Maren Hermanns-Clausen
University Medical Center Freiburg
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Featured researches published by Maren Hermanns-Clausen.
Addiction | 2013
Maren Hermanns-Clausen; Stefan Kneisel; Bela Szabo; Volker Auwärter
AIMS Recently, several synthetic cannabinoids were identified in herbal mixtures consumed as recreational drugs alternative to cannabis products. The aim was to characterize the acute toxicity of synthetic cannabinoids as experienced by emergency patients. DESIGN This was a retrospective study targeting patients seeking emergency treatment after recreational use of synthetic cannabinoids. SETTING AND PARTICIPANTS Patients were selected from the database of the Poisons Information Center Freiburg between September 2008 and February 2011. The inclusion criteria were: hospitalization, available clinical reports and analytical verification of synthetic cannabinoid uptake. In total, 29 patients were included (age 14-30 years, median 19; 25 males, four females). MEASUREMENTS Clinical reports were evaluated and synthetic cannabinoids and other drugs were determined analytically. FINDINGS CP-47,497-C8 (one), JWH-015 (one), JWH-018 (eight), JWH-073 (one), JWH-081 (seven), JWH-122 (11), JWH-210 (11), JWH-250 (four) and AM 694 (one) were quantified in blood samples. JWH-018 was most common in 2008-9, JWH-122 in 2010, and JWH-210 in 2011. Tachycardia, agitation, hallucination, hypertension, minor elevation of blood glucose, hypokalaemia and vomiting were reported most frequently. Chest pain, seizures, myoclonia and acute psychosis were also noted. CONCLUSIONS There appears to have been an increase in use of the extremely potent synthetic cannabinoids JWH-122 and JWH-210. Acute toxic symptoms associated with their use are also reported after intake of high doses of cannabis, but agitation, seizures, hypertension, emesis and hypokalaemia seem to be characteristic to the synthetic cannabinoids, which are high-affinity and high-efficacy agonists of the CB(1) receptor. Thus, these effects are due probably to a strong CB(1) receptor stimulation.
Journal of Medical Toxicology | 2011
Friedrich G. Kapp; Hans H. Maurer; Volker Auwärter; Martin Winkelmann; Maren Hermanns-Clausen
IntroductionKratom (Mitragyna speciosa) is a common medical plant in Thailand and is known to contain mitragynine as the main alkaloid. According to an increase in published reports and calls at German poison control centers, it has been used more frequently as a drug of abuse in the western hemisphere during the last couple of years. Despite this increase, reports of severe toxicity are rare within the literature.Case reportWe describe a case of a young man who presented with jaundice and pruritus after intake of kratom for 2 weeks in the absence of any other causative agent. Alkaloids of M. speciosa were detected in the urine.ConclusionWhile M. speciosa is gaining in popularity among illicit drug users, its adverse effects remain poorly understood. This is the first published case of intrahepatic cholestasis after kratom abuse.
