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Florida Department of Health
EPI UPDATE

A weekly publication by the Bureau of Epidemiology

For April 5, 2000

"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

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 Carina Blackmore, MS Vet. Med., PhD,

Zuber Mulla, MSPH,

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

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.

In this issue:

1. Notice: 1999 Disease Report Deadline is Friday, April 28th

2. Announcement: Communicable Disease Epidemiology Regional Training to be Held May 9th -10th in Lake City

3. Necrotizing Fasciitis Due to Photobacterium damsela in a Man Lashed by a Stingray

4. New Meningococcal Group C Vaccine Showing Success in the UK

5. Hepatitis C Virus One-Pager

6. Announcement: CDC Toll-Free International Travelers' Information Line

7. Epidemiology Grand Rounds Follow-up: Statistical Process Control

8. Announcement: A.G. Holley State Hospital Grand Rounds for April 2000

9. Weekly Disease Table: Week 13

1. Notice: 1999 Disease Report Deadline is Friday, April 28th

The Centers for Disease Control and Prevention (CDC) established May 12, 2000 as the deadline for 1999 disease reports from state epidemiology offices. County health departments should send all corrected and deleted records to the Bureau of Epidemiology by close of business Friday, April 28, so that the Bureau of Epidemiology may compile a complete report for CY 1999. Also, counties reporting to the Bureau electronically should send their final and complete week 53 reports (temp.zip) by close of business on April 28th, 2000.

We thank you in advance for your attention and support in this matter.

2. Announcement: Communicable Disease Epidemiology Regional Training to be Held May 9th -10th in Lake City

Melanie Black, LCSW, Bureau of Epidemiology

The Bureau of Epidemiology is pleased to announce the next training program for county health department staff members, which will be held in Lake City, Florida on May 9-10, 2000. The target audiences for the regional training programs are county health department staff members and partner agencies who are involved in epidemiology. County health directors and administrators are welcome to attend.

This program will provide an overview of epidemiological principles such as disease reporting, disease surveillance and communicable disease outbreak investigation. On-line registration is now available through Friday, April 28, 2000 on the Bureau of Epidemiology Intranet web page.

Space is limited so please register as soon as possible.

Additional information will be provided in the Epi Update and on the Bureau of Epidemiology Web page. We intend to offer training programs in other regions of the state this year. If you are interested in hosting one of the training sessions or have questions related to this program, please feel free to contact Melanie Black, Professional Training Coordinator for the Bureau of Epidemiology.

3. Necrotizing Fasciitis Due to Photobacterium damsela in a Man Lashed by a Stingray

The following letter appeared in the New England Journal of Medicine on March 16, 2000 (Vol. 342, No.11):

To the Editor:

A variety of vibrio species can cause gastroenteritis, wound infections, and primary septicemia as well as illness among marine organisms. (1,2) Photobacterium damsela (formerly Vibrio damsela) is similar to other species of the genus vibrio, which are halophilic, gram-negative bacilli. (3) We describe a 43-year-old man with necrotizing fasciitis as a result of a laceration inflicted by a stingray while he was stepping off his sailboat in Tampa Bay, Florida.

The patient first presented to the emergency department of another hospital, where the wound to his right tibialis anterior muscle was irrigated and sutured approximately six hours after admission. Antimicrobial therapy was not prescribed, and the patient was released from the emergency department. Three days later, fever developed and erythema appeared along the wound margins, followed within the next 24 hours by the appearance of a 2.5-cm, malodorous, fluctuant lesion. The patient then came to our emergency department. His oral temperature was 39°C, his white-cell count was 15,500 per cubic millimeter, and he had a septic appearance. There was necrotizing fasciitis of his right tibialis anterior muscle. Administration of intravenous doxycycline (400 mg per day), cefazolin (3 g per day), and tobramycin (6.5 mg per kilogram of body weight per day) was begun and was continued until his discharge, seven days later. Deep surgical debridement of skin, fascia, and muscle was performed on an emergency basis, and the wound was again debrided in the operating room the following morning. Wound cultures yielded P. damsela, which was sensitive to our battery of antibiotics for gram-negative organisms, with the exception of amikacin, to which it had intermediate sensitivity. As an outpatient he received oral doxycycline and cephalexin for two weeks. Subsequently, he required physical therapy and a split-thickness skin graft for wound closure.

