Serveur d'exploration COVID et hydrochloroquine

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Hydroxychloroquine and maintenance immunosuppression use in kidney transplant recipients: Analysis of linked US registry and claims data.

Identifieur interne : 001212 ( Main/Exploration ); précédent : 001211; suivant : 001213

Hydroxychloroquine and maintenance immunosuppression use in kidney transplant recipients: Analysis of linked US registry and claims data.

Auteurs : Krista L. Lentine [États-Unis] ; Ngan N. Lam [Canada] ; Yasar Caliskan [États-Unis] ; Tarek Alhamad [États-Unis] ; Huiling Xiao [États-Unis] ; Mark A. Schnitzler [États-Unis] ; Su-Hsin Chang [États-Unis] ; David Axelrod [États-Unis] ; Dorry L. Segev [États-Unis] ; Mara Mcadams-Demarco [États-Unis] ; Bertram L. Kasiske [États-Unis] ; Gregory P. Hess [États-Unis] ; Daniel C. Brennan [États-Unis]

Source :

RBID : pubmed:33048372

Descripteurs français

English descriptors

Abstract

Hydroxychloroquine (HCQ) is an antimalarial drug with immunomodulatory effects used to treat systemic lupus erythematosus (SLE) and scleroderma. The antiviral effects of HCQ have raised attention in the context of the COVID-19 pandemic, although safety is controversial. We examined linkages of national transplant registry data with pharmaceutical claims and Medicare billing claims to study HCQ use among Medicare-insured kidney transplant recipients with SLE or scleroderma (2008-2017; N = 1820). We compared three groups based on immunosuppression regimen 7 months-to-1 year post transplant: (a) tacrolimus (Tac) + mycophenolic acid (MPA) + prednisone (Pred) (referent group, 77.7%); (b) Tac + MPA + Pred + HCQ (16.5%); or (c) other immunosuppression + HCQ (5.7%). Compared to the referent group, recipients treated with other immunosuppression + HCQ had a 2-fold increased risk of abnormal ECG or QT prolongation (18.9% vs. 10.7%; aHR,1.12 1.963.42 , p = .02) and ventricular arrhythmias (15.2% vs. 11.4%; aHR,1.00 1.813.29 , p = .05) in the >1-to-3 years post-transplant. Tac + MPA + Pred + HCQ was associated with increased risk of ventricular arrhythmias (13.5% vs. 11.4%; aHR,1.02 1.542.31 , p = .04) and pancytopenia (35.9% vs. 31.4%; aHR,1.03 1.311.68 , p = .03) compared to triple immunosuppression without HCQ. However, HCQ-containing regimens were not associated with an increased risk of death or graft failure. HCQ may be used safely in selected kidney transplant recipients in addition to their maintenance immunosuppression, although attention to arrhythmias is warranted.

