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Early sedation with dexmedetomidine in ventilated critically ill patients and heterogeneity of treatment effect in the SPICE III randomised controlled trial

Early sedation with dexmedetomidine in ventilated critically ill patients and heterogeneity of treatment effect in the SPICE III randomised controlled trial
Early sedation with dexmedetomidine in ventilated critically ill patients and heterogeneity of treatment effect in the SPICE III randomised controlled trial
Purpose
To quantify potential heterogeneity of treatment effect (HTE), of early sedation with dexmedetomidine (DEX) compared with usual care, and identify patients who have a high probability of lower or higher 90-day mortality according to age, and other identified clusters.

Methods
Bayesian analysis of 3904 critically ill adult patients expected to receive invasive ventilation > 24 h and enrolled in a multinational randomized controlled trial comparing early DEX with usual care sedation.

Results
HTE was assessed according to age and clusters (based on 12 baseline characteristics) using a Bayesian hierarchical models. DEX was associated with lower 90-day mortality compared to usual care in patients > 65 years (odds ratio [OR], 0.83 [95% credible interval [CrI] 0.68–1.00], with 97.7% probability of reduced mortality across broad categories of illness severity. Conversely, the probability of increased mortality in patients ≤ 65 years was 98.5% (OR 1.26 [95% CrI 1.02–1.56]. Two clusters were identified: cluster 1 (976 patients) mostly operative, and cluster 2 (2346 patients), predominantly non-operative. There was a greater probability of benefit with DEX in cluster 1 (OR 0.86 [95% CrI 0.65–1.14]) across broad categories of age, with 86.4% probability that DEX is more beneficial in cluster 1 than cluster 2.

Conclusion
In critically ill mechanically ventilated patients, early sedation with dexmedetomidine exhibited a high probability of reduced 90-day mortality in older patients regardless of operative or non-operative cluster status. Conversely, a high probability of increased 90-day mortality was observed in younger patients of non-operative status. Further studies are needed to confirm these findings.

Take home message
The early use of dexmedetomidine for sedation of ventilated critically ill patients who are older than 65 years, and in those with an operative diagnosis, across broad range of age categories, has a high probability of reduced mortality. Conversely, younger patients with a non-operative diagnosis have a high probability of increased mortality. Thus, the early use of dexmedetomidine in this group of patients, outside controlled research, is not advised.
0342-4642
455 - 466
Shehabi, Y
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Serpa, Neto A
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Howe, BD
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Bellomo, R
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Arabi, YM
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Bailey, M
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Bass, FE
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Kadiman, SB
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McArthur, CJ
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Reade, MC
f19b9ad8-bf75-4f95-93d0-5c51556619de
Seppelt, IM
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Takala, J
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Wise, MP
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Webb, SA
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Investigators, SPICE III Study
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Shehabi, Y
8c1b9f49-e423-44d3-ac1f-8628fa3a6639
Serpa, Neto A
5c99f004-114f-4049-98ae-59fce2572ceb
Howe, BD
4593b70f-7f52-4275-8e7b-df4c04b9c143
Bellomo, R
3eca54ed-b548-4980-b7d2-ed8412d7af58
Arabi, YM
5ce91c95-2e17-4e76-a5ec-593d352b8169
Bailey, M
cb901712-61fe-4288-8955-b9aa3057f666
Bass, FE
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Kadiman, SB
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McArthur, CJ
35116db5-88ef-4ff1-a8ff-31f26feb7b7e
Reade, MC
f19b9ad8-bf75-4f95-93d0-5c51556619de
Seppelt, IM
27d38f50-c9fc-4d5c-bec1-45e69b6d3604
Takala, J
dab16220-8d7b-4428-a021-69a95fe0fc68
Wise, MP
8a4bd740-59d0-4758-9bd7-bba19785917d
Webb, SA
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Investigators, SPICE III Study
b47e277f-2756-4888-99fe-99130c65442c

Shehabi, Y, Serpa, Neto A, Howe, BD, Bellomo, R, Arabi, YM, Bailey, M, Bass, FE, Kadiman, SB, McArthur, CJ, Reade, MC, Seppelt, IM, Takala, J, Wise, MP, Webb, SA and Investigators, SPICE III Study (2021) Early sedation with dexmedetomidine in ventilated critically ill patients and heterogeneity of treatment effect in the SPICE III randomised controlled trial. Intensive Care Medicine, 455 - 466. (doi:10.1007/s00134-021-06356-8).

Record type: Article

Abstract

Purpose
To quantify potential heterogeneity of treatment effect (HTE), of early sedation with dexmedetomidine (DEX) compared with usual care, and identify patients who have a high probability of lower or higher 90-day mortality according to age, and other identified clusters.

Methods
Bayesian analysis of 3904 critically ill adult patients expected to receive invasive ventilation > 24 h and enrolled in a multinational randomized controlled trial comparing early DEX with usual care sedation.

Results
HTE was assessed according to age and clusters (based on 12 baseline characteristics) using a Bayesian hierarchical models. DEX was associated with lower 90-day mortality compared to usual care in patients > 65 years (odds ratio [OR], 0.83 [95% credible interval [CrI] 0.68–1.00], with 97.7% probability of reduced mortality across broad categories of illness severity. Conversely, the probability of increased mortality in patients ≤ 65 years was 98.5% (OR 1.26 [95% CrI 1.02–1.56]. Two clusters were identified: cluster 1 (976 patients) mostly operative, and cluster 2 (2346 patients), predominantly non-operative. There was a greater probability of benefit with DEX in cluster 1 (OR 0.86 [95% CrI 0.65–1.14]) across broad categories of age, with 86.4% probability that DEX is more beneficial in cluster 1 than cluster 2.

Conclusion
In critically ill mechanically ventilated patients, early sedation with dexmedetomidine exhibited a high probability of reduced 90-day mortality in older patients regardless of operative or non-operative cluster status. Conversely, a high probability of increased 90-day mortality was observed in younger patients of non-operative status. Further studies are needed to confirm these findings.

Take home message
The early use of dexmedetomidine for sedation of ventilated critically ill patients who are older than 65 years, and in those with an operative diagnosis, across broad range of age categories, has a high probability of reduced mortality. Conversely, younger patients with a non-operative diagnosis have a high probability of increased mortality. Thus, the early use of dexmedetomidine in this group of patients, outside controlled research, is not advised.

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Accepted/In Press date: 18 January 2021
Published date: 8 March 2021

Identifiers

Local EPrints ID: 477950
URI: http://eprints.soton.ac.uk/id/eprint/477950
ISSN: 0342-4642
PURE UUID: 641e7c25-7544-4f02-907e-5507397dbd0f

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Date deposited: 16 Jun 2023 16:52
Last modified: 17 Mar 2024 02:25

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Contributors

Author: Y Shehabi
Author: Neto A Serpa
Author: BD Howe
Author: R Bellomo
Author: YM Arabi
Author: M Bailey
Author: FE Bass
Author: SB Kadiman
Author: CJ McArthur
Author: MC Reade
Author: IM Seppelt
Author: J Takala
Author: MP Wise
Author: SA Webb
Author: SPICE III Study Investigators

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