|
State of Florida
Department of Health, Bureau of Epidemiology
EPI UPDATE
April 29, 1999
Richard S. Hopkins, M.D., M.S.P.H., Bureau Chief, State Epidemiologist
Don Ward, Surveillance Section Administrator, Epi Update Managing Editor
Natalie E. Tackett, Epi Update Editor
Bureau of Epidemiology Frequent Contributors:
Steven Wiersma, M.D., M.P.H., Deputy State Epidemiologist |
William J. Bigler, Ph.D., M.S. Senior Epidemiologist |
Jodi Baldy, M.P.H., Biological Scientist IV |
Ursula E. Bauer, Ph.D.,
Chronic Disease Epidemiologist |
John Werth, M.A.
Bureau Education Coordinator |
Lisa Conti, D.V.M., M.P.H., State Public Health Veterinarian |
| |
Regional
Epidemiologists |
Dolly
Katz, Ph.D., M.P.H.,
SE Florida |
Roger Sanderson, R.N., M.A.,
SW Florida |
Carina
Blackmore, M.S. Vet. Med., Ph.D., NE Florida |
Zuber Mulla, M.S.P.H.,
Central Florida |
Gérard
Krause, M.D., D.T.M.H.,
NW Florida |
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 (850/245-4401) PLEASE NOTE:
Consultation after 5 p.m. & on weekends is intended for emergencies.
Epi Update has a home on the World Wide Web at ---
http://www.doh.state.fl.us
The Florida Clean Indoor Air Act regulates smoking in indoor public
places.
To file a complaint call 1-800-337-3742
In this issue:
1. HIV Counseling and Testing Among Florida Women Who Have Had a Live
Birth
2. The Latest on Human Caliciviruses Presented at Recent CDC Conference
3. Investigation of Norwalk Outbreaks in Florida
4. Changes in CPT Code for Hepatitis Panel Causing Delayed Reports of
Acute Hepatitis
5. Influenza Summary Report
6. FDA Satellite Training: June 16-17, 1999
7. Vibrio parahaemolyticus
8. Febrile Viral Encephalitis in Malaysia
9. Florida Past: State Board Supports Creation of Poison Control Centers
10. Weekly Disease Table - Week 16
1. HIV Counseling and Testing Among Florida Women Who
Have Had a Live Birth
Chrissy Gest, M.A., Perinatal Epidemiologist
Research has shown that transmission of the HIV virus from mother to baby can be
reduced by approximately two-thirds if the mother and newborn are given Zidovudine (AZT).1
Zidovudine is more effective in preventing transmission of the HIV virus from mother to
baby the earlier it is given (but after the first trimester) in the pregnancy. The U.S.
Public Health Service has recommended routine HIV counseling and voluntary HIV testing for
all pregnant women.
In Florida,F.S.384.31 (serologic testing of pregnant women; duty of the attendant)
regarding HIV counseling and testing for pregnant women became effective on October 1,
1996. Health care providers must provide prenatal counseling on the benefits of HIV
testing and inform pregnant women about the options for HIV treatment if they are infected
with HIV. Health care providers must also offer HIV testing to all pregnant women
according to this statute.
The Bureau of Epidemiology recently completed a report on HIV testing and counseling on
HIV prevention and testing among pregnant women. Using data from the Pregnancy Risk
Assessment Monitoring System (PRAMS) the Bureau of Epidemiology analyzed the trends in HIV
counseling and testing in Florida for women receiving prenatal care in 1996 and 1997, and
found that certain groups of women are more likely to be counseled and offered testing in
Florida.
PRAMS is a population based, random sample mail/telephone survey of new mothers in
Florida. Each month we randomly select mothers from the states birth certificate
file. Statistical weights are applied to the data, so that inferences can be made about
all live births in Florida. Selected items from the birth certificate are included for
each respondent. The response rate was 80% in 1996 and 78% in 1997.
Some of the findings are:
- For women who recently had a live birth, both the percentage who reported a health care
provider talked to them about HIV testing and the percentage who were tested for HIV
showed statistically significant increases between 1996 and 1997. However, the percentage
receiving counseling on HIV prevention did not change at all.
- Women who were counseled on HIV testing were more likely to be tested for HIV. 91% of
women who reported they were counseled on HIV testing in 1997 were tested for HIV,
compared to 53% who reported they were not counseled on HIV testing.
