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Prepared Statement
Before the Senate
Committee on Governmental Affairs
Subcommittee on International Security, Proliferation and Federal
Services
17 October 2001
Amy E. Smithson, Ph.D.
Director, Chemical and Biological Weapons Nonproliferation Project
Henry L. Stimson Center
With the interplay of politics, institutional interests, and
differences of opinion, complex public policy decisions can be
difficult enough to make in times of peace and prosperity.
In times of turmoil and war, such decisions can be even
more challenging. In
recent weeks, US citizens have been on edge about the prospects of
chemical and biological terrorist attacks.
The occurrence of isolated anthrax incidents in Florida,
New York City, and now the nation’s capital has made it
difficult for the country to regain a sense of normalcy in the
aftermath of the September 11th tragedies.
Americans are looking to their leaders to make sage
decisions that will enhance the ability of local, state, and
federal assets to promptly and effectively respond to a chemical
calamity and to detect a disease outbreak in time to take
life-saving intervention. Mr.
Chairman, I know that this responsibility weighs heavily on the
minds of this committee’s members, as well as the broader Senate
membership, so I appreciate the invitation to testify on matters
that in light of recent events carry a sense of greater urgency
and importance.
No matter where one comes out in the debate about whether
terrorists can pull off a biological attack that causes massive
casualties, the debate itself is moot.
One need only consult public health journals to understand
that it is only a matter of time before a strain of influenza as
virulent as the one that swept this country in 1918 naturally
resurfaces. Further
confirmation of a looming public health crisis can be secured
through reports from the World Health Organization and the
Institutes of Medicine, which describe how a growing list of
common diseases (e.g., pneumonia, tuberculosis) are becoming
resistant to antibiotics. These
public health watchdogs are also justifiably worried about the
array of new diseases emerging as mankind ventures into previously
uninhabited areas. Even
with everything in the modern medical arsenal, public health
authorities will find it difficult to handle with disease
outbreaks in the future. Global
travel will facilitate the spread of communicable diseases through
huge population concentrations and will in turn hinder use of the
traditional means of containing a contagious disease outbreak,
namely quarantine.
As for the prospects of a large-scale chemical disaster, one needs
to keep in mind what America’s first responders and health care
workers have to deal with on a routine basis. According to the US Chemical Health and Safety Investigation Board,
between 1987 and 1996, a hazardous chemical incident of some
severity took place in 95 percent of US counties.
An average of 60,500 chemical incidents occurred per year
at fixed facilities and in transit, injuring or killing roughly
2,550 annually. This
country is peppered with roughly 850,000 facilities that work with
hazardous or extremely hazardous chemical substances.
While the chemical industry takes site security seriously
and emergency responders in many US cities began long ago take
extra security precautions with these sites, my main chemical
terrorism concern relates to the possible sabotage of these
industrial facilities.
Thus, there is a need for this nation’s front line
responders¾from firefighters, police, and paramedics to doctors, nurses, laboratory
workers, and public health officials¾to
be prepared to cope with chemical and biological disasters.
This need will remain constant for the indefinite future,
regardless of whether or not terrorists turn to chemical and
biological weapons to inflict mass casualties.
A Roadmap to Better Coordinated, More Cost-Effective Programs
The appointment of Governor Tom Ridge as Director of the new
Office of Homeland Security would seem to be a constructive step
that could put improved coordination and streamlining of the
federal response bureaucracy on a fast track. That may not be the
case, however, if he lacks sufficiently strong budgetary
authority. An initial review of section 3(k) of the Executive
Order establishing the Office of Homeland Security and the
Homeland Security Council does not appear to vest such power in
this new office. To
aid Governor Ridge in his efforts, Congress should grant him
czar-like budgetary authority.
Alone, Governor Ridge will have difficulty taming the
federal bureaucracy.
The other essential element of streamlining and coordinating
government programs lies here, in Congress.
Anyone that attempts to tally the number of congressional
committees with terrorism prevention and preparedness oversight
very quickly runs out of fingers and toes.
So long as that is the case, individual federal agencies
may continue to exploit the situation to the advantage of their
own institutional interests and the detriment of coordinated,
cost-effective programming. A
consolidation of congressional oversight committees is sorely
needed.
Also in order is a reassessment of the true value of politically
popular placebo programs like the National Guard’s Civil Support
Teams. I urge you to
consider the evaluation of these teams offered by the public
safety and health officials, including members of the National
Guard, that I interviewed in 33 cities in 25 states.