Drug Testing and Analysis | 2013
Maren Hermanns-Clausen; Stefan Kneisel; Melanie Hutter; Bela Szabo; Volker Auwärter
receptor-mediated effectsare changes in mood, pain perception, state of arousal, bodytemperature, cardiovascular regulation, and food intake.Recently, synthetic cannabinoids appeared on the drugmarket, mostly as undeclared additives in ‘herbal mixtures’ namedfor example ‘Spice’, ‘Lava Red’ or ‘Jamaican Gold’. The use ofsynthetic cannabinoids is driven by several factors. After the intro-duction of new compounds, their use is initially not restricted byprohibition. Moreover, their consumption cannot be verified bystandard drug tests, which is particularly interesting for peoplefacing regular drugtesting.Easy accessvia the Internetand afford-ability also contribute to the popularity of these drugs.Since their first detection in herbal mixtures,
Deutsches Arzteblatt International | 2009
Dominique Muller; Wolfgang Weinmann; Maren Hermanns-Clausen
BACKGROUND In recent years, the market for dietary supplements has grown. International products are readily available for purchase over the Internet. We report 17 cases of poisoning with a single product, said to be of purely herbal origin, that was bought over the Internet. A complete declaration of the ingredients was not available. METHODS We performed a retrospective study of cases of poisoning documented by the Göttingen and Freiburg poison information centers from 2005 to 2008. In 4 cases, we were able to perform toxicological analyses of leftover capsules and urine samples. RESULTS The manifestations of poisoning in the 17 documented cases included malaise, tachycardia, headache, agitation, arterial hypertension, nausea, vomiting, dyspnea, insomnia, left-sided chest pressure, elevated temperature, and, in two cases, psychosis after the substance was combined with atomoxetine and methylphenidate and with citalopram, olanzapine, and chlorprothixene. The frequency of cases rose markedly in the last year of the study. The toxicological analyses of all samples studied revealed sibutramine. The dose in each capsule was nearly twice the maximum daily dose sibutramine in the medication containing this substance that is licensed for use in Germany. CONCLUSIONS Products available without a prescription whose contents are claimed to be purely herbal may nonetheless contain synthetic substances in concentrations far above the therapeutic range and may be a cause of poisoning. When taking the history of a patient possibly suffering from an intoxication, the physician should ask specifically about drugs, dietary supplements, and so-called lifestyle products that were obtained without a prescription. It would be desirable for the contents of all such products to be declared, as required by law, so that their suitability for the market can be checked.
Clinical Toxicology | 2009
A. Schaper; Herbert Desel; Martin Ebbecke; L. de Haro; Michael Deters; Helmut Hentschel; Maren Hermanns-Clausen; C. Langer
Introduction. The presence of exotic, and sometimes venomous, pets in European homes is becoming more common. This phenomenon is the basis of a French-German cooperative evaluation of the species causing the injuries and the circumstances, severity, and treatment of the envenomations Methods. A retrospective, descriptive, cross-sectional, case series of data from 1996 to 2006. The study sample consists of all cases of bites and stings by exotic pets that were registered at four poisons European poisons centers. The inclusion criteria were bites and stings of human beings. Results. From 1996 to 2006 four poisons centers in Europe were consulted on 404 bites and stings by exotic pets. The average age of the patients was 36 (2 to 75) years and 73% of the patients were male. The severity of the envenomations, according to the Poisoning Severity Score, was as follows: 29 severe (7.1%), 55 moderate (14.2%) and 320 minor (78.7%). There were no fatalities in this case series. Exotic snakebites from rattlesnakes, cobras, mambas, and other venomous snakes caused 39% of envenomations, aquatic animals (mostly lionfish of the Pterois genus and stingrays) caused 30% of envenomations and arthropods (tarantulas and scorpions) caused 27% of envenomations. All severe envenomations were caused by venomous snakes. Conclusions. European healthcare professionals may encounter patients bitten or stung by exotic pets. Poisons center consultation can help manage these unusual presentations and help obtain rarely used antivenoms.
International Journal of Legal Medicine | 2009
Nerea Ferreirós; Sebastian Dresen; Maren Hermanns-Clausen; Volker Auwaerter; Annette Thierauf; Christoph W. Muller; R. Hentschel; Rainer Trittler; Gisela Skopp; Wolfgang Weinmann
This work presents two cases of codeine intoxication in 3-year-old monozygotic twin brothers while treated with a codeine slow-release formulation. One child had to be admitted to the hospital, whereas the other one died at home after aspiration of gastric content. The concentrations of codeine and major metabolites including morphine and corresponding glucuronide conjugates were measured by liquid chromatography–tandem mass spectrometry in serum, urine, cerebrospinal fluid, and brain tissue, respectively. A genetic polymorphism study was carried out in order to determine the ability of the children to metabolize codeine by O-demethylation. A pharmacokinetic calculation was also performed to estimate the administered dose of codeine in question. High concentrations of all substances were found in samples of both children. The pharmacokinetic estimate suggests an overdose of codeine, and the possible reasons for the high opiate concentrations are discussed. Furthermore, the postmortem distribution—during and after resuscitation—might play a major role in the interpretation of postmortem concentration levels.