DOI: 10.1111/ctr.14118
PubMed: 33048372


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<name sortKey="Segev, Dorry L" sort="Segev, Dorry L" uniqKey="Segev D" first="Dorry L" last="Segev">Dorry L. Segev</name>
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<name sortKey="Mcadams Demarco, Mara" sort="Mcadams Demarco, Mara" uniqKey="Mcadams Demarco M" first="Mara" last="Mcadams-Demarco">Mara Mcadams-Demarco</name>
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<name sortKey="Hess, Gregory P" sort="Hess, Gregory P" uniqKey="Hess G" first="Gregory P" last="Hess">Gregory P. Hess</name>
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<term>Aged, 80 and over (MeSH)</term>
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<term>Graft Rejection (prevention & control)</term>
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<term>Immunosuppresseurs (usage thérapeutique)</term>
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<term>Lupus érythémateux disséminé (mortalité)</term>
<term>Lupus érythémateux disséminé (traitement médicamenteux)</term>
<term>Mâle (MeSH)</term>
<term>Mémorisation et recherche des informations (MeSH)</term>
<term>Rejet du greffon (prévention et contrôle)</term>
<term>Résultat thérapeutique (MeSH)</term>
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<term>Sclérodermie systémique (traitement médicamenteux)</term>
<term>Sujet âgé (MeSH)</term>
<term>Sujet âgé de 80 ans ou plus (MeSH)</term>
<term>Survie du greffon (MeSH)</term>
<term>Transplantation rénale (MeSH)</term>
<term>États-Unis (MeSH)</term>
<term>Études rétrospectives (MeSH)</term>
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<term>Maintenance Chemotherapy</term>
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<term>Kidney Failure, Chronic</term>
<term>Lupus Erythematosus, Systemic</term>
<term>Scleroderma, Systemic</term>
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<term>Défaillance rénale chronique</term>
<term>Lupus érythémateux disséminé</term>
<term>Sclérodermie systémique</term>
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<keywords scheme="MESH" qualifier="méthodes" xml:lang="fr">
<term>Chimiothérapie de maintenance</term>
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<keywords scheme="MESH" qualifier="prevention & control" xml:lang="en">
<term>Graft Rejection</term>
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<term>Rejet du greffon</term>
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<term>Lupus érythémateux disséminé</term>
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<term>Hydroxychloroquine</term>
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<term>Sclérodermie systémique</term>
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<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr">
<term>Défaillance rénale chronique</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Adolescent</term>
<term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Drug Therapy, Combination</term>
<term>Female</term>
<term>Graft Survival</term>
<term>Humans</term>
<term>Information Storage and Retrieval</term>
<term>Insurance, Health</term>
<term>Kidney Transplantation</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Registries</term>
<term>Retrospective Studies</term>
<term>Treatment Outcome</term>
<term>Young Adult</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adolescent</term>
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Association de médicaments</term>
<term>Assurance maladie</term>
<term>Enregistrements</term>
<term>Femelle</term>
<term>Humains</term>
<term>Jeune adulte</term>
<term>Mâle</term>
<term>Mémorisation et recherche des informations</term>
<term>Résultat thérapeutique</term>
<term>Sujet âgé</term>
<term>Sujet âgé de 80 ans ou plus</term>
<term>Survie du greffon</term>
<term>Transplantation rénale</term>
<term>États-Unis</term>
<term>Études rétrospectives</term>
</keywords>
<keywords scheme="Wicri" type="geographic" xml:lang="fr">
<term>États-Unis</term>
</keywords>
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<front>
