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Brief Summary

GUIDELINE TITLE

Immunizations.

BIBLIOGRAPHIC SOURCE(S)

  • Institute for Clinical Systems Improvement (ICSI). Immunizations. Bloomington (MN): Institute for Clinical Systems Improvement (ICSI); 2008 Oct. 64 p. [67 references]

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version:

Institute for Clinical Systems Improvement (ICSI). Immunization update. Bloomington (MN): Institute for Clinical Systems Improvement (ICSI); 2007 Dec. 4 p.

Institute for Clinical Systems Improvement (ICSI). Immunizations. Bloomington (MN): Institute for Clinical Systems Improvement (ICSI); 2007 Oct. 67 p. [77 references]

BRIEF SUMMARY CONTENT

 
RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Notes from the National Guideline Clearinghouse (NGC) and the Institute for Clinical Systems Improvement (ICSI):

  • For a description of what has changed since the previous version of this guidance, refer to Summary of Changes Report -- October 2008.
  • The recommendations for immunizations are presented in the form of immunization schedules and an algorithm with a total of 30 components accompanied by detailed annotations. Clinical highlights and immunization schedules are provided below for: Immunization Schedule for Infants, Children, and Adolescents – Routine and High Risk and Immunization Schedule for Adult – Routine and High Risk. An algorithm for In-Clinic Immunization is provided in the original guideline document.
  • Vaccine shortages continue to occur in the United States and are the result of a number of factors including companies leaving the vaccine market, manufacturing or production problems, unexpected demand for new vaccines or to changes in vaccine recommendations. On occasion, shortages necessitate temporary changes in recommendations for their use. Information about the shortages including projected duration and recommendations for temporary changes in the immunization schedule are provided by the Advisory Committee on Immunization Practices. The work group recommends that all practitioners be kept abreast of the latest national information on vaccine shortage available at the Centers for Disease Control and Prevention Web site at http://www.cdc.gov/vaccines/news/default.htm.
  • Vaccines administered outside the United States can generally be accepted as valid if the schedule was similar to that recommended in the United States (i.e., minimum ages and intervals). Only written documentation should be accepted as evidence of previous vaccination. Written records are more likely to predict protection if the vaccines, dates of administration, intervals between doses, and the person's age at the time of vaccination are comparable to United States recommendations. If a question exists about whether vaccines administered outside the United States were immunogenic, repeating the vaccinations is usually safe and avoids the need to obtain and interpret serologic tests. If avoiding unnecessary injections is desired, serologic testing might be helpful in determining which vaccinations are needed.

Clinical Highlights

  • Utilize all clinical encounters as opportunities to assess a patient's immunization status. (Annotations #15, 16, 17; Aim #1 - see the original guideline document)
  • Administer at each clinical encounter all immunizations that are due or overdue unless true contraindications exist. (Annotations #20, 22, 23, 26; Aim #2 - see the original guideline document)
  • Educate patients (parents, if applicable) regarding the importance of infant, childhood, adolescent, and adult immunizations, the recommended schedule and the need to maintain a personal record of immunizations and childhood diseases. (Annotation #28 - see the original guideline document)
  • Document reasons for not administering immunizations that are clinically indicated, and flag the record for a recall appointment. (Annotations #23, 24 - see the original guideline document)
  • Document the future plan for administering immunizations. (Annotation #15, 26, 28; Aim #3 - see the original guideline document)

*Immunization Schedule for Infants, Children, and Adolescents – Routine and High Risk

Vaccine Birth 1 mo 2 mos 4 mos 6 mos 12 mos 15 mos 18 mos 24 mos 4-6 yrs 11-12 yrs 15-18 yrs
DTaP     X X X X   X Tdap  
IPV     X X X   X    
MMR (MMRV) See Annotation #3 in the original guideline document for information on combined measles, mumps, rubella and varicella vaccine (MMRV). X     X    
Varicella X     X   X
Verify second dose completed
Pneumococcal (PCV7)     X X X X          
Hib     X X X X          
Rotavirus     X X X            
Hep B
Schedule 1
X X   X          
Hep B
Schedule 2
  X X X        
Influenza       X
annually
Hep A         X
2 doses minimum 6 months interval
     
Meningococcal             X X
if previously not received
Human Papilloma Virus (HPV) (females)         X
(3-dose series)
X
(Catch up if appropriate, 3-dose series)

Abbreviations: DTaP, diphtheria, tetanus, acellular pertussis; Hep A, hepatitis A; Hep B, hepatitis B; Hib, Haemophilus influenzae type b; IPV, inactivated poliovirus vaccine; MMR, measles, mumps, and rubella; MMRV, measles, mumps, rubella, varicella; Tdap, tetanus-diphtheria-acellular pertussis

*Please check manufacturer specifications for dosing, as all time intervals may not be needed.

For additional information on immunizing high-risk patients, see Annotation #14 in the original guideline document.

