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The Epi-Log Newsletter
Volume 45, No. 10 - October 2005
Influenza Vaccination Recommendations 2005-2006, Including Information About Live Attenuated Influenza Vaccine (LAIV)
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The following priority groups should be vaccinated for influenza:
- persons aged > 65 years with comorbid conditions
- residents of long term care facilities
- persons aged 2 to 64 years with comorbid conditions
- persons aged > 65 years without comorbid conditions
- children aged 6 to 23 months
- pregnant women
- health-care personnel who provide direct patient care
- household contacts and out-of-home caregivers of children aged < 6 months
A change to this year’s recommendations is that comorbid conditions now specifically includes persons with any condition (e.g., cognitive dysfunction, spinal cord injuries, seizure disorders, or other neuromuscular disorders) that can compromise respiratory function or the handling of respiratory secretions or that can increase the risk for aspiration.
CDC has specified that, beginning October 24, flu vaccine can be offered to anyone, whether or not they are in one of these high-risk groups.
Inactivated Trivalent Influenza Vaccine (TIV)
Dosage recommendations for inactivated trivalent influenza vaccine (TIV) vary according to age group. For previously unvaccinated children aged < 9 years, 2 doses administered > 1 month apart are recommended. When possible, the second dose should be administered before December. If a child aged < 9 years receives vaccine for the first time one season and does not receive the second dose that season, only 1 dose of vaccine should be administered the following season. Inactivated influenza vaccine should not be administered to persons known to have anaphylactic hypersensitivity to eggs or to other components of the influenza vaccine without first consulting a physician.
Live, Attenuated Influenza Vaccine (LAIV)
For healthy persons aged 5 to 49 years of age, LAIV is a good option for influenza vaccination, including for persons in close contact with groups at high risk for influenza complications and most health-care workers. Possible advantages of LAIV include its potential to induce a broad mucosal and systemic immune response, its ease of administration, and the acceptability of an intranasal rather than intramuscular route of administration.
The following populations should not be vaccinated with LAIV:
- persons aged < 5 years or those aged > 50 years;
- persons with asthma, reactive airway disease or other chronic disorders of the pulmonary or cardiovascular systems; persons with other underlying medical conditions, including such metabolic diseases as diabetes, renal dysfunction, and hemoglobinopathies; or persons with known or suspected immunodeficiency diseases or who are receiving immunosuppressive therapies;
- children or adolescents receiving aspirin or other salicylates (because of the association of Reye syndrome with wild-type influenza infection);
- persons with a history of Guillain Barré Syndrome;
- pregnant women; or
- persons with a history of hypersensitivity, including anaphylaxis, to any of the components of LAIV or to eggs.
Severely Immunosuppressed Patients and Their Contacts
Inactivated influenza vaccine is preferred for vaccinating household members, health-care workers, and others who have close contact with severely immunosuppressed persons (e.g., patients with hematopoietic stem cell transplants) during those periods in which the immunosuppressed person requires care in a protective environment. Health-care workers who receive LAIV should refrain from contact with severely immunosup-pressed patients for 7 days after vaccine receipt. Hospital visitors who have received LAIV should also refrain from contact with severely immunosuppressed persons for 7 days after vaccination; however, such persons need not be excluded from visitation of patients who are not severely immunosuppressed.
Severely immunosuppressed persons should not administer LAIV. However, other persons at high risk for influenza complications, including persons with underlying medical conditions placing them at high risk or who are likely to be at risk, including pregnant women, persons with asthma, and persons aged > 50 years may administer LAIV
Children aged 58 years previously unvaccinated at any time with either LAIV or inactivated influenza vaccine should receive 2 doses of LAIV separated by at least 6 weeks. Children aged 5 to 8 years previously vaccinated at any time with either LAIV or inactivated influenza vaccine should receive 1 dose of LAIV and they do not require a second dose. Persons aged 9 to 49 years should receive 1 dose of LAIV. In accordance with CDC general recommendations on immunization, live vaccines, (i.e., MMR, varicella, LAIV), not administered on the same day should be administered at least 4 weeks apart.
Influenza Vaccine Supply Update
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On October 24th, the department of Health and Human Services held a press conference regarding influenza and influenza vaccine. The 70 million doses of influenza vaccine that will be produced this year (possibly more) should be adequate, reported the CDC. Chiron, the pharmaceutical company whose inactivated trivalent vaccine did not meet with FDA approval last year, has, so far, produced 2 million doses and additional vaccine is being approved on lot-by-lot basis.