<div type="abstract" xml:lang="en">Hydroxychloroquine (HCQ) is an antimalarial drug with immunomodulatory effects used to treat systemic lupus erythematosus (SLE) and scleroderma. The antiviral effects of HCQ have raised attention in the context of the COVID-19 pandemic, although safety is controversial. We examined linkages of national transplant registry data with pharmaceutical claims and Medicare billing claims to study HCQ use among Medicare-insured kidney transplant recipients with SLE or scleroderma (2008-2017; N = 1820). We compared three groups based on immunosuppression regimen 7 months-to-1 year post transplant: (a) tacrolimus (Tac) + mycophenolic acid (MPA) + prednisone (Pred) (referent group, 77.7%); (b) Tac + MPA + Pred + HCQ (16.5%); or (c) other immunosuppression + HCQ (5.7%). Compared to the referent group, recipients treated with other immunosuppression + HCQ had a 2-fold increased risk of abnormal ECG or QT prolongation (18.9% vs. 10.7%; aHR,
<sub>1.12</sub>
1.96
<sub>3.42</sub>
, p = .02) and ventricular arrhythmias (15.2% vs. 11.4%; aHR,
<sub>1.00</sub>
1.81
<sub>3.29</sub>
, p = .05) in the >1-to-3 years post-transplant. Tac + MPA + Pred + HCQ was associated with increased risk of ventricular arrhythmias (13.5% vs. 11.4%; aHR,
<sub>1.02</sub>
1.54
<sub>2.31</sub>
, p = .04) and pancytopenia (35.9% vs. 31.4%; aHR,
<sub>1.03</sub>
1.31
<sub>1.68</sub>
, p = .03) compared to triple immunosuppression without HCQ. However, HCQ-containing regimens were not associated with an increased risk of death or graft failure. HCQ may be used safely in selected kidney transplant recipients in addition to their maintenance immunosuppression, although attention to arrhythmias is warranted.</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">33048372</PMID>
<DateCompleted>
<Year>2021</Year>
<Month>01</Month>
<Day>04</Day>
</DateCompleted>
<DateRevised>
<Year>2021</Year>
<Month>01</Month>
<Day>04</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">1399-0012</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>34</Volume>
<Issue>12</Issue>
<PubDate>
<Year>2020</Year>
<Month>12</Month>
</PubDate>
</JournalIssue>
<Title>Clinical transplantation</Title>
<ISOAbbreviation>Clin Transplant</ISOAbbreviation>
</Journal>
<ArticleTitle>Hydroxychloroquine and maintenance immunosuppression use in kidney transplant recipients: Analysis of linked US registry and claims data.</ArticleTitle>
<Pagination>
<MedlinePgn>e14118</MedlinePgn>
</Pagination>
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<Abstract>
<AbstractText>Hydroxychloroquine (HCQ) is an antimalarial drug with immunomodulatory effects used to treat systemic lupus erythematosus (SLE) and scleroderma. The antiviral effects of HCQ have raised attention in the context of the COVID-19 pandemic, although safety is controversial. We examined linkages of national transplant registry data with pharmaceutical claims and Medicare billing claims to study HCQ use among Medicare-insured kidney transplant recipients with SLE or scleroderma (2008-2017; N = 1820). We compared three groups based on immunosuppression regimen 7 months-to-1 year post transplant: (a) tacrolimus (Tac) + mycophenolic acid (MPA) + prednisone (Pred) (referent group, 77.7%); (b) Tac + MPA + Pred + HCQ (16.5%); or (c) other immunosuppression + HCQ (5.7%). Compared to the referent group, recipients treated with other immunosuppression + HCQ had a 2-fold increased risk of abnormal ECG or QT prolongation (18.9% vs. 10.7%; aHR,
<sub>1.12</sub>
1.96
<sub>3.42</sub>
, p = .02) and ventricular arrhythmias (15.2% vs. 11.4%; aHR,
<sub>1.00</sub>
1.81
<sub>3.29</sub>
, p = .05) in the >1-to-3 years post-transplant. Tac + MPA + Pred + HCQ was associated with increased risk of ventricular arrhythmias (13.5% vs. 11.4%; aHR,
<sub>1.02</sub>
1.54
<sub>2.31</sub>
, p = .04) and pancytopenia (35.9% vs. 31.4%; aHR,
<sub>1.03</sub>
1.31
<sub>1.68</sub>
, p = .03) compared to triple immunosuppression without HCQ. However, HCQ-containing regimens were not associated with an increased risk of death or graft failure. HCQ may be used safely in selected kidney transplant recipients in addition to their maintenance immunosuppression, although attention to arrhythmias is warranted.</AbstractText>
<CopyrightInformation>© 2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Lentine</LastName>
<ForeName>Krista L</ForeName>
<Initials>KL</Initials>
<Identifier Source="ORCID">0000-0002-9423-4849</Identifier>
<AffiliationInfo>
<Affiliation>Center for Abdominal Transplantation, Saint Louis University, St. Louis, MO, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Lam</LastName>
<ForeName>Ngan N</ForeName>
<Initials>NN</Initials>
<Identifier Source="ORCID">0000-0002-0129-7091</Identifier>
<AffiliationInfo>
<Affiliation>University of Calgary, Calgary, AB, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Caliskan</LastName>
<ForeName>Yasar</ForeName>
<Initials>Y</Initials>
<AffiliationInfo>