- Women who are young, black, less educated, unmarried and/or poor, are more likely to
report being counseled about HIV prevention or HIV testing and to be tested for HIV during
pregnancy or delivery, than other women.
- 94% of black women who are 19 and older, unmarried and have less than a high school
education, reported they were tested for HIV, compared to 75% of women who are not black,
are 19 and older, are married and have more than a high school education.
- Rates of counseling on either HIV prevention or HIV testing and testing for HIV vary by
source of prenatal care and type of payment for prenatal care. All are lowest for women
receiving prenatal care in a private doctors office, in both 1996 and 1997.
While the numbers of pregnant women reporting they were counseled on HIV prevention or
testing, or who were tested for HIV, increased from 1996 to 1997, there is still room for
improvement. Much improvement needs to be made in counseling on HIV prevention. The number
of women counseled for HIV prevention was much lower than the numbers for both testing and
counseling for testing. Although Florida law does not mandate counseling on HIV
prevention, it should be included with prenatal counseling on HIV testing. Universal
counseling of pregnant woman on HIV testing is the law, but it is not the reality.
Once pregnant women are universally counseled on HIV testing, HIV testing during pregnancy
or delivery may increase.
1. Connor EM, Sperling RS, Gelber R, et al, for the Pediatric AIDS Clinical Trials
Group Protocol 076 Study Group. Reduction of Maternal-infant Transmission of Human
Immunodeficiency Virus Type 1 with Zidovudine Treatment. New England Journal of Medicine
1994; 331:1173-1180.
To receive a copy of the full report contact the Bureau of Epidemiology or visit the
Bureau of Epidemiologys web page at http://www.doh.state.fl.us
2. The Latest on Human Caliciviruses Presented at Recent CDC Conference
Dolly Katz, PhD, MPH, SE Regional Epidemiologist
Although human caliciviruses, more popularly known as Norwalk-like viruses, are a major
and underappreciated cause of diarrheal disease and morbidity worldwide, much remains to
be learned about this pathogen. The findings of recent research presented at an
international conference on caliciviruses held March 29-31 at the Centers for Disease
Control in Atlanta made it clear that: (1) Norwalk-like viruses are a much larger cause of
disease than our current limited surveillance data indicate and (2) much of what we
thought we knew about the virus and its effects is wrong.
For epidemiologists, the main take-home messages from the conference were:
- Calicivirus are a major cause of outbreaks
. Norwalk-like viruses are a principal
cause of sporadic and outbreak-associated enteric disease, and should be considered in the
investigation of any outbreak of diarrheal disease.
- Transmission can be person-to-person or foodborne/waterborne
Although food and water
are important vehicles in the transmission of Norwalk-like viruses, person to person
transmission appears to be the dominant mode
- Specimen testing essential for identification
. Collection of unpreserved, unfrozen
stool and vomitus samples for viral identification should be the first priority in any
outbreak investigation where Norwalk-like virus is a suspected cause.
Other new information presented was as follows:
- Role in outbreaks of enteric disease.
In the United States, caliciviruses cause 95%
of outbreaks of non-bacterial acute gastroenteritis, according to laboratory data from the
CDC's Viral Gastroenteritis Section. The true proportion of all gastrointestinal outbreaks
that are caused by caliciviruses in the U.S. is unknown, because the infection is not a
reportable disease and because most outbreaks are identified and investigated locally.
- Laboratory identification.
The explosion of knowledge about the true role of
Norwalk-like viruses in human disease is due to the vast improvement in laboratory
techniques in recent years. Relatively insensitive electron microscopy has been
supplemented by increasingly sensitive and specific molecular techniques that permit the
cloning and amplification of the virus's genetic material.
- Identification of Norwalk-like viruses in food and water.
Epidemiologic
investigations have been hampered by the inability of laboratories to consistently
identify caliciviruses in anything but human clinical samples and shellfish. New
genetically-based laboratory techniques increasingly are permitting the identification of
Norwalk-like viruses in environmental and food samples. Nevertheless, detection of
calicivirus in non-human samples remains difficult because no cell culture system
currently exists, the virus tends to be present only in low concentrations, multiple
primer sequences are necessary, and foods may contain enzymes that inhibit the polymerase
chain reaction technique used to amplify the virus.
- Animal to human transmission.
