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Is difficult, but may help us respond to new epidemics
The terror attacks on the World Trade Center in
Manhattan in 1993 and the Federal Building in Oklahoma City in 1995, together with the Sarin attack on the Tokyo subway in 1995, have forced upon America an unwanted awareness of its vulnerability to terror attack. So far there have been no biological attacks within the United
States, but many feel that this may only be a matter of time. Recently
the Institute of Medicine and the National Academy of Sciences have
made recommendations for research that would help in managing chemical
and biological terror attacks against the civilian
community.1
There are specific problems that are unique to biological attacks.
Firstly, whatever the agent, and however it is delivered, there will be
time lags between exposure and onset of the first symptoms and the
development of the full blown disease. Thus the disease will be
dispersed before we become aware that an attack has occurred (assuming
no public announcement by the terrorists). Since the population exposed
in a large community will approach the health system in many different
ways there may be no clumping of cases to trigger awareness of an attack.
Secondly, the early manifestations caused by virtually any of the
biological agents will look identical clinically. It is currently
impossible to distinguish viral from bacterial disease until a specific
organ pathophysiology declares itself, and this will probably be true
also for a biological weapon. Moreover, since many of the weapons will
be viral, the virulence of the attack weapon will probably be missed
until significant morbidity and mortality have occurred. As a result,
if there is no announcement of an attack, many patients will become
critically ill and die even if the agent is one for which there is a
specific diagnostic test and treatment. Conversely, if an attack is
announced, medical facilities risk being overwhelmed by the many people
who think they may have been exposed.
Thirdly, it is hard to raise money to defend against a problem that has
such a low incidence. Moreover, since it is unlikely that the same
community will be attacked repeatedly it is difficult to maintain an
effective disaster response.
Fourthly, even for those agents that have specific therapy there will
be huge problems in delivering it.
2 3
For example, though
there is an effective vaccine against anthrax, the supplies of vaccine
are limited, and no new vaccine is being produced. Anthrax is unique in
that if the diagnosis can be made before organ failure the disease can
be held in check with high doses of antibiotics while the
population at risk is immunised. Although spread of the agent can be
predicted to follow air and wind patterns,4 tracking its
spread will be made harder by the self dispersion of the exposed
population before they are aware of being ill. Moreover, even if we had
adequate supplies of anthrax vaccine, many citizens might refuse it.
Anthrax introduces another quandary in planning. It is one of the few
biological agents that actually has a treatment. Thus terrorists might
simply choose an agent less amenable to treatment. Another quandary is
involved in any discussion of smallpox. Although eradicated as a
worldwide disease, there remain two principal populations of smallpox
virus, one in Atlanta and one somewhere in Russia. Only small doses of
smallpox vaccine remain,1 and no agency is creating new
vaccine. While vaccination is effective in the first few days after
exposure, it is again unlikely that there will be enough vaccine to be
effective against a large population attack. Many elderly people were
once immunised but so long ago that their effective immunity must be
almost non-existent. Smallpox is also unique in being spread by
contiguous contact, so it potentially represents a severe and effective
weapon. We do not know whether any of the chemotherapeutic antiviral
agents would be effective against smallpox, and this was an area of
research recommended by the Institute of Medicine report.1
It has also become apparent that the management of any biological
attack must depend on systems already in place for managing new
diseases or new epidemics of old diseases. Unfortunately, US public
health surveillance systems are not modern, and there has been little
thought about how an epidemic might be recognised quickly. Most state
public health departments are underfunded and do not have the staff to
investigate anything more than a recognised epidemic.
Analysis of the Sarin attack in Tokyo shows that communication between
intelligence and law enforcement agencies and health agencies needs to
be improved. The medical community was never warned about an impending
attack in Tokyo, and doctors learnt about the cause of the problem from
another Japanese community that had sustained a Sarin attack a few
months earlier.5-8
Attacks may occur without warning, but there is every reason to think
that, given intelligence about potential attacks, a focused and
localised response could be achieved. An example would be to warn
emergency departments, primary care clinics, and local public health
agencies, as well as to build up supplies of any treatment that might
require stockpiling, such as antibiotics or vaccine. In light of the
above, there is a need for identification technologies that are quick
and accurate. Right now, there are none,1 and it is
difficult to envisage where the development is to occur given the lack
of opportunity to study these diseases other than theoretically or in
the laboratory.
