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USA: BioLab Unsafety Check

Giuseppe

Emeritus
Critics worry about duct-taped germ lab
Published: June 22, 2008 at 3:28 PM
ATLANTA, June 22 (UPI) --

A new Centers for Disease Control and Prevention laboratory is using duct tape to seal a room where deadly bacteria experiments are performed, officials say.

The duct tape was placed around the edges of the containment door at the $214 million Atlanta lab a year ago, after the building's ventilation system malfunctioned and pulled potentially contaminated air out of the lab and into a "clean" hallway, The Atlanta Journal-Constitution reported Sunday.

At the time, nine CDC workers were tested for potential exposure to the Q fever bacteria being studied in the lab, CDC officials said this week.

The CDC Q fever lab's air containment systems have since worked properly, agency officials said.

The lab is safe and poses no risk to workers, yet the duct tape remains in place.

"It's an enhancement," said Patrick Stockton, CDC safety and occupational health manager. "We could take it off."

Critics, however, are not so sure.

Rep. John Dingell, D-Mich., chairman of the House Committee on Energy and Commerce, said the duct tape use calls into question the CDC's self-inspection policy.

"I highly doubt that the CDC would accept duct-taped doors on the privately owned bio labs it inspects," Dingell said Friday.
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http://www.upi.com/Top_News/2008/06/22/Critics_worry_about_duct-taped_germ_lab/UPI-27711214162890/
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Re: _|USA: BIOLAB UNSAFETY CHECK|_

Re: _|USA: BIOLAB UNSAFETY CHECK|_

House committee airs safety concerns about biodefense labs.
L. Schnirring
http://www.cidrap.umn.edu/cidrap/content/bt/bioprepnews/oct0407hearing.html

Oct 4, 2007 (CIDRAP News) ? A US House of Representatives committee today explored problems at the nation's biodefense labs, including a lack of coordinated federal oversight and even a lack of knowledge of how many high-containment labs exist.

These concerns have been highlighted recently by aggressive efforts from the Sunshine Project, a watchdog group that monitors biodefense research safety, and by other media reports.

During the hearing, witnesses from the Government Accountability Office (GAO) released a preliminary report on oversight of new biosafety level (BSL) 3 and BSL 4 laboratories in the United States that includes several steps officials should take to address the problem. The hearing was available on a live Webcast.

Rep Bart Stupak, D-Mich., who led the hearing, said today's session was the first of a series of committee hearings on the subject, which will include biosafety at labs outside of the United States and the proposed closure of the BSL 4 facility at Plum Island, N.Y. He said that he hoped for input from the Department of Homeland Security, but that it had declined a request to appear at today's hearing.

In his opening statement, Stupak said it has become clear that no single federal agency is responsible for ensuring the security of the nation's high-containment labs. "No one in federal government knows how many there are, what research is going on in them, or how safe and secure they are," he said.

The rising number of BSL 3 and BSL 4 labs in the United States is unprecedented, he said, pointing out that the National Institutes of Health (NIH) has allocated $1 billion toward the construction of new BSL 3 and BSL 4 labs in the past few years.

"We need to assess the need before writing the checks to build them," Stupak said.

Rep Joe Barton, R-Tex., reminded the committee that, despite apparent gaps in federal oversight, it should keep in mind that the biodefense work is critical to the nation's health and security.

GAO releases preliminary findings
Testifying on behalf of the GAO, Keith Rhodes, PhD, chief technologist for the office's Center for Technology and Engineering, said because a baseline of human error will always be present in laboratory settings, the level of safety risks will rise as the number of labs increases. Since the 9/11 terrorist attacks, the number of BSL 4 labs has risen from 5 to 15, he said. The GAO estimated in its report that there are nearly 1,400 BSL 3 labs in the United States.

Of 12 agencies the GAO surveyed, none is responsible for tracking the number of BSL 3 and BSL 4 labs in the United States. "Consequently, no agency is responsible for determining the risks associated with the proliferation of these labs," the GAO report states.

Rep Michael Burgess, R-Tex., countered that it might be necessary to undertake some greater risks to gain greater national security in the form of better vaccines and countermeasures against bioterrorist attacks. "But are we doing a good job of managing that risk?" he asked.