<Affiliation>Center for Abdominal Transplantation, Saint Louis University, St. Louis, MO, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Alhamad</LastName>
<ForeName>Tarek</ForeName>
<Initials>T</Initials>
<AffiliationInfo>
<Affiliation>Washington University in Saint Louis, St. Louis, MO, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Xiao</LastName>
<ForeName>Huiling</ForeName>
<Initials>H</Initials>
<AffiliationInfo>
<Affiliation>Center for Abdominal Transplantation, Saint Louis University, St. Louis, MO, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Schnitzler</LastName>
<ForeName>Mark A</ForeName>
<Initials>MA</Initials>
<AffiliationInfo>
<Affiliation>Center for Abdominal Transplantation, Saint Louis University, St. Louis, MO, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Chang</LastName>
<ForeName>Su-Hsin</ForeName>
<Initials>SH</Initials>
<AffiliationInfo>
<Affiliation>Washington University in Saint Louis, St. Louis, MO, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Axelrod</LastName>
<ForeName>David</ForeName>
<Initials>D</Initials>
<Identifier Source="ORCID">0000-0001-5684-0613</Identifier>
<AffiliationInfo>
<Affiliation>University of Iowa, Iowa City, IA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Segev</LastName>
<ForeName>Dorry L</ForeName>
<Initials>DL</Initials>
<AffiliationInfo>
<Affiliation>Johns Hopkins University, Baltimore, MD, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>McAdams-DeMarco</LastName>
<ForeName>Mara</ForeName>
<Initials>M</Initials>
<Identifier Source="ORCID">0000-0003-3013-925X</Identifier>
<AffiliationInfo>
<Affiliation>Johns Hopkins University, Baltimore, MD, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Kasiske</LastName>
<ForeName>Bertram L</ForeName>
<Initials>BL</Initials>
<AffiliationInfo>
<Affiliation>Hennepin County Med Center, Minneapolis, MN, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Hess</LastName>
<ForeName>Gregory P</ForeName>
<Initials>GP</Initials>
<AffiliationInfo>
<Affiliation>Drexel University, Philadelphia, PA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Brennan</LastName>
<ForeName>Daniel C</ForeName>
<Initials>DC</Initials>
<AffiliationInfo>
<Affiliation>Johns Hopkins University, Baltimore, MD, USA.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
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<GrantID>R01-DK120518</GrantID>
<Acronym>DK</Acronym>
<Agency>NIDDK NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>HHSH250201000018C</GrantID>
<Acronym>HRSA</Acronym>
<Agency>HRSA HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>R01-DK120518</GrantID>
<Acronym>DK</Acronym>
<Agency>NIDDK NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>HHSH250201000018C</GrantID>
<Acronym>HRSA</Acronym>
<Agency>HRSA HHS</Agency>
<Country>United States</Country>
</Grant>
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<PublicationType UI="D052061">Research Support, N.I.H., Extramural</PublicationType>
</PublicationTypeList>
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<Year>2020</Year>
<Month>11</Month>
<Day>22</Day>
</ArticleDate>
</Article>
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<Country>Denmark</Country>
<MedlineTA>Clin Transplant</MedlineTA>
<NlmUniqueID>8710240</NlmUniqueID>
<ISSNLinking>0902-0063</ISSNLinking>
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<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D007166">Immunosuppressive Agents</NameOfSubstance>
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<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D000293" MajorTopicYN="N">Adolescent</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D000369" MajorTopicYN="N">Aged, 80 and over</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D004359" MajorTopicYN="N">Drug Therapy, Combination</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D006084" MajorTopicYN="N">Graft Rejection</DescriptorName>
<QualifierName UI="Q000517" MajorTopicYN="N">prevention & control</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D006085" MajorTopicYN="N">Graft Survival</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D006886" MajorTopicYN="N">Hydroxychloroquine</DescriptorName>
<QualifierName UI="Q000627" MajorTopicYN="Y">therapeutic use</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D007166" MajorTopicYN="N">Immunosuppressive Agents</DescriptorName>