P. damsela is a pathogen in both immunocompromised and healthy hosts and can cause rapid, fulminant infection with a high rate of death. (2,4) Clinicians should be aware of this organism and other vibrio species, particularly in cases of wounds exposed to salt or brackish water or wounds inflicted by marine animals living in such an environment.

Gerard R. Barber, R.Ph., M.P.H.
Jeffrey S. Swygert, M.D.
Lakeland Regional Medical Center
Lakeland, FL 33804

References

1. Morris JG Jr, Black RE. Cholera and other vibrioses in the United States. N Engl J Med 1985;312:343-50.

2. Shin JH, Shin MG, Suh SP, Ryang DW, Rew JS, Nolte FS. Primary Vibrio damsela septicemia. Clin Infect Dis 1996;22:856-7.

3. McLaughlin JC. Vibrio. In: Murray PR, Baron EJ, Pfaller MA, Tenover FC, Yolken PH, eds. Manual of clinical microbiology. 6th ed. Washington, D.C.: American Society for Microbiology, 1995:465-76.

4. Fraser SL, Purcell BK, Delgado B Jr, Baker AE, Whelen AC. Rapidly fatal infection due to Photobacterium (Vibrio) damsela. Clin Infect Dis 1997;25:935-6.

4. New Meningococcal Group C Vaccine Showing Success in the UK

Steven Wiersma, MD, MPH

A new conjugate vaccine against serogroup C meningococcal disease has been tested in the UK and, according to the following ProMed (serial online) posts, is showing promising results. This vaccine, technically similar to the HIB vaccine, is effective for use in young children and is designed for serogroup C disease, which accounts for approximately 45% of meningococcal disease in the U.S.

 

MENINGOCOCCUS GROUP C VACCINE SUCCESSFUL - UK

*********************************************

Date: Wed, 29 Mar 2000 00:03:54 -0500

From: Marjorie P. Pollack <pollackmp@mindspring.com>

Source: News media, 28 Mar 2000 [edited]

A new vaccine against meningitis introduced five months ago has slashed cases of the infectious disease in Britain by 75 percent among babies and teenagers, the government said Tuesday. "This is welcome news for parents and children. We are the first country in the world to have this new vaccine. It puts the UK in the forefront of tackling this devastating disease," Public Health Minister Yvette Cooper said in a statement.

The vaccine is for meningitis C, which accounts for 40 percent of cases of the disease and claimed the lives of 150 people in Britain in 1998. So far, the campaign has been limited to the highest risk groups because of short supplies of the vaccine, manufactured by Wyeth Vaccines, part of American Home Products Corp (AHP.N). Britain hopes to extend the program to all children under five by the summer.

"I hope that all parents take up the chance to have their children protected when their invitations arrive. A second vaccine has been licensed and is now being distributed. We aim to offer the vaccine to all young people under 18 by the autumn -- a target of 15 million children," Cooper said.

The Department of Health figures show that from December to March, cases [caused by group C meningococci] in 15- to 17-year-olds fell by 77 percent. Instead of the 70 cases expected by government health officials there have been only 16 confirmed cases. The numbers were equally good for babies under one year old. From the beginning of January to the middle of March only 10 cases were reported from an expected 37 cases, a drop of 73 percent.

The UK is [reported to be] the first country that has it available for patients. The drug was approved by the U.S. Federal Drug Administration in February but it is not yet readily available in the United States.

When the vaccine was tested in a clinical trial of 19 000 children it was 100 percent effective in preventing the disease.

