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1.
Public Health Rep ; 136(1_suppl): 87S-95S, 2021.
Article in English | MEDLINE | ID: mdl-34726980

ABSTRACT

OBJECTIVES: Increasing knowledge about the toxicology of drug overdose and substance misuse (DOSM) is important in improving our understanding of the epidemic. We describe the Minnesota Drug Overdose and Substance Use Pilot Surveillance Activity, which started collecting data on emergency department (ED) visits attributable to DOSM in 2017, with a focus on the toxicology results of a subset of clinical encounters. METHODS: From November 1, 2017, through January 30, 2020, we collected near-real-time data on DOSM-related ED encounters. The Minnesota Department of Health Public Health Laboratory tested leftover clinical specimens (blood and/or urine) for the presence of various substances for patients who died, were hospitalized, had an atypical clinical presentation, or were part of a local drug overdose cluster. Testing looked for >250 drugs or their metabolites, including those commonly misused (eg, methamphetamine, cocaine), prescription medications, synthetic cannabinoids and cathinones, and opioids. We describe characteristics of the overall group and a subgroup of clinical encounters with toxicology results. RESULTS: Specimens submitted from 6 EDs during the study period represented 239 clinical encounters. Methamphetamine was the most frequently detected substance (67.4%) but was suspected in only 45.6% of encounters. At least 1 opioid was detected in 42.5% of encounters but suspected in only 29.7%. Testing also detected potential adulterants and additives (eg, fentanyl, fentanyl analogues, levamisole) and showed frequent patient exposure to substances not reported by patients or suspected by clinicians. Nearly half (44.4%) of clinical encounters had >1 substance detected. CONCLUSIONS: ED surveillance for DOSM encounters, enhanced by toxicology testing, can provide local situational awareness on overdoses, prevent potential mischaracterization of the true drug overdose epidemic, and inform harm reduction and drug overdose prevention efforts.


Subject(s)
Biosurveillance/methods , Drug Overdose/diagnosis , Emergency Service, Hospital/statistics & numerical data , Adult , Drug Overdose/epidemiology , Emergency Service, Hospital/organization & administration , Female , Humans , Male , Middle Aged , Minnesota/epidemiology , Substance-Related Disorders/diagnosis , Substance-Related Disorders/epidemiology
2.
Article in English | MEDLINE | ID: mdl-28279874

ABSTRACT

Sulfur Mustard (HD) has a 100year history of use as a chemical warfare agent and recent events in the Middle East are causing it to once again be a potential concern. We report a new high-throughput method for the determination of HD exposure by the analysis of the ß-lyase metabolite 1,1'-sulfonylbis[2-(methylsulfinyl)ethane] (SBMSE) in human urine. This method features a hydrogen peroxide (H2O2) oxidative conversion of the ß-lyase metabolites to SBMSE, followed by sample extraction and concentration using solid phase extraction in 96-well plate format. Subsequent high performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS) analysis gave linear quantitation over a calibration range of 0.1-100ng/mL, with a method detection limit of 0.03ng/mL. Liquid chromatographic separation was achieved using a hydrophilic interaction liquid chromatography (HILIC) column with an analyte retention time of 0.9min and method time of 1.5min (cycle time=2.0min). Users of this method could prepare and analyze approximately 650 samples in 24h which would be important for an emergency response.


Subject(s)
Chemical Warfare Agents/metabolism , Chromatography, High Pressure Liquid/methods , Mustard Gas/metabolism , Sulfones/urine , Sulfoxides/urine , Tandem Mass Spectrometry/methods , Chromatography, High Pressure Liquid/instrumentation , Equipment Design , High-Throughput Screening Assays , Humans , Hydrogen Peroxide/metabolism , Limit of Detection , Lyases/metabolism , Oxidation-Reduction , Solid Phase Extraction/methods , Sulfones/metabolism , Sulfoxides/metabolism , Tandem Mass Spectrometry/instrumentation
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