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Rotavirus vaccine coverage and factors associated with uptake using linked data: Ontario, Canada.

Identifieur interne : 000048 ( Main/Exploration ); précédent : 000047; suivant : 000049

Rotavirus vaccine coverage and factors associated with uptake using linked data: Ontario, Canada.

Auteurs : Sarah E. Wilson [Canada] ; Hannah Chung [Canada] ; Kevin L. Schwartz [Canada] ; Astrid Guttmann [Canada] ; Shelley L. Deeks [Canada] ; Jeffrey C. Kwong [Canada] ; Natasha S. Crowcroft [Canada] ; Laura Wing [Canada] ; Karen Tu [Canada]

Source :

RBID : pubmed:29444167

Descripteurs français

English descriptors

Abstract

BACKGROUND

In August 2011, Ontario, Canada introduced a rotavirus immunization program using Rotarix™ vaccine. No assessments of rotavirus vaccine coverage have been previously conducted in Ontario.

METHODS

We assessed vaccine coverage (series initiation and completion) and factors associated with uptake using the Electronic Medical Record Administrative data Linked Database (EMRALD), a collection of family physician electronic medical records (EMR) linked to health administrative data. Series initiation (1 dose) and series completion (2 doses) before and after the program's introduction were calculated. To identify factors associated with series initiation and completion, adjusted odds ratios (aOR) and 95% confidence intervals (95%CI) were calculated using logistic regression.

RESULTS

A total of 12,525 children were included. Series completion increased each year of the program (73%, 79% and 84%, respectively). Factors associated with series initiation included high continuity of care (aOR = 2.15; 95%CI, 1.61-2.87), maternal influenza vaccination (aOR = 1.55; 95%CI,1.24-1.93), maternal immmigration to Canada in the last five years (aOR = 1.47; 95% CI, 1.05-2.04), and having no siblings (aOR = 1.62; 95%CI,1.30-2.03). Relative to the first program year, infants were more likely to initiate the series in the second year (aOR = 1.71; 95% CI 1.39-2.10) and third year (aOR = 2.02; 95% CI 1.56-2.61) of the program. Infants receiving care from physicians with large practices were less likely to initiate the series (aOR 0.91; 95%CI, 0.88-0.94, per 100 patients rostered) and less likely to complete the series (aOR 0.94; 95%CI, 0.91-0.97, per 100 patients rostered). Additional associations were identified for series completion.

CONCLUSIONS

Family physician delivery achieved moderately high coverage in the program's first three years. This assessment demonstrates the usefulness of EMR data for evaluating vaccine coverage. Important insights into factors associated with initiation or completion (i.e. high continuity of care, smaller roster sizes, rural practice location) suggest areas for research and potential program supports.


