggregate to form a granuloma, with lymphocytes surrounding the infected macrophages.
 
 
The granuloma functions not only to prevent dissemination of the mycobacteria, but also provides a local environment for communication of cells of the immune system. Within the granuloma, T lymphocytes secrete cytokines such as interferon gamma, which activates macrophages to destroy the bacteria with which they are infected.[38] Cytotoxic T cells can also directly kill infected cells, by secreting perforin and granulysin.[35]
 
 
Importantly, bacteria are not always eliminated within the granuloma, but can become dormant, resulting in a latent infection.[1] Another feature of the granulomas of human tuberculosis is the development of cell death, also called necrosis, in the center of tubercles. To the naked eye this has the texture of soft white cheese and was termed caseous necrosis.[39]
 
 
If TB bacteria gain entry to the bloodstream from an area of damaged tissue they spread through the body and set up many foci of infection,
 
all appearing as tiny white tubercles in the tissues. This severe form of TB disease is most common in infants and the elderly and is called miliary tuberculosis. Patients with this disseminated TB have a fatality rate near 100% if untreated. However, If treated early, the fatality rate is reduced to near 10%.[40]
 
In many patients the infection waxes and wanes.
 
Tissue destruction and necrosis are balanced by healing and fibrosis.[39] Affected tissue is replaced by scarring and cavities filled with cheese-like white necrotic material. During active disease, some of these cavities are joined to the air passages bronchi and this material can be coughed up. It contains living bacteria and can therefore pass on infection. Treatment with appropriate antibiotics kills bacteria and allows healing to take place. Upon cure, affected areas are eventually replaced by scar tissue.[39]
If untreated, infection with Mycobacterium tuberculosis can become lobar pneumonia.[41]
 
 
The children's camp is still in operation,
 
 
File:Glen%20Lake-02.JPG
 
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Post Options Post Options   Thanks (0) Thanks(0)   Quote Medclinician Quote  Post ReplyReply Direct Link To This Post Posted: December 29 2009 at 1:45am
beautiful tag post but completely ignores well now and news data.

This is 2 years old.

http://articles.latimes.com/2007/jun/01/nation/na-tb1


Border alert on TB patient disregarded

The Atlanta man defied instructions to stay put overseas after doctors realized he had a deadly strain of the disease.

The Nation

June 01, 2007|Jia-Rui Chong, Stephanie Simon and Nicholas Riccardi, Times Staff Writers

DENVER — A man infected with an extremely dangerous strain of tuberculosis was waved into the United States at a border crossing even after a routine check of his passport set off an urgent warning, authorities said Thursday.

Andrew Speaker, 31, a personal-injury lawyer from Atlanta, arrived at the Canadian border May 24 after disregarding explicit instructions from the Centers for Disease Control and Prevention to remain in Italy -- where he was on his honeymoon -- for fear of spreading his potentially deadly strain of TB.

Among the deadly maladies pouring across the border is tuberculosis, mostly wiped out in modern America, Cosman writes, "thanks to excellent hygiene and powerful modern drugs." But now, multidrug resistant tuberculosis has arrived in America via Mexico and other third-world countries. "MDR-TB MDR-TB Multi-Drug Resistant Tuberculosis
..... Click the link for more information.
," she explained, "takes 24 months [to cure] with many expensive drugs that cost around $250,000, with toxic side effects Side effects

Effects of a proposed project on other parts of the firm.
..... Click the link for more information.
. Each illegal with MDR-TB coughs and infects 10 to 30 people, who will not show symptoms immediately. Latent disease explodes later."

TB cases in Virginia jumped 17 percent in 2002, but Prince William County, alone, she reported, witnessed a 188-percent increase. And there's more:
   In 2001 the Indiana School of Medicine
studied an outbreak of MDRTB,
and traced it to Mexican illegal
aliens. The Queens, New York, health
department attributed 81 percent of
new TB cases in 2001 to immigrants.
The Centers for Disease Control and
Prevention ascribed 42 percent of all
new TB cases to foreign-born people
who have up to eight times higher
incidence. Apparently, 66 percent
of all TB cases coming to America
originate in Mexico, the Philippines,
and Vietnam. Virulent TB outbreaks
afflicted schoolteachers and children
in Michigan, adults and children in
Texas, and policemen in Minnesota.
Recently TB erupted in Portland,


Maine, and Del Rey Beach, Florida.


