
A weekly publication by the Bureau of Epidemiology
July 20, 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.
Steve Wiersma, MD, MPH, Acting Bureau Chief and State Epidemiologist
Don Ward, Surveillance Section Administrator, Epi Update Managing Editor
Jason Glisson, BS, Epi Editorial Assistant
Bureau of Epidemiology Frequent Contributors:
|
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.usFor information on diseases and conditions of public health importance go to
MyFlorida.com, click on Health and Human Services, then Consumers--Diseases and Conditions.In this issue:
1. Dr. Steven Wiersma Appointed as Acting Bureau Chief and State Epidemiologist
2. West Nile Virus Found in Georgia Bird; No Human Cases Found
New information from CDC4. Grand Rounds for Tuesday, July 31, 2001
1. Dr. Steven Wiersma Appointed as Acting Bureau Chief and State Epidemiologist
Don Ward, Surveillance Section Administrator
Steven Wiersma, MD, MPH, the Bureau of Epidemiology’s Executive Medical Director and Deputy State Epidemiologist has been officially appointed as the Acting Chief of the Bureau of Epidemiology and Acting State Epidemiologist. This follows the July 19 departure of Dr. Richard Hopkins who had previously served in both roles. Dr. Wiersma, who has been engaged in his present position for four years, brings a broad range of leadership experience to the Bureau. He is a nationally recognized expert in several areas including the epidemiology and prevention of hepatitis, Creutzfeldt Jakob disease and meningitis; international travel medicine; and bioterrorism preparedness and response. Dr. Wiersma serves as the member of a number of distinguished national level panels and policy development bodies. He is strongly committed to "providing the highest quality epidemiology program to the Department of Health." We welcome him to his new role.
2. West Nile Virus Found In Georgia Bird;
No Human Cases FoundLisa Conti, DVM, MPH, State Public Health Veterinarian,
from Barbara Joye,Georgia DHR Office of Communications"A crow infected with West Nile virus was found in Lowndes County, Georgia. This bird was found by a citizen on July 6 and died on July 7. The infection was confirmed today by the Centers for Disease Control and Prevention laboratory. This discovery is not unexpected, since Lowndes County is near Jefferson County, Florida where another infected crow was discovered in June. No West Nile virus infections in humans have been identified in Georgia.
Submitted by Steve Wiersma, MD, MPH, Acting Bureau Chief and State Epidemiologist
The Centers for Disease Control and Prevention has published "Updated U.S.
Public Health Service Guidelines for the Management of Occupational Exposures to HBV, HCV, and HIV and Recommendations for Postexposure Prophylaxis". MMWR 2001;50(RR-1):1-52. http://www.cdc.gov/mmwr/PDF/rr/rr5011.pdfIn addition the following information has been added to the DHQP web site:
1. UCLA interactive website to help in the management of healthcare workers
exposed to patient body fluids. http://www.cdc.gov/ncidod/hip/uclaweb.htm2. Updated information about the 2001-02 influenza season.
http://www.cdc.gov/ncidod/hip/INFECT/flu.htm3. Information about control of rubella outbreaks.
http://www.cdc.gov/ncidod/hip/INFECT/rubella.htm
4. Grand Rounds for Tuesday, July 31, 2001
Melanie Black, MSW, Professional Training Coordinator (reprinted from the previous week)
"Risk Factors for Hepatitis C (HCV) Among STD Clinic Clientele: Miami, Florida"
Weisbord JS1, Trepka MJ2, Zhang G2, Pandya-Smith I2, Whisenhunt S2, Brewer T3.
1 CDC Prevention Fellow assigned to the Miami-Dade County Health Department
2 Office of Epidemiology and Disease Control, Miami-Dade County Health Department
3 University of Miami
11:00 AM – 12:00 PM EST
Dial-in by 11:10 AM at (850) 487-8587 or SunCom 277-8587
Abstract
Background: Hepatitis C virus (HCV) is the most common blood borne infection in the United States. Injection drug use and history of blood transfusions prior to July 1992 are well-known risk factors for hepatitis C. Several studies have shown that HCV is transmitted through sex and through non-IV drug use. However, the extent to which HCV is spread through these routes is debated. The rate of HCV among the general population is 1.8%. Among persons reporting a history of an STD, the prevalence is 6%. We hypothesized that the prevalence of hepatitis infection among patients at the Miami-Dade County Health Department (MDCHC) STD clinic would be higher than the estimated 6%. Therefore, we undertook a study to assess the prevalence of, and risk factors for HCV among this population. We also sought to determine the sensitivity, specificity and positive predictive value (PPV) of screening criteria in this STD clinic clientele.
