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EPI UPDATE
A weekly publication by the Bureau of Epidemiology
"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.
For July 30, 1999
Richard S. Hopkins, MD, MSPH, Bureau Chief, State Epidemiologist
Don Ward, Surveillance Section Administrator, Epi Update Managing Editor
Jill H. Parker, MSP, Epi Update Editor
Bureau of Epidemiology Frequent Contributors:
Steven Wiersma, MD, MPH,
Deputy State Epidemiologist |
William J. Bigler, PhD, MS,
Senior Epidemiologist |
Jodi Baldy, MPH,
Biological Scientist IV |
Ursula
E. Bauer, PhD,
Chronic Disease Epidemiologist |
John
Werth, MA,
Bureau Education Coordinator |
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 |
Gérard
Krause, MD, DTMH,
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.
The Department of Health has a home on the World Wide Web at --- http://www.doh.state.fl.us
In this issue:
1. Vaccination of Infants Born to Hepatitis B Surface Antigen (HBsAg)
Negative Mothers
2. Editors' Corner
3. CDC Slide Series Entitled "Hepatitis A to E"
4. University of North Florida Plans MPH Program
5. Florida Past: Committee Censures County Pest House
6. Weekly Disease Table: Week 29
1. Vaccination of Infants Born to Hepatitis B Surface Antigen (HBsAg)
Negative Mothers
Information Submitted by Don Ward, Surveillance Section Administrator
In recent weeks, the American Academy of Pediatrics (AAP) and the Centers for Disease
Control have published separate guidelines on the use of thimerosal-containing vaccines.
The CDC guidelines address the vaccination of infants born to hepatitis B surface antigen
(HBsAg) negative mothers who belong to populations and groups with a high risk of early
childhood hepatitis B virus infection. The following information was excerpted from IAC
Express, Issue Number 98, July 20, 1999).
"When asked by IAC staff to clarify the difference between the United States
Public Health Service recommendation and the AAP recommendation, Dr. Harold S. Margolis,
Chief of the Hepatitis Branch of the Centers of Disease Control and Prevention, made the
following comment:
'CDC recommends that infants born to HBsAg negative women
who belong to populations and groups that have high risk of early childhood hepatitis B
virus infection be vaccinated as newborns. Although routine newborn vaccination is not the
current recommendation of the AAP, it is still a recommendation of the Advisory Committee
on Immunization Practices. However, if a hospital chooses to follow the AAP recommendation
and delay vaccination of these high-risk infants until two to six months, they should make
sure these infants receive their first dose by two months of age, even if COMVAX is not
available. This is definitely a situation in which the larger risk of not vaccinating
children far outweighs the much smaller theoretical risk of cumulative exposure to
thimerosal-containing vaccines over the first six months of life.'
"IAC EDITORS' NOTE: COMVAX is a thimerosal-free hepatitis B vaccine that also
contains a Hib component. It is licensed for use beginning at six weeks of age. It is also
anticipated that thimerosal-free, single-antigen hepatitis B vaccines will be available
during the month of September.
"The new CDC guidelines, which were released on July 15, 1999, and appear today on
the National Immunization Program's website, stress the importance of continuing to
vaccinate infants born to HBsAg negative women who belong to populations and groups that
have high risk of hepatitis B virus infection as well as infants born to HBsAg positive
mothers and to mothers whose status is not known.
"CDC GUIDELINES SAY TO VACCINATE THESE GROUPS OF INFANTS AT BIRTH:
"1. INFANTS BORN TO HBsAg POSITIVE MOTHERS
All infants born to HBsAg positive mothers need hepatitis B vaccine and hepatitis B
immune globulin (HBIG) within 12 hours of birth.
"2. INFANTS BORN TO MOTHERS WHOSE HBsAg STATUS IS UNKNOWN
All infants born to mothers whose HBsAg status is still unknown 12 hours after birth
need hepatitis B vaccine at that time. Draw the mother's blood upon admission and send it
to the lab ASAP. If the results cannot be obtained by 12 hours after the infant's birth,
the infant should be vaccinated at that time. If the mother is found to be HBsAg positive,
administer HBIG to the infant ASAP (no later than 7 days after birth).