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Post Options Post Options   Thanks (0) Thanks(0)   Quote Medclinician Quote  Post ReplyReply Direct Link To This Post Posted: December 29 2009 at 1:52am
Don't believe the .gov controlled search engines.. with a little investigation - you will find often 25 top rating articles are pure ficiton...

http://groups.google.com/group/alt.politics/browse_thread/thread/b7138928ceea86ae?pli=1


The buffer on this dates 1994 - 15 years ago

LANTANA, Fla. (AP) — It started with a cough, an autumn hack that
refused to go away.

Then came the fevers. They bathed and chilled the skinny frame of
Oswaldo Juarez, a 19-year-old Peruvian visiting to study English.
His lungs clattered, his chest tightened and he ached with every
gasp. During a wheezing fit at 4 a.m., Juarez felt a warm knot rise
from his throat. He ran to the bathroom sink and spewed a mouthful
of blood.

I’m dying, he told himself, “because when you cough blood, it’s
something really bad.”

It was really bad, and not just for him.

Doctors say Juarez’s incessant hack was a sign of what they have
both dreaded and expected for years — this country’s first case of
a contagious, aggressive, especially drug-resistant form of
tuberculosis. The Associated Press learned of his case, which until
now has not been made public, as part of a six-month look at the
soaring global challenge of drug resistance.

Juarez’s strain — so-called extremely drug-resistant (XXDR) TB —
has never before been seen in the U.S., according to Dr. David
Ashkin, one of the nation’s leading experts on tuberculosis. XXDR
tuberculosis is so rare that only a handful of other people in the
world are thought to have had it.

“He is really the future,” Ashkin said. “This is the new class that
people are not really talking too much about. These are the ones we
really fear because I’m not sure how we treat them.”
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http://www.npr.org/templates/story/story.php?storyId=9284375

April 2, 2007

Robert Daniels is being held in a detention ward at an Arizona hospital because he is infected with a deadly strain of tuberculosis. Daniels refused to comply with voluntary quarantine rules.

Rene Gutel of member station KJZZ reports, and Dr. Ross Upshur, head of the University of Toronto Joint Centre for Bioethics, argues that isolation is the only way to contain dangerous types of TB.


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TB Patient Isolated After Taking Two Flights

Dear Mr. Nigro:

Attached, please find an article published within today's edition of The New York Times entitled "TB Patient is Isolated After Taking Two Fights". Please note the report recounts the fact that theTB patient is infected with the same virulent strain of tuberculosis, XDR TB, of which CWA Local 1081 wrote to you within our attached letter of May 5, 2007 expressing our concern for the well being of our Union's members who might come into contact with clients knowingly, or unknowingly, infected with this deadly scourge.

Please note, as well, your attached written response of May 15, 2007 to our Union's letter written you of May 3, 2007 in which you downplayed the extent of the possible threat XDR TB poses to our members, this based upon statistics you personally researched. CWA Local 1081 responded to your letter within our attached missive of May 21, 2007, in which we took small solace with your assertion that you "'regularly visit the offices'", introduce yourself to clients "and shake their hands". Please recall that our Union emailed to the entirety of the employees of the Essex County Division of Welfare the attached article of May 28, 2007 published within The Chicago Tribune entitled "Study: Drug-resistant staph infections rise in poor neighborhoods".

Based upon all of the above, CWA Local 1081 is reiterating our respectfully fervent request you take a proactive approach to our concerns, particularly within the light of the recent published media reports we've furnished you, and that you soon arrange a meeting that shall include Essex County Health Office Michael Festa and a respective representation of the management of the Division of Welfare and CWA Local.

Sincerely,

David H. Weiner, President, CWA Local 1081

http://www.cwa1081.com/tbpatient_053007.php

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As Mary has mentioned-we are in the midst of multiple Pandemics. TB is one of them. Incredible lack of attention and focus has been placed on SARS, Avian, and Swine Flu- while Dengue-TB-Malaria and others ravage the planet with huge death tolls yearly.

It is my personal feeling this is a matter of race and elitism by developed countries against third world nations of color who suffer horrific conditions, lack of medical care, and disease and only when the problem becomes American or British or European- is it consider a real problem.