<QualifierName UI="Q000627" MajorTopicYN="Y">therapeutic use</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D016247" MajorTopicYN="N">Information Storage and Retrieval</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D007348" MajorTopicYN="N">Insurance, Health</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D007676" MajorTopicYN="N">Kidney Failure, Chronic</DescriptorName>
<QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName>
<QualifierName UI="Q000401" MajorTopicYN="N">mortality</QualifierName>
<QualifierName UI="Q000601" MajorTopicYN="Y">surgery</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D016030" MajorTopicYN="Y">Kidney Transplantation</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008180" MajorTopicYN="N">Lupus Erythematosus, Systemic</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName>
<QualifierName UI="Q000188" MajorTopicYN="Y">drug therapy</QualifierName>
<QualifierName UI="Q000401" MajorTopicYN="N">mortality</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D060046" MajorTopicYN="N">Maintenance Chemotherapy</DescriptorName>
<QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D012042" MajorTopicYN="N">Registries</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D012189" MajorTopicYN="N">Retrospective Studies</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D012595" MajorTopicYN="N">Scleroderma, Systemic</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName>
<QualifierName UI="Q000188" MajorTopicYN="Y">drug therapy</QualifierName>
<QualifierName UI="Q000401" MajorTopicYN="N">mortality</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D016896" MajorTopicYN="N">Treatment Outcome</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D014481" MajorTopicYN="N" Type="Geographic">United States</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D055815" MajorTopicYN="N">Young Adult</DescriptorName>
</MeshHeading>
</MeshHeadingList>
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<Keyword MajorTopicYN="Y">hydroxychloroquine</Keyword>
<Keyword MajorTopicYN="Y">immunosuppression</Keyword>
<Keyword MajorTopicYN="Y">kidney transplantation</Keyword>
<Keyword MajorTopicYN="Y">outcomes</Keyword>
<Keyword MajorTopicYN="Y">pharmacy claims</Keyword>
<Keyword MajorTopicYN="Y">registries</Keyword>
<Keyword MajorTopicYN="Y">scleroderma</Keyword>
<Keyword MajorTopicYN="Y">systemic lupus erythematosus</Keyword>
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<ReferenceList>
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<li>États-Unis</li>
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<li>Alberta</li>
<li>Iowa</li>
<li>Maryland</li>
<li>Minnesota</li>
<li>Missouri (État)</li>
<li>Pennsylvanie</li>
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<li>Calgary</li>
<li>Iowa City</li>
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<region name="Missouri (État)">
<name sortKey="Lentine, Krista L" sort="Lentine, Krista L" uniqKey="Lentine K" first="Krista L" last="Lentine">Krista L. Lentine</name>
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<name sortKey="Alhamad, Tarek" sort="Alhamad, Tarek" uniqKey="Alhamad T" first="Tarek" last="Alhamad">Tarek Alhamad</name>
<name sortKey="Axelrod, David" sort="Axelrod, David" uniqKey="Axelrod D" first="David" last="Axelrod">David Axelrod</name>
<name sortKey="Brennan, Daniel C" sort="Brennan, Daniel C" uniqKey="Brennan D" first="Daniel C" last="Brennan">Daniel C. Brennan</name>
<name sortKey="Caliskan, Yasar" sort="Caliskan, Yasar" uniqKey="Caliskan Y" first="Yasar" last="Caliskan">Yasar Caliskan</name>
<name sortKey="Chang, Su Hsin" sort="Chang, Su Hsin" uniqKey="Chang S" first="Su-Hsin" last="Chang">Su-Hsin Chang</name>
<name sortKey="Hess, Gregory P" sort="Hess, Gregory P" uniqKey="Hess G" first="Gregory P" last="Hess">Gregory P. Hess</name>
<name sortKey="Kasiske, Bertram L" sort="Kasiske, Bertram L" uniqKey="Kasiske B" first="Bertram L" last="Kasiske">Bertram L. Kasiske</name>
<name sortKey="Mcadams Demarco, Mara" sort="Mcadams Demarco, Mara" uniqKey="Mcadams Demarco M" first="Mara" last="Mcadams-Demarco">Mara Mcadams-Demarco</name>
<name sortKey="Schnitzler, Mark A" sort="Schnitzler, Mark A" uniqKey="Schnitzler M" first="Mark A" last="Schnitzler">Mark A. Schnitzler</name>
<name sortKey="Segev, Dorry L" sort="Segev, Dorry L" uniqKey="Segev D" first="Dorry L" last="Segev">Dorry L. Segev</name>
<name sortKey="Xiao, Huiling" sort="Xiao, Huiling" uniqKey="Xiao H" first="Huiling" last="Xiao">Huiling Xiao</name>
</country>
<country name="Canada">
<region name="Alberta">
<name sortKey="Lam, Ngan N" sort="Lam, Ngan N" uniqKey="Lam N" first="Ngan N" last="Lam">Ngan N. Lam</name>
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