GRADING OF RECOMMENDATIONS, ASSESSMENT, DEVELOPMENT, AND EVALUATION (GRADE) FOR ACAM2000: A LICENSED SMALLPOX VACCINE FOR PERSONS AT RISK FOR ORTHOPOXVIRUS DISEASE Público
Harms, Tiara Joy (2014)
Abstract
Despite smallpox eradication, orthopoxviruses still remain at the forefront of public health concern, as the potential for acquiring orthopoxvirus disease still exists; whether naturally, through inadvertent laboratory exposure, or intentional release. Protection is best achieved through vaccination with a vaccinia virus vaccine. In the United States (U.S.), the Advisory Committee on Immunization Practices (ACIP) is tasked with developing and providing expert written guidance on the use of vaccines and vaccine-related agents, approved by the Food and Drug Administration (FDA), for control of vaccine-preventable diseases in the U.S. civilian population. In 2008, ACAM2000 replaced Dryvax as the only FDA licensed and approved smallpox vaccine available for use in the U.S. for protection against orthopoxvirus disease. Despite ACAM2000 having been widely used since 2008, ACIP smallpox vaccination recommendations have not been updated since 2003. As the current recommendations are out of date, the need for development of new ACIP smallpox vaccination recommendations is paramount.
The purpose of this study was to utilize the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) approach to determine the evidence type (quality) for ACAM2000 within the context of the policy question considered by the ACIP Smallpox Vaccine Workgroup: "Should ACAM2000 be recommended routinely for persons at risk for Orthopoxvirus disease?" Critical outcomes were determined through a modified Delphi analysis, and a systematic review of literature was conducted. Data from five randomized controlled trials were pooled using meta-analysis. Pooled risk ratios for cutaneous response and mild adverse events (MAE) outcomes indicated there was no difference in these outcomes occurring in individuals vaccinated with ACAM2000 or Dryvax. Serious adverse events (SAE) and myo/pericarditis resolved with sequelae were each less likely to occur in those vaccinated with ACAM2000, while myo/pericarditis resolved without sequelae was more likely to occur among individuals vaccinated with ACAM2000. Using GRADE, the overall evidence quality across all critical outcomes was determined to be of moderate quality. The results of this study will be made available to ACIP for final consideration, and will aid in forming U.S. policy regarding smallpox vaccinations for persons at risk for orthopoxvirus disease.
Table of Contents
CHAPTER 1: INTRODUCTION
Introduction and
Rationale......................................................................1
Problem
Statement..............................................................................
2
Study
Framework................................................................................
3
Purpose
Statement..............................................................................
4
Significance
Statement.........................................................................
4
Definition of
Terms...............................................................................6
CHAPTER 2: REVIEW OF LITERATURE
Introduction.........................................................................................8
Review of
Literature..............................................................................8
Summary of Current Problem and Study
Relevance...................................14
CHAPTER 3: METHODOLOGY
Introduction........................................................................................16
Methods.............................................................................................16
Data
Analysis......................................................................................20
Study Limitations and
Delimitations.........................................................21
CHAPTER 4: RESULTS
Introduction.........................................................................................22
Findings.............................................................................................
22
Summary...........................................................................................
33
CHAPTER 5: CONCLUSIONS, IMPLICATIONS, AND
RECOMMENDATIONS
Introduction.........................................................................................35
Summary of
Study................................................................................35
Conclusions..........................................................................................37
Implications and
Recommendations..........................................................38
REFERENCES.......................................................................................42
APPENDICES
Appendix A: Rating of Outcome
Measures..................................................44
Appendix B: Literature Review Search
Criteria............................................45
Appendix C: Assessment of Risk of Bias for Randomized Controlled
Trials.......46
Appendix D: Determining Evidence
Type....................................................47
Appendix E: Reported Rates of Serious Adverse
Events................................48
Appendix F: Estimate Effects - Forest
Plots.................................................49
LIST OF FIGURES AND TABLES
Figure 1: Systematic Review
Approach......................................................18
Table 1: Rating of Outcome
Measures........................................................23
Table 2: Characteristics of Selected
Studies................................................25
Table 3: Evidence Table for Critical Outcomes:
Benefits................................27
Table 4: Evidence Table for Critical Outcomes:
Harms..................................29
Table 5: Summary of Findings Table: Evidence Type (Quality) for
ACAM2000....32
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GRADING OF RECOMMENDATIONS, ASSESSMENT, DEVELOPMENT, AND EVALUATION (GRADE) FOR ACAM2000: A LICENSED SMALLPOX VACCINE FOR PERSONS AT RISK FOR ORTHOPOXVIRUS DISEASE () | 2018-08-28 14:59:49 -0400 |
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