Resistant TB could wipe us out as effectively as any virus- and other diseases such as West Nile and Ebola simply mutated could destroy nations. In fact, many diseases such HIV in Africa are destroying nations and little is being done to really contain it or find an effective cure.

We focus on Swine Flu with a proclaimed CFR of .1% while Ebola is a wipe out the whole village pathogen.

With our wide open borders and a constant stream of sometimes diseased people who are not adequately medically screened- especially by jet (those who have money) we are long over due for some massive epidemics.

This is not the first case nor will it be the last. Some persons have been in isolation in the U.S. for some time.

Med
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THE XDR TB IS DIFFERENT THAN XXDR TB THAT THEY ARE CALLING THE FIRST
AM I CORRECT.
NOTICE ONE ARTICLE READS XXDR TB AND WHAT YOU POSTED  MARY 08 IS XDR TB
ITS SHORT ONE X.
IS THERE A DIFFERENCE
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Post Options Post Options   Thanks (0) Thanks(0)   Quote PrepGirl Quote  Post ReplyReply Direct Link To This Post Posted: December 29 2009 at 1:08pm

 

 

 

Alanna Shaikh's Blog

ns started in 2006. In July 2008, the Department of Field Support (DFS) launched the Misconduct Tracking System (MTS), a global database and confidential tracking system for all allegations of misconduct.

 there, it will be an impressive tool for ensuring accountability of peacekeepers and the UN. It will allow users to track allegations, investigations, and punitive action taken. If it allows activists to name and shame countries that don’t follow through on abuse allegations or discipline, it could have an enormous impact on reducing the incidence of abuse.

 I FOUND THIS ON THE INTERNET  PREPGIRL

Alanna Shaikh December 27, 2009 - 1:11 pm

Comment ( 2 )  

Until today, I hadn’t even heard of extremely drug resistant tuberculosis. There are only a handful of cases globally. The term was only defined in the last couple of years. It refers to TB bacteria that are resistant to all tuberculosis drugs and it’s almost always fatal. This is not the same as XDR TB (with one X), aka extensively drug resistant TB, which still responds to some third-line TB drugs and has a lower mortality rate.

According to WHO, there have been  two cases diagnosed of XXDR TB in Europe. Aidsmap mentions two cases in Italy in 2003, both fatal -. I assume they are the same cases mentioned by WHO. The AP reported Sunday on the first case of XXDR TB identified in the US. It was diagnosed in a Peruvian student named Oswaldo Juarez who was studying English in the US. The story is both reassuring and really, really scary.

The reassuring part is that they cured him. The process wasn’t easy. It took 19 months, and a drug regimen that left Juarez throwing up and thinking about suicide. He was transferred from regular TB care into isolation in a TB hospital in Florida, and his care cost the United States $500,000. But they did cure him of XXDR tuberculosis.

The scary part is that Juarez had never had tuberculosis before. Usually, drug resistant TB occurs when people undergo TB treatment that fails. It can fail because it’s a badly chosen treatment, the patient quits in the middle, or the drugs are expired or counterfeit. This failed treatment kills of the easily eliminated bacteria and leaves the stronger ones to thrive and develop resistance to TB drugs.

In the case of Oswaldo Juarez, he was somehow infected with XXDR TB without ever having had tuberculosis before. This is very bad. Doctors don’t even know how it happened. How did he get it? Peru has not been a major source of drug resistant TB and Juarez doesn’t recall any TB exposure.

If people are now getting extremely drug resistant TB – and without previous TB treatment - that could mean a major, extremely destructive, epidemic.

One final note – I was proud of the US government’s action here. They could have chartered a plane and deported to Juarez back to Peru. Hospitals do it all the time. Instead, they did the right thing, both morally and to protect public health. Letting Juarez spread XXDR TB in Peru would have been a death sentence for him and anyone on the plane with him, and it would have come back to the haunt the US when the disease spread here.

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I CLEAN THE ABOVE POST THE BEST I COULD
I HOPE IT HELPS WITH THE QUESTION OF XDR AND XXDR TB
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.
 
Hi... the problem is with the  Story Headline... not the difference between definitions of TB cases.
 
