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Clinical Research

Co-exposure to gamma-hydroxybutyrate is associated with attenuated neuropsychiatric and stimulant effects of metamfetamine

ORCID Icon, ORCID Icon, ORCID Icon, ORCID Icon & ORCID Icon
Received 18 Jan 2024, Accepted 03 May 2024, Published online: 17 Jun 2024

Figures & data

Table 1. Comparison of baseline characteristics between groups defined by analytical detections.

Figure 1. Median, interquartile range and range of metamfetamine blood concentrations at the time of hospital admission for each analytically defined exposure groups. *Median metafetamine blood concentration in groups with gamma-hydroxybutyrate detections was significantly greater than groups without gamma-hydroxybutyrate detected (P < 0.0004).

Figure 1. Median, interquartile range and range of metamfetamine blood concentrations at the time of hospital admission for each analytically defined exposure groups. *Median metafetamine blood concentration in groups with gamma-hydroxybutyrate detections was significantly greater than groups without gamma-hydroxybutyrate detected (P < 0.0004).

Figure 2. Median, interquartile range and range of gamma-hydroxybutyrate blood concentrations at the time of hospital admission for the analytically defined exposure groups. *Median gamma-hydroxybutyrate blood concentration was significantly greater in the metamfetamine plus gamma-hydroxybutyrate plus benzodiazepine group compared to the metamfetamine plus gamma-hydroxybutyrate group (P = 0.0004).

Figure 2. Median, interquartile range and range of gamma-hydroxybutyrate blood concentrations at the time of hospital admission for the analytically defined exposure groups. *Median gamma-hydroxybutyrate blood concentration was significantly greater in the metamfetamine plus gamma-hydroxybutyrate plus benzodiazepine group compared to the metamfetamine plus gamma-hydroxybutyrate group (P = 0.0004).

Figure 3. Median, interquartile range and range of presenting heart rates (beats per minute) for each analytically defined exposure group. *Median presenting heart rate in the gamma-hydroxybutyrate groups was significantly lower than groups without co-detection of gamma-hydroxybutyrate (P < 0.0001).

Figure 3. Median, interquartile range and range of presenting heart rates (beats per minute) for each analytically defined exposure group. *Median presenting heart rate in the gamma-hydroxybutyrate groups was significantly lower than groups without co-detection of gamma-hydroxybutyrate (P < 0.0001).

Table 2. Comparison of clinical effects recorded at the time of hospital presentation between groups defined by analytical detections.

Figure 4. Median, interquartile range and range of presenting temperature (degrees Celsius) for each analytically defined exposure group. *Median presenting temperature in the gamma-hydroxybutyrate groups was significantly lower than groups without co-detection of gamma-hydroxybutyrate (P ≤ 0.0001).

Figure 4. Median, interquartile range and range of presenting temperature (degrees Celsius) for each analytically defined exposure group. *Median presenting temperature in the gamma-hydroxybutyrate groups was significantly lower than groups without co-detection of gamma-hydroxybutyrate (P ≤ 0.0001).

Figure 5. Reported incidence of agitation on hospital presentation for each analytically defined exposure group. *Incidence of agitation in groups with co-detection of gamma-hydroxybutyrate or benzodiazepines was significantly lower compared to the lone metamfetamine group (P ≤ 0.0004).

Figure 5. Reported incidence of agitation on hospital presentation for each analytically defined exposure group. *Incidence of agitation in groups with co-detection of gamma-hydroxybutyrate or benzodiazepines was significantly lower compared to the lone metamfetamine group (P ≤ 0.0004).
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