DOI: 10.1371/journal.pone.0192809
PubMed: 29444167
PubMed Central: PMC5812625


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<keywords scheme="KwdEn" xml:lang="en">
<term>Child, Preschool (MeSH)</term>
<term>Cohort Studies (MeSH)</term>
<term>Confidence Intervals (MeSH)</term>
<term>Electronic Health Records (MeSH)</term>
<term>Family Practice (MeSH)</term>
<term>Female (MeSH)</term>
<term>Health Information Interoperability (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Immunization Programs (statistics & numerical data)</term>
<term>Infant (MeSH)</term>
<term>Infant, Newborn (MeSH)</term>
<term>Information Storage and Retrieval (MeSH)</term>
<term>Logistic Models (MeSH)</term>
<term>Male (MeSH)</term>
<term>Multivariate Analysis (MeSH)</term>
<term>Odds Ratio (MeSH)</term>
<term>Ontario (MeSH)</term>
<term>Rotavirus Infections (prevention & control)</term>
<term>Rotavirus Vaccines (therapeutic use)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Analyse multifactorielle (MeSH)</term>
<term>Dossiers médicaux électroniques (MeSH)</term>
<term>Enfant d'âge préscolaire (MeSH)</term>
<term>Femelle (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Infections à rotavirus (prévention et contrôle)</term>
<term>Interopérabilité des informations de santé (MeSH)</term>
<term>Intervalles de confiance (MeSH)</term>
<term>Modèles logistiques (MeSH)</term>
<term>Mâle (MeSH)</term>
<term>Médecine de famille (MeSH)</term>
<term>Mémorisation et recherche des informations (MeSH)</term>
<term>Nourrisson (MeSH)</term>
<term>Nouveau-né (MeSH)</term>
<term>Odds ratio (MeSH)</term>
<term>Ontario (MeSH)</term>
<term>Programmes de vaccination (statistiques et données numériques)</term>
<term>Vaccins anti-rotavirus (usage thérapeutique)</term>
<term>Études de cohortes (MeSH)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en">
<term>Rotavirus Vaccines</term>
</keywords>
<keywords scheme="MESH" qualifier="prevention & control" xml:lang="en">
<term>Rotavirus Infections</term>
</keywords>
<keywords scheme="MESH" qualifier="prévention et contrôle" xml:lang="fr">
<term>Infections à rotavirus</term>
</keywords>
<keywords scheme="MESH" qualifier="statistics & numerical data" xml:lang="en">
<term>Immunization Programs</term>
</keywords>
<keywords scheme="MESH" qualifier="statistiques et données numériques" xml:lang="fr">
<term>Programmes de vaccination</term>
</keywords>
<keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr">
<term>Vaccins anti-rotavirus</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Child, Preschool</term>
<term>Cohort Studies</term>
<term>Confidence Intervals</term>
<term>Electronic Health Records</term>
<term>Family Practice</term>
<term>Female</term>
<term>Health Information Interoperability</term>
<term>Humans</term>
<term>Infant</term>
<term>Infant, Newborn</term>
<term>Information Storage and Retrieval</term>
<term>Logistic Models</term>
<term>Male</term>
<term>Multivariate Analysis</term>
<term>Odds Ratio</term>
<term>Ontario</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Analyse multifactorielle</term>
<term>Dossiers médicaux électroniques</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Humains</term>
<term>Interopérabilité des informations de santé</term>
<term>Intervalles de confiance</term>
<term>Modèles logistiques</term>
<term>Mâle</term>
<term>Médecine de famille</term>
<term>Mémorisation et recherche des informations</term>
<term>Nourrisson</term>
<term>Nouveau-né</term>
<term>Odds ratio</term>
<term>Ontario</term>
<term>Études de cohortes</term>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>BACKGROUND</b>
</p>
<p>In August 2011, Ontario, Canada introduced a rotavirus immunization program using Rotarix™ vaccine. No assessments of rotavirus vaccine coverage have been previously conducted in Ontario.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>We assessed vaccine coverage (series initiation and completion) and factors associated with uptake using the Electronic Medical Record Administrative data Linked Database (EMRALD), a collection of family physician electronic medical records (EMR) linked to health administrative data. Series initiation (1 dose) and series completion (2 doses) before and after the program's introduction were calculated. To identify factors associated with series initiation and completion, adjusted odds ratios (aOR) and 95% confidence intervals (95%CI) were calculated using logistic regression.