Their views are presented fully in Ataxia: The Chemical and Biological Terrorism Threat and the US
Response, a report co-authored with Leslie-Anne Levy and
released last October and available at:
www.stimson.org/cwc.
Briefly, the message from the front line about these National
Guard teams is unified and clear: They have minuscule, if not
negative, utility. In
the mid-May 2000 TOPOFF exercise, the Civil Support Team in Denver
insisted that it had identified the mystery biological agent with
SMART tickets, which have such high false positive and false
negative rates that numerous cities have refused to buy them. The
team in Portsmouth lacked the technical expertise to understand
the minimal hazard posed by mustard on a chilly, 49-degree day.
To veterans of epidemiological investigations and hazardous
material operations, the absurdity of these two anecdotes is
readily apparent. The
deputy director of one city’s Office of Emergency Management
said, “The good thing about those teams is that it takes them as
long as it does to get here.”
To further illustrate the problem, called to duty after the planes
struck the World Trade Towers, the New York Civil Support Team
arrived at the scene roughly 12 hours later and proceeded to
conduct environmental monitoring that was redundant of efforts
undertaken hours earlier by New York City agencies as well as the
US Environmental Protection Agency. The dynamics of a chemical disaster response are such that
these teams cannot arrive in time to make a life-saving
difference. As for
their applicability to a biological disaster, their four-person
medical component is a drop in the bucket of what would be needed
in a major disease outbreak.
To those accustomed to overseeing billion dollar budgets, this
National Guard program might not seem so ill-advised. Please
consider how this program’s budget could be put to uses that
would make a real preparedness difference on the front lines, for
example, to begin fixing the glaring lack of decontamination
capacity in US hospitals that results in recurrent hospital
closures even after small hazmat incidents.
In most of the cities that I surveyed for Ataxia, the central game plan for hospitals in the event of a major
chemical catastrophe was to “lockdown,” meaning to shut their
doors to incoming patients. For the cost of standing up one
National Guard Civil Support Team, 2,333 hospitals or fire
stations could be outfitted with decontamination capabilities.
With the total 1999 budget for this program, 49,800 local
rescue and health facilities could have been armed for
decontamination. Civil
Support Team funds, in other words, could be used to make a
genuine preparedness difference were they applied to overcoming
the decontamination bottleneck at US hospitals.
Proposals are now circulating for each state to have its
own Civil Support Team. Common
sense calls for the existing teams to be disbanded, their
equipment to be disbursed within the respective states to
front-line rescue units and laboratories, where any leftover
training monies would also be placed.
The National Guard’s Civil Support Teams aside, both Congress
and Governor Ridge have their work cut out for them.
A series of expert studies and panels, as well as
Congress’ own General Accounting Office, have labeled the
federal preparedness programs a fractured mess and urged a
national strategy to guide programs better.
For the past several years, over 40 federal agencies have
been competing for the money and missions associated with
combating terrorism. The
section of chapter 7 in Ataxia
entitled “Preparedness Versus Pork” discusses in more detail
how lack of coordination and redundant programs handicap the
federal effort. This competition has been confusing for local and state
officials, who have difficulty figuring which agency is in charge,
not to mention how to decipher the varying sets of priorities and
guidelines that accompany the different federal grant programs.
In addition, this sparring among federal agencies has contributed
to a drift in the Domestic Preparedness Program away from the
initial objectives of its trio of Senate designers, Senators
Richard Lugar (R-Indiana), Sam Nunn (D-Georgia, ret.), and Pete
Domenici (R-New Mexico). The
initial objective was to enhance the readiness of local public
safety and public health officials to grapple with an
unconventional terrorism attack.
Instead, according to Office of Management and Budget
figures, this year federal government is spending $8.7 billion to
combat terrorism but only $311 million of that amount is making it
to the local level in the form of training, planning, and
equipment grants for unconventional attacks.
More specifically in the area of biodisaster readiness, in
2000, an estimated $206 million from the weapons of mass
destruction budget line items were put toward hospital
preparations, the public health infrastructure, and biomedical
research combined.
Those interested in a detailed breakdown of that spending
can consult table 7.2 in Ataxia.
