The Stanford Integrated Psychosocial Assessment for Transplant is Associated with Outcomes Before and After Liver Transplantation.
Identifieur interne : 000216 ( Main/Exploration ); précédent : 000215; suivant : 000217The Stanford Integrated Psychosocial Assessment for Transplant is Associated with Outcomes Before and After Liver Transplantation.
Auteurs : Sasha Deutsch-Link [États-Unis] ; Ethan M. Weinberg [États-Unis] ; Therese Bitterman [États-Unis] ; Mackenzie Mcdougal [États-Unis] ; Aniket Dhariwal [États-Unis] ; Lauren S. Jones [États-Unis] ; Robert M. Weinrieb [États-Unis] ; Arpita G. Banerjee [États-Unis] ; Senayish Addis [États-Unis] ; Marina Serper [États-Unis]Source :
- Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society [ 1527-6473 ] ; 2020.
Abstract
BACKGROUND
The Stanford Integrated Psychosocial Assessment for Transplant (SIPAT) is a standardized psychosocial evaluation tool used in liver transplant (LT) evaluation. Study aims were to assess the impact of the SIPAT score and sub-score domains on transplant waitlisting decisions and post-LT outcomes including immunosuppression (IS) non-adherence, biopsy-proven rejection, and mortality/graft failure.
METHODS
We conducted a single center observational cohort study of 1430 patients evaluated for LT. Patients were divided in two groups based on a SIPAT cutoff of score < or ≥ 21 (higher SIPAT scores indicate higher psychosocial risk). Tacrolimus coefficient of variation (CoV) was used to measure IS non-adherence. Regression models assessed the relationship between total SIPAT score and domain scores and waitlisting decisions, IS non-adherence, allograft rejection, and patient death/graft failure.
RESULTS
Patients with elevated total SIPAT and SIPAT domain scores were at higher risk of not being waitlisted for LT (total SIPAT ≥21 aOR=1.78, CI 1.36-2.33, readiness ≥5 aOR=2.01, CI 1.36-2.76, social support ≥4 aOR=1.50, CI 1.15-1.94, psychopathology ≥7 aOR=1.45, CI 1.07-1.94, and lifestyle/substance abuse ≥12 aOR=1.72, CI 1.23-2.39), and were more likely to experience IS non-adherence as measured by the tacrolimus CoV (total SIPAT ≥21 aOR=2.92, CI 1.69-5.03, readiness ≥5 aOR=3.26, CI 1.63-6.52, psychopathology ≥7 aOR=1.88, CI 1.00-3.50, and lifestyle substance abuse ≥ 12 aOR=3.03, CI 1.56-5.86). Patients with a SIPAT readiness score ≥5 were more likely to experience biopsy-proven allograft rejection (aOR=2.66, CI 1.20-5.91).
CONCLUSION
The SIPAT score was independently associated with LT listing decisions and IS non-adherence, and the readiness domain was associated with risk of allograft rejection. These findings offer insights into higher risk recipients that may require additional support prior to and after transplantation.
DOI: 10.1002/lt.25975
PubMed: 33320417
Affiliations:
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<affiliation wicri:level="3"><nlm:affiliation>Leonard Davis Institute of Health Economics, University of Pennsylvania Perelman School of Medicine, Philadelphia, USA.</nlm:affiliation>
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<series><title level="j">Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society</title>
<idno type="eISSN">1527-6473</idno>
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<front><div type="abstract" xml:lang="en"><p><b>BACKGROUND</b>
</p>
<p>The Stanford Integrated Psychosocial Assessment for Transplant (SIPAT) is a standardized psychosocial evaluation tool used in liver transplant (LT) evaluation. Study aims were to assess the impact of the SIPAT score and sub-score domains on transplant waitlisting decisions and post-LT outcomes including immunosuppression (IS) non-adherence, biopsy-proven rejection, and mortality/graft failure.</p>
</div>
<div type="abstract" xml:lang="en"><p><b>METHODS</b>
</p>
<p>We conducted a single center observational cohort study of 1430 patients evaluated for LT. Patients were divided in two groups based on a SIPAT cutoff of score < or ≥ 21 (higher SIPAT scores indicate higher psychosocial risk). Tacrolimus coefficient of variation (CoV) was used to measure IS non-adherence. Regression models assessed the relationship between total SIPAT score and domain scores and waitlisting decisions, IS non-adherence, allograft rejection, and patient death/graft failure.</p>
</div>
<div type="abstract" xml:lang="en"><p><b>RESULTS</b>
</p>
<p>Patients with elevated total SIPAT and SIPAT domain scores were at higher risk of not being waitlisted for LT (total SIPAT ≥21 aOR=1.78, CI 1.36-2.33, readiness ≥5 aOR=2.01, CI 1.36-2.76, social support ≥4 aOR=1.50, CI 1.15-1.94, psychopathology ≥7 aOR=1.45, CI 1.07-1.94, and lifestyle/substance abuse ≥12 aOR=1.72, CI 1.23-2.39), and were more likely to experience IS non-adherence as measured by the tacrolimus CoV (total SIPAT ≥21 aOR=2.92, CI 1.69-5.03, readiness ≥5 aOR=3.26, CI 1.63-6.52, psychopathology ≥7 aOR=1.88, CI 1.00-3.50, and lifestyle substance abuse ≥ 12 aOR=3.03, CI 1.56-5.86). Patients with a SIPAT readiness score ≥5 were more likely to experience biopsy-proven allograft rejection (aOR=2.66, CI 1.20-5.91).</p>
</div>
<div type="abstract" xml:lang="en"><p><b>CONCLUSION</b>
</p>
<p>The SIPAT score was independently associated with LT listing decisions and IS non-adherence, and the readiness domain was associated with risk of allograft rejection. These findings offer insights into higher risk recipients that may require additional support prior to and after transplantation.</p>
</div>
</front>
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<Day>15</Day>
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<Month>Dec</Month>