Until recently, humans were the only known reservoir
of Norwalk-like viruses. To date, approximately 40 distinct calicivirus genotypes have
been identified in 27 animal species, including pigs, cattle, dogs, fish, cats, and
rabbits. Whether animal to human transmission occurs is not yet known, but genetic studies
in the United Kingdom have determined that bovine caliciviruses are closely related to
human caliciviruses. Also a longitudinal study in Mexico found that contact with dogs is
associated with a six-fold increased risk of calcivirus infection in preschool children.
- Immunity,
seasonality, and identification of new strains. Limited studies
indicate that strain-specific, short-term immunity does exist, but that infection confirms
no long-term immunity. Although outbreaks occur year-round, they are more common in winter
and early spring worldwide. New strains are being identified and added to the
caliciviruses' increasingly intricate family tree as laboratory techniques improve. More
than two dozen human strains have been identified to date, but differences in nomenclature
and laboratory techniques make it difficult to determine how many of these are unique.
- Serodiagnosis.
Although stool and vomitus are the most common clinical specimens
used in laboratory diagnosis of infection, blood samples also can be used. The primary
advantage of blood is that serodiagnosis can detect antibodies weeks after infection,
while viruses are detectable in stool only for about two days after illness onset. The
primary disadvantage of blood is the difficulty of obtaining acute and convalescent sera
(although a single convalescent serum may be used for diagnosis).
3. Investigation of Norwalk Outbreaks in Florida
Dolly Katz, PhD, MPH, SE Regional Epidemiologist
The epidemiology of Norwalk-like virus may be different in Florida because of the
state's unique climate and large foreign-born population. Therefore, information on
outbreaks is critical to understanding and preventing Norwalk transmission in Florida.
While Norwalk-like virus infections are not in themselves reportable conditions in
Florida, all outbreaks, regardless of the cause, are reportable. Because caliciviruses
play a major role in the epidemiology of gastrointestinal outbreaks, epidemiologists
should consider Norwalk-like viruses in the investigation of any enteric outbreak.
Epidemiologists also should be aware that person-to-person transmission is probably more
common than food or waterborne transmission. However, we still have a lot to learn. Our
investigation of some outbreaks suggest that they may have started as foodborne and
eventually become person-to-person or vice versa.
During the past 5 years, we estimate that approximately 7% of our total food and
waterborne outbreaks and 20% of all cases reported for food and waterborne outbreaks have
been attributable to Norwalk-like viruses. When only confirmed outbreaks are considered
for the same time frame, approximately 12% of the outbreaks (24% of the cases) are related
to Norwalk-like viruses.
Also, since animals have not been ruled out as a source of Norwalk-like virus
infections, outbreak investigations should include questions about contact with animals,
particularly calves and dogs.
The state of Florida's Bureau of Laboratories now has the capacity to identify
Norwalk-like viruses in clinical samples. Samples should not be sent to the Centers for
Disease Control and Prevention for identification, as they were in the past. Instead,
stool and vomitus should be sent to the state's Tampa Branch Laboratory, 3952 West Dr.
M.L. King Jr. Blvd., Tampa, 33614. Ideally, 10 stool or vomitus samples should be
collected and sent together, using refrigerator ice packs to keep them cold. They should
be refrigerated during storage, but should NOT be frozen or preserved. Before sending
samples, please contact the laboratory at 813-871-7456; ask for Dr. Lillian, Stark,
Christopher Webb or Dr. Deno Kanzanis.
While water, food (other than oysters), and environmental samples are not routinely
tested for Norwalk-like viruses, laboratory techniques are improving rapidly, and such
testing may be appropriate under certain circumstances. If a specific food, water, or
environmental source is epidemologically linked to an outbreak, consult with the Tampa
branch laboratory about the possibility of testing.
4. Notice to Readers Changes in CPT Code for Hepatitis Panel Causing Delayed Reports
of Acute Hepatitis (MMWR April 30, 1999 / 48(16);338-9)
Submitted by Steven Wiersma, M.D., M.P.H., Deputy State Epidemiologist
During the last year, many county health department epidemiology staff members have
noticed that clinicians do not seem to be ordering IgM for hepatitis A and B as part of
their diagnostic work-up. This has made case confirmation and prevention of secondary
cases very difficult. The Bureau of Epidemiology and many CHDs have searched for reasons
to this change in hepatitis tests that removed IgM from standard panels. The CDC was aware
of this problem when contacted and our request for a full explanation are finally answered
in this brief MMWR report.