"3. INFANTS BORN TO HBsAg NEGATIVE MOTHERS BELONGING TO POPULATIONS OR GROUPS THAT
HAVE HIGH RISK OF EARLY CHILDHOOD HBV INFECTION
All infants born to HBsAg negative mothers belonging to populations or groups that have
high risk of early childhood HBV infection need hepatitis B vaccine prior to discharge.
These high-risk groups include, but are not limited to, Asian Pacific Islanders, immigrant
populations from countries in which HBV is of high or intermediate endemicity (see CDC's
"Health Information for International Travel, 1999"), and households with
persons with chronic HBV.
"NOTE: The AAP has no specific recommendation for infants who are born to women
belonging to groups or populations at high risk of early childhood hepatitis B virus
infection. Because of this, some hospitals are treating these high-risk infants no
differently from infants with low risk of infection and have written policies to delay
these infants' hepatitis B vaccination until 6 months of age.
"CDC recommends that if your hospital chooses to follow the recommendation of the
AAP, you should vaccinate all children who are born to HBsAg negative women in high-risk
communities at two months of age with thimerosal-free vaccine (COMVAX). However, if
thimerosal-free vaccine is not available, you should make sure that these high-risk
infants receive hepatitis B vaccine no later than two months of age, even if only
thimerosal-containing vaccine is available to you (Recombivax HB and Engerix-B).
"Do not wait until these at-risk children are six months old to give dose #1. The
need for these infants to receive hepatitis B vaccine by two months of age far outweighs
the much smaller theoretical risk of cumulative exposure to thimerosal-containing
vaccines.
"The complete guidelines, "Implementation Guidance for Immunization Grantees
During the Transition Period to Vaccines Without Thimerosal," can be downloaded
from CDC's.
"If you are unable to download these guidelines, call the immunization program
manager at your state health department. Your state health department received these
guidelines on July 15, 1999.
"CDC also has other important information on thimerosal and vaccines on
its website."
2. Editors' Corner
- Errata for last week's Epi Update (July 23, 1999), Article #3: Notifiable Disease
Rule Change Information to Be Sent to 1200 Clinical Laboratories in Florida:
Two errors appeared in an attachment (Current Reportable
Diseases/Conditions) to this article. The corrected version of the document is
attached below.
Current List of Reportable Diseases/Conditions in Florida
Epi Update Editor Change: As a reminder, please send future Epi Update
submissions to Jill Parker. Thank you.
3. CDC Slide Series Entitled "Hepatitis A to E"
Information Submitted by Jill Parker, MSP, Policy Analyst
The following information was summarized from IAC Express, Issue Number 101,
July 27, 1999.
A slide series entitled "Epidemiology and Prevention of Viral Hepatitis A to
E: An Overview" is offered on the Centers for Disease Control (CDC) website.
4. University of North Florida Plans MPH Program
Information Submitted by Richard S. Hopkins, MD, MSPH, Bureau Chief, State
Epidemiologist
The College of Health at the University of North Florida in Jacksonville is
developing a new Master of Public Health degree (MPH) program to begin next
year. The program will be oriented to working individuals, with off-campus
courses and advising available. Information regarding the planned program is
provided in the attached document.
5. FLORIDA PAST Committee Censures County Pest House
William J. Bigler, PhD
In the late 1800s, it was common for some communities to isolate cases of
infectious diseases in Pest Houses or isolation hospitals that were located away from the
general populace. When the State Board of Health came into existence, these facilities
were constructed at quarantine stations serving major ports, and many of the states
larger cities followed suit. It is not often we get a glimpse of the problems associated
with the operational side of this type of disease control practice. The following report
on sanitary conditions at the Orlando/Orange County Pest House circa 1910 was taken from
the archives of the Orange County Historical Society. It was kindly submitted by Mr. Bill
Toth, Epidemiologist, Orange County Health Department .
