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. 2020 Jun 18;7(7):e34. doi: 10.1016/S2215-0366(20)30238-8

Multidisciplinary research priorities for the COVID-19 pandemic

Shireen Najam a
PMCID: PMC7302782  PMID: 32563310

In their Position Paper1 in The Lancet Psychiatry, Emily Holmes and colleagues have laid out a comprehensive outline for mental health research, with a focus on a multidisciplinary approach to guide policy and practice using a bio-psychosocial approach, and have suggested research areas making use of existing research infrastructure and aligning ongoing research with COVID-19 priorities.

The authors have provided a nearly exhaustive list of issues within the psychological and social domains; however, the biological domain needs expansion. They have addressed a need to look at altered brain physiology, but not the psychotropic response in the context of infection with severe acute respiratory syndrome coronavirus 2 (SARS CoV-2).

Psychopharmacology is particularly important in acutely distressed patients,2 especially when staff–patient interactions are restricted by protective equipment and physical distancing. As Holmes and colleagues point out, evidence on the safety and efficacy of psychotropic drugs is likely to become available and be published in an uncoordinated way.

Much of the prescribing guidance has been based on knowledge published before the COVID-19 pandemic.3 Holmes and colleagues have looked at redeployment of medications, but this will not suffice. The safety of psychotropic drugs in patients is a major area of consultation liaison psychiatry. Laporte and Healy4 have highlighted that treatment of patients infected with SARS CoV-2 should avoid medicines that can increase the risk of pneumonia by depressing levels of consciousness, respiration, immunity, and other protective mechanisms, which includes antipsychotics, opioid analgesics, and additive effects of polypharmacy.

One way of tackling this potential problem would be to keep an electronic linked database of safety and efficacy of psychotropic drugs in various national and international centres, funded by private and public health agencies, in line with research on COVID-19 therapeutics in other specialties. At the hospital level, data can be retrieved through electronic health records. Song and colleagues5 have also described the role of hospital pharmacists in monitoring prescribed drugs in patients with SARS-CoV-2 infection. Previously unrecognised side-effects can be accounted for in retrospective case studies. The emerging data can then be used to test evidence in multicentre, blinded, pragmatic controlled trials, comparing it with pre-COVID-19 evidence on safety and efficacy, thereby increasing the sample size and gathering evidence in a relatively short timeframe.

The COVID-19 pandemic will last a long time. A concerted effort is needed to guide policy on the emerging effects of COVID-19 on the safety and efficacy of psychotropic drugs.

Acknowledgments

I declare no competing interests.

References


Articles from The Lancet. Psychiatry are provided here courtesy of Elsevier

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