Unfortunately, it looks like the problem will not be fixed until the dawn of the new
millennium. Fortunately, the root cause is being addressed and will give public health a
voice in future decisions made by the larger medical community. The important message here
is that clinicians need to order these tests separately in order to fully evaluate the
cause of infection in persons with acute hepatitis. The fact that the IgM tests are not in
the hepatitis panel does not mean that Medicaid or Medicare will not pay for needed
diagnostic tests; they just need to be ordered separately.
Current Procedural Terminology (CPT) codes are standardized codes developed and
maintained by the CPT Board of the American Medical Association for reporting medical
services. The Health Care Financing Administration requires use of these codes in the
Common Procedure Coding System when services are reported to Medicare and Medicaid for
reimbursement. Effective January 1, 1998, the CPT Board changed the hepatitis serology
panel (CPT#80059) to exclude the tests for IgM antibody to hepatitis A virus (IgM
anti-HAV) and IgM antibody to hepatitis B core antigen (IgM anti-HBc). These two tests
specifically identify recent infection with HAV and HBV, respectively. Many providers may
be unaware that these tests are not part of the standard hepatitis panel, and diagnoses of
cases of acute viral hepatitis are likely to be delayed by the need to perform additional
testing. As a result, reporting of cases to health departments may be delayed, and CDC has
received reports of instances of insufficient time to provide postexposure prophylaxis to
prevent transmission of HAV or HBV to susceptible contacts of the case-patient.
The CPT Board has revised the hepatitis serology panel to include both IgM tests that
were deleted. However, these modifications will not be implemented until the next CPT code
manual is issued on January 1, 2000. Until this change takes effect, health departments
should notify health-care practitioners and/or laboratories of the need to order
individual tests for IgM anti-HAV (CPT#86709) and IgM anti-HBc (CPT#86705) for accurate
determination of the cause of illness in patients with signs and/or symptoms of acute
viral hepatitis and for timely prophylaxis of contacts.
5. Influenza Summary Update Week 14 (week ending April 17 1999)
Carina Blackmore, MS Vet Med., PhD., Regional Epidemiologist, NE
Florida
National: Influenza morbidity peaked during February and has been declining during
March and early April. During week 15, there were no reports of widespread activity, but
three states (Alaska, Arizona and Tennessee) reported regional activity. During the
previous week, week 14, 5 states reported either widespread or regional activity. The WHO
laboratories reported that 15 % (12,156 of 79,008) of the specimens tested since October 4
have been positive for influenza. Seventy-seven percent (9,336) of these were influenza A.
Among the type A viruses, 26 % have been subtyped. Subtype A(H3N2) have predominated (99 %
of 2,370)). Twenty-one isolates have been subtyped as A(H1N1).
So far this season, influenza A has been the most common subtype in the U.S. overall
and in all of the nine regions; however the percentage of influenza type A viruses have
varied by region, ranging from 61 % in the East North Central and East South Central
regions to 91 % in the New England region. Of the total patient visits to sentinel
physicians, 1 % were due to ILI (influenza-like-illness) in the U.S. overall. The
percentage of patient visits was within baseline values of 0 %-3 % in all regions.
Nationally, influenza activity peaked during early to mid-February when 5 % of the total
patients' visits were due to influenza-like illness. The percentage of pneumonia and
influenza deaths reported from the 122 cities during Week 15 was 8.0 %, above the epidemic
threshold of 7.2 %. The percentage of deaths from pneumonia and influenza has declined
after peaking at 8.8 % during the week ending March 13 1999; however, pneumonia and
influenza deaths remained above the epidemic threshold for the twelve consecutive weeks.
Florida: During week 15 (11-17 April 1999) there were 2 laboratory-confirmed
isolates of influenza reported: Influenza AH3N2) was reported from Sarasota county and
influenza B was reported from Broward county. Since September 23 and to date, there have
been 226 isolates reported; 67 ( 30%) of these were type B 159 type A. Of the influenza A
isolates 74 were typed; 68 (30 %) were type A(H3N2) and 6 (3 %) were type A(H1N1).
Isolates have been reported from: Alachua (1), Brevard (5), Broward (27), Dade (5), Desoto
(1), Duval (14), Hillsborough (54), Indian River (5), Jackson (2), Leon (20), Martin (2)
Okaloosa (2), Orange (22), Osceola (1), Palm Beach (17), Pinellas (12), Polk (5), Sarasota
(24), Seminole (2), St. Johns (2) and Volusia (3) counties.