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<Title>Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society</Title>
<ISOAbbreviation>Liver Transpl</ISOAbbreviation>
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<ArticleTitle>The Stanford Integrated Psychosocial Assessment for Transplant is Associated with Outcomes Before and After Liver Transplantation.</ArticleTitle>
<ELocationID EIdType="doi" ValidYN="Y">10.1002/lt.25975</ELocationID>
<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">The Stanford Integrated Psychosocial Assessment for Transplant (SIPAT) is a standardized psychosocial evaluation tool used in liver transplant (LT) evaluation. Study aims were to assess the impact of the SIPAT score and sub-score domains on transplant waitlisting decisions and post-LT outcomes including immunosuppression (IS) non-adherence, biopsy-proven rejection, and mortality/graft failure.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">We conducted a single center observational cohort study of 1430 patients evaluated for LT. Patients were divided in two groups based on a SIPAT cutoff of score < or ≥ 21 (higher SIPAT scores indicate higher psychosocial risk). Tacrolimus coefficient of variation (CoV) was used to measure IS non-adherence. Regression models assessed the relationship between total SIPAT score and domain scores and waitlisting decisions, IS non-adherence, allograft rejection, and patient death/graft failure.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Patients with elevated total SIPAT and SIPAT domain scores were at higher risk of not being waitlisted for LT (total SIPAT ≥21 aOR=1.78, CI 1.36-2.33, readiness ≥5 aOR=2.01, CI 1.36-2.76, social support ≥4 aOR=1.50, CI 1.15-1.94, psychopathology ≥7 aOR=1.45, CI 1.07-1.94, and lifestyle/substance abuse ≥12 aOR=1.72, CI 1.23-2.39), and were more likely to experience IS non-adherence as measured by the tacrolimus CoV (total SIPAT ≥21 aOR=2.92, CI 1.69-5.03, readiness ≥5 aOR=3.26, CI 1.63-6.52, psychopathology ≥7 aOR=1.88, CI 1.00-3.50, and lifestyle substance abuse ≥ 12 aOR=3.03, CI 1.56-5.86). Patients with a SIPAT readiness score ≥5 were more likely to experience biopsy-proven allograft rejection (aOR=2.66, CI 1.20-5.91).</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">The SIPAT score was independently associated with LT listing decisions and IS non-adherence, and the readiness domain was associated with risk of allograft rejection. These findings offer insights into higher risk recipients that may require additional support prior to and after transplantation.</AbstractText>
<CopyrightInformation>This article is protected by copyright. All rights reserved.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Deutsch-Link</LastName>
<ForeName>Sasha</ForeName>
<Initials>S</Initials>
<Identifier Source="ORCID">https://orcid.org/0000-0002-0923-4300</Identifier>
<AffiliationInfo><Affiliation>Department of Gastroenterology & Hepatology, University of North Carolina - Chapel Hill, Chapel Hill, NC, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Weinberg</LastName>
<ForeName>Ethan M</ForeName>
<Initials>EM</Initials>
<AffiliationInfo><Affiliation>Division of Gastroenterology & Hepatology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Bitterman</LastName>
<ForeName>Therese</ForeName>
<Initials>T</Initials>
<AffiliationInfo><Affiliation>Division of Gastroenterology & Hepatology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>McDougal</LastName>
<ForeName>Mackenzie</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Drexel University College of Medicine, Philadelphia, PA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Dhariwal</LastName>
<ForeName>Aniket</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>University of Pennsylvania, Philadelphia, PA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Jones</LastName>
<ForeName>Lauren S</ForeName>
<Initials>LS</Initials>
<AffiliationInfo><Affiliation>Philadelphia College of Osteopathic Medicine, Philadelphia, PA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Weinrieb</LastName>
<ForeName>Robert M</ForeName>
<Initials>RM</Initials>
<AffiliationInfo><Affiliation>Department of Psychiatry, University of Pennsylvania Perelman School of medicine, Philadelphia, PA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Banerjee</LastName>
<ForeName>Arpita G</ForeName>
<Initials>AG</Initials>
<AffiliationInfo><Affiliation>Department of Psychiatry, University of Pennsylvania Perelman School of medicine, Philadelphia, PA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Addis</LastName>
<ForeName>Senayish</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>Division of Gastroenterology & Hepatology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Serper</LastName>
<ForeName>Marina</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Division of Gastroenterology & Hepatology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Leonard Davis Institute of Health Economics, University of Pennsylvania Perelman School of Medicine, Philadelphia, USA.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2020</Year>
<Month>12</Month>
<Day>15</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Liver Transpl</MedlineTA>
<NlmUniqueID>100909185</NlmUniqueID>
<ISSNLinking>1527-6465</ISSNLinking>
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<CitationSubset>IM</CitationSubset>
<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Allograft Rejection</Keyword>
<Keyword MajorTopicYN="N">SIPAT</Keyword>
<Keyword MajorTopicYN="N">Tacrolimus Coefficient of Variation</Keyword>
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