Evaluating the hip-flask defence in subjects with alcohol on board: An experimental study
Introduction
Driving under the influence of alcohol (DUI) is a major problem for traffic-safety. Drunk drivers are over-represented in statistics of injuries and deaths on the road. Among alcohol-impaired drivers a popular defence argument is alleged consumption after driving, commonly referred to as the hip-flask defence [1], [2]. In such cases the analysis and interpretation of a person’s blood-alcohol concentration (BAC) and urine alcohol concentration (UAC) are important tasks for forensic toxicologists. Therefore, knowledge about the pharmacokinetics of alcohol is important.
There is a considerable variation in pharmacokinetics of ethanol both within and between subjects [3], [4], [5]. In one study, the variation in mean maximum ethanol concentration (Cmax) was 23% between subjects and 24% within subject when subjects were fasted. Corresponding figures for the mean area under the ethanol concentration-time curve (AUC) were 21 and 22%, respectively [5]. In addition, both the absorption and elimination are affected by a number of factors, e.g. type of beverage, nutritional state, age, sex, body weight and genetic factors [4]. The speed of absorption of ethanol from the gut, which has bearing on the peak concentration of alcohol, depends on e.g. the concentration of ethanol in the beverage and in particular the fed or fasting state of the individual [5], [6]. In the above mentioned study [5], where 0.3 g ethanol/kg was given the Cmax in the fasting state was significantly greater than after a meal, 39.9 mg/dL vs 21.3 mg/dL. The same applied to the mean AUC, 54.8 mg/dL h vs 33.6 mg/dL h. Ethanol is distributed into the total body water and hence differences in age, sex and bodyweight will affect the concentration-time profile of ethanol [7]. The enzymes mainly responsible for the metabolism of ethanol are under genetic control. The alcohol dehydrogenase and aldehyde dehydrogenase responsible for converting ethanol to acetaldehyde and acetaldehyde to acetate, respectively shows polymorphism, which contributes to differences in enzyme activity and ethnic differences have been reported. Another ethanol metabolising enzyme, microsomal CYP2E1 is inducible and increases the clearance of ethanol in heavy drinkers. Feeding increases the rate of ethanol metabolism by enhancing enzyme activity. Women have shown to display a higher clearance of ethanol per unit of lean body mass [4].
Forensic toxicologists are often called as expert witnesses in drinking and driving cases where the suspect has claimed the hip-flask defence, to assess the credibility of the explanation. Several approaches to help the expert have been introduced [8]. Two consecutive blood samples have been used as well as congener analysis and recently the determination of ethyl glucuronide and ethyl sulphate concentrations in blood [9].
There is a number of controlled drinking experiments where peak BAC and times of reaching the peak after drinking known amounts of alcohol have been studied. In many of them the highest BAC was reached within 30 min after drinking ended. On the other hand there are other studies where individuals reached the highest concentration after 60 min or even 90 min after drinking was ended. Those variations explain why two blood samples taken 30–60 min apart are not enough to assess whether there has been a new intake of alcohol based on a BAC increase or decrease between samples [8].
In Sweden the preferred method is to take one blood sample and two urine samples within 60 min and then relate the blood concentrations to the urine concentrations. Approximately 0.5–2.5% of the total amount of alcohol ingested is excreted unchanged with the urine. Urine is produced at a rate of about 1 mL per minute and the expected UAC/BAC ratio for primary or ureter urine is 1.25:1 as expected from differences in water content (100/80 = 1.25). The BAC might show a rapid rise during absorption, depending on the dose, the speed of drinking and gastric emptying. By contrast, the UAC changes much more slowly and thus the UAC/BAC ratio for the first void is a lot lower than 1:25:1 [10], [11]. After finishing drinking the concentrations of ethanol in urine starts to exceed the concentrations in blood. During the entire post-absorptive phase of ethanol kinetics the urine alcohol concentration is always higher than in blood. If the ratio between urine alcohol and blood alcohol reaches 1.25 or more this indicates that the person is in the post-absorptive phase and that drinking ended at least 1–2 h earlier. If the second urine sample has a higher ethanol concentration than the first sample and a ratio between the concentration in the first urine sample and the concomitant blood sample close to unity, it indicates a recent intake (i.e. less than 2 h ago), supporting the hip-flask defence [12].
In 2017, the National Board of Forensic Medicine in Sweden received 4091 DUI cases. Expert opinion reports on the hip-flask defence were written in 237 cases in 2017. Hence, the hip-flask defence is a common claim from people suspected of driving under influence of alcohol. The scientific data used to support or challenge this is solely based on data from controlled single doses of ethanol administered during a short time and in abstinent subjects. In reality, we believe that even in drinking after driving cases, the subject many times has alcohol in the body at time of the hip-flask drink. This questions the usefulness of the two major parameters used to investigate the hip-flask defence; the relationship between two urinary voids and the UAC/BAC ratio. Therefore we aimed to investigate how these parameters vary after an initial drinking session of beer and then a subsequent hip-flask drink of three different doses of whiskey.