If you take no other message away from my testimony today, let it
be an understanding that the key to domestic preparedness lies not
in bigger federal bureaucracy, but in getting taxpayers’ dollars
channeled to readiness at the local level, where training and
enhanced response capacities will better arm public safety and
medical personnel to contend with disease outbreaks and chemical
incidents, whether natural, accidental, or intentional.
Federal spending priorities sorely need to be redressed,
and unless reforms are made and mindsets change on both ends of
Pennsylvania Avenue, a few years from now a great deal of money
will have been spent with marginal impact on front-line
preparedness.
The Route to Enhanced Readiness Nationwide
While the signs of a chemical disaster would materialize very
quickly, perhaps the first challenge facing the health care
community in a biological disaster would be figuring out that
something is amiss. Many
diseases present with flu-like symptoms, and the physicians and
nurses who could readily recognize the finer distinctions between
influenza and more exotic diseases are few in number indeed.
As medical science eradicated a series of diseases, medical
and nursing schools concentrated training on the ailments that
health care givers are more likely to see.
Exotic disease recognition problems are not limited to the medical
community. In the
nation’s laboratories, microbiologists and other technicians who
analyze the samples (e.g., blood, throat cultures) that physicians
order to help them figure out what ails their patients are much
more likely to have encountered exotic diseases in textbook
photographs rather than under their microscopes.
Thanks to the laboratory enhancement program initiated by
the Centers for Disease Control and Prevention (CDC), the ability
to identify out-of-the-ordinary diseases more rapidly is on the
rise in several dozen laboratories across the country.
However, such is not the case in the 158,000 laboratories
that serve hospitals, private physicians, and health maintenance
organizations and form the backbone of disease detection in this
nation. Enhanced training certainly contributed to the early
diagnosis of the first anthrax case in Florida.
A CDC official has noted that the Florida Department of
Health laboratory in Jacksonville where the blood sample taken
from Bob Stevens was identified as anthrax had recently completed
a special course in the identification of biowarfare diseases.
Still, an illustration of the need for better education of health
care professionals about bioterrorism matters can be found in the
far too many recent reports of physicians prescribing antibiotics
for patients worried about a possible bioterrorist attack.
Of all people, physicians should understand how such
prescriptions could backfire, not just in adverse reactions to the
antibiotics if citizens begin self-medicating their children and
themselves when they come down with the sniffles, but in the
lessened ability of those very drugs to help their patients in a
time of true medical need. Moreover,
over-prescription of antibiotics contributes to the rise in the
number of antibiotic-resistant diseases.
To date, Domestic Preparedness Program training, now administered
by the Justice Department, has managed to draw some health care
personnel, mostly emergency department physicians and nurses, into
the classroom in the cities where training is being provided.
To enhance the disease detection and treatment skills of
the medical community nationwide over the long term, however, a
different strategy is required.
If a long-term difference is to be made, then more
comprehensive instruction in medical, nursing, microbiology, and
other pertinent schools is required.
Knowledge of exotic diseases should be necessary to obtain
diplomas, and the topic should become a mainstay of the refresher
courses offered to maintain professional credentials.
Those involved in setting the curricula for these schools
should waste no time in adjusting their course offerings,
requirements, and other professional activities accordingly.
In the near term, compressed training should be made
available to all practicing US physicians via presentations during
grand rounds or via satellite hookup.
Both forms of training, by the way, already exist, so it is
just a matter of making it more widely available.
Moreover, in conjunction with the CDC and the Association
of Public Health Laboratories, the American Society of
Microbiology is developing protocols to assist clinical
microbiology laboratories in identifying bioterrorist agents. Although the protocols have yet to be published, volume
number 33 in the Cumulative
Techniques and Procedures in Clinical Microbiology series
addresses bioterrorism issues and is available from the American
Society of Microbiology.
Similarly, for chemical and biological disaster readiness,
preparedness standards need to be established for the various
response disciplines and training needs to be institutionalized in
fire and police academies, as well as in paramedic schools across
the country. Roughly
six years into the domestic preparedness effort, the time has
passed for Washington to turn training over to the appropriate
professional and local entities that will take preparedness
forward more systematically and cost effectively.
The hand-off should be concentrated in these organizations
(e.g., the National Fire Protection Association, the Accreditation
Council for Graduate Medical Education) and curtailed elsewhere,
so that various branches of the federal government, not to mention
enterprising contractors and universities, stop churning out
redundant training programs at taxpayers’ expense.