"We [sic] the undersigned committee appointed by the chairman to
investigate conditions at the County Pest House, have to report that we visited the Pest
House this morning and made as thorough an examination as possible, without entering the
building, which we could not do as there were five (5) patients in the house with
smallpox. We found the sanitary arrangements in a terrible condition, the drainage pipe
leading from the toilets and kitchen to the cesspool in such a shape that all the stuff
backs up and is deposited under the different parts of the building, causing a bad odor
and attracting swarms of flies and other insects. We found discarded clothing of the
patients lying all around the yard, also the discarded bedding.
"We questioned Mr. Goss, the man in charge, and got the following information as
to how the affairs of the institution are conducted: He is in charge, without any help
whatever; he is nurse, cook and everything else at a salary of $15.00 per month and boards
himself; he is unable to get any help so that he can get any laundry work done at the
hospital and in fact, none is ever done. We believe Mr. Goss to be doing all in his power,
with the limited means he is furnished with, to care for the patients, but we wish to
censure whoever is in control of the County Pest House for the unsanitary conditions
existing there, and for the criminal neglect of the unfortunate people who are obliged to
be taken there. And we recommend that the place be put in a sanitary condition at once.
J.D. Gill Chairman
Charles D. Prat
Hull Hurt
P.S. Heslington
G.L. Sands"
6. Weekly Disease Table - Week 29
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 |
39 |
31 |
32 |
34 |
91 |
27 |
| Anthrax |
0 |
0 |
0 |
0 |
0 |
0 |
| Botulism |
0 |
0 |
0 |
0 |
0 |
0 |
| Brucellosis |
5 |
0 |
1 |
2 |
3 |
0 |
| Campylobacteriosis |
589 |
505 |
389 |
494.3 |
975 |
482 |
| Ciguatera |
7 |
2 |
6 |
5 |
7 |
2 |
| Cryptosporidiosis |
74 |
56 |
61 |
63.7 |
203 |
63 |
| Cyclosporiasis |
154 |
56 |
5 |
71.7 |
6 |
2 |
| Dengue |
0 |
1 |
1 |
0.7 |
5 |
2 |
| Diphtheria |
0 |
0 |
0 |
0 |
0 |
0 |
| E. coli O157:H7 |
11 |
29 |
16 |
18.7 |
56 |
28 |
| E. coli, other (known serotype) |
2 |
5 |
2 |
3 |
12 |
12 |
| Ehrlichiosis, Human |
4 |
2 |
0 |
2 |
1 |
2 |
| Encephalitis, Eastern Equine |
0 |
0 |
0 |
0 |
0 |
0 |
| Encephalitis, St. Louis |
0 |
0 |
0 |
0 |
2 |
0 |
| Encephalitis, other (known organism) |
3 |
6 |
3 |
4 |
7 |
2 |
| Encephalitis, post-infectious* |
11 |
5 |
5 |
7 |
21 |
3 |
| Giardiasis (acute) |
832 |
727 |
634 |
731 |
1636 |
528 |
| Haemophilus influenzae*, invasive |
11 |
11 |
24 |
15.3 |
45 |
28 |
| Hansens Disease (Leprosy) |
1 |
0 |
3 |
1.3 |
4 |
2 |
| Hantavirus Infection |
0 |
0 |
0 |
0 |
0 |
0 |
| Hemolytic Uremic Syndrome |
0 |
2 |
3 |
1.7 |
12 |
3 |