*Immunization Schedule for Adults -- Routine and High-Risk

Vaccine 19-26 Years 27-39 Years 40-64 Years 65 Years and Older
Td/Tdap Tdap if previously not immunized, 1 dose Td booster every 10 years, substitute one dose of Tdap for Td Td booster
IPV Immunize if not previously immunized
MMR Persons born during or after 1957 should have 1-dose measles; a second dose may be required in special circumstances (see Annotation #3 in the original guideline document).  
Varicella X
Verify second dose completed
For all adults who do not have evidence of immunity to varicella, give two doses of varicella vaccine with at least 28 days between the first and second doses. (See Annotation #4 in the original guideline document.)
Pneumococcal (PPV23) Immunize high risk groups once. Re-immunize those at risk of losing immunity once after 5 years. Immunize at 65 if not done previously. Re-immunize once if 1st received >5 years ago and before age 65 or an appropriate immunocompromising condition is present.
Hep B Universal immunization Immunize those at high risk.
Influenza Annually during flu season for individuals age 50 and older, those at high risk, and others.
Hep A Immunize those in risk groups
Meningococcal X Immunize those in risk groups
Human Papilloma Virus (HPV) (females) X
Catch up, if appropriate
     
Herpes Zoster/Shingles     Immunize at age 60 and older

Abbreviations: Hep A, hepatitis A; Hep B, hepatitis B; IPV, inactivated polio vaccine; MMR, measles, mumps, rubella; Td, tetanus, diphtheria; Tdap, tetanus-diphtheria-acellular pertussis

*Please check manufacturer specifications for dosing, as all time intervals may not be needed.

For additional information on immunizing high-risk patients, see Annotation #14 in the original guideline document.

The Centers for Disease Control and Prevention (CDC) updates immunizations recommendations in January, July, and October -- please refer to the CDC website http://www.cdc.gov/vaccines for the most current schedule.

CLINICAL ALGORITHM(S)

A detailed and annotated clinical algorithm titled "In-Clinic Immunization Algorithm" is provided in the original guideline document.

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of supporting evidence is not stated for each recommendation.

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

  • Institute for Clinical Systems Improvement (ICSI). Immunizations. Bloomington (MN): Institute for Clinical Systems Improvement (ICSI); 2008 Oct. 64 p. [67 references]

ADAPTATION

Not applicable: The guideline was not adapted from another source.

DATE RELEASED

2007 Oct (revised 2008 Oct)

GUIDELINE DEVELOPER(S)

Institute for Clinical Systems Improvement - Private Nonprofit Organization

GUIDELINE DEVELOPER COMMENT

Organizations participating in the Institute for Clinical Systems Improvement (ICSI): Affiliated Community Medical Centers, Allina Medical Clinic, Altru Health System, Aspen Medical Group, Avera Health, CentraCare, Columbia Park Medical Group, Community-University Health Care Center, Dakota Clinic, ENT Specialty Care, Fairview Health Services, Family HealthServices Minnesota, Family Practice Medical Center, Gateway Family Health Clinic, Gillette Children's Specialty Healthcare, Grand Itasca Clinic and Hospital, HealthEast Care System, HealthPartners Central Minnesota Clinics, HealthPartners Medical Group and Clinics, Hutchinson Area Health Care, Hutchinson Medical Center, Lakeview Clinic, Mayo Clinic, Mercy Hospital and Health Care Center, MeritCare, Mille Lacs Health System, Minnesota Gastroenterology, Montevideo Clinic, North Clinic, North Memorial Care System, North Suburban Family Physicians, Northwest Family Physicians, Olmsted Medical Center, Park Nicollet Health Services, Pilot City Health Center, Quello Clinic, Ridgeview Medical Center, River Falls Medical Clinic, Saint Mary's/Duluth Clinic Health System, St. Paul Heart Clinic, Sioux Valley Hospitals and Health System, Southside Community Health Services, Stillwater Medical Group, SuperiorHealth Medical Group, University of Minnesota Physicians, Winona Clinic, Ltd., Winona Health

ICSI, 8009 34th Avenue South, Suite 1200, Bloomington, MN 55425; telephone, (952) 814-7060; fax, (952) 858-9675; e-mail: icsi.info@icsi.org; Web site: www.icsi.org.

SOURCE(S) OF FUNDING

The following Minnesota health plans provide direct financial support: Blue Cross and Blue Shield of Minnesota, HealthPartners, Medica, Metropolitan Health Plan, PreferredOne and UCare Minnesota. In-kind support is provided by the Institute for Clinical Systems Improvement's (ICSI) members.