Already, over 90 such training courses exist. Without such reform, ineffective spending will continue at
both the federal and local levels and training lacking in
standards will be implemented unevenly, in pockets.
Specification of standards and institutionalization of
training clearly make more sense than that.
Establishing an Early Warning Capability for Disease Outbreak
Detection
With modern data collection and analysis capabilities, one need
not rely solely on the ability of laboratories and medical
personnel to pick up the telltale early signs of a disease
outbreak. In a few
areas of the United States, public health and emergency management
officials are teaming to test ways to get a head start on
detection. The
concept focuses on early signs of syndromes (e.g., flu-like
illness, fever and skin rash) that might indicate the presence of
diseases of concern. They
are compiling historical databases to supply a baseline of normal
health patterns at various times of the year, against which
contemporary developments can be measured.
Since people feeling ill tend to take over-the-counter
medications, consult their physicians, or request emergency
medical care, some areas are beginning to track the status of
health in their communities via select Emergency Medical Services
call types (e.g., respiratory distress, adult asthma); sales of
certain medications (e.g., over-the-counter flu remedies); reports
from physicians, sentinel hospitals, and coroners about select
disease symptoms or unexplained deaths; or some combination of
these markers. This
tracking allows abnormal activity levels can be detected.
For instance, should EMS calls rise above the expected rate
in the fall season, public health officials and emergency managers
would get the earliest possible indication that something was
amiss, which would enable them to cue medical personnel and
laboratories to search more diligently for what might be causing a
possible disease outbreak. This
concept of syndrome surveillance will be key to allowing public
health officials to get the jump on prophylaxis and other control
measures. For more on
this approach, see the groundbreaking work of New York City’s
Department of Public Health and Office of Emergency Management,
which is summarized in box 6.7 of Ataxia.
What is now called for is a more systematic approach to
institutionalizing syndrome surveillance across the nation.
A model should be refined and then made available
nationally, along with funds to allow metropolitan areas to
conduct the necessary historical analysis and establish the
computer database, communications, and other components needed to
put syndrome surveillance in place.
Again, the data and the computing capabilities are
available; it is just a matter of harnessing them for the purposes
of early disease outbreak recognition.
In their own ways, the Kennedy-Frist and the Edwards-Hagel
bills address these matters.
Coordination of congressional action is necessary so that
the most readiness can be gained for taxpayers’ dollars.
The Need for Regional Hospital Planning
The next challenge facing a metropolitan area in the midst of a
chemical disaster or a major disease outbreak would be contending
with the flood of humanity that would seek health care services.
If one examines what transpired in Tokyo after Aum
Shinrikyo’s 20 March 1995 morning release of sarin in the
subway, demand for patient care would peaked rapidly and then
began subsiding by mid-afternoon on the day of the attack.
The best medical care in the world can be found in this
country, but in general US hospitals are at present poorly
prepared to handle either a chemical disaster or an epidemic.
With regard to a pandemic, those familiar with what is
happening on the front lines of health care in America know that
US hospitals already have difficulty handling the patient loads
that accompany a regular influenza season.
Ambulances wait for hours in emergency department bays,
unable to unload patients until bed space is available.
The press of genuinely ill and worried citizens clamoring
for medical attention in the midst of a plague or smallpox
epidemic would so far outstrip a normal flu season that local
health care systems could collapse.
To prevent hospitals from being quickly overwhelmed, it will be
critical for regional health care facilities to have a pre-agreed
plan that divides responsibilities and locks in arrangements to
bring emergency supplies in the interim until federal assistance
can arrive. In the
era of managed care, hospitals compete with each other for
business and rely on just-in-time supply of inventory, keeping an
average of two or three days supplies on hand.
Since community-wide hospital planning has fallen by the
wayside, precious time could be wasted if hospitals lack prior
agreement as to which facilities would convert to care of
infectious disease cases¾particularly
important if a communicable disease is involved¾and
which ones would attend to the other medical emergencies that
would persist throughout an epidemic.
Business competitors, in other words, must convert within
hours to work as a team.
Regionally, hospitals must plan to handle an overflow of patients
and provide prophylaxis to thousands upon thousands of people.
Whether the approach involves auxiliary facilities near major
hospitals, the conversion of civic or sporting arenas to impromptu
hospitals, or the use of fire stations or other neighborhood
facilities to conduct patient screening and prophylaxis, such a
plan needs to be put in place.