Rhodes said even some federal entities, particularly the Federal Bureau of Investigation (FBI) and intelligence agencies, have voiced concerns about the rapid expansion of biosafety labs. He pointed out that the FBI, for example, has said its workload has ballooned because it must do security checks on employees working at the high-containment labs, which takes time away from their other investigative duties.

Though the GAO's report was preliminary, Rhodes said GAO investigators have already identified six lessons, based on recent lab incidents in the United States, as well as at the Pirbright facility in the United Kingdom, which is thought to have triggered recent foot-and-mouth disease outbreaks. Health officials need to:

* identify and overcome barriers to reporting lab accidents
* improve the training of lab staff to ensure safety measures are followed
* inform medical providers about the agents that lab staff work with to ensure quick diagnosis and treatment
* clarify what constitutes an occupational exposure
* ensure that BSL 4 labs have safety and security measures that reflect the level of risk they present
* maintain the long-term physical integrity of high-containment labs

Some legislators asked why reports of laboratory accidents, such as the employee at Texas A&M University who was sickened by Brucella, came about through the efforts of the Sunshine Project, a nonprofit group based in Austin, Tex., rather than through Centers for Disease Control and Prevention (CDC) inspectors.

Sushil Sharma, PhD, the GAO's assistant director of applied research and methods, said the CDC inspectors depend on documentation and on people honestly reporting lab incidents.

Rhodes said the GAO would release a report detailing its recommendations in February, solicit comments from the public in March, and issue final recommendations in May.

CDC and NIH respond
Legislators had several questions about CDC's laboratory inspection protocols. Richard Besser, MD, who directs the CDC's office for terrorism preparedness and emergency response, said the labs are inspected every 3 years and more frequently if the facility changes the select agents it works with.

Besser said public concerns and questions about the labs were understandable and legitimate. "Just because there hasn't been a threat to the public, doesn't mean that an incident couldn't happen in the future," he said, adding that the CDC realizes it needs to improve inspections by interviewing more people at the labs, reviewing a broader range of documents, and releasing more outreach and training documents for labs.

The CDC has ordered an external review of its select agent program, and an audit of the CDC's select agent management practices by the Office of the Inspector General should be completed in 2008, Besser told the group.

Representing the National Institutes of Health (NIH) on the witness stand, Hugh Auchincloss, MD, deputy director of National Institute of Allergy and Infectious Diseases (NIAID), said the labs it funds are expected to follow good laboratory practices described in the Biosafety in Microbiological and Biomedical Laboratories manual , and that the agency monitors the work of local institutional biosafety committees (IBCs) that oversee recombinant DNA work in the labs, though he said there is no federal body that sets standards for IBCs.

He said the NIH is looking at several ways to strengthen its oversight of the labs and has set up an intergovernmental task force to analyze he current situation and develop recommendations for improving oversight.

A need for clarity and no-fault reporting
Texas A&M interim president Ed Davis, PhD, appeared on the stand to field questions about the lab accidents involving Brucella and Coxiella burnetti that were revealed in April by the Sunshine Project.

Davis said the university failed to report the Brucella incident in a timely manner and is taking the lab safety issues very seriously. However, he said episodes have exposed complex lab management issues. "There's a gap between understanding at the research compliance office and labs," he said, adding that clearer federal guidance is needed on what constitutes an occupational pathogen exposure.

Rep Burgess, along with Davis and other witnesses, said a no-fault reporting system, whereby laboratory employees and managers aren't penalized for reporting lab incidents, could improve lab safety.

"This would create a culture of not tolerating safety lapses and would allow employees, in a collaborative fashion, to learn from mistakes," Burgess said, pointing out that no-fault safety incident reporting has been successful in the federal aviation and aeronautics work environments.

Sunshine Project makes its case
Edward Hammond, director of the Sunshine Project, said the CDC has denied several of the group's freedom-of-information requests relating to lab safety issues. The Sunshine Project's goal, he said, is more government transparency, which he says would provide important benefits.

"There's a positive correlation between transparency and compliance and reporting," Hammond said, adding that the group's revelations about the lab incidents at Texas A&M have prompted a spike in reports from other labs to the CDC.

Legislators asked several of the witnesses if the federal government had ever assessed how many biosecurity labs were needed to conduct work toward its bioterror countermeasure development goals, but it was unclear if numbers were ever projected.

