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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 1800’s, 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 state’s 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

Hansen’s 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.

This page was last modified on: 10/25/2012 10:59:42