Other factors that regional hospital planning must address
are how to tap into local reserves of medical personnel (e.g.,
nursing students, retired physicians), how to break down and
distribute securely the national pharmaceutical stockpile, and how
to enable timely delivery of emergency supplies of everything from
intravenous fluids to sheets, tongue depressors, and food.
Obviously, regional hospital plans that address how to
overcome problems of decontamination, training, security, critical
medical supplies (e.g., respirators, antidotes), and
burden-sharing would also be of great utility should a chemical
disaster bring a surge of patients to health care facilities.
The Role of the Federal Government
Washington’s willingness to fund preparedness efforts at the
local level across the country will be critical to chemical or
biological disaster readiness.
With a few exceptions, the federal government’s role in
responding to a chemical or biological terrorism attack would fall
under the general heading of mid- to long-term disaster recovery
assistance. FEMA’s
capabilities have risen steadily over the last decade and little,
if anything, would need to be added to its existing capabilities
and regular Stafford Act assistance activities.
Local officials noted that they would probably call upon
federal assets to help decontaminate a site after a chemical
disaster, but that does not mean that additional federal capacity
needs to be built. Prior
to the 1995 Aum Shinrikyo attack, as chapter 4 of Ataxia
describes, numerous Pentagon and Environmental Protection Agency
teams that could be brought in to assist a stricken community
already existed. While
little, if any, additional federal capacity needs to be
constructed to aid local and state authorities in a chemical
disaster, appreciable work remains the area of biological disaster
readiness at the federal level. Aside from continuing to infuse
funds into the improvement of the public health system at the
local and state levels, the federal government needs to sort out
once and for all who is in charge and attend to its important
roles in the development and production of essential medicines and
in the provision of medical manpower during an emergency.
Calling the Shots in a Public Health Crisis
How many FBI special agents or Federal Emergency Management Agency
(FEMA) officials know off the top of their heads the appropriate
adult dosages of ciprofloxacin for prophylaxis in the event of a
terrorist release of anthrax?
Darned few, if any. No,
the FBI excels at catching criminals and FEMA at providing mid-
and long-term recovery support to communities stricken with all
manner of disasters. An
outbreak of disease is first and foremost a public health problem,
so let’s not be confused about who should be calling the shots
in an epidemic¾public
health officials. Yet, this simple fact is certainly not reflected in what is
taking place with regard to bioterrorism preparedness, inside or
outside the beltway.
Inside of Washington’s beltway, concepts of crisis and
consequence management not only linger, they predominate.
With an apparent lack of budgetary authority and proposals
circulating anew to have the Justice Department retain a
leadership and coordination role despite the Bush
administration’s earlier appointment of FEMA in this capacity,
it is fair to say that Governor Ridge’s office will have
difficulty presiding over the tug of war about which federal
agency should lead the federal component of unconventional
terrorism response. In
America’s cities, counties, and states there is also a fair
amount of jostling as to who exactly would have the authority to
make certain decisions during an epidemic.
Only a handful of states, unfortunately, have untangled the
cross-cutting jurisdictions left over from more than a century of
contradictory laws passed as authorities scrambled to deal with
the different diseases that were sweeping the country.
Prompt, decisive action could make a lifesaving difference
in the midst of an outbreak, but the experience of various
terrorism exercises and drills gives ample reason to believe that
precious time would be squandered as local, state, and federal
officials squabbled over who has the authority to do what.
These circumstances beg for a clear vision and a firm hand to
untangle this mess and put the people who know the most about
disease control and eradication¾public
health officials¾unquestionably
in charge of any biological disaster, whether natural or manmade.
FEMA, the FBI, the Pentagon, and other federal and local
agencies should be playing support roles, not reshaping and
second-guessing the directions of public health professionals as
they manage the crisis and
consequences of a major eruption of disease.
Research, Development, and Production of Medications
Long before the current concerns about bioterrorism, I was at a
loss to explain how the federal government could have known about
the extent of the Soviet Union’s biowarfare program—including
the production of tons of agents such as smallpox and antibiotic
resistant plague and anthrax—as early as 1992 and not kicked
this nation’s vaccine research, development, and production
programs into a higher gear until 1997.