[Byline: Emma Ducasse]

MENINGOCOCCUS GROUP C VACCINE - UK: CORRECTION

**********************************************

Date: 3 Apr 2000

From: Pratt, Douglas R. <prattd@cber.fda.gov>

In [an earlier ProMED-mail posting cited above] it was erroneously reported that the meningococcal conjugate manufactured by Wyeth-Lederle has been licensed in the U.S. Please note that the meningococcal type C conjugate vaccine manufactured by Wyeth-Lederle, currently being used in the U.K., is NOT licensed in the U.S. The correspondent apparently has confused the meningococcal C conjugate vaccine with a 7-valent pneumococcal conjugate vaccine, Prevnar, also manufactured by Wyeth-Lederle. The meningococcal C conjugate vaccine served as a control for Prevnar in the definitive

efficacy trial, however, the preventive efficacy of the meningococcal C vaccine was not evaluated. Prevnar was shown to be highly efficacious in preventing invasive pneumococcal disease, and was licensed 17 Feb 2000 in the US for use in infants and toddlers.

--

R. Douglas Pratt, M.D., M.P.H.

Division of Vaccines and Related Products Applications

Office of Vaccines Research and Review

Center for Biologics Evaluation and Research

Food and Drug Administration

Thanks to Dr. Pratt for setting the record straight concerning meningococcal type C conjugate vaccines in the US. It is noteworthy that there is a licensed quadrivalent capsular polysaccharide vaccine available in the US that provided coverage for type C disease. Dr. Pratt was also kind enough to provide a URL for a transcript of a public meeting conducted during September of 1999 at which the epidemiology of meningococcal disease for the US vs. Europe and technical issues related to evaluation of conjugate meningococcal vaccines were discussed at length. This is a very long document, but those with a special interest may find it at:

<http://www.fda.gov/ohrms/dockets/ac/99/transcpt/3544t2.rtf>. - Mod.ES]

es/ds

Visit ProMED-mail's web site at <http://www.promedmail.org>.

 

5. Hepatitis C Virus One-Pager

Dolly Katz, PhD, DOH, Bureau of Epidemiology

Hepatitis C virus (HCV) typically produces a symptomless liver infection that can lead, over decades, to severe liver disease, including cirrhosis and liver cancer. Most of those infected are unaware that they have the disease, and may serve as unknowing sources of transmission. HCV is the most common chronic bloodborne infection in the United States. An estimated 3.9 million Americans (1.8% of the population) have been infected with HCV, and most of those have chronic infections. The virus is transmitted primarily through direct injection of contaminated blood, most commonly by injecting drug use and, before 1992, by blood transfusion. No vaccine is available and no medications have proven effective in preventing infection after exposure, including exposure from accidental needle sticks.

After the acute infection, which produces jaundice or mild, nonspecific symptoms in 20-30% of patients, most people (75-85%) develop chronic infections, characterized by the persistence of viral RNA in the blood. Of those chronically infected, 60-70% have continuous or intermittent elevations of the liver enzyme alanine aminotransferase (ALT), indicating chronic active liver disease. Chronic cases may be diagnosed during blood donor screenings, from liver function tests performed for routine physical exams, or after onset of liver disease. The disease progresses very slowly; within 20 to 30 years after infection, 10% to 20% of those with chronic disease will develop cirrhosis, and 1% to 5%, liver cancer. HCV causes an estimated 8,000 to 10,000 deaths a year in the U.S., with more than $600 million in associated medical and work-loss costs.

Based on national estimates, approximately 220,000 Floridians are chronically infected with the hepatitis C virus, and approximately 2,000 new cases occur each year. However, because the initial stages of hepatitis C infection are either asymptomatic or associated only with mild symptoms, most new infections are not diagnosed. Hepatitis C was made a notifiable disease in Florida in July 1999. Prior to that time, all Hepatitis C cases were classified as hepatitis non-A/non-B, of which about 100 were reported each year. By the end of January 2000, only 49 confirmed new cases of hepatitis C had been reported to the Florida Department of Health for the last six months of 1999. Demographically, Florida cases are similar to the rest of the U.S.: incidence begins to rise in the teen years and peaks in 30-39 year olds, with similar rates among males and females.

The infection is diagnosed by detection of hepatitis C virus antibodies in blood, usually with an enzyme immunoassay (EIA) followed by a confirmatory recombinant immunoblot assay (RIBA) or polymerase chain reaction (PCR). Diagnosis can also be made by detection of viral RNA using gene amplification techniques.