| Hemorrhagic Fever |
0 |
0 |
0 |
0 |
0 |
0 |
| Hepatitis A |
232 |
226 |
278 |
245.3 |
539 |
345 |
| Hepatitis B |
271 |
194 |
201 |
222 |
466 |
223 |
| Hepatitis Non-A, Non-B |
41 |
45 |
45 |
43.7 |
95 |
5 |
| Hepatitis, unspecified |
2 |
3 |
4 |
3 |
26 |
9 |
| Histoplasmosis |
3 |
2 |
8 |
4.3 |
17 |
0 |
| Lead Poisoning |
1043 |
722 |
901 |
888.7 |
1805 |
358 |
| Legionellosis |
17 |
14 |
21 |
17.3 |
48 |
15 |
| Leptospirosis |
0 |
0 |
1 |
0.3 |
2 |
0 |
| Lyme Disease |
6 |
10 |
18 |
11.3 |
71 |
12 |
| Malaria |
39 |
37 |
31 |
35.7 |
96 |
45 |
| Measles |
1 |
3 |
2 |
2 |
2 |
1 |
| Meningococcal Disease (N. meningitidis) |
121 |
93 |
78 |
97.3 |
133 |
66 |
| Meningitis, Group B Streptococci |
13 |
10 |
10 |
11 |
22 |
8 |
| Meningitis, Haemophilus influenzae |
4 |
6 |
8 |
6 |
12 |
10 |
| Meningitis, Streptococcus pneumoniae |
62 |
48 |
54 |
54.7 |
96 |
68 |
| Meningitis, Listeria monocytogenes |
4 |
2 |
4 |
3.3 |
13 |
5 |
| Meningitis, other bacterial (including
unspecified) |
59 |
33 |
33 |
41.7 |
75 |
42 |
| Mercury Poisoning |
5 |
2 |
0 |
2.3 |
4 |
2 |
| Mumps |
4 |
8 |
9 |
7 |
11 |
2 |
| Paralytic Shellfish Poisoning |
0 |
0 |
0 |
0 |
0 |
0 |
| Pertussis |
45 |
41 |
22 |
36 |
39 |
32 |
| Pesticide Poisoning |
1 |
0 |
1 |
0.7 |
1 |
3 |
| Plague |
0 |
0 |
0 |
0 |
0 |
0 |
| Poliomyelitis |
0 |
0 |
0 |
0 |
0 |
0 |
| Psittacosis |
0 |
0 |
1 |
0.3 |
2 |
0 |
| Rabies, Animal |
121 |
168 |
118 |
135.7 |
215 |
98 |
| Rocky Mountain Spotted Fever |
1 |
2 |
1 |
1.3 |
2 |
2 |
| Rubella, including congenital |
10 |
0 |
3 |
4.3 |
4 |
0 |
| Salmonellosis |
1018 |
896 |
964 |
959.3 |
3038 |
1120 |
| Shigellosis |
736 |
588 |
1032 |
785.3 |
2343 |
754 |
| Streptococcal Disease, invasive Group A |
0 |
22 |
27 |
16.3 |
58 |
50 |
| Streptococcus pneumoniae, Drug
Resistant |
1 |
123 |
281 |
135 |
492 |
339 |
| Tetanus |
1 |
0 |
2 |
1 |
3 |
1 |
| Toxic Shock Syndrome |
0 |
1 |
3 |
1.3 |
4 |
3 |
| Toxoplasmosis |
5 |
3 |
6 |
4.7 |
15 |
7 |
| Typhoid Fever |
11 |
4 |
10 |
8.3 |
16 |
20 |
| Typhus (Louse & Murine) |
0 |
1 |
0 |
0.3 |
0 |
0 |
| Vibrio cholerae (serogrp O1) |
0 |
0 |
0 |
0 |
0 |
0 |
| Vibrio cholerae (serogrp Non-O1) |
1 |
5 |
6 |
4 |
11 |
5 |
| Vibrio vulnificus |
6 |
5 |
13 |
8 |
35 |
6 |
| Vibrio other (including unspecified) |
11 |
18 |
42 |
23.7 |
73 |
22 |
| Yellow Fever |
0 |
0 |
0 |
0 |
0 |
0 |
*Haemophilus influenzae can be the agent responsible
for disease under three of the reportable conditions listed-:
"Haemophilus influenzae, invasive" and
under "Encephalitis, post infectious." Cases of Haemophilus influenzae
meningitis are reported under
"Meningitis, H. influenzae."
Editors' Note: Kawasaki and Reye Syndrome were deleted from
the weekly disease table since cases are no longer required to be reported.
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