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A longitudinal study of post-traumatic stress, depressive, and anxiety symptoms trajectories in subjects with bipolar disorder during the COVID-19 pandemic

Published online by Cambridge University Press:  13 January 2022

Claudia Carmassi*
Affiliation:
Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy
Annalisa Cordone
Affiliation:
Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy
Carlo Antonio Bertelloni
Affiliation:
Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy
Andrea Cappelli
Affiliation:
Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy
Virginia Pedrinelli
Affiliation:
Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy
Gaia Sampogna
Affiliation:
Department of Psychiatry, University of Campania “L. Vanvitelli”, Naples, Italy
Gabriele Massimetti
Affiliation:
Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy
Valerio Dell’Oste
Affiliation:
Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy
Liliana Dell’Osso
Affiliation:
Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy
*
*Author for correspondence: Claudia Carmassi, E-mail: claudia.carmassi@unipi.it

Abstract

Background

Bipolar disorder (BD) is recognized to be at high risk for developing negative psychopathological sequelae to potentially traumatic events. Nevertheless, scant data are still available about the effects of the COVID-19 emergency on the clinical course of BD. The present study examined prospectively the development and trajectories of post-traumatic stress, depressive, and anxiety symptoms among subjects with BD that were followed in an outpatient psychiatric clinic at the time of pandemic onset.

Methods

A cohort of 89 subjects with BD was enrolled during the first wave of the COVID-19 pandemic, and assessed at baseline (T0), 2-months (T1), and 6-months (T2) follow-up. A K-means cluster analysis was used to identify distinct trajectories of depressive, anxiety, and post-traumatic stress symptoms during the three time points.

Results

We identified three trajectories: the Acute reaction (13.5%); the Increasing severity (23.6%); and the Low symptoms (62.9%) groups, respectively. In the Acute reaction group a significant prevalence of female gender was reported with respect to the Low symptoms one. Subjects in the Increasing severity group reported significantly lower employment rate, and higher rate of relatives at risk for COVID-19 medical complications. Subjects in the Increasing Severity group reported higher rates of previous hospitalization and manic symptoms at baseline than those included in the Low symptoms one.

Conclusions

Our results describe three distinct symptom trajectories during the COVID-19 emergency in a cohort of subjects suffering from BD, suggesting the need of a long-term follow-up for detecting the impact of the COVID-19 pandemic in this vulnerable population.

Information

Type
Research Article
Creative Commons
Creative Common License - CCCreative Common License - BYCreative Common License - NCCreative Common License - ND
This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives licence (http://creativecommons.org/licenses/by-nc-nd/4.0), which permits non-commercial re-use, distribution, and reproduction in any medium, provided that no alterations are made and the original article is properly cited. The written permission of Cambridge University Press must be obtained prior to any commercial use and/or adaptation of the article.
Copyright
© The Author(s), 2022. Published by Cambridge University Press on behalf of the European Psychiatric Association
Figure 0

Table 1. K-means cluster analysis features.

Figure 1

Figure 1. IES-R, GAD-7, and PHQ-9 mean scores among T0, T1, and T2 in the Acute reaction (N = 12), Increasing severity (N = 21), and Low symptoms (N = 56) groups.

Figure 2

Table 2. K-means cluster analysis features.

Figure 3

Table 3. Sociodemographic, clinical, and COVID-19 characteristics in the total sample (N = 89) and in the Acute reaction (N = 12), Increasing severity (N = 21), and Low symptoms (N = 56) groups.

Figure 4

Table 4. Comparison of IES-R, GAD-7, and PHQ-9, scores among T0, T1, and T2 in the total sample (N = 89) and in the Acute reaction (N = 12), Increasing severity (N = 21), and Low symptoms (N = 56) groups.

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