Since screening procedures for blood donors were instituted in the early 1980s, the predominant mode of HCV transmission in the U.S. has been injecting drug use, which accounts for an estimated 60% of new cases. Beginning in 1989, the estimated incidence of HCV infection dropped dramatically in the U.S., from an average of 230,000 new infections a year before 1989 to 36,000 in 1996. The decrease is correlated with a decline in cases among injecting drug users; the reasons for the decline are unclear, but may be related to risk-reduction behaviors among illegal drug users or to saturation of the injecting drug user population.

Although the prevalence of HCV infection is higher among persons with multiple sexual partners (9% among persons with 50 or more lifetime sexual partners), the risk of transmission between long-term steady partners is low. The risk of transmission from mother to child during birth is 5%-6%. Transmission among household contacts has been reported, but is uncommon. While hepatitis B is a well-recognized occupational hazard for health care workers, HCV appears to be less of a threat. Rates of HCV infection in health care workers are the same as or lower than rates in the general population, although unintentional needle stick injury still poses a risk. Previous studies of transmission have found no increased risk associated with medical, surgical or dental procedures; tattooing; acupuncture; ear piercing; or foreign travel, an indication either that these are not risk factors or that the excess risk is too low to detect.

Treatment with alpha-interferon and other drugs has low to moderate effectiveness in reducing ALT to normal levels and eradicating detectable viral RNA in serum. Treatment effectiveness depends greatly on the genotype of the virus; the most common genotype in the U.S is 1, which has the lowest response rate to therapy. Management of HCV infection also includes avoidance of alcohol and vaccination against hepatitis A and B. The effectiveness of treatment of infected persons in preventing transmission is unknown.

No vaccines are currently available to prevent HCV infection, and no medication has been approved for post-exposure prophylaxis. Prevention of HCV infection in the population currently depends on :

  • screening of blood and tissue donors;
  • risk-reduction counseling and services for high-risk groups like injecting drug users;
  • screening (identification, testing, and counseling) of persons at high risk for HCV infection;
  • improved population-based surveillance for acute and chronic HCV infection.

Screening programs should include persons who

  • ever, even once, injected illegal drugs, including those who injected once or a few times many years ago and do not consider themselves drug users;
  • received clotting factor concentrates produced before 1987;
  • were ever on chronic (long-term) hemodialysis;
  • have persistently abnormal ALT levels;
  • received organ transplants before July 1992;
  • received transfusions of blood or blood components before July 1992;
  • were notified that they received blood from a donor who later tested positive for HCV infection;
  • were born to HCV-positive women;
  • are healthcare, emergency medical, or public safety workers who had needle stick, sharps, or mucosal exposures to HCV-positive blood.

 

References 1/20/00

1. Centers for Disease Control and Prevention. Recommendations for prevention and control of hepaatitis C virus (HCV) infection and HCV-related chronic disease. MMWR 1998;47(No. RR-19).

6. Announcement: CDC Toll-Free International Travelers' Information Line

The following information was excerpted from IAC Express (serial online), Issue Number 154, April 3, 2000

April 3, 2000

CDC NOW HAS A TOLL-FREE TELEPHONE NUMBER FOR ITS INTERNATIONAL TRAVELERS' INFORMATION LINE

The Centers for Disease Control and Prevention (CDC) has a new toll-free number for its International Travelers' Information line. Callers can access recorded voice messages on diseases specific to international travel, request a list of publications on international travel available from CDC's automated fax information service, or order a copy of "Health Information for

International Travel" (the "Yellow Book").

The new toll-free number is (877) 394-8747 (877-FYI-TRIP). Travelers' health information can also be obtained from the National Center for Infectious Diseases' Travelers' Health website at: http://www.cdc.gov/travel

7. Epidemiology Grand Rounds Follow-up: Statistical Process Control

After our March Grand Rounds session, many participants had questions about the use of statistical process control. Heidi Orme, MSPH, provided the following list of references regarding this analytical method.

REFERENCES

 

Berger, R.W., Hart, T.H. Statistical Process Control (A Guide for Implementation). New York, N.Y.: Marcel Dekker, Inc. 1986

Doty, L.A. Statistical Process Control. New York, N.Y.: Industrial Press, Inc.; 1991.