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>A total of 12,525 children were included. Series completion increased each year of the program (73%, 79% and 84%, respectively). Factors associated with series initiation included high continuity of care (aOR = 2.15; 95%CI, 1.61-2.87), maternal influenza vaccination (aOR = 1.55; 95%CI,1.24-1.93), maternal immmigration to Canada in the last five years (aOR = 1.47; 95% CI, 1.05-2.04), and having no siblings (aOR = 1.62; 95%CI,1.30-2.03). Relative to the first program year, infants were more likely to initiate the series in the second year (aOR = 1.71; 95% CI 1.39-2.10) and third year (aOR = 2.02; 95% CI 1.56-2.61) of the program. Infants receiving care from physicians with large practices were less likely to initiate the series (aOR 0.91; 95%CI, 0.88-0.94, per 100 patients rostered) and less likely to complete the series (aOR 0.94; 95%CI, 0.91-0.97, per 100 patients rostered). Additional associations were identified for series completion.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>Family physician delivery achieved moderately high coverage in the program's first three years. This assessment demonstrates the usefulness of EMR data for evaluating vaccine coverage. Important insights into factors associated with initiation or completion (i.e. high continuity of care, smaller roster sizes, rural practice location) suggest areas for research and potential program supports.</p>
</div>
</front>
</TEI>
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<Year>2018</Year>
<Month>04</Month>
<Day>16</Day>
</DateCompleted>
<DateRevised>
<Year>2018</Year>
<Month>11</Month>
<Day>13</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">1932-6203</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>13</Volume>
<Issue>2</Issue>
<PubDate>
<Year>2018</Year>
</PubDate>
</JournalIssue>
<Title>PloS one</Title>
<ISOAbbreviation>PLoS ONE</ISOAbbreviation>
</Journal>
<ArticleTitle>Rotavirus vaccine coverage and factors associated with uptake using linked data: Ontario, Canada.</ArticleTitle>
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<Abstract>
<AbstractText Label="BACKGROUND">In August 2011, Ontario, Canada introduced a rotavirus immunization program using Rotarix™ vaccine. No assessments of rotavirus vaccine coverage have been previously conducted in Ontario.</AbstractText>
<AbstractText Label="METHODS">We assessed vaccine coverage (series initiation and completion) and factors associated with uptake using the Electronic Medical Record Administrative data Linked Database (EMRALD), a collection of family physician electronic medical records (EMR) linked to health administrative data. Series initiation (1 dose) and series completion (2 doses) before and after the program's introduction were calculated. To identify factors associated with series initiation and completion, adjusted odds ratios (aOR) and 95% confidence intervals (95%CI) were calculated using logistic regression.</AbstractText>
<AbstractText Label="RESULTS">A total of 12,525 children were included. Series completion increased each year of the program (73%, 79% and 84%, respectively). Factors associated with series initiation included high continuity of care (aOR = 2.15; 95%CI, 1.61-2.87), maternal influenza vaccination (aOR = 1.55; 95%CI,1.24-1.93), maternal immmigration to Canada in the last five years (aOR = 1.47; 95% CI, 1.05-2.04), and having no siblings (aOR = 1.62; 95%CI,1.30-2.03). Relative to the first program year, infants were more likely to initiate the series in the second year (aOR = 1.71; 95% CI 1.39-2.10) and third year (aOR = 2.02; 95% CI 1.56-2.61) of the program. Infants receiving care from physicians with large practices were less likely to initiate the series (aOR 0.91; 95%CI, 0.88-0.94, per 100 patients rostered) and less likely to complete the series (aOR 0.94; 95%CI, 0.91-0.97, per 100 patients rostered). Additional associations were identified for series completion.</AbstractText>
<AbstractText Label="CONCLUSIONS">Family physician delivery achieved moderately high coverage in the program's first three years. This assessment demonstrates the usefulness of EMR data for evaluating vaccine coverage. Important insights into factors associated with initiation or completion (i.e. high continuity of care, smaller roster sizes, rural practice location) suggest areas for research and potential program supports.</AbstractText>
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<LastName>Wilson</LastName>
<ForeName>Sarah E</ForeName>
<Initials>SE</Initials>
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<AffiliationInfo>
<Affiliation>Public Health Ontario, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
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<LastName>Chung</LastName>
<ForeName>Hannah</ForeName>
