Florida Department of HealthEPI UPDATE

A weekly publication by the Bureau of Epidemiology

 

June 15, 2001

"The reason for collecting, analyzing and disseminating information on a disease is to control that disease. Collection and analysis should not be allowed to consume resources if action does not follow."

--Foege WH et al. Int. J of Epidemiology 1976; 5:29-37.

Richard S. Hopkins, MD, MSPH, Bureau Chief, State Epidemiologist

Don Ward, Surveillance Section Administrator, Epi Update Managing Editor

Jason Glisson, BS, Epi Editorial Assistant

Bureau of Epidemiology Frequent Contributors:

Steven Wiersma, MD, MPH,

Deputy State Epidemiologist

Jodi Baldy, MPH,

Biological Scientist IV

Ursula E. Bauer, PhD,

Chronic Disease Epidemiologist

Lisa Conti, DVM, MPH,

State Public Health Veterinarian

Regional Epidemiologists:

Dolly Katz, PhD, MPH, SE Florida

Roger Sanderson, RN, MA, SW Florida

Carina Blackmore, MS Vet. Med., PhD, NE Florida

Zuber Mulla, MSPH,

Central Florida Carina Blackmore, MS Vet. Med., PhD,

Please print out this material and share with epidemiology staff, county health department directors, administrators, medical directors, nursing directors, environmental health directors and others with an interest in information of this type. Thank you.

The Bureau of Epidemiology is available 24 hours a day, 7 days a week for consultation at our main number (SunCom 205-4401 or 850/245-4401) PLEASE NOTE: Consultation after 5 p.m. & on weekends is intended for emergencies.

The Department of Health has a home on the World Wide Web at http://www.doh.state.fl.us

In this issue:

1. CSTE Meeting Notes

2. (New Mexico) State Labs Flunk Tests on Spotting Anthrax

3. Weekly Disease Table


 

1. CSTE Meeting Notes

Don Ward, Surveillance Section Administrator

I have just returned from the annual meeting of the Council of State and Territorial Epidemiologists (CSTE) which was held in Portland, Oregon (I was a guest of CSTE). As you probably know, CSTE has developed a strong role as an advisor to CDC and so has significant influence on the impact on public health policies and programs. On the long plane ride back, I took some time (interrupted by some terror over the Rockies) to reflect on how some of what I heard will or should influence communicable disease prevention efforts in Florida. My perspective is based on my attendance which was limited to communicable disease surveillance and epidemiology presentations.

Technology—The prospects of and planning for the electronic transmission of communicable disease related information was a high priority agenda. The CDC and states are working toward electronic case and laboratory results reporting, integrated database management and, in the long view, the electronic transmission of clinical data. We demonstrated the Merlin system, which was very well received. Under the auspices of the National Electronic Disease Surveillance System (NEDSS), the CDC is working on a "base system" (similar to Merlin) and modules for the various programs (STD, TB, HIV/AIDS). The Bureaus in the Division of Disease Control, the office of Health Planning Evaluation and Data Analysis and the information technology office are planning for the incorporation of the NEDSS architecture into the Florida DOH information systems.

Emerging and re-emerging infectious disease—The Director of the National Center for Infectious Diseases and several of the speakers made a clear and substantive case for the need to focus program attention on emerging infectious diseases: many chronic diseases have infectious origins (consider the recent discovery of the infectious cause of certain ulcers); there is significant potential for the international transmission of disease; and potential use as bioterrorist agents has renewed interest in several diseases. In addition, the development of antibiotic resistance by certain organisms is severely limiting the effectiveness of many therapies. Surveillance systems need to be able to identify and monitor the occurrence of all such problematic infectious diseases.

Epi-X—The CDC has developed an excellent web-based communications tool named Epi-X. This secure (by digital certificate) network allows registered public health professionals to post information that are expected to be useful to others. The purpose is to enable the communication of important public health data, as near real-time as possible without the restrictions of publication level data. Information may include outbreak notices that may begin with a suspect cluster and are followed through the intervention processes, epidemiologic data, and alerts. The alert function has a call-down feature that will contact key users through a variety of options. We, in the Bureau of Epidemiology, have asked CDC to assist us in the development of such a system for Florida. That network will connect hospitals, laboratories, major healthcare providers, county health departments and the state health office for the sharing of key public health information.