Section snippets
Chemicals and solutions
The following chemicals and solutions were used in the ethanol analysis: Ethanol 99.5%, ethanol 95% both from Kemetyl (Jordbro, Sweden) and n-propanol (analytical grade) from Merck (Darmstadt, Germany). From ethanol 99.5%, aqueous standards samples were in house prepared to final concentrations of 0.1, 0.2, 1.0, 2.5 and 5.0 mg/mL for calibration. From ethanol 95%, aqueous quality control samples were prepared in two steps to concentrations of 0.2 and 1.0 mg/mL. Together with the in house prepared
Results
The mean age and weight of the subjects were 30.5 years (20–66) and 72 kg (44.5–104.5) and there were no significant differences among the three dosing groups. After the first 1 h drinking session the participants Tmax (the time required to achieve the maximum concentration) occurred at 60–105 min (mean 81 min) and all participants were in the elimination phase when drinking session two began. First Cmax varied between 0.19‰ and 0.51‰ in blood and between 0.31‰ and 0.69‰ in urine. The drinking
Discussion
The main finding of our study was that the presence of alcohol in the urine from previous drinking does not preclude the interpretation of the hip-flask defence from parameters such as UAC/BAC and the difference between two consecutive urine samples. However, the inter-individual differences were large and should be addressed in testimonies and expert opinions.
Indeed, three of the subjects showed results not compatible with a recent drink using the criteria based on previous literature from
Conclusions
Our study showed that the difference between the ethanol concentrations in two consecutive urine samples, taken 1 h apart, is a more sensitive parameter than the urine to blood alcohol ratio to detect a recent intake when ethanol from previous intakes are present in the body. Out of 15 subjects, 3 showed unexpected results but when looking closer to especially the difference between two consecutive urine samples it was obvious that they were not normal and should easily be spotted by the trained
Author contributions
Christoffer Kronstrand applied for ethics approval and funding, supervised the subjects, obtained and analysed samples, analysed data and wrote draught manuscript.
Robert Kronstrand, designed the study, applied for ethics approval and funding, analysed data and wrote draught manuscript, and was corresponding author.
Gunnel Nilsson, supervised the subjects, obtained and analysed samples, analysed data and wrote manuscript.
Maria D. Chermà, supervised the subjects, analysed data and commented on
Acknowledgements
This research funded by the Swedish Trafikverket (grant TRV 2015/14589) and by the Swedish National Board of Forensic Medicine.
References (15)
The individual and the estimation of his blood alcohol concentration from intake: with particular reference to the “hip-flask” drink
J. Forensic Sci. Soc.
(1986)Evidence-based survey of the elimination rates of ethanol from blood with applications in forensic casework
Forensic Sci. Int.
(2010)- et al.
Evaluation of the hip-flask defence by determination of ethyl glucuronide and ethyl sulphate concentrations in blood
Forensic Sci. Int.
(2015) - et al.
Relationship between blood and urine alcohol concentrations in apprehended drivers who claimed consumption of alcohol after driving with and without supporting evidence
Forensic Sci. Int.
(2010) Top ten defence challenges among drinking drivers in Sweden
Med. Sci. Law
(1991)- et al.
Between-subject and within-subject variations in the pharmacokinetics of ethanol
Br. J. Clin. Pharmacol.
(1994) Inter-individual and intra-individual variability of ethanol concentration-time profiles: comparison of ethanol ingestion before or after an evening meal
Br. J. Clin. Pharmacol.
(1995)
Cited by (7)
Interpol review of toxicology 2019–2022
2023, Forensic Science International: SynergyCitation Excerpt :Experimental studies were carried out to assess hip-flask defense. A study investigated how blood and urine ethanol kinetics varied after an initial drinking session of beer and then a subsequent hip-flask drink of three different doses of whiskey [111]. Results supplemented the previous studies mainly based on data from administration of controlled single doses of ethanol.
Hip-flask defense: An experimental study in the Hungarian population
2021, Journal of Forensic and Legal MedicineCitation Excerpt :Therefore, collecting several urine samples and comparing them to the blood sample provides a more accurate information about the time of drinking and the phases of alcohol metabolism, making it possible to detect or exclude consumption after the act.5 A 2018 Swedish study showed that collecting one blood and two urine samples within 60–120 min after the act of driving is an effective method for determining alcohol metabolism.6 An UAC/BAC ratio exceeding 1.25 indicated that the absorption is complete, and the drink was consumed 1 or 2 h earlier.
Evaluating the hip-flask defence using analytical data from ethanol and ethyl glucuronide. A comparison of two models
2020, Forensic Science InternationalCitation Excerpt :Blood samples were analysed for ethanol the day of collection and urine samples analysed at the end of each study week (within 5 days). The method used has previously been validated for ethanol quantification in blood or urine samples from legal cases [19,20]. In brief, a 100 μL aliquot of study samples, calibration samples and control samples were diluted with 1000 μL internal solution in head-space vials, sealed with crimp caps and placed on an auto sampler for ethanol analysis by head-space gas chromatography and flame ionization detection.
Cycling under the influence of alcohol-criminal offenses in a German metropolis
2022, International Journal of Legal MedicineFORENSIC ISSUES RELATED TO ETHANOL DETERMINATION IN BIOLOGICAL SPECIMENS AS EVIDENCE FOR PROSECUTION OF TRAFFIC OFFENDERS WHEN STATUTORY CONCENTRATION LIMITS ARE ENFORCED
2022, Karch's Drug Abuse Handbook: Third EditionWhat the lab can and cannot do: clinical interpretation of drug testing results
2020, Critical Reviews in Clinical Laboratory Sciences