Clinical Toxicology | 2008
Jörg Pietsch; Ingrid Koch; Maren Hermanns-Clausen; Georg Hüller; Rafael Wagner; Jan Dressler
Introduction. Each year, 80,000 to 100,000 calls to the Poison Information Centres (PIC) concern pediatric exposures in Germany. Plant exposures are the fourth most common category, accounting for 22% of pediatric exposures. Methods. Information on plant exposures in children (0–14 years) was collected from annual reports of German PIC. The severity of pediatric plant exposures was classified using the number of ingestions and a calculated hazard factor. Results. A total of 58,641 cases involving 248 different plant genera were reported from 1998 to 2004. Most plant exposures were not associated with clinical effects at time of call, but 9.6% of cases had noticeable effects, including 0.4% classified as moderate and major effect. Conclusions. The majority of plant genera have low hazard factors. Most severe poisoning (highest hazard factors and exposures) in children involved Brugmansia, Laburnum, Phaseolus, and Thuja.
Journal of Clinical Pharmacy and Therapeutics | 2013
N. Toepfner; Ariane Wohlfarth; J. Naue; Volker Auwärter; R. Berner; Maren Hermanns-Clausen
What is known and Objective: Clozapine, a second generation antipsychotic which is relatively safe in overdose, has been used as an effective treatment alternative to traditional antipsychotics. The therapeutic use in children remains controversial. However, in accordance with the increasing prescription in adults, the accidental ingestion in childhood becomes more frequent. We report the youngest case of accidental clozapine ingestion.
Forensic Science International | 2013
M.A. Neukamm; S. Vogt; Maren Hermanns-Clausen; J. Naue; Annette Thierauf; V. Auwärter
The differentiation of intoxication courses is one of the most difficult challenges for forensic pathologists and toxicologists. The case of a 52-year-old female inpatient of a psychiatric clinic with multiple medications who died from doxepin intoxication is reported. Concentrations of doxepin metabolites and isomers, pharmacokinetic modelling and genotyping of the doxepin-metabolizing cytochrome P450 (CYP) enzymes led to the following conclusion: the lethal doxepin concentration of 2100 ng/mL was more likely to have been reached due to drug interactions and genetic peculiarities leading to a reduction of the metabolic capacity and not by an acute (suicidal) overdose.
Clinical Toxicology | 2016
Roland Elling; Marco Simon Spehl; Ariane Wohlfarth; Volker Auwaerter; Maren Hermanns-Clausen
Abstract Context: Repaglinide is a short-acting insulin secretagogue with high interindividual variability in pharmacokinetics due to genetic polymorphisms. Little is known about repaglinide overdoses, both with respect to pharmacokinetics and appropriate management. Given its short serum half-life of less than 1 h, hypoglycemic effects of repaglinide are expected to cease within a few hours post-ingestion. Case details: A 15-year-old girl ingested 10.5 mg of repaglinide in a suicide attempt. Few hours later, she developed a strong food craving, nausea, abdominal pain, and a headache. The lowest recorded serum glucose was 44 mg/dl (2.4 mmol/l) 14 h post-ingestion. Using liquid chromatography–mass spectrometry, we detected repaglinide serum levels of 5.3, 2.6, and 1.0 ng/ml at 14, 20, and 26 h post-ingestion, respectively. Discussion: This case illustrates that in the context of overdose, repaglinide can lead to prolonged hypoglycemia. We therefore recommend glucose monitoring and observation for 24 h in all patients who remain hypoglycemic or show symptoms of hypoglycemia for an unusually long period of time.