 
 
 
 
 
 
using these words

First Case of Highly Drug-Resistant TB Found in US
........................................................................................
 
for a Headline suggest that we have never had

Highly Drug-Resistant TB in the US

which is not true.   
 
 
 
................
 
 
  
 
Multi-drug resistant
India is a "Hot Zone"  for  MDR  ->  Multi-drug resistant TB.

And without proper care, new cases will become Highly resistant cases
as in...    XDR/XXDR TB
 

...Even if  "third-line drugs" are available for
treatment of XDR/XXDR TB today,
 
their improper use

can develop " XXXDR TB" !  
.....................................................
 

In 1952, Dubos and Dubos25 in their book

"The White Plague: Tuberculosis, Man andSociety"  wrote,

"However useful drugs, vaccines or

other options in cases, (they) cannot solve the problem

of TB.... It is through gross errors in organisation and

individual life that the problem (of TB) has reached

catastrophic levels that it has in Europe......and will

prevail in Asia....” Unfortunately, Rene and Dubois

proved very accurate in their estimate of the magnitude

of the problem of TB control and the reasons for it. DOT,

at present, therefore seems to be the only and Definite

Opportunity To Stop TB, a “ticking time bomb”.26
 
 
these could be considered highly resistant..
MDR TB
XDR TB
 
and this form of TB is defined as-
XXDR TB

 "extremely" drug resistant (XXDR) TB
has now been proposed for cases
resistant to all available first-and second-line drugs.6
...........................................................................................
 

.........................
 
 
Mary008
 
 
 
 
 
 
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Post Options Post Options   Thanks (0) Thanks(0)   Quote sjf53 Quote  Post ReplyReply Direct Link To This Post Posted: December 29 2009 at 8:46pm
Mary and Prep Girl, I found this also.......
 
Summarizing Below:  XXDR-TB is different......this form is resistant to all first and second line drugs.  This Mr. Juarez is a very lucky guy.
 
 
  • "Because XDR-TB is resistant to first- and second-line drugs, treatment options are seriously limited and so are the chances of cure. There is probably no difference between the speed of transmission of MDR-TB or XDR-TB and those of any other forms of TB
  • The first two cases of extremely drug-resistant TB (XXDR-TB) have been documented in Europe. This is a form of TB that is resistant to all first- and second-line drugs and so is virtually impossible to cure. "
  •  
    ------------------------------------------------------------------------------------------------
    WHO/ Europe Tuberculosis
     
    Multidrug-resistant and extensively drug-resistant tuberculosis
     

    The issue

    Tuberculosis (TB) can usually be treated with a course of four standard, or first-line, anti-TB drugs. If these are misused or mismanaged (that is, when drugs are taken in the wrong combination, are fewer than those prescribed, or are taken in insufficient doses or not at the proper time), multidrug-resistant TB (MDR-TB) can develop. MDR-TB is a form of disease resistant to the most important anti-TB drugs, i.e. isoniazid and rifampicin. MDR-TB takes longer to treat with second-line drugs, which are more expensive and have more side-effects. If these drugs are also misused or mismanaged, extensively drug-resistant TB (XDR-TB) can develop. Because XDR-TB is resistant to first- and second-line drugs, treatment options are seriously limited and so are the chances of cure.

    There is probably no difference between the speed of transmission of MDR-TB or XDR-TB and those of any other forms of TB. The spread of TB bacteria depends on factors such as the number and concentration of infectious people in any one place and the time of exposure, along with the presence of people with a higher risk of being infected, such as those with HIV.

    MDR-TB requires considerably more expensive and prolonged treatment and extensive patient supervision and support, than normal TB and has a higher fatality rate. Several countries with good TB control programmes have shown that up to 50–60% of people with MDR-TB can be cured. Much lower rates of success can be achieved in people with XDR-TB. Success also depends on the severity of the disease and whether the patient’s immune system is compromised.