Hammond contended that the necessary government projects could be done?and the nation would be safer?with one fifth of the current biosafety lab capacity.

"Our system can't absorb all of the labs coming online," he said.

See also: Oct '07 GAO preliminary report on high containment biosafety laboratories
http://www.gao.gov/new.items/d08108t.pdf
 
Re: _|USA: BIOLAB UNSAFETY CHECK|_

Re: _|USA: BIOLAB UNSAFETY CHECK|_

The lab is safe and poses no risk to workers, yet the duct tape remains in place.
"It's an enhancement," said Patrick Stockton, CDC safety and occupational health manager. "We could take it off."

Actually, if it was the old-time duct tape, it might very well have done a good job of sealing. That stuff used to stick just about anything together and I would think it is not porous. Most of the duct tape today is crap in comparison; trusting that to seal is iffy at best.
 
CDC lab: "experiments on bioterror bacteria in a room with a containment door sealed with duct tape"

CDC lab: "experiments on bioterror bacteria in a room with a containment door sealed with duct tape"

Comments from "EM" web site:

http://scienceblogs.com/effectmeasure/2008/06/dont_worry_the_cdc_labs_are_pe.php

Don't worry. The CDC labs are perfectly safe.

Category: BioterrorismCDC
Posted on: June 24, 2008 7:24 AM, by revere
<!--proximic_content_on-->The Atlanta Journal Constitution (AJC) newspaper is the Centers for Disease Control (CDC) worst nightmare because it continually runs in depth stories about why CDC is the worst nightmare for scientists concerned with laboratory safety. CDC is the agency supposedly ensuring the public's safety from laboratories researching contagious disease causing organisms. They have their own research labs which they need for identification of unknown organisms or scientific work on agents of special importance. In the Bush years, this has often meant CDC has worked on biowarfare agents. One of those agents is Coxiella burnettii, the cause of Q fever. Q fever is a possible biowarfare agent because it causes a debilitating acute disease and is relatively easy to disperse through the air. To our knowledge it has never been used militarily but work on it goes back to before World War II.




In 2005 CDC completed construction of a new Emerging Infectious Diseases Laboratory ("Building 18") that has specialized high containment facilities for research on agents like Q fever. It is touted as one of the safest laboratories in the world. Let's hope that's not true, because in its short operational lifetime it has suffered a series of embarrassing and potentially dangerous mishaps, as the AJC has reported. The latest installment involves duct taping the door seals of a Q fever lab after it was discovered that air was flowing out of the lab into a corridor rather than into the lab as it was designed:
At the Centers for Disease Control and Prevention's new $214 million infectious disease laboratory in Atlanta, scientists are conducting experiments on bioterror bacteria in a room with a containment door sealed with duct tape. The tape was applied around the edges of the door a year ago after the building's ventilation system malfunctioned and pulled potentially contaminated air out of the lab and into a "clean" hallway.​
Nine CDC workers were tested in May 2007 for potential exposure to the Q fever bacteria being studied in the lab, CDC officials said this week in response to questions from The Atlanta Journal-Constitution.​
The air-flow incident occurred very early in the morning, before the workday began. The blood tests were done out of an "abundance of caution," CDC spokesman Tom Skinner said, and they showed that none of the workers who arrived after the incident were infected. (Alison Young, AJC)​

The incident happened over a year ago but the duct tape is still there. Not to worry:
"It's an enhancement," said Patrick Stockton, CDC safety and occupational health manager, as he and four other agency officials took a reporter to see the door Wednesday. "We could take it off."​
"Enhancement" seems to be the new Bush administration all purpose word for explaining a screw up or misdeed, as in "enhanced interrogation" as a euphemism for torture. The tape is really unnecessary, CDC says, because the lab meets all applicable regulations. They don't even need the duct tape. Unnecessary. Superfluous.