The extent of the problem is illustrated by the fact that
only one company is under contract to produce the anthrax vaccine,
no company currently produces the plague vaccine, and it was not
until recently that steps were taken to meaningfully jumpstart
smallpox vaccine production. Such matters should have been promptly addressed if only to
enable protection of US combat troops, not to mention producing
enough vaccine to cover the responders on the domestic front
lines, namely the medical personnel, firefighters, police,
paramedics, public health officials, and emergency managers who
would be called upon to aid US citizens in the event of a
biological disaster.
As for the effort that was mounted, many nongovernmental experts
have been taken aback at the structuring and relatively meager
funding of the Joint Vaccine Acquisition Program.
With a $322 million budget over ten years, this program
aims to bring seven candidate biowarfare vaccines through the
clinical trials process. Giving
credit where it is due, one must acknowledge that this
program—as well as Defense Advanced Research Projects
Agency-sponsored research into innovative medical treatments—is
making headway. However,
the federal government must find ways to shrink the nine to 15
year timeline that it takes to bring a new drug through clinical
trials to the marketplace. Food
and Drug Administration officials are already wrestling with how
to adjust the clinical trials process for testing of new vaccines
and additional bumps are to be expected on the road ahead.
Next, the National Institutes of Health and the pharmaceutical
industry, not the Defense Department, are this country’s experts
at clinical testing and production of medications.
My point is not that the Defense Department should not have
a role—perhaps even a lead role since the candidate vaccines
originated with the US Army Medical Research Institute for
Infectious Diseases—but these other important players need to be
at the table if an accelerated program is to be achieved.
As I noted, Governor Ridge will have his hands full, no
matter which direction he turns. Moreover, close congressional oversight of this particular
aspect of the nation’s biological disaster readiness is
warranted.
On the chemical side of the house, by the way, the picture is
similarly discouraging. The
Pentagon now turns to one company for supply of the nerve agent
antidote kits, known as Mark 1 kits, that the Health and Human
Services Office of Emergency Preparedness has encouraged cities
participating in the Metropolitan Medical Response System program
to purchase. Many a
city is still waiting to receive the Mark 1 kits ordered long ago,
and when they do, these kits will have a considerably shorter
shelf life than the kits made available to the military.
Emergency Medical Manpower Needs During a Major Disease Outbreak
Secretary of Health and Human Services Tommy Thompson stated on
September 30th in an interview with “60 Minutes”
that his department has “7,000 medical personnel that are ready
to go” in the event of a bioterrorist attack.
While that statement may be true in theory, in practice it
may not hold. Somewhat
lost in the late 1990s rush to soup up federal teams for hot zone
rescues was the one major non-FEMA federal support capability that
would clearly be needed after an infectious disease outbreak and
perhaps after a chemical incident as well—medical assistance.
The National Disaster Medical System was one of several
improvements made to federal disaster recovery capabilities over
the last decade, a time during which the federal government
demonstrated that it could bring appreciable humanitarian and
logistical assets to bear after natural catastrophes and
conventional terrorist bombings.
While these events flexed the muscles of the FEMA-led
recovery system, including the deployment of Disaster Medical
Assistance Teams, they did not even approach the type of
monumental challenge that a full-fledged infectious disease
outbreak would present. Prior
to Secretary Thompson’s recent statement, officials from the
Health and Human Services Department and the Pentagon have also
stated that they could mobilize significant medical assets
quickly.
Yet considerable skepticism exists that these two departments
combined could have met the medical aid requests made from Denver
after the release of plague was simulated during the mid-May 2000
TOPOFF drill, much less a call for even more help.
During that hypothetical event, health care officials
quickly found their medical facilities sinking under the patient
load and concluded that 2,000 more medical personnel were needed
on the ground within a day to prevent the flight of citizens that
would have further spread the disease.
Getting that number of physicians and nurses to a city and
into hospitals and field treatment posts would be a tremendous
logistical achievement. No
one that interviewed for Ataxia,
including members of the Disaster Medical Assistance Teams and
other medical and public health professionals, felt that the
federal government could deliver 2,000 civilian medical
professionals within the required timeframe. For its part, the Pentagon has yet to articulate clearly or
commit to civilians at the federal or local level just how much
medical manpower it could deliver and in what timeframe.
Quite frankly, the time has come for the Pentagon to stop being
coy about what medical assets it could bring bear in a domestic
emergency. Articulation
of this capability, even if it needs to be done in classified
forums, is necessary for sound planning on the civilian side.