Ishikawa, K. Guide to Quality Control. 2nd ed. New York, N.Y.: Quality Resources; 1986.

Kume, H. Statistical Methods for Quality Improvement. Japan: 3A Corporation; 1985.

Oakland, J.S. Statistical Process Control (A Practical Guide). London: Heinemann; 1986.

Oakland, J.S. Statistical Process Control (A Really Practical Guide). 3rd ed. Oxford: Butterworth-Heinemann; 1996.

Wetherill, G.B., Brown, D.W. Statistical Process Control (Theory and Practice). New York, N.Y.: Chapman and Hall; 1991.

 

8. Announcement: A.G. Holley State Hospital Grand Rounds for April 2000

Topic: HIV Epidemiology Update

TB Update-1999 Review and Priorities for the Future

Speakers: Spencer Lieb, M.P.H., Epidemiologist, Florida Department of Health

Bureau of HIV/AIDS and Panel from the Florida Department of Health,

Bureau of TB & Refugee Health

Date: Wednesday, April 12, 2000

Place: Auditorium

A. G. Holley State Hospital, 1199 W. Lantana Rd., Lantana, FL

Time: 10:00 a.m. - 12:00 p. m. (EST)

Objectives: By the completion of the presentation, the participants will be able to:

  • Compare the HIV/AIDS epidemic in the context of the national and global epidemics.
  • Explain the magnitude and direction of the HIV/AIDS epidemic in Florida, including historic and current trends in morbidity and mortality.
  • Identify recent shifts in the demographics of the epidemic.
  • Demonstrate an understanding of the strengths and limitations of the HIV/AIDS data.

Lunch: Provided free - 12:00 p.m. (reservations required by 4/11 at 10 a.m.)

Sponsors: A. G. Holley State Hospital, American Lung Association of Florida, Inc.,

Florida Department of Health-Bureau of TB and Refugee Health, Florida Bureau of HIV/AIDS and the Everglades Area Health Education Center.

Credits: A. G. Holley is an approved Continuing Education provider by the Florida Board of Nursing, Provider # FBN 2137 - 2 contact hours (on-site attendees only). Approved continuing education credits for laboratorians will be provided through the Bureau of Laboratories, Provider # J.P. 0000110 - 2 contact hours (on-site attendees only).

Teleconference: For those unable to attend in person, you may listen to the lecture via a 30 line conference call # reserved for this purpose. Long distance charges may apply to your phone. Those able to use Suncom will be billed at the state rate of about 7 cents per minute. Please put your phone on mute so you won't disturb the speaker. Questions will be allowed at the end. If available, copies of speaker slides will be e-mailed to you when you register.

Future Topics: The next scheduled A.G. Holley Grand Rounds will be on Thursday, May 11, 2000. Lennox Jeffers, MD, University of Miami, School of Medicine will present "Treating Hepatitis C."

9. Weekly Disease Table: Week 13

County-Confirmed Cases, Sorted Alphabetically by Disease

(NR represents years that the disease lacked status as a reportable condition)

DISEASE

1997 TO DATE

1998 TO DATE

1999 TO DATE

3 YEAR AVERAGE

TO DATE

1999 TOTAL CASES

2000 TO DATE

Amebiasis

8

7

4

6.3

66

0

Anthrax

0

0

0

0

0

0

Botulism

0

0

0

0

4

0

Brucellosis

0

1

0

0.3

3

0

Campylobacteriosis

166

120

160

148.7

987

146

Ciguatera

2

0

0

0.7

2

0

Cryptosporidiosis

15

23

11

16.3

175

9

Cyclosporiasis

0

2

0

0.7

5

0

Dengue

0

1

1

0.7

5

2

Diphtheria

0

0

0

0

0

0

E. coli O157:H7

12

3

8

7.7

54

7

E. coli, other (known serotype)

2

2

5

3

16

2

Ehrlichiosis, Human

0

0

0

0

2

0

Encephalitis, Eastern Equine

0

0

0

0

2

0

Encephalitis, St. Louis

0

0

0

0

4

0

Encephalitis, other (known organism)