Of the total patient visits to sentinel physicians during Week 15, 1 % were due to ILI.
This is within the baseline levels of 0-3 %. Since October 4 the percentage has ranged
between 1 and 4 %. Influenza-like illness has been reported from health care providers in
20 of the 21 Florida counties represented (not Pasco) in the sentinel physician
surveillance network.
6. FDA Satellite Training: June 16-17, 1999
Submitted by Roberta Hammond, PhD
This message is being sent to all county health department
director/administrators, nursing directors, environmental health directors and regional
food and waterborne illness epidemiological investigators. This is an advanced course,
which discusses the steps involved in traceback investigations of foods implicated in
outbreaks. Previous attendance at FDA Satellite Courses on Food Microbiology and Foodborne
Illness Outbreak Investigations along with experience in foodborne outbreak investigations
is STRONGLY recommended. No nursing CEUs will be available for this course, however
nurses are welcome to attend. Approximately 9 CEUs will be awarded to environmental health
professionals. The registration deadline is June 1.
7. Vibrio parahaemolyticus
Carina Blackmore, MS Vet Med., PhD., Regional Epidemiologist, NE Florida
Vibrio parahaemolyticus is a gram-negative bacillus found in marine environments
worldwide. It colonizes filter-feeding animals such as oysters, crabs, mussles and fish
but can also be found free-living in seawater. Despite its broad distribution, most V
parahaemolyticus infections in the United States occur in the states bordering the
Gulf of Mexico as the bacilli multiply better in warm water where the water temperatures
in the summer generally exceed 70 ° F
People become infected with V. parahaemolyticus primarily through eating raw or
undercooked seafood. The bacteria grows very quickly at room temperature so contaminated
cooked seafood may also be a source. In Japan, V. parahaemolyticus is one of the
leading causes of foodborne illness1. Sporadic cases are common along the
coasts of the United States but outbreaks have also been reported 2. The most
recent outbreak occurred during the summer of 1998 when 416 people (including 52 Florida
residents and 10 visitors) became infected by consuming raw oysters from Galveston Bay,
Texas3. Other outbreaks in Florida have included two clusters associated with
cross-contamination of cooked blue crab with juices from the raw crab.
Vibrio parahaemolyticus is less virulent than V. vulnificus and the disease
is normally limited to a relatively mild gastroenteritis with diarrhea, abdominal cramps,
vomiting, headache and fever in otherwise healthy people. In people with underlying health
problems, particularly liver disease, the bacteria may spread into the blood and cause
septicemia. It can also cause wound infections. Some V. parahaemolyticus infections
may require hospitalization, however the disease is rarely fatal4.5.
Vibrio infections are reportable in Alabama, Florida, Mississippi, Louisiana and
Texas and V. parahaemolyticus is responsible for the majority of these cases in
Florida. On average 24 cases have been reported to date in the state each year from 1981
when the disease became reportable. Most cases occur between April and October. Records
from 1981-1993 (n=206) showed gastro-intestinal illness (58%) and wound infections (27%)
as the two most common forms of the disease in the state5. Males were 4 times
or more likely to get infected than females and 43% of all patients required
hospitalization.
In Florida, most people become infected by eating raw oysters. To prevent Vibrio
infections in high-risk groups, the state requires warning notices everywhere raw oysters
are sold. These urge people with chronic health problems to eat only fully cooked oysters.
References
- Oliver James D and Kaper James B. 1997. Vibrio species. In Food
Microbiology Fundamentals and Frontiers. Doyle Michael P., Beuchat Larry R. and Mintville
Thomas J. ed. American Society for Microbiology, Washington DC, 228-264.
- MMWR 1998 47(22) 457-462.
- Roberta Hammond, Bureau of Environmental epidemiology, Florida DOH, personal
communication
- Hally, RJ, Rubin RA, Fraimow HS and Hoffman-Terry ML. 1995. Fatal Vibrio parahemolyticus
septicemia in a patient with cirrhosis. A case report and review of the literature. Dig.
Dis. Sci. 40: 1257-60.
- Hlady, W.Gary.and Klontz Karl C. 1996. The epidemiology of Vibrio infections in Florida
1981-1993. J. Infect. Dis. 173: 1176-83.
8. Febrile Viral Encephalitis in Malaysia
Reprinted from the CDC Summary of health Information for International
Travel received April 28.