Menactra Vaccine Advisory
On September 30th, 2005, The CDC and FDA issued an alert regarding five reports of Guillain-Barré Syndrome (GBS) in teenagers, ages 17-18 years old, who had recently (14 to 31 days prior) received quadrivalent meningococcal conjugate vaccine (MCV4, Menactra® manufactured by sanofi pasteur). The rate of GBS, based on the reported number of cases, was not greater than would be expected due to chance alone; therefore, the CDC and FDA recommend that MCV4 should still be administered to high risk groups because of the protection it offers against meningococcal disease. Persons with a known history of GBS, who are not considered high-risk, are advised not to receive the vaccine.
Please report any clinically significant event following MCV4 vaccine, or any other vaccine, to the Public Health immunization section at 206-296-4774. Alternatively, you may report vaccine adverse events via the internet directly to the Vaccine Adverse Events Reporting System (VAERS) at: www.vaers.hhs.gov.
Communicable Disease Summary for 2003 and 2004 now Available
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The Communicable Disease Summary for the years 2003 and 2004 is now available on the web at: www.metrokc.gov/health/reports/cd-summary-2003-04.pdf
If you would like a hard copy of the summary, please contact Tiffany Acayan at 206-205-5812.
In the September 2005 issue of the EPI-LOG, use of Td vaccine was discussed in association with wound treatment for prevention of tetanus, however, the abbreviation “Td” was never defined. Td vaccine refers to the vaccine containing inactivated tetanus and diphtheria toxoids that is licensed for persons age 7 years and older. It contains a smaller amount of diphtheria toxoid than DTP, DTaP, or DT, hence the lower case “d”. For those aged 7 and older who have not received an initial series of tetanus and diptheria containing vaccine (DTP, DTaP, DT or Td), Td is recommended for beginning or completing the primary series. Td is recommended as a booster, every ten years throughout life. For information about prevention of tetanus, please see the September 2005 issue of the EPI-LOG at: www.metrokc.gov/health/epilog/vol4509.htm
Communicable Disease and Epidemiology contact information
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> Disease reporting
| AIDS |
(206) 296-4645 |
| Sexually Transmitted Diseases |
(206) 744-3954 |
| Tuberculosis |
(206) 744-4579 |
| Other Communicable Diseases |
(206) 296-4774 |
| Automated 24-hour reporting line for conditions not immediately notifiable |
(206) 296-4782 |
> Hotlines
| Communicable Disease Hotline |
(206) 296-4949 |
| HIV/STD Hotline |
(206) 205-7837 |
> For health providers:
- Health Provider homepage
Resources to fact sheets, updated news, vaccine information, health educational materials and external links.
www.metrokc.gov/health/providers
Reported Cases of Selected Diseases in Seattle and King County
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Cases reported
in September
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Cases reported through September
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2005
|
2004
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2005
|
2004
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| Campylobacteriosis |
41
|
22
|
259
|
200
|
| Cryptosporidiosis |
4
|
6
|
59
|
26
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| Chlamydial infections |
382
|
558
|
4,184
|
4,038
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Enterohemorrhagic
E. coli (non-O157) |
0
|
0
|
5
|
0
|
| E. coli O157: H7 |
12
|
7
|
27
|
33
|
| Giardiasis |
16
|
10
|
108
|
91
|
| Gonorrhea |
140
|
150
|
1,311
|
895
|
| Hæmophilus influenzæ (cases <6 years of age) |
0
|
0
|
2
|
2
|
| Hepatitis A |
1
|
3
|
15
|
9
|
| Hepatitis B (acute) |
0
|
0
|
16
|
16
|
| Hepatitis B (chronic) |
68
|
50
|
513
|
464
|
| Hepatitis C (acute) |
0
|
0
|
6
|
7
|
| Hepatitis C (chronic, confirmed/probable) |
92
|
66
|
952
|
908
|
| Hepatitis C (chronic, possible) |
37
|
22
|
320
|
257
|
| Herpes, genital (primary) |
36
|
65
|
579
|
554
|
| HIV and AIDS (includes only AIDS cases not previously reported as HIV) |
28
|
31
|
353
|
316
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| Measles |
1
|
0
|
1
|
6
|
| Meningococcal Disease |
0
|
3
|
13
|
14
|
| Mumps |
0
|
0
|
1
|
1
|
| Pertussis |
37
|
27
|
229
|
174
|
| Rubella |
0
|
0
|
1
|
0
|
| Rubella, congenital |
0
|
0
|
0
|
0
|
| Salmonellosis |
24
|
27
|
173
|
186
|
| Shigellosis |
9
|
7
|
54
|
50
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| Syphilis |
13
|
31
|
121
|
116
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| Syphilis, congenital |
0
|
0
|
0
|
0
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| Syphilis, late |
4
|
6
|
57
|
48
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| Tuberculosis |
11
|
10
|
88
|
99
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