Methods: Study participants were recruited from the downtown STD clinic of the MDCHD. Any client 18 years or older who presented to the STD clinic for a new problem, was eligible to participate in the study. If interested in being tested for HCV as part of the study, the participant gave informed consent, received education and counseling on HCV, and was interviewed using the questionnaire. The instrument assessed CDC screening criteria, as well as uncertain risk factors such as tattooing, body piercing, snorting drugs, exchanging sex for money, number of lifetime sex partners and history of an STD.
Results: A total of 710 hepatitis tests were performed as part of the study. The overall acceptance rate was 52%. We were unable to analyze twenty-one (3%) of the 710 tests performed due to an insufficient amount of blood. Analysis was performed on 689 completed questionnaires and corresponding laboratory results. The overall prevalence rate of hepatitis infection among our study population was 4.6%. In the multivariate analysis, four risk factors were significantly associated with being hepatitis infection, independent of confounding factors. These variables included IV drug use OR=29.1, 95% CI 7.7,106.5; a history of having spent at least one night in prison/jail OR=3.7, 95% CI 1.1,12.1; sexual contact with an HCV+ person OR=12.4, 95% CI 2.3,66.0, and older age OR=1.1, 95% CI 1.1, 1.2. The sensitivity of the CDC’s routine HCV screening criteria in this population was 69%, specificity 91% and PPV 28%. By adding a history of having spent at least one night in prison/jail to the CDC’s screening criteria, we increased the sensitivity from 69 to 91%, but decreased the specificity to 58%, and the PPV to 18%.
Conclusions: In our STD clinic population we found a prevalence of HCV similar to that found in other studies conducted in STD clinics. Having had a sexual contact with an HCV positive person was independently associated with HCV. We also found that a history of incarceration was independently associated with hepatitis C infection. This relationship should be further studied. CDC’s routine screening criteria were not sensitive in this STD population. Based on the study’s findings, we will consider including a history of incarceration, and sex with an HCV positive person to the routine screening criteria used it the STD clinic of the MDCHC.
Additional Information
Further details regarding the audio-conference call and PowerPoint files will be posted on the Bureau of Epidemiology Intranet web site. Be sure and register online for nursing CEU’s. Information about upcoming topics and presenters will also be posted in the Epi Update. If either of these access points is unavailable to you, please e-mail Melanie Black [Melanie-Black@doh.state.fl.us] or telephone (850) 245-4444 ext. 2448 (SunCom 205-4444 ext. 2448) to request presentation materials.
Important
While we realize you might not always be able to call in at 11:00 AM, it can be distracting to the speaker and others in the audience when participants dial-in throughout the hour. Please try to call in on time and remember to put your phones on mute so as not to disturb others. Thank you for your cooperation.
| DISEASE |
1999 TO |
2000 TO |
3-YEAR |
2000 |
2001 TO |
2001 |
|
Animal Rabies |
94 |
66 |
89.7 |
161 |
119 |
10 |
|
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 |
447 |
478 |
426 |
1026 |
444 |
33 |
|
Ciguatera |
2 |
1 |
3 |
14 |
0 |
0 |
|
Cryptosporidiosis |
57 |
33 |
49.3 |
180 |
39 |
1 |
|
