Which patients with bipolar depression receive antidepressant augmentation? Results from an observational multicenter study.


Journal

CNS spectrums
ISSN: 1092-8529
Titre abrégé: CNS Spectr
Pays: United States
ID NLM: 9702877

Informations de publication

Date de publication:
12 2022
Historique:
pubmed: 11 9 2021
medline: 7 12 2022
entrez: 10 9 2021
Statut: ppublish

Résumé

To identify demographic and clinical characteristics of bipolar depressed patients who require antidepressant (AD) augmentation, and to evaluate the short- and long-term effectiveness and safety of this therapeutic strategy. One hundred twenty-two bipolar depressed patients were consecutively recruited, 71.7% of them received mood stabilizers (MS)/second-generation antipsychotics (SGA) with AD-augmentation and 28.3% did not. Patients were evaluated at baseline, and after 12 weeks and 15 months of treatment. The AD-augmentation was significantly higher in patients with bipolar II compared with bipolar I diagnosis. Patients with MS/SGA + AD had often a seasonal pattern, depressive polarity onset, depressive index episode with anxious features, a low number of previous psychotic and (hypo)manic episodes and of switch. They had a low irritable premorbid temperament, a low risk of suicide attempts, and a low number of manic symptoms at baseline. After 12 weeks of treatment, 82% of patients receiving ADs improved, 58% responded and 51% remitted, 3.8% had suicidal thoughts or projects, 6.1% had (hypo)manic switch, and 4.1% needed hospitalization. During the following 12 months, 92% of them remitted from index episode, 25.5% did not relapse, and 11% needed hospitalization. Although at the start advantaged, patients with AD-augmentation, compared with those without AD-augmentation, did not significantly differ on any outcome as well on adverse events in the short- and long-term treatment. Our findings indicate that ADs, combined with MS and/or SGA, are short and long term effective and safe in a specific subgroup for bipolar depressed patients.

Sections du résumé

BACKGROUND
To identify demographic and clinical characteristics of bipolar depressed patients who require antidepressant (AD) augmentation, and to evaluate the short- and long-term effectiveness and safety of this therapeutic strategy.
METHODS
One hundred twenty-two bipolar depressed patients were consecutively recruited, 71.7% of them received mood stabilizers (MS)/second-generation antipsychotics (SGA) with AD-augmentation and 28.3% did not. Patients were evaluated at baseline, and after 12 weeks and 15 months of treatment.
RESULTS
The AD-augmentation was significantly higher in patients with bipolar II compared with bipolar I diagnosis. Patients with MS/SGA + AD had often a seasonal pattern, depressive polarity onset, depressive index episode with anxious features, a low number of previous psychotic and (hypo)manic episodes and of switch. They had a low irritable premorbid temperament, a low risk of suicide attempts, and a low number of manic symptoms at baseline. After 12 weeks of treatment, 82% of patients receiving ADs improved, 58% responded and 51% remitted, 3.8% had suicidal thoughts or projects, 6.1% had (hypo)manic switch, and 4.1% needed hospitalization. During the following 12 months, 92% of them remitted from index episode, 25.5% did not relapse, and 11% needed hospitalization. Although at the start advantaged, patients with AD-augmentation, compared with those without AD-augmentation, did not significantly differ on any outcome as well on adverse events in the short- and long-term treatment.
CONCLUSION
Our findings indicate that ADs, combined with MS and/or SGA, are short and long term effective and safe in a specific subgroup for bipolar depressed patients.

Identifiants

pubmed: 34505564
doi: 10.1017/S109285292100078X
pii: S109285292100078X
doi:

Substances chimiques

Antidepressive Agents 0
Antimanic Agents 0
Antipsychotic Agents 0
Antidepressive Agents, Second-Generation 0
Anticonvulsants 0

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

731-739

Auteurs

Laura Musetti (L)

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Antonio Tundo (A)

Istituto di Psicopatologia, Rome, Italy.

Erika Cambiali (E)

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Claudia Del Grande (C)

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Rocco De Filippis (R)

Istituto di Psicopatologia, Rome, Italy.

Caterina Franceschini (C)

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Luca Proietti (L)

Istituto di Psicopatologia, Rome, Italy.

Sophia Betrò (S)

Istituto di Psicopatologia, Rome, Italy.

Donatella Marazziti (D)

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Liliana Dell'Osso (L)

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

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Classifications MeSH