    The facts

    • The 13 countries with the highest prevalence of MDR-TB in the world are all in the WHO European Region.
    • It is estimated that there are nearly 70 000 cases of MDR-TB in Europe, of which 95% are in eastern Europe. They represent an average of 15% of all cases in the subregion, with peaks in some countries that are the highest rates in the world.
    • Of the cases of MDR-TB, a significant proportion have XDR-TB, which is almost untreatable. 
    • Trends in western Europe are greatly affected by immigration but generally remain low without any major increases. This is largely also true of the central European countries. In eastern Europe, there are trends showing a gradual decrease in MDR-TB where there is good TB control in place, such as in the Baltic states. Where TB control remains poor, the numbers rise.
    • The first two cases of extremely drug-resistant TB (XXDR-TB) have been documented in Europe. This is a form of TB that is resistant to all first- and second-line drugs and so is virtually impossible to cure.
    • Drug-resistant TB often occurs in socially vulnerable groups such as the homeless, alcohol and substance abusers and travellers. MDR-TB among prison inmates, particularly in countries of the former Soviet Union, also constitutes a considerable problem. In addition, certain population subgroups such as prisoners and injecting drug users are at risk of HIV infection as well as MDR-TB.

    The policy considerations

    Countries can prevent drug-resistant TB by ensuring that the work of their national TB control programmes, and all practitioners working with people with TB, is carried out according to the International standards for tuberculosis care. These include, in particular:

    • providing proper diagnosis and treatment to all TB patients, including those with drug-resistant TB;
    • ensuring regular, timely supplies of all anti-TB drugs;
    • properly managing anti-TB drugs and providing support to patients to maximize adherence to prescribed regimens; and
    • caring for people with MDR-TB and XDR-TB in centres with proper ventilation, and minimizing contact with other patients (particularly those with HIV), especially in the early stages before treatment has had a chance to reduce the infectiousness.

    Meanwhile, countries should promote the broad dissemination of The patients’ charter for tuberculosis care, which lists the rights and responsibilities of TB patients and their families.

    ------------------------------------------------------------
     
     
    Frequently asked questions: XDR-TB   (However, there is No mention of XXDR-TB in this article .)

    1. What is XDR-TB?

    XDR-TB is the abbreviation for extensively drug-resistant tuberculosis (TB). One in three people in the world is infected with dormant TB germs (i.e. TB bacteria). Only when the bacteria become active do people become ill with TB. Bacteria become active as a result of anything that can reduce the person’s immunity, such as HIV, advancing age, or some medical conditions. TB can usually be treated with a course of four standard, or first-line, anti-TB drugs. If these drugs are misused or mismanaged, multidrug-resistant TB (MDR-TB) can develop. MDR-TB takes longer to treat with second-line drugs, which are more expensive and have more side-effects. XDR-TB can develop when these second-line drugs are also misused or mismanaged and therefore also become ineffective. Because XDR-TB is resistant to first- and second-line drugs, treatment options are seriously limited. It is therefore vital that TB control is managed properly.

    2. What is MDR-TB?

    MDR-TB, or multidrug-resistant TB, is a specific form of drug-resistant TB. It occurs when the TB bacteria are resistant to at least isoniazid and rifampicin, the two most powerful anti-TB drugs. XDR-TB is TB that is resistant to at least three of the six classes of available second-line drugs, in addition to MDR-TB.

    3. How do people become infected with XDR-TB?

    People who are ill with pulmonary TB (i.e. TB of the lungs, the site most commonly affected) are often infectious and can spread the disease by coughing, or sneezing, or simply talking, as this propels TB bacteria into the air. A person needs only to breathe in a small number of these germs to become infected (although only a small proportion of people will become infected with TB disease). Sometimes the bacteria are already drug resistant if they come from a person who already has drug-resistant TB. A second way of developing MDR-TB or XDR-TB is when a patient’s own TB develops resistance. This can occur when anti-TB drugs are misused or mismanaged. This happens when TB control programmes are poorly managed, for example when patients are not properly supported to complete their full course of treatment; when health-care providers prescribe the wrong treatment, or the wrong dose, or for too short a period of time; when the supply of drugs to the clinics dispensing drugs is erratic; or when the drugs are of poor quality.

    4. How easily is XDR-TB spread?

    There is probably no difference between the speed of transmission of XDR-TB and any other forms of TB. The spread of TB bacteria depends on factors such as the number and concentration of infectious people in any one place together with the presence of people with a higher risk of being infected (such as those with HIV/AIDS). The risk of becoming infected increases the longer the time that a previously uninfected person spends in the same room as the infectious case. The risk of spread increases where there is a high concentration of TB bacteria, such as can occur in closed environments like overcrowded houses, hospitals or prisons. The risk will be further increased if ventilation is poor.
    WHO Stop TB Department
    October 2006
    The risk of spread will be reduced and eventually eliminated if infectious patients receive proper treatment.

