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Pharmacologic Treatment of Transplant Recipients Infected With SARS-CoV-2: Considerations Regarding Therapeutic Drug Monitoring and Drug-Drug Interactions.

Identifieur interne : 000950 ( Main/Exploration ); précédent : 000949; suivant : 000951

Pharmacologic Treatment of Transplant Recipients Infected With SARS-CoV-2: Considerations Regarding Therapeutic Drug Monitoring and Drug-Drug Interactions.

Auteurs : Laure Elens [Belgique] ; Loralie J. Langman [États-Unis] ; Dennis A. Hesselink [Pays-Bas] ; Stein Bergan [Norvège] ; Dirk Jan A R. Moes [Pays-Bas] ; Mariadelfina Molinaro [Italie] ; Raman Venkataramanan [États-Unis] ; Florian Lemaitre [France]

Source :

RBID : pubmed:32304488

Descripteurs français

English descriptors

Abstract

BACKGROUND

COVID-19 is a novel infectious disease caused by the severe acute respiratory distress (SARS)-coronavirus-2 (SARS-CoV-2). Several therapeutic options are currently emerging but none with universal consensus or proven efficacy. Solid organ transplant recipients are perceived to be at increased risk of severe COVID-19 because of their immunosuppressed conditions due to chronic use of immunosuppressive drugs (ISDs). It is therefore likely that solid organ transplant recipients will be treated with these experimental antivirals.

METHODS

This article is not intended to provide a systematic literature review on investigational treatments tested against COVID-19; rather, the authors aim to provide recommendations for therapeutic drug monitoring of ISDs in transplant recipients infected with SARS-CoV-2 based on a review of existing data in the literature.

RESULTS

Management of drug-drug interactions between investigational anti-SARS-CoV-2 drugs and immunosuppressants is a complex task for the clinician. Adequate immunosuppression is necessary to prevent graft rejection while, if critically ill, the patient may benefit from pharmacotherapeutic interventions directed at limiting SARS-CoV-2 viral replication. Maintaining ISD concentrations within the desired therapeutic range requires a highly individualized approach that is complicated by the pandemic context and lack of hindsight.

CONCLUSIONS

With this article, the authors inform the clinician about the potential interactions of experimental COVID-19 treatments with ISDs used in transplantation. Recommendations regarding therapeutic drug monitoring and dose adjustments in the context of COVID-19 are provided.


DOI: 10.1097/FTD.0000000000000761
PubMed: 32304488
PubMed Central: PMC7188032


Affiliations:


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Le document en format XML

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<p>
<b>BACKGROUND</b>
</p>
<p>COVID-19 is a novel infectious disease caused by the severe acute respiratory distress (SARS)-coronavirus-2 (SARS-CoV-2). Several therapeutic options are currently emerging but none with universal consensus or proven efficacy. Solid organ transplant recipients are perceived to be at increased risk of severe COVID-19 because of their immunosuppressed conditions due to chronic use of immunosuppressive drugs (ISDs). It is therefore likely that solid organ transplant recipients will be treated with these experimental antivirals.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>This article is not intended to provide a systematic literature review on investigational treatments tested against COVID-19; rather, the authors aim to provide recommendations for therapeutic drug monitoring of ISDs in transplant recipients infected with SARS-CoV-2 based on a review of existing data in the literature.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>Management of drug-drug interactions between investigational anti-SARS-CoV-2 drugs and immunosuppressants is a complex task for the clinician. Adequate immunosuppression is necessary to prevent graft rejection while, if critically ill, the patient may benefit from pharmacotherapeutic interventions directed at limiting SARS-CoV-2 viral replication. Maintaining ISD concentrations within the desired therapeutic range requires a highly individualized approach that is complicated by the pandemic context and lack of hindsight.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>With this article, the authors inform the clinician about the potential interactions of experimental COVID-19 treatments with ISDs used in transplantation. Recommendations regarding therapeutic drug monitoring and dose adjustments in the context of COVID-19 are provided.</p>
</div>
</front>
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<AbstractText Label="BACKGROUND">COVID-19 is a novel infectious disease caused by the severe acute respiratory distress (SARS)-coronavirus-2 (SARS-CoV-2). Several therapeutic options are currently emerging but none with universal consensus or proven efficacy. Solid organ transplant recipients are perceived to be at increased risk of severe COVID-19 because of their immunosuppressed conditions due to chronic use of immunosuppressive drugs (ISDs). It is therefore likely that solid organ transplant recipients will be treated with these experimental antivirals.</AbstractText>
<AbstractText Label="METHODS">This article is not intended to provide a systematic literature review on investigational treatments tested against COVID-19; rather, the authors aim to provide recommendations for therapeutic drug monitoring of ISDs in transplant recipients infected with SARS-CoV-2 based on a review of existing data in the literature.</AbstractText>
<AbstractText Label="RESULTS">Management of drug-drug interactions between investigational anti-SARS-CoV-2 drugs and immunosuppressants is a complex task for the clinician. Adequate immunosuppression is necessary to prevent graft rejection while, if critically ill, the patient may benefit from pharmacotherapeutic interventions directed at limiting SARS-CoV-2 viral replication. Maintaining ISD concentrations within the desired therapeutic range requires a highly individualized approach that is complicated by the pandemic context and lack of hindsight.</AbstractText>
<AbstractText Label="CONCLUSIONS">With this article, the authors inform the clinician about the potential interactions of experimental COVID-19 treatments with ISDs used in transplantation. Recommendations regarding therapeutic drug monitoring and dose adjustments in the context of COVID-19 are provided.</AbstractText>
</Abstract>
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<LastName>Elens</LastName>
<ForeName>Laure</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Louvain Drug Research Institute (LDRI), Integrated Pharmacometrics, Pharmacogenomics and Pharmacokinetics (PMGK), Université catholique de Louvain (UCLouvain), Brussels, Belgium.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Institut de Recherche Expérimentale et Clinique (IREC), Louvain Center for Toxicology and Applied Pharmacology (LTAP), Université catholique de Louvain (UCLouvain), Brussels, Belgium.</Affiliation>
</AffiliationInfo>
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<LastName>Langman</LastName>
<ForeName>Loralie J</ForeName>
<Initials>LJ</Initials>
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<Affiliation>Department of Laboratory Medicine and Pathology, Mayo Clinic College of Medicine, Rochester, Minnesota.</Affiliation>
</AffiliationInfo>
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<LastName>Hesselink</LastName>
<ForeName>Dennis A</ForeName>
<Initials>DA</Initials>
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<Affiliation>Division of Nephrology and Transplantation, Department of Internal Medicine, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Rotterdam Transplant Group.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Bergan</LastName>
<ForeName>Stein</ForeName>
<Initials>S</Initials>
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<Affiliation>Department of Pharmacology, Oslo University Hospital, Oslo, Norway.</Affiliation>
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<ForeName>Dirk Jan A R</ForeName>
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<Affiliation>Department of Clinical Pharmacy and Toxicology, Leiden University Medical Center, Leiden, the Netherlands.</Affiliation>
</AffiliationInfo>
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<ForeName>Mariadelfina</ForeName>
<Initials>M</Initials>
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<Affiliation>Clinical and Experimental Pharmacokinetics Lab, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.</Affiliation>
</AffiliationInfo>
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<ForeName>Raman</ForeName>
<Initials>R</Initials>
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<Affiliation>School of Pharmacy and Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.</Affiliation>
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<ForeName>Florian</ForeName>
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<Affiliation>Univ Rennes, CHU Rennes, Inserm, EHESP, Irset (Institut de recherche en sante[Combining Acute Accent], environnement et travail)-UMR_S 1085, Rennes, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>INSERM, Centre d'Investigation Clinique, CIC 1414, Rennes, France.</Affiliation>
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<Language>eng</Language>
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<Country>United States</Country>
<MedlineTA>Ther Drug Monit</MedlineTA>
<NlmUniqueID>7909660</NlmUniqueID>
<ISSNLinking>0163-4356</ISSNLinking>
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<Chemical>
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<SupplMeshName Type="Organism" UI="C000656484">severe acute respiratory syndrome coronavirus 2</SupplMeshName>
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<MeshHeading>
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<QualifierName UI="Q000031" MajorTopicYN="N">analogs & derivatives</QualifierName>
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<MeshHeading>
<DescriptorName UI="D000409" MajorTopicYN="N">Alanine</DescriptorName>
<QualifierName UI="Q000031" MajorTopicYN="N">analogs & derivatives</QualifierName>
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