This meeting was superb; there was much more than I reported. When the slides from the presentations are available, we will share them with you.

 

 

2. (New Mexico) State Labs Flunk Tests on Spotting Anthrax

By E. J. Mundell (From Haz--Mat-WMD Tuesday May 22)

ORLANDO (Reuters Health) - In a recent test, every medical laboratory that received a patient specimen containing the deadly anthrax bacterium failed to spot the organism or refer it to another lab, scientists report. The finding is worrisome, because "if Bacillus anthracis is used covertly in a bioterrorism attack, it will probably be first isolated in a clinical laboratory," according to Dr. Linda Nims and colleagues at the New Mexico State Laboratory in Albuquerque. Nims presented the findings here Monday at the annual meeting of the American Society for Microbiology. Speaking with Reuters Health, Nims explained that as a former clinical microbiologist, she suspected that most of her colleagues would dismiss an unexpected culture finding such as B. anthracis as an innocuous contaminant. "You feel like, 'well, it was on the skin but it's not causing the patient's infection," she said. The common response would be to abandon any further investigation of the bacillus. "I wanted to see if the laboratories in my city still did the same thing," Nims said. So, unannounced, she and her colleagues submitted four specimens-not from real patients-to four large New Mexico laboratories. Each contained a weakened form of B. anthracis. The result, Nims said, was "exactly what I thought-people just thought it was a contaminant. Three out of four laboratories turned it out as a contaminant or just 'Bacillus species.' One referred it to us--9 days after they first looked at the specimen." These types of mistakes and delays could have enormous public health consequences in the event of a real anthrax outbreak, the researchers warn.

Laboratories could "take a prolonged period of time to identify the organism or not identify it at all, which could result in increased illness and death in the population."

To address the problem locally, the New Mexico State Laboratory has presented training sessions in spotting and reporting B. anthracis for personnel at the four labs that flunked the test. The measure seems to have worked. In a second round of tests, all four labs correctly referred the bacillus to the state lab when it came across their desks, with three of the four doing so within a day. Nims believes this type of initiative may be needed nationwide, given the ongoing threat of bioterrorism. "I think that all laboratories have to be aware of it and probably ask their state health lab for help in training on it," she said.

 

 