On March 7, 1999, CDC was notified of an outbreak of an illness suspected to be
Japanese encephalitis among pig farmers, as well as severe disease in pigs in Malaysia in
the state of Negeri Sembilan, districts of Sikamat and Bukit Pelandok, and the state of
Perak, district of Kinta. According to the Malaysian Health Authorities, from October 1998
though March 1999, more than 200 human cases have been reported, with at least 80 deaths.
At the request of the Government of Malaysia, on March 21, CDC sent staff to Malaysia to
join local and international health officials in an investigation of the outbreak. To
date, all cases appear to be in persons who have had some contact with pigs; the majority
of cases have been in adult male pig farmers. Travelers to Malaysia should be aware of
this outbreak of febrile encephalitis, which thus far has involved only those closely
associated with pig farms. No travel restrictions are indicated at this time.
Because epidemiologic patterns were not totally consistent with Japanese encephalitis,
additional laboratory testing was performed in Malaysia. A subset of samples tested at CDC
confirmed the presence of a Hendra-like paramyxovirus (formerly called equine
morbillivirus). Hendra virus was first identified in 1994 in Australia and caused illness
in racehorses and three humans. Two of these patients died one of respiratory infection
and the other of meningoencephalitis. Al three previous human infections appear to have
been acquired from close contact with horses. However, other species demonstrated evidence
of infection with this virus. Researchers have shown that infected animals excrete the
virus in their urine.
Relatively little is know about the clinical syndrome of this new Hendra-like virus in
Malaysia. The illness apparently begins with fever, followed by drowsiness and coma. The
late stages are said to be accompanied by fluctuating blood pressure and body temperature.
Transmissibility of this Hendra-like virus is thought to be low for those not associated
with pig farming.
Persons anticipating travel to Malaysia should carefully follow the CDC regional
recommendations for Southeast Asia. These recommendations may be accessed on our (the CDC)
Internet website at http://www.cdc.gov/travel/index/htm or by calling toll-free on a
touch-tone phone for an autofax at 888-232-3299, then press '1' and enter document numbers
220200 and 380020. This information will be updated as more information becomes available.
Persons in Malaysia are advised to contact the Malaysian Health Authorities for
additional information and/or advice.
9. Florida Past: State Board Supports Creation of Poison Control
Centers William J. Bigler, PhD.
Thank you, Dr. Bigler, for your weekly contributions to the Epi Update. Congratulations
on your 34 years with the Department of Health. -Eds.
In the mid 1950s the State Board of Health, Bureau of Preventable Diseases, made
plans to expand the state epidemiologists responsibility to address
"Epidemiologic Studies in Non-communicable Disease." Among the activities
mentioned in the 1956 and 1957 annual reports was a chronicle of efforts to establish a
network of Poison Control Centers throughout the state. Apparently from the outset the
main objective of this initiative was to collect epidemiologic information that would be
used to develop prevention programs directed at reducing accidental poisonings,
particularly in children.
1956 Annual Report "The epidemiology of accidental poisoning in children
was the subject of considerable time and activity by the staff in 1956. In cooperation
with the Florida Pediatric Society, The Florida Chapter of the American Academy of
Pediatrics and the county health departments, assistance was given toward establishing a
statewide network of Poison Control Centers in 15 strategically located cities throughout
the state. The pediatricians in each city established a treatment center in the accident
room of a hospital, centered around a file of 1500 household products and their poisonous
ingredients. This file was prepared and distributed to the centers by Dr. Robert Grayson,
a Miami pediatrician, and his local committee. Cases of poisoning seen in the centers are
referred to county health departments for follow-up home visits. All data regarding the
case is recorded on forms prepared by the epidemiology staff. This information on these
forms is coded and tabulated, and used as a basis for preventive programs. The first
tabulation from the 267 forms received during 1956, from all the centers in operation is
shown in Table 4
(Summary information for the tabular presentation showed that
poisoning cases were mostly white 80%, less than 4 years of age 78%, and
evenly divided by sex - 48% male. The most common types of poisons were categorized as
internal medicines 37%, petroleum - 19%, insecticides 14%, and cleaning
agents 11%)
. The accumulation of this epidemiologic information on
accidental poisoning in children will be used to aid in the prevention of accidents, and
it is hoped, will serve as a stimulus for interest in general accident prevention
activities.
