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. Author manuscript; available in PMC: 2021 Apr 1.
Published in final edited form as: Alcohol Clin Exp Res. 2020 Mar 15;44(4):764–776. doi: 10.1111/acer.14305

Table 1.

Comparison of Ingestion and Infusion Paradigms

Aspect of Method Ingestion Intravenous Infusion
Control: controlled variable for alcohol administration Dose of alcohol ingested BrAC Trajectory
Control: main barrier to precision Uncontrollable absorption BrAC meter precision
Control: individual peak BrAC SD ~ 20-30% of intended mean SD ~ 3% of intended mean
Control: latency to peak BrAC SD ~ 25 min SD ~ 2 min
Control of overall BrAC trajectory Poor: see Figure 1A-1C Precise: see Figure 1D
Control: first pass metabolism Uncertain and uncontrollable None
Power: Influence on size of sample population required for adequate hypothesis testing Determined by concern for dealing with within-group variability in brain exposure to alcohol during analysis Maximized by elimination of absorption and individualized modeling of alcohol distribution and elimination kinetics
Safety: reservoir effect Unavoidable Does not exist
Safety: peak BrAC Mean value limited by uncertainty: absorption kinetics vs. toxicity Limited by toxicity only: investigator specifies a preset value that cannot be exceeded by participants.
Ability to control beverage characteristics, including concentration, amount, taste, aroma, texture, and temperature Excellent, but need to control them all, and to know relationship of each to subject’s preference No beverage, but important to know infusate alcohol concentration, and to control infusate temperature
Ability to blind the first data-collection technician regarding alcohol vs. control beverage Good Currently unavailable
Ability to control for expectancy effects with an effective placebo control Good to excellent depending on aspects of study design Good to excellent depending on aspects of study design
Use of preferred alcoholic beverages Feasible but uncommon Not applicable
Presence of sensory cues associated with alcohol consumption Excellent; olfactory and taste cues and behavioral responses (e.g., drinking from a glass). Limited on purpose, but can be added depending on experimental question
Documentation of BrAC achieved Stored, BrAC meter readings; unchecked if technician blinded Real-time, monitored BrAC meter readings and continuous estimate of BrAC
Documentation of events, comments Manual, changeable record Time-stamped, permanent record
Documentation of dosing schedule in each session Intermittent, by technician Continuous, by CAIS
Laboratory settings where research can be conducted Includes simulated bar, lab, simulated living room, fMRI, CT, etc. Includes simulated bar, lab, CT, SPECT, PET, and fMRI
Inclusion of social interaction as variable of interest Possible, limited, published currently limited, unpublished
Repeated within-session administrations Easy, but unreliable result Easy and reliable
Ability to study acute within-session tolerance Possible but typically confounded by limb effects Easy and reliable
Main domain of validity Ecological route of administration Ecological alcohol exposures
Cost; # technicians required for per-session data collection Minimum of 1; 2 if blinding required Minimum of 1; 2 if blinding required
Cost: preparation of beverage/alcohol administered Variable; usually by lab technician from readily available components Infusate: $150 – $300 per session; usually performed by a research pharmacy
Cost: optimization of alcohol delivery paradigm Variable depending on investigator experience 20 hours including free consultation using CAIS simulation mode
Cost: training of technicians Weeks on protocol Weeks on protocol + Days on CAIS
Cost: CAIS hardware $0 $2,500 - $4,000
Cost: CAIS software $0 $0 if paradigm used anywhere previously
Cost: CAIS bench testing $0 Free, but shipping at cost
Cost: CAIS training $0 ~ $500 a day + travel

Note. BrAC= Breath Alcohol Concentration; CAIS= Computer Assisted Infusion Software