4

3

2

3

5

2

Encephalitis, post-infectious1

2

0

1

1

14

1

Giardiasis (acute)

274

230

178

227.3

1319

194

Haemophilus influenzae, invasive1

4

14

10

9.3

48

13

Hansen’s Disease (Leprosy)

0

2

0

0.7

3

0

Hantavirus Infection

0

0

0

0

0

0

Hemolytic Uremic Syndrome

2

0

1

1

7

2

Hemorrhagic Fever

0

0

0

0

0

0

Hepatitis A

107

128

138

124.3

800

119

Hepatitis B

68

59

64

63.7

534

71

Hepatitis C2

NR

NR

7

NR

57

7

Hepatitis Non-A, Non-B

14

17

0

10.3

10

5

Hepatitis, perinatal B2

NR

NR

0

NR

 

0

Hepatitis, unspecified

0

0

1

0

16

4

Hepatitis, +HBsAg, pregnant woman2

NR

NR

1

NR

236

45

Lead Poisoning

268

336

93

232.3

896

166

Legionellosis

4

12

6

7.3

28

10

Leptospirosis

0

0

0

0

1

0

Listeriosis2

NR

NR

4

NR

32

5

Lyme Disease

3

4

2

3

50

3

Malaria

18

14

20

17.3

97

11

Measles

0

1

0

0.3

2

0

Meningococcal Disease (N. meningitidis)

54

41

30

41.7

122

31

Meningitis, Group B Streptococci

2

2

4

2.7

14

6

Meningitis, Haemophilus influenzae1

3

4

5

4

13

1

Meningitis, Streptococcus pneumoniae

27

35

32

31.3

98

30

Meningitis, Listeria monocytogenes

0

1

2

1

13

1

Meningitis, other bacterial (including unspecified)

11

10

13

11.3

60

15

Mercury Poisoning

0

0

1

0.3

7

1

Mumps

7

2

0

3

6

0

Neurotoxic Shellfish Poisoning2

0

0

0

0

0

0

Pertussis

18

11

4

11

85

5

Pesticide Poisoning

0

1

0

0.3

32

1

Plague

0

0

0

0

0

0

Poliomyelitis

0

0

0

0

0

0

Psittacosis

0

0

0

0

0

0

Rabies, Animal

73

57

35

55

176

31

Rocky Mountain Spotted Fever

1

1

1

1

2

0

Rubella, including congenital

0

0

0

0

1

1

Salmonellosis

280

297

322

299.7

3058

277

Shigellosis

224

256

306

262

1488

280

Smallpox2

NR

NR

0

NR

0

0

Staphylococcus aureus, (GISA/VISA)2

NR

NR

0

NR

0

0

Staphylococcus aureus, (GRSA/VRSA)2

NR

NR

0

NR

0

0

Streptococcal Disease, invasive Group A

6

12

10

9.3

93

36

Streptococcus pneumoniae, invasive disease

56

145

123

108

691

295

Tetanus

0

1

1

0.7

3

0

Toxic Shock Syndrome

0

2

2

1.3

6

0

Toxoplasmosis

1

4

3

2.7

16

2

Typhoid Fever

3

4

15

7.3

23

1

Vibrio cholerae (serogrp O1)

0

0

0

0

1

0

Vibrio cholerae (serogrp Non-O1)

2

1

2

1.7

9

1

Vibrio vulnificus

1

0

2

1

23

0

Vibrio other (including unspecified)

7

2

5

4.7

48

5

Yellow Fever

0

0

0

0

0

0

1 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."

2 The reportable disease rule was revised in July, 1999. Kawasaki Disease, Histoplasmosis, Reye Syndrome, and Typhus were deleted from the weekly disease table since cases are no longer reportable as of July 4, 1999. Hepatitis C; perinatal hepatitis B; hepatitis B +HbsAg, pregnant woman; listeriosis; smallpox, S. aureus (GISA/VISA) and S. aureus (GRSA/VRSA) were added to the reporting requirements as of July 4, 1999. Paralytic shellfish poisoning is now referred to as neurotoxic shellfish poisoning.

This page was last modified on: 10/29/2012 01:19:53