    5. Can XDR-TB be cured or treated?

    Yes, in some cases. Several countries with good TB control programmes have shown that cure is possible for up to 30% of affected people. But successful outcomes also depend greatly on the extent of the drug resistance, the severity of the disease and whether the patient’s immune system is compromised. It is vital that clinicians caring for TB patients are aware of the possibility of drug resistance and have access to laboratories that can provide early and accurate diagnosis so that effective treatment is provided as soon as possible. Effective treatment requires that all six classes of second-line drugs are available to clinicians who have special expertise in treating such cases.

    6. How common is XDR-TB?

    We do not know at the moment, but XDR-TB is rare. However, WHO estimates that there were almost half a million cases of MDR-TB worldwide in 2004, and MDR-TB usually has to occur before XDR-TB arises. We also know that findings from the only global study carried out so far showed that in some places perhaps as many as 19% of MDR-TB cases were in fact XDR-TB, but this is likely to be uncommon. Wherever second-line drugs to treat MDR-TB are being misused, the possibility of XDR-TB exists. Research is being carried out urgently to find out more.

    7. How can a person avoid becoming infected with XDR-TB?

    The majority of healthy people with normal immunity may never become ill with TB, unless they are heavily exposed to infectious cases who are not treated or who have been on treatment for less than about one week. Even then, 90% of people infected with TB bacteria never develop TB disease. This applies to XDR-TB as well as to “ordinary” TB. People with HIV infection, however, in close contact with a TB patient, are more likely to catch TB and fall ill. The TB patients whom they meet should be encouraged to follow good cough hygiene, for example, covering their mouths with a handkerchief when they cough, or even, in the early stages of treatment, using a surgical mask, especially in closed environments with poor ventilation. The risk of becoming infected with TB is very low outdoors in the open air. Overall, the chances of being infected with XDR-TB are even lower than with ordinary TB because cases of XDR-TB are still very rare.

    8. How can a person who already has ordinary TB, i.e. drug-sensitive TB, avoid getting XDR-TB?

    The most important thing is for a patient to continue taking all their treatment exactly as prescribed. No doses should be missed, but this is especially important if the course of treatment is meant to be taken every other day: so-called “intermittent treatment”. Above all, the treatment should be taken right through to the end. If a patient finds that side-effects are a problem, for example, the tablets make them feel sick, they should inform their clinician or nurse, because often there is a very simple solution. If they need to go away for any reason, patients should make sure they have enough tablets with them for the duration of the trip.

    9. Why have we never heard of XDR-TB before?

    For some years we have seen isolated cases of very highly resistant TB around the world that we would today call XDR-TB. All the drugs used against TB have been around for a long time. If they are not used carefully, then resistance can develop. It is only recently as we carry out regular surveys of drug resistance in more and more countries, and with improvements in laboratory capacity, that these
    WHO Stop TB Department
    October 2006
    cases are being reported in greater numbers. This has led to the problem being more closely examined and given a name.

    10. How do countries prevent XDR-TB?

    Countries can prevent XDR-TB by ensuring that the work of their national TB control programmes, and all practitioners working with people with TB, is carried out according to the International Standards for TB Care. These emphasize providing proper diagnosis and treatment to all TB patients, including those with drug-resistant TB; assuring regular, timely supplies of all anti-TB drugs; proper management of anti-TB drugs and providing support to patients to maximize adherence to prescribed regimens; caring for XDR-TB cases in a centre with proper ventilation, and minimizing contact with other patients, particularly those with HIV, especially in the early stages before treatment has had a chance to reduce the infectiousness.

    11. Can the TB vaccine, known as the BCG vaccine, prevent XDR-TB?

    The BCG vaccine prevents severe forms of TB in children, such as TB meningitis. It would be expected that BCG would have the same effect in preventing severe forms of TB in children, even if they were exposed to XDR-TB, but it may be less effective in preventing pulmonary TB in adults, the commonest and most infectious form of TB. The effect of BCG against XDR-TB would therefore likely be very limited. New vaccines are urgently needed, and WHO and members of the Stop TB Partnership are actively working on new vaccines.

