Chlormequat is a quaternary ammonium and choline chlorinated derivated is used as plant growth regulating agent. There are very few documented cases of poisoning in humans. We reported a case of non-fatal suicide attempt by chlormequat in France. A 34-year-old woman was admitted to hospital after deliberate consumption of plant growth regulator, C5 SUN, containing chlormequat chloride (460 g/L) and choline chloride (320 g/L). Immediately, she developed symptoms of respiratory distress and a cardiac massage was begun by her father. In this case report, we described the method for an accurate and reliable screening of chlormequat which was based on the combination of Target Analysis powerful software and a high performance TOF-MS (Impact HD from Bruker). After forced diuresis, the kinetic of elimination of chlormequat is biphasic: vascular phase diffusion (half-life of 5.6 hr) followed by a phase of free elimination (half-life of 16.2 h). Although chlormequat poisoning is clinically similar to that observed with anticholinesterase compounds, chlormequat chloride is not an acetylcholinesterase inhibitor. Chlormequat seems to be a weak substrat competitor for cholinesterase leading to acetylcholine accumulation and prolonged depolarization in muscular junction. Cardiac massage, artificial respiration and forced diuresis have significantly improved the prognosis of our patient.
Deliberate self-poisoning has become an increasingly common response to emotional distress in vulnerable persons, and it is now one of the most frequent reasons for emergency hospital admission. In rural zones, the substances most commonly used for self-poisoning are agricultural chemical products as pesticides [
In this view, we describe a case of non-fatal suicide attempt due to chlormequat intoxication by ingestion of C5 SUN composed by 460 g/L of chlormequat chloride and 320 g/L of choline chloride.
A woman of a 34-year-old was admitted to the emergency unit following intentional ingestion of C5 SUN for suicidal purpose following a family conflict. The woman presented both, cyanosis and consciousness disorders. She has a past psychiatric history and she was hospitalized for suicide attempt in July 2012 when she took an overdose of her medication (anti-depressive agents). According to his father present during the incident, immediately the symptoms began after consumption of chlormequat chloride and choline chloride. She suddenly lost consciousness and cyanosis appears leading to respiratory distress. For 15 minutes, her father performed an epigastric and thoracic cardiac massage causing emesis. During that time, she remained unresponsive but was breathing slowly. When firemen arrived, the patient had a circulatory activity without spontaneous ventilation.
On admission, vital signs revealed pulse rate of 85 beats/minute, blood pressure of 131/84 mmHg, respiratory rate of 15 per minute and his body temperature was 35.5˚C. The patient was set in artificial breathing after an orotracheal intubation. She required ventilator support for three days. She was treated with an antibiotic agent (Amoxicillin-Augmentin™) and was given by infusion at the rate of 2 g/6h. She was perfused by 500 mL of physiological serum to increase the diuresis. The patient was sedated by fentanyl (opiod analgesic) and midazolam (benzodiazepine) when signs of waking appeared. Response to the treatment was good and gradual improvement in biomarkers of inflammation was noticed (CRP and orosomucoid). Following recovery, she was evaluated by psychiatrist and revealed that ingestion of C5 SUN was an impulsive act due to poor social support from family. She exit the intensive care unit one week after her admission.
Her chest X-ray showed a right pulmonary alveolar infiltrate. A digestive investigation revealed an ulcerated esophagitis shallow and an erythematous gastric with minimal lesions. There were no neurological deficits and no cardiovascular disorders. Examination of other systems was normal. A medical examination at admission showed normal renal functions. Biological analyzes showed an increase of CPK (195 µL) and LDH (506 µL) likelyhood due to the effect of chlormequat chloride on the muscles. Furthermore a hypercalcemia, hyperglycemia (14.9 mmol∙L−1), acidosis (HCO3: 21.4 mmol∙L−1) with hypoxia (FIO2 81 and PEEP 3) occurred during the admission assessment. There was also an increase in lipase (189 µL). Cholinesterase activity was normal.
To measure and follow elimination of chlormequat, toxicological analysis were performed using a bench-top Ultra-High Resolution LC-MSMS system, Impact HD from Bruker Daltonics, France. LC-MSMS analysis was carried out on RSLC U30000. All chromatographic separation were achieved using an Acclaim™ RSLC C18 2.2 µM 2.1 × 100 mm column. A RSLC U3000 autosampler was used to inject 10 µL of extract into the LC-MS. Chromatographic separation was achieved using of two mobile phases; one consisting of 5 mM NH4 formiate in 0.01% formic acid solution in water; and a second mobile phase is a mix of water/MeOH (90:10). The total run time was 20 min at a flow rate of 0.2 mL/min. Mass spectrometry detection was performed by a Bruker Impact HD™ with electrospray ionization (ESI) performed in positive and negative mode. The mass spectrometer was tuned and calibrated using Na-formiate and acetate salt clusters. Samples were screened using a full scan mode.
Chlormequat quantities were determinate using an external calibration procedure. Based on the integrated peak areas for the reconstructed ion chromatograms corresponding at the 122 m/z (for chlormequat), a five-point calibration curve of relative response factor versus chlormequat concentration was established. Relative responses factors were calculated for each sample and the corresponding chlormequat concentration was determined from the calibration curve. Blood contents were analyzed for the intact chlormequat. The results of the analyses are presented in
Chlormequat is a quaternary ammonium. With choline chlorinated derivative, there are used as plant growth regulating agent. Generally, acute cholinergic symptoms due to anticholinergic pesticide poisoning manifests within 24 to 72 hours due to accumulation of acetylcholine at muscarinic and nicotinic sites. The intermediate syndrome which manifest after 24 to 96 hours due to prolonged activity of acetyl choline at nicotinic receptors resulting in weakness of ocular, neck, limb and respiratory muscles [
As far as use of atropine is considered as antidote, its role remains controversial because chlormequat is not an anticholinesterase agent. Database from TOXNET [
There is no antidote for chlormequat poisoning and treatment consisting of forced diuresis, earlier cardiac massage and artificial respiratory support, remains the only option. Aggressive primary decontamination with gastric lavage is required as early as possible. We did not assess the interest of activated charcoal in elimination of the chlormequat. Although chlormequat chloride poisoning resembles to the anticholinesterase agents’s poisoning. However, chlormequat chloride is not an acetyl cholinesterase inhibitor. Chlormequat was believed to be weak substrat competitor for cholinesterase leading to acetylcholine accumulation and prolonged depolarization in the diaphragm muscular junction; and produce clinical features similar to excessive stimulation of cholinergic receptors throughout the central and peripheral nervous system.
Although the accidental or intentional ingestion of chlormequat is rare and to our knowledge only three such cases have been described in literature. This is the first case in France describe in the last 2 years. Winek et al. [
In conclusion, the favorable prognosis of our patients is primarily due to rapid support by cardiac massage and also monitoring of cardiopulmonary function in intensive care unit by forcing the elimination of the product by diuresis. Toxicokinetic is a usefulness tool to monitor elimination of chlormequat and prevent any rebound.