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<AffiliationInfo>
<Affiliation>Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
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<LastName>Schwartz</LastName>
<ForeName>Kevin L</ForeName>
<Initials>KL</Initials>
<AffiliationInfo>
<Affiliation>Public Health Ontario, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.</Affiliation>
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<LastName>Guttmann</LastName>
<ForeName>Astrid</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Pediatrics, Hospital for Sick Children, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.</Affiliation>
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<LastName>Deeks</LastName>
<ForeName>Shelley L</ForeName>
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<Affiliation>Public Health Ontario, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.</Affiliation>
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<LastName>Kwong</LastName>
<ForeName>Jeffrey C</ForeName>
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<Affiliation>Public Health Ontario, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Family and Community Medicine, University of Toronto, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Crowcroft</LastName>
<ForeName>Natasha S</ForeName>
<Initials>NS</Initials>
<AffiliationInfo>
<Affiliation>Public Health Ontario, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Wing</LastName>
<ForeName>Laura</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Tu</LastName>
<ForeName>Karen</ForeName>
<Initials>K</Initials>
<AffiliationInfo>
<Affiliation>Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Family and Community Medicine, University of Toronto, Toronto, Ontario, Canada.</Affiliation>
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<name sortKey="Crowcroft, Natasha S" sort="Crowcroft, Natasha S" uniqKey="Crowcroft N" first="Natasha S" last="Crowcroft">Natasha S. Crowcroft</name>
<name sortKey="Crowcroft, Natasha S" sort="Crowcroft, Natasha S" uniqKey="Crowcroft N" first="Natasha S" last="Crowcroft">Natasha S. Crowcroft</name>
<name sortKey="Crowcroft, Natasha S" sort="Crowcroft, Natasha S" uniqKey="Crowcroft N" first="Natasha S" last="Crowcroft">Natasha S. Crowcroft</name>
<name sortKey="Deeks, Shelley L" sort="Deeks, Shelley L" uniqKey="Deeks S" first="Shelley L" last="Deeks">Shelley L. Deeks</name>
<name sortKey="Deeks, Shelley L" sort="Deeks, Shelley L" uniqKey="Deeks S" first="Shelley L" last="Deeks">Shelley L. Deeks</name>
<name sortKey="Guttmann, Astrid" sort="Guttmann, Astrid" uniqKey="Guttmann A" first="Astrid" last="Guttmann">Astrid Guttmann</name>
<name sortKey="Guttmann, Astrid" sort="Guttmann, Astrid" uniqKey="Guttmann A" first="Astrid" last="Guttmann">Astrid Guttmann</name>
<name sortKey="Guttmann, Astrid" sort="Guttmann, Astrid" uniqKey="Guttmann A" first="Astrid" last="Guttmann">Astrid Guttmann</name>
<name sortKey="Kwong, Jeffrey C" sort="Kwong, Jeffrey C" uniqKey="Kwong J" first="Jeffrey C" last="Kwong">Jeffrey C. Kwong</name>
<name sortKey="Kwong, Jeffrey C" sort="Kwong, Jeffrey C" uniqKey="Kwong J" first="Jeffrey C" last="Kwong">Jeffrey C. Kwong</name>
<name sortKey="Kwong, Jeffrey C" sort="Kwong, Jeffrey C" uniqKey="Kwong J" first="Jeffrey C" last="Kwong">Jeffrey C. Kwong</name>
<name sortKey="Kwong, Jeffrey C" sort="Kwong, Jeffrey C" uniqKey="Kwong J" first="Jeffrey C" last="Kwong">Jeffrey C. Kwong</name>
<name sortKey="Schwartz, Kevin L" sort="Schwartz, Kevin L" uniqKey="Schwartz K" first="Kevin L" last="Schwartz">Kevin L. Schwartz</name>
<name sortKey="Schwartz, Kevin L" sort="Schwartz, Kevin L" uniqKey="Schwartz K" first="Kevin L" last="Schwartz">Kevin L. Schwartz</name>
<name sortKey="Schwartz, Kevin L" sort="Schwartz, Kevin L" uniqKey="Schwartz K" first="Kevin L" last="Schwartz">Kevin L. Schwartz</name>
<name sortKey="Tu, Karen" sort="Tu, Karen" uniqKey="Tu K" first="Karen" last="Tu">Karen Tu</name>
<name sortKey="Tu, Karen" sort="Tu, Karen" uniqKey="Tu K" first="Karen" last="Tu">Karen Tu</name>
<name sortKey="Tu, Karen" sort="Tu, Karen" uniqKey="Tu K" first="Karen" last="Tu">Karen Tu</name>
<name sortKey="Wilson, Sarah E" sort="Wilson, Sarah E" uniqKey="Wilson S" first="Sarah E" last="Wilson">Sarah E. Wilson</name>
<name sortKey="Wilson, Sarah E" sort="Wilson, Sarah E" uniqKey="Wilson S" first="Sarah E" last="Wilson">Sarah E. Wilson</name>
<name sortKey="Wing, Laura" sort="Wing, Laura" uniqKey="Wing L" first="Laura" last="Wing">Laura Wing</name>
</country>
</tree>
</affiliations>
</record>

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