So does that mean this is a waste of money?
On Monday, designs were completed for a new self-sealing door to replace the one currently sealed with duct tape, said Ken Bowen, director of the CDC's Facilities Maintenance and Engineering Office. Even though it's not required, he said, the new door is being added "as a precaution." The construction to install the new door will begin sometime between November and next April, possibly sooner, depending on when there is a good stopping point in the experiments being conducted by the Q fever scientists.​

Is it an enhancement or a precaution? Precautions are what they are supposed to be taking in the first place. The lab is perfectly safe, CDC says. They just want to make it even more perfectly safe? Perfectly safe, like this?
A year ago, The Atlanta Journal-Constitution requested under the Freedom of Information Act that the CDC release records about safety issues at the lab building, including last June's power outage. So far the agency has not released any records. On Dec. 18, the building was evacuated after its new medical waste incinerator was started for a test, then vented smoke into the high-containment lab area, according to internal CDC memos recently obtained by the AJC. Excessive heat caused the failure of the incinerator's bypass stack, which tore away from its anchor bolts and fire caulk, the records show.​
I've only pulled a few small sections from a long and detailed AJC investigation. Go and read it, unless you scare easily. Alison Young and her colleagues at the AJC continue to do a superb job watching the watchers. The CDC's worst nightmare is making the CDC the worst nightmare for the rest of us.
 
Re: _|USA: BIOLAB UNSAFETY CHECK|_

Re: _|USA: BIOLAB UNSAFETY CHECK|_

Actually, if it was the old-time duct tape, it might very well have done a good job of sealing. That stuff used to stick just about anything together and I would think it is not porous. Most of the duct tape today is crap in comparison; trusting that to seal is iffy at best.
Yes, but using a "chewing gum sticking" technic in an:
"new $214 million infectious disease laboratory in Atlanta"
...
 
_|Leak from proposed ag lab could cost billions|_

_|Leak from proposed ag lab could cost billions|_

Leak from proposed ag lab could cost billions
Robert Roos News Editor

Jul 3, 2008 (CIDRAP News) ?

A leak of foot-and-mouth disease (FMD) virus at any of six proposed sites for a large federal laboratory to study foreign animal diseases could cost billions of dollars, according to a recent report by the US Department of Homeland Security (DHS).

Such a leak would be extremely unlikely, but, if it occurred, the estimated economic damage could range from $2.8 billion to $4.2 billion, depending on where the proposed lab is located, says the DHS report.

The economic impact would be smallest at the site of the US Department of Agriculture's existing Plum Island Animal Disease Center, located on a small island off Long Island in New York.

Estimates are higher for potential sites located closer to livestock industry operations, including sites in Kansas and Texas.

In-depth environmental impact statement
DHS released a lengthy environmental impact statement on the proposed National Bio and Agro-Defense Facility (NBAF) on Jun 20. The new lab would replace the Plum Island lab and would host research on the most dangerous foreign animal and zoonotic diseases, those requiring biosafety level (BSL) 3 and 4 containment.

The report says diseases likely to be studied at the lab include African swine fever, classical swine fever, contagious bovine pleuropneumonia, FMD, Japanese encephalitis, and Rift Valley fever?all requiring BSL-3 containment?and Hendra and Nipah viruses, which require BSL-4.

The Plum Island lab is the only US facility that can handle the FMD virus, but it is too small for current research needs and has an outdated structure that is unsuitable for BSL-4 research, according to DHS.

Currently the nation has no lab capable of doing BSL-4 studies on livestock.

"The proposed NBAF would enable us to meet the challenges posed by the intentional or unintentional introduction of a foreign animal or zoonotic disease that could threaten the US livestock industry, food supply, and public health," said Jay Cohen, DHS under secretary for science and technology, in a news release about the report.

Besides Plum Island, proposed sites for the facility are Manhattan, Kan.; San Antonio, Tex.; Flora (Madison County), Miss.; Athens, Ga.; and Butner (Granville County), N.C. Construction could start in early 2010 and would take about 4 years, according to DHS. However, a decision to build has not yet been made.

Risk for foreign bans on US meat
FMD is a highly contagious livestock disease that devastated the British cattle industry in 2001. DHS estimates the economic hit from an FMD virus leak at the proposed sites as follows: Plum Island, $2.8 billion; Georgia, $3.35 billion; Mississippi, $3.4 billion; North Carolina, $3.5 billion; Texas, $4.1 billion; and Kansas, $4.2 billion. For each site except Plum Island, the estimated loss from foreign bans on US meat amounts to $3.1 billion; for Plum Island the corresponding estimate is $2.7 billion.

