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Safety, Tolerability, and Real-World Effectiveness of Intravenous Ketamine in Older Adults With Treatment-Resistant Depression: A Case Series.

Authors :
Lipsitz, Orly
Di Vincenzo, Joshua D.
Rodrigues, Nelson B.
Cha, Danielle S.
Lee, Yena
Greenberg, David
Teopiz, Kayla M.
Ho, Roger C.
Cao, Bing
Lin, Kangguang
Subramaniapillai, Mehala
Flint, Alastair J.
Kratiuk, Kevin
McIntyre, Roger S.
Rosenblat, Joshua D.
Source :
American Journal of Geriatric Psychiatry; Sep2021, Vol. 29 Issue 9, p899-913, 15p
Publication Year :
2021

Abstract

<bold>Objective: </bold>To evaluate the safety, tolerability, and effectiveness of repeated doses of intravenous (IV) ketamine in older adults (i.e., ≥60 years of age) with treatment-resistant depression.<bold>Method: </bold>In this case series, fifty-three older adults (Mage = 67, SD = 6; 57% female [n = 30]) received 4 IV ketamine infusions, administered over 1-2 weeks. Effectiveness of IV ketamine was measured using the Quick Inventory for Depressive Symptomatology-Self Report 16 (QIDS-SR16) approximately 2 days after infusions 1-3, and 1-2 weeks after infusion 4. Safety was measured as hemodynamic changes before, during, immediately after, and 20 minutes after each infusion. Tolerability was assessed via systematic reporting of treatment-emergent adverse events during and after each infusion, in addition to symptoms of dissociation measured using the Clinician Administered Dissociative States Scale. Partial response (25%-50% symptomatic improvement from baseline), response (≥50% symptomatic improvement from baseline), clinically significant improvements (≥25% symptomatic improvement from baseline), and remission rates (QIDS-SR16 ≤5) were also calculated.<bold>Results: </bold>Participants reported significant decreases in depressive symptoms (i.e., as measured by the QIDS-SR16) with repeated ketamine infusions (F(4, 92) = 7.412, p <0.001). The mean QIDS-SR16 score was 17.12 (SD = 5.33) at baseline and decreased to 12.52 (SD = 5.79) following 4 infusions. After 4 infusions, 31% (n = 8) of participants partially responded to IV ketamine, 27% (n = 7) responded, 58% (n = 15) experienced clinically significant improvements, and 10% (n = 3) met remission criteria. Thirty-six participants (69%) experienced treatment-emergent hypertension during at least 1 infusion, and 10 (19%) required intervention with an antihypertensive. Drowsiness was the most commonly reported adverse event (50% of infusions; n = 73).<bold>Conclusion: </bold>Ketamine was associated with transient treatment-emergent hypertension. Response and remission rates were comparable to those reported in general adult samples. Findings are limited by the open-label, chart review nature of this study. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10647481
Volume :
29
Issue :
9
Database :
Supplemental Index
Journal :
American Journal of Geriatric Psychiatry
Publication Type :
Academic Journal
Accession number :
151913337
Full Text :
https://doi.org/10.1016/j.jagp.2020.12.032