    12. What is the link between XDR-TB and HIV/AIDS? Why in some places is XDR-TB so highly linked with or associated with HIV? Are most people with HIV-TB now infected with MDR-TB and XDR-TB?

    TB is one of the most common infections in people living with HIV/AIDS – because so many people are already infected with TB bacteria (see No. 1 above). In places where XDR-TB is most common, people living with HIV are at greater risk of becoming infected with XDR-TB, compared with people without HIV, because of their weakened immunity. If there are a lot of HIV-infected people in these places, then there will be a strong link between XDR-TB and HIV. Fortunately, in most of the places with high rates of HIV, XDR-TB is not widespread. For this reason, the majority of people with HIV who develop TB will have drug-susceptible or ordinary TB, and can be treated with standard first-line anti-TB drugs (see No. 1 above). For those with HIV infection, treatment with antiretroviral drugs will likely reduce the risk of becoming infected with XDR-TB, just as it does with ordinary TB.

    13. How do I know if I have TB or XDR-TB?

    Symptoms of XDR-TB are no different from ordinary or drug-susceptible TB: a cough with thick, cloudy mucus (or sputum), sometimes with blood, for more than 2 weeks; fever, chills, and night sweats; fatigue and muscle weakness; weight loss; and in some cases shortness of breath and chest pain. If you have these symptoms, it does not mean you have XDR-TB, but it does mean you must go and see a doctor for a check-up. If you are already a patient with TB and you are taking treatment , if after a few weeks of treatment at least some of these symptoms are not improving, you should inform your clinician or nurse.

    14. Is it safe to travel to places where XDR-TB has been identified?

    XDR-TB has been found in every region of the world, though it is still very rare. People who are at most risk, if they do come into contact with someone with XDR-TB, are those with reduced immunity to infectious diseases, such as those with HIV infection or other medical conditions that can weaken a
    WHO Stop TB Department
    October 2006
    person's immunity. It is also advised that such people should avoid high-risk areas where there are no infection control measures in place. Air travel itself carries only very minimal risks of infection with TB of any kind. Travellers with concerns about visiting countries with XDR-TB, or other health risks, should seek advice from their doctor, national authorities, or trusted travel web sites such as www.who.int/topics/travel.

    15. What should be done if a person has been in contact with a known or suspected case of XDR-TB?

    Anyone who has been in contact with someone known, or suspected of having, XDR-TB should consult their doctor or a local TB clinic and be screened to see if they have TB. This is most important if the person has any symptoms of TB (see No. 13 above). If they have a cough, they will be asked to provide a sample of sputum, which will be tested for evidence of TB. Several other tests will be performed in the clinic, including a skin test and a chest radiograph. If TB is found, treatment will be started with the drugs to which the person’s TB is most likely to respond. If there is any evidence of infection with TB bacteria but without TB disease, preventive treatment may be given (the choice of drugs will depend upon the known drug resistance pattern) or the person may simply be asked to attend regularly for a check up.
    16. What risks do health-care workers face with XDR-TB, particularly those who may be HIV-positive themselves?
    To protect health-care workers who may come into contact with infectious TB patients, appropriate and strict infection control measures must be implemented in health-care facilities at all times. Health-care workers are also encouraged to make sure they are aware of their HIV status so that they can avoid putting themselves at risk of exposure.

    17. How quickly can XDR-TB be diagnosed?

    This depends on the patient’s access to health-care services. If TB bacteria are found in the sputum, the diagnosis of TB can be made in a day or two, but this finding will not be able to distinguish between drug-susceptible and drug-resistant TB. To evaluate drug susceptibility, the bacteria need to be cultivated and tested in a suitable laboratory. Final diagnosis in this way for TB, and especially for XDR-TB, may take from 6 to 16 weeks. To reduce the time needed for diagnosis, new tools for rapid TB diagnosis are urgently needed.