Estimated losses from disruption of the livestock industry vary by site and are highest for Kansas, at just over $1 billion. "It is the size of the livestock industry in the affected state that serves as the main discriminator among the candidate sites in terms of economic losses," the report states.

The report also looks at the possible consequences of a leak of Rift Valley fever virus and Nipah virus from the various sites.

The document says DHS examined the potential for accidental or intentional release of a pathogen from the lab and the potential that the pathogen would spread from each site. "The evaluation considered the accident scenarios with and without measures to prevent and contain a release," it says. "The results indicate that for all sites the risk was none to low for all accident scenarios except an over-pressure fire, where an explosion would occur due to the buildup of a large amount of gas or flammable chemical in an enclosed area. The risk was moderate for all sites."

For all sites except Plum Island, the overall "risk rank" related to such a fire was classified as moderate "because of the potential easy spread of a disease through livestock or wildlife," the report states. The risk for Plum Island was "low or none due to the low likelihood of any disease getting off of the island."

Final decision months away
A Jun 21 Washington Post report, however, said the selection of Plum Island as the site is considered unlikely because the government "spent considerable time and money scouting new locations and because of financial concerns about operating from a location accessible only by ferry or helicopter."

DHS is taking comments on the report for 60 days and plans to hold a public meeting near each of the proposed sites later this summer, according to the news release. A final environmental impact statement is expected in late fall, and a decision on whether and where to build the NBAF is expected a month or more after the final report is issued.

See also:
Jun 20 DHS news release
http://www.dhs.gov/xnews/releases/pr_1213985419513.shtm
DHS general description of the NBAF
http://www.dhs.gov/xres/labs/editorial_0762.shtm
Table of contents page for the NBAF report
http://www.dhs.gov/xres/labs/gc_1187734676776.shtm
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http://www.cidrap.umn.edu/cidrap/content/bt/bioprep/news/jul0308lab-jw.html
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Re: _|USA: BIOLAB UNSAFETY CHECK|_

Re: _|USA: BIOLAB UNSAFETY CHECK|_

Airflow problems plague CDC bioterror lab

By Alison Young, USA TODAY
Updated 1d 16h ago

A $214 million bioterror germ lab at the Centers for Disease Control and Prevention in Atlanta has had repeated problems with airflow systems designed to help prevent the release of infectious agents, government documents and internal e-mails show.

While the agency says no one has been infected, a biosafety expert says the problems appear to be major violations of laboratory operating standards.

The area of the building with problems involves Biosafety Level 3 labs that can be used for experiments involving anthrax, dangerous strains of influenza, the SARS coronavirus, monkeypox and other microbes that have the potential to be used as bioweapons.

In February, air from inside a potentially contaminated lab briefly blew outward into a "clean" corridor where a group of visitors weren't wearing any protective gear which raised concern about exposure risks, according to e-mails reporting and discussing what happened. Research animals in the lab had not yet been infected at the time of the incident, the records say.

CDC engineers have raised written concerns about the air containment systems since at least 2010. At that time, scientists working with poxviruses, such as monkeypox, expressed concerns about airflow and said they "don't want to go into that facility because they don't feel comfortable with the way it is currently designed," according to minutes from a February 2010 meeting to discuss reversing the way air flowed through the labs and animal-holding areas.
...
In a statement, the CDC said there have been no releases of germs and no one has been injured. Experiments in the building's high-containment labs are "done in an environment with highly skilled staff, technical equipment, and safety systems that unfortunately, at times, experience challenges. Fortunately, this unique facility has multiple systems in place that provide appropriate redundancy, so when there is an incident, the public's safety, as well as worker safety, is not compromised." The agency said it always takes "appropriate steps" to address incidents when they occur, but provided no details.
...
The same lab building, which opened in 2005 and was touted by the agency as the world's most advanced laboratory, made news in 2007 when backup generators didn't work to keep airflow systems working during a power outage, then again in 2008 for a high-containment lab door that was being sealed with duct tape. The duct tape was applied after a 2007 incident where a ventilation system malfunctioned and pulled potentially contaminated air out of the lab and into a "clean" hallway; nine CDC workers were tested for potential exposure to Q fever bacteria. None were infected.

Full text:
http://www.usatoday.com/news/nation/story/2012-06-13/cdc-bioterror-lab/55557704/1
 
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