Another weakness in our response is the effective protection of medical
teams. People simply cannot work effectively for long in the protective
garments that currently exist, and without protection many health team
members will themselves become sick or die. There are no good methods
of decontamination after chemical, never mind biological, exposure, and
how to restrain the spread of a disease that has already started to
spread before it produces the first symptoms is a true
conundrum.9
One consequence of a terror attack is the residual psychological impact
on the community. This will include overload of medical facilities by
the "worried well," grief responses felt by
survivors,10 and anger at not being protected.
Moreover, the deaths of many adults might produce large numbers of
children with no one to care for them, who will overwhelm the
community's social agencies.
It is easy to become pessimistic about biological attacks, but the
Institute of Medicine committee thought it would be possible to lessen
the numbers of casualties and deaths through proper planning,
superposition of the disaster teams that already exist, and the
creation of special strike teams that could enter an attacked area,
bringing supplies of specific therapeutic agents with them. Most of the
problems are capable of being solved in part with an infusion of will,
money (already promised by the US president), and practice for the
unusual and infrequent event. Even if a terror attack is never
encountered society will benefit from attempting to solve the problems
of a biological attack because we will always be faced by such attacks
from nature. The efforts we make to respond will be useful in managing
new epidemics or re-emergent infections.
University of California San Diego Medical Center, San Diego,
CA 92103-8676, USA (psoc{at}aol.com)
| 1. | Institute of Medicine and National Research Council. Chemical and biological terrorism: research and development to improve civilian medical response. Washington, DC: National Academy Press, 1999. |
| 2. | Fainberg A. Debating policy priorities and implications. In: Roberts B, ed. Terrorism with chemical and biological weapons. Alexandria, VA: Chemical and Biological Arms Control Institute, 1997:75-93. |
| 3. | Franz DR, Jahrling PB, Friedlander AM, McClain DJ, Hoover DL, Byrne WR, et al. Clinical recognition and management of patients exposed to biological warfare agents. JAMA 1997; 278: 399-411[Abstract]. |
| 4. |
Meselson M, Guillemin J, Hugh-Jones M, Langmuir A, Popova I, Shelokov A, et al.
The Sverdlovsk anthrax outbreak of 1979.
Science
1994;
266:
1202-1208 |
| 5. | Morita H, Yanigasawa T, Shimizu M, Hirabayashi H, Okudera H, Nohara M, et al. Sarin poisioning in Matsumoto, Japan. Lancet 1995; 346: 290-293[CrossRef][Medline]. |
| 6. | Okumura T, Suzuki K, Kukuda A, Kohama A, Takasu N, Ishimatsu S, et al. The Tokyo subway sarin attack: disaster management, part 1: community emergency response. Acad Emerg Med 1998; 5: 613-617[Medline]. |
| 7. | Okumura T, Suzuki K, Kukuda A, Kohama A, Takasu N, Ishimatsu S, et al. The Tokyo subway sarin attack: disaster management, part 2: hospital response. Acad Emerg Med 1998; 5: 618-624[Medline]. |
| 8. | Okumura T, Suzuki K, Kukuda A, Kohama A, Takasu N, Ishimatsu S, et al. The Tokyo subway sarin attack: disaster management, part 3. Acad Emerg Med 1998; 5: 628-652[Medline]. |
| 9. | Belmonte RB. Tests of level A suits: protection against chemical and biological warfare agents and simulants: executive summary. Aberdeen Proving Ground, MD: Edgewood Research, Development, and Engineering Center, 1997. |
| 10. | Bowler RM, Huel D, Mergler G, Cone J. Psychological, psychosocial, and psycho-physiological sequelae in a community affected by a railroad chemical disaster. J Traumatic Stress 1994; 7: 601-624[CrossRef][Medline]. |
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