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

Ther Drug Monit. 2020 Jun;42(3):360-368 doi: 10.1097/FTD.0000000000000761.
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.

Metadata
Publication type: Review
Organ: Various; Kidney; Liver; Lung; Heart; Pancreas; Intestine; Simultaneous Kidney/Pancreas; Heart/Lung
Language: English
Country: International
MeSH terms: Adenosine Monophosphate; Alanine; Antibodies, Monoclonal, Humanized; Antiviral Agents; Betacoronavirus; COVID-19; Coronavirus Infections; Drug Interactions; Drug Monitoring; Glucocorticoids; Humans; Hydroxychloroquine; Immunosuppressive Agents; Pandemics; Pneumonia, Viral; Protease Inhibitors; SARS-CoV-2; Transplant Recipients; Liver Transplantation; Kidney Transplantation; Lung Transplantation; Heart Transplantation; Pancreas Transplantation; Heart-Lung Transplantation; 0 (Antibodies, Monoclonal, Humanized); 0 (Antiviral Agents); 0 (Glucocorticoids); 0 (Immunosuppressive Agents); 0 (Protease Inhibitors); 3QKI37EEHE (Remdesivir); 415SHH325A (Adenosine Monophosphate); 4QWG6N8QKH (Hydroxychloroquine); I031V2H011 (Tocilizumab); OF5P57N2ZX (Alanine); Covid-19