1957 Annual Report "Finally, the special project concerned
with the epidemiology of accidental poisoning was continued. A total of 1315 reports have
been processed by the epidemiology staff since the inception of the program in July 1956.
..A significant result of the activities of this program in 1957 was the discovery of
several cases of poisoning due to a thallium containing insecticide, which probably would
have gone unnoticed, due to dispersal over the state. The program also furnished
statistical facts for the continuing program of public education in the prevention of
accidental poisoning in children.
Editorial Note In 1962, the State Board of Health, Accident Prevention Program
formally assumed coordination of poison control activities in Florida. By 1971, the SBH
had been transformed into the Division of Health (DH) within the Department of Health and
Rehabilitative Services (HRS) and the Accident Prevention Program was providing liaison to
32 independently operating Poison Control Centers throughout the state. Apparently, In
1974, the legislature appropriated monies to operate a statewide poison information center
out of the University of Florida, but subsequent budget cuts eliminated that initiative.
In the early 1980s there were other attempts to establish statutory authority for
HRS to regulate poison control centers. Between 1985 and 1987 some state funding from the
Childrens Medical Services within HRS was helping to support the Tampa Bay Regional
Poison Center which was certified by the American Association of Poison Control Centers.
In 1989, the legislature authorized establishment of the three center Poison Information
Network. Thanks to a cooperative effort in the early 1990s that included the HRS
Children's Medical Services and the states medical schools we now have full-service
Poison Information Centers in Jacksonville, Tampa and Miami.
Today, Childrens Medical Services, within the Department of Health has statutory
authority to coordinate the activities of the Poison Information Center Network. The
program provides prevention and management information to consumers and health
practitioners throughout Florida on a 24-hours a day basis through a toll-free number
(1-800-282-3171). During 1998, 156,340 calls were handled by poison information
specialists who made 56,000 follow-up calls on exposure cases to determine the health
outcome of the victims. Approximately 60% of poisonings occurred in children under age
six.
Courtesy of Mary Beth Vickers, Mittie Moffett and Maxine Wenzinger at DOH/CMS.
10. Weekly Disease Table - Week 16
County-Confirmed Cases, Sorted Alphabetically by Disease
NR represents years that the disease lacked status as a reportable condition
DISEASE |
1996 TO DATE |
1997 TO DATE |
1998 TO DATE |
3 YEAR AVERAGE
TO DATE |
1998 TOTAL CASES |
1999 TO DATE |
| Amebiasis |
18 |
13 |
14 |
15 |
91 |
12 |
| Anthrax |
0 |
0 |
0 |
0 |
0 |
0 |
| Botulism |
0 |
0 |
0 |
0 |
0 |
0 |
| Brucellosis |
3 |
0 |
1 |
1.3 |
3 |
0 |
| Campylobacteriosis |
260 |
214 |
166 |
213.3 |
977 |
204 |
| Ciguatera |
7 |
2 |
0 |
3 |
7 |
0 |
| Cryptosporidiosis |
31 |
21 |
27 |
26.3 |
203 |
22 |
| Cyclosporiasis |