Cyclosporiasis |
2 |
3 |
3.3 |
9 |
25 |
1 |
|
Dengue Fever |
2 |
0 |
1 |
3 |
3 |
0 |
|
Diphtheria |
0 |
0 |
0 |
0 |
0 |
0 |
|
Ehrlichiosis, human |
1 |
0 |
0.3 |
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 |
0 |
|
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 |
5 |
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 |
27 |
28 |
23.7 |
95 |
16 |
1 |
|
Escherichia Coli, other |
11 |
6 |
6.3 |
13 |
6 |
0 |
|
Giardiasis |
500 |
583 |
559.3 |
1466 |
487 |
33 |
|
H. Influenzae Cellulitis |
0 |
0 |
0.7 |
1 |
0 |
0 |
|
H. Influenzae Epiglottitis |
0 |
0 |
0 |
1 |
0 |
0 |
|
H. Influenzae Meningitis |
10 |
1 |
6.3 |
11 |
6 |
0 |
|
H. Influenzae Pneumonia |
3 |
2 |
2.7 |
7 |
12 |
0 |
|
H. Influenzae Prim.Bacteremia |
13 |
21 |
14.7 |
57 |
43 |
0 |
|
H. Influenzae Septic Arthritis |
0 |
0 |
0 |
1 |
0 |
0 |
|
Hantaviris Infection |
0 |
0 |
0 |
0 |
0 |
0 |
|
Hemolytic Uremic Syndrome |
3 |
6 |
4 |
18 |
1 |
0 |
|
Hemorrhagic Fever |
0 |
0 |
0 |
0 |
0 |
0 |
|
Hepatitis A |
323 |
246 |
280.3 |
589 |
275 |
10 |
|
Hepatitis B |
210 |
232 |
212.7 |
525 |
206 |
8 |
|
Hepatitis B (+HbsAg in pregnant women) |
17 |
205 |
74 |
493 |
206 |
22 |
|
Hepatitis, Perinatal Hep B |
1 |
1 |
0.7 |
1 |
4 |
0 |
|
Hepatitis C |
26 |
9 |
11.7 |
19 |
12 |
0 |
|
Hepatitis, Non-A, Non-B |
2 |
5 |
17 |
6 |
2 |
0 |
|
Hepatitis, Other, including unspecified |
9 |
6 |
6.7 |
7 |
4 |
0 |
|
Lead Poisoning |
873 |
568 |
764 |
1219 |
329 |
17 |
|
Legionellosis |
10 |
21 |
17.3 |
51 |
31 |
5 |
|
Leprosy |
2 |
0 |
1.7 |
4 |
0 |
0 |
|
Leptospirosis |
0 |
1 |
0.3 |
2 |
0 |
0 |
|
Listeriosis |
11 |
12 |
7.7 |
32 |
10 |
0 |
|
Lyme Disease |
7 |
10 |
11.3 |
54 |
11 |
1 |
|
Malaria |
41 |
41 |
37.3 |
90 |
26 |
4 |
|
Measles |
1 |
1 |
1.3 |
2 |
0 |
0 |
|
Meningitis, Group B Strep |
8 |
8 |
8.7 |
21 |
8 |
1 |
|
Meningitis, List Monocytogenes |
5 |
2 |
3.7 |
7 |
0 |
0 |
|
Meningitis, Meningococcal |
25 |
18 |
23 |
41 |
36 |
2 |
|
Meningitis, other |
28 |
50 |
36.3 |
110 |
42 |
3 |
|
Meningitis, Strep Pneumoniae |
64 |
59 |
59 |
112 |
38 |
1 |
|
Meningococcemia, disseminated |
36 |
43 |
43 |
80 |
39 |
2 |
|
Mercury Poisoning |
2 |
6 |
2.7 |
11 |
2 |
0 |
|
Mumps |
2 |
2 |
4.3 |
4 |
2 |
0 |
|
Neurotoxic Shellfish Poisoning |
0 |
0 |
0 |
0 |
0 |
0 |
|
Pertussis |
30 |
33 |
28.3 |
48 |
12 |
2 |
|
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 |
1.7 |
2 |
1 |
0 |
|
Rubella, Congenital |
0 |
1 |
0.3 |
1 |
0 |
0 |
|
Salmonellosis |
1041 |
959 |
963.3 |
2755 |
1022 |
88 |
|
Shigellosis |
702 |
670 |
780 |
1292 |
380 |
30 |
|
Smallpox |
0 |
0 |
0 |
0 |
0 |
0 |
|
Staphylococcus Aureus (GISA/VISA) |
0 |
0 |
0 |
0 |
0 |
0 |
|
Staphylococcus Aureus (GRSA/VRSA) |
0 |
0 |
0 |
0 |
0 |
0 |
|
Streptococcal Disease, Invasive Group A |
30 |
69 |
41.7 |
146 |
89 |
6 |
|
Streptococcus Pneumoniae, Invasive |
301 |
584 |
388 |
1147 |
547 |
24 |
|
Tetanus |
1 |
0 |
1 |
1 |
2 |
0 |
|
Toxoplasmosis |
5 |
6 |
5.7 |
12 |
11 |
2 |
|
Trichinosis |
0 |
0 |
0 |
1 |
0 |
0 |
|
Tularemia |
0 |
0 |
0 |
0 |
0 |
0 |
|
Typhoid Fever |
20 |
5 |
11.7 |
12 |
3 |
0 |
|
Vibrio Alginolyticus |
5 |
6 |
4.3 |
15 |
1 |
0 |
|
Vibrio Cholerae Type 01 |
0 |
0 |
0 |
0 |
0 |
0 |
|
Vibrio Cholerae Non-01 |
4 |
3 |
4.3 |
4 |
3 |
0 |
|
Vibrio Fluvialis |
3 |
1 |
2.3 |
2 |
0 |
0 |
|
Vibrio Hollisae |
4 |
3 |
3 |
3 |
0 |
0 |
|
Vibrio Mimicus |
1 |
2 |
2 |
2 |
1 |
0 |
|
Vibrio, other |
1 |
0 |
0.7 |
2 |
0 |
0 |
|
Vibrio Parahaemolyticus |
8 |
4 |
14.3 |
16 |
5 |
0 |
|
Vibrio Vulnificus |
6 |
2 |
6.7 |
13 |
3 |
0 |
|
Yellow Fever |
0 |
0 |
0 |
0 |
0 |
0 |