Furthermore, there have been no large-scale dress
rehearsals to confirm whether civilian or military medical assets
could muster that many medical professionals that quickly, or even
over a few days. Even
so, the 2,000 figure from the Denver segment of TOPOFF seems
almost quaint when compared to one US city’s rough estimate that
45,000 health care providers—many of whom would have to be
imported—would be required to screen and treat its denizens.
The only way to find out whether the federal government is truly
up to the most important role it may have to perform after a
bioterrorist attack or a natural disease outbreak is to hold a
large-scale medical mobilization exercise.
Despite the expense, Congress should mandate a realistic
test of how much civilian and military medical assistance can be
delivered, how fast. Unlike
TOPOFF, where federal assets were pre-picked and pre-staged, the
terms of the exercise should specify that teams deploy as
notified. While the
general nature and identity of the exercise location(s) would
certainly be known beforehand and the timeframe of the drill
agreed within a window of several months, local officials should
trigger the onset of the exercise.
In short, dispense with the tabletop games that allow
everyone the comfort of claims of what they could do and see what
a real exercise brings. A
genuine and probably sobering measure of federal capabilities
could be taken, and the lessons of the exercise could inform the
structure of federal and local plans and programs.
Conclusions
In the 33-city survey done for Ataxia,
cities felt far better prepared to contend with a chemical
disaster than they did a biological one.
The higher state of chemical disaster preparedness is not
surprising given that over 650 hazmat teams, which would form the
core of an on-scene response, already existed nationwide prior to
the onset of federal domestic preparedness programs.
Local officials consistently identified the need for
enhancement of hospital readiness, the institutionalization of
training, the replenishment of personal protection gear, the
maintenance of key equipment items, and the regular conduct of
major field drills as critical to improving overall chemical
disaster preparedness.
When it comes to biological disaster readiness, one need not
resort to hyperbole when it comes to how difficult it would be for
major US cities to handle a pandemic; the truth is sobering
enough. Even though the basic components of the ability to handle a
disease outbreak¾hospitals, public health capabilities at the federal, state, and local
levels, and a wealth of medical professionals¾are
already in place, there is ample room for improvement.
The pragmatic steps that the federal government should take
are clear.
Mr. Chairman, Members of the Committee, Washington can take the
smart route to enhance chemical and biological disaster
preparedness nationwide or it can continue to go about this in an
expensive and inefficient way.
The keys to national chemical and biological disaster
readiness lie not in bigger budgets and more federal bureaucracy
but in common-sense policies and programs such as the following:
The sufficiency of existing federal programs, response teams, and
bureaucracies needs to be assessed and redundant and spurious ones
need to be eliminated. In
the interim until an assessment of the sufficiency of existing
assets is made, a government-wide moratorium on any new rescue
teams and bureaucracies should be declared, with the exception of
the enhanced intelligence, law enforcement, and airport security
measures that are being contemplated.
The bulk of federal funds need to be devoted to enhancing
readiness at the local level, where an increase in skills,
training, and equipment would make a genuine life-saving
difference. Even if terrorists never strike again in this country,
such investments would be well worthwhile because they would
improve the ability of hometown rescuers to respond to everyday
emergencies.
Defense Department programs related to the development and
production of new vaccines, antibiotics, and chemical antidotes
need to be put on a faster track, incorporating as appropriate
industrial expertise in such matters.
The federal government should continue to revive the nation’s
public health system, an endeavor that involves sending funds to
the local and state levels, not keeping them inside the beltway.
In addition, the federal government should fund regional
hospital planning grants and additional tests of disease syndrome
surveillance system, followed by plans and funds to establish such
capabilities nationwide.
Appropriate steps should be taken to see that firefighters,
police, paramedics, physicians, nurses, laboratory workers, and
public officials benefit from training that is institutionalized
in the nation’s training academies, universities, and schools.
Last, but certainly not least, Washington needs to develop a plan
to sustain preparedness over the long term.
Drills at the local and federal levels are necessary
because plans that sit on the shelf for extended periods of time
are often plans that do not work well when emergencies occur.
On behalf of the local public health and safety officials who have
shared their experience and common sense views with me, I urge
Congress to waste no time in passing legislation that brings the
burgeoning federal terrorism preparedness programs and
bureaucracies into line and points them in a more constructive,
cost-effective direction.
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