3. Weekly Disease Table (Week 23)

DISEASE

1999 TO
WEEK 23

2000 TO
WEEK 23

3-YEAR
AVERAGE
TO WEEK 23*

2000
TOTAL
CASES

2001 TO
WEEK 23

2001
WEEK 23
ONLY

Animal Rabies

75

59

74.7

161

97

5

Anthrax

0

0

0

0

0

0

Botulism, foodborne

0

0

0

0

0

0

Botulism, infant

0

0

0

0

0

0

Botulism, wound

0

0

0

0

0

0

Botulism, other

0

0

0

0

0

0

Brucellosis

0

1

0.7

2

1

0

Campylobacteriosis

353

339

318.7

1026

308

25

Ciguatera

1

0

2.3

14

0

0

Cryptosporidiosis

44

20

36

180

30

0

Cyclosporiasis

0

1

1.7

9

22

0

Dengue Fever

2

0

1

3

3

0

Diphtheria

0

0

0

0

0

0

Ehrlichiosis, human

0

0

0

0

0

0

Encephalitis, chickenpox

0

0

0

0

0

0

Encephalitis, Eastern Equine

0

0

0

0

0

0

Encephalitis, herpes

2

3

2.7

7

1

1

Encephalitis, influenza

0

1

0.3

1

0

0

Encephalitis, measles

0

0

0

0

0

0

Encephalitis, mumps

0

0

0

0

0

0

Encephalitis, other

3

4

3

8

2

0

Encephalitis, St. Louis

0

0

0

0

0

0

Encephalitis, Venezuelan

0

0

0

0

0

0

Encephalitis, Western Equine

0

0

0

0

0

0

Escherichia Coli 0157:H7

12

16

12.3

95

9

1

Escherichia Coli, other

9

5

5.3

13

2

0

Giardiasis

374

401

408.3

1466

358

15

H. Influenzae Cellulitis

0

0

0.7

1

0

0

H. Influenzae Epiglottitis

0

0

0

1

0

0

H. Influenzae Meningitis

10

1

6

11

4

0

H. Influenzae Pneumonia

2

2

2.3

7

12

1

H. Influenzae Prim.Bacteremia

11

16

11.7

57

41

4

H. Influenzae Septic Arthritis

0

0

0

1

0

0

Hantaviris Infection

0

0

0

0

0

0

Hemolytic Uremic Syndrome

1

4

2

18

1

0

Hemorrhagic Fever

0

0

0

0

0

0

Hepatitis A

267

202

234

589

213

11

Hepatitis B

161

164

160

525

163

15

Hepatitis B (+HbsAg in pregnant women)

5

158

54.3

493

143

12

Hepatitis, Perinatal Hep B

1

1

0.7

1

4

1

Hepatitis C

22

8

10

19

10

3

Hepatitis, Non-A, Non-B

1

4

13

6

1

0

Hepatitis, Other, including unspecified

9

5

6

7

4

0

Lead Poisoning

662

467

593.7

1219

250

20

Legionellosis

8

18

14.3

51

20

1

Leprosy

1

0

1.3

4

0

0

Leptospirosis

0

0

0

2

0

0

Listeriosis

5

10

5

32

7

0

Lyme Disease

6

8

9.3

54

4

0

Malaria

37

33

31

90

20

0

Measles

1

0

1

2

0

0

Meningitis, Group B Strep

6

7

6.3

21

5

1

Meningitis, List Monocytogenes

3

1

2.7

7

0

0

Meningitis, Meningococcal

21

15

19.3

41

29

0

Meningitis, other

19

40

28

110

32

8

Meningitis, Strep Pneumoniae

58

49

51.7

112

30

3

Meningococcemia, disseminated

31

36

35.7

80

33

2

Mercury Poisoning

2

3

1.7

11

2

0

Mumps

2

2

4.3

4

1

0

Neurotoxic Shellfish Poisoning

0

0

0

0

0

0

Pertussis

18

21

18

48

6

0

Plague, Bubonic

0

0

0

0

0

0

Plague, Pneumonic

0

0

0

0

0

0

Poliomyelitis

0

0

0

0

0

0

Psittacosis

0

0

0.3

3

0

0

Q Fever

0

0

0

0

0

0

Human Rabies

0

0

0

0

0

0

Rocky Mountain Spotted Fever

1

0

0.7

1

1

0

Rubella

0

2

1.3

2

1

0

Rubella, Congenital

0

0

0

1

0

0

Salmonellosis

733

620

658

2755

709

40

Shigellosis

595

486

576.7

1292

294

15

Smallpox

0

0

0

0

0

0

Staphylococcus Aureus (GISA/VISA)

0

0

0

0

1

0

Staphylococcus Aureus (GRSA/VRSA)

0

0

0

0

0

0

Streptococcal Disease, Invasive Group A

24

58

35.3

146

75

1

Streptococcus Pneumoniae, Invasive

264

465

326

1147

467

9

Tetanus

1

0

1

1

2

0

Toxoplasmosis

4

6

5.3

12

7

0

Trichinosis

0

0

0

1

0

0

Tularemia

0

0

0

0

0

0

Typhoid Fever

20

4

10.7

12

3

0

Vibrio Alginolyticus

3

3

2.3

15

1

0

Vibrio Cholerae Type 01

0

0

0

0

0

0

Vibrio Cholerae Non-01

3

3

3

4

1

1

Vibrio Fluvialis

1

0

1.3

2

0

0

Vibrio Hollisae

4

3

3

3

0

0

Vibrio Mimicus

1

1

1.7

2

0

0

Vibrio, other

1

0

0.7

2

0

0

Vibrio Parahaemolyticus

4

2

4.7

16

2

0

Vibrio Vulnificus

3

1

3.3

13

3

0

Yellow Fever

0

0

0

0

0

0


* The column of data representing the "3-year average to week ##" is the average of years 1998, 1999 and 2000 cases to the current listed week (##).