GUIDELINE COMMITTEE

Preventive Services Steering Committee

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Work Group Members: James Nordin, MD (Work Group Leader) (HealthPartners Medical Group) (Pediatrics); Emma Carlin, MD (Park Nicollet Health Services) (Family Medicine); Barbara Yawn, MD (Olmsted Medical Center) (Family Medicine); Abinash Virk, MD (Mayo Clinic) (Infectious Disease); Barb Ottis, RN (Park Nicollet Health Services) (Nursing); Renner Anderson, MD (Park Nicollet Health Services) (Pediatrics); Robert Jacobson, MD (Mayo Clinic) (Pediatrics); Sarah Rall, PharmD (Marshfield Clinic) (Pharmacy); Penny Fredrickson (Institute for Clinical Systems Improvement) (Measurement/Implementation Advisor); Melissa Marshall, MBA (Institute for Clinical Systems Improvement) (Facilitator)

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

The Institute for Clinical Systems Improvement (ICSI) has adopted a policy of transparency, disclosing potential conflict and competing interests of all individuals who participate in the development, revision and approval of ICSI documents (guidelines, order sets and protocols). This applies to all work groups (guidelines, order sets and protocols) and committees (Committee on Evidence-Based Practice, Cardiovascular Steering Committee, Women's Health Steering Committee, Preventive & Health Maintenance Steering Committee and Respiratory Steering Committee).

Participants must disclose any potential conflict and competing interests they or their dependents (spouse, dependent children, or others claimed as dependents) may have with any organization with commercial, proprietary, or political interests relevant to the topics covered by ICSI documents. Such disclosures will be shared with all individuals who prepare, review and approve ICSI documents.

Dr. Robert Jacobson serves on the data safety monitoring board for Kaiser Permanente of Southern California overseeing a Gardasil trial. He receives less than $10,000 for this commitment.

Barbara Ottis, RN holds stock in Merck and Baxter. She also received speaker fees from GSK in an amount less than $10,000.

Dr. Barbara Yawn negotiated research funds on behalf of Olmsted Medical Center from Merck. Dr. Yawn receives less than $10,000 from Merck for serving on the advisory board for Zostavax.

No other work group members have potential conflicts of interest to disclose.

ICSI's conflict of interest policy and procedures are available for review on ICSI's website at www.icsi.org.

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version:

Institute for Clinical Systems Improvement (ICSI). Immunization update. Bloomington (MN): Institute for Clinical Systems Improvement (ICSI); 2007 Dec. 4 p.

Institute for Clinical Systems Improvement (ICSI). Immunizations. Bloomington (MN): Institute for Clinical Systems Improvement (ICSI); 2007 Oct. 67 p. [77 references]

GUIDELINE AVAILABILITY

Electronic copies: Available from the Institute for Clinical Systems Improvement (ICSI) Web site.

Print copies: Available from ICSI, 8009 34th Avenue South, Suite 1200, Bloomington, MN 55425; telephone, (952) 814-7060; fax, (952) 858-9675; Web site: www.icsi.org; e-mail: icsi.info@icsi.org.

AVAILABILITY OF COMPANION DOCUMENTS

The following are available:

Print copies: Available from ICSI, 8009 34th Avenue South, Suite 1200, Bloomington, MN 55425; telephone, (952) 814-7060; fax, (952) 858-9675; Web site: www.icsi.org; e-mail: icsi.info@icsi.org.

PATIENT RESOURCES

None available

NGC STATUS

This summary was completed by ECRI on August 30, 1999. The information was verified by the guideline developer on October 11, 1999. This summary was updated by ECRI on May 15, 2000 and on October 22, 2001. This summary was updated by ECRI on December 4, 2002. The updated information was verified by the guideline developer on December 24, 2002. This summary was updated by ECRI on April 12, 2004, September 20, 2004, August 9, 2005, July 5, 2006, November, 30, 2006, and March 6, 2007. This summary was updated by ECRI Institute on July 9, 2007 following the FDA advisory on RotaTeq (Rotavirus, Live, Oral, Pentavalent) vaccine. This NGC summary was updated by ECRI Institute on December 18, 2007 and again on January 8, 2009.

COPYRIGHT STATEMENT

This NGC summary (abstracted ICSI Guideline) is based on the original guideline, which is subject to the guideline developer's copyright restrictions.

The abstracted ICSI Guidelines contained in this Web site may be downloaded by any individual or organization. If the abstracted ICSI Guidelines are downloaded by an individual, the individual may not distribute copies to third parties.

If the abstracted ICSI Guidelines are downloaded by an organization, copies may be distributed to the organization's employees but may not be distributed outside of the organization without the prior written consent of the Institute for Clinical Systems Improvement, Inc.

All other copyright rights in the abstracted ICSI Guidelines are reserved by the Institute for Clinical Systems Improvement, Inc. The Institute for Clinical Systems Improvement, Inc. assumes no liability for any adaptations or revisions or modifications made to the abstracts of the ICSI Guidelines.

DISCLAIMER

NGC DISCLAIMER

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Readers with questions regarding guideline content are directed to contact the guideline developer.


 

 

   
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