Variation in propofol induction doses administered to surgical patients over age 65.

dc.contributor.author

Schonberger, Robert B

dc.contributor.author

Bardia, Amit

dc.contributor.author

Dai, Feng

dc.contributor.author

Michel, George

dc.contributor.author

Yanez, David

dc.contributor.author

Curtis, Jeptha P

dc.contributor.author

Vaughn, Michelle T

dc.contributor.author

Burg, Matthew M

dc.contributor.author

Mathis, Michael

dc.contributor.author

Kheterpal, Sachin

dc.contributor.author

Akhtar, Shamsuddin

dc.contributor.author

Shah, Nirav

dc.date.accessioned

2024-06-11T13:47:06Z

dc.date.available

2024-06-11T13:47:06Z

dc.date.issued

2021-08

dc.description.abstract

Background/objectives

Advanced age is associated with increased susceptibility to acute adverse effects of propofol. The present study aimed to describe patterns of propofol dosing for induction of general anesthesia before endotracheal intubation in a nationwide sample of older adults presenting for surgery.

Design

Retrospective observational study using the Multicenter Perioperative Outcomes Group data set.

Setting

Thirty-six institutions across the United States.

Participants

A total of 350,766 patients aged over 65 years who received propofol for general anesthetic induction and endotracheal intubation between 2014 and 2018.

Intervention

None.

Measurements

Total induction bolus dose of propofol administered.

Results

The mean (SD) weight-adjusted propofol dose was 1.7 (0.6) mg/kg. The mean prevalent propofol induction dose exceeded the upper bound of what has been described as the typical geriatric dose requirement across every age category examined. The percent of patients receiving propofol induction doses above the described typical geriatric range was 64.8% (95% CI 64.6-65.0), varying from 73.8% among patients aged 65-69 to 45.8% among patients aged 80 and older.

Conclusion

The present study of a large multicenter cohort demonstrates that prevalent propofol dosing commonly falls above the published typically required dose range for patients aged ≥65 in nationwide anesthetic practice. Widespread variability in induction dose administration remains incompletely explained by known patient variables. The nature and clinical consequences of these unexplained dosing decisions remain important topics for further study. Observed discordance between expected and actual induction dosing raises the question of whether there should be reconsideration of widespread provider practice or, alternatively, whether what is published as the typical propofol induction dose range should be revisited.
dc.identifier.issn

0002-8614

dc.identifier.issn

1532-5415

dc.identifier.uri

https://hdl.handle.net/10161/31163

dc.language

eng

dc.publisher

Wiley

dc.relation.ispartof

Journal of the American Geriatrics Society

dc.relation.isversionof

10.1111/jgs.17139

dc.rights.uri

https://creativecommons.org/licenses/by-nc/4.0

dc.subject

Humans

dc.subject

Propofol

dc.subject

Anesthesia, General

dc.subject

Retrospective Studies

dc.subject

Intubation, Intratracheal

dc.subject

Age Factors

dc.subject

Dose-Response Relationship, Drug

dc.subject

Aged

dc.subject

Aged, 80 and over

dc.subject

United States

dc.subject

Female

dc.subject

Male

dc.title

Variation in propofol induction doses administered to surgical patients over age 65.

dc.type

Journal article

duke.contributor.orcid

Yanez, David|0000-0002-2501-5028

pubs.begin-page

2195

pubs.end-page

2209

pubs.issue

8

pubs.organisational-group

Duke

pubs.organisational-group

School of Medicine

pubs.organisational-group

Basic Science Departments

pubs.organisational-group

Biostatistics & Bioinformatics

pubs.organisational-group

Biostatistics & Bioinformatics, Division of Biostatistics

pubs.publication-status

Published

pubs.volume

69

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