    18. What is WHO doing to combat XDR-TB?

    First, WHO is ensuring that the health authorities responsible for TB control receive accurate information about XDR-TB. Second, WHO is emphasizing that good TB control prevents the emergence of drug resistance in the first place, and that the proper treatment of MDR-TB prevents the emergence of XDR-TB. This is completely in line with the new Stop TB Strategy launched in March 2006. Third, WHO is disseminating MDR-TB guidelines for national TB control programme managers published in May 2006 to help countries establish effective programmes to combat drug-resistant TB. Fourth, the WHO Stop TB and HIV departments are coordinating an international response through the XDR-TB Global Task Force, which will meet for the first time in October 2006. Major themes include rapid surveys to determine the geographical distribution of XDR-TB, surveillance, rapid diagnosis, treatment options, infection control and new drugs. Latest information and regular updates on XDR-TB, and related TB issues, will be published on the WHO Stop TB web site at www.who.int/tb and on the Stop TB Partnership web site at www.stoptb.org.
    WHO Stop TB Department
    October 2006
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    Post Options Post Options   Thanks (0) Thanks(0)   Quote Mary008 Quote  Post ReplyReply Direct Link To This Post Posted: December 29 2009 at 9:23pm
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    Did You Know?
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    Tuberculous prostatitis is sexually transmitted disease,
    so both partners should be treated simultaneously. Patients with
     
    prostatitis exactly need special examination on tuberculosis. The
    treatment of tuberculous prostatitis has to include laser therapy.

    source
    linkinghub.elsevier.com/retrieve/pii/S1158136008729724
     
     

    Tuberculosis continues to be a major health problem worldwide.
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    In 2008, the World Health Organization (WHO) estimated that

    one-third

    of the global population was infected with TB bacteria.

    8.8 million new cases of TB developed.

    1.6 million people died of this disease in 2005.

    Each person with untreated active TB will infect on average 10-15
    people each year.

    A new infection occurs every second.

     
     
    In 1993, the WHO declared tuberculosis a global emergency
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    TB Pandemic
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    All cases of TB are passed from person to person via droplets. When
    someone with TB infection coughs, sneezes, or talks, tiny droplets of
    saliva or mucus are expelled into the air, which can be inhaled by
    another person.
     
    Once infectious particles reach the alveoli (small saclike structures in
    the air spaces in the lungs), another cell, called the macrophage, engulfs
    the TB bacteria.

    Then the bacteria are transmitted to the lymphatic system and
    bloodstream and spread to other organs occurs.
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    The bacteria further multiply in organs that have high oxygen pressures,
    such as the
     
    upper lobes of the lungs,
     
    the kidneys,
     
    bone marrow, and
     
    meninges -- the membrane-like coverings of the brain and spinal cord.
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    When the bacteria cause clinically detectable disease, you have TB.

    People who have inhaled the TB bacteria, but in whom the disease is
    controlled, are referred to as infected.

    Their immune system has walled off the organism in an inflammatory

    focus known as a granuloma.

     
     
    They have no symptoms, frequently have a positive skin test for TB,
    yet cannot transmit the disease to others. This is referred to as latent
    tuberculosis infection or LTBI.
     
     
     
     
    LTBI
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    latent tuberculosis infection
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    efficient management of latent tuberculosis through screening and
    treatment is becoming increasingly important.

     
    In a review article available online March 1, 2005 in Rheumatology,

    Dr Joseph Keane (St James's Hospital and Trinity College Dublin, Ireland) discusses the many challenges this poses for clinicians [ 1 ].
    "The take-home message is screen everyone for latent tuberculosis

    infection (LTBI) and treat everyone, if possible." Keane told rheuma wire .
     
    Keane says that this should include a careful history looking for
    exposure to Mycobacterium tuberculosis, a tuberculin skin test (TST),
    and a chest radiograph. The presence of latent tuberculosis infection
    (LTBI) is considered likely if the
     TST ( tuberculin skin test ) is positive
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    and the chest x-ray is normal.
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    A positive TST means that you are infected with the TB bacillus.
     
     
    Once your doctor has evaluated you and made sure that you do not have any evidence of "
    active" TB disease (including a normal CXR) you are diagnosed with latent TB infection
     
    (LTBI).
     
    Persons with latent TB infection should take the medication to prevent them from
     
    developing active TB disease.
     
     
     
     
     
     
     
     
     
     
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    Mary008
     
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