0 |
1 |
2 |
1 |
7 |
0 |
| Dengue |
0 |
0 |
1 |
0.3 |
7 |
2 |
| Diphtheria |
0 |
0 |
0 |
0 |
0 |
0 |
| E. coli O157:H7 |
6 |
14 |
3 |
7.7 |
56 |
10 |
| E. coli, other (known serotype) |
2 |
2 |
2 |
2 |
12 |
7 |
| Ehrlichiosis, Human |
0 |
0 |
0 |
0 |
1 |
0 |
| Encephalitis, Eastern Equine |
0 |
0 |
0 |
0 |
0 |
0 |
| Encephalitis, St. Louis |
0 |
0 |
0 |
0 |
1 |
0 |
| Encephalitis, other (known organism) |
2 |
5 |
3 |
3.3 |
7 |
2 |
| Encephalitis, post-infectious* |
5 |
3 |
0 |
2.7 |
21 |
1 |
| Giardiasis (acute) |
389 |
349 |
284 |
340.7 |
1634 |
214 |
| Haemophilus influenzae*, invasive |
3 |
6 |
12 |
7 |
42 |
21 |
| Hansens Disease (Leprosy) |
0 |
0 |
3 |
1 |
4 |
0 |
| Hantavirus Infection |
0 |
0 |
0 |
0 |
0 |
0 |
| Hemolytic Uremic Syndrome |
0 |
2 |
0 |
0.7 |
12 |
1 |
| Hemorrhagic Fever |
0 |
0 |
0 |
0 |
0 |
0 |
| Hepatitis A |
94 |
127 |
163 |
128 |
547 |
166 |
| Hepatitis B |
99 |
96 |
104 |
99.7 |
504 |
88 |
| Hepatitis Non-A, Non-B |
19 |
20 |
21 |
20 |
101 |
5 |
| Hepatitis, unspecified |
1 |
0 |
0 |
0.3 |
25 |
2 |
| Histoplasmosis |
2 |
1 |
2 |
1.7 |
17 |
0 |
| Kawasaki |
7 |
6 |
14 |
9 |
53 |
0 |
| Lead Poisoning |
413 |
362 |
452 |
409 |
1850 |
168 |
| Legionellosis |
5 |
5 |
14 |
8 |
47 |
7 |
| Leptospirosis |
0 |
0 |
0 |
0 |
2 |
0 |
| Lyme Disease |
3 |
4 |
5 |
4 |
73 |
5 |
| Malaria |
19 |
18 |
16 |
17.7 |
96 |
22 |
| Measles |
1 |
1 |
1 |
1 |
2 |
1 |
| Meningococcal Disease (N. meningitidis) |
77 |
60 |
46 |
61 |
132 |
36 |
| Meningitis, Group B Streptococci |
7 |
4 |
5 |
5.3 |
21 |
5 |
| Meningitis, Haemophilus influenzae |
1 |
4 |
3 |
2.7 |
11 |
7 |
| Meningitis, Streptococcus pneumoniae |
39 |
30 |
40 |
36.3 |
94 |
39 |
| Meningitis, Listeria monocytogenes |
2 |
0 |
2 |
1.3 |
14 |
6 |
| Meningitis, other bacterial (including unspecified) |
29 |
13 |
16 |
19.3 |
80 |
21 |
| Mercury Poisoning |
1 |
0 |
0 |
0.3 |
4 |
1 |
| Mumps |
2 |
7 |
8 |
5.7 |
11 |
1 |
| Paralytic Shellfish Poisoning |
0 |
0 |
0 |
0 |
0 |
0 |
| Pertussis |
15 |
28 |
11 |
18 |
39 |
7 |
| Pesticide Poisoning |
0 |
0 |
1 |
0.3 |
1 |
1 |
| Plague |
0 |
0 |
0 |
0 |
0 |
0 |
| Poliomyelitis |
0 |
0 |
0 |
0 |
0 |
0 |
| Psittacosis |
0 |
0 |
0 |
0 |
2 |
0 |
| Rabies, Animal |
65 |
89 |
69 |
74.3 |
215 |
53 |
| Reye Syndrome |
0 |
0 |
1 |
0.3 |
1 |
0 |
| Rocky Mountain Spotted Fever |
0 |
1 |
1 |
0.7 |
3 |
1 |
| Rubella, including congenital |
10 |
0 |
1 |
3.7 |
4 |
0 |
| Salmonellosis |
445 |
388 |
384 |
405.7 |
3040 |
423 |
| Shigellosis |
254 |
285 |
370 |
303 |
2349 |
369 |
| Streptococcal Disease, invasive Group A |
0 |
12 |
15 |
9 |
55 |
20 |
| Streptococcus pneumoniae, Drug Resistant |
0 |
66 |
173 |
79.7 |
517 |
208 |
| Tetanus |
1 |
0 |
1 |
0.7 |
3 |
1 |
| Toxic Shock Syndrome |
0 |
0 |
3 |
1 |
4 |
3 |
| Toxoplasmosis |
4 |
2 |
4 |
3.3 |
15 |
4 |
| Typhoid Fever |
6 |
3 |
7 |
5.3 |
16 |
17 |
| Typhus (Louse & Murine) |
0 |
0 |
0 |
0 |
1 |
0 |
| Vibrio cholerae (serogrp O1) |
0 |
0 |
0 |
0 |
0 |
0 |
| Vibrio cholerae (serogrp Non-O1) |
1 |
3 |
1 |
1.7 |
12 |
2 |
| Vibrio vulnificus |
0 |
1 |
1 |
0.7 |
35 |
2 |
| Vibrio other (including unspecified) |
3 |
8 |
4 |
5 |
75 |
9 |
| Yellow Fever |
0 |
0 |
0 |
0 |
0 |
0 |
|